Science.gov

Sample records for ag nanoprism concentration

  1. Triangular Ag-Pd alloy nanoprisms: rational synthesis with high-efficiency for electrocatalytic oxygen reduction.

    PubMed

    Xu, Lin; Luo, Zhimin; Fan, Zhanxi; Zhang, Xiao; Tan, Chaoliang; Li, Hai; Zhang, Hua; Xue, Can

    2014-10-21

    We report the generation of triangular Ag-Pd alloy nanoprisms through a rationally designed synthetic strategy based on silver nanoprisms as sacrificial templates. The galvanic replacement between Ag nanoprisms and H2PdCl4 along with co-reduction of Ag(+)/Pd(2+) is responsible for the formation of final prismatic Ag-Pd alloy nanostructures. Significantly, these Ag-Pd alloy nanoprisms exhibited superior electrocatalytic activity for the oxygen reduction reaction (ORR) as compared with the commercial Pd/C catalyst. Such a high catalytic activity is attributed to not only the alloyed Ag-Pd composition but also the dominant {111} facets of the triangular Ag-Pd nanoprisms. This work demonstrates the rational design of bimetallic alloy nanostructures with control of selective crystal facets that are critical to achieve high catalytic activity for fuel cell systems.

  2. Triangular Ag-Pd alloy nanoprisms: rational synthesis with high-efficiency for electrocatalytic oxygen reduction

    NASA Astrophysics Data System (ADS)

    Xu, Lin; Luo, Zhimin; Fan, Zhanxi; Zhang, Xiao; Tan, Chaoliang; Li, Hai; Zhang, Hua; Xue, Can

    2014-09-01

    We report the generation of triangular Ag-Pd alloy nanoprisms through a rationally designed synthetic strategy based on silver nanoprisms as sacrificial templates. The galvanic replacement between Ag nanoprisms and H2PdCl4 along with co-reduction of Ag+/Pd2+ is responsible for the formation of final prismatic Ag-Pd alloy nanostructures. Significantly, these Ag-Pd alloy nanoprisms exhibited superior electrocatalytic activity for the oxygen reduction reaction (ORR) as compared with the commercial Pd/C catalyst. Such a high catalytic activity is attributed to not only the alloyed Ag-Pd composition but also the dominant {111} facets of the triangular Ag-Pd nanoprisms. This work demonstrates the rational design of bimetallic alloy nanostructures with control of selective crystal facets that are critical to achieve high catalytic activity for fuel cell systems.We report the generation of triangular Ag-Pd alloy nanoprisms through a rationally designed synthetic strategy based on silver nanoprisms as sacrificial templates. The galvanic replacement between Ag nanoprisms and H2PdCl4 along with co-reduction of Ag+/Pd2+ is responsible for the formation of final prismatic Ag-Pd alloy nanostructures. Significantly, these Ag-Pd alloy nanoprisms exhibited superior electrocatalytic activity for the oxygen reduction reaction (ORR) as compared with the commercial Pd/C catalyst. Such a high catalytic activity is attributed to not only the alloyed Ag-Pd composition but also the dominant {111} facets of the triangular Ag-Pd nanoprisms. This work demonstrates the rational design of bimetallic alloy nanostructures with control of selective crystal facets that are critical to achieve high catalytic activity for fuel cell systems. Electronic supplementary information (ESI) available. See DOI: 10.1039/c4nr03600j

  3. Plasmonic Ag@oxide nanoprisms for enhanced performance of organic solar cells.

    PubMed

    Du, Peng; Jing, Pengtao; Li, Di; Cao, Yinghui; Liu, Zhenyu; Sun, Zaicheng

    2015-05-01

    Localized surface plasmon resonance (LSPR), light scattering, and lowering the series resistance of noble metal nanoparticles (NPs) provide positive effect on the performance of photovoltaic device. However, the exciton recombination on the noble metal NPs accompanying above influences will deteriorate the performance of device. In this report, surface-modified Ag@oxide (TiO2 or SiO2 ) nanoprisms with 1-2 nm shell thickness are developed. The thin film composed of P3HT/Ag@oxides and P3HT:PCBM/Ag@oxides is investigated by absorption, photoluminescence (PL), and transient absorption spectroscopy. The results show a significant absorption, PL enhancement, and long-lived photogenerated polaron in the P3HT/Ag@TiO2 film, indicating the increase of photogenerated exciton population by LSPR of Ag nanoprisms. In the case of P3HT/Ag nanoprisms, partial PL quench and relatively short-lived photogenerated polaron are observed. That indicates that the oxides layer can effectively avoid the exciton recombination. When the Ag@oxide nanoprisms are introduced into the active layer of P3HT:PCBM photovoltaic devices, about 31% of power conversion efficiency enhancement is obtained relative to the reference cell. All these results indicate that Ag@oxides can enhance the performance of the cell, at the same time the ultrathin oxide shell prevents from the exciton recombination.

  4. ``Red-to-blue'' colorimetric detection of cysteine via anti-etching of silver nanoprisms

    NASA Astrophysics Data System (ADS)

    Li, Yonglong; Li, Zihou; Gao, Yuexia; Gong, An; Zhang, Yujie; Hosmane, Narayan S.; Shen, Zheyu; Wu, Aiguo

    2014-08-01

    The reported strategies for cysteine (Cys) colorimetric detection based on noble metal nanomaterials include triggering aggregation, etching or fluorescence quenching of nanomaterials by Cys. In this study, we propose a new strategy for Cys colorimetric detection, i.e. anti-etching of silver nanoprisms (AgNPRs). In the absence of Cys, iodide ions (I-) could etch the corners and edges of AgNPRs and induce the morphology transition from nanoprism to nanodisk, which results in color change of the AgNPR dispersion from blue to red. In its presence, however, Cys can prevent the AgNPRs from I- attack. In that case, the color of the AgNPR dispersion containing I- and Cys remains blue. The mechanism is confirmed by using UV-vis spectra, TEM, DLS, Raman spectra and XPS spectra. According to the sensing effect of the Cys detection system, the concentration of I- incubated with AgNPRs, incubation time of AgNPRs and I-, and pH of AgNPR dispersions are optimized to 5.0 μM, 10 min, and pH 6.2, respectively. Under the optimized conditions, the proposed Cys detection system has excellent selectivity and high sensitivity. The limit of detection (LOD) of our Cys detection system is 25 nM by the naked eye, which is much better than the reported lowest LOD by eye-vision (100 nM), and 10 nM by UV-vis spectroscopy. The results of Cys detection in rabbit urine or plasma samples reinforce that our Cys detection system is applicable for rapid colorimetric detection of Cys in real body fluid samples.The reported strategies for cysteine (Cys) colorimetric detection based on noble metal nanomaterials include triggering aggregation, etching or fluorescence quenching of nanomaterials by Cys. In this study, we propose a new strategy for Cys colorimetric detection, i.e. anti-etching of silver nanoprisms (AgNPRs). In the absence of Cys, iodide ions (I-) could etch the corners and edges of AgNPRs and induce the morphology transition from nanoprism to nanodisk, which results in color change of the

  5. Synthesis of gold hexagonal bipyramids directed by planar-twinned silver triangular nanoprisms.

    PubMed

    Personick, Michelle L; Langille, Mark R; Wu, Jinsong; Mirkin, Chad A

    2013-03-13

    The direct growth of planar-twinned Au nanoparticles (NPs) in high yield remains a challenge in shape-controlled NP synthesis largely because suitable planar-twinned seeds for Au NP growth have not been identified to date. Herein we describe the use of planar-twinned Ag triangular nanoprisms as a means to dictate Au NP twin structure. In a one-pot process, the Ag triangular nanoprisms first undergo oxidative Au replacement, forming Ag-Au alloy nanoframes and concomitantly releasing Ag(+) into solution, which then directs subsequent Au NP growth through an underpotential deposition process. The planar-twinned structure of the initial Ag nanoprism is maintained throughout particle growth. Using this method, we have successfully synthesized Au hexagonal bipyramids in high yield for the first time.

  6. Synthesis of silicon carbide hexagonal nanoprisms

    NASA Astrophysics Data System (ADS)

    Wu, R. B.; Yang, G. Y.; Pan, Y.; Chen, J. J.

    2007-02-01

    SiC hexagonal nanoprisms have been prepared by a reaction of multiwall carbon nanotubes and Si vapor in an Astro furnace at 1450 °C for 3 h. The polytype, morphology, crystal structure of the nanoprisms were studied by X-ray powder diffraction, scanning electron microscopy and high resolution transmission electron microscopy, showing their hexagonal nanoprism shapes with a 3C-SiC single crystal structure with a diameter of about 100 nm and 2 μm in length. The photoluminescence spectrum of the nanoprisms exhibits a significant blue-shift relative to bulk 3C-SiC and other nanostructured SiC. The possible growth mechanism that controls the nanostructure formation is also analysed.

  7. Metamorphosis-like photochemical growth route for silver nanoprisms synthesis via the unrevealed key intermediates of nanorods and nanotrapezoids

    NASA Astrophysics Data System (ADS)

    Zhu, Yingming; Yang, Shaobo; Cai, Jinmeng; Yu, Yifu; Meng, Ming; Li, Xingfei

    2014-10-01

    Photochemical synthesis is a promising strategy for the control of both the size and shape of silver nanoprisms; however, the mechanism of nanoprism formation under irradiation still remains as a mystery. Intermediates, which often contain abundant information about the reaction process, are significant to the understanding of reaction mechanisms. Unfortunately, intermediates are usually hard to be acquired due to the fast reaction rate. Herein, we successfully slow down the conversion rate of the photochemical reactions by enlarging the solution volume and removing morphology-directing agent bis(p-sulfonatophe-nyl) phenylphosphine dihydrate dipotassium. Nanorods and nanotrapezoids were found to be the key intermediates for the photoinduced formation of silver nanoprisms with 100 nm edge length, especially the nanorods which have never identified as the intermediates for silver nanoprism formation. Characterization methods including time-dependent ultraviolet-visible spectroscopy, high resolution transmission electron microscopy (TEM and HRTEM), and selected area electron diffraction were employed to characterize these intermediates. Based upon the revealed evidences, a plausible metamorphosis-like photochemical growth route for the formation of Ag nanoprisms via the intermediates of nanorods and nanotrapezoid is proposed.

  8. Creating gold nanoprisms directly on quartz crystal microbalance electrodes for mercury vapor sensing

    NASA Astrophysics Data System (ADS)

    Sabri, Y. M.; Ippolito, S. J.; O'Mullane, A. P.; Tardio, J.; Bansal, V.; Bhargava, S. K.

    2011-07-01

    A novel electrochemical route is used to form highly {111}-oriented and size-controlled Au nanoprisms directly onto the electrodes of quartz crystal microbalances (QCMs) which are subsequently used as mercury vapor sensors. The Au nanoprism loaded QCM sensors exhibited excellent response-concentration linearity with a response enhancement of up to ~ 800% over a non-modified sensor at an operating temperature of 28 °C. The increased surface area and atomic-scale features (step/defect sites) introduced during the growth of nanoprisms are thought to play a significant role in enhancing the sensing properties of the Au nanoprisms toward Hg vapor. The sensors are shown to have excellent Hg sensing capabilities in the concentration range of 0.123-1.27 ppmv (1.02-10.55 mg m - 3), with a detection limit of 2.4 ppbv (0.02 mg m - 3) toward Hg vapor when operating at 28 °C, and 17 ppbv (0.15 mg m - 3) at 89 °C, making them potentially useful for air monitoring applications or for monitoring the efficiency of Hg emission control systems in industries such as mining and waste incineration. The developed sensors exhibited excellent reversible behavior (sensor recovery) within 1 h periods, and crucially were also observed to have high selectivity toward Hg vapor in the presence of ethanol, ammonia and humidity, and excellent long-term stability over a 33 day operating period.

  9. Silver nanoprisms self-assembly on differently functionalized silica surface

    NASA Astrophysics Data System (ADS)

    Pilipavicius, J.; Chodosovskaja, A.; Beganskiene, A.; Kareiva, A.

    2015-03-01

    In this work colloidal silica/silver nanoprisms (NPRs) composite coatings were made. Firstly colloidal silica sols were synthesized by sol-gel method and produced coatings on glass by dip-coating technique. Next coatings were silanized by (3-Aminopropyl)triethoxysilane (APTES), N-[3-(Trimethoxysilyl)propyl]ethylenediamine (AEAPTMS), (3- Mercaptopropyl)trimethoxysilane (MPTMS). Silver NPRs where synthesized via seed-mediated method and high yield of 94±15 nm average edge length silver NPRs were obtained with surface plasmon resonance peak at 921 nm. Silica-Silver NPRs composite coatings obtained by selfassembly on silica coated-functionalized surface. In order to find the most appropriate silanization way for Silver NPRs self-assembly, the composite coatings were characterized by scanning electron microscopy (SEM), dynamic light scattering (DLS), water contact angle (CA) and surface free energy (SFE) methods. Results have showed that surface functionalization is necessary to achieve self-assembled Ag NPRs layer. MPTMS silanized coatings resulted sparse distribution of Ag NPRs. Most homogeneous, even distribution composite coatings obtained on APTES functionalized silica coatings, while AEAPTMS induced strong aggregation of Silver NPRs.

  10. Effects of the position of silver nanoprisms on the performance of organic solar cells

    NASA Astrophysics Data System (ADS)

    Zhang, Qiang; Qin, Wen-jing; Cao, Huan-qi; Yang, Li-ying; Zhang, Feng-ling; Yin, Shou-gen

    2014-07-01

    Silver nanoprisms (AgNPs) affect the performance of organic solar cells (OSCs) in different ways depending on their positions in the device. To investigate this issue, we incorporate AgNPs in different positions of OSCs and compare their performance. The power conversion efficiency (PCE) is improved by 23.60% to 3.98% when the AgNPs are incorporated in front of the active layer. On the other hand, when AgNPs are incorporated in the back of the active layer, the short-circuit current density ( J SC) is improved by 17.44% to 10.84 mA/cm2. However, if AgNPs are incorporated in the active layer, both open-circuit voltage ( V OC) and J SC are decreased. We discuss the position effect on the device performance, clarify the absorption shadow and exciton recombination caused by AgNPs, and finally indicate that the optimal position of plasmonic AgNPs is in front of the active layer.

  11. The isotopic composition and concentration of Ag in iron meteorites and the origin of exotic silver

    NASA Technical Reports Server (NTRS)

    Kaiser, T.; Wasserburg, G. J.

    1983-01-01

    The isotopic composition of Ag and the concentration of Ag and Pd in Canyon Diablo (IA), Grant (IIIB), Santa Clara, Tlacotepec and Warburton Range (IVB), Pinon and Deep Springs (anom) were analyzed. Troilite from Santa Clara and from Grant was also studied. With the exception of IA, all the meteorites were enriched in Ag-107 by about 2%-212% and the ratio of Ag-107/Ag-109 in the metal phase was found to be greater than the terrestrial value. Ag of anomalous isotopic composition was found to be common in all IVB and anomalous meteorites. A correlation of Ag-107/Ag-109 with Pd/Ag was established except for the iron meteorite of Santa Clara. The excess Ag-107 is thought to result from the decay of Pd-107. The Grant data appear to represent a Pd-107-Ag-107 isochron and indicate that the cooling rate at elevated temperatures was rapid enough to preserve the isotopic differences between metal and troilite. The data suggest that Ag in Santa Clara is made up of almost pure Ag-107 produced from Pd-107 decay and Ag-109 produced by nuclear reactions with only a small amount of 'normal' Ag. This indicates an intense energetic particle bombardment history in the early solar system which occurred after the formation of small planetary bodies.

  12. Potassium permanganate-glutaraldehyde chemiluminescence system catalyzed by gold nanoprisms toward selective determination of fluoride.

    PubMed

    Abolhasani, Jafar; Hassanzadeh, Javad; Ghorbani-Kalhor, Ebrahim

    2016-02-01

    Gold and silver nanoparticles (NPs) are shown to exert a positive effect on the chemiluminescence (CL) reaction of permanganate aldehydes. Interestingly, between various shapes examined, Au nanoprisms have the highest beneficial effect. This effect is even more notable in the presence of sodium dodecyl sulfate (SDS) surfactant. UV-vis spectra and transmission electron microscopy were used to characterize the NP shapes and sizes. Furthermore, it was observed that iron(III) ions can slightly increase CL emission of this system. This intensification is very effective in the presence of fluoride ions (F(-)). These observations form the basis of the method for the high sensitive determination of F(-) in the 6-1200 nmol L(-1) concentration range, with a detection limit of 2.1 nmol L(-1). The proposed method has good precision and was satisfactorily used in the selective determination of low concentrations of fluoride ion in real samples.

  13. Glancing angle deposition of Fe triangular nanoprisms consisting of vertically-layered nanoplates

    NASA Astrophysics Data System (ADS)

    Li, Jianghao; Li, Liangliang; Ma, Lingwei; Zhang, Zhengjun

    2016-10-01

    Fe triangular nanoprisms consisting of vertically-layered nanoplates were synthesized on Si substrate by glancing angle deposition (GLAD) with an electron beam evaporation system. It was found that Fe nanoplates with a crystallographic plane index of BCC (110) were stacked vertically to form triangular nanoprisms and the axial direction of the nanoprisms, BCC <001>, was normal to the substrate. The effects of experimental parameters of GLAD on the growth and morphology of Fe nanoprisms were systematically studied. The deposition rate played an important role in the morphology of Fe nanoprisms at the same length, the deposition angle just affected the areal density of nanoprisms, and the rotation speed of substrate had little influence within the parameter range we investigated. In addition, the crystal growth mechanism of Fe nanoprisms was explained with kinetically-controlled growth mechanism and zone model theory. The driving force of crystal growth was critical to the morphology and microstructure of Fe nanoprisms deposited by GLAD. Our work introduced an oriented crystal structure into the nanomaterials deposited by GLAD, which provided a new approach to manipulate the properties and functions of nanomaterials.

  14. Electromagnetic properties of Bi-2223/Ag concentric tapes

    SciTech Connect

    Majoros, M.; Polak, M.; Kvitkovic, J.; Suchon, D.; Martini, L.; Ottoboni, V.; Zannella, S.

    1996-07-01

    It is well established that near the silver interface highly textured Bi-2223 layers compared to the inner ceramic core may be obtained. Thus Bi-2223 multilayered concentric tapes with silver matrix are very promising in increasing transport critical current densities. In the present work the authors report on the electromagnetic characterization of short tapes having in their cross-section a very thin HTS flattened ring with Ag inside and outside of it. The samples were prepared by the powder in tube method and have self-field critical current densities J{sub c} of the order of 3 {times} 10{sup 4} A/cm{sup 2} at 77 K. Transport and SQUID magnetization measurements revealed weak link nature of the samples in low magnetic fields. Large transport J{sub c}(B) hysteresis was observed at 4.2 K and magnetic fields up to 20 T. Magnetic field profiles measurements with miniature Hall sensors are in qualitative accordance with model calculations supposing homogeneous current density distribution across the superconducting core.

  15. Crystallinity effects on scaling properties of photoinduced modes in silver nanoprisms

    SciTech Connect

    Ng, Ming-Yaw; Ho, I-Lin; Chang, Yia-Chung

    2015-02-21

    The crystallinity effects on scaling properties of photoinduced modes in crystalline silver nanoprisms with C{sub 3v} symmetry are studied using a realistic atomistic model and group theory. Among all vibrational modes, photoinduced modes can be identified as those vibrational modes which possess larger in-phase radial atomic displacement and can be projected out by the projected density of states method. We found that the properties of vibrations in silver nanoprisms strongly depend on the particle’s aspect ratio (bisector length over thickness). By considering crystallinity of silver nanoprisms, the dominant modes with the in-plane oscillation become several closely spaced modes, and become obvious for nanoprisms with a smaller aspect ratio. The oscillation spectra show that the dominant planar modes are insensitive to thickness change. On the contrary, the atomic displacements show significantly different patterns for nanoprisms of different thicknesses. We also found that, for nanoprisms with same aspect ratio that is larger than 4, the vibrational properties of dominant modes exhibit scaling similarity. By using a simple linear transformation, the vibration frequencies for large-sized nanoprisms of aspect ratio 6 can be obtained by a corresponding scaling factor. The calculated results are in good agreement with experimental data.

  16. Effect of Ag nanoparticle concentration on the electrical and ferroelectric properties of Ag/P(VDF-TrFE) composite films

    DOE PAGES

    Paik, Haemin; Choi, Yoon -Young; Hong, Seungbum; ...

    2015-09-04

    We investigated the effect of the Ag nanoparticles on the ferroelectric and piezoelectric properties of Ag/poly(vinylidenefluoride-trifluoroethylene) (P(VDF-TrFE)) composite films. We found that the remanent polarization and direct piezoelectric coefficient increased up to 12.14 μC/cm2 and 20.23 pC/N when the Ag concentration increased up to 0.005 volume percent (v%) and decreased down to 9.38 μC/cm2 and 13.45 pC/N when it increased up to 0.01 v%. Further increase in Ag concentration resulted in precipitation of Ag phase and significant leakage current that hindered any meaningful measurement of the ferroelectric and piezoelectric properties. 46% increase of the remanent polarization value and 27% increasemore » of the direct piezoelectric coefficient were observed in the film with the 0.005 v% of the Ag nanoparticles added without significant changes to the crystalline structure confirmed by both X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) experiments. The enhancements of both the ferroelectric and piezoelectric properties are attributed to the increase in the effective electric field induced by the reduction in the effective volume of P(VDF-TrFE) that results in more aligned dipoles.« less

  17. Effect of Ag nanoparticle concentration on the electrical and ferroelectric properties of Ag/P(VDF-TrFE) composite films

    SciTech Connect

    Paik, Haemin; Choi, Yoon -Young; Hong, Seungbum; No, Kwangsoo

    2015-09-04

    We investigated the effect of the Ag nanoparticles on the ferroelectric and piezoelectric properties of Ag/poly(vinylidenefluoride-trifluoroethylene) (P(VDF-TrFE)) composite films. We found that the remanent polarization and direct piezoelectric coefficient increased up to 12.14 μC/cm2 and 20.23 pC/N when the Ag concentration increased up to 0.005 volume percent (v%) and decreased down to 9.38 μC/cm2 and 13.45 pC/N when it increased up to 0.01 v%. Further increase in Ag concentration resulted in precipitation of Ag phase and significant leakage current that hindered any meaningful measurement of the ferroelectric and piezoelectric properties. 46% increase of the remanent polarization value and 27% increase of the direct piezoelectric coefficient were observed in the film with the 0.005 v% of the Ag nanoparticles added without significant changes to the crystalline structure confirmed by both X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) experiments. The enhancements of both the ferroelectric and piezoelectric properties are attributed to the increase in the effective electric field induced by the reduction in the effective volume of P(VDF-TrFE) that results in more aligned dipoles.

  18. Systematic control of edge length, tip sharpness, thickness, and localized surface plasmon resonance of triangular Au nanoprisms

    NASA Astrophysics Data System (ADS)

    Noda, Yuta; Hayakawa, Tomokatsu

    2016-10-01

    Triangular gold (Au) nanoprisms of various sizes were synthesized in a controlled way using a modified three-step seed-mediated method with different volumes of starting seed solution and subsequent first step's growth solution. The structures and optical properties of the triangular Au nanoprisms were investigated using transmission electron microscopy (TEM), atomic force microscopy, and UV-Vis-NIR spectrophotometry. The Au nanoprisms synthesized also varied in optical response frequency of localized surface plasmon resonance (LSPR) owing to electric dipole polarizations of the Au nanoprisms. This variation depended nonlinearly on the volume of the seed solution. From optical extinction spectra and careful TEM observations, the dipole LSPR peak frequency was found to be linearly proportional to the edge length of the Au nanoprisms. Consequently, it was experimentally shown that the LSPR optical response frequency of their colloidal solutions could be controlled in the near-infrared region (700-1200 nm), corresponding to an edge length of 40-180 nm of the Au nanoprisms. It was also demonstrated that the tip sharpness of triangular Au nanoprisms was improved by using fine Au seeds instead of coarse Au seeds, and the resulting Au nanoprisms were smaller and thinner. A formation mechanism of triangular Au nanoprisms shall also be discussed with a prospect of synthesizing very tiny Au nanoprisms.

  19. Influence of Ag doping concentration on structural and optical properties of CdS thin film

    SciTech Connect

    Kumar, Pragati; Saxena, Nupur; Gupta, Vinay; Agarwal, Avinash

    2015-05-15

    This work shows the influence of Ag concentration on structural properties of pulsed laser deposited nanocrystalline CdS thin film. X-ray photoelectron spectroscopy (XPS) studies confirm the dopant concentration in CdS films and atomic concentration of elements. XPS studies show that the samples are slightly sulfur deficient. GAXRD scan reveals the structural phase transformation from cubic to hexagonal phase of CdS without appearance of any phase of CdO, Ag{sub 2}O or Ag{sub 2}S suggesting the substitutional doping of Ag ions. Photoluminescence studies illustrate that emission intensity increases with increase in dopant concentration upto 5% and then decreases for higher dopant concentration.

  20. The isotopic composition and concentration of AG in iron meteorites and the origin of exotic silver

    NASA Astrophysics Data System (ADS)

    Kaiser, T.; Wasserburg, G. J.

    1983-01-01

    The isotopic composition of Ag and the concentration of Ag and Pd have been determined in Canyon Diablo (IA), Grant (IIIB), Hoba, Santa Clara, Tlacotepec and Warburton Range (IVB), Piñon and Deep Springs (anom.). Troilite from Grant and Santa Clara have also been analyzed. All of these meteorites, with the exception of Canyon Diablo, give 107Ag/109Ag in the metal phase that is greater than the terrestrial value with the enrichments of 107Ag ranging from ≡2% to 212%. These data show that Ag of anomalous isotopic composition is common to all IVB and anomalous meteorites. The results on Grant suggest that the anomalies may be widespread including more common meteorite groups. There is a general correlation of 107Ag/109Ag with Pd/Ag except for the data from FeS of Santa Clara. The data suggest that Ag in Santa Clara and possibly other IVB meteorites is made up of almost pure 107Ag produced from 107Pd decay and 109Ag produced by nuclear reactions with only a small amount of "normal" Ag. This indicates an intense energetic particle bombardment history in the early solar system (≡1020 p/m2) which occurred after the formation of small planetary bodies. The authors infer that a T-Tauri activity by the early sun contributed to some late stage "nucleosynthesis" and the heating of a dust cloud. In addition, implications on the early thermal evolution of iron meteorites are presented based on 107Pd decay and models of the cooling history.

  1. Charge carrier mobility and concentration as a function of composition in AgPO3-AgI glasses

    NASA Astrophysics Data System (ADS)

    Rodrigues, Ana Candida Martins; Nascimento, Marcio Luis Ferreira; Bragatto, Caio Barca; Souquet, Jean-Louis

    2011-12-01

    Conductivity data of the xAgI(1 - x)AgPO3 system (0 ≤ x ≤ 0.5) were collected in the liquid and glassy states. The difference in the dependence of ionic conductivity on temperature below and above their glass transition temperatures (Tg) is interpreted by a discontinuity in the charge carrier's mobility mechanisms. Charge carrier displacement occurs through an activated mechanism below Tg and through a Vogel-Fulcher-Tammann-Hesse mechanism above this temperature. Fitting conductivity data with the proposed model allows one to determine separately the enthalpies of charge carrier formation and migration. For the five investigated compositions, the enthalpy of charge carrier formation is found to decrease, with x, from 0.86 to 0.2 eV, while the migration enthalpy remains constant at ≈0.14 eV. Based on these values, the charge carrier mobility and concentration in the glassy state can then be calculated. Mobility values at room temperature (≈10-4 cm2 V-1 s-1) do not vary significantly with the AgI content and are in good agreement with those previously measured by the Hall-effect technique. The observed increase in ionic conductivity with x would thus only be due to an increase in the effective charge carrier concentration. Considering AgI as a weak electrolyte, the change in the effective charge carrier concentration is justified and is correlated to the partial free energy of silver iodide forming a regular solution with AgPO3.

  2. Modal engineering of Surface Plasmons in apertured Au Nanoprisms

    NASA Astrophysics Data System (ADS)

    Cuche, Aurélien; Viarbitskaya, Sviatlana; Sharma, Jadab; Arbouet, Arnaud; Girard, Christian; Dujardin, Erik

    2015-11-01

    Crystalline gold nanoprisms of sub-micrometric size sustain high order plasmon modes in the visible and near infrared range that open a new realm for plasmon modal design, integrated coplanar devices and logic gates. In this article, we explore the tailoring of the surface plasmon local density of states (SP-LDOS) by embedding a single defect, namely a small hole, carved in the platelet by focused ion beam (FIB). The change in the SP-LDOS of the hybrid structure is monitored by two-photon luminescence (TPL) microscopy. The dependency of the two-dimensional optical field intensity maps on the linear polarization of the tightly focused femtosecond laser beam reveals the conditions for which the hole defect significantly affects the initial modes. A detailed numerical analysis of the spectral characteristics of the SP-LDOS based on the Green dyadic method clearly indicates that the hole size and location can be exploited to tune or remove selected SP modes.

  3. Glucose-functionalized Au nanoprisms for optoacoustic imaging and near-infrared photothermal therapy

    NASA Astrophysics Data System (ADS)

    Han, Jishu; Zhang, Jingjing; Yang, Meng; Cui, Daxiang; de La Fuente, Jesus M.

    2015-12-01

    Targeted imaging and tumor therapy using nanomaterials has stimulated research interest recently, but the high cytotoxicity and low cellular uptake of nanomaterials limit their bioapplication. In this paper, glucose (Glc) was chosen to functionalize Au nanoprisms (NPrs) for improving the cytotoxicity and cellular uptake of Au@PEG-Glc NPrs into cancer cells. Glucose is a primary source of energy at the cellular level and at cellular membranes for cell recognition. A coating of glucose facilitates the accumulation of Au@PEG-Glc NPrs in a tumor region much more than Au@PEG NPrs. Due to the high accumulation and excellent photoabsorbing property of Au@PEG-Glc NPrs, enhanced optoacoustic imaging of a tumor in vivo was achieved, and visualization of the tumor further guided cancer treatment. Based on the optical-thermal conversion performance of Au@PEG-Glc NPrs, the tumor in vivo was effectively cured through photothermal therapy. The current work demonstrates the great potential of Au@PEG-Glc NPrs in optoacoustic imaging and photothermal cancer therapy in future.Targeted imaging and tumor therapy using nanomaterials has stimulated research interest recently, but the high cytotoxicity and low cellular uptake of nanomaterials limit their bioapplication. In this paper, glucose (Glc) was chosen to functionalize Au nanoprisms (NPrs) for improving the cytotoxicity and cellular uptake of Au@PEG-Glc NPrs into cancer cells. Glucose is a primary source of energy at the cellular level and at cellular membranes for cell recognition. A coating of glucose facilitates the accumulation of Au@PEG-Glc NPrs in a tumor region much more than Au@PEG NPrs. Due to the high accumulation and excellent photoabsorbing property of Au@PEG-Glc NPrs, enhanced optoacoustic imaging of a tumor in vivo was achieved, and visualization of the tumor further guided cancer treatment. Based on the optical-thermal conversion performance of Au@PEG-Glc NPrs, the tumor in vivo was effectively cured through

  4. Study of the tryptophan-terbium FRET pair coupled to silver nanoprisms for biosensing applications.

    PubMed

    di Gennaro, Ane K; Gurevich, Leonid; Skovsen, Esben; Overgaard, Michael T; Fojan, Peter

    2013-06-14

    Plasmonic coupling between fluorophores and metal surfaces has become a focal point of optical research during the last two decades, however, the interactions of FRET couples with metal surfaces remain relatively unexplored. In this study, interactions of the tryptophan-Tb(3+) FRET pair with silver nanoprisms for potential biosensor development have been investigated. For this purpose an engineered lanthanide binding peptide (LBTtrp) containing tryptophan as the sensitizer for bound lanthanide ions (Tb(3+)) as well as a trypsin cleavage site was synthesized. The modified LBTtrp peptide contained two N-terminal cysteine residues to provide a stronger coupling to the silver nanoprisms (~6 nm high, ~50 nm wide). This study investigated the interaction between tryptophan, chelated Tb(3+) ions, and silver nanoprisms in solution using fluorescence and transient absorption spectroscopy. We have found that Tb(3+) luminescence decreases upon binding of the LBTtrp-Tb(3+) to silver nanoprisms and increases upon trypsin cleavage. The transient absorption spectroscopy measurements showed a significant decrease in the lifetime of the excited singlet state of tryptophan upon Tb(3+) chelation, while coupling to the silver nanoprisms did not show a significant effect on tryptophan. The results obtained in this work demonstrate a first proof of concept for a new sensitive optical biosensor in solution.

  5. Structural and Optical Properties of Discrete Dendritic Pt Nanoparticles on Colloidal Au Nanoprisms

    PubMed Central

    2016-01-01

    Catalytic and optical properties can be coupled by combining different metals into nanoscale architectures in which both the shape and the composition provide fine-tuning of functionality. Here, discrete, small Pt nanoparticles (diameter = 3–6 nm) were grown in linear arrays on Au nanoprisms, and the resulting structures are shown to retain strong localized surface plasmon resonances. Multidimensional electron microscopy and spectroscopy techniques (energy-dispersive X-ray spectroscopy, electron tomography, and electron energy-loss spectroscopy) were used to unravel their local composition, three-dimensional morphology, growth patterns, and optical properties. The composition and tomographic analyses disclose otherwise ambiguous details of the Pt-decorated Au nanoprisms, revealing that both pseudospherical protrusions and dendritic Pt nanoparticles grow on all faces of the nanoprisms (the faceted or occasionally twisted morphologies of which are also revealed), and shed light on the alignment of the Pt nanoparticles. The electron energy-loss spectroscopy investigations show that the Au nanoprisms support multiple localized surface plasmon resonances despite the presence of pendant Pt nanoparticles. The plasmonic fields at the surface of the nanoprisms indeed extend into the Pt nanoparticles, opening possibilities for combined optical and catalytic applications. These insights pave the way toward comprehensive nanoengineering of multifunctional bimetallic nanostructures, with potential applications in plasmon-enhanced catalysis and in situ monitoring of chemical processes via surface-enhanced spectroscopy. PMID:27688821

  6. Study on electrostatic resonance of nanoprisms with sharp corners

    NASA Astrophysics Data System (ADS)

    Chan, Wai Soen; Ng, Ka Ki; Yu, Kin Wah

    2015-03-01

    We have studied the electrostatic resonance of metal nanoprisms with sharp corners numerically. We consider an infinite metal cylinder with polygonal base, e.g. square. The incident electric field lies in the plane of cross-section of the cylinder. Yu and co-workers proposed Green's function formalism (GFF) to numerically calculate the electric potential and field distribution in plasmonic systems. We will adopt the scheme to demonstrate the effect of sharp corners, particularly on the effect of electrostatic resonance spectrum, as in the spectral analysis proposed by Bergman and Milton. Hetherington and Thorpe investigated the conductivity of a sheet containing dilute inclusion with sharp corners, they made use of a conformal mapping approach to calculate the conductivity from circular inclusions. Helsing, McPhedran and Milton also investigated the optical properties of a metamaterial lattice with inclusions having sharp corners. We study the possibility of improving numerical accuracy by combining the conformal mapping approach and GFF. We may extend similar approach to investigate the properties of plasmonic systems, for examples nanoboties and nanostars.

  7. Modal engineering of Surface Plasmons in apertured Au Nanoprisms

    PubMed Central

    Cuche, Aurélien; Viarbitskaya, Sviatlana; Sharma, Jadab; Arbouet, Arnaud; Girard, Christian; Dujardin, Erik

    2015-01-01

    Crystalline gold nanoprisms of sub-micrometric size sustain high order plasmon modes in the visible and near infrared range that open a new realm for plasmon modal design, integrated coplanar devices and logic gates. In this article, we explore the tailoring of the surface plasmon local density of states (SP-LDOS) by embedding a single defect, namely a small hole, carved in the platelet by focused ion beam (FIB). The change in the SP-LDOS of the hybrid structure is monitored by two-photon luminescence (TPL) microscopy. The dependency of the two-dimensional optical field intensity maps on the linear polarization of the tightly focused femtosecond laser beam reveals the conditions for which the hole defect significantly affects the initial modes. A detailed numerical analysis of the spectral characteristics of the SP-LDOS based on the Green dyadic method clearly indicates that the hole size and location can be exploited to tune or remove selected SP modes. PMID:26563677

  8. Determining the Concentration Dependent Transformations of Ag Nanoparticles in Complex Media: Using SP-ICP-MS and Au@Ag Core-Shell Nanoparticles as Tracers.

    PubMed

    Merrifield, Ruth C; Stephan, Chady; Lead, Jamie

    2017-03-01

    The fate, behavior, and impact of engineered nanoparticles (NPs) in toxicological and environmental media are driven by complex processes which are difficult to quantify. A key limitation is the ability to perform measurements at low and environmentally relevant concentrations, since concentration may be a key factor determining fate and effects. Here, we use single particle inductively coupled mass spectroscopy (SP-ICP-MS) to measure directly NP diameter and particle number concentration of suspensions containing gold-silver core-shell (Au@Ag) NPs in EPA moderately hard water (MHW) and MHW containing 2.5 mg L(-1) Suwannee River fulvic acid. The Au core of the Au@Ag NPs acts as an internal standard, and aids in the analysis of the complex Ag transformations. The high sensitivity of SP-ICP-MS, along with the Au@Ag NPs, enabled us to track the NP transformations in the range 0.01 and 50 μg L(-1), without further sample preparation. On the basis of the analysis of both Au and Ag parameters (size, size distribution, and particle number), concentration was shown to be a key factor in NP behavior. At higher concentration, NPs were in an aggregation-dominated regime, while at the lower and environmentally representative concentrations, dissolution of Ag was dominant and aggregation was negligible. In addition, further formation of ionic silver as Ag NPs in the form of AgS or AgCl was shown to occur. Between 1 and 10 μg L(-1), both aggregation and dissolution were important. The results suggest that, under realistic conditions, the role of NP homoaggregation may be minimal. In addition, the complexity of exposure and dose in dose-response relationships is highlighted.

  9. NIR femtosecond laser induced hyper-Rayleigh scattering and luminescence from silver nanoprisms.

    PubMed

    Jain, Beena; Srivastava, Arvind Kumar; Uppal, Abha; Gupta, Pradeep Kumar; Das, Kaustuv

    2010-09-01

    The nonlinear response of silver nanoprisms (edge length 40 +/- 5 nm and thickness 4.5 +/- 0.5 nm) was studied by exciting with NIR femtosecond pulses (780-880 nm). These nanostructures were observed to generate hyper-Rayleigh scattering (HRS) and broadband luminescence. While HRS showed the expected second order power dependence, the luminescence was observed to follow a third order excitation power dependence. Both HRS and luminescence were observed to be dipolar in nature. The first hyperpolarizability of the nanoprisms was found to be an order of magnitude higher than approximately 15 nm sized nanospheres.

  10. Just What Is It That Makes Silver Nanoprisms So Different, So Appealing?

    ERIC Educational Resources Information Center

    Panzarasa, Guido

    2015-01-01

    Thanks to their unique physicochemical properties (e.g., surface plasmon resonance), noble metal nanoparticles are at the cornerstone of nanotechnology. Silver triangular nanoprisms are presented here as an ideal playground to introduce students to nanochemistry concepts such as the formation of shape-controlled nanostructures. Not only a reliable…

  11. Polyvinylpyrrolidone-induced anisotropic growth of gold nanoprisms in plasmon-driven synthesis

    SciTech Connect

    Zhai, Yueming; DuChene, Joseph S.; Wang, Yi-Chung; Qiu, Jingjing; Johnston-Peck, Aaron C.; You, Bo; Guo, Wenxiao; DiCiaccio, Benedetto; Qian, Kun; Zhao, Evan W.; Ooi, Frances; Hu, Dehong; Su, Dong; Stach, Eric A.; Zhu, Zihua; Wei, Wei David

    2016-07-04

    After more than a decade, it is still unknown whether the plasmon-mediated growth of silver nanostructures can be extended to the synthesis of other noble metals, as the molecular mechanisms governing the growth process remain elusive. In this paper, we demonstrate the plasmon-driven synthesis of gold nanoprisms and elucidate the details of the photochemical growth mechanism at the single-nanoparticle level. Our investigation reveals that the surfactant polyvinylpyrrolidone preferentially adsorbs along the nanoprism perimeter and serves as a photochemical relay to direct the anisotropic growth of gold nanoprisms. This discovery confers a unique function to polyvinylpyrrolidone that is fundamentally different from its widely accepted role as a crystal-face-blocking ligand. Additionally, we find that nanocrystal twinning exerts a profound influence on the kinetics of this photochemical process by controlling the transport of plasmon-generated hot electrons to polyvinylpyrrolidone. Finally, these insights establish a molecular-level description of the underlying mechanisms regulating the plasmon-driven synthesis of gold nanoprisms.

  12. Polyvinylpyrrolidone-induced anisotropic growth of gold nanoprisms in plasmon-driven synthesis

    DOE PAGES

    Zhai, Yueming; DuChene, Joseph S.; Wang, Yi-Chung; ...

    2016-07-04

    After more than a decade, it is still unknown whether the plasmon-mediated growth of silver nanostructures can be extended to the synthesis of other noble metals, as the molecular mechanisms governing the growth process remain elusive. In this paper, we demonstrate the plasmon-driven synthesis of gold nanoprisms and elucidate the details of the photochemical growth mechanism at the single-nanoparticle level. Our investigation reveals that the surfactant polyvinylpyrrolidone preferentially adsorbs along the nanoprism perimeter and serves as a photochemical relay to direct the anisotropic growth of gold nanoprisms. This discovery confers a unique function to polyvinylpyrrolidone that is fundamentally different frommore » its widely accepted role as a crystal-face-blocking ligand. Additionally, we find that nanocrystal twinning exerts a profound influence on the kinetics of this photochemical process by controlling the transport of plasmon-generated hot electrons to polyvinylpyrrolidone. Finally, these insights establish a molecular-level description of the underlying mechanisms regulating the plasmon-driven synthesis of gold nanoprisms.« less

  13. Polyvinylpyrrolidone-induced anisotropic growth of gold nanoprisms in plasmon-driven synthesis

    SciTech Connect

    Zhai, Yueming; DuChene, Joseph S.; Wang, Yi-Chung; Qiu, Jingjing; Johnston-Peck, Aaron C.; You, Bo; Guo, Wenxiao; DiCiaccio, Benedetto; Qian, Kun; Zhao, Evan W.; Ooi, Frances; Hu, Dehong; Su, Dong; Stach, Eric A.; Zhu, Zihua; Wei, Wei David

    2016-07-04

    After more than a decade, it is still unknown whether the plasmon-mediated growth of silver nanostructures can be extended to the synthesis of other noble metals, as the molecular mechanisms governing the growth process remain elusive. Herein, we demonstrate the plasmon-driven synthesis of gold nanoprisms and elucidate the details of the photochemical growth mechanism at the single-nanoparticle level. Our investigation reveals that the surfactant polyvinylpyrrolidone preferentially adsorbs along the nanoprism perimeter and serves as a photochemical relay to direct the anisotropic growth of gold nanoprisms. This discovery confers a unique function to polyvinylpyrrolidone that is fundamentally diferent from its widely accepted role as a crystal-face-blocking ligand. Additionally, we find that nanocrystal twinning exerts a profound influence on the kinetics of this photochemical process by controlling the transport of plasmon-generated hot electrons to polyvinylpyrrolidone. These insights establish a molecular-level description of the underlying mechanisms regulating the plasmon-driven synthesis of gold nanoprisms.

  14. Yb doping concentration and temperature influence on Yb:LuAG thermal lensing

    NASA Astrophysics Data System (ADS)

    Veselský, Karel; Šulc, Jan; Jelínková, Helena; Nejezchleb, Karel; Škoda, Václav

    2016-03-01

    The aim of this study was to investigate whether refractive power of thermal lens for Yb:LuAG crystal at cryogenic temperatures depends on Yb doping concentration which has not been examined yet. The three measured Yb:LuAG laser rods samples (length of 3 mm, diameter 3 mm, AR @ 0.94 μm and 1.03 μm, doping concentration 5.4, 8.4 and 16.6 at. % Yb/Lu) were mounted in the temperature controlled copper holder of the liquid nitrogen cryostat. Samples were longitudinally pumped with fiber coupled CW laser diode at 0.930 μm with the focal point 0.4 mm in diameter. The 38 mm long semi-hemispherical laser resonator consisted of a flat pump mirror (HR @ 1.03 μm and HT 0.94 μm) and curved output coupler (r=500 mm) of reflectivity 94 % @ 1.06 μm. The refractive power of thermal lens was estimated indirectly by measuring of change in the position of focused laser beam focal point. The measurement was performed for constant absorbed power of 10 W in temperature range from 80 up to 240 K. It was observed that cryogenic cooling caused reduction of thermal lens power, which increased linearly with increasing temperature. For temperatures from 80 to 160 K refractive power was identical for all concentration. For higher temperature the refractive power of thermal lens increased with increasing Yb3+ concentration. Presented study shows that application of cryogenic temperature leads to reduction of thermal effect even for high dopant concentration in Yb:LuAG crystal. This is essential for reaching of high output power while maintaining high beam quality.

  15. Influence of the Ag concentration on the medium-range order in a CuZrAlAg bulk metallic glass

    PubMed Central

    Gammer, C.; Escher, B.; Ebner, C.; Minor, A. M.; Karnthaler, H. P.; Eckert, J.; Pauly, S.; Rentenberger, C.

    2017-01-01

    Fluctuation electron microscopy of bulk metallic glasses of CuZrAl(Ag) demonstrates that medium-range order is sensitive to minor compositional changes. By analyzing nanodiffraction patterns medium-range order is detected with crystal-like motifs based on the B2 CuZr structure and its distorted structures resembling the martensitic ones. This result demonstrates some structural homology between the metallic glass and its high temperature crystalline phase. The amount of medium-range order seems slightly affected with increasing Ag concentration (0, 2, 5 at.%) but the structural motifs of the medium-range ordered clusters become more diverse at the highest Ag concentration. The decrease of dominant clusters is consistent with the destabilization of the B2 structure measured by calorimetry and accounts for the increased glass-forming ability. PMID:28322304

  16. Influence of the Ag concentration on the medium-range order in a CuZrAlAg bulk metallic glass

    NASA Astrophysics Data System (ADS)

    Gammer, C.; Escher, B.; Ebner, C.; Minor, A. M.; Karnthaler, H. P.; Eckert, J.; Pauly, S.; Rentenberger, C.

    2017-03-01

    Fluctuation electron microscopy of bulk metallic glasses of CuZrAl(Ag) demonstrates that medium-range order is sensitive to minor compositional changes. By analyzing nanodiffraction patterns medium-range order is detected with crystal-like motifs based on the B2 CuZr structure and its distorted structures resembling the martensitic ones. This result demonstrates some structural homology between the metallic glass and its high temperature crystalline phase. The amount of medium-range order seems slightly affected with increasing Ag concentration (0, 2, 5 at.%) but the structural motifs of the medium-range ordered clusters become more diverse at the highest Ag concentration. The decrease of dominant clusters is consistent with the destabilization of the B2 structure measured by calorimetry and accounts for the increased glass-forming ability.

  17. Controllable galvanic synthesis of triangular Ag-Pd alloy nanoframes for efficient electrocatalytic methanol oxidation.

    PubMed

    Xu, Lin; Luo, Zhimin; Fan, Zhanxi; Yu, Sijia; Chen, Junze; Liao, Yusen; Xue, Can

    2015-06-08

    Triangular Ag-Pd alloy nanoframes were successfully synthesized through galvanic replacement by using Ag nanoprisms as sacrificial templates. The ridge thickness of the Ag-Pd alloy nanoframes could be readily tuned by adjusting the amount of the Pd source during the reaction. These obtained triangular Ag-Pd alloy nanoframes exhibit superior electrocatalytic activity for the methanol oxidation reaction as compared with the commercial Pd/C catalyst due to the alloyed Ag-Pd composition as well as the hollow-framed structures. This work would be highly impactful in the rational design of future bimetallic alloy nanostructures with high catalytic activity for fuel cell systems.

  18. Synthesis and Characterization of Varying Concentrations of Ag-doped ZnO Thin Films

    NASA Astrophysics Data System (ADS)

    Hachlica, Justin; Wadie-Ibrahim, Patrick; Sahiner, M. Alper

    Silver doped ZnO is a promising compound for photovoltaic solar cell use. Doping this compound with varying amounts of silver will theoretically make this type of thin film more efficient by reducing the overall resistance and increasing the voltage and current output. The extent of this promise is being tested experimentally, by analysis of both the electrical and the surface roughness properties of the cells. Ag-doped Zinc Oxide is deposited by method of Pulsed Laser Deposition (PLD) onto Indium Tin Oxide (ITO) coated Glass. Annealing effects were also observed by varying the temperature at which the annealing occurred after synthesis of the sample. Thickness is confirmed by use of Ellipsometery. X-Ray Diffraction (XRD) measurements confirmed a ZnO crystal structure on the thin films. The active dopant carrier concentrations were determined using a Hall Effect Measuring System. Finally, the photovoltaic properties of the film are recorded by using a Keithley Source Meter. The structural characterization and electrical results of the effect of Ag doping on ZnO will then be discussed.

  19. Influence of temperature and precursor concentration on the synthesis of HDA-capped Ag{sub 2}Se nanoparticles

    SciTech Connect

    Mlambo, M.; Moloto, M.J.; Moloto, N.; Mdluli, P.S.

    2013-06-01

    Graphical abstract: The temperature effect on the growth and size of silver selenide nanoparticles with the size distribution and XRD patterns. Highlights: ► The HDA-capped Ag{sub 2}Se nanoparticles were synthesized via the colloidal route. ► Temperature and monomer concentration of the reaction were varied. ► The concentration as a factor influenced particles with a decrease observed as the amount of Ag{sup +} ion source is increased. ► Temperature has expected influence on the growth of particles resulting in increase as the temperature is increased. ► TEM images shows spherical particles and their orthorhombic phase from structural analysis by XRD. - Abstract: The size dependent of temperature and precursor concentration on the synthesis of hexadecylamine capped Ag{sub 2}Se nanoparticles via the colloidal route were studied using the combination of optical and structural analysis. The as-prepared Ag{sub 2}Se nanoparticles showed the quantum confinement with all the obtained absorption band edges blue-shifted from the bulk and their corresponding emission maxima displaying a red-shift from band edges characterised by UV–vis absorption and photoluminescence spectroscopy. The particle sizes were obtained from transmission electron microscopy analysis. The increase in precursor concentration resulted in a decrease in nanoparticle sizes. The increase in reaction temperature showed an increase in the nanoparticle sizes, when the critical temperature at 160 °C was reached, the nanoparticle sizes decreased.

  20. Gold Triangular Nanoprisms and Nanodecahedra: Synthesis and Interaction Studies with Luminol toward Biosensor Applications.

    PubMed

    Naveenraj, Selvaraj; Mangalaraja, Ramalinga Viswanathan; Wu, Jerry J; Asiri, Abdullah M; Anandan, Sambandam

    2016-11-15

    Gold triangular nanoprisms and nanodecahedra (pentagonal bipyramids) were synthesized in the absence and presence of nanoseeds by a simple solvothermal synthesis through the reduction of Auric Chloride (HAuCl4) with poly(vinylpyrrolidone) (PVP) in N,N-dimethylformamide (DMF), respectively. These gold nanoparticles exhibit two plasmon resonance bands. The interaction of these gold nanoparticles with luminol was investigated using UV-vis and fluorescence spectroscopy since hefty number of environmental and biological sensors are based on the combination of luminol and gold nanoparticles. The gold nanoparticles quenches the fluorescence of luminol through a static quenching mechanism, i.e., ground state complex formation, which was confirmed by both absorption spectroscopy as well as time-resolved fluorescence spectroscopy. The Stern-Volmer quenching constant and the effective quenching constant determine that gold nanodecahedra has more interaction with luminol than that of triangular gold nanoprisms. The distance between the gold nanoparticles and luminol, calculated using FRET theory, is less than 8 nm, which indicates efficient energy transfer during interaction. These results are expected to be useful for the development of novel sensors.

  1. Removal of gas phase low-concentration toluene over Mn, Ag and Ce modified HZSM-5 catalysts by periodical operation of adsorption and non-thermal plasma regeneration.

    PubMed

    Wang, Wenzheng; Wang, Honglei; Zhu, Tianle; Fan, Xing

    2015-07-15

    Ag/HZSM-5, Mn/HZSM-5, Ce/HZSM-5, Ag-Mn/HZSM-5 and Ce-Mn/HZSM-5 were prepared by impregnation method. Both their adsorption capacity and catalytic activity were investigated for the removal of gas phase low-concentration toluene by periodical operation of adsorption and non-thermal plasma regeneration. Results show that catalysts loaded with Ag (Ag/HZSM-5 and Ag-Mn/HZSM-5) had larger adsorption capacity for toluene than the other catalysts. And Ag-Mn/HZSM-5 displayed the best catalytic performance for both toluene oxidation by non-thermal plasma and byproducts suppression. On the other hand, the deactivated catalyst can be fully regenerated by calcining in air stream when its adsorption capacity and catalytic activity of the Ag-Mn/HZSM-5 catalyst was found to be decreased after 10 cycles of periodical adsorption and non-thermal regeneration.

  2. Fabrication and characterisation of the graphene ring micro electrode (GRiME) with an integrated, concentric Ag/AgCl reference electrode.

    PubMed

    Dickinson, James W; Bromley, Michael; Andrieux, Fabrice P L; Boxall, Colin

    2013-03-14

    We report the fabrication and characterisation of the first graphene ring micro electrodes with the addition of a miniature concentric Ag/AgCl reference electrode. The graphene ring electrode is formed by dip coating fibre optics with graphene produced by a modified Hummers method. The reference electrode is formed using an established photocatalytically initiated electroless deposition (PIED) plating method. The performance of the so-formed graphene ring micro electrodes (GRiMEs) and associated reference electrode is studied using the probe redox system ferricyanide and electrode thicknesses assessed using established electrochemical methods. Using 220 µm diameter fibre optics, a ~15 nm thick graphene ring electrode is obtained corresponding to an inner to outer radius ratio of >0.999, so allowing for use of extant analytical descriptions of very thin ring microelectrodes in data analysis. GRiMEs are highly reliable (current response invariant over >3,000 scans), with the concentric reference electrode showing comparable stability (current response invariant over >300 scans). Furthermore the micro-ring design allows for efficient use of electrochemically active graphene edge sites and the associated nA scale currents obtained neatly obviate issues relating to the high resistivity of undoped graphene. Thus, the use of graphene in ring microelectrodes improves the reliability of existing micro-electrode designs and expands the range of use of graphene-based electrochemical devices.

