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Sample records for ag doped tio2

  1. Structural, morphological, optical and photocatalytic investigation of Ag-doped TiO2

    NASA Astrophysics Data System (ADS)

    Kundu, Virender Singh; Singh, Davender; Maan, A. S.; Tanwar, Amit

    2016-05-01

    The pure and Ag-doped TiO2 nanoparticles were prepared by using Titanium isoproxide (TTIP), silver nitrate sodium hydroxide and sodium hydroxide. The calcined nanoparticles at 400°C were characterized by means of X-ray diffraction (XRD). XRD analyses reveal that the nanoparticles of various doping concentration were having anatase phase. The particle size was calculated by Scherrer formula and was found 11.08 nm for pure TiO2 and 8.86 nm for 6 mol % Ag doped TiO2. The morphology and nature of nanoparticles was analyzed by using scanning electron microscope (SEM), the optical absorption spectra of pure TiO2 and Ag-doped TiO2 nanoparticles showed that absorption edge increases towards longer wavelength from 390 nm (pure) to 450 nm (doped), also band gap energy calculated from Tauc's plot decrease from 3.20eV to 2.92eV with increase in doing. The measurement of photocatalytic properties of pure TiO2 and Ag-doped TiO2 nanoparticles showed that Ag-doped TiO2 degrades MB dye more efficiently than pure TiO2.

  2. The Synthesis of Ag-Doped Mesoporous TiO2

    SciTech Connect

    Li, Xiaohong S.; Fryxell, Glen E.; Wang, Chong M.; Engelhard, Mark H.

    2008-04-15

    Ag-doped mesoporous titanium oxide was prepared using non-ionic surfactants and easily handled titanium precursors, under mild reaction conditions. In contrast to the stabilizing effect of Cd-doping on mesoporous TiO2, Ag-doping was found to significantly destabilize the mesoporous structure.

  3. Fabrication and photocatalytic activity of TiO2 derived nanotubes with Ag ions doping.

    PubMed

    Liu, Fang; Lai, Shuting; Huang, Peilin; Liu, Yingju; Xu, Yuehua; Fang, Yueping; Zhou, Wuyi

    2012-11-01

    Ag/TiO2 nanotubes with uniform distribution were successfully prepared by a hydrothermal-dipping method. The synthesized samples were characterized by XRD, TEM and FTIR, respectively. The results exhibited that the morphological structure of the TiO2 nanotubes was improved by the doping of Ag ions. The photocatalytic degradation experiment indicated that the photocatalytic activity of the Ag/TiO2 nanotubes indicated better photocatalytic activity than pure TiO2 nanotubes since silver was able to help the electron-hole separation by attracting photoelectrons. The optimal mol ration of TiO2 and AgNO3 was 25:1.

  4. Photocatalytic antibacterial performance of TiO2 and Ag-doped TiO2 against S. aureus. P. aeruginosa and E. coli.

    PubMed

    Gupta, Kiran; Singh, R P; Pandey, Ashutosh; Pandey, Anjana

    2013-01-01

    This paper reports the structural and optical properties and comparative photocatalytic activity of TiO2 and Ag-doped TiO2 nanoparticles against different bacterial strains under visible-light irradiation. The TiO2 and Ag-doped TiO2 photocatalysts were synthesized by acid catalyzed sol-gel technique and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-vis spectroscopy and photoluminescence (PL). The XRD pattern revealed that the annealed sample of TiO2 has both anatase and rutile phases while only an anatase phase was found in Ag-doped TiO2 nanoparticles. The decreased band-gap energy of Ag-doped TiO2 nanoparticles in comparison to TiO2 nanoparticles was investigated by UV-vis spectroscopy. The rate of recombination and transfer behaviour of the photoexcited electron-hole pairs in the semiconductors was recorded by photoluminescence. The antimicrobial activity of TiO2 and Ag-doped TiO2 nanoparticles (3% and 7%) was investigated against both gram positive (Staphylococcus aureus) and gram negative (Pseudomonas aeruginosa, Escherichia coli) bacteria. As a result, the viability of all three microorganisms was reduced to zero at 60 mg/30 mL culture in the case of both (3% and 7% doping) concentrations of Ag-doped TiO2 nanoparticles. Annealed TiO2 showed zero viability at 80 mg/30 mL whereas doped Ag-TiO2 7% showed zero viability at 40 mg/30 mL culture in the case of P. aeruginosa only.

  5. Assessment of antimicrobial activity of nanosized Ag doped TiO(2) colloids.

    PubMed

    Yaşa, Ihsan; Lkhagvajav, Natsag; Koizhaiganova, Meruyert; Celik, Erdal; Sarı, Ozcan

    2012-07-01

    In the present research, the antimicrobial effects of nanosized silver (Ag) doped TiO(2) colloidal solutions prepared using a sol-gel technique were investigated. In order to determine the solution characteristics, the turbidity, viscosity and pH of the colloidal solutions were measured. Differential thermal analysis-thermogravimetry equipment was used to determine the chemical structures and reaction types of the films formed from these solutions. The morphology of Ag doped TiO(2) nanoparticles was evaluated by atomic force microscopy. The disc diffusion method was employed to explore antimicrobial activity, and the Broth Microdilution method was used to obtain MIC values of nanosized Ag doped TiO(2) colloidal solutions against the test microorganisms Escherichia coli, Staphylococcus aureus, Candida albicans, Bacillus subtilis, and Salmonella typhimurium. It was found that the silver doped TiO(2) nanoparticles inhibited the growth and multiplication of the test microorganisms, including the fungus C. albicans. Antimicrobial activity was observed against all tested microorganisms at a very low concentration of 1.125-2.81 μg/ml of nano silver in 1-25 % Ag-TiO(2) solutions.

  6. Contact potential barriers and characterization of Ag-doped composite TiO2 nanotubes

    NASA Astrophysics Data System (ADS)

    Li, Jingling; Chen, Wenzhe; Yu, Hualiang; Wu, Bo; Huang, Wenbo; Wang, Mingxiu; Huang, Shizhen; Lin, Wei; Zhang, Likun; Li, Shiping

    2014-04-01

    Ag-doping TiO2 composite nanotubes (Ag-TNTs) were synthesized by alkaline fusion followed by hydrothermal treatment. The microstructure and morphology of the materials were characterized by XRD, TEM, XPS, SPS (surface photovoltage spectroscopy), FISPS (electric field-induced surface photovoltage spectroscopy) and Raman spectroscopy. First-principles calculations based on density-functional theory (DFT) showed the formation of several impurity levels near the top of the valence band in the band gap (Eg) of rutile TiO2 due to Ag doping. A "double junction" is proposed, involving a Schottky junction and p-n junction (denoted as "Ag-p-n junction") occurring between the Ag particles and the nanotube surface, as well as forming inside TiO2 nanotubes, respectively. The strongly built-in electric field of the junctions promotes the separation of photo-holes and photoelectrons, enhancing the photocatalytic efficiency. XRD results indicated that the composite Ag-TNTs exist as a mixture of anatase and rutile phases. XPS results showed that Ti4+ is the primary state of Ti. Raman spectral analysis of Ag-TNTs revealed the presence of a new peak at 271 cm-1. The red-shift of the absorption light wavelength of Ag-TNTs was 0.16 eV (20 nm) due to a considerable narrowing of Eg by the existing impurity levels.

  7. TiO2 nanowire and TiO2 nanowire doped Ag-PVP nanocomposite for antimicrobial and self-cleaning cotton textile.

    PubMed

    Hebeish, A A; Abdelhady, M M; Youssef, A M

    2013-01-16

    The TiO(2) nanowire (TiO(2) Nw) was successfully prepared via hydrothermal method through TiO(2) nanoparticle (TiO(2) Np). TiO(2) Np doped silver and TiO(2) Nw doped silver were prepared via photo-reducing Ag(+) ions to Ag metal on the TiO(2) Np or TiO(2) Nw surfaces. The prepared nanomaterials were evaluated using X-ray (XRD) diffraction pattern, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Bleached untreated cotton fabric and PVP treated cotton fabrics were coated with the synthesized nanomaterials using pad-dry-cure method. Photocatalytic activity of untreated and coated cotton fabrics with TiO(2) nanomaterials was investigated through the fabric self cleaning of MB dye stains. Also, the PVP finished cotton fabric modified by nanomaterials demonstrated antimicrobial activity against Gram positive bacteria, Gram negative bacteria and fungi. The mechanical properties of coated cotton fabric (tear strength, surface roughness, tensile strength and elongation at break) were examined.

  8. Antibacterial Activity of As-Annealed TiO2 Nanotubes Doped with Ag Nanoparticles against Periodontal Pathogens.

    PubMed

    Yeniyol, Sinem; He, Zhiming; Yüksel, Behiye; Boylan, Robert Joseph; Urgen, Mustafa; Ozdemir, Tayfun; Ricci, John Lawrence

    2014-01-01

    It is important to develop functional transmucosal implant surfaces that reduce the number of initially adhering bacteria and they need to be modified to improve the anti-bacterial performance. Commercially pure Ti sheets were anodized in an electrolyte containing ethylene glycol, distilled water and ammonium fluoride at room temperature to produce TiO2 nanotubes. These structures were then annealed at 450°C to transform them to anatase. As-annealed TiO2 nanotubes were then treated in an electrolyte containing 80.7 g/L NiSO4 ·7H2O, 41 g/L MgSO4 ·7H2O, 45 g/L H3BO3, and 1.44 g/L Ag2SO4 at 20°C by the application of 9 V AC voltage for doping them with silver. As-annealed TiO2 nanotubes and as-annealed Ag doped TiO2 nanotubes were evaluated by SEM, FESEM, and XRD. Antibacterial activity was assessed by determining the adherence of A. actinomycetemcomitans, T. forsythia, and C. rectus to the surface of the nanotubes. Bacterial morphology was examined using an SEM. As-annealed Ag doped TiO2 nanotubes revealed intense peak of Ag. Bacterial death against the as-annealed Ag doped TiO2 nanotubes were detected against A. actinomycetemcomitans, T. forsythia, and C. rectus indicating antibacterial efficacy.

  9. Photocatalytic comparison of Cu- and Ag-doped TiO2/GF for bioaerosol disinfection under visible light

    NASA Astrophysics Data System (ADS)

    Pham, Thanh-Dong; Lee, Byeong-Kyu

    2015-12-01

    Photocatalysts, TiO2/glass fiber (TiO2/GF), Cu-doped TiO2/glass fiber (Cu-TiO2/GF) and Ag-doped TiO2/glass fiber (Ag-TiO2/GF), were synthesized by a sol-gel method. They were then used to disinfect Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) in bioaerosols under visible light irradiation. TiO2/GF did not show any significant disinfection effect. Both Cu and Ag acted as intermediate agents to enhance separation efficiency of electron-hole pairs of TiO2, leading to improved photocatalytic activity of Cu-TiO2/GF and Ag-TiO2/GF under visible light. Cu in Cu-TiO2/GF acted as a defective agent, increasing the internal quantum efficiency of TiO2, while Ag in Ag-TiO2/GF acted as a sensitive agent, enhancing the transfer efficiency of the electrons generated. The highest disinfection efficiencies of E. coli and S. aureus by Cu-TiO2/GF were 84.85% and 65.21%, respectively. The highest disinfection efficiencies of E. coli and S. aureus by Ag-TiO2/GF were 94.46% and 73.12%, respectively. Among three humidity conditions - 40±5% (dry), 60±5% (moderate), and 80±5% (humid) - the moderate humidity condition showed the highest disinfection efficiency for both E. coli and S. aureus. This study also showed that a Gram-negative bacterium (E. coli) were more readily disinfected by the photocatalysts than a Gram-positive bacterium (S. aureus).

  10. Antibacterial Activity of As-Annealed TiO2 Nanotubes Doped with Ag Nanoparticles against Periodontal Pathogens

    PubMed Central

    Yeniyol, Sinem; He, Zhiming; Yüksel, Behiye; Boylan, Robert Joseph; Ürgen, Mustafa; Özdemir, Tayfun; Ricci, John Lawrence

    2014-01-01

    It is important to develop functional transmucosal implant surfaces that reduce the number of initially adhering bacteria and they need to be modified to improve the anti-bacterial performance. Commercially pure Ti sheets were anodized in an electrolyte containing ethylene glycol, distilled water and ammonium fluoride at room temperature to produce TiO2 nanotubes. These structures were then annealed at 450°C to transform them to anatase. As-annealed TiO2 nanotubes were then treated in an electrolyte containing 80.7 g/L NiSO4·7H2O, 41 g/L MgSO4·7H2O, 45 g/L H3BO3, and 1.44 g/L Ag2SO4 at 20°C by the application of 9 V AC voltage for doping them with silver. As-annealed TiO2 nanotubes and as-annealed Ag doped TiO2 nanotubes were evaluated by SEM, FESEM, and XRD. Antibacterial activity was assessed by determining the adherence of A. actinomycetemcomitans, T. forsythia, and C. rectus to the surface of the nanotubes. Bacterial morphology was examined using an SEM. As-annealed Ag doped TiO2 nanotubes revealed intense peak of Ag. Bacterial death against the as-annealed Ag doped TiO2 nanotubes were detected against A. actinomycetemcomitans, T. forsythia, and C. rectus indicating antibacterial efficacy. PMID:25202230

  11. Improved performance of Ag-doped TiO2 synthesized by modified sol-gel method as photoanode of dye-sensitized solar cell

    NASA Astrophysics Data System (ADS)

    Gupta, Arun Kumar; Srivastava, Pankaj; Bahadur, Lal

    2016-08-01

    Ag-doped TiO2 with Ag content ranging from 1 to 7 mol% was synthesized by a modified sol-gel route, and its performance as the photoanode of dye-sensitized solar cells (DSSCs) was compared with undoped TiO2 photoanode. Titanium(IV)isopropoxide was used as precursor and hexamethylenetetramine as the capping agent. XRD results show the formation of TiO2 nanoparticles with an average crystallite size of 5 nm (1 % Ag-doped TiO2) and 9 nm (undoped TiO2), respectively. The TiO2 nanopowder was used to prepare its thin film photoelectrode using doctor's blade method. Significant improvement in light-to-energy conversion efficiency was achieved when thin films of 1 % Ag-doped TiO2 were applied as photoanode in DSSC taking N719 as the sensitizer dye. As evidenced by EIS measurements, the electron lifetime of DSSC with Ag-doped TiO2 increased from 1.33 (for undoped TiO2) to 2.05 ms. The short-circuit current density ( J sc), open-circuit voltage ( V oc), fill factor (FF) and the overall energy conversion efficiency ( η) were 1.07 mA cm-2, 0.72 V, 0.73 and 0.40 %, respectively, with the use of 1 % Ag-doped TiO2 photoanode, whereas with undoped TiO2 under similar conditions, J sc = 0.63 mA cm-2, V oc = 0.70 V, fill factor 0.45 and conversion efficiency 0.14 % could be obtained. Therefore, compared with the reference DSSC containing an undoped TiO2 photoanode, the power conversion efficiency of the cell based on Ag-doped TiO2 has been remarkably enhanced by ~70 %. The substantial improvement in the device performance is attributed to the reduced band-gap energy, retarded charge recombination and greater surface coverage of the sensitizing dye over Ag-doped TiO2, which ultimately resulted in improved IPCE, J SC and η values.

  12. Photocatalytic characteristics for the nanocrystalline TiO2 on the Ag-doped CaAl2O4:(Eu,Nd) phosphor

    NASA Astrophysics Data System (ADS)

    Kim, Jung-Sik; Sung, Hyun-Je; Kim, Bum-Joon

    2015-04-01

    This study investigated the photocatalytic behavior of nanocrystalline TiO2 deposited on Ag-doped long-lasting phosphor (CaAl2O4:Eu2+,Nd3+). The CaAl2O4:Eu2+,Nd3+ phosphor powders were prepared via conventional sintering using CaCO3, Al2O3, Eu2O3, and Nd2O3 as raw materials according to the appropriate molar ratios. Silver nanoparticles were loaded on the phosphor by mixing with an aqueous Ag-dispersion solution. Nanocrystalline TiO2 was deposited on Ag-doped CaAl2O4:Eu2+,Nd3+ powders via low-pressure chemical vapor deposition (LPCVD). The TiO2 coated on the phosphor was actively photo-reactive under irradiation with visible light and showed much faster benzene degradation than pure TiO2, which is almost non-reactive. The coupling of TiO2 with phosphor may result in an energy band bending in the junction region, which then induces the TiO2 crystal at the interface to be photo-reactive under irradiation with visible light. In addition, the intermetallic compound of CaTiO3 that formed at the interface between TiO2 and the CaAl2O4:(Eu2+,Nd3+) phosphor results in the formation of oxygen vacancies and additional electrons that promote the photodecomposition of benzene gas. The addition of Ag nanoparticles enhanced the photocatalytic reactivity of the TiO2/CaAl2O4:Eu2+,Nd3+ phosphor. TiO2 on the Ag-doped phosphor presented a higher benzene gas decomposition rate than the TiO2 did on the phosphor without Ag-doping under both irradiation with ultraviolet and visible light.

  13. Synthesis of Ag-doped TiO2 nanoparticles by combining laser decomposition of titanium isopropoxide and ablation of Ag for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Al-Kamal, Ahmed Kamal

    Nanostructured powders of TiO2 and Ag-doped TiO2 are synthesized by a novel pulsed-laser process that combines laser ablation of a silver (Ag) disc with laser decomposition of a titanium tetra-isopropoxide (TTIP) solution. Nanoparticles are formed by rapid condensation of vaporized species in the plasma plume generated by the high power laser, resulting in the formation of rapidly quenched Ag-doped TiO2 nanoparticles that have far-from-equilibrium or metastable structures. The uniqueness of the new ablation process is that it is a one-step process, in contrast to the two-step process developed by previous researchers in the field. Moreover, its ability to synthesize an extended-solid solution phase of Ag in TiO 2 may also be unique. The present work implies that other oxide phases, such as Al2O3, MgO and MgAl2O4, can be doped with normally insoluble metals, such as Pt and Ir, thus opening new opportunities for catalytic applications. Again, there is the prospect of being able to synthesize nanopowders of diamond, c-BN, and mixtures thereof, which are of interest for applications in machine tools, rock-drill bits, and lightweight armor. A wet-chemistry method is also investigated, which has much in common with that adopted by previous workers in the field. However, photo-voltaic properties do not measure up to expectations based on published data. A possible explanation is that the selected Ag concentrations are too high, so that recombination of holes and electrons occurs via a quantum-tunneling mechanism reduces photo-activity. Future work, therefore, will investigate lower concentrations of Ag dopant in TiO2, while also examining the effects of metastable states, including extended solid solution, amorphous, and semi-crystalline structures.

  14. Enhancement of the photoelectric performance of dye-sensitized solar cells using Ag-doped TiO2 nanofibers in a TiO2 film as electrode.

    PubMed

    Jin, En Mei; Zhao, Xing Guan; Park, Ju-Young; Gu, Hal-Bon

    2012-01-01

    For high solar conversion efficiency of dye-sensitized solar cells [DSSCs], TiO2 nanofiber [TN] and Ag-doped TiO2 nanofiber [ATN] have been extended to be included in TiO2 films to increase the amount of dye loading for a higher short-circuit current. The ATN was used on affected DSSCs to increase the open circuit voltage. This process had enhanced the exit in dye molecules which were rapidly split into electrons, and the DSSCs with ATN stop the recombination of the electronic process. The conversion efficiency of TiO2 photoelectrode-based DSSCs was 4.74%; it was increased to 6.13% after adding 5 wt.% ATN into TiO2 films. The electron lifetime of DSSCs with ATN increased from 0.29 to 0.34 s and that electron recombination was reduced.

  15. Synthesis and characterization of cube-like Ag@AgCl-doped TiO2/fly ash cenospheres with enhanced visible-light photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Liu, Shaomin; Zhu, Jinglin; Yang, Qing; Xu, Pengpeng; Ge, Jianhua; Guo, Xuetao

    2016-03-01

    A cube-like Ag@AgCl-doped TiO2/fly ash cenosphere composite (denoted Ag@AgCl-TiO2/fly ash cenospheres) was successfully synthesized via a two-step approach. The as-prepared catalysts were characterized by scanning electron microscopy, X-ray diffraction, diffuse reflectance ultraviolet-visible spectroscopy, Brunauer-Emmett-Teller, and X-ray photoelectron spectroscopy. The photocatalytic experiment showed that the rhodamine B degradation rate with Ag@AgCl-TiO2/fly ash cenospheres was 1.56 and 1.33 times higher than that with AgCl-TiO2/fly ash cenospheres and Ag@AgCl, respectively. The degradation ratio of rhodamine B with Ag@AgCl-TiO2/fly ash cenospheres was nearly 100% within 120 min under visible light. Analysis of active species indicated that radO2- and h+ dominated the reaction, and radOH participated in the photocatalytic reactions as an active species. A mechanism for the photocatalytic degradation by the Ag@AgCl-TiO2/fly-ash cenospheres was also proposed based on the experimental results.

  16. Ag doped hollow TiO2 nanoparticles as an effective green fungicide against Fusarium solani and Venturia inaequalis phytopathogens

    NASA Astrophysics Data System (ADS)

    Sankar Boxi, Siddhartha; Mukherjee, Khushi; Paria, Santanu

    2016-02-01

    Chemical-based pesticides are widely used in agriculture to protect crops from insect infestation and diseases. However, the excessive use of highly toxic pesticides causes several human health (neurological, tumor, cancer) and environmental problems. Therefore nanoparticle-based green pesticides have become of special importance in recent years. The antifungal activities of pure and Ag doped (solid and hollow) TiO2 nanoparticles are studied against two potent phytopathogens, Fusarium solani (which causes Fusarium wilt disease in potato, tomato, etc) and Venturia inaequalis (which causes apple scab disease) and it is found that hollow nanoparticles are more effective than the other two. The antifungal activities of the nanoparticles were further enhanced against these two phytopathogens under visible light exposure. The fungicidal effect of the nanoparticles depends on different parameters, such as particle concentration and the intensity of visible light. The minimum inhibitory dose of the nanoparticles for V. inaequalis and F. solani are 0.75 and 0.43 mg/plate. The presence of Ag as a dopant helps in the formation of stable Ag-S and disulfide bonds (R-S-S-R) in cellular protein, which leads to cell damage. During photocatalysis generated •OH radicals loosen the cell wall structure and this finally leads to cell death. The mechanisms of the fungicidal effect of nanoparticles against these two phytopathogens are supported by biuret and triphenyl tetrazolium chloride analyses and field emission electron microscopy. Apart from the fungicidal effect, at a very low dose (0.015 mg/plate) the nanoparticles are successful in arresting production of toxic napthoquinone pigment for F. solani which is related to the fungal pathogenecity. The nanoparticles are found to be effective in protecting potatoes affected by F. solani or other fungi from spoiling.

  17. Ag doped hollow TiO2 nanoparticles as an effective green fungicide against Fusarium solani and Venturia inaequalis phytopathogens.

    PubMed

    Boxi, Siddhartha Sankar; Mukherjee, Khushi; Paria, Santanu

    2016-02-26

    Chemical-based pesticides are widely used in agriculture to protect crops from insect infestation and diseases. However, the excessive use of highly toxic pesticides causes several human health (neurological, tumor, cancer) and environmental problems. Therefore nanoparticle-based green pesticides have become of special importance in recent years. The antifungal activities of pure and Ag doped (solid and hollow) TiO2 nanoparticles are studied against two potent phytopathogens, Fusarium solani (which causes Fusarium wilt disease in potato, tomato, etc) and Venturia inaequalis (which causes apple scab disease) and it is found that hollow nanoparticles are more effective than the other two. The antifungal activities of the nanoparticles were further enhanced against these two phytopathogens under visible light exposure. The fungicidal effect of the nanoparticles depends on different parameters, such as particle concentration and the intensity of visible light. The minimum inhibitory dose of the nanoparticles for V. inaequalis and F. solani are 0.75 and 0.43 mg/plate. The presence of Ag as a dopant helps in the formation of stable Ag-S and disulfide bonds (R-S-S-R) in cellular protein, which leads to cell damage. During photocatalysis generated (•)OH radicals loosen the cell wall structure and this finally leads to cell death. The mechanisms of the fungicidal effect of nanoparticles against these two phytopathogens are supported by biuret and triphenyl tetrazolium chloride analyses and field emission electron microscopy. Apart from the fungicidal effect, at a very low dose (0.015 mg/plate) the nanoparticles are successful in arresting production of toxic napthoquinone pigment for F. solani which is related to the fungal pathogenecity. The nanoparticles are found to be effective in protecting potatoes affected by F. solani or other fungi from spoiling. PMID:26808118

  18. Ag doped hollow TiO2 nanoparticles as an effective green fungicide against Fusarium solani and Venturia inaequalis phytopathogens.

    PubMed

    Boxi, Siddhartha Sankar; Mukherjee, Khushi; Paria, Santanu

    2016-02-26

    Chemical-based pesticides are widely used in agriculture to protect crops from insect infestation and diseases. However, the excessive use of highly toxic pesticides causes several human health (neurological, tumor, cancer) and environmental problems. Therefore nanoparticle-based green pesticides have become of special importance in recent years. The antifungal activities of pure and Ag doped (solid and hollow) TiO2 nanoparticles are studied against two potent phytopathogens, Fusarium solani (which causes Fusarium wilt disease in potato, tomato, etc) and Venturia inaequalis (which causes apple scab disease) and it is found that hollow nanoparticles are more effective than the other two. The antifungal activities of the nanoparticles were further enhanced against these two phytopathogens under visible light exposure. The fungicidal effect of the nanoparticles depends on different parameters, such as particle concentration and the intensity of visible light. The minimum inhibitory dose of the nanoparticles for V. inaequalis and F. solani are 0.75 and 0.43 mg/plate. The presence of Ag as a dopant helps in the formation of stable Ag-S and disulfide bonds (R-S-S-R) in cellular protein, which leads to cell damage. During photocatalysis generated (•)OH radicals loosen the cell wall structure and this finally leads to cell death. The mechanisms of the fungicidal effect of nanoparticles against these two phytopathogens are supported by biuret and triphenyl tetrazolium chloride analyses and field emission electron microscopy. Apart from the fungicidal effect, at a very low dose (0.015 mg/plate) the nanoparticles are successful in arresting production of toxic napthoquinone pigment for F. solani which is related to the fungal pathogenecity. The nanoparticles are found to be effective in protecting potatoes affected by F. solani or other fungi from spoiling.

  19. Enhanced photo-catalytic activity of Sr and Ag co-doped TiO2 nanoparticles for the degradation of Direct Green-6 and Reactive Blue-160 under UV & visible light.

    PubMed

    Naraginti, Saraschandra; Thejaswini, T V L; Prabhakaran, D; Sivakumar, A; Satyanarayana, V S V; Arun Prasad, A S

    2015-10-01

    This work is focused on sol-gel synthesis of silver and strontium co-doped TiO2 nanoparticles and their utilization as photo-catalysts in degradation of two textile dyes. Effect of pH, intensity of light, amount of photo-catalyst, concentration of dye, sensitizers, etc., were studied to optimize conditions for obtaining enhanced photo-catalytic activity of synthesized nanoparticles. XRD, BET, HR-TEM, EDAX and UV-Vis (diffused reflectance mode) techniques were used to characterize the nanoparticles. Interestingly, band gap of Sr and Ag co-doped TiO2 nanoparticles showed considerable narrowing (2.6 eV) when compared to Ag doped TiO2 (2.7 eV) and undoped TiO2 (3.17 eV) nanoparticles. Incorporation of Ag and Sr in the lattice of TiO2 could bring isolated energy levels near conduction and valence bands thus narrowing band gap. The XRD analysis shows that both Ag and Sr nanoparticles are finely dispersed on the surface of titania framework, without disturbing its crystalline structure. TEM images indicate that representative grain sizes of Ag-doped TiO2 & Sr and Ag co-doped TiO2 nanoparticles are in the range of 8-20 nm and 11-25 nm, respectively. Effective degradation of Direct Green-6 (DG-6) and Reactive Blue-160 (RB-160) under UV and visible light has been achieved using the photo-catalysts. Sr and Ag co-doped TiO2 photo-catalysts showed higher catalytic activity during degradation process in visible region when compared to Ag-doped and undoped TiO2 nanoparticles which could be attributed to the interactive effect caused by band gap narrowing and enhancement in charge separation. For confirming degradation of the dyes, total organic carbon (TOC) content was monitored periodically.

  20. Visible-Light-Responsive Photocatalysis: Ag-Doped TiO2 Catalyst Development and Reactor Design Testing

    NASA Technical Reports Server (NTRS)

    Coutts, Janelle L.; Hintze, Paul E.; Meier, Anne; Shah, Malay G.; Devor, Robert W.; Surma, Jan M.; Maloney, Phillip R.; Bauer, Brint M.; Mazyck, David W.

    2016-01-01

    In recent years, the alteration of titanium dioxide to become visible-light-responsive (VLR) has been a major focus in the field of photocatalysis. Currently, bare titanium dioxide requires ultraviolet light for activation due to its band gap energy of 3.2 eV. Hg-vapor fluorescent light sources are used in photocatalytic oxidation (PCO) reactors to provide adequate levels of ultraviolet light for catalyst activation; these mercury-containing lamps, however, hinder the use of this PCO technology in a spaceflight environment due to concerns over crew Hg exposure. VLR-TiO2 would allow for use of ambient visible solar radiation or highly efficient visible wavelength LEDs, both of which would make PCO approaches more efficient, flexible, economical, and safe. Over the past three years, Kennedy Space Center has developed a VLR Ag-doped TiO2 catalyst with a band gap of 2.72 eV and promising photocatalytic activity. Catalyst immobilization techniques, including incorporation of the catalyst into a sorbent material, were examined. Extensive modeling of a reactor test bed mimicking air duct work with throughput similar to that seen on the International Space Station was completed to determine optimal reactor design. A bench-scale reactor with the novel catalyst and high-efficiency blue LEDs was challenged with several common volatile organic compounds (VOCs) found in ISS cabin air to evaluate the system's ability to perform high-throughput trace contaminant removal. The ultimate goal for this testing was to determine if the unit would be useful in pre-heat exchanger operations to lessen condensed VOCs in recovered water thus lowering the burden of VOC removal for water purification systems.

  1. Necrosis of Staphylococcus aureus by the Electrospun Fe- and Ag-Doped TiO2 Nanofibers

    PubMed Central

    Aboelzahab, Asem; Azad, Abdul-Majeed; Goel, Vijay

    2012-01-01

    Postsurgery infections cause prolonged hospitalization, incurring increased patient and hospital costs, making it increasingly vital to develop an effective solution for the mitigation and elimination of infection buildup at these sites. Incorporation of a bactericidal device at the infection-prone sites provides the capability of attacking bacterial growth even after the patient has left the hospital. Polycrystalline titanium dioxide (TiO2) is photoactive and possesses antibacterial properties that can mitigate the onset of these infections and aid in wound healing. In this work, TiO2 nanofibers were synthesized by electrospinning. Doping with iron as well as with silver (5 wt% and 1 wt%, resp.) was also carried out to increase their effectiveness towards bactericidal properties. The electrospun fibers were processed and tested in the presence of light in the suspensions of methicillin-susceptible Staphylococcus aureus (MSSA) bacteria, which are the leading infection-inducing bacteria among hospital patients. It was found that upon brief activation (cf. 30 s) by an infrared laser source, greater than 90% of the S. aureus was rendered inactive within cf. 10 min. of exposure, thereby showing the potential of titania nanofibers for effective mitigation of infection. PMID:24977085

  2. Tuning the charge state of Ag and Au atoms and clusters deposited on oxide surfaces by doping: a DFT study of the adsorption properties of nitrogen- and niobium-doped TiO2 and ZrO2.

    PubMed

    Schlexer, Philomena; Ruiz Puigdollers, Antonio; Pacchioni, Gianfranco

    2015-09-14

    The charge state of Ag and Au atoms and clusters (Ag4 and Au4, Ag5 and Au5) adsorbed on defective TiO2 anatase(101) and tetragonal ZrO2(101) has been systematically investigated as a function of oxide doping and defectivity using a DFT+U approach. As intrinsic defects, we have considered the presence of oxygen vacancies. As extrinsic defects, substitutional nitrogen- and niobium-doping have been investigated, respectively. Both surface and sub-surface defects and dopants have been considered. Whereas on surfaces with oxygen vacancies or Nb-doping, atoms and clusters may become negatively charged, N-doping always leads to the formation of positively charged adsorbates, independently of the supporting material (TiO2 or ZrO2). This suggests the possibility to tune the electronic properties of supported metal clusters by selective doping of the oxide support, an effect that may result in complete changes in chemical reactivity.

  3. Evolution of structural and magnetic properties of Co-doped TiO2 thin films irradiated with 100 MeV Ag7+ ions

    NASA Astrophysics Data System (ADS)

    Mohanty, P.; Singh, V. P.; Mishra, N. C.; Ojha, S.; Kanjilal, D.; Rath, Chandana

    2014-08-01

    In continuation to our earlier studies where we have shown room temperature ferromagnetism observed in TiO2 and Co-doped TiO2 (CTO) thin films independent of their phase (Mohanty et al 2012 J. Phys. D: Appl. Phys. 45 325301), here the modifications in structure and magnetic properties in CTO thin films using 100 MeV Ag7+ ion irradiation are reported. Owing to the important role of defects in tailoring the magnetic properties of the material, we vary the ion fluence from 5 × 1011 to 1 × 1012 ions cm-2 to create post-deposition defects. While the film deposited under 0.1 mTorr oxygen partial pressure retains its crystallinity showing radiation-resistant behaviour even at a fluence of 1 × 1012 ions cm-2, films deposited under 1 to 300 mTorr oxygen partial pressure becomes almost amorphous at the same fluence. Using Poisson's law, the diameter of the amorphized region surrounding the ion path is calculated to be ˜4.2 nm from the x-ray diffraction peak intensity ((1 1 0) for rutile phase) as a function of ion fluence. The saturation magnetization (Ms) decreases exponentially similar to the decrease in x-ray peak intensity with fluence, indicating magnetic disordered region surrounding the ion path. The diameter of the magnetic disordered region is found to be ˜6.6 nm which is larger than the diameter of the amorphized latent track. Therefore, it is confirmed that swift heavy ion irradiation induces a more significant magnetic disorder than the structural disorder.

  4. Influence of silver doping on surface defect characteristics of TiO2

    NASA Astrophysics Data System (ADS)

    Tripathi, S. K.; Rani, Mamta

    2015-08-01

    In the present work, we proposed a novel silver doped TiO2 polyethylene conjugated films to improve the performance of DSSCs. Oxides nanoparticles dispersed in a semiconducting polymer form the active layer of a solar cell. Localized surface plasmon resonance effects associated with spatially dispersed silver (Ag) nanoparticles can be exploited to enhance the light-harvesting efficiency, the photocurrent density and the overall light-to electrical-energy-conversion efficiency of high-area DSSCs based TiO2 photoanodes. Silver doped titanium dioxide (TiO2:Ag) is prepared by sol-gel technique and deposited on fluorine doped indium oxide (FTO) coated glass substrates by using doctor blade technique at 550°C from aqueous solutions of titanium butoxide and silver nitrate precursors. The effect of Ag doping on electrical properties of films is studied. The Ag-TiO2 films are about 548 times more photosensitive as compare to the pure TiO2 sample. The presence of metallic Ag nanoparticles and oxygen vacancy on the surface of TiO2 nanoparticles promotes the separation of photogenerated electron-hole pairs and thus enhances the photosensitivity. Photoconduction mechanism of all prepared samples is investigated by performing transient photoconductivity measurements on TiO2 and Ag-TiO2 films keeping intensity of light constant.

  5. Synthesis and visible light photoactivity of anatase Ag, and garlic loaded TiO2 nanocrystalline catalyst

    EPA Science Inventory

    An excellent visible light activated Ag and S doped TiO2 nanocatalyst was prepared by using AgNO3 and garlic (Allium sativum) as Ag+ and sulfur sources, respectively. The catalyst resisted the change from anatase to rutile phase even at calcination at 700 oC. The photocatalytic e...

  6. Antibacterial activity of single crystalline silver-doped anatase TiO2 nanowire arrays

    NASA Astrophysics Data System (ADS)

    Zhang, Xiangyu; Li, Meng; He, Xiaojing; Hang, Ruiqiang; Huang, Xiaobo; Wang, Yueyue; Yao, Xiaohong; Tang, Bin

    2016-05-01

    Well-ordered, one-dimensional silver-doped anatase TiO2 nanowire (AgNW) arrays have been prepared through a hydrothermal growth process on the sputtering-deposited AgTi layers. Electron microscope analyses reveal that the as-synthesized AgNW arrays exhibit a single crystalline phase with highly uniform morphologies, diameters ranging from 85 to 95 nm, and lengths of about 11 μm. Silver is found to be doped into TiO2 nanowire evenly and mainly exists in the zerovalent state. The AgNW arrays show excellent efficient antibacterial activity against Escherichia coli (E. coli), and all of the bacteria can be killed within 1 h. Additionally, the AgNW arrays can still kill E. coli after immersion for 60 days, suggesting the long-term antibacterial property. The technique reported here is environmental friendly for formation of silver-containing nanostructure without using any toxic organic solvents.

  7. Novel phosphorus doped carbon nitride modified TiO2 nanotube arrays with improved photoelectrochemical performance

    NASA Astrophysics Data System (ADS)

    Su, Jingyang; Geng, Ping; Li, Xinyong; Zhao, Qidong; Quan, Xie; Chen, Guohua

    2015-10-01

    Novel phosphorus-doped graphitic-carbon nitride (P-C3N4) modified vertically aligned TiO2 nanotube arrays (NTs) were designed and synthesized. They can significantly enhance the conduction and utilization of photogenerated charge carriers of TiO2 NTs. The heterostructure was successfully fabricated through a three-step process: electrochemical anodization and wet-dipping followed by thermal polymerization. The prepared P-C3N4/TiO2 NTs exhibit enhanced light-absorption characteristics and improved charge separation and transfer ability, thus resulting in a 3-fold photocurrent (1.98 mA cm-2 at 0 V vs. Ag/AgCl) compared with that of pure TiO2 NTs (0.66 mA cm-2 at 0 V vs. Ag/AgCl) in 1 M NaOH solution. The prepared P-C3N4/TiO2 NT photoelectrodes also present excellent photocatalytic and photoelectrocatalytic capabilities in the degradation of methylene blue (MB). The kinetic rate of P-C3N4/TiO2 NTs in the photoelectrocatalytic process for MB is 2.7 times that of pristine TiO2 NTs. Furthermore, the prepared sample was used as a photoanode for solar-driven water splitting, giving a H2 evolution rate of 36.6 μmol h-1 cm-2 at 1.0 V vs. RHE under simulated solar light illumination. This novel structure with a rational design for a visible light response shows potential for metal free materials in photoelectrochemical applications.Novel phosphorus-doped graphitic-carbon nitride (P-C3N4) modified vertically aligned TiO2 nanotube arrays (NTs) were designed and synthesized. They can significantly enhance the conduction and utilization of photogenerated charge carriers of TiO2 NTs. The heterostructure was successfully fabricated through a three-step process: electrochemical anodization and wet-dipping followed by thermal polymerization. The prepared P-C3N4/TiO2 NTs exhibit enhanced light-absorption characteristics and improved charge separation and transfer ability, thus resulting in a 3-fold photocurrent (1.98 mA cm-2 at 0 V vs. Ag/AgCl) compared with that of pure TiO2 NTs (0

  8. Doping of TiO2 for sensitized solar cells.

    PubMed

    Roose, Bart; Pathak, Sandeep; Steiner, Ullrich

    2015-11-21

    This review gives a detailed summary and evaluation of the use of TiO2 doping to improve the performance of dye sensitized solar cells. Doping has a major effect on the band structure and trap states of TiO2, which in turn affect important properties such as the conduction band energy, charge transport, recombination and collection. The defect states of TiO2 are highly dependent on the synthesis method and thus the effect of doping may vary for different synthesis techniques, making it difficult to compare the suitability of different dopants. High-throughput methods may be employed to achieve a rough prediction on the suitability of dopants for a specific synthesis method. It was however found that nearly every employed dopant can be used to increase device performance, indicating that the improvement is not so much caused by the dopant itself, as by the defects it eliminates from TiO2. Furthermore, with the field shifting from dye sensitized solar cells to perovskite solar cells, the role doping can play to further advance this emerging field is also discussed.

  9. Removal of 4-Nitrophenol from Water Using Ag-N-P-Tridoped TiO2 by Photocatalytic Oxidation Technique.

    PubMed

    Achamo, Temesgen; Yadav, O P

    2016-01-01

    Photocatalytic oxidation using semiconductor nanoparticles is an efficient, eco-friendly, and cost-effective process for the removal of organic pollutants, such as dyes, pesticides, phenols, and their derivatives in water. In the present study, nanosize Ag-N-P-tridoped titanium(IV) oxide (TiO2) was prepared by using sol-gel-synthesized Ag-doped TiO2 and soybean (Glycine max) or chickpea (Cicer arietinum) seeds as nonmetallic bioprecursors. As-synthesized photocatalysts were characterized using X-ray diffraction, Fourier transform infrared, and ultra violet (UV)-visible spectroscopic techniques. Average crystallite size of the studied photocatalysts was within 39-46 nm. Whereas doped Ag in TiO2 minimized the photogenerated electron-hole recombination, doped N and P extended its photoabsorption edge to visible region. Tridoping of Ag, N, and P in TiO2 exhibited synergetic effect toward enhancing its photocatalytic degradation of 4-nitrophenol (4-NP), separately, under UV and visible irradiations. At three hours, degradations of 4-NP over Ag-N-P-tridoped TiO2 under UV and visible radiations were 73.8 and 98.1%, respectively.

  10. Removal of 4-Nitrophenol from Water Using Ag-N-P-Tridoped TiO2 by Photocatalytic Oxidation Technique.

    PubMed

    Achamo, Temesgen; Yadav, O P

    2016-01-01

    Photocatalytic oxidation using semiconductor nanoparticles is an efficient, eco-friendly, and cost-effective process for the removal of organic pollutants, such as dyes, pesticides, phenols, and their derivatives in water. In the present study, nanosize Ag-N-P-tridoped titanium(IV) oxide (TiO2) was prepared by using sol-gel-synthesized Ag-doped TiO2 and soybean (Glycine max) or chickpea (Cicer arietinum) seeds as nonmetallic bioprecursors. As-synthesized photocatalysts were characterized using X-ray diffraction, Fourier transform infrared, and ultra violet (UV)-visible spectroscopic techniques. Average crystallite size of the studied photocatalysts was within 39-46 nm. Whereas doped Ag in TiO2 minimized the photogenerated electron-hole recombination, doped N and P extended its photoabsorption edge to visible region. Tridoping of Ag, N, and P in TiO2 exhibited synergetic effect toward enhancing its photocatalytic degradation of 4-nitrophenol (4-NP), separately, under UV and visible irradiations. At three hours, degradations of 4-NP over Ag-N-P-tridoped TiO2 under UV and visible radiations were 73.8 and 98.1%, respectively. PMID:27081309

  11. Structural, Optical and Thermal Investigations of TiO2 and S-Doped TiO2 Nanoparticles

    NASA Astrophysics Data System (ADS)

    Bhatnagar, Divyanshu; Kumar, Ashavani

    2011-12-01

    Titanium dioxide (TiO2) and sulfur doped titanium dioxide (S-doped TiO2) nanoparticles are synthesized by Coprecipitation technique using titanium trichloride (TiCl3) as precursor, ammonium hydroxide (NH4OH) as solvent and sodium sulfite as source of sulfur. The X-ray diffraction (xrd) pattern reveals that TiO2 Nanoparticles are in anatase phase and anatase content decreases with increasing S-doping. The Differential Scanning Calorimetry (DSC) analysis elucidates the metastable anatase phase changes to stable rutile phase at 746 °C temperature. The UV/Vis study predicts larger band gap of TiO2 Nanoparticles as compare to bulk and blue shift with increasing S-doping.

  12. Preparation and characterization of Cu-doped TiO2 materials for electrochemical, photoelectrochemical, and photocatalytic applications

    NASA Astrophysics Data System (ADS)

    Ganesh, Ibram; Kumar, Polkampally P.; Annapoorna, Ibram; Sumliner, Jordan M.; Ramakrishna, Mantripragada; Hebalkar, Neha Y.; Padmanabham, Gade; Sundararajan, Govindan

    2014-02-01

    The Cu-doped TiO2 (Cu = 0-50 wt.%) powders and thin films were prepared by following a homogeneous co-precipitation method and sol-gel dip-coating technique, respectively, and were treated through 400-800 °C, and then thoroughly investigated by following various characterization techniques. The characterization results suggest that the pure TiO2 powder formed at 550 °C is in rutile phase, whereas the 0.1-10 wt.% Cu-doped TiO2 powders formed at 550 °C are mainly in anatase phase. These latter powders possess low band-gap energies (3.247-3.265 eV) and flat-band potentials amenable to water oxidation reaction. The 0.5-wt.% Cu-doped TiO2 thin film formed at 550 °C exhibited n-type semiconducting behavior and considerable photocurrent among various investigated powders. The CO2 reduction with a Faradaic efficiency of 82% and ˜ 96% CO selectivity in a two-compartment electrochemical cell was noted at -2500 mV (vs. Ag/Ag+) on pre-reduced (at -2000 mV vs. Ag/AgCl) 50 wt.% Cu-doped TiO2 thin film electrode in conjunction with an ionic liquid. The UV-light-induced TiO2 was found to be responsible for photocatalytic methylene blue (MB) degradation, and TiO2 is not sensitized by MB. The in situ formed compounds of TiO2 and CuO/Cu2O were found to absorb visible light, but showed little visible-light-induced photocatalytic activity.

  13. Au-loaded TiO2 and Ag-loaded TiO2 synthesized by modified sol-gel/impregnation method as photocatalysts

    NASA Astrophysics Data System (ADS)

    Ninsonti, Hathaithip; Sriwichai, Saengrawee; Wetchakun, Natda; Kangwansupamonkon, Wiyong; Phanichphant, Sukon

    2016-02-01

    In this work, Au-loaded TiO2 and Ag-loaded TiO2 nanoparticles were synthesized by modified sol-gel method together with impregnation method. The samples were characterized by their physicochemical properties using X-ray diffraction (XRD) and X-ray photoelectron spectroscopy in order to obtain the correlation between structure and photocatalytic properties. XRD results indicated unloaded TiO2, Au-loaded TiO2 and Ag-loaded TiO2 nanoparticles were all in the anatase phase with average crystallite size in the range of 10-13 nm. In addition, XPS analysis confirmed the presence of Au and Ag elements in Au-loaded TiO2 and Ag-loaded TiO2 nanoparticles, respectively. The photocatalytic activities of TiO2, Au-loaded TiO2 and Ag-loaded TiO2 nanoparticles were evaluated through the mineralization of formic acid under UV-light illumination. The results showed that Au-loading and Ag-loading could effectively improve the photocatalytic activities of TiO2. Furthermore, Au-loaded TiO2 exhibited a higher photocatalytic activity than Ag-loaded TiO2.

  14. Density functional theory calculations for the investigation of (Ag, N) codoping effect on the electronic and optical properties of anatase TiO2

    NASA Astrophysics Data System (ADS)

    Khan, Matiullah; Cao, Wenbin; Li, Jing; Zaman, Muhammad Iqbal; Manan, Abdul

    2014-04-01

    Efficient absorption of light in visible range and enhance separation of photoexcited electron-hole pairs (EHPs) are crucial for improving the photoactivity of metal nonmetal codoped TiO2. By using density functional theory (DFT) calculations, an effective metal (Ag) and nonmetal (N) codoping approach is described to modify the photoelectrochemical properties of titanium dioxide ( TiO2). Nitrogen (N) doping introduces isolated N-2p states above the valence band maximum (VBM) which acts as an electron trap to promote EHP recombination. For Ag-doped TiO2, Ag-4d states are introduced above the VBM which leads to the band gap narrowing. Silver (Ag) and nitrogen codoped TiO2 possess stable configuration, narrowed band gap and best visible light absorption. Defect pair binding energy calculation shows that individual dopants, located at a distance of 8.951 Å bind each other, which indicates that the defect pair is stable compared to the isolated impurities in the host lattice. Ag and N codoped TiO2 shows better visible light absorption as compared to other doped models due to the reduced band gap. N doping reduces the band gap of TiO2 while Ag doping enhances the EHPs separation, so their combined presence in a sample would improve the photocatalytic activity due to their synergistic codoping effect. Our calculations provide reasonable explanation for the experimental findings.

  15. TiO2 doped with nitrogen: synthesis and characterization.

    PubMed

    Abazović, Nadica D; Montone, Amelia; Mirenghi, Luciana; Janković, Ivana A; Comor, Mirjana I

    2008-02-01

    In this study, nitrogen-doped titanium dioxide (TiO2) powders were synthesized in two ways: by heating of titanium hydroxide with urea and by direct hydrolysis of titanium tetraisopropoxide (TTIP) with ammonium hydroxide. The samples were characterized by structural (XRD), analytical (XPS), optical (UV/Vis absorption/reflection and Raman spectroscopy) and morphological (SEM, TEM) techniques. The characterization suggested that the doped materials have anatase crystalline form without any detectable peaks that correspond to dopants. The absorption threshold of titanium dioxide was moved in the visible range of optical spectrum from 3.2 eV to 2.20 eV. Particle sizes of synthesized powders were obtained from XRD measurements and from TEM data ranging from 6-20 nm. XPS and Raman spectroscopy were used for detection of nitrogen in doped samples. PMID:18464379

  16. Origin of unexpected magnetism in Cu-doped TIO2

    NASA Astrophysics Data System (ADS)

    Li, Q. K.; Wang, B.; Woo, C. H.; Wang, H.; Zhu, Z. Y.; Wang, R.

    2008-01-01

    Cu-doped TiO2 has recently been found to exhibit unexpected room temperature ferromagnetism. In the present work, possible defect structures and the associated magnetism are calculated within the generalized gradient approximation using the projector augmented wave method (PAW). In particular, structures of the vacancy-Cu impurity complex are studied. Our results show that the magnetism is caused by: 1) the hybridization of p-d orbitals between the Cu and O ions, and 2) the spin polarization of the 3d orbital of Cu and of the 2p orbital of O ions.

  17. Ag Nanorods Coated with Ultrathin TiO2 Shells as Stable and Recyclable SERS Substrates

    NASA Astrophysics Data System (ADS)

    Ma, Lingwei; Huang, Yu; Hou, Mengjing; Xie, Zheng; Zhang, Zhengjun

    2015-10-01

    TiO2-coated Ag nanorods (Ag@TiO2 NRs) have been fabricated as multifunctional surface-enhanced Raman scattering (SERS) substrates. Uniform TiO2 shells could sufficiently protect the internal Ag NRs against oxidation and sulfuration, thus the temporal stability of SERS substrates was markedly improved. Meanwhile, due to the synergetic effect between crystalline TiO2 and Ag, the nanocomposites could clean themselves via photocatalytic degradation of the adsorbed molecules under ultraviolet irradiation and water dilution, making the SERS substrates renewable. Such Ag@TiO2 NRs were shown to serve as outstanding SERS sensors featuring high sensitivity, superior stability and recyclability.

  18. Ag Nanorods Coated with Ultrathin TiO2 Shells as Stable and Recyclable SERS Substrates

    PubMed Central

    Ma, Lingwei; Huang, Yu; Hou, Mengjing; Xie, Zheng; Zhang, Zhengjun

    2015-01-01

    TiO2-coated Ag nanorods (Ag@TiO2 NRs) have been fabricated as multifunctional surface-enhanced Raman scattering (SERS) substrates. Uniform TiO2 shells could sufficiently protect the internal Ag NRs against oxidation and sulfuration, thus the temporal stability of SERS substrates was markedly improved. Meanwhile, due to the synergetic effect between crystalline TiO2 and Ag, the nanocomposites could clean themselves via photocatalytic degradation of the adsorbed molecules under ultraviolet irradiation and water dilution, making the SERS substrates renewable. Such Ag@TiO2 NRs were shown to serve as outstanding SERS sensors featuring high sensitivity, superior stability and recyclability. PMID:26486994

  19. Ag nanoparticle-deposited TiO2 nanotube arrays for electrodes of Dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Kawamura, Go; Ohmi, Hayato; Tan, Wai Kian; Lockman, Zainovia; Muto, Hiroyuki; Matsuda, Atsunori

    2015-05-01

    Dye-sensitized solar cells composed of a photoanode of Ag nanoparticle (NP)-deposited TiO2 nanotube (TNT) arrays were fabricated. The TNT arrays were prepared by anodizing Ti films on fluorine-doped tin oxide (FTO)-coated glass substrates. Efficient charge transportation through the ordered nanostructure of TNT arrays should be carried out compared to conventional particulate TiO2 electrodes. However, it has been a big challenge to grow TNT arrays on FTO glass substrates with the lengths needed for sufficient light-harvesting (tens of micrometers). In this work, we deposited Ag nanoparticles (NPs) on the wall of TNT arrays to enhance light-harvesting property. Dye-sensitized solar cells with these Ag NP-deposited TNT arrays yielded a higher power conversion efficiency (2.03 %) than those without Ag NPs (1.39 %).

  20. Fabrication N, F, and N/F-Doped TiO2 Photoelectrodes for Dye-Sensitized Solar Cells.

    PubMed

    Park, Su Kyung; Yun, Tae Kwan; Bae, Jae Young

    2015-08-01

    In this study, pure TiO2, N-doped TiO2, F-doped TiO2, and N/F-doped TiO2 particles were successfully synthesized through the hydrolysis of TiCl4 in the presence of ammonia water and NH4F, respectively. The introduction of doping materials did not affect the crystalline structure. No absorption peak for pure TiO2 was observed above the wavelength of 400 nm. However, the N-doped TiO2 and N/F-doped TiO2 powders exhibited a new absorption peak in the visible light region between 400 and 530 nm. The Jsc value of DSSCs based on the N/F-doped TiO2 electrode was increased by 10% compared to DSSCs using a pure TiO2 electrode, and the energy conversion efficiency was increased by 12%.

  1. A comparative study of doped and un-doped sol-gel TiO2 and P25 TiO2 (photo)electrodes.

    PubMed

    Pooarporn, Y; Worayingyong, A; Wörner, M; Songsiriritthigul, P; Braun, A M

    2007-01-01

    Doped and undoped titanium dioxide films have been deposited on indium tin oxide glass using the sol-gel technique. The percentage of rutile in the prepared TiO2, calcined at 823 K and determined by X-ray diffraction, was 23% compared to 24% of rutile in P25-TiO2. Cerium doped TiO2 showed mainly the anatase phase, as characterised by both X-ray diffraction and Raman spectroscopy. The electrochemical and photoelectrochemical properties of the films were studied by cyclic voltammetry and electrochemical impedance spectroscopy. The (photo)electrochemical characteristics of the different films are reported and discussed.

  2. Effects of TiO2 coating dosage and operational parameters on a TiO2/Ag photocatalysis system for decolorizing Procion red MX-5B.

    PubMed

    Lin, Yu-Chih; Lee, Ho-Shan

    2010-07-15

    In this study, titanium dioxide (TiO(2)) powder was coated onto the surface of a dendritic silver (Ag) carrier to synthesize TiO(2)/Ag for decolorizing Procion red MX-5B (MX-5B), and related operation factors were also studied. The results showed that even without ultraviolet-A (UVA) irradiation, the Ag carrier from the TiO(2)/Ag catalyst had oxidizing ability, which could effectively degrade MX-5B color, but TiO(2) was ineffective. In addition, TiO(2) from TiO(2)/Ag demonstrated photocatalysis performance when irradiated, and the Ag carrier further showed an electron-scavenging ability to mitigate electron-hole pair recombination, which can improve the photocatalytic efficacy. With the oxidization and electron-scavenging ability of Ag and the photocatalysis ability of TiO(2), TiO(2)/Ag can decolor MX-5B more efficiently than TiO(2). The heavier Ag carrier also improves the solid-liquid separation of nano-TiO(2), making TiO(2)/Ag more suitable for application in slurry systems of photocatalytic water treatment. When the TiO(2)/Ag coating ratio was 50% by weight, there was a sufficient amount of TiO(2) on Ag's surface with a good distribution, and it exhibited a good photocatalysis decolorizing effect. In a study of how operational factors impact the decolorizing of MX-5B in the TiO(2)/Ag photocatalysis system with UVA irradiation (UVA-TiO(2)/Ag), the decolorization efficiency was optimal when the solution was maintained at pH 6.35. The addition of 0.01 M hydrogen peroxide (H(2)O(2)) aided the photocatalysis decolorization efficiency, although excessive H(2)O(2) reacted with hydroxyl free radicals and decreased the active groups in the system, thereby reducing the photocatalysis activity. An operating temperature of 40 degrees C was conducive to MX-5B decolorization, which was better than operating at room temperature.

  3. N-doped TiO 2: Theory and experiment

    NASA Astrophysics Data System (ADS)

    Di Valentin, Cristiana; Finazzi, Emanuele; Pacchioni, Gianfranco; Selloni, Annabella; Livraghi, Stefano; Paganini, Maria Cristina; Giamello, Elio

    2007-10-01

    Nitrogen doped titanium dioxide is attracting a continuously increasing attention because of its potential as material for environmental photocatalysis. In this paper we review experimental and theoretical work done on this system in our groups in recent years. The analysis is largely based on electron paramagnetic resonance (EPR) spectra and on their interpretation based on high-level ab initio calculations. N-doped anatase TiO 2 contains thermally stable single N-atom impurities either as charged diamagnetic Nb- centers or as neutral paramagnetic Nbrad centers (b stays for bulk). The N-atoms can occupy both interstitial or substitutional positions in the solid, with some evidence for a preference for interstitial sites. All types of N b centers give rise to localized states in the band-gap of the oxide, thus accounting for the related reduction of absorption band edge. The relative abundance of these species depends on the oxidation state of the solid. In fact, upon reduction, oxygen vacancies form and transfer electrons from Ti 3+ ions to the Nbrad with formation of Ti 4+ and Nb-. EPR spectra measured under irradiation show that the N b centers are responsible for visible light absorption with promotion of electrons from the localized N-impurity states to the conduction band or to electron scavengers like O 2 adsorbed on the surface. These results provide an unambiguous characterization of the electronic states associated with N-impurities in TiO 2 and a realistic picture of the processes occurring in the solid under irradiation with visible light.

  4. Electrochromic properties of spray deposited TiO 2-doped WO 3 thin films

    NASA Astrophysics Data System (ADS)

    Patil, P. S.; Mujawar, S. H.; Inamdar, A. I.; Sadale, S. B.

    2005-08-01

    TiO 2-doped WO 3 thin films were deposited onto fluorine-doped tin oxide coated conducting glass substrates using spray pyrolysis technique at 525 °C. The volume percentage of TiO 2 dopant was varied from 13% to 38%. The thin film samples were transparent, uniform and strongly adherent to the substrates. Electrochromical properties of TiO 2-doped WO 3 thin films were studied with the help of cyclic voltammetry (CV), chronoamperometry (CA) and chronocoulometry (CC) techniques. It has been found that TiO 2 doping in WO 3 enhances its electrochromic performance. Colouration efficiency becomes almost double and samples exhibit increasingly high reversibility with TiO 2 doping concentrations, in the studied range.

  5. Feasibility of Silver Doped TiO2/Glass Fiber Photocatalyst under Visible Irradiation as an Indoor Air Germicide

    PubMed Central

    Pham, Thanh-Dong; Lee, Byeong-Kyu

    2014-01-01

    This study investigated the feasibility of using Ag-TiO2 photocatalyst supported on glass fiber (Ag-TiO2/GF) prepared by a sol-gel method as an indoor air germicide. An experimental model was designed to investigate the bacterial disinfection efficiency of Staphylococcus (Staph), the most popular bacterium in hospitals in Korea, by the Ag-TiO2/GF photocatalyst. The silver content in Ag/TiO2 was altered from 1 to 10% to investigate the optimal ratio of Ag doped on TiO2/glass fiber (TiO2/GF) for photocatalytic disinfection of Staph. This study confirmed that Ag in Ag-TiO2/GF could work as an electron sink or donor to increase photocatalytic activity and promote the charge separation of electron-hole pairs generated from TiO2 after photon absorption. Ag also acts as an intermediate agent for the transfer of photo-generated electrons from the valence band of TiO2 to an acceptor (O2 gas) to promote photo-oxidation processes. The photocatalytic disinfection activity of Ag-TiO2/GF under visible light increased with the increase in silver content up to 7.5% and then slightly decreased with further increasing silver content. The highest disinfection efficiency and disinfection capacity of Staph using 7.5% Ag-TiO2/GF were 75.23% and 20 (CFU∙s−1∙cm−2) respectively. The medium level of humidity of 60% ± 5% showed better photocatalytic disinfection than the lower (40% ± 5%) or higher (80% ± 5%) levels. PMID:24658408

  6. Synergetic effects in novel hydrogenated F-doped TiO2 photocatalysts

    NASA Astrophysics Data System (ADS)

    Samsudin, Emy Marlina; Abd Hamid, Sharifah Bee; Juan, Joon Ching; Basirun, Wan Jefrey; Centi, Gabriele

    2016-05-01

    The synergistic effect between fluorine and hydrogen in hydrogenated F-doped TiO2 photocatalysts is evaluated for the photocatalytic degradation of atrazine. The interaction between fluorine and hydrogen species in hydrogenated F-doped TiO2 overcomes the limitations of individual F-doped TiO2 and hydrogenated TiO2 photocatalyst properties. Hydrogenated F-doped TiO2 is photo-active under UV, visible and infrared light illumination with efficient electrons and holes separations. The optimized concentration of surface vacancies and Ti3+ centers coupled with enhanced surface hydrophilicity facilitates the production of surface-bound and free hydroxyl radicals. The surface of the catalyst contains dbnd Tisbnd F, dbnd Tisbnd OH, dbnd Tisbnd Ovacancy and dbnd Tisbnd H bonds as evidenced by XPS, Raman, FTIR and HR-TEM analysis. This combination also triggers the formation of new Ti3+ occupied states under the conduction band of hydrogenated F-doped TiO2. Moreover, the change in the pore structure from cylindrical to slits and larger surface area facilitates surface charge interactions. The thermal stability is also enhanced and a single anatase phase is obtained. The size of the particles of hydrogenated F-doped TiO2 is also uniform with defined and homogeneous crystal structure. This synergetic effect between fluorine and hydrogen opens up new alternatives in improving the properties of TiO2 and its photocatalytic activity.

  7. Photocatalysis with chromium-doped TiO2: bulk and surface doping.

    PubMed

    Ould-Chikh, Samy; Proux, Olivier; Afanasiev, Pavel; Khrouz, Lhoussain; Hedhili, Mohamed N; Anjum, Dalaver H; Harb, Moussab; Geantet, Christophe; Basset, Jean-Marie; Puzenat, Eric

    2014-05-01

    The photocatalytic properties of TiO2 modified by chromium are usually found to depend strongly on the preparation method. To clarify this problem, two series of chromium-doped titania with a chromium content of up to 1.56 wt % have been prepared under hydrothermal conditions: the first series (Cr:TiO2) is intended to dope the bulk of TiO2, whereas the second series (Cr/TiO2) is intended to load the surface of TiO2 with Cr. The catalytic properties have been compared in the photocatalytic oxidation of formic acid. Characterization data provides evidence that in the Cr/TiO2 catalysts chromium is located on the surface of TiO2 as amorphous CrOOH clusters. In contrast, in the Cr:TiO2 series, chromium is mostly dissolved in the titania lattice, although a minor part is still present on the surface. Photocatalytic tests show that both series of chromium-doped titania demonstrate visible-light-driven photo-oxidation activity. Surface-doped Cr/TiO2 solids appear to be more efficient photocatalysts than the bulk-doped Cr:TiO2 counterparts.

  8. Photodegradation of phenanthrene by N-doped TiO2 photocatalyst.

    PubMed

    Sirisaksoontorn, Weekit; Thachepan, Surachai; Songsasen, Apisit

    2009-07-15

    The photodegradation of phenanthrene has been catalyzed by nanostructures of TiO2 doped with nitrogen, N-doped TiO2. The N-doped TiO2 was prepared from the sol-gel reaction of Titanium(IV) bis(ethyl acetoacetato)diisopropoxide with 25% ammonia solution. The N-doped TiO2 was calcined at various temperatures from 300 to 700 degrees C. X-ray diffraction (XRD) results showed that N-doped TiO2 remained amorphous at 300 degrees C but anatase-to-rutile transformation started at 400 degrees C and was complete at 700 degrees C. The average particle size calculated from Scherrer's equation was in the range of 9-51 nm with surface area (S(BET)) of 253.7-4.8 m2/g. X-ray photoelectron spectroscopy (XPS) results confirmed the incorporation of nitrogen atoms (Ti-N bond) in the N-doped catalyst. Moreover, the percentage of nitrogen determined by Elemental analysis was 0.236% of N-doped calcined at 400 degrees C. UV-Vis reflection spectra indicated that N-doped TiO2 calcined at 400 degrees C shifted to the higher absorption edge in the range of visible light. N-doped TiO2 calcined at 400 degrees C successfully catalyzed the photodegradation of phenanthrene (80% conversion) whereas N-doped TiO2 calcined at 500 degrees C and P25 TiO2 failed as catalysts.

  9. Both Enhanced Biocompatibility and Antibacterial Activity in Ag-Decorated TiO2 Nanotubes

    PubMed Central

    Lan, Ming-Ying; Liu, Chia-Pei; Huang, Her-Hsiung; Lee, Sheng-Wei

    2013-01-01

    In this study, Ag is electron-beam evaporated to modify the topography of anodic TiO2 nanotubes of different diameters to obtain an implant with enhanced antibacterial activity and biocompatibility. We found that highly hydrophilic as-grown TiO2 nanotubes became poorly hydrophilic with Ag incorporation; however they could effectively recover their wettability to some extent under ultraviolet light irradiation. The results obtained from antibacterial tests suggested that the Ag-decorated TiO2 nanotubes could greatly inhibit the growth of Staphylococcus aureus. In vitro biocompatibility evaluation indicated that fibroblast cells exhibited an obvious diameter-dependent behavior on both as-grown and Ag-decorated TiO2 nanotubes. Most importantly, of all samples, the smallest diameter (25-nm-diameter) Ag-decorated nanotubes exhibited the most obvious biological activity in promoting adhesion and proliferation of human fibroblasts, and this activity could be attributed to the highly irregular topography on a nanometric scale of the Ag-decorated nanotube surface. These experimental results demonstrate that by properly controlling the structural parameters of Ag-decorated TiO2 nanotubes, an implant surface can be produced that enhances biocompatibility and simultaneously boosts antibacterial activity. PMID:24124484

  10. Both enhanced biocompatibility and antibacterial activity in Ag-decorated TiO2 nanotubes.

    PubMed

    Lan, Ming-Ying; Liu, Chia-Pei; Huang, Her-Hsiung; Lee, Sheng-Wei

    2013-01-01

    In this study, Ag is electron-beam evaporated to modify the topography of anodic TiO2 nanotubes of different diameters to obtain an implant with enhanced antibacterial activity and biocompatibility. We found that highly hydrophilic as-grown TiO2 nanotubes became poorly hydrophilic with Ag incorporation; however they could effectively recover their wettability to some extent under ultraviolet light irradiation. The results obtained from antibacterial tests suggested that the Ag-decorated TiO2 nanotubes could greatly inhibit the growth of Staphylococcus aureus. In vitro biocompatibility evaluation indicated that fibroblast cells exhibited an obvious diameter-dependent behavior on both as-grown and Ag-decorated TiO2 nanotubes. Most importantly, of all samples, the smallest diameter (25-nm-diameter) Ag-decorated nanotubes exhibited the most obvious biological activity in promoting adhesion and proliferation of human fibroblasts, and this activity could be attributed to the highly irregular topography on a nanometric scale of the Ag-decorated nanotube surface. These experimental results demonstrate that by properly controlling the structural parameters of Ag-decorated TiO2 nanotubes, an implant surface can be produced that enhances biocompatibility and simultaneously boosts antibacterial activity.

  11. Characteristics of ionic polymer-metal composite with chemically doped TiO2 particles

    NASA Astrophysics Data System (ADS)

    Jung, Youngsoo; Kim, Seong Jun; Kim, Kwang J.; Lee, Deuk Yong

    2011-12-01

    Many studies have investigated techniques to improve the bending performance of ionic polymer-metal composite (IPMC) actuators, including 'doping' of metal particles in the polymer membrane usually by means of physical processes. This study is mainly focused on the characterization of the physical, electrochemical and electromechanical properties of TiO2-doped ionic polymer membranes and IPMCs prepared by the sol-gel method, which results in a uniform distribution of the particles inside the polymer membrane. X-ray and UV-visible spectra indicate the presence of anatase-TiO2 in the modified membranes. TiO2-doped membranes (0.16 wt%) exhibit the highest level of water uptake. The glass transition temperature of these membranes, measured using differential scanning calorimetry (DSC), increases with the increase of the amount of TiO2 in the membrane. Dynamic mechanical analysis (DMA) demonstrated that the storage modulus of dried TiO2-doped ionic polymer membranes increases as the amount of TiO2 in the membrane increases, whereas the storage modulus of hydrated samples is closely related to the level of water uptake. Electrochemical impedance spectroscopy (EIS) shows that the conductivity of TiO2-doped membranes decreases with increasing TiO2 content in spite of an internal resistance drop in the samples. Above all, bending deflection of TiO2-doped IPMC decreased with higher TiO2 content in the membrane while the blocking force of each sample increased with the higher TiO2 content. Additionally, it was determined that the lifetime of IPMC is strongly dependent on the level of water uptake.

  12. Nitrogen doped TiO2 nano-particles: Phase control by solution combustion method

    NASA Astrophysics Data System (ADS)

    Bapna, Komal; Choudhary, R. J.; Phase, D. M.; Shastri, Sheetal; Prasad, R.; Ahuja, B. L.

    2016-05-01

    N-doped TiO2 nano powders were prepared by sol-gel solution combustion method. The influence of different fuels (urea and citric acid) used in obtaining N-TiO2 nano particles in similar conditions (heat treatment, amount of precursors) has been investigated. The growth of different phases of TiO2 (anatase and rutile) is strongly affected by the ligands and the dehydration reaction. Reduction in the band gap of TiO2 and features observed in the XPS spectra confirm the incorporation of N into TiO2 matrix.

  13. Tailoring of antibacterial Ag nanostructures on TiO2 nanotube layers by magnetron sputtering.

    PubMed

    Uhm, Soo-Hyuk; Song, Doo-Hoon; Kwon, Jae-Sung; Lee, Sang-Bae; Han, Jeon-Geon; Kim, Kyoung-Nam

    2014-04-01

    To reduce the incidence of postsurgical bacterial infection that may cause implantation failure at the implant-bone interface, surface treatment of titanium implants with antibiotic materials such as silver (Ag) has been proposed. The purpose of this work was to create TiO2 nanotubes using plasma electrolytic oxidation (PEO), followed by formation of an antibacterial Ag nanostructure coating on the TiO2 nanotube layer using a magnetron sputtering system. PEO was performed on commercially pure Ti sheets. The Ag nanostructure was added onto the resulting TiO2 nanotube using magnetron sputtering at varying deposition rates. Field emission scanning electron microscopy and transmission electron microscopy were used to characterize the surface, and Ag content on the TiO2 nanotube layer was analyzed by X-ray diffraction and X-ray photoelectron spectroscopy. Scanning probe microscopy for surface roughness and contact angle measurement were used to indirectly confirm enhanced TiO2 nanotube hydrophilicity. Antibacterial activity of Ag ions in solution was determined by inductively coupled plasma mass spectrometry and antibacterial testing against Staphylococcus aureus (S. aureus). In vitro, TiO2 nanotubes coated with sputtered Ag resulted in significantly reduced S. aureus. Cell viability assays showed no toxicity for the lowest sputtering time group in the osteoblastic cell line MC3T3-E1. These results suggest that a multinanostructured layer with a biocompatible TiO2 nanotube and antimicrobial Ag coating is a promising biomaterial that can be tailored with magnetron sputtering for optimal performance.

  14. Synthesis, characterization and photocatalytic activity of fluorine doped TiO2 nanoflakes synthesized using solid state reaction method.

    PubMed

    Umadevi, M; Parimaladevi, R; Sangari, M

    2014-01-01

    Fluorine doped TiO2 were synthesized by solid state reaction method. Optical and structural properties of fluorine doped TiO2 were investigated by X-ray diffraction, Fourier transform infrared spectroscopy, UV-vis diffusion reflectance spectroscopy and scanning electron microscopic techniques. The prepared fluorine doped TiO2 was smaller in size with respect to pure TiO2 and it is tetragonal in crystalline structure. Nanoflakes like structure of pure and fluorine doped TiO2 was confirmed from SEM image. Fluorine doped TiO2 shows smaller band gap, high strain and dislocation density when compared to pure TiO2. It also has higher photocatalytic activity with respect to pure TiO2.

  15. Controllable Synthesis and Tunable Photocatalytic Properties of Ti3+-doped TiO2

    PubMed Central

    Ren, Ren; Wen, Zhenhai; Cui, Shumao; Hou, Yang; Guo, Xiaoru; Chen, Junhong

    2015-01-01

    Photocatalysts show great potential in environmental remediation and water splitting using either artificial or natural light. Titanium dioxide (TiO2)-based photocatalysts are studied most frequently because they are stable, non-toxic, readily available, and highly efficient. However, the relatively wide band gap of TiO2 significantly limits its use under visible light or solar light. We herein report a facile route for controllable synthesis of Ti3+-doped TiO2 with tunable photocatalytic properties using a hydrothermal method with varying amounts of reductant, i.e., sodium borohydride (NaBH4). The resulting TiO2 showed color changes from light yellow, light grey, to dark grey with the increasing amount of NaBH4. The present method can controllably and effectively reduce Ti4+ on the surface of TiO2 and induce partial transformation of anatase TiO2 to rutile TiO2, with the evolution of nanoparticles into hierarchical structures attributable to a high pressure and strong alkali environment in the synthesis atmosphere; in this way, the photocatalytic activity of Ti3+-doped TiO2 under visible-light can be tuned. The as-developed strategy may open up a new avenue for designing and functionalizing TiO2 materials for enhancing visible light absorption, narrowing band gap, and improving photocatalytic activity. PMID:26044406

  16. Controllable Synthesis and Tunable Photocatalytic Properties of Ti(3+)-doped TiO2.

    PubMed

    Ren, Ren; Wen, Zhenhai; Cui, Shumao; Hou, Yang; Guo, Xiaoru; Chen, Junhong

    2015-06-05

    Photocatalysts show great potential in environmental remediation and water splitting using either artificial or natural light. Titanium dioxide (TiO2)-based photocatalysts are studied most frequently because they are stable, non-toxic, readily available, and highly efficient. However, the relatively wide band gap of TiO2 significantly limits its use under visible light or solar light. We herein report a facile route for controllable synthesis of Ti(3+)-doped TiO2 with tunable photocatalytic properties using a hydrothermal method with varying amounts of reductant, i.e., sodium borohydride (NaBH4). The resulting TiO2 showed color changes from light yellow, light grey, to dark grey with the increasing amount of NaBH4. The present method can controllably and effectively reduce Ti(4+) on the surface of TiO2 and induce partial transformation of anatase TiO2 to rutile TiO2, with the evolution of nanoparticles into hierarchical structures attributable to a high pressure and strong alkali environment in the synthesis atmosphere; in this way, the photocatalytic activity of Ti(3+)-doped TiO2 under visible-light can be tuned. The as-developed strategy may open up a new avenue for designing and functionalizing TiO2 materials for enhancing visible light absorption, narrowing band gap, and improving photocatalytic activity.

  17. Deposition of Co-doped TiO2 Thin Films by sol-gel method

    NASA Astrophysics Data System (ADS)

    Boutlala, A.; Bourfaa, F.; Mahtili, M.; Bouaballou, A.

    2016-03-01

    Cobalt doped TiO2 thin films have been prepared by sol-gel method onto glass substrate at room temperature. in this present work, we are interesting to study the effect of Cobalt doped TiO2 thin films.the concentration of Co was varied from 0 to 6%at .The obtained films have been annealed at 500°C for 2 hours. X-ray diffraction patterns showed that Co: TiO2 films are polycrystalline with a tetragonal anatase and orthorhombic brookite types structures. The surface morphologies of the TiO2 doped with cobalt thin films were evaluated by Atomic Force Microscopy (AFM). The optical properties were studied by mean of UV-visible and near infrared spectroscopy.The calculated optical band gap decreases from 3.30 to 2.96 eV with increasing Co doping.

  18. Enhanced hydrogen evolution from water splitting using Fe-Ni codoped and Ag deposited anatase TiO2 synthesized by solvothermal method

    NASA Astrophysics Data System (ADS)

    Sun, Tao; Liu, Enzhou; Liang, Xuhua; Hu, Xiaoyun; Fan, Jun

    2015-08-01

    In this paper, the Fe-Ni co-doped and Ag deposited anatase TiO2 (Fe-Ni/Ag/TiO2) nanocomposites were successfully prepared by a simple one-pot solvothermal approach. The investigations indicated that all as-prepared TiO2 samples were single anatase phase, and the impurity level was generated due to the Fe3+ or Ni2+ being located in the intrinsic band gap of TiO2, while the Ag+ ions could be transformed into metallic silver due to the reduction reaction and then loaded onto the surface of TiO2. Compared with pure TiO2, Fe-Ni/Ag/TiO2 composites with the sizes of Ag nanoparticles from 1.0 to 3.0 nm displayed the well optical property including higher visible light absorption activity and lower electron-hole pair recombination rate, and its absorption wavelength edge moved remarkably with a red shift to 700 nm. The photocatalytic water splitting was performed to produce H2 over the samples, and the experimental results indicate that Fe-Ni/Ag/TiO2 composites presented the highest H2 evolution rate, it can reach up to 793.86 μmol h-1 gcat-1 (λ > 400 nm for 6 h, energy efficiency is 0.25%), which was much higher than that of pure TiO2 for 9.57 μmol h-1 gcat-1. In addition, a tentative photocatalytic mechanism is proposed to understand the enhancement mechanism over Fe-Ni codoped and Ag deposited anatase TiO2.

  19. Characterization and photocatalytic performance evaluation of various metal ion-doped microstructured TiO2 under UV and visible light.

    PubMed

    Sahoo, Chittaranjan; Gupta, Ashok K

    2015-01-01

    Commercially available microcrystalline TiO2 was doped with silver, ferrous and ferric ion (1.0 mol %) using silver nitrate, ferrous sulfate and ferric nitrate solutions following the liquid impregnation technology. The catalysts prepared were characterised by FESEM, XRD, FTIR, DRS, particle size and micropore analysis. The photocatalytic activity of the prepared catalysts was tested on the degradation of two model dyes, methylene blue (3,7-bis (Dimethylamino)-phenothiazin-5-ium chloride, a cationic thiazine dye) and methyl blue (disodium;4-[4-[[4-(4-sulfonatoanilino)phenyl]-[4-(4-sulfonatophenyl)azaniumylidenecyclohexa-2,5-dien-1-ylidene]methyl]anilino]benzene sulfonate, an anionic triphenyl methane dye) under irradiation by UV and visible light in a batch reactor. The efficiency of the photocatalysts under UV and visible light was compared to ascertain the light range for effective utilization. The catalysts were found to have the anatase crystalline structure and their particle size is in a range of 140-250 nm. In the case of Fe(2+) doped TiO2 and Fe(3+) doped TiO2, there was a greater shift in the optical absorption towards the visible range. Under UV light, Ag(+) doped TiO2 was the most efficient catalyst and the corresponding decolorization was more than 99% for both the dyes. Under visible light, Fe(3+) doped TiO2 was the most efficient photocatalyst with more than 96% and 90% decolorization for methylene blue and methyl blue, respectively. The kinetics of the reaction under both UV and visible light was investigated using the Langmuir-Hinshelwood pseudo-first-order kinetic model. Kinetic measurements confirmed that, Ag(+) doped TiO2 was most efficient in the UV range, while Fe(3+) doped TiO2 was most efficient in the visible range.

  20. Bacterial responses to Cu-doped TiO(2) nanoparticles.

    PubMed

    Wu, Bing; Huang, Rick; Sahu, Manoranjan; Feng, Xueyang; Biswas, Pratim; Tang, Yinjie J

    2010-03-01

    The toxicity of Cu-doped TiO(2) nanoparticles (NPs, 20nm), synthesized by a flame aerosol reactor, to Mycobacterium smegmatis and Shewanella oneidensis MR-1, is the primary focus of this study. Both doped and non-doped TiO(2) NPs (20nm) tended to agglomerate in the medium solution, and therefore did not penetrate into the cell and damage cellular structures. TiO(2) particles (<100mg/L) did not apparently interfere with the growth of the two species in aqueous cultures. Cu-doped TiO(2) NPs (20mg/L) significantly reduced the M. smegmatis growth rate by three fold, but did not affect S. oneidensis MR-1 growth. The toxicity of Cu-doped TiO(2) NPs was driven by the release of Cu(2+) from the parent NPs. Compared to equivalent amounts of Cu(2+), Cu-doped TiO(2) NPs exhibited higher levels of toxicity to M. smegmatis (P-value<0.1). Addition of EDTA in the culture appeared to significantly decrease the anti-mycobacterium activity of Cu-doped TiO(2) NPs. S. oneidensis MR-1 produced a large amount of extracellular polymeric substances (EPS) under NP stress, especially extracellular protein. Therefore, S. oneidensis MR-1 was able to tolerate a much higher concentration of Cu(2+) or Cu-doped TiO(2) NPs. S. oneidensis MR-1 also adsorbed NPs on cell surface and enzymatically reduced ionic copper in culture medium with a remediating rate of 61microg/(liter x OD(600) x hour) during its early exponential growth phase. Since the metal reducing Shewanella species can efficiently "clean" metal-oxide NPs, the activities of such environmentally relevant bacteria may be an important consideration for evaluating the ecological risk of metal-oxide NPs. PMID:19931887

  1. Doping of TiO 2 Polymorphs for Altered Optical and Photocatalytic Properties

    DOE PAGES

    Nie, Xiliang; Zhuo, Shuping; Maeng, Gloria; Sohlberg, Karl

    2009-01-01

    Tmore » his paper reviews recent investigations of the influence of dopants on the optical properties of TiO 2 polymorphs.he common undoped polymorphs of TiO 2 are discussed and compared.he results of recent doping efforts are tabulated, and discussed in the context of doping by elements of the same chemical group. Dopant effects on the band gap and photocatalytic activity are interpreted with reference to a simple qualitative picture of the TiO 2 electronic structure, which is supported with first-principles calculations.« less

  2. N-doped TiO2 Prepared by RF DBD Plasma

    NASA Astrophysics Data System (ADS)

    Sun, Zhi-Guang; Liu, Jing-Lin; Li, Xiao-Song; Zhai, Zhao-Jun; Zhu, Ai-Min; Laboratory of Plasma Physical Chemistry Team

    2014-10-01

    TiO2 is the most promising photocatalyst because of its chemical stable, nontoxic, low cost, high photocatalytic activity and other attractive properties. Anatase has the highest photocatalytic activity among the three crystal form of TiO2. However, the 3.2 eV bandgap of anatase TiO2 makes it can only utilize the ultraviolet part of solar spectrum. Nitrogen doping is an effective method to extend the absorption range of anatase to visible light. N-doped TiO2 preparation methods, such as heat treatment under NH3 flow, the hydrolytic precipitation and the sol-gel process, have been reported. In this work, preparation of N-doped TiO2 was explored by radio-frequency (RF) dielectric barrier discharge (DBD) plasma using Ar as discharge gas. TiCl4, O2 and N2 were used as Ti, O and N precursors, respectively. In addition, H2 was added to the plasma. X-ray photoelectron spectra (XPS) showed nitrogen was successfully doped into the as-prepared TiO2. Further investigations on structure, composition and optical property of the as-prepared TiO2 samples were conducted by X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) and UV-Vis absorption spectra techniques.

  3. Fabrication of plasmonic AgBr/Ag nanoparticles-sensitized TiO2 nanotube arrays and their enhanced photo-conversion and photoelectrocatalytic properties

    NASA Astrophysics Data System (ADS)

    Wang, Qingyao; Qiao, Jianlei; Jin, Rencheng; Xu, Xiaohui; Gao, Shanmin

    2015-03-01

    Plasmonic photosensitizer AgBr/Ag nanospheres supported on TiO2 nanotube arrays (TiO2 NTs) are prepared by successive ionic layer adsorption and reaction (SILAR) technique followed by photoreduction methods. The structural and surface morphological properties of AgBr/Ag nanoparticles sensitized TiO2 NTs and their photoelectrochemical performance are investigated and discussed. A detailed formation mechanism of the TiO2 NTs/AgBr/Ag is proposed. The TiO2 NTs/AgBr/Ag exhibit excellent photocurrent and photoelectrocatalytic activities under visible light irradiation. Efficient utilization of solar energy to create electron-hole pairs is attributed to the significant visible light response and surface plasmon resonance of Ag nanoparticles. This finding indicates that the high photosensitivity of the TiO2 NTs-based surface plasmon resonance materials could be applied toward the development of new plasmonic visible-light-sensitive photovoltaic fuel cells and photocatalysts.

  4. Photoelectrocatalytic degradation of benzoic acid using Au doped TiO2 thin films.

    PubMed

    Mohite, V S; Mahadik, M A; Kumbhar, S S; Hunge, Y M; Kim, J H; Moholkar, A V; Rajpure, K Y; Bhosale, C H

    2015-01-01

    Highly transparent pure and Au doped TiO2 thin films are successfully deposited by using simple chemical spray pyrolysis technique. The effect of Au doping onto the structural and physicochemical properties has been investigated. The PEC study shows that, both short circuit current (Isc) and open circuit voltage (Voc) are (Isc=1.81mA and Voc=890mV) relatively higher at 3at.% Au doping percentage. XRD study shows that the films are nanocrystalline in nature with tetragonal crystal structure. FESEM images show that the film surface covered with a smooth, uniform, compact and rice shaped nanoparticles. The Au doped thin films exhibit indirect band gap, decreases from 3.23 to 3.09eV with increase in Au doping. The chemical composition and valence states of pure and Au doped TiO2 films are studied by using X-ray photoelectron spectroscopy. The photocatalytic degradation effect is 49% higher in case 3at.% Au doped TiO2 than the pure TiO2 thin film photoelectrodes in the degradation of benzoic acid. It is revealed that Au doped TiO2 can be reused for five cycles of experiments without a requirement of post-treatment while the degradation efficiency was retained.

  5. Photoelectrocatalytic degradation of benzoic acid using Au doped TiO2 thin films.

    PubMed

    Mohite, V S; Mahadik, M A; Kumbhar, S S; Hunge, Y M; Kim, J H; Moholkar, A V; Rajpure, K Y; Bhosale, C H

    2015-01-01

    Highly transparent pure and Au doped TiO2 thin films are successfully deposited by using simple chemical spray pyrolysis technique. The effect of Au doping onto the structural and physicochemical properties has been investigated. The PEC study shows that, both short circuit current (Isc) and open circuit voltage (Voc) are (Isc=1.81mA and Voc=890mV) relatively higher at 3at.% Au doping percentage. XRD study shows that the films are nanocrystalline in nature with tetragonal crystal structure. FESEM images show that the film surface covered with a smooth, uniform, compact and rice shaped nanoparticles. The Au doped thin films exhibit indirect band gap, decreases from 3.23 to 3.09eV with increase in Au doping. The chemical composition and valence states of pure and Au doped TiO2 films are studied by using X-ray photoelectron spectroscopy. The photocatalytic degradation effect is 49% higher in case 3at.% Au doped TiO2 than the pure TiO2 thin film photoelectrodes in the degradation of benzoic acid. It is revealed that Au doped TiO2 can be reused for five cycles of experiments without a requirement of post-treatment while the degradation efficiency was retained. PMID:25550120

  6. Enhanced photocatalysis by coupling of anatase TiO2 film to triangular Ag nanoparticle island.

    PubMed

    Xu, Jinxia; Xiao, Xiangheng; Ren, Feng; Wu, Wei; Dai, Zhigao; Cai, Guangxu; Zhang, Shaofeng; Zhou, Juan; Mei, Fei; Jiang, Changzhong

    2012-01-01

    In order to overcome the low utilization ratio of solar light and high electron-hole pair recombination rate of TiO2, the triangular Ag nanoparticle island is covered on the surface of the TiO2 thin film. Enhancement of the photocatalytic activity of the Ag/TiO2 nanocomposite system is observed. The increase of electron-hole pair generation is caused by the enhanced near-field amplitudes of localized surface plasmon of the Ag nanoparticles. The efficiently suppressed recombination of electron-hole pair caused by the metal-semiconductor contact can also enhance the photocatalytic activity of the TiO2 film. PMID:22548875

  7. Enhanced photocatalysis by coupling of anatase TiO2 film to triangular Ag nanoparticle island

    PubMed Central

    2012-01-01

    In order to overcome the low utilization ratio of solar light and high electron-hole pair recombination rate of TiO2, the triangular Ag nanoparticle island is covered on the surface of the TiO2 thin film. Enhancement of the photocatalytic activity of the Ag/TiO2 nanocomposite system is observed. The increase of electron-hole pair generation is caused by the enhanced near-field amplitudes of localized surface plasmon of the Ag nanoparticles. The efficiently suppressed recombination of electron-hole pair caused by the metal-semiconductor contact can also enhance the photocatalytic activity of the TiO2 film. PMID:22548875

  8. High Mobility of Graphene-Based Flexible Transparent Field Effect Transistors Doped with TiO2 and Nitrogen-Doped TiO2.

    PubMed

    Wu, Yu-Hsien; Tseng, Po-Yuan; Hsieh, Ping-Yen; Chou, Hung-Tao; Tai, Nyan-Hwa

    2015-05-13

    Graphene with carbon atoms bonded in a honeycomb lattice can be tailored by doping various species to alter the electrical properties of the graphene for fabricating p-type or n-type field-effect transistors (FETs). In this study, large-area and single-layer graphene was grown on electropolished Cu foil using the thermal chemical vapor deposition method; the graphene was then transferred onto a poly(ethylene terephthalate) (PET) substrate to produce flexible, transparent FETs. TiO2 and nitrogen-doped TiO2 (N-TiO2) nanoparticles were doped on the graphene to alter its electrical properties, thereby enhancing the carrier mobility and enabling the transistors to sense UV and visible light optically. The results indicated that the electron mobility of the graphene was 1900 cm(2)/(V·s). Dopings of TiO2 and N-doped TiO2 (1.4 at. % N) lead to n-type doping effects demonstrating extremely high carrier mobilities of 53000 and 31000 cm(2)/(V·s), respectively. Through UV and visible light irradiation, TiO2 and N-TiO2 generated electrons and holes; the generated electrons transferred to graphene channels, causing the FETs to exhibit n-type electric behavior. In addition, the Dirac points of the graphene recovered to their original state within 5 min, confirming that the graphene-based FETs were photosensitive to UV and visible light. In a bending state with a radius of curvature greater than 2.0 cm, the carrier mobilities of the FETs did not substantially change, demonstrating the application possibility of the fabricated graphene-based FETs in photosensors.

  9. Investigation of photocatalytic degradation of phenol by Fe(III)-doped TiO2 and TiO2 nanoparticles

    PubMed Central

    2014-01-01

    In this study Fe (III)-doped TiO2 nanoparticles were synthesized by sol–gel method at two atomic ratio of Fe/Ti, 0.006 and 0.034 percent. Then the photoactivity of them was investigated on degradation of phenol under UV (<380 nm) irradiation and visible light (>380 nm). Results showed that at appropriate atomic ratio of Fe to Ti (% 0.034) photoactivity of Fe(III)–doped TiO2 nanoparticles increased. In addition, the effects of various operational parameters on photocatalytic degradation, such as pH, initial concentration of phenol and amount of photocatalyst were examined and optimized. At all different initial concentration, highest degradation efficiency occurred at pH = 3 and 0.5 g/L Fe(III)–doped TiO2 dosage. With increase in initial concentration of phenol, photocatalytic degradation efficiency decreased. Photoactivity of Fe (III)-doped TiO2 under UV irradiation and visible light at optimal condition (pH = 3 and catalyst dosage = and 0.5 g/L) was compared with P25 TiO2 nanoparticles. Results showed that photoactivity of Fe(III)-doped TiO2 under visible light was more than P25 TiO2 photoactivity, but it was less than P25 TiO2 photoactivity under UV irradiation. Also efficiency of UV irradiation alone and amount of phenol adsorption on Fe(III)-doped TiO2 at dark condition was investigated. PMID:25105016

  10. Investigation of photocatalytic degradation of phenol by Fe(III)-doped TiO2 and TiO2 nanoparticles.

    PubMed

    Hemmati Borji, Saeedeh; Nasseri, Simin; Mahvi, Amir Hossein; Nabizadeh, Ramin; Javadi, Amir Hossein

    2014-01-01

    In this study Fe (III)-doped TiO2 nanoparticles were synthesized by sol-gel method at two atomic ratio of Fe/Ti, 0.006 and 0.034 percent. Then the photoactivity of them was investigated on degradation of phenol under UV (<380 nm) irradiation and visible light (>380 nm). Results showed that at appropriate atomic ratio of Fe to Ti (% 0.034) photoactivity of Fe(III)-doped TiO2 nanoparticles increased. In addition, the effects of various operational parameters on photocatalytic degradation, such as pH, initial concentration of phenol and amount of photocatalyst were examined and optimized. At all different initial concentration, highest degradation efficiency occurred at pH = 3 and 0.5 g/L Fe(III)-doped TiO2 dosage. With increase in initial concentration of phenol, photocatalytic degradation efficiency decreased. Photoactivity of Fe (III)-doped TiO2 under UV irradiation and visible light at optimal condition (pH = 3 and catalyst dosage = and 0.5 g/L) was compared with P25 TiO2 nanoparticles. Results showed that photoactivity of Fe(III)-doped TiO2 under visible light was more than P25 TiO2 photoactivity, but it was less than P25 TiO2 photoactivity under UV irradiation. Also efficiency of UV irradiation alone and amount of phenol adsorption on Fe(III)-doped TiO2 at dark condition was investigated.

  11. First-principles study on transition metal-doped anatase TiO2.

    PubMed

    Wang, Yaqin; Zhang, Ruirui; Li, Jianbao; Li, Liangliang; Lin, Shiwei

    2014-01-28

    The electronic structures, formation energies, and band edge positions of anatase TiO2 doped with transition metals have been analyzed by ab initio band calculations based on the density functional theory with the planewave ultrasoft pseudopotential method. The model structures of transition metal-doped TiO2 were constructed by using the 24-atom 2 × 1 × 1 supercell of anatase TiO2 with one Ti atom replaced by a transition metal atom. The results indicate that most transition metal doping can narrow the band gap of TiO2, lead to the improvement in the photoreactivity of TiO2, and simultaneously maintain strong redox potential. Under O-rich growth condition, the preparation of Co-, Cr-, and Ni-doped TiO2 becomes relatively easy in the experiment due to their negative impurity formation energies, which suggests that these doping systems are easy to obtain and with good stability. The theoretical calculations could provide meaningful guides to develop more active photocatalysts with visible light response.

  12. Doping concentration dependence of microstructure and magnetic behaviours in Co-doped TiO2 nanorods

    PubMed Central

    2014-01-01

    Co-doped titanium dioxide (TiO2) nanorods with different doping concentrations were fabricated by a molten salt method. It is found that the morphology of TiO2 changes from nanorods to nanoparticles with increasing doping concentration. The mechanism for the structure and phase evolution is investigated in detail. Undoped TiO2 nanorods show strong ferromagnetism at room temperature, whereas incorporating of Co deteriorates the ferromagnetic ordering. X-ray photoelectron spectroscopy (XPS) and electron spin resonance (ESR) results demonstrate that the ferromagnetism is associated with Ti vacancy. PMID:25593558

  13. [Spectrum characterization and fine structure of copper phthalocyanine-doped TiO2 microcavities].

    PubMed

    Liu, Cheng-lin; Zhang, Xin-yi; Zhong, Ju-hua; Zhu, Yi-hua; He, Bo; Wei, Shi-qiang

    2007-10-01

    Copper phthalocyanine-doped TiO2 microcavities were fabricated by chemistry method. Their spectrum characterization was studied by Fourier transform infrared (FTIR) and Raman spectroscopy, and their fine structure was analyzed by X-ray absorption fine structure (XAFS). The results show that there is interaction of copper phthalocyanine (CuPc) and TiO2 microcavities after TiO2 microcavities was doped with CuPc. For example, there is absorption at 900.76 cm(-1) in FTIR spectra, and the "red shift" of both OH vibration at 3392.75 cm(-1) and CH vibration at 2848.83 cm(-1). There exist definite peak shifts and intensity changes in infrared absorption in the C-C or C-N vibration in the planar phthalocyanine ring, the winding vibration of C-H inside and C-N outside plane of benzene ring. In Raman spectrum, there are 403.4, 592.1 and 679.1 cm(-1) characterized peaks of TiO2 in CuPc-doped TiO2 microcavities, but their wave-numbers show shifts to anatase TiO2. The vibration peaks at 1586.8 and 1525.6 cm(-1) show that there exists the composite material of CuPc and TiO2. These changes are related to the plane tropism of the molecule structure of copper phthalocyanine. XAFS showed tetrahedron TiO4 structure of Ti in TiO2 microcavities doped with copper phthalocyanine, and the changes of inner "medial distances" and the surface structure of TiO2 microcavities.

  14. Interstitial Boron-Doped TiO2 Thin Films: The Significant Effect of Boron on TiO2 Coatings Grown by Atmospheric Pressure Chemical Vapor Deposition.

    PubMed

    Quesada-González, Miguel; Boscher, Nicolas D; Carmalt, Claire J; Parkin, Ivan P

    2016-09-28

    The work presented here describes the preparation of transparent interstitial boron-doped TiO2 thin-films by atmospheric pressure chemical vapor deposition (APCVD). The interstitial boron-doping, on TiO2, proved by X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD), is shown to enhance the crystallinity and significantly improve the photocatalytic activity of the TiO2 films. The synthesis, highly suitable for a reel-to-reel process, has been carried out in one step. PMID:27622709

  15. Interstitial Boron-Doped TiO2 Thin Films: The Significant Effect of Boron on TiO2 Coatings Grown by Atmospheric Pressure Chemical Vapor Deposition.

    PubMed

    Quesada-González, Miguel; Boscher, Nicolas D; Carmalt, Claire J; Parkin, Ivan P

    2016-09-28

    The work presented here describes the preparation of transparent interstitial boron-doped TiO2 thin-films by atmospheric pressure chemical vapor deposition (APCVD). The interstitial boron-doping, on TiO2, proved by X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD), is shown to enhance the crystallinity and significantly improve the photocatalytic activity of the TiO2 films. The synthesis, highly suitable for a reel-to-reel process, has been carried out in one step.

  16. Structural, electrical and optical properties of TiO 2 doped WO 3 thin films

    NASA Astrophysics Data System (ADS)

    Patil, P. S.; Mujawar, S. H.; Inamdar, A. I.; Shinde, P. S.; Deshmukh, H. P.; Sadale, S. B.

    2005-12-01

    TiO 2 doped WO 3 thin films were deposited onto glass substrates and fluorine doped tin oxide (FTO) coated conducting glass substrates, maintained at 500 °C by pyrolytic decomposition of adequate precursor solution. Equimolar ammonium tungstate ((NH 4) 2WO 4) and titanyl acetyl acetonate (TiAcAc) solutions were mixed together at pH 9 in volume proportions and used as a precursor solution for the deposition of TiO 2 doped WO 3 thin films. Doping concentrations were varied between 4 and 38%. The effect of TiO 2 doping concentration on structural, electrical and optical properties of TiO 2 doped WO 3 thin films were studied. Values of room temperature electrical resistivity, thermoelectric power and band gap energy ( Eg) were estimated. The films with 38% TiO 2 doping in WO 3 exhibited lowest resistivity, n-type electrical conductivity and improved electrochromic performance among all the samples. The values of thermoelectric power (TEP) were in the range of 23-56 μV/K and the direct band gap energy varied between 2.72 and 2.86 eV.

  17. Effect of metal-ion doping on the characteristics and photocatalytic activity of TiO2 nanotubes for the removal of toluene from water.

    PubMed

    Yuan, Rongfang; Zhou, Beihai; Hua, Duo; Shi, Chunhong; Ma, Li

    2014-01-01

    Toluene is an extensively used reagent that could cause water pollution and endanger human health. In this work, an O3/UV/ion-doped TiO2 nanotubes process was investigated to obtain the optimum TiO2 nanotubes for effective toluene decomposition. Photocatalytic activity is found to be influenced by the doped-ion type by affecting the ionic radius, valence state, and configuration of the dopant. The calcination temperature and doping concentration, which change the weight fractions of the anatase phase (fA), the Brunauer-Emmett-Teller surface area (SBET), and the energy band gap (Eg) of the catalyst, also affect the photocatalytic activity. When TiO2 is doped with ions, SBET decreases and Eg becomes narrower. The photocatalytic activities of TiO2 for toluene removal increase after doping with Ag(+), Al(3+), Cu(2+), Fe(3+), Mn(2+), Ni(2+), V(5+), and Zn(2+). Moreover, the 1.0% Fe(3+)-doped TiO2 nanotubes calcined at 550 °C have the highest catalytic activity, with a toluene removal efficiency of 70.7%.

  18. Structure and high photocatalytic activity of (N, Ta)-doped TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Le, N. T. H.; Thanh, T. D.; Pham, V.-T.; Phan, T. L.; Lam, V. D.; Manh, D. H.; Anh, T. X.; Le, T. K. C.; Thammajak, N.; Hong, L. V.; Yu, S. C.

    2016-10-01

    A hydrothermal method was used to prepare three nano-crystalline samples of TiO2 (S1), N-doped TiO2 (S2), and (N, Ta)-codoped TiO2 (S3) with average crystallite sizes (D) of 13-25 nm. X-ray diffraction studies confirmed a single phase of the samples with a tetragonal/anatase structure. A slight increase in the lattice parameters was observed when N and/or Ta dopants were doped into the TiO2 host lattice. Detailed analyses of extended X-ray absorption spectra indicated that N- and/or Ta-doping into TiO2 nanoparticles influenced the co-ordination number and radial distance (R) of Ti ions in the anatase structure. Concerning their absorption spectra, (N, Ta)-doping narrowed the band gap (Eg) of TiO2 from 3.03 eV for S1 through 2.94 eV for S2 to 2.85 eV for S3. Such results revealed the applicability of these nanoparticles in the photocatalytic field working in the ultraviolet (UV)-visible region. Among these, photocatalytic activity of S3 was the strongest. By using S3 as a catalyst powder, the degradation efficiency of methylene blue solution was about 99% and 93% after irradiation of UV-visible light for 75 min and visible-light for 180 min, respectively.

  19. Equilibration Kinetics and Chemical Diffusion of Indium-Doped TiO2.

    PubMed

    Nowotny, Janusz; Alim, Mohammad A

    2015-04-30

    The present work reports the gas/solid equilibration kinetics for In-doped TiO2 (0.4 atom % In) at elevated temperatures (1023-1273 K) in the gas phase of controlled oxygen activity [10(-13) Pa < p(O2) < 10(5) Pa]. Thus, the determined chemical diffusion coefficient is considered in terms of a microdiffusion coefficient that is reflective of the transport kinetics within very narrow ranges of oxygen activities. In analogy to pure TiO2, the chemical diffusion coefficient for In-doped TiO2 exhibits a maximum at the n-p transition point. The activation energy of the chemical diffusion exhibits a decrease with temperature from 200 kJ/mol at 1023 K to an insignificant value at 1273 K. This effect is reflective of a segregation-induced electrical potential barrier blocking the transport of defects. The absolute value of the chemical diffusion coefficient for In-doped TiO2 is larger from that of pure TiO2 by a factor of approximately 10. The effect of indium on the diffusion rate is considered in terms of the associated concentration of oxygen vacancies, which are formed in order to satisfy the charge neutrality for In-doped TiO2.

  20. Comparative study of (N, Fe) doped TiO2 photocatalysts

    NASA Astrophysics Data System (ADS)

    Larumbe, S.; Monge, M.; Gómez-Polo, C.

    2015-02-01

    The effect of N and Fe doping on the structural, optical, photocatalytic and magnetic properties of TiO2 nanoparticles is analyzed. Undoped, N and Fe doped TiO2 nanoparticles were synthesized by sol-gel method. Titanium tetraisopropoxide (TTIP) was used as the alkoxyde precursor and iron (III) nitrate and urea were the employed precursors to obtain Fe and N doped TiO2 nanoparticles, respectively. Differential Scanning Calorimetry (DSC) and Thermogravimetrical Analysis (TGA) enabled the analysis of the thermal decomposition process and the final calcination temperature. X-Ray Diffraction patterns of the calcined nanoparticles displayed a monophasic anatase structure in all the samples with mean crystallite diameter around 4-6 nm. The introduction of Fe or N induced a red-shift in the absorption spectra. Such a red-shift is characterized by a decrease in the band-gap energy and the occurrence of an absorption (Urbach) tail in the visible region. Finally, the photocatalytic efficiency was evaluated under UV and Visible light, obtaining an improvement of the kinetic constants in the nitrogen doped TiO2 nanoparticles with respect to undoped and Fe doped TiO2. The differences in the photocatalytic response under Fe and N doping are also analyzed in terms of the magnetic response of the analyzed photocatalysts.

  1. Synthesis and characterization of Ag deposited TiO2 particles by laser ablation in water

    NASA Astrophysics Data System (ADS)

    Liu, C. H.; Hong, M. H.; Zhou, Y.; Chen, G. X.; Saw, M. M.; Hor, A. T. S.

    2007-12-01

    Ag deposited TiO2 (Ag/TiO2) particles were synthesized by laser ablation of silver and titanium targets in de-ionized (DI) water. Post-annealing makes the structure stable and the materials change to crystalline state. It is a new approach to form Ag/TiO2 particles with a simple system and non-toxic materials. TiO2 particles with size from 20 to 30 nm coated with silver nano-clusters were observed. The silver nano-clusters can enhance the absorption capability of TiO2 photocatalysts. UV-vis spectrum analysis shows that there is a strong absorption peak at around 400 nm. It is attributed to Ag nanoparticles surface plasmon resonance (SPR) effect. This effect helps to improve the spectral characteristics of TiO2 nanoparticles with its absorption spectra shifted to a longer wavelength region. From the above properties, Ag/TiO2 nanoparticles would have new potential applications in photocatalyst and photo-anode.

  2. Effects of Mn doping on surface enhanced Raman scattering properties of TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Xue, Xiangxin; Ji, Wei; Mao, Zhu; Li, Zhishi; Ruan, Weidong; Zhao, Bing; Lombardi, John R.

    2012-09-01

    TiO2 and Mn-doped TiO2 (1%, 3% and 5%) nanoparticles (NPs) were synthesized by a sol-hydrothermal method for surface-enhanced Raman spectroscopy study. When using the 4-mercaptobenzoic acid (4-MBA) as the probing molecule, optimum SERS signals were observed on the Mn-TiO2 (3%) samples. On the 3% Mn doped TiO2 substrate, 4-MBA molecules exhibit a higher SERS intensity by a factor of six as compared with the native enhancement of 4-MBA adsorbed on pure TiO2 NPs. The possible mechanism for the phenomena is also discussed. This study opens up a new dimension for the family of SERS substrates.

  3. Mussel-Directed Synthesis of Nitrogen-Doped Anatase TiO2.

    PubMed

    Xie, Jingjing; Xie, Hao; Su, Bao-Lian; Cheng, Yi-Bing; Du, Xiaodong; Zeng, Hui; Wang, Menghu; Wang, Weimin; Wang, Hao; Fu, Zhengyi

    2016-02-24

    Structure-forming processes leading to biominerals are well worth learning in pursuit of new synthetic techniques. Strategies that attempt to mimic nature in vitro cannot replace an entire complex natural organism, requiring ingenuity beyond chemists' hands. A "bioprocess-inspired synthesis" is demonstrated for fabrication of N-doped TiO2 materials at ambient temperature by direct implantation of precursor into living mussels. The amorphous precursor transforms into N-doped anatase TiO2 with a hierarchical nanostructure. Synthetic TiO2 exhibits high phase stability and enhanced visible-light photocatalytic activity as a result of modifications to its band gap during in vivo mineralization. Intracellular proteins were found to be involved in TiO2 mineralization. Our findings may inspire material production by new synthetic techniques, especially under environmentally benign conditions.

  4. Eco-friendly synthesis of TiO2, Au and Pt doped TiO2 nanoparticles for dye sensitized solar cell applications and evaluation of toxicity

    NASA Astrophysics Data System (ADS)

    Gopinath, K.; Kumaraguru, S.; Bhakyaraj, K.; Thirumal, S.; Arumugam, A.

    2016-04-01

    Driven by the demand of pure TiO2, Au and Pt doped TiO2 NPs were successfully synthesized using Terminalia arjuna bark extract. The eco-friendly synthesized NPs were characterized by UV-Vis-DRS, ATR-FT-IR, PL, XRD, Raman, SEM with EDX and TEM analysis. The synthesized NPs were investigation for dye sensitized solar cell applications. UV-Vis-Diffused Reflectance Spectra clearly showed that the expected TiO2 inter band absorption below 306 nm, incorporation of gold shows surface plasma resonant (SPR) near 555 nm and platinum incorporated TiO2 NPs shows absorbance at 460 nm. The energy conversion efficiency for Au doped TiO2 NPs when compared to pure and Pt doped TiO2 NPs. In addition to that, Au noble metal present TiO2 matrix and an improve open-circuit voltage (Voc) of DSSC. Synthesized NPs was evaluated into antibacterial and antifungal activities by disk diffusion method. It is observed that NPs have not shown any activities in all tested bacterial and fungal strains. In this eco-friendly synthesis method to provide non toxic and environmental friendly nanomaterials can be used for solar energy device application.

  5. Controlled synthesis and photocatalysis of sea urchin-like Fe3O4@TiO2@Ag nanocomposites

    NASA Astrophysics Data System (ADS)

    Zhao, Yilin; Tao, Chengran; Xiao, Gang; Wei, Guipeng; Li, Linghui; Liu, Changxia; Su, Haijia

    2016-02-01

    Based on the synergistic photocatalytic activities of nano-sized TiO2 and Ag, as well as the magnetic properties of Fe3O4, a sea urchin-like Fe3O4@TiO2@Ag nanocomposite (Fe3O4@TiO2@Ag NCs) is controllably synthesized with tunable cavity size, adjustable shell layer of TiO2 nanofiber, higher structural stability and larger specific surface area. Here, Fe3O4@TiO2@Ag NCs are obtained with Fe3O4 as the core and nanofiber TiO2/Fe3O4/Ag nanoheterojunctions as the shell; and Ag nanoparticles with diameter of approximately 4 nm are loaded both on TiO2 nanofibers and inside the cavities of sea urchin-like Fe3O4@TiO2 nanocomposites uniformly. Ag nanoparticles lead to the production of more photogenerated charges in the TiO2/Fe3O4/Ag heterojunction via LSPR absorption, and enhance the band-gap absorption of TiO2, while the Fe3O4 cocatalyst provides the active sites for oxygen reduction by the effective transfer of photogenerated electrons to oxygen. So the photocatalytic performance is improved due to the synergistic effect of TiO2/Fe3O4/Ag nanoheterojunctions. As photocatalysts under UV and visible irradiation, the as-synthesized nanocomposites display enhanced photocatalytic and recycling properties for the degradation of ampicillin. Moreover, they present better broad-spectrum antibiosis under visible irradiation. The enhanced photocatalytic activity and excellent chemical stability, in combination with the magnetic recyclability, makes this multifunctional nanostructure a promising candidate for antibiosis and remediation in aquatic environmental contamination in the future.Based on the synergistic photocatalytic activities of nano-sized TiO2 and Ag, as well as the magnetic properties of Fe3O4, a sea urchin-like Fe3O4@TiO2@Ag nanocomposite (Fe3O4@TiO2@Ag NCs) is controllably synthesized with tunable cavity size, adjustable shell layer of TiO2 nanofiber, higher structural stability and larger specific surface area. Here, Fe3O4@TiO2@Ag NCs are obtained with Fe3O4 as the

  6. Electronic, optical and photocatalytic behavior of Mn, N doped and co-doped TiO2: Experiment and simulation

    NASA Astrophysics Data System (ADS)

    Zhao, Ya Fei; Li, Can; Lu, Song; Liu, Ru Xi; Hu, Ji Yuan; Gong, Yin Yan; Niu, Leng Yuan

    2016-03-01

    The crystal phase structure, surface morphology, chemical states and optical properties of Mn, N mono-doped and co-doped TiO2 nanoparticles were investigated by X-ray powder diffractometry, Raman spectra, scanning electron microscopy, X-ray photoelectron spectroscopy and UV-vis diffuse reflectance spectroscopy. Meanwhile, geometry structures, formation energies, electronic and optical properties of all systems have been also analyzed by density functional theory. The results showed that the band gap values and the carrier mobility in the valence band, conduction band and impurity levels have a synergetic influence on the visible-light absorption and photocatalytic activity of the doped TiO2. The number and the carrier mobility of impurity level jointly influence the photocatalytic activity of catalyst under visible-light. Especially, the photocatalytic activity of Mn-2N co-doped TiO2 beyond three-fold than that of pure TiO2 under visible-light.

  7. QD co-sensitized and nitrogen doped TiO2 nanocomposite for photoelectrochemical hydrogen generation

    NASA Astrophysics Data System (ADS)

    Hensel, Jennifer; Canin, Max; Zhang, Jin Z.

    2010-08-01

    Metal oxides are promising for solar energy conversion applications since they are less expensive and easier to produce than conventional single crystal silicon. In this paper we focused on CdSe and CdS quantum dot (QD) co-sensitized and nitrogen doped TiO2 (N:TiO2) nanocomposite photoanodes for photoelectrochemical (PEC) water splitting for hydrogen generation. PEC, UV-vis and scanning electron microscopy (SEM) characterizations of the nanostructured films were carried out. The QD co-sensitized and N-doped TiO2 photoanodes exhibits increased photocurrent compared to cosensitized TiO2 without N-doping This is tentatively attributed to enhanced hole transport by oxygen vacancy states that are increased upon nitrogen doping. The enhanced hole transport facilitates overall charge transfer and transport and thereby results in improved photocurrent.

  8. Modulating TiO2 photocatalyst by Al doping: Density functional theory approach

    NASA Astrophysics Data System (ADS)

    Zhao, Ya Fei; Li, Can; Lu, Song; Gong, Yin Yan; Niu, Leng Yuan; Liu, Xin Juan

    2016-06-01

    In this work, systematic study of the thermal stability, crystal structure and electronic properties of Al doped TiO2 were studied by the first principles calculations. The results showed that Al atoms preferentially occupying the interstitial site under Ti-rich condition, but substituting the Ti atom under O-rich condition. In contrast to pure TiO2, the values of VBM and CBM are reduced for Al substituting Ti doped mode, but increased for Al interstitial atom doped mode. Thus, we can modulate the preparation condition and dosage concentration for preparing the optimal photocatalyst.

  9. Characterization and improved solar light activity of vanadium doped TiO2/diatomite hybrid catalysts.

    PubMed

    Wang, Bin; Zhang, Guangxin; Leng, Xue; Sun, Zhiming; Zheng, Shuilin

    2015-03-21

    V-doped TiO2/diatomite composite photocatalysts with different vanadium concentrations were synthesized by a modified sol-gel method. The diatomite was responsible for the well dispersion of TiO2 nanoparticles on the matrix and consequently inhibited the agglomeration. V-TiO2/diatomite hybrids showed red shift in TiO2 absorption edge with enhanced absorption intensity. Most importantly, the dopant energy levels were formed in the TiO2 bandgap due to V(4+) ions substituted to Ti(4+) sites. The 0.5% V-TiO2/diatomite photocatalyst displayed narrower bandgap (2.95 eV) compared to undoped sample (3.13 eV) and other doped samples (3.05 eV) with higher doping concentration. The photocatalytic activities of V doped TiO2/diatomite samples for the degradation of Rhodamine B under stimulated solar light illumination were significantly improved compared with the undoped sample. In our case, V(4+) ions incorporated in TiO2 lattice were responsible for increased visible-light absorption and electron transfer to oxygen molecules adsorbed on the surface of TiO2 to produce superoxide radicals ˙O2(-), while V(5+) species presented on the surface of TiO2 particles in the form of V2O5 contributed to e(-)-h(+) separation. In addition, due to the combination of diatomite as support, this hybrid photocatalyst could be separated from solution quickly by natural settlement and exhibited good reusability.

  10. Characterization and improved solar light activity of vanadium doped TiO2/diatomite hybrid catalysts.

    PubMed

    Wang, Bin; Zhang, Guangxin; Leng, Xue; Sun, Zhiming; Zheng, Shuilin

    2015-03-21

    V-doped TiO2/diatomite composite photocatalysts with different vanadium concentrations were synthesized by a modified sol-gel method. The diatomite was responsible for the well dispersion of TiO2 nanoparticles on the matrix and consequently inhibited the agglomeration. V-TiO2/diatomite hybrids showed red shift in TiO2 absorption edge with enhanced absorption intensity. Most importantly, the dopant energy levels were formed in the TiO2 bandgap due to V(4+) ions substituted to Ti(4+) sites. The 0.5% V-TiO2/diatomite photocatalyst displayed narrower bandgap (2.95 eV) compared to undoped sample (3.13 eV) and other doped samples (3.05 eV) with higher doping concentration. The photocatalytic activities of V doped TiO2/diatomite samples for the degradation of Rhodamine B under stimulated solar light illumination were significantly improved compared with the undoped sample. In our case, V(4+) ions incorporated in TiO2 lattice were responsible for increased visible-light absorption and electron transfer to oxygen molecules adsorbed on the surface of TiO2 to produce superoxide radicals ˙O2(-), while V(5+) species presented on the surface of TiO2 particles in the form of V2O5 contributed to e(-)-h(+) separation. In addition, due to the combination of diatomite as support, this hybrid photocatalyst could be separated from solution quickly by natural settlement and exhibited good reusability. PMID:25497036

  11. Fe doped TiO2-graphene nanostructures: synthesis, DFT modeling and photocatalysis

    NASA Astrophysics Data System (ADS)

    Farhangi, Nasrin; Ayissi, Serge; Charpentier, Paul A.

    2014-08-01

    In this work, Fe-doped TiO2 nanoparticles ranging from a 0.2 to 1 weight % were grown from the surface of graphene sheet templates containing -COOH functionalities using sol-gel chemistry in a green solvent, a mixture of water/ethanol. The assemblies were characterized by a variety of analytical techniques, with the coordination mechanism examined theoretically using the density functional theory (DFT). Scanning electron microscopy and transmission electron microscopy images showed excellent decoration of the Fe-doped TiO2 nanoparticles on the surface of the graphene sheets >5 nm in diameter. The surface area and optical properties of the Fe-doped photocatalysts were measured by BET, UV and PL spectrometry and compared to non-graphene and pure TiO2 analogs, showing a plateau at 0.6% Fe. Interactions between graphene and Fe-doped anatase TiO2 were also studied theoretically using the Vienna ab initio Simulation Package based on DFT. Our first-principles theoretical investigations validated the experimental findings, showing the strength in the physical and chemical adsorption between the graphene and Fe-doped TiO2. The resulting assemblies were tested for photodegradation under visible light using 17β-estradiol (E2) as a model compound, with all investigated catalysts showing significant enhancements in photocatalytic activity in the degradation of E2.

  12. Improved efficiency of dye-sensitized solar cells applied with nanostructured N-F doped TiO2 electrode

    NASA Astrophysics Data System (ADS)

    Yang, Shuming; Xue, Hongbin; Wang, Hongjun; Kou, Huizhi; Wang, Jichao; Zhu, Guanghui

    2012-07-01

    Dye-sensitized solar cells (DSSCs) were fabricated with N-F-doped TiO2 electrodes. The XRD pattern of the N-F-doped TiO2 is almost the same as that of pure TiO2, showing that N and F doping has little influence on the formation of anatase titania. The influence of dopant N and F on band energetics and photoelectrochemical properties of nanostructured TiO2 electrodes were investigated. Compared with pure TiO2 electrodes, the Efb of N-F-doped TiO2 electrodes shifted a little in electrolytes containing LiClO4. However the total trap densities were remarkably decreased as TiO2 electrodes were doped with N and F. Finally the N-F-doped TiO2 electrodes were sensitized with N3 and their photoelectrochemical properties were studied. Experimental results showed that the photoelectric conversion efficiency of N3 sensitized N-F-doped TiO2 electrodes was 8.61% under irradiation of 100 mW cm-2 white light, about 17.1% higher than that of a pure TiO2 electrode.

  13. First-principles study of Cu-doping and oxygen vacancy effects on TiO2 for water splitting

    NASA Astrophysics Data System (ADS)

    Zhang, Huamin; Yu, Xiaohui; McLeod, John A.; Sun, Xuhui

    2014-09-01

    We investigate the electronic structures and optical properties of Cu-doped TiO2-x using density functional theory (DFT) calculations. We find that Cu doping creates an empty impurity band lying above the valence band of TiO2, which bridges most of the gap between the valence band maximum and conduction band minimum in undoped TiO2. The results also show that oxygen vacancies produce a similar effect and that Cu-doping can increase the stability of oxygen vacancies. We propose that Cu-doped TiO2-x improves light harvesting and could be a promising visible-light photocatalyst.

  14. Antibacterial ability and osteogenic activity of porous Sr/Ag-containing TiO2 coatings.

    PubMed

    He, Xiaojing; Zhang, Xiangyu; Bai, Long; Hang, Ruiqiang; Huang, Xiaobo; Qin, Lin; Yao, Xiaohong; Tang, Bin

    2016-01-01

    Implant-associated infection and poor osseointegration remains a major clinical challenge in Ti-based implant materials. A versatile strategy to endow Ti-based implants with long-term antibacterial ability as well as better osteogenic activity is highly desirable for high quality implantation. Strontium (Sr) has been shown to be a significant element to favor bone growth by promoting new bone formation and inhibiting bone resorption. In this study, a novel duplex-treatment technique encompassing magnetron sputtering with micro-arc oxidation is utilized to fabricate porous Sr/Ag-containing TiO2 coatings loaded with different concentrations of Ag and Sr. All coatings are porous with pore size less than 5 µm. Ag is primarily distributed homogeneously inside the pores, and the concentrations of Ag in Sr/Ag-containing TiO2 coatings with low and high Ag contents are 0.40 at.% and 0.83 at.% respectively. We have demonstrated that this kind of coating displays long-lasting antibacterial ability even up to 28 d due to the incorporation of Ag. Further, Sr/Ag-containing TiO2 coatings with optimum Ag and Sr contents revealed good cytocompatibility, enhanced osteoblast spreading and osseointegration, which stemmed primarily from the synergistic effect exerted by the porous surface topography and the bioactive element Sr. However, this study has also identified, for the first time, that proper addition of Ag would further facilitate osteogenic effects. Besides, Sr may be able to alleviate the potential cytotoxic effect of excessive Ag. Thus, integration of optimum functional elements Ag and Sr into Ti-based implant materials would be expected to expedite osseointegration while simultaneously sustaining long-term antibacterial activity, which would provide new insights for relevant fundamental investigations and biomedical applications. PMID:27508428

  15. Effect of sulfur doped TiO2 on photovoltaic properties of dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Seo, Hyunwoong; Nam, Sang-Hun; Itagaki, Naho; Koga, Kazunori; Shiratani, Masaharu; Boo, Jin-Hyo

    2016-07-01

    In a dye-sensitized solar cell (DSC), a nano-porous semiconductor layer plays an important role in the performance. It determines open-circuit voltage and it affects the dye adsorption capacity and charge transfer, which are closely associated with photocurrent and overall performance. TiO2 is the most proper material for nano-porous layer since the first development of DSCs. This work focuses on the enhancement of TiO2 by doping. Sulfur (S) doping enhances charge transfer and the photoconversion of TiO2. Therefore, the increase in photocurrent and efficiency is expected by S doping. S is doped into TiO2 by hydrolysis method. The amount of S is varied and their photo-responses are verified. The most effective S doped TiO2 is applied to DSCs. Overall performance of DSC is enhanced by the addition of S doped TiO2. Especially, the photocurrent is much increased by the improvement on charge transfer, electron lifetime, and photo-conversion. The photovoltaic properties of DSCs are investigated with various ratios of undoped and S doped TiO2. Finally, a DSC based on undoped and S doped TiO2 ratio of 1:1 has the highest efficiency, better than that of a standard DSC based on undoped TiO2. [Figure not available: see fulltext.

  16. Synthesis and photocatalytic activities of Nd-doped TiO2 mesoporous microspheres

    NASA Astrophysics Data System (ADS)

    Liu, Xijian; Sun, Yangang; Wang, Yeying; Zhang, Lijuan; Lu, Jie

    2016-11-01

    Nd-doped TiO2 mesoporous microspheres with possessing regular micro/nanostructure were synthesized by a simple and facile method. The structure and optical properties of the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N2 adsorption-desorption isotherms and UV-Visible absorbance spectroscopy. It was revealed that Nd-doped TiO2 mesoporous microspheres are composed of primary nanoparticles with a particle size of ˜25nm. The photocatalytic activities of all the samples were evaluated by degradation methyl orange (MO) in aqueous solution as a model reaction under xenon lamp light irradiation. The results showed that the doped samples demonstrated a higher photocatalytic activity than TiO2 mesoporous microspheres, and the MO of 10mg/mL almost could be completely degraded by the Nd-doped TiO2 mesoporous sample (the dosage of Nd salt to TiO2 is 6%) under xenon lamp light irradiation within 1h.

  17. Raman spectral analysis of TiO2 thin films doped with rare-earth samarium.

    PubMed

    Yang, Chang-Hu; Ma, Zhong-Quan

    2012-08-01

    TiO(2) thin films doped with rare-earth samarium were prepared on a quartz plate by the sol-gel/spin-coating technique. The samples were annealed at 700 °C to 1100 °C, and the Raman spectra of the samples were obtained. Analyses of Raman spectra show that samarium doping can inhibit the anatase-rutile phase transition. Samarium doping can refine grains of TiO(2) thin films and increase the internal stress, thereby preventing lattice vibration. Nanocrystalline TiO(2) thin films obviously show the phonon confinement effect, i.e., the blueshift of characteristic Raman peak and full width at half-height increase, and the peak shapes asymmetrically broaden with a decrease in the grain sizes of the samples.

  18. Effect of silver-doping on the crystal structure, morphology and photocatalytic activity of TiO2 nanofibers

    NASA Astrophysics Data System (ADS)

    Barakat, N. A. M.; Kim, H. Y.

    2012-09-01

    In this study, effect of sliver-doping on the crystal structure, the nanofibrous morphology and the photocatalytic activity of titanium oxide nanofibers have been investigated. Silver-doped TiO2 nanofibers having different silver contents were prepared by calcination of electrospun nanofiber mats consisting of silver nitrate, titanium isopropoxide and poly(vinyl acetate) at 600 °C. The results affirmed formation of silver-doped TiO2 nanofibers composed of anatase and rutile when the silver nitrate content in the original electrospun solution was more than 3 wt%. The rutile phase content was directly proportional with the AgNO3 concentration in the electrospun solution. Negative impact of the silver-doping on the nanofibrous morphology was observed as increase the silver content caused to decrease the aspect ratio, i.e. producing nanorods rather nanofibers. However, silver-doping leads to modify the surface roughness. Study of the photocatalytic degradation of methylene blue dye clarified that increase the silver content strongly enhances the dye oxidation process.

  19. Synthesis and Modification of Zn-doped TiO2 Nanoparticles for the Photocatalytic Degradation of Tetracycline.

    PubMed

    Pang, Shuo; Huang, Ji-Guo; Su, Yun; Geng, Bo; Lei, Su-Yuan; Huang, Yu-Ting; Lyu, Cong; Liu, Xing-Juan

    2016-09-01

    The synthesis of Zn-doped TiO2 nanoparticles by solgel method was investigated in this study, as well as its modification by H2 O2 . The catalyst was characterized by transmission electron microscopy, X-ray diffraction, Brunauer-Emmett-Teller, UV-visible reflectance spectra and X-ray photoelectron spectroscopy (XPS). The results indicated that doping Zn into TiO2 nanoparticles could inhibit the transformation from anatase phase to rutile phase. Zn existed as the second valence oxidation state in the Zn-doped TiO2 . Zn-doped TiO2 that was synthesized by 5% Zn doping at 450°C exhibited the best photocatalytic activity. Then, the H2 O2 modification further enhanced the photocatalytic activity. Zn doping and H2 O2 modifying narrowed the band gap and efficiently increased the optical absorption in visible region. The optimal degradation rate of tetracycline by Zn-doped TiO2 and H2 O2 modified Zn-doped TiO2 was 85.27% and 88.14%. Peroxide groups were detected in XPS analysis of H2 O2 modified Zn-doped TiO2 , favoring the adsorption of visible light. Furthermore, Zn-doped TiO2 modified by H2 O2 had relatively good reusability, exhibiting a potential practical application for tetracycline's photocatalytic degradation.

  20. Photoluminescence studies of nitrogen-doped TiO2 powders prepared by annealing with urea

    NASA Astrophysics Data System (ADS)

    Kawai, T.; Kishimoto, Y.; Kifune, K.

    2012-11-01

    Photoluminescence and excitation spectra have been investigated for undoped and nitrogen-doped TiO2 powders at low temperatures. A broad luminescence band peaking at 2.25 eV is observed in the undoped TiO2 powders. The 2.25 eV luminescence band exhibits a sharp rise from 3.34 eV in the excitation spectrum reflecting the fundamental absorption edge of anatase TiO2. On the other hand, the N-doped TiO2 powders obtained by annealing with urea at 350 and 500°C exhibit broad luminescence bands around 2.89 and 2.63 eV, respectively. The excitation spectra for these luminescence bands rise from the lower energy side of the fundamental absorption edge of anatase TiO2. The origin of the luminescence bands and N-related energy levels formed in the band-gap of TiO2 are discussed.

  1. Preparation of magnetic Fe3O4/TiO2/Ag composite microspheres with enhanced photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Zhang, Li; Wu, Zheng; Chen, Liangwei; Zhang, Lianjie; Li, Xuelian; Xu, Haifeng; Wang, Hongyan; Zhu, Guang

    2016-02-01

    The novel three-component Fe3O4/TiO2/Ag composite mircospheres were prepared via a facile chemical deposition route. The Fe3O4/TiO2 mircospheres were first prepared by the solvothermal method, and then Ag nanoparticles were anchored onto the out-layer of TiO2 by the tyrosine-reduced method. The as-prepared magnetic Fe3O4/TiO2/Ag composite mircospheres were applied as photocatalysis for the photocatalytic degradation of methylene blue. The results indicate that the photocatalytic activity of Fe3O4/TiO2/Ag composite microspheres is superior to that of Fe3O4/TiO2 due to the dual effects of the enhanced light absorption and reduction of photoelectron-hole pair recombination in TiO2 with the introduction of Ag NPs. Moreover, these magnetic Fe3O4/TiO2/Ag composite microspheres can be completely removed from the dispersion with the help of magnetic separation and reused with little or no loss of catalytic activity.

  2. Fe-Doped TiO2 Thin Films for CO Gas Sensing

    NASA Astrophysics Data System (ADS)

    Kumar, Mukesh; Kumar, Dinesh; Gupta, Anil Kumar

    2015-01-01

    Fe-doped TiO2 thin films were prepared by the sol-gel technique on silicon substrate. The thin films were evaluated for detection of carbon monoxide (CO) gas at room temperature. The TiO2 films were characterized by x-ray diffraction (XRD) analysis, field-emission scanning electron microscopy, and ultraviolet-visible (UV) spectroscopy. The characterization revealed that, as the doping concentration was increased, the grain size decreased. XRD patterns revealed the phase transition from rutile to anatase with addition of different percentages (weight/volume) of Fe. The bandgap determined from UV spectroscopy was found to decrease with increasing Fe doping concentration. Fe doping was observed to have a significant effect on the resistivity of the doped TiO2 thin films. The gas sensing behavior of the films was studied by exposure to different concentrations of CO gas with measurement of the electrical resistance. It was observed that Fe-doped (7% weight/volume) TiO2 exhibited high sensitivity and good response/recovery on exposure to CO gas in the concentration range from 100 ppm to 900 ppm in Ar.

  3. Formation of hydroxyl radicals and kinetic study of 2-chlorophenol photocatalytic oxidation using C-doped TiO2, N-doped TiO2, and C,N Co-doped TiO2 under visible light.

    PubMed

    Ananpattarachai, Jirapat; Seraphin, Supapan; Kajitvichyanukul, Puangrat

    2016-02-01

    This work reports on synthesis, characterization, adsorption ability, formation rate of hydroxyl radicals (OH(•)), photocatalytic oxidation kinetics, and mineralization ability of C-doped titanium dioxide (TiO2), N-doped TiO2, and C,N co-doped TiO2 prepared by the sol-gel method. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and UV-visible spectroscopy were used to analyze the titania. The rate of formation of OH(•) for each type of titania was determined, and the OH-index was calculated. The kinetics of as-synthesized TiO2 catalysts in photocatalytic oxidation of 2-chlorophenol (2-CP) under visible light irradiation were evaluated. Results revealed that nitrogen was incorporated into the lattice of titania with the structure of O-Ti-N linkages in N-doped TiO2 and C,N co-doped TiO2. Carbon was joined to the Ti-O-C bond in the C-doped TiO2 and C,N co-doped TiO2. The 2-CP adsorption ability of C,N co-doped TiO2 and C-doped TiO2 originated from a layer composed of a complex carbonaceous mixture at the surface of TiO2. C,N co-doped TiO2 had highest formation rate of OH(•) and photocatalytic activity due to a synergistic effect of carbon and nitrogen co-doping. The order of photocatalytic activity per unit surface area was the same as that of the formation rate of OH(•) unit surface area in the following order: C,N co-doped TiO2 > C-doped TiO2 > N-doped TiO2 > undoped TiO2.

  4. Zirconium doped TiO2 thin films deposited by chemical spray pyrolysis

    NASA Astrophysics Data System (ADS)

    Juma, A.; Oja Acik, I.; Oluwabi, A. T.; Mere, A.; Mikli, V.; Danilson, M.; Krunks, M.

    2016-11-01

    Chemical spray pyrolysis (CSP) is a flexible deposition technique that allows for mixing of the precursor solutions in different proportions suitable for doping thin films. The CSP method was used to dope TiO2 thin films with Zr by adding zirconium(IV) acetylacetonate into a solution of titanium(IV) isopropoxide in ethanol stabilized by acetylacetone at [Zr]/[Ti] of 0, 5, 10 and 20 at%. The Zr-doped TiO2 thin films were uniform and homogeneous showing much smaller grains than the undoped TiO2 films. Zr stabilized the anatase phase to temperatures above 800 °C depending on Zr concentration in the spray solution. The concentration of Zr determined by XPS was 6.4 at% for the thin film deposited from the 20 at% solution. According to AFM studies, Zr doping decreased the root mean square roughness of TiO2 film from 5.9 to 1.1 nm. An XRD study of samples with the highest Zr amount showed the ZrTiO4 phase started forming after annealing at 800 °C. The optical band gap for TiO2 decreased from 3.3 eV to 3.0 eV after annealing at 800 °C but for the TiO2:Zr(20) film it remained at 3.4 eV. The dielectric constant increased by more than four times with Zr-doping and this was associated with the change in the bond formations caused by substitution of Ti by Zr in the lattice.

  5. [Performance of solar/S-doped TiO2 on the decomposition of bisphenol A].

    PubMed

    Liu, Cheng; Chen, Wei; Tao, Hui; Lin, Tao

    2009-06-15

    Removal efficiency and influencing factors of bisphenol A by the combined process of solar irradiation and S-doped TiO2 were studied in detail, in which S-doped TiO2 photo-catalyst with high activity was prepared by acid catalyzed hydrolysis method using thiourea as sulfur source. Results showed that bisphenol A could be more effectively oxidized by the solar/S-doped TiO2 process than by solar/TiO2 process, whose removal effect were 79% and 49% after 30 min's irradiation, respectively. Pseudo-first-order model could be used to simulate the oxidation process in which the degradation rate coefficients were independent of the initial concentration of bisphenol A. Degradation rate could be greatly affected by the concentration of H2O2, and the optimum concentration for the system of solar/S-doped TiO2 was found to be 20 mg/L, which was 5 mg/L higher than that of solar/TiO2 system. Lower water pH favored the degradation of bisphenol A, whose degradation rate coefficients at pH 5.5 were about 50% higher than that at pH 8.5. Humic acids decreased both the degradation rate of the two processes, and the influence could be fitted by second-order equation. In addition, solar/S-doped TiO2 process was more easily affected, for the humic acids could not only compete with molecular bisphenol-A for radicals but also adsorb part of visible sunlight which can excite radical with TiO2.

  6. Paramagnetic behavior of Co doped TiO2 nanocrystals controlled by self-purification mechanism

    NASA Astrophysics Data System (ADS)

    Anitha, B.; Khadar, M. Abdul; Banerjee, Alok

    2016-07-01

    Doping in nanocrystals is a challenging process because of the self- purification mechanism which tends to segregate out the dopants resulting in a greater dopant concentration near the surface than at the interior of nanocrystals. In the present work nanocrystals of TiO2 doped with different atom % of Co were synthesized by peroxide gel method. XRD analysis confirmed the tetragonal anatase structure and HRTEM images showed the rod-like morphology of the samples. Raman modes of anatase phase of TiO2 along with weak intensity peaks of Co3O4 for higher Co dopant concentrations were observed for the samples. EPR measurements revealed the presence of cobalt in +2 oxidation state in the TiO2 matrix. SQUID measurements indicated paramagnetic behavior of the Co doped TiO2 nanocrystals. The paramagnetic behavior is attributed to an increased concentration of Co2+ ions and an increased presence of Co3O4 phase near the surface of the TiO2 nanocrystals due to self-purification mechanism.

  7. Electronic and optical properties study on Fesbnd B co-doped anatase TiO2

    NASA Astrophysics Data System (ADS)

    Li, Xuechao; Shi, Jianhao; Chen, Hao; Wan, Rundong; Leng, Chongyan; Lei, Ying

    2016-09-01

    We investigate the density of states and optical properties for Fe, 2B and (Fe, 2B) doped TiO2 with DFT calculations. The calculated results reveal mono-doping introduces midgap states which are half-occupied and easy to become the recombination centers of charge carriers, thus inhibiting the enhancement of photocatalystic activity. The coupling of 2p-3d states in the (Fe, 2B) compensated co-doped TiO2 makes gap states couple with the valence bands edge, thus greatly causing the band gap narrowing and higher visible light absorption. Moreover, the gap states cannot become recombination centers of the photoexcited carriers, thus promoting the separation of electron-hole pairs, prolonging the lifetime of carriers. The analysis of electron density indicates more electrons from Fe transfer to adjacent B, realizing the charge compensation and forming a stronger Fesbnd B bond. Therefore, the (Fe, 2B) compensated co-doped TiO2 exhibits the higher visible-light photocatalystic activity than those of pure and solely doped TiO2.

  8. Preparation and photoelectrocatalytic performance of N-doped TiO2/NaY zeolite membrane composite electrode material.

    PubMed

    Cheng, Zhi-Lin; Han, Shuai

    2016-01-01

    A novel composite electrode material based on a N-doped TiO2-loaded NaY zeolite membrane (N-doped TiO2/NaY zeolite membrane) for photoelectrocatalysis was presented. X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-visible (UV-vis) and X-ray photoelectron spectroscopy (XPS) characterization techniques were used to analyze the structure of the N-doped TiO2/NaY zeolite membrane. The XRD and SEM results verified that the N-doped TiO2 nanoparticles with the size of ca. 20 nm have been successfully loaded on the porous stainless steel-supported NaY zeolite membrane. The UV-vis result showed that the N-doped TiO2/NaY zeolite membrane exhibited a more obvious red-shift than that of N-TiO2 nanoparticles. The XPS characterization revealed that the doping of N element into TiO2 was successfully achieved. The photoelectrocatalysis performance of the N-doped TiO2/NaY zeolite membrane composite electrode material was evaluated by phenol removal and also the effects of reaction conditions on the catalytic performance were investigated. Owing to exhibiting an excellent catalytic activity and good recycling stability, the N-doped TiO2/NaY zeolite membrane composite electrode material was of promising application for photoelectrocatalysis in wastewater treatment. PMID:26877029

  9. Preparation and photoelectrocatalytic performance of N-doped TiO2/NaY zeolite membrane composite electrode material.

    PubMed

    Cheng, Zhi-Lin; Han, Shuai

    2016-01-01

    A novel composite electrode material based on a N-doped TiO2-loaded NaY zeolite membrane (N-doped TiO2/NaY zeolite membrane) for photoelectrocatalysis was presented. X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-visible (UV-vis) and X-ray photoelectron spectroscopy (XPS) characterization techniques were used to analyze the structure of the N-doped TiO2/NaY zeolite membrane. The XRD and SEM results verified that the N-doped TiO2 nanoparticles with the size of ca. 20 nm have been successfully loaded on the porous stainless steel-supported NaY zeolite membrane. The UV-vis result showed that the N-doped TiO2/NaY zeolite membrane exhibited a more obvious red-shift than that of N-TiO2 nanoparticles. The XPS characterization revealed that the doping of N element into TiO2 was successfully achieved. The photoelectrocatalysis performance of the N-doped TiO2/NaY zeolite membrane composite electrode material was evaluated by phenol removal and also the effects of reaction conditions on the catalytic performance were investigated. Owing to exhibiting an excellent catalytic activity and good recycling stability, the N-doped TiO2/NaY zeolite membrane composite electrode material was of promising application for photoelectrocatalysis in wastewater treatment.

  10. Preparation of Fe-doped TiO2 nanoparticles immobilized on polyamide fabric

    NASA Astrophysics Data System (ADS)

    Zhang, Hui; Zhu, Hong

    2012-10-01

    A thin layer of nano-scaled Fe-doped TiO2 particles prepared by hydrothermal method is immobilized on the surface of polyamide 6 (PA6) fiber using tetrabutyl titanate as the precursor, ferric trichloride as the doping agent and chitosan as the dispersant agent. The morphology, crystal structure, thermal behavior, composition and chemical structure of PA6 fabric before and after treatments are characterized by means of scanning electron microscope, transmission electron microscope, X-ray diffraction, X-ray photoelectron spectroscopy, differential scanning calorimetry and thermal gravimetric analysis techniques. The properties of diffuse reflectance spectrum, tensile, air permeability, whiteness, yellowness and photocatalytic activity are also analyzed. It is found that the anatase phase Fe-doped TiO2 nanoparticles with crystal size of 12 nm or so are synthesized, and simultaneously grafted onto the fiber surface during the processing. Compared with the TiO2-coated fabric, the thermal stability of the Fe-doped TiO2-coated fabric changes a little. The absorption ability to ultraviolet (UV) rays and visible light is greatly improved. The breaking force and breaking elongation increase to some extent because of the shrinkage of fabric. The air permeability decreases distinctly. The color of PA6 fabric changes from white to light brownish because of the introduction of ferric trichloride. The photocatalytic activity of methylene blue decolorization is enhanced under sunlight and UV irradiation.

  11. Visible light induced photobleaching of methylene blue over melamine-doped TiO2 nanocatalyst

    EPA Science Inventory

    TiO2 doping with N-rich melamine produced a stable, active and visible light sentisized nanocatalyst that showed a remarkable efficiency towards the photobleaching of a model compound – methylene blue (MB) in aqueous solution. The photobleaching followed a mixed reaction order ki...

  12. Preparation and Characterization of Fe-Doped TiO2 Films Covered on Silicagel

    NASA Astrophysics Data System (ADS)

    Nghia, Nguyen Manh; Hue, Nguyen Thi; Thu, Ma Thi Anh; Len, Phung Thi; Thu, Vu Thi; Lam, Tran Dai

    2016-07-01

    This study describes sol-gel preparation of (TiO2:Fe x )/SiO2 ( x = 0-0.8%) on silicagel grains using titanium tetraisopropoxide and iron (III) chloride as titanium precursor and doping agent, respectively. The structural properties, morphology, and chemical composition of the samples were thoroughly studied using x-ray diffraction, field emission scanning electron microscopy, and energy-dispersive x-ray spectroscopy, respectively. The results demonstrated the formation of highly pure anatase TiO2:Fe x crystals with diameters of several tens of nanometers. With increasing doping level, no significant change in porosity of TiO2 material was observed, whereas the decrease in crystalline size was easily recorded. In addition, the bandgap (observed by UV-Vis) was dramatically shifted from 2.9 eV to 1.7 eV as doping with TiO2 with Fe at doping content as low as 0.8%. The use of silicagel as a solid support to carry photocatalytic crystals enables recycling of the material. These findings represent a simple pathway to design reusable catalyst for highly effective water detoxification under visible illumination.

  13. Self-referenced luminescence thermometry with Sm(3+) doped TiO2 nanoparticles.

    PubMed

    Dramićanin, M D; Antić, Ž; Ćulubrk, S; Ahrenkiel, S P; Nedeljković, J M

    2014-12-01

    The performance of Sm(3+) doped TiO2 nanoparticles for luminescence temperature sensing was tested over a temperature range from room to 110 °C. The Sm(3+) ions were incorporated into TiO2 nanocrystals using hydrolytic sol-gel route. Microstructural characterization of the obtained material was performed using transmission electron microscopy and x-ray diffraction measurements. Luminescence emission spectra of Sm(3+) doped TiO2 nanoparticles consists of two distinct spectral regions: the high energy region associated with the trap emission of the TiO2 host, and the low energy region with well-resolved emission peaks of the Sm(3+) ions. The ratio between Sm(3+) emission and TiO2 trap emission shows strong temperature dependence, and is tested for temperature sensing. The relative sensor sensitivity was found to be higher than 1% °C(-1) over given temperature range with the maximum value of 10.54% °C(-1) at 57.5 °C. Lifetime data derived from the Sm(3+) emission decay revealed that time-resolved measurements provide comparable quality of temperature sensing as corresponding ratiometric measurements, with a maximum relative sensitivity of 10.14% °C(-1) at 66.5 °C.

  14. Ag-loaded TiO2/reduced graphene oxide nanocomposites for enhanced visible-light photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Vasilaki, E.; Georgaki, I.; Vernardou, D.; Vamvakaki, M.; Katsarakis, N.

    2015-10-01

    In this work, Ag nanoparticles were loaded by chemical reduction onto TiO2 P25 under different loadings ranging from 1 up to 4 wt% and hydrothermally deposited on reduced graphene oxide sheets. Chemical reduction was determined to be an effective preparation approach for Ag attachment to titania, leading to the formation of small silver nanoparticles with an average diameter of 4.2 nm. The photocatalytic performance of the hybrid nanocomposite materials was evaluated via methylene blue (MB) dye removal under visible-light irradiation. The rate of dye decolorization was found to depend on the metal loading, showing an increase till a threshold value of 3 wt%, above which the rate drops. Next, the as prepared sample of TiO2/Ag of better photocatalytic response, i.e., at a 3 wt% loading value, was hydrothermally deposited on a platform of reduced graphene oxide (rGO) of tunable content (mass ratio). TiO2/Ag/rGO coupled nanocomposite presented significantly enhanced photocatalytic activity compared to the TiO2/Ag, TiO2/rGO composites and bare P25 titania semiconductor photocatalysts. In particular, after 45 min of irradiation almost complete decolorization of the dye was observed for the TiO2/Ag/rGO nanocatalyst, while the respective removal efficiency was 92% for TiO2/Ag, 93% for TiO2/rGO and only 80% for the bare TiO2 nanoparticles. This simple step by step preparation strategy allows for optimum exploitation of the advanced properties of metal plasmonic effect and reduced graphene oxide as the critical host for boosting the overall photocatalytic activity towards visible-light.

  15. Microstructure and dielectric properties of (Nb + In) co-doped rutile TiO2 ceramics

    NASA Astrophysics Data System (ADS)

    Li, Jinglei; Li, Fei; Zhuang, Yongyong; Jin, Li; Wang, Linghang; Wei, Xiaoyong; Xu, Zhuo; Zhang, Shujun

    2014-08-01

    The (Nb + In) co-doped TiO2 ceramics recently attracted considerable attention due to their colossal dielectric permittivity (CP) (˜100,000) and low dielectric loss (˜0.05). In this research, the 0.5 mol. % In-only, 0.5 mol. % Nb-only, and 0.5-7 mol. % (Nb + In) co-doped TiO2 ceramics were synthesized by standard conventional solid-state reaction method. Microstructure studies showed that all samples were in pure rutile phase. The Nb and In ions were homogeneously distributed in the grain and grain boundary. Impedance spectroscopy and I-V behavior analysis demonstrated that the ceramics may compose of semiconducting grains and insulating grain boundaries. The high conductivity of grain was associated with the reduction of Ti4+ ions to Ti3+ ions, while the migration of oxygen vacancy may account for the conductivity of grain boundary. The effects of annealing treatment and bias filed on electrical properties were investigated for co-doped TiO2 ceramics, where the electric behaviors of samples were found to be susceptible to the annealing treatment and bias field. The internal-barrier-layer-capacitance mechanism was used to explain the CP phenomenon, the effect of annealing treatment and nonlinear I-V behavior for co-doped rutile TiO2 ceramics. Compared with CaCu3Ti4O12 ceramics, the high activation energy of co-doped rutile TiO2 (3.05 eV for grain boundary) was thought to be responsible for the low dielectric loss.

  16. Synthesis and Characterization of Rutile TiO2Nanopowders Doped with Iron Ions

    PubMed Central

    2009-01-01

    Titanium dioxide nanopowders doped with different amounts of Fe ions were prepared by coprecipitation method. Obtained materials were characterized by structural (XRD), morphological (TEM and SEM), optical (UV/vis reflection and photoluminescence, and Raman), and analytical techniques (XPS and ICP-OES). XRD analysis revealed rutile crystalline phase for doped and undoped titanium dioxide obtained in the same manner. Diameter of the particles was 5–7 nm. The presence of iron ions was confirmed by XPS and ICP-OES. Doping process moved absorption threshold of TiO2into visible spectrum range. Photocatalytic activity was also checked. Doped nanopowders showed normal and up-converted photoluminescence. PMID:20596442

  17. Research Update: Doping ZnO and TiO2 for solar cells

    NASA Astrophysics Data System (ADS)

    Hoye, Robert L. Z.; Musselman, Kevin P.; MacManus-Driscoll, Judith L.

    2013-12-01

    ZnO and TiO2 are two of the most commonly used n-type metal oxide semiconductors in new generation solar cells due to their abundance, low-cost, and stability. ZnO and TiO2 can be used as active layers, photoanodes, buffer layers, transparent conducting oxides, hole-blocking layers, and intermediate layers. Doping is essential to tailor the materials properties for each application. The dopants used and their impact in solar cells are reviewed. In addition, the advantages, disadvantages, and commercial potential of the various fabrication methods of these oxides are presented.

  18. Defect generation, d- d transition, and band gap reduction in Cu-doped TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Choudhury, Biswajit; Dey, Munmun; Choudhury, Amarjyoti

    2013-04-01

    TiO2 doped with Cu2+ initiates the formation of brookite phase along with anatase. Doping of Cu2+ introduces structural defects into TiO2. The direct evidence is the low intense and broad diffraction peaks. Raman peaks of doped TiO2 are also broad and are blueshifted. Pure TiO2 exhibits an absorption in the UV region, the position of which is shifted towards the visible region on incorporation of Cu into it. The visible absorption peaks arise due to the d- d transition of Cu2+ in the crystalline environment of TiO2. Incorporation of Cu2+ distorts the local structure of TiO2, resulting in the loss of octahedral symmetry surrounding Cu2+. The Jahn-Teller distortion splits the 2 E g and 2 T 2g state of Cu2+ into several d states. Interaction of light excites the electron from ground to several of the excited states and gives the visible absorption peaks in the framework of TiO2. These Cu2+ d states and oxygen defects create band states, thereby favoring electronic transition to these levels and resulting in lowering of band gap of TiO2. A direct confirmation is the increase in the magnitude of Urbach energy with the reduction in the band gap of doped TiO2.

  19. Revisiting the mechanism of photocatalytic activities in N-doped TiO2

    NASA Astrophysics Data System (ADS)

    Umezawa, Naoto; Ye, Jinhua

    2012-02-01

    Photocatalysis possesses a great potential for environmental remediation and fuel production [1]. Nitrogen doped TiO2 is a well-known visible-light sensitive photocatalyst where deep impurity states associated with substitutional nitrogen at oxygen sites (NO) are believed to be the source of the red shift in photo-absorption edge. However, such a deep level should trap hole carriers, degrading oxidation process. The contradiction between the deep NO level and rather a high oxidation power of N-doped TiO2 has been an unsolved puzzle. Here, we propose a convincing mechanism which successfully solves the riddle. NO strongly binds with a titanium atom at an interstitial site, forming a defect-impurity band, which consists of bonding and anti-bonding states of nitrogen p and titanium d and narrows the band gap. Such a newly formed band, which is connected to the valence band maximum of the host TiO2, becomes the migration path of photo-induced hole carriers, assisting carrier transfer to the surface. This clearly explains the photocatalytic activity of N-doped TiO2 both for the visible-light absorption and the oxidation reaction. [1] Hua Tong, Shuxin Ouyang, Yingpu Bi, Naoto Umezawa, Mitsutake Oshikiri, and Jinhua Ye, Advanced Materials DOI: 10.1002/adma.20110275

  20. Photocatalytic Activity of W-Doped TiO2 Nanofibers for Methylene Blue Dye Degradation.

    PubMed

    Song, Yo-Seung; Cho, Nam-Ihn; Lee, Myung-Hyun; Kim, Bae-Yeon; Lee, Deuk Yong

    2016-02-01

    Photocatalytic degradation of methylene blue (MB) in water was examined using W-doped TiO2 nanofibers prepared by a sol-gel derived electrospinning and subsequent calcination for 4 h at 550 degrees C. Different concentrations of W dopant in the range of 0 to 8 mol% were synthesized to evaluate the effect of W concentration on the photocatalytic activity of TiO2. XRD results indicated that the undoped TiO2 is composed of anatase and rutile phases. The rutile phase was transformed to anatase phase completely with the W doping. Among W-TiO2 catalysts, the 2 mol% W-TiO2 catalyst showed the highest MB degradation rate. The degradation kinetic constant increased from 1.04 x 10(-3) min(-1) to 3.54 x 10(-3) min(-1) with the increase of W doping from 0 to 2 mol%, but decreased down to 1.77 x 10(-3) min(-1) when the W content was 8 mol%. It can be concluded that the degradation of MB under UV radiation was more efficient with W-TiO2 catalysts than with pure TiO2-

  1. Photocatalytic Activity of W-Doped TiO2 Nanofibers for Methylene Blue Dye Degradation.

    PubMed

    Song, Yo-Seung; Cho, Nam-Ihn; Lee, Myung-Hyun; Kim, Bae-Yeon; Lee, Deuk Yong

    2016-02-01

    Photocatalytic degradation of methylene blue (MB) in water was examined using W-doped TiO2 nanofibers prepared by a sol-gel derived electrospinning and subsequent calcination for 4 h at 550 degrees C. Different concentrations of W dopant in the range of 0 to 8 mol% were synthesized to evaluate the effect of W concentration on the photocatalytic activity of TiO2. XRD results indicated that the undoped TiO2 is composed of anatase and rutile phases. The rutile phase was transformed to anatase phase completely with the W doping. Among W-TiO2 catalysts, the 2 mol% W-TiO2 catalyst showed the highest MB degradation rate. The degradation kinetic constant increased from 1.04 x 10(-3) min(-1) to 3.54 x 10(-3) min(-1) with the increase of W doping from 0 to 2 mol%, but decreased down to 1.77 x 10(-3) min(-1) when the W content was 8 mol%. It can be concluded that the degradation of MB under UV radiation was more efficient with W-TiO2 catalysts than with pure TiO2- PMID:27433681

  2. Zirconium and silver co-doped TiO2 nanoparticles as visible light catalyst for reduction of 4-nitrophenol, degradation of methyl orange and methylene blue

    NASA Astrophysics Data System (ADS)

    Naraginti, Saraschandra; Stephen, Finian Bernard; Radhakrishnan, Adhithya; Sivakumar, A.

    2015-01-01

    Catalytic activity of Zr and Ag co-doped TiO2 nanoparticles on the reduction of 4-nitrophenol, degradation of methylene blue and methyl orange was studied using sodium borohydride as reducing agent. The nanoparticles were characterized using X-ray diffraction, energy dispersive X-ray, high resolution transmission electron microscopy, selected area electron diffraction and UV-Vis spectroscopy. The rate of the reduction/degradation was found to increase with increasing amount of the photocatalyst which could be attributed to higher dispersity and small size of the nanoparticles. The catalytic activity of Zr and Ag co-doped TiO2 nanoparticles showed no significant difference even after recycling the catalyst four times indicating a promising potential for industrial application of the prepared photocatalyst.

  3. N-doped TiO2/C nanocomposites and N-doped TiO2 synthesised at different thermal treatment temperatures with the same hydrothermal precursor.

    PubMed

    Wang, Jia; Fan, Chenyao; Ren, Zhimin; Fu, Xinxin; Qian, Guodong; Wang, Zhiyu

    2014-09-28

    A hydrothermal precursor was first obtained by isopropyl titanate reacting with tetramethylammonium hydroxide (TMAOH), which acts as a source of nitrogen and carbon. A facile post-thermal treatment was employed to enhance the crystallinity and visible light photocatalytic activity of the as-prepared precursor. The resulting products of post-thermal treatment between 200 °C and 700 °C display different colours from brown to white. Black N-doped TiO2 nanoparticles modified with carbon (denoted as N-TiO2/C) were obtained at 300 °C, while yellow N-doped TiO2 nanoparticles (denoted as N-TiO2) were obtained at 500 °C. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS) were applied to characterize N-TiO2/C, N-TiO2 and the evolution process during thermal treatment. The results show that for both N-TiO2/C and N-TiO2, nitrogen was doped into the lattice, thus narrowing the band gap and increasing the absorption in the visible light region. Moreover, for N-TiO2/C, the carbon species modified on the surface and between the nanocrystals enhanced the visible light harvesting and increased the adsorption of the dye in the photodegradation measurement. The photocatalytic performance under visible light irradiation is N-TiO2/C > N-TiO2 > undoped TiO2.

  4. Ag@helical chiral TiO2 nanofibers for visible light photocatalytic degradation of 17α-ethinylestradiol.

    PubMed

    Zhang, Chi; Li, Yi; Wang, Dawei; Zhang, Wenlong; Wang, Qing; Wang, Yuming; Wang, Peifang

    2015-07-01

    Ag-modified helical chiral TiO2 NFs (Ag@chiral TiO2 NFs) were fabricated and characterized by ultraviolet-visible absorption spectroscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy. This novel material exhibited efficient photocatalytic activity for the degradation of 17α-ethinylestradiol (EE2) in water under visible light irradiation with an optimum size of deposited silver nanoparticles (Ag NPs) in the range of 12 ∼ 14 nm. The pseudo-first-order rate constant (k obs) for EE2 photodegradation by Ag@chiral TiO2 NFs increased by up to a factor of 20.1 when compared with that of pure chiral TiO2 NFs. The high photocatalytic activity can be attributed to the interactions between helical chiral TiO2 NFs and surface plasmon resonance effect of Ag NPs. The new catalyst retains its photocatalytic activity at least up to five consecutive cycles. The results clearly demonstrate the feasibility of using Ag@chiral TiO2 NFs for the photocatalytic removal of EE2 and other endocrine-disrupting chemicals from water. PMID:25721529

  5. Controlled synthesis of Ag-coated TiO2 nanofibers and their enhanced effect in photocatalytic applications

    NASA Astrophysics Data System (ADS)

    Guan, Hongyu; Wang, Xiaohong; Guo, Yihang; Shao, Changlu; Zhang, Xintong; Liu, Yichun; Louh, Rong-Fuh

    2013-09-01

    Novel nanostructured Ag/TiO2 hybrid nanofibers (NFs) have been successfully prepared via a simple electrospinning process combined with silver mirror reaction. The Ag/TiO2 NFs demonstrated a unique morphology with evenly distributed Ag nanoparticles uniformly deposited onto the surface of each individual TiO2 NFs. The loading capacity and size of Ag NPs can be easily controlled by varying the silver mirror reaction time. Compared with pristine TiO2 NFs, such heterogeneous Ag/TiO2 nanocomposites exhibited preferable photocatalytic activity during photocatalytic degradation of rhodamine-B under the simulated sunlight irradiation and this enhanced photocatalytic performance was driven by combination and interaction between TiO2 and Ag NPs.

  6. In situ surface hydrogenation synthesis of Ti3+ self-doped TiO2 with enhanced visible light photoactivity

    NASA Astrophysics Data System (ADS)

    Huo, Junchao; Hu, Yanjie; Jiang, Hao; Li, Chunzhong

    2014-07-01

    A novel one-step, vapor-fed aerosol flame synthetic process (VAFS) has been developed to prepare Ti3+ self-doped titanium dioxide (TiO2). The freshly formed TiO2 was in situ surface hydrogenated during the condensation stage by introducing H2 above the flame, and Ti3+ ions were created near the surface of TiO2. The relative content of Ti3+ ions near the surface of TiO2 is estimated to be 8%. Because of the high absorption of visible light and suppression of charge recombination, the photocurrent density and decomposition of MB under visible light irradiation were remarkably enhanced. This study demonstrates a simple, potential method to produce Ti3+ self-doped TiO2 with effective photoactivity in visible light.A novel one-step, vapor-fed aerosol flame synthetic process (VAFS) has been developed to prepare Ti3+ self-doped titanium dioxide (TiO2). The freshly formed TiO2 was in situ surface hydrogenated during the condensation stage by introducing H2 above the flame, and Ti3+ ions were created near the surface of TiO2. The relative content of Ti3+ ions near the surface of TiO2 is estimated to be 8%. Because of the high absorption of visible light and suppression of charge recombination, the photocurrent density and decomposition of MB under visible light irradiation were remarkably enhanced. This study demonstrates a simple, potential method to produce Ti3+ self-doped TiO2 with effective photoactivity in visible light. Electronic supplementary information (ESI) available: Schematic setup for Ti3+ self-doped TiO2 nanoparticles is shown in Fig. S1. The BET specific surface and pore-size distribution of Ti3+ self-doped TiO2 is shown in Fig. S2. XRD patterns of pristine TiO2 and Ti3+ self-doped TiO2 are shown in Fig. S3. HRTEM image of Ti3+ self-doped TiO2 with mixture phase is shown in Fig. S4. The photographs of different colors of Ti3+ self-doped TiO2 with different flow rates of hydrogen are shown in Fig. S5. TEM images of Ti3+ self-doped TiO2 samples with different

  7. Synthesis of rare earth doped TiO2 nanorods as photocatalysts for lignin degradation.

    PubMed

    Song, Liang; Zhao, Xueyuan; Cao, Lixin; Moon, Ji-Won; Gu, Baohua; Wang, Wei

    2015-10-28

    A two-step process is developed to synthesize rare earth doped titania nanorods (RE-TiO2 NRs) as photocatalysts for efficient degradation of lignin under simulated sunlight irradiation. In this approach, protonated titanate nanotubes with layered structures were first prepared by a hydrothermal approach, and rare earth metal ions were subsequently bound to the negatively charged surface of the synthesized titanate via electrostatic incorporation. The as-synthesized RE-TiO2 NRs after calcination generally showed much higher photocatalytic efficiencies than those of undoped TiO2 NRs or the commercial P25 TiO2 photocatalyst. Using methyl orange (MO) as a probing molecule, we demonstrate that Eu-TiO2 NRs are among the best for degrading MO, with an observed rate constant of 4.2 × 10(-3) s(-1). The La(3+), Sm(3+), Eu(3+) and Er(3+) doped TiO2 NRs also showed higher photocatalytic efficiencies in degrading MO than the commercial P25 TiO2. We further demonstrate that lignin can be photodegraded effectively and rapidly at room temperature under simulated sunlight through two reaction routes, which could be important in controlling ways of lignin depolymerization or the formation of reaction products. PMID:26400095

  8. Synthesis of rare earth doped TiO2 nanorods as photocatalysts for lignin degradation

    DOE PAGES

    Song, Liang; Zhao, Xueyuan; Cao, Lixin; Moon, Ji-Won; Gu, Baohua; Wang, Wei

    2015-09-10

    In this paper, a two-step process is developed to synthesize rare earth doped titania nanorods (RE–TiO2 NRs) as photocatalysts for efficient degradation of lignin under simulated sunlight irradiation. In this approach, protonated titanate nanotubes with layered structures were first prepared by a hydrothermal approach, and rare earth metal ions were subsequently bound to the negatively charged surface of the synthesized titanate via electrostatic incorporation. The as-synthesized RE–TiO2 NRs after calcination generally showed much higher photocatalytic efficiencies than those of undoped TiO2 NRs or the commercial P25 TiO2 photocatalyst. Using methyl orange (MO) as a probing molecule, we demonstrate that Eu–TiO2more » NRs are among the best for degrading MO, with an observed rate constant of 4.2 × 10-3 s-1. The La3+, Sm3+, Eu3+ and Er3+ doped TiO2 NRs also showed higher photocatalytic efficiencies in degrading MO than the commercial P25 TiO2. Finally, we further demonstrate that lignin can be photodegraded effectively and rapidly at room temperature under simulated sunlight through two reaction routes, which could be important in controlling ways of lignin depolymerization or the formation of reaction products.« less

  9. Synthesis of rare earth doped TiO2 nanorods as photocatalysts for lignin degradation.

    PubMed

    Song, Liang; Zhao, Xueyuan; Cao, Lixin; Moon, Ji-Won; Gu, Baohua; Wang, Wei

    2015-10-28

    A two-step process is developed to synthesize rare earth doped titania nanorods (RE-TiO2 NRs) as photocatalysts for efficient degradation of lignin under simulated sunlight irradiation. In this approach, protonated titanate nanotubes with layered structures were first prepared by a hydrothermal approach, and rare earth metal ions were subsequently bound to the negatively charged surface of the synthesized titanate via electrostatic incorporation. The as-synthesized RE-TiO2 NRs after calcination generally showed much higher photocatalytic efficiencies than those of undoped TiO2 NRs or the commercial P25 TiO2 photocatalyst. Using methyl orange (MO) as a probing molecule, we demonstrate that Eu-TiO2 NRs are among the best for degrading MO, with an observed rate constant of 4.2 × 10(-3) s(-1). The La(3+), Sm(3+), Eu(3+) and Er(3+) doped TiO2 NRs also showed higher photocatalytic efficiencies in degrading MO than the commercial P25 TiO2. We further demonstrate that lignin can be photodegraded effectively and rapidly at room temperature under simulated sunlight through two reaction routes, which could be important in controlling ways of lignin depolymerization or the formation of reaction products.