  3. Fabrication and Characterisation of the Graphene Ring Micro Electrode (GRiME) with an Integrated, Concentric Ag/AgCl Reference Electrode

    PubMed Central

    Dickinson, James W.; Bromley, Michael; Andrieux, Fabrice P. L.; Boxall, Colin

    2013-01-01

    We report the fabrication and characterisation of the first graphene ring micro electrodes with the addition of a miniature concentric Ag/AgCl reference electrode. The graphene ring electrode is formed by dip coating fibre optics with graphene produced by a modified Hummers method. The reference electrode is formed using an established photocatalytically initiated electroless deposition (PIED) plating method. The performance of the so-formed graphene ring micro electrodes (GRiMEs) and associated reference electrode is studied using the probe redox system ferricyanide and electrode thicknesses assessed using established electrochemical methods. Using 220 μm diameter fibre optics, a ∼15 nm thick graphene ring electrode is obtained corresponding to an inner to outer radius ratio of >0.999, so allowing for use of extant analytical descriptions of very thin ring microelectrodes in data analysis. GRiMEs are highly reliable (current response invariant over >3,000 scans), with the concentric reference electrode showing comparable stability (current response invariant over >300 scans). Furthermore the micro-ring design allows for efficient use of electrochemically active graphene edge sites and the associated nA scale currents obtained neatly obviate issues relating to the high resistivity of undoped graphene. Thus, the use of graphene in ring microelectrodes improves the reliability of existing micro-electrode designs and expands the range of use of graphene-based electrochemical devices. PMID:23493126

  4. Negative index optical chiral metamaterial based on asymmetric hexagonal arrays of metallic triangular nanoprisms

    NASA Astrophysics Data System (ADS)

    Giloan, M.; Astilean, S.

    2014-03-01

    Nanostructures made of two layers of metallic triangular nanoprisms arranged in hexagonal lattice separated by a dielectric layer are theoretically analyzed as chiral metamaterial slabs. Transmitted and reflected electromagnetic field of normally incident circular polarized plane waves are computed using a tri-dimensional (3D) finite-difference time domain (FDTD) algorithm. Chirality and effective constitutive parameters are calculated using the modified S-parameter retrieval method for chiral metamaterials. Different hybridized plasmon modes are induced by the left and right circularly polarized light leading to a chiral behavior of the asymmetric type metamaterials. Negative refractive index due to chirality is obtained in the near infrared range of the spectrum for either left or right polarization.

  5. Sculpturing patterns of plasmonic silver nanoprisms by means of photocatalytic lithography.

    PubMed

    Panzarasa, Guido; Soliveri, Guido; Marra, Gianluigi; Meda, Laura; Savoini, Alberto; Ardizzone, Silvia; Salvalaggio, Mario

    2017-04-18

    The controlled shaping of nanoparticles' morphology is one of the pillars of nanotechnology. Here, we demonstrate that photocatalytic lithography, a technique already proved to be useful in materials science, can act as a dry etching technique for noble metal nanoparticles. Triangular silver nanoprisms are self-assembled on titanium dioxide films and photocatalytically shaped into discoidal particles upon irradiation with near-UV light. The obtained patterned surfaces show a dramatically different surface-enhanced Raman scattering response, suggesting the utility of our approach for the development of sensors. The photocatalytic nature of the particle shaping is demonstrated and a plausible mechanism drawn by performing photocatalysis in different configurations (direct and remote) and by irradiating in different solvents.

  6. Sculpturing patterns of plasmonic silver nanoprisms by means of photocatalytic lithography

    NASA Astrophysics Data System (ADS)

    Panzarasa, Guido; Soliveri, Guido; Marra, Gianluigi; Meda, Laura; Savoini, Alberto; Ardizzone, Silvia; Salvalaggio, Mario

    2017-04-01

    The controlled shaping of nanoparticles’ morphology is one of the pillars of nanotechnology. Here, we demonstrate that photocatalytic lithography, a technique already proved to be useful in materials science, can act as a dry etching technique for noble metal nanoparticles. Triangular silver nanoprisms are self-assembled on titanium dioxide films and photocatalytically shaped into discoidal particles upon irradiation with near-UV light. The obtained patterned surfaces show a dramatically different surface-enhanced Raman scattering response, suggesting the utility of our approach for the development of sensors. The photocatalytic nature of the particle shaping is demonstrated and a plausible mechanism drawn by performing photocatalysis in different configurations (direct and remote) and by irradiating in different solvents.

  7. Cobalt carbide nanoprisms for direct production of lower olefins from syngas.

    PubMed

    Zhong, Liangshu; Yu, Fei; An, Yunlei; Zhao, Yonghui; Sun, Yuhan; Li, Zhengjia; Lin, Tiejun; Lin, Yanjun; Qi, Xingzhen; Dai, Yuanyuan; Gu, Lin; Hu, Jinsong; Jin, Shifeng; Shen, Qun; Wang, Hui

    2016-10-06

    Lower olefins-generally referring to ethylene, propylene and butylene-are basic carbon-based building blocks that are widely used in the chemical industry, and are traditionally produced through thermal or catalytic cracking of a range of hydrocarbon feedstocks, such as naphtha, gas oil, condensates and light alkanes. With the rapid depletion of the limited petroleum reserves that serve as the source of these hydrocarbons, there is an urgent need for processes that can produce lower olefins from alternative feedstocks. The 'Fischer-Tropsch to olefins' (FTO) process has long offered a way of producing lower olefins directly from syngas-a mixture of hydrogen and carbon monoxide that is readily derived from coal, biomass and natural gas. But the hydrocarbons obtained with the FTO process typically follow the so-called Anderson-Schulz-Flory distribution, which is characterized by a maximum C2-C4 hydrocarbon fraction of about 56.7 per cent and an undesired methane fraction of about 29.2 per cent (refs 1, 10, 11, 12). Here we show that, under mild reaction conditions, cobalt carbide quadrangular nanoprisms catalyse the FTO conversion of syngas with high selectivity for the production of lower olefins (constituting around 60.8 per cent of the carbon products), while generating little methane (about 5.0 per cent), with the ratio of desired unsaturated hydrocarbons to less valuable saturated hydrocarbons amongst the C2-C4 products being as high as 30. Detailed catalyst characterization during the initial reaction stage and theoretical calculations indicate that preferentially exposed {101} and {020} facets play a pivotal role during syngas conversion, in that they favour olefin production and inhibit methane formation, and thereby render cobalt carbide nanoprisms a promising new catalyst system for directly converting syngas into lower olefins.

  8. Cobalt carbide nanoprisms for direct production of lower olefins from syngas

    NASA Astrophysics Data System (ADS)

    Zhong, Liangshu; Yu, Fei; An, Yunlei; Zhao, Yonghui; Sun, Yuhan; Li, Zhengjia; Lin, Tiejun; Lin, Yanjun; Qi, Xingzhen; Dai, Yuanyuan; Gu, Lin; Hu, Jinsong; Jin, Shifeng; Shen, Qun; Wang, Hui

    2016-10-01

    Lower olefins—generally referring to ethylene, propylene and butylene—are basic carbon-based building blocks that are widely used in the chemical industry, and are traditionally produced through thermal or catalytic cracking of a range of hydrocarbon feedstocks, such as naphtha, gas oil, condensates and light alkanes. With the rapid depletion of the limited petroleum reserves that serve as the source of these hydrocarbons, there is an urgent need for processes that can produce lower olefins from alternative feedstocks. The ‘Fischer-Tropsch to olefins’ (FTO) process has long offered a way of producing lower olefins directly from syngas—a mixture of hydrogen and carbon monoxide that is readily derived from coal, biomass and natural gas. But the hydrocarbons obtained with the FTO process typically follow the so-called Anderson-Schulz-Flory distribution, which is characterized by a maximum C2-C4 hydrocarbon fraction of about 56.7 per cent and an undesired methane fraction of about 29.2 per cent (refs 1, 10, 11, 12). Here we show that, under mild reaction conditions, cobalt carbide quadrangular nanoprisms catalyse the FTO conversion of syngas with high selectivity for the production of lower olefins (constituting around 60.8 per cent of the carbon products), while generating little methane (about 5.0 per cent), with the ratio of desired unsaturated hydrocarbons to less valuable saturated hydrocarbons amongst the C2-C4 products being as high as 30. Detailed catalyst characterization during the initial reaction stage and theoretical calculations indicate that preferentially exposed {101} and {020} facets play a pivotal role during syngas conversion, in that they favour olefin production and inhibit methane formation, and thereby render cobalt carbide nanoprisms a promising new catalyst system for directly converting syngas into lower olefins.

  9. Dipole plasmon resonance induced large third-order optical nonlinearity of Au triangular nanoprism in infrared region.

    PubMed

    Chen, Ziyu; Dai, Hongwei; Liu, Jiaming; Xu, Hui; Li, Zixuan; Zhou, Zhang-Kai; Han, Jun-Bo

    2013-07-29

    Au triangular nanoprisms with strong dipole plasmon absorption peak at 1240 nm were prepared by wet chemical methods. Both numerical calculations and experiments were carried out to investigate the optical properties of the samples. Finite difference time domain (FDTD) and Local Density of States (LDOS) calculations demonstrate that strong electric field enhancement and large LDOS can be obtained at tip areas of the Au triangular nanoprisms. Z scan techniques were used to characterize the nonlinear absorption, nonlinear refraction, as well as one- and two-photon figures of merit (W and T, respectively) of the sample. The results show that maximum nonlinear refractive index can be obtained around the resonance absorption wavelength of 1240 nm, detuning the wavelength from the absorption peak will lead to the decrease of the nonlinear refractive index n(2), while the nonlinear absorption coefficient β doesn't change much with the wavelength. This large wavelength dependence of n(2) and small change of β enable the sample to satisfy the all-optical switching demand of W> 1 and T< 1 easily in a large wavelength range of 1200-1300 nm. These significant nonlinear properties of the sample imply that Au triangular nanoprism is a good candidate for future optical switches in infrared optical communication wavelength region.

  10. Growth of different morphologies (quantum dots to nanorod) of Ag-nanoparticles: role of cysteine concentrations.

    PubMed

    Khan, Zaheer; Talib, Abou

    2010-03-01

    This work describes an easy chemical method for the preparation of orange-red color silver sol by the cysteine reduction of silver (I) in the presence of cetyltrimethylammonium bromide (CTAB). The obtained sol was found to have very small particles in the order of quantum dots for the first time. Transmission electron microscope (TEM) images show that the silver sol consists of aggregated as well as cross-linking arrangement of spherical silver quantum dots (size in the range ca. Ag-nanoparticles from quantum dots to nanorod of diameter 60nm and pearl-necklace shaped which occurred due to the cross-linking aggregation of silver quantum dots. For a certain reaction time, i.e., 100min, the absorbance of reaction mixture first increased until it reached a maximum, then decreased with [cysteine]. The rate of Ag-nanoparticles formation decreases with the increase in [cysteine] whereas [CTAB] and [Ag(+)] have no effect on the reaction rate. Interestingly, at higher [cysteine] (>or=20.0x10(-4)mol dm(-3)), white precipitate was formed instead of transparent silver sol. Cysteine acts as a reducing, cross-linking, stabilizing and buffering agent during the growth of different shape and size of silver nanoparticles.

  11. Effects of concentration of Ag nanoparticles on surface structure and in vitro biological responses of oxide layer on pure titanium via plasma electrolytic oxidation

    NASA Astrophysics Data System (ADS)

    Shin, Ki Ryong; Kim, Yeon Sung; Kim, Gye Won; Yang, Hae Woong; Ko, Young Gun; Shin, Dong Hyuk

    2015-08-01

    This study was to investigate how Ag nanoparticles with various concentrations affect the surface structure and in vitro biological properties of oxide layers on the pure titanium produced by a plasma electrolytic oxidation (PEO) process. For this aim, PEO processes were carried out at an AC current density of 100 mA/cm2 for 300 s in potassium pyrophosphate (K4P2O7) electrolytes containing 0, 0.1, 0.3 and 0.5 g/l Ag nanoparticles. Structural investigations using scanning electron microscopy evidenced that the oxide layers showed the successful incorporation of Ag nanoparticles, and the topographical deformation of the porous surface was found when the concentration of Ag nanoparticles was more than 0.1 g/l. Based on the anti-bacterial activity of all oxide layers, the Ag nanoparticles uniformly spread were of considerable importance in triggering the disinfection of E. coli bacteria. The bone forming abilities and cell (MC3T3-E1) proliferation rates of oxide layers produced in electrolytes containing 0 and 0.1 g/l Ag nanoparticles were higher than those containing 0.3 and 0.5 g/l Ag nanoparticles. Consequently, the oxide layer on pure titanium via PEO process in the electrolyte with 0.1 g/l Ag nanoparticles exhibited better the bioactivity accompanying the anti-bacterial activity.

  12. Microfluidic synthesis of Ag@Cu2O core-shell nanoparticles with enhanced photocatalytic activity.

    PubMed

    Tao, Sha; Yang, Mei; Chen, Huihui; Ren, Mingyue; Chen, Guangwen

    2017-01-15

    A microfluidic-based method for the continuous synthesis of Ag@Cu2O core-shell nanoparticles (NPs) has been developed. It only took 32s to obtain Ag@Cu2O core-shell NPs, indicating a high efficiency of this microfluidic-based method. Triangular Ag nanoprisms were employed as the cores for the overgrowth of Cu2O through the reduction of Cu(OH)4(2-) with ascorbic acid. The as-synthesized samples were characterized by XRD, TEM, SEM, HAADF-STEM, EDX, HRTEM, UV-vis spectra and N2 adsorption-desorption. The characterization results revealed that the as-synthesized Ag@Cu2O core-shell NPs exhibited a well-defined core-shell nanostructure with a polycrystalline shell, which was composed of numbers of Cu2O domains epitaxially growing on the triangular Ag nanoprism. It was concluded that the synthesis parameters such as the molar ratio of trisodium citrate to AgNO3, H2O2 to AgNO3, NaOH to CuSO4, ascorbic acid to CuSO4 and AgNO3 to CuSO4 had significant effect on the synthesis of Ag@Cu2O core-shell NPs. Moreover, Ag@Cu2O core-shell NPs exhibited superior catalytic activity in comparison with pristine Cu2O NPs towards the visible light-driven degradation of methyl orange. This enhanced photocatalytic activity of Ag@Cu2O core-shell NPs was attributed to the larger BET surface area and improved charge separation efficiency. The trapping experiment indicated that holes and superoxide anion radicals were the major reactive species in the photodegradation of methyl orange over Ag@Cu2O core-shell NPs. In addition, Ag@Cu2O core-shell NPs showed no obvious deactivation in the cyclic test.

  13. Dissecting the molecular mechanism of apoptosis during photothermal therapy using gold nanoprisms.

    PubMed

    Pérez-Hernández, Marta; Del Pino, Pablo; Mitchell, Scott G; Moros, María; Stepien, Grazyna; Pelaz, Beatriz; Parak, Wolfgang J; Gálvez, Eva M; Pardo, Julián; de la Fuente, Jesús M

    2015-01-27

    The photothermal response of plasmonic nanomaterials can be exploited for a number of biomedical applications in diagnostics (biosensing and optoacoustic imaging) and therapy (drug delivery and photothermal therapy). The most common cellular response to photothermal cancer treatment (ablation of solid tumors) using plasmonic nanomaterials is necrosis, a process that releases intracellular constituents into the extracellular milieu producing detrimental inflammatory responses. Here we report the use of laser-induced photothermal therapy employing gold nanoprisms (NPRs) to specifically induce apoptosis in mouse embryonic fibroblast cells transformed with the SV40 virus. Laser-irradiated "hot" NPRs activate the intrinsic/mitochondrial pathway of apoptosis (programmed cell death), which is mediated by the nuclear-encoded proteins Bak and Bax through the activation of the BH3-only protein Bid. We confirm that an apoptosis mechanism is responsible by showing how the NPR-mediated cell death is dependent on the presence of caspase-9 and caspase-3 proteins. The ability to selectively induce apoptotic cell death and to understand the subsequent mechanisms provides the foundations to predict and optimize NP-based photothermal therapy to treat cancer patients suffering from chemo- and radioresistance.

  14. Two-Dimensional Au-Nanoprism/Reduced Graphene Oxide/Pt-Nanoframe as Plasmonic Photocatalysts with Multiplasmon Modes Boosting Hot Electron Transfer for Hydrogen Generation.

    PubMed

    Lou, Zaizhu; Fujitsuka, Mamoru; Majima, Tetsuro

    2017-02-16

    Two-dimensional Au-nanoprism/reduced graphene oxide (rGO)/Pt-nanoframe was synthesized as plasmonic photocatalyt, exhibiting activity of photocatalytic hydrogen generation greater than those of Au-nanorod/rGO/Pt-nanoframe and metallic plasmonic photocatalyst Pt-Au. The single-particle plasmonic photoluminescence study demonstrated that Au-nanorod has only a longitudinal plasmon resonance mode for hot electron transfer to rGO, while Au-nanoprism has in-plane dipole and multipole surface plasmon resonance modes for hot electron transfer, leading to highly efficient charge separation for hydrogen generation.

  15. Effect of Aluminum Concentration on the Interfacial Reactions of Sn-3.0Ag- xAl Solders with Copper and ENIG Metallizations

    NASA Astrophysics Data System (ADS)

    Xia, Y. H.; Jee, Y. K.; Yu, J.; Lee, T. Y.

    2008-12-01

    Aluminum was added into Sn-3.0Ag (wt.%) solder to investigate the effect of aluminum concentration on the interfacial reaction of Sn-3.0Ag- xAl solders with copper or electroless nickel immersion gold (ENIG) metallizations. Four different Sn-3.0Ag- xAl solders ( x = 0 wt.%, 0.1 wt.%, 0.5 wt.%, and 1.0 wt.%) were used for comparison. It was found that the composition, morphology, and thickness of interfacial reaction products were strongly dependent on aluminum concentration. At low aluminum concentration (0.1 wt.%), the typical Cu6Sn5 layer was formed at the interface. When the aluminum concentration was 0.5 wt.%, a continuous CuAl2 layer spalled off from the interfacial Cu-Sn intermetallic compound (IMC) layer. Only a planar CuAl2 layer was observed at the interface when the aluminum concentration was increased to 1.0 wt.%. In Sn-Ag-Al/ENIG reactions, Ni3Sn4 was formed and spallation occurred near the interface in the Sn-3.0Ag and Sn-3.0Ag-0.1Al solder joints. When the aluminum concentration was higher than 0.1 wt.%, a thin planar AuAl compound formed at the interface. There was no P-rich phase formation that retarded the spalling phenomenon. The aluminum additive in Sn-Ag solder inhibited the growth of IMCs in the reaction with copper or ENIG metallizations, which was favorable for the reliability of solder joints.

  16. Dispensing of high concentration Ag nano-particles ink for ultra-low resistivity paper-based writing electronics.

    PubMed

    Wang, Fuliang; Mao, Peng; He, Hu

    2016-02-17

    Paper-based writing electronics has received a lot of interest recently due to its potential applications in flexible electronics. To obtain ultra-low resistivity paper-based writing electronics, we developed a kind of ink with high concentration of Ag Nano-particles (up to 80 wt%), as well as a related dispensing writing system consisting an air compressor machine and a dispenser. Additionally, we also demonstrated the writability and practical application of our proposed ink and writing system. Based on the study on the effect of sintering time and pressure, we found the optimal sintering time and pressure to obtain high quality Ag NPs wires. The electrical conductivity of nano-silver paper-based electronics has been tested using the calculated resistivity. After hot-pressure sintering at 120 °C, 25 MPa pressure for 20 minutes, the resistivity of silver NPs conductive tracks was 3.92 × 10(-8) (Ωm), only 2.45 times of bulk silver. The mechanical flexibility of nano-silver paper-based electronics also has been tested. After 1000 bending cycles, the resistivity slightly increased from the initial 4.01 × 10(-8) to 5.08 × 10(-8) (Ωm). With this proposed ink preparation and writing system, a kind of paper-based writing electronics with ultra-low resistivity and good mechanical flexibility was achieved.

  17. Plant-Scale Concentration Column Designs for SHINE Target Solution Utilizing AG 1 Anion Exchange Resin

    SciTech Connect

    Stepinski, Dominique C.; Vandegrift, G. F.

    2015-09-30

    Argonne is assisting SHINE Medical Technologies (SHINE) in their efforts to develop SHINE, an accelerator-driven process that will utilize a uranyl-sulfate solution for the production of fission product Mo-99. An integral part of the process is the development of a column for the separation and recovery of Mo-99, followed by a concentration column to reduce the product volume from 15-25 L to <1 L. Argonne has collected data from batch studies and breakthrough column experiments to utilize the VERSE (Versatile Reaction Separation) simulation program (Purdue University) to design plant-scale product recovery and concentration processes.

  18. Synthesis of Silver Nanoprisms with Variable Size and Investigation of Their Optical Properties: A First-Year Undergraduate Experiment Exploring Plasmonic Nanoparticles

    ERIC Educational Resources Information Center

    Frank, Andrew J.; Cathcart, Nicole; Maly, Kenneth E.; Kitaev, Vladimir

    2010-01-01

    A robust and reasonably simple experiment is described that introduces students to the visualization of nanoscale properties and is intended for a first-year laboratory. Silver nanoprisms (NPs) that display different colors due to variation of their plasmonic absorption with respect to size are prepared. Control over the size of the silver…

  19. Effects of Ge replacement in GeTe by Ag or Sb on the Seebeck coefficient and carrier concentration modified by local electron imbalance

    NASA Astrophysics Data System (ADS)

    Levin, E. M.; Howard, A.; Straszheim, W. E.

    2015-03-01

    XRD, SEM, EDS, 125Te NMR, Seebeck coefficient, and electrical resistivity of AgxGe50-xTe50 and SbxGe50-xTe50 alloys have been studied. Replacement of Ge in GeTe by Sb significantly increases the Seebeck coefficient, while replacement by Ag decreases it. These effects can be attributed to a change in carrier concentration observed via 125Te NMR spin-lattice relaxation measurements and NMR signal position, which mostly depends on the Knight shift. Variation in carrier concentration in AgxGe50-xTe50 and SbxGe50-xTe50 can be attributed to different electron configurations of valence electrons of Ag (4d105s1) and Sb (5s25p3) compared to that of Ge (4s24p2) resulting in local electron imbalances and changing the concentration of charge carrier (holes) generated by Ge vacancies. In contrast, our 125Te NMR and Seebeck coefficient data for Ag2Sb2Ge46Te50 are similar to those observed for GeTe. This shows that effects from Ag and Sb compensate each other and indicates the existence of [Ag +Sb] pairs. The effects of Ge replacement in GeTe by Ag, Sb, or [Ag +Sb] on rhombohedral lattice distortion also have been analyzed. Interplay between the Seebeck coefficient and electrical resistivity in these alloys results in variation of power factor; the value of 45 mW/cm K2, the highest among known tellurides, was found for Sb2Ge48Te50.

  20. Preparation of a novel PAN/cellulose acetate-Ag based activated carbon nanofiber and its adsorption performance for low-concentration SO2

    NASA Astrophysics Data System (ADS)

    Wu, Yan-bo; Bi, Jun; Lou, Ting; Song, Tie-ben; Yu, Hong-quan

    2015-04-01

    Polyacrylonitrile (PAN), PAN/cellulose acetate (CA), and PAN/CA-Ag based activated carbon nanofiber (ACNF) were prepared using electrostatic spinning and further heat treatment. Thermogravimetry-differential scanning calorimetry (TG-DSC) analysis indicated that the addition of CA or Ag did not have a significant impact on the thermal decomposition of PAN materials but the yields of fibers could be improved. Scanning electron microscopy (SEM) analysis showed that the micromorphologies of produced fibers were greatly influenced by the viscosity and conductivity of precursor solutions. Fourier transform infrared spectroscopy (FT-IR) analysis proved that a cyclized or trapezoidal structure could form and the carbon scaffold composed of C=C bonds appeared in the PAN-based ACNFs. The characteristic diffraction peaks in X-ray diffraction (XRD) spectra were the evidence of a turbostratic structure and silver existed in the PAN/CA-Ag based ACNF. Brunner-Emmett-Teller (BET) analysis showed that the doping of CA and Ag increased surface area and micropore volume of fibers; particularly, PAN/CA-Ag based ACNF exhibited the best porosity feature. Furthermore, SO2 adsorption experiments indicated that all the three fibers had good adsorption effects on lower concentrations of SO2 at room temperature; especially, the PAN/CA-Ag based ACNF showed the best adsorption performance, and it may be one of the most promising adsorbents used in the fields of chemical industry and environment protection.

  1. Dispensing of high concentration Ag nano-particles ink for ultra-low resistivity paper-based writing electronics

    PubMed Central

    Wang, Fuliang; Mao, Peng; He, Hu

    2016-01-01

    Paper-based writing electronics has received a lot of interest recently due to its potential applications in flexible electronics. To obtain ultra-low resistivity paper-based writing electronics, we developed a kind of ink with high concentration of Ag Nano-particles (up to 80 wt%), as well as a related dispensing writing system consisting an air compressor machine and a dispenser. Additionally, we also demonstrated the writability and practical application of our proposed ink and writing system. Based on the study on the effect of sintering time and pressure, we found the optimal sintering time and pressure to obtain high quality Ag NPs wires. The electrical conductivity of nano-silver paper-based electronics has been tested using the calculated resistivity. After hot-pressure sintering at 120 °C, 25 MPa pressure for 20 minutes, the resistivity of silver NPs conductive tracks was 3.92 × 10−8 (Ωm), only 2.45 times of bulk silver. The mechanical flexibility of nano-silver paper-based electronics also has been tested. After 1000 bending cycles, the resistivity slightly increased from the initial 4.01 × 10−8 to 5.08 × 10−8 (Ωm). With this proposed ink preparation and writing system, a kind of paper-based writing electronics with ultra-low resistivity and good mechanical flexibility was achieved. PMID:26883558

  2. Effects of Ge substitution in GeTe by Ag or Sb on the Seebeck coefficient and carrier concentration derived from 125Te NMR

    NASA Astrophysics Data System (ADS)

    Levin, E. M.

    2016-01-01

    GeTe, a self-doping p -type semiconductor where the high free hole concentration is determined by Ge vacancies is a well-known base for high-efficiency A gxS bxG e50 -2 xT e50 (a tellurium-antimony-germanium-silver series) thermoelectric materials. Here it is shown that the replacement of Ge by Ag in GeTe (a A gxG e50 -xT e50 system) significantly decreases the Seebeck coefficient, whereas the replacement by Sb (S bxG e50 -xT e50 ) increases it. These effects can be attributed to a change in carrier concentration and consistent with 125Te NMR spin-lattice relaxation measurements and NMR signal position, which is mostly dependent on the Knight shift. Opposite changes in carrier concentration in A gxG e50 -xT e50 and S bxG e50 -xT e50 can be explained by different valence electron configurations of Ag and Sb compared to that of Ge, which results in a different local electron imbalance and/or in a change in Ge vacancy formation energy and affects the total carrier concentration. Comparison of our data for GeTe, A g2G e48T e50 , and S b2G e48T e50 with those for A g2S b2G e46T e50 shows that the effects from Ag and Sb compensate for each other and supports the formation of [Ag +Sb ] atomic pairs suggested earlier based on theoretical calculations.

  3. AgI alloying in SnTe boosts the thermoelectric performance via simultaneous valence band convergence and carrier concentration optimization

    NASA Astrophysics Data System (ADS)

    Banik, Ananya; Biswas, Kanishka

    2016-10-01

    SnTe, a Pb-free analogue of PbTe, was earlier assumed to be a poor thermoelectric material due to excess p-type carrier concentration and large energy separation between light and heavy hole valence bands. Here, we report the enhancement of the thermoelectric performance of p-type SnTe by Ag and I co-doping. AgI (1-6 mol%) alloying in SnTe modulates its electronic structure by increasing the band gap of SnTe, which results in decrease in the energy separation between its light and heavy hole valence bands, thereby giving rise to valence band convergence. Additionally, iodine doping in the Te sublattice of SnTe decreases the excess p-type carrier concentration. Due to significant decrease in hole concentration and reduction of the energy separation between light and heavy hole valence bands, significant enhancement in Seebeck coefficient was achieved at the temperature range of 600-900 K for Sn1-xAgxTe1-xIx samples. A maximum thermoelectric figure of merit, zT, of ~1.05 was achieved at 860 K in high quality crystalline ingot of p-type Sn0.95Ag0.05Te0.95I0.05.

  4. The influence of particle size and AgNO3 concentration in the ionic exchange process on the fungicidal action of antimicrobial glass.

    PubMed

    Mendes, E; Piletti, R; Barichello, T; Oliveira, C M; Kniess, C T; Angioletto, E; Riella, H G; Fiori, M A

    2012-08-01

    Antimicrobial materials have long been used as an effective means of reducing the risks posed to humans by fungi, bacteria and other microorganisms. These materials are essential in environments where cleanliness, comfort and hygiene are the predominate concerns. This work presents preliminary results for the development of a fungicidal vitreous material that is produced by the incorporation of a silver ionic specimen through ionic exchange reactions. Silver ions were incorporated into powdered glass via ionic exchange in an ionic medium containing silver species with different concentrations of AgNO3. The fungicidal efficiency of the samples was studied as a function of the AgNO3 concentration and the particle size of the glass using the agar diffusion test for the microbiological analysis of the fungus species Candida albicans. The samples were examined by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and X-ray diffraction (XRD). The experimental results showed that the fungicidal effect was dependent on the AgNO3 concentration in the ionic exchange medium but was not dependent on the particle size of the glass.

  5. Kinetically controlled overgrowth of Ag or Au on Pd nanocrystal seeds: from hybrid dimers to nonconcentric and concentric bimetallic nanocrystals.

    PubMed

    Zhu, Cun; Zeng, Jie; Tao, Jing; Johnson, Matthew C; Schmidt-Krey, Ingeborg; Blubaugh, Lynn; Zhu, Yimei; Gu, Zhongze; Xia, Younan

    2012-09-26

    This article describes a systematic study of the nucleation and growth of Ag (and Au) on Pd nanocrystal seeds. By carefully controlling the reaction kinetics, the newly formed Ag atoms could be directed to selectively nucleate and then epitaxially grow on a specific number (ranging from one to six) of the six faces on a cubic Pd seed, leading to the formation of bimetallic nanocrystals with a variety of different structures. In addition to changing the injection rate of precursor, we also systematically investigated other reaction parameters including the capping agent, reductant, and reaction temperature. Our results suggest that the site-selective growth of Ag on cubic Pd seeds could be readily realized by optimizing these reaction parameters. On the basis of the positions of Pd seeds inside the bimetallic nanocrystals as revealed by TEM imaging and elemental mapping, we could identify the exact growth pathways and achieve a clear and thorough understanding of the mechanisms. We have successfully applied the same strategy based on kinetic control to cubic Pd seeds with different sizes and octahedral Pd seeds of one size to generate an array of novel bimetallic nanocrystals with well-controlled structures. With cubic Pd seeds as an example, we have also extended this strategy to the Pd-Au system. We believe this work will provide a promising route to the fabrication of bimetallic nanocrystals with novel structures and properties for applications in plasmonics, catalysis, and other areas.

  6. Gold-reinforced silver nanoprisms on optical fiber tapers—A new base for high precision sensing

    NASA Astrophysics Data System (ADS)

    Wieduwilt, T.; Zeisberger, M.; Thiele, M.; Doherty, B.; Chemnitz, M.; Csaki, A.; Fritzsche, W.; Schmidt, M. A.

    2016-09-01

    Due to their unique optical properties, metallic nanoparticles offer a great potential for important applications such as disease diagnostics, demanding highly integrated device solutions with large refractive index sensitivity. Here we introduce a new type of monolithic localized surface plasmon resonance (LSPR) waveguide sensor based on the combination of an adiabatic optical fiber taper and a high-density ensemble of immobilized gold-reinforced silver nanoprisms, showing sensitivities up to 900 nm/RIU. This result represents the highest value reported so far for a fiber optic sensor using the LSPR effect and exceeds the corresponding value of the bulk solution by a factor of two. The plasmonic resonance is efficiently excited via the evanescent field of the propagating taper mode, leading to pronounced transmission dips (-20 dB). The particle density is so high (approx. 210 particle/μm2) that neighboring particles are able to interact, boosting the sensitivity, as confirmed by qualitative infinite element simulations. We additionally introduce a qualitative model explaining the interaction of plasmon resonance and taper mode on the basis of light extinction, allowing extracting key parameters of the plasmonic taper (e.g., modal attenuation). Due to the monolithic design and the extremely high sensitivity we expect our finding to be relevant in fields such as biomedicine, disease diagnostics, and molecular sensing.

  7. Combined three-dimensional electromagnetic and device modeling of surface plasmon-enhanced organic solar cells incorporating low aspect ratio silver nanoprisms

    NASA Astrophysics Data System (ADS)

    Jiang, Wenjun; Salvador, Michael; Dunham, Scott T.

    2013-10-01

    We investigate silver nanoparticle enhanced organic solar cells by coupling three-dimensional electromagnetic and electronic device simulations. For active layer thicknesses of less than 50 nm, an array of optimized silver nanoprisms with 10 nm edge length, 15 nm thickness, and 17 nm period length can enhance the power conversion efficiency (PCE) by more than 25% when embedded in a bulk heterojunction polymer blend. For thicker layers, optical losses associated with the particles outweigh the increased absorption and reduce the PCE. Additionally, we find that the nanoparticle's work function determines the current-voltage behavior of plasmonic devices.

  8. Environmental geochemistry of shale-hosted Ag-Pb-Zn massive sulfide deposits in northwest Alaska: Natural background concentrations of metals in water from mineralized areas

    USGS Publications Warehouse

    Kelley, K.D.; Taylor, C.D.

    1997-01-01

    Red Dog, Lik and Drenchwater are shale-hosted stratiform Ag-Pb-Zn massive sulfide deposits in the northwestern Brooks Range. Natural background concentrations of metals in waters from the undisturbed (unmined) Drenchwater prospect and Lik deposit were compared to pre-mining baseline studies conducted at Red Dog. The primary factors affecting water chemistry are the extent of exposure of the deposits, the grade of mineralization, the presence of carbonate reeks in the section, and the proportion of Fe-sulfide in the ore. Surface water samples from the Drenchwater prospect, which has pyrite-dominant mineralization exposed in outcrop, have pH values as low as 2.8 and high dissolved concentrations of metals including as much as 95 mg 1-1 Al, 270 mg 1-1 Fe, 8 ??1-1 Cd, 10 ??1-1 Pb, and 2600 ??1-1 Zn, with As up to 26 ??g1-1. Surface waters from the Red Dog deposit prior to mining were also acidic and metal-rich, however, dissolved metal concentrations in Red Dog waters were many times greater. The higher metal concentrations in Red Dog waters reflect the high Zn grades and the abundant sphalerite, pyrite, and galena that were present in outcrop prior to mining. In contrast, despite significant mineralization at the Lik deposit, carbonate rocks in the section buffer the system, resulting in less acidic, mostly near-neutral pH values with low concentrations of most metals except Zn.

  9. An empirical investigation on thermal characteristics and pressure drop of Ag-oil nanofluid in concentric annular tube

    NASA Astrophysics Data System (ADS)

    Abbasian Arani, A. A.; Aberoumand, H.; Aberoumand, S.; Jafari Moghaddam, A.; Dastanian, M.

    2016-08-01

    In this work an experimental study on Silver-oil nanofluid was carried out in order to present the laminar convective heat transfer coefficient and friction factor in a concentric annulus with constant heat flux boundary condition. Silver-oil nanofluid prepared by Electrical Explosion of Wire technique with no nanoparticles agglomeration during nanofluid preparation process and experiments. The average sizes of particles were 20 nm. Nanofluids with various particle Volume fractions of 0.011, 0.044 and 0.171 vol% were employed. The nanofluid flowing between the tubes is heated by an electrical heating coil wrapped around it. The effects of different parameters such as flow Reynolds number, tube diameter ratio and nanofluid particle concentration on heat transfer coefficient are studied. Results show that, heat transfer coefficient increased by using nanofluid instead of pure oil. Maximum enhancement of heat transfer coefficient occurs in 0.171 vol%. In addition the results showed that, there are slight increases in pressure drop of nanofluid by increasing the nanoparticle concentration of nanofluid in compared to pure oil.

  10. Preparation and antibacterial activities of Ag/Ag+/Ag3+ nanoparticle composites made by pomegranate (Punica granatum) rind extract

    NASA Astrophysics Data System (ADS)

    Yang, Hui; Ren, Yan-yu; Wang, Tao; Wang, Chuang

    Nano-silver and its composite materials are widely used in medicine, food and other industries due to their strong conductivity, size effect and other special performances. So far, more microbial researches have been applied, but a plant method is rarely reported. In order to open up a new way to prepare AgNP composites, pomegranate peel extract was used in this work to reduce Ag+ to prepare Ag/Ag+/Ag3+ nanoparticle composites. UV-Vis was employed to detect and track the reduction of Ag+ and the forming process of AgNPs. The composition, structure and size of the crystal were analyzed by XRD and TEM. Results showed that, under mild conditions, pomegranate peel extract reacted with dilute AgNO3 solution to produce Ag/Ag+/Ag3+ nanoparticle composites. At pH = 8 and 10 mmol/L of AgNO3 concentration, the size of the achieved composites ranged between 15 and 35 nm with spherical shapes and good crystallinity. The bactericidal experiment indicated that the prepared Ag/Ag+/Ag3+ nanoparticles had strong antibacterial activity against gram positive bacteria and gram negative bacteria. FTIR analysis revealed that biological macromolecules with groups of sbnd NH2, sbnd OH, and others were distributed on the surface of the newly synthesized Ag/Ag+/Ag3+ nanoparticles. This provided a useful clue to further study the AgNP biosynthesis mechanism.

  11. Separation of PS-PMMA block copolymers from PS precursors via selective adsorption on nanoprous silica

    NASA Astrophysics Data System (ADS)

    Ryu, Chang Yeol

    2005-03-01

    We report a simple adsorption-based separation method using nanoporous silica in solution via controlling solvent quality to remove polystyrene (PS) homopolymers from polystyrene-poly(methyl methacrylate) (PS-PMMA) diblock copolymers. In particular, the solvent quality is controlled by employing binary mixed solvents of THF (good solvent) and isooctane (nonsolvent for both PS and PMMA). The aim of this work is to qualitatively study the competitive adsorption between PS and PS-PMMA and to provide a correlative understanding of polymer adsorption in nanopores with interaction chromatography techniques. In addition, the quantitative understanding of polymer adsorption is further employed to develop a simple polymer separation scheme for manipulating polymer adsorption via solvent quality. In particular, concentration changes of PS and PS-PMMA in the supernatant solution have been quantitatively measured for the adsorption studies using solvent gradient interaction chromatography techniques. We found that the PS-PMMA (43k-32k) selectively adsorb over PS (43k) precursors at the THF composition window between 42 % and 55% in THF/IO (v/v) mixed solvents. For THF/IO solvents with composition higher than 60 % THF, polymers did not adsorb to the nanoporous silica due to the good solvent quality.

  12. Biosynthesis of Au, Ag and Au-Ag nanoparticles using edible mushroom extract

    NASA Astrophysics Data System (ADS)

    Philip, Daizy

    2009-07-01

    Integration of green chemistry principles to nanotechnology is one of the key issues in nanoscience research. There is growing need to develop environmentally benign metal nanoparticle synthesis process that do not use toxic chemicals in the synthesis protocols to avoid adverse effects in medical applications. Here, it is a report on extracellular synthesis method for the preparation of Au, Ag and Au-Ag nanoparticles in water, using the extract of Volvariella volvacea, a naturally occurring edible mushroom, as reducing and protecting agents. Gold nanoparticles of different sizes (20-150 nm) and shapes from triangular nanoprisms to nearly spherical and hexagonal are obtained by this novel method. The size and shape of gold nanoparticles are also found to depend on temperature of the extract. The silver nanoparticles are spherical with size ˜15 nm. There is increased productivity of nanoparticles as shown by sharp and intense surface plasmon resonance bands for the nanoparticles prepared using an excess of the extract. The Au-Ag nanoparticles prepared by co-reduction has only one plasmon band due to alloying of the constituents. All the synthesized nanoparticles are found to be photoluminescent and are highly crystalline as shown by SAED and XRD patterns with fcc phase oriented along the (1 1 1) plane. FTIR measurements were carried out to identify the possible biomolecules responsible for capping and efficient stabilization of the nanoparticles. It is found that Au nanoparticles are bound to proteins through free amino groups and silver nanoparticles through the carboxylate group of the amino acid residues. The position and intensity of the emission band is found to depend on composition of the nanoparticles indicating the possible use in therapeutic applications.

  13. Facile synthesis, structure, and properties of Ag2S/Ag heteronanostructure

    NASA Astrophysics Data System (ADS)

    Sadovnikov, S. I.; Gusev, A. I.

    2016-09-01

    Ag2S/Ag heteronanostructure has been produced by a simple one-stage chemical deposition from aqueous solutions of silver nitrate, sodium sulfide, and sodium citrate with the use of monochromatic light irradiation. For simultaneous synthesis of Ag2S and Ag nanoparticles, deposition has been performed from reaction mixtures with reduced sodium sulfide concentration. The size of Ag2S and Ag nanoparticles is 45-50 and 15-20 nm, respectively. It is established that in the contact layer between silver sulfide and silver, nonconducting α-Ag2S acanthite transforms into superionic β-Ag2S argentite under the action of external electric field. The scheme of the operation of a resistive switch based on an Ag2S/Ag heteronanostructure is proposed. The UV-Vis optical absorption spectra of colloidal solutions of Ag2S/Ag heteronanostructures have been studied.

  14. Towards high quality triangular silver nanoprisms: improved synthesis, six-tip based hot spots and ultra-high local surface plasmon resonance sensitivity

    NASA Astrophysics Data System (ADS)

    Xue, Bin; Wang, Dan; Zuo, Jing; Kong, Xianggui; Zhang, Youlin; Liu, Xiaomin; Tu, Langping; Chang, Yulei; Li, Cuixia; Wu, Fei; Zeng, Qinghui; Zhao, Haifeng; Zhao, Huiying; Zhang, Hong

    2015-04-01

    The great application potential of triangular silver nanoprisms (TSNPRs, also referred to as triangular silver nanoplates) is hampered by the lack of methods to produce well-defined tips with high monodispersity, with easily removable ligands. In this work, a simple one-step plasmon-mediated method was developed to prepare monodisperse high-quality TSNPRs. In this approach, the sole surface capping agent was the easily removable trisodium citrate. Differing from common strategies using complex polymers, OH- ions were used to improve the monodispersity of silver seeds, as well as to control the growth process through inhibiting the oxidation of silver nanoparticles. Using these monodisperse high-quality TSNPRs as building blocks, self-assembled TSNPRs consisting of six-tip based ``hot spots'' were realized for the first time as demonstrated in a high enhancement (~107) of surface-enhanced Raman scattering (SERS). From the plasmon band shift versus the refractive index, ultra-high local surface plasmon resonance sensitivity (413 nm RIU-1 or 1.24 eV RIU-1, figure of merit (FOM) = 4.59) was reached at ~630 nm, making these materials promising for chemical/biological sensing applications.The great application potential of triangular silver nanoprisms (TSNPRs, also referred to as triangular silver nanoplates) is hampered by the lack of methods to produce well-defined tips with high monodispersity, with easily removable ligands. In this work, a simple one-step plasmon-mediated method was developed to prepare monodisperse high-quality TSNPRs. In this approach, the sole surface capping agent was the easily removable trisodium citrate. Differing from common strategies using complex polymers, OH- ions were used to improve the monodispersity of silver seeds, as well as to control the growth process through inhibiting the oxidation of silver nanoparticles. Using these monodisperse high-quality TSNPRs as building blocks, self-assembled TSNPRs consisting of six-tip based ``hot

  15. Towards high quality triangular silver nanoprisms: improved synthesis, six-tip based hot spots and ultra-high local surface plasmon resonance sensitivity.

    PubMed

    Xue, Bin; Wang, Dan; Zuo, Jing; Kong, Xianggui; Zhang, Youlin; Liu, Xiaomin; Tu, Langping; Chang, Yulei; Li, Cuixia; Wu, Fei; Zeng, Qinghui; Zhao, Haifeng; Zhao, Huiying; Zhang, Hong

    2015-05-07

    The great application potential of triangular silver nanoprisms (TSNPRs, also referred to as triangular silver nanoplates) is hampered by the lack of methods to produce well-defined tips with high monodispersity, with easily removable ligands. In this work, a simple one-step plasmon-mediated method was developed to prepare monodisperse high-quality TSNPRs. In this approach, the sole surface capping agent was the easily removable trisodium citrate. Differing from common strategies using complex polymers, OH(-) ions were used to improve the monodispersity of silver seeds, as well as to control the growth process through inhibiting the oxidation of silver nanoparticles. Using these monodisperse high-quality TSNPRs as building blocks, self-assembled TSNPRs consisting of six-tip based "hot spots" were realized for the first time as demonstrated in a high enhancement (∼10(7)) of surface-enhanced Raman scattering (SERS). From the plasmon band shift versus the refractive index, ultra-high local surface plasmon resonance sensitivity (413 nm RIU(-1) or 1.24 eV RIU(-1), figure of merit (FOM) = 4.59) was reached at ∼630 nm, making these materials promising for chemical/biological sensing applications.

  16. Loading effect of Ag/AgO on the photocatalytic performance of ZnO rods

    NASA Astrophysics Data System (ADS)

    Samsuddin, Aida Fitri; Aziz, Siti Nor Qurratu Aini Abd; Pung, Swee-Yong

    2017-01-01

    The photocatalytic performance of ZnO rods in degradation of Rhodamine B dye under UV light was improved by 7.3% via deposition of Ag/AgO using 1.0 × 10-3 g mL-1 of silver nitrate solution. However, its photodegradation efficiency decreased with the increase in silver nitrate concentration which was used to prepare the Ag/AgO-ZnO rods. This result suggests that the loading of Ag/AgO on the surface of ZnO rods affected the photocatalytic performance differently. The scavenger study indicates that the main reactive species responsible for the degradation of Rhodamine B dye by Ag-/AgO-deposited ZnO rods were holes, followed by superoxide anion free radicals, hydroxyl free radicals and electrons. Based on these findings, a refined photodegradation mechanism of Rhodamine B by Ag/AgO-ZnO rods is proposed.

  17. Effects of soil and dietary exposures to Ag nanoparticles and AgNO₃ in the terrestrial isopod Porcellionides pruinosus.

    PubMed

    Tourinho, Paula S; van Gestel, Cornelis A M; Jurkschat, Kerstin; Soares, Amadeu M V M; Loureiro, Susana

    2015-10-01

    The effects of Ag-NPs and AgNO3 on the isopod Porcellionides pruinosus were determined upon soil and dietary exposures. Isopods avoided Ag in soil, with EC50 values of ∼16.0 and 14.0 mg Ag/kg for Ag-NPs and AgNO3, respectively. Feeding inhibition tests in soil showed EC50s for effects on consumption ratio of 127 and 56.7 mg Ag/kg, respectively. Although similar EC50s for effects on biomass were observed for nanoparticulate and ionic Ag (114 and 120 mg Ag/kg dry soil, respectively), at higher concentrations greater biomass loss was found for AgNO3. Upon dietary exposure, AgNO3 was more toxic, with EC50 for effects on biomass change being >1500 and 233 mg Ag/kg for Ag-NPs and AgNO3, respectively. The difference in toxicity between Ag-NPs and AgNO3 could not be explained from Ag body concentrations. This suggests that the relation between toxicity and bioavailability of Ag-NPs differs from that of ionic Ag in soils.

  18. Morphology and mechanical properties of nanocrystalline Cu/Ag alloy

    NASA Astrophysics Data System (ADS)

    Li, Ao; Szlufarska, Izabela

    2017-04-01

    Hybrid Monte Carlo (MC)/molecular dynamics (MD) simulations are conducted to study the microstructures of nanocrystalline (nc) Cu/Ag alloys with various Ag concentrations. When the Ag concentration is below 50 Ag atoms/nm!, an increase in Ag concentration leads to a gradual growth of monolayer grain boundary (GB) complexions into nanolayer complexions. Above the concentration of 50 Ag atoms/nm!, wetting layers with a bulk crystalline phase are observed. The effects of Ag on mechanical properties and deformation mechanisms of nc Cu/Ag alloys are investigated in MD simulations of uniaxial tension. GB sliding resistance is found to first increase and then decrease with an increase in Ag concentration. Surprisingly, we also find that the dislocation density decreases monotonically with an increase in Ag concentration, which suggests that the grain interiors are softened by the introduction of Ag dopants at GBs. In addition, there is a critical Ag concentration that maximizes flow stress of nc Cu/Ag alloys. The flow stress, GB sliding resistance, and the intragranular dislocation densities become less sensitive to Ag dopants when the grain diameter increases from 5nm to 40nm.

  19. Antibacterial activity and reusability of CNT-Ag and GO-Ag nanocomposites

    NASA Astrophysics Data System (ADS)

    Kim, Ji Dang; Yun, Hyosuk; Kim, Gwui Cheol; Lee, Chul Won; Choi, Hyun Chul

    2013-10-01

    A facile approach to the synthesis of novel CNT-Ag and GO-Ag antibacterial materials, in which thiol groups are utilized as linkers to secure silver (Ag) nanoparticles to the CNT and GO surfaces without agglomeration, is reported. The resulting CNT-Ag and GO-Ag samples were characterized by performing TEM, XRD, Auger, XPS, and Raman measurements, which revealed that in these antibacterial materials size-similar and quasi-spherical Ag nanoparticles are anchored to the CNT and GO surfaces. The Ag nanoparticles in CNT-Ag and GO-Ag have narrow size distributions with average diameters of 2.6 and 3.5 nm respectively. The antibacterial activities of CNT-Ag and GO-Ag against Escherichia coli were assessed with the paper-disk diffusion method and by determining the minimal inhibitory concentrations (MICs). CNT-Ag was found to have higher antibacterial activity than the reference Ag colloid. Moreover, both CNT-Ag and GO-Ag retain more than 50% of their original antibacterial activities after 20 washes with detergent, which indicates their potential as antibacterial materials for laboratory and medical purposes.

  20. Synthesis of vinyl-terminated Au nanoprisms and nanooctahedra mediated by 3-butenoic acid: direct Au@pNIPAM fabrication with improved SERS capabilities

    NASA Astrophysics Data System (ADS)

    Casado-Rodriguez, M. A.; Sanchez-Molina, M.; Lucena-Serrano, A.; Lucena-Serrano, C.; Rodriguez-Gonzalez, B.; Algarra, M.; Diaz, A.; Valpuesta, M.; Lopez-Romero, J. M.; Perez-Juste, J.; Contreras-Caceres, R.

    2016-02-01

    Here we describe the first seedless synthesis of vinyl-terminated Au nanotriangular prisms (AuNTPs) and nanooctahedra (AuNOC) in aqueous media. This synthesis is performed by chemical reduction of chloroauric acid (HAuCl4) with 3-butenoic acid (3BA) in the presence of benzyldimethylammonium chloride (BDAC). The principal novelties of the presented method are the use of a mixture of 3BA and BDAC, the synthesis of gold prisms and octahedra with controllable size, and the presence of terminal double bonds on the metal surface. Initially this method produces a mixture of triangular gold nanoprisms and octahedra; however, both morphologies are successfully separated by surfactant micelle induced depletion interaction, reaching percentages up to ~90%. Moreover, the alkene moieties present on the gold surface are exploited for the fabrication of hybrid core@shell particles. Gold octahedra and triangular prisms are easily encapsulated by free radical polymerization of N-isopropylacrylamide (NIPAM). Finally, in order to obtain a gold core with the most number of tips, AuNTP@pNIPAM microgels were subjected to gold core overgrowth, thus resulting in star-shaped nanoparticles (AuSTs@pNIPAM). We use 4-amino-benzenethiol as the model analyte for SERS investigations. As expected, gold cores with tips and high curvature sites produced the highest plasmonic responses.Here we describe the first seedless synthesis of vinyl-terminated Au nanotriangular prisms (AuNTPs) and nanooctahedra (AuNOC) in aqueous media. This synthesis is performed by chemical reduction of chloroauric acid (HAuCl4) with 3-butenoic acid (3BA) in the presence of benzyldimethylammonium chloride (BDAC). The principal novelties of the presented method are the use of a mixture of 3BA and BDAC, the synthesis of gold prisms and octahedra with controllable size, and the presence of terminal double bonds on the metal surface. Initially this method produces a mixture of triangular gold nanoprisms and octahedra; however

  1. Toxicokinetics of Ag in the terrestrial isopod Porcellionides pruinosus exposed to Ag NPs and AgNO₃ via soil and food.

    PubMed

    Tourinho, Paula S; van Gestel, Cornelis A M; Morgan, A John; Kille, Peter; Svendsen, Claus; Jurkschat, Kerstin; Mosselmans, J Fred W; Soares, Amadeu M V M; Loureiro, Susana

    2016-03-01

    Silver nanoparticles (Ag NPs) have been used in numerous consumer products and may enter the soil through the land application of biosolids. However, little is known about the relationship between Ag NP exposure and their bioavailability for soil organisms. This study aims at comparing the uptake and elimination kinetics of Ag upon exposures to different Ag forms (NPs and ionic Ag (as AgNO3)) in the isopod Porcellionides pruinosus. Isopods were exposed to contaminated Lufa 2.2 soil or alder leaves as food. Uptake and elimination rate constants for soil exposure did not significantly differ between Ag NPs and ionic Ag at 30 and 60 mg Ag/kg. For dietary exposure, the uptake rate constant was up to 5 times higher for Ag NPs than for AgNO3, but this was related to feeding activity and exposure concentrations, while no difference in the elimination rate constants was found. When comparing both routes, dietary exposure resulted in lower Ag uptake rate constants but elimination rate constants did not differ. A fast Ag uptake was observed from both routes and most of the Ag taken up seemed not to be eliminated. Synchrotron X-ray fluorescence showed Ag in the S-cells of the hepatopancreas, thus supporting the observations from the kinetic experiment (i.e. low elimination). In addition, our results show that isopods have an extremely high Ag accumulation capacity, suggesting the presence of an efficient Ag storage compartment.

  2. Visible light driven photocatalysis and antibacterial activity of AgVO{sub 3} and Ag/AgVO{sub 3} nanowires

    SciTech Connect

    Singh, Anamika; Dutta, Dimple P.; Ballal, A.; Tyagi, A.K.; Fulekar, M.H.

    2014-03-01

    Graphical abstract: - Highlights: • Ag/AgVO{sub 3} and pure AgVO{sub 3} nanowires synthesized by sonochemical process. • Characterization done using XRD, SEM, TEM, EDX and BET analysis. • Visible light degradation of RhB by Ag/AgVO{sub 3} within 45 min. • Antibacterial activity of Ag/AgVO{sub 3} demonstrated. - Abstract: Ag/AgVO{sub 3} nanowires and AgVO{sub 3} nanorods were synthesized in aqueous media via a facile sonochemical route. The as-synthesized products were characterized by X-ray diffraction, Brunauer–Emmett–Teller surface area analysis, scanning electron microscopy together with an energy dispersion X-ray spectrum analysis, transmission electron microscopy and UV–vis diffuse reflectance spectroscopy. The results revealed that inert atmosphere promotes the formation of Ag/AgVO{sub 3} nanowires. The photocatalytic studies revealed that the Ag/AgVO{sub 3} nanowires exhibited complete photocatalytic degradation of Rhodamine B within 45 min under visible light irradiation. The antibacterial activity of Ag/AgVO{sub 3} nanowires was tested against Escherechia coli and Bacillus subtilis. The minimum growth inhibitory concentration value was found to be 50 and 10 folds lower than for the antibiotic ciprofloxacin for E. coli and B. subtilis, respectively. The antibacterial properties of the β-AgVO{sub 3} nanorods prove that in case of the Ag dispersed Ag/AgVO{sub 3} nanowires, the enhanced antibacterial action is also due to contribution from the AgVO{sub 3} support.

  3. Spin coating of Ag nanoparticles: Effect of reduction

    SciTech Connect

    Ansari, A. A. Sartale, S. D.

    2014-04-24

    A surfactant free method for the growth of Ag nanoparticles on glass substrate by spin coating of Ag ions solution followed by chemical reduction in aqueous hydrazine hydrate (HyH) solution has been presented. Appearance of surface plasmon resonance confirms the formation of Ag nanoparticles. Morphology and absorbance spectra of Ag nanoparticles films are used to examine effect of hydrazine concentration on the growth of Ag nanoparticles. SEM images show uniformly distributed Ag nanoparticles. Rate constant was found to be dependent on HyH concentration as a consequence influence particle size.

  4. Optimization of SHINE Process: Design and Verification of Plant-Scale AG 1 Anion-Exchange Concentration Column and Titania Sorbent Pretreatment

    SciTech Connect

    Stepinski, Dominique C.; Abdul, Momen; Youker, Amanda J.; Rotsch, David A.; Tkac, Peter; Chemerisov, Sergey; Vandegrift, George F.

    2016-06-01

    Argonne National Laboratory has developed a Mo-recovery and -purification system for the SHINE medical technologies process, which uses a uranyl sulfate solution for the accelerator-driven production of Mo-99. The objective of this effort is to reduce the processing time for the acidification of the Mo-99 product prior to loading onto a concentration column and concentration of the Mo-99 product solution. Two methods were investigated: (1) the replacement of the titania concentration column by an anion-exchange column to decrease processing time and increase the radioiodine-decontamination efficiency and (2) pretreatment of the titania sorbent to improve its effectiveness for the Mo-recovery and -concentration columns. Promising results are reported for both methods.

  5. On the measurement of /sup 107/Ag//sup 109/Ag ratios in meteorites

    SciTech Connect

    Kutschera, W.; Faestermann, T.; Gillitzer, A.; Fortuna, G.

    1986-01-01

    The detection of stable Ag isotopes in meteorites at the ppB level was attempted in an AMS experiment using the Munich MP tandem accelerator in conjunction with a time-of-flight detection system. The sensitivity of detecting Ag at this level was established by observing a counting rate of 17 ions of /sup 107/Ag per sec from a Au sample, which had been spiked with the radioisotope /sup 105/Ag (T/sub 1/2/ = 41 d) at a concentration of 1.0 ppB. A blank Ta sample gave no /sup 105/Ag counts in 13 min, which corresponds to a detection limit of 7.5 x 10/sup -5/ ppB. Although this sensitivity was clearly sufficient to perform /sup 107/Ag and /sup 109/Ag measurements in the desired concentration range, experiments with these isotopes were hampered by a currently irreducable background of stable Ag in the ppM range, possibly originating from the ion source itself. Indications of extraordinarily high Ag concentrations, far above this background, were observed in some of the investigated meteorites, but conclusions on their actual existence must await a better understanding of the origin of the general Ag background. 10 refs., 4 figs., 3 tabs.

  6. Photo-catalytic activity of Plasmonic Ag@AgCl nanoparticles (synthesized via a green route) for the effective degradation of Victoria Blue B from aqueous phase.

    PubMed

    Devi, Th Babita; Begum, Shamima; Ahmaruzzaman, M

    2016-07-01

    This study reports a green process for the fabrication of Ag@AgCl (silver@silver chloride) nanoparticles by using Aquilaria agallocha (AA) leaves juice without using any external reagents. The effect of various reaction parameters, such as reaction temperature, reaction time and concentration of Aquilaria agallocha leaves juice in the formation of nanoparticles have also been investigated. From the FTIR spectra of leaves juice and phytochemicals test, it was found that flavonoids present in the leaves are responsible for the reduction of Ag(+) ions to Ag(0) species and leads to the formation of Ag@AgCl NPs. The synthesized Ag@AgCl NPs were utilized for the removal of toxic and hazardous dyes, such as Victoria Blue B from aqueous phase. Approximately, 99.46% degradation of Victoria Blue B dye were observed with Ag@AgCl NPs. Furthermore, the photocatalytic activity of the Ag@AgCl nanoparticles was unchanged after 5cycles of operation.

  7. Equilibrium adsorption isotherm studies of Cu (II) and Co (II) in high concentration aqueous solutions on Ag-TiO2-modified kaolinite ceramic adsorbents

    NASA Astrophysics Data System (ADS)

    Ajenifuja, E.; Ajao, J. A.; Ajayi, E. O. B.

    2016-03-01

    Photocatalytic ceramic adsorbents were prepared from locally sourced kaolinite clay minerals for the removal of copper and cobalt ions from high concentration aqueous solutions. The minerals were treated with mild acid before modification using silver nanoparticles sources and titanium-oxide nanoparticles. Batch adsorption experiment was carried out on the targeted ions and the results were analyzed by Langmuir and Freundlich equation at different concentrations (100-1000 mg/l). As-received raw materials do not exhibit any adsorption capacity. However, the adsorption isotherms for modified kaolinite clay ceramic adsorbents could be fitted well by the Langmuir model for Cu2+ and Co2+ with correlation coefficient (R) of up to 0.99705. The highest and lowest monolayer coverage (q max) were 93.023 and 30.497 mg/g for Cu2+ and Co2+, respectively. The separation factor (R L ) was less than one (<1), indicating that the adsorption of metal ions on modified ceramic adsorbent is favorable. The highest adsorbent adsorption capacity (K f ) and intensity (n) constants obtained from Freundlich model are 14.401 (Cu2+ on KLN-T) and 6.057 (Co2+ on KLN-T).

  8. Study of the oxygen transport through Ag (110), Ag (poly), and Ag 2.0 Zr

    NASA Technical Reports Server (NTRS)

    Outlaw, R. A.; Wu, D.; Davidson, M. R.; Hoflund, Gar B.

    1992-01-01

    The transport of oxygen through high-purity membranes of Ag (110), Ag (poly), Ag (nano), and Ag 2.0 Zr has been studied by an ultrahigh vacuum permeation method over the temperature range of 400-800 C. The data show that there are substantial deviations from ordinary diffusion-controlled transport. A surface limitation has been confirmed by glow-discharge studies where the upstream O2 supply has been partially converted to atoms, which, for the same temperature and pressure, gave rise to over an order of magnitude increase in transport flux. Further, the addition of 2.0 wt percent Zr to the Ag has provided increased dissociative adsorption rates, which, in turn, increased the transport flux by a factor of 2. It was also observed that below a temperature of 630 C, the diffusivity exhibits an increase in activation energy of over 4 kcal/mol, which has been attributed to trapping of the atomic oxygen and/or kinetic barriers at the surface and subsurface of the vacuum interface. Above 630 C, the activation barrier decreases to the accepted value of about 11 kcal/mol for Ag (poly), consistent with zero concentration at the vacuum interface.

  9. Silver nanoparticle toxicity to Daphnia magna is a function of dissolved silver concentration.

    PubMed

    Newton, Kim M; Puppala, Hema L; Kitchens, Christopher L; Colvin, Vicki L; Klaine, Stephen J

    2013-10-01

    The most persistent question regarding the toxicity of silver nanoparticles (AgNPs) is whether this toxicity is due to the nanoparticles themselves or the silver ions (Ag(+)) they release. The present study investigates the role of surface coating and the presence of dissolved organic carbon on the toxicity of AgNPs to Daphnia magna and tests the hypothesis that the acute toxicity of AgNPs is a function of dissolved Ag produced by nanoparticle dissolution. Toxicity of silver nitrate (AgNO3) and AgNPs with surface coatings-gum arabic (AgGA), polyethylene glycol (AgPEG), and polyvinylpyrrolidone (AgPVP)-at 48 h was assessed in US Environmental Protection Agency moderately hard reconstituted water alone and augmented with Suwannee River dissolved organic carbon (DOC). As expected, AgNO3 was the most toxic to D. magna and AgPVPs were the least toxic. In general, Suwannee River DOC presence reduced the toxicity of AgNO3, AgGAs, and AgPEG, while the toxicity of AgPVPs was unaffected. The measured dissolved Ag concentrations for all AgNPs and AgNO3 at the 48-h median lethal concentration in moderately hard reconstituted water were similar. The presence of Suwannee River DOC decreased the ratio of measured dissolved Ag to measured total Ag concentration. These results support the hypothesis that toxicity of AgNPs to D. magna is a function of dissolved Ag concentration from these particles.

  10. Graphene Nanopres for DNA Fingerprinting

    NASA Astrophysics Data System (ADS)

    Ahmed, Towfiq; Balatsky, Alexander V.; Haraldsen, J. T.; Schuller, Ivan K.; di Ventra, M.; Wikfeldt, K. T.

    2013-03-01

    The recent progress in nanopore experiments with transverse current is important for the development of fast, accurate and cheap finger-printing techniques for single nucleotide. Despite its enormous potential for the next generation DNA sequencing technology, the presence of large noise in the temporal spectrum of transverse current remains a big challenge for getting highly accurate interpretation of data. In this paper we present our abinitio calculations, and propose graphene based device for DNA fingerprinting. We calculate transmission current through graphene for each DNA base (A,C,G,T). As shown in our work, a proper time-series analysis of a signal provides a higher quality information in identifying single bio-molecule is translocating through the nanopores. This work is supported by LANL, Nordita, US DOE, AFOSR, and NIH.

  11. Fluorescence switch for silver ion detection utilizing dimerization of DNA-Ag nanoclusters.

    PubMed

    Lee, Jihyun; Park, Juhee; Hee Lee, Hong; Park, Hansoo; Kim, Hugh I; Kim, Won Jong

    2015-06-15

    A fluorescence switch that consists of DNA-templated silver nanoclusters (DNA-AgNCs) triggered by silver ion (Ag(+)) is developed to detect Ag(+). The mechanism of the fluorescence switching of DNA-AgNCs is investigated by fluorescence spectroscopy, circular dichroism spectroscopy, DNA hybridization assay and mass spectrometry. Ag(+) induces a dimeric structure of Cyt12-AgNCs by forming a bridge between two Cyt12-AgNCs, where Cyt12 is cytosine 12-mer; this dimer formation causes the fluorescence change of Cyt12-AgNCs from red to green. Using this Ag(+)-triggered fluorescence switch, we successfully detected Ag(+) at concentrations as low as 10nM. Furthermore, we quantitatively detected the Ag(+) in the Silmazin(®), which is dermatological burn ointment having silver sulfadiazine. Ag(+) detection using this fluorescence switch has high selectivity and sensitivity, and short response time, and can be used successfully even in the presence of other metal ions.

  12. Effect of cysteine and humic acids on bioavailability of Ag from Ag nanoparticles to a freshwater snail

    USGS Publications Warehouse

    Luoma, Samuel N.; Tasha Stoiber,; Croteau, Marie-Noele; Isabelle Romer,; Ruth Merrifeild,; Lead, Jamie

    2016-01-01

    Metal-based engineered nanoparticles (NPs) will undergo transformations that will affect their bioavailability, toxicity and ecological risk when released to the environment, including interactions with dissolved organic material. The purpose of this paper is to determine how interactions with two different types of organic material affect the bioavailability of silver nanoparticles (AgNPs). Silver uptake rates by the pond snail Lymnaea stagnalis were determined after exposure to 25 nmol l-1 of Ag as PVP AgNPs, PEG AgNPs or AgNO3, in the presence of either Suwannee River humic acid or cysteine, a high-affinity thiol-rich organic ligand. Total uptake rate of Ag from the two NPs was either increased or not strongly affected in the presence of 1 – 10 mg 1-1 humic acid. Humic substances contain relatively few strong ligands for Ag explaining their limited effects on Ag uptake rate. In contrast, Ag uptake rate was substantially reduced by cysteine. Three components of uptake from the AgNPs were quantified in the presence of cysteine using a biodynamic modeling approach: uptake of dissolved Ag released by the AgNPs, uptake of a polymer or large (>3kD) Ag-cysteine complex and uptake of the nanoparticle itself. Addition of 1:1 Ag:cysteine reduced concentrations of dissolved Ag, which contributed to, but did not fully explain the reductions in uptake. A bioavailable Ag-cysteine complex (> 3kD) appeared to be the dominant avenue of uptake from both PVP AgNPs and PEG AgNPs in the presence of cysteine. Quantifying the different avenues of uptake sets the stage for studies to assess toxicity unique to NPs.

  13. Silver bioaccumulation dynamics in a freshwater invertebrate after aqueous and dietary exposures to nanosized and ionic Ag

    USGS Publications Warehouse

    le Croteau, Marie-Noe; Misra, Superb K.; Luoma, Samuel N.; Valsami-Jones, Eugenia

    2011-01-01

    We compared silver (Ag) bioavailability and toxicity to a freshwater gastropod after exposure to ionic silver (Ag+) and to Ag nanoparticles (Ag NPs) capped with citrate or with humic acid. Silver form, exposure route, and capping agent influence Ag bioaccumulation dynamics in Lymnaea stagnalis. Snails efficiently accumulated Ag from all forms after either aqueous or dietary exposure. For both exposure routes, uptake rates were faster for Ag+ than for Ag NPs. Snails efficiently assimilated Ag from Ag NPs mixed with diatoms (assimilation efficiency (AE) ranged from 49 to 58%) and from diatoms pre-exposed to Ag+ (AE of 73%). In the diet, Ag NPs damaged digestion. Snails ate less and inefficiently processed the ingested food, which adversely impacted their growth. Loss rates of Ag were faster after waterborne exposure to Ag NPs than after exposure to dissolved Ag+. Once Ag was taken up from diet, whether from Ag+ or Ag NPs, Ag was lost extremely slowly. Large Ag body concentrations are thus expected in L. stagnalis after dietborne exposures, especially to citrate-capped Ag NPs. Ingestion of Ag associated with particulate materials appears as the most important vector of uptake. Nanosilver exposure from food might trigger important environmental risks.

  14. The Ratio of 2-AG to Its Isomer 1-AG as an Intrinsic Fine Tuning Mechanism of CB1 Receptor Activation

    PubMed Central

    Dócs, Klaudia; Mészár, Zoltán; Gonda, Sándor; Kiss-Szikszai, Attila; Holló, Krisztina; Antal, Miklós; Hegyi, Zoltán

    2017-01-01

    Endocannabinoids are pleiotropic lipid messengers that play pro-homeostatic role in cellular physiology by strongly influencing intracellular Ca2+ concentration through the activation of cannabinoid receptors. One of the best-known endocannabinoid ‘2-AG’ is chemically unstable in aqueous solutions, thus its molecular rearrangement, resulting in the formation of 1-AG, may influence 2-AG-mediated signaling depending on the relative concentration and potency of the two isomers. To predict whether this molecular rearrangement may be relevant in physiological processes and in experiments with 2-AG, here we studied if isomerization of 2-AG has an impact on 2-AG-induced, CB1-mediated Ca2+ signaling in vitro. We found that the isomerization-dependent drop in effective 2-AG concentration caused only a weak diminution of Ca2+ signaling in CB1 transfected COS7 cells. We also found that 1-AG induces Ca2+ transients through the activation of CB1, but its working concentration is threefold higher than that of 2-AG. Decreasing the concentration of 2-AG in parallel to the prevention of 1-AG formation by rapid preparation of 2-AG solutions, caused a significant diminution of Ca2+ signals. However, various mixtures of the two isomers in a fix total concentration – mimicking the process of isomerization over time – attenuated the drop in 2-AG potency, resulting in a minor decrease in CB1 mediated Ca2+ transients. Our results indicate that release of 2-AG into aqueous medium is accompanied by its isomerization, resulting in a drop of 2-AG concentration and simultaneous formation of the similarly bioactive isomer 1-AG. Thus, the relative concentration of the two isomers with different potency and efficacy may influence CB1 activation and the consequent biological responses. In addition, our results suggest that 1-AG may play role in stabilizing the strength of cannabinoid signal in case of prolonged 2-AG dependent cannabinoid mechanisms. PMID:28265242

  15. Ag/ZnO heterostructure nanocrystals: synthesis, characterization, and photocatalysis.

    PubMed

    Zheng, Yuanhui; Zheng, Lirong; Zhan, Yingying; Lin, Xingyi; Zheng, Qi; Wei, Kemei

    2007-08-20

    A high yield of the dimer-type heterostructure of Ag/ZnO nanocrystals with different Ag contents is successfully prepared through a simple solvothermal method in the absence of surfactants. The samples are characterized by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, UV-vis spectroscopy, and IR spectroscopy. The results show that all samples are composed of metallic Ag and ZnO; Ag nanoparticles locate on the surface of ZnO nanorods; the binding energy of Ag 3d(5/2) for the Ag/ZnO sample with a Ag content of 5.0 atom % shifts remarkably to the lower binding energy compared with the corresponding value of pure metallic Ag because of the interaction between Ag and ZnO nanocrystals; the concentration of oxygen vacancy for the as-synthesized samples varies with the increasing Ag content, and the Ag/ZnO sample with a Ag content of 5.0 atom % has the largest density of oxygen vacancy. In addition, the relationship between their structure and photocatalytic property is investigated in detail. It is found that the photocatalytic property is closely related to its structure, such as heterostructure, oxygen defect, and crystallinity. The presence of metallic Ag nanoparticles and oxygen vacancy on the surface of ZnO nanorods promotes the separation of photogenerated electron-hole pairs and thus enhances the photocatalytic activity.

  16. The Antimicrobial Properties of Silver Nanoparticles in Bacillus subtilis Are Mediated by Released Ag+ Ions

    PubMed Central

    Hsueh, Yi-Huang; Lin, Kuen-Song; Ke, Wan-Ju; Hsieh, Chien-Te; Chiang, Chao-Lung; Tzou, Dong-Ying; Liu, Shih-Tung

    2015-01-01

    The superior antimicrobial properties of silver nanoparticles (Ag NPs) are well-documented, but the exact mechanisms underlying Ag-NP microbial toxicity remain the subject of intense debate. Here, we show that Ag-NP concentrations as low as 10 ppm exert significant toxicity against Bacillus subtilis, a beneficial bacterium ubiquitous in the soil. Growth arrest and chromosomal DNA degradation were observed, and flow cytometric quantification of propidium iodide (PI) staining also revealed that Ag-NP concentrations of 25 ppm and above increased membrane permeability. RedoxSensor content analysis and Phag-GFP expression analysis further indicated that reductase activity and cytosolic protein expression decreased in B. subtilis cells treated with 10–50 ppm of Ag NPs. We conducted X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) analyses to directly clarify the valence and fine structure of Ag atoms in B. subtilis cells placed in contact with Ag NPs. The results confirmed the Ag species in Ag NP-treated B. subtilis cells as Ag2O, indicating that Ag-NP toxicity is likely mediated by released Ag+ ions from Ag NPs, which penetrate bacterial cells and are subsequently oxidized intracellularly to Ag2O. These findings provide conclusive evidence for the role of Ag+ ions in Ag-NP microbial toxicity, and suggest that the impact of inappropriately disposed Ag NPs to soil and water ecosystems may warrant further investigation. PMID:26669836

  17. Pd effect on reliability of Ag bonding wires in microelectronic devices in high-humidity environments

    NASA Astrophysics Data System (ADS)

    Cho, Jong-Soo; Yoo, Kyung-Ah; Moon, Jeong-Tak; Son, Seoung-Bum; Lee, Se-Hee; Oh, Kyu Hwan

    2012-10-01

    We investigated the effect of Pd concentration in Pd-doped Ag wires on the humidity reliability and interfacial corrosion characteristics between Ag wire and Al metallization. Additionally, we confirmed no corrosion problem between Ag wire and noble metal (Pd, Au) metallization, even after a pressure cooker test (PCT). The chemical composition of the tested Ag wires was pure Ag, Ag-1wt% Pd and Ag-3wt% Pd. These wires were bonded to Al and noble metal (Au, Pd) metallization using a thermo-sonic bonder. The interfaces were characterized by focused ion beam (FIB), high resolution transmission electron microscope (HRTEM) and energy dispersive X-ray spectroscopy (EDS). The interface corrosion of Pd doped Ag wires was significantly reduced as the Pd concentration in the Ag wires increased. Furthermore, the Ag wires on the noble metal (Au, Pd) metallization exhibited stable reliability during the PCT.

  18. Biotic and abiotic interactions in aquatic microcosms determine fate and toxicity of Ag nanoparticles: part 2-toxicity and Ag speciation.

    PubMed

    Bone, Audrey J; Colman, Benjamin P; Gondikas, Andreas P; Newton, Kim M; Harrold, Katherine H; Cory, Rose M; Unrine, Jason M; Klaine, Stephen J; Matson, Cole W; Di Giulio, Richard T

    2012-07-03

    To study the effects of complex environmental media on silver nanoparticle (AgNP) toxicity, AgNPs were added to microcosms with freshwater sediments and two species of aquatic plants (Potamogeton diversifolius and Egeria densa), followed by toxicity testing with microcosm surface water. Microcosms were designed with four environmental matrices in order to determine the contribution of each environmental compartment to changes in toxicity: water only (W), water + sediment (WS), water + plants (WP), and water + plants + sediment (WPS). Silver treatments included AgNPs with two different coatings, gum arabic (GA-AgNPs) or polyvinylpyrollidone (PVP-AgNPs), as well as AgNO(3). Water samples taken from the microcosms at 24 h postdosing were used in acute toxicity tests with two standard model organisms, early life stage zebrafish (Danio rerio) and Daphnia magna. Speciation of Ag in these samples was analyzed using Ag L3-edge X-ray absorption near edge spectroscopy (XANES). Silver speciation patterns for the nanoparticle treatments varied significantly by coating type. While PVP-AgNPs were quite stable and resisted transformation across all matrices (>92.4% Ag(0)), GA-AgNP speciation patterns suggest significantly higher transformation rates, especially in treatments with plants (<69.2% and <58.8% Ag(0) in WP and WPS, respectively) and moderately increased transformation with sediments (<85.6% Ag(0)). Additionally, the presence of plants in the microcosms (with and without sediments) reduced both the concentration of Ag in the water column and toxicity for all Ag treatments. Reductions in toxicity may have been related to decreased water column concentrations as well as changes in the surface chemistry of the particles induced by organic substances released from the plants.

  19. AGS experiments - 1994, 1995, 1996

    SciTech Connect

    Depken, J.C.

    1997-01-01

    This report contains the following information on the Brookhaven AGS Accelerator complex: FY 1996 AGS schedule as run; FY 1997 AGS schedule (working copy); AGS beams 1997; AGS experimental area FY 1994 physics program; AGS experimental area FY 1995 physics program; AGS experimental area FY 1996 physics program; AGS experimental area FY 1997 physics program (in progress); a listing of experiments by number; two-phage summaries of each experiment begin here, also ordered by number; listing of publications of AGS experiments begins here; and listing of AGS experimenters begins here.

  20. Surface-enhanced Raman spectroscopy for DNA detection by the self-assembly of Ag nanoparticles onto Ag nanoparticle-graphene oxide nanocomposites.

    PubMed

    Lin, Tsung-Wu; Wu, Hong-Yi; Tasi, Ting-Ti; Lai, Ying-Huang; Shen, Hsin-Hui

    2015-07-28

    A novel surface-enhanced Raman scattering (SERS) sensing system which operates by the self-assembly of Ag nanoparticles (AgNPs) onto the nanocomposite of AgNPs and graphene oxide (AgNP-GO) in the presence of two complementary DNAs has been developed. In this system, AgNP-GO serves as a SERS-active substrate. The AgNPs with the modification of non-fluorescent 4-mercaptobenzoic acid (4-MBA) act as highly efficient Raman probes for DNA hybridization. When probe DNAs on AgNP-GO are complementary to target DNAs on AgNPs functionalized with 4-MBA, the DNA hybridization occurring directs the self-assembly of AgNPs onto AgNP-GO, leading to the creation of SERS hot spots. Due to the fact that partial 4-MBA molecules are located in the region of the hot spots, their SERS signals are greatly enhanced, indicating successful DNA hybridization. It is noteworthy that the size of AgNPs contributes significantly to the enhancement of SERS activity. The detection limit of the target DNAs at the pM level can be achieved through the self-assembly of large sized AgNPs onto AgNP-GO. More importantly, the AgNP-AgNP-GO system shows reproducible SERS signals in proportion to the logarithm of the target DNA concentrations spanning from 10(-6) to 10(-12) M and the excellent capability for multiplex DNA detection.

  1. Mechanisms of Toxicity of Ag Nanoparticles in Comparison to Bulk and Ionic Ag on Mussel Hemocytes and Gill Cells.

    PubMed

    Katsumiti, Alberto; Gilliland, Douglas; Arostegui, Inmaculada; Cajaraville, Miren P

    2015-01-01

    Silver nanoparticles (Ag NPs) are increasingly used in many products and are expected to end up in the aquatic environment. Mussels have been proposed as marine model species to evaluate NP toxicity in vitro. The objective of this work was to assess the mechanisms of toxicity of Ag NPs on mussel hemocytes and gill cells, in comparison to ionic and bulk Ag. Firstly, cytotoxicity of commercial and maltose stabilized Ag NPs was screened in parallel with the ionic and bulk forms at a wide range of concentrations in isolated mussel cells using cell viability assays. Toxicity of maltose alone was also tested. LC50 values were calculated and the most toxic Ag NPs tested were selected for a second step where sublethal concentrations of each Ag form were tested using a wide array of mechanistic tests in both cell types. Maltose-stabilized Ag NPs showed size-dependent cytotoxicity, smaller (20 nm) NPs being more toxic than larger (40 and 100 nm) NPs. Maltose alone provoked minor effects on cell viability. Ionic Ag was the most cytotoxic Ag form tested whereas bulk Ag showed similar cytotoxicity to the commercial Ag NPs. Main mechanisms of action of Ag NPs involved oxidative stress and genotoxicity in the two cell types, activation of lysosomal AcP activity, disruption of actin cytoskeleton and stimulation of phagocytosis in hemocytes and increase of MXR transport activity and inhibition of Na-K-ATPase in gill cells. Similar effects were observed after exposure to ionic and bulk Ag in the two cell types, although generally effects were more marked for the ionic form. In conclusion, results suggest that most observed responses were due at least in part to dissolved Ag.

  2. Mechanisms of Toxicity of Ag Nanoparticles in Comparison to Bulk and Ionic Ag on Mussel Hemocytes and Gill Cells

    PubMed Central

    Katsumiti, Alberto; Gilliland, Douglas; Arostegui, Inmaculada; Cajaraville, Miren P.

    2015-01-01

    Silver nanoparticles (Ag NPs) are increasingly used in many products and are expected to end up in the aquatic environment. Mussels have been proposed as marine model species to evaluate NP toxicity in vitro. The objective of this work was to assess the mechanisms of toxicity of Ag NPs on mussel hemocytes and gill cells, in comparison to ionic and bulk Ag. Firstly, cytotoxicity of commercial and maltose stabilized Ag NPs was screened in parallel with the ionic and bulk forms at a wide range of concentrations in isolated mussel cells using cell viability assays. Toxicity of maltose alone was also tested. LC50 values were calculated and the most toxic Ag NPs tested were selected for a second step where sublethal concentrations of each Ag form were tested using a wide array of mechanistic tests in both cell types. Maltose-stabilized Ag NPs showed size-dependent cytotoxicity, smaller (20 nm) NPs being more toxic than larger (40 and 100 nm) NPs. Maltose alone provoked minor effects on cell viability. Ionic Ag was the most cytotoxic Ag form tested whereas bulk Ag showed similar cytotoxicity to the commercial Ag NPs. Main mechanisms of action of Ag NPs involved oxidative stress and genotoxicity in the two cell types, activation of lysosomal AcP activity, disruption of actin cytoskeleton and stimulation of phagocytosis in hemocytes and increase of MXR transport activity and inhibition of Na-K-ATPase in gill cells. Similar effects were observed after exposure to ionic and bulk Ag in the two cell types, although generally effects were more marked for the ionic form. In conclusion, results suggest that most observed responses were due at least in part to dissolved Ag. PMID:26061169

  3. Highly selective and quantitative colorimetric detection of mercury(II) ions by carrageenan-functionalized Ag/AgCl nanoparticles.

    PubMed

    Narayanan, Kannan Badri; Han, Sung Soo

    2017-03-15

    The natural algal polysaccharide carrageenan was used for the greener synthesis of silver/silver chloride nanoparticles (Carr-Ag/AgCl NPs) without any toxic chemicals. We report the robust, highly selective, and sensitive colorimetric sensing of Hg(2+) ions using Carr-Ag/AgCl NPs without any further surface modification. The dark-brown color of a solution of Carr-Ag/AgCl NPs turned to white in a concentration-dependent manner with the addition of Hg(2+) ions, confirming the interaction of Carr-Ag/AgCl NPs with Hg(2+) ions. The plot of the extinction ratio of absorbance at 350nm to 450nm (A350/A450) for Carr-Ag/AgCl NPs against the concentration of [Hg(2+)] ions was linear, and the calibration curve was A350/A450=1.05254+0.00318×CHg with a lower detection limit of 1μM. This portable and cost-effective method for mercury(II) ion sensing is widely applicable in on-field qualitative and quantitative measurements of [Hg(2+)] ions in environmental or biological samples.

  4. Exposure Medium: Key in Identifying Free Ag+ as the Exclusive Species of Silver Nanoparticles with Acute Toxicity to Daphnia magna

    PubMed Central

    Shen, Mo-Hai; Zhou, Xiao-Xia; Yang, Xiao-Ya; Chao, Jing-Bo; Liu, Rui; Liu, Jing-Fu

    2015-01-01

    It is still not very clear what roles the various Ag species play in the toxicity of silver nanoparticles (AgNPs). In this study, we found that traditional exposure media result in uncontrollable but consistent physicochemical transformation of AgNPs, causing artifacts in determination of median lethal concentration (LC50) and hindering the identification of Ag species responsible for the acute toxicity of AgNPs to Daphnia magna. This obstacle was overcome by using 8 h exposure in 0.1 mmol L−1 NaNO3 medium, in which we measured the 8-h LC50 of seven AgNPs with different sizes and coatings, and determined the concentrations of various Ag species. The LC50 as free Ag+ of the seven AgNPs (0.37–0.44 μg L−1) agreed very well with that of AgNO3 (0.40 μg L−1), and showed the lowest value compared to that as total Ag, total Ag+, and dissolved Ag, demonstrating free Ag+ is exclusively responsible for the acute toxicity of AgNPs to D. magna, while other Ag species in AgNPs have no contribution to the acute toxicity. Our results demonstrated the great importance of developing appropriate exposure media for evaluating risk of nanomaterials. PMID:25858866

  5. Exposure Medium: Key in Identifying Free Ag+ as the Exclusive Species of Silver Nanoparticles with Acute Toxicity to Daphnia magna

    NASA Astrophysics Data System (ADS)

    Shen, Mo-Hai; Zhou, Xiao-Xia; Yang, Xiao-Ya; Chao, Jing-Bo; Liu, Rui; Liu, Jing-Fu

    2015-04-01

    It is still not very clear what roles the various Ag species play in the toxicity of silver nanoparticles (AgNPs). In this study, we found that traditional exposure media result in uncontrollable but consistent physicochemical transformation of AgNPs, causing artifacts in determination of median lethal concentration (LC50) and hindering the identification of Ag species responsible for the acute toxicity of AgNPs to Daphnia magna. This obstacle was overcome by using 8 h exposure in 0.1 mmol L-1 NaNO3 medium, in which we measured the 8-h LC50 of seven AgNPs with different sizes and coatings, and determined the concentrations of various Ag species. The LC50 as free Ag+ of the seven AgNPs (0.37-0.44 μg L-1) agreed very well with that of AgNO3 (0.40 μg L-1), and showed the lowest value compared to that as total Ag, total Ag+, and dissolved Ag, demonstrating free Ag+ is exclusively responsible for the acute toxicity of AgNPs to D. magna, while other Ag species in AgNPs have no contribution to the acute toxicity. Our results demonstrated the great importance of developing appropriate exposure media for evaluating risk of nanomaterials.

  6. Synthesis of AG@AgCl Core-Shell Structure Nanowires and Its Photocatalytic Oxidation of Arsenic (III) Under Visible Light.

    PubMed

    Qin, Yanyan; Cui, Yanping; Tian, Zhen; Wu, Yangling; Li, Yilian

    2017-12-01

    Ag@AgCl core-shell nanowires were synthesized by oxidation of Ag nanowires with moderate FeCl3, which exhibited excellent photocatalytic activity for As(III) oxidation under visible light. It was proved that the photocatalytic oxidation efficiency was significantly dependent on the mole ratio of Ag:AgCl. The oxidation rate of As(III) over Ag@AgCl core-shell nanowires first increased with the decrease of Ag(0) percentage, up until the optimized synthesis mole ratio of Ag nanowires:FeCl3 was 2.32:2.20, with 0.023 mg L(-1) min(-1) As(III) oxidation rate; subsequently, the oxidation rate dropped with the further decrease of Ag(0) percentage. Effects of the pH, ionic strength, and concentration of humic acid on Ag@AgCl photocatalytic ability were also studied. Trapping experiments using radical scavengers confirmed that h(+) and ·O2(-) acted as the main active species during the visible-light-driven photocatalytic process for As(III) oxidation. The recycling experiments validated that Ag@AgCl core-shell nanowires were a kind of efficient and stable photocatalyst for As(III) oxidation under visible-light irradiation.

  7. Uptake pathway for Ag bioaccumulation in three benthic invertebrates exposed to contaminated sediments

    USGS Publications Warehouse

    Yoo, H.; Lee, J.-S.; Lee, B.-G.; Lee, I.T.; Schlekat, C.E.; Koh, C.-H.; Luoma, S.N.

    2004-01-01

    We exposed 3 benthic invertebrates, the clam Macoma balthica, the polychaete Neanthes arenaceodentata and the amphipod Leptocheirus plumulosus, to Ag-contaminated sediments to evaluate the relative importance of various uptake routes (sediments, porewater or overlying water, and supplementary food) for Ag bioaccumulation. Silver bioaccumulation was evaluated at 4 levels of sediment Ag (0.1, 0,3, 1,2 and 3.3 ??mol Ag g-1) and 2 levels of acid-volatile sulfide (AVS), <0.5 or ???40 ??mol g-1, and compared among food treatments with or without Ag contamination, or with different food rations. L. plumulosus were incubated for 35 d in the Ag-contaminated sediments after 3 mo of Ag-sediment equilibration, and M. balthica and N. arenaceodentata for 19 d after 5 mo equilibration. Ag bioaccumulation in the 3 organisms was significantly correlated with 1N HCl-extractable Ag concentrations (Ag-SEM: simultaneously extracted Ag with AVS) in sediments. The Ag concentrations in porewater and overlying water were greatest in the sediments with least AVS, consistent with previous studies. Nevertheless, the amphipod and clam exposed to oxic sediments (<0.5 ??mol AVS g-1) accumulated amounts of Ag similar to those accumulated by organisms exposed to anoxic sediments (???40 ??mol AVS g-1), when Ag-SEM levels were comparable. The dissolved Ag source was important for bioaccumulation in the polychaete N. arenaceodentata. Amphipods fed Ag-contaminated food contained ???1.8-fold more tissue Ag concentrations than those fed uncontaminated food. As suggested in kinetic (DYMBAM) modeling studies, ingestion of contaminated sediments and food were the principle routes of Ag bioaccumulation by the benthic invertebrates during chronic exposure, but the relative importance of each uptake route differed among species.

  8. Quasi four-level Tm:LuAG laser

    NASA Technical Reports Server (NTRS)

    Jani, Mahendra G. (Inventor); Barnes, Norman P. (Inventor); Hutcheson, Ralph L. (Inventor); Rodriguez, Waldo J. (Inventor)

    1997-01-01

    A quasi four-level solid-state laser is provided. A laser crystal is disposed in a laser cavity. The laser crystal has a LuAG-based host material doped to a final concentration between about 2% and about 7% thulium (Tm) ions. For the more heavily doped final concentrations, the LuAG-based host material is a LuAG seed crystal doped with a small concentration of Tm ions. Laser diode arrays are disposed transversely to the laser crystal for energizing the Tm ions.

  9. AgRISTARS

    NASA Technical Reports Server (NTRS)

    1984-01-01

    An introduction to the overall AgRISTARS program, a general statement on progress, and separate summaries of the activities of each project, with emphasis on the technical highlights are presented. Organizational and management information on AgRISTARS is included in the appendices, as is a complete bibliography of publication and reports.

  10. AGS experiments: 1993 - 1994 - 1995

    SciTech Connect

    Depken, J.C.

    1996-04-01

    This report contains: FY 1995 AGS Schedule as Run; FY 1996-97 AGE Schedule (working copy); AGS Beams 1995; AGS Experimental Area FY 1993 Physics Program; AGS Experimental Area FY 1994 Physics Program; AGS Experimental Area FY 1995 Physics Program; AGS Experimental Area FY 1996 Physics Program (In progress); A listing of experiments by number; Two-page summaries of each experiment begin here, also ordered by number; Listing of publications of AGS experiments begins here; and Listing of AGS experimenters begins here. This is the twelfth edition.

  11. The isotopic composition of AG in meteorites and the presence of Pd-107 in protoplanets

    NASA Astrophysics Data System (ADS)

    Chen, J. H.; Wasserburg, G. J.

    1990-06-01

    Results are presented on the isotopic composition of Ag and the concentrations of Pd and Ag in metal and sulfide phases in iron meteorites Gibeon, Derrick Peak, and Mundrabilla and in schereibersite in Derrick Peak. It was found that almost all iron meteorite samples with a ratio of Pd-108/Ag-109 greater than about 400 had an excess of Ag-107. The results, in conjunction with the data of Chen and Wasserburg (1983) on IIIA-IIIB meteorites, demonstrate the widespread occurrence of excess Ag-107 in diverse types of small early planetary bodies. The excess Ag-107 is believed to be produced by the decay of Pd-107.

  12. Thermoelectric Properties of Ag-Doped Bi2(Se,Te)3 Compounds: Dual Electronic Nature of Ag-Related Lattice Defects.

    PubMed

    Lu, Meng-Pei; Liao, Chien-Neng; Huang, Jing-Yi; Hsu, Hung-Chang

    2015-08-03

    Effects of Ag doping and thermal annealing temperature on thermoelectric transport properties of Bi2(Se,Te)3 compounds are investigated. On the basis of the comprehensive analysis of carrier concentration, Hall mobility, and lattice parameter, we identified two Ag-related interstitial (Agi) and substitutional (AgBi) defects that modulate in different ways the thermoelectric properties of Ag-doped Bi2(Se,Te)3 compounds. When Ag content is less than 0.5 wt %, Agi plays an important role in stabilizing crystal structure and suppressing the formation of donor-like Te vacancy (VTe) defects, leading to the decrease in carrier concentration with increasing Ag content. For the heavily doped Bi2(Se,Te)3 compounds (>0.5 wt % Ag), the increasing concentration of AgBi is held responsible for the increase of electron concentration because formation of AgBi defects is accompanied by annihilation of hole carriers. The analysis of Seebeck coefficients and temperature-dependent electrical properties suggests that electrons in Ag-doped Bi2(Se,Te)3 compounds are subject to a mixed mode of impurity scattering and lattice scattering. A 10% enhancement of thermoelectric figure-of-merit at room temperature was achieved for 1 wt % Ag-doped Bi2(Se,Te)3 as compared to pristine Bi2(Se,Te)3.

  13. @AuAg nanostructures

    NASA Astrophysics Data System (ADS)

    Singh, Rina; Soni, R. K.

    2014-09-01

    Bimetallic and trimetallic nanoparticles have attracted significant attention in recent times due to their enhanced electrochemical and catalytic properties compared to monometallic nanoparticles. The numerical calculations using Mie theory has been carried out for three-layered metal nanoshell dielectric-metal-metal (DMM) system consisting of a particle with a dielectric core (Al@Al2O3), a middle metal Ag (Au) layer and an outer metal Au (Ag) shell. The results have been interpreted using plasmon hybridization theory. We have also prepared Al@Al2O3@Ag@Au and Al@Al2O3@AgAu triple-layered core-shell or alloy nanostructure by two-step laser ablation method and compared with calculated results. The synthesis involves temporal separations of Al, Ag, and Au deposition for step-by-step formation of triple-layered core-shell structure. To form Al@Ag nanoparticles, we ablated silver for 40 min in aluminium nanoparticle colloidal solution. As aluminium oxidizes easily in water to form alumina, the resulting structure is core-shell Al@Al2O3. The Al@Al2O3 particle acts as a seed for the incoming energetic silver particles for multilayered Al@Al2O3@Ag nanoparticles is formed. The silver target was then replaced by gold target and ablation was carried out for different ablation time using different laser energy for generation of Al@Al2O3@Ag@Au core-shell or Al@Al2O3@AgAu alloy. The formation of core-shell and alloy nanostructure was confirmed by UV-visible spectroscopy. The absorption spectra show shift in plasmon resonance peak of silver to gold in the range 400-520 nm with increasing ablation time suggesting formation of Ag-Au alloy in the presence of alumina particles in the solution.

  14. Corrosion behavior of Ti-Ag alloys used in dentistry in lactic acid solution

    NASA Astrophysics Data System (ADS)

    Takahashi, Masatoshi; Kikuchi, Masafumi; Takada, Yukyo

    2011-02-01

    The purpose of this study was to evaluate the corrosion resistance of experimental Ti-Ag alloys used as dental materials. An elution test and a rest-potential measurement of alloys with 5-30 mass.% Ag were performed in a 1 % lactic acid solution. The amount of Ti ions released from the α phase of the Ti-Ag alloys decreased as the Ag concentration increased. TiAg present in the alloys dissolved preferentially, but Ti2Ag did not. The rest potentials of the Ti-Ag alloys were significantly higher than that of pure titanium. The elution test and the rest-potential measurement revealed that the Ti-Ag alloys, which formed a single α-titanium structure or contained a titanium and Ti2Ag, had excellent corrosion resistance that was comparable or superior to that of pure titanium.

  15. Plasmon-assisted site-selective growth of Ag nanotriangles and Ag-Cu2O hybrids.

    PubMed

    Xie, Ying; Ma, Liang; Cheng, Zi-Qiang; Yang, Da-Jie; Zhou, Li; Hao, Zhong-Hua; Wang, Qu-Quan

    2017-03-21

    We report a plasmon-assisted growth of metal and semiconductor onto the tips of Ag nanotriangles (AgNTs) under light irradiation. The site-selective growth of Ag onto AgNTs are firstly demonstrated on the copper grids and amine-coated glass slides. As the irradiation time increases, microscopic images indicate that AgNTs gradually touch with each other and finally "weld" tip-to-tip together into the branched chains. Meanwhile, the redshift of plasmon band is observed in the extinction spectra, which agrees well the growth at the tips of AgNTs and the decrease of the gaps between the adjacent nanotriangles. We also synthesize AgNT-Cu2O nanocomposites by using a photochemical method and find that the Cu2O nanoparticles preferably grow on the tips of AgNTs. The site-selective growth of Ag and Cu2O is interpreted by the local field concentration at the tips of AgNTs induced by surface plasmon resonance under light excitation.

  16. Plasmon-assisted site-selective growth of Ag nanotriangles and Ag-Cu2O hybrids

    NASA Astrophysics Data System (ADS)

    Xie, Ying; Ma, Liang; Cheng, Zi-Qiang; Yang, Da-Jie; Zhou, Li; Hao, Zhong-Hua; Wang, Qu-Quan

    2017-03-01

    We report a plasmon-assisted growth of metal and semiconductor onto the tips of Ag nanotriangles (AgNTs) under light irradiation. The site-selective growth of Ag onto AgNTs are firstly demonstrated on the copper grids and amine-coated glass slides. As the irradiation time increases, microscopic images indicate that AgNTs gradually touch with each other and finally “weld” tip-to-tip together into the branched chains. Meanwhile, the redshift of plasmon band is observed in the extinction spectra, which agrees well the growth at the tips of AgNTs and the decrease of the gaps between the adjacent nanotriangles. We also synthesize AgNT-Cu2O nanocomposites by using a photochemical method and find that the Cu2O nanoparticles preferably grow on the tips of AgNTs. The site-selective growth of Ag and Cu2O is interpreted by the local field concentration at the tips of AgNTs induced by surface plasmon resonance under light excitation.

  17. Plasmon-assisted site-selective growth of Ag nanotriangles and Ag-Cu2O hybrids

    PubMed Central

    Xie, Ying; Ma, Liang; Cheng, Zi-Qiang; Yang, Da-Jie; Zhou, Li; Hao, Zhong-Hua; Wang, Qu-Quan

    2017-01-01

    We report a plasmon-assisted growth of metal and semiconductor onto the tips of Ag nanotriangles (AgNTs) under light irradiation. The site-selective growth of Ag onto AgNTs are firstly demonstrated on the copper grids and amine-coated glass slides. As the irradiation time increases, microscopic images indicate that AgNTs gradually touch with each other and finally “weld” tip-to-tip together into the branched chains. Meanwhile, the redshift of plasmon band is observed in the extinction spectra, which agrees well the growth at the tips of AgNTs and the decrease of the gaps between the adjacent nanotriangles. We also synthesize AgNT-Cu2O nanocomposites by using a photochemical method and find that the Cu2O nanoparticles preferably grow on the tips of AgNTs. The site-selective growth of Ag and Cu2O is interpreted by the local field concentration at the tips of AgNTs induced by surface plasmon resonance under light excitation. PMID:28322264

  18. Radiolytic formation of Ag clusters in aqueous polyvinyl alcohol solution and hydrogel matrix

    NASA Astrophysics Data System (ADS)

    Kumar, Manmohan; Varshney, Lalit; Francis, Sanju

    2005-05-01

    Ag+ ions, in aqueous polyvinyl alcohol (PVA) solution and in PVA hydrogel matrix have been gamma radiolytically reduced to produce Ag clusters. UV-visible absorption spectral characteristics of Ag clusters obtained under different gamma dose, Ag+ concentration, PVA concentration and crosslinking density of the gel used have been studied. The effect of Ag+ ions on the radiation crosslinking of the PVA chains, have also been investigated by viscosity measurements. The radiation-induced Ag+ ion reduction was followed by crosslinking of the PVA chains. PVA was found to be a very efficient stabilizer to prevent aggregation of Ag clusters. The clusters produced in the hydrogel matrix were expected to be smaller than the pore size (∼2-20 nm) of the gels used in the study. These Ag clusters were unable to reduce methyl viologen (MV2+) chloride and were stable in air.

  19. Photoluminescence Behaviour of Sm3+ Ions in presence of Ag Nanoparticles in Methanol

    NASA Astrophysics Data System (ADS)

    Dehingia, N.; Gogoi, P.; Boruah, A.; Kakoti, D.; Rajkonwar, N.; Dutta, P.

    2016-10-01

    In the present work, capped Ag NPs prepared by reduction of Ag (NO3)3 by Dimethyl Formamide is doped with Sm3+ in methanol and its photoluminescence behavior is studied. Significant modifications of the Sm3+ ions’ emission as well as quantum yield, were observed with the concentration of Ag NPs. Local field enhancement induced by neutral Ag NPs were found to be responsible for enhancement in efficiency of the Sm3+ ions.

  20. ZnWO4 nanorods decorated with Ag/AgBr nanoparticles as highly efficient visible-light-responsive photocatalyst for dye AR18 photodegradation

    NASA Astrophysics Data System (ADS)

    Li, Kebin; Xue, Jie; Zhang, Yanhui; Wei, Hong; Liu, Yalan; Dong, Chengxing

    2014-11-01

    A novel Ag-AgBr/ZnWO4 nanorod heterostructure composite was prepared via a facile deposition-precipitation method with ZnWO4 nanorods as the substrate, and characterized by XRD, SEM-EDX, TEM, XPS, and DRS to confirm its structure, morphology, composition, and optical property. The composite was used as a photocatalyst to destroy azo dye Acid Red 18 (AR18) under visible light irradiation. The effects of catalyst composition, solution pH, catalyst loading, and initial dye concentration on photocatalytic degradation rate and efficiency were examined. It was revealed that the photocatalytic activity of Ag-AgBr/ZnWO4 nanojunction system was higher than that of the single ZnWO4 or Ag-AgBr for AR18 degradation under visible light irradiation. The optimal content of Ag-AgBr in Ag-AgBr/ZnWO4 composite was 0.58:1 of Ag/W molar ratio using in the catalyst preparation. Acid pH and decreasing dye initial concentration were favorable to AR18 photodegradation, but the catalyst loading had an optimal value. The catalyst was stable and recyclable, after five successive cycles the photoactivity was fully maintained and the XRD patterns of AgBr displayed no evident change. Photoluminescence spectra revealed the enhanced photocatalytic activity and stability were closely related to the efficient separation of photogenerated carriers in Ag-AgBr/ZnWO4 nanojunction system. Superoxide radicals and holes were found to be main active species for AR18 photodegradation. Finally, the possible mechanism for AR18 degradation over Ag-AgBr/ZnWO4 nanorods under visible light irradiation was proposed as well.

  1. The role of exopolymeric substances in the bioaccumulation and toxicity of Ag nanoparticles to algae

    PubMed Central

    Zhou, Kaijun; Hu, Yi; Zhang, Luqing; Yang, Kun; Lin, Daohui

    2016-01-01

    Exopolymeric substances (EPS) have an important role in bioaccumulation and toxicity of nanoparticles (NPs) to algae, which warrants specific studies. The interaction of EPS with citrate and polyvinyl pyrrolidone (PVP) coated AgNPs (C-AgNPs and P-AgNPs, respectively) and its roles in bioaccumulation and toxicity of the AgNPs to Chlorella pyrenoidosa were investigated. The amino and aromatic carboxylic groups in the EPS were involved in the EPS-AgNP interactions. Compared with Ag+, C-AgNPs had comparable total bioaccumulation but greater absorption by intact algae with EPS; P-AgNPs had the smallest total bioaccumulation and were mainly adsorbed on algal surfaces. With EPS removed, the total bioaccumulations and surface adsorptions for the three Ag species decreased but the cell internalizations increased; the 96 h half growth inhibition concentrations decreased, indicating EPS alleviated the algal toxicity of Ag. The cell-internalized but not the adsorbed AgNPs could contribute to the nanotoxicity. The EPS could bind both AgNPs and Ag+, and thus inhibited the cell internalization and the nanotoxicity. However, the EPS-bound Ag on the cell surfaces would migrate along with the algae and be biologically amplified in the aquatic food chains, presenting ecological risks. These results are helpful for understanding the fate and ecological effects of NPs. PMID:27615743

  2. The role of exopolymeric substances in the bioaccumulation and toxicity of Ag nanoparticles to algae

    NASA Astrophysics Data System (ADS)

    Zhou, Kaijun; Hu, Yi; Zhang, Luqing; Yang, Kun; Lin, Daohui

    2016-09-01

    Exopolymeric substances (EPS) have an important role in bioaccumulation and toxicity of nanoparticles (NPs) to algae, which warrants specific studies. The interaction of EPS with citrate and polyvinyl pyrrolidone (PVP) coated AgNPs (C-AgNPs and P-AgNPs, respectively) and its roles in bioaccumulation and toxicity of the AgNPs to Chlorella pyrenoidosa were investigated. The amino and aromatic carboxylic groups in the EPS were involved in the EPS-AgNP interactions. Compared with Ag+, C-AgNPs had comparable total bioaccumulation but greater absorption by intact algae with EPS; P-AgNPs had the smallest total bioaccumulation and were mainly adsorbed on algal surfaces. With EPS removed, the total bioaccumulations and surface adsorptions for the three Ag species decreased but the cell internalizations increased; the 96 h half growth inhibition concentrations decreased, indicating EPS alleviated the algal toxicity of Ag. The cell-internalized but not the adsorbed AgNPs could contribute to the nanotoxicity. The EPS could bind both AgNPs and Ag+, and thus inhibited the cell internalization and the nanotoxicity. However, the EPS-bound Ag on the cell surfaces would migrate along with the algae and be biologically amplified in the aquatic food chains, presenting ecological risks. These results are helpful for understanding the fate and ecological effects of NPs.

  3. The role of exopolymeric substances in the bioaccumulation and toxicity of Ag nanoparticles to algae.

    PubMed

    Zhou, Kaijun; Hu, Yi; Zhang, Luqing; Yang, Kun; Lin, Daohui

    2016-09-12

    Exopolymeric substances (EPS) have an important role in bioaccumulation and toxicity of nanoparticles (NPs) to algae, which warrants specific studies. The interaction of EPS with citrate and polyvinyl pyrrolidone (PVP) coated AgNPs (C-AgNPs and P-AgNPs, respectively) and its roles in bioaccumulation and toxicity of the AgNPs to Chlorella pyrenoidosa were investigated. The amino and aromatic carboxylic groups in the EPS were involved in the EPS-AgNP interactions. Compared with Ag(+), C-AgNPs had comparable total bioaccumulation but greater absorption by intact algae with EPS; P-AgNPs had the smallest total bioaccumulation and were mainly adsorbed on algal surfaces. With EPS removed, the total bioaccumulations and surface adsorptions for the three Ag species decreased but the cell internalizations increased; the 96 h half growth inhibition concentrations decreased, indicating EPS alleviated the algal toxicity of Ag. The cell-internalized but not the adsorbed AgNPs could contribute to the nanotoxicity. The EPS could bind both AgNPs and Ag(+), and thus inhibited the cell internalization and the nanotoxicity. However, the EPS-bound Ag on the cell surfaces would migrate along with the algae and be biologically amplified in the aquatic food chains, presenting ecological risks. These results are helpful for understanding the fate and ecological effects of NPs.