  10. Effect of doping level of colored TiO2 nanotube arrays fabricated by electrochemical self-doping on electrochemical properties.

    PubMed

    Kim, Choonsoo; Kim, Seonghwan; Hong, Sung Pil; Lee, Jaehan; Yoon, Jeyong

    2016-06-01

    Recently, two types of TiO2 nanotube arrays (NTAs) (blue- and black-colored TiO2 NTAs), which are easily fabricated by electrochemical self-doping, have gained much attention due particularly to their enhanced capacitive and oxidant-generating properties. These enhanced electrochemical properties mean that they have potential as basic materials for energy and environmental applications, such as in supercapacitors and anodes for water treatment. However, the understanding of the effect of the doping level of these TiO2 NTAs on their electrochemical properties is limited because there is no direct comparison or relevant discussion of their respective electrochemical properties under the same conditions, despite the similar surface characteristics of the TiO2 NTAs obtained by comparable electrochemical doping. Therefore, the objective of this study was to investigate the effect of the doping level of blue and black TiO2 NTAs on their electrochemical properties, including the capacitive and oxidant-generating properties. Although no significant difference in their surface properties was found using SEM, XRD and XPS, the black TiO2 NTA revealed a slightly higher doping level than the blue TiO2 NTA, which is caused by the order of the electrochemical self-doping and annealing conditions. With the different doping levels of the two TiO2 NTAs, the black TiO2 NTA showed a higher areal capacitance, indicating good capacitive properties, and better service life in oxidant-generation than that of the blue TiO2 NTA. The blue TiO2 NTA exhibited a larger oxygen evolution overpotential and higher chlorine evolution efficiency than that of the black TiO2 NTA. We report that the new knowledge on blue and black TiO2 NTAs from this study can contribute to the further development of supercapacitors and oxidant-generating anodes for water treatment. PMID:27169417

  11. Effect of doping level of colored TiO2 nanotube arrays fabricated by electrochemical self-doping on electrochemical properties.

    PubMed

    Kim, Choonsoo; Kim, Seonghwan; Hong, Sung Pil; Lee, Jaehan; Yoon, Jeyong

    2016-06-01

    Recently, two types of TiO2 nanotube arrays (NTAs) (blue- and black-colored TiO2 NTAs), which are easily fabricated by electrochemical self-doping, have gained much attention due particularly to their enhanced capacitive and oxidant-generating properties. These enhanced electrochemical properties mean that they have potential as basic materials for energy and environmental applications, such as in supercapacitors and anodes for water treatment. However, the understanding of the effect of the doping level of these TiO2 NTAs on their electrochemical properties is limited because there is no direct comparison or relevant discussion of their respective electrochemical properties under the same conditions, despite the similar surface characteristics of the TiO2 NTAs obtained by comparable electrochemical doping. Therefore, the objective of this study was to investigate the effect of the doping level of blue and black TiO2 NTAs on their electrochemical properties, including the capacitive and oxidant-generating properties. Although no significant difference in their surface properties was found using SEM, XRD and XPS, the black TiO2 NTA revealed a slightly higher doping level than the blue TiO2 NTA, which is caused by the order of the electrochemical self-doping and annealing conditions. With the different doping levels of the two TiO2 NTAs, the black TiO2 NTA showed a higher areal capacitance, indicating good capacitive properties, and better service life in oxidant-generation than that of the blue TiO2 NTA. The blue TiO2 NTA exhibited a larger oxygen evolution overpotential and higher chlorine evolution efficiency than that of the black TiO2 NTA. We report that the new knowledge on blue and black TiO2 NTAs from this study can contribute to the further development of supercapacitors and oxidant-generating anodes for water treatment.

  12. Flame-made Nb-doped TiO2 ethanol and acetone sensors.

    PubMed

    Phanichphant, Sukon; Liewhiran, Chaikarn; Wetchakun, Khatcharin; Wisitsoraat, Anurat; Tuantranont, Adisorn

    2011-01-01

    Undoped TiO(2) and TiO(2) nanoparticles doped with 1-5 at.% Nb were successfully produced in a single step by flame spray pyrolysis (FSP). The phase and crystallite size were analyzed by XRD. The BET surface area (SSA(BET)) of the nanoparticles was measured by nitrogen adsorption. The trend of SSA(BET) on the doping samples increased and the BET equivalent particle diameter (d(BET)) (rutile) increased with the higher Nb-doping concentrations while d(BET) (anatase) remained the same. The morphology and accurate size of the primary particles were further investigated by high-resolution transmission electron microscopy (HRTEM). The crystallite sizes of undoped and Nb-doped TiO(2) spherical were in the range of 10-20 nm. The sensing films were prepared by spin coating technique. The mixing sample was spin-coated onto the Al(2)O(3) substrates interdigitated with Au electrodes. The gas sensing of acetone (25-400 ppm) was studied at operating temperatures ranging from 300-400 °C in dry air, while the gas sensing of ethanol (50-1,000 ppm) was studied at operating temperatures ranging from 250-400 °C in dry air. PMID:22346586

  13. Photoelectrochemical oxidation of ibuprofen via Cu2O-doped TiO2 nanotube arrays.

    PubMed

    Sun, Qiannan; Peng, Yen-Ping; Chen, Hanlin; Chang, Ken-Lin; Qiu, Yang-Neng; Lai, Shiau-Wu

    2016-12-01

    A p-n junction based Cu2O-doped TiO2 nanotube arrays (Cu2O-TNAs) were synthesized and used as a working anode in a photoelectrochemical (PEC) system. The results revealed that the Cu2O-TNAs were dominated by the anatase phase and responded significantly to visible light. XPS analyses indicated that with an amount of 24.79% Cu doping into the structure, the band gap of Cu2O-TNAs was greatly reduced. SEM images revealed that the supported TiO2 nanotubes had diameters of approximately 80nm and lengths of about 2.63μm. Upon doping with Cu2O, the TiO2 nanotubes maintained their structural integrity, exhibiting no significant morphological change, favoring PEC applications. Under illumination, the photocurrent from Cu2O/TNAs was 2.4 times larger than that from TNAs, implying that doping with Cu2O significantly improved electron mobility by reducing the rate of recombination of electron-hole pairs. The EIS and Bode plot revealed that the estimated electron lifetimes, τel, of TNAs and Cu2O/TNAs were 6.91 and 26.26ms, respectively. The efficiencies of degradation of Ibuprofen by photoelectrochemical, photocatalytic (PC), electrochemical (EC) and photolytic (P) methods were measured. PMID:27021261

  14. Ni-doped TiO2 nanotubes for wide-range hydrogen sensing

    PubMed Central

    2014-01-01

    Doping of titania nanotubes is one of the efficient way to obtain improved physical and chemical properties. Through electrochemical anodization and annealing treatment, Ni-doped TiO2 nanotube arrays were fabricated and their hydrogen sensing performance was investigated. The nanotube sensor demonstrated a good sensitivity for wide-range detection of both dilute and high-concentration hydrogen atmospheres ranging from 50 ppm to 2% H2. A temperature-dependent sensing from 25°C to 200°C was also found. Based on the experimental measurements and first-principles calculations, the electronic structure and hydrogen sensing properties of the Ni-doped TiO2 with an anatase structure were also investigated. It reveals that Ni substitution of the Ti sites could induce significant inversion of the conductivity type and effective reduction of the bandgap of anatase oxide. The calculations also reveal that the resistance change for Ni-doped anatase TiO2 with/without hydrogen absorption was closely related to the bandgap especially the Ni-induced impurity level. PMID:24624981

  15. Electronic structure and room temperature ferromagnetism of C doped TiO2

    NASA Astrophysics Data System (ADS)

    Ablat, Abduleziz; Wu, Rong; Mamat, Mamatrishat; Ghupur, Yasin; Aimidula, Aimierding; Bake, Muhammad Ali; Gholam, Turghunjan; Wang, Jiaou; Qian, Haijie; Wu, Rui; Ibrahim, Kurash

    2016-10-01

    C-doped TiO2 nanoparticles were successfully synthesized using a simple hydrothermal synthesis method. After this preparation, a portion of the samples were annealed separately in air on the one hand, and in argon on the other, and another portion remained untreated. The results of X-ray diffraction show that the untreated samples primarily display anatase and rutile structures. However, after annealing, the samples displayed the rutile structure only. The Ti K-edge and L-edge Near Edge X-ray Absorption Fine Structure analyses clearly show that C atoms were successfully incorporated into the TiO2 host lattice. All doped samples exhibit ferromagnetism at room temperature. The saturation magnetization (Ms) and coercive fields (Hc) tend to decrease after the samples are annealed in argon and in air. The maximum Ms of the untreated samples was approximately 0.038 emu/g.

  16. Experimental study of transition metal ion doping on TiO2 with photocatalytic behavior.

    PubMed

    Siddhapara, K S; Shah, D V

    2014-08-01

    In this research, we have studied the doping behaviors of three transition metal ion dopants on the crystal phase, particle sizes, XRD patterns, EDAX spectra, and photoreactivity of TiO2 nanoparticles. Test metal ion concentrations ranged from 1% to 4 at.%, we report the growth of [Fe, Co and Mn]xTiO2 nanocrystals prepared by Sol-Gel technique, followed by freeze-drying treatment at -30 °C temperature for 12 hrs. The obtained Gel was thermally treated at different temperature like 200 °C, 400 °C, 600 °C, 800 °C. Thermal gravimetric analysis (TGA) shows that dopant concentration affects thermal decomposition. The photoreactivities of transition metal ion-doped TiO2 nanoparticles under UV irradiation were quantified by the degradation of formaldehyde.

  17. Silver-loaded nitrogen-doped yolk-shell mesoporous TiO2 hollow microspheres with enhanced visible light photocatalytic activity.

    PubMed

    Jiang, Zhifeng; Wei, Wei; Mao, Danjun; Chen, Cheng; Shi, Yunfei; Lv, Xiaomeng; Xie, Jimin

    2015-01-14

    Silver-loaded nitrogen-doped yolk-shell mesoporous TiO2 hollow microspheres (Ag-N-TiO2-YSM) were prepared by employing acetic acid as the hollowing controller and triethanolamine as the N source for the first time. Ag nanoparticles (NPs) were uniformly deposited by a simple in situ photo-reduction method, which can prevent the aggregation of Ag NPs. The efficiency of the as-prepared samples was investigated by monitoring the degradation of rhodamine B and ciprofloxacin under visible light irradiation. The experimental results indicate that N-doped yolk-shell mesoporous TiO2 hollow microspheres show higher photocatalytic activity than P25 TiO2 under visible light irradiation because of N doping and the unique yolk-shell structure. In addition, Ag-N-TiO2-YSM shows enhanced activity compared with N-TiO2-YSM due to the SPR absorption of silver NPs and the fast generation, separation and transportation of the photogenerated carriers. Moreover, the Ag contents can affect the photocatalytic activity of the Ag-N-TiO2-YSM composite. A suitable amount of Ag deposition gives the highest photocatalytic activity. A higher loading does not improve the photocatalytic activity of N-TiO2-YSM further. The active species generated in the photocatalytic system were also investigated. Based on our experimental results, a possible photocatalytic mechanism was proposed. The strategy presented here gives a promising route towards the development of delicate metal@hollow semiconductor composites for many applications in photocatalysis.

  18. Reduced graphene oxide and Ag wrapped TiO2 photocatalyst for enhanced visible light photocatalysis

    NASA Astrophysics Data System (ADS)

    Leong, Kah Hon; Sim, Lan Ching; Bahnemann, Detlef; Jang, Min; Ibrahim, Shaliza; Saravanan, Pichiah

    2015-10-01

    A well-organised reduced graphene oxide (RGO) and silver (Ag) wrapped TiO2 nano-hybrid was successfully achieved through a facile and easy route. The inherent characteristics of the synthesized RGO-Ag/TiO2 were revealed through crystalline phase, morphology, chemical composition, Raman scattering, UV-visible absorption, and photoluminescence analyses. The adopted synthesis route significantly controlled the uniform formation of silver nanoparticles and contributed for the absorption of light in the visible spectrum through localized surface plasmon resonance effects. The wrapped RGO nanosheets triggered the electron mobility and promoted visible light shift towards red spectrum. The accomplishment of synergised effect of RGO and Ag well degraded Bisphenol A under visible light irradiation with a removal efficiency of 61.9%.

  19. Performance improvement of TiO2/Ag/TiO2 multilayer transparent conducting electrode films for application on photodetectors

    NASA Astrophysics Data System (ADS)

    Zhu, Meng-Qi; Jin, Han-Dong; Bi, Peng-Qing; Zong, Fu-Jian; Ma, Jin; Hao, Xiao-Tao

    2016-03-01

    TiO2/Ag/TiO2 (TAT) multilayer transparent conducting electrodes were deposited onto glass substrates by room temperature sputtering. The impact of Ag sputtering current on the film morphology, and the optical and electrical properties were discussed. The increase in the sputtering current led to a more continuous Ag middle layer. As the Ag middle layer became continuous, the TAT electrodes had lower sheet resistance and higher transmittance. In addition, an optimized TAT electrode with a figure of merit of 15.97× {{10}-2}{{Ω }-1} was obtained at an Ag thickness of 16 nm and a sputtering current of 0.48 A. Finally, organic photodetectors were also fabricated based on TAT electrodes and the performance is comparable to reference devices with commercially purchased Sn-doped In2O3 (ITO) electrodes.

  20. Microwave-assisted self-doping of TiO2 photonic crystals for efficient photoelectrochemical water splitting.

    PubMed

    Zhang, Zhonghai; Yang, Xiulin; Hedhili, Mohamed Nejib; Ahmed, Elaf; Shi, Le; Wang, Peng

    2014-01-01

    In this article, we report that the combination of microwave heating and ethylene glycol, a mild reducing agent, can induce Ti(3+) self-doping in TiO2. A hierarchical TiO2 nanotube array with the top layer serving as TiO2 photonic crystals (TiO2 NTPCs) was selected as the base photoelectrode. The self-doped TiO2 NTPCs demonstrated a 10-fold increase in visible-light photocurrent density compared to the nondoped one, and the optimized saturation photocurrent density under simulated AM 1.5G illumination was identified to be 2.5 mA cm(-2) at 1.23 V versus reversible hydrogen electrode, which is comparable to the highest values ever reported for TiO2-based photoelectrodes. The significant enhancement of photoelectrochemical performance can be ascribed to the rational coupling of morphological and electronic features of the self-doped TiO2 NTPCs: (1) the periodically morphological structure of the photonic crystal layer traps broadband visible light, (2) the electronic interband state induced from self-doping of Ti(3+) can be excited in the visible-light region, and (3) the captured light by the photonic crystal layer is absorbed by the self-doped interbands.

  1. Photocatalytic activity of multielement doped TiO 2 in the degradation of congo red

    NASA Astrophysics Data System (ADS)

    Ramakrishnan, R.; Kalaivani, S.; Amala Infant Joice, J.; Sivakumar, T.

    2012-01-01

    TiO2 although considered a promising photocatalyst for the degradation of aqueous pollutants, it suffers from poor absorption in the visible region and hence requires ultraviolet (UV) light for activation. To make TiO2 a visible active photocatalyst, multielement (C, N, B, and F) doping has been done. The synthesised CNBF/TiO2 catalysts were calcined at different temperatures and characterized by XRD, BET surface area, UV DRS, XPS, HRSEM-EDAX, and TEM techniques. These catalysts found to show less band gap values when compared to bare TiO2. These catalysts were tested for their catalytic activity towards the degradation of a textile dye - congo red (CR) under different reaction conditions. It was found that the photocatalytic activity was dependent on both doping of multielement and the calcination temperature of CNBF/TiO2. The co-doped catalysts which were calcined at 400 °C and 600 °C (100% intensity in anatase phase) were found to be the best catalysts (100% decolourisation of CR in 21/2 h and 2 h respectively). TOC analysis carried out for the samples at the reaction time of 5 h showed very high percentage (83%) degradation of CR over CNBF/TiO2 catalysts calcined at 600 °C when compared to the other catalysts calcined at different temperatures. CNBF/TiO2 (1000 °C) showed very less photocatalytic activity due to the formation of rutile phase.

  2. C-doped mesoporous anatase TiO2 comprising 10nm crystallites.

    PubMed

    Xie, Chong; Yang, Shenghui; Li, Beibei; Wang, Hongkong; Shi, Jian-Wen; Li, Guodong; Niu, Chunming

    2016-08-15

    We report a C-doped mesoporous anatase TiO2 with high surface area synthesized using multi-walled carbon nanotube (MWCNT) mat as a "rigid" template and carbon doping source. The characterization by SEM, HRTEM, X-ray diffraction and nitrogen adsorption revealed that TiO2 samples have a porous structure which are figuratively a inverse copy of MWCNT network and pore walls are formed by interconnected TiO2 nanoparticles with average diameter of ∼10nm. We found that annealing temperatures from 400 to 1000°C before MWCNT template removal had very limited effect on particle size (∼10nm), surface area (112-129m(2)/g) and total pore volume (0.74-0.85m(2)/g) of the samples through a significantly delayed phase transition from anatase to rutile started at 800°C, resulting in only ∼9.1% conversion at 1000°C. The pore size distribution is in mesopore range from 6 to 60nm peaked at ∼24nm. XPS analysis showed a relatively strong C1s peak at 288.4eV, indicating C doping at Ti sites, which is responsible for red shift of adsorption edge of UV-vis spectra and photocatalytic activity in visible-light region. PMID:27179173

  3. Photocatalytic and superhydrophilicity properties of N-doped TiO 2 nanothin films

    NASA Astrophysics Data System (ADS)

    Chekini, M.; Mohammadizadeh, M. R.; Vaez Allaei, S. M.

    2011-06-01

    Pure TiO 2 and nitrogen doped titanium dioxide (N-TiO 2) thin films were prepared by sol-gel method through spin coating on soda lime glass substrates. TiCl 4 and urea were used as Ti and N sources in the sol. XRD results showed nitrogen doping has retarded anatase to rutile phase transformation. The doping also leads to a decrease in roughness of the samples from 4 nm (TiO 2) to 1 nm (N-TiO 2). However, surface analysis by statistical methods reveals that both surfaces have self-affine structure. Optical band gap of thin films was shifted from 3.65 eV (TiO 2) to 3.47 eV (N-TiO 2). Hydrophilic conversion and photocatalytic degradation properties of thin films were investigated and exhibited that N-TiO 2 thin film has more preferable hydrophilicity and photocatalytic properties under UV illumination.

  4. Synthesis of iron-doped TiO2 for degradation of reactive Orange16

    PubMed Central

    2014-01-01

    In this study the optimum conditions for preparing the iron-doped TiO2 nanoparticles were investigated. Samples were synthesized by sol–gel impregnation method. Three effective parameters were optimized using Taguchi method, consisted of: (i) atomic ratios of Fe to Ti; (ii) sintering temperature; (iii) sintering time. The characterization of samples was determined using X-ray diffraction, BET- specific surface area, UV- Vis reflectance spectra (DRS) and scanning electron microscope (SEM). The XRD patterns of the samples indicated the existence of anatase crystal phase in structure. UV- Vis reflectance spectra showed an enhancement in light absorbance in the visible region (wavelength > 400 nm) for iron-doped samples. The photocatalytic activity of samples was investigated by the degradation of RO 16 (RO 16) dye under UV irradiation. The results illustrated that the photocatalytic activity of iron-doped TiO2 was more than pure TiO2, because of the smaller crystal size, grater BET surface area and higher light absorption ability. PMID:24405975

  5. Huge low-frequency dielectric response of (Nb,In)-doped TiO2 ceramics

    NASA Astrophysics Data System (ADS)

    Wu, Y. Q.; Zhao, X.; Zhang, J. L.; Su, W. B.; Liu, J.

    2015-12-01

    The (Nb,In)-doped TiO2 ceramics have drawn considerable attention as a type of promising giant-permittivity dielectric materials in recent years. However, a significant controversy concerning the giant dielectric mechanism currently exists, and clarifying it is vitally important from both scientific and technological viewpoints. This letter reports the results of a systematical comparison study, where two kinds of (Nb,In)-doped TiO2 ceramics with a substantial difference in dielectric loss are used. Dielectric properties and complex impedance are investigated over a broad frequency band of 3 mHz-110 MHz. A huge low-frequency dielectric response in addition to the giant dielectric relaxation appearing above 1 MHz is observed for both kinds of (Nb,In)-doped TiO2 ceramics in dielectric dispersion. The huge dielectric response observed in the low frequency range can be ascribed to a non-ohmic electrode-contact, and the dielectric relaxation appearing above 1 MHz can be attributed to an internal barrier layer capacitance effect. An electrical equivalent circuit model suggested can well describe the observed dielectric properties and electrical behaviors.

  6. C-doped mesoporous anatase TiO2 comprising 10nm crystallites.

    PubMed

    Xie, Chong; Yang, Shenghui; Li, Beibei; Wang, Hongkong; Shi, Jian-Wen; Li, Guodong; Niu, Chunming

    2016-08-15

    We report a C-doped mesoporous anatase TiO2 with high surface area synthesized using multi-walled carbon nanotube (MWCNT) mat as a "rigid" template and carbon doping source. The characterization by SEM, HRTEM, X-ray diffraction and nitrogen adsorption revealed that TiO2 samples have a porous structure which are figuratively a inverse copy of MWCNT network and pore walls are formed by interconnected TiO2 nanoparticles with average diameter of ∼10nm. We found that annealing temperatures from 400 to 1000°C before MWCNT template removal had very limited effect on particle size (∼10nm), surface area (112-129m(2)/g) and total pore volume (0.74-0.85m(2)/g) of the samples through a significantly delayed phase transition from anatase to rutile started at 800°C, resulting in only ∼9.1% conversion at 1000°C. The pore size distribution is in mesopore range from 6 to 60nm peaked at ∼24nm. XPS analysis showed a relatively strong C1s peak at 288.4eV, indicating C doping at Ti sites, which is responsible for red shift of adsorption edge of UV-vis spectra and photocatalytic activity in visible-light region.

  7. Room temperature ferromagnetism in non-magnetic doped TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Gómez-Polo, C.; Larumbe, S.; Pastor, J. M.

    2013-05-01

    Room-temperature ferromagnetism in non-magnetic doped TiO2 semiconductor nanoparticles is analyzed in the present work. Undoped and N-doped TiO2 nanoparticles were obtained employing sol-gel procedure using urea as the nitrogen source. The obtained gels were first dried at 70 °C and afterwards calcined in air at 300 °C. A residual carbon concentration was retained in the samples as a consequence of the organic decomposition process. Post-annealing treatments at 300 °C under air and vacuum conditions were also performed. The crystallographic structure of nanoparticles was analyzed by X-ray diffraction, obtaining a single anatase crystalline phase after the calcinations (mean nanoparticle diameters around 5-8 nm). SQUID magnetometry was employed to analyze the magnetic response of the samples. Whereas for the undoped samples synthesized with hydrolysis rate h = 6, paramagnetic like behavior is observed at room temperature, the N-doped nanoparticles (h = 3) show a weak ferromagnetic response (saturation magnetization ≈10-3 emu/g). Moreover, a clear reinforcement of the room-temperature ferromagnetism response is found with the post-annealing treatments, in particular that performed in vacuum. Thus, the results indicate the dominant role of the oxygen stoichiometry and the oxygen vacancies in the room temperature ferromagnetic response of these TiO2 nanoparticles.

  8. Boron-Doped Anatase TiO2 as a High-Performance Anode Material for Sodium-Ion Batteries.

    PubMed

    Wang, Baofeng; Zhao, Fei; Du, Guodong; Porter, Spencer; Liu, Yong; Zhang, Peng; Cheng, Zhenxiang; Liu, Hua Kun; Huang, Zhenguo

    2016-06-29

    Pristine and boron-doped anatase TiO2 were prepared via a facile sol-gel method and the hydrothermal method for application as anode materials in sodium-ion batteries (SIBs). The sol-gel method leads to agglomerated TiO2, whereas the hydrothermal method is conducive to the formation of highly crystalline and discrete nanoparticles. The structure, morphology, and electrochemical properties were studied. The crystal size of TiO2 with boron doping is smaller than that of the nondoped crystals, which indicates that the addition of boron can inhibit the crystal growth. The electrochemical measurements demonstrated that the reversible capacity of the B-doped TiO2 is higher than that for the pristine sample. B-doping also effectively enhances the rate performance. The capacity of the B-doped TiO2 could reach 150 mAh/g at the high current rate of 2C and the capacity decay is only about 8 mAh/g over 400 cycles. The remarkable performance could be attributed to the lattice expansion resulting from B doping and the shortened Li(+) diffusion distance due to the nanosize. These results indicate that B-doped TiO2 can be a good candidate for SIBs.

  9. Synthesis and photocatalytic property of N-doped TiO 2 nanorods and nanotubes with high nitrogen content

    NASA Astrophysics Data System (ADS)

    He, Z.; He, H. Y.

    2011-11-01

    Nano N-doped TiO2 nanotubes were fabricated by hydrothermally treating N-doped TiO2 nanorods in a 8 M NaOH solution at 110 °C for 20 h. The N-doped TiO2 nanorods were synthesized by a solvothermal process with precursor solution containing titanium sulfate, urea, and dichloroethane. The N-doped TiO2 nanorods and nanotubes were characterized with X-ray diffraction, transmission electron microscopy, and UV-vis spectrophotometry. The nitrogen contents of the N-doped TiO2 nanorods and nanotubes were reached to high values of 36.9 at.% and 25.7 at.%, respectively. The nitrogen doping narrowed the band gap of the N-doped TiO2 nanorods and nanotubes and introduced indirect band gap to the powders, which respectively extended the absorption edge to visible light and infrared region. The nanotubes showed larger specific surface area and greater degradation efficiency to methyl orange than the nanorods.

  10. Enhanced visible-light photocatalytic performances of Ag3PO4 surface-modified with small amounts of TiO2 and Ag

    NASA Astrophysics Data System (ADS)

    Wang, Desong; Li, Lei; Luo, Qingzhi; An, Jing; Li, Xueyan; Yin, Rong; Zhao, Mangmang

    2014-12-01

    A novel approach has been developed to prepare an efficient visible-light photocatalyst using Ag3PO4 and TiO2 sol as precursors. First, Ag3PO4 particles were dipped into TiO2 sol for 5 min and were filtered quickly. Second, Ag3PO4 particles adsorbing a small amount of TiO2 sol were aged for 24 h to form TiO2 gel on their surface. Finally, Ag3PO4 particles covered by TiO2 gel were calcined at 450 °C for 2 h to obtain the surface-modified Ag3PO4 sample. The surface-modified Ag3PO4 was characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, UV-vis diffuse reflection spectroscopy, X-ray photoelectron spectroscopy, and electrochemical impedance spectroscopy. The visible-light photocatalytic performances of the surface-modified Ag3PO4 were evaluated by the photodegradation of methyl orange or phenol solution. The results showed that the surface-modified Ag3PO4 exhibited much higher visible-light photocatalytic activity and stability than pure Ag3PO4. As the amount of TiO2 gel on the Ag3PO4 surface increased, the visible-light photocatalytic activity increased first and then decreased. The surface-modification of Ag3PO4 obviously decreased its solubility in water environment due to the protection of TiO2 and Ag nanocrystals on the surface. The visible-light photocatalytic mechanism of the surface-modified Ag3PO4 has been discussed.

  11. Improved conversion efficiency of dye sensitized solar cell using Zn doped TiO2-ZrO2 nanocomposite

    NASA Astrophysics Data System (ADS)

    Tomar, Laxmi J.; Bhatt, Piyush J.; Desai, Rahul K.; Chakrabarty, B. S.; Panchal, C. J.

    2016-05-01

    TiO2-ZrO2 and Zn doped TiO2-ZrO2 nanocomposites were prepared by hydrothermal method for dye sensitized solar cell (DSSC) application. The structural and optical properties were investigated by X -ray diffraction (XRD) and UV-Visible spectroscopy respectively. XRD results revealed the formation of material in nano size. The average crystallite size is 22.32 nm, 17.41 nm and 6.31 nm for TiO2, TiO2-ZrO2 and Zn doped TiO2-ZrO2 nanocomposites respectively. The optical bandgap varies from 2.04 eV to 3.75 eV. Dye sensitized solar cells were fabricated using the prepared material. Pomegranate juice was used as a sensitizer and graphite coated conducting glass plate was used as counter electrode. The I - V characteristics were recorded to measure photo response of DSSC. Photovoltaic parameter like open circuit voltage, power conversion efficiency, and fill factor were evaluated for fabricated solar cell. The power conversion efficiency of DSSC fabricated with TiO2, TiO2-ZrO2 and Zn doped TiO2-ZrO2 nanocomposites were found 0.71%, 1.97% and 4.58% respectively.

  12. Mesoporous nitrogen-doped TiO2 sphere applied for quasi-solid-state dye-sensitized solar cell

    PubMed Central

    2011-01-01

    A mesoscopic nitrogen-doped TiO2 sphere has been developed for a quasi-solid-state dye-sensitized solar cell [DSSC]. Compared with the undoped TiO2 sphere, the quasi-solid-state DSSC based on the nitrogen-doped TiO2 sphere shows more excellent photovoltaic performance. The photoelectrochemistry of electrodes based on nitrogen-doped and undoped TiO2 spheres was characterized with Mott-Schottky analysis, intensity modulated photocurrent spectroscopy, and electrochemical impedance spectroscopy, which indicated that both the quasi-Fermi level and the charge transport of the photoelectrode were improved after being doped with nitrogen. As a result, a photoelectric conversion efficiency of 6.01% was obtained for the quasi-solid-state DSSC. PMID:22115421

  13. Chemical assembly of TiO2 and TiO2@Ag nanoparticles on silk fiber to produce multifunctional fabrics.

    PubMed

    Li, Guohong; Liu, Hong; Zhao, Hongshi; Gao, Yuqiang; Wang, Jiyang; Jiang, Huaidong; Boughton, R I

    2011-06-01

    A carefully designed surface modification technique for the manufacture of multifunctional silk textile nanocomposite materials is successfully developed by the functionalization of silk with TiO(2) and TiO(2)@Ag nanoparticles (NPs). The NPs are assembled onto a silk substrate through covalent linkages, including enediol ligand-metal oxide bonding, resin dehydration and the acylation of silk. Owing to the strong chemical bonding, silk fibroin fabric (SFF) and the NPs form a stable composite system. The functionalized SFF, especially TiO(2)@Ag NP-functionalized SFF are endowed with remarkable UV protection properties, and an efficient anti-bacterial capability toward Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. Furthermore, the nearly total photodegradation of methylene orange (MO) under UV illumination illustrates that functionalized SFF possesses high photocatalytic and self-cleaning capability. This multifunctional silk material satisfies the market demand for natural "smart" products, and is a promising practical material for use in the textile industry, hospital sterilization and environmental cleanup. PMID:21419419

  14. The effects of n-type doping on lithium storage in TiO2.

    PubMed

    Shin, Ji-Yong; Joo, Jong Hoon; Adepalli, Kiran K; Samuelis, Dominik; Maier, Joachim

    2016-04-01

    In this report, we discuss the Li-storage performance of niobium-doped TiO2 nanostructures (Ti(1-y)Nb(y)O(2+δ)), with a special focus on the effects of ionic/electronic charge carrier concentration (defect chemistry) on Li storage and transport properties. By Nb-doping, Li storage kinetics of titania electrode material is significantly improved mainly due to the increased electronic charge carrier concentration (n-type doping). However, it was found that there is a maximum beyond which further doping is rather detrimental to Li diffusion kinetics. Defect chemical analysis indicates that this limited doping effect is due to the trapping of free lithium ions by the critical electron-ion association reactions at room temperature such as Li(i)(•) + e' ⇌ Li(i)(×) and Nb(Ti)(•) + e' ⇌ Nb(Ti)(×). PMID:26961152

  15. Origin of leakage paths driven by electric fields in Al-doped TiO2 films.

    PubMed

    Park, Gyeong-Su; Park, Seong Yong; Heo, Sung; Kwon, Ohseong; Cho, Kyuho; Han, Kwan-Young; Kang, Sung Jin; Yoon, Aram; Kim, Miyoung

    2014-12-23

    The growth of leakage current paths in Al-doped TiO2 (ATO) films is observed by in situ TEM under negative bias stress. Through systematic HAADF-STEM, STEM-EDS, and STEM-EELS studies, it is confirmed that the electric field-induced growth of the Ru-doped TiO2 phase is the main reason for the ATO film's negative leakage.

  16. Electrical Conductivity, Thermoelectric Power, and Equilibration Kinetics of Nb-Doped TiO2.

    PubMed

    Nowotny, Janusz; Bak, Tadeusz; Dickey, Elisabeth C; Sigmund, Wolfgang; Alim, Mohammad A

    2016-09-01

    This work considers the equilibration kinetics of Nb-doped TiO2 single crystal (0.066 atom % Nb) during oxidation and reduction within a wide range of temperature (1073-1298 K) and oxygen activity (10(-14)-10(5) Pa). The associated semiconducting properties were determined using simultaneous measurements of both electrical conductivity and thermoelectric power. It is shown that the chemical diffusion coefficient in the strongly reducing regime, p(O2) < 10(-5) Pa, is 4 orders of magnitude larger than that in the reducing and oxidizing regimes, 10 Pa < p(O2) < 22 kPa. The derived theoretical model considers the gas/solid kinetics for the TiO2/O2 system in terms of two diffusion regimes: the fast regime related to fast defects (oxygen vacancies and titanium interstitials) and leading to quasi-equilibrium, and the slow regime associated with slow defects (titanium vacancies) resulting in the gas/solid equilibrium. It has been shown that incorporation of donor-type elements, such as niobium, and imposition of oxygen activity above a certain critical value, results in a substantial reduction in the concentration of high mobility defects and leads to slowing down the equilibration kinetics. In consequence, the fast kinetic regime is not observed. Comparison of the kinetic data for Nb-doped TiO2 single crystal (this work) and polycrystalline Nb-doped TiO2 (reported before) indicates that the gas/solid kinetics for the polycrystalline specimen at higher oxygen activities is rate controlled by the transport of oxygen within individual grains.

  17. Electrical Conductivity, Thermoelectric Power, and Equilibration Kinetics of Nb-Doped TiO2.

    PubMed

    Nowotny, Janusz; Bak, Tadeusz; Dickey, Elisabeth C; Sigmund, Wolfgang; Alim, Mohammad A

    2016-09-01

    This work considers the equilibration kinetics of Nb-doped TiO2 single crystal (0.066 atom % Nb) during oxidation and reduction within a wide range of temperature (1073-1298 K) and oxygen activity (10(-14)-10(5) Pa). The associated semiconducting properties were determined using simultaneous measurements of both electrical conductivity and thermoelectric power. It is shown that the chemical diffusion coefficient in the strongly reducing regime, p(O2) < 10(-5) Pa, is 4 orders of magnitude larger than that in the reducing and oxidizing regimes, 10 Pa < p(O2) < 22 kPa. The derived theoretical model considers the gas/solid kinetics for the TiO2/O2 system in terms of two diffusion regimes: the fast regime related to fast defects (oxygen vacancies and titanium interstitials) and leading to quasi-equilibrium, and the slow regime associated with slow defects (titanium vacancies) resulting in the gas/solid equilibrium. It has been shown that incorporation of donor-type elements, such as niobium, and imposition of oxygen activity above a certain critical value, results in a substantial reduction in the concentration of high mobility defects and leads to slowing down the equilibration kinetics. In consequence, the fast kinetic regime is not observed. Comparison of the kinetic data for Nb-doped TiO2 single crystal (this work) and polycrystalline Nb-doped TiO2 (reported before) indicates that the gas/solid kinetics for the polycrystalline specimen at higher oxygen activities is rate controlled by the transport of oxygen within individual grains. PMID:27490974

  18. Large Enhancement in Electrorheological Activity of Mesoporous Cerium-Doped TIO2 from High Surface Area and Robust Pore Walls

    NASA Astrophysics Data System (ADS)

    Yin, Jianbo; Zhao, Xiaopeng

    Considering the importance of large interfacial or surface polarization to strong electrorheological (ER) effect, we developed a high surface area mesoporous doped TiO2 ER material by using block-copolymer. By comparing the ER experiments between samples with mesopore and without mesopore, we demonstrate a very large enhancement in ER activity of mesoporous ER material and its yield stress is 100 times that of the pure TiO2 ER material and 5-8 times that of single doped TiO2 without mesoporous structure. We give a preliminary discussion about the improvement in ER activity based on previous dielectric analysis.

  19. Understanding the dispersion of Ag on high surface area TiO2 supports using XPS intensity ratios

    NASA Astrophysics Data System (ADS)

    Davis, Zenda D.; Tatarchuk, Bruce J.

    2015-10-01

    Silver-titania (Ag/TiO2) adsorbents, in the range of 4 wt% Ag, display high selectivity toward sulfur heterocyclic compounds from complex fuel streams containing other aromatics. An experimental investigation of Ag on TiO2 has been undertaken to understand the state of dispersion and growth of Ag. XPS is one of the more promising characterization tools for the state of dispersion. Silver loading from 1 wt% to 20 wt% on 150 m2/g titania was investigated. Ag/Ti intensity ratios increased linearly with Ag content up to 4 wt% and increased less significantly thereafter from 8 wt% to 20 wt% indicating nucleation and growth of Ag crystallites. Inelastic mean free path (IMFP) calculations were used to estimate Ag crystallite size based on the attenuation of the Ag signal, realizing in this regime there is insufficient Ag to attenuate background titania. At 4, 8, 12, and 20 wt% the estimated average crystallite sizes were 0.35, 0.71, 0.84, and 1.11 nm respectively. Ag loadings up to 4 wt% were present in the form of Ag+1 adatoms presumably occupying TiO2 surface defects. Saturation of surface TiO2 defects is in good agreement with quantitative sulfur heterocycle adsorption.

  20. Preparation of Ag deposited TiO2 (Ag/TiO2) composites and investigation on visible-light photocatalytic degradation activity in magnetic field

    NASA Astrophysics Data System (ADS)

    Zhang, L.; Ma, C. H.; Wang, J.; Li, S. G.; Li, Y.

    2014-12-01

    In this study, Ag deposited TiO2 (Ag/TiO2) composites were prepared by three different methods (Ultraviolet Irradiation Deposition (UID), Vitamin C Reduction (VCR) and Sodium Borohydride Reduction (SBR)) for the visible-light photocatalytic degradation of organic dyes in magnetic field. And then the prepared Ag deposited TiO2 (Ag/TiO2) composites were characterized physically by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The visible-light photocatalytic activities of these three kinds of Ag deposited TiO2 (Ag/TiO2) composites were examined and compared through the degradation of several organic dyes under visible-light irradiation in magnetic field. In addition, some influence factors such as visible-light irradiation time, organic dye concentration, revolution speed, magnetic field intensity and organic dye kind on the visible-light photocatalytic activity of Ag deposited TiO2 (Ag/TiO2) composite were reviewed. The research results showed that the presence of magnetic field significantly enhanced the visible-light photocatalytic activity of Ag deposited TiO2 (Ag/TiO2) composites and then contributed to the degradation of organic dyes.

  1. Effect on Electron Structure and Magneto-Optic Property of Heavy W-Doped Anatase TiO2.

    PubMed

    Hou, Qingyu; Zhao, Chunwang; Guo, Shaoqiang; Mao, Fei; Zhang, Yue

    2015-01-01

    The spin or nonspin state of electrons in W-doped anatase TiO2 is very difficult to judge experimentally because of characterization method limitations. Hence, the effect on the microscopic mechanism underlying the visible-light effect of W-doped anatase TiO2 through the consideration of electronic spin or no-spin states is still unknown. To solve this problem, we establish supercell models of W-doped anatase TiO2 at different concentrations, followed by geometry optimization and energy calculation based on the first-principle planewave norm conserving pseudo-potential method of the density functional theory. Calculation results showed that under the condition of nonspin the doping concentration of W becomes heavier, the formation energy becomes greater, and doping becomes more difficult. Meanwhile, the total energy increases, the covalent weakens and ionic bonds strengthens, the stability of the W-doped anatase TiO2 decreases, the band gap increases, and the blue-shift becomes more significant with the increase of W doping concentration. However, under the condition of spin, after the band gap correction by the GGA+U method, it is found that the semimetal diluted magnetic semiconductors can be formed by heavy W-doped anatase TiO2. Especially, a conduction electron polarizability of as high as near 100% has been found for the first time in high concentration W-doped anatase TiO2. It will be able to be a promising new type of dilute magnetic semiconductor. And the heavy W-doped anatase TiO2 make the band gap becomes narrower and absorption spectrum red-shift. PMID:25955308

  2. Effect on Electron Structure and Magneto-Optic Property of Heavy W-Doped Anatase TiO2.

    PubMed

    Hou, Qingyu; Zhao, Chunwang; Guo, Shaoqiang; Mao, Fei; Zhang, Yue

    2015-01-01

    The spin or nonspin state of electrons in W-doped anatase TiO2 is very difficult to judge experimentally because of characterization method limitations. Hence, the effect on the microscopic mechanism underlying the visible-light effect of W-doped anatase TiO2 through the consideration of electronic spin or no-spin states is still unknown. To solve this problem, we establish supercell models of W-doped anatase TiO2 at different concentrations, followed by geometry optimization and energy calculation based on the first-principle planewave norm conserving pseudo-potential method of the density functional theory. Calculation results showed that under the condition of nonspin the doping concentration of W becomes heavier, the formation energy becomes greater, and doping becomes more difficult. Meanwhile, the total energy increases, the covalent weakens and ionic bonds strengthens, the stability of the W-doped anatase TiO2 decreases, the band gap increases, and the blue-shift becomes more significant with the increase of W doping concentration. However, under the condition of spin, after the band gap correction by the GGA+U method, it is found that the semimetal diluted magnetic semiconductors can be formed by heavy W-doped anatase TiO2. Especially, a conduction electron polarizability of as high as near 100% has been found for the first time in high concentration W-doped anatase TiO2. It will be able to be a promising new type of dilute magnetic semiconductor. And the heavy W-doped anatase TiO2 make the band gap becomes narrower and absorption spectrum red-shift.

  3. Enhanced photoelectrochemical water splitting performance of TiO2 nanotube arrays coated with an ultrathin nitrogen-doped carbon film by molecular layer deposition.

    PubMed

    Tong, Xili; Yang, Peng; Wang, Yunwei; Qin, Yong; Guo, Xiangyun

    2014-06-21

    Vertically oriented TiO2 nanotube arrays (TNTAs) were conformally coated with an ultrathin nitrogen-doped (N-doped) carbon film via the carbonization of a polyimide film deposited by molecular layer deposition and simultaneously hydrogenated, thereby creating a core/shell nanostructure with a precisely controllable shell thickness. The core/shell nanostructure provides a larger heterojunction interface to substantially reduce the recombination of photogenerated electron-hole pairs, and hydrogenation enhances solar absorption of TNTAs. In addition, the N-doped carbon film coating acts as a high catalytic active surface for oxygen evolution reaction, as well as a protective film to prevent hydrogen-treated TiO2 nanotube oxidation by electrolyte or air. As a result, the N-doped carbon film coated TNTAs displayed remarkably improved photocurrent and photostability. The TNTAs with a N-doped carbon film of ∼ 1 nm produces a current density of 3.6 mA cm(-2) at 0 V vs. Ag/AgCl under the illumination of AM 1.5 G (100 mW cm(-2)), which represents one of the highest values achieved with modified TNTAs. Therefore, we propose that ultrathin N-doped carbon film coating on materials is a viable approach to enhance their PEC water splitting performance.

  4. Effects of TiO2 and Ag nanoparticles on polyhydroxybutyrate biosynthesis by activated sludge bacteria.

    PubMed

    Priester, John H; Van De Werfhorst, Laurie C; Ge, Yuan; Adeleye, Adeyemi S; Tomar, Shivira; Tom, Lauren M; Piceno, Yvette M; Andersen, Gary L; Holden, Patricia A

    2014-12-16

    Manufactured nanomaterials (MNMs) are increasingly incorporated into consumer products that are disposed into sewage. In wastewater treatment, MNMs adsorb to activated sludge biomass where they may impact biological wastewater treatment performance, including nutrient removal. Here, we studied MNM effects on bacterial polyhydroxyalkanoate (PHA), specifically polyhydroxybutyrate (PHB), biosynthesis because of its importance to enhanced biological phosphorus (P) removal (EBPR). Activated sludge was sampled from an anoxic selector of a municipal wastewater treatment plant (WWTP), and PHB-containing bacteria were concentrated by density gradient centrifugation. After starvation to decrease intracellular PHB stores, bacteria were nutritionally augmented to promote PHB biosynthesis while being exposed to either MNMs (TiO2 or Ag) or to Ag salts (each at a concentration of 5 mg L(-1)). Cellular PHB concentration and PhyloChip community composition were analyzed. The final bacterial community composition differed from activated sludge, demonstrating that laboratory enrichment was selective. Still, PHB was synthesized to near-activated sludge levels. Ag salts altered final bacterial communities, although MNMs did not. PHB biosynthesis was diminished with Ag (salt or MNMs), indicating the potential for Ag-MNMs to physiologically impact EBPR through the effects of dissolved Ag ions on PHB producers. PMID:25409530

  5. Photocatalytic antibacterial effect of TiO(2) film formed on Ti and TiAg exposed to Lactobacillus acidophilus.

    PubMed

    Choi, Jung-Yoon; Kim, Kyung-Ho; Choy, Kwang-Chul; Oh, Keun-Taek; Kim, Kyoung-Nam

    2007-02-01

    When irradiated under near-ultraviolet (UV) light, TiO(2) exhibits strong bactericidal activity. The TiO(2) photocatalyst would be effective on orthodontic appliances after its antibacterial effect on the carcinogenic microorganism Lactobacillus acidophilus is evaluated. To compare the antibacterial effect of two crystalline forms of TiO(2), rutile and anatase, thermal oxidation and anodic oxidation were employed to form each structure, respectively. The antibacterial effect of TiO(2) film on TiAg was also compared with that on Ti. Bacterial solutions were pipetted onto the TiO(2)-coated specimen and illuminated with UVA (2 x 15 W, black light, 356 nm) up to 100 min and the reaction solutions were incubated to count the colony-forming units. The antibacterial activity of the coated specimens was similar to that of the uncoated group. The antibacterial activity of the coated specimens of TiAg was not different from that of Ti. TiO(2) coatings formed on both Ti and TiAg specimens did not exhibit cytotoxicity on the L-929 cells of mice. PMID:16850466

  6. Preparation, testing and characterization of doped TiO2 active in the peroxidation of biomolecules under visible light.

    PubMed

    Bacsa, Revathi; Kiwi, John; Ohno, Teruhisa; Albers, Peter; Nadtochenko, Victor

    2005-03-31

    Doped TiO2 samples using different preparative procedures were synthesized using either urea or thiourea leading to N- or S-doped TiO2. Photocatalytic peroxidation and oxidation (mineralization) of phosphatidylethanolamine (PE) lipid with doped TiO2 were carried out under light irradiation lambda > 410 nm. The formation of conjugated double bonds in PE molecules was followed to detect the formation of peroxy radicals (peroxidation index) under light excitation (lambda > 410 nm) when doped TiO2 was used. The kinetics of CO2 production was monitored during the mineralization of PE. Colored TiO2 powders were studied in detail by different and complementary physicochemical techniques. The band gap energies of colored TiO2 were determined by diffuse reflectance spectroscopy (DRS). The visible absorption shoulder of TiO2 was observed to follow Urbach's law. The variation of the transient decay after 354 nm laser pulse excitation does not correlate with the different N- and S-TiO2 doping levels introduced by the addition of urea or thiourea. This suggests that the states (recombination centers or traps) introduced by the doping are not effective in varying the decay kinetics within the nanosecond and microsecond time scale. Elemental analysis shows comparable amounts of S- and N-doping of TiO2 when thiourea is used as dopant. X-ray diffraction reveals no rutile in S-TiO2 samples heated to 600 degrees C, suggesting that the addition of sulfur precludes rutilization during sample crystallization. X-ray photoelectron spectroscopy (XPS) of the S-TiO2 samples confirms the preferential localization of S on the 20 topmost layers of S-TiO2 upon calcination at 500 degrees C for 2 h.

  7. Charge compensation in trivalent cation doped bulk rutile TiO2

    NASA Astrophysics Data System (ADS)

    Iwaszuk, Anna; Nolan, Michael

    2011-08-01

    Doping of TiO2 is a very active field, with a particularly large effort expended using density functional theory (DFT) to model doped TiO2; this interest has arisen from the potential for doping to be used in tuning the band gap of TiO2 for photocatalytic applications. Doping is also of importance for modifying the reactivity of an oxide. Finally, dopants can also be unintentionally incorporated into an oxide during processing, giving unexpected electronic properties. To unravel properly how doping impacts on the properties of a metal oxide requires a modelling approach that can describe such systems consistently. Unfortunately, DFT, as used in the majority of studies, is not suitable for application here and in many cases cannot even yield a qualitatively consistent description. In this paper we investigate the doping of bulk rutile TiO2 with trivalent cations, Al, Ga and In, using DFT, DFT corrected for on-site Coulomb interactions (DFT + U, with U on oxygen 2p states) and hybrid DFT (the screened exchange HSE06 exchange correlation functional) in an effort to better understand the performance of DFT in describing such fundamental doping scenarios and to analyse the process of charge compensation with these dopants. With all dopants, DFT delocalizes the oxygen hole polaron that results from substitution of Ti with the lower valence cation. DFT also finds an undistorted geometry and does not produce the characteristic polaron state in the band gap. DFT + U and hybrid DFT both localize the polaron, and this is accompanied by a distortion to the structure around the oxygen hole site. DFT + U and HSE06 both give a polaron state in the band gap. The band gap underestimation present in DFT + U means that the offset of the gap state from both the valence and the conduction band cannot be properly described, while the hybrid DFT offsets should be correct. We have investigated dopant charge compensation by formation of oxygen vacancies. Due to the large number of

  8. Charge compensation in trivalent cation doped bulk rutile TiO2.

    PubMed

    Iwaszuk, Anna; Nolan, Michael

    2011-08-24

    Doping of TiO(2) is a very active field, with a particularly large effort expended using density functional theory (DFT) to model doped TiO(2); this interest has arisen from the potential for doping to be used in tuning the band gap of TiO(2) for photocatalytic applications. Doping is also of importance for modifying the reactivity of an oxide. Finally, dopants can also be unintentionally incorporated into an oxide during processing, giving unexpected electronic properties. To unravel properly how doping impacts on the properties of a metal oxide requires a modelling approach that can describe such systems consistently. Unfortunately, DFT, as used in the majority of studies, is not suitable for application here and in many cases cannot even yield a qualitatively consistent description. In this paper we investigate the doping of bulk rutile TiO(2) with trivalent cations, Al, Ga and In, using DFT, DFT corrected for on-site Coulomb interactions (DFT + U, with U on oxygen 2p states) and hybrid DFT (the screened exchange HSE06 exchange correlation functional) in an effort to better understand the performance of DFT in describing such fundamental doping scenarios and to analyse the process of charge compensation with these dopants. With all dopants, DFT delocalizes the oxygen hole polaron that results from substitution of Ti with the lower valence cation. DFT also finds an undistorted geometry and does not produce the characteristic polaron state in the band gap. DFT + U and hybrid DFT both localize the polaron, and this is accompanied by a distortion to the structure around the oxygen hole site. DFT + U and HSE06 both give a polaron state in the band gap. The band gap underestimation present in DFT + U means that the offset of the gap state from both the valence and the conduction band cannot be properly described, while the hybrid DFT offsets should be correct. We have investigated dopant charge compensation by formation of oxygen vacancies. Due to the large number of

  9. Sequential laser and ultrasonic wave generation of TiO2@Ag core-shell nanoparticles and their anti-bacterial properties.

    PubMed

    Hamad, Abubaker Hassan; Li, Lin; Liu, Zhu; Zhong, Xiang Li; Wang, Tao

    2016-02-01

    Core-shell nanoparticles have unusual physical, chemical and biological properties. Until now, for the Ag and TiO2 combination, only Ag core and TiO2 shell nanoparticles have been practically demonstrated. In this investigation, novel TiO2@Ag core-shell (TiO2 core and Ag shell) nanoparticles were produced via ultrasonic vibration of Ag-TiO2 compound nanoparticles. A bulk Ti/Ag alloy plate was used to generate colloidal Ag-TiO2 compound nanoparticles via picosecond laser ablation in deionised water. The colloidal nanoparticles were then sonicated in an ultrasonic bath to generate TiO2@Ag core-shell nanoparticles. They were characterised using a UV-VIS spectrometer, transmission electron microscopy (TEM), high-angle annular dark-field-Scanning transmission electron microscopy (HAADF-STEM), energy-dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD). The Ag-TiO2 compound and the TiO2@Ag core-shell nanoparticles were examined for their antibacterial activity against Escherichia coli (E. coli) JM109 strain bacteria and compared with those of Ag and TiO2 nanoparticles. The antibacterial activity of the core-shell nanoparticles was slightly better than that of the compound nanoparticles at the same concentration under standard laboratory light conditions and both were better than the TiO2 nanoparticles but not as good as the Ag nanoparticles.

  10. Characterization of nanocrystalline cobalt doped TiO2 sol-gel material

    NASA Astrophysics Data System (ADS)

    Siddhapara, Kirit; Shah, Dimple

    2012-08-01

    Nanocrystalline 1%, 2% and 4% Cobalt-doped TiO2 were prepared by sol-gel technique, followed by freeze-drying treatment at -30 °C temperature for 12 h. The obtained gels were thermally treated at 200, 400, 600 and 800 °C. X-ray Powder Diffraction (XRD), Scanning Electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDAX) were used to study its structural properties. The XRD pattern shows the coexistence of anatase phase and minor brookite phase. UV-vis Spectroscopy and Photoluminescence (PL) were used to study its optical properties. Optical band gap was calculated with the incorporation of different concentrations of cobalt. UV-visible spectroscopy shows variation in band gap for the sample treated at different temperatures for same concentration. All Cobalt doped TiO2 nanostructures show an appearance of Red shift relative to the bulk TiO2. The determination of magnetic properties was also carried out by Gouy balance method.

  11. Towards TiO2sbnd Ag porous nanocomposites based SERS sensors for chemical pollutant detection

    NASA Astrophysics Data System (ADS)

    Iancu, Vlad; Baia, Lucian; Tarcea, Nicolae; Popp, Jürgen; Baia, Monica

    2014-09-01

    Since the TiO2 environmental friendly character and the affinity of a large variety of molecules to bind to the silver surfaces are well-known, novel porous nanoarchitectures based on TiO2 aerogel and Ag colloidal particles deposited on a poly(methyl methacrylate) (PMMA) substrate were obtained. The ability of the deposited porous structures to detect by surface-enhanced Raman spectroscopy (SERS) contaminant species adsorbed from aqueous media was tested. The morphological particularities of the bulk samples during the deposition on the PMMA substrates were preserved. The SERS detection efficiency was assessed by using congo red as a test molecule. No matter the average size of the Ag nanoparticles, the lowest detectable concentrations were found be of around 5 × 10-6 M for all samples. The morphological parameters such as median pore diameter and cumulative pore volume were also taken into consideration when discussing the detection performances. Moreover, calibration curves have been obtained in order to estimate an unknown concentration of the analyte. The obtained results show the real potential of the prepared porous composites for further use in the development of new SERS-based sensors for monitoring of water quality, especially when the contaminants are dye molecules.

  12. Effective nitrogen doping into TiO2 (N-TiO2) for visible light response photocatalysis.

    PubMed

    Yoshida, Tomoko; Niimi, Satoshi; Yamamoto, Muneaki; Nomoto, Toyokazu; Yagi, Shinya

    2015-06-01

    The thickness-controlled TiO2 thin films are fabricated by the pulsed laser deposition (PLD) method. These samples function as photocatalysts under UV light irradiation and the reaction rate depends on the TiO2 thickness, i.e., with an increase of thickness, it increases to the maximum, followed by decreasing to be constant. Such variation of the reaction rate is fundamentally explained by the competitive production and annihilation processes of photogenerated electrons and holes in TiO2 films, and the optimum TiO2 thickness is estimated to be ca. 10nm. We also tried to dope nitrogen into the effective depth region (ca. 10nm) of TiO2 by an ion implantation technique. The nitrogen doped TiO2 enhanced photocatalytic activity under visible-light irradiation. XANES and XPS analyses indicated two types of chemical state of nitrogen, one photo-catalytically active N substituting the O sites and the other inactive NOx (1⩽x⩽2) species. In the valence band XPS spectrum of the high active sample, the additional electronic states were observed just above the valence band edge of a TiO2. The electronic state would be originated from the substituting nitrogen and be responsible for the band gap narrowing, i.e., visible light response of TiO2 photocatalysts.

  13. Antifungal activity of Ag:hydroxyapatite thin films synthesized by pulsed laser deposition on Ti and Ti modified by TiO2 nanotubes substrates

    NASA Astrophysics Data System (ADS)

    Eraković, S.; Janković, A.; Ristoscu, C.; Duta, L.; Serban, N.; Visan, A.; Mihailescu, I. N.; Stan, G. E.; Socol, M.; Iordache, O.; Dumitrescu, I.; Luculescu, C. R.; Janaćković, Dj.; Miškovic-Stanković, V.

    2014-02-01

    Hydroxyapatite (HA) is a widely used biomaterial for implant thin films, largely recognized for its excellent capability to chemically bond to hard tissue inducing the osteogenesis without immune response from human tissues. Nowadays, intense research efforts are focused on development of antimicrobial HA doped thin films. In particular, HA doped with Ag (Ag:HA) is expected to inhibit the attachment of microbes and contamination of metallic implant surface. We herewith report on nano-sized HA and Ag:HA thin films synthesized by pulsed laser deposition on pure Ti and Ti modified with 100 nm diameter TiO2 nanotubes (fabricated by anodization of Ti plates) substrates. The HA-based thin films were characterized by SEM, AFM, EDS, FTIR, and XRD. The cytotoxic activity was tested with HEp2 cells against controls. The antifungal efficiency of the deposited layers was tested against the Candida albicans and Aspergillus niger strains. The Ti substrates modified with TiO2 nanotubes covered with Ag:HA thin films showed the highest antifungal activity.

  14. Photocatalytic activity of Cr-doped TiO2 nanoparticles deposited on porous multicrystalline silicon films

    PubMed Central

    2014-01-01

    This work deals with the deposition of Cr-doped TiO2 thin films on porous silicon (PS) prepared from electrochemical anodization of multicrystalline (mc-Si) Si wafers. The effect of Cr doping on the properties of the TiO2-Cr/PS/Si samples has been investigated by means of X-ray diffraction (XRD), atomic force microcopy (AFM), photoluminescence, lifetime, and laser beam-induced current (LBIC) measurements. The photocatalytic activity is carried out on TiO2-Cr/PS/Si samples. It was found that the TiO2-Cr/PS/mc-Si type structure degrades an organic pollutant (amido black) under ultraviolet (UV) light. A noticeable degradation of the pollutant is obtained for a Cr doping of 2 at. %. This result is discussed in light of LBIC and photoluminescence measurements. PMID:25313302

  15. Preparation of Co-doped TiO2 thin films deposited by sol-gel method

    NASA Astrophysics Data System (ADS)

    Mahtali, M.; Boudjema, E.-H.; Boutelala, A.; Bourfaa, F.; Mahcene, F.; Hanini, F.; Bouabellou, A.

    2012-09-01

    Cobalt doped TiO2 thin films (Co: TiO2, Co: 0-2-4-6 at. %) have been prepared by sol-gel method onto glass substrate at room temperature. The obtained films have been annealed at 500°C for 2 hours. X-ray diffraction patterns showed that all Al: TiO2 films are polycrystalline with a tetragonal anatase and orthorhombic brookite types structures. The surface morphologies of the TiO2 doped with cobalt thin films were evaluated by atomic force microscopy (AFM). The calculated optical band gap decreases from 3.03 to 2.96 eV with increasing Co doping.

  16. Synthesis and photocatalytic activity of N-doped TiO2 produced in a solid phase reaction

    NASA Astrophysics Data System (ADS)

    Xin, Gang; Pan, Hongfei; Chen, Dan; Zhang, Zhihua; Wen, Bin

    2013-02-01

    N-doped TiO2 was synthesized by calcining a mixture of titanic acid and graphitic carbon nitride (g-C3N4) at temperatures above 500 °C. The final samples were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), electron energy loss spectroscopy (EELS), and UV-vis diffuse reflectance spectra. The photocatalytic activity of N-doped TiO2 was studied by assessing the degradation of methylene blue in an aqueous solution, under visible light and UV light irradiation. It was found that the N-doped TiO2 displayed higher photocatalytic activity than pure TiO2, under both visible and UV light.

  17. Photocatalytic activity of Cr-doped TiO2 nanoparticles deposited on porous multicrystalline silicon films.

    PubMed

    Hajjaji, Anouar; Trabelsi, Khaled; Atyaoui, Atef; Gaidi, Mounir; Bousselmi, Latifa; Bessais, Brahim; El Khakani, My Ali

    2014-01-01

    This work deals with the deposition of Cr-doped TiO2 thin films on porous silicon (PS) prepared from electrochemical anodization of multicrystalline (mc-Si) Si wafers. The effect of Cr doping on the properties of the TiO2-Cr/PS/Si samples has been investigated by means of X-ray diffraction (XRD), atomic force microcopy (AFM), photoluminescence, lifetime, and laser beam-induced current (LBIC) measurements. The photocatalytic activity is carried out on TiO2-Cr/PS/Si samples. It was found that the TiO2-Cr/PS/mc-Si type structure degrades an organic pollutant (amido black) under ultraviolet (UV) light. A noticeable degradation of the pollutant is obtained for a Cr doping of 2 at. %. This result is discussed in light of LBIC and photoluminescence measurements.

  18. Effect of Nb doping on structural, optical and photocatalytic properties of flame-made TiO2 nanopowder.

    PubMed

    Michalow, Katarzyna A; Flak, Dorota; Heel, Andre; Parlinska-Wojtan, Magdalena; Rekas, Mieczyslaw; Graule, Thomas

    2012-11-01

    TiO(2):Nb nanopowders within a dopant concentration in the range of 0.1-15 at.% were prepared by one-step flame spray synthesis. Effect of niobium doping on structural, optical and photocatalytic properties of titanium dioxide nanopowders was studied. Morphology and structure were investigated by means of Brunauer-Emmett-Teller isotherm, X-ray diffraction and transmission electron microscopy. Diffuse reflectance and the resulting band gap energy were determined by diffuse reflectance spectroscopy. Photocatalytic activity of the investigated nanopowders was revised for the photodecomposition of methylene blue (MB), methyl orange (MO) and 4-chlorophenol under UVA and VIS light irradiation. Commercial TiO(2)-P25 nanopowder was used as a reference. The specific surface area of the powders was ranging from 42.9 m(2)/g for TiO(2):0.1 at.% Nb to 90.0 m(2)/g for TiO(2):15 at.% Nb. TiO(2):Nb particles were nanosized, spherically shaped and polycrystalline. Anatase was the predominant phase in all samples. The anatase-related transition was at 3.31 eV and rutile-related one at 3.14 eV. TiO(2):Nb nanopowders exhibited additional absorption in the visible range. In comparison to TiO(2)-P25, improved photocatalytic activity of TiO(2):Nb was observed for the degradation of MB and MO under both UVA and VIS irradiation, where low doping level (Nb < 1 at.%) was the most effective. Niobium doping affected structural, optical and photocatalytic properties of TiO(2). Low dopant level enhanced photocatalytic performance under UVA and VIS irradiation. Therefore, TiO(2):Nb (Nb < 1 at.%) can be proposed as an efficient selective solar light photocatalyst. PMID:23054731

  19. Contributions of Ag Nanowires to the Photoelectric Conversion Efficiency Enhancement of TiO2 Dye-Sensitized Solar Cells.

    PubMed

    Liu, Yunyu; She, Guangwei; Qi, Xiaopeng; Mu, Lixuan; Wang, Xuesong; Shi, Wensheng

    2015-09-01

    Ag nanowires (AgNWs) were employed in mesoporous TiO2 dye-sensitized solar cells (DSSCs) to enhance the photoelectric conversion efficiency (PCE). The possible reasons for PCE improvement, i.e., improvement in electron transport and light harvesting due to light scattering and plasmonic resonance effect of AgNWs are investigated. Electrochemical impedance spectra (EIS) study proved that addition of AgNWs can enhance the conductivity of TiO2 thin film photoanode, which is an important reason for the increase of photocurrent. Furthermore, through the comparison experiments as well as the UV-Vis absorption and IPCE characterization, contributions of the light scattering and plasmonic resonance effect to the enhancement of light harvest, and thus PCE of the DSSCs were demonstrated. It was found that fast electron transport of AgNWs played more important role for the PCE improvement than the light harvest enhancement due to light scattering and plasmonic effect. Based on these investigations, the AgNWs modified TiO2 thin film DSSCs were optimized. After integrating AgNWs into the photoanode, the photocurrent increased significantly and PCE increased -50% comparing with the pure TiO2-based DSSCs.

  20. Contributions of Ag Nanowires to the Photoelectric Conversion Efficiency Enhancement of TiO2 Dye-Sensitized Solar Cells.

    PubMed

    Liu, Yunyu; She, Guangwei; Qi, Xiaopeng; Mu, Lixuan; Wang, Xuesong; Shi, Wensheng

    2015-09-01

    Ag nanowires (AgNWs) were employed in mesoporous TiO2 dye-sensitized solar cells (DSSCs) to enhance the photoelectric conversion efficiency (PCE). The possible reasons for PCE improvement, i.e., improvement in electron transport and light harvesting due to light scattering and plasmonic resonance effect of AgNWs are investigated. Electrochemical impedance spectra (EIS) study proved that addition of AgNWs can enhance the conductivity of TiO2 thin film photoanode, which is an important reason for the increase of photocurrent. Furthermore, through the comparison experiments as well as the UV-Vis absorption and IPCE characterization, contributions of the light scattering and plasmonic resonance effect to the enhancement of light harvest, and thus PCE of the DSSCs were demonstrated. It was found that fast electron transport of AgNWs played more important role for the PCE improvement than the light harvest enhancement due to light scattering and plasmonic effect. Based on these investigations, the AgNWs modified TiO2 thin film DSSCs were optimized. After integrating AgNWs into the photoanode, the photocurrent increased significantly and PCE increased -50% comparing with the pure TiO2-based DSSCs. PMID:26716285

  1. the effect of electron doping in TiO2 assessed by ARPES

    NASA Astrophysics Data System (ADS)

    Moreschini, Luca; Moser, Simon; Jacimovic, Jacim; Barisic, Osor; Berger, Helmut; Magrez, Arnaud; Chang, Young Jun; Kim, Keun Su; Bostwick, Aaron; Forro, Laszlo; Rotenberg, Eli; Grioni, Marco

    2013-03-01

    The titanium oxide TiO2 has been object of extensive studies because of its suitability in many practical fields, ranging from photovoltaic applications, to catalysis, memristors, and others. As for many other transition metal oxides, great attention has been devoted to the impact on the electronic structure of different doping mechanisms, either extrinsic or due to the creation of oxygen vacancies. Here we report an angle-resolved photoemission (ARPES) work on TiO2 single crystals and epitaxial films grown wIth the in situ pulsed-laser-deposition (PLD) system available on beamline 7.0.1 at the Advanced Light Source. We show the evolution of the electronic structure as a function of the amount of oxygen vacancies induced by the photon beam.

  2. TiO2 nanoparticles doped SiO2 films with ordered mesopore channels: a catalytic nanoreactor.

    PubMed

    Saha, Jony; Mitra, Anuradha; Dandapat, Anirban; De, Goutam

    2014-04-01

    Titanium dioxide (TiO2) incorporated ordered 2D hexagonal mesoporous silica (SiO2) films on a glass substrate were fabricated for use as a catalytic nanoreactor. Films were prepared using a tetraethyl orthosilicate (TEOS) derived SiO2 sol and a commercially available dispersion of TiO2 nanoparticles (NPs) in the presence of pluronic P123 as the structure directing agent. The effect of TiO2 doping (4-10 mol% with respect to the equivalent SiO2) into the ordered mesoporous SiO2 matrix was thoroughly investigated. The undoped SiO2 film showed a mesostructural transformation after heat-treatment at 350 °C whereas incorporation of TiO2 restricted such a transformation. Among all the TiO2 incorporated films, TEM showed that the 7 equivalent mol% TiO2 doped SiO2 film (ST-7) had an optimal composition which could retain the more organized 2D hexagonal (space group p6mm)-like mesostructures after heat-treatment. The catalytic activities of the TiO2 doped (4-10 mol%) films were investigated for the reduction of toxic KMnO4 in an aqueous medium. ST-7 film showed the maximum catalytic activity, as well as reusability. A TEM study on the resultant solution after KMnO4 reduction revealed the formation of MnO2 nanowires. It was understood that the embedded TiO2 NPs bonded SiO2 matrix increased the surface hydroxyl groups of the composite films resulting in the generation of acidic sites. The catalytic process can be explained by this enhanced surface acidity. The mesoporous channel of the ST-7 films with TiO2 doping can be used as a nanoreactor to form extremely thin MnO2 nanowires.

  3. High power TiO2 and high capacity Sn-doped TiO2 nanomaterial anodes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Lübke, Mechthild; Johnson, Ian; Makwana, Neel M.; Brett, Dan; Shearing, Paul; Liu, Zhaolin; Darr, Jawwad A.

    2015-10-01

    A range of phase-pure anatase TiO2 (∼5 nm) and Sn-doped TiO2 nanoparticles with the formula Ti1-xSnxO2 (where x = 0, 0.06, 0.11 and 0.15) were synthesized using a continuous hydrothermal flow synthesis (CHFS) reactor. Charge/discharge cycling tests were carried out in two different potential ranges of 3 to 1 V and also a wider range of 3 to 0.05 V vs Li/Li+. In the narrower potential range, the undoped TiO2 nanoparticles display superior electrochemical performance to all the Sn-doped titania crystallites. In the wider potential range, the Sn-doped samples perform better than undoped TiO2. The sample with composition Ti0.85Sn0.15O2, shows a capacity of ca. 350 mAh g-1 at an applied constant current of 100 mA g-1 and a capacity of 192.3 mAh g-1 at a current rate of 1500 mA g-1. After 500 charge/discharge cycles (at a high constant current rate of 382 mA g-1), the same nanomaterial anode retains a relatively high specific capacity of 240 mAh g-1. The performance of these nanomaterials is notable, particularly as they are processed into electrodes, directly from the CHFS process (after drying) without any post-synthesis heat-treatment, and they are made without any conductive surface coating.

  4. Enhanced dopant solubility and visible-light absorption in Cr-N co-doped TiO2 nanoclusters

    SciTech Connect

    Chiodi, Dr Mirco; Cheney, Christine; Vilmercati, Paolo; Cavaliere, Emanuele; Mannella, Norman; Gavioli, Luca; Weitering, Harm H

    2012-01-01

    A major obstacle toward employing TiO2 as an efficient photoactive material is related to its large optical band gap, strongly limiting visible light absorption. Substitutional doping with both donors and acceptors (co-doping) potentially leads to a significant band gap reduction, but the effectiveness of the co-doping approach remains limited by the low solubility of dopants inside TiO2. Here we show that nanostructured Cr and N co-doped TiO2 thin films can be obtained by Supersonic Cluster Beam Deposition (SCBD) with a high concentration of dopants and a strongly reduced band gap. Complementary spectroscopic investigations show that doping effectively occurs into substitutional lattice sites, inducing dopant levels in the gap that are remarkably delocalized. The high surface-to-volume ratio, typical of SCBD nanostructured films, likely facilitates the dopant incorporation. The present results indicate that SCBD films are highly promising photoactive nanophase materials.

  5. Synthesis of Ag-decorated porous TiO2 nanowires through a sunlight induced reduction method and its enhanced photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Yao, Yun-Chang; Dai, Xin-Rong; Hu, Xiao-Ye; Huang, Su-Zhen; Jin, Zhen

    2016-11-01

    In this work, Ag-decorated porous TiO2 nanowires were successfully synthesized via a facile and low-cost sunlight induced reduction method. The cooperation of sunlight irradiation and ethanol reduction results the formation and decoration of the Ag nanoparticles on the porous TiO2 nanowires. The structure of the Ag-decorated porous TiO2 nanowires were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Energy dispersive spectroscopy (EDS) measurements. It can be seen that the Ag nanoparticles are well dispersed within the porous TiO2 nanowires. The as-prepared Ag-decorated porous TiO2 nanowires exhibits excellent photocatalytic properties. The photocatalytic tests show that 10 ppm methylene blue can be photodegraded within 60 min. And the photodegradation ratio of the Ag-decorated porous TiO2 nanowires much higher than that of P25 and porous TiO2 nanowires. Moreover, the Ag-decorated porous TiO2 nanowires also reveal good photocatalytic activity towards to other organic pollutions, such as phenol and R6G. Therefore, it is believed that the Ag-decorated porous TiO2 nanowires can be used as a potential high performance photocatalyst in wastewater treatment.

  6. Effective passivation of Ag nanowire-based flexible transparent conducting electrode by TiO2 nanoshell

    NASA Astrophysics Data System (ADS)

    Lee, Dong Geon; Lee, Dongjun; Yoo, Jin Sun; Lee, Sangwook; Jung, Hyun Suk

    2016-08-01

    Silver nanowire-based flexible transparent electrodes have critical problem, in spite of their excellent electrical and optical properties, that the electrical conductance and transparency degrade within several days in air because of oxidation of silver. To prevent the degradation of the silver nanowire, we encapsulated Ag-NWs with thin TiO2 barrier. Bar-coated silver nanowires on flexible polymer substrate were laminated at 120 °C, followed by atomic layer deposition of TiO2 nanoshell. With 20 nm of TiO2 nanoshells on silver nanowires, the transparent electrode keeps its electrical and optical properties over 2 months. Moreover, the TiO2-encapsulated silver nanowire-based transparent electrodes exhibit excellent bending durability.

  7. Preparation and use of photocatalytically active segmented Ag|ZnO and coaxial TiO2-Ag nanowires made by templated electrodeposition.

    PubMed

    Maijenburg, A Wouter; Rodijk, Eddy J B; Maas, Michiel G; Ten Elshof, Johan E

    2014-05-02

    Photocatalytically active nanostructures require a large specific surface area with the presence of many catalytically active sites for the oxidation and reduction half reactions, and fast electron (hole) diffusion and charge separation. Nanowires present suitable architectures to meet these requirements. Axially segmented Ag|ZnO and radially segmented (coaxial) TiO2-Ag nanowires with a diameter of 200 nm and a length of 6-20 µm were made by templated electrodeposition within the pores of polycarbonate track-etched (PCTE) or anodized aluminum oxide (AAO) membranes, respectively. In the photocatalytic experiments, the ZnO and TiO2 phases acted as photoanodes, and Ag as cathode. No external circuit is needed to connect both electrodes, which is a key advantage over conventional photo-electrochemical cells. For making segmented Ag|ZnO nanowires, the Ag salt electrolyte was replaced after formation of the Ag segment to form a ZnO segment attached to the Ag segment. For making coaxial TiO2-Ag nanowires, a TiO2 gel was first formed by the electrochemically induced sol-gel method. Drying and thermal annealing of the as-formed TiO2 gel resulted in the formation of crystalline TiO2 nanotubes. A subsequent Ag electrodeposition step inside the TiO2 nanotubes resulted in formation of coaxial TiO2-Ag nanowires. Due to the combination of an n-type semiconductor (ZnO or TiO2) and a metal (Ag) within the same nanowire, a Schottky barrier was created at the interface between the phases. To demonstrate the photocatalytic activity of these nanowires, the Ag|ZnO nanowires were used in a photocatalytic experiment in which H2 gas was detected upon UV illumination of the nanowires dispersed in a methanol/water mixture. After 17 min of illumination, approximately 0.2 vol% H2 gas was detected from a suspension of ~0.1 g of Ag|ZnO nanowires in a 50 ml 80 vol% aqueous methanol solution.

  8. Preparation and Use of Photocatalytically Active Segmented Ag|ZnO and Coaxial TiO2-Ag Nanowires Made by Templated Electrodeposition

    PubMed Central

    Maijenburg, A. Wouter; Rodijk, Eddy J.B.; Maas, Michiel G.; ten Elshof, Johan E.

    2014-01-01

    Photocatalytically active nanostructures require a large specific surface area with the presence of many catalytically active sites for the oxidation and reduction half reactions, and fast electron (hole) diffusion and charge separation. Nanowires present suitable architectures to meet these requirements. Axially segmented Ag|ZnO and radially segmented (coaxial) TiO2-Ag nanowires with a diameter of 200 nm and a length of 6-20 µm were made by templated electrodeposition within the pores of polycarbonate track-etched (PCTE) or anodized aluminum oxide (AAO) membranes, respectively. In the photocatalytic experiments, the ZnO and TiO2 phases acted as photoanodes, and Ag as cathode. No external circuit is needed to connect both electrodes, which is a key advantage over conventional photo-electrochemical cells. For making segmented Ag|ZnO nanowires, the Ag salt electrolyte was replaced after formation of the Ag segment to form a ZnO segment attached to the Ag segment. For making coaxial TiO2-Ag nanowires, a TiO2 gel was first formed by the electrochemically induced sol-gel method. Drying and thermal annealing of the as-formed TiO2 gel resulted in the formation of crystalline TiO2 nanotubes. A subsequent Ag electrodeposition step inside the TiO2 nanotubes resulted in formation of coaxial TiO2-Ag nanowires. Due to the combination of an n-type semiconductor (ZnO or TiO2) and a metal (Ag) within the same nanowire, a Schottky barrier was created at the interface between the phases. To demonstrate the photocatalytic activity of these nanowires, the Ag|ZnO nanowires were used in a photocatalytic experiment in which H2 gas was detected upon UV illumination of the nanowires dispersed in a methanol/water mixture. After 17 min of illumination, approximately 0.2 vol% H2 gas was detected from a suspension of ~0.1 g of Ag|ZnO nanowires in a 50 ml 80 vol% aqueous methanol solution. PMID:24837535

  9. Optical and structural characterization of TiO2 films doped with silver nanoparticles obtained by sol-gel method

    NASA Astrophysics Data System (ADS)

    Ivanova, T.; Harizanova, A.; Koutzarova, T.; Vertruyen, B.

    2013-12-01

    Nanostructured titanium oxide films with incorporated Ag nanoparticles were deposited by sol-gel spin coating method. The films were annealed at 300 °C, 400 °C, 500 °C and 600 °C in oxygen and nitrogen ambient. X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and UV-VIS spectroscopy had been applied for studying the influence of the thermal treatments and the gas ambient on the structural and optical properties of TiO2 and TiO2:Ag films. The XRD analysis revealed the presence of metallic Ag phase without traces of silver oxides and these results were confirmed by FTIR spectra. It has been revealed that the annealing temperatures and the ambient, where the annealing is carried out is crucial for TiO2 crystallization, when there is Ag incorporation and especially for appearance of anatase and rutile phase. The nitrogen and oxygen ambient influences quite different the crystallization of TiO2:Ag films. Transmission and absorption spectra have been analyzed. Optical band gap values were evaluated for pure titania and Ag incorporated TiO2 films.

  10. Carbon coating stabilized Ti(3+)-doped TiO2 for photocatalytic hydrogen generation under visible light irradiation.

    PubMed

    Fu, Gao; Zhou, Peng; Zhao, Meiming; Zhu, Weidong; Yan, Shicheng; Yu, Tao; Zou, Zhigang

    2015-07-28

    Self-doping by Ti(3+) is a useful method to expand the light response of TiO2 into the visible light region. However, to obtain a stable Ti(3+)-doped TiO2 seems to be a challenge due to the easy oxidation of Ti(3+) during the heterogeneous reaction. Here, we propose a simple carbon coating route to stabilize the Ti(3+)-doped TiO2, in which both the Ti(3+) and precursor of the carbon coating layer were in situ formed from the hydrothermal hydrolysis of titanium isopropoxide. The carbon coated Ti(3+)-doped TiO2 exhibited excellent stability for photocatalytic hydrogen production. Based on electron paramagnetic resonance (EPR) analysis, the proposed stabilizing mechanism is that the conductive carbon coating layer as a barrier layer prevents the H2O and O2 from diffusing into the surface of the photocatalyst, which can oxidize the surface O vacancies and Ti(3+) in TiO2. Our findings offer a simple route to prepare a highly stable TiO2-based photocatalyst with visible light response.

  11. Highly active Ag clusters stabilized on TiO2 nanocrystals for catalytic reduction of p-nitrophenol

    NASA Astrophysics Data System (ADS)

    Wang, Xin; Zhao, Zhe; Ou, Dingrong; Tu, Baofeng; Cui, Daan; Wei, Xuming; Cheng, Mojie

    2016-11-01

    Ag/TiO2 nanocomposites comprising of Ag clusters on TiO2 nanocrystal surfaces are of great significance in catalysts and advanced functional materials. Herein a novel method to synthesize Ag/TiO2 nanocomposites with Ag clusters under 2 nm on TiO2 nanocrystal surfaces have been developed. The success of this method relies on a silver mirror reaction in toluene, which refers to the reduction of silver-dodecylamine complexes by acetaldehyde in the presence of mono-dispersed TiO2 nanocrystals. The prepared Ag/TiO2 nanocomposites have been characterized by FT-IR spectra, UV-vis absorption spectra, X-ray diffraction (XRD) analysis, ultra high resolution scanning electron microscope (Ultra-HRSEM), high resolution transmission electron microscope (HRTEM) and X-ray photoelectron spectra (XPS). Catalytic activity of Ag/TiO2 nanocomposites is evaluated for the reduction of p-nitrophenol (4-NP) into p-aminophenol (4-AP) by NaBH4. Results demonstrate that Ag/TiO2 nanocomposites have shown an outstanding catalytic activity as well as a good stability in successive reduction of 4-NP. Noticeably, TOF of Ag/TiO2-0.75 nanocomposites obtained in this work is the highest among Ag based catalysts previously reported.

  12. Toxicological aspects of photocatalytic degradation of selected xenobiotics with nano-sized Mn-doped TiO2.

    PubMed

    Ozmen, Murat; Güngördü, Abbas; Erdemoglu, Sema; Ozmen, Nesrin; Asilturk, Meltem

    2015-08-01

    The toxic effects of two selected xenobiotics, bisphenol A (BPA) and atrazine (ATZ), were evaluated after photocatalytic degradation using nano-sized, Mn-doped TiO2. Undoped and Mn-doped TiO2 nanoparticles were synthesized. The samples were characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM), UV-vis-diffuse reflectance spectra (DRS), X-ray fluorescence spectroscopy (XRF), and BET surface area. The photocatalytic efficiency of the undoped and Mn-doped TiO2 was evaluated for BPA and ATZ. The toxicity of the synthesized photocatalysts and photocatalytic by-products of BPA and ATZ was determined using frog embryos and tadpoles, zebrafish embryos, and bioluminescent bacteria. Possible toxic effects were also evaluated using selected enzyme biomarkers. The results showed that Mn-doped TiO2 nanoparticles did not cause significant lethality in Xenopus laevis embryos and tadpoles, but nonfiltered samples caused lethality in zebrafish. Furthermore, Mn-doping of TiO2 increased the photocatalytic degradation capability of nanoparticles, and it successfully degraded BPA and AZT, but degradation of AZT caused an increase of the lethal effects on both tadpoles and fish embryos. Degradation of BPA caused a significant reduction of lethal effects, especially after 2-4h of degradation. However, biochemical assays showed that both Mn-doped TiO2 and the degradation by-products caused a significant change of selected biomarkers on X. laevis tadpoles; thus, the ecological risks of Mn-doped TiO2 should be considered due to nanomaterial applications and for spilled nanoparticles in an aquatic ecosystem. Also, the risk of nanoparticles should be considered using indicator reference biochemical markers to verify the environmental health impacts. PMID:26037099

  13. Toxicological aspects of photocatalytic degradation of selected xenobiotics with nano-sized Mn-doped TiO2.

    PubMed

    Ozmen, Murat; Güngördü, Abbas; Erdemoglu, Sema; Ozmen, Nesrin; Asilturk, Meltem

    2015-08-01

    The toxic effects of two selected xenobiotics, bisphenol A (BPA) and atrazine (ATZ), were evaluated after photocatalytic degradation using nano-sized, Mn-doped TiO2. Undoped and Mn-doped TiO2 nanoparticles were synthesized. The samples were characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM), UV-vis-diffuse reflectance spectra (DRS), X-ray fluorescence spectroscopy (XRF), and BET surface area. The photocatalytic efficiency of the undoped and Mn-doped TiO2 was evaluated for BPA and ATZ. The toxicity of the synthesized photocatalysts and photocatalytic by-products of BPA and ATZ was determined using frog embryos and tadpoles, zebrafish embryos, and bioluminescent bacteria. Possible toxic effects were also evaluated using selected enzyme biomarkers. The results showed that Mn-doped TiO2 nanoparticles did not cause significant lethality in Xenopus laevis embryos and tadpoles, but nonfiltered samples caused lethality in zebrafish. Furthermore, Mn-doping of TiO2 increased the photocatalytic degradation capability of nanoparticles, and it successfully degraded BPA and AZT, but degradation of AZT caused an increase of the lethal effects on both tadpoles and fish embryos. Degradation of BPA caused a significant reduction of lethal effects, especially after 2-4h of degradation. However, biochemical assays showed that both Mn-doped TiO2 and the degradation by-products caused a significant change of selected biomarkers on X. laevis tadpoles; thus, the ecological risks of Mn-doped TiO2 should be considered due to nanomaterial applications and for spilled nanoparticles in an aquatic ecosystem. Also, the risk of nanoparticles should be considered using indicator reference biochemical markers to verify the environmental health impacts.

  14. Synthesis and characterization of high photocatalytic activity and stable Ag3PO4/TiO2 fibers for photocatalytic degradation of black liquor

    NASA Astrophysics Data System (ADS)

    Cai, Li; Long, Qiyi; Yin, Chao

    2014-11-01

    The TiO2 fiber was prepared by using cotton fiber as a template, and then Ag3PO4/TiO2 fibers were synthesized via in situ Ag3PO4 particles onto the surface of TiO2 fiber. Their structure and physical properties were characterized by means of scanning electron microscopy (SEM), specific surface analyzer, X-ray diffraction (XRD), UV-vis absorption spectra and photoluminescence spectra (PL). SEM analysis indicated that the well-defined surface morphology of natural cotton fiber was mostly preserved in TiO2 and Ag3PO4/TiO2 fibers. Compared with TiO2 fiber, the absorbance wavelengths of Ag3PO4/TiO2 fibers were apparently red shifted and the PL intensities revealed a significant decrease. By using the photocatalytic degradation of black liquor as a model reaction, the visible light and ultraviolet light catalytic efficiencies of TiO2, Ag3PO4 and Ag3PO4/TiO2 fibers were evaluated. The reaction results showed that Ag3PO4/TiO2 fibers had stronger photocatalytic activity and excellent chemical stability in repeated and long-term applications. Therefore, the prepared Ag3PO4/TiO2 fibers could act as an efficient catalyst for the photocatalytic degradation of black liquor, which suggested their promising applications. It was proposed that the •OH radicals played the leading role in the photocatalytic degradation of the black liquor by Ag3PO4/TiO2 fibers system.

  15. Enhancement removal of tartrazine dye using HCl-doped polyaniline and TiO2-decorated PANI particles

    NASA Astrophysics Data System (ADS)

    Elsayed, M. A.; Gobara, Mohamed

    2016-08-01

    HCl-doped polyaniline (HCl-PANI) and titanium dioxide decorated with polyaniline (TiO2-decorated PANI) with different TiO2:PANI ratios were chemically prepared and utilized for the removal of tartrazine (TZ) dye from a synthetic aqueous solution. The mechanism of preparation of the sample suggested that aniline was adsorbed on the TiO2 surface before the polymerization process took place. Samples were characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, energy dispersive x-ray spectroscopy and x-ray diffraction. The results showed that HCl-PANI and TiO2-decorated PANI have an amorphous structure. The thermal stability of the prepared samples was characterized using thermo-gravimetric (TG) analysis. HCl-PANI is stable up to 200 °C and the relative weight per cent of PANI in the TiO2-decorated PANI was 20, 25, 40 and 45%. The removal activity of TiO2-decorated PANI via TZ azo dye was investigated under UV light irradiations and compared with HCl-PANI and TiO2 particles. The results indicated the superiority of the TiO2-decorated PANI over pure HCl-PANI and TiO2. However, the excessive PANI percentage tends to form a relatively thick layer, and even aggregates on the surface of TiO2. This hinders the migration of excited electrons from the outer PANI layer to the inner TiO2 particles, which consequently leads to a decrease in the removal efficiency. A possible mechanism for the removal oxidative degradation is also mentioned.

  16. Enhancement removal of tartrazine dye using HCl-doped polyaniline and TiO2-decorated PANI particles

    NASA Astrophysics Data System (ADS)

    Elsayed, M. A.; Gobara, Mohamed

    2016-08-01

    HCl-doped polyaniline (HCl-PANI) and titanium dioxide decorated with polyaniline (TiO2-decorated PANI) with different TiO2:PANI ratios were chemically prepared and utilized for the removal of tartrazine (TZ) dye from a synthetic aqueous solution. The mechanism of preparation of the sample suggested that aniline was adsorbed on the TiO2 surface before the polymerization process took place. Samples were characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, energy dispersive x-ray spectroscopy and x-ray diffraction. The results showed that HCl-PANI and TiO2-decorated PANI have an amorphous structure. The thermal stability of the prepared samples was characterized using thermo-gravimetric (TG) analysis. HCl-PANI is stable up to 200 °C and the relative weight per cent of PANI in the TiO2-decorated PANI was 20, 25, 40 and 45%. The removal activity of TiO2-decorated PANI via TZ azo dye was investigated under UV light irradiations and compared with HCl-PANI and TiO2 particles. The results indicated the superiority of the TiO2-decorated PANI over pure HCl-PANI and TiO2. However, the excessive PANI percentage tends to form a relatively thick layer, and even aggregates on the surface of TiO2. This hinders the migration of excited electrons from the outer PANI layer to the inner TiO2 particles, which consequently leads to a decrease in the removal efficiency. A possible mechanism for the removal oxidative degradation is also mentioned.

  17. Defect Complex Effect in Nb Doped TiO2 Ceramics with Colossal Permittivity

    NASA Astrophysics Data System (ADS)

    Li, Fuchao; Shang, Baoqiang; Liang, Pengfei; Wei, Lingling; Yang, Zupei

    2016-10-01

    Donor-doped Nb x Ti1- x O2 ( x = 1%, 2%, 4%, 6%, and 8%) ceramics with giant permittivity (>104) and a very low dielectric loss (˜0.05) were sintered under flowing N2 at 1400°C for 10 h. By increasing Nb doping concentration, two different dielectric responses were evidenced in the frequency dependence of dielectric properties of Nb doped TiO2 ceramics, which corresponded to the space charge polarization and the electron-pinned defect-dipoles effect, respectively. Especially, combined with the x-ray photoelectron spectroscopy results, the electron-pinned defect-dipoles induced by the 2({Nb}^{5 + } )_{{Ti}}^{ bullet } to 4({Ti}^{3 + } )^'_{{Ti}} leftarrow {V}_{{o}}^{ bullet bullet } defect complex were further confirmed to give rise to both their high ɛr and low tan δ in the high frequency range for the Nb x Ti1- x O2 ceramics with x > 4%.

  18. Modification mechanism of praseodymium doping for the photocatalytic performance of TiO2: a combined experimental and theoretical study.

    PubMed

    Duan, Zhi-Gang; Zhao, Zong-Yan; Shi, Qing-Nan

    2015-07-15

    Impurity doping is a simple and efficient modification method to improve the photocatalytic performance of wide band gap photocatalysts. However, some basic and important issues about the mechanism of impurity doping modification still need to be further confirmed and explained. In the present work, Pr-doped TiO2 with a mono-phase crystal structure was prepared by a sol-gel method. Then, the crystal structure, binding information, optical absorption, and photocatalytic activity were systematically investigated. The experimental results show that Pr doping could significantly enhance the photocatalytic activity of TiO2, and the effects of modification on rutile TiO2 are more obvious than for anatase TiO2. In order to understand the underlying mechanism, density functional theory was utilized to calculate the crystal structure and electronic structure of pure and Pr-doped TiO2. The differences in electronic structure between anatase and rutile phases lead to the above photocatalytic performance. The experimental measurements and theoretical calculations mutually support each other in the present work. Two points are confirmed: the position of the band edge determines the redox activity of the photocatalyst, and the shallow energy bands induced by impurity doping could improve the photocatalytic performance.

  19. Modification mechanism of praseodymium doping for the photocatalytic performance of TiO2: a combined experimental and theoretical study.

    PubMed

    Duan, Zhi-Gang; Zhao, Zong-Yan; Shi, Qing-Nan

    2015-07-15

    Impurity doping is a simple and efficient modification method to improve the photocatalytic performance of wide band gap photocatalysts. However, some basic and important issues about the mechanism of impurity doping modification still need to be further confirmed and explained. In the present work, Pr-doped TiO2 with a mono-phase crystal structure was prepared by a sol-gel method. Then, the crystal structure, binding information, optical absorption, and photocatalytic activity were systematically investigated. The experimental results show that Pr doping could significantly enhance the photocatalytic activity of TiO2, and the effects of modification on rutile TiO2 are more obvious than for anatase TiO2. In order to understand the underlying mechanism, density functional theory was utilized to calculate the crystal structure and electronic structure of pure and Pr-doped TiO2. The differences in electronic structure between anatase and rutile phases lead to the above photocatalytic performance. The experimental measurements and theoretical calculations mutually support each other in the present work. Two points are confirmed: the position of the band edge determines the redox activity of the photocatalyst, and the shallow energy bands induced by impurity doping could improve the photocatalytic performance. PMID:26130404

  20. FTIR spectra and thermal properties of TiO2-doped iron phosphate glasses

    NASA Astrophysics Data System (ADS)

    Lu, Mingwei; Wang, Fu; Liao, Qilong; Chen, Kuiru; Qin, Jianfa; Pan, Sheqi

    2015-02-01

    Structure and thermal properties of xTiO2·(90 - x) (60P2O5-40Fe2O3)ṡ10CaF2 (x = 0, 5, 10, 15, 20 and 25 mol%) glasses are investigated in detail by Fourier Transform Infrared Spectrum (FTIR) and Differential Thermal Analysis (DTA), respectively. It is found that incorporation of TiO2 increase the density and glass transition temperature of iron phosphate system glass. The increment of doped-TiO2 can also strengthen phosphate network chains due to increasing O/P ratios and more orthophosphate (Q0) units formed in the glass structure at expense of pyrophosphate (Q1) units and metaphosphate (Q2) groups. Moreover, the structure of iron phosphate glass with TiO2 content contain distorted octahedral [TiO6] linked to phosphate unit through Psbnd Osbnd Ti bonds, thus enhanced structure cohesion and increased density obtained. The knowledge provides an improved understanding of the role of TiO2 in the structure of iron phosphate glasses.

  1. Theoretical investigations of Ni- and Cu-doped TiO2

    NASA Astrophysics Data System (ADS)

    Esakki muthuraju, M.; Mahesh, R.; Sreekanth, T.; Venugopal Reddy, P.

    2014-03-01

    The electronic, magnetic and optical properties of rutile Ti1-xTMxO2 (where TM: Ni, Cu and x = 0.25) have been investigated by the density functional theory with the plane wave self consistent field method. For the calculation of exchange correlation potential, the local density approximation along with Hubbard correction (LDA +U) was used. Electronic, magnetic and optical properties were calculated using 12 atoms supercell of rutile TiO2 with one Ti atom replaced by a dopant transition metal atom. The band structure of doped rutile phase indicates the reduction of band gap leading to improvement in the photocatalytic properties of TiO2 as well as enhancement in its magnetic properties. The observed magnetism is explained on the basis of spin polarization of d states of Ti with dopants. Optical calculations by full potential, linear augmented plane wave plus local orbital (FP-LAPW+lo) method with ELK code established the presence of optical transitions in the visible light region. These theoretical calculations gave a meaningful information and excellent prediction to develop TiO2 for spintronics applications and photocatalytic applications in the visible region.

  2. Visible light photocatalytic antibacterial activity of Ni-doped and N-doped TiO2 on Staphylococcus aureus and Escherichia coli bacteria.

    PubMed

    Ananpattarachai, Jirapat; Boonto, Yuphada; Kajitvichyanukul, Puangrat

    2016-03-01

    The Ni-doped and N-doped TiO2 nanoparticles were investigated for their antibacterial activities on Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) bacteria. Their morphological features and characteristics such as particle size, surface area, and visible light absorbing capacity were compared and discussed. Scanning electron microscopy, X-ray diffraction, and UV-visible spectrophotometry were used to characterize both materials. The inactivation of E. coli (as an example of Gram-negative bacteria) and S. aureus (as an example of Gram-positive bacteria) with Ni-doped and N-doped TiO2 was investigated in the absence and presence of visible light. Antibacterial activity tests were conducted using undoped, Ni-doped, and N-doped TiO2. The N-doped TiO2 nanoparticles show higher antibacterial activity than Ni-doped TiO2. The band gap narrowing of N-doped TiO2 can induce more visible light absorption and leads to the superb antibacterial properties of this material. The complete inactivation time for E. coli at an initial cell concentration of 2.7 × 10(4) CFU/mL was 420 min which is longer than the 360 min required for S. aureus inactivation. The rate of inactivation of S. aureus using the doped TiO2 nanoparticles in the presence of visible light is greater than that of E. coli. The median lethal dose (LD50) values of S. aureus and E. coli by antibacterial activity under an 18-W visible light intensity were 80 and 350 mg/ml for N-doped TiO2, respectively.

  3. TiO2 doped UO2 fuels sintered by spark plasma sintering

    NASA Astrophysics Data System (ADS)

    Yao, Tiankai; Scott, Spencer M.; Xin, Guoqing; Lian, Jie

    2016-02-01

    UO2 fuels doped with oxide additives Cr2O3 and TiO2 display larger grain size, improving fission product retention capability and thus accident tolerance. Spark plasma sintering (SPS) was applied to consolidate TiO2-doped UO2 fuel pellets with 0.5 wt % dopant concentration, above its solubility, in order to induce eutectic phase formation and promote sintering kinetics. The grain size can reach 80 μm by sintering at 1700 °C for 20 min, and liquid U-Ti-O eutectic phase occurs at the triple junction of grain boundaries and significantly improves grain growth during sintering. The oxide additive also impedes the reduction of the initial hyperstoichiometric fuel powders to more stoichiometric fuel pellets upon SPS process. Thermal-mechanical properties of the sintered doped fuel pellets including thermal conductivity and hardness are measured and compared with undoped fuel pellets. The enlarged grain size (80 μm) and densification within short sintering duration highlight the immense possibility of SPS in fabricating large grained UO2 fuel pellets to improve fuel performance.

  4. Europium Doped TiO2 Hollow Nanoshells: Two-Photon Imaging of Cell Binding

    PubMed Central

    Sandoval, Sergio; Yang, Jian; Alfaro, Jesus G.; Liberman, Alexander; Makale, Milan; Chiang, Casey E.; Schuller, Ivan K.

    2012-01-01

    A simple scalable method to fabricate luminescent monodisperse 200 nm europium doped hollow TiO2 nanoshell particles is reported. Fluorophore reporter, Eu3+ ions, are incorporated directly in the NS matrix, leaving the surface free for functionalization and the core free for payload encapsulation. Amine functionalized polystyrene beads were used as templates, and the porous walls of europium doped titania nanoshells were synthesized using titanium(IV) t-butoxide and europium(III) nitrate as reactants. X-ray diffraction analysis identified anatase as the predominant titania phase of the rigid nanoshell wall structure, and photoluminescence spectra showed that the Eu(III) doped TiO2 nanoshells exhibited a red emission at 617 nm due to an atomic f-f transition. Nanoshell interactions with HeLa cervical cancer cells in vitro were visualized using two-photon microscopy of the Eu(III) emission, and studied using a luminescence ratio analysis to assess nanoshell adhesion and endocytosis. PMID:23185106

  5. Fabrication of bioactive, antibacterial TiO2 nanotube surfaces, coated with magnetron sputtered Ag nanostructures for dental applications.

    PubMed

    Uhm, Soo-Hyuk; Lee, Sang-Bae; Song, Doo-Hoon; Kwon, Jae-Sung; Han, Jeon-Geon; Kim, Kyoung-Nam

    2014-10-01

    We investigated whether a silver coating on an anodic oxidized titania (TiO2) nanotube surface would be useful for preventing infections in dental implants. We used a magnetron sputtering process to deposit Ag nanoparticles onto a TiO2 surface. We studied different sputtering input power densities and maintained other parameters constant. We used scanning electron microscopy, X-ray diffraction, and contact angle measurements to characterize the coated surfaces. Staphylococcus aureus was used to evaluate antibacterial activity. The X-ray diffraction analysis showed peaks that corresponded to metallic Ag, Ti, O, and biocompatible anatase phase TiO2 on the examined surfaces. The contact angles of the Ag nanoparticle-loaded surfaces were significantly lower at 2.5 W/cm2 input power under pulsed direct current mode compared to commercial, untreated Ti surfaces. In vitro antibacterial analysis indicated that a significantly reduced number of S. aureus were detected on an Ag nanoparticle-loaded TiO2 nanotube surface compared to control untreated surfaces. No cytotoxicity was noted, except in the group treated with 5 W/cm2 input power density, which was the highest input of power density we tested for the magnetron sputtering process. Overall, we concluded that it was feasible to create antibacterial Ag nanoparticle-loaded titanium nanotube surfaces with magnetron sputtering. PMID:25942879

  6. Comparative x-ray absorption spectroscopy study of Co-doped SnO2 and TiO2

    NASA Astrophysics Data System (ADS)

    Lussier, A.; Dvorak, J.; Idzerda, Y. U.; Ogale, S. B.; Shinde, S. R.; Choudary, R. J.; Venkatesan, T.

    2004-06-01

    We performed x-ray absorption spectroscopy measurements at the cobalt L2,3 edge and the oxygen K edge of Co-doped SnO2 and Co-doped TiO2. Our measurements confirm that doped cobalt atoms are in the same local environment in both compounds. Furthermore, the results support the idea that cobalt atoms occupy substitutional cation sites. Additionally, the oxygen spectral shapes offer insight into a possible cause for the observed giant magnetic moment of cobalt atoms present in SnO2, but not in TiO2.

  7. Preparation and photocatalytic activity of B, Ce Co-doped TiO2 hollow fibers photocatalyst

    NASA Astrophysics Data System (ADS)

    Qiu, Jingping; Sun, Xiaogang; Xing, Jun; Liu, Xiaobo

    2014-07-01

    A series of B, Ce co-doped TiO2 (B, Ce-TiO2) photocatalytic materials with a hollow fiber structure were successfully prepared by template method using boric acid, ammonium ceric nitrate and tetrabutyltitanate as precursors and cotton fibers as template, followed by calcination at 500°C in an N2 atmosphere for 2 h. Scanning electron microscopy (SEM), X-ray diffraction (XRD), nitrogen adsorption-desorption measurements, and UV-visible spectroscopy (UV-Vis) were employed to characterize the morphology, crystal structure, surface structure, and optical absorption properties of the samples. The photocatalytic performance of the samples was studied by photodegradation phenol in water under UV light irradiation. The results showed that the TiO2 fiber materials have hollow structures, and the fiber structure materials showed better photocatalytic properties for the degradation of phenol than pure TiO2 under UV light. In the experiment condition, the photocatalytic activity of B, Ce co-doped TiO2 fibers was optimal of all the prepared samples. In addition, the possibility of cyclic usage of B, Ce co-doped TiO2 fiber photocatalyst was also confirmed, the photocatalytic activity of TiO2 fibers remained above 90% of that of the fresh sample after being used four times. The material was easily removed by centrifugal separation from the medium. It can therefore be potentially applied for the treatment of water contaminated by organic pollutants.

  8. Low Temperature Hydrothermal Synthesis of Visible-Light-Activated I-Doped TiO2 for Improved Dye Degradation.

    PubMed

    Wang, Dongting; Li, Jianwen; Zhou, Guangsheng; Wang, Wenxu; Zhang, Xianxi; Pan, Xu

    2016-06-01

    Iodine doped TiO2 with different iodine/Ti molar ratios has been firstly synthesized with a low temperature hydrothermal route and has been studied systematically in photocatalysis under visible light condition. The resulting iodine doped TiO2 were characterized by X-ray diffraction (XRD), high resolution transmission electron microscopy (TEM), diffuse reflectance spectrum (DRS), and X-ray photoelectron spectroscopy (XPS). The photocatalytic performance investigations were conducted by means of the degradation of Rhodamine B (RhB) under the visible light irradiation in aqueous solution. Under an optimized I/Ti doping ratio of 10 mol%, the photocatalytic performance is greatly better, with degradation efficiency of 95%, which is almost double that of pure TiO2. The superior photocatalytic activity of iodine-doped TiO2 could be mainly attributed to extended visible light absorption originated from the formation of continuous states existed in the band gap of the doped TiO2 introduced by iodine. Active oxygen species, that is, *OH and O2-, were evidenced to be involved in the degradation process and a possible mechanism was also proposed.

  9. Low Temperature Hydrothermal Synthesis of Visible-Light-Activated I-Doped TiO2 for Improved Dye Degradation.

    PubMed

    Wang, Dongting; Li, Jianwen; Zhou, Guangsheng; Wang, Wenxu; Zhang, Xianxi; Pan, Xu

    2016-06-01

    Iodine doped TiO2 with different iodine/Ti molar ratios has been firstly synthesized with a low temperature hydrothermal route and has been studied systematically in photocatalysis under visible light condition. The resulting iodine doped TiO2 were characterized by X-ray diffraction (XRD), high resolution transmission electron microscopy (TEM), diffuse reflectance spectrum (DRS), and X-ray photoelectron spectroscopy (XPS). The photocatalytic performance investigations were conducted by means of the degradation of Rhodamine B (RhB) under the visible light irradiation in aqueous solution. Under an optimized I/Ti doping ratio of 10 mol%, the photocatalytic performance is greatly better, with degradation efficiency of 95%, which is almost double that of pure TiO2. The superior photocatalytic activity of iodine-doped TiO2 could be mainly attributed to extended visible light absorption originated from the formation of continuous states existed in the band gap of the doped TiO2 introduced by iodine. Active oxygen species, that is, *OH and O2-, were evidenced to be involved in the degradation process and a possible mechanism was also proposed. PMID:27427614

  10. Facile synthesis and enhanced visible light photocatalytic activity of N and Zr co-doped TiO2 nanostructures from nanotubular titanic acid precursors.

    PubMed

    Zhang, Min; Yu, Xinluan; Lu, Dandan; Yang, Jianjun

    2013-01-01

    Zr/N co-doped TiO2 nanostructures were successfully synthesized using nanotubular titanic acid (NTA) as precursors by a facile wet chemical route and subsequent calcination. These Zr/N-doped TiO2 nanostructures made by NTA precursors show significantly enhanced visible light absorption and much higher photocatalytic performance than the Zr/N-doped P25 TiO2 nanoparticles. Impacts of Zr/N co-doping on the morphologies, optical properties, and photocatalytic activities of the NTA precursor-based TiO2 were thoroughly investigated. The origin of the enhanced visible light photocatalytic activity is discussed in detail.

  11. Facile synthesis and enhanced visible light photocatalytic activity of N and Zr co-doped TiO2 nanostructures from nanotubular titanic acid precursors

    NASA Astrophysics Data System (ADS)

    Zhang, Min; Yu, Xinluan; Lu, Dandan; Yang, Jianjun

    2013-12-01

    Zr/N co-doped TiO2 nanostructures were successfully synthesized using nanotubular titanic acid (NTA) as precursors by a facile wet chemical route and subsequent calcination. These Zr/N-doped TiO2 nanostructures made by NTA precursors show significantly enhanced visible light absorption and much higher photocatalytic performance than the Zr/N-doped P25 TiO2 nanoparticles. Impacts of Zr/N co-doping on the morphologies, optical properties, and photocatalytic activities of the NTA precursor-based TiO2 were thoroughly investigated. The origin of the enhanced visible light photocatalytic activity is discussed in detail.

  12. Antimicrobial activity and cytocompatibility of Ag plasma-modified hierarchical TiO2 film on titanium surface.

    PubMed

    Li, Jinhua; Liu, Xuanyong; Qiao, Yuqin; Zhu, Hongqin; Ding, Chuanxian

    2014-01-01

    To improve the antimicrobial ability and cytocompatibility of biomedical titanium implants, many efforts have been made to modify their surface topography and chemical composition. In this work, Ag plasma-modified hierarchical TiO2 film was fabricated on titanium surface via acid etching to produce micropit, hydrothermal treatment to generate TiO2 nanorod and subsequent plasma immersion ion implantation process to impregnate Ag into TiO2 surface. In view of the potential clinical applications, their antimicrobial activity, bioactivity and cytocompatibility were systematically evaluated. The hierarchical TiO2 film showed enhanced bioactivity and bacteriostatic effect on both microbes due to more negative zeta potential, constructing the first defense line against microbial adhesion by electrostatic repulsion. Addition of embedded Ag remarkably enhanced the antimicrobial efficiency toward both microbes based on Schottky contact without Ag(+) release, establishing the second defense line targeting microbial membrane. Furthermore, the addition of Ag degraded the bioactivity very little and exerted nearly no adverse or even promoted effect on MG63 cell functions, including adhesion, spreading and proliferation. This work illustrates a two-defense-line antimicrobial activity in darkness with both prior electrostatic repulsion to inhibit most microbes adhesion and posterior biocidal action to kill residual ones that luckily infiltrated through the first defense line, and provide proof of concept using both clinically relevant human pathogens. In conclusion, the Ag-embedded hierarchical TiO2 film with excellent antimicrobial activity, bioactivity and cytocompatibility provides a promising candidate for orthopedic and dental implants. PMID:24077111

  13. Niobium Doping Effects on TiO2 Mesoscopic Electron Transport Layer-Based Perovskite Solar Cells.

    PubMed

    Kim, Dong Hoe; Han, Gill Sang; Seong, Won Mo; Lee, Jin-Wook; Kim, Byeong Jo; Park, Nam-Gyu; Hong, Kug Sun; Lee, Sangwook; Jung, Hyun Suk

    2015-07-20

    Perovskite solar cells (PSCs) are the most promising candidates as next-generation solar energy conversion systems. To design a highly efficient PSC, understanding electronic properties of mesoporous metal oxides is essential. Herein, we explore the effect of Nb doping of TiO2 on electronic structure and photovoltaic properties of PSCs. Light Nb doping (0.5 and 1.0 at %) increased the optical band gap slightly, but heavy doping (5.0 at %) distinctively decreased it. The relative Fermi level position of the conduction band is similar for the lightly Nb-doped TiO2 (NTO) and the undoped TiO2 whereas that of the heavy doped NTO decreased by as much as ∼0.3 eV. The lightly doped NTO-based PSCs exhibit 10 % higher efficiency than PSCs based on undoped TiO2 (from 12.2 % to 13.4 %) and 52 % higher than the PSCs utilizing heavy doped NTO (from 8.8 % to 13.4 %), which is attributed to fast electron injection/transport and preserved electron lifetime, verified by transient photocurrent decay and impedance studies.

  14. Cu-doped TiO(2) nanoparticles for photocatalytic disinfection of bacteria under visible light.

    PubMed

    Karunakaran, C; Abiramasundari, G; Gomathisankar, P; Manikandan, G; Anandi, V

    2010-12-01

    Two percent Cu-doped TiO(2) nanoparticles were prepared by a modified ammonia-evaporation-induced synthetic method, calcined at 450°C, and characterized by powder X-ray diffraction, energy dispersive X-ray analysis, ESR spectroscopy, scanning electron microscopy, UV-visible diffuse reflectance spectrum, photoluminescence spectroscopy, and electrochemical impedance spectroscopy. Doping shifts the optical absorption edge to the visible region but increases the charge-transfer resistance and decreases the capacitance. Under visible light, the composite nanoparticles very efficiently catalyze the disinfection of Escherichia coli. The prepared oxide is selective in photocatalysis; under UV light, its photocatalytic activity to degrade sunset yellow, rhodamine B, and methylene blue dyes is less than that of the undoped one. PMID:20832079

  15. Origin of magnetism and quasiparticles properties in Cr-doped TiO2.

    PubMed

    Da Pieve, F; Di Matteo, S; Rangel, T; Giantomassi, M; Lamoen, D; Rignanese, G-M; Gonze, X

    2013-03-29

    Combining the local spin density approximation (LSDA)+U and an analysis of superexchange interactions beyond density functional theory, we describe the magnetic ground state of Cr-doped TiO2, an intensively studied and debated dilute magnetic oxide. In parallel, we correct our LSDA+U (+ superexchange) ground state through GW corrections (GW@LSDA+U) that reproduce the position of the impurity states and the band gaps in satisfying agreement with experiments. Because of the different topological coordinations of Cr-Cr bonds in the ground states of rutile and anatase, superexchange interactions induce either ferromagnetic or antiferromagnetic couplings of Cr ions. In Cr-doped anatase, this interaction leads to a new mechanism which stabilizes a (nonrobust) ferromagnetic ground state, in keeping with experimental evidence, without the need to invoke F-center exchange. The interplay between structural defects and vacancies in contributing to the superexchange is also unveiled.

  16. Linear and nonlinear optical studies of bare and copper doped TiO2 nanoparticles via sol gel technique

    NASA Astrophysics Data System (ADS)

    Rajamannan, B.; Mugundan, S.; Viruthagiri, G.; Praveen, P.; Shanmugam, N.

    2014-01-01

    In general, the nanoparticles of TiO2 may exist in the phases of anatase, rutile and brookite. In the present work, we used titanium terta iso propoxide and 2-propanol as a common starting material to prepare the precursors of bare and copper doped nanosized TiO2. Then the synthesized products were calcinated at 500 °C and after calcination the pure TiO2 nanoparticles in anatase phase were harvested. The crystallite sizes of bare and copper doped TiO2 nanoparticles were calculated from X-ray diffraction analysis. The existence of functional groups of the samples was identified by Fourier transform infrared spectroscopy. The optical properties of bare and doped samples were carried out using UV-DRS and photoluminescence measurements. The surface morphology and the element constitution of the copper doped TiO2 nanoparticles were studied by scanning electron microscope fitted with energy dispersive X-ray spectrometer arrangement. The nonlinear optical properties of the products were confirmed by Kurtz second harmonic generation (SHG) test and the output power generated by the nanoparticle was compared with that of potassium di hydrogen phosphate (KDP).

  17. Linear and nonlinear optical studies of bare and copper doped TiO2 nanoparticles via sol gel technique.

    PubMed

    Rajamannan, B; Mugundan, S; Viruthagiri, G; Praveen, P; Shanmugam, N

    2014-01-24

    In general, the nanoparticles of TiO2 may exist in the phases of anatase, rutile and brookite. In the present work, we used titanium terta iso propoxide and 2-propanol as a common starting material to prepare the precursors of bare and copper doped nanosized TiO2. Then the synthesized products were calcinated at 500°C and after calcination the pure TiO2 nanoparticles in anatase phase were harvested. The crystallite sizes of bare and copper doped TiO2 nanoparticles were calculated from X-ray diffraction analysis. The existence of functional groups of the samples was identified by Fourier transform infrared spectroscopy. The optical properties of bare and doped samples were carried out using UV-DRS and photoluminescence measurements. The surface morphology and the element constitution of the copper doped TiO2 nanoparticles were studied by scanning electron microscope fitted with energy dispersive X-ray spectrometer arrangement. The nonlinear optical properties of the products were confirmed by Kurtz second harmonic generation (SHG) test and the output power generated by the nanoparticle was compared with that of potassium di hydrogen phosphate (KDP).

  18. Non-metal doped TiO2 nanotube arrays for high efficiency photocatalytic decomposition of organic species in water

    NASA Astrophysics Data System (ADS)

    Szkoda, Mariusz; Siuzdak, Katarzyna; Lisowska-Oleksiak, Anna

    2016-10-01

    Titanium dioxide is a well-known photoactive semiconductor with a variety of possible applications. The procedure of pollutant degradation is mainly performed using TiO2 powder suspension. It can also be exploited an immobilized catalyst on a solid support. Morphology and chemical doping have a great influence on TiO2 activity under illumination. Here we compare photoactivity of titania nanotube arrays doped with non-metal atoms: nitrogen, iodine and boron applied for photodegradation of organic dye - methylene blue and terephtalic acid. The doped samples act as a much better photocatalyst in the degradation process of methylene blue and lead to the formation of much higher amount of hydroxyl radicals (•OH) than undoped TiO2 nanotube arrays. The use of a catalyst active under solar light illumination in the form of thin films on a stable substrate can be scaled up for an industrial application.

  19. Rutile to anatase phase transition induced by N doping in highly oriented TiO2 films.

    PubMed

    Breeson, Andrew C; Sankar, Gopinathan; Goh, Gregory Kia Liang; Palgrave, Robert G

    2016-09-21

    Highly oriented TiO2 thin films were deposited onto Al2O3(0001), SrTiO3(001), and LaAlO3(001) substrates by spin coating a titanium alkoxide precursor solution followed by annealing. The films were nitrogen doped by two different routes: either by adding tetramethyethylenediamine (TMEDA) to the precursor solution or alternatively by high temperature ammonolysis. Undoped TiO2 films were highly oriented and the phase was dependent on the substrate. N doping by ammonolysis led to transformation of rutile films to anatase, confirmed by XRD and by XPS valence band spectroscopy. Significant differences were observed in the spatial distribution of the nitrogen dopant depending upon which synthesis method was used. These two factors may shed light on the increased photocatalytic efficiencies reported in N doped TiO2. PMID:27546382

  20. Photochromism-based detection of volatile organic compounds by W-doped TiO2 nanofibers.

    PubMed

    Jin, Ming; Zhang, Xintong; Pu, Hongting; Nishimoto, Shunsuke; Murakami, Taketoshi; Fujishima, Akira

    2011-10-01

    W-doped TiO(2) nanofibers with various compositions (W/Ti: 2-8%) were fabricated by the electrospinning method from respective precursor solutions containing tungsten(V) pentaethoxide, titanium tetraisopropoxide (TTIP), and polyvinylpyrrolidone (PVP), followed with calcination at 550 °C. Morphological and structural characteristics of these nanofibers were studied with SEM, XRD and XPS. W-doping inhibited the crystal growth and anatase-to-rutile transformation of TiO(2) nanofibers. W-doped TiO(2) nanofiber mats showed good photocatalytic oxidation abilities for acetone. Obvious color change from white to blue of mats during the photocatalysis process can be detected by naked eyes, which provides a good way in detection of pollutants in indoor air, especially for the volatile organic compounds (VOCs). PMID:21741658

  1. Zn-doped nanocrystalline TiO2 films for CdS quantum dot sensitized solar cells.

    PubMed

    Zhu, Guang; Cheng, Zujun; Lv, Tian; Pan, Likun; Zhao, Qingfei; Sun, Zhuo

    2010-07-01

    Quantum dot-sensitized solar cells based on Zn-doped TiO(2) (Zn-TiO(2)) film photoanode and polysulfide electrolyte were fabricated. Zn-TiO(2) nanoparticles were obtained via a hydrothermal method and screen printed on the fluorine-doped tin oxide glass to prepare the photoanode. The structure, morphology and impedance of the Zn-TiO(2)/CdS film and the photovoltaic performance of the Zn-TiO(2)/CdS cell were investigated. It was found that the photovoltaic efficiency was improved by 24% when the Zn-TiO(2) film was adopted as the photoanode of CdS QDSSCs instead of only the TiO(2) layer. The improvement was ascribed to the reduction of electron recombination and the enhancement of electron transport in the TiO(2) film by Zn doping.

  2. Preparation and Solar Light Photocatalytic Activity of N-Doped TiO2-Loaded Halloysite Nanotubes Nanocomposites

    NASA Astrophysics Data System (ADS)

    Cheng, Zhi-Lin; Sun, Wei

    2015-10-01

    A novel method to prepare N-doped TiO2-loaded halloysite nanotubes (N-TiO2/HNTs) nanocomposites was achieved by using the chemical vapor deposition in autoclave. The N-TiO2/HNTs nanocomposites obtained by the different form of the doping N source were studied through a series of characterizations. The XRD, SEM, and TEM characterizations verified the anatase structure of TiO2 nanoparticles with the size of ca.20nm loaded on the outer surface of HNTs. The UV-vis characterization of the N-TiO2/HNTs presented a further red-shift compared to the pure N-TiO2 nanoparticles.. The XPS characterizations confirmed the N element doped into the crystal structure of TiO2 nanoparticles. The photocatalytic activities of N-TiO2/HNTs nanocomposites prepared were evaluated by degradation of phenol at room temperature under simulated solar light irradiation.

  3. Energetic, electronic and optical properties of lanthanide doped TiO2: An ab initio LDA+U study

    NASA Astrophysics Data System (ADS)

    Mulwa, Winfred M.; Ouma, Cecil N. M.; Onani, Martin O.; Dejene, Francis B.

    2016-05-01

    Substitutional energies, thermodynamic charge transition levels and optical properties of lanthanide doped anatase TiO2 has been investigated using local density approximation with the Hubbard U correction (LDA+U) within the density functional theory formalism. All the lanthanides apart from La introduced impurity states in the host band gap on doping. The calculated substitutional energies indicate that it is possible to dope TiO2 with lanthanide ions. The optimal doping percentage was predicted to be ~3% and dopant levels resulting from Ce, Nd, Sm, Gd and Tm doping were found to possess negative U characteristics. In addition the calculated thermodynamic transition levels predicted Lu as not having any possible charge transitions within the host band gap. The calculated optical absorption coefficients indicate that lanthanide doping led to optical absorption in the visible regime.

  4. Bacteria Adherence Properties of Nitrogen-Doped TiO2 Coatings by Plasma Surface Alloying Technique

    NASA Astrophysics Data System (ADS)

    Wang, Hefeng; Tang, Bin; Li, Xiuyan; Fan, Ailan

    Titanium nitride coatings on 316L stainless steel (S. S) were obtained by plasma surface alloying technique. Nitrogen-doped titanium dioxide (TiO2-xNx) was synthesized by oxidative annealing the resulted TiNx coatings in air. The reference TiO2 samples were also prepared by oxidation of sputtered Ti coatings. The as-prepared coatings were characterized by X-ray diffraction, glow discharge optical emission spectrometer (GDOES), scanning electron microscopy, X-ray hotoelectron spectroscopy and UV-Vis spectrophotometry, respectively. The bacteria adherence property of the TiO2-xNx coatings on stainless steel on the oral bacteria Streptococcus Mutans was investigated and compared with that of stainless steel by fluorescence microscopy. The mechanism of the bacteria adherence was discussed. The results show that the TiO2-xNx coatings are composed of anatase crystalline structure. SEM measurement indicates a rough surface morphology with three-dimensional homogenous protuberances after annealing treatment. Optical properties reveal an extended tailing of the absorption edge toward the visible region due to nitrogen presence. The band gap of the N-doped sample is reduced from 2.29 eV to 1.90 eV compared with the pure TiO2 one. Because of the different roughness and microstructure, the TiO2-xNx coatings inhibit the bacteria adherence.

  5. Flexible N-doped TiO2/C ultrafine fiber mat and its photocatalytic activity under simulated sunlight

    NASA Astrophysics Data System (ADS)

    Wu, Nan; Wang, Yingde; Lei, Yongpeng; Wang, Bing; Han, Cheng

    2014-11-01

    Flexible N-doped TiO2/C ultrafine fiber (NTCf) mat has been produced via electrospinning and subsequent heat treatment, analyzed by a combination of characterizations. The nitrogen content can be modulated by the addition of urea. The composite fiber with mean diameter of around 500 nm exhibits outstanding mechanical flexibility. The TiO2 in the fiber obtained at 700 °C is anatase with a mass ratio of 23 wt%. In the photodegradation experiment under simulated sunlight, the as-prepared flexible mat demonstrates remarkable efficiency in the degradation of methylene blue (MB) due to the well-proportioned distribution of TiO2 nanoparticles and the improvement of charge transfer process. The nitrogen species in TiO2 lattice and the nitrogen functional groups on the surface of the fiber play crucial impacts on the photocatalytic activity.

  6. Improved electrochemical performance of nitrogen doped TiO2-B nanowires as anode materials for Li-ion batteries.

    PubMed

    Zhang, Yongquan; Fu, Qiang; Xu, Qiaoling; Yan, Xiao; Zhang, Rongyu; Guo, Zhendong; Du, Fei; Wei, Yingjin; Zhang, Dong; Chen, Gang

    2015-07-28

    N-doped TiO2-B nanowires are prepared by the solvothermal method using TiN nanoparticles as the starting material. X-ray photoelectron spectroscopy shows that the N dopants preferentially occupy the interstitial sites of TiO2-B up to a content of ∼0.55 at%. Above this critical value, the N dopants will substitute the oxygen atoms which improve the electronic conductivity of TiO2-B. The maximum proportion of substituted-N in the TiO2-B nanowires is ∼1.3 at%. Raman scattering shows that the substituted-N strengthens the Ti(1)-O1-Ti(2) and O1-Ti(1)-O3 bonds of TiO2-B. This improves the stability of the corresponding local structures, thus reducing the distortion of the Li(+) diffusion channel along the b-axis of TiO2-B. As a result, the substituted-N has more of an impact on the electrochemical properties of TiO2-B than the interstitial-N does. The TiO2-B nanowires containing substituted-N dopants exhibit a remarkably enhanced electrochemical performance compared to pure TiO2-B. They show a discharge capacity of 153 mA h g(-1) at the 20 C rate with a capacity retention of 76% after 1000 cycles. In addition, they can deliver a discharge capacity of 100 mA h g(-1) at an ultra-high rate of 100 C, indicating their great potential in high power lithium ion batteries.

  7. Low-temperature preparation of F-doped TiO 2 film and its photocatalytic activity under solar light

    NASA Astrophysics Data System (ADS)

    Xu, Jingjing; Ao, Yanhui; Fu, Degang; Yuan, Chunwei

    2008-03-01

    A novel and simple method for preparing F-doped anatase TiO 2 (defined as FTO) film with high photocatalytic activity was developed using titanium- n-butoxide and NH 4F as TiO 2 and fluorine precursors under mild condition, i.e. low temperature (lower than 373 K) and ambient pressure. The prepared samples were characterized by XRD, SEM, X-ray photoelectron spectroscopy (XPS), diffuse reflectance spectrum (DRS), photoluminescence spectrum (PL) and TG-DSC analysis. The photocatalytic activity was evaluated by decomposing X-3B under artificial solar light. The results showed that the crystallinity of TiO 2 was improved by F-doping. F - ions can prevent the grain growth, and the transformation of anatase to rutile phase was also inhibited. The doped fluorine atoms existed in two chemical forms, and the ones incorporated into TiO 2 lattice might take a positive role in photocatalysis. Compared with surface fluorination samples, FTO film exhibited better photocatalytic activity. The high photocatalytic activity of FTO may due to extrinsic absorption through the creation of oxygen vacancies rather than the excitation of the intrinsic absorption band of bulk TiO 2. Furthermore, the FTO can be recycled with little photocatalytic activity depression. Without any further treatment besides rinsing, after 6 recycle utilization, the photocatalytic activity of FTO film was still higher than 79%.

  8. Preparation and Characterization of Ni-Doped TiO2 Materials for Photocurrent and Photocatalytic Applications

    PubMed Central

    Ganesh, Ibram; Gupta, A. K.; Kumar, P. P.; Sekhar, P. S. C.; Radha, K.; Padmanabham, G.; Sundararajan, G.

    2012-01-01

    Different amounts of Ni-doped TiO2 (Ni = 0.1 to 10%) powders and thin films were prepared by following a conventional coprecipitation and sol-gel dip coating techniques, respectively, at 400 to 800°C, and were thoroughly characterized by means of XRD, FT-IR, FT-Raman, DRS, UV-visible, BET surface area, zeta potential, flat band potential, and photocurrent measurement techniques. Photocatalytic abilities of Ni-doped TiO2 powders were evaluated by means of methylene blue (MB) degradation reaction under simulated solar light. Characterization results suggest that as a dopant, Ni stabilizes TiO2 in the form of anatase phase, reduces its bandgap energy, and adjusts its flat band potentials such that this material can be employed for photoelectrochemical (PEC) oxidation of water reaction. The photocatalytic activity and photocurrent ability of TiO2 have been enhanced by doping of Ni in TiO2. The kinetic studies revealed that the MB degradation reaction follows the Langmuir-Hinshelwood first-order reaction relationship. PMID:22619580

  9. Facile synthesis of the Ti3+ self-doped TiO2-graphene nanosheet composites with enhanced photocatalysis

    PubMed Central

    Qiu, Bocheng; Zhou, Yi; Ma, Yunfei; Yang, Xiaolong; Sheng, Weiqin; Xing, Mingyang; Zhang, Jinlong

    2015-01-01

    This study developed a facile approach for preparing Ti3+ self-doped TiO2-graphene photocatalyst by a one-step vacuum activation technology involved a relative lower temperature, which could be activated by the visible light owing to the synergistic effect among Ti3+ doping, some new intersurface bonds generation and graphene oxide reduction. Compared with the traditional methods, the vacuum activation involves a low temperature and low-costing, which can achieve the reduction of GO, the self doping of Ti3+ in TiO2 and the loading of TiO2 nanoparticles on GR surface at the same time. These resulting TiO2-graphene composites show the high photodegradation rate of MO, high hydrogen evolution activity and excellent IPCE in the visible light irradiation. The facile vacuum activation method can provide an effective and practical approach to improve the performance of TiO2-graphene and other metal oxides-graphene towards their practical photocatalytic applications. PMID:25716132

  10. A new dielectric ta-C film coating of Ag-nanoparticle hybrids to enhance TiO2 photocatalysis

    NASA Astrophysics Data System (ADS)

    Liu, Fanxin; Tang, Chaojun; Wang, Zhenlin; Sui, Chenghua; Ma, Hongtao

    2014-03-01

    We have demonstrated a novel method to enhance TiO2 photocatalysis by adopting a new ultrathin tetrahedral-amorphous-carbon (ta-C) film coating on Ag nanoparticles to create strong plasmonic near-field enhancement. The result shows that the decomposition rate of methylene blue on the Ag/10 Å ta-C/TiO2 composite photocatalyst is ten times faster than that on a TiO2 photocatalyst and three times faster than that on a Ag/TiO2 photocatalyst. This can be ascribed to the simultaneous realization of two competitive processes: one that excites the surface plasmons (SPs) of the ta-C-film/Ag-nanoparticle hybrid and provides a higher electric field near the ta-C/TiO2 interface compared to Ag nanoparticles alone, while the other takes advantage of the dense diamond-like ta-C layer to help reduce the transfer of photogenerated electrons from the conduction band of TiO2 to the metallic surface, since any electron transfer will suppress the excitation of SP modes in the metal nanoparticles.

  11. Structural and electronic properties of Mg and Mg-Nb co-doped TiO2 (101) anatase surface

    NASA Astrophysics Data System (ADS)

    Sasani, Alireza; Baktash, Ardeshir; Mirabbaszadeh, Kavoos; Khoshnevisan, Bahram

    2016-10-01

    In this paper, by using density functional theory, Mg and Nb-Mg co-doping of TiO2 anatase (101) surfaces are studied. By studying the formation energy of the defects and the bond length distribution of the surface, it is shown that Mg defects tend to stay as far as possible to induce least possible lattice distortion while Nb and Mg defects stay close to each other to cause less stress to the surface. By investigating band structure of the surface and changes stemmed from the defects, potential effects of Mg and Mg-Nb co-doping of TiO2 surface on dye-sensitized solar cells are investigated. In this study, it is shown that the Nb-Mg co-doping could increase JSC of the surface while slightly decreasing VOC compared to Mg doped surface, which might result in an increase in efficiency of the DSSCs compared to Nb or Mg doped surfaces.

  12. Enhanced electron transport in Nb-doped TiO2 nanoparticles via pressure-induced phase transitions.

    PubMed

    Lü, Xujie; Yang, Wenge; Quan, Zewei; Lin, Tianquan; Bai, Ligang; Wang, Lin; Huang, Fuqiang; Zhao, Yusheng

    2014-01-01

    Anatase TiO2 is one of the most important energy materials but suffers from poor electrical conductivity. Nb doping has been considered as an effective way to improve its performance in the applications of photocatalysis, solar cells, Li batteries, and transparent conducting oxide films. Here, we report the further enhancement of electron transport in Nb-doped TiO2 nanoparticles via pressure-induced phase transitions. The phase transition behavior and influence of Nb doping in anatase Nb-TiO2 have been systematically investigated by in situ synchrotron X-ray diffraction and Raman spectroscopy. The bulk moduli are determined to be 179.5, 163.3, 148.3, and 139.0 GPa for 0, 2.5, 5.0, and 10.0 mol % Nb-doped TiO2, respectively. The Nb-concentration-dependent stiffness variation has been demonstrated: samples with higher Nb concentrations have lower stiffness. In situ resistance measurements reveal an increase of 40% in conductivity of quenched Nb-TiO2 in comparison to the pristine anatase phase. The pressure-induced conductivity evolution is discussed in detail in terms of the packing factor model, which provides direct evidence for the rationality of the correlation of packing factors with electron transport in semiconductors. Pressure-treated Nb-doped TiO2 with unique properties surpassing those in the anatase phase holds great promise for energy-related applications.

  13. Enhanced lithium ion storage in TiO2 nanoparticles, induced by sulphur and carbon co-doping

    NASA Astrophysics Data System (ADS)

    Ivanov, Svetlozar; Barylyak, Adriana; Besaha, Khrystyna; Dimitrova, Anna; Krischok, Stefan; Bund, Andreas; Bobitski, Jaroslav

    2016-09-01

    Sulphur and carbon codoped anatase nanoparticles are synthesized by one-step approach based on interaction between thiourea and metatitanic acid. Electron microscopy shows micrometer-sized randomly distributed crystal aggregates, consisting of many 25-40 nm TiO2 nanoparticles. The obtained phase composition and chemical states of the elements in the structure are analyzed by means of X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). XRD shows that after doping the tetragonal anatase structure is preserved. Further data assessment by Rietveld refinement allows detection of a slight increase of the c lattice parameter and volume related to incorporation of the doping elements. XPS confirms the coexistence of both elemental and oxide carbon forms, which are predominantly located on the TiO2 particle surface. According to XPS analysis sulphur occupies titanium sites and the element is present in S6+ sulfate environment. Analysis based on cyclic voltammetry and galvanostatic intermittent titration (GITT) suggests an accelerated Li+ transport in the doped TiO2 structure. The synthesized S and C co-doped anatase has an excellent electrochemical performance in terms of capacity and very fast lithiation kinetics, superior to the non-doped TiO2. The material displays 83% capacity retention for 500 galvanostatic cycles and nearly 100% current efficiency.

  14. Enhanced photoelectrochemical water splitting performance of TiO2 nanotube arrays coated with an ultrathin nitrogen-doped carbon film by molecular layer deposition

    NASA Astrophysics Data System (ADS)

    Tong, Xili; Yang, Peng; Wang, Yunwei; Qin, Yong; Guo, Xiangyun

    2014-05-01

    Vertically oriented TiO2 nanotube arrays (TNTAs) were conformally coated with an ultrathin nitrogen-doped (N-doped) carbon film via the carbonization of a polyimide film deposited by molecular layer deposition and simultaneously hydrogenated, thereby creating a core/shell nanostructure with a precisely controllable shell thickness. The core/shell nanostructure provides a larger heterojunction interface to substantially reduce the recombination of photogenerated electron-hole pairs, and hydrogenation enhances solar absorption of TNTAs. In addition, the N-doped carbon film coating acts as a high catalytic active surface for oxygen evolution reaction, as well as a protective film to prevent hydrogen-treated TiO2 nanotube oxidation by electrolyte or air. As a result, the N-doped carbon film coated TNTAs displayed remarkably improved photocurrent and photostability. The TNTAs with a N-doped carbon film of ~1 nm produces a current density of 3.6 mA cm-2 at 0 V vs. Ag/AgCl under the illumination of AM 1.5G (100 mW cm-2), which represents one of the highest values achieved with modified TNTAs. Therefore, we propose that ultrathin N-doped carbon film coating on materials is a viable approach to enhance their PEC water splitting performance.Vertically oriented TiO2 nanotube arrays (TNTAs) were conformally coated with an ultrathin nitrogen-doped (N-doped) carbon film via the carbonization of a polyimide film deposited by molecular layer deposition and simultaneously hydrogenated, thereby creating a core/shell nanostructure with a precisely controllable shell thickness. The core/shell nanostructure provides a larger heterojunction interface to substantially reduce the recombination of photogenerated electron-hole pairs, and hydrogenation enhances solar absorption of TNTAs. In addition, the N-doped carbon film coating acts as a high catalytic active surface for oxygen evolution reaction, as well as a protective film to prevent hydrogen-treated TiO2 nanotube oxidation by

  15. Microcystin-LR removal from aqueous solutions using a magnetically separable N-doped TiO2 nanocomposite under visible light irradiation

    EPA Science Inventory

    The performance of magnetically separable N-doped TiO2 was found to be significantly improved when compared with a non-magnetic N-doped TiO2 for the aqueous removal of cyanotoxin Microcystin-LR. The observed enhanced photocatalytic activity may be related to the presence of ferri...

  16. Electrical Properties and Defect Chemistry of In-Doped TiO2 in Terms of the Jonker Formalism.

    PubMed

    Nowotny, Janusz; Bak, Tadeusz; Ionescu, Mihail; Alim, Mohammad A

    2015-04-30

    The present work considers the semiconducting properties of In-doped TiO2 in terms of the Jonker formalism applied for both electrical conductivity and thermoelectric power data determined simultaneously in equilibrium with the gas phase of controlled oxygen activity. It is shown that the electrical properties of In-doped TiO2 annealed in oxidizing conditions [p(O2) > 10 Pa] can be described by the Jonker formalism very well. However, annealing of In-doped TiO2 in strongly reducing conditions [p(O2) < 10(-10) Pa], imposed by the gas phase involving hydrogen, results in a deviation of the experimental data from the Jonker's theoretical model derived for the Maxwell-Boltzmann statistics. This departure is considered in terms of the effect of hydrogen on the formation of structural domains, which are expected to be entirely different from those of oxidized TiO2 in terms of its electronic properties. It is argued that In-doped TiO2 annealed in the gas phase involving hydrogen exhibits a high concentration of donor-type ionic defects, which lead to the formation of high concentration of electrons. The related semiconducting properties are inconsistent with the model of classical semiconductor where the electrons are described by the Maxwell-Boltzmann statistics. It is concluded that strong interactions within the electron gas lead, in consequence, to the behavior resembling correlated transport of electrons. The obtained results suggest that indium incorporation into the rutile structure of TiO2 results in the formation of structural properties that exhibit extraordinary charge transport.

  17. Effects of acceptor-donor complexes on electronic structure properties in co-doped TiO2: A first-principles study

    NASA Astrophysics Data System (ADS)

    Zhang, L.; Cai, L. L.; Yuan, X. B.; Hu, G. C.; Ren, J. F.

    2016-07-01

    We theoretically investigate the doping effects induced by impurity complexes on the electronic structures of anatase TiO2 based on the density functional theory. Mono-doping and co-doping effects are discussed separately. The results show that the impurity doping can make the band-edges shift. The induced defect levels in the band gaps by impurity doping reduce the band gap predominantly. The compensated acceptor-donor pairs in the co-doped TiO2 will improve the photoelectrochemical activity. From the calculations, it is also found that (S+Zr)-co-doped TiO2 has the ideal band gap and band edge, at the same time, the binding energy is higher than other systems, so (S+Zr)-co-doping in TiO2 is more promise in photoelectrochemical experiments.

  18. Nitrogen-doped carbon-embedded TiO2 nanofibers as promising oxygen reduction reaction electrocatalysts

    NASA Astrophysics Data System (ADS)

    Hassen, D.; Shenashen, M. A.; El-Safty, S. A.; Selim, M. M.; Isago, H.; Elmarakbi, A.; El-Safty, A.; Yamaguchi, H.

    2016-10-01

    The development of inexpensive and effective electrocatalysts for oxygen reduction reaction (ORR) as a substitute for commercial Pt/C catalyst is an important issue in fuel cells. In this paper, we report on novel fabrication of self-supported nitrogen-doped carbon-supported titanium nanofibers (Nsbnd TiO2@C) and carbon-supported titanium (TiO2@C) electrocatalysts via a facile electrospinning route. The nitrogen atom integrates physically and homogenously into the entire carbon-titanium structure. We demonstrate the catalytic performance of Nsbnd TiO2@C and TiO2@C for ORR under alkaline conditions in comparison with Pt/C catalyst. The Nsbnd TiO2@C catalyst shows excellent ORR reactivity and durability. Interestingly, among all the catalysts used in this ORR, Nsbnd TiO2@C-0.75 exhibits remarkable competitive oxygen reduction activity in terms of current density and onset potential, as well as superior methanol tolerance. Such tolerance attributes to maximizing the diffusion of trigger pulse electrons during catalytic reactions because of enhanced electronic features. Results indicate that our fabrication strategy can provide an opportunity to produce a simple, efficient, cost-effective, and promising ORR electrocatalyst for practical applications in energy conversion and storage technologies.

  19. Fabrication and characterization of CdS doped TiO2 nanotube composite and its photocatalytic activity for the degradation of methyl orange.

    PubMed

    Chung, Jinwook; Kim, Seu-Run; Kim, Jong-Oh

    2015-01-01

    CdS doped TiO2 nanotube composite was fabricated by chemical bath deposition, and was characterized by the structural, spectral and photoelectrochemical properties. The results of the structural and spectral properties showed that CdS particles were successfully deposited onto the surface of TiO2 nanotube. It is demonstrated that CdS doped TiO2 nanotube composite improved the light harvesting ability. Power conversion efficiency of about 0.32% was observed. This value is about 2.9 times higher than that of pure TiO2 nanotube. The CdS doped TiO2 nanotube composite possesses relatively higher photocatalytic activity and photodegradation efficiency than that of pure TiO2 nanotube under UV light irradiation, and the degradation efficiency of methyl orange was about 42% at UV intensity of 32 W.

  20. Photodeposition of Ag2S on TiO2 nanorod arrays for quantum dot-sensitized solar cells

    PubMed Central

    2013-01-01

    Ag2S quantum dots were deposited on the surface of TiO2 nanorod arrays by a two-step photodeposition. The prepared TiO2 nanorod arrays as well as the Ag2S deposited electrodes were characterized by X-ray diffraction, scanning electron microscope, and transmission electron microscope, suggesting a large coverage of Ag2S quantum dots on the ordered TiO2 nanorod arrays. UV–vis absorption spectra of Ag2S deposited electrodes show a broad absorption range of the visible light. The quantum dot-sensitized solar cells (QDSSCs) based on these electrodes were fabricated, and the photoelectrochemical properties were examined. A high photocurrent density of 10.25 mA/cm2 with a conversion efficiency of 0.98% at AM 1.5 solar light of 100 mW/cm2 was obtained with an optimal photodeposition time. The performance of the QDSSC at different incident light intensities was also investigated. The results display a better performance at a lower incident light level with a conversion efficiency of 1.25% at 47 mW/cm2. PMID:23286551

  1. Highly Active TiO2-Based Visible-Light Photocatalyst with Nonmetal Doping and Plasmonic Metal Decoration

    SciTech Connect

    Zhang, Qiao; Lima, Diana Q.; Chi, Miaofang; Yin, Yadong

    2011-01-01

    A sandwich-structured photocatalyst shows an excellent performance in degradation reactions of a number of organic compounds under UV, visible light, and direct sunlight (see picture). The catalyst was synthesized by a combination of nonmetal doping and plasmonic metal decoration of TiO2 nanocrystals, which improves visible-light activity and enhances light harvesting and charge separation, respectively.

  2. Carbamazepine degradation using a N-doped TiO2 coated photocatalytic membrane reactor: Influence of physical parameters.

    PubMed

    Horovitz, Inna; Avisar, Dror; Baker, Mark A; Grilli, Rossana; Lozzi, Luca; Di Camillo, Daniela; Mamane, Hadas

    2016-06-01

    Commercial α-Al2O3 photocatalytic membranes with a pore size of 200 and 800-nm were coated with N-doped TiO2 photocatalytic film using a sol-gel technique for concurrent bottom-up filtration and photocatalytic oxidation. X-ray diffraction confirmed that the deposited N-doped TiO2 films are in the form of anatase with 78-84% coverage of the membrane surface. The concentration of N found by X-ray photoelectron spectroscopy was in the range of 0.3-0.9 atomic percentage. Membrane permeability after coating decreased by 50% and 12% for the 200- and 800-nm membrane substrates, respectively. The impact of operational parameters on the photocatalytic activity (PCA) of the N-doped TiO2-coated membranes was examined in a laboratory flow cell based on degradation of the model micropollutant carbamazepine, using a solar simulator as the light source. The significant gap in degradation rate between flow through the membrane and flow on the surface of the membrane was attributed both to the hydraulic effect and in-pore PCA. N-doped TiO2-coated membranes showed enhanced activity for UV wavelengths, in addition to activity under visible light. Experiments of PCA under varying flow rates concluded that the process is in the mass-transfer control regime. Carbamazepine removal rate increased with temperature, despite the decrease in dissolved oxygen concentration. PMID:26900981

  3. Synthesis of N-doped TiO2 Using Guanidine Nitrate: An Excellent Visible Light Photocatalyst

    EPA Science Inventory

    An excellent visible light active nitrogen-rich TiO2 photocatalyst have been synthesized by using guanidine nitrate as the doping material. The catalytic efficiency of the catalyst has been demonstrated by the decomposition of the dye, methyl orange (MO), and the pollutant, 2,4 d...

  4. Carbamazepine degradation using a N-doped TiO2 coated photocatalytic membrane reactor: Influence of physical parameters.

    PubMed

    Horovitz, Inna; Avisar, Dror; Baker, Mark A; Grilli, Rossana; Lozzi, Luca; Di Camillo, Daniela; Mamane, Hadas

    2016-06-01

    Commercial α-Al2O3 photocatalytic membranes with a pore size of 200 and 800-nm were coated with N-doped TiO2 photocatalytic film using a sol-gel technique for concurrent bottom-up filtration and photocatalytic oxidation. X-ray diffraction confirmed that the deposited N-doped TiO2 films are in the form of anatase with 78-84% coverage of the membrane surface. The concentration of N found by X-ray photoelectron spectroscopy was in the range of 0.3-0.9 atomic percentage. Membrane permeability after coating decreased by 50% and 12% for the 200- and 800-nm membrane substrates, respectively. The impact of operational parameters on the photocatalytic activity (PCA) of the N-doped TiO2-coated membranes was examined in a laboratory flow cell based on degradation of the model micropollutant carbamazepine, using a solar simulator as the light source. The significant gap in degradation rate between flow through the membrane and flow on the surface of the membrane was attributed both to the hydraulic effect and in-pore PCA. N-doped TiO2-coated membranes showed enhanced activity for UV wavelengths, in addition to activity under visible light. Experiments of PCA under varying flow rates concluded that the process is in the mass-transfer control regime. Carbamazepine removal rate increased with temperature, despite the decrease in dissolved oxygen concentration.

  5. Important role of surface fluoride in nitrogen-doped TiO2 nanoparticles with visible light photocatalytic activity.

    PubMed

    Brauer, Jonathan I; Szulczewski, Greg

    2014-12-11

    Nitrogen-doped TiO2 nanoparticles have been synthesized using sol-gel methods and subsequently fluorinated at room temperature by aging in acidic solutions of NaF. The nanoparticles were characterized by X-ray photoelectron spectroscopy, X-ray diffraction, UV-vis, and IR diffuse reflectance spectroscopy. After aging at room temperature in NaF solutions, the Ti-OH groups on the surface of the TiO2 nanoparticles were replaced by Ti-F bonds, which resulted in a decrease of the point of zero charge from pH 5.4 to 2.8. Most importantly, the nitrogen dopants were retained after the fluorination process, and the amorphous nanoparticles were partially converted into the anatase phase. Annealing the photocatalysts resulted in a decrease of both the nitrogen and fluoride atomic concentration. Diffuse reflectance spectra show an increase in absorbance above 400 nm after annealing the F,N-doped TiO2, which suggests the formation of color centers. The photoactivity of the F,N-doped and N-doped TiO2 catalysts were evaluated by monitoring by the decolorization of methylene blue with visible light. Mass spectrometric analysis revealed that methylene blue undergoes successive demethylation, and more importantly, the rate of decolorization depends on the fluoride concentration. These results show the importance of a two-step synthesis method to independently control the nitrogen and fluoride concentration.

  6. Novel Fe doped mesoporous TiO 2 microspheres: Ultrasonic-hydrothermal synthesis, characterization, and photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Li, Haibin; Liu, Guocong; Chen, Shuguang; Liu, Qicheng

    2010-04-01

    Novel Fe doped mesoporous TiO 2 microspheres were fabricated by an ultrasonic-hydrothermal method when tetrabutyl titanate was used as a precursor and octadecylamine was used as a structure-directing agent. The mesoporous materials were characterized by XRD, SEM, TEM, N 2 adsorption-desorption measurements, XPS, FL, and UV-vis. The results suggest that both ultrasonic treatment and hydrothermal procedure are critical for the fabrication of Fe doped mesoporous TiO 2 microspheres with a combination of regular morphology, large specific surface area, high crystallinity, and high thermal stability. Low-angle XRD and TEM images indicate that the disordered wormhole-like mesostructure of Fe doped TiO 2 microspheres with diameters of about 300-400 nm is actually formed by the agglomerization of nanoparticles with an average size of about 10 nm. The photocatalytic activity of Fe doped mesoporous TiO 2 microspheres was evaluated by the photodegradation of methyl orange. A small amount of Fe 3+ can obviously enhance their photocatalytic activity. The optimal atomic ratio of Fe to Ti for photocatalytic activity is about 0.5 at%.

  7. Nanostructured microtubes based on TiO2 doped by Zr and Hf oxides with the anatase structure

    NASA Astrophysics Data System (ADS)

    Zheleznov, VV; Voit, EI; Sushkov, YV; Sarin, SA; Kuryavyi, VG; Opra, DP; Gnedenkov, SV; Sinebryukhov, SL; Sokolov, AA

    2016-01-01

    The nanostructured microtubes based on TiO2 have been prepared on the carbon fiber template using the sol-gel method. The microtubes consist of nanoparticles of metal oxides: TiO2/ZrO2 and TiO2/HfO2. The dependence of microtubes morphology and nanoparticles structure on the synthesis conditions has been studied using the methods of SEM, SAXS, and Raman spectroscopy. It has been demonstrated that at the stoichiometric ratio of up to 0.04 for Zr/Ti and up to 0.06 for Hf/Ti microtubes consist of uniform nanoparticles with the anatase structure. Along with further increase of the dopants content in the microtubes composition, nanoparticles acquire the core-shell structure. It has been suggested that nanoparticles have a core composed of the solid solutions Ti1-xZrxO2 or Ti1-xHfxO2 and a shell consisting of zirconium or hafnium titanate. The fabricated Zr- and Hf-doped TiO2 materials were investigated in view of their possible use as anode materials for Li-ion batteries. Charge- discharge measurements showed that the doped samples manifested significantly higher reversibility in comparison with the undoped TiO2. The method opens new prospects in synthesis of nanostructured materials for Li-ion batteries application.

  8. Efficiency enhancements in Ag nanoparticles-SiO2-TiO2 sandwiched structure via plasmonic effect-enhanced light capturing

    PubMed Central

    2013-01-01

    TiO2-SiO2-Ag composites are fabricated by depositing TiO2 films on silica substrates embedded with Ag nanoparticles. Enhancement of light absorption of the nanostructural composites is observed. The light absorption enhancement of the synthesized structure in comparison to TiO2 originated from the near-field enhancement caused by the plasmonic effect of Ag nanoparticles, which can be demonstrated by the optical absorption spectra, Raman scattering investigation, and the increase of the photocatalytic activity. The embedded Ag nanoparticles are formed by ion implantation, which effectively prevents Ag to be oxidized through direct contact with TiO2. The suggested incorporation of plasmonic nanostructures shows a great potential application in a highly efficient photocatalyst and ultra-thin solar cell. PMID:23402586

  9. Synthesis and visible-light-induced catalytic activity of Ag2S-coupled TiO2 nanoparticles and nanowires

    NASA Astrophysics Data System (ADS)

    Xie, Yi; Heo, Sung Hwan; Kim, Yong Nam; Yoo, Seung Hwa; Cho, Sung Oh

    2010-01-01

    We present the synthesis and visible-light-induced catalytic activity of Ag2S-coupled TiO2 nanoparticles (NPs) and TiO2 nanowires (NWs). Through a simple wet chemical process from a mixture of peroxo titanic acid (PTA) solution, thiourea and AgAc, a composite of Ag2S NPs and TiO2 NPs with sizes of less than 7 nm was formed. When the NP composite was further treated with NaOH solution followed by annealing at ambient conditions, a new nanocomposite material comprising Ag2S NPs on TiO2 NWs was created. Due to the coupling with such a low bandgap material as Ag2S, the TiO2 nanocomposites could have a visible-light absorption capability much higher than that of pure TiO2. As a result, the synthesized Ag2S/TiO2 nanocomposites exhibited much higher catalytic efficiency for the decomposition of methyl orange than commercial TiO2 (Degussa P25, Germany) under visible light.

  10. Synthesis and characterization of UV-treated Fe-doped bismuth lanthanum titanate-doped TiO2 layers in dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Song, Myoung Geun; Bark, Chung Wung

    2016-06-01

    Dye-sensitized solar cells (DSSCs) based on titanium dioxide (TiO2) have been extensively studied because they constitute promising low-cost alternatives to their conventional semiconductor-based counterparts. However, much of the effort aimed at achieving high conversion efficiencies has focused on dye and liquid electrolytes. In this work, we report the photovoltaic characteristics of DSSCs fabricated by mixing TiO2 with Fe-doped bismuth lanthanum titanate (Fe-BLT). These nanosized Fe-BLT powders were prepared by using a high-energy ball-milling process. In addition, we used a UV radiation-ozone (UV-O3) treatment to change the surface wettability of TiO2 from hydrophobic to hydrophilic and thereby prevented the easy separation of the Fe-BLT-mixed TiO2 from the fluorine-doped tin-oxide (FTO) coating glass.

  11. Enhanced capacitance of composite TiO2 nanotube/boron-doped diamond electrodes studied by impedance spectroscopy.

    PubMed

    Siuzdak, K; Bogdanowicz, R; Sawczak, M; Sobaszek, M

    2015-01-14

    We report on novel composite nanostructures based on boron-doped diamond thin films grown on top of TiO2 nanotubes. The nanostructures made of BDD-modified titania nanotubes showed an increase in activity and performance when used as electrodes in electrochemical environments. The BDD thin films (∼200-500 nm) were deposited using microwave plasma assisted chemical vapor deposition (MW PA CVD) onto anodically fabricated TiO2 nanotube arrays. The influence of boron-doping level, methane admixture and growth time on the performance of the Ti/TiO2/BDD electrode was studied in detail. Scanning electron microscopy (SEM) was applied to investigate the surface morphology and grain size distribution. Moreover, the chemical composition of TiO2/BDD electrodes was investigated by means of micro-Raman spectroscopy. The composite electrodes TiO2/BDD are characterized by a significantly higher capacitive current compared to BDD films deposited directly onto a Ti substrate. The novel composite electrode of TiO2 nanotube arrays overgrown by boron-doped diamond (BDD) immersed in 0.1 M NaNO3 can deliver a specific capacitance of 2.10, 4.79, and 7.46 mF cm(-2) at a scan rate of 10 mV s(-1) for a [B]/[C] ratio of 2k, 5k and 10k, respectively. The substantial improvement of electrochemical performance and the excellent rate capability could be attributed to the synergistic effect of TiO2 treatment in CH4 : H2 plasma and the high electrical conductivity of BDD layers. The analysis of electrochemical impedance spectra using an electric equivalent circuit allowed us to determine the surface area on the basis of the value of constant phase element.

  12. Enhanced capacitance of composite TiO2 nanotube/boron-doped diamond electrodes studied by impedance spectroscopy

    NASA Astrophysics Data System (ADS)

    Siuzdak, K.; Bogdanowicz, R.; Sawczak, M.; Sobaszek, M.

    2014-12-01

    We report on novel composite nanostructures based on boron-doped diamond thin films grown on top of TiO2 nanotubes. The nanostructures made of BDD-modified titania nanotubes showed an increase in activity and performance when used as electrodes in electrochemical environments. The BDD thin films (~200-500 nm) were deposited using microwave plasma assisted chemical vapor deposition (MW PA CVD) onto anodically fabricated TiO2 nanotube arrays. The influence of boron-doping level, methane admixture and growth time on the performance of the Ti/TiO2/BDD electrode was studied in detail. Scanning electron microscopy (SEM) was applied to investigate the surface morphology and grain size distribution. Moreover, the chemical composition of TiO2/BDD electrodes was investigated by means of micro-Raman spectroscopy. The composite electrodes TiO2/BDD are characterized by a significantly higher capacitive current compared to BDD films deposited directly onto a Ti substrate. The novel composite electrode of TiO2 nanotube arrays overgrown by boron-doped diamond (BDD) immersed in 0.1 M NaNO3 can deliver a specific capacitance of 2.10, 4.79, and 7.46 mF cm-2 at a scan rate of 10 mV s-1 for a [B]/[C] ratio of 2k, 5k and 10k, respectively. The substantial improvement of electrochemical performance and the excellent rate capability could be attributed to the synergistic effect of TiO2 treatment in CH4 : H2 plasma and the high electrical conductivity of BDD layers. The analysis of electrochemical impedance spectra using an electric equivalent circuit allowed us to determine the surface area on the basis of the value of constant phase element.

  13. N-doped TiO2 based visible light activated label-free photoelectrochemical biosensor for detection of Hg(2+) through quenching of photogenerated electrons.

    PubMed

    Han, Qianqian; Wang, Kewei; Xu, Lijun; Yan, Xiang; Zhang, Kunchi; Chen, Xing; Wang, Qinglin; Zhang, Lan; Pei, Renjun

    2015-06-21

    A novel photoelectrochemical (PEC) biosensor was fabricated based on N-doped TiO2 for the detection of Hg(2+) through the quenching of photogenerated electrons. The N-doped TiO2 was synthesized by a sol-gel method with urea and tetrabutyl titanate as the N and Ti sources. Compared with the undoped TiO2, the N-doped TiO2 showed an enhanced photocurrent response under visible light (λ > 420 nm). The sensing surface was functionalized with 5'-amino-modified T-rich oligonucleotides. The photoelectrochemical biosensor bound Hg(2+) on the surface by a highly specific T-Hg(2+)-T recognition. Hg(2+) on the surface of the N-doped TiO2 film withdrew the photogenerated electrons and decreased the recorded current signal. The dynamic linear range for Hg(2+) has been determined to be as low as 2-6 μM.

  14. Improve efficiency of perovskite solar cells by using Magnesium doped ZnO and TiO2 compact layers

    NASA Astrophysics Data System (ADS)

    Baktash, Ardeshir; Amiri, Omid; Sasani, Alireza

    2016-05-01

    Here the effect of Magnesium doped TiO2 and ZnO as hole blocking layers (HBLs) are investigated by using solar cell capacitance simulator (SCAPS). The Impact of Magnesium concentration into the TiO2 and ZnO and effect of operating temperature on the performance of the perovskite solar cell are investigated. Best cell performance for both TiO2 and ZnO HBLs (with cell efficiencies of 19.86% and 19.57% respectively) are concluded for the doping level of 10% of Mg into the structure of HBLs. Increase in operating temperature from 300 K to 400 K are decreased the performance of the perovskite solar cell with both pure and Mg-doped HBLs. However, the cells with pure ZnO layer and with Zn0.9 Mg0.1O layer show the highest (with a decline of 8.88% in efficiency) and the lowest stability (with a decline of 50.49% in efficiency) at higher temperatures respectively. Moreover, the cell with Ti0.9 Mg0.1O2 layer shows better stability (with 21.85% reduction in efficiency) than the cell with pure TiO2 compact layer (with 23.28% reduction in efficiency) at higher operating temperatures.

  15. Combination study of DFT calculation and experiment for photocatalytic properties of S-doped anatase TiO2

    NASA Astrophysics Data System (ADS)

    Liu, Rujun; Zhou, Xiaosong; Yang, Fan; Yu, Ying

    2014-11-01

    Although there are many publications about S-doped TiO2, the related mechanism is still not well elucidated. In order to investigate the origin and trend of S substituting for O in TiO2 crystal lattice with proper dopant concentration, a combination of DFT calculation and experiment was used. Bader charge and electronic location function analysis indicate that the largely ionic character between Ti and S bonding in titanium dioxide decreases and there is free electron gas like behavior around S and neighbor Ti for the S-doped anatase TiO2. From DFT calculation, ST2.78 model is found to stabilize the structure of S substitution for lattice O with lower formation energy and its absorbance in visible light increases. Experiment results demonstrate that the sulfur doping results in the shift of the absorption edge for TiO2 to lower energy region, which leads to the nanoparticles active within the wavelength range of 650 nm.

  16. Synthesis and characterization of undoped and cobalt-doped TiO2 nanoparticles via sol-gel technique

    NASA Astrophysics Data System (ADS)

    Mugundan, S.; Rajamannan, B.; Viruthagiri, G.; Shanmugam, N.; Gobi, R.; Praveen, P.

    2015-04-01

    TiO2 nanoparticles doped with different concentrations of cobalt (4, 8, 12 and 16 %) were synthesized by sol-gel method at room temperature with appropriate reactants. In general, TiO2 can exist in anatase, rutile, and brookite phases. In this present study, we used titanium tetra iso propoxide and 2-propanol as a common starting materials and the obtained products were calcined at 500 °C and 800 °C to get anatase and rutile phases, respectively. The crystalline sizes of the doped and undoped TiO2 nanoparticles were observed with X-ray diffraction (XRD) analysis. The functional groups of the samples were identified by Fourier transform infrared spectroscopy (FTIR). From UV-VIS diffuse reflectance spectra (DRS), the band gap energy and excitation wavelength of doped and undoped TiO2 nanoparticles were identified. The defect oriented emissions were seen from photoluminescence (PL) study. The spherical uniform size distribution of particles and elements present in the samples was determined using two different techniques viz., scanning electron microscopy (SEM) with energy-dispersive spectrometer (EDX) and transmission electron microscope (TEM) with selected area electron diffraction (SAED) pattern. The second harmonic generation (SHG) efficiency was also found and the obtained result was compared with potassium di hydrogen phosphate (KDP).

  17. Decorated TiO2 Nanoparticles with La and Ag Elements to Improve Photocatalytic Activity Under Visible Light for the Degradation of MO.

    PubMed

    Wang, Qinghua; Gao, Xuechuan; Zhang, Renfei; Shen, Beibei; Tan, Zhibing; Li, Zhao; Yu, Shiyong

    2016-04-01

    Visible-light photocatalyst of TiO2/La/Ag nanocomposites were successfully synthesized via the conventional sol-gel method and reducing agent of Ag+. The photocatalytic activities were evaluated by methyl orange (MO) degradation. They have remarkable photocatalytic activities compared to TiO2-Anatase, which is thanks to the separation of electron-hole pairs by Ag nanoparticles and lanthanum. The products were characterized by a series of techniques such as X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and Uv-vis. The results show that spherical nanocomposites have been prepared with the size 300 nm and Ag nanoparticles (~10 nm) are dispersed uniformly onto the surface of TiO2/La, which forms TiO2/La/Ag nanocomposites. TiO2/La/Ag nanocomposites have good absorption in the visible region (700 nm > λ > 400 nm). The reasons are as follows: (1) the efficient separation of photogenerated electrons and holes of the photocatalysts on the surface of TiO2/La/Ag nanocomposites and (2) a wide visible-light photoabsorption range (700 nm > λ > 400 nm). Therefore, this study may provide some new idea for the rational design and the facile synthesis of composite catalysts with a green, efficient pathway. PMID:27451670

  18. Enhanced sunlight photocatalytic activity of Ag3PO4 decorated novel combustion synthesis derived TiO2 nanobelts for dye and bacterial degradation.

    PubMed

    Eswar, Neerugatti KrishnaRao; Ramamurthy, Praveen Chandrashekarapura; Madras, Giridhar

    2015-07-01

    This study demonstrates the synthesis of TiO2 nanobelts using solution combustion derived TiO2 with enhanced photocatalytic activity for dye degradation and bacterial inactivation. Hydrothermal treatment of combustion synthesized TiO2 resulted in unique partially etched TiO2 nanobelts and Ag3PO4 was decorated using the co-precipitation method. The catalyst particles were characterized using X-ray diffraction analysis, BET surface area analysis, diffuse reflectance and electron microscopy. The photocatalytic properties of the composites of Ag3PO4 with pristine combustion synthesized TiO2 and commercial TiO2 under sunlight were compared. Therefore the studies conducted proved that the novel Ag3PO4/unique combustion synthesis derived TiO2 nanobelt composites exhibited extended light absorption, better charge transfer mechanism and higher generation of hydroxyl and hole radicals. These properties resulted in enhanced photodegradation of dyes and bacteria when compared to the commercial TiO2 nanocomposite. These findings have important implications in designing new photocatalysts for water purification.