  4. Nanosilver on nanostructured silica: Antibacterial activity and Ag surface area

    PubMed Central

    Sotiriou, Georgios A.; Teleki, Alexandra; Camenzind, Adrian; Krumeich, Frank; Meyer, Andreas; Panke, Sven; Pratsinis, Sotiris E.

    2013-01-01

    Nanosilver is one of the first nanomaterials to be closely monitored by regulatory agencies worldwide motivating research to better understand the relationship between Ag characteristics and antibacterial activity. Nanosilver immobilized on nanostructured silica facilitates such investigations as the SiO2 support hinders the growth of nanosilver during its synthesis and, most importantly, its flocculation in bacterial suspensions. Here, such composite Ag/silica nanoparticles were made by flame spray pyrolysis of appropriate solutions of Ag-acetate or Ag-nitrate and hexamethyldisiloxane or tetraethylorthosilicate in ethanol, propanol, diethylene glucolmonobutyl ether, acetonitrile or ethylhexanoic acid. The effect of solution composition on nanosilver characteristics and antibacterial activity against the Gram negative Escherichia coli was investigated by monitoring their recombinantly synthesized green fluorescent protein. Suspensions with identical Ag mass concentration exhibited drastically different antibacterial activity pointing out that the nanosilver surface area concentration rather than its mass or molar or number concentration determine best its antibacterial activity. Nanosilver made from Ag-acetate showed a unimodal size distribution, while that made from inexpensive Ag-nitrate exhibited a bimodal one. Regardless of precursor composition or nanosilver size distribution, the antibacterial activity of nanosilver was correlated best with its surface area concentration in solution. PMID:23730198

  5. Nanosilver on nanostructured silica: Antibacterial activity and Ag surface area.

    PubMed

    Sotiriou, Georgios A; Teleki, Alexandra; Camenzind, Adrian; Krumeich, Frank; Meyer, Andreas; Panke, Sven; Pratsinis, Sotiris E

    2011-06-01

    Nanosilver is one of the first nanomaterials to be closely monitored by regulatory agencies worldwide motivating research to better understand the relationship between Ag characteristics and antibacterial activity. Nanosilver immobilized on nanostructured silica facilitates such investigations as the SiO2 support hinders the growth of nanosilver during its synthesis and, most importantly, its flocculation in bacterial suspensions. Here, such composite Ag/silica nanoparticles were made by flame spray pyrolysis of appropriate solutions of Ag-acetate or Ag-nitrate and hexamethyldisiloxane or tetraethylorthosilicate in ethanol, propanol, diethylene glucolmonobutyl ether, acetonitrile or ethylhexanoic acid. The effect of solution composition on nanosilver characteristics and antibacterial activity against the Gram negative Escherichia coli was investigated by monitoring their recombinantly synthesized green fluorescent protein. Suspensions with identical Ag mass concentration exhibited drastically different antibacterial activity pointing out that the nanosilver surface area concentration rather than its mass or molar or number concentration determine best its antibacterial activity. Nanosilver made from Ag-acetate showed a unimodal size distribution, while that made from inexpensive Ag-nitrate exhibited a bimodal one. Regardless of precursor composition or nanosilver size distribution, the antibacterial activity of nanosilver was correlated best with its surface area concentration in solution.

  6. Synthesis, characterization and antimycobacterial activity of Ag(I)-aspartame, Ag(I)-saccharin and Ag(I)-cyclamate complexes.

    PubMed

    Cavicchioli, Maurício; Leite, Clarice Q F; Sato, Daisy N; Massabni, Antonio C

    2007-10-01

    The present work describes the synthesis and antimycobacterial activity of three Ag(I)-complexes with the sweeteners aspartame, saccharin, and cyclamate as ligands, with the aim of finding new candidate substances for fighting tuberculosis and other mycobacterial infections. The minimal inhibitory concentration of these three complexes was investigated in order to determine their in-vitro antimycobacterial activity against Mycobacterium tuberculosis, Mycobacterium avium, Mycobacterium intracellulare, Mycobacterium malmoense, and Mycobacterium kansasii. The MIC values were determined using the Microplate Alamar Blue Assay. The best MIC values found for the complexes were 9.75 microM for Ag(I)-aspartame against M. kansasii and 15.7 microM for Ag(I)-cyclamate against M. tuberculosis.

  7. AgSTAR Partners

    EPA Pesticide Factsheets

    AgSTAR’s Partner Program builds stronger relationships with state and non-governmental stakeholders to support all phases of anaerobic digester projects: planning, deployment, and long-term success.

  8. Ag-Al-Ca

    NASA Astrophysics Data System (ADS)

    Carow-Watamura, U.; Louzguine, D. V.; Takeuchi, A.

    This document is part of Part 1 http://dx.doi.org/10.1007/97.etType="URL"/> 'Systems from Ag-Al-Ca to Au-Pd-Si' of Subvolume B 'Physical Properties of Ternary Amorphous Alloys' of Volume 37 'Phase Diagrams and Physical Properties of Nonequilibrium Alloys' of Landolt-Börnstein - Group III 'Condensed Matter'. It contains the Chapter 'Ag-Al-Ca' with the content:

  9. Adsorption and visible light-driven photocatalytic degradation of Rhodamine B in aqueous solutions by Ag@AgBr/SBA-15

    NASA Astrophysics Data System (ADS)

    Hu, Longxing; Yuan, Hang; Zou, Lianpei; Chen, Feiyan; Hu, Xing

    2015-11-01

    A novel composite, Ag@AgBr/SBA-15, was successfully synthesized by dispersion of AgBr on mesoporous silica SBA-15, characterized by several techniques, such as XRD, N2 adsorption-desorption, SEM & EDS, UV-vis spectrum and XPS, and utilized for visible light photocatalytic degradation of dye Rhodamine B (RhB) in aqueous solutions. The results showed that for the various AgBr loadings in the composites, RhB photocatalytic degradation efficiency arrived at the maximum of 77% at 50% loading, or with 50Ag@AgBr/SBA-15. Under the combined mode, the RhB removal reached 88% at 0.3 g/L of 50Ag@AgBr/SBA-15 dosage, 20 mg L-1 of initial RhB concentration, 4.28 of unadjusted initial pH and 20 °C. The RhB photocatalytic degradation followed well with the second-order kinetics, and the increase of the 50Ag@AgBr/SBA-15 dosage, the decrease of the initial RhB concentration and the optimal initial solution pH would be favorable to RhB photocatalytic degradation. The quenching tests demonstrated that the RhB photocatalytic degradation was mainly attributed to the generation of active species such as O2-,bigdot OH and h+. Moreover, the adsorption characteristics of 50Ag@AgBr/SBA-15 were investigated, with its pHpzc of 6.21 acquired and the conclusion that the RhB adsorption isotherm well followed Langmuir model drawn. Additionally, photocatalyst 50Ag@AgBr/SBA-15 can be effectively regenerated with the H2O2 solutions under visible light irradiation, and reused for up to five runs for the degradation of RhB in the presence of visible light, with RhB removal more than 75% and Ag+ leaching undetected for each run.

  10. Influence of Ag thickness on structural, optical, and electrical properties of ZnS/Ag/ZnS multilayers prepared by ion beam assisted deposition

    NASA Astrophysics Data System (ADS)

    Leng, Jian; Yu, Zhinong; Xue, Wei; Zhang, Ting; Jiang, Yurong; Zhang, Jie; Zhang, Dongpu

    2010-10-01

    The structural, optical, and electrical characteristics of zinc sulfide (ZnS)/Ag/ZnS (ZAZ) multilayer films prepared by ion beam assisted deposition on k9 glass have been investigated as a function of Ag layer thickness. The characteristics of ZAZ multilayer are significantly improved up insertion of optimal Ag thickness between ZnS layers. The results show that due to bombardment of Ar ion beam, distinct Ag islands evolve into continuous Ag films at a thin Ag thickness of about 4 nm. The thinner Ag film as a thickness of 2 nm leads to high sheet resistance and low transmittance for the interface scattering induced by the Ag islands or noncontinuous films; and when the Ag thickness is over 4 nm, the ZAZ multilayer exhibits a remarkably reduced sheet resistance between 7-80 Ω/sq for the increase in carrier concentration and mobility of Ag layer, and a high transmittance over 90% for the interference phenomena of multilayers and low absorption and surface scattering of Ag layer. The ZAZ multilayer with 14 nm Ag film has a figure of merit up to 6.32×10-2 Ω-1, an average transmittance over 92% and a sheet resistance of 7.1 Ω/sq. The results suggest that ZAZ film has better optoelectrical properties than conditional indium tin oxide single layer.

  11. In vitro corrosion of dental Ag-based alloys in polyvinylpyrrolidone iodine solution.

    PubMed

    Ochi, Morio; Endo, Kazuhiko; Ohno, Hiroki; Takasusuki, Norio; Matsubara, Hideki; Maida, Takeo

    2005-09-01

    The corrosion and tarnish behaviors of three Ag-based alloys (Ag-Pd-Cu-Au alloy, Ag-In alloy, and Ag-Sn-Zn alloy) in polyvinylpyrrolidone iodine (povidone-iodine) solution were examined. The degree of tarnish was evaluated by visible-ray spectrocolorimetry. Corrosion potential measurements and analyses of corrosion products by X-ray diffractometry were carried out to elucidate the corrosion mechanism. The corrosion rate of the three Ag-based alloys in povidone-iodine solution at its practical concentration used as a gargle solution was so fast that the alloys tarnished within 10 seconds of immersion with the formation of AgI. Thermodynamic consideration and the results of surface analysis by X-ray diffractometry revealed that the main anodic and cathodic reactions were Ag + I(-)-->AgI + e- and I2 + 2e(-)-->2I- respectively.

  12. Synthesis of Ag modified vanadium oxide nanotubes and their antibacterial properties

    SciTech Connect

    Li Jing; Zheng Lifang; Zhang Kaifeng; Feng Xiaoqiang; Su Zhongxing Ma Jiantai

    2008-10-02

    Vanadium oxide nanotubes (VO{sub x}-NTs) modified by highly dispersed Ag nanoparticles have been synthesized via a facile silver-mirror reaction. The crucial factors that affected the preparation of the Ag modified vanadium oxide nanotubes (Ag/VO{sub x}-NTs) have been also studied. The dispersion and structure of Ag nanoparticles in the obtained materials were characterized by transmission electron microscopy (TEM), electron diffraction (ED) and X-ray diffraction (XRD). The results showed the distribution and size of the formed Ag particles were greatly influenced by the concentration of AgNO{sub 3} solution. Typically, Ag nanoparticles were well dispersed on the VO{sub x}-NTs with the size range from 3 to 10 nm. The corresponding antibacterial tests demonstrated the as-synthesized Ag/VO{sub x}-NTs exhibited strong antibacterial activity against Escherichia coli (E. coli)

  13. Application of a new coordination compound for the preparation of AgI nanoparticles

    SciTech Connect

    Mohandes, Fatemeh; Salavati-Niasari, Masoud

    2013-10-15

    Graphical abstract: Silver iodide nanoparticles have been sonochemically synthesized by using silver salicylate complex, [Ag(HSal)], as silver precursor. A series of control experiments were carried out to investigate the effects of solvent, surfactant concentration, sonication time and temperature on the morphology of AgI nanostructures. - Highlights: • Silver salicylate as a new precursor was applied to fabricate γ-AgI nanoparticles. • To further decrease the particle size of AgI, SDS was used as surfactant. • The effect of preparation parameters on the particle size of AgI was investigated. - Abstract: AgI nanoparticles have been sonochemically synthesized by using silver salicylate, [Ag(HSal)], as silver precursor. To investigate the effects of solvent, surfactant concentration, sonication time and temperature on the morphology of AgI nanostructures, several experiments were carried out. The products were characterized by SEM, TEM, XRD, TGA/DTA, UV–vis, and FT-IR. Based on the experimental findings in this research, it was found that the size of AgI nanoparticles was dramatically dependent on the silver precursor, sonochemical irradiation, and surfactant concentration. Sodium dodecyl sulfate (SDS) was applied as surfactant. When the concentration of SDS was 0.055 mM, very uniform sphere-like AgI nanoparticles with grain size of about 25–30 nm were obtained. These results indicated that the high concentration of SDS could prevent the aggregation between colloidal nanoparticles due to its steric hindrance effect.

  14. Nanostructured Ag surface fabricated by femtosecond laser for surface-enhanced Raman scattering.

    PubMed

    Chang, Han-Wei; Tsai, Yu-Chen; Cheng, Chung-Wei; Lin, Cen-Ying; Lin, Yen-Wen; Wu, Tzong-Ming

    2011-08-01

    Femtosecond laser was employed to fabricate nanostructured Ag surface for surface-enhanced Raman scattering (SERS) application. The prepared nanostructured Ag surface was characterized by field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The FESEM images demonstrate the formation of nanostructure-covered femtosecond laser-induced periodic surface structure, also termed as ripples, on the Ag surface. The AFM images indicate that the surface roughness of the produced nanostructured Ag substrate is larger than the untreated Ag substrate. The XRD and XPS of the nanostructured Ag surface fabricated by femtosecond laser show a face centered cubic phase of metallic Ag and no impurities of Ag oxide species. The application of the produced nanostructured Ag surface in SERS was investigated by using rhodamine 6G (R6G) as a reference chemical. The SERS intensity of R6G in aqueous solution at the prepared nanostructured Ag surface is 15 times greater than that of an untreated Ag substrate. The Raman intensities vary linearly with the concentrations of R6G in the range of 10(-8)-10(-4)M. The present methodology demonstrates that the nanostructured Ag surface fabricated by femtosecond laser is potential for qualification and quantification of low concentration molecules.

  15. Heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalyst with enhanced photocatalytic activity and stability under visible light

    NASA Astrophysics Data System (ADS)

    Wang, Wan-Sheng; Du, Hong; Wang, Rui-Xia; Wen, Tao; Xu, An-Wu

    2013-03-01

    A heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalyst was prepared by a rational in situ ion exchange reaction between Ag3PO4 micro-cubes and Br- in aqueous solution followed by photoreduction. The photocatalytic activities of obtained photocatalysts were measured by the degradation of methyl orange (MO) and methylene blue (MB) under visible light irradiation (λ >= 400 nm). Compared to AgBr/Ag, Ag3PO4/AgBr heterocrystals and pure Ag3PO4 crystals, the heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalysts exhibit much higher photocatalytic activity and stability. This enhanced photocatalytic activity suggests that the synergetic effects of the heterostructured Ag3PO4/AgBr/Ag and the strong SPR of Ag NPs on the surface result in the high efficiencies of the photocatalytic activity and the improved stability. With the assistance of Ag3PO4/AgBr/Ag heterostructures, only 8 min and 12 min are taken to completely decompose MO and MB molecules under visible-light irradiation, respectively. Furthermore, the photodegradation rate does not show an obvious decrease during ten successive cycles, indicating that our heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalysts are extremely stable under visible-light irradiation.A heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalyst was prepared by a rational in situ ion exchange reaction between Ag3PO4 micro-cubes and Br- in aqueous solution followed by photoreduction. The photocatalytic activities of obtained photocatalysts were measured by the degradation of methyl orange (MO) and methylene blue (MB) under visible light irradiation (λ >= 400 nm). Compared to AgBr/Ag, Ag3PO4/AgBr heterocrystals and pure Ag3PO4 crystals, the heterostructured Ag3PO4/AgBr/Ag plasmonic photocatalysts exhibit much higher photocatalytic activity and stability. This enhanced photocatalytic activity suggests that the synergetic effects of the heterostructured Ag3PO4/AgBr/Ag and the strong SPR of Ag NPs on the surface result in the high

  16. A novel P/Ag/Ag2O/Ag3PO4/TiO2 composite film for water purification and antibacterial application under solar light irradiation.

    PubMed

    Zhu, Qi; Hu, Xiaohong; Stanislaus, Mishma S; Zhang, Nan; Xiao, Ruida; Liu, Na; Yang, Yingnan

    2017-01-15

    TiO2-based thin films have been intensively studied in recent years to develop efficient photocatalyst films to degrade refractory organics and inactivate bacteria for wastewater treatment. In the present work, P/Ag/Ag2O/Ag3PO4/TiO2 composite films on the inner-surface of glass tube were successfully prepared via sol-gel approach. P/Ag/Ag2O/Ag3PO4/TiO2 composite films with 3 coating layers, synthesized at 400°C for 2h, showed the optimal photocatalytic performance for rhodamine B (Rh B) degradation. The results indicated that degradation ratio of Rh B by P/Ag/Ag2O/Ag3PO4/TiO2 composite film reached 99.9% after 60min under simulated solar light, while just 67.9% of Rh B was degraded by pure TiO2 film. Moreover, repeatability experiments indicated that even after five recycling runs, the photodegradation ratio of Rh B over composite film maintained at 99.9%, demonstrating its high stability. Photocatalytic inactivation of E. coli with initial concentration of 10(7)CFU/mL also showed around 100% of sterilization ratio under simulated solar light irradiation in 5min by the composite film. The radical trapping experiments implied that the major active species of P/Ag/Ag2O/Ag3PO4/TiO2 composite films were photo-generated holes and O2(-) radicals. The proposed photocatalytic mechanism shows that the transfer of photo-induced electrons and holes may reduce the recombination efficiency of electron-hole pairs and potential photodecomposition of composite film, resulting in enhanced photocatalytic ability of P/Ag/Ag2O/Ag3PO4/TiO2 composite films.

  17. Silver sulfide nanoparticles (Ag2S-NPs) are taken up by plants and are phytotoxic.

    PubMed

    Wang, Peng; Menzies, Neal W; Lombi, Enzo; Sekine, Ryo; Blamey, F Pax C; Hernandez-Soriano, Maria C; Cheng, Miaomiao; Kappen, Peter; Peijnenburg, Willie J G M; Tang, Caixian; Kopittke, Peter M

    2015-01-01

    Silver nanoparticles (NPs) are used in more consumer products than any other nanomaterial and their release into the environment is unavoidable. Of primary concern is the wastewater stream in which most silver NPs are transformed to silver sulfide NPs (Ag2S-NPs) before being applied to agricultural soils within biosolids. While Ag2S-NPs are assumed to be biologically inert, nothing is known of their effects on terrestrial plants. The phytotoxicity of Ag and its accumulation was examined in short-term (24 h) and longer-term (2-week) solution culture experiments with cowpea (Vigna unguiculata L. Walp.) and wheat (Triticum aestivum L.) exposed to Ag2S-NPs (0-20 mg Ag L(-1)), metallic Ag-NPs (0-1.6 mg Ag L(-1)), or ionic Ag (AgNO3; 0-0.086 mg Ag L(-1)). Although not inducing any effects during 24-h exposure, Ag2S-NPs reduced growth by up to 52% over a 2-week period. This toxicity did not result from their dissolution and release of toxic Ag(+) in the rooting medium, with soluble Ag concentrations remaining below 0.001 mg Ag L(-1). Rather, Ag accumulated as Ag2S in the root and shoot tissues when plants were exposed to Ag2S-NPs, consistent with their direct uptake. Importantly, this differed from the form of Ag present in tissues of plants exposed to AgNO3. For the first time, our findings have shown that Ag2S-NPs exert toxic effects through their direct accumulation in terrestrial plant tissues. These findings need to be considered to ensure high yield of food crops, and to avoid increasing Ag in the food chain.

  18. Transport of engineered silver (Ag) nanoparticles through partially fractured sandstones

    NASA Astrophysics Data System (ADS)

    Neukum, Christoph; Braun, Anika; Azzam, Rafig

    2014-08-01

    Transport behavior and fate of engineered silver nanoparticles (AgNP) in the subsurface is of major interest concerning soil and groundwater protection in order to avoid groundwater contamination of vital resources. Sandstone aquifers are important groundwater resources which are frequently used for public water supply in many regions of the world. The objective of this study is to get a better understanding of AgNP transport behavior in partially fractured sandstones. We executed AgNP transport studies on partially fissured sandstone drilling cores in laboratory experiments. The AgNP concentration and AgNP size in the effluent were analyzed using flow field-flow fractionation mainly. We employed inverse mathematical models on the measured AgNP breakthrough curves to identify and quantify relevant transport processes. Physicochemical filtration, time-dependent blocking due to filling of favorable attachment sites and colloid-facilitated transport were identified as the major processes for AgNP mobility. Physicochemical filtration was found to depend on solute chemistry, mineralogy, pore size distribution and probably on physical and chemical heterogeneity. Compared to AgNP transport in undisturbed sandstone matrix reported in the literature, their mobility in partially fissured sandstone is enhanced probably due to larger void spaces and higher hydraulic conductivity.

  19. Structural Characterization of the Ag/ybco Interface

    NASA Astrophysics Data System (ADS)

    Tidjani, Mohammed Elkhamis

    1990-01-01

    The present research is intended to characterize the interface microstructure and long term stability of the deposited silver metal in contact to the superconducting oxide YBa_2Cu_3O _{rm 7-x} (YBCO). High resolution transmission electron microscopy (HRTEM) observations of the interfacial regions reveal that Ag contacts to YBCO occurred without any intermediate phase formation at the interface. The Ag metal exhibits a preferred orientation relationship with YBCO, in which the densely packed planes and directions of the metal are parallel to those of the superconductor. The formation of (111) interfaces and facets during deposition indicates that these planes are associated with the lowest interfacial energy. The as-deposited Ag film exhibits a granular morphology, and the Ag grains are often twinned along the (111) plane while the surface of YBCO is mostly rough and structurally unstable. Annealing of the Ag/YBCO interface resulted in outdiffusion of yttrium and oxygen at regions where the surface of YBCO was rough. This diffusion, however, did not result in the formation of continuous layers at the Ag/YBCO interface but only to growth of Ag_2 Y and Ag_2O inclusions. Thus it is believed that the stability of the Ag/YBCO depends on the quality of the surface of YBCO, especially its structure. Treatment of the surface of YBCO by ion-bombardment yielded flat surfaces but damaged a layer of about 30A. Such a cleaning process improved the quality of the deposited Ag since the Ag grains were larger and contained low defects concentration. The same orientation relationships between Ag and YBCO were observed after cleaning the surface of YBCO which implied that the destruction of the structure at the surface is only partial. Deposition of Ag in the same chamber where YBCO was initially grown, to minimize the contamination of the surface of YBCO, also was not effective in enhancing the structure of the Ag/YBCO interface. The roughness of the surface of YBCO did not decrease

  20. Application of a Newly Developed High-Sensitivity HBsAg Chemiluminescent Enzyme Immunoassay for Hepatitis B Patients with HBsAg Seroclearance

    PubMed Central

    Shinkai, Noboru; Matsuura, Kentaro; Sugauchi, Fuminaka; Watanabe, Tsunamasa; Murakami, Shuko; Iio, Etsuko; Ogawa, Shintaro; Nojiri, Shunsuke; Joh, Takashi

    2013-01-01

    We modified and automated a highly sensitive chemiluminescent enzyme immunoassay (CLEIA) for surface antigen (HBsAg) detection using a combination of monoclonal antibodies, each for a specific epitope of HBsAg, and by improving an earlier conjugation technique. Of 471 hepatitis B virus (HBV) carriers seen in our hospital between 2009 and 2012, 26 were HBsAg seronegative as determined by the Abbott Architect assay. The Lumipulse HBsAg-HQ assay was used to recheck those 26 patients who demonstrated seroclearance by the Abbott Architect assay. The performance of the Lumipulse HBsAg-HQ assay was compared with that of a quantitative HBsAg detection system (Abbott Architect) and the Roche Cobas TaqMan HBV DNA assay (CTM) (lower limit of detection, 2.1 log copies/ml) using blood serum samples from patients who were determined to be HBsAg seronegative by the Abbott Architect assay. Ten patients had spontaneous HBsAg loss. Of 8 patients treated with nucleotide analogues (NAs), two were HBsAg seronegative after stopping lamivudine therapy and 6 were HBsAg seronegative during entecavir therapy. Eight acute hepatitis B (AH) patients became HBsAg seronegative. Of the 26 patients, 16 were HBsAg positive by the Lumipulse HBsAg-HQ assay but negative by the Abbott Architect assay. The differences between the two assays in terms of detectable HBsAg persisted over the long term in the spontaneous loss group (median, 10 months), the NA-treated group (2.5 months), and the AH group (0.5 months). In 9 patients, the Lumipulse HBsAg-HQ assay detected HBsAg when HBV DNA was negative by the CTM assay. HBsAg was also detected by the Lumipulse HBsAg-HQ assay in 4 patients with an anti-HBs concentration of >10 mIU/ml, 3 of whom had no HBsAg escape mutations. The automatic, highly sensitive HBsAg CLEIA Lumipulse HBsAg-HQ is a convenient and precise assay for HBV monitoring. PMID:23946517

  1. Influence of Ag contents on structure and tribological properties of TiSiN-Ag nanocomposite coatings on Ti-6Al-4V

    NASA Astrophysics Data System (ADS)

    Dang, Chaoqun; Li, Jinlong; Wang, Yue; Yang, Yitao; Wang, Yongxin; Chen, Jianmin

    2017-02-01

    TiSiN-Ag nanocomposite coatings with different Ag contents were deposited on Ti-6Al-4V using reactive co-sputtering in multi-arc ion plating system. Influence of Ag contents on structure and tribological properties of TiSiN-Ag nanocomposite coatings was investigated. The TiSiN-Ag coatings were found to have unique nanocomposite structures composed of nanocrystallite and amorphous nc-TiN/nc-Ag/a-Si3N4. When the silver content was 1.4 at.%, the coating exhibited high hardness (36 GPa), but poor wear resistance. When the silver content was increased from 5.3 to 8.7 at.%, the coatings possessed homogeneous distribution and small variation in hardness. Although these coatings revealed obvious decrease in hardness, significantly reduced in the friction coefficient and possessed excellent tribological properties, besides, the coating with the Ag content of 5.3 at.% showed best wear resistance in artificial seawater and the coating (7.9 at.% Ag) revealed the best wear resistance in ambient air. However, with a further increased incorporation of Ag into the TiSiN-Ag coating (17.0 at.%) resulted in the formation of a large volume fraction of metallic silver, which caused a decrease both in hardness and wear resistance. The coating containing highest Ag concentration (21.0 at.%) exhibited low friction coefficient both in ambient air and artificial seawater, although possessing low hardness.

  2. Synthesis of silver nanoparticles deposited on silica by γ-irradiation and preparation of PE/Ag nano compound masterbatches

    NASA Astrophysics Data System (ADS)

    Nguyen, Thi Kim Lan; Trinh Nguyen, Thuy Ai; Phu Dang, Van; Duy Nguyen, Ngoc; Le, Anh Quoc; Hien Nguyen, Quoc

    2013-12-01

    Silver nanoparticles (AgNPs) deposited on silica were synthesized by gamma Co-60 irradiation of Ag+ dispersion in silica/ethanol/water mixture (9/80/20:w/v/v). The reduction of Ag+ is occurred by hydrated electron (e-aq) and hydrogen atom (H•) generated during radiolysis of ethanol/water. The conversion doses (Ag+ → Ag0) were determined by UV-Vis spectroscopy. The synthesized AgNPs/silica were characterized by transmission electron microscopy (TEM) and x-ray diffraction (XRD), which showed the size of AgNPs to be in the range of 5-40 nm for Ag+ concentrations from 5 to 20 mM. Masterbatches of PE/AgNPs/silica compound with silver content from 250 to 1000 mg kg-1 were also prepared. These masterbatches can be suitably used for various applications such as antimicrobial food containers and packing films, etc.

  3. Preparation of AgBr Nanoparticles in Microemulsions Via Reaction of AgNO3 with CTAB Counterion

    NASA Astrophysics Data System (ADS)

    Husein, Maen M.; Rodil, Eva; Vera, Juan H.

    2007-10-01

    Nanoparticles of AgBr were prepared by precipitating AgBr in the water pools of microemulsions consisting of CTAB, n-butanol, isooctane and water. An aqueous solution of AgNO3 added to the microemulsion was the source of Ag+ ions. The formation of AgBr nanoparticles in microemulsions through direct reaction with the surfactant counterion is a novel approach aimed at decreasing the role of intermicellar nucleation on nanoparticle formation for rapid reactions. The availability of the surfactant counterion in every reverse micelle and the rapidity of the reaction with the counterion trigger nucleation within individual reverse micelles. The effect of the following variables on the particle size and size distribution was investigated: the surfactant and cosurfactant concentrations, moles of AgNO3 added, and water to surfactant mole ratio, R. High concentration of the surfactant or cosurfactant, or high water content of the microemulsion favored intermicellar nucleation and resulted in the formation of large particles with broad size distribution, while high amounts of AgNO3 favored nucleation within individual micelles and resulted in small nanoparticles with narrow size distribution. A blue shift in the UV absorption threshold corresponding to a decrease in the particle size was generally observed. Notably, the variation of the absorption peak size with the nanoparticle size was opposite to those reported by us in previous studies using different surfactants.

  4. Highly dynamic PVP-coated silver nanoparticles in aquatic environments: chemical and morphology change induced by oxidation of Ag(0) and reduction of Ag(+).

    PubMed

    Yu, Su-Juan; Yin, Yong-Guang; Chao, Jing-Bo; Shen, Mo-Hai; Liu, Jing-Fu

    2014-01-01

    The fast growing and abundant use of silver nanoparticles (AgNPs) in commercial products alerts us to be cautious of their unknown health and environmental risks. Because of the inherent redox instability of silver, AgNPs are highly dynamic in the aquatic system, and the cycle of chemical oxidation of AgNPs to release Ag(+) and reconstitution to form AgNPs is expected to occur in aquatic environments. This study investigated how inevitable environmentally relevant factors like sunlight, dissolved organic matter (DOM), pH, Ca(2+)/Mg(2+), Cl(-), and S(2-) individually or in combination affect the chemical transformation of AgNPs. It was demonstrated that simulated sunlight induced the aggregation of AgNPs, causing particle fusion or self-assembly to form larger structures and aggregates. Meanwhile, AgNPs were significantly stabilized by DOM, indicating that AgNPs may exist as single particles and be suspended in natural water for a long time or delivered far distances. Dissolution (ion release) kinetics of AgNPs in sunlit DOM-rich water showed that dissolved Ag concentration increased gradually first and then suddenly decreased with external light irradiation, along with the regeneration of new tiny AgNPs. pH variation and addition of Ca(2+) and Mg(2+) within environmental levels did not affect the tendency, showing that this phenomenon was general in real aquatic systems. Given that a great number of studies have proven the toxicity of dissolved Ag (commonly regarded as the source of AgNP toxicity) to many aquatic organisms, our finding that the effect of DOM and sunlight on AgNP dissolution can regulate AgNP toxicity under these conditions is important. The fact that the release of Ag(+) and regeneration of AgNPs could both happen in sunlit DOM-rich water implies that previous results of toxicity studies gained by focusing on the original nature of AgNPs should be reconsidered and highlights the necessity to monitor the fate and toxicity of AgNPs under more

  5. Inputs, dynamics and potential impacts of silver (Ag) from urban wastewater to a highly turbid estuary (SW France).

    PubMed

    Deycard, Victoria N; Schäfer, Jörg; Petit, Jérôme C J; Coynel, Alexandra; Lanceleur, Laurent; Dutruch, Lionel; Bossy, Cécile; Ventura, Alexandre; Blanc, Gérard

    2017-01-01

    Although silver (Ag) has been listed as a priority pollutant for the aquatic environment by the European Union (Directive 2006/11/EC), the use of Ag-based products with antimicrobial effects is increasing in Europe, as well as North America and Asia. This study investigates personal care products (PCP) as a potential source of Ag in wastewater, as well as the dynamics and fate of Ag in the influent and effluent of a major urban wastewater treatment plant (WWTP) located on the fluvial part of the Gironde Estuary. Typical household PCPs marked as using Ag contained concentrations of up to 0.4 mg kg(-1) making them likely contributors to urban Ag released into the aquatic environment. Silver concentrations in influent wastewater generally occurred during mid-week working hours and decreased during the night and on weekends clearly indicating the dominance of urban sources. Up to 90% of the total Ag in wastewater was bound to particles and efficiently (>80%) removed by the treatment process, whereas 20% of Ag was released into the fluvial estuary. Silver concentrations in wastewater effluents clearly exceeded estuarine concentrations and may strongly amplify the local Ag concentrations and fluxes, especially during summer rainstorms in low river discharge conditions. Further work should focus on environmental effects and fate of urban Ag release due to immediate localized outfall and/or the adsorption on estuarine particles and subsequent release as dissolved Ag chloro-complexes within the estuarine salinity gradient.

  6. AGS experiments -- 1991, 1992, 1993. Tenth edition

    SciTech Connect

    Depken, J.C.

    1994-04-01

    This report contains: (1) FY 1993 AGS schedule as run; (2) FY 1994--95 AGS schedule; (3) AGS experiments {ge} FY 1993 (as of 30 March 1994); (4) AGS beams 1993; (5) AGS experimental area FY 1991 physics program; (6) AGS experimental area FY 1992 physics program; (7) AGS experimental area FY 1993 physics program; (8) AGS experimental area FY 1994 physics program (planned); (9) a listing of experiments by number; (10) two-page summaries of each experiment; (11) listing of publications of AGS experiments; and (12) listing of AGS experiments.

  7. AGS experiments -- 1995, 1996 and 1997

    SciTech Connect

    Depken, J.C.; Presti, P.L.

    1997-12-01

    This report contains (1) FY 1995 AGS schedule as run; (2) FY 1996 AGS schedule as run; (3) FY 1997 AGS schedule as run; (4) FY 1998--1999 AGS schedule (proposed); (5) AGS beams 1997; (6) AGS experimental area FY 1995 physics program; (7) AGS experimental area FY 1996 physics program; (8) AGS experimental area FY 1997 physics program; (9) AGS experimental area FY 1998--1999 physics program (proposed); (10) a listing of experiments by number; (11) two-page summaries of each experiment, in order by number; and (12) listing of publications of AGS experiments.

  8. Size- and shape-dependent growth of fluorescent ZnS nanorods and nanowires using Ag nanocrystals as seeds

    NASA Astrophysics Data System (ADS)

    Shen, Huaibin; Shang, Hangying; Niu, Jinzhong; Xu, Weiwei; Wang, Hongzhe; Li, Lin Song

    2012-09-01

    High-quality, monodisperse, and size-controlled Ag-ZnS nanorods or nanowires have been synthesized successfully using Ag nanocrystals as seeds. Such one-dimensional colloidal Ag-ZnS nanorods or nanowires having a purposefully controlled diameter in the range of 5-9 nm and a length of 18-600 nm were obtained by altering the reaction conditions, such as concentration, reaction time, reaction temperature, and diameter of Ag nanocrystals. The conjunction interface of Ag-ZnS nanorods or nanowires consists of the (200) plane of Ag nanocrystal and (101) plane of ZnS rod or wire, the <101> directions of ZnS nanorods grow preferentially. Based on the photoluminescence and lifetime of Ag-ZnS nanorods, it was found that Ag nanocrystals enhanced the radiative rate eventually, the fluorescence intensity of Ag-ZnS nanorods can be tuned by changing the size of the Ag seeds. The Ag-ZnS nanorods or nanowires showed greatly improved optical properties as compared to ZnS nanocrystals, the maximum emission was around 402 nm and the photoluminescence quantum yield was up to 30% when 5 nm Ag nanocrystals were used as seeds.High-quality, monodisperse, and size-controlled Ag-ZnS nanorods or nanowires have been synthesized successfully using Ag nanocrystals as seeds. Such one-dimensional colloidal Ag-ZnS nanorods or nanowires having a purposefully controlled diameter in the range of 5-9 nm and a length of 18-600 nm were obtained by altering the reaction conditions, such as concentration, reaction time, reaction temperature, and diameter of Ag nanocrystals. The conjunction interface of Ag-ZnS nanorods or nanowires consists of the (200) plane of Ag nanocrystal and (101) plane of ZnS rod or wire, the <101> directions of ZnS nanorods grow preferentially. Based on the photoluminescence and lifetime of Ag-ZnS nanorods, it was found that Ag nanocrystals enhanced the radiative rate eventually, the fluorescence intensity of Ag-ZnS nanorods can be tuned by changing the size of the Ag seeds. The Ag

  9. Transport and separation of Ag(+) and Zn(2+) by donnan dialysis through a monovalent cation selective membrane.

    PubMed

    Cherif, A T; Gavach, C; Molenat, J; Elmidaoui, A

    1998-08-01

    Donnan Dialysis of Ag(+) and Zn(2+) was investigated through a cation exchange membrane (CMS Neosepta) when a proton concentration difference was maintained between the two sides of the membrane. Developed for the production of brine from sea water, CMS Neosepta showed a higher permeability to monovalent than to bivalent cations. Several physico-chemical parameters have been determined (electrical resistance, membrane potential, sorption of electrolytes, Zn(2+) and Ag(+) diffusion coefficients). The flux of Ag(+) and the diffusion potential in the membrane increase with HNO(3) concentrations. Ag(+) and Zn(2+) can be separated because of the preferential membrane transfer for Ag(+).

  10. Synthesis, characterization and photocatalytic behavior of Ag doped TiO2 thin film

    NASA Astrophysics Data System (ADS)

    Bensouici, F.; Souier, T.; Dakhel, A. A.; Iratni, A.; Tala-Ighil, R.; Bououdina, M.

    2015-09-01

    In this study, structure, microstructure, optical properties and photocatalytic degradation of Rhodamine B (RhB) have been investigated in an aqueous heterogeneous media containing pure and Ag doped TiO2 nanostructures thin films which were prepared by a simple sol-gel route. Thermal analysis demonstrated that Ag content decreased the temperature of anatase-to-rutile phase transformation. X-ray diffraction analysis confirmed that the prepared nanostructures crystallize within anatase-type structure and that the dopant Ag ions were not fully incorporated within TiO2 host lattice, meanwhile both the refractive index and optical band gap were affected by Ag concentration. The photodegradation of Rhodamine B under UV-C radiation by using pure and Ag-doped TiO2 nanostructures showed that Ag played an important role in a significant improvement of the photodegradation efficiency and that the optimum content of Ag ions was found to be 0.5% molar ratio.

  11. Mechanism and experimental study on the photocatalytic performance of Ag/AgCl @ chiral TiO2 nanofibers photocatalyst: the impact of wastewater components.

    PubMed

    Wang, Dawei; Li, Yi; Li Puma, Gianluca; Wang, Chao; Wang, Peifang; Zhang, Wenlong; Wang, Qing

    2015-03-21

    The effect of the water matrix components of a secondary effluent of a urban wastewater treatment plant on the photocatalytic activity of Ag/AgCl @ chiral TiO2 nanofibers and the undergoing reaction mechanisms were investigated. These effects were evaluated through the water components-induced changes on the net rate of hydroxyl radical (˙OH) generation and modeled using a relative rate technique. Dissolved organic matter DOM (k=-2.8×10(8) M(-1) s(-1)) scavenged reactive oxygen species, Cl(-) (k=-5.3×10(8) M(-1) s(-1)) accelerated the transformation from Ag to AgCl (which is not photocatalytically active under visible-light irradiation), while Ca(2+) at concentrations higher than 50 mM (k=-1.3×10(9) M(-1) s(-1)) induced aggregation of Ag/AgCl and thus all of them revealed inhibitory effects. In contrast, NO3(-) (k=6.9×10(8) M(-1) s(-1)) and CO3(2-) (k=3.7×10(8) M(-1) s(-1)) improved the photocatalytic activity of Ag/AgCl slightly by improving the rate of HO˙ generation. Other ubiquitous secondary effluent components including SO4(2-) (k=3.9×10(5) M(-1) s(-1)), NH3(+) (k=3.5×10(5) M(-1) s(-1)) and Na(+) (k=2.6×10(4) M(-1) s(-1)) had negligible effects. 90% of 17-α-ethynylestradiol (EE2) spiked in the secondary effluent was removed within 12 min, while the structure and size of Ag/AgCl @ chiral TiO2 nanofibers remained stable. This work may be helpful not only to uncover the photocatalytic mechanism of Ag/AgCl based photocatalyst but also to elucidate the transformation and transportation of Ag and AgCl in natural water.

  12. Effects of Ag Nanoparticles on Growth and Fat Body Proteins in Silkworms (Bombyx mori).

    PubMed

    Meng, Xu; Abdlli, Nouara; Wang, Niannian; Lü, Peng; Nie, Zhichao; Dong, Xin; Lu, Shuang; Chen, Keping

    2017-03-30

    Ag nanoparticles (AgNPs), a widely used non-antibiotic, antibacterial material, have shown toxic and other potentially harmful effects in mammals. However, the deleterious effects of AgNPs on insects are still unknown. Here, we studied the effects of AgNPs on the model invertebrate organism Bombyx mori. After feeding silkworm larvae different concentrations of AgNPs, we evaluated the changes of B. mori body weights, survival rates, and proteomic differences. The results showed that low concentrations (<400 mg/L) of AgNPs promoted the growth and cocoon weights of B. mori. Although high concentrations (≥800 mg/L) of AgNPs also improved B. mori growth, they resulted in silkworm death. An analysis of fat body proteomic differences revealed 13 significant differences in fat body protein spots, nine of which exhibited significantly downregulated expression, while four showed significantly upregulated expression. Reverse transcription-polymerase chain reaction results showed that at an AgNP concentration of 1600 mg/L, the expression levels of seven proteins were similar to the transcription levels of their corresponding genes. Our results suggest that AgNPs lowered the resistance to oxidative stress, affected cell apoptosis, and induced cell necrosis by regulating related protein metabolism and metabolic pathways in B. mori.

  13. Studies on electrochemical recovery of silver from simulated waste water from Ag(II)/Ag(I) based mediated electrochemical oxidation process.

    PubMed

    Chandrasekara Pillai, K; Chung, Sang Joon; Moon, Il-Shik

    2008-11-01

    In the Ag(II)/Ag(I) based mediated electrochemical oxidation (MEO) process, the spent waste from the electrochemical cell, which is integrated with the scrubber columns, contains high concentrations of precious silver as dissolved ions in both the anolyte and the catholyte. This work presents an electrochemical developmental study for the recovery of silver from simulated waste water from Ag(II)/Ag(I) based MEO process. Galvanostatic method of silver deposition on Ti cathode in an undivided cell was used, and the silver recovery rate kinetics of silver deposition was followed. Various experimental parameters, which have a direct bearing on the metal recovery efficiency, were optimized. These included studies with the nitric acid concentration (0.75-6M), the solution stirring rate (0-1400 rpm), the inter-electrode distance between the anode and the cathode (2-8 cm), the applied current density (29.4-88.2 mA cm(-2)), and the initial Ag(I) ion concentration (0.01-0.2M). The silver recovered by the present electrodeposition method was re-dissolved in 6M nitric acid and subjected to electrooxidation of Ag(I) to Ag(II) to ascertain its activity towards Ag(II) electrogeneration from Ag(I), which is a key factor for the efficient working of MEO process. Our studies showed that the silver metal recovered by the present electrochemical deposition method could be reused repeatedly for MEO process with no loss in its electrochemical activity. Some work on silver deposition from sulfuric acid solution of different concentrations was also done because of its promising features as the catholyte in the Ag(II) generating electrochemical cell used in MEO process, which include: (i) complete elimination of poisonous NO(x) gas liberation in the cathode compartment, (ii) reduced Ag(+) ion migration across Nafion membrane from anolyte to catholyte thereby diminished catholyte contamination, and (iii) lower cell voltage and hence lesser power consumption.

  14. Biological synthesis of triangular gold nanoprisms

    NASA Astrophysics Data System (ADS)

    Shankar, S. Shiv; Rai, Akhilesh; Ankamwar, Balaprasad; Singh, Amit; Ahmad, Absar; Sastry, Murali

    2004-07-01

    The optoelectronic and physicochemical properties of nanoscale matter are a strong function of particle size. Nanoparticle shape also contributes significantly to modulating their electronic properties. Several shapes ranging from rods to wires to plates to teardrop structures may be obtained by chemical methods; triangular nanoparticles have been synthesized by using a seeded growth process. Here, we report the discovery that the extract from the lemongrass plant, when reacted with aqueous chloroaurate ions, yields a high percentage of thin, flat, single-crystalline gold nanotriangles. The nanotriangles seem to grow by a process involving rapid reduction, assembly and room-temperature sintering of 'liquid-like' spherical gold nanoparticles. The anisotropy in nanoparticle shape results in large near-infrared absorption by the particles, and highly anisotropic electron transport in films of the nanotriangles.

  15. 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.

  16. Ag/AgO Nanoparticles Grown via Time Dependent Double Mechanism in a 2D Layered Ni-PCP and Their Antibacterial Efficacy

    PubMed Central

    Agarwal, Rashmi A.; Gupta, Neeraj K.; Singh, Rajan; Nigam, Shivansh; Ateeq, Bushra

    2017-01-01

    A simple synthesis route for growth of Ag/AgO nanoparticles (NPs) in large quantitative yields with narrow size distribution from a functional, non-activated, Ni (II) based highly flexible porous coordination polymer (PCP) as a template has been demonstrated. This template is a stable storage media for the NPs larger than the pore diameters of the PCP. From EPR study it was concluded that NPs were synthesized via two mechanisms i.e. acid formation and the redox activity of the framework. Size range of Ag/AgO NPs is sensitive to choice of solvent and reaction time. Direct use of Ag/AgO@Ni-PCP shows influential growth inhibition towards Escherichia coli and the pathogen Salmonella typhimurium at extremely low concentrations. The pristine template shows no cytotoxic activity, even though it contains Ni nodes in the framework. PMID:28322256

  17. Ag/AgO Nanoparticles Grown via Time Dependent Double Mechanism in a 2D Layered Ni-PCP and Their Antibacterial Efficacy

    NASA Astrophysics Data System (ADS)

    Agarwal, Rashmi A.; Gupta, Neeraj K.; Singh, Rajan; Nigam, Shivansh; Ateeq, Bushra

    2017-03-01

    A simple synthesis route for growth of Ag/AgO nanoparticles (NPs) in large quantitative yields with narrow size distribution from a functional, non-activated, Ni (II) based highly flexible porous coordination polymer (PCP) as a template has been demonstrated. This template is a stable storage media for the NPs larger than the pore diameters of the PCP. From EPR study it was concluded that NPs were synthesized via two mechanisms i.e. acid formation and the redox activity of the framework. Size range of Ag/AgO NPs is sensitive to choice of solvent and reaction time. Direct use of Ag/AgO@Ni-PCP shows influential growth inhibition towards Escherichia coli and the pathogen Salmonella typhimurium at extremely low concentrations. The pristine template shows no cytotoxic activity, even though it contains Ni nodes in the framework.

  18. Enhancement of stability of N-doped TiO2 photocatalysts with Ag loading

    NASA Astrophysics Data System (ADS)

    Gao, Yuanpeng; Fang, Pengfei; Chen, Feitai; Liu, Yang; Liu, Zhi; Wang, Dahai; Dai, Yiqun

    2013-01-01

    Various contents of Ag nanoparticles were successfully introduced into the N-doped TiO2 photocatalysts via a hydrothermal procedure in the silver-ammonia solutions with different Ag concentrations. Effects of Ag loading on the structure and properties of N-doped TiO2 photocatalysts were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, fluorescence spectroscopy (FL), UV-vis spectroscopy, X-ray photoelectron spectroscopy (XPS), and N2 physical adsorption analysis. The relationship between the stability of N dopants in TiO2 lattice and the Ag loading content was investigated for the first time. The results confirm that Ag nanoparticles loading on TiO2 surfaces significantly restrain the escape of the N dopants from the oxide during the hydrothermal process, and the escape rate of N dopants decreased gradually with the increase of Ag loading amount. The dependence of photocatalytic activity on Ag content was also investigated through degradation of rhodamine B (RhB) under visible light irradiation. It was found that the photocatalytic activity increases gradually with increasing Ag content first, and then decreases after exceeding the optimal Ag content. Therefore, the photocatalytic activity of Ag/N co-modified TiO2 photocatalysts can be adjusted by the Ag content.

  19. Microstructure of Cu-Ag Uniform Nanoparticulate Films on Polyurethane 3D Catheters: Surface Properties.

    PubMed

    Rtimi, Sami; Sanjines, Rosendo; Pulgarin, Cesar; Kiwi, John

    2016-01-13

    The preparation, characterization, and antibacterial testing of Cu-Ag sputtered polyurethane (PU) catheters are addressed in this study. PU catheters with different atomic ratios Cu:Ag have been sputtered and led to different optical properties as followed by diffuse reflectance spectroscopy (DRS) and the surface redox properties were also different for different Cu-Ag ratios as observed by X-ray photoelectron spectroscopy (XPS). The surface atomic percentage concentration of the oxidized/reduced C-species originating from bacterial cultures before and after bacterial inactivation were determined on the Cu-Ag PU catheters. The crystallographic properties were determined by X-ray diffraction (XRD). The XRD-diffractogram showed the presence of Cu2O (111), Cu (200), CuO (020), and Ag (111) indicating that Cu nanoparticles present a more crystalline character compared to Ag nanoparticles. Increasing the percentage of Ag in the Cu-Ag films, bigger Ag-particle agglomerates were detected by scanning transmission electron microscopy (STEM) microanalysis confirming the results obtained by AFM. The bacterial inactivation kinetics of the sputtered Cu-Ag films on PU catheters was investigated in detail. Quasi-instantaneous bacterial inactivation kinetics was induced by the sputtered films on PU catheters after optimization of the Cu-Ag film thickness.

  20. Morphological and electrochemical characterization of electrodeposited Zn–Ag nanoparticle composite coatings

    SciTech Connect

    Punith Kumar, M.K.; Srivastava, Chandan

    2013-11-15

    Silver nanoparticles with an average size of 23 nm were chemically synthesized and used to fabricate Zn–Ag composite coatings. The Zn–Ag composite coatings were generated by electrodeposition method using a simple sulfate plating bath dispersed with 0.5, 1 and 1.5 g/l of Ag nanoparticles. Scanning electron microscopy, X-ray diffraction and texture co-efficient calculations revealed that Ag nanoparticles appreciably influenced the morphology, micro-structure and texture of the deposit. It was also noticed that agglomerates of Ag nanoparticles, in the case of high bath load conditions, produced defects and dislocations on the deposit surface. Ag nanoparticles altered the corrosion resistance property of Zn–Ag composite coatings as observed from Tafel polarization, electrochemical impedance analysis and an immersion test. Reduction in corrosion rate with increased charge transfer resistance was observed for Zn–Ag composite coatings when compared to a pure Zn coating. However, the particle concentration in the plating bath and their agglomeration state directly influenced the surface morphology and the subsequent corrosion behavior of the deposits. - Highlights: • Synthesis of Ag nanoparticles with an average size of 23 nm • Fabrication of Zn/nano Ag composite coating on mild steel • Composite coatings showed better corrosion resistance. • Optimization of particle concentration is necessary.

  1. Quantifying the origin of released Ag+ ions from nanosilver.

    PubMed

    Sotiriou, Georgios A; Meyer, Andreas; Knijnenburg, Jesper T N; Panke, Sven; Pratsinis, Sotiris E

    2012-11-13

    Nanosilver is most attractive for its bactericidal properties in modern textiles, food packaging, and biomedical applications. Concerns, however, about released Ag(+) ions during dispersion of nanosilver in liquids have limited its broad use. Here, nanosilver supported on nanostructured silica is made with closely controlled Ag size both by dry (flame aerosol) and by wet chemistry (impregnation) processes without any surface functionalization that could interfere with its ion release. It is characterized by electron microscopy, atomic absorption spectroscopy, and X-ray diffraction, and its Ag(+) ion release in deionized water is monitored electrochemically. The dispersion method of nanosilver in solutions affects its dissolution rate but not the final Ag(+) ion concentration. By systematically comparing nanosilver size distributions to their equilibrium Ag(+) ion concentrations, it is revealed that the latter correspond precisely to dissolution of one to two surface silver oxide monolayers, depending on particle diameter. When, however, the nanosilver is selectively conditioned by either washing or H(2) reduction, the oxide layers are removed, drastically minimizing Ag(+) ion leaching and its antibacterial activity against E. coli . That way the bactericidal activity of nanosilver is confined to contact with its surface rather than to rampant ions. This leads to silver nanoparticles with antibacterial properties that are essential for medical tools and hospital applications.

  2. Controlled formation of ag nanoparticles by means of long-chain sodium polyacrylates in dilute solution.

    PubMed

    Huber, Klaus; Witte, Thomas; Hollmann, Jutta; Keuker-Baumann, Susanne

    2007-02-07

    A new tool is presented to control formation of Ag nanoparticles. Small amounts of silver ions were added to dilute solutions of long-chain sodium polyacrylates (NaPA). Four NaPA samples covering a molar mass regime of 97 kD < or = Mw < or = 650 kD have been used. With amounts of added Ag(+) as low as 1-2% of the COO(-) groups of the polyanionic chains, significant changes could already be induced in the NaPA coils with 650 kD. If the NaPA concentration was kept below 0.1 g/L, the coils with 650 kD exhibited a significant coil shrinking in stable solutions. At larger NaPA concentrations, addition of Ag+ initiates an aggregation of the polyacrylate coils toward compact structures. Coil shrinking and aggregation was revealed by means of time-resolved static light scattering. If exposed to UV-radiation, small Ag particles formed within the shrunken anionic polyacrylate coils. The Ag nanoparticles were identified by means of an enhanced light scattering and a characteristic plasmon absorption band around 410 nm. No such Ag particle formation could be observed even at 5 times larger concentrations of Ag(+) and NaPA if the two smallest polyacrylate samples have been used under otherwise equal conditions. This molar mass sensitive response of NaPA to Ag(+)-addition suggests an interesting phenomenon: if the coil size of the NaPa chains, which act as Ag(+) collectors, is large enough, local Ag(+) concentration in these coil-shaped Ag(+) containers exceeds a critical value, and irradiation with UV generates Ag nanoparticles.

  3. Heterojunction double dumb-bell Ag2Te-Te-Ag2Te nanowires

    NASA Astrophysics Data System (ADS)

    Som, Anirban; Pradeep, T.