  19. Mechanism of strong visible light photocatalysis by Ag2O-nanoparticle-decorated monoclinic TiO2(B) porous nanorods

    NASA Astrophysics Data System (ADS)

    Paul, Kamal Kumar; Ghosh, Ramesh; Giri, P. K.

    2016-08-01

    We report on the ultra-high rate of photodegradation of organic dyes under visible light illumination on Ag2O-nanoparticle-decorated (NP) porous pure B-phase TiO2 (TiO2(B)) nanorods (NRs) grown by a solvothermal route. The as-grown TiO2(B) NRs are found to be nanoporous in nature and the Ag2O NPs are uniformly decorated over its surface, since most of the pores work as nucleation sites for the growth of Ag2O NPs. The effective band gap of the TiO2(B)/Ag2O heterostructure (HS), with a weight ratio of 1:1, has been significantly reduced to 1.68 eV from the pure TiO2(B) band gap of 2.8 eV. Steady state and time-resolved photoluminescence (PL) studies show the reduced intensity of visible PL and slower recombination dynamics in the HS samples. The photocatalytic degradation efficiency of the TiO2(B)/Ag2O HS has been investigated using aqueous methyl orange and methylene blue as reference dyes under visible light (390–800 nm) irradiation. It is found that photodegradation by the TiO2(B)/Ag2O HS is about one order of magnitude higher than that of bare TiO2(B) NRs and Ag2O NPs. The optimized TiO2(B)/Ag2O HS exhibited the highest photocatalytic efficiency, with 88.2% degradation for 30 min irradiation. The corresponding first order degradation rate constant is 0.071 min‑1, which is four times higher than the reported values. Furthermore, cyclic stability studies show the high stability of the HS photocatalyst for up to four cycles of use. The major improvement in photocatalytic efficiency has been explained on the basis of enhanced visible light absorption and band-bending-induced efficient charge separation in the HS. Our results demonstrate the long-term stability and superiority of the TiO2(B)/Ag2O HS over the bare TiO2(B) NRs and other TiO2-based photocatalysts for its cutting edge application in hydrogen production and environmental cleaning driven by solar light photocatalysis.

  20. Mechanism of strong visible light photocatalysis by Ag2O-nanoparticle-decorated monoclinic TiO2(B) porous nanorods

    NASA Astrophysics Data System (ADS)

    Paul, Kamal Kumar; Ghosh, Ramesh; Giri, P. K.

    2016-08-01

    We report on the ultra-high rate of photodegradation of organic dyes under visible light illumination on Ag2O-nanoparticle-decorated (NP) porous pure B-phase TiO2 (TiO2(B)) nanorods (NRs) grown by a solvothermal route. The as-grown TiO2(B) NRs are found to be nanoporous in nature and the Ag2O NPs are uniformly decorated over its surface, since most of the pores work as nucleation sites for the growth of Ag2O NPs. The effective band gap of the TiO2(B)/Ag2O heterostructure (HS), with a weight ratio of 1:1, has been significantly reduced to 1.68 eV from the pure TiO2(B) band gap of 2.8 eV. Steady state and time-resolved photoluminescence (PL) studies show the reduced intensity of visible PL and slower recombination dynamics in the HS samples. The photocatalytic degradation efficiency of the TiO2(B)/Ag2O HS has been investigated using aqueous methyl orange and methylene blue as reference dyes under visible light (390-800 nm) irradiation. It is found that photodegradation by the TiO2(B)/Ag2O HS is about one order of magnitude higher than that of bare TiO2(B) NRs and Ag2O NPs. The optimized TiO2(B)/Ag2O HS exhibited the highest photocatalytic efficiency, with 88.2% degradation for 30 min irradiation. The corresponding first order degradation rate constant is 0.071 min-1, which is four times higher than the reported values. Furthermore, cyclic stability studies show the high stability of the HS photocatalyst for up to four cycles of use. The major improvement in photocatalytic efficiency has been explained on the basis of enhanced visible light absorption and band-bending-induced efficient charge separation in the HS. Our results demonstrate the long-term stability and superiority of the TiO2(B)/Ag2O HS over the bare TiO2(B) NRs and other TiO2-based photocatalysts for its cutting edge application in hydrogen production and environmental cleaning driven by solar light photocatalysis.

  1. Mechanism of strong visible light photocatalysis by Ag2O-nanoparticle-decorated monoclinic TiO2(B) porous nanorods.

    PubMed

    Paul, Kamal Kumar; Ghosh, Ramesh; Giri, P K

    2016-08-01

    We report on the ultra-high rate of photodegradation of organic dyes under visible light illumination on Ag2O-nanoparticle-decorated (NP) porous pure B-phase TiO2 (TiO2(B)) nanorods (NRs) grown by a solvothermal route. The as-grown TiO2(B) NRs are found to be nanoporous in nature and the Ag2O NPs are uniformly decorated over its surface, since most of the pores work as nucleation sites for the growth of Ag2O NPs. The effective band gap of the TiO2(B)/Ag2O heterostructure (HS), with a weight ratio of 1:1, has been significantly reduced to 1.68 eV from the pure TiO2(B) band gap of 2.8 eV. Steady state and time-resolved photoluminescence (PL) studies show the reduced intensity of visible PL and slower recombination dynamics in the HS samples. The photocatalytic degradation efficiency of the TiO2(B)/Ag2O HS has been investigated using aqueous methyl orange and methylene blue as reference dyes under visible light (390-800 nm) irradiation. It is found that photodegradation by the TiO2(B)/Ag2O HS is about one order of magnitude higher than that of bare TiO2(B) NRs and Ag2O NPs. The optimized TiO2(B)/Ag2O HS exhibited the highest photocatalytic efficiency, with 88.2% degradation for 30 min irradiation. The corresponding first order degradation rate constant is 0.071 min(-1), which is four times higher than the reported values. Furthermore, cyclic stability studies show the high stability of the HS photocatalyst for up to four cycles of use. The major improvement in photocatalytic efficiency has been explained on the basis of enhanced visible light absorption and band-bending-induced efficient charge separation in the HS. Our results demonstrate the long-term stability and superiority of the TiO2(B)/Ag2O HS over the bare TiO2(B) NRs and other TiO2-based photocatalysts for its cutting edge application in hydrogen production and environmental cleaning driven by solar light photocatalysis. PMID:27333816

  2. Enhanced electronic properties in mesoporous TiO2 via lithium doping for high-efficiency perovskite solar cells

    NASA Astrophysics Data System (ADS)

    Giordano, Fabrizio; Abate, Antonio; Correa Baena, Juan Pablo; Saliba, Michael; Matsui, Taisuke; Im, Sang Hyuk; Zakeeruddin, Shaik M.; Nazeeruddin, Mohammad Khaja; Hagfeldt, Anders; Graetzel, Michael

    2016-01-01

    Perovskite solar cells are one of the most promising photovoltaic technologies with their extraordinary progress in efficiency and the simple processes required to produce them. However, the frequent presence of a pronounced hysteresis in the current voltage characteristic of these devices arises concerns on the intrinsic stability of organo-metal halides, challenging the reliability of technology itself. Here, we show that n-doping of mesoporous TiO2 is accomplished by facile post treatment of the films with lithium salts. We demonstrate that the Li-doped TiO2 electrodes exhibit superior electronic properties, by reducing electronic trap states enabling faster electron transport. Perovskite solar cells prepared using the Li-doped films as scaffold to host the CH3NH3PbI3 light harvester produce substantially higher performances compared with undoped electrodes, improving the power conversion efficiency from 17 to over 19% with negligible hysteretic behaviour (lower than 0.3%).

  3. Enhanced electronic properties in mesoporous TiO2 via lithium doping for high-efficiency perovskite solar cells.

    PubMed

    Giordano, Fabrizio; Abate, Antonio; Correa Baena, Juan Pablo; Saliba, Michael; Matsui, Taisuke; Im, Sang Hyuk; Zakeeruddin, Shaik M; Nazeeruddin, Mohammad Khaja; Hagfeldt, Anders; Graetzel, Michael

    2016-01-01

    Perovskite solar cells are one of the most promising photovoltaic technologies with their extraordinary progress in efficiency and the simple processes required to produce them. However, the frequent presence of a pronounced hysteresis in the current voltage characteristic of these devices arises concerns on the intrinsic stability of organo-metal halides, challenging the reliability of technology itself. Here, we show that n-doping of mesoporous TiO2 is accomplished by facile post treatment of the films with lithium salts. We demonstrate that the Li-doped TiO2 electrodes exhibit superior electronic properties, by reducing electronic trap states enabling faster electron transport. Perovskite solar cells prepared using the Li-doped films as scaffold to host the CH3NH3PbI3 light harvester produce substantially higher performances compared with undoped electrodes, improving the power conversion efficiency from 17 to over 19% with negligible hysteretic behaviour (lower than 0.3%). PMID:26758549

  4. Enhanced electronic properties in mesoporous TiO2 via lithium doping for high-efficiency perovskite solar cells

    PubMed Central

    Giordano, Fabrizio; Abate, Antonio; Correa Baena, Juan Pablo; Saliba, Michael; Matsui, Taisuke; Im, Sang Hyuk; Zakeeruddin, Shaik M.; Nazeeruddin, Mohammad Khaja; Hagfeldt, Anders; Graetzel, Michael

    2016-01-01

    Perovskite solar cells are one of the most promising photovoltaic technologies with their extraordinary progress in efficiency and the simple processes required to produce them. However, the frequent presence of a pronounced hysteresis in the current voltage characteristic of these devices arises concerns on the intrinsic stability of organo-metal halides, challenging the reliability of technology itself. Here, we show that n-doping of mesoporous TiO2 is accomplished by facile post treatment of the films with lithium salts. We demonstrate that the Li-doped TiO2 electrodes exhibit superior electronic properties, by reducing electronic trap states enabling faster electron transport. Perovskite solar cells prepared using the Li-doped films as scaffold to host the CH3NH3PbI3 light harvester produce substantially higher performances compared with undoped electrodes, improving the power conversion efficiency from 17 to over 19% with negligible hysteretic behaviour (lower than 0.3%). PMID:26758549

  5. First-principles study of the electronic structure of nonmetal-doped anatase TiO2

    NASA Astrophysics Data System (ADS)

    Wang, Yuan; Ma, Jing; Zhou, Jian-Ping; Chen, Xiao-Ming; Wang, Jing-Zhou

    2016-02-01

    In this paper, we present a detailed study of the structure, defect formation energy, and electronic and magnetic properties of nonmetal-doped TiO2 by using the first-principles projector augmented wave (PAW) potential within the generalized gradient approximation (GGA). The formation energy reduces with increasing electronegativity of the dopant. After doping with nonmetal elements, some band gaps of the doped-TiO2 become narrow, and others become wide, in which impurity states appear in the band gap. The relative positions of the impurity states are much different, mainly caused by the different electronegativities of the nonmetal elements F, O, B, C and N. When H is added to achieve a charge balance, the impurity states approach the valence band maximum, because the electronegativity difference among the nonmetal elements is decreased. Therefore, nonmetal and H codoping is an effective way to improve the visible-light catalytic activity of anatase TiO2. In addition, N-doping and C-doping can cause spin polarization of the TiO2 electronic structure and form 1.0 μ B and 2.0 μ B magnetic moment, respectively.

  6. Synthesis, characterization and photocatalytic applications of Zn-doped TiO2 nanoparticles by sol-gel method

    NASA Astrophysics Data System (ADS)

    Aware, Dinkar V.; Jadhav, Shridhar S.

    2016-10-01

    Mesoporous, nanocrystalline, Zinc-doped TiO2 nanoparticles were synthesized by surfactant-assisted sol-gel method. The X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET), and UV-VIS spectrometer techniques were used to characterize the synthesized products. XRD results confirm the formation of the anatase phase for the TiO2 nanoparticles, with crystallite sizes in the range of 12.6-18.1 nm. The small crystallite size and doping with Zinc ion inhibit phase transformation and promote the growth of the TiO2 anatase phase. The SEM and TEM micrographs revealed the spherical-like morphology with average diameter of about 12-18 nm which is in agreement with XRD results. The optical study shows that doping ions lead to an increase in the absorption edge wavelength and a decrease in the band gap energy of titania. Photocatalytic activity of the synthesized nanomaterials was successfully tested for photodegradation of methyl red as model pollutant under UV light. The photocatalytic activity results confirm that the doped nanoparticles show higher activity than undoped titania. The small grain size, high crystallinity, high specific surface area and decrease in the band gap energy of doped titania may be responsible for the high photocatalytic activity.

  7. Synthesis of Metal Ion-Doped TiO2 Nanoparticles Using Two-Phase Method and Their Photocatalytic Activity Under Visible Light Irradiation.

    PubMed

    Nguyen, Duy-Trinh; Hong, Seong-Soo

    2016-02-01

    In this study, TiO2 and metal ion-doped TiO2 nanoparticles were successfully synthesized by solvothermal reaction of titanium butoxide precursor in the presence of oleic acid, oleylamine and vapor water and they were characterized by XRD, Raman, TEM and DRS. We also investigated the photocatalytic activity of these oxides for the decomposition of Rhodamine B. From XRD and Raman results, doping of the metal ion in the crystal lattice did not change the high crystallinity of the TiO2 structure, and all the metal ions were incorporated into the structures of titania as well as replaced titanium ion or located at interstitial site. The absorption band shifted to a higher wavelength on the metal ion-doped TiO2 samples compared to the pure TiO2 sample. The Ce ion- doped TiO2 catalysts showed the higher photocatalytic activity compared to the pure TiO2 and a commercial P-25 catalysts and 1% Ce-doped TiO2 showed the highest photocatalytic activity.

  8. Synthesis of Metal Ion-Doped TiO2 Nanoparticles Using Two-Phase Method and Their Photocatalytic Activity Under Visible Light Irradiation.

    PubMed

    Nguyen, Duy-Trinh; Hong, Seong-Soo

    2016-02-01

    In this study, TiO2 and metal ion-doped TiO2 nanoparticles were successfully synthesized by solvothermal reaction of titanium butoxide precursor in the presence of oleic acid, oleylamine and vapor water and they were characterized by XRD, Raman, TEM and DRS. We also investigated the photocatalytic activity of these oxides for the decomposition of Rhodamine B. From XRD and Raman results, doping of the metal ion in the crystal lattice did not change the high crystallinity of the TiO2 structure, and all the metal ions were incorporated into the structures of titania as well as replaced titanium ion or located at interstitial site. The absorption band shifted to a higher wavelength on the metal ion-doped TiO2 samples compared to the pure TiO2 sample. The Ce ion- doped TiO2 catalysts showed the higher photocatalytic activity compared to the pure TiO2 and a commercial P-25 catalysts and 1% Ce-doped TiO2 showed the highest photocatalytic activity. PMID:27433699

  9. Photocatalytic degradation of acephate in pak choi, Brassica chinensis, with Ce-doped TiO2.

    PubMed

    Liu, Xiangying; Wang, Lifeng; Zhou, Xiaomao; Liu, Kailin; Bai, Lianyang; Zhou, Xuguo

    2015-01-01

    The photocatalytic degradation of acephate was investigated using Ce-doped TiO2 (TiO2/Ce) hydrosol. In contrast to previous research conducted under artificial light in the laboratory, this study investigated the decomposition of acephate in a field trial. The results show that acephate can be efficiently degraded by the TiO2/Ce system under natural field conditions; the degradation efficiency was affected by the dosage of the photocatalyst and acephate. The optimum dosage of TiO2/Ce was 2400 g a.i.ha(-1), and the photodegradation efficiency of acephate reached 93.5% after 20 h at an acephate dosage of 675 g a.i.ha(-1). Ultra-performance liquid chromatography/mass spectrometry (UPLC/MS) analysis detected and identified four degradation products-methamidophos, phosphorothioic acid O,O,S-trimethyl ester, S-methyl methanethiosulfonate and phosphorous acid-that were formed during the TiO2/Ce photodegradation of acephate. Based on the structural identification of the degradation products, a probable photodegradation pathway was proposed, and the first decomposition step may be the cleavage of the C‒N bond of acephate. Subsequently, the P‒S and P‒O bonds may be oxidized gradually or simultaneously to complete the mineralization.

  10. Structural phase analysis, band gap tuning and fluorescence properties of Co doped TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Alamgir; Khan, Wasi; Ahmad, Shabbir; Mehedi Hassan, M.; Naqvi, A. H.

    2014-12-01

    This paper reports on structural and optical properties of Co (0, 3, 5 & 7 mol%) doped TiO2 (titania) nanoparticles (NPs) synthesized by employing acid modified sol-gel method. The crystalline phase of the pure and doped NPs was observed with X-ray diffraction (XRD) followed by Raman scattering technique. Field emission scanning electron microscope and transmission electron microscopy give the morphological details. Fourier transform infrared spectra indicate the bonding interactions of Co ions with the titania lattice framework. Optical studies were attained with UV-visible absorption and fluorescence emission spectroscopy. XRD analysis reveals that all prepared samples have pure anatase phase with tetragonal symmetry devoid of any other secondary phase. The average crystallite size of all samples was calculated using Scherrer's formula and was found to vary from 8 to 10 nm with doping concentration of Co. The Raman spectroscopy further confirmed the formation of TiO2 in anatase structure in both pure and Co doped TiO2 NPs. The most intense Raman active Eg peak of TiO2 NPs shifted to higher energy on doping. Both UV-visible and fluorescence spectra show a blue shift in their absorption and band edge emission subsequently on increasing with Co percentage in titania host matrix, wherever there is an indication of quantum confinement effect with widening of band gap on decreasing in NPs size. There is also a possibility of strong Coulomb interaction effect on the optical processes involving the Co ions. However, the intensities of different emission spectra are not the same but decrease profoundly for doping samples due to concentration quenching effect.

  11. Influence of transition metal doping on the structural, optical, and magnetic properties of TiO2 films deposited on Si substrates by a sol–gel process

    PubMed Central

    2013-01-01

    Transition metal (TM)-doped TiO2 films (TM = Co, Ni, and Fe) were deposited on Si(100) substrates by a sol–gel method. With the same dopant content, Co dopants catalyze the anatase-to-rutile transformation (ART) more obviously than Ni and Fe doping. This is attributed to the different strain energy induced by the different dopants. The optical properties of TM-doped TiO2 films were studied with spectroscopic ellipsometry data. With increasing dopant content, the optical band gap (EOBG) shifts to lower energy. With the same dopant content, the EOBG of Co-doped TiO2 film is the smallest and that of Fe-doped TiO2 film is the largest. The results are related to electric disorder due to the ART. Ferromagnetic behaviors were clearly observed for TM-doped TiO2 films except the undoped TiO2 film which is weakly magnetic. Additionally, it is found that the magnetizations of the TM-doped TiO2 films decrease with increasing dopant content. PMID:24350904

  12. Mesoporous TiO2 nanoparticles containing Ag ion with excellent antimicrobial activity at remarkable low silver concentrations.

    PubMed

    Naik, Kshipra; Chatterjee, Amrita; Prakash, Halan; Kowshik, Meenal

    2013-04-01

    Mesoporous Ag-TiO2 nanoparticles with TiO2 homogenous anatase crystalline phase was synthesized using a one-pot sol-gel method. The sample was calcined at 100 degrees C and characterized by XRD, HR TEM, EDAX, IR spectroscopy, DRS, N2 adsorption-desorption isotherm and Brunauer-Emmett-Teller (BET) analysis. The BET surface area of the sample was 266 m2/g and the crystallite size as calculated using Scherrer formula was 3.76 nm. The Ag-TiO2 nanoparticles exhibited excellent antimicrobial activity against representative Gram-positive and Gram-negative bacterial cultures and Candida albicans. Complete inhibition of microorganisms was achieved at a very low Ag-TiO2 concentration, in the range of 1.0 to 20 microg/mL (effective Ag concentrations were 11.7 to 234 ppb) in less than 2 h under ambient conditions, without the requirement of photoactivation. Silver ion release studies showed that about 18% of silver ions were present in solution. Thus, it may be inferred that the antimicrobial activity is due to Ag ions released from the TiO2 matrix. The mesoporous nature and antimicrobial activity at low concentrations without photoactivation are important aspects which make this material an excellent candidate for potential application as disinfectant and/or antimicrobial agent.

  13. Synergistic effect on the visible light activity of Ti3+ doped TiO2 nanorods/boron doped graphene composite

    PubMed Central

    Xing, Mingyang; Li, Xiao; Zhang, Jinlong

    2014-01-01

    TiO2/graphene (TiO2-x/GR) composites, which are Ti3+ self-doped TiO2 nanorods decorated on boron doped graphene sheets, were synthesized via a simple one-step hydrothermal method using low-cost NaBH4 as both a reducing agent and a boron dopant on graphene. The resulting TiO2 nanorods were about 200 nm in length with exposed (100) and (010) facets. The samples were characterized by X-ray diffraction (XRD), UV-visible diffuse reflectance spectroscopy, X-band electron paramagnetic resonance (EPR), X-ray photoelectron spectra (XPS), transmission electron microscope (TEM), Raman, and Fourier-transform infrared spectroscopy (FTIR). The XRD results suggest that the prepared samples have an anatase crystalline structure. All of the composites tested exhibited improved photocatalytic activities as measured by the degradation of methylene blue and phenol under visible light irradiation. This improvement was attributed to the synergistic effect of Ti3+ self-doping on TiO2 nanorods and boron doping on graphene. PMID:24974890

  14. Electrochemical reduction induced self-doping of Ti3+ for efficient water splitting performance on TiO2 based photoelectrodes.

    PubMed

    Zhang, Zhonghai; Hedhili, Mohamed Nejib; Zhu, Haibo; Wang, Peng

    2013-10-01

    Hetero-element doping (e.g., N, F, C) of TiO2 is inevitably accompanied by significantly increased structural defects due to the dopants' nature being foreign impurities. Very recently, in situ self-doping with homo-species (e.g., Ti(3+)) has been emerging as a rational solution to enhance TiO2 photoactivity within both UV and visible light regions. Herein we demonstrate that conventional electrochemical reduction is indeed a facile and effective strategy to induce in situ self-doping of Ti(3+) into TiO2 and the self-doped TiO2 photoelectrodes showed remarkably improved and very stable water splitting performance. In this study, hierarchical TiO2 nanotube arrays (TiO2 NTs) were chosen as TiO2 substrates and then electrochemically reduced under varying conditions to produce Ti(3+) self-doped TiO2 NTs (ECR-TiO2 NTs). The optimized saturation photocurrent density and photoconversion efficiency on the ECR-TiO2 NTs under simulated AM 1.5G illumination were identified to be 2.8 mA cm(-2) at 1.23 V vs. RHE and 1.27% respectively, which are the highest values ever reported for TiO2 based photoelectrodes. The electrochemical impedance spectra measurement confirms that the electrochemical induced Ti(3+) self-doping improved the electrical conductivity of the ECR-TiO2 NTs. The versatility and effectiveness of the electrochemical reduction method for Ti(3+) self-doping in P25 based TiO2 was also examined and confirmed.

  15. UV-visible light-activated Ag-decorated, monodisperse TiO2 aggregates for treatment of the pharmaceutical oxytetracycline.

    PubMed

    Han, Changseok; Likodimos, Vlassis; Khan, Javed Ali; Nadagouda, Mallikarjuna N; Andersen, Joel; Falaras, Polycarpos; Rosales-Lombardi, Pablo; Dionysiou, Dionysios D

    2014-10-01

    Noble metal Ag-decorated, monodisperse TiO2 aggregates were successfully synthesized by an ionic strength-assisted, simple sol-gel method and were used for the photocatalytic degradation of the antibiotic oxytetracycline (OTC) under both UV and visible light (UV-visible light) irradiation. The synthesized samples were characterized by X-ray diffraction analysis (XRD); UV-vis diffuse reflectance spectroscopy; environmental scanning electron microscopy (ESEM); transmission electron microscopy (TEM); high-resolution TEM (HR-TEM); micro-Raman, energy-dispersive X-ray spectroscopy (EDS); and inductively coupled plasma optical emission spectrometry (ICP-OES). The results showed that the uniformity of TiO2 aggregates was finely tuned by the sol-gel method, and Ag was well decorated on the monodisperse TiO2 aggregates. The absorption of the samples in the visible light region increased with increasing Ag loading that was proportional to the amount of Ag precursor added in the solution over the tested concentration range. The Brunauer, Emmett, and Teller (The BET) surface area slightly decreased with increasing Ag loading on the TiO2 aggregates. Ag-decorated TiO2 samples demonstrated enhanced photocatalytic activity for the degradation of OTC under UV-visible light illumination compared to that of pure TiO2. The sample containing 1.9 wt% Ag showed the highest photocatalytic activity for the degradation of OTC under both UV-visible light and visible light illumination. During the experiments, the detected Ag leaching for the best TiO2-Ag photocatalyst was much lower than the National Secondary Drinking Water Regulation for Ag limit (0.1 mg L(-1)) issued by the US Environmental Protection Agency.

  16. Preparation of TiO(2)/Ag colloids with ultraviolet resistance and antibacterial property using short chain polyethylene glycol.

    PubMed

    Su, W; Wei, S S; Hu, S Q; Tang, J X

    2009-12-30

    TiO(2)/Ag nano-antibacterial material was prepared at low temperature using polyethylene glycol (PEG-600) as reducing and stabilizing agent. The size and shape as well as the optical properties of the nano-materials were characterized with transmission electron microscopy (TEM) and UV-vis spectroscopy (UV-vis). The results showed that the average particle size of TiO(2) among these nano-materials was around 50-150 nm, and the average particle size of nano-silver was around 20 nm. Formation of Ag nano-particles on the surface of TiO(2) was confirmed by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS), and the antibacterial activity was also investigated. By the antibacterial activity study and ultraviolet resistance test, it is noted that growth inhibition rates against E. coli was 99.99% as the concentration of nano-particles dispersion solution was 10 ppm, the minimum UV protective effect could be achieved as the concentration was 290 ppm.

  17. Carbonate Doping in TiO2 Microsphere: The Key Parameter Influencing Others for Efficient Dye Sensitized Solar Cell

    PubMed Central

    Seddigi, Zaki S.; Ahmed, Saleh A.; Sardar, Samim; Pal, Samir Kumar

    2016-01-01

    Four key parameters namely light trapping, density of light harvesting centre, photoinduced electron injection and electron transport without self-recombination are universally important across all kinds of solar cells. In the present study, we have considered the parameters in the context of a model Dye Sensitized Solar Cell (DSSC). Our experimental studies reveal that carbonate doping of TiO2 mesoporous microspheres (doped MS) makes positive influence to all the above mentioned key parameters responsible for the enhanced solar cell efficiency. A simple method has been employed to synthesize the doped MS for the photoanode of a N719 (ruthenium dye)-based DSSC. A detail electron microscopy has been used to characterize the change in morphology of the MS upon doping. The optical absorption spectrum of the doped MS reveals significant shift of TiO2 (compared to that of the MS without doping) towards maximum solar radiance (~500 nm) and the excellent scattering in the entire absorption band of the sensitizing dye (N719). Finally, and most importantly, for the first time we have demonstrated that the solar cells with doped MS offers better efficiency (7.6%) in light harvesting compared to MS without doping (5.2%) and also reveal minimum self recombination of photoelectrons in the redox chain. PMID:26984765

  18. Characterization of Ni-doped TiO2 thin films deposited by dip-coating technique

    NASA Astrophysics Data System (ADS)

    Kharoubi, Abdelmalek; Bouaza, A.; Benrabah, B.; Ammari, A.; Khiali, A.

    2015-12-01

    Undoped and Ni-doped TiO2 thin films have been prepared by sol-gel dip-coating method on glass and silicon substrates. X-ray diffraction studies show that both TiO2 and Ni-doped TiO2 thin films are of anatase phase with (1 0 1) as preferential orientation. From the UV-visible spectroscopy analysis, all films exhibits a high transparency ~ 80% and shows that the optical band gap decreases from 3.66 to 3.59 eV, which may be related with the phase composition and impurities. Fourier transformed infrared spectroscopy (FTIR) study confirms the presence of Ti-O, Ti=O and O-H bands. Thermal analysis by differential scanning calorimetriy (DSC) shows endothermic reactions between 30 °C and 280 °C and exothermic reactions between 370 °C and 540 °C corresponding to the crystallization of TiO2 in the anatase phase. The Nyquist plots suggests that the equivalent circuit of the films is an RpCp parallel circuit and shows an increase in resistance Rp with increasing the Ni concentration and a decrease in capacity Cp.

  19. Characteristics and anticorrosion performance of Fe-doped TiO2 films by liquid phase deposition method

    NASA Astrophysics Data System (ADS)

    Liu, Yu; Xu, Chao; Feng, ZuDe

    2014-09-01

    Fe-doped TiO2 thin films were fabricated by liquid phase deposition (LPD) method, using Fe(III) nitrate as both Fe element source and fluoride scavenger instead of commonly-used boric acid (H3BO3). Scanning electron microscopy (SEM), X-ray diffraction (XRD), and UV-vis spectrum were employed to examine the effects of Fe element on morphology, structure and optical characteristics of TiO2 films. The as-prepared films were served as photoanode applied to photogenerated cathodic protection of SUS304 stainless steel (304SS). It was observed that the photoelectrochemical properties of the as-prepared films were enhanced with the addition of Fe element compared to the undoped TiO2 film. The highest photoactivity was achieved for Ti13Fe (Fe/Ti = 3 molar ratio) film prepared in precursor bath containing 0.02 M TiF4 + 0.06 M Fe(NO3)3 under white-light illumination. The effective anticorrosion behaviors can be attributed to the Fe element incorporation which decreases the probability of photogenerated charge-carrier recombination and extends the light response range of Fe-doped TiO2 films appeared to visible-light region.

  20. Cu-doped TiO(2) nanoparticles enhance survival of Shewanella oneidensis MR-1 under ultraviolet light (UV) exposure.

    PubMed

    Wu, Bing; Zhuang, Wei-Qin; Sahu, Manoranjan; Biswas, Pratim; Tang, Yinjie J

    2011-10-01

    It has been shown that photocatalytic TiO(2) nanoparticles (NPs) can be used as an efficient anti-microbial agent under UV light due to generation of reactive oxygen species (ROS), while Shewanella oneidensis MR-1 is a metal-reducing bacterium highly susceptible to UV radiation. Interestingly, we found that the presence of Cu-doped TiO(2) NPs in the cultural medium dramatically increased the survival rates (based on colony-forming unit) of strain MR-1 by over 10,000-fold (incubation without shaking) and ~200 fold (incubation with shaking) after a 2-h exposure to UV light. Gene expression results (via qPCR measurement) indicated that the DNA repair gene recA in MR-1 was significantly induced by UV exposure (indicating cellular damage under UV stress), but the influence of NPs on recA expression was not statistically evident. Plausible explanations to NP attenuation of UV stresses are: 1. TiO(2) based NPs are capable of scattering and absorbing UV light and thus create a shading effect to protect MR-1 from UV radiation; 2. more importantly, Cu-doped TiO(2) NPs can co-agglomerate with MR-1 to form large flocs that improves cells' survival against the environmental stresses. This study improves our understanding of NP ecological impacts under natural solar radiation and provides useful insights to application of photocatalytic-NPs for bacterial disinfection. PMID:21855961

  1. TiS2 transformation into S-doped and N-doped TiO2 with visible-light catalytic activity

    NASA Astrophysics Data System (ADS)

    Lin, Yu-Chen; Chien, Tzu-En; Lai, Po-Chih; Chiang, Yu-Hsien; Li, Kun-Lin; Lin, Jong-Liang

    2015-12-01

    S-doped rutile has been prepared for the first time by hydrothermal reaction of TiS2 in hydrochloric acid at a low temperature (180 °C), with the S atoms in three states of Tisbnd Ssbnd Ti, Tisbnd Ssbnd O and SO4. TiS2 in nitric acid can also be transformed into TiO2, but with mixed phases of anatase and rutile, containing nitrogen atoms at interstitial sites in the form of Tisbnd Osbnd N or Tisbnd Nsbnd O. The Ssbnd TiO2 catalyst shows a better visible-light reactivity toward adsorbed methylene blue (MB) photodegradation and hydroxylation of terephthalic acid with respect to the Nsbnd TiO2. The possible reasons leading to the high photoactivity of the Ssbnd TiO2 are discussed in terms of the incorporated sulfur states.

  2. Effects of Fe Doping on the Structural, Optical, and Magnetic Properties of TiO2 Nanoparticles

    NASA Astrophysics Data System (ADS)

    Thu, Dang Xuan; Trung, Vu Quoc; Nghia, Nguyen Manh; Khang, Nguyen Cao; Lam, Tran Dai

    2016-08-01

    Fe-doped TiO2 nanoparticles have been prepared by the hydrolysis method. The effects of Fe doping on the structural, optical, and magnetic properties of the Ti1-x Fe x O2 (x = 0.00, 0.03, 0.06, 0.10, 0.13) materials were thoroughly investigated by a combination of various methods, including transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET) analysis, x-ray diffraction (XRD) analysis, ultraviolet-visible (UV-Vis) reflectance spectroscopy, Raman spectroscopy, and vibrating-sample magnetometry. Analysis of the TEM and XRD measurements showed that the resulting powders had nanoscale particle size. The Fe-doped samples were found to be paramagnetic at room temperature (by magnetization measurements), with Fe acting as substitutional impurity at Ti sites in the anatase TiO2 phase. Substitution of Fe at Ti sites was also confirmed by Raman spectra. The paramagnetic nature of the Ti1-x Fe x O2 samples was further investigated using density functional theory calculations of their electronic band structure and density of states. Finally, the photocatalytic activity of the Fe-doped TiO2 samples was studied by investigating their photocatalytic decomposition of methylene blue.

  3. Effects of Fe Doping on the Structural, Optical, and Magnetic Properties of TiO2 Nanoparticles

    NASA Astrophysics Data System (ADS)

    Thu, Dang Xuan; Trung, Vu Quoc; Nghia, Nguyen Manh; Khang, Nguyen Cao; Lam, Tran Dai

    2016-11-01

    Fe-doped TiO2 nanoparticles have been prepared by the hydrolysis method. The effects of Fe doping on the structural, optical, and magnetic properties of the Ti1- x Fe x O2 ( x = 0.00, 0.03, 0.06, 0.10, 0.13) materials were thoroughly investigated by a combination of various methods, including transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET) analysis, x-ray diffraction (XRD) analysis, ultraviolet-visible (UV-Vis) reflectance spectroscopy, Raman spectroscopy, and vibrating-sample magnetometry. Analysis of the TEM and XRD measurements showed that the resulting powders had nanoscale particle size. The Fe-doped samples were found to be paramagnetic at room temperature (by magnetization measurements), with Fe acting as substitutional impurity at Ti sites in the anatase TiO2 phase. Substitution of Fe at Ti sites was also confirmed by Raman spectra. The paramagnetic nature of the Ti1- x Fe x O2 samples was further investigated using density functional theory calculations of their electronic band structure and density of states. Finally, the photocatalytic activity of the Fe-doped TiO2 samples was studied by investigating their photocatalytic decomposition of methylene blue.

  4. Photocatalytic Properties of TiO2 Thin Films Modified with Ag and Pt Nanoparticles Deposited by Gas Flow Sputtering.

    PubMed

    Maicu, M; Glöss, D; Frach, Peter; Hecker, D; Gerlach, G; Córdoba, José M

    2015-09-01

    In this work, a gas flow sputtering (GFS) process which allows the production and deposition of metal nanoparticles (NPs) in a vacuum environment is described. Aim of the study is to prove the potential of this technology for the fabrication of new TiO2 films with enhanced photocatalytic properties. For this purpose, Ag and Pt NPs have been produced and deposited on photocatalytic float glass coated with TiO2 thin films by magnetron sputtering. The influence of the process parameters and of the metal amount on the final properties of the particles (quantity, size, size distribution, oxidation state etc.,) was widely investigated. Moreover, the effect of the NPs on the photocatalytic activity of the resulting materials was evaluated for the case of the decomposition of stearic acid (SA) during UV-A irradiation. The reduction of the water contact angle (WCA) during the irradiation period was measured in order to test the photo-induced super-hydrophilicity (PSH).

  5. Improved conversion efficiency of Ag2S quantum dot-sensitized solar cells based on TiO2 nanotubes with a ZnO recombination barrier layer

    PubMed Central

    2011-01-01

    We improve the conversion efficiency of Ag2S quantum dot (QD)-sensitized TiO2 nanotube-array electrodes by chemically depositing ZnO recombination barrier layer on plain TiO2 nanotube-array electrodes. The optical properties, structural properties, compositional analysis, and photoelectrochemistry properties of prepared electrodes have been investigated. It is found that for the prepared electrodes, with increasing the cycles of Ag2S deposition, the photocurrent density and the conversion efficiency increase. In addition, as compared to the Ag2S QD-sensitized TiO2 nanotube-array electrode without the ZnO layers, the conversion efficiency of the electrode with the ZnO layers increases significantly due to the formation of efficient recombination layer between the TiO2 nanotube array and electrolyte. PMID:21777458

  6. Microstructure and antibacterial properties of Cu-doped TiO2 coating on titanium by micro-arc oxidation

    NASA Astrophysics Data System (ADS)

    Yao, Xiaohong; Zhang, Xiangyu; Wu, Haibo; Tian, Linhai; Ma, Yong; Tang, Bin

    2014-02-01

    Infection associated with titanium implants remains the most common serious complication after surgery. In this work, Cu-doped antibacterial TiO2 coating was synthesized by micro-arc oxidation of titanium in an electrolyte bearing Cu nanoparticles. Surface morphology and structure of the coating were characterized with scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The results indicated that Cu nanoparticles were not only distributed on the surface and inside the pores but also embedded in the coating. Cu mainly exists in the Cu2+ state in the TiO2 coating. The Cu-doped coating exhibited excellent antibacterial activities against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus).

  7. Study on the catalytic activity of vanadium doped TiO2: Anatase-to-rutile phase transition

    NASA Astrophysics Data System (ADS)

    Zhang, Huiming; Bian, He; Zhang, Shiguo

    2016-01-01

    The catalytic activity of vanadium doped TiO2 in the ethylbenzene oxidative dehydrogenation with CO2 was studied experimentally and theoretically. The experimental results showed that the reduction of ethylbenzene conversion and the styrene selectivity was caused by the transition of anatase to rutile phase. Theoretical results showed that the transition of the anatase to rutile phase was mainly caused by vanadium ions and oxygen vacancies.

  8. Near-infrared electroluminescence from light-emitting devices based on Nd-doped TiO2/p+-Si heterostructures

    NASA Astrophysics Data System (ADS)

    Yang, Yang; Lv, Chunyan; Zhu, Chen; Li, Si; Ma, Xiangyang; Yang, Deren

    2014-05-01

    We report on near-infrared (NIR) electroluminescence (EL) from the light-emitting devices based on Nd-doped TiO2/p+-Si heterostructures. NIR emissions peaking at ˜910, 1090, and 1370 nm, originated from intra-4f transitions in Nd3+ ions, can be activated by a forward bias voltage as low as ˜5 V. Such NIR EL is triggered by the energy transferred from TiO2 host to Nd3+ ions. It is found that the coexistence of anatase and rutile phases in the TiO2 host enables the device to exhibit pronounced Nd-related EL without concurrent emission from the TiO2 host itself, quite other than the case of existing only anatase phase in TiO2 host. We tentatively suggest that the anatase/rutile interface states play important role in the energy transfer from TiO2 host to Nd3+ ions.

  9. Characterization of TiO2-Doped Yttria-Stabilized Zirconia (YSZ) for Supercritical Water-Cooled Reactor Insulator Application

    NASA Astrophysics Data System (ADS)

    Barrett, F.; Huang, X.; Guzonas, Dave

    2013-06-01

    In this study, TiO2-doped YSZ samples were tested in supercritical water (SCW) to evaluate their corrosion behavior. The doped samples were produced by mechanically alloying standard 7 wt.% Y2O3-ZrO2 with 5, 10, and 15 wt.% of TiO2 first. The bulk sample pieces were then obtained using plasma spraying of the alloyed powder materials followed by sintering. The results showed that the weight changes for 5TiYSZ and 10TiYSZ after 1000 h of exposure in SCW were negligible and the sample surfaces did not exhibit any indication of corrosion. In comparison to the reference materials (Al2O3 and 7YSZ) processed using the same method, the rate of weight change followed the order of Al2O3 > 7YSZ, 15TiYSZ > 10TiYSZ > 5TiYSZ. As several TiO2-doped 7SYZ compositions also display increased fracture toughness and reduced thermal conductivity, they may be considered as potential candidates for thermal insulation in a SCW-cooled nuclear reactor.

  10. Hydrogen-doped Brookite TiO2 Nanobullets Array as a Novel Photoanode for Efficient Solar Water Splitting

    PubMed Central

    Choi, Mingi; Lee, June Ho; Jang, Youn Jeong; Kim, Donghyung; Lee, Jae Sung; Jang, Hyun Myung; Yong, Kijung

    2016-01-01

    As a representative photocatalyst for photoelectrochemical solar water splitting, TiO2 has been intensively studied but most researches have focused on the rutile and anatsase phases because brookite, another important crystalline polymorph of TiO2, rarely exists in nature and is difficult to synthesize. In this work, hydrogen doped brookite (H:brookite) nanobullet arrays were synthesized via a well-designed solution reaction for the first time. H:brookite shows highly improved PEC properties with excellent stability, enhanced photocurrent, and significantly high Faradaic efficiency for overall solar water splitting. To support the experimental data, ab initio density functional theory calculations were also conducted. At the interstitial doping site that has minimum formation energy, the hydrogen atoms act as shallow donors and exist as H+. which has the minimum formation energy among three states of hydrogen (H+. H0, and H−). The calculated density of states of H:brookite shows a narrowed bandgap and an increased electron density compared to the pristine brookite. The combined experimental and theoretical results provide frameworks for the exploration of the PEC properties of doped brookite and extend our knowledge regarding the undiscovered properties of brookite of TiO2. PMID:27782198

  11. Tungsten Doped TiO2 with Enhanced Photocatalytic and Optoelectrical Properties via Aerosol Assisted Chemical Vapor Deposition

    NASA Astrophysics Data System (ADS)

    Sathasivam, Sanjayan; Bhachu, Davinder S.; Lu, Yao; Chadwick, Nicholas; Althabaiti, Shaeel A.; Alyoubi, Abdulrahman O.; Basahel, Sulaiman N.; Carmalt, Claire J.; Parkin, Ivan P.

    2015-06-01

    Tungsten doped titanium dioxide films with both transparent conducting oxide (TCO) and photocatalytic properties were produced via aerosol-assisted chemical vapor deposition of titanium ethoxide and dopant concentrations of tungsten ethoxide at 500 °C from a toluene solution. The films were anatase TiO2, with good n-type electrical conductivities as determined via Hall effect measurements. The film doped with 2.25 at.% W showed the lowest resistivity at 0.034 Ω.cm and respectable charge carrier mobility (14.9 cm3/V.s) and concentration (×1019 cm-3). XPS indicated the presence of both W6+ and W4+ in the TiO2 matrix, with the substitutional doping of W4+ inducing an expansion of the anatase unit cell as determined by XRD. The films also showed good photocatalytic activity under UV-light illumination, with degradation of resazurin redox dye at a higher rate than with undoped TiO2.

  12. Tungsten Doped TiO2 with Enhanced Photocatalytic and Optoelectrical Properties via Aerosol Assisted Chemical Vapor Deposition

    PubMed Central

    Sathasivam, Sanjayan; Bhachu, Davinder S.; Lu, Yao; Chadwick, Nicholas; Althabaiti, Shaeel A.; Alyoubi, Abdulrahman O.; Basahel, Sulaiman N.; Carmalt, Claire J.; Parkin, Ivan P.

    2015-01-01

    Tungsten doped titanium dioxide films with both transparent conducting oxide (TCO) and photocatalytic properties were produced via aerosol-assisted chemical vapor deposition of titanium ethoxide and dopant concentrations of tungsten ethoxide at 500 °C from a toluene solution. The films were anatase TiO2, with good n-type electrical conductivities as determined via Hall effect measurements. The film doped with 2.25 at.% W showed the lowest resistivity at 0.034 Ω.cm and respectable charge carrier mobility (14.9 cm3/V.s) and concentration (×1019 cm−3). XPS indicated the presence of both W6+ and W4+ in the TiO2 matrix, with the substitutional doping of W4+ inducing an expansion of the anatase unit cell as determined by XRD. The films also showed good photocatalytic activity under UV-light illumination, with degradation of resazurin redox dye at a higher rate than with undoped TiO2. PMID:26042724

  13. Growth, differentiation, and migration of osteoblasts on transparent Ni doped TiO2 thin films deposited on borosilicate glass.

    PubMed

    Dhayal, Marshal; Kapoor, Renu; Sistla, Pavana Goury; Kant, Chander; Pandey, Ravi Ranjan; Govind; Saini, Krishan Kumar; Pande, Gopal

    2012-05-01

    A simple and cost effective dip coating method was used to deposit thin films of amorphous (AM) or anatase (AN) titanium dioxide (TiO(2)) on borosilicate glass substrates, either with or without prior doping of TiO(2) with nickel (Ni) cations by a specially designed sol gel technique. The objective of the study was to compare the physicochemical and biological properties of these films and assess their use in orthopedic implants or for in vitro cell biological studies. Analytical techniques such as XRD and XPS, in combination with ATR-FTIR and SEM revealed that only AN films, prepared by controlled heating up to 450°C, irrespective of prior doping with Ni, contained significant crystalline structures of variable morphologies. This observation could be linked to the carbon and oxygen contents and the availability of functional groups in the films. Cell biological studies revealed that Ni doping of TiO(2) in both AM and AN films improved the adhesion, spreading, proliferation, differentiation, and migration of MC3T3 cells. Our studies provide a new approach to prepare optically transparent metal surfaces, with tunable physicochemical properties, which could be suitable for eliciting optimal osteoinductive cell responses and permit the detailed in vitro cell biological studies of osteoblasts.

  14. Photocatalytic degradation of Orange G on nitrogen-doped TiO2 catalysts under visible light and sunlight irradiation.

    PubMed

    Sun, Jianhui; Qiao, Liping; Sun, Shengpeng; Wang, Guoliang

    2008-06-30

    In this paper, the degradation of an azo dye Orange G (OG) on nitrogen-doped TiO2 photocatalysts has been investigated under visible light and sunlight irradiation. Under visible light irradiation, the doped TiO2 nanocatalysts demonstrated higher activity than the commercial Dugussa P25 TiO2, allowing more efficient utilization of solar light, while under sunlight, P25 showed higher photocatalytic activity. According to the X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and UV-vis spectra analyses, it was found that both the nanosized anatase structure and the appearance of new absorption band in the visible region caused by nitrogen doping were responsible for the significant enhancement of OG degradation under visible light. In addition, the photosensitized oxidation mechanism originated from OG itself was also considered contributing to the higher visible-light-induced degradation efficiency. The effect of the initial pH of the solution and the dosage of hydrogen peroxide under different light sources was also investigated. Under visible light and sunlight, the optimal solution pH was both 2.0, while the optimal dosage of H2O2 was 5.0 and 15.0 mmol/l, respectively.

  15. Enhancement of Photo-Oxidation Activities Depending on Structural Distortion of Fe-Doped TiO2 Nanoparticles.

    PubMed

    Kim, Yeonwoo; Yang, Sena; Jeon, Eun Hee; Baik, Jaeyoon; Kim, Namdong; Kim, Hyun Sung; Lee, Hangil

    2016-12-01

    To design a high-performance photocatalytic system with TiO2, it is necessary to reduce the bandgap and enhance the absorption efficiency. The reduction of the bandgap to the visible range was investigated with reference to the surface distortion of anatase TiO2 nanoparticles induced by varying Fe doping concentrations. Fe-doped TiO2 nanoparticles (Fe@TiO2) were synthesized by a hydrothermal method and analyzed by various surface analysis techniques such as transmission electron microscopy, Raman spectroscopy, X-ray diffraction, scanning transmission X-ray microscopy, and high-resolution photoemission spectroscopy. We observed that Fe doping over 5 wt.% gave rise to a distorted structure, i.e., Fe2Ti3O9, indicating numerous Ti(3+) and oxygen-vacancy sites. The Ti(3+) sites act as electron trap sites to deliver the electron to O2 as well as introduce the dopant level inside the bandgap, resulting in a significant increase in the photocatalytic oxidation reaction of thiol (-SH) of 2-aminothiophenol to sulfonic acid (-SO3H) under ultraviolet and visible light illumination.

  16. Enhancement of Photo-Oxidation Activities Depending on Structural Distortion of Fe-Doped TiO2 Nanoparticles

    NASA Astrophysics Data System (ADS)

    Kim, Yeonwoo; Yang, Sena; Jeon, Eun Hee; Baik, Jaeyoon; Kim, Namdong; Kim, Hyun Sung; Lee, Hangil

    2016-01-01

    To design a high-performance photocatalytic system with TiO2, it is necessary to reduce the bandgap and enhance the absorption efficiency. The reduction of the bandgap to the visible range was investigated with reference to the surface distortion of anatase TiO2 nanoparticles induced by varying Fe doping concentrations. Fe-doped TiO2 nanoparticles (Fe@TiO2) were synthesized by a hydrothermal method and analyzed by various surface analysis techniques such as transmission electron microscopy, Raman spectroscopy, X-ray diffraction, scanning transmission X-ray microscopy, and high-resolution photoemission spectroscopy. We observed that Fe doping over 5 wt.% gave rise to a distorted structure, i.e., Fe2Ti3O9, indicating numerous Ti3+ and oxygen-vacancy sites. The Ti3+ sites act as electron trap sites to deliver the electron to O2 as well as introduce the dopant level inside the bandgap, resulting in a significant increase in the photocatalytic oxidation reaction of thiol (-SH) of 2-aminothiophenol to sulfonic acid (-SO3H) under ultraviolet and visible light illumination.

  17. A stable and high resolution optical waveguide biosensor based on dense TiO2/Ag multilayer film

    NASA Astrophysics Data System (ADS)

    Jin, Zhao; Guan, Weiming; Liu, Chang; Xue, Tianyu; Wang, Qiyu; Zheng, Weitao; Cui, Xiaoqiang

    2016-07-01

    Optical waveguide (OWG) biosensor has attracted much attention according to the high sensitivity and resolution compared with conventional surface plasmon resonance (SPR) biosensor. Nanoporous materials are usually used as the waveguide layer for absorbing analytes into the porous structure and enhancing the sensor signal. However, this kind of waveguide layer provides poor protection to the metal film and leads to the damage of the biosensor. Ag film can provide great sensitivity in SPR sensing comparing to other metal but was rarely used because of its poor chemical stability. Fabricating high stability Ag based SPR biosensor is still a challenge. In this work we produce an OWG biosensor using a dense TiO2 film as the waveguide layer which provides high resolution and remarkable protection to the metal film. This waveguide structure makes long time detection possible using Ag as the metal layer and is able to lead an enhancement of sensitivity comparing to the Au-based biosensor.

  18. Kinetics stabilized doping: computational optimization of carbon-doped anatase TiO2 for visible-light driven water splitting.

    PubMed

    Sun, Yi-Yang; Zhang, Shengbai

    2016-01-28

    Using density functional theory calculation we investigate the carbon doping of anatase TiO2, a technique widely studied for visible-light driven water splitting. By a detailed analysis of the thermodynamics of C defects in TiO2, we show that any significant concentration of C dopants in the TiO2 lattice must be a result of non-equilibrium doping, which emphasizes the importance of kinetics stabilized C defects. Based on the band gaps calculated using hybrid density functionals, we exclude the possibility of C occupying Ti lattice sites or interstitial sites to enhance visible-light absorption of TiO2, as extensively discussed in the literature. Also, the recently proposed defect with a CO species occupying two O sites yields a too small band gap for water splitting. Two defects that can effectively reduce the band gap for the water splitting application are identified to be: (1) the CO-VO complex, i.e., a C substituting for O (CO) paired with an O vacancy (VO) and (2) the (C2)2O complex with a C dimer (C2) occupying two neighboring O vacancies. Compared with the CO-VO complex, (C2)2O exhibits strong binding (greater than 2.5 eV) between the two C atoms, which could significantly enhance its kinetic stability to survive from high temperature annealing. With a reduced band gap of about 1.4 eV, carbon dimers could be ideal for kinetic doping of anatase TiO2 to enhance its visible-light activity in photocatalytic reactions. Molecular doping using C2H2 or C2H4 as C precursors has been proposed to introduce the carbon dimers into TiO2.

  19. Bismuth-doped ordered mesoporous TiO2: visible-light catalyst for simultaneous degradation of phenol and chromium.

    PubMed

    Sajjad, Shamaila; Leghari, Sajjad A K; Chen, Feng; Zhang, Jinlong

    2010-12-10

    A controllable and reproducible synthesis of highly ordered two-dimensional hexagonal mesoporous, crystalline bismuth-doped TiO(2) nanocomposites with variable Bi ratios is reported here. Analyses by transmission electron microscopy, X-ray diffraction, Raman, and X-ray photoelectron spectroscopy reveal that the well-ordered mesostructure is doped with Bi, which exists as Bi(3+) and Bi((3+x+)). The Bi-doped mesoporous TiO(2) (ms-TiO(2)) samples exhibit improved photocatalytic activities for simultaneous phenol oxidation and chromium reduction in aqueous suspension under visible and UV light over the pure ms-TiO(2), P-25, and conventional Bi-doped titania. The high catalytic activity is due to both the unique structural characteristics and the Bi doping. This new material extends the spectral response from UV to the visible region, and reduces electron-hole recombination, which renders the 2.0% Bi-doped ms-TiO(2) photocatalyst highly responsive to visible light. PMID:20957621

  20. Fabrication of N-doped TiO2 coatings on nanoporous Si nanopillar arrays through biomimetic layer by layer mineralization.

    PubMed

    Yan, Yong; Wang, Dong; Schaaf, Peter

    2014-06-14

    Si/N-doped TiO2 core/shell nanopillar arrays with a nanoporous structure are fabricated through a simple protein-mediated TiO2 deposition process. The Si nanopillar arrays are used as templates and alternatively immersed in aqueous solutions of catalytic molecules (protamine, PA) and the titania precursor (titanium(iv) bis(ammonium lactato)dihydroxide, Ti-BALDH) for the layer by layer mineralization of a PA/TiO2 coating. After a subsequent calcination, a N-doped TiO2 layer is formed, and its thickness could be controlled by varying the cycles of deposition. Moreover, the nanoporous structure of the Si nanopillars strongly affects the formation of the TiO2 layer. The obtained Si/TiO2 nanocomposites show significantly improved solar absorption compared with commercially purchased TiO2 nanoparticles.

  1. In situ plasmonic Ag nanoparticle anchored TiO2 nanotube arrays as visible-light-driven photocatalysts for enhanced water splitting

    NASA Astrophysics Data System (ADS)

    Ge, Ming-Zheng; Cao, Chun-Yan; Li, Shu-Hui; Tang, Yu-Xin; Wang, Lu-Ning; Qi, Ning; Huang, Jian-Ying; Zhang, Ke-Qin; Al-Deyab, S. S.; Lai, Yue-Kun

    2016-02-01

    An ultrasonication-assisted in situ deposition strategy was utilised to uniformly decorate plasmonic Ag nanoparticles on vertically aligned TiO2 nanotube arrays (NTAs) to construct a Ag@TiO2 NTA composite. The Ag nanoparticles act as efficient surface plasmon resonance (SPR) photosensitizers to drive photocatalytic water splitting under visible light irradiation. The Ag nanoparticles were uniformly deposited on the surface and inside the highly oriented TiO2 nanotubes. The visible-light-driven hydrogen production activities of silver nanoparticle anchored TiO2 nanotube array photocatalysts were evaluated using methanol as a sacrificial reagent in water under a 500 W Xe lamp with a UV light cutoff filter (λ >= 420 nm). It was found that the hydrogen production rate of the Ag@TiO2 NTAs prepared with ultrasonication-assisted deposition for 5 min was approximately 15 times higher than that of its pristine TiO2 NTAs counterpart. The highly efficient photocatalytic hydrogen evolution is attributed to the SPR effect of Ag for enhanced visible light absorption and boosting the photogenerated electron-hole separation/transfer. This strategy is promising for the design and construction of high efficiency TiO2 based photocatalysts for solar energy conversion.An ultrasonication-assisted in situ deposition strategy was utilised to uniformly decorate plasmonic Ag nanoparticles on vertically aligned TiO2 nanotube arrays (NTAs) to construct a Ag@TiO2 NTA composite. The Ag nanoparticles act as efficient surface plasmon resonance (SPR) photosensitizers to drive photocatalytic water splitting under visible light irradiation. The Ag nanoparticles were uniformly deposited on the surface and inside the highly oriented TiO2 nanotubes. The visible-light-driven hydrogen production activities of silver nanoparticle anchored TiO2 nanotube array photocatalysts were evaluated using methanol as a sacrificial reagent in water under a 500 W Xe lamp with a UV light cutoff filter (λ >= 420 nm

  2. Effect of TiO2-Ag2O additives on the formation of calcium phosphate based functionally graded bioceramics.

    PubMed

    Manjubala, I; Sampath Kumar, T S

    2000-10-01

    The combined effect of titanium dioxide and silver oxide on the in situ formation of biphasic calcium phosphate ceramics was investigated. Titania (5-20 mol%) was mixed with pure hydroxyapatite (HA) or HA containing Ag2O (10-20 mol%) and was heated to 900 degrees C for 12 h. The sintered samples were found to contain tricalcium phosphate (beta-TCP) and other phases along with HA depending upon the amount as well as the type of the additives used as evidenced by X-ray powder diffraction (XRD) and fourier transform infrared (FT-IR) spectroscopic studies. Enhanced TCP formation with reduced impurity phases was observed with TiO2-Ag2O addition. In vitro solubility study in phosphate buffer at physiological conditions shows the resorbable nature of these materials. A functionally graded material (FGM) structure was formed by spreading TiO2-Ag2O mixture on the surface of the HA green compact and heating at 900 degrees C. The FGM shows gradient structure of TCP and HA from the surface to the interior of the pellet in addition to titania and silver phases.

  3. Highly Visible Light Activity of Nitrogen Doped TiO2 Prepared by Sol-Gel Approach

    NASA Astrophysics Data System (ADS)

    Than, Le Dien; Luong, Ngo Sy; Ngo, Vu Dinh; Tien, Nguyen Manh; Dung, Ta Ngoc; Nghia, Nguyen Manh; Loc, Nguyen Thai; Thu, Vu Thi; Lam, Tran Dai

    2016-09-01

    A simple approach was explored to prepare N-doped anatase TiO2 nanoparticles (N-TiO2 NPs) from titanium chloride (TiCl4) and ammonia (NH3) via sol-gel method. The effects of important process parameters such as calcination temperatures, NH3/TiCl4 molar ratio (R N) on crystallite size, structure, phase transformation, and photocatalytic activity of titanium dioxide (TiO2) were thoroughly investigated. The as-prepared samples were characterized by ultraviolet-visible spectroscopy, x-ray diffraction, transmission electron microscopy, energy dispersive x-ray spectroscopy, and x-ray photoelectron spectroscopy. The photocatalytic activity of the samples was evaluated upon the degradation of methylene blue aqueous solution under visible-light irradiation. The results demonstrated that both calcination temperatures and NH3/TiCl4 molar ratios had significant impacts on the formation of crystallite nanostructures, physicochemical, as well as catalytic properties of the obtained TiO2. Under the studied conditions, calcination temperature of 600°C and NH3/TiCl4 molar ratio of 4.2 produced N-TiO2 with the best crystallinity and photocatalytic activity. The high visible light activity of the N-TiO2 nanomaterials was ascribed to the interstitial nitrogen atoms within TiO2 lattice units. These findings could provide a practical pathway capable of large-scale production of a visible light-active N-TiO2 photocatalyst.

  4. In situ plasmonic Ag nanoparticle anchored TiO2 nanotube arrays as visible-light-driven photocatalysts for enhanced water splitting.

    PubMed

    Ge, Ming-Zheng; Cao, Chun-Yan; Li, Shu-Hui; Tang, Yu-Xin; Wang, Lu-Ning; Qi, Ning; Huang, Jian-Ying; Zhang, Ke-Qin; Al-Deyab, S S; Lai, Yue-Kun

    2016-03-01

    An ultrasonication-assisted in situ deposition strategy was utilised to uniformly decorate plasmonic Ag nanoparticles on vertically aligned TiO2 nanotube arrays (NTAs) to construct a Ag@TiO2 NTA composite. The Ag nanoparticles act as efficient surface plasmon resonance (SPR) photosensitizers to drive photocatalytic water splitting under visible light irradiation. The Ag nanoparticles were uniformly deposited on the surface and inside the highly oriented TiO2 nanotubes. The visible-light-driven hydrogen production activities of silver nanoparticle anchored TiO2 nanotube array photocatalysts were evaluated using methanol as a sacrificial reagent in water under a 500 W Xe lamp with a UV light cutoff filter (λ ≥ 420 nm). It was found that the hydrogen production rate of the Ag@TiO2 NTAs prepared with ultrasonication-assisted deposition for 5 min was approximately 15 times higher than that of its pristine TiO2 NTAs counterpart. The highly efficient photocatalytic hydrogen evolution is attributed to the SPR effect of Ag for enhanced visible light absorption and boosting the photogenerated electron-hole separation/transfer. This strategy is promising for the design and construction of high efficiency TiO2 based photocatalysts for solar energy conversion. PMID:26878901

  5. Role of Zn doping in oxidative stress mediated cytotoxicity of TiO2 nanoparticles in human breast cancer MCF-7 cells

    PubMed Central

    Ahamed, Maqusood; Khan, M. A. Majeed; Akhtar, Mohd Javed; Alhadlaq, Hisham A.; Alshamsan, Aws

    2016-01-01

    We investigated the effect of Zn-doping on structural and optical properties as well as cellular response of TiO2 nanoparticles (NPs) in human breast cancer MCF-7 cells. A library of Zn-doped (1–10 at wt%) TiO2 NPs was prepared. Characterization data indicated that dopant Zn was incorporated into the lattice of host TiO2. The average particle size of TiO2 NPs was decreases (38 to 28 nm) while the band gap energy was increases (3.35 eV–3.85 eV) with increasing the amount of Zn-doping. Cellular data demonstrated that Zn-doped TiO2 NPs induced cytotoxicity (cell viability reduction, membrane damage and cell cycle arrest) and oxidative stress (reactive oxygen species generation & glutathione depletion) in MCF-7 cells and toxic intensity was increases with increasing the concentration of Zn-doping. Molecular data revealed that Zn-doped TiO2 NPs induced the down-regulation of super oxide dismutase gene while the up-regulation of heme oxygenase-1 gene in MCF-7 cells. Cytotoxicity induced by Zn-doped TiO2 NPs was efficiently prevented by N-acetyl-cysteine suggesting that oxidative stress might be the primarily cause of toxicity. In conclusion, our data indicated that Zn-doping decreases the particle size and increases the band gap energy as well the oxidative stress-mediated toxicity of TiO2 NPs in MCF-7 cells. PMID:27444578

  6. Role of Zn doping in oxidative stress mediated cytotoxicity of TiO2 nanoparticles in human breast cancer MCF-7 cells

    NASA Astrophysics Data System (ADS)

    Ahamed, Maqusood; Khan, M. A. Majeed; Akhtar, Mohd Javed; Alhadlaq, Hisham A.; Alshamsan, Aws

    2016-07-01

    We investigated the effect of Zn-doping on structural and optical properties as well as cellular response of TiO2 nanoparticles (NPs) in human breast cancer MCF-7 cells. A library of Zn-doped (1–10 at wt%) TiO2 NPs was prepared. Characterization data indicated that dopant Zn was incorporated into the lattice of host TiO2. The average particle size of TiO2 NPs was decreases (38 to 28 nm) while the band gap energy was increases (3.35 eV–3.85 eV) with increasing the amount of Zn-doping. Cellular data demonstrated that Zn-doped TiO2 NPs induced cytotoxicity (cell viability reduction, membrane damage and cell cycle arrest) and oxidative stress (reactive oxygen species generation & glutathione depletion) in MCF-7 cells and toxic intensity was increases with increasing the concentration of Zn-doping. Molecular data revealed that Zn-doped TiO2 NPs induced the down-regulation of super oxide dismutase gene while the up-regulation of heme oxygenase-1 gene in MCF-7 cells. Cytotoxicity induced by Zn-doped TiO2 NPs was efficiently prevented by N-acetyl-cysteine suggesting that oxidative stress might be the primarily cause of toxicity. In conclusion, our data indicated that Zn-doping decreases the particle size and increases the band gap energy as well the oxidative stress-mediated toxicity of TiO2 NPs in MCF-7 cells.

  7. Solvothermal synthesis of carbon coated N-doped TiO2 nanostructures with enhanced visible light catalytic activity

    NASA Astrophysics Data System (ADS)

    Yan, Xue-Min; Kang, Jialing; Gao, Lin; Xiong, Lin; Mei, Ping

    2013-01-01

    Visible light-active carbon coated N-doped TiO2 nanostructures(CTS-TiO2) were prepared by a facile one-step solvothermal method with chitosan as carbon and nitrogen resource at 180 °C. The as-prepared samples were characterized by transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), N2 adsorption-desorption analysis, X-ray photoelectron spectroscopy (XPS), and ultraviolet-visible (UV-vis) diffuse reflectance spectroscopy. The CTS-TiO2 nanocomposites possess anatase phase of nanocrystalline structure with average particle size of about 5-7 nm. A wormhole mesostructure can be observed in the CTS-TiO2 nanocomposites due to the constituent agglomerated of nanoparticles. It has been evidenced that the nitrogen was doped into the anatase titania lattice and the carbon species were modified on the surface of TiO2. The photocatalytic activities of the as-prepared photocatalysts were measured by the degradation of methylene blue (MB) under visible light irradiation at λ ≥ 400 nm. The results show that CTS-TiO2 nanostructures display a higher visible light photocatalytic activity than pure TiO2, commercial P25 and C-coated TiO2 (C-TiO2) photocatalysts. The higher photocatalytic activity could be attributed to the band-gap narrowed by N-doping and the accelerated separation of the photo-generated electrons and holes by carbon modification.

  8. Nitrogen-Doped Ordered Mesoporous Anatase TiO2 Nanofibers as Anode Materials for High Performance Sodium-Ion Batteries.

    PubMed

    Wu, Ying; Liu, Xiaowu; Yang, Zhenzhong; Gu, Lin; Yu, Yan

    2016-07-01

    Nitrogen-doped ordered mesoporous TiO2 nanofibers (N-MTO) have been fabricated by electrospinning and subsequent nitridation treatment. The N-doping in TiO2 leads to the formation of Ti(3+) , resulting in the improved electron conductivity of TiO2 . In addition, one-dimensional (1D) N-MTO nanostructure possesses very short diffusion length of Na(+) /e(-) in N-MTO, easy access of electrolyte, and high conductivity transport of electrons along the percolating fibers. The N-MTO shows excellent sodium storage performance.

  9. Energy Storage: Nitrogen-Doped Ordered Mesoporous Anatase TiO2 Nanofibers as Anode Materials for High Performance Sodium-Ion Batteries (Small 26/2016).

    PubMed

    Wu, Ying; Liu, Xiaowu; Yang, Zhenzhong; Gu, Lin; Yu, Yan

    2016-07-01

    On page 3522, Y. Yu and co-workers fabricate nitrogen-doped ordered mesoporous TiO2 nanofibers (denoted as N-MTO) by electrospinning and subsequent nitridation treatment. Nitrogen atoms are successfully doped into the TiO2 lattice, accompanied by the formation of Ti(3+) and oxygen vacancies, contributing to the improvement of electronic conductivity of TiO2 . When used as an anode for a sodium-ion battery, the N-MTO demonstrates excellent rate capability and superior long cycling performance. PMID:27383035

  10. Energy Storage: Nitrogen-Doped Ordered Mesoporous Anatase TiO2 Nanofibers as Anode Materials for High Performance Sodium-Ion Batteries (Small 26/2016).

    PubMed

    Wu, Ying; Liu, Xiaowu; Yang, Zhenzhong; Gu, Lin; Yu, Yan

    2016-07-01

    On page 3522, Y. Yu and co-workers fabricate nitrogen-doped ordered mesoporous TiO2 nanofibers (denoted as N-MTO) by electrospinning and subsequent nitridation treatment. Nitrogen atoms are successfully doped into the TiO2 lattice, accompanied by the formation of Ti(3+) and oxygen vacancies, contributing to the improvement of electronic conductivity of TiO2 . When used as an anode for a sodium-ion battery, the N-MTO demonstrates excellent rate capability and superior long cycling performance.

  11. Combined Embedding of N/F-Doping and CaCO3 Surface Modification in the TiO2 Photoanode for Dye-Sensitized Solar Cells.

    PubMed

    Park, Su Kyung; Yun, Tae Kwan; Bae, Jae Young

    2016-03-01

    N/F-doping and CaCO3 surface modification was carried out in TiO2 photoelectrodes for dye-sensitized solar cells (DSSCs). The combined effect of the N/F doped TiO2 and the CaCO3 coating showed a great increase of the short-circuit current (J(sc)), and photoelectric conversion efficiency (η) of the prepared cells; the efficiency (η) was improved from 7.00% of a commercial TiO2 photoelectrode to 7.90% of an uncoated N/F-doped electrode, and to 9.09% of a N/F-doped and CaCO3 surface modified electrode. An enhanced photoresponse in N/F-doped TiO2 nanoparticles generate more photo-excited electrons, as supported by measured UV-Vis diffuse reflectance spectra. A successive CaCO3 surface modification then forms a barrier on the surface of the N/F-doped TiO2 particles; the higher basicity of the CaCO3 modified TiO2 facilitates the dye adsorption, as supported by the direct measurement of the amount of adsorbed dye.

  12. Combined Embedding of N/F-Doping and CaCO3 Surface Modification in the TiO2 Photoanode for Dye-Sensitized Solar Cells.

    PubMed

    Park, Su Kyung; Yun, Tae Kwan; Bae, Jae Young

    2016-03-01

    N/F-doping and CaCO3 surface modification was carried out in TiO2 photoelectrodes for dye-sensitized solar cells (DSSCs). The combined effect of the N/F doped TiO2 and the CaCO3 coating showed a great increase of the short-circuit current (J(sc)), and photoelectric conversion efficiency (η) of the prepared cells; the efficiency (η) was improved from 7.00% of a commercial TiO2 photoelectrode to 7.90% of an uncoated N/F-doped electrode, and to 9.09% of a N/F-doped and CaCO3 surface modified electrode. An enhanced photoresponse in N/F-doped TiO2 nanoparticles generate more photo-excited electrons, as supported by measured UV-Vis diffuse reflectance spectra. A successive CaCO3 surface modification then forms a barrier on the surface of the N/F-doped TiO2 particles; the higher basicity of the CaCO3 modified TiO2 facilitates the dye adsorption, as supported by the direct measurement of the amount of adsorbed dye. PMID:27455671

  13. Improved visible light photocatalytic activity of fluorine and nitrogen co-doped TiO2 with tunable nanoparticle size

    NASA Astrophysics Data System (ADS)

    Cheng, Junyang; Chen, Jin; Lin, Wei; Liu, Yandong; Kong, Yan

    2015-03-01

    Fluorine and nitrogen co-doped TiO2 (F-N-TiO2) photocatalysts with enhanced photocatalytic activities were facilely synthesized by a simple one-step hydrothermal method using Ti(SO4)2 as an economical precursor, and hydrofluoric acid and ammonia as F and N source, respectively. The structure, morphology, and optical properties of produced nanoparticles were characterized by X-ray diffraction (XRD), N2 adsorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectra (FT-IR) methods. The synergistic effects of F and N doping were systematically examined by changing the molar ratio of F/N. Compared with the un-doped F or N mono-doped TiO2, the co-doped samples exhibited significantly improved photocatalytic performance due to their synergistic effects under visible light. It was shown that F dopant promoted the crystal growth and crystallinity of samples, while N dopant hindered it to some extent, which resulted in the tunable particle size of obtained F-N-TiO2 materials. The effects of F and N dopants on the enhanced photocatalytic activity of modified TiO2 materials were also discussed. The degradation rate of methylene blue (MB) was achieved at 97.31% after 5 h reaction under visible light over the optimized sample of FN3.5T. The materials also showed excellent stability according to the recycling tests of the photodegradation of MB.

  14. Photocatalytic degradation of 17α-ethinylestradiol (EE2) in the presence of TiO2-doped zeolite.

    PubMed

    Pan, Zhong; Stemmler, Elizabeth A; Cho, Hong Je; Fan, Wei; LeBlanc, Lawrence A; Patterson, Howard H; Amirbahman, Aria

    2014-08-30

    Current design limitations and ineffective remediation techniques in wastewater treatment plants have led to concerns about the prevalence of pharmaceutical and personal care products (PPCPs) in receiving waters. A novel photocatalyst, TiO2-doped low-silica X zeolite (TiO2-LSX), was used to study the degradation of the pharmaceutical compound, 17α-ethinylestradiol (EE2). The catalyst was synthesized and characterized using XRD, BET surface analysis, SEM-EDAX, and ICP-OES. The effects of different UV light intensities, initial EE2 concentrations, and catalyst dosages on the EE2 removal efficiency were studied. A higher EE2 removal efficiency was attained with UV-TiO2-LSX when compared with UV-TiO2 or UV alone. The EE2 degradation process followed pseudo-first-order kinetics. A comprehensive empirical model was developed to describe the EE2 degradation kinetics under different conditions using multiple linear regression analysis. The EE2 degradation mechanism was proposed based on molecular calculations, identification of photoproducts using HPLC-MS/MS, and reactive species quenching experiments; the results showed that oxidative degradation pathways initiated by hydroxyl radicals were predominant. This novel TiO2-doped zeolite system provides a promising application for the UV disinfection process in wastewater treatment plants.

  15. Improvement of Charge Transportation in Si Quantum Dot-Sensitized Solar Cells Using Vanadium Doped TiO2.

    PubMed

    Seo, Hyunwoong; Ichida, Daiki; Hashimoto, Shinji; Itagaki, Naho; Koga, Kazunori; Shiratani, Masaharu; Nam, Sang-Hun; Boo, Jin-Hyo

    2016-05-01

    The multiple exciton generation characteristics of quantum dots have been expected to enhance the performance of photochemical solar cells. In previous work, we first introduced Si quantum dot for sensitized solar cells. The Si quantum dots were fabricated by multi-hollow discharge plasma chemical vapor deposition, and were characterized optically and morphologically. The Si quantum dot-sensitized solar cells had poor performance due to significant electron loss by charge recombination. Although the large Si particle size resulted in the exposure of a large TiO2 surface area, there was a limit to ho much the particle size could be decreased due to the reduced absorbance of small particles. Therefore, this work focused on decreasing the internal impedance to improve charge transfer. TiO2 was electronically modified by doping with vanadium, which can improve electron transfer in the TiO2 network, and which is stable in the redox electrolyte. Photogenerated electrons can more easily arrive at the conductive electrode due to the decreased internal impedance. The dark photovoltaic properties confirmed the reduction of charge recombination, and the photon-to-current conversion efficiency reflected the improved electron transfer. Impedance analysis confirmed a decrease in internal impedance and an increased electron lifetime. Consequently, these improvements by vanadium doping enhanced the overall performance of Si quantum dot-sensitized solar cells. PMID:27483838

  16. Efficiency enhancement of dye-sensitized solar cells by use of ZrO2-doped TiO2 nanofibers photoanode.

    PubMed

    Mohamed, Ibrahim M A; Dao, Van-Duong; Barakat, Nasser A M; Yasin, Ahmed S; Yousef, Ahmed; Choi, Ho-Suk

    2016-08-15

    Due to the good stability and convenient optical properties, TiO2 nanostructures still the prominent photoanode materials in the Dye Sensitized Solar Cells (DSCs). However, the well-known low bandgap energy and weak adsorption affinity for the dye distinctly constrain the wide application. This work discusses the impact of Zr-doping and nanofibrous morphology on the performance and physicochemical properties of TiO2. Zr-doped TiO2 nanofibers (NFs), with various zirconia content (0, 0.5, 1, 1.5 and 2wt%) were prepared by calcination of electrospun mats composed of polyvinyl acetate, titanium isopropoxyl and zirconium n-propoxyl. For all formulations, the results have shown that the prepared materials are continuous, randomly oriented, and good morphology nanofibers. The average diameter decreased from 353.85nm to 210.78nm after calcination without a considerable influence on the nanofibrous structure regardless the zirconia content. XRD result shows that there is no Rutile nor Brookite phases in the obtained material and the average crystallite size of the sample is affected by the presence of Zr-doping and changed from 23.01nm to 37.63nm for TiO2 and Zr-doped TiO2, respectively. Optical studies have shown Zr-doped TiO2 NFs have more absorbance in the visible region than that of pristine TiO2 NFs; the maximum absorbance is corresponding to the NFs having 1wt% zirconia. The improved spectra of Zr-doped TiO2 in the visible region is attributed to the heterostructure composition resulting from Zr-doping. The absorption bandgaps were calculated using Tauc model as 3.202 and 3.217 for pristine and Zr (1wt%)-doped TiO2 NFs, respectively. Furthermore, in Dye-sensitized Solar Cells, utilizing Zr (1wt%)-doped TiO2 nanofibers achieved higher efficiency of 4.51% compared to the 1.61% obtained from the pristine TiO2 NFs.

  17. Nitrogen-doping of bulk and nanotubular TiO2 photocatalysts by plasma-assisted atomic layer deposition

    NASA Astrophysics Data System (ADS)

    Zhang, Yi; Creatore, Mariadriana; Ma, Quan-Bao; El Boukili, Aishah; Gao, Lu; Verheijen, Marcel A.; Verhoeven, M. W. G. M. (Tiny); Hensen, Emiel. J. M.

    2015-03-01

    Plasma-assisted atomic layer deposition (PA-ALD) was adopted to deposit TiO2-xNx ultrathin layers on Si wafers, calcined Ti foils and nanotubular TiO2 arrays. A range of N content and chemical bond configurations were obtained by varying the background gas (O2 or N2) during the Ti precursor exposure, while the N2/H2-fed inductively coupled plasma exposure time was varied between 2 and 20 s. On calcined Ti foils, a positive effect from N doping on photocurrent density was observed when O2 was the background gas with a short plasma exposure time (5 and 10 s). This correlates with the presence of interstitial N states in the TiO2 with a binding energy of 400 eV (Ninterst) as measured by X-ray photoelectron spectroscopy. A longer plasma time or the use of N2 as background gas results in formation of N state with a binding energy of 396 eV (Nsubst) and very low photocurrents. These Nsubst are linked to the presence of Ti3+, which act as detrimental recombination center for photo-generated electron-hole pairs. On contrary, PA-ALD treated nanotubular TiO2 arrays show no variation of photocurrent density (with respect to the pristine nanotubes) upon different plasma exposure times and when the O2 recipe was adopted. This is attributed to constant N content in the PA-ALD TiO2-xNx, regardless of the adopted recipe.

  18. Highly oriented and physical properties of sprayed anatase Sn-doped TiO2 thin films with an enhanced antibacterial activity

    NASA Astrophysics Data System (ADS)

    Dhanapandian, S.; Arunachalam, A.; Manoharan, C.

    2016-03-01

    Pristine TiO2 and Sn-doped TiO2 thin films with different Sn doping levels (2, 4, 6 and 8 at.%) were deposited by employing a simplified spray pyrolysis technique. The XRD pattern of the films confirmed tetragonal structure with the polycrystalline nature. The films exhibited a pure anatase titanium dioxide (TiO2) with a strong orientation along (101) plane. The scanning electron microscopy image of 6 at.% Sn-doped TiO2 thin film depicted nanosized grains with porous nature. The atomic force microscopy study had shown the columnar arrangement of grains with the increase in particle size and surface roughness for 6 at.% Sn-doped TiO2 thin films. The optical transmittance was increased with the decrease in the optical energy band gap. The optical constants such as extinction coefficient and refractive index were determined. The intensity of the photoluminescence emission was observed at 398 nm for doped films. The resistivity decreased with the increasing carrier concentration and Hall mobility. The incorporation of Sn into TiO2 matrix yielded a well-pronounced antibacterial activity for Bacillus subtilis.

  19. Photocatalytic performance of nitrogen, osmium co-doped TiO2 for removal of eosin yellow in water under simulated solar radiation.

    PubMed

    Kuvarega, Alex T; Krause, Rui W M; Mamba, Bhekie B

    2013-07-01

    Nitrogen, osmium co-doped TiO2 photocatalysts were prepared by a modified sol-gel method using ammonia as the nitrogen source and osmium tetroxide as the source of osmium. The role of rutile phase OsO2 in enhancing the photocatalytic activity of rutile TiO2 towards the degradation of Eosin Yellow was investigated. The materials were characterised by various techniques that include FTIR, Raman, XRD, SEM, EDS, TEM, TGA and DRUV-Vis. The amorphous, oven dried sample was transformed to the anatase and then the rutile phase with increasing calcination temperature. DRUV-Vis analysis revealed a red shift in absorption with increasing calcination temperature, confirmed by a decrease in the band gap of the material. The photocatalytic activity of N, Os co-doped TiO2 was evaluated using eosin yellow degradation and activity increased with increase in calcination temperature under simulated solar irradiation. The rutile phase of the co-doped TiO2 was found to be more effective in degrading the dye (k(a) = 1.84 x 10(-2) min(-1)) compared to the anatase co-doped phase (k(a) = 9.90 x 10(-3) min(-1)). The enhanced photocatalytic activity was ascribed to the synergistic effects of rutile TiO2 and rutile OsO2 in the N, Os co-doped TiO2. PMID:23901525

  20. Photocatalytic performance of nitrogen, osmium co-doped TiO2 for removal of eosin yellow in water under simulated solar radiation.

    PubMed

    Kuvarega, Alex T; Krause, Rui W M; Mamba, Bhekie B

    2013-07-01

    Nitrogen, osmium co-doped TiO2 photocatalysts were prepared by a modified sol-gel method using ammonia as the nitrogen source and osmium tetroxide as the source of osmium. The role of rutile phase OsO2 in enhancing the photocatalytic activity of rutile TiO2 towards the degradation of Eosin Yellow was investigated. The materials were characterised by various techniques that include FTIR, Raman, XRD, SEM, EDS, TEM, TGA and DRUV-Vis. The amorphous, oven dried sample was transformed to the anatase and then the rutile phase with increasing calcination temperature. DRUV-Vis analysis revealed a red shift in absorption with increasing calcination temperature, confirmed by a decrease in the band gap of the material. The photocatalytic activity of N, Os co-doped TiO2 was evaluated using eosin yellow degradation and activity increased with increase in calcination temperature under simulated solar irradiation. The rutile phase of the co-doped TiO2 was found to be more effective in degrading the dye (k(a) = 1.84 x 10(-2) min(-1)) compared to the anatase co-doped phase (k(a) = 9.90 x 10(-3) min(-1)). The enhanced photocatalytic activity was ascribed to the synergistic effects of rutile TiO2 and rutile OsO2 in the N, Os co-doped TiO2.

  1. Photocatalytic degradation of gaseous toluene over Ag-doping TiO₂ nanotube powder prepared by anodization coupled with impregnation method.

    PubMed

    Li, Xinyong; Zou, Xuejun; Qu, Zhenping; Zhao, Qidong; Wang, Lianzhou

    2011-04-01

    In this work, Ag-doping TiO(2) nanotubes were prepared and employed as the photocatalyst for the degradation of toluene. The TiO(2) nanotube powder was produced by the rapid-breakdown potentiostatic anodization of Ti foil in chloride-containing electrolytes, and then doped with Ag through an incipient wetness impregnation method. The samples were characterized by scanning electron microscope, high-resolution transmission electron microscopy, X-ray diffraction, surface photovoltage measurements, X-ray photoelectron spectroscopy and N(2) adsorption. The nanotubular TiO(2) photocatalysts showed an outer diameter of approximately 40nm, fine mesoporous structure and high specific surface area. The photocatalytic activity of Ag-doping TiO(2) nanotube powder was evaluated through photooxidation of gaseous toluene. The results indicated that the degradation efficiency of toluene could get 98% after 4h reaction using the Ag-doping TiO(2) nanotubes as the photocatalyst under UV light illumination, which was higher than that of the pure TiO(2) nanotubes, Ag-doping P25 or P25. Benzaldehyde species could be observed during the photocatalytic oxidation monitored by in situ FTIR, and the formed benzaldehyde intermediate during reaction would be partially oxidized into CO(2) and H(2)O. PMID:21435692

  2. Physical properties of Zn doped TiO2 thin films with spray pyrolysis technique and its effects in antibacterial activity.

    PubMed

    Arunachalam, A; Dhanapandian, S; Manoharan, C; Sivakumar, G

    2015-03-01

    Zinc doped Titanium dioxide (TiO2: Zn) thin films were deposited onto glass substrates by the spray pyrolysis technique with the substrate temperature 450°C. The structural, optical, photoluminescence (PL) properties and morphological studies were investigated for the films deposited with various doping concentration (0, 2, 4, 6 and 8at.%) of zinc. The results of X-ray diffraction (XRD) had shown the presence of anatase peak with a strong orientation along (101) plane at 8at.% of Zn-doped TiO2 film. Scanning electron microscopy (SEM) study showed the uniform distribution of grains with porous nature. Atomic force microscopy (AFM) observations indicated the tetragonal shape at 8at.% of Zn-doped TiO2 with the particle size and decrease in surface roughness. The emission at 398nm was observed at the 8at.% of Zn-doped TiO2 thin film. The carrier concentration and Hall mobility was increased with doping. The antibacterial activity was highly yielded for the Zn-doped TiO2 thin films.

  3. Structure and Property of Nano-TiO2 Doped with Ag+ Membrane Photocatalyst.

    PubMed

    Liu, Fang; He, Ting; Cao, Qingyun; Xu, Yuehua; Liu, Wei; Zhou, Wuyi

    2015-04-01

    Highly transparent silver incorporated titania (Ag/TiO2) composite nanomembranes were fabricated by a simple, reproducible dip-coating process on ceramic substrates. The obtained membrane samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectrometer (EDX), X-ray photoelectron spectroscopy (XPS). The photocatalytic activity of the Ag/TiO2 nanomembranes was assessed by the degradation of methylene blue under visible light irradiation. Compared with pure TiO2 nanomembranes, no significant shift in the TiO2 crystal structure was detected after doping with silver ions. The results from the SEM and EDX analyses showed that homogeneous spherical silver nanoparticles were produced and scattered on the surface of the TiO2 nanomembrane that was coated on the surface of the ceramic substrates. The doping with silver ions could effectively improve the photocatalytic activity of TiO2 under visible light irradiation. The Ag/TiO2 composite nanomembrane also exhibited improved hydrophilicity compared to that of a pure TiO2 nanomembrane.

  4. Interfacial n-Doping Using an Ultrathin TiO2 Layer for Contact Resistance Reduction in MoS2.

    PubMed

    Kaushik, Naveen; Karmakar, Debjani; Nipane, Ankur; Karande, Shruti; Lodha, Saurabh

    2016-01-13

    We demonstrate a low and constant effective Schottky barrier height (ΦB ∼ 40 meV) irrespective of the metal work function by introducing an ultrathin TiO2 ALD interfacial layer between various metals (Ti, Ni, Au, and Pd) and MoS2. Transmission line method devices with and without the contact TiO2 interfacial layer on the same MoS2 flake demonstrate reduced (24×) contact resistance (RC) in the presence of TiO2. The insertion of TiO2 at the source-drain contact interface results in significant improvement in the on-current and field effect mobility (up to 10×). The reduction in RC and ΦB has been explained through interfacial doping of MoS2 and validated by first-principles calculations, which indicate metallic behavior of the TiO2-MoS2 interface. Consistent with DFT results of interfacial doping, X-ray photoelectron spectroscopy (XPS) data also exhibit a 0.5 eV shift toward higher binding energies for Mo 3d and S 2p peaks in the presence of TiO2, indicating Fermi level movement toward the conduction band (n-type doping). Ultraviolet photoelectron spectroscopy (UPS) further corroborates the interfacial doping model, as MoS2 flakes capped with ultrathin TiO2 exhibit a reduction of 0.3 eV in the effective work function. Finally, a systematic comparison of the impact of selective doping with the TiO2 layer under the source-drain metal relative to that on top of the MoS2 channel shows a larger benefit for transistor performance from the reduction in source-drain contact resistance.

  5. Atomic Layer Deposition of p-Type Epitaxial Thin Films of Undoped and N-Doped Anatase TiO2.

    PubMed

    Vasu, K; Sreedhara, M B; Ghatak, J; Rao, C N R

    2016-03-01

    Employing atomic layer deposition, we have grown p-type epitaxial undoped and N-doped anatase TiO2(001) thin films on c-axis Al2O3 substrate. From X-ray diffraction and transmission electron microscopy studies, crystallographic relationships between the film and the substrate are found to be (001)TiO2//(0001)Al2O3 and [1̅10]TiO2//[011̅0]Al2O3. N-doping in TiO2 thin films enhances the hole concentration and mobility. The optical band gap of anatase TiO2 (3.23 eV) decreases to 3.07 eV upon N-doping. The epitaxial films exhibit room-temperature ferromagnetism and photoresponse. A TiO2-based homojunction diode was fabricated with rectification from the p-n junction formed between N-doped p-TiO2 and n-TiO2. PMID:26963716

  6. Atomic Layer Deposition of p-Type Epitaxial Thin Films of Undoped and N-Doped Anatase TiO2.

    PubMed

    Vasu, K; Sreedhara, M B; Ghatak, J; Rao, C N R

    2016-03-01

    Employing atomic layer deposition, we have grown p-type epitaxial undoped and N-doped anatase TiO2(001) thin films on c-axis Al2O3 substrate. From X-ray diffraction and transmission electron microscopy studies, crystallographic relationships between the film and the substrate are found to be (001)TiO2//(0001)Al2O3 and [1̅10]TiO2//[011̅0]Al2O3. N-doping in TiO2 thin films enhances the hole concentration and mobility. The optical band gap of anatase TiO2 (3.23 eV) decreases to 3.07 eV upon N-doping. The epitaxial films exhibit room-temperature ferromagnetism and photoresponse. A TiO2-based homojunction diode was fabricated with rectification from the p-n junction formed between N-doped p-TiO2 and n-TiO2.

  7. Preparation and Optical Absorption Performance of Si Single Quantum Dots and Si/Ge Double Quantum Dots Doped TiO2 Films.

    PubMed

    Chen, Lixia; He, Fang; Sun, Zuwen; Zhang, Yan; Li, Fengjiao; Huang, Yuan; Gu, Ruisona

    2015-02-01

    Si single quantum dots (QDs) and Si/Ge double QDs doped TiO2 films were successfully fabricated via layer-by-layer ion beam sputtering assisted by annealing treatment, and their morphology and optical absorption performance were analyzed in this paper. TEM images show that Si QDs and Si/Ge double QDs prepared in the TiO2 matrix are in a uniform size distribution and high density, especially after annealed at 500 °C. XPS results indicate that Si in the TiO2 films mainly exists in the form of elemental Si and SiO2, and Ge is in elemental form. From the optical absorption spectra, the optical response of the TiO2 films is shifted from ultraviolet to visible and near infrared region when they are doped by the QDs, and the Si/Ge double QDs co-doped TiO2 films show better optical response compared with the Si QDs doped TiO2 films, suggesting a hybrid enhanced effect of double QDs.

  8. Effect of Ce doping of TiO2 support on NH3-SCR activity over V2O5-WO3/CeO2-TiO2 catalyst.

    PubMed

    Cheng, Kai; Liu, Jian; Zhang, Tao; Li, Jianmei; Zhao, Zhen; Wei, Yuechang; Jiang, Guiyuan; Duan, Aijun

    2014-10-01

    CeO2-TiO2 composite supports with different Ce/Ti molar ratios were prepared by a homogeneous precipitation method, and V2O5-WO3/CeO2-TiO2 catalysts for the selective catalytic reduction (SCR) of NOx with NH3 were prepared by an incipient-wetness impregnation method. These catalysts were characterized by means of BET, XRD, UV-Vis, Raman and XPS techniques. The results showed that the catalytic activity of V2O5-WO3/TiO2 was greatly enhanced by Ce doping (molar ratio of Ce/Ti=1/10) in the TiO2 support. The catalysts that were predominantly anatase TiO2 showed better catalytic performance than the catalysts that were predominantly fluorite CeO2. The Ce additive could enhance the surface adsorbed oxygen and accelerate the SCR reaction. The effects of O2 concentration, ratio of NH3/NO, space velocity and SO2 on the catalytic activity were also investigated. The presence of oxygen played an important role in NO reduction. The optimal ratio of NH3/NO was 1/1 and the catalyst had good resistance to SO2 poisoning. PMID:25288555

  9. Effect of Ce doping of TiO2 support on NH3-SCR activity over V2O5-WO3/CeO2-TiO2 catalyst.

    PubMed

    Cheng, Kai; Liu, Jian; Zhang, Tao; Li, Jianmei; Zhao, Zhen; Wei, Yuechang; Jiang, Guiyuan; Duan, Aijun

    2014-10-01

    CeO2-TiO2 composite supports with different Ce/Ti molar ratios were prepared by a homogeneous precipitation method, and V2O5-WO3/CeO2-TiO2 catalysts for the selective catalytic reduction (SCR) of NOx with NH3 were prepared by an incipient-wetness impregnation method. These catalysts were characterized by means of BET, XRD, UV-Vis, Raman and XPS techniques. The results showed that the catalytic activity of V2O5-WO3/TiO2 was greatly enhanced by Ce doping (molar ratio of Ce/Ti=1/10) in the TiO2 support. The catalysts that were predominantly anatase TiO2 showed better catalytic performance than the catalysts that were predominantly fluorite CeO2. The Ce additive could enhance the surface adsorbed oxygen and accelerate the SCR reaction. The effects of O2 concentration, ratio of NH3/NO, space velocity and SO2 on the catalytic activity were also investigated. The presence of oxygen played an important role in NO reduction. The optimal ratio of NH3/NO was 1/1 and the catalyst had good resistance to SO2 poisoning.

  10. Theoretical and photo-electrochemical studies of surface plasmon induced visible light absorption of Ag loaded TiO2 nanotubes for water splitting

    NASA Astrophysics Data System (ADS)

    Gross, P. A.; Javahiraly, N.; Geraldini Sabat, N.; Cottineau, T.; Savinova, E. R.; Keller, V.

    2016-10-01

    Vertically aligned TiO2 nanotubes (TiO2-NTs), obtained by anodization in organic electrolyte, are decorated with 15 nm Ag nanoparticles prepared by a micro-wave assisted polyol synthesis. The Ag/TiO2 system is characterized by electronic microscopies in order to build a Finite Differential Time Domain (FDTD) model to simulate the interaction of light with the system. By combining UV-visible spectroscopy and FDTD simulations, the observed red shift in the surface plasmon resonance wavelength of the Ag nanoparticles, deposited on TiO2, is explained. The Ag/TiO2-NT system is used as photoanode in a photoelectrochemical water splitting setup and shows an increasing Incident Photon to Current Conversion Efficiency (IPCE) in the visible light domain with an increasing amount of deposited Ag. The spectral position of this activity enhancement coincides with the one expected from the FDTD calculations for the surface plasmon resonance of the Ag nanoparticles deposited on TiO2.

  11. Migration of Ag- and TiO2-(Nano)particles from textiles into artificial sweat under physical stress: experiments and exposure modeling.

    PubMed

    von Goetz, N; Lorenz, C; Windler, L; Nowack, B; Heuberger, M; Hungerbühler, K

    2013-09-01

    Engineered nanoparticles (ENP) are increasingly used to functionalize textiles taking advantage, e.g., of the antimicrobial activity of silver (Ag)-ENP or the UV-absorption of titania (TiO2)-ENP. Mobilization and migration of ENPs from the textile into human sweat can result in dermal exposure to these nanoobjects and their aggregates and agglomerates (NOAA). In this study we assessed exposure to NOAA migrating from commercially available textiles to artificial sweat by an experimental setup that simulates wear-and-tear during physical activity. By combining physical stress with incubation in alkaline and acidic artificial sweat solutions we experimentally realized a worst case scenario for wearing functionalized textiles during sports activities. This experimental approach is not limited to NOAA, but can be used for any other textile additive. Out of four investigated textiles, one T-shirt and one pair of trousers with claimed antimicrobial properties were found to release Ag <450 nm in detectable amounts (23-74 μg/g/L). Textiles containing TiO2 for UV protection did not release significant amounts of TiO2 <450 nm, but the antimicrobial T-shirt released both TiO2 and Ag <450 nm. The silver was present in dissolved and particulate form, whereas TiO2 was mainly found as particulate. On the basis of our experimental results we calculated external dermal exposure to Ag and TiO2 for male and female adults per use. For silver, maximal amounts of 17.1 and 8.2 μg/kg body weight were calculated for total and particulate Ag <450 nm, respectively. For TiO2, the exposure levels amount to maximal 11.6 μg/kg body weight for total (mainly particulate) TiO2. In comparison with other human exposure pathways, dermal exposure to NOAA from textiles can be considered comparably minor for TiO2-NOAA, but not for Ag-NOAA.

  12. Catalyst performance and mechanism of catalytic combustion of dichloromethane (CH2Cl2) over Ce doped TiO2.

    PubMed

    Cao, Shuang; Wang, Haiqiang; Yu, Feixiang; Shi, Mengpa; Chen, Shuang; Weng, Xiaole; Liu, Yue; Wu, Zhongbiao

    2016-02-01

    TiO2 and Ce/TiO2 were synthesized and subsequently used for the catalytic combustion of DCM. TiO2 had abundant Lewis acid sites and was responsible for the adsorption and the rupture of C-Cl bonds. However, TiO2 tended to be inactivated because of chloride poisoning due to the adsorption and accumulation of Cl species over the surface. While, Ce/TiO2 obtained total oxidation of CH2Cl2 at 335°C and exhibited stable DCM removal activity on 100h long-time stability tests at 330°C without any catalyst deactivation. The doped cerium generated Ce(3+) chemical states and surface active oxygen, and therefore played important roles from two aspects as follows. First of all, the poisoning of Cl for Ce/TiO2 was inhibited to some extent by CeO2 due to the rapid removal of Cl on the surface of CeO2, which has been verified by NH3-IR characterization. In the other hand, CeO2 enhanced the further deep oxidation of C-H from byproducts and retained the certain oxidation of CO to CO2. Based on the DRIFT characterization and the catalysts activity tests, a two-step reaction pathway for the catalytic combustion of DCM on Ce/TiO2 catalyst was proposed. PMID:26550781

  13. Catalyst performance and mechanism of catalytic combustion of dichloromethane (CH2Cl2) over Ce doped TiO2.

    PubMed

    Cao, Shuang; Wang, Haiqiang; Yu, Feixiang; Shi, Mengpa; Chen, Shuang; Weng, Xiaole; Liu, Yue; Wu, Zhongbiao

    2016-02-01

    TiO2 and Ce/TiO2 were synthesized and subsequently used for the catalytic combustion of DCM. TiO2 had abundant Lewis acid sites and was responsible for the adsorption and the rupture of C-Cl bonds. However, TiO2 tended to be inactivated because of chloride poisoning due to the adsorption and accumulation of Cl species over the surface. While, Ce/TiO2 obtained total oxidation of CH2Cl2 at 335°C and exhibited stable DCM removal activity on 100h long-time stability tests at 330°C without any catalyst deactivation. The doped cerium generated Ce(3+) chemical states and surface active oxygen, and therefore played important roles from two aspects as follows. First of all, the poisoning of Cl for Ce/TiO2 was inhibited to some extent by CeO2 due to the rapid removal of Cl on the surface of CeO2, which has been verified by NH3-IR characterization. In the other hand, CeO2 enhanced the further deep oxidation of C-H from byproducts and retained the certain oxidation of CO to CO2. Based on the DRIFT characterization and the catalysts activity tests, a two-step reaction pathway for the catalytic combustion of DCM on Ce/TiO2 catalyst was proposed.

  14. Insight into visible light-driven photocatalytic degradation of diesel oil by doped TiO2-PS floating composites.

    PubMed

    Wang, Xin; Wang, Wei; Wang, Xuejiang; Zhao, Jianfu; Zhang, Jing; Song, Jingke

    2016-09-01

    TiO2-pearlstone (PS) floatable photocatalysts were synthesized using a facile sol-gel method and confirmed by XRD, N2 adsorption-desorption, SEM, EDX, TEM, FT-IR, XPS, and UV-vis DRS measurements. It has been found that the photocatalysts composed of anatase TiO2 deposited on the surface of PS and formed mesoporous structure. By N or B/N doping, the band gap of the photocatalyst has been narrowed. The obtained floatable photocatalysts can be applied to solar light-driven remediation of oil-contaminated water. Diesel oil was chosen as the model pollutant to evaluate the photocatalytic activity. The results showed B/N-TiO2-PS exhibited the highest photocatalytic activity for diesel oil under visible light irradiation, which is 48 % removal rate for 9 h. The reaction rate constant k of B/N-TiO2-PS is 0.08423 h(-1), which is four times larger than that of pure TiO2-PS. Moreover, the characteristic of floatable makes the photocatalysts easier to separate and reuse, which showed great potential for practical applications in the field of environmental cleanup and solar energy conversion.

  15. Enhanced photoelectric property and visible activity of nitrogen doped TiO2 synthesized from different nitrogen dopants

    NASA Astrophysics Data System (ADS)

    Cheng, Xiuwen; Yu, Xiujuan; Xing, Zipeng

    2013-03-01

    N doped TiO2 nano-particles were synthesized through simple sol-gel reactions from different nitrogen dopants. The resulting materials were characterized by X-ray diffraction (XRD), Raman spectra, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS) and surface photovoltage spectroscopy (SPS). Furthermore, the photoelectric property and activity enhanced mechanism were investigated in detail. It was found that the introduction of N dopants could effectively inhibit the crystal growth of TiO2 nano-particles, enhance the light absorption in visible region, possess more surface hydroxyl groups and separate the photoinduced charge carriers. The effects of dopants on the photocatalytic activity for the degradation of rhodamine B (RhB) were investigated in detail. It is clearly demonstrated that the photocatalytic activity of N)-TiO nano-particle was higher than that of NCl)-TiO and undoped TiO2. The enhanced photocatalytic activity could be attributed to the smaller crystal size, more hydroxyl groups on surface of the catalyst, stronger light absorption in visible region and higher separation efficiency of photoinduced charge carriers.

  16. Insight into visible light-driven photocatalytic degradation of diesel oil by doped TiO2-PS floating composites.

    PubMed

    Wang, Xin; Wang, Wei; Wang, Xuejiang; Zhao, Jianfu; Zhang, Jing; Song, Jingke

    2016-09-01

    TiO2-pearlstone (PS) floatable photocatalysts were synthesized using a facile sol-gel method and confirmed by XRD, N2 adsorption-desorption, SEM, EDX, TEM, FT-IR, XPS, and UV-vis DRS measurements. It has been found that the photocatalysts composed of anatase TiO2 deposited on the surface of PS and formed mesoporous structure. By N or B/N doping, the band gap of the photocatalyst has been narrowed. The obtained floatable photocatalysts can be applied to solar light-driven remediation of oil-contaminated water. Diesel oil was chosen as the model pollutant to evaluate the photocatalytic activity. The results showed B/N-TiO2-PS exhibited the highest photocatalytic activity for diesel oil under visible light irradiation, which is 48 % removal rate for 9 h. The reaction rate constant k of B/N-TiO2-PS is 0.08423 h(-1), which is four times larger than that of pure TiO2-PS. Moreover, the characteristic of floatable makes the photocatalysts easier to separate and reuse, which showed great potential for practical applications in the field of environmental cleanup and solar energy conversion. PMID:27259962

  17. Synthesis, characterization and photocatalytic evaluation of visible light activated C-doped TiO2 nanoparticles.

    PubMed

    Liu, Guanglong; Han, Changseok; Pelaez, Miguel; Zhu, Duanwei; Liao, Shuijiao; Likodimos, Vlassis; Ioannidis, Nikolaos; Kontos, Athanassios G; Falaras, Polycarpos; Dunlop, Patrick S M; Byrne, J Anthony; Dionysiou, Dionysios D

    2012-07-27

    We have demonstrated heterogeneous photocatalytic degradation of microcystin-LR (MC-LR) by visible light activated carbon doped TiO(2) (C-TiO(2)) nanoparticles, synthesized by a modified sol-gel route based on the self-assembly technique exploiting oleic acid as a pore directing agent and carbon source. The C-TiO(2) nanoparticles crystallize in anatase phase despite the low calcination temperature of 350 °C and exhibit a highly porous structure that can be optimized by tuning the concentration of the oleic acid surfactant. The carbon modified nanomaterials exhibited enhanced absorption in the broad visible light region together with an apparent red shift in the optical absorption edge by 0.5 eV (2.69 eV), compared to the 3.18 eV of reference anatase TiO(2). Carbon species were identified by x-ray photoelectron spectroscopy analysis through the formation of both Ti-C and C-O bonds, indicative of substitution of carbon for oxygen atoms and the formation of carbonates, respectively. Electron paramagnetic resonance spectroscopy revealed the formation of two carbon related paramagnetic centers in C-TiO(2), whose intensity was markedly enhanced under visible light illumination, pointing to the formation of localized states within the anatase band gap, following carbon doping. The photocatalytic activity of C-TiO(2) nanomaterials was evaluated for the degradation of MC-LR at pH 3.0 under visible light (λ > 420 nm) irradiation. The doped materials showed a higher MC-LR degradation rate than reference TiO(2), behavior that is attributed to the incorporation of carbon into the titania lattice.

  18. Synthesis, characterization and photocatalytic evaluation of visible light activated C-doped TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Liu, Guanglong; Han, Changseok; Pelaez, Miguel; Zhu, Duanwei; Liao, Shuijiao; Likodimos, Vlassis; Ioannidis, Nikolaos; Kontos, Athanassios G.; Falaras, Polycarpos; Dunlop, Patrick S. M.; Byrne, J. Anthony; Dionysiou, Dionysios D.

    2012-07-01

    We have demonstrated heterogeneous photocatalytic degradation of microcystin-LR (MC-LR) by visible light activated carbon doped TiO2 (C-TiO2) nanoparticles, synthesized by a modified sol-gel route based on the self-assembly technique exploiting oleic acid as a pore directing agent and carbon source. The C-TiO2 nanoparticles crystallize in anatase phase despite the low calcination temperature of 350 °C and exhibit a highly porous structure that can be optimized by tuning the concentration of the oleic acid surfactant. The carbon modified nanomaterials exhibited enhanced absorption in the broad visible light region together with an apparent red shift in the optical absorption edge by 0.5 eV (2.69 eV), compared to the 3.18 eV of reference anatase TiO2. Carbon species were identified by x-ray photoelectron spectroscopy analysis through the formation of both Ti-C and C-O bonds, indicative of substitution of carbon for oxygen atoms and the formation of carbonates, respectively. Electron paramagnetic resonance spectroscopy revealed the formation of two carbon related paramagnetic centers in C-TiO2, whose intensity was markedly enhanced under visible light illumination, pointing to the formation of localized states within the anatase band gap, following carbon doping. The photocatalytic activity of C-TiO2 nanomaterials was evaluated for the degradation of MC-LR at pH 3.0 under visible light (λ > 420 nm) irradiation. The doped materials showed a higher MC-LR degradation rate than reference TiO2, behavior that is attributed to the incorporation of carbon into the titania lattice.

  19. Optical properties analysis of Ta-doped TiO2 thin films on LaAlO3 substrates

    NASA Astrophysics Data System (ADS)

    Nurfani, Eka; Sutjahja, Inge M.; Winata, Toto; Rusydi, Andrivo; Darma, Yudi

    2015-09-01

    We study optical properties of Ta-doped TiO2 thin film on LaAlO3 substrate using spectroscopy ellipsometry (SE) analysis at energy range of 0.5 - 6.5 eV. Room temperature SE data for Ψ (amplitude ratio) and Δ (phase difference) between p- and s- polarized light waves are taken with multiple incident angles at several spots on the samples. Here, absorption coefficient has been extracted from SE measurements at photon incident angle of 70° for different Ta concentration (0.01, 0.4, and 5 at. %). Multilayer modelling is performed which takes into account reflections at each interface through Fresnel coefficients to obtain reasonably well the fitting of Ψ and Δ data simultaneously. As the results, we estimate that film thickness increases by increasing Ta concentration accompanied by the formation of a new electronic structure. By increasing Ta impurities, the blueshift of absorption coefficient (α) peaks is observable. This result indicates that TiO2 thin film becomes optically resistive by introducing Ta doping. Schematic model of interband transition inTiO2:Ta will be proposed base on obtained optical properties. This study enables us to predict the role of Ta doping on the electronic and optical band structures of TiO2 thin film. Due to a processing error by AIP Publishing, an incorrect version of the above article was published on 30 September 2015 that omitted the name of author Toto Winata. AIP Publishing apologizes for this error. All online versions of the article were corrected on 7 October 2015. The author names and affiliations appear correctly above.

  20. Disinfection of Escherichia coli Gram negative bacteria using surface modified TiO2: optimization of Ag metallization and depiction of charge transfer mechanism.

    PubMed

    Gomathi Devi, LakshmipathiNaik; Nagaraj, Basavalingaiah

    2014-01-01

    The antibacterial activity of silver deposited TiO2 (Ag-TiO2 ) against Gram negative Escherichia coli bacteria was investigated by varying the Ag metal content from 0.10 to 0.50% on the surface of TiO2 . Ag depositions by the photoreduction method were found to be stable. Surface silver metallization was confirmed by EDAX and XPS studies. Photoluminescence studies show that the charge carrier recombination is less for 0.1% Ag-TiO2 and this catalyst shows superior bactericidal activity under solar light irradiation compared to Sol gel TiO2 (SG-TiO2 ) due to the surface plasmon effect. The energy levels of deposited Ag are dependent on the Ag content and it varies from -4.64 eV to -1.30 eV with respect to the vacuum energy level based on atomic silver to bulk silver deposits. The ability of electron transfer from Ag deposit to O2 depends on the position of the energy levels. The 0.25% and 0.50% Ag depositions showed detrimental effect on bactericidal activity due to the mismatch of energy levels. The effect of the EROS (External generation of the Reactive Oxygen Species by 0.1% Ag-TiO2 ) and IROS (Interior generation of Reactive Oxygen Species within the bacteria) on the bactericidal inactivation is discussed in detail. PMID:24995499

  1. Folic acid-conjugated TiO2-doped mesoporous carbonaceous nanocomposites loaded with Mitoxantrone HCl for chemo-photodynamic therapy.

    PubMed

    Li, Zhi; Ou-Yang, Ya; Liu, Yang; Wang, Yi-Qiu; Zhu, Xia-Li; Zhang, Zhen-Zhong

    2015-06-01

    Recently, porous carbons have showed great potential in many areas. In this study, TiO2-doped mesoporous carbonaceous (TiO2@C) nanoparticles were obtained by a simple one-pot hydrothermal treatment, folic acid (FA) was conjugated to TiO2@C through an amide bond, then Mitoxantrone HCl (MTX) was adsorbed onto TiO2@C-FA and a drug delivery system, TiO2@C-FA/MTX was obtained. TiO2@C-FA/MTX showed a much faster MTX release at pH 4.5 than at pH 6.0 and pH 7.4. Furthermore, compared with free MTX, this drug delivery system showed a dose-dependent cytotoxicity by varying the irradiance, and afforded higher antitumor efficacy in cultured PC3 cells in vitro. The ability of TiO2@C-FA/MTX to combine chemotherapy with photodynamic activity enhanced the cancer cell killing effect in vitro, demonstrating that TiO2@C-FA/MTX has a great potential for cancer therapy in the future.

  2. TiO(2) doping by hydroxyurea at the nucleation stage: towards a new photocatalyst in the visible spectral range.

    PubMed

    Azouani, R; Tieng, S; Chhor, K; Bocquet, J-F; Eloy, P; Gaigneaux, E M; Klementiev, K; Kanaev, A V

    2010-10-01

    We report an original method of preparation of OCN-doped TiO(2) for photocatalysis in the visible spectral range. The preparation is achieved by a sol-gel route using titanium tetraisopropoxide precursor. Special attention was paid to fluid micromixing, which enables homogeneous reaction conditions in the reactor bulk and monodispersity of the produced clusters/nanoparticles. The dopant hydroxyurea (HyU, CH(4)N(2)O(2)) is injected into the reactive fluid at the nucleation stage, which lasts tens of milliseconds. The doping results in a strong yellow coloration of the nanocolloids due to the absorption band in the spectral range 380-550 nm and accelerates the aggregation kinetics of both nuclei at the induction stage and sub-nuclei units (clusters) at the nucleation stage. FTIR, Raman and UV-visible absorption analyses show the formation of a stable HyU-TiO(2) complex. EXAFS spectra indicate no appreciable changes of the first-shell Ti atom environment. The doping agent takes available surface sites of TiO(2) clusters/nanoparticles attaining ∼10% molar loading. The reaction kinetics then accelerates due to a longer collisional lifetime between nanoparticles induced by the formation of a weak [double bond, length as m-dash]OTi bond. The OCN-group bonding to titanium atoms produces a weakening of the C[double bond, length as m-dash]O double bond and a strengthening of the C-N and N-O bonds.

  3. Preparation of K-doped TiO2 nanostructures by wet corrosion and their sunlight-driven photocatalytic performance

    NASA Astrophysics Data System (ADS)

    Shin, Eunhye; Jin, Saera; Kim, Jiyoon; Chang, Sung-Jin; Jun, Byung-Hyuk; Park, Kwang-Won; Hong, Jongin

    2016-08-01

    K-doped TiO2 nanowire networks were prepared by the corrosion reaction of Ti nanoparticles in an alkaline (potassium hydroxide: KOH) solution. The prepared nanostructures were characterized by scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) analysis, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, X-ray diffraction (XRD) and photoluminescence (PL) spectra. Their sunlight-driven photocatalytic activity was also investigated with differently charged dye molecules, such as methylene blue, rhodamine B and methyl orange. The adsorption of the dye molecules on the photocatalyst surface would play a critical role in their selective photodegradation under sunlight illumination.

  4. Inkjet printable luminescent Eu3+-TiO2 doped in sol gel matrix for paper tagging.

    PubMed

    Attia, M S; Elsaadany, Soad A; Ahmed, Kawther A; El-Molla, Mohamed M; Abdel-Mottaleb, M S A

    2015-01-01

    Europium (III) with different concentrations (0.2, 0.4 and 0.8 %)-TiO(2) doped silica composite systems were sensitized by sol-gel method. Different spectroscopic and microscopic tools characterized the composites. The Europium ion incorporated into the liquid silica-titania solution acts as red light emission center in the luminescent materials. This luminescent nano composite pigment has great potential of application in preparing luminescent ink. Inkjet printer loaded with the prepared ink to show its potential usage as tagging material performed the printing test on a white paper.

  5. Improvement of sintering, nonlinear electrical, and dielectric properties of ZnO-based varistors doped with TiO2

    NASA Astrophysics Data System (ADS)

    Osama, A. Desouky; K, E. Rady

    2016-06-01

    The effects of TiO2 on sintering and nonlinear electrical properties of (98.5 ‑ x)ZnO–0.5MnO2–0.5Co,2O3‑0.5Bi2O3–xTiO2 (x = 0.3, 0.5, 0.7, 0.9 mol%) ceramic varistors prepared by the ceramic technique are investigated in this work. The optimum sintering temperature of the prepared samples is deduced by determining the firing shrinkage and water absorption percentages. The optimum sintering temperature is found to be 1200 °C, at which each of the samples shows a maximum firing shrinkage and minimum water absorption. Also minimum water absorption appears in a sample of x = 0.9 mol%. Higher sintering temperature and longer sintering time give rise to a reduction in bulk density due to the increased amount of porosity between the large grains of ZnO resulting from the rapid grain growth induced by the liquid phase sintering. The crystal size of ZnO decreases with increasing TiO2 doping. The addition of TiO2 improves the nonlinear coefficient and attains its maximum value at x = 0.7 mol% of TiO2, further addition negatively affects it. A decrease in capacitance consequently in the dielectric constant is recorded with increasing the frequency in a range of 30 kHz–200 kHz. The temperature and composition dependences of the dielectric constant and AC conductivity are also studied. The increase of temperature raises the dielectric constant because it increases ionic response to the field at any particular frequency.

  6. Photodecolorization of Rhodamine B on tungsten-doped TiO2/activated carbon under visible-light irradiation.

    PubMed

    Li, Youji; Zhou, Xiaoming; Chen, Wei; Li, Leiyong; Zen, Mengxiong; Qin, Shidong; Sun, Shuguo

    2012-08-15

    Tungsten-doped TiO(2)/activated carbon catalysts have been prepared by a supercritical-pretreatment-assisted sol-gel process. The structural features of the photocatalysts have been investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV/Vis diffuse-reflectance spectroscopy (DRS), electron dispersive X-ray (EDX), photoluminescence spectroscopy, and Brunauer-Emmett-Teller (BET) analysis. The results revealed that a W-TiO(2) layer was coated on the AC surface, and had higher surface area and smaller crystallite size than TiO(2)/AC obtained by a similar route. The W dopant was responsible for narrowing the band gap of TiO(2) and shifting its optical response from the ultraviolet (UV) to the visible-light region. The photocatalytic performances of the supported catalysts have been evaluated for the degradation of Rhodamine B (RhB) solution under visible-light irradiation. Compared with bulk W-TiO(2), the photoactivity was obviously enhanced when it was coated onto AC. In addition, it was found that the reactivity showed a significant relationship with the amount of W dopant, and the photoactivity order of the catalysts from weak to strong showed good agreement with their PL intensities. The effects of TiO(2) content, tungsten ion content, catalyst amount, pH, and initial RhB concentration have been examined as operational parameters. The photocatalytic reactions followed pseudo-first-order kinetics and are discussed in terms of the Langmuir-Hinshelwood model.

  7. Photocatalyzed degradation of flumequine by doped TiO2 and simulated solar light.

    PubMed

    Nieto, J; Freer, J; Contreras, D; Candal, R J; Sileo, E E; Mansilla, H D

    2008-06-30

    Titanium dioxide was obtained in its pure form (TiO2) and in the presence of urea (u-TiO2) and thiourea (t-TiO2) using the sol-gel technique. The obtained powders were characterized by BET surface area analysis, Infrared Spectroscopy, Diffuse Reflectance Spectroscopy and the Rietveld refinement of XRD measurements. All the prepared catalysts show high anatase content (>99%). The a and b-cell parameters of anatase increase in the order TiO2u-TiO2>TiO2. The photocatalytic activities of the samples were determined on flumequine under solar-simulated irradiation. The most active catalysts were u-TiO2 and t-TiO2, reaching values over 90% of flumequine degradation after 15 min irradiation, compared with values of 55% for the pure TiO2 catalyst. Changing simultaneously the catalyst amount (t-TiO2) and pH, multivariate analysis using the response surface methodology was used to determine the roughly optimal conditions for flumequine degradation. The optimized conditions found were pH below 7 and a catalyst amount of 1.6 g L(-1).

  8. Photocatalytic Properties of TiO2 Thin Films Modified with Ag and Pt Nanoparticles Deposited by Gas Flow Sputtering.

    PubMed

    Maicu, M; Glöss, D; Frach, Peter; Hecker, D; Gerlach, G; Córdoba, José M

    2015-09-01

    In this work, a gas flow sputtering (GFS) process which allows the production and deposition of metal nanoparticles (NPs) in a vacuum environment is described. Aim of the study is to prove the potential of this technology for the fabrication of new TiO2 films with enhanced photocatalytic properties. For this purpose, Ag and Pt NPs have been produced and deposited on photocatalytic float glass coated with TiO2 thin films by magnetron sputtering. The influence of the process parameters and of the metal amount on the final properties of the particles (quantity, size, size distribution, oxidation state etc.,) was widely investigated. Moreover, the effect of the NPs on the photocatalytic activity of the resulting materials was evaluated for the case of the decomposition of stearic acid (SA) during UV-A irradiation. The reduction of the water contact angle (WCA) during the irradiation period was measured in order to test the photo-induced super-hydrophilicity (PSH). PMID:26716202

  9. High-rate performance of Ti(3+) self-doped TiO2 prepared by imidazole reduction for Li-ion batteries.

    PubMed

    Seok, Dong-Il; Wu, Mihye; Shim, Kwang Bo; Kang, Yongku; Jung, Ha-Kyun

    2016-10-28

    Ti(3+) self-doped TiO2 nanoparticles were prepared via a simple imidazole reduction process and developed as an anode material for Li-ion batteries. Introducing the Ti(3+)-state on TiO2 nanoparticles resulted in superior rate performances that the capacity retention of 88% at 50 C. The enhanced electrochemical performances were attributed to the resulting lower internal resistance and improved electronic conductivity, based on galvanostatic intermittent titration technique and electrochemical impedance spectroscopy analyses.

  10. High-rate performance of Ti(3+) self-doped TiO2 prepared by imidazole reduction for Li-ion batteries.

    PubMed

    Seok, Dong-Il; Wu, Mihye; Shim, Kwang Bo; Kang, Yongku; Jung, Ha-Kyun

    2016-10-28

    Ti(3+) self-doped TiO2 nanoparticles were prepared via a simple imidazole reduction process and developed as an anode material for Li-ion batteries. Introducing the Ti(3+)-state on TiO2 nanoparticles resulted in superior rate performances that the capacity retention of 88% at 50 C. The enhanced electrochemical performances were attributed to the resulting lower internal resistance and improved electronic conductivity, based on galvanostatic intermittent titration technique and electrochemical impedance spectroscopy analyses. PMID:27651352

  11. High-rate performance of Ti3+ self-doped TiO2 prepared by imidazole reduction for Li-ion batteries

    NASA Astrophysics Data System (ADS)

    Seok, Dong-il; Wu, Mihye; Shim, Kwang Bo; Kang, Yongku; Jung, Ha-Kyun

    2016-10-01

    Ti3+ self-doped TiO2 nanoparticles were prepared via a simple imidazole reduction process and developed as an anode material for Li-ion batteries. Introducing the Ti3+-state on TiO2 nanoparticles resulted in superior rate performances that the capacity retention of 88% at 50 C. The enhanced electrochemical performances were attributed to the resulting lower internal resistance and improved electronic conductivity, based on galvanostatic intermittent titration technique and electrochemical impedance spectroscopy analyses.

  12. Synthesis and characterization of TiO 2/Ag/polymer ternary nanoparticles via surface-initiated atom transfer radical polymerization

    NASA Astrophysics Data System (ADS)

    Park, Jung Tae; Koh, Joo Hwan; Seo, Jin Ah; Cho, Yong Soo; Kim, Jong Hak

    2011-08-01

    We report on the novel ternary hybrid materials consisting of semiconductor (TiO 2), metal (Ag) and polymer (poly(oxyethylene methacrylate) (POEM)). First, a hydrophilic polymer, i.e. POEM, was grafted from TiO 2 nanoparticles via the surface-initiated atom transfer radical polymerization (ATRP) technique. These TiO 2-POEM brush nanoparticles were used to template the formation of Ag nanoparticles by introduction of a AgCF 3SO 3 precursor and a NaBH 4 aqueous solution for reduction process. Successful grafting of polymeric chains from the surface of TiO 2 nanoparticles and the in situ formation of Ag nanoparticles within the polymeric chains were confirmed using transmission electron microscopy (TEM), UV-vis spectroscopy, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). FT-IR spectroscopy also revealed the specific interaction of Ag nanoparticles with the C dbnd O groups of POEM brushes. This study presents a simple route for the in situ synthesis of both metal and polymer confined within the semiconductor, producing ternary hybrid inorganic-organic nanomaterials.

  13. Design of Ag@C@SnO2@TiO2 yolk-shell nanospheres with enhanced photoelectric properties for dye sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Zhao, Peilu; Li, Dan; Yao, Shiting; Zhang, Yiqun; Liu, Fengmin; Sun, Peng; Chuai, Xiaohong; Gao, Yuan; Lu, Geyu

    2016-06-01

    The hierarchical Ag@C@SnO2@TiO2 nanospheres (ACSTS) have been successfully synthesized by deposition of SnO2 and TiO2 on the Ag@C templates layer by layer. The size of ACSTS is ca. 360 nm while the Ag@C cores have an average diameter of about 300 nm. The rough and porous shell structure consisting of SnO2 and TiO2 ensures a large specific surface area (115.5 m2 g-1). To demonstrate how such a unique structure might lead to more excellent photovoltaic property, several kinds of dye-sensitized solar cells (DSSCs) are also fabricated using different nanospheres based photoanodes. It is found that the ACSTS based DSSC exhibits an obvious improvement in cell performance. According to various technical characterization, the ACSTS can provide dual-functions of light absorption and charge transfer, hence resulting in an enhanced short-circuit photocurrent density of 18.68 mA cm-2 and a higher FF of 63% compared with other DSSCs. The ACSTS cell finally obtains a PCE of up to 8.62%, increasing by 70.4% and 10.2% than hollow TiO2 nanospheres and Ag@C@TiO2 nanospheres based cells, respectively. The improved photovoltaic properties of ACSTS cell can be mainly ascribed to the unique microstructure and the synergistic effect of the encapsulated Ag@C cores.

  14. Nanostructured N-doped TiO2 marigold flowers for an efficient solar hydrogen production from H2S

    NASA Astrophysics Data System (ADS)

    Chaudhari, Nilima S.; Warule, Sambhaji S.; Dhanmane, Sushil A.; Kulkarni, Milind V.; Valant, Matjaz; Kale, Bharat B.

    2013-09-01

    Nitrogen-doped TiO2 nanostructures in the form of marigold flowers have been synthesized for the first time using a facile solvothermal method. The structural analysis has shown that such an N-doped TiO2 system crystallizes in the anatase structure. The optical absorption spectra have clearly shown the shift in the absorption edge towards the visible-light range, which indicates successful nitrogen doping. The nitrogen doping has been further confirmed by photoluminescence and photoemission spectroscopy. Microscopy studies have shown the thin nanosheets (petals) of N-TiO2 with a thickness of ~2-3 nm, assembled in the form of the marigold flower with a high surface area (224 m2 g-1). The N-TiO2 nanostructure with marigold flowers is an efficient photocatalyst for the decomposition of H2S and production of hydrogen under solar light. The maximum hydrogen evolution obtained is higher than other known N-TiO2 systems. It is noteworthy that photohydrogen production using the unique marigold flowers of N-TiO2 from abundant H2S under solar light is hitherto unattempted. The proposed synthesis method can also be utilized to design other hierarchical nanostructured N-doped metal oxides.Nitrogen-doped TiO2 nanostructures in the form of marigold flowers have been synthesized for the first time using a facile solvothermal method. The structural analysis has shown that such an N-doped TiO2 system crystallizes in the anatase structure. The optical absorption spectra have clearly shown the shift in the absorption edge towards the visible-light range, which indicates successful nitrogen doping. The nitrogen doping has been further confirmed by photoluminescence and photoemission spectroscopy. Microscopy studies have shown the thin nanosheets (petals) of N-TiO2 with a thickness of ~2-3 nm, assembled in the form of the marigold flower with a high surface area (224 m2 g-1). The N-TiO2 nanostructure with marigold flowers is an efficient photocatalyst for the decomposition of H2S and

  15. N-Doped TiO2 Nanobelts with Coexposed (001) and (101) Facets and Their Highly Efficient Visible-Light-Driven Photocatalytic Hydrogen Production.

    PubMed

    Sun, Shuchao; Gao, Peng; Yang, Yurong; Yang, Piaoping; Chen, Yujin; Wang, Yanbo

    2016-07-20

    To narrow the band gap (3.2 eV) of TiO2 and extend its practical applicability under sunlight, the doping with nonmetal elements has been used to tune TiO2 electronic structure. However, the doping also brings new recombination centers among the photoinduced charge carriers, which results in a quantum efficiency loss accordingly. It has been proved that the {101} facets of anatase TiO2 are beneficial to generating and transmitting more reductive electrons to promote the H2-evolution in the photoreduction reaction, and the {001} facets exhibit a higher photoreactivity to accelerate the reaction involved of photogenerated hole. Thus, it was considered by us that using the surface heterojunction composed of both {001} and {101} facets may depress the disadvantage of N doping. Fortunately, we successfully synthesized anatase N-doped TiO2 nanobelts with a surface heterojunction of coexposed (101) and (001) facets. As expected, it realized the charge pairs' spatial separation and showed higher photocatalytic activity under a visible-light ray: a hydrogen generation rate of 670 μmol h(-1) g(-1) (much higher than others reported previously in literature of N-doped TiO2 nanobelts).

  16. A nitrogen doped TiO2 layer on Ti metal for the enhanced formation of apatite.

    PubMed

    Hashimoto, Masami; Kashiwagi, Kazumi; Kitaoka, Satoshi

    2011-09-01

    Biomedical titanium metals subjected to gas under precisely regulated oxygen partial pressures (P(O2)) from 10(-18) to 10(5) Pa at 973 K for 1 h were soaked in a simulated body fluid (SBF), whose ion concentrations were nearly equal to those of human blood plasma, at 36.5°C for up to 7 days. The effect of oxygen partial pressures on apatite formation was assessed using X-ray diffraction (XRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) measurements. After heating, the weight of the oxide layer (mainly TiO(2)) formed on the titanium metal was found to increase with increased oxygen partial pressure. Nitrogen (N)-doped TiO(2) (Interstitial N) was formed under a P(O2) of 10(-14) Pa. At lower P(O2) (10(-18) Pa), only a titanium nitride layer (TiN and Ti(2)N) was formed. After soaking in SBF, apatite was detected on heat-treated titanium metal samples. The most apatite was formed, based on the growth rate calculated from the apatite coverage ratio, on the titanium metal heated under a P(O2) of 10(-14) Pa, followed by the sample heated under a P(O2) of 10 and 10(4) Pa (in N(2)). The titanium metal heated under a P(O2) of 10(5) Pa (in O(2)) experienced far less apatite formation than the former three titanium samples. Similarly, very little weight change was observed for the titanium metal heated under a P(O2) of 10(-18) Pa (in N(2)). During the experimental observation period (5 days, 36.5°C, SBF), the following relationship held: The growth rate of apatite decreased in the order P(O2) of 10(-14) Pa > P(O2) of 10 Pa ≥ P(O2) of 10(4) Pa > P(O2) of 10(5) Pa > > P(O2) of 10(-18) Pa. These results suggest that N-doped TiO(2) (Interstitial N) strongly induces apatite formation but samples coated only with titanium nitride do not. Thus, controlling the formation of N-doped TiO(2) is expected to improve the bioactivity of biomedical titanium metal.

  17. Fabrication of bidirectionally doped β-Bi2O3/TiO2-NTs with enhanced photocatalysis under visible light irradiation.

    PubMed

    Li, Deyi; Zhang, Yonggang; Zhang, Yalei; Zhou, Xuefei; Guo, Sujin

    2013-08-15

    Stable β-Bi2O3/TiO2-NTs photocatalyst with excellent visible-light-activity is successfully prepared by bidirectional doping. Stake structure of the TiO2-NTs provides a larger specific surface area and makes the contact area between the TiO2-NTs and β-Bi2O3 much larger; The stake structure of TiO2-NTs not only leads to a firmer combination of TiO2-NTs and β-Bi2O3, but also makes them dope one another deeply. The modification of Bi species into TiO2-NTs can form Bi-O-Ti chemical absorption bonds, then a localized impurity level is generated within the band gap. Electrons can be excited and transferred from the Bi(3+) impurity level to the conduction band (CB) of TiO2, similar to narrowing the band-gap of TiO2-NTs, resulting in a red shift of the absorption edge and an enhancement in visible-light activity. During annealing, Bi atoms are partially replaced by Ti atoms. The lattice of β-Bi2O3 is compressed around the Ti impurity, making the lattice dislocate and distort. This dislocation and distortion leads to an increase in the β-Bi2O3 valance band (VB), from 2.02 to 2.28 eV. Accordingly, the weak oxidability of β-Bi2O3 is improved, and its photocatalytic ability is further enhanced. Moreover, this lattice dislocation and distortion changes the Bi-O distances, thus remarkably improving the stability of the β-Bi2O3/TiO2-NTs.

  18. Rapid flame synthesis of internal Mo6+ doped TiO2 nanocrystals in situ decorated with highly dispersed MoO3 clusters for lithium ion storage

    NASA Astrophysics Data System (ADS)

    Li, Yunfeng; Hu, Yanjie; Shen, Jianhua; Jiang, Haibo; Min, Guoquan; Qiu, Shengjie; Song, Zhitang; Sun, Zhuo; Li, Chunzhong

    2015-11-01

    The rational design of nanoheterostructured materials has attracted much attention because of its importance for developing highly efficient LIBs. Herein, we have demonstrated that internal Mo6+ doped TiO2 nanocrystals in situ decorated with highly dispersed MoO3 clusters have been realized by a facile and rapid flame spray pyrolysis route for electrochemical energy storage. In such intriguing nanostructures, internal Mo6+ doping can improve the conductivity of electrode materials and facilitate rapid Li+ intercalation and ion transport and the heteroassembly of highly dispersed ultrafine MoO3 clusters with excellent electrochemical activity endows the TiO2 with extra Li+ ion storage ability as well as incorporates Mo6+. Thus, the as-prepared nanohybrid electrodes exhibit a high specific capacity and superior rate capability due to the maximum synergetic effect of TiO2, Mo6+ and ultrafine MoO3 clusters. Moreover, the aerosol flame process with a unique temperature gradient opens a new strategy to design novel hybrid materials by the simultaneous doping and heteroassembly engineering for next-generation LIBs.The rational design of nanoheterostructured materials has attracted much attention because of its importance for developing highly efficient LIBs. Herein, we have demonstrated that internal Mo6+ doped TiO2 nanocrystals in situ decorated with highly dispersed MoO3 clusters have been realized by a facile and rapid flame spray pyrolysis route for electrochemical energy storage. In such intriguing nanostructures, internal Mo6+ doping can improve the conductivity of electrode materials and facilitate rapid Li+ intercalation and ion transport and the heteroassembly of highly dispersed ultrafine MoO3 clusters with excellent electrochemical activity endows the TiO2 with extra Li+ ion storage ability as well as incorporates Mo6+. Thus, the as-prepared nanohybrid electrodes exhibit a high specific capacity and superior rate capability due to the maximum synergetic effect

  19. Nitrogen doped TiO2-Cu(x)O core-shell mesoporous spherical hybrids for high-performance dye-sensitized solar cells.

    PubMed

    Guo, Enyan; Yin, Longwei

    2015-01-01

    We report on high-performance dye-sensitized solar cells (DSSCs) based on nitrogen doped anatase TiO2-CuxO core-shell mesoporous hybrids synthesized through a facile and controlled combined sol-gel and hydrothermal process in the presence of hexadecylamine as the structure-directing agent. The matching of band edges between CuxO and TiO2 to form a semiconductor heterojunction plays an important role in effective separation of light induced electrons and holes, providing a promising photoanode for DSSCs because of its wide absorption spectrum, high electron injection efficiency, and fast electron transference. DSSCs based on the mesoporous TiO2-CuxO core-shell hybrids show a high short-circuit current density of 9.60 mA cm(-2) and a conversion efficiency of 3.86% under one sun illumination. While DSSCs based on the N-doped mesoporous TiO2-CuxO hybrids exhibit the higher short-circuit current density of 13.24 mA cm(-2) and a conversion efficiency of 4.57% under one sun illumination. In comparison with un-doped TiO2-CuxO hybrids, the doping of nitrogen into the lattice of TiO2 can extend the light absorption in the ultraviolet range to the visible light region and effectively decrease the recombination rate of photo-generated electrons and holes. The presented N-doped mesoporous TiO2-CuxO hybrids as photoanodes could find potential applications for high performance DSSCs.

  20. New insight into the enhanced visible-light photocatalytic activities of B-, C- and B/C-doped anatase TiO2 by first-principles.

    PubMed

    Yu, Jiaguo; Zhou, Peng; Li, Qin

    2013-08-01

    The geometry structures, formation energies and electronic properties of the B-, C- and B/C-doped anatase TiO2 were investigated by the density functional theory (DFT) calculations of first-principles. The results indicated that the visible-light absorption and photocatalytic activities of the B-, C- and B/C-doped anatase TiO2 were not only influenced by the energy gaps (Eg) and the distributions of impurity states, but also affected by the locations of Fermi levels (EF) and the energies of the edges of band gaps (Ev for the top of valence bands and Ec for the bottom of conduction bands). However, the above four factors changed with the doped models of TiO2. The impurity states in the band gaps reduced the maximum energy gaps in the band gaps, which is responsible for the absorption of visible light. The Fermi levels at the bottom of conduction bands indicated the existence of Ti(3+) ions, which enhanced the separation rates of photogenerated electrons and holes. Further, the energies of the edges of band gaps, determining the dominant types of oxidants (O2(-), hole, ˙OH) in the photocatalytic degradation, were discussed. Moreover, the stability of the doped TiO2 depended on its growth conditions (O-rich or Ti-rich environment). The O-rich growth condition is beneficial to the substitutional B and C atoms to Ti atoms, while the Ti-rich growth condition is favorable to the other doped TiO2 including the most stable co-doped TiO2 with the interstitial B atom and the substitutional C atom to O atom. In addition, our results also showed that the B/C-doped TiO2 inherited the partial electronic properties of single-doped TiO2, but also exhibited many new electronic properties, implying that the electronic properties of co-doped systems are not a mechanical mixture of those of both single-doped systems.

  1. Nb doped TiO2 as a Cathode Catalyst Support Material for Polymer Electrolyte Membrane Fuel Cells

    NASA Astrophysics Data System (ADS)

    O'Toole, Alexander W.

    In order to reduce the emissions of greenhouse gases and reduce dependence on the use of fossil fuels, it is necessary to pursue alternative sources of energy. Transportation is a major contributor to the emission of greenhouse gases due to the use of fossil fuels in the internal combustion engine. To reduce emission of these pollutants into the atmosphere, research is needed to produce alternative solutions for vehicle transportation. Low temperature polymer electrolyte membrane fuel cells are energy conversion devices that provide an alternative to the internal combustion engine, however, they still have obstacles to overcome to achieve large scale implementation. T he following work presents original research with regards to the development of Nb doped TiO2 as a cathode catalyst support material for low temperature polymer electrolyte membrane fuel cells. The development of a new process to synthesize nanoparticles of Nb doped TiO2 with controlled compositions is presented as well as methods to scale up the process and optimize the synthesis for the aforementioned application. In addition to this, comparison of both electrochemical activity and durability with current state of the art Pt on high surface area carbon black (Vulcan XC-72) is investigated. Effects of the strong metal-support interaction on the electrochemical behavior of these materials is also observed and discussed.

  2. Comparing Cr, and N only doping with (Cr,N)-codoping for enhancing visible light reactivity of TiO2

    SciTech Connect

    Li, Yuan; Wang, Wei; Qiu, Xiaofeng; Meyer III, Harry M; Paranthaman, Mariappan Parans; Eres, Gyula; Zhang, Zhenyu; Gu, Baohua

    2011-01-01

    The photoreactivity of titania (TiO2) nanoclusters with varying levels of N or Cr-doping, or (Cr,N)-codoping, was systematically investigated using photodegradation of methyl orange in aqueous suspensions. The shifting of the TiO2 absorption edge into the visible spectral region that is primarily attributable to band gap narrowing was found to be a reliable metric for estimating the photoreactivity of the doped nanoclusters. Compared to the weak response with undoped and N-doped TiO2, Cr-doping and (Cr, N)-codoping were found to significantly enhance photodegradation of methyl orange under visible light. The initial reaction rates increase from about 0 to above 1.6 10-2 min-1 when the doping concentration of Cr in TiO2 increases from 0 to 5%. In stark contrast, under UV irradiation, doping is not only ineffective but detrimental to the photoreactivity, and all doping including N or Cr only and (Cr, N)-codoping were found to reduce photoreactivity.

  3. Direct view at colossal permittivity in donor-acceptor (Nb, In) co-doped rutile TiO2

    NASA Astrophysics Data System (ADS)

    Mandal, Suman; Pal, Somnath; Kundu, Asish K.; Menon, Krishnakumar S. R.; Hazarika, Abhijit; Rioult, Maxime; Belkhou, Rachid

    2016-08-01

    Topical observations of colossal permittivity (CP) with low dielectric loss in donor-acceptor cations co-doped rutile TiO2 have opened up several possibilities in microelectronics and energy-storage devices. Yet, the precise origin of the CP behavior, knowledge of which is essential to empower the device integration suitably, is highly disputed in the literature. From spectromicroscopic approach besides dielectric measurements, we explore that microscopic electronic inhomogeneities along with the nano-scale phase boundaries and the low temperature polaronic relaxation are mostly responsible for such a dielectric behavior, rather than electron-pinned defect-dipoles/grain-boundary effects as usually proposed. Donor-acceptor co-doping results in a controlled carrier-hopping inevitably influencing the dielectric loss while invariably upholding the CP value.

  4. Photocatalytic enhancement of TiO2 by B and Zr co-doping and modulation of microstructure

    NASA Astrophysics Data System (ADS)

    Fu, Chengxin; Gong, Yinyan; Wu, Yitao; Liu, Jiaqi; Zhang, Zhen; Li, Can; Niu, Lengyuan

    2016-08-01

    Visible-light photodegradation test revealed that B and Zr co-doping can raise the photocatalytic ability of the undoped TiO2 by a fold. XRD crystallography and Raman phonon spectroscopy measurements suggest that the Zr4+ ions replace the Ti4+ ions while the B3+ ions occupy the interstitial sites, expanding the unit-cell volume and reducing crystallite size. The incorporation of interstitial boron dopants creates oxygen vacancies (Ovrad rad) and reduce Ti4+ to Ti3+ to form [Ovrad rad -Ti3+]+, which traps the carriers and prolongs carrier lifetime. Moreover, Zr4+ ions replace Ti4+ ions and form impurity levels, which could improve visible light response. The co-doped samples are benefited from both B interstitials and Zr substitutes.

  5. N incorporation and electronic structure in N-doped TiO2(110) rutile

    SciTech Connect

    Cheung, Sau H.; Nachimuthu, Ponnusamy; Joly, Alan G.; Engelhard, Mark H.; Bowman, Michael K.; Chambers, Scott A.

    2007-02-08

    Epitaxial TiO2-xNx film growth under anion-rich conditions is characterized by nearly balanced incorporation rates for substitutional N (NO) and interstitial Ti (Tii). Tii donors fully compensate and stabilize N3-, but preclude the formation of p-type material. Hybridization occurs between Tii(IV) and NO3-, but the value of x is limited to ~0.02 under these conditions. Tii(IV)-NO3- states occur above the valence band maximum of pure TiO2, riving rise to enhanced optical absorption in the visible up to ~2.5 eV. Much higher NO and Tii concentrations result from using cation-rich conditions.

  6. A First-Principle Study of Synergized O2 Activation and CO Oxidation by Ag Nanoparticles on TiO2(101) Support.

    PubMed

    Jia, Chuanyi; Zhang, Guozhen; Zhong, Wenhui; Jiang, Jun

    2016-04-27

    We performed density functional theory (DFT) calculations to investigate the synergized O2 activation and CO oxidation by Ag8 cluster on TiO2(101) support. The excellent catalytic activity of the interfacial Ag atoms in O2 dissociation is ascribed to the positive polarized charges, upshift of Ag d-band center, and assistance of surface Ti5c atoms. CO oxidation then takes place via a two-step mechanism coupled with O2 dissociation: (i) CO + O2 → CO2 + O and (ii) CO + O → CO2. The synergistic effect of CO and O2 activations reduces the oxidation energy barrier (Ea) of reaction (i), especially for the up-layered Ag atoms not in contact with support. It is found that the coadsorbed CO and O2 on the up-layered Ag atoms form a metal-stable four-center O-O-CO structure motif substantially promoting CO oxidation. On the oxygen defective Ag8/TiO2(101) surface, because of the decreased positive charges and the down-shift of d-band centers in Ag, the metal cluster exhibits low O2 adsorption and activation abilities. Although the dissociation of O2 is facilitated by the TiO2(101) defect sites, the dissociated O atoms would cover the defects so strongly that further CO oxidation would be prohibited unless much extra energy is introduced to recreate oxygen defects. PMID:27049335

  7. Electrodeposited AgInSe2 onto TiO2 films for semiconductor-sensitized solar cell application: The influence of electrodeposited time

    NASA Astrophysics Data System (ADS)

    Chen, Lung-Chuan; Ho, Yi-Ching; Yang, Ru-Yuan; Chen, Jean-Hong; Huang, Chao-Ming

    2012-06-01

    The influence of electrodeposited time (EDT) on Ag-In-Se species growth onto TiO2 films for possible semiconductor-sensitized solar cells (SSSCs) application was investigated. XRD analysis illustrated that the Ag-In-Se film was predominantly comprised by AgInSe2 species with tetragonal body structure and crystal size of 6.05-7.50 nm when EDT was in the region of 15-60 min at a bias of -1.25 V (verse Hg/Hg2SO4 (MSE)). Scanning electron microscope (SEM) indicated a high porosity of AgInSe2/ITO morphology, permitting electrolytes freely percolated through these films. The prepared AgInSe2 films exhibited n-type semiconductor behavior with two band gap energies at 1.27 and 1.80 eV. Photoelectrochemical measurement reflected that open circuit potential varied little with EDT, however, significant change was associated with short circuit current and fill factor (FF), causing the AgInSe2/TiO2 films with EDT of 45 min exhibited the best solar to electricity conversion efficiency of 0.26%. The AgInSe2/TiO2 films with EDT of 45 min demonstrated the longest electron lifetime according to the open circuit voltage decay analysis.

  8. Facile synthesis of hierarchical Ag3PO4/TiO2 nanofiber heterostructures with highly enhanced visible light photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Xie, Jinlei; Yang, Yefeng; He, Haiping; Cheng, Ding; Mao, Minmin; Jiang, Qinxu; Song, Lixin; Xiong, Jie

    2015-11-01

    Heterostructured semiconductor nanostructures have provoked great interest in the areas of energy, environment and catalysis. Herein, we report a novel hierarchical Ag3PO4/TiO2 heterostructure consisting of nearly spherical Ag3PO4 particles firmly coupled on the surface of TiO2 nanofibers (NFs). The construction of Ag3PO4/TiO2 heterostructure with tailored morphologies, compositions and optical properties was simply achieved via a facile and green synthetic strategy involving the electrospinning and solution-based processes. Owing to the synergetic effects of the components, the resulting hybrid heterostructures exhibited much improved visible light photocatalytic performance, which could degrade the RhB dye completely in 7.5 min. In addition, the coupling of Ag3PO4 particles with UV-light-sensitive TiO2 NFs enabled full utilization of solar energy and less consumption of noble metals, significantly appealing for their practical use in new energy sources and environmental issues. The developed synthetic strategy was considered to be applicable for the rational design and construction of other heterostructured catalysts.

  9. Antibacterial property of Ag nanoparticle-impregnated N-doped titania films under visible light

    NASA Astrophysics Data System (ADS)

    Wong, Ming-Show; Chen, Chun-Wei; Hsieh, Chia-Chun; Hung, Shih-Che; Sun, Der-Shan; Chang, Hsin-Hou

    2015-07-01

    Photocatalysts produce free radicals upon receiving light energy; thus, they possess antibacterial properties. Silver (Ag) is an antibacterial material that disrupts bacterial physiology. Our previous study reported that the high antibacterial property of silver nanoparticles on the surfaces of visible light-responsive nitrogen-doped TiO2 photocatalysts [TiO2(N)] could be further enhanced by visible light illumination. However, the major limitation of this Ag-TiO2 composite material is its durability; the antibacterial property decreased markedly after repeated use. To overcome this limitation, we developed TiO2(N)/Ag/TiO2(N) sandwich films in which the silver is embedded between two TiO2(N) layers. Various characteristics, including silver and nitrogen amounts, were examined in the composite materials. Various analyses, including electron microscopy, energy dispersive spectroscopy, X-ray diffraction, and ultraviolet-visible absorption spectrum and methylene blue degradation rate analyses, were performed. The antibacterial properties of the composite materials were investigated. Here we revealed that the antibacterial durability of these thin films is substantially improved in both the dark and visible light, by which bacteria, such as Escherichia coli, Streptococcus pyogenes, Staphylococcus aureus, and Acinetobacter baumannii, could be efficiently eliminated. This study demonstrated a feasible approach to improve the visible-light responsiveness and durability of antibacterial materials that contain silver nanoparticles impregnated in TiO2(N) films.

  10. Antibacterial property of Ag nanoparticle-impregnated N-doped titania films under visible light

    PubMed Central

    Wong, Ming-Show; Chen, Chun-Wei; Hsieh, Chia-Chun; Hung, Shih-Che; Sun, Der-Shan; Chang, Hsin-Hou

    2015-01-01

    Photocatalysts produce free radicals upon receiving light energy; thus, they possess antibacterial properties. Silver (Ag) is an antibacterial material that disrupts bacterial physiology. Our previous study reported that the high antibacterial property of silver nanoparticles on the surfaces of visible light-responsive nitrogen-doped TiO2 photocatalysts [TiO2(N)] could be further enhanced by visible light illumination. However, the major limitation of this Ag-TiO2 composite material is its durability; the antibacterial property decreased markedly after repeated use. To overcome this limitation, we developed TiO2(N)/Ag/TiO2(N) sandwich films in which the silver is embedded between two TiO2(N) layers. Various characteristics, including silver and nitrogen amounts, were examined in the composite materials. Various analyses, including electron microscopy, energy dispersive spectroscopy, X-ray diffraction, and ultraviolet–visible absorption spectrum and methylene blue degradation rate analyses, were performed. The antibacterial properties of the composite materials were investigated. Here we revealed that the antibacterial durability of these thin films is substantially improved in both the dark and visible light, by which bacteria, such as Escherichia coli, Streptococcus pyogenes, Staphylococcus aureus, and Acinetobacter baumannii, could be efficiently eliminated. This study demonstrated a feasible approach to improve the visible-light responsiveness and durability of antibacterial materials that contain silver nanoparticles impregnated in TiO2(N) films. PMID:26156001

  11. Antibacterial property of Ag nanoparticle-impregnated N-doped titania films under visible light.

    PubMed

    Wong, Ming-Show; Chen, Chun-Wei; Hsieh, Chia-Chun; Hung, Shih-Che; Sun, Der-Shan; Chang, Hsin-Hou

    2015-07-09

    Photocatalysts produce free radicals upon receiving light energy; thus, they possess antibacterial properties. Silver (Ag) is an antibacterial material that disrupts bacterial physiology. Our previous study reported that the high antibacterial property of silver nanoparticles on the surfaces of visible light-responsive nitrogen-doped TiO2 photocatalysts [TiO2(N)] could be further enhanced by visible light illumination. However, the major limitation of this Ag-TiO2 composite material is its durability; the antibacterial property decreased markedly after repeated use. To overcome this limitation, we developed TiO2(N)/Ag/TiO2(N) sandwich films in which the silver is embedded between two TiO2(N) layers. Various characteristics, including silver and nitrogen amounts, were examined in the composite materials. Various analyses, including electron microscopy, energy dispersive spectroscopy, X-ray diffraction, and ultraviolet-visible absorption spectrum and methylene blue degradation rate analyses, were performed. The antibacterial properties of the composite materials were investigated. Here we revealed that the antibacterial durability of these thin films is substantially improved in both the dark and visible light, by which bacteria, such as Escherichia coli, Streptococcus pyogenes, Staphylococcus aureus, and Acinetobacter baumannii, could be efficiently eliminated. This study demonstrated a feasible approach to improve the visible-light responsiveness and durability of antibacterial materials that contain silver nanoparticles impregnated in TiO2(N) films.

  12. Controllable growth of vertically aligned Bi-doped TiO2 nanorod arrays for all-oxide solid-state DSSCs

    NASA Astrophysics Data System (ADS)

    Asemi, Morteza; Ghanaatshoar, Majid

    2016-09-01

    In this study, vertically aligned Bi-doped TiO2 nanorod arrays as photoanodes were successfully grown on the fluorine-doped tin oxide by hydrothermal method. Structural analysis showed that bismuth was successfully incorporated into the TiO2 lattice at low concentration, but at higher concentration, phase segregation of Bi2O3 in the TiO2 matrix was occurred. TiO2 nanorods with 3 % bismuth concentration had minimum electrical resistivity. As the solid-state electrolyte, Mg-doped CuCrO2 nanoparticles with p-type conductivity were synthesized by sol-gel method. The fabricated all-oxide solid-state dye-sensitized solar cells with Bi-doped TiO2 nanorods displayed better photovoltaic performance due to the presence of Bi. The improved cell performance was correlated with the higher dye loading, slower charge recombination rate and the higher electrical conductivity of the photoanodes. After mechanical pressing, the all-oxide solid-state DSSC exhibited enhanced photovoltaic performance due to the formation of the large neck between adjacent nanoparticles by mechanical sintering. The open-circuit photovoltage decay measurement of the devices and electrical conductivity of the nanoparticles before and after pressing revealed that the mechanical pressing technique reduces charge recombination rate and facilitates electron transport through the interconnected nanoparticles.

  13. Ultrasonic-assisted sol-gel synthesis of samarium, cerium co-doped TiO2 nanoparticles with enhanced sonocatalytic efficiency.

    PubMed

    Eskandarloo, Hamed; Badiei, Alireza; Behnajady, Mohammad A; Ziarani, Ghodsi Mohammadi

    2015-09-01

    In this work, pure TiO2 and samarium, cerium mono-doped and co-doped TiO2 catalysts were synthesized by an ultrasonic-assisted sol-gel method and their sonocatalytic efficiency studied toward removal of Methyl Orange as a model organic pollutant from the textile industry. The relationship of structure and sonocatalytic performance of catalysts was established by using various techniques, such as XRD, TEM, SEM, EDX, DRS, and PL. A comparison on the removal efficiency of sonolysis alone and sonocatalytic processes was performed. The results showed that the samarium, cerium co-doped TiO2 catalyst with narrower band gap energy and smaller particle size leads to a rapid removal of pollutant. It was believed that Sm(3+) and Ce(4+) ions can serve as superficial trapping for electrons at conduction band of TiO2 and prolonged the lifetime of electron-hole pairs. Finally, the effect of synthesis and operational variables on the sonocatalytic activity of co-doped TiO2 catalyst was studied and optimized using response surface methodology as a statistical technique. The results showed that the maximum removal efficiency (96.33%) was achieved at the optimum conditions: samarium content of 0.6 wt%, cerium content of 0.82 wt%, initial pollutant concentration of 4.31 mg L(-1), catalyst dosage of 0.84 mg L(-1), ultrasonic irradiation power of 700 W, and irradiation time of 50 min.

  14. Promotional effect of Si-doped V2O5/TiO2 for selective catalytic reduction of NOx by NH3.

    PubMed

    Pan, Yanxiao; Zhao, Wei; Zhong, Qin; Cai, Wei; Li, Hongyu

    2013-08-01

    TiO2 supports doped with different amounts of Si were prepared by a sol-gel method, and 1 wt% vanadia (V2O5) loaded on Si-doped TiO2 was obtained by an impregnation method. The mole ratio of Si/Ti was 0.2, NOx conversion exceeds 94% at 300 degrees C and GHSV of 41,324 hr(-1), which is about 20% higher than pure V2O5/TiO2. The catalysts were characterized by XRD, BET, TEM, FT-IR, NH3-TPD, XPS, H2-TPR, Raman and in situ DRIFTS. The results of FT-IR and XPS indicated that Si was doped into the TiO2 lattice successfully and a solid solution was obtained. V2O5 active component could be dispersed well on the support with the increasing of surface area of the catalyst, which was confirmed by Raman and XRD results. Above all, the numbers of acid sites (especially the Brønsted-acid) and oxidation properties were enhanced for Si-doped V2O5/TiO2 catalysts, which improved the deNOx catalytic activity.

  15. Efficient removal of herbicide 2,4-dichlorophenoxyacetic acid from water using Ag/reduced graphene oxide co-decorated TiO2 nanotube arrays.

    PubMed

    Tang, Yanhong; Luo, Shenglian; Teng, Yarong; Liu, Chengbin; Xu, Xiangli; Zhang, Xilin; Chen, Liang

    2012-11-30

    A new photocatalyst, Ag nanoparticles (NPs) and reduced graphene oxide (RGO) co-decorated TiO(2) nanotube arrays (NTs) (Ag/RGO-TiO(2) NTs), was designed and facilely produced by combining electrodeposition and photoreduction processes. The structures and properties of the photocatalysts were characterized. The ternary catalyst exhibited almost 100% photocatalytic removal efficiency of typical herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) from water under simulated solar light irradiation. The photodegradation rate toward 2,4-D over Ag/RGO-TiO(2) NTs is 11.3 times that over bare TiO(2) NTs. After 10 successive cycles with 1600 min of irradiation, Ag/RGO-TiO(2) NTs maintained as high 2,4-D removal efficiency as 97.3% with excellent stability and easy recovery, which justifies the photocatalytic system a promising application for herbicide removal from water. PMID:23062512

  16. Efficient removal of herbicide 2,4-dichlorophenoxyacetic acid from water using Ag/reduced graphene oxide co-decorated TiO2 nanotube arrays.

    PubMed

    Tang, Yanhong; Luo, Shenglian; Teng, Yarong; Liu, Chengbin; Xu, Xiangli; Zhang, Xilin; Chen, Liang

    2012-11-30

    A new photocatalyst, Ag nanoparticles (NPs) and reduced graphene oxide (RGO) co-decorated TiO(2) nanotube arrays (NTs) (Ag/RGO-TiO(2) NTs), was designed and facilely produced by combining electrodeposition and photoreduction processes. The structures and properties of the photocatalysts were characterized. The ternary catalyst exhibited almost 100% photocatalytic removal efficiency of typical herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) from water under simulated solar light irradiation. The photodegradation rate toward 2,4-D over Ag/RGO-TiO(2) NTs is 11.3 times that over bare TiO(2) NTs. After 10 successive cycles with 1600 min of irradiation, Ag/RGO-TiO(2) NTs maintained as high 2,4-D removal efficiency as 97.3% with excellent stability and easy recovery, which justifies the photocatalytic system a promising application for herbicide removal from water.

  17. High visible light photocatalytic property of Co2+-doped TiO2 nanoparticles with mixed phases

    NASA Astrophysics Data System (ADS)

    Zhao, Cong; Shu, Xin; Zhu, Da-chuan; Wei, Shang-hai; Wang, Yu-xin; Tu, Ming-jing; Gao, Wei

    2015-12-01

    Mixed phases Co2+-doped TiO2 nanoparticles have been prepared by a novel method combined with sol-gel and hydrothermal methods. The section of sol-gel method, sol, provides an unstable colloidal reaction system for the next reaction process. The hydrothermal method is to treat the above reaction system to prepare undoped and doped samples. The as-prepared samples have been characterized by XRD, SEM, TEM, HRTEM and UV-vis spectroscopy. The results show that the as-prepared samples contain three titania polymorphs: brookite, rutile and anatase phases. These titania polymorphs probably form polymorph-junctions that can extend the lifetime of photogenerated electron-hole pairs. The photocatalytic activity has been evaluated by the photocatalytic degradation of Rhodamine B in air under visible-light irradiation. The degradation results indicate that the photocatalytic activity of as-prepared samples is higher than that of Degussa P25, especially the doped sample. This is ascribed to the fact that the phases with smaller band gap can enhance visible-light photocatalytic activity, the polymorph-junctions effectively extend the photoelectron lifetime and the nano size effect and Co-doping induce the shift of the absorption edge into the visible-light region. Furthermore, the XRD, SEM, and TEM data indicate that Co2+-doping results in the decrease of particle size.

  18. Synthesis and spectroscopic characterization of nanoparticles of TiO2 doped with Pt produced via the self-combustion route

    NASA Astrophysics Data System (ADS)

    Lopera, A. A.; Chavarriaga, E. A.; Estupiñan, H. A.; Valencia, I. C.; Paucar, C.; Garcia, C. P.

    2016-05-01

    Titanium oxide (TiO2) is the most important semiconductor used in photocatalysis. For that reason, most recent scientific studies have focused on improving the absorbance of this material in the visible region. In this paper, we report on the production of nanopowders of TiO2 doped with platinum via the solution combustion synthesis method, using glycine as a fuel at concentrations of 0.3, 0.6, 0.9, and 1.2% w/w of Pt with respect to TiO2 (Pt / TiO2), in order to study the influence of the dopant content on the absorbance spectrum in the visible region. The structure of the samples was characterized using x-ray diffraction and Raman spectroscopy, which confirmed the production of a pure anatase phase. VIS diffuse reflectance spectroscopy confirmed that in the visible region the samples doped with Pt absorb within the range of 400 nm to 800 nm. Field emission scanning electron microscopy and transmission electron microscopy showed the formation of TiO2 nanoparticles with an average size of 13 nm and with spherical morphology. Colorimetry (Commission Internationale de l’Eclairage L *, a *, b *) confirmed photocatalytic activity for the degradation of rhodamine B using visible light. It was concluded that the route of synthesis and the Pt content play important roles in the absorbance spectrum and the activation energy of TiO2.

  19. Sonophotocatalytic degradation of dye C.I. Acid Orange 7 by TiO2 and Ag nanoparticles immobilized on corona pretreated polypropylene non-woven fabric.

    PubMed

    Marković, Darka; Šaponjić, Zoran; Radoičić, Marija; Radetić, Tamara; Vodnik, Vesna; Potkonjak, Branislav; Radetić, Maja

    2015-05-01

    This study discusses the possibility of using corona pre-treated polypropylene (PP) non-woven fabric as a support for immobilization of colloidal TiO2 and Ag nanoparticles in order to remove dye C.I. Acid Orange 7 from aqueous solution. Dye removal efficiency by sonocatalysis, photocatalysis and sonophotocatalysis was evaluated on corona pre-treated fabric loaded with TiO2 nanoparticles, corona pre-treated fabric double loaded with TiO2 nanoparticles and corona pre-treated fabrics loaded with TiO2 nanoparticles before and after deposition of Ag nanoparticles. In addition, the stability of PP non-woven fabric during these processes was investigated. The substrates were characterized by SEM, EDX and AAS analyses. The change of the dye concentration was evaluated by UV-VIS spectrophotometry. Unlike sonocatalysis and photocatalysis, complete dye removal from both solution and non-woven fabric was obtained already after 240-270 min of sonophotocatalysis. Corona pre-treated PP non-woven fabric loaded with Ag nanoparticles prior to deposition of TiO2 nanoparticles provided excellent degradation efficiency and superior reusability. Sonophotocatalytic degradation of dye in the presence of all investigated samples was the most prominent in acidic conditions. Although this nanocomposite system ensured fast discoloration of dye solution, TOC values of water measured after sonophotocatalysis were not satisfactory because of PP degradation. Therefore, it is suggested to include TOC evaluation in each case study where different supports for TiO2 nanoparticles are used since these nanoparticles may guarantee the dye removal from solution but the stability of support could be problematic causing even more serious environmental impact.

  20. Multiscale anode materials in lithium ion batteries by combining micro- with nanoparticles: design of mesoporous TiO2 microfibers@nitrogen doped carbon composites

    NASA Astrophysics Data System (ADS)

    Cheng, Wei; Rechberger, Felix; Primc, Darinka; Niederberger, Markus

    2015-08-01

    TiO2 has been considered as a promising anode material for lithium ion batteries. However, its poor rate capability originating from the intrinsically low lithium ion diffusivity and its poor electronic conductivity hampers putting such an application into practice. Both issues can be addressed by nanostructure engineering and conductive surface coating. Herein, we report a template-assisted synthesis of micron sized TiO2 fibers consisting of a mesoporous network of anatase nanoparticles of about 7.5 nm and coated by N doped carbon. In a first step, an amorphous layer of TiO2 was deposited on cobalt silicate nanobelts and subsequently transformed into crystalline anatase nanoparticles by hydrothermal treatment. The N doped carbon coating was realized by in situ polymerization of dopamine on the crystalline TiO2 followed by annealing under N2. After removal of the template, we obtained the final mesoporous TiO2 fibers@N doped carbon composite. Electrochemical tests revealed that the composite electrode exhibited excellent electrochemical properties in terms of specific capacity, rate performance and long term stability.TiO2 has been considered as a promising anode material for lithium ion batteries. However, its poor rate capability originating from the intrinsically low lithium ion diffusivity and its poor electronic conductivity hampers putting such an application into practice. Both issues can be addressed by nanostructure engineering and conductive surface coating. Herein, we report a template-assisted synthesis of micron sized TiO2 fibers consisting of a mesoporous network of anatase nanoparticles of about 7.5 nm and coated by N doped carbon. In a first step, an amorphous layer of TiO2 was deposited on cobalt silicate nanobelts and subsequently transformed into crystalline anatase nanoparticles by hydrothermal treatment. The N doped carbon coating was realized by in situ polymerization of dopamine on the crystalline TiO2 followed by annealing under N2. After

  1. In vitro degradation, cytocompatibility and hemolysis tests of CaF2 doped TiO2-SiO2 composite coating on AZ31 alloy

    NASA Astrophysics Data System (ADS)

    Li, Bing; Chen, Yun; Huang, Wei; Yang, Wenzhong; Yin, Xiaoshuang; Liu, Ying

    2016-09-01

    In this study, a CaF2 doped TiO2-SiO2 composite coating was successfully coated onto AZ31 alloy by sol-gel method. Electrochemical tests, in vitro degradation, direct cellular experiment and hemolysis tests were conducted and the results showed that the CaF2 doped TiO2-SiO2 composite coating can not only improve the corrosion resistance, but also enhance the biocompatibility of AZ31 alloy. XRD, SEM and EDX were also performed to characterize the crystalline structures, morphologies and chemical compositions of the coatings.

  2. Dual-Wavelength Irradiation and Dox Delivery for -Cancer Cell Ablation with Photocatalytic Pr Doped TiO2 /NGO -Hybrid Nanocomposite.