    2012-07-01

    Growth of isolated axial heterojunction nanowires by a solution phase growth process is reported. The dumb-bell shaped nanowires contain two silver telluride sections at the extremes joined by a tellurium section. Reaction of silver nitrate with tellurium NWs in aqueous solution at a molar ratio of 1 : 1 leads to the formation of amorphous partially silver reacted Te NWs. Low temperature (75 °C) solution phase annealing of these silver deficient NWs results in phase segregation producing crystalline Ag2Te and Te phases with clear phase boundaries along the wire axis. Structural characterization of these dumb-bell shaped NWs was performed with different microscopic and spectroscopic tools. Solution phase silver concentration over the course of annealing indicated leaching of silver into the solution during the formation of biphasic NWs. Similar Ag : Te ratios were observed in both partially silver reacted Te NWs and phase segregated Ag2Te-Te-Ag2Te NWs and this was attributed to redeposition of leached silver on the amorphous NW tips which eventually resulted in complete phase segregation. Successful integration of different chemical components in single NWs is expected to open up new application possibilities as physical and chemical properties of the heterostructure can be exploited.Growth of isolated axial heterojunction nanowires by a solution phase growth process is reported. The dumb-bell shaped nanowires contain two silver telluride sections at the extremes joined by a tellurium section. Reaction of silver nitrate with tellurium NWs in aqueous solution at a molar ratio of 1 : 1 leads to the formation of amorphous partially silver reacted Te NWs. Low temperature (75 °C) solution phase annealing of these silver deficient NWs results in phase segregation producing crystalline Ag2Te and Te phases with clear phase boundaries along the wire axis. Structural characterization of these dumb-bell shaped NWs was performed with different microscopic and spectroscopic

  4. Ultrasound aided photochemical synthesis of Ag loaded TiO2 nanotube arrays to enhance photocatalytic activity.

    PubMed

    Sun, Lan; Li, Jing; Wang, Chenglin; Li, Sifang; Lai, Yuekun; Chen, Hongbo; Lin, Changjian

    2009-11-15

    This work presents a novel approach for preparing TiO(2) nanotube array photocatalyst loaded with highly dispersed Ag nanoparticles through an ultrasound aided photochemical route. The Ag content loaded on the array was controlled by changing the concentration of AgNO(3) solution. The Ag-TiO(2) nanotube arrays were characterized by SEM, XRD, XPS and UV-vis absorption. The effects of Ag content on the photoelectrochemical (PEC) property and photocatalytic activity of TiO(2) nanotube array electrode were studied. The results showed that Ag loading significantly enhanced the photocurrent and photocatalytic degradation rate of TiO(2) nanotube array under UV-light irradiation. The photocurrent and photocatalytic degradation rate of Ag-TiO(2) nanotube array prepared in 0.006 M AgNO(3) solution were about 1.2 and 3.7 times as that of pure TiO(2) nanotube array, respectively.

  5. Contribution of Eu ions on the precipitation of silver nanoparticles in Ag-Eu co-doped borate glasses

    SciTech Connect

    Jiao, Qing; Qiu, Jianbei; Zhou, Dacheng; Xu, Xuhui

    2014-03-01

    Graphical abstract: - Highlights: • Silver nanoparticles are precipitated from the borate glasses during the melting process without any further heat treatment. • The reduction of Eu{sup 3+} ions to Eu{sup 2+} ions is presented in this material. • The intensity of Ag{sup +} luminescence. • The introduction of Eu ions accelerated the reaction between Eu{sup 2+} ions and silver ions inducing the silver clusters formation. - Abstract: Ag{sup +} doped sodium borate glasses with different Eu ions concentration were prepared by the melt-quenching method. The absorption at about 410 nm which was caused by the surface plasmon resonance (SPR) of Ag nanoparticles (NPs) is promoted with increasing of Eu ions concentration. Meanwhile, the luminescent spectra showed that the emission intensity of Ag{sup +} decreased while that of the Ag aggregates increased simultaneously. The results indicated that the Ag ions intend to form the high-polymeric state such as Ag aggregates and nanoparticles with increasing of europium ions. Owing to the self-reduction of Eu{sup 3+} to Eu{sup 2+} in our glass system, it revealed that Ag{sup +} has been reduced by the neighboring Eu{sup 2+} which leads to the formation of Ag aggregates and the precipitation of Ag NPs in the matrix. In addition, energy transfer (ET) process from Ag{sup +}/Ag aggregates to the Eu{sup 3+} was investigated for the enhancement of Eu{sup 3+} luminescence.

  6. The Intermetallic Compound Formation for the Wire Bond Between an Al Pad and Ag-xPd Alloy Wire

    NASA Astrophysics Data System (ADS)

    Huang, Wei-Hsiang; Lin, Kwang-Lung; Lin, Yu-Wei; Cheng, Yun-Kai

    2016-12-01

    Silver-palladium alloy wire has been shown as an economical and reliable substitute for gold wire in various applications in the electronic packaging industry. The success of wire bonding relies on the formation of an interfacial intermetallic compound (IMC). This study is aimed to investigate the formation behavior of IMCs between an Al pad and Ag-Pd alloy wire with various Pd concentrations of 1.0-6.0% for the as-bonded commercial Ag/Al joint. The interfacial IMCs were investigated with scanning electron microscopy and energy-dispersive x-ray spectroscopy. The IMCs formed are separate (Ag, Pd)2Al and (Ag, Pd)3Al2 for a Ag6Pd wire bond, while (Ag, Pd)2Al and (Ag, Pd)3Al2 are mixed for the other Ag(1-4.5)Pd alloy wire bonds. The thickness of the total IMC layer varies from 0.65 μm for Ag1Pd to 0.91 μm for Ag6Pd, yet a minimum of 0.44 μm exists for Ag3.5Pd. The compound formation behavior was found to correspond with the Ag-Al phase diagram. After pressure cooker tests, a less stable IMC (Ag, Pd)3Al formed at the AgxPd/Al interface.

  7. Ag/AgCl reference electrode in thionyl chloride electrolytes

    NASA Astrophysics Data System (ADS)

    Delnick, F. M.; Cieslak, W. R.

    1985-07-01

    Thionyl chloride is the active cathode and electrolyte solvent in Li/SOCl2 primary battery systems. To evaluate charge-transfer reactions in this solvent system, a reference electrode is required. This report describes the fabrication and characterization of Ag/AgCl microreference electrodes that can be used in SOCl2 battery electrolytes.

  8. Ag-Air Service

    NASA Technical Reports Server (NTRS)

    1981-01-01

    Econ, Inc.'s agricultural aerial application, "ag-air," involves more than 10,000 aircraft spreading insecticides, herbicides, fertilizer, seed and other materials over millions of acres of farmland. Difficult for an operator to estimate costs accurately and decide what to charge or which airplane can handle which assignment most efficiently. Computerized service was designed to improve business efficiency in choice of aircraft and determination of charge rates based on realistic operating cost data. Each subscriber fills out a detailed form which pertains to his needs and then receives a custom-tailored computer printout best suited to his particular business mix.

  9. Construction of Ag/AgCl nanostructures from Ag nanoparticles as high-performance visible-light photocatalysts

    NASA Astrophysics Data System (ADS)

    Yang, Fan; Liu, Dongzhi; Wang, Tianyang; Li, Wei; Hu, Wenping; Zhou, Xueqin

    2016-11-01

    A combined strategy of in situ oxidation and assembly is developed to prepare Ag/AgCl nanospheres and nanocubes from Ag nanoparticles under room temperature. It is a new facile way to fabricate Ag/AgCl with small sizes and defined morphologies. Ag/AgCl nanospheres with an average size of 80 nm were achieved without any surfactants, while Ag/AgCl nanocubes with a mean edge length of 150 nm were obtained by introduction of N-dodecyl- N, N-dimethyl-2-ammonio-acetate. The possible formation mechanism involves the self-assembly of AgCl nanoparticles, Ostwald ripening and photoreduction of Ag+ into Ag0 by the room light. The as-prepared Ag/AgCl nanospheres and nanocubes exhibit excellent photocatalytic activity and stability toward degradation of organic pollutants under visible-light irradiation. It is demonstrated that Ag/AgCl nanocubes display enhanced photocatalytic activity in comparison with Ag/AgCl nanospheres due to the more efficient charge transfer. This work may pave an avenue to construct various functional materials via the assembly strategy using nanoparticles as versatile building blocks.

  10. Long-term transformation and fate of manufactured ag nanoparticles in a simulated large scale freshwater emergent wetland.

    PubMed

    Lowry, Gregory V; Espinasse, Benjamin P; Badireddy, Appala Raju; Richardson, Curtis J; Reinsch, Brian C; Bryant, Lee D; Bone, Audrey J; Deonarine, Amrika; Chae, Soryong; Therezien, Mathieu; Colman, Benjamin P; Hsu-Kim, Heileen; Bernhardt, Emily S; Matson, Cole W; Wiesner, Mark R

    2012-07-03

    Transformations and long-term fate of engineered nanomaterials must be measured in realistic complex natural systems to accurately assess the risks that they may pose. Here, we determine the long-term behavior of poly(vinylpyrrolidone)-coated silver nanoparticles (AgNPs) in freshwater mesocosms simulating an emergent wetland environment. AgNPs were either applied to the water column or to the terrestrial soils. The distribution of silver among water, solids, and biota, and Ag speciation in soils and sediment was determined 18 months after dosing. Most (70 wt %) of the added Ag resided in the soils and sediments, and largely remained in the compartment in which they were dosed. However, some movement between soil and sediment was observed. Movement of AgNPs from terrestrial soils to sediments was more facile than from sediments to soils, suggesting that erosion and runoff is a potential pathway for AgNPs to enter waterways. The AgNPs in terrestrial soils were transformed to Ag(2)S (~52%), whereas AgNPs in the subaquatic sediment were present as Ag(2)S (55%) and Ag-sulfhydryl compounds (27%). Despite significant sulfidation of the AgNPs, a fraction of the added Ag resided in the terrestrial plant biomass (~3 wt % for the terrestrially dosed mesocosm), and relatively high body burdens of Ag (0.5-3.3 μg Ag/g wet weight) were found in mosquito fish and chironomids in both mesocosms. Thus, Ag from the NPs remained bioavailable even after partial sulfidation and when water column total Ag concentrations are low (<0.002 mg/L).

  11. Defects responsible for abnormal n-type conductivity in Ag-excess doped PbTe thermoelectrics

    SciTech Connect

    Ryu, Byungki Lee, Jae Ki; Lee, Ji Eun; Joo, Sung-Jae; Kim, Bong-Seo; Min, Bok-Ki; Lee, Hee-Woong; Park, Su-Dong; Oh, Min-Wook

    2015-07-07

    Density functional calculations have been performed to investigate the role of Ag defects in PbTe thermoelectric materials. Ag-defects can be either donor, acceptor, or isovalent neutral defect. When Ag is heavily doped in PbTe, the neutral (Ag-Ag) dimer defect at Pb-site is formed and the environment changes to the Pb-rich/Te-poor condition. Under Pb-rich condition, the ionized Ag-interstitial defect (Ag{sub I}{sup +}) becomes the major donor. The formation energy of Ag{sub I}{sup +} is smaller than other native and Ag-related defects. Also it is found that Ag{sub I}{sup +} is an effective dopant. There is no additional impurity state near the band gap and the conduction band minimum. The charge state of Ag{sub I}{sup +} defect is maintained even when the Fermi level is located above the conduction band minimum. The diffusion constant of Ag{sub I}{sup +} is calculated based on the temperature dependent Fermi level, formation energy, and migration energy. When T > 550 K, the diffusion length of Ag within a few minutes is comparable to the grain size of the polycrystalline PbTe, implying that Ag is dissolved into PbTe and this donor defect is distributed over the whole lattice in Ag-excess doped polycrystalline PbTe. The predicted solubility of Ag{sub I}{sup +} well explains the increased electron carrier concentration and electrical conductivity reported in Ag-excess doped polycrystalline PbTe at T = 450–750 K [Pei et al., Adv. Energy Mater. 1, 291 (2011)]. In addition, we suggest that this abnormal doping behavior is also found for Au-doped PbTe.

  12. Communication: Structure, formation, and equilibration of ensembles of Ag-S complexes on an Ag surface

    SciTech Connect

    Russell, Selena M.; Kim, Yousoo; Liu, Da-Jiang; Evans, J. W.; Thiel, P. A.

    2013-02-15

    We have utilized conditions of very low temperature (4.7 K) and very low sulfur coverage to isolate and identify Ag-S complexes that exist on the Ag(111) surface. The experimental conditions are such that the complexes form at temperatures above the temperature of observation. These complexes can be regarded as polymeric chains of varying length, with an Ag4S pyramid at the core of each monomeric unit. Steps may catalyze the formation of the chains and this mechanism may be reflected in the chain length distribution.

  13. The impact of Ag nanoparticles on the parameters of DSS- cells sensitized by Z907

    NASA Astrophysics Data System (ADS)

    Ibrayev, N. Kh; Aimukhanov, A. K.; Zeinidenov, A. K.

    2016-02-01

    Research of influence of Ag nanoparticles are in-process undertaken on absorption and on parameters CVC DSS-cells sensitized Z907. It is set that with the height of concentration Ag nanoparticles in tape to the concentration of 0.3% wt%. the absorbance of Z907 in a short-wave stripe grew to the value 1,6. It is set that under reaching the concentration of Ag nanoparticles in the cell of value the 0.3% wt%. efficiency of cell increased to 2.2%.

  14. Localized surface plasmon resonance and surface enhanced Raman scattering responses of Au@Ag core-shell nanorods with different thickness of Ag shell.

    PubMed

    Ma, Yanan; Zhou, Jun; Zou, Weibo; Jia, Zhenhong; Petti, Lucia; Mormile, Pasquale

    2014-06-01

    The properties of the localized surface plasmon resonance (LSPR) and the surface enhanced Raman scattering (SERS) of the core-shell bimetallic nanostructures, that is the monodisperse Au@Ag core-shell nanorods with different thickness of Ag shell, are theoretically and experimental researched. The UV-vis-NIR absorption spectra of the Au@Ag core-shell nanorods are measured and displayed their blue-shifts of the longitudinal plasmon resonance peaks with increasing of Ag concentrations in the colloidal solution. And the absorption spectra of the Au@Ag core-shell nanorods are simulated by the Finite Element Method (FEM), which are in agreement with the experimental measurements and reveal their LSPR mechanism as the varying structures. In addition, Rhodamine 6G, as a Raman reporter molecule, is used to investigate SERS of gold nanorods and Au@Ag core-shell nanorods. It is found that Au@Ag core-shell nanorods have better SERS responses, comparing with those of Au nanorods, and their SERS intensities are increased with the increases of the Ag shell thickness, which demonstrate that the chemisorptive bond effect and the morphology of the nanoparticle play key roles to the SERS signals. It is significant to design the biosensor based on the properties of Au@Ag core-shell nanorods.

  15. AGS Experiments: 1989, 1990, 1991

    SciTech Connect

    Depken, J.C.

    1992-02-01

    This report contains: Experimental areas layout; table of beam parameters and fluxes; experiment schedule as run''; proposed 1992 schedule; a listing of experiments by number; two-page summaries of each experiment begin here, also ordered by number; publications of AGS Experiments begin here; and list of AGS Experimenters begins here.

  16. AGS Experiments: 1989, 1990, 1991

    SciTech Connect

    Depken, J.C.

    1992-02-01

    This report contains: Experimental areas layout; table of beam parameters and fluxes; experiment schedule ``as run``; proposed 1992 schedule; a listing of experiments by number; two-page summaries of each experiment begin here, also ordered by number; publications of AGS Experiments begin here; and list of AGS Experimenters begins here.

  17. What Is Ag-Ed?

    ERIC Educational Resources Information Center

    Lindley, Judy

    Ag-Ed is an agricultural education project aimed at upper primary students, held in conjunction with the Toowoomba Show (similar to a county fair) in Queensland, Australia. The program achieves its purpose of helping children understand the impact and relevance that agriculture has on their everyday lives through two components, an Ag-Ed day and a…

  18. Fabrication and Formation Mechanism of Ag Nanoplate-Decorated Nanofiber Mats and Their Application in SERS.

    PubMed

    Jia, Peng; Chang, Jiao; Wang, Jianqiang; Zhang, Pan; Cao, Bing; Geng, Yuting; Wang, Xiuxing; Pan, Kai

    2016-01-01

    We report a new simple method to fabricate a highly active SERS substrate consisting of poly-m-phenylenediamine/polyacrylonitrile (PmPD/PAN) decorated with Ag nanoplates. The formation mechanism of Ag nanoplates is investigated. The synthetic process of the Ag nanoplate-decorated PmPD/PAN (Ag nanoplates@PmPD/PAN) nanofiber mats consists of the assembly of Ag nanoparticles on the surface of PmPD/PAN nanofibers as crystal nuclei followed by in situ growth of Ag nanoparticles exclusively into nanoplates. Both the reducibility of the polymer and the concentration of AgNO3 are found to play important roles in the formation and the density of Ag nanoplates. The optimized Ag nanoplates@PmPD/PAN nanofiber mats exhibit excellent activity and reproducibility in surface-enhanced Raman scattering (SERS) detection of 4-mercaptobenzoic acid (4-MBA) with a detection limit of 10(-10)  m, making the Ag nanoplates@PmPD/PAN nanofiber mats a promising substrate for SERS detection of chemical molecules. In addition, this work also provides a design and fabrication process for a 3D SERS substrate made of a reducible polymer with noble metals.

  19. The disinfection performance and mechanisms of Ag/lysozyme nanoparticles supported with montmorillonite clay.

    PubMed

    Jiang, Jing; Zhang, Chang; Zeng, Guang-Ming; Gong, Ji-Lai; Chang, Ying-Na; Song, Biao; Deng, Can-Hui; Liu, Hong-Yu

    2016-11-05

    The fabrication of montmorillonite (Mt) decorated with lysozyme-modified silver nanoparticles (Ag/lyz-Mt) was reported. The lysozyme (lyz) was served as both reducing and capping reagent. Coupling the bactericidal activity of the lyz with AgNPs, along with the high porous structure and large specific surface area of the Mt, prevented aggregation of AgNPs and promoted nanomaterial-bacteria interactions, resulting in a greatly enhanced bactericidal capability against both Gram positive and Gram negative bacteria. This paper systematically elucidated the bactericidal mechanisms of Ag/lyz-Mt. Direct contact between the Ag/lyz-Mt surface and the bacterial cell was essential to the disinfection. Physical disruption of bacterial membrane was considered to be one of the bactericidal mechanisms of Ag/lyz-Mt. Results revealed that Ag(+) was involved in the bactericidal activity of Ag/lyz-Mt via tests conducted using Ag(+) scavengers. A positive ROS (reactive oxygen species) scavenging test indirectly confirmed the involvement of ROS (O2(-), H2O2, and OH) in the bactericidal mechanism. Furthermore, the concentrations of individual ROS were quantified. Results showed that Ag/lyz-Mt nanomaterial could be a promising bactericide for water disinfection.

  20. Origin of metallicity in atomic Ag wires on Si(557)

    NASA Astrophysics Data System (ADS)

    Krieg, U.; Lichtenstein, T.; Brand, C.; Tegenkamp, C.; Pfnür, H.

    2015-04-01

    We investigated the metallicity of Ag-\\sqrt{3} ordered atomic wires close to one monolayer (ML) coverage, which are formed on Si(557) via self assembly. For this purpose we combined high resolution electron energy loss spectroscopy with tunneling microscopy. By extending the excess Ag coverage up to 0.6 ML on samples annealed at high temperatures where partial desorption occurs, we demonstrate that one-dimensional metallicity in the Ag-\\sqrt{3}× \\sqrt{3} R30° ordered atomic wires on the (111) mini-terraces originates only from Ag atoms in excess of (local) monolayer coverage, which are adsorbed and localized at the highly stepped parts of the Si(557) surface. Thus these Ag atoms act as extrinsic dopants on the atomic scale, causing coverage dependent subband filling and increasing localization as a function of doping concentration. The second layer lattice gas as well as Ag islands on the (111) terraces turn out not to be relevant as dopants. We simulated the peculiar saturation behavior within a modified lattice gas model and give evidence that the preparation dependent saturation of doping is due to changes of average terrace size and step morphology induced by high temperature treatment.

  1. Probing ultrafast energy transfer between excitons and plasmons in the ultrastrong coupling regime

    NASA Astrophysics Data System (ADS)

    Balci, Sinan; Kocabas, Coskun; Küçüköz, Betül; Karatay, Ahmet; Akhüseyin, Elif; Gul Yaglioglu, H.; Elmali, Ayhan

    2014-08-01

    We investigate ultrafast energy transfer between excitons and plasmons in ensembles of core-shell type nanoparticles consisting of metal core covered with a concentric thin J-aggregate (JA) shell. The high electric field localization by the Ag nanoprisms and the high oscillator strength of the JAs allow us to probe this interaction in the ultrastrong plasmon-exciton coupling regime. Linear and nonlinear optical properties of the coupled system have been measured using transient absorption spectroscopy revealing that the hybrid system shows half-plasmonic and half-excitonic properties. The tunability of the nanoprism plasmon resonance provides a flexible platform to study the dynamics of the hybrid state in a broad range of wavelengths.

  2. Plasmonic Ag2MoO4/AgBr/Ag composite: Excellent photocatalytic performance and possible photocatalytic mechanism

    NASA Astrophysics Data System (ADS)

    Wang, Zhongliao; Zhang, Jinfeng; Lv, Jiali; Dai, Kai; Liang, Changhao

    2017-02-01

    Plasmonic Ag2MoO4/AgBr/Ag composite is fabricated by in-situ ion exchange and reduction methods at room temperature. The samples are characterized by X-ray diffraction (XRD), UV-vis diffuse reflectance (DRS), energy-dispersive X-ray spectroscopy (EDS), scanning electron microscope (SEM) and photoluminescence (PL) measurements. The results show that butterfly-like Ag2MoO4 nanosheets served as the precursor, and Ag2MoO4/AgBr/Ag is formed in phase transformation with MoO42- displaced by Br-. The ternary Ag2MoO4/AgBr/Ag composite photocatalysts show greatly enhanced photocatalytic activity in photodegrading methylene blue (MB) under visible light irradiation compared with AgBr and Ag2MoO4. The pseudo-first-order rate constant kapp of Ag2MoO4/AgBr/Ag is 0.602 min-1, which is 11.6 and 18.3 times as high as that of AgBr and Ag2MoO4, respectively. Meanwhile, the efficiency of degradation still kept 90% after ten times cyclic experiments. Eventually, possible photocatalytic mechanism was proposed.

  3. Effect of toxicity of Ag nanoparticles on SERS spectral variance of bacteria

    NASA Astrophysics Data System (ADS)

    Cui, Li; Chen, Shaode; Zhang, Kaisong

    2015-02-01

    Ag nanoparticles (NPs) have been extensively utilized in surface-enhanced Raman scattering (SERS) spectroscopy for bacterial identification. However, Ag NPs are toxic to bacteria. Whether such toxicity can affect SERS features of bacteria and interfere with bacterial identification is still unknown and needed to explore. Here, by carrying out a comparative study on non-toxic Au NPs with that on toxic Ag NPs, we investigated the influence of nanoparticle concentration and incubation time on bacterial SERS spectral variance, both of which were demonstrated to be closely related to the toxicity of Ag NPs. Sensitive spectral alterations were observed on Ag NPs with increase of NPs concentration or incubation time, accompanied with an obvious decrease in number of viable bacteria. In contrast, SERS spectra and viable bacterial number on Au NPs were rather constant under the same conditions. A further analysis on spectral changes demonstrated that it was cell response (i.e. metabolic activity or death) to the toxicity of Ag NPs causing spectral variance. However, biochemical responses to the toxicity of Ag were very different in different bacteria, indicating the complex toxic mechanism of Ag NPs. Ag NPs are toxic to a great variety of organisms, including bacteria, fungi, algae, protozoa etc., therefore, this work will be helpful in guiding the future application of SERS technique in various complex biological systems.

  4. Radiochemical synthesis of 105gAg-labelled silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Ichedef, C.; Simonelli, F.; Holzwarth, U.; Bagaria, J. Piella; Puntes, V. F.; Cotogno, G.; Gilliland, D.; Gibson, N.

    2013-11-01

    A method for synthesis of radiolabelled silver nanoparticles is reported. The method is based on proton activation of silver metal powder, enriched in 107Ag, with a 30.7 MeV proton beam. At this proton energy 105gAg is efficiently created, mainly via the 107Ag(p,3n)105Cd → 105gAg reaction. 105gAg has a half-life of 41.29 days and emits easily detectable gamma radiation on decay to 105Pd. This makes it very useful as a tracing radionuclide for experiments over several weeks or months. Following activation and a period to allow short-lived radionuclides to decay, the powder was dissolved in concentrated nitric acid in order to form silver nitrate (AgNO3), which was used to synthesise radiolabelled silver nanoparticles via the process of sodium borohydride reduction. For comparison, non-radioactive silver nanoparticles were synthesised using commercially supplied AgNO3 in order to check if the use of irradiated Ag powder as a starting material would alter in any way the final nanoparticle characteristics. Both nanoparticle types were characterised using dynamic light scattering, zeta-potential and X-ray diffraction measurements, while additionally the non-radioactive samples were analysed by transmission electron microscopy and UV-Vis spectrometry. A hydrodynamic diameter of about 16 nm was determined for both radiolabelled and non-radioactive nanoparticles, while the electron microscopy on the non-radioactive samples indicated that the physical size of the metal NPs was (7.3 ± 1.4) nm.

  5. Approaches for Controlled Ag(+) Ion Release: Influence of Surface Topography, Roughness, and Bactericide Content.

    PubMed

    Sukhorukova, I V; Sheveyko, A N; Shvindina, N V; Denisenko, E A; Ignatov, S G; Shtansky, D V

    2017-02-01

    Silver is the most famous bactericidal element known from ancient times. Its antibacterial and antifungal effects are typically associated with the Ag ionization and concentration of Ag(+) ions in a bacterial culture. Herein we thoroughly studied the influence of surface topography and roughness on the rate of Ag(+) ion release. We considered two types of biocompatible and bioactive TiCaPCON-Ag films with 1 and 2 at. % of Ag and nine types of Ti surfaces with an average roughness varying in the range from 5.4 × 10(-2) to 12.6 μm and different topographic features obtained through polishing, sandblasting, laser treatment, and pulsed electrospark deposition. It is demonstrated that the Ag(+) ion release rates do not depend on the Ag content in the films as the main parameter, and it is other factors, such as the state of Ag agglomeration, surface topography and roughness, as well as kinetics of surface oxidation, that play a critical role. The obtained results clearly show a synergistic effect of the Ag content in the film and surface topography and roughness on Ag(+) ion release. By changing the surface topographical features at a constant content of bactericidal element, we showed that the Ag(+) ion release can be either accelerated by 2.5 times or almost completely suppressed. Despite low Ag(+) ion concentration in physiological solution (<40 ppb), samples with specially fabricated surface reliefs (flakes or holes) showed a pronounced antibacterial effect already after 3 h of immersion in E. coli bacterial culture. Thus, our results open up new possibilities for the production of cost-effective, scalable, and biologically safe implants with pronounced antibacterial characteristics for future applications in the orthopedic field.

  6. Cellular Energy Allocation to Assess the Impact of Nanomaterials on Soil Invertebrates (Enchytraeids): The Effect of Cu and Ag.

    PubMed

    Gomes, Susana I L; Scott-Fordsmand, Janeck J; Amorim, Mónica J B

    2015-06-16

    The effects of several copper (Cu) and silver (Ag) nanomaterials were assessed using the cellular energy allocation (CEA), a methodology used to evaluate the energetic status and which relates with organisms' overall condition and response to toxic stress. Enchytraeus crypticus (Oligochatea), was exposed to the reproduction effect concentrations EC20/50 of several Cu and Ag materials (CuNO3, Cu-Field, Cu-Nwires and Cu-NPs; AgNO3, Ag NM300K, Ag-NPs Non-coated and Ag-NPs PVP-coated) for 7 days (0-3-7d). The parameters measured were the total energy reserves available (protein, carbohydrate and lipid budgets) and the energy consumption (Ec) integrated to obtain the CEA. Results showed that these parameters allowed a clear discrimination between Cu and Ag, but less clearly within each of the various materials. For Cu there was an increase in Ec and protein budget, while for Ag a decrease was observed. The results corroborate known mechanisms, e.g., with Cu causing an increase in metabolic rate whereas Ag induces mitochondrial damage. The various Cu forms seem to activate different mechanisms with size and shape (e.g., Cu-NPs versus Cu-Nwires), causing clearly different effects. For Ag, results are in line with a slower oxidation rate of Ag-NMs in comparison with Ag-salt and hence delayed effects.

  7. In vitro cytotoxicity evaluation of porous TiO₂-Ag antibacterial coatings for human fetal osteoblasts.

    PubMed

    Necula, B S; van Leeuwen, J P T M; Fratila-Apachitei, L E; Zaat, S A J; Apachitei, I; Duszczyk, J

    2012-11-01

    Implant-associated infections (IAIs) may be prevented by providing antibacterial properties to the implant surface prior to implantation. Using a plasma electrolytic oxidation (PEO) technique, we produced porous TiO₂ coatings bearing various concentrations of Ag nanoparticles (Ag NPs) (designated as 0 Ag, 0.3 Ag and 3.0 Ag) on a Ti-6Al-7Nb biomedical alloy. This study investigates the cytotoxicity of these coatings using a human osteoblastic cell line (SV-HFO) and evaluates their bactericidal activity against methicillin-resistant Staphylococcus aureus (MRSA). The release of Ag and the total amount of Ag in the coatings were determined using a graphite furnace atomic absorption spectrometry technique (GF-AAS) and flame-AAS, respectively. Cytotoxicity was evaluated using the AlamarBlue assay coupled with the scanning electron microscopy (SEM) observation of seeded cells and by fluorescence microscopy examination of the actin cytoskeleton and nuclei after 48 h of incubation. Antibacterial activity was assessed quantitatively using a direct contact assay. AlamarBlue viability assay, SEM and fluorescence microscopy observation of the SV-HFO cells showed no toxicity for 0 Ag and 0.3 Ag specimens, after 2, 5 and 7 days of culture, while 3.0 Ag surfaces appeared to be extremely cytotoxic. All Ag-bearing surfaces had good antibacterial activity, whereas Ag-free coatings showed an increase in bacterial numbers. Our results show that the 0.3 Ag coatings offer conditions for optimum cell growth next to antibacterial properties, which makes them extremely useful for the development of new antibacterial dental and orthopedic implants.

  8. AgH, Ag/sub 2/, and AgO revisited: Basis set extensions

    SciTech Connect

    Martin, R.L.

    1987-05-01

    An extended basis set has been developed for Ag which significantly improves the agreement between theoretical and experimental spectroscopic parameters for AgH, AgO, and Ag/sub 2/. The major improvement comes about as a result of the improved treatment of electron correlation in the Ag d shell upon the introduction of f functions. Their inclusion produces very slight differences at the SCF level, but significant reductions in r/sub e/ and increases in ..omega../sub e/ and D/sub e/ in the Mo-dash-barller--Plesset perturbation theory expansion. At the MP4(SDTQ) level, typical results are 0.02 A too long for r/sub e/, 4% too low for ..omega../sub e/, and 10 kcal too small for D/sub e/. From a pragmatic standpoint, MP2 give results very similar to this at a much reduced level of effort.

  9. A convenient phase transfer route for Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Zhao, Shi-Yong; Chen, Shen-Hao; Li, De-Gang; Yang, Xue-Geng; Ma, Hou-Yi

    2004-06-01

    Generally, phase transfer of metal nanoparticles between aqueous phase and organic phase need two reagents at last. One is stabilizer of nanoparticles, the other is phase-transfer agent (Chem. Lett. 21 (1992) 1527; J. Colloid Interface Sci. 161 (1993) 471; J. Phys. Chem B 101 (1997) 9876; Chem. Commun. (1997) 537; Langmuir 14 (1998) 602; J. Phys. Chem B 103 (1999) 7238; Chem. Mater. 13 (2001) 4692; Langmuir 17 (2001) 733; Langmuir 16 (2000) 9775; Langmuir 18 (2002) 3364; J. Am. Chem. Soc. 123 (2001) 11148). In this paper, Ag nanoparticle prepared by tannic acid reduction of AgNO 3 in aqueous medium were transferred to chloroform solution via a remarkably simple one-step route under the effect of phase-transfer inducer dimethyldioctadecylammonium chloride (DDAC), where no special stabilizer was required. Monolayer of Ag nanoparticles is obtained on carbon film by self-assembly using chloroform organosol. The effect of the inducer DDAC concentration is checked, and it was found that 5×10 -3 mol dm -3 of DDAC was the optimum concentration for phase transfer of Ag nanoparticles. The organosol, Ag nanoparticle self-assembled monolayer and phase transfer were characterized by UV-vis spectra, TEM, ED and TF-IR.

  10. THE AGS ELECTROSTATIC SEPTUM.

    SciTech Connect

    HOCK,J.RUSSO,T.GLEN,J.BROWN,K.

    2003-05-12

    The previous slow beam extraction electro static septum in the AGS was designed in 1981. Research documented at the Fermi Laboratory was used as the base line for this design. The septum consisted of a ground plane of .002 inch diameter wire tungsten-rhenium alloy (75%W 25%Re) with a hollow welded titanium cathode assembly. The vacuum chamber is stationary and the septum is moved with a pair of high vacuum linear feed throughs. After years of beam time, the frequency of failures increased. The vacuum system design was poor by today's standards and resulted in long pump down times after repairs. The failures ranged from broken septum wires to a twisted cathode. In addition to the failures, the mechanical drive system had too much backlash, making the operating position difficult to repeat. The new septum needed to address all of these issues in order to become a more reliable septum.

  11. A new photothermal therapeutic agent: core-free nanostructured Au x Ag1-x dendrites.

    PubMed

    Hu, Kuo-Wei; Huang, Chih-Chia; Hwu, Jih-Ru; Su, Wu-Chou; Shieh, Dar-Bin; Yeh, Chen-Sheng

    2008-01-01

    A new class of Au(x)Ag(1-x) nanostructures with dendrite morphology and a hollow interior were synthesized by using a replacement reaction between Ag dendrites and an aqueous solution of HAuCl(4). The Ag nanostructured dendrites were generated by the reaction of AgNO(3) with ascorbic acid in a methanol/water system. The dendrites resemble a coral shape and are built up of many stems with an asymmetric arrangement. Each stem is approximately 400 nm in length and 65 nm in diameter. The bimetallic composition of Au(x)Ag(1-x) can be tuned by the addition of different amounts of HAuCl(4) to the Ag dendritic solution. The hollowing process resulted in tubular structures with a wall thickness of 10.5 nm in Au(0.3)Ag(0.7) dendrites. The UV/Vis spectra indicate that the strongest NIR absorption among the resulting hollow Au(x)Ag(1-x) dendrites was in Au(0.3)Ag(0.7). The MTT assay was conducted to evaluate the cytotoxicity of Ag dendrites, hollow Au(0.06)Ag(0.94) and Au(0.3)Ag(0.7) dendrites, and Au nanorods. It was found that hollow Au(0.06)Ag(0.94) and Au(0.3)Ag(0.7) dendrites exhibited good biocompatibility, while both Ag dendrites and Au nanorods showed dose-dependent toxicity. Because of absorption in the NIR region, hollow Au(0.3)Ag(0.7) dendrites were used as photothermal absorbers for destroying A549 lung cancer cells. Their photothermal performance was compared to that of Au nanorod photothermal therapeutic agents. As a result, the particle concentration and laser power required for efficient cancer cell damage were significantly reduced for hollow Au(0.3)Ag(0.7) dendrites relative to those used for Au nanorods. The hollow Au(0.3)Ag(0.7) nanostructured dendrites show potential in photothermolysis for killing cancer cells.

  12. The AGS-Booster lattice

    SciTech Connect

    Lee, Y.Y.; Barton, D.S.; Claus, J.; Cottingham, J.G.; Courant, E.D.; Danby, G.T.; Dell, G.F.; Forsyth, E.B.; Gupta, R.C.; Kats, J.

    1987-01-01

    The AGS Booster has three objectives. They are to increase the space charge limit of the AGS, to increase the intensity of the polarized proton beam by accumulating many linac pulses (since the intensity is limited by the polarized ion source), and to reaccelerate heavy ions from the BNL Tandem Van de Graaff before injection into the AGS. The machine is capable of accelerating protons at 7.5 Hertz from 200 MeV to 1.5 GeV or to lower final energies at faster repetition rates. The machine will also be able to accelerate heavy ions from as low as 1 MeV/nucleon to a magnetic rigidity as high as 17.6 Tesla-meters with a one second repetition rate. As an accumulator for polarized protons, the Booster should be able to store the protons at 200 MeV for several seconds. We expect that the Booster will increase the AGS proton intensity by a factor of four, polarized proton intensity by a factor of twenty to thirty, and will also enable the AGS to accelerate all species of heavy ions (at present the AGS heavy ion program is limited to the elements lighter than sulfur because it can only accelerate fully stripped ions). The construction project started in FY 1985 and is expected to be completed in 1989. The purpose of this paper is to provide a future reference for the AGS Booster lattice.

  13. Low-temperature ferromagnetic properties in Co-doped Ag{sub 2}Se nanoparticles

    SciTech Connect

    Yang, Fengxia E-mail: xia9020@hust.edu.cn; Yu, Gen; Han, Chong; Liu, Tingting; Zhang, Duanming; Xia, Zhengcai E-mail: xia9020@hust.edu.cn

    2014-01-06

    β-Ag{sub 2}Se is a topologically nontrivial insulator. The magnetic properties of Co-doped Ag{sub 2}Se nanoparticles with Co concentrations up to 40% were investigated. The cusp of zero-field-cooling magnetization curves and the low-temperature hysteresis loops were observed. With increasing concentration of Co{sup 2+} ions mainly substituting Ag{sub I} sites in the Ag{sub 2}Se structure, the resistivity, Curie temperature T{sub c}, and magnetization increased. At 10 T, a sharp drop of resistance near T{sub c} was detected due to Co dopants. The ferromagnetic behavior in Co-doped Ag{sub 2}Se might result from the intra-layer ferromagnetic coupling and surface spin. This magnetic semiconductor is a promising candidate in electronics and spintronics.

  14. Distortion induced band gap and phase transformation in Tix Ag(1 - x) O2 system

    NASA Astrophysics Data System (ADS)

    Mathpal, Mohan Chandra; Tripathi, Anand Kumar; Kumar, Promod; Agrahari, Vivek; Singh, Manish Kumar; Agarwal, Arvind

    2014-10-01

    The polymorphic crystallization and optical properties of Ag-doped TiO2 nanoparticles have been investigated. Sol-gel method has been used to prepare anatase, rutile, and the anatase-rutile mixed phase of TiO2 nanoparticles by Ag doping on Ti(4+) sites. The doped TiO2 nanoparticles exhibit different phase of TiO2 for the different concentration of dopants. The Ag-doping affects the luminescence and morphological properties of TiO2 nanoparticles. The anatase to rutile phase transformation temperature (ART) has reduced significantly. The Ag doping in TiO2 lattice gives a large red shift for a particular concentration of Ag dopants.

  15. Phase diagrams of the Tb-Ag-In and Dy-Ag-In systems at 870 K

    SciTech Connect

    Demchyna, M.; Belan, B.; Manyako, M.; Pietraszko, A.; Kalychak, Ya.

    2012-08-15

    The phase equilibria of Tb-Ag-In and Dy-Ag-In ternary systems have been studied at 870 K in the whole concentration range by means of X-ray powder, single crystal X-ray diffraction and EDX analyses. Isothermal sections of Tb-Ag-In and Dy-Ag-In phase diagrams at this temperature have been constructed. Both systems are characterized by formation of three ternary compounds: REAg{sub 3}In{sub 3} (YbAg{sub 2}In{sub 4}-type, space group Im-3), REAg{sub 2}In (MnCu{sub 2}Al-type, space group Fm-3m) and RE{sub 2}AgIn{sub 3} (CaIn{sub 2}-type, space group P6{sub 3}/mmc) RE=Tb, Dy. Homogeneity ranges of the ternary phases with CaIn{sub 2} structure type lies from 35 to 60 at% of In for Tb-containing phase and from 39 to 50 at% of In for Dy-containing phase. The existence of solid solutions based on REAg (CsCl-type, space group Pm-3m) binary compounds up to 30 at% of In and REIn{sub 3} (AuCu{sub 3}-type, space group Pm-3 m) binary compounds up to 5 at% of Ag has been found. - Graphical Abstract: Phase relations in the ternary systems Tb-Ag-In and Dy-Ag-In have been established for the isothermal section at T=870 K based on X-ray powder and single crystal diffraction analyses. The existence of three ternary compounds in each system were observed. Highlights: Black-Right-Pointing-Pointer Isothermal section of Tb-Ag-In system at T=870 K was constructed. Black-Right-Pointing-Pointer Isothermal section of Dy-Ag-In system at T=870 K was constructed. Black-Right-Pointing-Pointer Three ternary compounds and two solid solutions in each system were detected.

  16. Ordered array of Ag semishells on different diameter monolayer polystyrene colloidal crystals: An ultrasensitive and reproducible SERS substrate

    PubMed Central

    Yi, Zao; Niu, Gao; Luo, Jiangshan; Kang, Xiaoli; Yao, Weitang; Zhang, Weibin; Yi, Yougen; Yi, Yong; Ye, Xin; Duan, Tao; Tang, Yongjian

    2016-01-01

    Ag semishells (AgSS) ordered arrays for surface-enhanced Raman scattering (SERS) spectroscopy have been prepared by depositing Ag film onto polystyrene colloidal particle (PSCP) monolayer templates array. The diversified activity for SERS activity with the ordered AgSS arrays mainly depends on the PSCP diameter and Ag film thickness. The high SERS sensitivity and reproducibility are proved by the detection of rhodamine 6G (R6G) and 4-aminothiophenol (4-ATP) molecules. The prominent enhancements of SERS are mainly from the “V”-shaped or “U”-shaped nanogaps on AgSS, which are experimentally and theoretically investigated. The higher SERS activity, stability and reproducibility make the ordered AgSS a promising choice for practical SERS low concentration detection applications. PMID:27586562

  17. Ordered array of Ag semishells on different diameter monolayer polystyrene colloidal crystals: An ultrasensitive and reproducible SERS substrate

    NASA Astrophysics Data System (ADS)

    Yi, Zao; Niu, Gao; Luo, Jiangshan; Kang, Xiaoli; Yao, Weitang; Zhang, Weibin; Yi, Yougen; Yi, Yong; Ye, Xin; Duan, Tao; Tang, Yongjian

    2016-09-01

    Ag semishells (AgSS) ordered arrays for surface-enhanced Raman scattering (SERS) spectroscopy have been prepared by depositing Ag film onto polystyrene colloidal particle (PSCP) monolayer templates array. The diversified activity for SERS activity with the ordered AgSS arrays mainly depends on the PSCP diameter and Ag film thickness. The high SERS sensitivity and reproducibility are proved by the detection of rhodamine 6G (R6G) and 4-aminothiophenol (4-ATP) molecules. The prominent enhancements of SERS are mainly from the “V”-shaped or “U”-shaped nanogaps on AgSS, which are experimentally and theoretically investigated. The higher SERS activity, stability and reproducibility make the ordered AgSS a promising choice for practical SERS low concentration detection applications.

  18. Controlled growth of thermally stable uniform-sized Ag nanoparticles on flat support and their electrochemical activity

    NASA Astrophysics Data System (ADS)

    Ansari, A. A.; Sartale, S. D.

    2015-05-01

    A method consisting of spin coating of Ag+ ions (AgNO3) solution followed by chemical reduction in aqueous hydrazine solution has been presented for controlled growth of thermally stable uniform-sized Ag nanoparticles on flat substrate. Scanning electron microscopy images and local surface plasmon resonance absorption studies imply that most of the Ag nanoparticles grow with unique preferable size. This preferable size can be controlled by changing AgNO3 solution characteristics (drop size and concentration), spin-coating parameters (rpm and ramp) and annealing temperatures. With increase in rpm or ramp, particle size decreases with enhanced particles density. The Ag nanoparticles are thermally stable up to 450 °C, and the preferable size is increased with annealing temperature. The grown particles are catalytic active for oxygen reduction reaction, and activity was found to be dependent on size and density of Ag nanoparticles.

  19. Photovoltaic concentrators

    NASA Astrophysics Data System (ADS)

    Boes, E. C.

    1980-01-01

    A status report on photovoltaic (PV) concentrators technology is presented. The major topics covered are as follows: (1) current PV concentrator arrays; designs, performances, and costs; (2) current PV concentrator array components; cells and cell assemblies, optical concentrators, support structures, tracking, and drive; (3) design of PV concentrator arrays; and (4) array manufacturing technology.

  20. Preparation and characterization of Ag-cluster in poly(methylmethacrylate)

    SciTech Connect

    Yanagihara, Naohisa; Ishii, Yoshitaka; Kawase, Takanori; Kaneko, Toshimare; Horie, Hisashi; Hara, Toru

    1997-09-01

    Solid sols of silver in poly(methylmethacrylate), Ag/PMMA, were prepared by bulk polymerization of methyl methacrylate (MMA) with benzoyl peroxide (BPO) as an initiator in the presence of silver(I) trifluoroacetate. Ag/PMMAs were characterized by visible spectroscopy. Effects of the concentration of initiator, the concentration of silver(I) complex and the heat-treatment time on the formation of silver cluster were studied in detail.

  1. Sodium cholate-templated blue light-emitting Ag subnanoclusters: in vivo toxicity and imaging in zebrafish embryos.

    PubMed

    Chandirasekar, Shanmugam; Chandrasekaran, Chandramouli; Muthukumarasamyvel, Thangavel; Sudhandiran, Ganapasam; Rajendiran, Nagappan

    2015-01-28

    We report a novel green chemical approach for the synthesis of blue light-emitting and water-soluble Ag subnanoclusters, using sodium cholate (NaC) as a template at a concentration higher than the critical micelle concentration (CMC) at room temperature. However, under photochemical irradiation, small anisotropic and spherically shaped Ag nanoparticles (3-11 nm) were obtained upon changing the concentration of NaC from below to above the CMC. The matrix-assisted laser desorption ionization time-of-flight and electrospray ionization mass spectra showed that the cluster sample was composed of Ag4 and Ag6. The optical properties of the clusters were studied by UV-visible and luminescence spectroscopy. The lifetime of the synthesized fluorescent Ag nanoclusters (AgNCs) was measured using a time-correlated single-photon counting technique. High-resolution transmission electron microscopy was used to assess the size of clusters and nanoparticles. A protocol for transferring nanoclusters to organic solvents is also described. Toxicity and bioimaging studies of NaC templated AgNCs were conducted using developmental stage zebrafish embryos. From the survival and hatching experiment, no significant toxic effect was observed at AgNC concentrations of up to 200 μL/mL, and the NC-stained embryos exhibited blue fluorescence with high intensity for a long period of time, which shows that AgNCs are more stable in living system.

  2. Thermodynamic Properties of Liquid Ag-Au-Sn Alloys

    NASA Astrophysics Data System (ADS)

    Hindler, M.; Knott, S.; Mikula, A.

    2010-10-01

    The thermodynamic properties of liquid Ag-Au-Sn alloys were studied with an electromotive force (EMF) method using the eutectic mixture of KCl/LiCl as a liquid electrolyte. Activities of Sn in the liquid alloys were measured at three cross-sections with constant molar ratios of Ag:Au = 2:1, 1:1, and 1:2 with tin in the concentration range between 20 at.% and 90 at.% from the liquidus of the samples up to 1030 K. The integral Gibbs energies at 973 K and the integral enthalpies were calculated by Gibbs-Duhem integration.

  3. Pb-free Sn-Ag-Cu ternary eutectic solder

    DOEpatents

    Anderson, I.E.; Yost, F.G.; Smith, J.F.; Miller, C.M.; Terpstra, R.L.

    1996-06-18

    A Pb-free solder includes a ternary eutectic composition consisting essentially of about 93.6 weight % Sn-about 4.7 weight % Ag-about 1.7 weight % Cu having a eutectic melting temperature of about 217 C and variants of the ternary composition wherein the relative concentrations of Sn, Ag, and Cu deviate from the ternary eutectic composition to provide a controlled melting temperature range (liquid-solid ``mushy`` zone) relative to the eutectic melting temperature (e.g. up to 15 C above the eutectic melting temperature). 5 figs.

  4. Pb-free Sn-Ag-Cu ternary eutectic solder

    DOEpatents

    Anderson, Iver E.; Yost, Frederick G.; Smith, John F.; Miller, Chad M.; Terpstra, Robert L.

    1996-06-18

    A Pb-free solder includes a ternary eutectic composition consisting essentially of about 93.6 weight % Sn-about 4.7 weight % Ag-about 1.7 weight % Cu having a eutectic melting temperature of about 217.degree. C. and variants of the ternary composition wherein the relative concentrations of Sn, Ag, and Cu deviate from the ternary eutectic composition to provide a controlled melting temperature range (liquid-solid "mushy" zone) relative to the eutectic melting temperature (e.g. up to 15.degree. C. above the eutectic melting temperature).

  5. Spin dynamics simulations at AGS

    SciTech Connect

    Huang, H.; MacKay, W.W.; Meot, F.; Roser, T.

    2010-05-23

    To preserve proton polarization through acceleration, it is important to have a correct model of the process. It has been known that with the insertion of the two helical partial Siberian snakes in the Alternating Gradient Synchrotron (AGS), the MAD model of AGS can not deal with a field map with offset orbit. The stepwise ray-tracing code Zgoubi provides a tool to represent the real electromagnetic fields in the modeling of the optics and spin dynamics for the AGS. Numerical experiments of resonance crossing, including spin dynamics in presence of the snakes and Q-jump, have been performed in AGS lattice models, using Zgoubi. This contribution reports on various results so obtained.

  6. The effect of dielectric constants on noble metal/semiconductor SERS enhancement: FDTD simulation and experiment validation of Ag/Ge and Ag/Si substrates.

    PubMed

    Wang, Tao; Zhang, Zhaoshun; Liao, Fan; Cai, Qian; Li, Yanqing; Lee, Shuit-Tong; Shao, Mingwang

    2014-02-11

    The finite-difference time-domain (FDTD) method was employed to simulate the electric field distribution for noble metal (Au or Ag)/semiconductor (Ge or Si) substrates. The simulation showed that noble metal/Ge had stronger SERS enhancement than noble metal/Si, which was mainly attributed to the different dielectric constants of semiconductors. In order to verify the simulation, Ag nanoparticles with the diameter of ca. 40 nm were grown on Ge or Si wafer (Ag/Ge or Ag/Si) and employed as surface-enhanced Raman scattering substrates to detect analytes in solution. The experiment demonstrated that both the two substrates exhibited excellent performance in the low concentration detection of Rhodamine 6G. Besides, the enhancement factor (1.3 × 10(9)) and relative standard deviation values (less than 11%) of Ag/Ge substrate were both better than those of Ag/Si (2.9 × 10(7) and less than 15%, respectively), which was consistent with the FDTD simulation. Moreover, Ag nanoparticles were grown in-situ on Ge substrate, which kept the nanoparticles from aggregation in the detection. To data, Ag/Ge substrates showed the best performance for their sensitivity and uniformity among the noble metal/semiconductor ones.

  7. Silica Cladding of Ag Nanoparticles for High Stability and Surface-Enhanced Raman Spectroscopy Performance

    NASA Astrophysics Data System (ADS)

    Zhao, Miaomiao; Guo, Hao; Liu, Wenyao; Tang, Jun; Wang, Lei; Zhang, Binzhen; Xue, Chenyang; Liu, Jun; Zhang, Wendong

    2016-09-01

    For high-precision biochemical sensing, surface-enhanced Raman spectroscopy (SERS) has been demonstrated to be a highly sensitive spectroscopic analytical method and Ag is considered to be the best material for SERS performance. Due to the high surface activity of Ag nanoparticles, the high stability of Ag nanostructures, especially in moist environments, is one of the key issues that need to be solved. A method for silica (SiO2) cladding of Ag nanoparticles (NPs) is demonstrated here for high sensitivity and long-term stability when putted in aqueous solution. The chemically inert, transparent, hydrophilic, and bio-compatible SiO2 surface acts as the protection layer for the Ag nanoparticles, which can also enhance the Raman intensity to a certain extent. In our study, the Ag@SiO2 core-shell substrate can detect crystal violet solutions with molar concentrations down to 10-12 M. After 24 h of immersion, the reduction in Raman scattering intensity is about 85 % for sole Ag NP films, compared to 12 % for the Ag coated with a 10-nm SiO2 layer. This thickness was found to be optimum for Ag@SiO2 core-shell substrates with long-term stability and high SERS activity.

  8. Ag-Pd-Si (009)

    NASA Astrophysics Data System (ADS)

    Carow-Watamura, U.; Louzguine, D. V.; Takeuchi, A.

    This document is part of Part 1 http://dx.doi.org/10.1007/97.etType="URL"/> 'Systems from Ag-Al-Ca to Au-Pd-Si' of Subvolume B 'Physical Properties of Ternary Amorphous Alloys' of Volume 37 'Phase Diagrams and Physical Properties of Nonequilibrium Alloys' of Landolt-Börnstein - Group III 'Condensed Matter'. It contains the Chapter 'Ag-Pd-Si (009)' with the content:

  9. Silver concentrations in Colorado, USA, watersheds using improved methodology.

    PubMed

    Wen, Liang-Saw; Santschi, Peter H; Gill, Gary A; Tang, Degui

    2002-10-01

    River water samples were collected at five sites in the state of Colorado, USA, to assess the impact of municipal and industrial discharges on Ag concentrations and speciation in surface waters. Samples were collected and analyzed for total (unfiltered collections), filtered (0.1 and 0.4 microm), particulate (> or = 0.45 microm), and colloidal Ag (3 kDa-0.1 m) using ultraclean protocols. A series of laboratory experiments were conducted to assess bias from sample storage, digestion, and preconcentration protocols. In general, upstream unfiltered and particulate Ag concentrations fell within a fairly narrow range, 3.1 to 21 ng/L and 0.2 to 1.7 microg/g, respectively. Downstream unfiltered and particulate Ag concentrations showed a more broad range, 2.8 to 1,110 ng/L and 0.5 to 104 microg/g, respectively, and reflected attenuated impacts of Ag-laden discharge effluents. However, Ag concentrations in the 0.1-microm filter-passing fraction 0.8 to 1.2 km downstream from major treatment plant effluents were all below the chronic silver criteria. On average, more than 60% of the 0.1-microm filter-passing Ag was associated with colloidal macromolecular organic matter. Silver concentrations in colloids (microg/g) were, on average, the same as those in suspended particulate matter. The percentage abundance of colloidal Ag was similar to that of dissolved organic carbon, suggesting that strong Ag binding ligands exist in both the colloidal and the particle size fractions, as these macromolecular ligands likely play a major role in Ag speciation.

  10. Preparation and antibacterial properties of Ag@polydopamine/graphene oxide sheet nanocomposite

    NASA Astrophysics Data System (ADS)

    Zhou, Hao; Liu, Yunfang; Chi, Weidong; Yu, Changyuan; Yu, Yingjie

    2013-10-01

    Immobilization of silver nanoparticles (Ag NPs) on poly-dopamine (PDA) functionalized graphene oxide sheets (GOSs) were carried out by an easy in situ reduction method. The PDA layer was coated on the surface of the GOSs via the self-polymerization of dopamine under atmosphere condition. The PDA layer not only works as the chemisorption and reduction sites for silver ions to form Ag NPs but also stabilizes them. High-resolution transmission electron microscopy observation shows that the average size of the Ag NPs anchored on the PDA/GOS composite is about 2.8 nm. The inhibition zone diameter of the Ag@PDA/GOS nanocomposite is about 23.7 mm, whereas said diameter of the Ag NPs is only 18.5 mm. The minimum bactericidal concentration of the Ag@PDA/GOS nanocomposite is about 25 μg/ml that is only half of said concentration of the Ag NPs. The Ag@PDA/GOS nanocomposite exhibits an excellent antibacterial property.

  11. Growth of Ag nanoparticles using plasma-modified multi-walled carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Tseng, Chun-Hao; Chen, Chuh-Yung

    2008-01-01

    This study presents a novel method for preparing multi-walled carbon nanotubes (MWNTs) grafted with a poly(2-hydroxyethyl methacrylate) (HEMA)-silver complex (CNTs-HEMA-Ag complex) through plasma-induced grafting polymerization. The characteristics of the MWNTs after being grafted with HEMA polymer are monitored by Fourier transform infrared (FT-IR) spectroscopy. The chelating groups in the HEMA polymer grafted on the surface of the CNTs-HEMA are the coordination sites for chelating silver ions, and are further used as nanotemplates for the growing of Ag nanoparticles (quantum dots). Transmission electron microscopy (TEM) reveals that the particle size of Ag nanoparticles on the CNT surfaces increases with the Ag+ chelating concentration, reaction time, and reaction temperature. Moreover, the crystalline phase of Ag nanoparticles is identified by using x-ray diffraction (XRD). In addition, high-resolution x-ray photoelectron spectroscopy (XPS) is used to characterize the functional groups on the surface of the MWNTs after chemical modification through plasma treatment; it demonstrates that the growing amount of the Ag nanoparticles on the nanotubes increases with the Ag+ chelating concentration due to the blocking effect of the Ag particles forming on the MWNTs.

  12. Enhanced photocatalytic activity of Ag-TiO2/Ag heterogeneous films

    NASA Astrophysics Data System (ADS)

    Liang, Ying; Wang, ShaoHua; Guo, PengFeng

    2015-11-01

    Ag-deposited TiO2 and Ag (Ag-TiO2/Ag) films coated on glass substrates were prepared using a simple sol-gel and dip-coating method. The Ag chemical state was investigated through X-ray diffractometry and X-ray photoelectron spectroscopy. Results showed that the Ag mainly exists in metallic state in the Ag-TiO2 film. Ag-TiO2/Ag exhibits higher photocatalytic activity than individual Ag-TiO2 and TiO2/Ag films. This enhanced photocatalytic activity was attributed to high surface plasmon resonance effects and separation rates of photoinduced electron-hole pairs of Ag nanoparticles. Results were verified by photoluminescence and UV-Vis spectroscopy.

  13. Sonochemical synthesis of Ag nanoclusters: electrogenerated chemiluminescence determination of dopamine.

    PubMed

    Liu, Tao; Zhang, Lichun; Song, Hongjie; Wang, Zhonghui; Lv, Yi

    2013-01-01

    We report a facile one-pot sonochemical approach to preparing highly water-soluble Ag nanoclusters (NCs) using bovine serum albumin as a stabilizing agent and reducing agent in aqueous solution. Intensive electrogenerated chemiluminescence (ECL) was observed from the as-prepared Ag (NCs) and successfully applied for the ECL detection of dopamine with high sensitivity and a wide detection range. A possible ECL mechanism is proposed for the preparation of Ag NCs. With this method, the dopamine concentration was determined in the range of 8.3 × 10(-9) to 8.3 × 10(-7) mol/L without the obvious interference of uric acid, ascorbic acid and some other neurotransmitters, such as serotonin, epinephrine and norepinephrine, and the detection limit was 9.2 × 10(-10) mol/L at a signal/noise ratio of 3.

  14. Exploration of silver decoration concentration to enhance photocatalytic efficiency of titanium dioxide photocatalysts

    NASA Astrophysics Data System (ADS)

    Chang, Lee-Hong; Cho, Chun-Pei

    2016-12-01

    Ag decoration on TiO2 is favorable to absorption of visible light and wider absorption range. Ag nanoparticles playing the role of electron receivers on TiO2 surface enhance photodegradation. However, excess Ag nanoparticles caused reduced specific surface area of photocatalysts and increased probability of charge recombination, resulting in lower photocatalytic efficiency. In this study, the influence of various Ag decoration concentrations on photocatalytic activity was investigated. Surface treatment by nitric acid after Ag decoration was performed to avoid excessive Ag deposition. The extent of Ag elimination and its impacts on photocatalytic activity were also explored. An optimum Ag content in the photocatalyst was achieved and photocatalytic efficiency was obviously improved. It was found that the number of calcination times affected the crystallinity and stability of photocatalysts. Better photocatalytic efficiency could be obtained after twice calcinations.

  15. Ag-graphene hybrid conductive ink for writing electronics

    NASA Astrophysics Data System (ADS)

    Xu, L. Y.; Yang, G. Y.; Jing, H. Y.; Wei, J.; Han, Y. D.

    2014-02-01

    With the aim of preparing a method for the writing of electronics on paper by the use of common commercial rollerball pens loaded with conductive ink, hybrid conductive ink composed of Ag nanoparticles (15 wt%) and graphene-Ag composite nanosheets (0.15 wt%) formed by depositing Ag nanoparticles (˜10 nm) onto graphene sheets was prepared for the first time. Owing to the electrical pathway effect of graphene and the decreased contact resistance of graphene junctions by depositing Ag nanoparticles (NPs) onto graphene sheets, the concentration of Ag NPs was significantly reduced while maintaining high conductivity at a curing temperature of 100 ° C. A typical resistivity value measured was 1.9 × 10-7 Ω m, which is 12 times the value for bulk silver. Even over thousands of bending cycles or rolling, the resistance values of writing tracks only increase slightly. The stability and flexibility of the writing circuits are good, demonstrating the promising future of this hybrid ink and direct writing method.

  16. Chestnut extract induces apoptosis in AGS human gastric cancer cells.

    PubMed

    Lee, Hyun Sook; Kim, Eun Ji; Kim, Sun Hyo

    2011-06-01

    In Korea, chestnut production is increasing each year, but consumption is far below production. We investigated the effect of chestnut extracts on antioxidant activity and anticancer effects. Ethanol extracts of raw chestnut (RCE) or chestnut powder (CPE) had dose-dependent superoxide scavenging activity. Viable numbers of MDA-MD-231 human breast cancer cells, DU145 human prostate cancer cells, and AGS human gastric cancer cells decreased by 18, 31, and 69%, respectively, following treatment with 200 µg/mL CPE for 24 hr. CPE at various concentrations (0-200 µg/mL) markedly decreased AGS cell viability and increased apoptotic cell death dose and time dependently. CPE increased the levels of cleaved caspase-8, -7, -3, and poly (ADP-ribose) polymerase in a dose-dependent manner but not cleaved caspase-9. CPE exerted no effects on Bcl-2 and Bax levels. The level of X-linked inhibitor of apoptosis protein decreased within a narrow range following CPE treatment. The levels of Trail, DR4, and Fas-L increased dose-dependently in CPE-treated AGS cells. These results show that CPE decreases growth and induces apoptosis in AGS gastric cancer cells and that activation of the death receptor pathway contributes to CPE-induced apoptosis in AGS cells. In conclusion, CPE had more of an effect on gastric cancer cells than breast or prostate cancer cells, suggesting that chestnuts would have a positive effect against gastric cancer.

  17. Hydrogels of Superlong Helices to Synthesize Hybrid Ag-Helical Nanomaterials.

    PubMed

    Li, Guihua; Wang, Yitong; Wang, Ling; Song, Aixin; Hao, Jingcheng

    2016-11-22

    The gelation behavior of mixtures of sodium deoxycholate (NaDC) and glutathione (GSH) in water is investigated. The system exhibits a structural transition of self-assembled hydrogels from nanofibers to nanohelix structures, and then to helical ribbons with increasing GSH concentration. Superlong helical nanofibers with left- and right-handed orientations are produced by tuning the concentration of GSH at a fixed concentration of NaDC. Random coil and β-sheet structures are significant for the formation of the helical structures, and are indicated by circular dichroism (CD) and Fourier transform infrared (FT-IR) spectra. The mechanical strength of the "weak" hydrogels is enhanced by the introduction of appropriate suitable amount of AgNO3. Furthermore, the controlled growth of Ag nanoparticles at spatially arranged locations along the nanohelices (hybrid Ag-helical nanomaterial) is readily achieved by UV reduction of Ag (I) ions on the supramolecular helical templates.

  18. Growth Mechanism and Electrical and Magnetic Properties of Ag-Fe₃O₄ Core-Shell Nanowires.

    PubMed

    Ma, Jingjing; Wang, Kai; Zhan, Maosheng

    2015-07-29

    One-dimensional Ag-Fe3O4 core-shell heteronanowires have been synthesized by a facile and effective coprecipitation method, in which silver nanowires (AgNWs) were used as the nucleation site for growth of Fe3O4 in aqueous solution. The size and morphology control of the core-shell nanowires were achieved by simple adjustments of reaction conditions including FeCl3/FeCl2 concentration, poly(vinylpyrrolidone) (PVP) concentration, reaction temperature, and time. It was found that the Fe3O4 shell thickness could be tuned from 6 to 76 nm with the morphology variation between nanopheres and nanorods. A possible growth mechanism of Ag-Fe3O4 core-shell nanowires was proposed. First, the C═O derived from PVP on the surface of AgNWs provided nucleation points and in situ oxidation reaction between AgNWs and FeCl3/FeCl2 solution promoted the accumulation of Fe(3+) and Fe(2+) on the AgNWs surface. Second, Fe3O4 nanoparticles nucleated on the AgNWs surface. Lastly, Fe3O4 nanoparticles grew on the AgNWs surface by using up the reagents. Higher FeCl3/FeCl2 concentration or higher temperature led to faster nucleation and growth, resulting in the formation of Fe3O4 nanorods, whereas lower concentration or lower temperature resulted in slower nucleation and growth, leading to the formation of Fe3O4 nanospheres. Furthermore, the Ag-Fe3O4 core-shell nanowires exhibited good electrical properties and ferromagnetic properties at room temperature. Particularly, the magnetic saturation values (Ms) increased from 5.7 to 26.4 emu g(-1) with increasing Fe3O4 shell thickness from 9 to 76 nm. This growth of magnetic nanoparticles on 1D metal nanowires is meaningful from both fundamental and applied perspectives.

  19. Enhanced Electrical Properties of La(CaSr) MnO Polycrystalline Composites with Ag Addition

    NASA Astrophysics Data System (ADS)

    Yue, Xuejiao; Zhan, Yanhong; Liu, Xiang; Gu, Gang; Wang, Qiangshen; Yin, Xuepeng

    2015-09-01

    La(CaSr)MnO:Ag(LCSMO:Ag, x = 0, 0.1, 0.2 and 0.3, mol%) polycrystalline composites were prepared by a solid-state reaction method. With the increasing of Ag addition, the temperature coefficient of resistance (TCR) and the metal-to-insulator transition temperature () reach the maximum values of 9.1 % K and 258 K for LCSMO:Ag ( x = 0.3) sample, which can be used as a candidate of bolometer or infrared detectors. The improvement of Mn concentration and grain connectivity by Ag addition is responsible for the enhancement of and TCR values. The fitting curves of electrical resistivity show that the low temperature region () is fitted with grain/domain boundary, electron-electron, and magnon scattering mechanisms, as well as the high temperature region () is fitted with adiabatic small-polaron hopping mechanism.

  20. DNA/Ag Nanoparticles as Antibacterial Agents against Gram-Negative Bacteria

    PubMed Central

    Takeshima, Tomomi; Tada, Yuya; Sakaguchi, Norihito; Watari, Fumio; Fugetsu, Bunshi

    2015-01-01

    Silver (Ag) nanoparticles were produced using DNA extracted from salmon milt as templates. Particles spherical in shape with an average diameter smaller than 10 nm were obtained. The nanoparticles consisted of Ag as the core with an outermost thin layer of DNA. The DNA/Ag hybrid nanoparticles were immobilized over the surface of cotton based fabrics and their antibacterial efficiency was evaluated using E. coli as the typical Gram-negative bacteria. The antibacterial experiments were performed according to the Antibacterial Standard of Japanese Association for the Functional Evaluation of Textiles. The fabrics modified with DNA/Ag nanoparticles showed a high enough inhibitory and killing efficiency against E. coli at a concentration of Ag ≥ 10 ppm. PMID:28347012

  1. Green fabrication of quaternized chitosan/rectorite/Ag NP nanocomposites with antimicrobial activity.

    PubMed

    Luo, Jiwen; Xie, Meijia; Wang, Xiaoying

    2014-02-01

    Silver nanoparticles (Ag NPs) were synthesized rapidly in one pot via the Tollens reaction, in which quaternized chitosan (QCS) and rectorite (REC) acted as the reducing and stabilizing agent, while other chemical reducing and stabilizing agents and the surfactant were not included. X-ray diffraction, scanning electron microscopy and transmission electron microscopy results showed that spherical Ag NPs with uniform sizes were obtained, the layers of clay were peeled and thus exfoliated QCS/REC/Ag NP (QCRAg) nanocomposite was achieved. Moreover, Ag NPs dispersed well in the exfoliated nanocomposite matrix, some Ag NPs even entered into the interlayer of REC. QCRAg nanocomposites showed strong antimicrobial activity; the lowest minimum inhibitory concentration against Staphyloccocus aureus was only 0.0001% (w/v). The study reveals that the obtained QCRAg nanocomposites have great potential for biomedical applications.

  2. Evaluation of bimetallic catalyst PtAg/C as a glucose-tolerant oxygen reduction cathode

    NASA Astrophysics Data System (ADS)

    Guerra-Balcázar, M.; Cuevas-Muñiz, F. M.; Álvarez-Contreras, L.; Arriaga, L. G.; Ledesma-García, J.

    2012-01-01

    PtAg/C nanoparticles were synthesized by chemical reduction and evaluated for the oxygen reduction reaction (ORR) in the absence and presence of glucose. PtAg/C catalyst formed onion-like layered structures, which are uniformly distributed on the support. PtAg/C showed activity comparable to that of Pt/C ETEK for ORR. Further, the catalyst exhibited high selectivity for ORR in the presence of glucose. PtAg/C was evaluated as cathode in a microfluidic fuel cell operated with high concentration of glucose (100 mM) as fuel. The results demonstrated that the use of PtAg/C as cathode electrode achieved higher selectivity and better performance compared with Pt/C catalyst.

  3. Self-assembled dendrite Ag arrays with tunable morphologies for surface-enhanced Raman scattering

    NASA Astrophysics Data System (ADS)

    Huang, Pingping; Wang, Zhezhe; Lin, Lin; Feng, Zhuohong; Wen, Xin; Zheng, Zhiqiang

    2016-11-01

    Highly ordered dendrite Ag arrays are fabricated by using photosensitive sol-gel and electrochemical reaction self-assembly strategy to achieve large field enhancement for Surface-Enhanced Raman scattering (SERS) application. The effects of applied voltage, reaction time and KH550 have been investigated to tailor the growth of Ag dendrite. At an applied voltage of 25 V and reaction time of 30 min, orderly dendrite Ag arrays are obtained and show strong SERS effect. Meanwhile, the additive KH550 also shows a unique effect on the morphologies of Ag dendrite and contributes to increase the SERS. This kind of substrate can be used to detect R6G with the concentration of as low as 10-13 M obviously. Our results suggest that the dendrite Ag arrays as SERS substrate with strong SERS effect having vast potential applications in biosensors and nanodevices with molecule-level detection.

  4. Thermoelectric properties of n-type Nb-doped Ag8SnSe6

    NASA Astrophysics Data System (ADS)

    Zhang, Xiao; Zhang, Cheng-Long; Lin, Siqi; Lu, Hong; Pei, Yanzhong; Jia, Shuang

    2016-04-01

    Electrical and thermoelectric (TE) properties for n-type Ag8SnSe6 and ( Ag1- x Nb x ) 8 SnSe 6 are investigated. Ag8SnSe6 has the thermoelectric figure of merit (ZT) close to 1.1 at 803 K due to its intrinsic ultralow thermal conductivity ˜ 0.3 Wm - 1 K - 1 , relatively low resistivity ˜0.01 Ω cm, and high Seebeck coefficient ˜-200 μV/K. The ZT for pure Ag8SnSe6 drops to 0.02 at room temperature due to its large resistivity. Niobium doping increases the carrier concentration nearly 10 times and thus enhances its ZT to 0.11 at room temperature. Ag8SnSe6 is a promising n-type candidate of TE materials which needs further elaborations.

  5. Phytostimulation of poplars and Arabidopsis exposed to silver nanoparticles and Ag⁺ at sublethal concentrations.

    PubMed

    Wang, Jing; Koo, Yeonjong; Alexander, Anne; Yang, Yu; Westerhof, Samantha; Zhang, Qingbo; Schnoor, Jerald L; Colvin, Vicki L; Braam, Janet; Alvarez, Pedro J J

    2013-05-21

    The increasing likelihood of silver nanoparticle (AgNP) releases to the environment highlights the importance of understanding AgNP interactions with plants, which are cornerstones of most ecosystems. In this study, poplars (Populus deltoides × nigra) and Arabidopsis thaliana were exposed hydroponically to nanoparticles of different sizes (PEG-coated 5 and 10 nm AgNPs, and carbon-coated 25 nm AgNPs) or silver ions (Ag(+), added as AgNO₃) at a wide range of concentrations (0.01 to 100 mg/L). Whereas all forms of silver were phytotoxic above a specific concentration, a stimulatory effect was observed on root elongation, fresh weight, and evapotranspiration of both plants at a narrow range of sublethal concentrations (e.g., 1 mg/L of 25 nm AgNPs for poplar). Plants were most susceptible to the toxic effects of Ag(+) (1 mg/L for poplar, 0.05 mg/L for Arabidopsis), but AgNPs also showed some toxicity at higher concentrations (e.g., 100 mg/L of 25 nm AgNPs for poplar, 1 mg/L of 5 nm AgNPs for Arabidopsis) and this susceptibility increased with decreasing AgNP size. Both poplars and Arabidopsis accumulated silver, but silver distribution in shoot organs varied between plant species. Arabidopsis accumulated silver primarily in leaves (at 10-fold higher concentrations than in the stem or flower tissues), whereas poplars accumulated silver at similar concentrations in leaves and stems. Within the particle subinhibitory concentration range, silver accumulation in poplar tissues increased with exposure concentration and with smaller AgNP size. However, compared to larger AgNPs, the faster silver uptake associated with smaller AgNPs was offset by their toxic effect on evapotranspiration, which was exerted at lower concentrations (e.g., 1 mg/L of 5 nm AgNPs for poplar). Overall, the observed phytostimulatory effects preclude generalizations about the phytotoxicity of AgNPs and encourage further mechanistic research.

  6. Sublethal concentrations of silver nanoparticles affect the mechanical stability of biofilms.

    PubMed

    Grün, Alexandra Y; Meier, Jutta; Metreveli, George; Schaumann, Gabriele E; Manz, Werner

    2016-12-01

    Bacterial biofilms are most likely confronted with silver nanoparticles (Ag NPs) as a pollutant stressor in aquatic systems. In this study, biofilms of Aquabacterium citratiphilum were exposed for 20 h to 30 and 70 nm citrate stabilized Ag NPs in low-dose concentrations ranging from 600 to 2400 μg l(-1), and the Ag NP-mediated effects on descriptive, structural, and functional biofilm characteristics, including viability, protein content, architecture, and mechanical stability, were investigated. Viability, based on the bacterial cell membrane integrity of A. citratiphilum, as determined by epifluorescence microscopy, remained unaffected after Ag NP exposure. Moreover, in contrast to information in the current literature, protein contents of cells and extracellular polymeric substances (EPS) and biofilm architecture, including dry mass, thickness, and density, were not significantly impacted by exposure to Ag NPs. However, the biofilms themselves served as effective sinks for Ag NPs, exhibiting enrichment factors from 5 to 8. Biofilms showed a greater capacity to accumulate 30 nm sized Ag NPs than 70 nm Ag NPs. Furthermore, Ag NPs significantly threatened the mechanical stability of biofilms, as determined by a newly developed assay. For 30 nm Ag NPs, the mechanical stability of biofilms decreased as the Ag NP concentrations applied to them increased. In contrast, 70 nm Ag NPs produced a similar decrease in mechanical stability for each applied concentration. Overall, this finding demonstrates that exposure to Ag NPs triggers remarkable changes in biofilm adhesion and/or cohesiveness. Because of biofilm-mediated ecological services, this response raises environmental concerns regarding Ag NP release into freshwater systems, even in sublethal concentrations.

  7. Effect of Ag Templates on the Formation of Au-Ag Hollow/Core-Shell Nanostructures.

    PubMed

    Tsai, Chi-Hang; Chen, Shih-Yun; Song, Jenn-Ming; Haruta, Mitsutaka; Kurata, Hiroki

    2015-12-01

    Au-Ag alloy nanostructures with various shapes were synthesized using a successive reduction method in this study. By means of galvanic replacement, twined Ag nanoparticles (NPs) and single-crystalline Ag nanowires (NWs) were adopted as templates, respectively, and alloyed with the same amount of Au(+) ions. High angle annular dark field-scanning TEM (HAADF-STEM) images observed from different rotation angles confirm that Ag NPs turned into AuAg alloy rings with an Au/Ag ratio of 1. The shifts of surface plasmon resonance and chemical composition reveal the evolution of the alloy ring formation. On the other hand, single-crystalline Ag NWs became Ag@AuAg core-shell wires instead of hollow nanostructure through a process of galvanic replacement. It is proposed that in addition to the ratio of Ag templates and Au ion additives, the twin boundaries of the Ag templates were the dominating factor causing hollow alloy nanostructures.

  8. Probing the rupture of a Ag atomic junction in a Ag-Au mixed electrode

    NASA Astrophysics Data System (ADS)

    Kim, Taekyeong

    2015-09-01

    We probed that the atomic junction in Ag part ruptures during stretching of atomic sized contacts of Ag-Au mixed electrodes, resulting in Ag-Ag electrodes through a scanning tunneling microscope breaking junction (STM-BJ) technique. We observed that the conductance and tunneling decay constant for a series of amine-terminated oligophenyl molecular junctions are essentially the same for the Ag-Au mixed and the Ag-Ag electrodes. We also found the molecular plateau length and the evolution patterns with the Ag-Au mixed electrodes are similar to those with Ag-Ag electrodes rather than the Au-Au electrodes in the molecular junction elongation. This result is attributed to the smaller binding energy of Ag atoms compared to that of Au atoms, so the Ag junction part is more easily broken than that of Au part in stretching of Ag-Au mixed electrodes. Furthermore, we successfully observed that the rupture force of the atomic junction for the Ag-Au mixed electrodes was identical to that for the Ag-Ag electrodes and smaller than that for the Au-Au electrodes. This study may advance the understanding of the electrical and the mechanical properties in molecular devices with Ag and Au electrodes in future.

  9. Electronic transport in heavily doped Ag/n-Si composite films

    NASA Astrophysics Data System (ADS)

    Bates, Clayton W.; Zhang, Chichang

    2013-10-01

    Hall measurements characterized Ag/n-Si composite films 1 micron thick produced by magnetron co-sputtering onto high resistivity Si (111) substrates at 550°C. The targets were Ag and n-type Si doped with 3 × 1019/cm3 of antimony. Films were prepared with 13, 16 and 22 at. % Ag and measured over a temperature range 77-500°K. Conduction takes place at low temperatures by variable rang hopping in localized states at the Fermi level and by thermal activation over grain boundaries at higher temperatures. The Log Resistivity vs 1/kT curves for the three Ag concentrations vary in a similar manner, but decrease in magnitude with increasing Ag due to the smaller number of grain boundaries between Ag nanoparticles occurring with increasing Ag concentration. At low temperatures Hall mobilities are essentially independent of temperature as the carrier densities for the three Ag concentrations are constant from 77 to slightly under 300°K with resistivities varying by small amounts. The mobilities at all Ag concentrations increase with temperature and approach each other as the effects of grain boundaries become less important. This work presents for the first time the effects of metal particles embedded in a semiconductor on the transport properties of carriers in the semiconductor. Though these effects are for a given average particle size most of the results are expected to hold over a range of particle sizes. Free electrons produced in films containing 13 and 16 at. % Ag result in concentrations of 1.5 × 1019/cm3, one half the antimony doping, while those with 22 at. % Ag, the carrier concentrations are three orders of magnitude higher. These constant carrier concentrations are due to the metal-insulator transition that occurs in doped crystalline and polycrystalline silicon for carrier densities nc >3.9 × 1018/cm3. The three orders of magnitude higher carrier concentration produced in films with 22 at. % Ag is argued to be due to doping of the Si matrix by the Ag

  10. Morphology-dependent bactericidal activities of Ag/CeO2 catalysts against Escherichia coli.

    PubMed

    Wang, Lian; He, Hong; Yu, Yunbo; Sun, Li; Liu, Sijin; Zhang, Changbin; He, Lian

    2014-06-01

    Silver-loaded CeO2 nanomaterials (Ag/CeO2) including Ag/CeO2 nanorods, nanocubes, nanoparticles were prepared with hydrothermal and impregnation methods. Catalytic inactivation of Escherichia coli with Ag/CeO2 catalysts through the formation of reactive oxygen species (ROS) was investigated. For comparison purposes, the bactericidal activities of CeO2 nanorods, nanocubes and nanoparticles were also studied. There was a 3-4 log order improvement in the inactivation of E. coli with Ag/CeO2 catalysts compared with CeO2 catalysts. Temperature-programmed reduction of H2 showed that Ag/CeO2 catalysts had higher catalytic oxidation ability than CeO2 catalysts, which was the reason for that Ag/CeO2 catalysts exhibited stronger bactericidal activities than CeO2 catalysts. Further, the bactericidal activities of CeO2 and Ag/CeO2 depend on their shapes. Results of 5,5-dimethyl-1-pyrroline-N-oxide spin-trapping measurements by electron spin resonance and addition of catalase as a scavenger indicated the formation of OH, O2(-), and H2O2, which caused the obvious bactericidal activity of catalysts. The stronger chemical bond between Ag and CeO2 nanorods led to lower Ag(+) elution concentrations. The toxicity of Ag(+) eluted from the catalysts did not play an important role during the bactericidal process. Experimental results also indicated that Ag/CeO2 induced the production of intracellular ROS and disruption of the cell wall and cell membrane. A possible production mechanism of ROS and bactericidal mechanism of catalytic oxidation were proposed.

  11. Optimizing Au/Ag core-shell nanorods: purification, stability, and surface modification

    NASA Astrophysics Data System (ADS)

    Ma, Yanan; Zhou, Jun; Shu, Lei; Li, Tianhua; Petti, Lucia; Mormile, Pasquale

    2014-06-01

    The purification, stability, and surface modification of Au/Ag core-shell nanorods (Au/Ag NRs) in a biological buffer solution were systematically studied for the first time. In this study, Au/Ag NRs were synthesized by chemically reducing silver on the surface of gold nanorods using cetyltrimethylammonium bromide as surfactant and then purified by centrifugation washing. Based on the analysis of UV-Vis absorption spectra, TEM images, Raman spectra, and the ξ-potential, it was observed that after the second washing step, the Au/Ag NRs displayed good stability and high surface-enhanced Raman scattering (SERS) enhancement. When the as-prepared Au/Ag NRs were centrifuged more than twice, a structural transition in the surfactant layer was manifested with a sudden increase in the Raman signal intensities at 760 and 1,455 cm-1. Moreover, 4-mercaptobenzoic acid (4MBA) was used as a Raman reporter molecule to investigate the SERS characteristics of the purified Au/Ag NRs. The Raman signal intensity was enhanced with increasing the concentration of 4MBA and reached its highest intensity at the saturation concentration of 1.0 µM 4MBA in a 5 ml solution of the purified Au/Ag NRs. To prevent significant aggregation of the 4MBA-tagged Au/Ag NRs, a poly(styrenesulfonate) (PSS) layer was assembled on the nanorod surfaces by electrostatic adsorption for further surface modification, which made the 4MBA-tagged Au/Ag NRs suitable for the labeled biosensing. Subsequently, the characteristics of the PSS-coated Au/Ag NRs were demonstrated for the potential applications of label-free biosensing.

  12. Pd-Ag chronology of volatile depletion, crystallization and shock in the Muonionalusta IVA iron meteorite and implications for its parent body

    NASA Astrophysics Data System (ADS)

    Horan, M. F.; Carlson, R. W.; Blichert-Toft, J.

    2012-10-01

    Muonionalusta, a Group IVA iron meteorite, was analyzed for its 107Pd-107Ag isotope systematics by multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) in order to better constrain the initial Solar System abundance of 107Pd and to provide high resolution chronology of the evolution of its parent body. Six metal samples from Muonionalusta yield Ag abundances between 0.1012 and 1.461 ng/g, 107Ag/109Ag between 1.131 and 1.805, with 108Pd/109Ag ratios of 2201 to 52,300. The metal Pd/Ag and Ag isotopic data are correlated with a slope corresponding to a 107Pd/108Pd of (2.15±0.30)×10-5. If the Pd-Ag and Pb-Pb isotope systems closed at the same time in Muonionalusta, i.e., 2-3 Ma after CAI formation, then an initial Solar System ratio of 107Pd/108Pd=(2.8±0.5)×10-5 can be inferred. One troilite sample contains 8.478 ng/g Ag and has a 107Ag/109Ag ratio of 1.0833; its Pd concentration is 205.2 ng/g corresponding to a low 108Pd/109Ag of 13.56. The Pd-Ag results for this troilite plot near the extrapolation of the line passing through the metal points and define an initial 107Ag/109Ag that is substantially higher than chondritic, indicating that Muonionalusta formed from a precursor with high Pd/Ag. Pd and Ag concentrations in Muonionalusta metal suggest fractional crystallization from a source having Pd/Ag>4500, but the initial Ag isotopic composition for Muonionalusta troilite limits the duration of the high Pd/Ag to an interval of ≤0.6 Ma before cooling to closure of the Pd-Ag system. This result suggests that depletion of Ag and other volatile elements occurred shortly before accretion and cooling of the IVA parent body, and may have been associated with violent disruption of a progenitor to the IVA parent. Another troilite sample, its chromite inclusions and adjacent metal were isotopically homogenized locally after 107Pd had decayed, possibly by a later episode of shock >50 Ma after Solar System formation.

  13. A new Schiff base based on vanillin and naphthalimide as a fluorescent probe for Ag+ in aqueous solution

    NASA Astrophysics Data System (ADS)

    Zhou, Yanmei; Zhou, Hua; Ma, Tongsen; Zhang, Junli; Niu, Jingyang

    2012-03-01

    A new Schiff base based on vanillin and naphthalimide was designed and synthesized as fluorescent probe. The probe showed high selectivity for Ag+ over other metal ions such as Pb2+, Na+, K+, Cd2+, Ba2+, Cr3+, Zn2+, Cu2+, Ni2+, Ca2+, Al3+ and Mg2+ in aqueous solution. A new fluorescence emission was observed at 682 nm in the presence of Ag+ ion. The fluorescence intensity quenched with increasing the concentration of Ag+ at 682 nm. The method of job's plot confirmed the 1:2 complex between Ag+ and probe, and the mechanism was proposed.

  14. Quantitative determination of melamine in milk using Ag nanoparticle monolayer film as SERS substrate

    NASA Astrophysics Data System (ADS)

    Li, Ruoping; Yang, Jingliang; Han, Junhe; Liu, Junhui; Huang, Mingju

    2017-04-01

    A Raman method employing silver nanoparticle (Ag NP) monolayer film as Surface-enhanced Raman Scattering (SERS) substrate was presented to rapidly detect melamine in milk. The Ag NPs with 80 nm diameter were modified by polyvinylpyrrolidone to improve their uniformity and chemical stability. The treatment procedure of liquid milk required only addition of acetic acid and centrifugation, and required time is less than 15 min. The Ag NP monolayer film significantly enhanced Raman signal from melamine and allowed experimentally reproducible determination of the melamine concentration. A good linear relationship (R2=0.994) between the concentration and Raman peak intensity of melamine at 681 cm-1 was obtained for melamine concentrations between 0.10 mg L-1 and 5.00 mg L-1. This implies that this method can detect melamine concentrations below 1.0 mg L-1, the concentration currently considered unsafe.

  15. Halloysite Nanotubes Supported Ag and ZnO Nanoparticles with Synergistically Enhanced Antibacterial Activity.

    PubMed

    Shu, Zhan; Zhang, Yi; Yang, Qian; Yang, Huaming

    2017-12-01

    Novel antimicrobial nanocomposite incorporating halloysite nanotubes (HNTs) and silver (Ag) into zinc oxide (ZnO) nanoparticles is prepared by integrating HNTs and decorating Ag nanoparticles. ZnO nanoparticles (ZnO NPs) and Ag nanoparticles (Ag NPs) with a size of about 100 and 8 nm, respectively, are dispersively anchored onto HNTs. The synergistic effects of ZnO NPs, Ag NPs, and HNTs led to the superior antibacterial activity of the Ag-ZnO/HNTs antibacterial nanocomposites. HNTs facilitated the dispersion and stability of ZnO NPs and brought them in close contact with bacteria, while Ag NPs could promote the separation of photogenerated electron-hole pairs and enhanced the antibacterial activity of ZnO NPs. The close contact with cell membrane enabled the nanoparticles to produce the increased concentration of reactive oxygen species and the metal ions to permeate into the cytoplasm, thus induced quick death of bacteria, indicating that Ag-ZnO/HNTs antibacterial nanocomposite is a promising candidate in the antibacterial fields.

  16. Halloysite Nanotubes Supported Ag and ZnO Nanoparticles with Synergistically Enhanced Antibacterial Activity

    NASA Astrophysics Data System (ADS)

    Shu, Zhan; Zhang, Yi; Yang, Qian; Yang, Huaming

    2017-02-01

    Novel antimicrobial nanocomposite incorporating halloysite nanotubes (HNTs) and silver (Ag) into zinc oxide (ZnO) nanoparticles is prepared by integrating HNTs and decorating Ag nanoparticles. ZnO nanoparticles (ZnO NPs) and Ag nanoparticles (Ag NPs) with a size of about 100 and 8 nm, respectively, are dispersively anchored onto HNTs. The synergistic effects of ZnO NPs, Ag NPs, and HNTs led to the superior antibacterial activity of the Ag-ZnO/HNTs antibacterial nanocomposites. HNTs facilitated the dispersion and stability of ZnO NPs and brought them in close contact with bacteria, while Ag NPs could promote the separation of photogenerated electron-hole pairs and enhanced the antibacterial activity of ZnO NPs. The close contact with cell membrane enabled the nanoparticles to produce the increased concentration of reactive oxygen species and the metal ions to permeate into the cytoplasm, thus induced quick death of bacteria, indicating that Ag-ZnO/HNTs antibacterial nanocomposite is a promising candidate in the antibacterial fields.

  17. Direct electrochemical oxidation of S-captopril using gold electrodes modified with graphene-AuAg nanocomposites

    PubMed Central

    Pogacean, Florina; Biris, Alexandru R; Coros, Maria; Lazar, Mihaela Diana; Watanabe, Fumiya; Kannarpady, Ganesh K; Al Said, Said A Farha; Biris, Alexandru S; Pruneanu, Stela

    2014-01-01

    In this paper, we present a novel approach for the electrochemical detection of S-captopril based on graphene AuAg nanostructures used to modify an Au electrode. Multi-layer graphene (Gr) sheets decorated with embedded bimetallic AuAg nanoparticles were successfully synthesized catalytically with methane as the carbon source. The two catalytic systems contained 1.0 wt% Ag and 1.0 wt% Au, while the second had a larger concentration of metals (1.5 wt% Ag and 1.5 wt% Au) and was used for the synthesis of the Gr-AuAg-1 and Gr-AuAg-1.5 multicomponent samples. High-resolution transmission electron microscopy analysis indicated the presence of graphene flakes that had regular shapes (square or rectangular) and dimensions in the tens to hundreds of nanometers. We found that the size of the embedded AuAg nanoparticles varied between 5 and 100 nm, with the majority being smaller than 20 nm. Advanced scanning transmission electron microscopy studies indicated a bimetallic characteristic of the metallic clusters. The resulting Gr-AuAg-1 and Gr-AuAg-1.5 samples were used to modify the surface of commonly used Au substrates and subsequently employed for the direct electrochemical oxidation of S-captopril. By comparing the differential pulse voltammograms recorded with the two modified electrodes at various concentrations of captopril, the peak current was determined to be well-defined, even at relatively low concentration (10−5 M), for the Au/Gr-AuAg-1.5 electrode. In contrast, the signals recorded with the Au/Gr-AuAg-1 electrode were poorly defined within a 5×10−6 to 5×10−3 M concentration range, and many of them overlapped with the background. Such composite materials could find significant applications in nanotechnology, sensing, or nanomedicine. PMID:24596464

  18. Direct electrochemical oxidation of S-captopril using gold electrodes modified with graphene-AuAg nanocomposites.

    PubMed

    Pogacean, Florina; Biris, Alexandru R; Coros, Maria; Lazar, Mihaela Diana; Watanabe, Fumiya; Kannarpady, Ganesh K; Al Said, Said A Farha; Biris, Alexandru S; Pruneanu, Stela

    2014-01-01

    In this paper, we present a novel approach for the electrochemical detection of S-captopril based on graphene AuAg nanostructures used to modify an Au electrode. Multi-layer graphene (Gr) sheets decorated with embedded bimetallic AuAg nanoparticles were successfully synthesized catalytically with methane as the carbon source. The two catalytic systems contained 1.0 wt% Ag and 1.0 wt% Au, while the second had a larger concentration of metals (1.5 wt% Ag and 1.5 wt% Au) and was used for the synthesis of the Gr-AuAg-1 and Gr-AuAg-1.5 multicomponent samples. High-resolution transmission electron microscopy analysis indicated the presence of graphene flakes that had regular shapes (square or rectangular) and dimensions in the tens to hundreds of nanometers. We found that the size of the embedded AuAg nanoparticles varied between 5 and 100 nm, with the majority being smaller than 20 nm. Advanced scanning transmission electron microscopy studies indicated a bimetallic characteristic of the metallic clusters. The resulting Gr-AuAg-1 and Gr-AuAg-1.5 samples were used to modify the surface of commonly used Au substrates and subsequently employed for the direct electrochemical oxidation of S-captopril. By comparing the differential pulse voltammograms recorded with the two modified electrodes at various concentrations of captopril, the peak current was determined to be well-defined, even at relatively low concentration (10(-5) M), for the Au/Gr-AuAg-1.5 electrode. In contrast, the signals recorded with the Au/Gr-AuAg-1 electrode were poorly defined within a 5×10(-6) to 5×10(-3) M concentration range, and many of them overlapped with the background. Such composite materials could find significant applications in nanotechnology, sensing, or nanomedicine.

  19. AG Draconis - a symbiotic mystery

    NASA Astrophysics Data System (ADS)

    Galis, R.; Hric, L.; Smelcer, L.

    2015-02-01

    Symbiotic system AG Draconis regularly undergoes quiescent and active stages which consist of the series of individual outbursts. The period analysis of new and historical photometric data, as well as radial velocities, confirmed the presence of the two periods. The longer one (~550 d) is related to the orbital motion and the shorter one (~355 d) could be due to pulsation of the cool component of AG Dra. In addition, the active stages change distinctively, but the outbursts are repeated with periods from 359 - 375 d.

  20. Contents of Ag and other metals in food-contact plastics with nanosilver or Ag ion and their migration into food simulants.

    PubMed

    Ozaki, Asako; Kishi, Eri; Ooshima, Tomoko; Hase, Atsushi; Kawamura, Yoko

    2016-09-01

    Six nanosilver-labelled products and five silver ion (Ag(+))-labelled products were investigated to measure the migration of Ag from food-contact plastics, including nanosilver into various food simulants. The products were obtained in Japanese markets in 2012. Zinc (Zn), another major antimicrobial agent, and three harmful metals, cadmium (Cd), lead (Pb) and arsenic (As), were also examined. Ag and Zn were detected in all six nanosilver products at concentrations of 21-200 and 8.4-140 mg kg(-1), respectively. These metals were also detected in all five Ag(+) products at the same level as nanosilver products. Cd, Pb and As were not detected in any sample. Migrations of Ag and Zn were highest in 4% acetic acid, but also observed in water and 20% ethanol. Big differences were not observed in the migration ratio between nanosilver products and Ag(+) products. The ultrafiltration experiments suggested that the Ag that migrated from nanosilver products into 4% acetic acid was in its ionic form, while that into water and 20% ethanol was in its nanoparticle form.

  1. Photocatalytic degradation of lignin on synthesized Ag-AgCl/ZnO nanorods under solar light and preliminary trials for methane fermentation.

    PubMed

    Li, Huifang; Lei, Zhongfang; Liu, Chunguang; Zhang, Zhenya; Lu, Baowang

    2015-01-01

    New photocatalysts, Ag-AgCl/ZnO nanorods, were successfully synthesized in this study by using microwave assisted chemical precipitation and deposition-precipitation-photoreduction methods. The optimal preparation condition was determined as pH 9 in distilled water and 40min for UV light photoreduction of Ag (i.e. Ag40-AgCl/ZnO) by degradation of methyl orange. This work investigated the feasibility of using Ag40-AgCl/ZnO to degrade lignin under natural solar light and then subsequent methane production with influencing factors like solution pH, dosage of catalyst and initial lignin concentration being considered. OH radicals were found to play the most important role in the photocatalytic process, and the new prepared catalyst possessed stable photocatalytic activity after 7 cycles' utilization. During the subsequent biogasification, the degraded lignin obtained from 120min photocatalysis yielded 184ml methane and 325ml biogas for per gram of removed total organic carbon, increased by 10.9% and 23.1%, respectively compared to the control.

  2. Studies of induced radioactivity at the AGS

    SciTech Connect

    Brown, K.A.; Tanaka, M.

    1987-01-01

    With the goals of higher proton intensities, along with the many modes the AGS now runs and those being commissioned to run, we have begun detailed studies of the beam induced radioactivity in the AGS.

  3. Ag nanowires: large-scale synthesis via a trace-salt-assisted solvothermal process and application in transparent electrodes

    NASA Astrophysics Data System (ADS)

    Jiu, Jinting; Sugahara, Tohru; Nogi, Masaya; Suganuma, Katsuaki

    2013-04-01

    Ag nanowire (AgNW) films are receiving increasing attention as new transparent conductive films poised to replace indium tine oxide materials. However, coating of AgNW surfaces with polyvinylpyrrolidone (PVP) and other impurities during synthesis causes large contact resistance between the wires leading to low conductivities in the absence of additional treatments to fuse the overlapped AgNWs together. In the present work, we demonstrated a simple method to synthesize AgNWs by the reduction of AgNO3 using PVP as the reducing agent assisted by trace amounts of salts in ethanol. The shape and yield of the AgNWs depended significantly on the concentrations of these trace salts and on reaction temperatures. The silver nanowires were about 5-20 μm in length and showed a uniform diameter of about 70 nm. A detailed growth mechanism of the AgNWs has been proposed on the basis of the observations recorded by varying these synthesis parameters. Further, the AgNWs were used to form a transparent film, which without any additional treatments showed a sheet resistance of 10.4 Ω/sq and a transmittance of 81.9 % at 550 nm. The performance of the films was attributed to the trace amounts of residual impurities on the surface of the AgNWs and to the special V-shaped morphology of the wires prepared with the solvothermal process.

  4. Structural evolution of NiAg heterogeneous alloys upon annealing

    NASA Astrophysics Data System (ADS)

    Proux, O.; Mimault, J.; Revenant-Brizard, C.; Regnard, J. R.; Mevel, B.

    1999-01-01

    NiAg heterogeneous alloys were studied by x-ray diffraction and x-ray absorption spectroscopy at the Ni K-edge using a total electron yield detection. In the as-deposited 0953-8984/11/1/013/img8 alloys of 0.10 and 0.15 Ni atomic fraction, most of the Ni atoms are in substitutional sites in the Ag matrix. At higher Ni concentration, the Ni atoms outside the Ag-rich phase become numerous enough to group together in small clusters. An important disorder in the neighbourhood of Ni atoms is demonstrated. At low annealing temperature (up to 0953-8984/11/1/013/img9C), in 0953-8984/11/1/013/img10 and 0953-8984/11/1/013/img11, some Ni atoms are still present in substitutional sites in the Ag matrix and the small Ni particles are under strain. A very short-range order exists in this state. After a 0953-8984/11/1/013/img9C annealing, the Ni particles grow, and the Ag-rich phase remains in a steady structural state. After a higher annealing (0953-8984/11/1/013/img13C), the local Ni atomic environment becomes well ordered and typical of the pure Ni FCC phase. The Ag-rich crystallites are impoverished in Ni atoms and grow with elimination of defects. Ni grains are generally smaller than 1 nm for as-deposited alloys and reach several nanometres after a 0953-8984/11/1/013/img13C annealing for 10 min.

  5. The synthesis and characterization of Ag-N dual-doped p-type ZnO: experiment and theory.

    PubMed

    Duan, Li; Wang, Pei; Yu, Xiaochen; Han, Xiao; Chen, Yongnan; Zhao, Peng; Li, Donglin; Yao, Ran

    2014-03-07

    Ag-N dual-doped ZnO films have been fabricated by a chemical bath deposition method. The p-type conductivity of the dual-doped ZnO:(Ag, N) is stable over a long period of time, and the hole concentration in the ZnO:(Ag, N) is much higher than that in mono-doped ZnO:Ag or ZnO:N. We found that this is because AgZn-NO complex acceptors can be formed in ZnO:(Ag, N). First-principles calculations show that the complex acceptors generate a fully occupied band above the valance band maximum, so the acceptor levels become shallower and the hole concentration is increased. Furthermore, the binding energy of the Ag-N complex in ZnO is negative, so ZnO:(Ag, N) can be stable. These results indicate that the Ag-N dual-doping may be expected to be a potential route to achieving high-quality p-type ZnO for use in a variety of devices.

  6. Seed-mediated synthesis and structural analysis of hierarchical silver microparticles (HiAgMPs) with highly nanotextured surfaces

    SciTech Connect

    Han, Sang Hun; Cheon, Jae Yeong; Joo, Sang Hoon; Lee, Jae-Seung

    2013-06-01

    Highlights: • Hierarchical silver microparticles (HiAgMPs) were synthesized by the seed-mediated method using silver nanoplates as seeds. • The growth of HiAgMPs under various synthetic conditions was analyzed by time-dependent scanning electron microscopy. • The internal structure of HiAgMPs was thoroughly investigated by direct electron microscopic observation and N{sub 2} isotherm. - Abstract: We developed a novel method to synthesize hierarchical silver microparticles (HiAgMPs) with highly nanotextured surfaces based on the seed-mediated synthesis by using silver nanoplates as seeds. The synthetic conditions for the resultant HiAgMPs were intensively investigated with various types and concentrations of nanoparticle seeds at different Ag{sup +} concentrations. The growth mechanism of the HiAgMPs was studied by monitoring the morphological evolution at different growth phases. Importantly, we, for the first time, analyzed the internal structure of the HiAgMPs, which are composed of a packed core surrounded by a grooved shell. The catalytic properties of the HiAgMPs were investigated and determined to be highly active for the reduction of 4-nitrophenol.

  7. Ag nanotubes and Ag/AgCl electrodes in nanoporous membranes.

    PubMed

    Davenport, Matthew; Healy, Ken; Siwy, Zuzanna S

    2011-04-15

    Miniaturization of the entire experimental setup is a key requirement for widespread application of nanodevices. For nanopore biosensing, integrating electrodes onto the nanopore membrane and controlling the pore length is important for reducing the complexity and improving the sensitivity of the system. Here we present a method to achieve these goals, which relies on electroless plating to produce Ag nanotubes in track-etched polymer nanopore templates. By plating from one side only, we create a conductive nanotube that does not span the full length of the pore, and thus can act as a nanoelectrode located inside the nanopore. To give optimal electrochemical behavior for sensing, we coat the Ag nanotube with a layer of AgCl. We characterize the behavior of this nanoelectrode by measuring its current-voltage response and find that, in most cases, the response is asymmetric. The plated nanopores have initial diameters between 100 and 300 nm, thus a range suitable for detection of viruses.

  8. Label free detection of DNA on Au/ZnO/Ag hybrid structure based SERS substrate

    NASA Astrophysics Data System (ADS)

    Pal, Anil Kumar; Mohan, D. Bharathi

    2016-04-01

    Au/ZnO/Ag based SERS substrate was fabricated for the label free detection of DNA of Escherichia Coli bacteria. The SERS substrate was fabricated by growing ZnO nanorod arrays on thermally evaporated ultrathin Ag film of 5 nm thickness using hydrothermal process. Non-spherical like Au nanoparticles were decorated on ZnO nanorod arrays by sputtering technique with sputtering time of 45 sec. The surface of Au/ZnO/Ag was observed to be nearly superhydrophobic exhibiting the contact angle of 144 °. A low volume (5 µl) of aqueous solution of DNA of laboratory strain Escherichia Coli with very low concentration was adsorbed on fabricated SERS substrate by drop casting. The SERS detection of DNA molecules was achieved up to lower concentration of 10-8 M due to strong local electric field enhancement at the nanometer gap among Au nanoparticles and superhydrophobic nature of Au/ZnO/Ag surface.

  9. Characterization of nanocomposite a-C:H/Ag thin films synthesized by a hybrid deposition process

    NASA Astrophysics Data System (ADS)

    Venkatesh, M.; Taktak, S.; Meletis, E. I.

    2015-08-01

    Silver containing amorphous carbon films were deposited on Si wafer using a hybrid deposition process combining d.c. magnetron sputtering and PECVD. The concentration of Ag in the films was varied from 1.3 to 8.3 at % by changing d.c. magnetron current of Ag target. The influence of incorporated Ag in the a-C:H on the atomic bond structure of the films were investigated by XPS, FTIR, Raman, and HRTEM methods of analysis. The XPS, FTIR, and Raman studies demonstrated that as the silver concentration increased in the a-C:H, sp2 bonding content increased and a-C:H films changed to more graphitic structure. The high resolution TEM cross sectional studies revealed that crystalline Ag particles formed with a size in the range of 2-4 nm throughout an amorphous a-C:H matrix.

  10. Tuning the transmittance of colloidal solution by changing the orientation of Ag nanoplates in ferrofluid.

    PubMed

    Mao, Yiwu; Liu, Jing; Ge, Jianping

    2012-09-11

    Ag nanoplates and Fe(3)O(4) nanoparticle-based ferrofluids were utilized to fabricate a magnetic field controlled optic switch. The changing of light transmittance (LT) is caused by the rotation of Ag nanoplates, whose long axis always follows the orientation of external magnetic field to minimize the potential energy. The sensitivity of switching was optimized by choosing Ag nanoplates with appropriate size and concentration. The switching of transmission is proved to be fast and fully reversible. This phenomenon not only indicates an effective method to adjust the propagation of optical signals, but also reveals the possibility and great potential to develop magnetic controlled functional devices.

  11. AGS experiments: 1990, 1991, 1992. Ninth edition

    SciTech Connect

    Depken, J.C.

    1993-04-01

    This report contains a description of the following: AGS Experimental Area - High Energy Physics FY 1993 and Heavy Ion Physics FY 1993; Table of Beam Parameters and Fluxes; Experiment Schedule ``as run``; Proposed 1993 Schedule; A listing of experiments by number; Two-page summaries of each experiment begin here, also ordered by number; Publications of AGS Experiments; and List of AGS Experimenters.

  12. Selective turn-on fluorescence sensor for Ag+ using cysteamine capped CdS quantum dots: determination of free Ag+ in silver nanoparticles solution.

    PubMed

    Khantaw, Thitima; Boonmee, Chanida; Tuntulani, Thawatchai; Ngeontae, Wittaya

    2013-10-15

    Cadmium sulfide quantum dots capped with cysteamine (Cys-CdS QDs) were demonstrated as a selective fluorescence probe for sensing of free trace silver ions. The fluorescence intensity of the Cys-CdS QDs can be enhanced only in the presence of free Ag(+) and the fluorescence spectrum was slightly red shift from the original spectra. In addition, the fluorescence intensities were linearly increased upon increasing Ag(+) concentration. At the optimized condition for Ag(+) detection, when adding other metal ions to the Cys-CdS QDs solution, fluorescence spectra of Cys-CdS QDs did not change significantly revealing good selectivity of the sensors towards Ag(+). The working linear concentration range was found to be 0.1-1.5 µM with LOD of 68 nM. The proposed sensor was then applied to detect free Ag(+) in the silver nanoparticles solution. The results showed that the proposed sensor can be efficiently used with good accuracy and precision providing the simple method for detection of free Ag(+) in silver nanoparticles of quality control products.

  13. Novel process for simultaneous removal of NO(x) and SO2 from simulated flue gas by using a sustainable Ag(I)/Ag(II) redox mediator.

    PubMed

    Raju, Thasan; Chung, Sang Joon; Moon, Il Shik

    2008-10-01

    The objective of this work is to develop a sustainable process for simultaneous removal of waste gases such as NO, NO2, and SO2 by an electrochemically generated Ag(I)/Ag(II) redox mediator system. High removal efficiency was achieved for NO and SO2 by the wet scrubbing method at room temperature and atmospheric pressure. This removal is achieved through oxidation and absorption by contacting the gaseous stream with redox mediator ions that offer specific or selective solubility for the solute gases to be recovered in a wet scrubber. The process parameters such as gas velocity, liquid velocity, Ag(I) concentration, and HNO3 concentration were investigated to explore the possibility of complete removal of waste gases. The Ag(I)/Ag(II)-based mediated electrochemical oxidation process proved to be quite effective for simultaneous removal of NO, NO(x), and SO2 from the simulated flue gas mixtures containing NO and SO2 over a wide concentration range of 100-400 ppm. Studies were carried out with individual gas components for the mixture, and the effect of input NO and input SO2 concentrations on the NO(x) and SO2 removal efficiencies at 20 degrees C was examined. Complete oxidation of NO to NO2 with 100% NO removal efficiency and 92% NO(x) removal efficiency was achieved along with 100% SO2 removal efficiency, highlighting a potentially far greater efficiency of the Ag(I)/Ag(II)-based system in functionality and selectivity. Active research work in this direction is anticipated in the near future.