    PubMed

    Jang, Hongje; Choi, Myung-Ho; Yim, Yeajee; Kim, Young-Kwan; Min, Dal-Hee

    2015-08-26

    Herein, hybrid nanocomposite of praseodymium doped TiO2 nanocrystals and graphene oxide nanosheets are prepared by facile hydrothermal treatment. As-synthesized Pr-TiO2 /NGO hybrid nanocomposite exhibits enhanced photocatalytic activity under visible light irradiation by the intact graphene oxide and doped lanthanide mediated band gap narrowing compared to TiO2 . Moreover, high payload and controlled release of doxorubicin by charge reversal of hybrid nanocomposite at endosomal pH and near-infrared irradiation mediated efficient photothermal conversion provide highly favorable features in therapeutic applications. Through the combination of these three distinctive therapeutic modalities, highly efficient trimodal cancer cell ablation is demonstrated. PMID:26085286

  3. A novel ethanol gas sensor based on TiO2/Ag0.35V2O5 branched nanoheterostructures

    NASA Astrophysics Data System (ADS)

    Wang, Yuan; Liu, Lixin; Meng, Chuanmin; Zhou, Yun; Gao, Zhao; Li, Xuhai; Cao, Xiuxia; Xu, Liang; Zhu, Wenjun

    2016-09-01

    Much greater surface-to-volume ratio of hierarchical nanostructures renders them attract considerable interest as prototypical gas sensors. In this work, a novel resistive gas sensor based on TiO2/Ag0.35V2O5 branched nanoheterostructures is fabricated by a facile one-step synthetic process and the ethanol sensing performance of this device is characterized systematically, which shows faster response/recovery behavior, better selectivity, and higher sensitivity of about 9 times as compared to the pure TiO2 nanofibers. The enhanced sensitivity of the TiO2/Ag0.35V2O5 branched nanoheterostructures should be attributed to the extraordinary branched hierarchical structures and TiO2/Ag0.35V2O5 heterojunctions, which can eventually result in an obvious change of resistance upon ethanol exposure. This study not only indicates the gas sensing mechanism for performance enhancement of branched nanoheterostructures, but also proposes a rational approach to design nanostructure based chemical sensors with desirable performance.

  4. A novel ethanol gas sensor based on TiO2/Ag0.35V2O5 branched nanoheterostructures.

    PubMed

    Wang, Yuan; Liu, Lixin; Meng, Chuanmin; Zhou, Yun; Gao, Zhao; Li, Xuhai; Cao, Xiuxia; Xu, Liang; Zhu, Wenjun

    2016-01-01

    Much greater surface-to-volume ratio of hierarchical nanostructures renders them attract considerable interest as prototypical gas sensors. In this work, a novel resistive gas sensor based on TiO2/Ag0.35V2O5 branched nanoheterostructures is fabricated by a facile one-step synthetic process and the ethanol sensing performance of this device is characterized systematically, which shows faster response/recovery behavior, better selectivity, and higher sensitivity of about 9 times as compared to the pure TiO2 nanofibers. The enhanced sensitivity of the TiO2/Ag0.35V2O5 branched nanoheterostructures should be attributed to the extraordinary branched hierarchical structures and TiO2/Ag0.35V2O5 heterojunctions, which can eventually result in an obvious change of resistance upon ethanol exposure. This study not only indicates the gas sensing mechanism for performance enhancement of branched nanoheterostructures, but also proposes a rational approach to design nanostructure based chemical sensors with desirable performance. PMID:27615429

  5. A novel ethanol gas sensor based on TiO2/Ag0.35V2O5 branched nanoheterostructures

    PubMed Central

    Wang, Yuan; Liu, Lixin; Meng, Chuanmin; Zhou, Yun; Gao, Zhao; Li, Xuhai; Cao, Xiuxia; Xu, Liang; Zhu, Wenjun

    2016-01-01

    Much greater surface-to-volume ratio of hierarchical nanostructures renders them attract considerable interest as prototypical gas sensors. In this work, a novel resistive gas sensor based on TiO2/Ag0.35V2O5 branched nanoheterostructures is fabricated by a facile one-step synthetic process and the ethanol sensing performance of this device is characterized systematically, which shows faster response/recovery behavior, better selectivity, and higher sensitivity of about 9 times as compared to the pure TiO2 nanofibers. The enhanced sensitivity of the TiO2/Ag0.35V2O5 branched nanoheterostructures should be attributed to the extraordinary branched hierarchical structures and TiO2/Ag0.35V2O5 heterojunctions, which can eventually result in an obvious change of resistance upon ethanol exposure. This study not only indicates the gas sensing mechanism for performance enhancement of branched nanoheterostructures, but also proposes a rational approach to design nanostructure based chemical sensors with desirable performance. PMID:27615429

  6. Ab initio studies of Nb-N-S tri-doped TiO2 with enhanced visible light photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Ren, Dahua; Cheng, Junxia; Cheng, Xinlu

    2016-06-01

    The electronic and optical properties of Nb-N-S tri-doped anatase TiO2 were investigated within the frame of the density functional theory (DFT) plus U method. Results show that a significant red-shift effect and improvement of visible-light absorption for Nb-N-S tri-doped TiO2 are observed with respect to pure TiO2 and S-N codoped TiO2. At the same time, the enhanced visible-light photocatalytic activity of tri-doped TiO2 is derived from the narrowing band gap, the appearance of Nb 4d state at the bottom of conduction band and the mixture of N 2p, S 3p states forming new defect levels at the top of valance band, which is excellently consistent with the previous experiment. Moreover, S ion leads to the lattice distortion and promotes the visible-light photocatalytic activity. Furthermore, the absorbance of 1.39NbNS-TiO2 accords well with the experimental result in the visible region. It is also found that the 2.78NbNS-TiO2 can be easily grown under O-rich condition and have the strongest absorbance from 2.0 to 4.2 eV among four models.

  7. Multiscale anode materials in lithium ion batteries by combining micro- with nanoparticles: design of mesoporous TiO2 microfibers@nitrogen doped carbon composites.

    PubMed

    Cheng, Wei; Rechberger, Felix; Primc, Darinka; Niederberger, Markus

    2015-09-01

    TiO2 has been considered as a promising anode material for lithium ion batteries. However, its poor rate capability originating from the intrinsically low lithium ion diffusivity and its poor electronic conductivity hampers putting such an application into practice. Both issues can be addressed by nanostructure engineering and conductive surface coating. Herein, we report a template-assisted synthesis of micron sized TiO2 fibers consisting of a mesoporous network of anatase nanoparticles of about 7.5 nm and coated by N doped carbon. In a first step, an amorphous layer of TiO2 was deposited on cobalt silicate nanobelts and subsequently transformed into crystalline anatase nanoparticles by hydrothermal treatment. The N doped carbon coating was realized by in situ polymerization of dopamine on the crystalline TiO2 followed by annealing under N2. After removal of the template, we obtained the final mesoporous TiO2 fibers@N doped carbon composite. Electrochemical tests revealed that the composite electrode exhibited excellent electrochemical properties in terms of specific capacity, rate performance and long term stability.

  8. Preparation of Carbon-Doped TiO2 and Its Application as a Photoelectrodes in Dye-Sensitized Solar Cells.

    PubMed

    Park, Su Kyung; Jeong, Jin Seong; Yun, Tae Kwan; Bae, Jae Young

    2015-02-01

    In this study, C-doped TiO2 particles were successfully synthesized by a hydrothermal method. Three binding energy peaks were observed at 284.6, 286.2, and 288.5 eV in the C is region of the XPS. The signals at 286.2 and 288.5 eV were attributed to chemically bound C-O and Ti-C-O linkages within the crystalline TiO2 lattice, respectively. The introduction of carbon did not affect the crystallite structure or BET surface area of TiO2. The JSC value of DSSCs based on a C-doped TiO2 electrode was increased by 20% compared to DSSCs using a pure TiO2 electrode, and the energy conversion efficiency was increased by 23%. This was due to the enhancement of dye adsorption and high electrical conductivity of the carbon. High energy conversion efficiency was achieved with the DSSCs based on the C-doped TiC2 electrode.

  9. Removal of toluene from water by photocatalytic oxidation with activated carbon supported Fe(3+)-doped TiO2 nanotubes.

    PubMed

    Yuan, Rongfang; Zhou, Beihai; Ma, Li

    2014-01-01

    In this work, activated carbon (AC)-supported TiO2 containing 1.0% (mass percent) of 1.0 at.% (atomic percent) Fe(3+)-doped TiO2 nanotubes (Fe-TNTs) were successfully synthesized. The catalyst was used to effectively decompose toluene in water under O3/UV conditions, and some properties including the morphology, X-ray photoelectron spectroscopy, X-ray diffraction patterns, specific surface area and UV-visible diffuse reflectance spectroscopy were analyzed. A removal efficiency of 90.7% was achieved in the presence of fresh AC-supported Fe-TNTs calcined at 550 °C, with a pseudo-first-order rate constant of 0.038/min. The removal efficiency of toluene was reduced when the catalysts were repeatedly used, since the amount of adsorption sites of the supporting substrates decreased. However, even after AC-supported catalyst was used four times, the removal efficiency of toluene was still sufficient in water treatment. The enhanced photocatalytic activity of AC-supported Fe-TNTs was related to the synergistic effect of AC adsorption and Fe-TNTs photocatalytic ozonation. The water from a petrochemical company in China was used to obtain the removal efficiency of the pollutants, and the toluene and total organic carbon removal efficiencies were 69.9% and 58.3%, respectively.

  10. Enhanced photocatalytic degradation of humic acids using Al and Fe co-doped TiO2 nanotubes under UV/ozonation for drinking water purification.

    PubMed

    Yuan, Rongfang; Zhou, Beihai; Hua, Duo; Shi, Chunhong

    2013-11-15

    O3/UV/TiO2 was used to effectively decompose humic acids (HAs) in drinking water. To obtain a large specific surface area and low band gap energy, Al and Fe co-doped TiO2 nanotubes were successfully synthesized using the hydrothermal method. The effect of the optimal co-doped TiO2 nanotubes catalyst on the HAs removal efficiency through O3/UV/co-doped TiO2 process was investigated. The highest HAs removal efficiency (79.4%) that exhibited a pseudo-first-order rate constant of 0.172 min(-1) was achieved, in the presence of 550 °C calcined 1.0% co-doped TiO2 nanotubes with an Al:Fe ratio of 0.25:0.75. The effects of calcination temperature and doping concentration on anatase phase weight fractions, average crystallite sizes, Brunauer-Emmett-Teller surface area, catalyst band gap energy, and catalyst photocatalytic activity were also discussed. The inorganic anions also affected the catalyst photocatalytic ability. In a neutral solution, SO4(2-) slightly promoted HAs removal. However, HCO3(-) was found to significantly inhibit the catalyst activity, whereas Cl(-) had negligible effect on photocatalytic ability.

  11. Effect of Cu2O Doping in TiO2 Films on Device Performance of Dye-Sensitized Solar Cells

    NASA Astrophysics Data System (ADS)

    Koo, Horng-Show; Wang, Der-Tsuey; Yu, Yi-Kuei; Ho, Shao-Hung; Jhang, Jia-Yu; Chen, Mi; Tai, Ming-Fong

    2012-10-01

    We demonstrated the effects of Cu2O doping at various weight ratios in TiO2 photoanode films on the photovoltaic performance of dye-sensitized solar cells (DSSCs). The photovoltaic characteristics, namely, open-circuit voltage, short-circuit current, fill factor, and energy conversion efficiency, of DSSCs with 0.3 wt % Cu2O doping in the photoanode are 690 mV, 4.55 mA/cm2, 52.0%, and 1.96%, respectively. The photovoltaic parameters of the sample with 0.3 wt % Cu2O doping are better than those of other Cu2O-doped samples, which are inferior to undoped TiO2-based DSSCs. The measured cell performance shows that the addition of Cu2O to the TiO2 photoanode in DSSCs results in the reduction of photovoltaic parameters. The degradation mechanism upon Cu2O doping in the TiO2 photoanode of DSSCs may be attributed to the variations in the valence numbers of copper and titanium ions during calcination and the reduction-oxidation reaction, resulting in the formation of oxygen vacancy-Ti+3 defects and related recombination centers.

  12. Joint Effects of Photoactive TiO2 and Fluoride-Doping on SnO2 Inverse Opal Nanoarchitecture for Solar Water Splitting.

    PubMed

    Gun, Yun; Song, Gwang Yeom; Quy, Vu Hong Vinh; Heo, Jaeyeong; Lee, Hyunjung; Ahn, Kwang-Soon; Kang, Soon Hyung

    2015-09-16

    Inverse opal (IO) films of tin dioxide (SnO2) were fabricated on polystyrene (PS) beads (diameter=350 nm (±20 nm) with a spin coating method. To compensate for the large band gap (Eg=3.8 eV), a thin TiO2 shell was deposited on the SnO2-IO films with atomic layer deposition (ALD), which produced shells with thicknesses of 10-40 nm. The morphological changes and crystalline properties of the SnO2 and TiO2-coated SnO2 (herein after referred to as TiO2/SnO2) IO films were investigated with field-emission scanning electron microscopy and X-ray diffraction, respectively. The photoelectrochemical (PEC) behavior of the samples was tested in a 0.1 M KOH solution under 1 sun illumination (100 mW/cm2 with an AM 1.5 filter). The highest PEC performance was obtained with the TiO2(10 nm)/SnO2 IO films, which produced a photocurrent density (Jsc) of 4.67 mA/cm2 at 0.5 V (vs NHE) and was sequentially followed by the TiO2(20 nm)/SnO2-IO, TiO2(30 nm)/SnO2-IO, TiO2 (40 nm)/SnO2-IO and SnO2 IO films. Overall, the thin TiO2 shell covered on the SnO2-IO core enhanced Jsc by 3 orders of magnitude, which in turn the PEC activity. This is mainly ascribed to the extremely low charge-transfer resistance (Rct) in the photoelectrode/electrolyte and at the TiO2/SnO2 interface, as well as the contribution of the photoactive TiO2 layer, which has an Eg of 3.2 eV. Moreover, to improve the electrical conductivity of the core SnO2 IO film, the films were doped with 10 mol % of F. The F- doped films were labeled as the FTO IO film. The Rct of the FTO-IO films decreased because of the improved electronic conductivity, enhancing the PEC performance of the TiO2(10 nm)/FTO-IO films by approximately 20%. The core-shell nanowire mesh nanoarchitecture is therefore suggested to provide an insight for designing the peculiar structure based on the material's properties and the engineering of their band gap energy for highly efficient PEC performance. PMID:26322646

  13. Joint Effects of Photoactive TiO2 and Fluoride-Doping on SnO2 Inverse Opal Nanoarchitecture for Solar Water Splitting.

    PubMed

    Gun, Yun; Song, Gwang Yeom; Quy, Vu Hong Vinh; Heo, Jaeyeong; Lee, Hyunjung; Ahn, Kwang-Soon; Kang, Soon Hyung

    2015-09-16

    Inverse opal (IO) films of tin dioxide (SnO2) were fabricated on polystyrene (PS) beads (diameter=350 nm (±20 nm) with a spin coating method. To compensate for the large band gap (Eg=3.8 eV), a thin TiO2 shell was deposited on the SnO2-IO films with atomic layer deposition (ALD), which produced shells with thicknesses of 10-40 nm. The morphological changes and crystalline properties of the SnO2 and TiO2-coated SnO2 (herein after referred to as TiO2/SnO2) IO films were investigated with field-emission scanning electron microscopy and X-ray diffraction, respectively. The photoelectrochemical (PEC) behavior of the samples was tested in a 0.1 M KOH solution under 1 sun illumination (100 mW/cm2 with an AM 1.5 filter). The highest PEC performance was obtained with the TiO2(10 nm)/SnO2 IO films, which produced a photocurrent density (Jsc) of 4.67 mA/cm2 at 0.5 V (vs NHE) and was sequentially followed by the TiO2(20 nm)/SnO2-IO, TiO2(30 nm)/SnO2-IO, TiO2 (40 nm)/SnO2-IO and SnO2 IO films. Overall, the thin TiO2 shell covered on the SnO2-IO core enhanced Jsc by 3 orders of magnitude, which in turn the PEC activity. This is mainly ascribed to the extremely low charge-transfer resistance (Rct) in the photoelectrode/electrolyte and at the TiO2/SnO2 interface, as well as the contribution of the photoactive TiO2 layer, which has an Eg of 3.2 eV. Moreover, to improve the electrical conductivity of the core SnO2 IO film, the films were doped with 10 mol % of F. The F- doped films were labeled as the FTO IO film. The Rct of the FTO-IO films decreased because of the improved electronic conductivity, enhancing the PEC performance of the TiO2(10 nm)/FTO-IO films by approximately 20%. The core-shell nanowire mesh nanoarchitecture is therefore suggested to provide an insight for designing the peculiar structure based on the material's properties and the engineering of their band gap energy for highly efficient PEC performance.

  14. Role of Ag2S coupling on enhancing the visible-light-induced catalytic property of TiO2 nanorod arrays

    PubMed Central

    Li, Zhengcao; Xiong, Shan; Wang, Guojing; Xie, Zheng; Zhang, Zhengjun

    2016-01-01

    In order to obtain a better photocatalytic performance under visible light, Ag2S-coupled TiO2 nanorod arrays (NRAs) were prepared through the electron beam deposition with glancing angle deposition (GLAD) technique, annealing in air, followed by the successive ionic layer absorption and reaction (SILAR) method. The properties of the photoelectrochemical and photocatalytic degradation of methyl orange (MO) were thus conducted. The presence of Ag2S on TiO2 NRAs was observed to have a significant improvement on the response to visible light. It’s resulted from that Ag2S coupling can improve the short circuit photocurrent density and enhance the photocatalytic activity remarkably. PMID:26790759

  15. Annealing effects on structure and magnetic properties of Mn-doped TiO2

    NASA Astrophysics Data System (ADS)

    Ahmed, S. A.

    2016-03-01

    Ti1-xMnxO2 powder samples with nominal manganese concentration x=0.02 were synthesized by a solid state reaction route. Thermal treatment of the samples was carried out in air at temperatures of 500, 600 and 700 °C. The samples were investigated by x-ray diffraction, photoluminescence and magnetization measurements. Photoluminescence studies indicated presence of oxygen vacancy defects in TiO2 lattice. Room temperature M-H loops showed a ferromagnetic behavior for all Ti1-xMnxO2 samples, and the magnetization of samples decreases with increasing annealing temperature. Temperature-dependent magnetization measurements showed evidence for ordering temperature of >420 K. However, the experimental results indicate that the ferromagnetism observed in Ti1-xMnxO2 samples is intrinsic rather than associated with secondary phases. It seems that the ferromagnetic phase could originate from interactions between manganese ions and oxygen vacancies and/or defects incorporated in the TiO2 crystal lattice during the thermal treatment of the samples.

  16. Photodegradation of ibuprofen by TiO2 co-doping with urea and functionalized CNT irradiated with visible light - Effect of doping content and pH.

    PubMed

    Yuan, Ching; Hung, Chung-Hsuang; Li, Huei-Wen; Chang, Wei-Hsian

    2016-07-01

    Ibuprofen (IBP) is one kind of non-steroidal anti-inflammatory drugs (NSAIDs), which are classified as Pharmaceuticals and Personal Care Products (PPCPs). IBP possesses bioactive property and the substantial use of IBP results in a harmful impact on bioreceptors even in small concentrations. Accordingly, the treatment of these wastewaters is important before discharging them into the ecosystem. The photodegradation of IBP with TiO2 co-doped with functionalized CNTs (CNT-COOH and CNT-COCl) and urea, named as N-doping CNT/TiO2, irradiated with visible light of 410 nm was investigated in this study. The titanium tetrachloride was used as the precursor of Ti. The N-doping CNT-COCl/TiO2 photocatalysts exhibited a better crystalline structure and smaller crystal size than the N-doping CNT-COOH/TiO2 photocatalyst. It might largely ascribe to strong binding between acyl chloride functional group and TiO2. About 85.0%-86.0% of IBP was degraded with N-doping CNT/TiO2 within 120 min at natural condition, which obeyed the pseudo first order reaction and the rate constant was 4.45 × 10(-3)-1.22 × 10(-2) min(-1) and 5.03 × 10(-3)-1.47 × 10(-2) min(-1) for N-doping CNT-COOH/TiO2 and N-doping CNT-COCl/TiO2, respectively. The best IBP degradation of 87.9%-89.0% was found at pH 5, which indicated superoxide radicals (O2(-)) played a key role. The optimal pH was majorly dominated by the nature of IBP and N-doping CNT/TiO2. A successful synergy effect of TiO2 and dopants was exhibited and this mainly attributed to the strong binding strength by functional group of acyl chloride (COCl) and carboxylic acid (COOH). In summary, IBP could be effectively photodegraded by the fabricated N-doping CNT/TiO2 photocatalysts.

  17. Preparation and photoelectric properties of Fe-doped mesoporous TiO2 thick films used in DSSC

    NASA Astrophysics Data System (ADS)

    Xie, Yian; Shen, Yue; Gu, Feng; Lu, Huina; Wu, Mingming; Wang, Linjun

    2009-08-01

    Fe-doped mesoporous TiO2 (M-TiO2-Fe) thick films were prepared by sol-gel and screen printing process. Raman characteristics results show that the M-TiO2-Fe thick film possesses a certain degree of the anatase phase, which may have advantages on photocatalysis and photovoltaic ability. Derived from small angel X-Ray diffraction (SAXRD), the films exhibit mesoporous structure with pore size around 7-8 nm. Eg of the films was obviously narrowed from 3.4 eV to 3.0 eV, which allows the thick films using more light to initiate photovoltaic process. Dye-sensitized solar cell (DSSC) based on M-TiO2-Fe was structured and chlorophyl was used as sensitizers. The solar cells have an open circuit voltage above 260mV.

  18. Anticorrosion Performance of Electrochemically Produced Zn-1% Mn-Doped TiO2 Nanoparticle Composite Coatings

    NASA Astrophysics Data System (ADS)

    Punith Kumar, M. K.; Venkatesha, T. V.; Pavithra, M. K.; Nithyananda Shetty, A.

    2015-05-01

    The Zn-TiO2 composite coatings were electrodeposited on mild steel using sulfate plating bath dispersed with 1% Mn-doped TiO2 nanoparticles. The agglomeration state and charge on the particles in plating condition were analyzed by zeta potential and particle size distribution measurements. The change in microstructure and morphology in composite coatings was analyzed by x-ray diffraction, energy-dispersive x-ray diffraction, and Scanning electron microscopic analyses. The corrosion behavior of the coatings was tested by electrochemical methods such as Tafel polarization and Electrochemical Impedance study. The increased charge transfer resistance with reduced corrosion rate was observed for composite coatings compared to pure zinc coating. The morphology and corrosion behavior of the composite coatings are correlated with pure zinc coating properties.

  19. Half-metallic behaviour in doped TiO2 (rutile) with double impurities: ab initio calculation

    NASA Astrophysics Data System (ADS)

    Fakhim Lamrani, A.; Belaiche, M.; Benyoussef, A.; El Kenz, A.

    2013-12-01

    Dilute magnetic oxides are without doubt among the most interesting classes of magnetic materials. However, the nature of their electronic structure and magnetic exchange is far from understood. Here, we apply the ab initio augmented spherical wave (ASW) method, with corrected generalised gradient approximation to study the electronic structure and magnetic properties of doped TiO2 rutile with double impurities. The study reveals a half-metallic ferromagnetic behaviour for Ti1-2x Cr x Mo x O2, and the local magnetic moments of the impurities and their oxidation states agree with the charge transfer between Cr and Mo, which would lead to the ferromagnetic state through the double-exchange mechanism in transition metal oxides.

  20. Solution-Processed Polyfluorene:Naphthalenediimide-N-Doped TiO2 Hybrids for Ultraviolet Photodetector Applications

    NASA Astrophysics Data System (ADS)

    Memisoglu, Gorkem; Varlikli, Canan; Diker, Halide

    2013-12-01

    In this study, highly efficient ultraviolet (UV) photodetectors based on a solution-processed system are introduced. Nitrogen-doped TiO2 nanoparticles are embedded in poly(9,9-dioctylfluorenyl-2,7-yleneethynylene) (PFE): N, N'-bis- n-butyl-1,4,5,8-naphthalenediimide (BNDI) (3:1 wt.%) blends. An UV- active layer of [(PFE:BNDI)(3:1):ammonium hydroxide-TiO2] [9:1 wt.%] gave a photoresponsivity value of 545 ± 6.92 mA/W at -4 V under 1 mW/cm2 UV light at 365 nm, and this value was increased to 597 ± 9.22 mA/W on annealing the active layer at 60°C. The efficiencies obtained are strongly dependent on the nitrogen source nature, their donor-acceptor relationship, and the morphological interaction with the PFE:BNDI blend.

  1. SiO(2) /TiO(2) hollow nanoparticles decorated with Ag nanoparticles: enhanced visible light absorption and improved light scattering in dye-sensitized solar cells.

    PubMed

    Hwang, Sun Hye; Shin, Dong Hoon; Yun, Juyoung; Kim, Chanhoi; Choi, Moonjung; Jang, Jyongsik

    2014-04-01

    Hollow SiO2 /TiO2 nanoparticles decorated with Ag nanoparticles (NPs) of controlled size (Ag@HNPs) were fabricated in order to enhance visible-light absorption and improve light scattering in dye-sensitized solar cells (DSSCs). They exhibited localized surface plasmon resonance (LSPR) and the LSPR effects were significantly influenced by the size of the Ag NPs. The absorption peak of the LSPR band dramatically increased with increasing Ag NP size. The LSPR of the large Ag NPs mainly increased the light absorption at short wavelengths, whereas the scattering from the SiO2 /TiO2 HNPs improved the light absorption at long wavelengths. This enabled the working electrode to use the full solar spectrum. Furthermore, the SiO2 layer thickness was adjusted to maximize the LSPR from the Ag NPs and avoid corrosion of the Ag NPs by the electrolyte. Importantly, the power conversion efficiency (PCE) increased from 7.1 % with purely TiO2 -based DSSCs to 8.1 % with HNP-based DSSCs, which is an approximately 12 % enhancement and can be attributed to greater light scattering. Furthermore, the PCEs of Ag@HNP-based DSSCs were 11 % higher (8.1 vs. 9.0 %) than the bare-HNP-based DSSCs, which can be attributed to LSPR. Together, the PCE of Ag@HNP-based DSSCs improved by a total of 27 %, from 7.1 to 9.0 %, due to these two effects. This comparative research will offer guidance in the design of multifunctional nanomaterials and the optimization of solar-cell performance.

  2. Identification of the arsenic resistance on MoO3 doped CeO2/TiO2 catalyst for selective catalytic reduction of NOx with ammonia.

    PubMed

    Li, Xiang; Li, Xiansheng; Li, Junhua; Hao, Jiming

    2016-11-15

    Arsenic resistance on MoO3 doped CeO2/TiO2 catalysts for selective catalytic reduction of NOx with NH3 (NH3-SCR) is investigated. It is found that the activity loss of CeO2-MoO3/TiO2 caused by As oxide is obvious less than that of CeO2/TiO2 catalysts. The fresh and poisoned catalysts are compared and analyzed using XRD, Raman, XPS, H2-TPR and in situ DRIFTS. The results manifest that the introduction of arsenic oxide to CeO2/TiO2 catalyst not only weakens BET surface area, surface acid sites and adsorbed NOx species, but also destroy the redox circle of Ce(4+) to Ce(3+) because of interaction between Ce and As. When MoO3 is added into CeO2/TiO2 system, the main SCR reaction path are found to be changed from the reaction between coordinated NH3 and ad-NOx species to that between an amide and gaseous NO. Additionally, for CeO2-MoO3/TiO2 catalyst, As toxic effect on active sites CeO2 can be released because of stronger As-Mo interaction. Moreover, not only are the reactable Brønsted and Lewis acid sites partly restored, but the cycle of Ce(4+) to Ce(3+) can also be free to some extent.

  3. Novel adsorption and photocatalytic oxidation for removal of gaseous toluene by V-doped TiO2/PU under visible light.

    PubMed

    Pham, Thanh-Dong; Lee, Byeong-Kyu

    2015-12-30

    In this study, V was used as a dopant to defect into the TiO2 lattice, leading to formation of Ti(3+) and V(4+) in the lattice. The presence of Ti(3+) and V(4+) introduced into the TiO2 lattice increased the electron-hole pair generation capacity and electron-hole pair separation efficiency of the TiO2, leading to enhancement of the photocatalytic activity of the photocatalyst. Porous polyurethane (PU) was used to immobilize the V-doped TiO2 by creating chemical bonds. The use of porous substrate contributed to the increased adsorption ability of the enhanced photocatalyst, as well as expanded its application for the removal of toluene from aerosols. Under dark conditions, the V-TiO2/PU only exhibited adsorption ability for toluene treatment in aerosol. Under visible light conditions, the V-TiO2/PU exhibited high photocatalytic oxidation ability for the removal of toluene in aerosol. The photocatalytic oxidation ability was found to depend on the V to TiO2 ratio. The optimal V content in V/TiO2 for enhancing the photocatalytic activity of TiO2 was determined to be 6 wt%. Even under visible light irradiation, the 6% V-TiO2/PU sample could photocatalytically remove 80% of the toluene in 200-ppmV inlet gas, while 89.3% of the removed amount was mineralized into CO2 and H2O.

  4. Treatment of olive mill wastewater by photooxidation with ZrO2-doped TiO2 nanocomposite and its reuse capability.

    PubMed

    Sponza, Delia Teresa; Oztekin, Rukiye

    2016-01-01

    Zirconium dioxide (zirconia, ZrO2)-doped TiO2 (TiO2/ZrO2) nanocomposite was used for the photocatalytic oxidation of pollutant parameters [COD components (CODtotal, CODdissolved and CODinert)], polyphenols (catechol, 3-hydroxybenzoic acid, tyrosol and 4-hydroxybenzoic acid) and total polyaromatic amines [aniline, 4-nitroaniline, o-toluidine and o-anisidine] from the olive mill effluent wastewaters at different operational conditions such as at different mass ratios of ZrO2 (50, 25, 14, 10 and 5 wt%) in the TiO2/ZrO2 nanocomposite, at different TiO2/ZrO2 photocatalyst concentrations (1, 4, 15 and 50 mg/L) and pH values (4.0-7.0-10.0) under 300 W UV irradiations, respectively. Under the optimized conditions (pH = 4.6, 15 mg/L ZrO2/TiO2 nanocomposite with a ZrO2 mass ratio of 14 wt%, 300 W UV light, after 60 min photooxidation time, at 21°C), the maximum CODdissolved, total phenol and total aromatic amines photooxidation yields were 99%, 89% and 95%, respectively. High pollutant removal (89%) yields after sequential five times utilization of ZrO2/TiO2 nanocomposite show that this catalyst can be effectively used commercially in the treatment of olive mill effluent.

  5. Oxygen vacancy induced phase formation and room temperature ferromagnetism in undoped and Co-doped TiO2 thin films

    NASA Astrophysics Data System (ADS)

    Mohanty, P.; Mishra, N. C.; Choudhary, R. J.; Banerjee, A.; Shripathi, T.; Lalla, N. P.; Annapoorni, S.; Rath, Chandana

    2012-08-01

    TiO2 and Co-doped TiO2 (CTO) thin films deposited at various oxygen partial pressures by pulsed laser deposition exhibit room temperature ferromagnetism (RTFM) independent of their phase. Films deposited at 0.1 mTorr oxygen partial pressure show a complete rutile phase confirmed from glancing angle x-ray diffraction and Raman spectroscopy. At the highest oxygen partial pressure, i.e. 300 mTorr, although the TiO2 film shows a complete anatase phase, a small peak corresponding to the rutile phase along with the anatase phase is identified in the case of CTO film. An increase in O to Ti/(Ti+Co) ratio with increase in oxygen partial pressure is observed from Rutherford backscattering spectroscopy. It is revealed from x-ray photoelectron spectroscopy (XPS) that oxygen vacancies are found to be higher in the CTO film than TiO2, while the valency of cobalt remains in the +2 state. Therefore, the CTO film deposited at 300 mTorr does not show a complete anatase phase unlike the TiO2 film deposited at the same partial pressure. We conclude that RTFM in both films is not due to impurities/contaminants, as confirmed from XPS depth profiling and cross-sectional transmission electron microscopy (TEM), but due to oxygen vacancies. The magnitude of moment, however, depends not only on the phase of TiO2 but also on the crystallinity of the films.

  6. Correlations of Optical Absorption, Charge Trapping, and Surface Roughness of TiO2 Photoanode Layer Loaded with Neat Ag-NPs for Efficient Perovskite Solar Cells.

    PubMed

    Yang, Dongwook; Jang, Jae Gyu; Lim, Joohyun; Lee, Jin-Kyu; Kim, Sung Hyun; Hong, Jong-In

    2016-08-24

    We systematically investigated the effect of silver nanoparticles (Ag-NPs) on the power conversion efficiency (PCE) of perovskite solar cells (PSCs). Neat, spherical Ag-NPs at loading levels of 0.0, 0.5, 1.0, and 2.0 wt % were embedded into the titanium dioxide (TiO2) photoanode layer. The plasmonic effect of the Ag-NPs strongly enhanced the incident light absorption over a wide range of the visible wavelength region in addition to the inherent absorbance of the perovskite sensitizer. The low conduction energy level of the Ag-NPs compared to that of TiO2 provides trap sites for free charge carriers. Thus, the correlation between the enhancement of the optical absorption and the number of charge traps provided by the Ag-NPs is critical to determine the device performance, especially current density (Jsc) and PCE. This is confirmed by the quantitative comparison of the incident light absorption and the time-resolved photoluminescence decay according to the loading levels of the Ag-NPs in the TiO2 layer. The absorption enhancement from 380 to 750 nm in the UV-visible spectrum is proportional to the increase in the loading levels of the Ag-NPs. However, the Jsc increases with the device with 0.5 wt % Ag-NPs and gradually decreases with increases in the loading level above 0.5 wt % because of the different contributions to the absorbance and the charge trapping by different Ag-NP loading levels. In addition, the suppression of the surface roughness with dense packing by the Ag-NPs helps to improve the Jsc and the following PCE. Consequently, the PCE of the PSC with 0.5 wt % Ag-NPs is increased to 11.96%. These results are attributed to the balance between increased absorbance by the localized surface plasmon resonance and the decreased charge trapping as well as the decreased surface roughness of the TiO2 layer with the Ag-NPs. PMID:27471777

  7. Preparation and characterization of TiO2 and Si-doped octacalcium phosphate composite coatings on zirconia ceramics (Y-TZP) for dental implant applications

    NASA Astrophysics Data System (ADS)

    Bao, Lei; Liu, Jingxiao; Shi, Fei; Jiang, Yanyan; Liu, Guishan

    2014-01-01

    In order to prevent the low temperature degradation and improve the bioactivity of zirconia ceramic implants, TiO2 and Si-doped octacalcium phosphate composite coating was prepared on zirconia substrate. The preventive effect on low temperature degradation and surface morphology of the TiO2 layer were studied. Meanwhile, the structure and property changes of the bioactive coating after doping Si were discussed. The results indicate that the dense TiO2 layer, in spite of some microcracks, inhibited the direct contact of the water vapor with the sample's surface and thus prevented the low temperature degradation of zirconia substrates. The acceleration aging test shows that the ratio of the monoclinic phase transition decreased from 10% for the original zirconia substrate to 4% for the TiO2-coated substrate. As to the Si-doped octacalcium phosphate coating prepared by biomimetic method, the main phase composition of the coating was octacalcium phosphate. The morphology of the coating was lamellar-like, and the surface was uniform and continuous with no cracks being observed. It is suggested that Si was added into the coating both through substituting for PO43- and doping as NaSiO3.

  8. Fabrication of Fe-doped TiO2 nanoparticles and investigation of photocatalytic decolorization of reactive red 198 under visible light irradiation.

    PubMed

    Moradi, Halimeh; Eshaghi, Akbar; Hosseini, Seyed Rahman; Ghani, Kamal

    2016-09-01

    In this research, Fe-doped TiO2 nanoparticles with various Fe concentrations (0. 0.1, 1, 5 and 10wt%) were prepared by a sol-gel method. Then, nanoparticles were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray analysis (EDX), BET surface area, photoluminescence (PL) spectroscopy and UV-vis diffuse reflectance spectroscopy (DRS). The photocatalytic activity of the nano-particles was evaluated through degradation of reactive red 198 (RR 198) under UV and visible light irradiations. XRD results revealed that all samples contained only anatase phase. DRS showed that the Fe doping in the titania induced a significant red shift of the absorption edge and then the band gap energy decreased from 3 to 2.1eV. Photocatalytic results indicated that TiO2 had a highest photocatalytic decolorization of the RR 198 under UV irradiation whereas photocatalytic decolorization of the RR 198 under visible irradiation increased in the presence of Fe-doped TiO2 nanoparticles. Among the samples, Fe-1wt% doped TiO2 nanoparticles showed the highest photocatalytic decolorization of RR198 under visible light irradiation.

  9. Preparation of N doped TiO2 via microwave-assisted method and its photocatalytic activity for degradation of Malathion.

    PubMed

    Kadam, A N; Dhabbe, R S; Kokate, M R; Gaikwad, Y B; Garadkar, K M

    2014-12-10

    We report herein, nitrogen doped TiO2 nanostructure synthesized by simple microwave assisted method, where ammonia was used as hydrolyzing agent. The synthesized nanomaterials were characterized by means of X-ray diffraction (XRD) which demonstrated that N-doped TiO2 is in anatase phase with average crystallite size of 10nm. Doping of N into the lattice of TiO2 was supported by X-ray photoelectron spectroscopy (XPS), Fourier transform-infrared spectroscopy (FT-IR), CHNS analysis, energy dispersive spectroscopy (EDS). The diffuse reflectance spectroscopy (DRS) showed shifting of absorption edge toward the visible region. Thermogravimetric-differential thermal analysis (TGA-DTA) points out N-doped TiO2 nanoparticles are thermally stable. In order to achieve maximum degradation efficiency, the effect of catalyst loading, pH and light sources (UV and sunlight) were studied. A maximum 97% degradation efficiency was achieved under optimized conditions. A 80% reduction in the chemical oxygen demand (COD) was observed after 150min that indicated mineralization of Malathion. The cytotoxicological studies indicate that photocatalytically degraded products were less toxic as compared to Malathion.

  10. A robust super-paramagnetic TiO2:Fe3O4:Ag nanocomposite with enhanced photo and bio activities on polyester fabric via one step sonosynthesis.

    PubMed

    Harifi, Tina; Montazer, Majid

    2015-11-01

    High intensity ultrasound was used for the synthesis and simultaneous deposition of TiO2:Fe3O4:Ag nanocomposites on polyester surface providing a feasible route for imparting magnetic and enhanced antibacterial and self-cleaning activities with controllable hydrophilicity/hydrophobicity at low temperature. Synergistic impact of sonochemistry and physical effects of ultrasound originating from implosive collapse of bubbles were responsible for the formation and adsorption of nanomaterials on the fabric surface during ultrasound irradiation. The increase in photocatalytic activity of TiO2 was obtained attributing to the co-operation of iron oxide and silver nanoparticles nucleated on TiO2 surface boosting the electron-hole pair separation and prolonging their recombination rate. The process was further optimized in terms of reagents concentrations including Fe(2+)/TiO2 and Ag/TiO2 molar ratios using central composite design in order to achieve the best self-cleaning property of the treated fabric. The magnetic measurements indicated the super-paramagnetic behavior of the treated fabric with saturation magnetization of 4.5 (emu/g). Findings suggest the potential of the proposed facial method in producing an intelligent fabric with durable multi-functional activities that can be suitable for various applications including medical, military, bio-separation, bio-sensors, magneto graphic printing, magnetic screens and magnetic filters.

  11. A robust super-paramagnetic TiO2:Fe3O4:Ag nanocomposite with enhanced photo and bio activities on polyester fabric via one step sonosynthesis.

    PubMed

    Harifi, Tina; Montazer, Majid

    2015-11-01

    High intensity ultrasound was used for the synthesis and simultaneous deposition of TiO2:Fe3O4:Ag nanocomposites on polyester surface providing a feasible route for imparting magnetic and enhanced antibacterial and self-cleaning activities with controllable hydrophilicity/hydrophobicity at low temperature. Synergistic impact of sonochemistry and physical effects of ultrasound originating from implosive collapse of bubbles were responsible for the formation and adsorption of nanomaterials on the fabric surface during ultrasound irradiation. The increase in photocatalytic activity of TiO2 was obtained attributing to the co-operation of iron oxide and silver nanoparticles nucleated on TiO2 surface boosting the electron-hole pair separation and prolonging their recombination rate. The process was further optimized in terms of reagents concentrations including Fe(2+)/TiO2 and Ag/TiO2 molar ratios using central composite design in order to achieve the best self-cleaning property of the treated fabric. The magnetic measurements indicated the super-paramagnetic behavior of the treated fabric with saturation magnetization of 4.5 (emu/g). Findings suggest the potential of the proposed facial method in producing an intelligent fabric with durable multi-functional activities that can be suitable for various applications including medical, military, bio-separation, bio-sensors, magneto graphic printing, magnetic screens and magnetic filters. PMID:25899439

  12. The effect of F --doping and temperature on the structural and textural evolution of mesoporous TiO 2 powders

    NASA Astrophysics Data System (ADS)

    Yu, Jia-Guo; Yu, Jimmy C.; Cheng, Bei; Hark, S. K.; Iu, Kwansai

    2003-09-01

    Mesoporous F --doped TiO 2 powders were prepared by hydrolysis of titanium tetraisopropoxide (TTIP) in a mixed NH 4F-H 2O solution. Effects of F - ion content and calcination temperatures on the phase composition and porosity of mesoporous titania were investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and BET surface areas. The results showed the BET surface area ( SBET) of the pure and doped powders dried at 100°C ranged from 260 to 310 m 2/g as determined by nitrogen adsorption. With increasing calcination temperatures, the SBET values of the calcined titania powders decreased due to the increase in crystalline size. The pore size distribution was bimodal with fine intra-particle pore and larger inter-particle pore as determined by nitrogen adsorption isotherms. The peak pore diameter of intra-particle pore increases with increasing F - ion content. At 700°C, all the titania powders exhibit monomodal pore size distributions due to the complete collapse of the intra-particle pores. The crystallization of anatase was obviously enhanced due to F --doping at 400°C and 500°C. Moreover, with increasing F - ion concent, F - ions not only suppressed the formation of brookite phase at low temperature, but also prevented phase transition of anatase to rutile at high temperature.

  13. Crystal Structure and Photocatalytic Activity of Al-Doped TiO2 Nanofibers for Methylene Blue Dye Degradation.

    PubMed

    Lee, Deuk Yong; Lee, Myung-Hyun; Kim, Bae-Yeon; Cho, Nam-Ihn

    2016-05-01

    Al-TiO2 nanofibers were prepared using a sol-gel derived electrospinning by varying the Al/Ti molar ratio from 0 to 0.73 to investigate the effect of Al doping on the crystal structure and the photocatalytic activity of Al-TiO2 for methylene blue (MB) degradation. XRD results indicated that as the Al/Ti molar ratio rose, crystal structure of Al-TiO2 was changed from anatase/rutile (undoped), anatase (0.07-0.18), to amorphous phase (0.38-0.73), which was confirmed by XPS and Raman analysis. The degradation kinetic constant increased from 7.3 x 10(-4) min(-1) to 4.5 x 10(-3) min(-1) with the increase of Al/Ti molar ratios from 0 to 0.38, but decreased to 3.4 x 10(-3) min(-1) when the Al/Ti molar ratio reached 0.73. The Al-TiO2 catalyst doped with 0.38 Al/Ti molar ratio demonstrated the best MB degradation. Experimental results indicated that the Al doping in Al-TiO2 was mainly attributed to the crystal structure of TiO2 and the photocatalytic degradation of MB.

  14. Crystal Structure and Photocatalytic Activity of Al-Doped TiO2 Nanofibers for Methylene Blue Dye Degradation.

    PubMed

    Lee, Deuk Yong; Lee, Myung-Hyun; Kim, Bae-Yeon; Cho, Nam-Ihn

    2016-05-01

    Al-TiO2 nanofibers were prepared using a sol-gel derived electrospinning by varying the Al/Ti molar ratio from 0 to 0.73 to investigate the effect of Al doping on the crystal structure and the photocatalytic activity of Al-TiO2 for methylene blue (MB) degradation. XRD results indicated that as the Al/Ti molar ratio rose, crystal structure of Al-TiO2 was changed from anatase/rutile (undoped), anatase (0.07-0.18), to amorphous phase (0.38-0.73), which was confirmed by XPS and Raman analysis. The degradation kinetic constant increased from 7.3 x 10(-4) min(-1) to 4.5 x 10(-3) min(-1) with the increase of Al/Ti molar ratios from 0 to 0.38, but decreased to 3.4 x 10(-3) min(-1) when the Al/Ti molar ratio reached 0.73. The Al-TiO2 catalyst doped with 0.38 Al/Ti molar ratio demonstrated the best MB degradation. Experimental results indicated that the Al doping in Al-TiO2 was mainly attributed to the crystal structure of TiO2 and the photocatalytic degradation of MB. PMID:27483928

  15. Role of Fe doping in tuning the band gap of TiO2 for the photo-oxidation-induced cytotoxicity paradigm.

    PubMed

    George, Saji; Pokhrel, Suman; Ji, Zhaoxia; Henderson, Bryana L; Xia, Tian; Li, LinJiang; Zink, Jeffrey I; Nel, André E; Mädler, Lutz

    2011-07-27

    UV-light-induced electron-hole (e(-)/h(+)) pair generation with free radical production in TiO(2)-based nanoparticles is a major conceptual paradigm for biological injury. However, to date, this hypothesis has been difficult to experimentally verify due to the high energy of UV light that is intrinsically highly toxic to biological systems. Here, a versatile flame spray pyrolysis (FSP) synthetic process has been exploited to synthesize a library of iron-doped (0-10 wt%) TiO(2) nanoparticles. These particles have been tested for photoactivation-mediated cytotoxicity using near-visible light exposure. The reduction in TiO(2) band gap energy with incremental levels of Fe loading maintained the nanoparticle crystalline structure in spite of homogeneous Fe distribution (demonstrated by XRD, HRTEM, SAED, EFTEM, and EELS). Photochemical studies showed that band gap energy was reciprocally tuned proportional to the Fe content. The photo-oxidation capability of Fe-doped TiO(2) was found to increase during near-visible light exposure. Use of a macrophage cell line to evaluate cytotoxic and ROS production showed increased oxidant injury and cell death in parallel with a decrease in band gap energy. These findings demonstrate the importance of band gap energy in the phototoxic response of the cell to TiO(2) nanoparticles and reflect the potential of this material to generate adverse effects in humans and the environment during high-intensity light exposure. PMID:21678906

  16. Role of Fe doping in tuning the band gap of TiO2 for photo-oxidation induced cytotoxicity paradigm

    PubMed Central

    George, Saji; Pokhrel, Suman; Ji, Zhaoxia; Henderson, Bryana L.; Xia, Tian; Li, LinJiang; Zink, Jeffrey I.; Nel, André E.; Mädler, Lutz

    2014-01-01

    UV-Light induced electron-hole (e−/h+) pair generation and free radical production in TiO2 based nanoparticles is a major conceptual paradigm for biological injury. However, to date, this hypothesis has been difficult to experimentally verify due to the high energy of UV light that is intrinsically highly toxic to biological systems. Here, a versatile flame spray pyrolysis (FSP) synthetic process has been exploited to synthesize a library of iron doped (0–10 at wt%) TiO2 nanoparticles. These particles have been tested for photoactivation-mediated cytotoxicity using near-visible light exposure. The reduction in TiO2 band gap energy with incremental levels of Fe loading maintained the nanoparticle crystalline structure in spite of homogeneous Fe distribution (demonstrated by XRD, HRTEM, SAED, EFTEM, and EELS). Photochemical studies showed that band gap energy was reciprocally tuned proportional to the Fe content. The photo-oxidation capability of Fe-doped TiO2 was found to increase during near-visible light exposure. Use of a macrophage cell line to evaluate cytotoxic and ROS production showed increased oxidant injury and cell death in parallel with a decrease in band gap energy. These findings demonstrate the importance of band gap energy in the phototoxic response of the cell to TiO2 nanoparticles and reflect the potential of this material to generate adverse effects in humans and the environment during high intensity light exposure. PMID:21678906

  17. Bonding and Anti-bonding Modes of Plasmon Coupling Effects in TiO2-Ag Core-shell Dimers

    PubMed Central

    Li, Quanshui; Zhang, Zhili

    2016-01-01

    Bonding and anti-bonding modes of plasmon coupling effects are numerically investigated in TiO2-Ag core-shell nano dimers. First, splitting phenomena of the coupled anti-bonding modes are observed under the longitudinal polarization when the distance between the monomers decreases to a certain level. Second, one of the split resonance modes is identified to be formed by the dipole anti-bonding mode of the monomers from charge density distribution patterns. Those split modes have similar redshift behaviors as the coupled dipole bonding modes in the same situations. Furthermore, the intensities of those anti-bonding modes weaken with decreasing distance between the monomers, because of the interaction of the induced dipole moment in the monomers and the charge distribution variation on the facing surfaces of the gap by the coulomb attraction. Other split bands are the higher-order mode (octupole-like or triakontadipole-like), which do not have obvious peak-shift behavior, and the intensities have very little attenuation with decreasing distance. Finally, the coupling of the bonding and anti-bonding modes under the longitudinal polarization is symmetric (bonding). PMID:26763719

  18. Bonding and Anti-bonding Modes of Plasmon Coupling Effects in TiO2-Ag Core-shell Dimers.

    PubMed

    Li, Quanshui; Zhang, Zhili

    2016-01-01

    Bonding and anti-bonding modes of plasmon coupling effects are numerically investigated in TiO2-Ag core-shell nano dimers. First, splitting phenomena of the coupled anti-bonding modes are observed under the longitudinal polarization when the distance between the monomers decreases to a certain level. Second, one of the split resonance modes is identified to be formed by the dipole anti-bonding mode of the monomers from charge density distribution patterns. Those split modes have similar redshift behaviors as the coupled dipole bonding modes in the same situations. Furthermore, the intensities of those anti-bonding modes weaken with decreasing distance between the monomers, because of the interaction of the induced dipole moment in the monomers and the charge distribution variation on the facing surfaces of the gap by the coulomb attraction. Other split bands are the higher-order mode (octupole-like or triakontadipole-like), which do not have obvious peak-shift behavior, and the intensities have very little attenuation with decreasing distance. Finally, the coupling of the bonding and anti-bonding modes under the longitudinal polarization is symmetric (bonding). PMID:26763719

  19. Promotion effect of Pd on TiO2 for visible light photocatalytic degradation of gaseous formaldehyde.

    PubMed

    Wu, Ren-Jang; Liu, Yung-Shiuan; Lai, Hsiao-Fang; Wang, Jhe-Hao; Chavali, Murthy

    2014-09-01

    TiO2 and Pd doped TiO2 (Pd/TiO2) nanoparticles were prepared by sol gel method. Pd/TiO2 material was characterized by XRD, TEM, TPR, XPS and BET. From XRD data, the crystalline type of TiO2 is known to as Anatase type. TiO2 and Pd/TiO2 were in the order of 9-10 nm and 10-13 nm respectively. The photocatalytic activities of the TiO2 and Pd/TiO2 nanomaterials were evaluated and compared for the photodegradation of formaldehyde (HCHO). HCHO degradation on Pd/TiO2 catalyst, at 60 min, the degradation rate of gaseous HCHO is 95%. Using Pd/TiO2, the rate was faster than TiO2 or doped with other metals (Au/TiO2; Ag/TiO2; Pt/TiO2).

  20. A systematic study on visible-light N-doped TiO2 photocatalyst obtained from ethylenediamine by sol-gel method

    NASA Astrophysics Data System (ADS)

    Li, Hui; Hao, Yubao; Lu, Haiqiang; Liang, Liping; Wang, Yuanyang; Qiu, Jianhao; Shi, Xianchao; Wang, Ying; Yao, Jianfeng

    2015-07-01

    N-doped titania is prepared using ethylenediamine as the nitrogen source by a sol-gel method. The preparation conditions, such as the volume ratio of ethylenediamine to sol, and the heat temperature on the nitrogen doping are systematically examined. UV results indicate the N-doped TiO2 catalysts have enhanced absorption in the visible light region, and exhibit high activities on the visible light photocatalytic reactions to the hydrogen production and methyl orange degradation. X-ray diffraction (XRD) and FT-IR results reveal that N species have been incorporated into the TiO2 lattice at a high N-doping level. N-doped titania prepared with an ethylenediamine to sol volume ratio of 1:1 and sintering temperature of 500 °C performed the highest hydrogen production rate (2.98 mmol g-1 h-1) and best methyl orange degradation performance. A conceivable structure change of N-doped TiO2 sintered at different temperature was proposed.

  1. Visible-light-driven photoelectrochemical and photocatalytic performances of Cr-doped SrTiO3/TiO2 heterostructured nanotube arrays

    PubMed Central

    Jiao, Zhengbo; Chen, Tao; Xiong, Jinyan; Wang, Teng; Lu, Gongxuan; Ye, Jinhua; Bi, Yingpu

    2013-01-01

    Well-aligned TiO2 nanotube arrays have become of increasing significance because of their unique highly ordered array structure, high specific surface area, unidirectional charge transfer and transportation features. However, their poor visible light utilization as well as the high recombination rate of photoexcited electron-hole pairs greatly limited their practical applications. Herein, we demonstrate the fabrication of visible-light-responsive heterostructured Cr-doped SrTiO3/TiO2 nanotube arrays by a simple hydrothermal method, which facilitate efficient charge separation and thus improve the photoelectrochemical as well as photocatalytic performances. PMID:24056587

  2. Effect of Nb and Sc doping on the phase transformation of sol-gel processed TiO2 nanoparticles.

    PubMed

    Ahmad, A; Buzby, S; Ni, C; Ismat Shah, S

    2008-05-01

    Nb and Sc doped TiO2 nanoparticles were synthesized via sol-gel technique. Dopant concentration of each element was varied from 0.5 to 1.5 atomic%. The effect of metal ion doping and calcination temperatures on anatase to rutile phase transformation has been investigated. Samples were analyzed by various analytical methods such as X-ray diffraction (XRD), Transmission Electron Microscope (TEM), X-ray Photoelectron Spectroscopy (XPS) and Energy Dispersive X-ray Spectroscopy (EDS). XRD analyses showed that Nb and Sc doped samples calcined at 300 degrees C and 350 degrees C, respectively, were crystalline and had an anatase structure. Results showed that anatase was stable up to 700 degrees C annealing temperature for samples doped with 0.5 atomic% Nb. There was a sharp transition from anatase to rutile phase above 700 degrees C and complete rutile structure was obtained at 750 degrees C. However, the transformation from anatase to rutile was not so sharp in samples doped with 1.0 atomic% and 1.5 atomic% Nb. Results indicated that higher concentration of Nb helps to stabilize the anatase phase. For samples doped with 0.5 atomic% Sc, anatase phase is stable up to 650 degrees C. Transformation from anatase to rutile starts at temperature above 650 degrees C and 100% rutile phase was obtained at 800 degrees C while for samples doped with 1.0 atomic% and 1.5 atomic% Sc, the complete transformation from anatase to rutile takes place at an even higher temperature. Results indicate that increasing the calcination time from 0.5 to 2.0 hours at 500 degrees C does not affect the stability of anatase phase. However, TEM and XRD data showed that the increase in the annealing time leads to an increase in particles size. The rutile to anatase concentration ratio increased with temperature above the phase transformation temperature. The activation energy for the phase transformation from anatase to rutile for doped and undoped samples was also measured. There was a general rise in

  3. Photochemically deposited nano-Ag/sol-gel TiO2-In2O3 mixed oxide mesoporous-assembled nanocrystals for photocatalytic dye degradation.

    PubMed

    Sreethawong, Thammanoon; Ngamsinlapasathian, Supachai; Yoshikawa, Susumu

    2014-05-01

    This work focused on the improvement of the photocatalytic activity for Congo Red (CR) azo dye degradation of mesoporous-assembled 0.95 TiO2-0.05 In2O3 mixed oxide photocatalyst (with a TiO2-to-In2O3 molar ratio of 0.95:0.05) by loading with Ag nanoparticles. The mesoporous-assembled 0.95TiO2-0.05In2O3 mixed oxide photocatalyst was synthesized by a hydrolytic sol-gel method with the aid of a structure-directing surfactant, prior to loading with various Ag contents (0.5-2 wt.%) by a photochemical deposition method. The optimum Ag loading content was found to be 1.5 wt.%, exhibiting a great increase in photocatalytic CR dye degradation activity. The 1.5 wt.% Ag-loaded 0.95TiO2-0.05In2O3 mixed oxide photocatalyst was further applied for the CR dye degradation in the presence of water hardness. Different types (Ca2+ and Ca2+ -Mg2+ mixture) and concentrations (200 and 500 mg/l) of water hardness were investigated. The results showed that the water hardness reduced the photocatalytic CR dye degradation activity, particularly for the extremely hard water with 500 mg/l of Ca2+ -Mg2+ mixture. The adjustment of initial solution pH of the CR dye-containing hard water to an appropriate value was found to improve the photocatalytic CR dye degradation activity under the identical reaction conditions.

  4. Gas Sensitivity and Sensing Mechanism Studies on Au-Doped TiO2 Nanotube Arrays for Detecting SF6 Decomposed Components

    PubMed Central

    Zhang, Xiaoxing; Yu, Lei; Tie, Jing; Dong, Xingchen

    2014-01-01

    The analysis to SF6 decomposed component gases is an efficient diagnostic approach to detect the partial discharge in gas-insulated switchgear (GIS) for the purpose of accessing the operating state of power equipment. This paper applied the Au-doped TiO2 nanotube array sensor (Au-TiO2 NTAs) to detect SF6 decomposed components. The electrochemical constant potential method was adopted in the Au-TiO2 NTAs' fabrication, and a series of experiments were conducted to test the characteristic SF6 decomposed gases for a thorough investigation of sensing performances. The sensing characteristic curves of intrinsic and Au-doped TiO2 NTAs were compared to study the mechanism of the gas sensing response. The results indicated that the doped Au could change the TiO2 nanotube arrays' performances of gas sensing selectivity in SF6 decomposed components, as well as reducing the working temperature of TiO2 NTAs. PMID:25330053

  5. Photooxidation of different organic dyes (RB, MO, TB, and BG) using Fe(III)-doped TiO 2 nanophotocatalyst prepared by novel chemical method

    NASA Astrophysics Data System (ADS)

    Ghorai, Tanmay K.; Biswas, Soumya K.; Pramanik, Panchanan

    2008-09-01

    The nano-structured Fe(III)-doped TiO 2 photocatalysts with anatase phase have been developed for the oxidation of non-biodegradable different organic dyes like methyl orange (MO), rhodamine B (RB), thymol blue (TB) and bromocresol green (BG) using UV-Hg-lamp. The different compositions of Fe xTi 1- xO 2 ( x = 0.005, 0.01, 0.05, and 0.1) nanocatalysts synthesized by chemical method (CM), have been characterized by X-ray diffraction (XRD), UV-vis diffuse reflectance spectra, specific surface area (BET), transmission electronic microscopy (TEM) analysis, XPS, ESR and zeta potential. From XRD analysis, the results indicate that all the compositions of Fe(III) doped in TiO 2 catalysts gives only anatase phase not rutile phase. For complete degradation of all the solutions of the dyes (MO, RB, TB, and BG), the composition with x = 0.005 is more photoactive compared all other compositions of Fe xTi 1- xO 2, and degussa P25. The decolorization rate of different dyes decreases as Fe(III) concentration in TiO 2 increases. The energy band gap of Fe(III)-doped TiO 2 is found to be 2.38 eV. The oxidation state of iron has been found to be 3+ from XPS and ESR show that Fe 3+ is in low spin state.

  6. Three-dimensional ruthenium-doped TiO2 sea urchins for enhanced visible-light-responsive H2 production.

    PubMed

    Nguyen-Phan, Thuy-Duong; Luo, Si; Vovchok, Dimitriy; Llorca, Jordi; Sallis, Shawn; Kattel, Shyam; Xu, Wenqian; Piper, Louis F J; Polyansky, Dmitry E; Senanayake, Sanjaya D; Stacchiola, Dario J; Rodriguez, José A

    2016-06-21

    Three-dimensional (3D) monodispersed sea urchin-like Ru-doped rutile TiO2 hierarchical architectures composed of radially aligned, densely-packed TiO2 nanorods have been successfully synthesized via an acid-hydrothermal method at low temperature without the assistance of any structure-directing agent and post annealing treatment. The addition of a minuscule concentration of ruthenium dopants remarkably catalyzes the formation of the 3D urchin structure and drives the enhanced photocatalytic H2 production under visible light irradiation, not possible on undoped and bulk rutile TiO2. Increasing ruthenium doping dosage not only increases the surface area up to 166 m(2) g(-1) but also induces enhanced photoresponse in the regime of visible and near infrared light. The doping introduces defect impurity levels, i.e. oxygen vacancy and under-coordinated Ti(3+), significantly below the conduction band of TiO2, and ruthenium species act as electron donors/acceptors that accelerate the photogenerated hole and electron transfer and efficiently suppress the rapid charge recombination, therefore improving the visible-light-driven activity. PMID:27240884

  7. Effect of Nb-doped TiO2 on nanocomposited aligned ZnO nanorod/TiO2:Nb for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Saurdi, I.; Shafura, A. K.; Azhar, N. E. A.; Ishak, A.; Malek, M. F.; Alrokayan, A. H. Salman; Khan, Haseeb A.; Mamat, M. H.; Rusop, M.

    2016-07-01

    The Nb-doped TiO2 films were deposited on glass substrate at different Nb concentrations of 0 at.%, 1 at.%, 3 at.%, 5 at.% and 7 at.%, respectively and their electrical and structural properties were investigated. Subsequently, the Nb-doped TiO2 films were deposited on top of aligned ZnO Nanorod on ITO glass substrates using spin coating technique. The nanocomposited aligned ZnO nanorod/Nb-doped TiO2 (TiO2:Nb) were coated with different Nb concentrations of 0 at.%, 1 at.%, 3 at.%, 5 at.% and 7 at.%, respectively. The Dye-sensitized solar cells were fabricated from the nanocomposited aligned ZnO nanorod/TiO2:Nb photoanodes and their effects on the performance of the DSSCs were investigated. From the solar simulator measurement of DSSC the solar energy conversion efficiency (η) of 5.376% under AM 1.5 was obtained for the ZnO nanorod/TiO2:Nb-5at.%.

  8. Marked enhancement of photocatalytic activity and photochemical stability of N-doped TiO2 nanocrystals by Fe3+/Fe2+ surface modification.

    PubMed

    Dong, Fan; Wang, Haiqiang; Wu, Zhongbiao; Qiu, Jinfeng

    2010-03-01

    N-doped TiO(2) (N-TiO(2)) nanocrystals with anatase and rutile mixed phases were prepared by partial oxidation of TiN. The samples were further modified by Fe-ions through incipient wetness impregnation method. The as-prepared samples were characterized by XRD, TEM, XPS, Raman, EPR, UV-vis DRS, and PL in detail. The results indicated that Fe mainly existed as Fe(3+)/Fe(2+) ions on the catalyst surface. The addition of small amounts of Fe-ions to N-TiO(2) nanocrystals caused several times enhancement of the photocatalytic activity under visible, UV and UV-vis light irradiation in degradation of gaseous toluene. The optimized Fe-ions content in this investigation was 0.02 wt.%. EPR and PL clearly showed that Fe(3+)/Fe(2+) redox cycle facilitated electron/hole charge separation, and contributed to the enhanced photocatalytic performance. Moreover, the photochemical stability of N-TiO(2) nanocrystals under visible light was improved due to the stabilization of nitrogen atoms in TiO(2) lattice by surface Fe-ions modification. The N-doped TiO(2) nanocrystals without Fe-ions modification suffered from a gradual deactivation due mainly to the loss of lattice-nitrogen during the photocatalytic reaction. The way to modification of nonmetal-doped TiO(2) nanomaterials brought new concept in enhancing the photocatalytic performance from the viewpoint of practical application. PMID:19969303

  9. Doped TiO2 anodic layers of enhanced antibacterial properties.

    PubMed

    Arenas, María A; Pérez-Jorge, Concepción; Conde, Ana; Matykina, Endzhe; Hernández-López, Juan M; Pérez-Tanoira, Ramón; de Damborenea, Juan J; Gómez-Barrena, Enrique; Esteba, Jaime

    2013-05-01

    Ti-6Al-4V joint replacement implants foster uncemented fixation in orthopaedic surgery. However, bacterial colonization competes with host cells and ultimately may produce implant-related difficult-to-treat infections, justifying the efforts to obtain infection-resistant materials. In a previous work, the authors demonstrated the antibacterial properties of anodic fluoride-TiO2 nanostructured layers on Ti-6Al-4V alloy. In this work, the anodizing bath has been modified in order to grow fluoride-TiO2 barrier layers (FBL). A bacterial adherence protocol, run with reference and six different clinical strains of Staphylococcus aureus and Staphylococcus epidermidis, showed a statistically significant decrease in the percentage of covered surface (p<0.0001, Kruskal-Wallis test) for FBL specimens when compared with non fluoride-containing specimens, i.e. chemically polished Ti-6Al-4V and F-free TiO2 barrier layers. The results obtained on the F-barrier layers allowed discrimination between the effects of the presence of fluoride in the layer and the layer nanostructure on bacterial adhesion. PMID:23357736

  10. Photocatalytic characteristic and photodegradation kinetics of toluene using N-doped TiO2 modified by radio frequency plasma.

    PubMed

    Shie, Je-Lueng; Lee, Chiu-Hsuan; Chiou, Chyow-San; Chen, Yi-Hung; Chang, Ching-Yuan

    2014-01-01

    This study investigates the feasibility of applications of the plasma surface modification of photocatalysts and the removal of toluene from indoor environments. N-doped TiO2 is prepared by precipitation methods and calcined using a muffle furnace (MF) and modified by radio frequency plasma (RF) at different temperatures with light sources from a visible light lamp (VLL), a white light-emitting diode (WLED) and an ultraviolet light-emitting diode (UVLED). The operation parameters and influential factors are addressed and prepared for characteristic analysis and photo-decomposition examination. Furthermore, related kinetic models are established and used to simulate the experimental data. The characteristic analysis results show that the RF plasma-calcination method enhanced the Brunauer Emmett Teller surface area of the modified photocatalysts effectively. For the elemental analysis, the mass percentages of N for the RF-modified photocatalyst are larger than those of MF by six times. The aerodynamic diameters of the RF-modifiedphotocatalyst are all smaller than those of MF. Photocatalytic decompositions of toluene are elucidated according to the Langmuir-Hinshelwood model. Decomposition efficiencies (eta) of toluene for RF-calcined methods are all higher than those of commercial TiO2 (P25). Reaction kinetics ofphoto-decomposition reactions using RF-calcined methods with WLED are proposed. A comparison of the simulation results with experimental data is also made and indicates good agreement. All the results provide useful information and design specifications. Thus, this study shows the feasibility and potential use of plasma modification via LED in photocatalysis.

  11. Photocatalytic characteristic and photodegradation kinetics of toluene using N-doped TiO2 modified by radio frequency plasma.

    PubMed

    Shie, Je-Lueng; Lee, Chiu-Hsuan; Chiou, Chyow-San; Chen, Yi-Hung; Chang, Ching-Yuan

    2014-01-01

    This study investigates the feasibility of applications of the plasma surface modification of photocatalysts and the removal of toluene from indoor environments. N-doped TiO2 is prepared by precipitation methods and calcined using a muffle furnace (MF) and modified by radio frequency plasma (RF) at different temperatures with light sources from a visible light lamp (VLL), a white light-emitting diode (WLED) and an ultraviolet light-emitting diode (UVLED). The operation parameters and influential factors are addressed and prepared for characteristic analysis and photo-decomposition examination. Furthermore, related kinetic models are established and used to simulate the experimental data. The characteristic analysis results show that the RF plasma-calcination method enhanced the Brunauer Emmett Teller surface area of the modified photocatalysts effectively. For the elemental analysis, the mass percentages of N for the RF-modified photocatalyst are larger than those of MF by six times. The aerodynamic diameters of the RF-modifiedphotocatalyst are all smaller than those of MF. Photocatalytic decompositions of toluene are elucidated according to the Langmuir-Hinshelwood model. Decomposition efficiencies (eta) of toluene for RF-calcined methods are all higher than those of commercial TiO2 (P25). Reaction kinetics ofphoto-decomposition reactions using RF-calcined methods with WLED are proposed. A comparison of the simulation results with experimental data is also made and indicates good agreement. All the results provide useful information and design specifications. Thus, this study shows the feasibility and potential use of plasma modification via LED in photocatalysis. PMID:24645445

  12. TiO2-doped phosphate glass microcarriers: A stable bioactive substrate for expansion of adherent mammalian cells

    PubMed Central

    Guedes, Joana C; Park, Jeong-Hui; Lakhkar, Nilay J; Kim, Hae-Won; Knowles, Jonathan C

    2013-01-01

    Scalable expansion of cells for regenerative cell therapy or to produce large quantities for high-throughput screening remains a challenge for bioprocess engineers. Laboratory scale cell expansion using t-flasks requires frequent passaging that exposes cells to many poorly defined bioprocess forces that can cause damage or alter their phenotype. Microcarriers offer a potential solution to scalable production, lending themselves to cell culture processes more akin to fermentation, removing the need for frequent passaging throughout the expansion period. One main problem with microcarrier expansion, however, is the difficulty in harvesting cells at the end of the process. Therefore, therapies that rely on cell delivery using biomaterial scaffolds could benefit from a microcarrier expansion system whereby the cells and microcarriers are transplanted together. In the current study, we used bioactive glass microcarriers doped with 5% TiO2 that display a controlled rate of degradation and conducted experiments to assess biocompatibility and growth of primary fibroblast cells as a model for cell therapy products. We found that the microcarriers are highly biocompatible and facilitate cell growth in a gradual controlled manner. Therefore, even without additional biofunctionalization methods, Ti-doped bioactive glass microcarriers offer potential as a cell expansion platform. PMID:22935537

  13. Influence of calcination parameters on the synthesis of N-doped TiO2 by the polymeric precursors method

    NASA Astrophysics Data System (ADS)

    Dawson, Margaret; Soares, Gabriela Byzynski; Ribeiro, Caue

    2014-07-01

    In this paper, the influence of calcination parameters on the synthesis of N:TiO2 catalysts obtained through the polymeric precursors method was evaluated. The powders were prepared by annealing Ti4+ precursor resins at different temperature-time conditions in air, resulting in powders with different degrees of crystallinity for N doping, which was done by adding urea to the as-prepared powders and calcining in N2 atmosphere. The N doping process resulted in band gap narrowing of TiO2 and, varying annealing temperature and time, can be an alternative method for preferential formation of substitutional N or interstitial N. It was found that the percentage of interstitial N increased with an increase in annealing temperature, resulting in the complete absence of substitutional N at 400 °C. The photocatalytic performance of the powders was evaluated using Rhodamine-B and Atrazine solutions under ultraviolet and visible irradiations. The coefficients revealed that interstitial N had a positive correlation to both ultraviolet and visible photoactivity. In contrast, substitutional N showed a negative correlation. Further, the ratio of substitutional N to interstitial N indicated a strong negative correlation to ultraviolet light photoactivity and no correlation to visible light photoactivity. However, substitutional N should be controlled for better photocatalytic properties.

  14. Titanium atoms dimerization phenomenon and magnetic properties of titanium-antisite (TiO) and chromium doped rutile TiO2, ab-initio calculation

    NASA Astrophysics Data System (ADS)

    Zarhri, Z.; Ziat, Y.; El Rhazouani, O.; Benyoussef, A.; Elkenz, A.

    2016-07-01

    The ab-initio calculations based on the Korringa Kohn Rostoker approximation approach combined with coherent potential approximation (KKR-CPA), were used to study the magnetic properties of the titanium anti-site (TiO) and chromium (Cr) doped TiO2. In the considered systems, we used different concentrations for TiO defect and Cr doping. In TiO2(0.98)(TiO)0.02, the obtained results indicate that TiO is a donor having half-metal behavior. TiO[3d] band is located at the Fermi level, although isn't 100% polarized, the ferromagnetic (FM) state is verified as being more stable than disordered local moment (DLM) state. For Ti0.98Cr0.02O2 the Cr doping introduced new states which give the material half-metallic feature. The majority spin of Cr impurities are located at the Fermi level and the conduction electrons around the Fermi level are 100% spin polarized. This indicates the stability of (FM) state. Moreover, in Ti0.98Cr0.02O2(0.98)(TiO)0.02, the top of the valence band is shifted to lower energy compared to pure TiO2, and the n-type of TiO2 is verified. The majority spin of Cr[3d] are located at 0.025 Ry close to the Fermi level. The predicted Curie temperatures (Tc) were calculated using the mean field approximation (MFA) and we predicted that TiO defect in Cr doped TiO2 makes Tc higher. This kind of defect makes the material useful for spinotronics's applications and devices.

  15. CeO2 doped anatase TiO2 with exposed (001) high energy facets and its performance in selective catalytic reduction of NO by NH3

    NASA Astrophysics Data System (ADS)

    Wang, Haiqiang; Cao, Shuang; Fang, Zheng; Yu, Feixiang; Liu, Yue; Weng, Xiaole; Wu, Zhongbiao

    2015-03-01

    Ceria doped on anatase TiO2 with high energy (001) facets was synthesized in this paper, which was subsequently utilized for selective catalytic reduction (SCR) of NO by NH3. After subjected to a range of analytical techniques, such as XRD, BET, TEM, XPS ESR, H2-TPR and NH3-TPD, it was found that compared with Ce/P25 catalyst, the presence of (001) facets over the TiO2 support had yielded a remarkably high activity at 390-490 °C for NO removal. The unique feature of active-energy (001) facets had enhanced the thermal stability of CeO2 whilst the presence of Ti3+ over the TiO2 surface had effectively facilitated the SCR process, both of which resulted in the remarkable catalytic performance for the catalyst.

  16. Strategies to prepare TiO2 thin films, doped with transition metal ions, that exhibit specific physicochemical properties to support osteoblast cell adhesion and proliferation.

    PubMed

    Dhayal, Marshal; Kapoor, Renu; Sistla, Pavana Goury; Pandey, Ravi Ranjan; Kar, Satabisha; Saini, Krishan Kumar; Pande, Gopal

    2014-04-01

    Metal ion doped titanium oxide (TiO2) thin films, as bioactive coatings on metal or other implantable materials, can be used as surfaces for studying the cell biological properties of osteogenic and other cell types. Bulk crystallite phase distribution and surface carbon-oxygen constitution of thin films, play an important role in determining the biological responses of cells that come in their contact. Here we present a strategy to control the polarity of atomic interactions between the dopant metal and TiO2 molecules and obtain surfaces with smaller crystallite phases and optimal surface carbon-oxygen composition to support the maximum proliferation and adhesion of osteoblast cells. Our results suggest that surfaces, in which atomic interactions between the dopant metals and TiO2 were less polar, could support better adhesion, spreading and proliferation of cells.

  17. Multivalence Charge Transfer in Doped and Codoped Photocatalytic TiO2.

    PubMed

    Ren, Hangjuan; Koshy, Pramod; Cao, Fuyang; Sorrell, Charles Christopher

    2016-08-15

    The present work reports data for the mineralogical and chemical properties of anatase thin films individually doped or codoped with chromium and vanadium, fabricated by sol-gel spin coating on glass substrates and annealing at 450 °C for 2 h. X-ray photoelectron spectroscopy data indicated the presence of Ti(4+), Ti(3+), Cr(3+), and possibly Cr(4+) in the Cr-doped thin films; Ti(4+), Ti(3+), V(3+), V(4+), and possibly V(5+) in the V-doped thin films; and Ti(4+), Ti(3+), Cr(3+), Cr(4+), V(3+), V(4+), and possibly V(5+) in the codoped thin films. While the thermodynamically stable valences Ti(4+), Cr(3+), and V(5+) would be expected to have formed, the presence of the nonequilibrium valences Ti(3+), Cr(4+), V(3+), and V(4+) is considered to have resulted from intervalence charge transfer for the Cr-doped and V-doped systems but from multivalence charge transfer (MVCT) for the codoped system. The latter phenomenon, which is introduced as a new conceptual term, describes the nature of the mutual exchange of electrons during valence changes of both dopant (Cr, V) and matrix (Ti) ions during annealing. In the present case, MVCT appears to be a transient metastable condition that acts during annealing, but subsequent UV irradiation can alter its effects. PMID:27487225

  18. Enhancement of photocatalytic properties of TiO2 nanoparticles doped with CeO2 and supported on SiO2 for phenol degradation

    NASA Astrophysics Data System (ADS)

    Hao, Chunjing; Li, Jing; Zhang, Zailei; Ji, Yongjun; Zhan, Hanhui; Xiao, Fangxing; Wang, Dan; Liu, Bin; Su, Fabing

    2015-03-01

    A series of CeO2-TiO2 and CeO2-TiO2/SiO2 composites were prepared with TiCl4 and Ce (NO3)3·6H2O as precursors via a facile co-precipitation method. The obtained samples were characterized by various techniques such as X-ray diffraction (XRD), nitrogen adsorption (N2-BET), Fourier transformation infrared spectrum (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV-Vis spectroscopy measurements. The results indicated that TiO2 doped with CeO2 and supported on SiO2 could reduce the crystallite size, inhibit the phase transformation, enhance the thermal stability, and effectively extend the spectral response from UV to visible range. When applied to the phenol photodegradation on a homemade batch reactor with an external cooling jacket, the CeO2-TiO2/SiO2 catalysts exhibited significantly enhanced photodegradation efficiency in comparison with commercial Degussa P25 and CeO2-TiO2. The unique catalytic properties of CeO2-TiO2/SiO2 were ascribed to improved electron-hole pairs separation efficiency and formation of more reactive oxygen species owing to the presence of Ce3+/Ce4+, as well as high dispersion of active component of CeO2-TiO2 as a result of the introduction of SiO2 support. Furthermore, the catalysts can be easily recovered from the reaction solution by centrifugation and reused for four cycles without significant loss of activity.

  19. Photovoltaic performances of Cu2-xTe sensitizer based on undoped and indium(3+)-doped TiO2 photoelectrodes and assembled counter electrodes.

    PubMed

    Srathongluan, Pornpimol; Kuhamaneechot, Rattanakorn; Sukthao, Prapatsawan; Vailikhit, Veeramol; Choopun, Supab; Tubtimtae, Auttasit

    2016-02-01

    Novel binary Cu2-xTe nanoparticles based on undoped and indium-doped TiO2 photoelectrodes were synthesized using a successive ionic layer adsorption and reaction (SILAR) technique as a sensitizer for liquid-junction solar cells. A larger diameter of TiO2 promoted a narrower energy band gap after indium doping, attributing to yield a broader absorption range of nanoparticle sensitizer due to the increasing amount of Cu2-xTe NPs on TiO2 surface. The atomic percentages showed the stoichiometric formation of Cu2Te incorporated in a Cu2-xTe structure. The best photovoltaic performance with the lower SILAR cycle, i.e., n=13 was performed after indium doping in both of carbon and Cu2S CEs and revealed that the efficiency of 0.73% under the radiant 100mW/cm(2) (AM 1.5G). The electrochemical impedance spectroscopy (EIS) was used to investigate the electrical properties via effect of material doping and counter electrodes with a lower charge-transfer resistance (Rct) and it was also found that the electron lifetime was improved after the sample doped with indium and assembled with carbon CE. PMID:26524258

  20. Visible Light Absorption of N-Doped TiO2 Rutile Using (LR/RT)-TDDFT and Active Space EOMCCSD Calculations

    SciTech Connect

    Govind, Niranjan; Lopata, Kenneth A.; Rousseau, Roger J.; Andersen, Amity; Kowalski, Karol

    2011-11-03

    We have performed detailed ground and excited state calculations of pure and N-doped TiO2 rutile to model and analyze the experimentally observed UV/Vis spectrum. Using our embedding model we have performed both linear-response (LR) and real-time (RT) TDDFT calculations of the excited states of the pure and N-doped systems. We have also studied the lowest excitations using high-level active space equation-of-motion coupled cluster (EOMCC) approaches involving all single and inter-band double excitations. We compare and contrast the nature of the excitations in detail for the pure and doped systems and also provide an analysis of the excited-state density using our RT-TDDFT calculations. Our calculations indicate a lowering of the band gap and verify the role of the N3- states on the observed spectrum of N-doped TiO2 rutile as suggested by experimental findings. Both RT-TDDFT and EOMCC calculations show that the excitations in pure TiO2 are more delocalized compared with the N-doped system.

  1. Low temperature synthesis of N-doped TiO2 with rice-like morphology through peroxo assisted hydrothermal route: Materials characterization and photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Bakar, Shahzad Abu; Ribeiro, Caue

    2016-07-01

    Nanorice-shaped N:TiO2 photocatalysts have been prepared by the peroxo assisted hydrothermal method using stabilized titanium complex as a precursor and urea as a N source. The N:TiO2 nanorices were characterised by XRD, FE-SEM, HRTEM, XPS, UV-vis spectroscopy, Raman spectroscopy and measurements of photocatalytic degradation of organic molecules (atrazine and RhB dye) under the UV and visible-light irradiation. XRD analyses showed that pristine TiO2 crystallizes into anatase polymorph and that the N-doping process at 5% introduced a degree of disorder on the TiO2 crystalline structure. XPS study revealed the successful incorporation of the nitrogen atoms at the interstitial sites of the TiO2 crystal lattice. Microscopy studies revealed that the particle size was in the range 50-80 nm for the pristine TiO2. The photocatalysts were assembled in the form of nanorices with a high surface area (102 m2 g-1). The successful incorporation of nitrogen atoms into the TiO2 crystal lattice is expected to be responsible for enhanced photocatalytic activity of the as-prepared samples for the degradation of pollutants (RhB and atrazine) under UV and visible light irradiation. The rate of rad OH radicals formation under visible-light irradiation was examined and found to be correlated with the photocatalytic activity per unit surface area. The N:TiO2 particles with nanorice morphology was efficient photocatalysts for decomposition of organic dyes under UV and visible-light exposure while pristine TiO2 photocatalyst did not show any significant photocatalytic activity when stimulated by visible-light. The 3% doped N:TiO2 sample exhibited the highest photocatalytic activity among all synthesized photocatalysts.

  2. Kinetic study of formic acid degradation by Fe3+ doped TiO2 self-cleaning nanostructure surfaces prepared by cold spray

    NASA Astrophysics Data System (ADS)

    Sayyar, Zahra; Akbar Babaluo, Ali; Shahrouzi, Javad Rahbar

    2015-04-01

    A self-cleaning solution was introduced in this paper based on sol-gel and was applied for preparing self-cleaning TiO2. Fe3+ ions have been doped into the TiO2 crystal lattice. XRD analysis indicated that the obtained TiO2 powder contains mainly the anatase phase and TiO2 powder has a crystallite size distribution of 10-12 nm. SEM micrographs have also confirmed nanometric distribution of the obtained powder. A series of uniform and transparent TiO2 and Fe/TiO2 films were prepared by cold spray technique which may result in high uniformity in the final coated surfaces. Photocatalytic activity of the thin films was investigated through degradation of aqueous formic acid under UV-visible light. The Langmuir-Hinshelwood kinetic model was used to interpret quantitatively the observed kinetic experimental result. Comparative study of the obtained coated surfaces with those of uncoated surfaces, demonstrated a remarkable performance. The Fe/TiO2 films and their calcination at 650 °C demonstrated the highest photocatalytic activity.