  14. High-value utilization of lignin to synthesize Ag nanoparticles with detection capacity for Hg²⁺.

    PubMed

    Shen, Zuguang; Luo, Yuqiong; Wang, Qun; Wang, Xiaoying; Sun, Runcang

    2014-09-24

    This study reports the rapid preparation of silver nanoparticles (AgNPs) from Tollens' reagent under microwave irradiation. In the synthesis, lignin with reducing groups and spatial three-dimensional structure was used as reducing and stabilizing agents without other chemical reagents, and the effects of the ratio of lignin to Ag(+), reaction temperature, and heating time on the synthesis of AgNPs were investigated. The obtained AgNPs were further characterized by UV-vis, Malvern particle size, TEM, XRD, and XPS analyses. The structural changes of lignin before and after reaction were also studied by FT-IR, (1)H NMR, (13)C NMR, and GC-MS. The results revealed that the obtained AgNPs were mostly spherical with diameters of around 24 nm. The optimum reaction conditions were a ratio 50 mg of lignin to 0.3 mM of Ag(+), a microwave irradiation temperature of 60 °C, and a heating time of 10 min. Moreover, AgNPs redispersed well in water and ethanol after centrifugation for the removal of lignin. During the formation of AgNPs, lignin was oxidized, and the side chains of lignin were partly disrupted into small molecules, such as hydrocarbon and alcohol. The resultant lignin-AgNPs showed highly selective sensing detection for Hg(2+), and the color of the lignin-AgNP solution containing Hg(2+) decreased gradually with increasing amounts of Hg(2+) within seconds, but the other 19 metal ions had little effect on the color and surface plasmon absorption band of the lignin-AgNPs. Also, there was a linear relationship between the absorbance and Hg(2+) concentration, with a limit of detection concentration of 23 nM. This study provides not only a new way to take advantage of agricultural and forestry residues, but also a green and rapid method for the synthesis of AgNPs to detect the toxic ion Hg(2+) selectively and sensitively.

  15. Activation properties of Ag+-ion conduction in bulk amorphous AgI: estimation from extrapolation of the AgI composition dependence in AgI Ag2O P2O5 glasses

    NASA Astrophysics Data System (ADS)

    Hanaya, M.; Hatate, A.; Oguni, M.

    2003-06-01

    AgI-based fast-ion conducting glasses with very high AgI compositions from the (AgI)x(AgPO3)1-x, (AgI)x(Ag2PO3.5)1-x, and (AgI)x(Ag3PO4)1-x systems were prepared successfully by using a rapid-press quenching and a twin-roller quenching method. The ac dielectric measurements showed common relaxation properties of Ag+-ion conduction in the glasses independently of the species of the glass network formers of AgPO3, Ag2PO3.5, and Ag3PO4, and the activation energies, Δɛa, for Ag+-ion conduction were observed to converge upon the same magnitude of ~26 kJ mol-1 at the AgI composition limit of x = 1. This indicates the formation of amorphous AgI regions in the glasses, and the value of Δɛa = 26 +/- 1 kJ mol-1 estimated at x = 1 was concluded to correspond to that for bulk amorphous AgI which has never been obtained experimentally.

  16. AGS 20th anniversary celebration

    SciTech Connect

    Baggett, N.V.

    1980-05-22

    On May 22, 1980, a symposium was held at Brookhaven to celebrate the 20th birthday of the AGS, to recall its beginnings, and to review major discoveries that have been made with its beams. The talks at the symposium are recorded in this volume.

  17. AGS experiments, 1988, 1989, 1990

    SciTech Connect

    Depken, J.C.

    1991-04-01

    This report contains: experimental areas layout; table of beam parameters and fluxes; experiment schedule as run''; experiment long range schedule; a listing of experiments by number; two-page summaries of each experiment begin here, also ordered by number; publications of AGS experiments; and list of experimenters.

  18. AGS experiments: 1985, 1986, 1987

    SciTech Connect

    Depken, J.C.

    1987-01-01

    This report contains: Experimental areas layout, table of beam parameters and fluxes, experiment schedule ''as run,'' experiment long range schedule, a listing of experiments by number, two-page summaries of each experiment, also ordered by number, and publications of AGS experiments, 1982-1987.

  19. 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.

  20. Pd@Ag Nanosheets in Combination with Amphotericin B Exert a Potent Anti-Cryptococcal Fungicidal Effect

    PubMed Central

    Wang, Guizhen; Fang, Wei; Ye, Chen; Hu, Hanhua; Fa, Zhenzong; Yi, Jiu; Liao, Wan-qing

    2016-01-01

    Silver nanoparticles have received considerable interest as new “nanoantibiotics” with the potential to kill drug-resistant microorganisms. Recently, a class of new core-shell nanostructures, Pd@Ag nanosheets (Pd@Ag NSs), were created using deposition techniques and demonstrated excellent inhibitory effects on various bacteria in vitro. In this study, we evaluated the antifungal activity of Pd@Ag NSs against common invasive fungal pathogens. Among these organisms, Cryptococcus neoformans complex species was most susceptible to Pd@Ag NSs, which exhibited potent antifungal activity against various molecular types or sources of cryptococcal strains including fluconazole-resistant isolates. The anticryptococcal activity of Pd@Ag NSs was significantly greater than fluconazole and similar to that of amphotericin B (AmB). At relatively high concentrations, Pd@Ag NSs exhibited fungicidal activity against Cryptococcus spp., which can likely be attributed to the disruption of cell integrity, intracellular protein synthesis, and energy metabolism. Intriguingly, Pd@Ag NSs also exhibited strong synergistic anti-cryptococcal fungicidal effects at low concentrations in combination with AmB but exhibited much better safety in erythrocytes than AmB, even at the minimal fungicidal concentration. Therefore, Pd@Ag NSs may be a promising adjunctive agent for treating cryptococcosis, and further investigation for clinical applications is required. PMID:27271376

  1. Comparative Study of Antimicrobial Activity of AgBr and Ag Nanoparticles (NPs)

    PubMed Central

    Suchomel, Petr; Kvitek, Libor; Panacek, Ales; Prucek, Robert; Hrbac, Jan; Vecerova, Renata; Zboril, Radek

    2015-01-01

    The diverse mechanism of antimicrobial activity of Ag and AgBr nanoparticles against gram-positive and gram-negative bacteria and also against several strains of candida was explored in this study. The AgBr nanoparticles (NPs) were prepared by simple precipitation of silver nitrate by potassium bromide in the presence of stabilizing polymers. The used polymers (PEG, PVP, PVA, and HEC) influence significantly the size of the prepared AgBr NPs dependently on the mode of interaction of polymer with Ag+ ions. Small NPs (diameter of about 60–70 nm) were formed in the presence of the polymer with low interaction as are PEG and HEC, the polymers which interact with Ag+ strongly produce nearly two times bigger NPs (120–130 nm). The prepared AgBr NPs were transformed to Ag NPs by the reduction using NaBH4. The sizes of the produced Ag NPs followed the same trends – the smallest NPs were produced in the presence of PEG and HEC polymers. Prepared AgBr and Ag NPs dispersions were tested for their biological activity. The obtained results of antimicrobial activity of AgBr and Ag NPs are discussed in terms of possible mechanism of the action of these NPs against tested microbial strains. The AgBr NPs are more effective against gram-negative bacteria and tested yeast strains while Ag NPs show the best antibacterial action against gram-positive bacteria strains. PMID:25781988

  2. Flashlamp-pumped Ho:Tm:Cr:LuAG laser

    NASA Technical Reports Server (NTRS)

    Jani, Mahendra G. (Inventor); Barnes, Norman P. (Inventor); Murray, Keith E. (Inventor); Kokta, Milan R. (Inventor)

    1997-01-01

    A room temperature solid-state laser is provided. A laser crystal is disposed in a laser cavity. The laser crystal has a LuAG host material doped with a concentration of about 0.35% Ho ions, about 5.57% Tm ions and at least about 1.01% Cr ions. A broadband energizing source such as a flashlamp is disposed transversely to the laser crystal to energize the Ho ions, Tm ions and Cr ions.

  3. Concentrating collectors

    SciTech Connect

    Not Available

    1981-06-01

    Selected specifications from sixteen concentrating collector manufacturers are tabulated. Eleven are linear parabolic trough collectors, and the others include slats, cylindrical trough, linear Fresnel lens, parabolic cylindrical Fresnel lens, and two point focus parabolic dish collectors. Also included is a brief discussion of the operating temperatures and other design considerations for concentrating collectors. (LEW)

  4. Characterization of spark plasma sintered Ag nanopowders.

    PubMed

    Fu, Y Q; Shearwood, C; Xu, B; Yu, L G; Khor, K A

    2010-03-19

    The low temperature sintering behaviour of nanocrystalline Ag powder (with an average size of 70 nm) was characterized. Using spark plasma sintering (SPS), the Ag nanopowders can be successfully sintered at low pressure for only 5 min without external heating, and the sintering density increases and porosity decreases significantly with increase in the sintering temperature. Nanoindentation has been used to characterize the SPS sintered Ag samples. The mechanisms of the low sintering temperature behaviour of the nano-Ag powder and the nanoscale mechanical performance have been discussed. Compression tests were also used to characterize the mechanical properties of the sintered Ag sample with a maximum strain up to 15%.

  5. Structural, optical and electronic properties of Ag-TiO2 nanocomposite thin film

    NASA Astrophysics Data System (ADS)

    Sharma, Himanshu; Singhal, R.; Siva Kumar, V. V.; Asokan, K.

    2016-12-01

    Nanocomposite thin films of Ag nanoparticles in TiO2 matrices were synthesised by RF magnetron co-sputtering and characterised by X-ray diffraction (XRD), Rutherford back scattering (RBS) spectrometry, UV-Vis, high-resolution transmission electron microscopy (HR-TEM) and X-ray photoelectron spectroscopy (XPS). The composition of Ag was varied from 0 to 45 at.%. The thickness and the concentrations of Ag in the nanocomposite thin film were revealed by RBS. XRD analysis confirmed that the TiO2 matrix is in anatase phase and shows change in phase with Ag concentration. The UV-visible absorption spectroscopy revealed low-intense and broad surface plasmon resonance (SPR) peak at 500 nm for the thin film with 33 at.% Ag content that was red-shifted to 525 nm with increasing its intensity for 45 at.% of Ag. The red shift in SPR peak understood by Maxwell-Garnett theory and explained further nonexistence of SPR by interparticle separation from HR-TEM images and crystallinity. This HR-TEM image analysis confirmed the formation of Ag nanoparticles, and average radii were 5, 12, 15 nm. The Tauc plot reveals reduction in band gap from 3.05 to 2.25 eV with increase in Ag content. Above results are understood based on the XPS analysis which shows a strong interaction between the Ag nanoparticle and TiO2. This decrease in band gap was advantageous to enhance the properties like photocatalytic and bioactivities through SPR.

  6. Transparent conductive PVP/AgNWs films for flexible organic light emitting diodes by spraying method

    NASA Astrophysics Data System (ADS)

    Hu, Jun-tao; Mei, Wen-juan; Ye, Kang-li; Wei, Qing-qing; Hu, Sheng

    2016-05-01

    In this study, a simple spraying method is used to prepare the transparent conductive films (TCFs) based on Ag nanowires (AgNWs). Polyvinylpyrrolidone (PVP) is introduced to modify the interface of substrate. The transmittance and bending performance are improved by optimizing the number of spraying times and the solution concentration and controlling the annealing time. The spraying times of 20, the concentration of 2 mg/mL and the annealing time of 10 min are chosen to fabricate the PVP/AgNWs films. The transmittance of PVP/AgNWs films is 53.4%—67.9% at 380—780 nm, and the sheet resistance is 30 Ω/□ which is equivalent to that of commercial indium tin oxide (ITO). During cyclic bending tests to 500 cycles with bending radius of 5 mm, the changes of resistivity are negligible. The performance of PVP/AgNW transparent electrodes has little change after being exposed to the normal environment for 1 000 h. The adhesion to polymeric substrate and the ability to endure bending stress in AgNWs network films are both significantly improved by introducing PVP. Spraying method makes AgNWs form a stratified structure on large-area polymer substrates, and the vacuum annealing method is used to weld the AgNWs together at junctions and substrates, which can improve the electrical conductivity. The experimental results indicate that PVP/AgNW transparent electrodes can be used as transparent conductive electrodes in flexible organic light emitting diodes (OLEDs).

  7. A mixture toxicity approach to predict the toxicity of Ag decorated ZnO nanomaterials.

    PubMed

    Azevedo, S L; Holz, T; Rodrigues, J; Monteiro, T; Costa, F M; Soares, A M V M; Loureiro, S

    2017-02-01

    Nanotechnology is a rising field and nanomaterials can now be found in a vast variety of products with different chemical compositions, sizes and shapes. New nanostructures combining different nanomaterials are being developed due to their enhancing characteristics when compared to nanomaterials alone. In the present study, the toxicity of a nanostructure composed by a ZnO nanomaterial with Ag nanomaterials on its surface (designated as ZnO/Ag nanostructure) was assessed using the model-organism Daphnia magna and its toxicity predicted based on the toxicity of the single components (Zn and Ag). For that ZnO and Ag nanomaterials as single components, along with its mixture prepared in the laboratory, were compared in terms of toxicity to ZnO/Ag nanostructures. Toxicity was assessed by immobilization and reproduction tests. A mixture toxicity approach was carried out using as starting point the conceptual model of Concentration Addition. The laboratory mixture of both nanomaterials showed that toxicity was dependent on the doses of ZnO and Ag used (immobilization) or presented a synergistic pattern (reproduction). The ZnO/Ag nanostructure toxicity prediction, based on the percentage of individual components, showed an increase in toxicity when compared to the expected (immobilization) and dependent on the concentration used (reproduction). This study demonstrates that the toxicity of the prepared mixture of ZnO and Ag and of the ZnO/Ag nanostructure cannot be predicted based on the toxicity of their components, highlighting the importance of taking into account the interaction between nanomaterials when assessing hazard and risk.

  8. Electrochemical Migration of Fine-Pitch Nanopaste Ag Interconnects

    NASA Astrophysics Data System (ADS)

    Tsou, Chia-Hung; Liu, Kai-Ning; Lin, Heng-Tien; Ouyang, Fan-Yi

    2016-12-01

    With the development of intelligent electronic products, usage of fine-pitch interconnects has become mainstream in high performance electronic devices. Electrochemical migration (ECM) of interconnects would be a serious reliability problem under temperature, humidity and biased voltage environments. In this study, ECM behavior of nanopaste Ag interconnects with pitch size from 20 μm to 50 μm was evaluated by thermal humidity bias (THB) and water drop (WD) tests with deionized water through in situ leakage current-versus-time (CVT) curve. The results indicate that the failure time of ECM in fine-pitch samples occurs within few seconds under WD testing and it increases with increasing pitch size. The microstructure examination indicated that intensive dendrite formation of Ag through the whole interface was found to bridge the two electrodes. In the THB test, the CVT curve exhibited two stages, incubation and ramp-up; failure time of ECM was about 173.7 min. In addition, intensive dendrite formation was observed only at the protrusion of the Ag interconnects due to the concentration of the electric field at the protrusion of the Ag interconnects.

  9. An Investigative Study on the Effect of Silver Nanoparticles on E.Coli K12 in Various Sodium Chloride Concentrations

    NASA Astrophysics Data System (ADS)

    Levard, C.; Mitra, S.; Badireddy, A.; Jew, A. D.; Brown, G. E.

    2011-12-01

    Engineered nanomaterials have had an increasing presence in consumer products. Consequently, their release in wastewater systems is believed to pose a viable threat to the environment. NPs are used for drug delivery devices, imaging agents, and consumer products like sunscreens, paints, and cosmetics. Among the major types of manufactured nanoparticles, silver nanoparticles (Ag-NPs) are currently the most widely used in the nanotechnology industry. These particles have unique antibacterial, antiviral, and antifungal properties and as a result, there is a growing concern about the environmental impact of released Ag nanoparticles, particularly their unintended impact on organisms and ecosystems. Even though the toxicity of Ag-NPs has been extensively studied, the environmental transformations that the Ag-NPs may experience once released in the environment have not been considered. These transformations can readily impact their properties and therefore their behavior in terms of reactivity and toxicity. For example, it is known that silver strongly react with Chloride (Cl), which is ubiquitous in natural waters. At a low Cl/Ag ratio, Cl may precipitate on the surface and partly inhibit dissolution. On the contrary, for a high Cl/Ag ratio, chloride may enhance dissolution and therefore toxicity since soluble Ag species are a main source of toxicity. In this context, the focus of this study is on understanding the toxicity of coated Ag-NPs at various concentrations (1ppb-100ppm) on E.Coli (K12) in deionized water and various sodium chloride concentrations that mimic natural conditions (.5, .1 and .01 M NaCl). Ag+ ions (100 ppm-1ppb) were also tested in these salt concentrations as a control. Samples were inoculated in bacteria and incubated for 24 hours. Based on this test, we inferred that increasing concentrations of Ag+ ions/ AgNps played a role in the inhibition of growth of E.Coli K12. A live-dead staining test has shown the correlation between inhibition of

  10. Synergistic effect of interfacial lattice Ag(+) and Ag(0) clusters in enhancing the photocatalytic performance of TiO2.

    PubMed

    Xu, Liming; Zhang, Dandan; Ming, Lufei; Jiao, Yanchao; Chen, Feng

    2014-09-28

    An interfacial lattice Ag(+) doped on TiO2 (Ag(+)/TiO2) was prepared by eluting Ag(0) clusters from a hydrothermally prepared Ag(0)/Ag(+)/TiO2 composite. An Ag(+)/TiO2@Ag(0) composite photocatalyst was subsequently obtained via a secondary Ag(0) clusters loading process to the Ag(+)/TiO2. The photocatalytic activity of Ag(+)/TiO2@Ag(0) was greatly improved compared to Ag(0)/Ag(+)/TiO2 and Ag(+)/TiO2. X-ray photoelectron spectroscopy (XPS) and cyclic voltammetry (CV) testing verified that Ag(+) ions occur as an interfacial lattice Ag(+) species in the composites. The enhancement effect of the interfacial lattice Ag(+) species is exhibited by the newly-formed Ag(+)/TiO2@Ag(0) as the interfacial lattice Ag(+) is fully exposed but not overlapped with the re-loaded Ag(0) clusters. The interfacial lattice Ag(+) ions and Ag(0) clusters are both responsible for the photocatalytic performance improvement of the catalyst, in either the photocatalytic degradation of methyl orange or photocurrent measurement.

  11. Enhancing the ag precipitation by surface mechanical attrition treatment on Cu-Ag alloys

    NASA Astrophysics Data System (ADS)

    Liu, Jiabin; Zhang, Lehao; Liu, Jingjing; Huang, Liuyi; Gu, Hao; Fang, Youtong; Meng, Liang; Zhang, Jian

    2016-09-01

    The influence of surface mechanical attrition treatment (SMAT) on Ag precipitation in Cu-Ag alloys was investigated. Cu-6 wt% Ag was melt, cold rolled and solution treated to be Cu-Ag solid solution, which was either aged at 250 and 350 °C for 24 h directly or SMAT-ed before aging. Ag precipitates were hard be found in the directly aged Cu-Ag sample while they were observed clearly in the SMAT-ed counterpart at 250 °C. The Ag precipitates formed in the surface layer by SMAT are much coarser than those in the un-SMAT-ed sample. It is obvious that the precipitating behavior of Ag was promoted significantly by SMAT approach. A large number of defects were generated by SMAT and they were acting as fast atomic diffusion channels that facilitated the atomic diffusion of Ag.

  12. Effect of nanomaterial and media physicochemical properties on Ag NM aggregation kinetics.

    PubMed

    Afshinnia, Kamelia; Sikder, Mithun; Cai, Bo; Baalousha, Mohammed

    2017-02-01

    Nanomaterial (NM) aggregation is a key process determining their environmental, fate behavior and effects. Nanomaterials are typically engineered to remain kinetically stable; however, in environmental and toxicological media, NMs are prone to aggregation. The aggregation kinetics of NM is typically quantified by measuring their attachment efficiency (α) and critical coagulation concentration (CCC). Several studies measured α and CCC for Ag NMs with a major focus on investigating the effects of ionic strength, ion valency and natural organic matter, with few studies investigating other environmental factors such as light and dissolved oxygen and none investigating the effect of particle size, buffer type and concentration, or surface coverage by capping agent. A survey of recent research articles reporting CCC values for Ag NMs reveals substantial variation in experimental conditions and particle stability with CCC values of monovalent and divalent counterions covering a wide range (ca. 25 to infinity for monovalent counterions and 1.6 to infinity for divalent counterions). Here, we rationalize the differences in the CCC values for Ag NMs based on the variability in the experimental conditions, which includes NM and medium physicochemical properties. Capping agents determines NM stability mechanism with citrate, sodium dodecyl sulfate (SDS), and alginate stabilizing NM by electrostatic mechanism; whereas polyvinylpyrrolidone (PVP), casein, dextrin, tween, branched polyethyleneimine (BPEI), and Gum Arabic stabilizing NMs by steric mechanisms. The CCC values for Ag NMs with different capping agents follow the order citrate∼alginate∼SDSAg NMs, the CCC increases with the decrease in NM size and buffer concentration and decreases with light irradiation. For sterically stabilized PVP-Ag NMs, the CCC increases with the coating concentration/surface coverage and completely

  13. Potential nanosilver impact on anaerobic digestion at moderate silver concentrations.

    PubMed

    Yang, Yu; Chen, Qian; Wall, Judy D; Hu, Zhiqiang

    2012-03-15

    Silver nanoparticles (AgNPs, nanosilver) entering the sewers and wastewater treatment plants (WWTPs) are mostly accumulated in the sludge. In this study, we determined the impact of AgNPs on anaerobic glucose degradation, sludge digestion and methanogenic assemblages. At ambient (22 °C) and mesophilic temperatures (37 °C), there was no significant difference in biogas and methane production between the sludge treated with AgNPs at the concentrations up to 40 mg Ag/L (13.2 g silver/Kg biomass COD) and the control. In these anaerobic digestion samples, acetate and propionic acid were the only detectable volatile fatty acids (VFAs) and they were depleted in 3 days. On the other hand, more than 90% of AgNPs was removed from the liquid phase and associated with the sludge while almost no silver ions were released from AgNPs under anaerobic conditions. Quantitative PCR results indicated that Methanosaeta and Methanomicrobiales were the dominant methanogens, and the methanogenic diversity and population remained largely unchanged after nanosilver exposure and anaerobic digestion. The results suggest that AgNPs at moderate concentrations (e.g., ≤40 mg/L) have negligible impact on anaerobic digestion and methanogenic assemblages because of little to no silver ion release.

  14. Green Synthesis of AgNPs Stabilized with biowaste and their antimicrobial activities

    PubMed Central

    Jasuja, Nakuleshwar Dut; Gupta, Deepak Kumar; Reza, Mohtashim; Joshi, Suresh C.

    2014-01-01

    In the present study, rapid reduction and stabilization of Ag+ ions with different NaOH molar concentration (0.5 mM, 1.0 mM and 1.5 mM) has been carried out in the aqueous solution of silver nitrate by the bio waste peel extract of P.granatum. Generally, chemical methods used for the synthesis of AgNPs are quite toxic, flammable and have adverse effect in medical application but green synthesis is a better option due to eco-friendliness, non-toxicity and safe for human. Stable AgNPs were synthesized by treating 90 mL aqueous solution of 2 mM AgNO3 with the 5 mL plant peels extract (0.4% w/v) at different NaOH concentration (5 mL). The synthesized AgNPs were characterized by UV-Vis spectroscopy, TEM and SEM. Further, antimicrobial activities of AgNPs were performed on Gram positive i.e. Staphylococcus aureus, Bacillus subtilius and Gram negative i.e. E. coli, Pseudomonas aeruginosa bacteria. The AgNPs synthesized at 1.5 mM NaOH concentration had shown maximum zone of inhibition (ZOI) i.e. 49 ± 0.64 in E. coli, whereas Pseudomonas aeruginosa, Staphylococcus aureus and Bacillus subtilius had shown 40 ± 0.29 mm, 28 ± 0.13 and 42 ± 0.49 mm ZOI respectively. The MIC value of 30 μg/mL observed for E. coli Whereas, Staphylococcus aureus, Bacillus subtilius and Pseudomonas aeruginosa had shown 45 μg/mL, 38 μg/mL, 35 μg/mL respectively. The study revealed that AgNPs had shown significant antimicrobial activity as compared to Streptomycin. PMID:25763037

  15. Concentrating Radioactivity

    ERIC Educational Resources Information Center

    Herrmann, Richard A.

    1974-01-01

    By concentrating radioactivity contained on luminous dials, a teacher can make a high reading source for classroom experiments on radiation. The preparation of the source and its uses are described. (DT)

  16. Bacterial response to a continuous long-term exposure of silver nanoparticles at sub-ppm silver concentrations in a membrane bioreactor activated sludge system.

    PubMed

    Zhang, Chiqian; Liang, Zhihua; Hu, Zhiqiang

    2014-03-01

    Silver nanoparticles (nanosilver or AgNPs) have excellent antimicrobial properties. Because of their increasing use, there is a concern about the potential impact of AgNPs in wastewater treatment systems. This study investigated the long-term effects of AgNPs (continuous loading for more than 60 days) on membrane bioreactor (MBR) activated sludge performance. At the influent AgNP concentration of 0.10 mg Ag/L, there was no significant difference in effluent water quality or bacterial activities before and after AgNP exposure. Nitrifying bacterial community structure was relatively stable before and after the long-term AgNP loading. Both ammonia-oxidizing bacteria (AOB) Nitrosomonas spp. and Nitrosospira spp. were present while Nitrospira spp. was the dominant nitrite-oxidizing bacterial species throughout this study. Abundance of silver resistance gene silE in the MBR, however, increased by 50-fold 41 days after the AgNP exposure, and then decreased with continuous AgNP exposure. The long-term nanosilver exposure did not change the membrane fouling rate although extracellular polymeric substances (EPS) concentration increased significantly after nanosilver dosing. The results suggest that AgNPs at the influent concentrations of 0.10 mg/L and below have almost no impact on activated sludge wastewater treatment performance, as activated sludge can effectively reduce nanosilver toxicity by adsorbing or precipitating AgNPs and silver ions (Ag(+)) released from the dissolution of AgNPs.

  17. Structure and electronic behavior of 26-atom Cu-Ag and Cu-Au nanoalloys

    NASA Astrophysics Data System (ADS)

    Guzmán-Ramírez, Gregorio; Robles, Juvencio; Aguilera-Granja, Faustino

    2016-09-01

    We hereby present a density functional theory (DFT) study of the structural, energetic, and electronic properties of the binary clusters Cu n X26- n (with X = Ag and Au). Our electronic calculations were performed with the DFT package GAUSSIAN 09, and we chose the BPW91 exchange correlation functional in combination with an effective core potential LANL2DZ basis set as our level of theory. We find that in the case of these clusters and in a completely different way - as compared to the bulk chemical order observed in both alloys CuAg (segregation) and CuAu (ordering) -, for small n both Ag and Au clusters exhibit a similar chemical order, finding the Cu atoms in the center of the cluster with the tendency to form core shell structures. On the other hand, for large n values the Ag and Au atoms tend to occupy surface positions forming separated surface islands that keep the two metal atoms separated as long as the concentration allows it. Concerning the structural properties, a clear increase in the interatomic distance of the Ag-Ag and Au-Au surface pairs is observed, particularly in the equiatomic region. In conclusion, both nanoalloys CuAg and CuAu behave quite similarly in contrast to their respective bulk cases.

  18. Tailoring the structural and optical properties of TiN thin films by Ag ion implantation

    NASA Astrophysics Data System (ADS)

    Popović, M.; Novaković, M.; Rakočević, Z.; Bibić, N.

    2016-12-01

    Titanium nitride (TiN) thin films thickness of ∼260 nm prepared by dc reactive sputtering were irradiated with 200 keV silver (Ag) ions to the fluences ranging from 5 × 1015 ions/cm2 to 20 × 1015 ions/cm2. After implantation TiN layers were annealed 2 h at 700 °C in a vacuum. Ion irradiation-induced microstructural changes were examined by using Rutherford backscattering spectrometry, X-ray diffraction and transmission electron microscopy, while the surface topography was observed using atomic force microscopy. Spectroscopic ellipsometry was employed to get insights on the optical and electronic properties of TiN films with respect to their microstructure. The results showed that the irradiations lead to deformation of the lattice, increasing disorder and formation of new Ag phase. The optical results demonstrate the contribution of surface plasmon resonace (SPR) of Ag particles. SPR position shifted in the range of 354.3-476.9 nm when Ag ion fluence varied from 5 × 1015 ions/cm2 to 20 × 1015 ions/cm2. Shift in peak wavelength shows dependence on Ag particles concentration, suggesting that interaction between Ag particles dominate the surface plasmon resonance effect. Presence of Ag as second metal in the layer leads to overall decrease of optical resistivity of TiN.

  19. AgBr/nanoAlMCM-41 visible light photocatalyst for degradation of methylene blue dye.

    PubMed

    Pourahmad, A; Sohrabnezhad, Sh; Kashefian, E

    2010-12-01

    A novel photocatalytic material was synthesized by dispersion of AgBr in nanoAlMCM-41 material. The AgBr/nanoAlMCM-41 sample shows strong absorption in the visible region because of the plasmon resonance of Ag nanoparticles in AgBr/nanoAlMCM-41. The catalysts were characterized using XRD (X-ray diffraction), UV-visible diffused reflectance spectra (UV-vis DRS) and scanning electron microscopy (SEM). The photocatalytic activity and stability of the synthesized catalysts were evaluated for methylene blue (MB) degradation in aqueous solution in the presence of 200 W tungsten filament Philips lamp. Several parameters were examined, catalyst amount, pH and initial concentration of MB, AgBr loading. The effect of dosage of photocatalyst was studied in the range 0.05-1.00 g/L. It was seen that 0.1 g/L of photocatalyst is an optimum value for the dosage of photocatalyst. The support size was obtained about 9-100 nm. In the same way, the average size of AgBr nanoparticles was about 10nm before visible radiation. After visible radiation the average size of AgBr nanoparticles was about 25 nm.

  20. Water-soluble Ag(2)S quantum dots for near-infrared fluorescence imaging in vivo.

    PubMed

    Jiang, Peng; Zhu, Chun-Nan; Zhang, Zhi-Ling; Tian, Zhi-Quan; Pang, Dai-Wen

    2012-07-01

    A one-step method for synthesizing water-soluble Ag(2)S quantum dots terminated with carboxylic acid group has been reported. The crystal structure and surface of the prepared Ag(2)S quantum dots were characterized. The prepared Ag(2)S quantum dots exhibited bright photoluminescence and excellent photostabilities. The photoluminescence emissions could be tuned from visible region to near-infrared (NIR) region (from 510 nm to 1221 nm). Ultra-small sized Ag(2)S nanoclusters were synthesized with high initial monomer concentration in the current system. The in vivo imaging experiments of nude mice showed that the NIR photoluminescence of the prepared Ag(2)S quantum dots could penetrate the body of mice. Compared to the conventional NIR quantum dots, the Ag(2)S quantum dots don't contain toxic elements to body (such as Cd and Pb), thus, the prepared Ag(2)S quantum dots could serve as excellent NIR optical imaging probes and would open the opportunity to study nanodiagnostics and imaging in vivo.

  1. Optical properties of a-C:H thin films modified by Ti and Ag

    NASA Astrophysics Data System (ADS)

    Prikhodko, Oleg Yu.; Mikhailova, Svetlana L.; Mukhametkarimov, Ershan C.; Maksimova, Suyumbika Ya.; Manabaev, Nurlan K.; Dauthan, Kuanysh

    2016-09-01

    Structure and optical properties of amorphous diamond-like carbon (a-C: H) thin films modified with Ag, Ti and Ag + Ti metal impurities are studied. The films were prepared by ion-plasma magnetron sputtering of combined polycrystalline graphite and metal target in the mixture of Ar and CH4 gases. AFM, SEM and TEM methods show that a-C:H<Ag+Ti> films are heterogeneous, nanostructured and characterized by the presence of silver nanoclusters on the surface sized 60 nm and both Ti and Ag nanoclusters with a mean size (2 ÷ 3) nm in the bulk of films. It was found that in a- C:H<Ag+Ti> films as well as in a-C:H<Ag> films plasma resonance absorption due to excitation of surface plasmons in silver nanoclusters in the visible region of spectrum takes place. Intensity of the resonance absorption in the a- C:H<Ag+Ti> films increases with increase in concentration of silver. The results are important for produce of nanomaterials with nonlinear optical properties based on the amorphous diamond-like carbon films containing metal nanoclusters.

  2. Oxidative degradation of acid orange 7 using Ag-doped zinc oxide thin films.

    PubMed

    Shinde, S S; Bhosale, C H; Rajpure, K Y

    2012-12-05

    Ag-doped ZnO thin films with preferred c-axis orientation along (002) have been prepared by spray pyrolysis technique in aqueous medium on to the corning glass substrates. The effect of Ag-doping on to the photoelectrochemical, structural, morphological, optical, luminescence, electrical and thermal properties has been investigated. XRD and Raman study indicates that the films have hexagonal (wurtzite) crystal structure. The effect of Ag loading on the photocatalytic activity of Ag-doped ZnO in the degradation of azo dye is studied and results are compared with pure ZnO. The results show that the rate of degradation of azo dye over Ag-doped ZnO is much higher as compared to pure ZnO. Ag doping in ZnO is highly effective and can significantly enhance the photocatalytic degradation and mineralization of azo dye. The enhancement of photocatalytic activity of Ag-doped ZnO thin films is mainly due to their smaller crystallite size and capability for reducing the electron-hole pair recombination. Kinetic parameters have been investigated in terms of a first order rate equation. The rate constant (-k) for this heterogeneous photocatalysis is evaluated as a function of the initial concentration of original species. Substantial reduction in azo dye is achieved as analyzed from COD and TOC studies.

  3. Fabrication LSPR sensor chip of Ag NPs and their biosensor application based on interparticle coupling

    NASA Astrophysics Data System (ADS)

    Ghodselahi, T.; Neishaboorynejad, T.; Arsalani, S.

    2015-07-01

    We introduce a simple method to synthesize localized surface plasmon resonance (LSPR) sensor chip of Ag NPs on the hydrogenated amorphous carbon by co-deposition of RF-Sputtering and RF-PECVD. The X-ray photoelectron spectroscopy revealed the content of Ag and C atoms. X-ray diffraction profile and atomic force microscopy indicate that the Ag NPs have fcc crystal structure and spherical shape and by increasing deposition time, particle sizes do not vary and only Ag NPs aggregation occurs, resulting in LSPR wavelength shift. Firstly, by increasing Ag NPs content, in-plan interparticles coupling is dominant and causes redshift in LSPR. At the early stage of agglomeration, out-plane coupling occurs and in-plane coupling is reduced, resulting a blueshift in the LSPR. By further increasing of Ag NPs content, agglomeration is completed on the substrate and in-plan coupling rises, resulting significant redshift in the LSPR. Results were used to implement biosensor application of chips. Detection of DNA primer at fM concentration was achieved based on breaking interparticles coupling of Ag NPs. A significant wavelength shift sensitivity of 30 nm and a short response time of 30 min were obtained, where both of these are prerequisite for biosensor applications.

  4. Possible mechanism for the inhibition of gastric (H+ + K+)-adenosine triphosphatase by the proton pump inhibitor AG-1749

    SciTech Connect

    Nagaya, H.; Satoh, H.; Kubo, K.; Maki, Y.

    1989-02-01

    Mechanisms related to the inhibition of (H+ + K+)-adenosine triphosphatase (ATPase) by 2-(((3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl)methyl) sulfinyl)-1H-benzimidazole (AG-1749) were studied using canine gastric microsomes. AG-1749 (1-100 microM) inhibited the K+-stimulated ATP hydrolysis and vesicular accumulation of H+. AG-1749 bound to the microsomes concentration-dependently and decreased the number of free SH groups; the binding correlating with the enzyme inhibition. Both the binding and inhibition were antagonized by dithiothreitol. N-ethylmaleimide inhibited the (H+ + K+)-ATPase and decreased the binding of (/sup 14/C)AG-1749 to the microsomes. The inhibitory effect of AG-1749 gradually increased with incubation time, and was enhanced by lowering the pH. AG-2000 and AG-1812, acid-induced rearrangement products of AG-1749, inhibited (H+ + K+)-ATPase potently, rapidly and independently of pH; the inhibition was antagonized by dithiothreitol. We propose that AG-1749 is transformed into its active forms within the acidic compartment of the parietal cells and that the active compounds inhibit (H+ + K+)-ATPase activity by reacting with the SH groups of the enzyme.

  5. Photocatalytic activity of Ag/ZnO core–shell nanoparticles with shell thickness as controlling parameter under green environment

    NASA Astrophysics Data System (ADS)

    Rajbongshi, Himanshu; Bhattacharjee, Suparna; Datta, Pranayee

    2017-02-01

    Plasmonic Ag/ZnO core–shell nanoparticles have been synthesized via a simple two-step wet chemical method for application in Photocatalysis. The morphology, size, crystal structure, composition and optical properties of the nanoparticles are investigated by x-ray diffraction, transmission electron microscopy (TEM), FTIR spectroscopy, ultraviolet–visible (UV–Vis) absorption spectroscopy and photoluminescence (PL) spectroscopy. The shell thicknesses are varied by varying the concentration of zinc nitrate hexa-hydrate and triethanolamine. The ZnO shell coating over Ag core enhances the charge separation, whereas the larger shell thickness and increased refractive index of surrounding medium cause red shifts of surface Plasmon resonance (SPR) peak of Ag core. The photoluminescence (PL) spectra of Ag/ZnO core–shell show that the larger shell thickness quenches the near band edge UV emission of ZnO. The electrochemical impedance spectra (EIS) i.e. Nyquist plots also confirm the higher charge transfer efficiency of the Ag/ZnO core–shell nanoparticles. The Photocatalytic activities of Ag/ZnO core–shell nanoparticles are investigated by the degradation of methylene blue (MB) dye under direct sunlight irradiation. Compared to pure ZnO nanoparticles (NPs), Ag/ZnO core–shell NPs display efficient sunlight plasmonic photocatalytic activity because of the influence of SPR of Ag core and the electron sink effect. The photocatalytic activity of Ag/ZnO core–shell NPs is found to be enhanced with increase in shell thickness.

  6. Ag@Au core-shell dendrites: a stable, reusable and sensitive surface enhanced Raman scattering substrate

    PubMed Central

    Jun Yin, Hong; Yang Chen, Zhao; Mei Zhao, Yong; Yang Lv, Ming; An Shi, Chun; Long Wu, Zheng; Zhang, Xin; Liu, Luo; Li Wang, Ming; Jun Xu, Hai

    2015-01-01

    Surface enhanced Raman scattering (SERS) substrate based on fabricated Ag@Au core-shell dendrite was achieved. Ag dendrites were grown on Si wafer by the hydrothermal corrosion method and Au nanofilm on the surface of Ag dendritic nanostructure was then fabricated by chemical reduction. With the help of sodium borohydride in water, Au surface absorbates such as thiophene, adenine, rhodamine, small anions (Br– and I–), and a polymer (PVP, poly(N-vinylpyrrolidone)) can be completely and rapidly removed. After four repeatable experiments, the substrate SERS function did not decrease at all, indicating that the Ag@Au dendrite should be of great significance to SERS application because it can save much resource. Six-month-duration stability tests showed that the Ag@Au core-shell dendrite substrate is much more stable than the Ag dendrite substrates. We have also experimented on fast detection of Cd2+ at 10−8  M concentration by decorating single-stranded DNA containing adenine and guanine bases on the surface of this Ag@Au dendrite. Finite-difference time-domain simulations were carried out to investigate the influence of Au nanolayer on Ag dendrites, which showed that the local electric fields and enhancement factor are hardly affected when a 4 nm Au nanolayer is coated on Ag dendrite surface. PMID:26412773

  7. Polymorphism of LiAg

    NASA Astrophysics Data System (ADS)

    Pavlyuk, V. V.; Dmytriv, G. S.; Tarasiuk, I. I.; Chumak, I. V.; Pauly, H.; Ehrenberg, H.

    2010-02-01

    A phase transition from the cubic CsCl-type structure (Pm-3m space group) into a tetragonal UPb-type structure (I4 1/amd) is observed for the LiAg binary compound at ambient conditions. The crystal structure of the tetragonal modification of the LiAg binary compound was solved by direct methods in SHELXS on the base of structure factors which were extracted from a powder diffraction pattern and refined by SHELXL and the Rietveld method ( a = 3.9605(1), c = 8.2825(2) Å, Bragg R-factor = 4.81, Rf-factor = 4.87). Elevated temperatures and/or a small Li-excess versus the equimolar composition favour the cubic structure whereas ambient and lower temperatures and/or a small Li-deficiency stabilize the tetragonal structure. This reconstructive transition is reversible but proceeds slowly.

  8. Graphene oxide-Ag nanoparticles-pyramidal silicon hybrid system for homogeneous, long-term stable and sensitive SERS activity

    NASA Astrophysics Data System (ADS)

    Guo, Jia; Xu, Shicai; Liu, Xiaoyun; Li, Zhe; Hu, Litao; Li, Zhen; Chen, Peixi; Ma, Yong; Jiang, Shouzhen; Ning, Tingyin

    2017-02-01

    In our work, few layers graphene oxide (GO) were directly synthesized on Ag nanoparticles (AgNPs) by spin-coating method to fabricate a GO-AgNPs hybrid structure on a pyramidal silicon (PSi) substrate for surface-enhanced Raman scattering (SERS). The GO-AgNPs-PSi substrate showed excellent Raman enhancement effect, the minimum detected concentration for Rhodamine 6G (R6G) can reach 10-12 M, which is one order of magnitude lower than the AgNPs-PSi substrate and two order of magnitude lower than the GO-AgNPs-flat-Si substrate. The linear fit calibration curve with error bars is presented and the value of R2 of 612 and 773 cm-1 can reach 0.986 and 0.980, respectively. The excellent linear response between the Raman intensity and R6G concentrations prove that the prepared GO-AgNPs-PSi substrates can serve as good SERS substrate for molecule detection. The maximum deviations of SERS intensities from 20 positions of the GO-AgNPs-PSi substrate are less than 8%, revealing the high homogeneity of the SERS substrate. The excellent homogeneity of the enhanced Raman signals can be attributed to well-separated pyramid arrays of PSi, the uniform morphology of AgNPs and multi-functions of GO layer. Besides, the uniform GO film can effectively protect AgNPs from oxidation and endow the hybrid system a good stability and long lifetime. This GO-AgNPs-PSi substrate may provide a new way toward practical applications for the ultrasensitive and label-free SERS detection in areas of medicine, food safety and biotechnology.

  9. An efficient visible-light photocatalyst prepared by modifying AgBr particles with a small amount of activated carbon

    SciTech Connect

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

    2016-04-15

    Highlights: • An efficient visible-light photocatalyst was prepared by modifying AgBr particles. • A small amount of activated carbon was used to modify AgBr particles. • The modified AgBr exhibited improved visible-light photocatalytic performances. - Abstract: An efficient visible-light photocatalyst was successfully prepared by modifying AgBr particles with a small amount of activated carbon (AC) via a simple chemical precipitation approach. The AC/AgBr composite was characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, UV–vis diffuse reflection spectroscopy, photoluminescence spectroscopy, electrochemical impedance spectroscopy. The photocatalytic performances of the AC/AgBr composite were investigated by evaluating photodegradation of methyl orange (MO) and phenol under visible light irradiation, and the effects of the AC content in the composite, concentrations of AC/AgBr composite and MO, carrier scavengers on MO photodegradation rate were systematically investigated. The results indicated that the modification of AC can hardly change the crystalline and crystal size of AgBr particles, while significantly improve their specific surface areas, visible-light absorption and separation efficiency of photogenerated electron–hole pairs. Compared with pure AgBr, the AC/AgBr composite exhibited drastically enhanced visible-light photocatalytic activity and stability. The photogenerated electrons and holes, hydroxyl radicals are responsible to the photodegradation of organic pollutants, and the photogenerated holes are the main active species. On the basis of the results and the properties of AC and AgBr, the visible-light photocatalytic mechanism of the AC/AgBr composite was discussed.

  10. The importance of evaluating the real metal concentration in nanoparticles post-synthesis for their applications: A case-study using silver nanoparticles.

    PubMed

    Galazzi, Rodrigo Moretto; Santos, Elias de Barros; Caurin, Tatiana; Pessôa, Gustavo de Souza; Mazali, Italo Odone; Arruda, Marco Auréli Zezzio

    2016-01-01

    To determine whether the effect observed in a study is related to the nanoparticle only or to their synergic effect with the "free" metal ions, the real concentration of silver (104±8 and 100±2 mg L(-1)) after AgNP synthesis is obtained through ICP-MS and ICP OES in the solution after the AgNP synthesis and in different fractions after centrifugation (at 8100 g for 40 min). From the resuspension of the AgNP contained in the solution (AgNP-total) after synthesis (AgNP-res), concentrations of 49±3 and 51±3 mg L(-1) are found and concentrations of 50±7 and 47±2 mg L(-1) in the supernatant (Ag-sup) are found using ICP-MS and ICP OES respectively. The characterization of AgNP-total, AgNP-res and Ag-sup is performed by HRTEM and UV-vis, corroborating the results in terms of Ag determination, and indicates that half of the total silver concentration is in the AgNP form and that the other half is in the "free" silver form. The results of the stability test of the NPs indicate a 7% decrease in Ag as NP three months after its synthesis.

  11. Mixed messages from benthic microbial communities exposed to nanoparticulate and ionic silver: 3D structure picks up nano-specific effects, while EPS and traditional endpoints indicate a concentration-dependent impact of silver ions.

    PubMed

    Kroll, Alexandra; Matzke, Marianne; Rybicki, Marcus; Obert-Rauser, Patrick; Burkart, Corinna; Jurkschat, Kerstin; Verweij, Rudo; Sgier, Linn; Jungmann, Dirk; Backhaus, Thomas; Svendsen, Claus

    2016-03-01

    Silver nanoparticles (AgNP) are currently defined as emerging pollutants in surface water ecosystems. Whether the toxic effects of AgNP towards freshwater organisms are fully explainable by the release of ionic silver (Ag(+)) has not been conclusively elucidated. Long-term effects to benthic microbial communities (periphyton) that provide essential functions in stream ecosystems are unknown. The effects of exposure of periphyton to 2 and 20 μg/L Ag(+) (AgNO3) and AgNP (polyvinylpyrrolidone stabilised) were investigated in artificial indoor streams. The extracellular polymeric substances (EPS) and 3D biofilm structure, biomass, algae species, Ag concentrations in the water phase and bioassociated Ag were analysed. A strong decrease in total Ag was observed within 4 days. Bioassociated Ag was proportional to dissolved Ag indicating a rate limitation by diffusion across the diffusive boundary layer. Two micrograms per liter of AgNO3 or AgNP did not induce significant effects despite detectable bioassociation of Ag. The 20-μg/L AgNO3 affected green algae and diatom communities, biomass and the ratio of polysaccharides to proteins in EPS. The 20-μg/L AgNO3 and AgNP decreased biofilm volume to about 50 %, while the decrease of biomass was lower in 20 μg/L AgNP samples than the 20-μg/L AgNO3 indicating a compaction of the NP-exposed biofilms. Roughness coefficients were lower in 20 μg/L AgNP-treated samples. The more traditional endpoints (biomass and diversity) indicated silver ion concentration-dependent effects, while the newly introduced parameters (3D structure and EPS) indicated both silver ion concentration-dependent effects and effects related to the silver species applied.

  12. Data Concentrator

    NASA Technical Reports Server (NTRS)

    Willett, Mike

    2015-01-01

    Orbital Research, Inc., developed, built, and tested three high-temperature components for use in the design of a data concentrator module in distributed turbine engine control. The concentrator receives analog and digital signals related to turbine engine control and communicates with a full authority digital engine control (FADEC) or high-level command processor. This data concentrator follows the Distributed Engine Controls Working Group (DECWG) roadmap for turbine engine distributed controls communication development that operates at temperatures at least up to 225 C. In Phase I, Orbital Research developed detailed specifications for each component needed for the system and defined the total system specifications. This entailed a combination of system design, compiling existing component specifications, laboratory testing, and simulation. The results showed the feasibility of the data concentrator. Phase II of this project focused on three key objectives. The first objective was to update the data concentrator design modifications from DECWG and prime contractors. Secondly, the project defined requirements for the three new high-temperature, application-specific integrated circuits (ASICs): one-time programmable (OTP), transient voltage suppression (TVS), and 3.3V. Finally, the project validated each design by testing over temperature and under load.

  13. Capacitive deionization of seawater effected by nano Ag and Ag@C on graphene.

    PubMed

    Cai, P-F; Su, C-J; Chang, W-T; Chang, F-C; Peng, C-Y; Sun, I-W; Wei, Y-L; Jou, C-J; Wang, H Paul

    2014-08-30

    Drinking water shortage has become worse in recent decades. A new capacitive deionization (CDI) method for increasing water supplies through the effective desalination of seawater has been developed. Silver as nano Ag and Ag@C which was prepared by carbonization of the Ag(+)-β-cyclodextrin complex at 573 K for 30 min can add the antimicrobial function into the CDI process. The Ag@C and Ag nanoparticles dispersed on reduced graphene oxide (Ag@C/rGO and nano Ag/rGO) were used as the CDI electrodes. The nano Ag/rGO and Ag@C/rGO electrodes can reduce the charging resistant, and enhance the electrosorption capability. Better CDI efficiencies with the nano Ag/rGO and Ag@C/rGO electrodes can therefore be obtained. When reversed the voltage, the electrodes can be recovered up to 90% within 5 min. This work presents the feasibility for the nano Ag and Ag@C on rGO electrodes applied in CDI process to produce drinking water from seawater or saline water.

  14. Detection of Ag+ using graphite carbon nitride nanosheets based on fluorescence quenching

    NASA Astrophysics Data System (ADS)

    Bian, Wei; Zhang, Hao; Yu, Qing; Shi, Meijuan; Shuang, Shaomin; Cai, Zongwei; Choi, Martin M. F.

    2016-12-01

    The graphite carbon nitride (g-C3N4) nanosheets were synthesized and applied for the detection of Ag+ ion in aqueous solutions. Transmission electron microscopy, Fourier infrared spectroscopy, x-ray diffraction, ultraviolet/visible and photoluminescence spectroscopy were used for characterization of g-C3N4 nanosheets. The fluorescence intensity of g-C3N4 nanosheets decreases with the increase in the concentration of Ag+. The fluorescence probe can be applied for detection of Ag+. The results show that it has high selectivity to Ag+ and exhibits a good linearity over the concentration range 0.020-2.0 μM with a detection limit of 27 nM. Most cations do not have any interference on the detection of Ag+. The quenching process is assessed and discussed. Finally, the g-C3N4 nanosheets have been successfully used for the detection of Ag+ in real water samples. The recoveries of spiked water samples are > 97%.

  15. Silver nanoparticles (AgNPs) biosynthesized using pod extract of Cola nitida enhances antioxidant activity and phytochemical composition of Amaranthus caudatus Linn

    NASA Astrophysics Data System (ADS)

    Azeez, Luqmon; Lateef, Agbaje; Adebisi, Segun A.

    2017-02-01

    This study investigates the influence of different concentrations of AgNPs biologically synthesized using pod extract of Cola nitida on antioxidant activity, phenolic contents, flavonoid contents and compositions of Amaranthus caudatus L. AgNPs of 25, 50, 75, 100 and 150 ppm were utilized in growing A. caudatus while water was used as control. Delayed germination for two days was observed for A. caudatus grown with 150 ppm of AgNPs, while others showed no difference. There were 43.3, 38.7, 26.7 and 6.48% improvements in the 2,2-diphenyl-1-picrylhydrazyl (DPPH) antioxidant activity of A. caudatus grown with 25, 50, 75 and 100 ppm of AgNPs, respectively, compared to control. Antioxidant activity of A. caudatus grown with AgNPs reduced with increase in the concentrations of AgNPs. A. caudatus grown with 50 ppm of AgNPs was the most potent with the least IC50 of 0.67 mg/ml. Significant improvements obtained for phenolic and flavonoid contents grown with AgNPs were concentration dependent. Enhancements of 21.9, 68.19, and 1.98% in phenolic contents were achieved in treatments with 25, 50 and 75 ppm AgNPs, respectively, while 32.58, 35.80, and 7.20% improvement in flavonoids were obtained for 25, 50 and 100 ppm treatments, respectively. Kaempferol and quercetin were the most abundant flavonoids in A. caudatus treated with 50 ppm of AgNPs, showing the highest flavonoid composition. This further confirms A. caudatus grown with 50 ppm of AgNPs as the most potent. This study has shown that concentration-dependent AgNPs can be used to boost antioxidant activity and phytochemical contents of vegetables.

  16. Silver nanoparticles (AgNPs) biosynthesized using pod extract of Cola nitida enhances antioxidant activity and phytochemical composition of Amaranthus caudatus Linn

    NASA Astrophysics Data System (ADS)

    Azeez, Luqmon; Lateef, Agbaje; Adebisi, Segun A.

    2017-01-01

    This study investigates the influence of different concentrations of AgNPs biologically synthesized using pod extract of Cola nitida on antioxidant activity, phenolic contents, flavonoid contents and compositions of Amaranthus caudatus L. AgNPs of 25, 50, 75, 100 and 150 ppm were utilized in growing A. caudatus while water was used as control. Delayed germination for two days was observed for A. caudatus grown with 150 ppm of AgNPs, while others showed no difference. There were 43.3, 38.7, 26.7 and 6.48% improvements in the 2,2-diphenyl-1-picrylhydrazyl (DPPH) antioxidant activity of A. caudatus grown with 25, 50, 75 and 100 ppm of AgNPs, respectively, compared to control. Antioxidant activity of A. caudatus grown with AgNPs reduced with increase in the concentrations of AgNPs. A. caudatus grown with 50 ppm of AgNPs was the most potent with the least IC50 of 0.67 mg/ml. Significant improvements obtained for phenolic and flavonoid contents grown with AgNPs were concentration dependent. Enhancements of 21.9, 68.19, and 1.98% in phenolic contents were achieved in treatments with 25, 50 and 75 ppm AgNPs, respectively, while 32.58, 35.80, and 7.20% improvement in flavonoids were obtained for 25, 50 and 100 ppm treatments, respectively. Kaempferol and quercetin were the most abundant flavonoids in A. caudatus treated with 50 ppm of AgNPs, showing the highest flavonoid composition. This further confirms A. caudatus grown with 50 ppm of AgNPs as the most potent. This study has shown that concentration-dependent AgNPs can be used to boost antioxidant activity and phytochemical contents of vegetables.