  3. Synthesis and characterization of anionic/nonionic surfactant-interceded iron-doped TiO2 to enhance sorbent/photo-catalytic properties

    NASA Astrophysics Data System (ADS)

    Sharma, Ajit; Lee, Byeong-Kyu

    2015-09-01

    We investigated the synthesis, characterization, and application of surfactant-interceded Fe nanoparticle-doped TiO2 (TiO2/Fe-S1 and TiO2/Fe-S2) that were used as adsorbents and photo-catalysts for the removal of As(V) ions from aqueous media. Two types of surfactant (anionic (sodium dodecyl sulfate), S1 and non-ionic (Triton X-100), S2) were used to obtain the separation and mono-dispersion of Fe(III) ions in the reaction solution. The nanocomposites were characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), UV-vis, scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDX) and elemental mapping analysis before and after As(V) removal. The Langmuir capacities (qe, mg/g) of the sodium dodecyl sulfate (SDS) and Triton X-100 interceded nanocomposites (TiO2/Fe-S1 and TiO2/Fe-S2, respectively) for arsenic removal were determined to be 65.79 and 50.76 mg/g, respectively, in aqueous media with As(V) concentration ranges of 0-10 mg/L at pH 6.5.

  4. Porous immobilized C coated N doped TiO2 containing in-situ generated polyenes for enhanced visible light photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Sabri, N. A.; Nawi, M. A.; Nawawi, W. I.

    2015-10-01

    Carbon coated nitrogen-doped Degussa P25TiO2 (or C,N-P25TiO2) was successfully immobilized on a glass plate using epoxidized natural rubber (ENR-50) and polyvinyl chloride (PVC) as the organic binders. Photo-etching of the fabricated system for 10 h oxidized its PVC binder into polyenes as well as forming a highly porous surface. The band gap energy (Eg) of the photo-etched immobilized photocatalyst system (C,N-P25TiO2/ENR/PVC-10 h) was reduced from 2.91 to 2.86 eV. Its photocatalytic activity was studied via photocatalytic degradation of 2,4-dichlorophenoxyacetic acid (2,4-D) under a 45 W visible light fluorescent lamp. C,N-P25TiO2/ENR/PVC-10 h with polyenes performed better than its slurry counterpart under visible light irradiation where the conjugated double bonds acted as photo sensitizers. The immobilized C,N-P25TiO2/ENR/PVC-10 h has excellent reusability and sustainable with an average k value of 0.056 ± 0.011 min-1 and average percent removal of 99.18 ± 0.54%.

  5. Evaluation of bimetal doped TiO2 in dye fragmentation and its comparison to mono-metal doped and bare catalysts

    NASA Astrophysics Data System (ADS)

    Malika, Manjakuppam; Rao, Ch. Venkatanarasimha; Das, Raj Kumar; Giri, Ardhendu Sekhar; Golder, Animes Kumar

    2016-04-01

    There are instances that bimetal doped semiconductor materials impart superior photocatalytic activity than bare and mono-metal doping. In this study, visible light responsive mono- (Cu/TiO2 and Ni/TiO2) and bi-metal doped (Cu-Ni/TiO2) TiO2 photocatalysts with wide band gap energy were synthesized via co-precipitation method with an equal mass ratio of Cu and Ni. The catalyst characterization was performed using Diffuse Reflectance UV-visible (DR-UV-vis) spectroscopy, Fourier Transform Infrared (FTIR) spectroscopy, X-ray Diffraction (XRD), zeta-potential and Transmission Electron Microscopy (TEM) analyzes. The charge balancing effect of Cu and Ni caused a notable reduction in the optical band gap of TiO2 to 2.91 eV with Cu-Ni/TiO2. The synthesis method increased the anatase phase significantly along with the crystallite size. Cu-Ni/TiO2 displayed a lesser destabilization tendency, and the absolute value of zeta-potentials increased much at pH > pHzpc resulted from the higher oxygen vacancies. The activity of Ni/TiO2, Cu/TiO2, and Cu-Ni/TiO2 was tested for the degradation dynamics and kinetics of Eriochrome Cyanine Red (ECR), an anionic dye. Cu doping exhibited a better dye decomposition because of the low recombination rate of electron/hole pair as a full 3d sub-level of Cu is energetically more favorable than a full 4s sub-level of Ni. The mechanism of dye decomposition releasing inorganic ions is also proposed and validated from the mass spectra.

  6. Dopant location identification in Nd3+ doped TiO2 nanoparticles

    SciTech Connect

    Li, W.; Frenkel, A.; Woicik, J.; Ni, C.; Shah, S.

    2010-12-03

    Large band gap semiconductors are typically doped in order to enhance their photocatalytic, photovoltaic, and other chemical and optoelectronic properties. The identification of dopant position and its local environment are essential to explore the effect of doping. X ray techniques, including extended x ray absorption fine structure, x ray photoelectron spectroscopy, and x ray diffraction, were performed to analyze the Nd (0 to 1.5 at. %) dopant location and the structural changes associated with the doping in anatase TiO{sub 2} nanoparticles, which were synthesized by metalorganic chemical vapor deposition. Nd ions were determined to have a trivalent chemical state and substitute for Ti{sup 4+} in the TiO{sub 2} structure. The substitutional Nd{sup 3+} ions cause anatase lattice expansion along c direction with a maximum value of 0.15 {angstrom} at 1.5% Nd doping level and the local structure of the dopants changes towards rutile like configuration. The lengths of the nearest neighbor Nd-O and Nd-Ti bonds increase by 0.5-0.8 {angstrom} compared to their counterparts in the pure TiO{sub 2} host structure. The substitutional nature of Nd{sup 3+} dopants explains why they are efficient not only for charge carrier separation but also for visible light absorption in TiO{sub 2}.

  7. Green synthesis of Pt-doped TiO2 nanocrystals with exposed (001) facets and mesoscopic void space for photo-splitting of water under solar irradiation.

    PubMed

    Banerjee, Biplab; Amoli, Vipin; Maurya, Abhayankar; Sinha, Anil Kumar; Bhaumik, Asim

    2015-06-21

    We report a non-trivial facile chemical approach using ionic liquid ([bmim][Cl]) as a porogen for the synthesis of (001) faceted TiO2 nanocrystals having mesoscopic void space. This faceted TiO2 nanomaterial has been doped with Pt nanoclusters through chemical impregnation. The resulting Pt-doped TiO2 nanomaterials are thoroughly characterized by powder X-ray diffraction (PXRD), Raman spectroscopy, field emission scanning electron microscopy (FE-SEM), ultra high resolution transmission electron microscopy (UHR-TEM), energy dispersive X-ray spectrometry (EDX), UV-vis diffuse reflection spectroscopy (DRS) and N2 sorption studies. These Pt/TiO2 nanocrystals with (001) exposed facets are employed as efficient and benign catalysts for hydrogen production from pure water and methanol-water systems under one AM 1.5G sunlight illumination. The effect of platinum loading and methanol-water ratio on the photocatalytic activity of the faceted TiO2 nanocrystals are investigated and it is found that hydrogen evolution rates have been enhanced significantly upon Pt loading. Under optimized reaction conditions the highest photocatalytic activity of 11.2 mmol h(-1) g(-1) has been achieved over ca. 1.0 wt% Pt loaded Pt/TiO2 nanocrystals with (001) exposed facets, which is one of the highest hydrogen evolution rates over the noble metal/TiO2 system reported to date in the literature.

  8. Improved performance of dye sensitized solar cells using Cu-doped TiO2 as photoanode materials: Band edge movement study by spectroelectrochemistry

    NASA Astrophysics Data System (ADS)

    Zhou, Li; Wei, Liguo; Yang, Yulin; Xia, Xue; Wang, Ping; Yu, Jia; Luan, Tianzhu

    2016-08-01

    Cu-doped TiO2 nanoparticles are prepared and used as semiconductor materials of photoanode to improve the performance of dye sensitized solar cells (DSSCs). UV-Vis spectroscopy and variable temperature spectroelectrochemistry study are used to characterize the influence of copper dopant with different concentrations on the band gap energies of TiO2 nanoparticles. The prepared Cu-doped TiO2 semiconductor has avoided the formation of CuO during hydrothermal process and lowered the conduction band position of TiO2, which contribute to increase the short circuit current density of DSSCs. At the optimum Cu concentration of 1.0 at.%, the short circuit current density increased from 12.54 to 14.98 mA cm-2, full sun solar power conversion efficiencies increased from 5.58% up to 6.71% as compared to the blank DSSC. This showed that the presence of copper in DSSCs leads to improvements of up to 20% in the conversion efficiency of DSSCs.

  9. Enhanced visible-light absorption of mesoporous TiO2 by co-doping with transition-metal/nitrogen ions

    SciTech Connect

    Mathis, John; Bi, Zhonghe; Bridges, Craig A; Kidder, Michelle; Paranthaman, Mariappan Parans

    2013-01-01

    Titanium (IV) oxide, TiO2, has been the object of intense scrutiny for energy applications. TiO2 is inexpensive, non-toxic, and has excellent corrosion resistance when exposed to electrolytes. A major drawback preventing the widespread use TiO2 for photolysis is its relatively large band gap of ~3eV. Only light with wavelengths shorter than 400 nm, which is in the ultraviolet portion of the spectrum, has sufficient energy to be absorbed. Less than 14 percent of the solar irradiation reaching the earth s surface has energy exceeding this band gap. Adding dopants such as transition metals has long been used to reduce the gap and increase photocatalytic activity by accessing the visible part of the solar spectrum. The degree to which the band gap is reduced using transition metals depends in part on the overlap of the d-orbitals of the transition metals with the oxygen p-orbitals. Therefore, doping with anions such as nitrogen to modify the cation-anion orbital overlap is another approach to reduce the gap. Recent studies suggest that using a combination of transition metals and nitrogen as dopants is more effective at introducing intermediate states within the band gap, effectively narrowing it. Here we report the synthesis of mesoporous TiO2 spheres, co-doped with transition metals and nitrogen that exhibit a nearly flat absorbance response across the visible spectrum extending into the near infrared.

  10. Study on the water durability of zinc boro-phosphate glasses doped with MgO, Fe2O3, and TiO2

    NASA Astrophysics Data System (ADS)

    Hwang, Moon Kyung; Ryu, Bong Ki

    2016-07-01

    The water durability of zinc boro-phosphate (PZB) glasses with the composition 60P2O5-20ZnO-20B2O3- xMeO ( x = 0, 2, 4, 6 and MeO = MgO, Fe2O3, or TiO2) (mol%) was measured, and PZB glass was studied in terms of its thermal properties, density, and FTIR characteristics. The surface conditions and corrosion byproducts were analyzed using scanning electron microscopy. When MgO, Fe2O3, and TiO2 were doped into the PZB glass, Q2 was decreased and Q1 was increased in the phosphate structure, while the number of BO4 structures increased with increasing MeO content. The density of the PZB glass was increased by the addition of Fe2O3 and TiO2, while the glass transition temperature ( T g ) and dilatometric softening temperature ( T d ) were increased when additional MgO, Fe2O3, and TiO2 were added. From the weight loss analysis (95 ◦ C, 96 h), TiO2 doped glass showed the lowest weight loss (1.70 × 10 -3 g/cm2) while MgO doped glass showed the highest value (2.44 × 10 -3 g/cm2), compared with PZB glass (3.07 × 10 -3 g/cm2). These results were discussed in terms of the Me n+ ions in the glass structure, and their different coordination numbers and bonding strengths.

  11. Plasmon-exciton coupling at Ag nanocluster decorated TiO2(110) surface studied by time-resolved two-photon photoemission spectroscopy

    NASA Astrophysics Data System (ADS)

    Tan, Shijing; Argondizzo, Adam; Petek, Hrvoje

    We study the spectroscopy and electron dynamics at Ag nanocluster decorated TiO2(110) surface upon photoexcitation of plasmonic modes by two-photon photoemission spectroscopy (2PP). Depositing Ag onto a reduced rutile TiO2(110) surface at room temperature forms pancake-like Ag particles with an average diameter of 4 nm and height of 1.5 nm. Measurements of the 2PP yield from Ag/TiO2 surface with tunable femtosecond laser excitation show enhancement at plasmonic resonances. Exciting with s-polarization (S -->) the plasmonic resonance enhancement has a single peak at 3.1 eV, whereas with p-polarization (P -->) there is an additional more intense resonance at 3.8 eV. We attribute the 3.1 and 3.8 eV peaks to the in-plane and the surface-normal plasmon modes respectively. Crystal azimuth orientation dependent excitation with (S -->) shows an anisotropy in the 2PP spectra for the 3.1 eV in-plane plasmon mode when the laser electric field is aligned in the [001] vs. [ 1 1 0 ] directions. The existence of two plasmon modes and the in-plane plasmon anisotropy imply that the plasmon modes are perturbed by coherent coupling with excitons in the rutile TiO2 substrate. We speculate that plasmon-exciton resonant energy transfer could play an important role in the plasmonically enhanced photocatalysis at the Ag/TiO2 surface.

  12. Multi-functional TiO2/Si/Ag(Cr)/TiNx coatings for low-emissivity and hydrophilic applications

    NASA Astrophysics Data System (ADS)

    Loka, Chadrasekhar; Park, Kyoung Ryeol; Lee, Kee-Sun

    2016-02-01

    Multi-functional (coatings with some additional functional properties such as high transparency, antireflection, hydrophilicity and antifogging) coatings are indispensable for the modern energy saving systems. In this regard, we deposited TiO2/Si/Ag(Cr)/TiNx multilayer thin films on soda-lime glass by using RF and DC magnetron sputtering to achieve a multi-functional thin film stack with the combination low-emissivity (low-e) and hydrophilicity properties in addition to the high transparency. Primary deposition of Ag(Cr)/TiNx was tried for the low-e effect and successfully obtained a very low emissivity value of 0.067, and then Si and TiO2 films with different bandgap were subsequently deposited to provide the hydrophilic properties. X-ray diffraction results revealed the anatase phase formation of TiO2 after annealing the films at 673 K by using the rapid thermal annealing system. Rutherford Backscattering Spectrometry (RBS) was carried out to determine the chemical composition and elemental depth distribution. The multilayer stack exhibited superhydrophilicity with a water contact angle of about 5° after irradiation by UV light. A Heterojunction film with wide and narrow bandgap semiconductor materials was effective to improve the hydrophilicity. The films exhibited a high visible transmittance (∼85.5%, at 550 nm) and low infrared transmittance (7%, at 2000 nm) including low-e and superhydrophilicity.

  13. Synthesize and characterize of Ag3VO4/TiO2 nanorods photocatalysts and its photocatalytic activity under visible light irradiation

    NASA Astrophysics Data System (ADS)

    Zou, Xuejun; Dong, Yuying; Zhang, Xiaodong; Cui, Yubo

    2016-03-01

    In this paper, in order to expand the light response range of TiO2, Ag3VO4/TiO2 nanorods photocatalysts were fabricated by a simple sol-gel method with microwave and hydrothermal method. The as-prepared samples were characterized by XRD, SEM, DRS, XPS and N2 adsorption-desorption. Meanwhile, their photocatalytic properties were investigated by the degradation of toluene under visible light irradiation. The degradation conversation of toluene had gotten to about 70% in 1% Ag3VO4/TiO2 nanorods after reaction 4 h. The predominant photocatalytic activity can be attributed to its strong absorption in visible light region and excellent charge separation characteristics. By using in situ FTIR, benzyl alcohol and benzaldehyde species could be observed during the reaction and the formed intermediates would be partially oxidized into CO2 and H2O. Electron spin resonance confirmed that OHrad and O2rad - were involved in the photocatalytic degradation of toluene.

  14. Outstanding supercapacitive properties of Mn-doped TiO2 micro/nanostructure porous film prepared by anodization method

    PubMed Central

    Ning, Xuewen; Wang, Xixin; Yu, Xiaofei; Zhao, Jianling; Wang, Mingli; Li, Haoran; Yang, Yang

    2016-01-01

    Mn-doped TiO2 micro/nanostructure porous film was prepared by anodizing a Ti-Mn alloy. The film annealed at 300 °C yields the highest areal capacitance of 1451.3 mF/cm2 at a current density of 3 mA/cm2 when used as a high-performance supercapacitor electrode. Areal capacitance retention is 63.7% when the current density increases from 3 to 20 mA/cm2, and the capacitance retention is 88.1% after 5,000 cycles. The superior areal capacitance of the porous film is derived from the brush-like metal substrate, which could greatly increase the contact area, improve the charge transport ability at the oxide layer/metal substrate interface, and thereby significantly enhance the electrochemical activities toward high performance energy storage. Additionally, the effects of manganese content and specific surface area of the porous film on the supercapacitive performance were also investigated in this work. PMID:26940546

  15. Enhanced photocatalytic activity of nitrogen doped TiO2 photocatalysts sensitized by metallo Co, Ni-porphyrins

    NASA Astrophysics Data System (ADS)

    Niu, Jinfen; Yao, Binghua; Chen, Yuanqing; Peng, Chao; Yu, Xiaojiao; Zhang, Jian; Bai, Guanghai

    2013-04-01

    Nitrogen doped anatase TiO2 powders (N-TiO2) were sensitized by four kinds of metalloporphyrins (CoTHPP, CoTPP, NiTHPP, and NiTPP). The resulting materials were characterized by XRD, TEM, XPS, DRS and N2 adsorption. The results showed that the crystal structure and morphology of N-TiO2 were not affected by the existence of porphyrin on its surface, but the surface area increased after the N-TiO2 sensitized by metalloporphyrins. The photocatalytic degradation of methyl blue (MB) experiments showed that the metalporphyrins sensitized N-TiO2 composite catalysts, especially the CoTHPP/N-TiO2 and CoTPP/N-TiO2, exhibited higher degradation efficiency than the unsentisized N-TiO2 powders. In addition, the photocatalytic degradations of MB using the composite catalysts were all demonstrated to follow first-order kinetic model. The composite catalysts can be recycled four times without significant loss of photocatalytic activity.

  16. Identification of the arsenic resistance on MoO3 doped CeO2/TiO2 catalyst for selective catalytic reduction of NOx with ammonia.

    PubMed

    Li, Xiang; Li, Xiansheng; Li, Junhua; Hao, Jiming

    2016-11-15

    Arsenic resistance on MoO3 doped CeO2/TiO2 catalysts for selective catalytic reduction of NOx with NH3 (NH3-SCR) is investigated. It is found that the activity loss of CeO2-MoO3/TiO2 caused by As oxide is obvious less than that of CeO2/TiO2 catalysts. The fresh and poisoned catalysts are compared and analyzed using XRD, Raman, XPS, H2-TPR and in situ DRIFTS. The results manifest that the introduction of arsenic oxide to CeO2/TiO2 catalyst not only weakens BET surface area, surface acid sites and adsorbed NOx species, but also destroy the redox circle of Ce(4+) to Ce(3+) because of interaction between Ce and As. When MoO3 is added into CeO2/TiO2 system, the main SCR reaction path are found to be changed from the reaction between coordinated NH3 and ad-NOx species to that between an amide and gaseous NO. Additionally, for CeO2-MoO3/TiO2 catalyst, As toxic effect on active sites CeO2 can be released because of stronger As-Mo interaction. Moreover, not only are the reactable Brønsted and Lewis acid sites partly restored, but the cycle of Ce(4+) to Ce(3+) can also be free to some extent. PMID:27474851

  17. Synthesis of activated charcoal supported Bi-doped TiO2 nanocomposite under solar light irradiation for enhanced photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Chandraboss, V. L.; Kamalakkannan, J.; Senthilvelan, S.

    2016-11-01

    In this study, activated charcoal (AC) supported bismuth (Bi)-doped Titanium dioxide (TiO2) nanocomposite was synthesized by precipitation method. The photocatalytic activity of AC-Bi/TiO2 was investigated for the degradation of methylene blue (MB) in aqueous solution under solar light irradiation. The incorporation of Bi3+ into the TiO2 lattice shifts the absorbance of TiO2 to the visible region then the addition of high adsorption capacity activated charcoal to improve the efficiency of TiO2. AC-Bi/TiO2 is found to be more efficient than Bi/TiO2 and undoped TiO2 for the degradation of MB under solar light irradiation. Surface morphology and bulk composition of the composite was obtained using high resolution-scanning electron microscopy with energy dispersive X-ray analysis. The crystal structure evolution and elemental composition were analyzed by combining Fourier transform-Raman spectroscopy, X-ray diffraction and X-ray photoelectron spectroscopy. The ultraviolet-visible (UV-vis) absorption spectra show that the absorption edge for the composite with Bi3+ has red shift as compared with that of undoped TiO2. UV-vis diffuse reflectance spectra demonstrated a decrease in the direct band gap of AC-Bi/TiO2. BET surface area, pore radius and pore volume of the materials were calculated by applying the BET equation to the sorption isotherms. The production of hydroxyl radicals (rad OH) on the surface of solar light irradiated materialswere detected by photoluminescence technique using coumarin as a probe molecule. The mechanism of photocatalytic effect of the AC-Bi/TiO2 was proposed for the degradation of MB under solar light irradiation.

  18. Simultaneous observation of up/down conversion photoluminescence and colossal permittivity properties in (Er+Nb) co-doped TiO2 materials

    NASA Astrophysics Data System (ADS)

    Tse, Mei-Yan; Tsang, Ming-Kiu; Wong, Yuen-Ting; Chan, Yi-Lok; Hao, Jianhua

    2016-07-01

    We have investigated the optical and dielectric properties of rutile TiO2 doped with Nb and Er, i.e., (Er0.5Nb0.5)xTi1-xO2. The up/downconversion photoluminescence was observed in the visible and near-infrared region from the materials under 980 nm laser diode excitation. The upconversion emissions are attributed to the energy transfer between Er ions in the excited states. Moreover, the dielectric measurements indicate that the fabricated materials simultaneously present colossal permittivity properties with relatively low dielectric loss. Our work demonstrates the coexistence of both interesting luminescence and attractive dielectric characteristics in (Er+Nb) co-doped TiO2, showing the potential for multifunctional applications.

  19. Effective role of trifluoroacetic acid (TFA) to enhance the photocatalytic activity of F-doped TiO2 prepared by modified sol-gel method

    NASA Astrophysics Data System (ADS)

    Samsudin, Emy Marlina; Hamid, Sharifah Bee Abd; Juan, Joon Ching; Basirun, Wan Jefrey; Kandjani, Ahmad Esmaielzadeh; Bhargava, Suresh K.

    2016-03-01

    Highly photoactive mesoporous F-doped TiO2 with improved physico-chemical characteristics is achieved using modified sol-gel method. The usage of trifluoroacetic as fluorine precursor significantly modifies the morphology, size, pore shape, crystal phase, crystal structure, surface chemical state and to a lesser extent, {1 0 1} and {0 0 1} facets. The accessibility of fluoride ions on Tisbnd Osbnd Ti polymer chains during crystal growth during the sol-gel process remarkably influences the properties of catalyst. To the best of our knowledge, preparation of F-doped TiO2 using modified sol-gel and trifluoroacetic acid are limited, and still not enough. Thus this work provides additional insight by using an approach which is less hazardous, less costly and practical for large scale agile development in the photocatalysis industry.

  20. A new preparation of doped photocatalytic TiO2 anatase nanoparticles: a preliminary study for the removal of pollutants in confined museum areas

    NASA Astrophysics Data System (ADS)

    Greco, Enrico; Ciliberto, Enrico; Cirino, Antonio M. E.; Capitani, Donatella; Di Tullio, Valeria

    2016-05-01

    The use of nanotechnology in conservation is a relatively new concept. Usually, classical cleanup methods take into account the use of other chemicals: On the one hand they help the environment destroying pollutants, but on the other hand they often become new pollutants. Among the new oxidation methods called advanced oxidation processes, heterogeneous photocatalysis has appeared an emerging technology with several economic and environmental advantages. A new sol-gel method of synthesis of TiO2 anatase is reported in this work using lithium and cobalt (II) salts. The activation energy of the doped photocatalyst was analyzed by solid-state UV-Vis spectrophotometer. The mobility of Li ions on TiO2 NPs surface was studied by 7Li MAS NMR spectroscopy. Use of doped nanotitania is suggested from authors for the removal of pollutants in confined areas containing goods that must be preserved from decomposition and aging phenomena.

  1. CO 2 Adsorption on Anatase TiO 2 (101) Surfaces in the Presence of Subnanometer Ag/Pt Clusters: Implications for CO 2 Photoreduction

    DOE PAGES

    Yang, Chi-Ta; Wood, Brandon C.; Bhethanabotla, Venkat R.; Joseph, Babu

    2014-10-20

    We show how CO2 adsorption on perfect and reduced anatase TiO2 (101) surfaces can be substantially modified by the presence of surface Ag and Pt octamer clusters, using density functional theory calculations. Furthermore, we found that adsorption was affected even at sites where the adsorbate was not in direct contact with the octamer, which we attributed to charge donation to CO2 from the Ag/Pt-modified surface, as well as an electrostatic competition between attractive (Ti–O) and repulsive (Ti–C) interactions. Additionally, TiO2-supported Pt octamers offer key advantages that could be leveraged for CO2 photoreduction, including providing additional stable adsorption sites for bentmore » CO2 species and facilitating charge transfer to aid in CO2– anion formation. Electronic structure analysis suggests these factors arise primarily from the hybridization of the bonding molecular orbitals of CO2 with d orbitals of the Pt atoms. Our results show that, for adsorption on TiO2-supported Pt octamers, the O–C–O bending and C–O asymmetric stretching frequencies can be used as reliable indicators of the presence of the CO2– anion intermediate as well as to distinguish unique adsorption geometries or sites. Finally, we suggest a possible pathway for subsequent CO2 dissociation to CO at the surface of a reduced anatase TiO2 (101)-supported Pt octamer, which has a computed energy barrier of 1.01 eV.« less

  2. Effect of reaction conditions on methyl red degradation mediated by boron and nitrogen doped TiO2

    NASA Astrophysics Data System (ADS)

    Galenda, A.; Crociani, L.; Habra, N. El; Favaro, M.; Natile, M. M.; Rossetto, G.

    2014-09-01

    Nowadays the employment of renewable and sustainable energy sources, and solar light as main option, becomes an urgent need. Photocatalytic processes received great attention in wastewater treatment due to their cheapness, environmental compatibility and optimal performances. Despite the general low selectivity of the photocatalysts, an accurate optimisation of the operational parameters needs to be carried out in order to maximise the process yield. Because of this reason, the present contribution aims to deepen either the knowledge in boron and/or nitrogen doped TiO2-based systems and their employment in methyl red removal from aqueous solutions. The samples were obtained by coprecipitation and characterised by XRD, SEM, BET specific surface area, UV-vis and XPS techniques. The catalytic activity was for the first time carefully evaluated with respect to methyl red photodegradation in different conditions as a function of working pH, counter-ions and pre-adsorption time. An ad-hoc study was performed on the importance of the pre-adsorption of the dye, suggesting that an extended adsorption is useless for the catalyst photoactivity, while a partial coverage is preferable. The photocatalytic tests demonstrate the positive influence of boron doping in photo-activated reactions and the great importance of the operational parameters with respect to the simple methyl red bleaching rather than the overall pollutant mineralisation. It is proved, indeed, that different working pH, acidifying means and substrate pre-adsorption time can enhance or limit the catalyst performances with respect to the complete pollutant degradation rather than its partial breakage.

  3. TiO2 nanotube composite layers as delivery system for ZnO and Ag nanoparticles - an unexpected overdose effect decreasing their antibacterial efficacy.

    PubMed

    Roguska, A; Belcarz, A; Pisarek, M; Ginalska, G; Lewandowska, M

    2015-06-01

    Enhancement of biocompatibility and antibacterial properties of implant materials is potentially beneficial for their practical value. Therefore, the use of metallic and metallic oxide nanoparticles as antimicrobial coatings components which induce minimized antibacterial resistance receives currently particular attention. In this work, TiO2 nanotubes layers loaded with ZnO and Ag nanoparticles were designed for biomedical coatings and delivery systems and evaluated for antimicrobial activity. TiO2 nanotubes themselves exhibited considerable and diameter-dependent antibacterial activity against planktonic Staphylococcus epidermidis cells but favored bacterial adhesion. Loading of nanotubes with moderate amount of ZnO nanoparticles significantly diminished S. epidermidis cell adhesion and viability just after 1.5h contact with modified surfaces. However, an increase of loaded ZnO amount unexpectedly altered the structure of nanoparticle-nanolayer, caused partial closure of nanotube interior and significantly reduced ZnO solubility and antibacterial efficacy. Co-deposition of Ag nanoparticles enhanced the antibacterial properties of synthesized coatings. However, the increase of ZnO quantity on Ag nanoparticles co-deposited surfaces favored the adhesion of bacterial cells. Thus, ZnO/Ag/TiO2 nanotube composite layers may be promising delivery systems for combating post-operative infections in hard tissue replacement procedures. However, the amount of loaded antibacterial agents must be carefully balanced to avoid the overdose and reduced efficacy.

  4. Bioinspired anchoring AgNPs onto micro-nanoporous TiO2 orthopedic coatings: Trap-killing of bacteria, surface-regulated osteoblast functions and host responses.

    PubMed

    Jia, Zhaojun; Xiu, Peng; Li, Ming; Xu, Xuchen; Shi, Yuying; Cheng, Yan; Wei, Shicheng; Zheng, Yufeng; Xi, Tingfei; Cai, Hong; Liu, Zhongjun

    2016-01-01

    The therapeutic applications of silver nanoparticles (AgNPs) against biomedical device-associated infections (BAI), by local delivery, are encountered with risks of detachment, instability and nanotoxicity in physiological milieus. To firmly anchor AgNPs onto modified biomaterial surfaces through tight physicochemical interactions would potentially relieve these concerns. Herein, we present a strategy for hierarchical TiO2/Ag coating, in an attempt to endow medical titanium (Ti) with anticorrosion and antibacterial properties whilst maintaining normal biological functions. In brief, by harnessing the adhesion and reactivity of bioinspired polydopamine, silver nanoparticles were easily immobilized onto peripheral surface and incorporated into interior cavity of a micro/nanoporous TiO2 ceramic coating in situ grown from template Ti. The resulting coating protected the substrate well from corrosion and gave a sustained release of Ag(+) up to 28 d. An interesting germicidal effect, termed "trap-killing", was observed against Staphylococcus aureus strain. The multiple osteoblast responses, i.e. adherence, spreading, proliferation, and differentiation, were retained normal or promoted, via a putative surface-initiated self-regulation mechanism. After subcutaneous implantation for a month, the coated specimens elicited minimal, comparable inflammatory responses relative to the control. Moreover, this simple and safe functionalization strategy manifested a good degree of flexibility towards three-dimensional sophisticated objects. Expectedly, it can become a prospective bench to bedside solution to current challenges facing orthopedics.

  5. Conductive and transparent multilayer films for low-temperature TiO2/Ag/SiO2 electrodes by E-beam evaporation with IAD

    PubMed Central

    2014-01-01

    Conductive and transparent multilayer thin films consisting of three alternating layers (TiO2/Ag/SiO2, TAS) have been fabricated for applications as transparent conducting oxides. Metal oxide and metal layers were prepared by electron-beam evaporation with ion-assisted deposition, and the optical and electrical properties of the resulting films as well as their energy bounding characteristics and microstructures were carefully investigated. The optical properties of the obtained TAS material were compared with those of well-known transparent metal oxide glasses such as ZnO/Ag/ZnO, TiO2/Ag/TiO2, ZnO/Cu/ZnO, and ZnO/Al/ZnO. The weathering resistance of the TAS film was improved by using a protective SiO2 film as the uppermost layer. The transmittance spectra and sheet resistance of the material were carefully measured and analyzed as a function of the layer thickness. By properly adjusting the thickness of the metal and dielectric films, a low sheet resistance of 6.5 ohm/sq and a high average transmittance of over 89% in the 400 to 700 nm wavelength regions were achieved. We found that the Ag layer played a significant role in determining the optical and electrical properties of this film. PMID:24433437

  6. TiO2 nanotube composite layers as delivery system for ZnO and Ag nanoparticles - an unexpected overdose effect decreasing their antibacterial efficacy.

    PubMed

    Roguska, A; Belcarz, A; Pisarek, M; Ginalska, G; Lewandowska, M

    2015-06-01

    Enhancement of biocompatibility and antibacterial properties of implant materials is potentially beneficial for their practical value. Therefore, the use of metallic and metallic oxide nanoparticles as antimicrobial coatings components which induce minimized antibacterial resistance receives currently particular attention. In this work, TiO2 nanotubes layers loaded with ZnO and Ag nanoparticles were designed for biomedical coatings and delivery systems and evaluated for antimicrobial activity. TiO2 nanotubes themselves exhibited considerable and diameter-dependent antibacterial activity against planktonic Staphylococcus epidermidis cells but favored bacterial adhesion. Loading of nanotubes with moderate amount of ZnO nanoparticles significantly diminished S. epidermidis cell adhesion and viability just after 1.5h contact with modified surfaces. However, an increase of loaded ZnO amount unexpectedly altered the structure of nanoparticle-nanolayer, caused partial closure of nanotube interior and significantly reduced ZnO solubility and antibacterial efficacy. Co-deposition of Ag nanoparticles enhanced the antibacterial properties of synthesized coatings. However, the increase of ZnO quantity on Ag nanoparticles co-deposited surfaces favored the adhesion of bacterial cells. Thus, ZnO/Ag/TiO2 nanotube composite layers may be promising delivery systems for combating post-operative infections in hard tissue replacement procedures. However, the amount of loaded antibacterial agents must be carefully balanced to avoid the overdose and reduced efficacy. PMID:25842121

  7. Design of N-doped anatase TiO2 photocatalyst with visible-light-response based on Ti-O bond weakening

    NASA Astrophysics Data System (ADS)

    Yin, L.-C.; Liu, G.; Cheng, H.-M.; Advanced Carbon Division Team

    2013-03-01

    Nitrogen bulk doping is an effective strategy to change the electronic structures of anatase TiO2 photocatalyst for visible light response improvement. Unfortunately, it is hard to achieve nitrogen bulk doping in practice, due to both limited thermodynamic solubility of substitutional nitrogen and N-induced recombination centers. It remains challenging yet highly desirable to develop new doping approach to increase nitrogen solubility in bulk. This challenge is originally stemmed from both strong Ti-O bond and charge difference (O2- versus N3-) between lattice oxygen and nitrogen dopant. In this work, we propose a new doping approach to promote the bulk substitution of lattice oxygen with nitrogen in bulk anatase TiO2, based on the Ti-O bond weakening by pre-implanted interstitial boron.1 By using the first-principles calculations, we study the interstitial boron induced Ti-O bonding weakening and the thermodynamics/kinetics changes for nitrogen bulk doping.2 In experiment, we realize to synthesize a bulk gradient B-N co-doping red anatase TiO2 microsphere which has an extended absorption edge up to ca. 700 nm covering the full visible light spectrum and has a bandgap varying from 1.94 eV on its surface to 3.22 eV in its core by gradually elevating VBM. This approach could be extended to modify other electronic materials that demand bulk substitutional doping. 1. G. Liu, J. Pan, L. C. Yin et al., Adv. Funct. Mater., 2012, 22, 3233. 2. G. Liu, L. C. Yin, J. Q. Wang et al., Energy Environ. Sci. 2012, 5, 9603. Financial support from Ministry of Science and Technology of China (no. 2009CB220001), NSFC (no. 50921004, 51002160, 21090343, 51172243, 51202255), CAS China (KJCX2-YW-H21-01).

  8. Biomimetic layer-by-layer deposition assisted synthesis of Cu, N co-doped TiO2 nanosheets with enhanced visible light photocatalytic performance.

    PubMed

    Wang, Xiaobo; Yan, Yong; Hao, Bo; Chen, Ge

    2014-10-01

    In this paper, a Cu, N co-doped TiO2 nanosheet with increased visible light photocatalytic activity was successfully synthesized using a biomimetic layer-by-layer deposition process. The polymer, branched-polyethyleneimine (b-PEI) was used as an induction agent for the hydrolysis of titanium bis(ammonium lactato)-dihydroxide (Ti-BALDH) as well as for a nitrogen resource, and the graphene oxide (GO) was used as a two-dimensional nano-template. The positively charged b-PEI will bind to the negatively charged GO and titania. In a typical layer-by-layer deposition process, GO nanosheets are exposed in an alternating fashion to aqueous b-PEI, CuCl2 and Ti-BALDH solutions, thus, making the layer-by-layer deposition of a conformal b-PEI/Cu-Ti-O coating on the GO. Subsequent b-PEI and GO pyrolysis at 550 °C under air yielded Cu, N co-doped TiO2 nanosheets. The materials obtained were comprehensively investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-Vis diffuse reflectance spectroscopy, Raman spectra, photoluminescence spectra and electron paramagnetic resonance. The Cu, N co-doped TiO2 nanosheets showed obviously enhanced photocatalytic activity which was evaluated by degradation of methylene blue under visible light irradiation. This research might provide some new insights for the "green synthesis" of the simultaneous doping of two kinds of foreign atoms into TiO2 with controlled morphology and photocatalytic properties.

  9. Influence of difference quantity La-doped TiO2 photoanodes on the performance of dye-sensitized solar cells: A strategy for choosing an appropriate doping quantity

    NASA Astrophysics Data System (ADS)

    Zhang, Zige; Li, Guoxiang; Cui, Zijian; Zhang, Kaiyue; Feng, Yaqing; Meng, Shuxian

    2016-05-01

    Facilitated by TiO2 particles adsorbing lanthanide ions in hydrosol, La-doped TiO2 was produced by a hydrothermal method. The structure, optical and photoluminescence properties of down-converting photoelectrode with the La3+ were characterized by X-ray (XRD), Scanning electron microscopy (SEM), Energy dispersive X-ray detector (EDX) and N2 adsorption-desorption isotherms measurement. The photoelectric conversion efficiency of dye-sensitized solar cells (DSSCs) fabricated with 0.05 g-La/TiO2 reached 7.02%, which gave an efficiency improved by 10.36% compared with that of cells fabricated from pure TiO2. The improvement in efficiency was ascribed to more dyes adsorbed on the surface of TiO2.

  10. Carbon-Dot-Sensitized, Nitrogen-Doped TiO2 in Mesoporous Silica for Water Decontamination through Nonhydrophobic Enrichment-Degradation Mode.

    PubMed

    Cheng, Chen; Tan, Xianjun; Lu, Deli; Wang, Lingzhi; Sen, Tapas; Lei, Juying; El-Toni, Ahmed Mohamed; Zhang, Jinlong; Zhang, Fan; Zhao, Dongyuan

    2015-12-01

    Mesoporous silica synthesized from the cocondensation of tetraethoxysilane and silylated carbon dots containing an amide group has been adopted as the carrier for the in situ growth of TiO2 through an impregnation-hydrothermal crystallization process. Benefitting from initial complexation between the titania precursor and carbon dot, highly dispersed anatase TiO2 nanoparticles can be formed inside the mesoporous channel. The hybrid material possesses an ordered hexagonal mesostructure with p6mm symmetry, a high specific surface area (446.27 m(2)  g(-1) ), large pore volume (0.57 cm(3)  g(-1) ), uniform pore size (5.11 nm), and a wide absorption band between λ=300 and 550 nm. TiO2 nanocrystals are anchored to the carbon dot through TiON and TiOC bonds, as revealed by X-ray photoelectron spectroscopy. Moreover, the nitrogen doping of TiO2 is also verified by the formation of the TiN bond. This composite shows excellent adsorption capabilities for 2,4-dichlorophenol and acid orange 7, with an electron-deficient aromatic ring, through electron donor-acceptor interactions between the carbon dot and organic compounds instead of the hydrophobic effect, as analyzed by the contact angle analysis. The composite can be photocatalytically recycled through visible-light irradiation after adsorption. The narrowed band gap, as a result of nitrogen doping, and the photosensitization effect of carbon dots are revealed to be coresponsible for the visible-light activity of TiO2 . The adsorption capacity does not suffer any clear losses after being recycled three times. PMID:26487497

  11. Enhancing the photocatalytic activity of TiO2 co-doping of graphene-Fe3+ ions for formaldehyde removal.

    PubMed

    Low, Wasu; Boonamnuayvitaya, Virote

    2013-09-30

    In the present work, graphene and Fe(3+) ions were doped to enhance the photocatalytic activity of a TiO2 photocatalyst with the expectation of synergistic effects on the specific surface area and electronic conductivity due to the formation of Ti-O-C bonds preventing charge recombination contributed by graphene and band gap energy narrowing by doping with Fe(3+) ions. GR/Fe(3+)-TiO2 was successfully synthesized by the refluxed peroxo titanic acid (PTA) method and was tested for gaseous formaldehyde removal. The results show that graphene contributed to formaldehyde adsorption since the equilibrium adsorption capacity increased with an increasing weight ratio of graphene. The GR/Fe(3+)-TiO2 photocatalyst with a weight ratio of graphene to TiO2 (PTA) of 1:50 and the Fe(3+) dopant at 0.12 wt% was optimal. An equilibrium formaldehyde adsorption capacity of 10.2 mg(HCHO) g(-1)catalyst and photodegradation efficiency of about 50.3% and 25.5% under UV and visible light irradiation for 90 min, respectively, were obtained. It was observed that the adsorption property of the catalyst was increased by adding graphene and the extendable absorption edge of light to longer wavelengths was attributed to the synergistic effect of graphene and Fe(3+) dopants on the band gap energy of the catalyst. The greater photocatalytic activity of GR/Fe(3+)-TiO2 compared to GR-TiO2 resulted from more hydroxyl (OH) and superoxide [Formula: see text] radicals produced via redox reactions with Fe ions. PMID:23694821

  12. A nanotechnology based new approach for chemotherapy of Cutaneous Leishmaniasis: TIO2@AG nanoparticles - Nigella sativa oil combinations.

    PubMed

    Abamor, Emrah Sefik; Allahverdiyev, Adil M

    2016-07-01

    Since toxicity and resistance are the major drawbacks of current antileishmanial drugs, studies have been recently focused on combination therapy in fight against leishmaniasis. Combination therapy generally provides opportunity to decrease toxicity of applied agents and enhance their antimicrobial performance. Moreover, this method can be effective in preventing drug resistance. Highly antileishmanial effects of silver doped titanium dioxide nanoparticles (TiAgNps) and Nigella sativa oil were demonstrated in previous studies. However, toxicity is still an important factor preventing use of these molecules in clinic. By considering high antileishmanial potential of each agent and basic principles of combination therapy, we propose that use of combinations including non-toxic concentrations of TiAgNps and N. sativa oil may compose more effective and safer formulations against Leishmania parasites. Therefore, the main goal of the present study was to investigate antileishmanial effects of non-toxic concentrations of TiAgNps and Nigella sativa oil combinations on promastigote and amastigote-macrophage culture systems and also to develop nanotechnology based new antileishmanial strategies against Cutaneous Leishmaniasis. Numerous parameters such as proliferation, metabolic activity, apoptosis, amastigote-promastigote conversion, infection index analysis and nitric oxide production were used to detect antileishmanial efficacies of combinations. Investigated all parameters demonstrated that TiAgNps-N. sativa oil combinations had significant antileishmanial effect on each life forms of parasites. Tested combinations were found to decrease proliferation rates of Leishmania tropica promastigotes in a range between 1,5-25 folds and metabolic activity values between 2 and 4 folds indicating that combination applications lead to virtually inhibition of promastigotes and elimination of parasites were directly related to apoptosis manner. TiAgNps-N. sativa combinations also

  13. A nanotechnology based new approach for chemotherapy of Cutaneous Leishmaniasis: TIO2@AG nanoparticles - Nigella sativa oil combinations.

    PubMed

    Abamor, Emrah Sefik; Allahverdiyev, Adil M

    2016-07-01

    Since toxicity and resistance are the major drawbacks of current antileishmanial drugs, studies have been recently focused on combination therapy in fight against leishmaniasis. Combination therapy generally provides opportunity to decrease toxicity of applied agents and enhance their antimicrobial performance. Moreover, this method can be effective in preventing drug resistance. Highly antileishmanial effects of silver doped titanium dioxide nanoparticles (TiAgNps) and Nigella sativa oil were demonstrated in previous studies. However, toxicity is still an important factor preventing use of these molecules in clinic. By considering high antileishmanial potential of each agent and basic principles of combination therapy, we propose that use of combinations including non-toxic concentrations of TiAgNps and N. sativa oil may compose more effective and safer formulations against Leishmania parasites. Therefore, the main goal of the present study was to investigate antileishmanial effects of non-toxic concentrations of TiAgNps and Nigella sativa oil combinations on promastigote and amastigote-macrophage culture systems and also to develop nanotechnology based new antileishmanial strategies against Cutaneous Leishmaniasis. Numerous parameters such as proliferation, metabolic activity, apoptosis, amastigote-promastigote conversion, infection index analysis and nitric oxide production were used to detect antileishmanial efficacies of combinations. Investigated all parameters demonstrated that TiAgNps-N. sativa oil combinations had significant antileishmanial effect on each life forms of parasites. Tested combinations were found to decrease proliferation rates of Leishmania tropica promastigotes in a range between 1,5-25 folds and metabolic activity values between 2 and 4 folds indicating that combination applications lead to virtually inhibition of promastigotes and elimination of parasites were directly related to apoptosis manner. TiAgNps-N. sativa combinations also

  14. Rapid flame synthesis of internal Mo(6+) doped TiO2 nanocrystals in situ decorated with highly dispersed MoO3 clusters for lithium ion storage.

    PubMed

    Li, Yunfeng; Hu, Yanjie; Shen, Jianhua; Jiang, Haibo; Min, Guoquan; Qiu, Shengjie; Song, Zhitang; Sun, Zhuo; Li, Chunzhong

    2015-11-28

    The rational design of nanoheterostructured materials has attracted much attention because of its importance for developing highly efficient LIBs. Herein, we have demonstrated that internal Mo(6+) doped TiO2 nanocrystals in situ decorated with highly dispersed MoO3 clusters have been realized by a facile and rapid flame spray pyrolysis route for electrochemical energy storage. In such intriguing nanostructures, internal Mo(6+) doping can improve the conductivity of electrode materials and facilitate rapid Li(+) intercalation and ion transport and the heteroassembly of highly dispersed ultrafine MoO3 clusters with excellent electrochemical activity endows the TiO2 with extra Li(+) ion storage ability as well as incorporates Mo(6+). Thus, the as-prepared nanohybrid electrodes exhibit a high specific capacity and superior rate capability due to the maximum synergetic effect of TiO2, Mo(6+) and ultrafine MoO3 clusters. Moreover, the aerosol flame process with a unique temperature gradient opens a new strategy to design novel hybrid materials by the simultaneous doping and heteroassembly engineering for next-generation LIBs. PMID:26490363

  15. Tm-doped TiO2 and Tm2Ti2O7 pyrochlore nanoparticles: enhancing the photocatalytic activity of rutile with a pyrochlore phase

    PubMed Central

    De los Santos, Desiré M; Aguilar, Teresa; Sánchez-Coronilla, Antonio; Fernández-Lorenzo, Concha; Alcántara, Rodrigo; Piñero, Jose Carlos; Blanco, Ginesa; Martín-Calleja, Joaquín

    2015-01-01

    Summary Tm-doped TiO2 nanoparticles were synthesized using a water-controlled hydrolysis reaction. Analysis was performed in order to determine the influence of the dopant concentration and annealing temperature on the phase, crystallinity, and electronic and optical properties of the resulting material. Various characterization techniques were utilized such as X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy and UV–vis spectroscopy. For the samples annealed at 773 and 973 K, anatase phase TiO2 was obtained, predominantly internally doped with Tm3+. ICP–AES showed that a doping concentration of up to 5.8 atom % was obtained without reducing the crystallinity of the samples. The presence of Tm3+ was confirmed by X-ray photoelectron spectroscopy and UV–vis spectroscopy: the incorporation of Tm3+ was confirmed by the generation of new absorption bands that could be assigned to Tm3+ transitions. Furthermore, when the samples were annealed at 1173 K, a pyrochlore phase (Tm2Ti2O7) mixed with TiO2 was obtained with a predominant rutile phase. The photodegradation of methylene blue showed that this pyrochlore phase enhanced the photocatalytic activity of the rutile phase. PMID:25821701

  16. LED and low level laser therapy association in tooth bleaching using a novel low concentration H2O2/N-doped TiO2 bleaching agent

    NASA Astrophysics Data System (ADS)

    Bezerra Dias, Hércules; Teixeira Carrera, Emanuelle; Freitas Bortolatto, Janaína; Ferrarezi de Andrade, Marcelo; Nara de Souza Rastelli, Alessandra

    2016-01-01

    Since low concentration bleaching agents containing N-doped TiO2 nanoparticles have been introduced as an alternative to conventional agents, it is important to verify their efficacy and the hypersensitivity effect in clinical practice. Six volunteer patients were evaluated for color change and hypersensitivity after bleaching using 35% H2O2 (one session of two 12 min applications) and 6% H2O2/N-doped TiO2 (one session of three 12 min applications) and after low level laser therapy application (LLLT) (780 nm, 40 mW, 10 J.cm-2, 10 s). Based on this case study, the nanobleaching agent provided better or similar aesthetic results than the conventional agent under high concentration, and its association with LLLT satisfactorily decreased the hypersensitivity. The 6% H2O2/N-doped TiO2 agent could be used instead of conventional in-office bleaching agents under high concentrations to fulfill the rising patient demand for aesthetics.

  17. Evidences of grain boundary capacitance effect on the colossal dielectric permittivity in (Nb + In) co-doped TiO2 ceramics

    PubMed Central

    Li, Jinglei; Li, Fei; Li, Chao; Yang, Guang; Xu, Zhuo; Zhang, Shujun

    2015-01-01

    The (Nb + In) co-doped TiO2 ceramics were synthesized by conventional solid-state sintering (CSSS) and spark plasma sintering (SPS) methods. The phases and microstructures were studied by X-ray diffraction, Raman spectra, field-emission scanning electron microscopy and transmission electron microscopy, indicating that both samples were in pure rutile phase while showing significant difference in grain size. The dielectric and I–V behaviors of SPS and CSSS samples were investigated. Though both possess colossal permittivity (CP), the SPS samples exhibited much higher dielectric permittivity/loss factor and lower breakdown electric field when compared to their CSSS counterparts. To further explore the origin of CP in co-doped TiO2 ceramics, the I–V behavior was studied on single grain and grain boundary in CSSS sample. The nearly ohmic I–V behavior was observed in single grain, while GBs showed nonlinear behavior and much higher resistance. The higher dielectric permittivity and lower breakdown electric field in SPS samples, thus, were thought to be associated with the feature of SPS, by which reduced space charges and/or impurity segregation can be achieved at grain boundaries. The present results support that the grain boundary capacitance effect plays an important role in the CP and nonlinear I–V behavior of (Nb + In) co-doped TiO2 ceramics. PMID:25656713

  18. Synthesis, Characterization, and Tribological Evaluation of TiO2-Reinforced Boron and Nitrogen co-Doped Reduced Graphene Oxide Based Hybrid Nanomaterials as Efficient Antiwear Lubricant Additives.

    PubMed

    Jaiswal, Vinay; Kalyani; Umrao, Sima; Rastogi, Rashmi B; Kumar, Rajesh; Srivastava, Anchal

    2016-05-11

    The microwave-synthesized reduced graphene oxide (MRG), boron-doped reduced graphene oxide (B-MRG), nitrogen-doped reduced graphene oxide (N-MRG), boron-nitrogen-co-doped reduced graphene oxide (B-N-MRG), and TiO2-reinforced B-N-MRG (TiO2-B-N-MRG) nanomaterials have been synthesized and characterized by various state-of-the-art techniques, like Raman spectroscopy, powder X-ray diffraction, scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy, high-resolution transmission electron microscopy, and X-ray photoelectron spectroscopy. Furthermore, the tribological properties of prepared nanomaterials as antiwear additives in neutral paraffin oil have been evaluated using a four-ball machine at an optimized additive concentration (0.15% w/v). The tribological parameters, like mean wear scar diameter, coefficient of friction, and wear rates, revealed that these nanomaterials have potential to be developed as environmentally friendly sulfated-ash-, phosphorus-, and sulfur-free antiwear lubricant additives. The friction- and wear-reducing behavior of MRG increased upon successive doping of nitrogen, boron, and both nitrogen and boron. Among these additives, B-N-co-doped MRG shows superior tribological behavior in paraffin base oil. Besides this, the load-carrying properties of B-N-co-doped MRG have significantly improved after its reinforcement with TiO2 nanoparticles. A comparative study of the surface morphology of a lubricated track in the presence of various additives has been assessed by SEM and contact-mode atomic force microscopy. The X-ray photoelectron spectroscopy studies have proved that the excellent lubrication properties of TiO2-B-N-MRG are due to the in situ formation of a tribofilm composed of boron nitride, adsorbed graphene layers, and tribosintered TiO2 nanoparticles during the tribocontact. Being sulfur-, halogen-, and phosphorus-free, these graphene-based nanomaterials act as green antiwear additives, protecting interacting

  19. In situ fabrication of Ag3PO4/TiO2 nanotube heterojunctions with enhanced visible-light photocatalytic activity.

    PubMed

    Tong, Zhen Wei; Yang, Dong; Sun, Yuan Yuan; Tian, Yao; Jiang, Zhong Yi

    2015-05-14

    Ag3PO4/TiO2 nanotube (TNT) heterojunctions were fabricated via a facile in situ growth method. Hemispherical Ag3PO4 nanocrystals were uniformly grown on the TNT surface, and their size was confined to 5-10 nm. A joint area was distinctly observed between the Ag3PO4 nanocrystals and TNT, indicating the formation of a Ag3PO4/TNT heterojunction. Compared with pure Ag3PO4, the Ag3PO4/TNT heterojunction possesses more active sites, less bulk defects, more efficient electron-hole separation, as well as better dye adsorption properties, and thus exhibits a significantly elevated photocatalytic activity for Rhodamine B (RhB) degradation. The study of the reactive species demonstrates that the photocatalytic degradation of RhB over the Ag3PO4/TNT heterojunction is primarily driven by both photogenerated h(+) and ˙OH radicals. This easily-fabricated Ag3PO4/TNT heterojunction with promising photocatalytic activity may find potential applications in energy and environmental related areas. PMID:25884048

  20. In situ fabrication of Ag3PO4/TiO2 nanotube heterojunctions with enhanced visible-light photocatalytic activity.

    PubMed

    Tong, Zhen Wei; Yang, Dong; Sun, Yuan Yuan; Tian, Yao; Jiang, Zhong Yi

    2015-05-14

    Ag3PO4/TiO2 nanotube (TNT) heterojunctions were fabricated via a facile in situ growth method. Hemispherical Ag3PO4 nanocrystals were uniformly grown on the TNT surface, and their size was confined to 5-10 nm. A joint area was distinctly observed between the Ag3PO4 nanocrystals and TNT, indicating the formation of a Ag3PO4/TNT heterojunction. Compared with pure Ag3PO4, the Ag3PO4/TNT heterojunction possesses more active sites, less bulk defects, more efficient electron-hole separation, as well as better dye adsorption properties, and thus exhibits a significantly elevated photocatalytic activity for Rhodamine B (RhB) degradation. The study of the reactive species demonstrates that the photocatalytic degradation of RhB over the Ag3PO4/TNT heterojunction is primarily driven by both photogenerated h(+) and ˙OH radicals. This easily-fabricated Ag3PO4/TNT heterojunction with promising photocatalytic activity may find potential applications in energy and environmental related areas.

  1. The synthesis of nitrogen/sulfur co-doped TiO2 nanocrystals with a high specific surface area and a high percentage of {001} facets and their enhanced visible-light photocatalytic performance

    PubMed Central

    2012-01-01

    Nitrogen/sulfur co-doped anatase TiO2 nanocrystals with a high specific surface area and a high percentage of {001} facets were synthesized by a solvent-thermal process followed by the calcination with thiourea at an optimum heat treatment temperature. Under current experimental conditions, the optimum heat treatment temperature was found at 300°C, which successfully introduced nitrogen and sulfur dopants into the anatase lattice to replace a small portion of oxygen atoms while preserving the geometry of these anatase TiO2 nanocrystals to maintain a high percentage of {001} facets. These nitrogen/sulfur co-doped anatase TiO2 nanocrystals demonstrated a largely enhanced light absorption in the whole visible-light range and exhibited much higher photocatalytic performance than both P25 TiO2 nanoparticles and anatase TiO2 nanocrystals with a high percentage of {001} facets under visible-light illumination. PMID:23095371

  2. Direct Synthesis of Carbon-Doped TiO2-Bronze Nanowires as Anode Materials for High Performance Lithium-Ion Batteries.

    PubMed

    Goriparti, Subrahmanyam; Miele, Ermanno; Prato, Mirko; Scarpellini, Alice; Marras, Sergio; Monaco, Simone; Toma, Andrea; Messina, Gabriele C; Alabastri, Alessandro; De Angelis, Francesco; Manna, Liberato; Capiglia, Claudio; Zaccaria, Remo Proietti

    2015-11-18

    Carbon-doped TiO2-bronze nanowires were synthesized via a facile doping mechanism and were exploited as active material for Li-ion batteries. We demonstrate that both the wire geometry and the presence of carbon doping contribute to the high electrochemical performance of these materials. Direct carbon doping for example reduces the Li-ion diffusion length and improves the electrical conductivity of the wires, as demonstrated by cycling experiments, which evidenced remarkably higher capacities and superior rate capability over the undoped nanowires. The as-prepared carbon-doped nanowires, evaluated in lithium half-cells, exhibited lithium storage capacity of ∼306 mA h g(-1) (91% of the theoretical capacity) at the current rate of 0.1C as well as excellent discharge capacity of ∼160 mAh g(-1) even at the current rate of 10 C after 1000 charge/discharge cycles.

  3. Characterisation, phase stability and surface chemical properties of photocatalytic active Zr and Y co-doped anatase TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Mattsson, Andreas; Lejon, Christian; Bakardjieva, Snejana; Štengl, Vaclav; Österlund, Lars

    2013-03-01

    We report on the characterization, phase stability, surface chemical and photocatalytic properties of Zr and Y co-doped anatase TiO2 nanoparticles prepared by homogenous hydrolysis methods using urea as precipitating agent. The materials were analyzed by scanning electron microscopy, X-ray diffraction, Raman spectroscopy, BET isotherm and BJH pore size distribution measurements. It is shown that Y and Zr ions replace Ti ions in the anatase TiO2 structures up to a critical total dopant concentration of approximately 13 wt%. The co-doped particles show increased phase stability compared to pure anatase TiO2 nanoparticles. The anatase to rutile phase transformation is shown to be preceded by cation segregation and dissolution with concomitant precipitation of Y2Ti2-xZrxO7 and ZrTiO4. Co-doping modifies the optical absorption edge with a resulting attenuation of the Urbach tail. The band gap is slightly blue-shifted at high doping concentrations, and red shifted at lower doping concentrations. Formic acid adsorption was used as a probe molecule to investigate surface chemical properties and adsorbate structures. It was found that the relative abundance of monodentate formate compared to bidentate coordinated formate decreases with increasing doping concentration. This is attributed to an increased surface acidity with increasing dopant concentration. Photodegradation of formic acid occurred on all samples. With mode-resolved in situ FTIR spectroscopy it is shown that the rate of photodegradation of monodentate formate species are higher than for bidentate formate species. Thus our results show that the trend of decreasing photo-degradation rate with increasing dopant concentration can be explained by the adsorbate structure, which is controlled by the acidity of the surface.

  4. Magnetically separable Fe3O4@SiO2@TiO2-Ag microspheres with well-designed nanostructure and enhanced photocatalytic activity.

    PubMed

    Chi, Yue; Yuan, Qing; Li, Yanjuan; Zhao, Liang; Li, Nan; Li, Xiaotian; Yan, Wenfu

    2013-11-15

    Major efforts in modern material chemistry are devoted to the design and fabrication of nanostructured systems with tunable physical-chemical properties for advanced catalytic applications. Here, a novel Fe3O4@SiO2@TiO2-Ag nanocomposite has been synthesized and characterized by a series of techniques including SEM, TEM, XRD, XPS as well as magnetization measurement and subsequently tested for the photocatalytic activities. The well-designed nanocomposite exhibits significantly superior activity to that of the commercial Degussa P25 thanks to the suppression of electron-hole pairs from recombination by Ag nanoparticles, and can be easily recycled by applying an external magnetic field while maintaining the catalytic activity without significant decrease even after running 10 times. The unique nanostructure makes Fe3O4@SiO2@TiO2-Ag a highly efficient, recoverable, stable, and cost-effective photocatalytic system offering broad opportunities in the field of catalyst synthesis and application. PMID:24076477

  5. UV-vis light activated Ag decorated monodisperse TiO2 for treatment of pharmaceuticals in water

    EPA Science Inventory

    Recently, many researchers have made a lot of effort to utilize the visible light portion of the solar spectrum to activate TiO2 photocatalyst for environmental applications, such as water, air, and soil remediation. The deposition of noble metals on photocatalysts is of great in...

  6. Highly efficient and recyclable triple-shelled Ag@Fe3O4@SiO2@TiO2 photocatalysts for degradation of organic pollutants and reduction of hexavalent chromium ions

    NASA Astrophysics Data System (ADS)

    Su, Jianwei; Zhang, Yunxia; Xu, Sichao; Wang, Shuan; Ding, Hualin; Pan, Shusheng; Wang, Guozhong; Li, Guanghai; Zhao, Huijun

    2014-04-01

    Herein, we demonstrate the design and fabrication of the well-defined triple-shelled Ag@Fe3O4@SiO2@TiO2 nanospheres with burr-shaped hierarchical structures, in which the multiple distinct functional components are integrated wonderfully into a single nanostructure. In comparison with commercial TiO2 (P25), pure TiO2 microspheres, Fe3O4@SiO2@TiO2 and annealed Ag@Fe3O4@SiO2@TiO2 nanocomposites, the as-obtained amorphous triple-shelled Ag@Fe3O4@SiO2@TiO2 hierarchical nanospheres exhibit a markedly enhanced visible light or sunlight photocatalytic activity towards the photodegradation of methylene blue and photoreduction of hexavalent chromium ions in wastewater. The outstanding photocatalytic activities of the plasmonic photocatalyst are mainly due to the enhanced light harvesting, reduced transport paths for both mass and charge transport, reduced recombination probability of photogenerated electrons/holes, near field electromagnetic enhancement and efficient scattering from the plasmonic nanostructure, increased surface-to-volume ratio and active sites in three dimensional (3D) hierarchical porous nanostructures, and improved photo/chemical stability. More importantly, the hierarchical nanostructured Ag@Fe3O4@SiO2@TiO2 photocatalysts could be easily collected and separated by applying an external magnetic field and reused at least five times without any appreciable reduction in photocatalytic efficiency. The enhanced photocatalytic activity and excellent chemical stability, in combination with the magnetic recyclability, make these multifunctional nanostructures promising candidates to remediate aquatic contaminants and meet the demands of future environmental issues.Herein, we demonstrate the design and fabrication of the well-defined triple-shelled Ag@Fe3O4@SiO2@TiO2 nanospheres with burr-shaped hierarchical structures, in which the multiple distinct functional components are integrated wonderfully into a single nanostructure. In comparison with commercial TiO2

  7. Synthesis, characterization and degradation of Bisphenol A using Pr, N co-doped TiO 2 with highly visible light activity

    NASA Astrophysics Data System (ADS)

    Yang, Juan; Dai, Jun; Li, Jiantong

    2011-08-01

    Praseodymium and nitrogen co-doped titania (Pr/N-TiO 2) photocatalysts, which could degrade Bisphenol A (BPA) under visible light irradiation, were prepared by the modified sol-gel process. Tetrabutyl titanate, urea and praseodymium nitrate were used as the sources of titanium, nitrogen and praseodymium, respectively. The resulting materials were investigated by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), UV-vis absorbance spectroscopy, X-ray photoelectron spectroscopy (XPS), N 2 adsorption-desorption isotherm and Fourier transform infrared spectra (FTIR). It was found that Pr doping inhibited the growth of crystalline size and the transformation from anatase to rutile. The degradation of BPA under visible light illumination was taken as probe reaction to evaluate the photo-activity of the co-doped photocatalyst. In our experiments, the optimal dopant amount of Pr was 1.2 mol% and the calcination temperature was 500 °C for the best photocatalytic activity. Pr/N-TiO 2 samples exhibited enhanced visible-light photocatalytic activity compared to N-TiO 2, undoped TiO 2 and commercial P25. The nitrogen atoms were incorporated into the crystal of titania and could narrow the band gap energy. Pr doping could slow the radiative recombination of photogenerated electrons and holes in TiO 2. The improvement of photocatalytic activity was ascribed to the synergistic effects of nitrogen and Pr co-doping.

  8. Synthesis of Cu-Doped Mixed-Phase TiO2 with the Assistance of Ionic Liquid by Atmospheric-Pressure Cold Plasma

    NASA Astrophysics Data System (ADS)

    Zhan, Zhibin; Di, Lanbo; Zhang, Xiuling; Li, Yanchun

    2016-05-01

    An atmospheric-pressure dielectric barrier discharge (DBD) gas-liquid cold plasma was employed to synthesize Cu-doped TiO2 nanoparticles in an aqueous solution with the assistance of [C2MIM]BF4 ionic liquid (IL) and using air as the working gas. The influences of the discharge voltage, IL and the amount of copper nitrite were investigated. X-ray diffraction, N2 adsorption-desorption measurements and UV-Vis spectroscopy were adopted to characterize the samples. The results showed that the specific surface area of TiO2 was promoted with Cu-doping (from 57.6 m2·g‑1 to 106.2 m2·g‑1 with 3% Cu-doping), and the content of anatase was increased. Besides, the band gap energy of TiO2 with Cu-doping decreased according to the UV-Vis spectroscopy test. The 3%Cu-IL-TiO2 samples showed the highest efficiency in degrading methylene blue (MB) dye solutions under simulated sunlight with an apparent rate constant of 0.0223 min‑1, which was 1.2 times higher than that of non-doped samples. According to the characterization results, the reasons for the high photocatalytic activity were discussed. supported by National Natural Science Foundation of China (Nos. 21173028, 11505019), the Science and Technology Research Project of Liaoning Provincial Education Department (No. L2013464), the Scientific Research Foundation for the Doctor of Liaoning Province (No. 20131004), the Program for Liaoning Excellent Talents in University (No. LR2012042), and Dalian Jinzhou New District Science and Technology Plan Project (No. KJCX-ZTPY-2014-0001)

  9. Synthesis of Cu-Doped Mixed-Phase TiO2 with the Assistance of Ionic Liquid by Atmospheric-Pressure Cold Plasma

    NASA Astrophysics Data System (ADS)

    Zhan, Zhibin; Di, Lanbo; Zhang, Xiuling; Li, Yanchun

    2016-05-01

    An atmospheric-pressure dielectric barrier discharge (DBD) gas-liquid cold plasma was employed to synthesize Cu-doped TiO2 nanoparticles in an aqueous solution with the assistance of [C2MIM]BF4 ionic liquid (IL) and using air as the working gas. The influences of the discharge voltage, IL and the amount of copper nitrite were investigated. X-ray diffraction, N2 adsorption-desorption measurements and UV-Vis spectroscopy were adopted to characterize the samples. The results showed that the specific surface area of TiO2 was promoted with Cu-doping (from 57.6 m2·g-1 to 106.2 m2·g-1 with 3% Cu-doping), and the content of anatase was increased. Besides, the band gap energy of TiO2 with Cu-doping decreased according to the UV-Vis spectroscopy test. The 3%Cu-IL-TiO2 samples showed the highest efficiency in degrading methylene blue (MB) dye solutions under simulated sunlight with an apparent rate constant of 0.0223 min-1, which was 1.2 times higher than that of non-doped samples. According to the characterization results, the reasons for the high photocatalytic activity were discussed. supported by National Natural Science Foundation of China (Nos. 21173028, 11505019), the Science and Technology Research Project of Liaoning Provincial Education Department (No. L2013464), the Scientific Research Foundation for the Doctor of Liaoning Province (No. 20131004), the Program for Liaoning Excellent Talents in University (No. LR2012042), and Dalian Jinzhou New District Science and Technology Plan Project (No. KJCX-ZTPY-2014-0001)

  10. A mini-review on rare earth metal-doped TiO2 for photocatalytic remediation of wastewater.

    PubMed

    Saqib, Najm Us; Adnan, Rohana; Shah, Irfan

    2016-08-01

    Titanium dioxide (TiO2) has been considered a useful material for the treatment of wastewater due to its non-toxic character, chemical stability and excellent electrical and optical properties which contribute in its wide range of applications, particularly in environmental remediation technology. However, the wide band gap of TiO2 photocatalyst (anatase phase, 3.20 eV) limits its photocatalytic activity to the ultraviolet region of light. Besides that, the electron-hole pair recombination has been found to reduce the efficiency of the photocatalyst. To overcome these problems, tailoring of TiO2 surface with rare earth metals to improve its surface, optical and photocatalytic properties has been investigated by many researchers. The surface modifications with rare earth metals proved to enhance the efficiency of TiO2 photocatalyts by way of reducing the band gap by shifting the working wavelength to the visible region and inhibiting the anatase-to-rutile phase transformations. This review paper summarises the attempts on modification of TiO2 using rare earth metals describing their effect on the photocatalytic activities of the modified TiO2 photocatalyst. PMID:27335012

  11. A mini-review on rare earth metal-doped TiO2 for photocatalytic remediation of wastewater.

    PubMed

    Saqib, Najm Us; Adnan, Rohana; Shah, Irfan

    2016-08-01

    Titanium dioxide (TiO2) has been considered a useful material for the treatment of wastewater due to its non-toxic character, chemical stability and excellent electrical and optical properties which contribute in its wide range of applications, particularly in environmental remediation technology. However, the wide band gap of TiO2 photocatalyst (anatase phase, 3.20 eV) limits its photocatalytic activity to the ultraviolet region of light. Besides that, the electron-hole pair recombination has been found to reduce the efficiency of the photocatalyst. To overcome these problems, tailoring of TiO2 surface with rare earth metals to improve its surface, optical and photocatalytic properties has been investigated by many researchers. The surface modifications with rare earth metals proved to enhance the efficiency of TiO2 photocatalyts by way of reducing the band gap by shifting the working wavelength to the visible region and inhibiting the anatase-to-rutile phase transformations. This review paper summarises the attempts on modification of TiO2 using rare earth metals describing their effect on the photocatalytic activities of the modified TiO2 photocatalyst.

  12. The role of transition metal impurities and oxygen vacancies in the formation of ferromagnetism in Co-doped TiO2

    NASA Astrophysics Data System (ADS)

    Anisimov, V. I.; Korotin, M. A.; Nekrasov, I. A.; Mylnikova, A. S.; Lukoyanov, A. V.; Wang, J. L.; Zeng, Z.

    2006-02-01

    We have investigated the role of transition metal impurities and oxygen vacancies in the formation of ferromagnetism in Co-doped TiO2 using the LSDA +U approach which takes into account strong on-site Coulomb correlations for electronic structure calculations. Several model supercells of rutile TiO2, with a Co2+ ion in high-spin state substituted into the titanium site and with oxygen vacancies, were considered. We found that the exchange interaction of Co magnetic ions is ferromagnetic, but very weak due to the large average impurity-impurity distance. However, it becomes three times stronger when there is a magnetic vacancy nearby. The magnetic moment values are 3 μB for Co2+ and -1 μB for vacancy. Our investigation showed that the exchange interaction energy of Co and vacancy moments varies from 330 to 40 meV depending on the distance between them in the supercell. We assume that the strong interaction between Co and vacancy moments should be taken into account to explain the high Curie temperature value in Co-doped TiO2.

  13. Extremely fast dark adsorption rate of carbon and nitrogen co-doped TiO2 prepared by a relatively fast, facile and low-cost microwave method

    NASA Astrophysics Data System (ADS)

    Du, Chun; Zhou, Jiangshan; Li, Fangzhou; Li, Wei; Wang, Yinzhen; He, Qinyu

    2016-07-01

    A facile and low-cost microwave method was used to prepare C and N co-doped TiO2 in just 8 min. The prepared samples were thoroughly characterized and were found to have favourable features such as surface adsorption of pollutants and photocatalysis. The rapid decomposition of CH5N3HCl under microwave irradiation led to mesopores and surface roughness in the as-prepared particles, resulting in large surface adsorption of pollutant and good photodegradation. The best sample is the one with the ratio of TiO2/CH2N3HCl at 3:1, which adsorbed 86.3 % of a methylene orange (MO) solution (20 mg L-1) in 10 min.

  14. Nonlinear optical absorption and switching properties of gold nanoparticle doped SiO2-TiO2 sol-gel films.

    PubMed

    Venkatram, N; Kumar, R Sai Santosh; Rao, D Narayana; Medda, S K; De, Sucheta; De, Goutam

    2006-07-01

    The nonlinear optical absorption and switching properties of sol-gel derived of Au nanoparticle doped SiO2-TiO2 sol-gel films having different Au-surface plasmon absorption positions are reported in this paper. The Au nanoparticles are embedded in SiO2 and SiO2-TiO2 mixed glassy film matrices with different refractive index values. To study the nonlinear absorption properties, lasers with three different wavelengths are used. The optical switching behavior is studied by using the pump-probe technique with 532 nm as the excitation wavelength. Ground state conduction band, surface plasmon band, and the free carrier band are taken as three level model to explain theoretically the obtained RSA and SA behaviors.

  15. Green synthesis of Pt-doped TiO2 nanocrystals with exposed (001) facets and mesoscopic void space for photo-splitting of water under solar irradiation

    NASA Astrophysics Data System (ADS)

    Banerjee, Biplab; Amoli, Vipin; Maurya, Abhayankar; Sinha, Anil Kumar; Bhaumik, Asim

    2015-06-01

    We report a non-trivial facile chemical approach using ionic liquid ([bmim][Cl]) as a porogen for the synthesis of (001) faceted TiO2 nanocrystals having mesoscopic void space. This faceted TiO2 nanomaterial has been doped with Pt nanoclusters through chemical impregnation. The resulting Pt-doped TiO2 nanomaterials are thoroughly characterized by powder X-ray diffraction (PXRD), Raman spectroscopy, field emission scanning electron microscopy (FE-SEM), ultra high resolution transmission electron microscopy (UHR-TEM), energy dispersive X-ray spectrometry (EDX), UV-vis diffuse reflection spectroscopy (DRS) and N2 sorption studies. These Pt/TiO2 nanocrystals with (001) exposed facets are employed as efficient and benign catalysts for hydrogen production from pure water and methanol-water systems under one AM 1.5G sunlight illumination. The effect of platinum loading and methanol-water ratio on the photocatalytic activity of the faceted TiO2 nanocrystals are investigated and it is found that hydrogen evolution rates have been enhanced significantly upon Pt loading. Under optimized reaction conditions the highest photocatalytic activity of 11.2 mmol h-1 g-1 has been achieved over ca. 1.0 wt% Pt loaded Pt/TiO2 nanocrystals with (001) exposed facets, which is one of the highest hydrogen evolution rates over the noble metal/TiO2 system reported to date in the literature.We report a non-trivial facile chemical approach using ionic liquid ([bmim][Cl]) as a porogen for the synthesis of (001) faceted TiO2 nanocrystals having mesoscopic void space. This faceted TiO2 nanomaterial has been doped with Pt nanoclusters through chemical impregnation. The resulting Pt-doped TiO2 nanomaterials are thoroughly characterized by powder X-ray diffraction (PXRD), Raman spectroscopy, field emission scanning electron microscopy (FE-SEM), ultra high resolution transmission electron microscopy (UHR-TEM), energy dispersive X-ray spectrometry (EDX), UV-vis diffuse reflection spectroscopy (DRS) and

  16. Time-resolved imaging of positive pulsed corona-induced surface streamers on TiO2 and γ-Al2O3-supported Ag catalysts

    NASA Astrophysics Data System (ADS)

    Kim, Hyun-Ha; Teramoto, Yoshiyuki; Ogata, Atsushi

    2016-10-01

    We report the first instance of time-resolved imaging of surface streamers in air propagating on the surface of titanium dioxide (TiO2) and alumina (γ-Al2O3) beads at ambient temperature and atmospheric pressure. The propagation velocity of primary streamers was found to be dependent primarily on the applied voltage and the type of catalyst. The presence of Ag nanoparticles enhanced the propagation velocity of primary streamers in both TiO2 and γ-Al2O3. Some of the primary streamers passed through a partial discharge, which resulted in enhanced discharge intensity. Through successive steps, the partial discharge served as a staging point for primary streamers, and promoted their propagation toward the next catalyst bead. For a given configuration and catalyst, the velocity of the primary streamer was largely influenced by applied voltage and catalyst type. For a mesh-to-mesh reactor with Ag/ TiO2 catalyst, the primary streamer reached about 660 km s‑1. Secondary streamers occurred with much slower velocities after the primary streamer had disappeared. In contrast to primary streamers, secondary streamer velocities were almost completely independent of the applied voltage on both TiO2 (150  ±  50 km s‑1) and γ-Al2O3 (70  ±  10 km s‑1). Detailed time-resolved imaging data on surface streamers can provide important insight into understanding and modeling plasma-catalysis, which can accelerate the progress of research and development in this area.

  17. Synergy of metal and nonmetal dopants for visible-light photocatalysis: a case-study of Sn and N co-doped TiO2.

    PubMed

    Zhuang, Huaqiang; Zhang, Yingguang; Chu, Zhenwei; Long, Jinlin; An, Xiaohan; Zhang, Hongwen; Lin, Huaxiang; Zhang, Zizhong; Wang, Xuxu

    2016-04-14

    This paper mainly focuses on the synergistic effect of Sn and N dopants to enhance the photocatalytic performance of anatase TiO2 under visible light or simulated solar light irradiation. The Sn and N co-doped TiO2 (SNT-x) photocatalysts were successfully prepared by the facile sol-gel method and the post-nitridation route in the temperature range of 400-550 °C. All the as-prepared samples were characterized in detail by X-ray diffraction, UV-vis diffuse reflectance spectroscopy, transmission electron microscopy, X-ray photoelectron and electron spin resonance spectroscopy and photoelectrochemical measurements. The characterization results reveal that the co-incorporation of Sn and N atoms remarkably modifies the electronic structure of TiO2, which gives rise to a prominent separation of photogenerated charge carriers and more efficient interfacial charge-transfer reactions in a photocatalytic process. The enhanced photocatalytic activity is attributed to the intensified active oxygen species including hydroxyl radicals (˙OH) and superoxide anion radicals (O2˙(-)) for degradation of organic pollutants. And the result of photocatalytic hydrogen production further confirms the existence of the synergistic effect in the SNT-x samples, because they exhibit higher photocatalytic activity than the sum of N/TiO2 and Sn/TiO2. This work provides a paradigm to consolidate the understanding of the synergistic effect of metal and non-metal co-doped TiO2 in domains of photocatalysis and photoelectrochemistry.

  18. Interplay of dopant, defects and electronic structure in driving ferromagnetism in Co-doped oxides: TiO(2), CeO(2) and ZnO.

    PubMed

    Ali, Bakhtyar; Shah, Lubna R; Ni, C; Xiao, J Q; Shah, S Ismat

    2009-11-11

    A comprehensive study of the defects and impurity (Co)-driven ferromagnetism is undertaken in the oxide semiconductors: TiO(2), ZnO and CeO(2). The effect of magnetic (Co(2+)) and non-magnetic (Cu(2+)) impurities in conjunction with defects, such as oxygen vacancies (V(o)), have been thoroughly investigated. Analyses of the x-ray diffraction (XRD) and x-ray photoelectron spectroscopy (XPS) data reveal the incorporation of cobalt in the lattice, with no signature of cobalt segregation. It is shown that oxygen vacancies are necessary for the ferromagnetic coupling in the Co-doped oxides mentioned above. The possible exchange mechanisms responsible for the ferromagnetism are discussed in light of the energy levels of dopants in the host oxides. In addition, Co and Cu co-doped TiO(2) samples are studied in order to understand the role of point defects in establishing room temperature ferromagnetism. The parameters calculated from the bound magnetic polaron (BMP) and Jorgensen's optical electronegativity models offer a satisfactory explanation of the defect-driven ferromagnetism in the doped/co-doped samples.

  19. Effect of Sn doping on the structural, optical and electrical properties of TiO2 films prepared by spray pyrolysis

    NASA Astrophysics Data System (ADS)

    Arunachalam, A.; Dhanapandian, S.; Manoharan, C.

    2016-02-01

    In this work, highly oriented pure and Tin-doped Titanium dioxide (Sn-doped TiO2) with porous nature photoelectrodes were deposited on ITO glass plates using spray pyrolysis technique. The XRD pattern revealed the formation of anatase TiO2 with the maximum intensity of (101) plane while doping 6 at% of Sn. The morphological studies depicted the porous nature with the uniform arrangement of small-sized grains. The presence of tin confirmed with the EDX spectra. The size of particles of 13 nm was observed from High Resolution Transmission Electron Microscopy (HR-TEM) analysis. The average transmittance was about 85% for the doped photoelectrode and was observed for the photoelectrode deposited with 6 at% of tin, with decreased energy band gap. The PL study showed the emission peak at 391 nm. The maximum carrier concentration and Hall mobility was observed for the photoelectrode deposited with 6 at% of tin. With these studies, the DSSCs were prepared separately with the dye extracted from Hibiscus Rosasinesis and Hibiscus Surttasinesis and their efficiency was maximum for the DSSC prepared with 6 at% of tin.

  20. Adhesion and inactivation of Gram-negative and Gram-positive bacteria on photoreactive TiO2/polymer and Ag-TiO2/polymer nanohybrid films

    NASA Astrophysics Data System (ADS)

    Tallósy, Szabolcs Péter; Janovák, László; Nagy, Elisabeth; Deák, Ágota; Juhász, Ádám; Csapó, Edit; Buzás, Norbert; Dékány, Imre

    2016-05-01

    The aim of this study was to develop photoreactive surface coatings, possessing antibacterial properties and can be activated under visible light illumination (λmax = 405 nm) using LED-light source. The photocatalytically active titanium dioxide (TiO2) was functionalized with silver nanoparticles (Ag NPs) and immobilized in polyacrylate based nanohybrid thin film in order to facilitate visible light activity (λAg/TiO2,max = 500 nm). First, the photocatalytic activity was modelled by following ethanol vapor degradation. The plasmonic functionalization resulted in 15% enhancement of the activity compared to pure TiO2. The photoreactive antimicrobial (5 log reduction of cfu in 2 h) surface coatings are able to inactivate clinically relevant pathogen strains (methicillin resistant Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa) within short time (60-120 min) due to the formed and quantified reactive oxygen species (ROS). The existence of electrostatic interactions between the negatively charged bacteria (from -0.89 to -3.19 μeq/109 cfu) and positively charged photocatalyst particles (in the range of +0.38 and +12.3 meq/100 g) was also proven by charge titration measurements. The surface inactivation of the bacteria and the photocatalytic degradation of the cell wall component were also confirmed by fluorescence and transmission electron microscopic observations, respectively. According to the results an effective sterilizing system and prevention strategy can be developed and carried out against dangerous microorganisms in health care.