  17. Facile synthesis of S-Ag nanocomposites and Ag2S short nanorods by the interaction of sulfur with AgNO3 in PEG400

    NASA Astrophysics Data System (ADS)

    Zhang, Yan-Li; Xie, Xin-Yuan; Liang, Ming; Xie, Shu-Ming; Chen, Jie-Mei; Zheng, Wen-Jie

    2016-06-01

    A facile, eco-friendly and inexpensive method to prepare Ag2S short nanorods and S-Ag nanocomposites using sublimed sulfur, AgNO3, PVP and PEG400 was studied. According to x-ray diffraction and scanning electron microscopy of the Ag2S, the products are highly crystalline and pure Ag2S nanorods with diameters of 70-160 nm and lengths of 200-360 nm. X-ray diffraction of the S-Ag nanocomposites shows that we obtained cubic Ag and S nanoparticles. Transmission electron microscopy shows that the molar ratio of PVP to Ag+ plays an important role in controlling the size and morphology of the S-Ag nanocomposites. When the molar ratio of PVP to Ag+ was 10:1, smaller sizes, better dispersibility and narrower distribution of S-Ag nanocomposites with diameters of 10-40 nm were obtained. The formation mechanism of the S-Ag nanocomposites was studied by designing a series of experiments using ultraviolet-visible measurement, and it was found that S nanoparticles are produced first and act as seed crystals; then Ag+ becomes Ag nanocrystals on the surfaces of the S nanoparticles by the reduction of PVP. PEG400 acts as a catalyzer, accelerating the reaction rate, and protects the S-Ag nanocomposites from reacting to produce Ag2S. The antimicrobial experiments show that the S-Ag nanocomposites have greater antimicrobial activity on Staphylococcus aureus, Aspergillus niger and blue mold than Ag nanoparticles.

  18. Silver nanoparticle toxicity is related to coating materials and disruption of sodium concentration regulation.

    PubMed

    Kwok, Kevin W H; Dong, Wu; Marinakos, Stella M; Liu, Jie; Chilkoti, Ashutosh; Wiesner, Mark R; Chernick, Melissa; Hinton, David E

    2016-11-01

    Silver nanoparticles (AgNPs) have been increasingly commercialized and their release into the environment is imminent. Toxicity of AgNP has been studied with a wide spectrum of organisms, yet the mechanism of toxicity remains largely unknown. This study systematically compared toxicity of 10 AgNPs of different particle diameters and coatings to Japanese medaka (Oryzias latipes) larvae to understand how characteristics of AgNP relate to toxicity. Dissolution of AgNPs was largely dependent on particle size, but their aggregation behavior and toxicity were more dependent on coating materials. 96 h lethal concentration 50% (LC50) values correlated with AgNP aggregate size rather than size of individual nanoparticles. Of the AgNPs studied, the dissolved Ag concentration in the test suspensions did not account for all of the observed toxicity, indicating the role of NP-specific characteristics in resultant toxicity. Exposure to AgNP led to decrease of sodium concentration in the tissue and increased expression of Na(+)/K(+ )ATPase. Gene expression patterns also suggested that toxicity was related to disruption of sodium regulation and not to oxidative stress.

  19. Characterization of nanostructured TiO2:Ag films: structural and optical properties

    NASA Astrophysics Data System (ADS)

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

    2016-10-01

    TiO2:Ag nanocomposites have been prepared by sol-gel method with varying silver concentration. Different technological approaches are employed to study the formation of Ag nanoparticles in titanium dioxide matrix. The obtained thin films are either thermally treated at temperatures from 300 to 600oC or UV irradiated for 15 minutes between layer deposition. XRD and FTIR studies reveal that Ag is incorporated in TiO2 films as nanoparticles and no Ag oxide phases are detected. Optical characterization performed by UV-VIS spectroscopy confirms the formation of silver nanoparticles. The influence of thermal treatment and UV radiation on the optical and structural properties is studied.

  20. Atomic force microscopy of AgBr crystals and adsorbed gelatin films

    SciTech Connect

    Haugstad, G.; Gladfelter, W.L.; Keyes, M.P.; Weberg, E.B.

    1993-06-01

    Atomic force microscopy of the (111) surface of macroscopic AgBr crystals revealed steps ranging in height from two atomic layers up to 10 nm, lying predominantly along the (110) and (112) families of crystal directions. Rods of elemental Ag, formed via photoreduction, were observed along the (110) family of directions. Images of adsorbed gelatin films revealed circular pores with diameters of order 10-100 nm, extending to the AgBr surface. The length of deposition time, the pH and concentration of the gelatin solution, and the presence of steps on the AgBr surface were observed to affect the size, number, and location of pores in the gelatin films. 12 refs., 7 figs.

  1. Photodegradation of Acid Violet 7 with AgBr-ZnO under highly alkaline conditions.

    PubMed

    Krishnakumar, B; Swaminathan, M

    2012-12-01

    The photocatalytic activity of AgBr-ZnO was investigated for the degradation of Acid Violet 7 (AV 7) in aqueous solution using UV-A light. AgBr-ZnO is found to be more efficient than commercial ZnO and prepared ZnO at pH 12 for the mineralization of AV 7. The effects of operational parameters such as the amount of photocatalyst, dye concentration, initial pH on photo mineralization have been analyzed. Expect oxone, other oxidants decrease the degradation efficiency. Addition of metal ions and anions decrease the degradation efficiency of AgBr-ZnO significantly. The mineralization of AV 7 has also been confirmed by COD measurements. The mechanism of degradation by AgBr-ZnO is proposed to explain its higher activity under UV light. The catalyst is found to be reusable.

  2. Prediction of Phase Formation in Nanoscale Sn-Ag-Cu Solder Alloy

    NASA Astrophysics Data System (ADS)

    Wu, Min; Lv, Bailin

    2016-01-01

    In a dynamic nonequilibrium process, the effective heat of formation allows the heat of formation to be calculated as a function of concentrations of the reacting atoms. In this work, we used the effective heat of formation rule to predict the formation and size of compound phases in a nanoscale Sn-Ag-Cu lead-free solder. We calculated the formation enthalpy and effective formation enthalpy of compounds in the Sn-Ag, Sn-Cu, and Ag-Cu systems by using the Miedema model and effective heat of formation. Our results show that, considering the surface effect of the nanoparticle, the effective heat of formation rule successfully predicts the phase formation and sizes of Ag3Sn and Cu6Sn5 compounds, which agrees well with experimental data.

  3. AgI/Ag{sub 3}PO{sub 4} hybrids with highly efficient visible-light driven photocatalytic activity

    SciTech Connect

    Katsumata, Hideyuki; Hayashi, Takahiro; Taniguchi, Masanao; Suzuki, Tohru; Kaneco, Satoshi

    2015-03-15

    Highlights: • AgI/Ag{sub 3}PO{sub 4} hybrid was prepared via an in situ anion-exchange method. • AgI/Ag{sub 3}PO{sub 4} displays the excellent photocatalytic activity under visible light. • AgI/Ag{sub 3}PO{sub 4} readily transforms to be Ag@AgI/Ag{sub 3}PO{sub 4} system. • h{sup +} and O{sub 2}{sup ·−} play the major role in the AO 7 decolorization over AgI/Ag{sub 3}PO{sub 4}. • The activity enhancement is ascribed to a Z-scheme system composed of Ag{sub 3}PO{sub 4}, Ag and AgI. - Abstract: Highly efficient visible-light-driven AgI/Ag{sub 3}PO{sub 4} hybrid photocatalysts with different mole ratios of AgI were prepared via an in situ anion-exchange method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV–vis diffuse reflectance spectroscopy (DRS) and photoluminescence (PL) technique. Under visible light irradiation (>420 nm), the AgI/Ag{sub 3}PO{sub 4} photocatalysts displayed the higher photocatalytic activity than pure Ag{sub 3}PO{sub 4} and AgI for the decolorization of acid orange 7 (AO 7). Among the hybrid photocatalysts, AgI/Ag{sub 3}PO{sub 4} with 80% of AgI exhibited the highest photocatalytic activity for the decolorization of AO 7. X-ray photoelectron spectroscopy (XPS) results revealed that AgI/Ag{sub 3}PO{sub 4} readily transformed to be Ag@AgI/Ag{sub 3}PO{sub 4} system while the photocatalytic activity of AgI/Ag{sub 3}PO{sub 4} remained after 5 recycling runs. In addition, the quenching effects of different scavengers displayed that the reactive h{sup +} and O{sub 2}{sup ·−} play the major role in the AO 7 decolorization. The photocatalytic activity enhancement of AgI/Ag{sub 3}PO{sub 4} hybrids can be ascribed to the efficient separation of electron–hole pairs through a Z-scheme system composed of Ag{sub 3}PO{sub 4}, Ag and AgI, in which Ag nanoparticles act as the charge separation center.

  4. Study on swift heavy ions induced modifications of Ag-ZnO nanocomposite thin film

    NASA Astrophysics Data System (ADS)

    Singh, S. K.; Singhal, R.; Siva Kumar, V. V.

    2017-03-01

    In the present work, swift heavy ion (SHI) irradiation induced modifications in structural and optical properties of Ag-ZnO nanocomposite thin films have been investigated. Ag-ZnO nanocomposite (NCs) thin films were synthesized by RF magnetron sputtering technique and irradiated with 100 MeV Ag7+ ions at three different fluences 3 × 1012, 1 × 1013 and 3 × 1013 ions/cm2. Rutherford Backscattering Spectrometry revealed Ag concentration to be ∼8.0 at.%, and measured thickness of the films was ∼55 nm. Structural properties of pristine and irradiated films have been analyzed by X-ray diffraction analysis and found that variation in crystallite size of the film with ion irradiation. X-ray photoelectron spectroscopy (XPS) indicates the formation of Ag-ZnO nanocomposite thin film with presence of Ag, Zn and O elements. Oxidation state of Ag and Zn also estimated by XPS analysis. Surface plasmon resonance (SPR) of Ag nanoparticle has appeared at ∼475 nm in the pristine thin film, which is blue shifted by ∼30 nm in film irradiated at fluence of 3 × 1012 ions/cm2 and completely disappeared in film irradiated at higher fluences, 1 × 1013 and 3 × 1013 ions/cm2. A marginal change in the optical band gap of Ag-ZnO nanocomposite thin film is also found with increasing ion fluence. Surface morphology of pristine and irradiated films have been studied using Atomic Force Microscopy (AFM). Raman and Photo-luminance (PL) spectra of nanocomposite thin films have been investigated to understand the ion induced modifications such as lattice defects and disordering in the nanocomposite thin film.

  5. Building novel Ag/CeO{sub 2} heterostructure for enhancing photocatalytic activity

    SciTech Connect

    Leng, Qiang; Yang, Dezhi; Yang, Qi; Hu, Chenguo; Kang, Yue; Wang, Mingjun; Hashim, Muhammad

    2015-05-15

    Highlights: • Ag nanoparticle is designed to building Schottky heterojunction on CeO{sub 2} nanocube. • The photocatalytic activity of Ag/CeO{sub 2} heterostructure is much enhanced. • 95.33% of MB can be effectively degraded within half an hour. • Ag as acceptor of photoelectrons blocks the recombination of electron–hole pairs. - Abstract: Stable and recyclable photocatalysts with high efficiency to degrade organic contamination are important and widely demanded under the threat of the environment pollution. Ag/CeO{sub 2} heterostructure is designed as a photocatalyst to degrade organic dye under the simulated sunlight. The catalytic activity of CeO{sub 2} nanocubes (NCs) to degrade methylene blue (MB) is obviously enhanced when Ag nanoparticles (NPs) are deposited on the surface of them. The weight ratio of Ag and CeO{sub 2} in forming high efficiency catalyst, the amount of Ag/CeO{sub 2} catalyst used in degradation process, and the dye concentration and pH value of the initial MB solution are examined systematically. 95.33% of MB can be effectively degraded within half an hour when 50 mg of Ag/CeO{sub 2} catalyst in an optimal weight ratio of 1:3, is added to the 100 mL of MB solution (c{sub 0} = 1 × 10{sup −5} mol L{sup −1}, pH 6.2). The mechanism of the enhanced catalytic activity of Ag/CeO{sub 2} heterostructure is discussed. The photocatalytic degradation rate is found to obey pseudo-first-order kinetics equations according to Langmuir–Hinshelwood model. The intermediate products in different stages during the degradation of MB are analyzed.

  6. Preclinical pharmacokinetics and distribution to tissue of AG1343, an inhibitor of human immunodeficiency virus type 1 protease.

    PubMed

    Shetty, B V; Kosa, M B; Khalil, D A; Webber, S

    1996-01-01

    AG1343, a potent inhibitor of human immunodeficiency virus type 1 (HIV-1) protease (Ki = 2 nM), was designed by protein structure-based drug design techniques. AG1343 has potent antiviral activity (95% effective dose = 0.04 microgram/ml) against a number of HIV-1 strains in acute and chronic models of infection. As part of its preclinical development, the oral bioavailability of AG1343 in rats, dogs, monkeys, and marmosets was determined and its tissue distribution in rats was evaluated. There were no major interspecies differences in AG1343 pharmacokinetics. Following intravenous administration, the elimination half-life of AG1343 ranged from 1 to 1.4 hr. The total volume of distribution (2 to 7 liters/kg) exceeded the volume of total body water, indicating extensive tissue distribution. Systemic clearance of AG1343 (1 to 4 liters/kg) in the different species corresponded to hepatic blood flow, suggesting possible hepatic involvement in the elimination of AG1343. Following oral administration, peak levels in plasma ranged from 0.34 microgram/ml after treatment with 10 mg/kg of body weight in the dog to 1.7 micrograms/ml after dosing with 50 mg/kg in the rat. Because of the slow absorption of AG1343, plasma concentrations of AG1343 exceeding that required for 95% inhibition of HIV-1 replication were maintained for up to 7 h after a single oral dose in all species evaluated. Average oral bioavailability of AG1343 ranged from 17% in the marmoset to 47% in the dog. Studies of distribution to tissue in the rat after oral administration of 14C-AG1343 established extensive distribution with concentrations in most tissues exceeding that found in plasma. Of particular significance were high levels of AG1343 equivalent in mesenteric lymph nodes (32.05 micrograms/g) and spleen tissue (9.33 micrograms/g). The major excretory route for AG1343 was via feces, with 100% of the dose recovered by 48 h. Results from these studies demonstrate that AG1343 is orally bioavailable and

  7. Preclinical pharmacokinetics and distribution to tissue of AG1343, an inhibitor of human immunodeficiency virus type 1 protease.

    PubMed Central

    Shetty, B V; Kosa, M B; Khalil, D A; Webber, S

    1996-01-01

    AG1343, a potent inhibitor of human immunodeficiency virus type 1 (HIV-1) protease (Ki = 2 nM), was designed by protein structure-based drug design techniques. AG1343 has potent antiviral activity (95% effective dose = 0.04 microgram/ml) against a number of HIV-1 strains in acute and chronic models of infection. As part of its preclinical development, the oral bioavailability of AG1343 in rats, dogs, monkeys, and marmosets was determined and its tissue distribution in rats was evaluated. There were no major interspecies differences in AG1343 pharmacokinetics. Following intravenous administration, the elimination half-life of AG1343 ranged from 1 to 1.4 hr. The total volume of distribution (2 to 7 liters/kg) exceeded the volume of total body water, indicating extensive tissue distribution. Systemic clearance of AG1343 (1 to 4 liters/kg) in the different species corresponded to hepatic blood flow, suggesting possible hepatic involvement in the elimination of AG1343. Following oral administration, peak levels in plasma ranged from 0.34 microgram/ml after treatment with 10 mg/kg of body weight in the dog to 1.7 micrograms/ml after dosing with 50 mg/kg in the rat. Because of the slow absorption of AG1343, plasma concentrations of AG1343 exceeding that required for 95% inhibition of HIV-1 replication were maintained for up to 7 h after a single oral dose in all species evaluated. Average oral bioavailability of AG1343 ranged from 17% in the marmoset to 47% in the dog. Studies of distribution to tissue in the rat after oral administration of 14C-AG1343 established extensive distribution with concentrations in most tissues exceeding that found in plasma. Of particular significance were high levels of AG1343 equivalent in mesenteric lymph nodes (32.05 micrograms/g) and spleen tissue (9.33 micrograms/g). The major excretory route for AG1343 was via feces, with 100% of the dose recovered by 48 h. Results from these studies demonstrate that AG1343 is orally bioavailable and

  8. Lasting antibacterial activities of Ag-TiO2/Ag/a-TiO2 nanocomposite thin film photocatalysts under solar light irradiation.

    PubMed

    Akhavan, O

    2009-08-01

    Photodegradation of Escherichia coli bacteria in presence of Ag-TiO(2)/Ag/a-TiO(2) nanocomposite film with an effective storage of silver nanoparticles was investigated in the visible and the solar light irradiations. The nanocomposite film was synthesized by sol-gel deposition of 30 nm Ag-TiO(2) layer on approximately 200 nm anatase(a-)TiO(2) film previously doped by silver nanoparticles. Both Ag/a-TiO(2) and Ag-TiO(2)/Ag/a-TiO(2) films were transparent with a SPR absorption band at 412 nm. Depth profile X-ray photoelectron spectroscopy showed metallic silver nanoparticles with diameter of 30 nm and fcc crystalline structure were self-accumulated on the film surface at depth of 5 nm of the TiO(2) layer and also at the interface of the Ag-TiO(2) and a-TiO(2) films (at depth of 30 nm). Both OH(-) bounds and H(2)O contents were concentrated on the film surface and at the interface, as a profit in releasing more ionic (not metallic) silver nanoparticles. Antibacterial activity of the nanocomposite film against E. coli bacteria was 5.1 times stronger than activity of the a-TiO(2), in dark. Photo-antibacterial activity of the nanocomposite film exposed by the solar light was measured 1.35 and 6.90 times better than activity of the Ag/a-TiO(2) and a-TiO(2), respectively. The main mechanism for silver ion releasing was inter-diffusion of water and silver nanoparticles through pores of the TiO(2) layer. Durability of the nanocomposite film was at least 11 times higher than the Ag/a-TiO(2) film. Therefore, the Ag-TiO(2)/Ag/a-TiO(2) photocatalyst can be nominated as one of the effective and long-lasting antibacterial nanocomposite materials.

  9. The cardiovascular response to the AGS

    NASA Technical Reports Server (NTRS)

    Cardus, David; Mctaggart, Wesley G.

    1993-01-01

    This paper reports the preliminary results of experiments on human subjects conducted to study the cardiovascular response to various g-levels and exposure times using an artificial gravity simulator (AGS). The AGS is a short arm centrifuge consisting of a turntable, a traction system, a platform and four beds. Data collection hardware is part of the communication system. The AGS provides a steep acceleration gradient in subjects in the supine position.

  10. CrCuAgN PVD nanocomposite coatings: Effects of annealing on coating morphology and nanostructure

    NASA Astrophysics Data System (ADS)

    Liu, Xingguang; Iamvasant, Chanon; Liu, Chang; Matthews, Allan; Leyland, Adrian

    2017-01-01

    CrCuAgN PVD nanocomposite coatings were produced using pulsed DC unbalanced magnetron sputtering. This investigation focuses on the effects of post-coat annealing on the surface morphology, phase composition and nanostructure of such coatings. In coatings with nitrogen contents up to 16 at.%, chromium exists as metallic Cr with N in supersaturated solid solution, even after 300 °C and 500 °C post-coat annealing. Annealing at 300 °C did not obviously change the phase composition of both nitrogen-free and nitrogen-containing coatings; however, 500 °C annealing resulted in significant transformation of the nitrogen-containing coatings. The formation of Ag aggregates relates to the (Cu + Ag)/Cr atomic ratio (threshold around 0.2), whereas the formation of Cu aggregates relates to the (Cu + Ag + N)/Cr atomic ratio (threshold around 0.5). The primary annealing-induced changes were reduced solubility of Cu, Ag and N in Cr, and the composition altering from a mixed ultra-fine nanocrystalline and partly amorphous phase constitution to a coarser, but still largely nanocrystalline structure. It was also found that, with sufficient Cu content (>12 at.%), annealing at a moderately high temperature (e.g. 500 °C) leads to transportation of both Cu and Ag (even at relatively low concentrations of Ag, ≤3 at.%) from inside the coating to the coating surface, which resulted in significant reductions in friction coefficient, by over 50% compared to that of the substrate (from 0.31 to 0.14 with a hemispherical diamond indenter, and from 0.83 to 0.40 with an alumina ball counterface, respectively). Results indicate that the addition of both Cu and Ag (in appropriate concentrations) to nitrogen-containing chromium is a viable strategy for the development of 'self-replenishing' silver-containing thin film architectures for temperature-dependent solid lubrication requirements or antimicrobial coating applications.

  11. Multiple Partial Siberian Snakes in the AGS

    NASA Astrophysics Data System (ADS)

    Takano, J.; Ahrens, L. A.; Bai, M.; Brown, K.; Courant, E. D.; Gardner, C. J.; Glenn, J. W.; Hattori, T.; Huang, H.; Lin, F.; Luccio, A. U.; MacKay, W. W.; Okamura, M.; Roser, T.; Tepikian, S.; Tsoupas, N.; Yip, K.; Zelenski, A.; Zeno, K.

    2007-06-01

    Polarized protons are accelerated up to 24.3 GeV in the Alternating Gradient Synchrotron (AGS) at Brookhaven National Laboratory (BNL). To accelerate the beam with preserving the polarization, two different types of helical dipole partial Siberian snake have been installed to the AGS. One is a superconducting magnet (Cold Snake, CSNK), and the other is a normal conducting one (Warm Snake, WSNK). With these snake magnets, the polarization at the AGS extraction achieved 65%. However, the AGS has spin mismatches at the injection and extraction. This description shows calculated results to have better spin matching with using two or three snakes.

  12. Multiple Partial Siberian Snakes in the AGS

    SciTech Connect

    Takano, J.; Ahrens, L. A.; Bai, M.; Brown, K.; Courant, E. D.; Gardner, C. J.; Glenn, J. W.; Huang, H.; Luccio, A. U.; MacKay, W. W.; Okamura, M.; Roser, T.; Tepikian, S.; Tsoupas, N.; Yip, K.; Zelenski, A.; Zeno, K.; Hattori, T.; Lin, F.

    2007-06-13

    Polarized protons are accelerated up to 24.3 GeV in the Alternating Gradient Synchrotron (AGS) at Brookhaven National Laboratory (BNL). To accelerate the beam with preserving the polarization, two different types of helical dipole partial Siberian snake have been installed to the AGS. One is a superconducting magnet (Cold Snake, CSNK), and the other is a normal conducting one (Warm Snake, WSNK). With these snake magnets, the polarization at the AGS extraction achieved 65%. However, the AGS has spin mismatches at the injection and extraction. This description shows calculated results to have better spin matching with using two or three snakes.

  13. Transformation from Ag@Ag3PO4 to Ag@Ag2SO4 hybrid at room temperature: preparation and its visible light photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Wei, Ting; Gao, Shanmin; Wang, Qingyao; Xu, Hui; Wang, Zeyan; Huang, Baibiao; Dai, Ying

    2017-02-01

    In the present study, Ag/Ag2SO4 hybrid photocatalysts were obtained via a facile redox-precipitation reaction approach by using Ag@Ag3PO4 nanocomposite as the precursor and KMnO4 as the oxidant. Multiple techniques, such as X-ray diffraction pattern (XRD), transmission electron microscope (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS) and Brunauer-Emmett-Teller (BET), photocurrent and electrochemical impedance spectroscopy (EIS), were applied to investigate the structures, morphologies, optical, and electronic properties of as-prepared samples. The photocatalytic activities were evaluated by photodegradation of organic rhodamine B (RhB) and methyl orange (MO) under visible light irradiation. It was found that pure Ag2SO4 can partially transform into metallic Ag during the photocatalytic degradation of organic pollutants, but the Ag/Ag2SO4 hybrids can maintain its structure stability and show enhanced visible light photocatalytic activity because of the surface plasma resonance effect of the metallic Ag.

  14. Silver toxicity across salinity gradients: the role of dissolved silver chloride species (AgCl x ) in Atlantic killifish (Fundulus heteroclitus) and medaka (Oryzias latipes) early life-stage toxicity.

    PubMed

    Matson, Cole W; Bone, Audrey J; Auffan, Mélanie; Lindberg, T Ty; Arnold, Mariah C; Hsu-Kim, Heileen; Wiesner, Mark R; Di Giulio, Richard T

    2016-08-01

    The influence of salinity on Ag toxicity was investigated in Atlantic killifish (Fundulus heteroclitus) early life-stages. Embryo mortality was significantly reduced as salinity increased and Ag(+) was converted to AgCl(solid). However, as salinity continued to rise (>5 ‰), toxicity increased to a level at least as high as observed for Ag(+) in deionized water. Rather than correlating with Ag(+), Fundulus embryo toxicity was better explained (R(2) = 0.96) by total dissolved Ag (Ag(+), AgCl2 (-), AgCl3 (2-), AgCl4 (3-)). Complementary experiments were conducted with medaka (Oryzias latipes) embryos to determine if this pattern was consistent among evolutionarily divergent euryhaline species. Contrary to Fundulus data, medaka toxicity data were best explained by Ag(+) concentrations (R(2) = 0.94), suggesting that differing ionoregulatory physiology may drive observed differences. Fundulus larvae were also tested, and toxicity did increase at higher salinities, but did not track predicted silver speciation. Alternatively, toxicity began to increase only at salinities above the isosmotic point, suggesting that shifts in osmoregulatory strategy at higher salinities might be an important factor. Na(+) dysregulation was confirmed as the mechanism of toxicity in Ag-exposed Fundulus larvae at both low and high salinities. While Ag uptake was highest at low salinities for both Fundulus embryos and larvae, uptake was not predictive of toxicity.

  15. Single step electrochemical synthesis of hydrophilic/hydrophobic Ag5 and Ag6 blue luminescent clusters.

    PubMed

    Santiago González, Beatriz; Blanco, M C; López-Quintela, M Arturo

    2012-12-21

    Well-defined Ag(5) and Ag(6) dodecanethiol/tetrabutyl ammonium-protected clusters were prepared by a one-pot electrochemical method. Ag clusters show bright and photostable emissions. The presence of a dual capping renders the silver clusters soluble in both organic and aqueous solvents.

  16. Synthesis of Cu-Ag@Ag particles using hyperbranched polyester as template

    NASA Astrophysics Data System (ADS)

    Han, Wen-Song

    2015-07-01

    In this manuscript, the third-generation hyperbranched polyester was synthesized with 2, 2-dimethylol propionic acid as AB2 monomer and pentaerythrite as core molecule by using step by step polymerization process at first. Then, the Cu-Ag particles were prepared by co-reduction of silver nitrate and copper nitrate with ascorbic acid in the aqueous solution using hyperbranched polyester as template. Finally, the Cu-Ag@Ag particles were prepared by coating silver on the surface of Cu-Ag particles by reduction of silver nitrate. The synthesized hyperbranched polyester and Cu-Ag@Ag particles were characterized by Fourier transform infrared (FT-IR) spectroscopy, UV-vis spectra, x-ray diffraction, Laser light scattering, thermogravimetric analysis (TGA) and SEM. UV-vis spectra results showed that the Cu-Ag@Ag particles had a strong absorption band at around 420 nm. Laser light scattering and SEM studies confirmed that the most frequent particle sizes of Cu-Ag@Ag particles were 1.2 um. TGA results indicated that the Cu-Ag@Ag particles had good thermal stability. [Figure not available: see fulltext.

  17. An Au/AgBr-Ag heterostructure plasmonic photocatalyst with enhanced catalytic activity under visible light.

    PubMed

    Purbia, Rahul; Paria, Santanu

    2017-01-17

    This study reports an easy synthesis protocol of a novel bimetallic silver halide (Au/AgBr-Ag) plasmonic heterostructure as a visible light induced photocatalyst. In this process, first CTAB capped Au NPs were coated with AgBr, and then Ag nanoparticles were formed on the surface of AgBr by photoreduction, while exposing to daylight at room temperature. The presence of Au and Ag improves the visible absorption ability of NPs and avoids charge recombination of the semiconductor AgBr during photoexcitation, which in turn enhances 16 and 8.9 fold the photocatalytic efficiency of Rhodamine B dye degradation under visible light irradiation compared to that of pure AgBr and AgBr/Ag, respectively. The recycling tests of the photocatalyst show only ∼8.7% decrease in efficiency after the 5(th) cycle of reuse without changing the morphology. During the photocatalytic process, active superoxide radicals (O2˙(-)) play a major role, proved through scavenger trapping and photoluminescence experiments. The presence of two plasmonic metals (Au and Ag) in the heterostructure helps to improve visible light absorption as well as avoid charge recombination of the semiconductor AgBr to act as a better photocatalyst. Since this heteronanostructure can be easily synthesized by a one-step method, this study could provide a new approach for the development of efficient bimetallic/semiconductor halide plasmonic photocatalysts with enhanced visible absorption and better charge separation.

  18. Highly efficient visible light plasmonic photocatalyst Ag@Ag(Br,I).

    PubMed

    Wang, Peng; Huang, Baibiao; Zhang, Qianqian; Zhang, Xiaoyang; Qin, Xiaoyan; Dai, Ying; Zhan, Jie; Yu, Jiaoxian; Liu, Haixia; Lou, Zaizhu

    2010-09-03

    The new plasmonic photocatalyst Ag@Ag(Br,I) was synthesized by the ion-exchange process between the silver bromide and potassium iodide, then by reducing some Ag(+) ions in the surface region of Ag(Br,I) particles to Ag(0) species. Ag nanoparticles are formed from Ag(Br,I) by the light-induced chemical reduction reaction. The Ag@Ag(Br,I) particles have irregular shapes with their sizes varying from 83 nm to 1 mum. The as-grown plasmonic photocatalyst shows strong absorption in the visible light region because of the plasmon resonance of Ag nanoparticles. The ability of this compound to reduce Cr(VI) under visible light was compared with those of other reference photocatalyst. The plasmonic photocatalyst is shown to be highly efficient under visible light. The stability of the photocatalyst was examined by X-ray diffraction and X-ray photoelectron spectroscopy. The XRD pattern and XPS spectra prove the stability of the plasmonic photocatalyst Ag@Ag(Br,I).

  19. Antibacterial and antifouling activities of chitosan/TiO2/Ag NPs nanocomposite films against packaged drinking water bacterial isolates.

    PubMed

    Natarajan, Saravanan; Bhuvaneshwari, M; Lakshmi, D Shanthana; Mrudula, P; Chandrasekaran, N; Mukherjee, Amitava

    2016-10-01

    TiO2 and Ag NPs are widely used as antibacterial agents against many bacterial pathogens. Chitosan (polymer) itself acts as a strong antibacterial agent. Hence, chitosan/TiO2/Ag NPs incorporated nanocomposite film was prepared against packed drinking water bacterial strains. A concentration-dependent increase in the reduction of cell viability was observed in all the isolates under UV-C and dark exposure conditions. The bacteria consortium showed greater resistance against antibacterial effects of chitosan/TiO2/Ag nanocomposite as compared to single isolates. Glycocalyx test and mass assessment conclude the effective antibacterial activity by inhibiting bacterial adhesion on the film surface. The release of LDH and generation of ROS act as the predominant antibacterial mechanism induced by TiO2/Ag NPs. Surface characterization of chitosan/TiO2/Ag nanocomposite was studied by FTIR and XRD analyses and SEM analysis after interaction with the bacteria.

  20. Green synthesis of asymmetrically textured silver meso-flowers (AgMFs) as highly sensitive SERS substrates.

    PubMed

    Nhung, Tran Thi; Lee, Sang-Wha

    2014-12-10

    Highly asymmetrical "flower-like" micron silver particles, so-called hierarchical silver meso-flowers (AgMFs), were facilely synthesized using ascorbic acid at room temperature in the presence of chitosan biopolymer. The time-evolution of TEM images and XRD analysis confirmed the anisotropic growth of AgMFs with single crystalline phase of which the formation mechanism was described in detail. The morphology and size of as-prepared AgMFs were tunable simply by changing the concentration of chitosan biopolymer and/or AgNO3 precursor under otherwise identical conditions. The asymmetrically textured AgMFs dramatically enhanced Raman signals of probe molecules (2-chlorothiophenol, 4-aminothiophenol) even at a single particle level because of their surface morphologies consisting of numerous nanoedges and crevices.

  1. Facile and low-cost fabrication of Ag-Cu substrates via replacement reaction for highly sensitive SERS applications

    NASA Astrophysics Data System (ADS)

    Hu, Litao; Liu, Yan Jun; Xu, Shicai; Li, Zhe; Guo, Jia; Gao, Saisai; Lu, Zhengyi; Si, Haipeng; Jiang, Shouzhen; Wang, Shuyun

    2017-01-01

    In this work, we demonstrated facile and low-cost fabrication of highly sensitive SERS substrates via replacement reaction by immersing Cu foils into a AgNO3 solution. Different morphologies of Ag nanostructures were observed on the substrate surface by controlling the reaction time. The growth mechanism of Ag nanostructures on the Cu substrates was also analyzed based on the nanostructure evolution. The Ag-Cu substrates showed optimum SERS enhancement at certain reaction time, and the minimum detected concentration of Rhodamine 6G is as low as 10-13 M. The easy and low-cost fabrication makes the Ag-Cu SERS substrates promising for rapid, sensitive detection of targeted analytes, such as biomolecules, pollutants, and explosives in the environment.

  2. Negligible shift of 3Ag- potential in longer-chain carotenoids as revealed by a single persistent peak of 3Ag-→1Ag- stimulated emission followed by 3Ag-←1Ag- transient-absorption

    NASA Astrophysics Data System (ADS)

    Li, Chunyong; Miki, Takeshi; Kakitani, Yoshinori; Koyama, Yasushi; Nagae, Hiroyoshi

    2007-12-01

    Upon excitation of lycopene, anhydrorhodovibrin or spirilloxanthin to the 1Bu+(0) state, stimulated emission followed by transient-absorption was observed as a single peak with the 3Ag-(0) energy that had been determined by measurement of resonance-Raman excitation profiles. This observation was explained in terms of negligible shift of the 3Ag- potential, in reference to the 1Ag- potential, where only the 3Ag-(υ)→1Ag-(υ) emission and the 3Ag-(υ)←1Ag-(υ) absorption become allowed during the vibrational relaxation of υ = 2 → 1 → 0, starting from the 3Ag-(2) level generated by diabatic internal conversion from the 1Bu+(0) level, in anhydrorhodovibrin, for example.

  3. Half-life determination for 108Ag and 110Ag

    NASA Astrophysics Data System (ADS)

    Zahn, Guilherme S.; Genezini, Frederico A.

    2014-11-01

    In this work, the half-life of the short-lived silver radionuclides 108Ag and 110Ag were measured by following the activity of samples after they were irradiated in the IEA-R1 reactor. The results were then fitted using a non-paralizable dead time correction to the regular exponential decay and the individual half-life values obtained were then analyzed using both the Normalized Residuals and the Rajeval techniques, in order to reach the most exact and precise final values. To check the validity of dead-time correction, a second correction method was also employed by means of counting a long-lived 60Co radioactive source together with the samples as a livetime chronometer. The final half-live values obtained using both dead-time correction methods were in good agreement, showing that the correction was properly assessed. The results obtained are partially compatible with the literature values, but with a lower uncertainty, and allow a discussion on the last ENSDF compilations' values.

  4. Progress with the AGS Booster

    SciTech Connect

    Weng, W.T.

    1988-01-01

    Rare K-decay, neutrino and heavy ion physics demands that a rapid- cycling high vacuum and high intensity Booster be built for the AGS at Brookhaven. For each mode of operation there are corresponding accelerator physics and design issues needing special attention. Problems pertinent to any single mode of operation have been encountered and solved before, but putting high intensity proton requirements and high vacuum heavy ion requirements into one machine demands careful design considerations and decisions. The lattice design and magnet characteristics will be briefly reviewed. Major design issues will be discussed and design choices explained. Finally, the construction status and schedule will be presented. 6 refs., 6 figs.

  5. Photocatalytic oxidation removal of Hg0 using ternary Ag/AgI-Ag2CO3 hybrids in wet scrubbing process under fluorescent light

    NASA Astrophysics Data System (ADS)

    Zhang, Anchao; Zhang, Lixiang; Chen, Xiaozhuan; Zhu, Qifeng; Liu, Zhichao; Xiang, Jun

    2017-01-01

    A series of ternary Ag/AgI-Ag2CO3 photocatalysts synthesized using a facile coprecipitation method were employed to investigate their performances of Hg0 removal in a wet scrubbing reactor. The hybrids were characterized by N2 adsorption-desorption, XRD, SEM-EDS, HRTEM, XPS, DRS and ESR. The photocatalytic activities of Hg0 removal were evaluated under fluorescent light. The results showed that AgI content, fluorescent light irradiation, reaction temperature all showed significant influences on Hg0 removal. NO exhibited significant effect on Hg0 removal in comparison to SO2. Among these ternary Ag/AgI-Ag2CO3 hybrids, Ag/AgI(0.1)-Ag2CO3 showed the highest Hg0 removal efficiency, which could be ascribed to the effective separation of photogenerated electron-hole pairs between AgI and Ag2CO3 and the surface plasmon resonance (SPR) effect in the visible region by metallic silver nanoparticles (Ag0 NPs). The trapping studies of reactive radicals showed that the superoxide radicals (rad O2-) may play a key role in Hg0 removal under fluorescent light. According to the experimental and characterization results, a possible photocatalytic oxidation mechanism for enhanced Hg0 removal over Ag/AgI(0.1)-Ag2CO3 hybrid under fluorescent light was proposed.

  6. The alloying effect and AgCl-directing growth for synthesizing a trimetallic nanoring with improved SERS

    NASA Astrophysics Data System (ADS)

    Han, Shuhua; Zhou, Guangju; Fu, Yunzhi; Ma, Ying; Xu, Li; Zou, Chao; Chen, Wei; Yang, Yun; Huang, Shaoming

    2015-12-01

    We report the synthesis of high quality trimetallic Au/Ag/Pt nanorings (TAAPNs) by using Au/Ag alloy decahedra (AAAD) as templates. The alloying effect and AgCl-directing growth have been investigated in detail during the formation of TAAPN. It was found that the doping of Ag in AAAD changes the surrounding environment of Au atoms and decreases the oxidization reduction potential (ORP) of [AuCl2]-/Au because of the alloying effect, resulting in the dissolved O2 molecules that serve as an effective etchant for oxidizing Au to Au(i). Ascorbic acid (AA) and chloroplatinic acid (H2PtCl6) are weak acids which can accelerate the etching by increasing the concentration of H+. The AgCl selectively absorbs on {100} of the decahedra and induces the preferential deposition of H2PtCl6 here via their complexing interaction. AA reduces Pt(iv) and Ag(i) to atoms which grow on {100} facets. The formed Pt/Ag layer changes the etching direction from along [100] to [111] and generates the TAAPN. Besides, it has been noted that the TAAPNs exhibit good Surface Enhanced Raman Scattering (SERS) performance.We report the synthesis of high quality trimetallic Au/Ag/Pt nanorings (TAAPNs) by using Au/Ag alloy decahedra (AAAD) as templates. The alloying effect and AgCl-directing growth have been investigated in detail during the formation of TAAPN. It was found that the doping of Ag in AAAD changes the surrounding environment of Au atoms and decreases the oxidization reduction potential (ORP) of [AuCl2]-/Au because of the alloying effect, resulting in the dissolved O2 molecules that serve as an effective etchant for oxidizing Au to Au(i). Ascorbic acid (AA) and chloroplatinic acid (H2PtCl6) are weak acids which can accelerate the etching by increasing the concentration of H+. The AgCl selectively absorbs on {100} of the decahedra and induces the preferential deposition of H2PtCl6 here via their complexing interaction. AA reduces Pt(iv) and Ag(i) to atoms which grow on {100} facets. The formed

  7. Sensitive and selective detection of Hg2+ and Cu2+ ions by fluorescent Ag nanoclusters synthesized via a hydrothermal method

    NASA Astrophysics Data System (ADS)

    Liu, Jing; Ren, Xiangling; Meng, Xianwei; Fang, Zheng; Tang, Fangqiong

    2013-09-01

    An easily prepared fluorescent Ag nanoclusters (Ag NCs) probe for the sensitive and selective detection of Hg2+ and Cu2+ ions was developed here. The Ag NCs were synthesized by using polymethacrylic acid sodium salt as a template via a convenient hydrothermal process. The as-prepared fluorescent Ag NCs were monodispersed, uniform and less than 2 nm in diameter, and can be quenched in the presence of mercury (Hg2+) or copper (Cu2+) ions. Excellent linear relationships existed between the quenching degree of the Ag NCs and the concentrations of Hg2+ or Cu2+ ions in the range of 10 nM to 20 μM or 10 nM to 30 μM, respectively. By using ethylenediaminetetraacetate (EDTA) as the masking agent of Cu2+, Hg2+ was exclusively detected in coexistence with Cu2+ with high sensitivity (LOD = 10 nM), which also provided a reusable detection method for Cu2+. Furthermore, the different quenching phenomena caused by the two metals ions such as changes in visible colour, shifts of UV absorbance peaks and changes in size of Ag NCs make it easy to distinguish between them. Therefore the easily synthesized fluorescent Ag NCs may have great potential as Hg2+ and Cu2+ ions sensors.An easily prepared fluorescent Ag nanoclusters (Ag NCs) probe for the sensitive and selective detection of Hg2+ and Cu2+ ions was developed here. The Ag NCs were synthesized by using polymethacrylic acid sodium salt as a template via a convenient hydrothermal process. The as-prepared fluorescent Ag NCs were monodispersed, uniform and less than 2 nm in diameter, and can be quenched in the presence of mercury (Hg2+) or copper (Cu2+) ions. Excellent linear relationships existed between the quenching degree of the Ag NCs and the concentrations of Hg2+ or Cu2+ ions in the range of 10 nM to 20 μM or 10 nM to 30 μM, respectively. By using ethylenediaminetetraacetate (EDTA) as the masking agent of Cu2+, Hg2+ was exclusively detected in coexistence with Cu2+ with high sensitivity (LOD = 10 nM), which also provided a

  8. Easy deposition of Ag onto polystyrene beads for developing surface-enhanced-Raman-scattering-based molecular sensors.

    PubMed

    Kim, Kwan; Lee, Hyang Bong; Park, Hyoung Kun; Shin, Kuan Soo

    2008-02-15

    We describe a very simple electroless plating method that can be used to prepare Ag-coated polystyrene beads. Robust Ag nanostructures are reproducibly fabricated by soaking polystyrene beads in ethanolic solutions of AgNO(3) and butylamine. When the molar ratio of butylamine to AgNO(3) is far below 1.0, distinct nanosized Ag particles are formed on the polystyrene beads, but by increasing the amount of butylamine, network-like Ag nanostructures are formed that possess very broad UV/vis absorption characteristics extending from the near-UV to near-infrared regions. In conformity with the UV/vis absorption characteristics, the Ag-deposited polystyrene beads were highly efficient surface-enhanced Raman scattering (SERS) substrates, with an enhancement factor estimated using 4-aminobenzenethiol (4-ABT) as a model adsorbate to be larger than 1.1x10(6). On the basis of the nature of the SERS peaks of 4-ABT, those Ag-deposited polystyrene beads were confirmed, after attaching biotin groups over 4-ABT, to selectively recognize streptavidin molecules down to concentrations of 10(-11) g mL(-1) (i.e., approximately 0.2 pM). Since a number of different molecules can be used as SERS-marker molecules (such as 4-ABT), multiple bioassays are readily accomplished via SERS after attaching appropriate host or guest molecules onto them.

  9. Thermoelectric properties of p-type PbTe/Ag{sub 2}Te bulk composites by extrinsic phase mixing

    SciTech Connect

    Lee, Min Ho; Rhyee, Jong-Soo

    2015-12-15

    We investigated the thermoelectric properties of PbTe/Ag{sub 2}Te bulk composites, synthesized by hand milling, mixing, and hot press sintering. From x-ray diffraction and energy dispersive x-ray spectroscopy measurements, we observed Ag{sub 2}Te phase separation in the PbTe matrix without Ag atom diffusion. In comparison with previously reported pseudo-binary (PbTe){sub 1−x}(Ag{sub 2}Te){sub x} composites, synthesized by high temperature phase separation, the PbTe/Ag{sub 2}Te bulk composites fabricated with a low temperature phase mixing process give rise to p-type conduction of carriers with significantly decreased electrical conductivity. This indicates that Ag atom diffusion in the PbTe matrix changes the sign of the Seebeck coefficient to n-type and also increases the carrier concentration. Effective p-type doping with low temperature phase separation by mixing and hot press sintering can enhance the thermoelectric performance of PbTe/Ag{sub 2}Te bulk composites, which can be used as a p-type counterpart of n-type (PbTe){sub 1−x}(Ag{sub 2}Te){sub x} bulk composites.

  10. Facile one-pot synthesis of uniform TiO2-Ag hybrid hollow spheres with enhanced photocatalytic activity.

    PubMed

    Wang, Sunli; Qian, Huanhuan; Hu, Yong; Dai, Wei; Zhong, Yijun; Chen, Jiafu; Hu, Xiao

    2013-01-28

    TiO(2)-Ag hybrid hollow spheres (about 700 nm in diameter) with a highly uniform morphology and good structural stability were facilely prepared via a one-pot hydrothermal method, using carbon spheres as templates followed by an annealing treatment. Through this route, the as-prepared hybrid hollow spheres preserved the uniformity of the initial carbon sphere templates and the loading amount of the Ag nanocrystals can be conveniently varied or controlled by the concentration of the Ag precursor. The investigation of the photocatalytic ability demonstrated that the as-prepared TiO(2)-Ag hybrid hollow spheres possess excellent photocatalytic activity, superior to commercial TiO(2) nanoparticles (Degussa P25), for the degradation of rhodamine B (RhB) and methyl orange (MO) dyes under visible-light illumination. Furthermore, the ˙OH radicals formed during photocatalysis with different Ag content hybrids were revealed by means of a terephthalic acid fluorescence probe method, which uncovers that the Ag content in the TiO(2)-Ag hybrids was crucial to obtain an optimal synergistic effect between the Ag and TiO(2) for the degradation of organic pollutants. Accordingly, the optimum matching for the best photocatalytic activity was investigated thoroughly and a reasonable mechanism was also proposed.

  11. Recovery of silver metal from low concentrated wastewater by photocatalysis

    NASA Astrophysics Data System (ADS)

    Ding, Mali; Han, Jie; Qiu, Wei; Zhang, Weijun; Gao, Wei

    2015-03-01

    This work studies the photocatalytic activity of zinc oxide (ZnO) nanopowder to recover silver (Ag) metal from low Ag+ concentrated solution under artificial ultraviolet (UV) light. Benchmark titanium dioxide (P25 TiO2) was used for comparison purpose. Experimental results indicated that ZnO exhibited superior performance for Ag recovery compared to TiO2. Under optimal catalyst loading, the achieved Ag removal efficiencies were 100% and 99.94% at 0.2 g/L ZnO (1 h) and 2 g/L TiO2 (2 h), respectively. An induction period at low concentration of TiO2 (0.1 g/L) was observed and a mechanism was proposed. The photodissolution of ZnO was assessed and proved to be negligible. Recovered pure Ag metal was characterized by X-ray diffractometry (XRD) and scanning electron microscopy (SEM), showing a promising effective Ag recovery technology using ZnO photocatalyst.

  12. AgRISTARS documents tracking list report

    NASA Technical Reports Server (NTRS)

    Hawkins, J. L.

    1983-01-01

    A quarterly listing of documents issued and placed in the AgRISTARS tracking system is provided. The technical publications are arranged by type of documents. The reference AgRISTARS document number, title and date of publication, the issuing organization, and the National Technical Information Service reference number is given.

  13. The AGS synchrotron with four helical magnets

    SciTech Connect

    Tsoupas N.; Huang, H.; Roser, T.; MacKay, W.W.; Trbojevic, D.

    2012-05-20

    The idea of using two partial helical magnets was applied successfully to the AGS synchrotron to preserve the proton beam polarization. In this paper we explore in details the idea of using four helical magnets placed symmetrically in the AGS ring. The placement of four helical magnets in the AGS ring provides many advantages over the present setup of the AGS which uses two partial helical magnets. First, the symmetric placement of the four helical magnets allows for a better control of the AGS optics with reduced values of the beta functions especially near beam injection, second, the vertical spin direction during beam injection and extraction is closer to vertical, and third, it provides for a larger 'spin tune gap', which allows the vertical and horizontal tunes to be placed, and prevent the horizontal and vertical intrinsic spin resonances of the AGS to occur during the acceleration cycle. Although the same spin gap can be obtained with a single or two partial helices, the required high field strength of a single helix makes its use impractical, and that of the double helix rather difficult. In this paper we will provide results on the spin tune and on the optics of the AGS with four partial helical magnets, and compare these results with the present setup of the AGS that uses two partial helical magnets.

  14. AgPO2F2 and Ag9(PO2F2)14: the first Ag(i) and Ag(i)/Ag(ii) difluorophosphates with complex crystal structures.

    PubMed

    Malinowski, Przemysław J; Kurzydłowski, Dominik; Grochala, Wojciech

    2015-12-07

    The reaction of AgF2 with P2O3F4 yields a mixed valence Ag(I)/Ag(II) difluorophosphate salt with AgAg(PO2F2)14 stoichiometry - the first Ag(ii)-PO2F2 system known. This highly moisture sensitive brown solid is thermally stable up to 120 °C, which points at further feasible extension of the chemistry of Ag(ii)-PO2F2 systems. The crystal structure shows a very complex bonding pattern, comprising of polymeric Ag(PO2F2)14(4-) anions and two types of Ag(I) cations. One particular Ag(II) site present in the crystal structure of Ag9(PO2F2)14 is the first known example of square pyramidal penta-coordinated Ag(ii) in an oxo-ligand environment. Ag(i)PO2F2 - the product of the thermal decomposition of Ag9(PO2F2)14 - has also been characterized by thermal analysis, IR spectroscopy and X-ray powder diffraction. It has a complicated crystal structure as well, which consists of infinite 1D [Ag(I)O4/2] chains which are linked to more complex 3D structures via OPO bridges. The PO2F2(-) anions bind to cations in both compounds as bidentate oxo-ligands. The terminal F atoms tend to point inside the van der Waals cavities in the crystal structure of both compounds. All important structural details of both title compounds were corroborated by DFT calculations.

  15. Maximizing the photo catalytic and photo response properties of multimodal plasmonic Ag/WO(3-x) heterostructure nanorods by variation of the Ag size.

    PubMed

    Ghosh, Sirshendu; Saha, Manas; Paul, Sumana; De, S K

    2015-11-21

    High quality nearly monodisperse colloidal WO3-x nanorods with an aspect ratio ∼18 were synthesized using the thermal decomposition technique. The effects of a capping agent and an activating agent on the nanorod aspect ratio have been studied. Excess carrier concentration due to large oxygen vacancy and smaller width of the nanorods compared to the Bohr exciton radius gives rise to an increase of the band gap. Shape anisotropy in nanorods results in two plasmonic absorbance bands at about 890 nm and 5900 nm corresponding to short axis and long axis plasmon modes. The short axis mode reveals an excellent plasmonic sensitivity of ∼345 nm per refractive index. A plasmonic photocatalysis process based on WO3-x nanorods has been developed to synthesize Ag/WO3-x heterostructures consisting of multiple Ag dots with ∼2 nm size, randomly decorated on the surface of the WO3-x nanorods. Long time irradiation leads to an increase in the size (5 nm) of Ag nanocrystals concomitant with decrease in the number of Ag nanocrystals attached per WO3-x nanorod. Plasmonic photocatalysis followed by thermal annealing produces only one Ag nanocrystal of size ∼10 nm on each WO3-x nanorod. Red shifting and broadening of plasmon bands of Ag nanocrystals and WO3-x nanorods confirm the formation of heterostructures between the metal and semiconductor. Detailed transmission electron micrograph analysis indicates the epitaxial growth of Ag nanocrystals onto WO3-x nanorods. A high photocurrent gain of about 4000 is observed for Ag (10 nm)/WO3-x heterostructures. The photodegradation rate for Rhodamine-B and methylene blue is maximum for Ag (10 nm)/WO3-x heterostructures due to efficient electron transfer from WO3-x nanorods to Ag nanocrystals. Metal plasmon-semiconductor exciton coupling, prominent plasmon absorbance of metal nanoparticles, and formation of an epitaxial interface are found to be the important factors to achieve the maximum photocatalytic activity and fabrication of a

  16. Ligand and counterion control of Ag(I) architectures: assembly of a {Ag8} ring cluster mediated by hydrophobic and Ag...Ag interactions.

    PubMed

    Fielden, John; Long, De-liang; Slawin, Alexandra M Z; Kögerler, Paul; Cronin, Leroy

    2007-10-29

    A strategy combining ligand design and counterion variation has been used to investigate the assembly of silver(I) complexes. As a result, dinuclear, octanuclear, and polymeric silver(I) species have been synthesized by complexation of the rigid aliphatic amino ligands cis-3,5-diamino-trans-hydroxycyclohexane (DAHC), cis-3,5-diamino-trans-methoxycyclohexane (DAMC), and cis-3,5-diamino-trans-tert-butyldimethylsilylanyloxycyclohexane (DATC) with silver(I) triflate, nitrate, and perchlorate. The compositions of these aggregates, established by X-ray crystallography and elemental analysis, are [{Ag(DAHC)}2](CF3SO3)2 (1), [{Ag(DAMC)}2](CF3SO3)2 (2), [{Ag(DAMC)}2](NO3)2 (3), [{Ag(DATC)}6{Ag(DAHC)}2](NO3)8 (4), and [{Ag(DATC}n](NO3)n (5), where the DAHC present in 4 is formed by in situ hydrolysis of the acid labile silyl ether group. The type of aggregate formed depends both upon the noncoordinating O-substituent of the ligand and the (also noncoordinating) counterion, with the normal preference of the ligand topology for forming Ag2L2 structures being broken by introduction of the bulky, lipophilic O-tert-butyldimethylsilyl (TBDMS) group. Of particular note is the octanuclear silver ring structure 4, which is isolated only when both the O-TBDMS group and the nitrate counteranion are present and is formed from four Ag2L2 dimers connected by Ag...Ag and hydrogen-bonding interactions. Diffusion rate measurement of this {Ag8} complex by 1H NMR (DOSY) indicates dissociation in CD3OD and CD3CN, showing that this supramolecular ring structure is formed upon crystallization, and establishing a qualitative limit to the strength of Ag...Ag interactions in solution. When solutions of the {Ag8} cluster in methanol are kept for several days though, a new UV-vis absorption is observed at around 430 nm, consistent with the formation of silver nanoparticles.

  17. Diffusivities and Atomic Mobilities of Sn-Ag and Sn-In Melts

    NASA Astrophysics Data System (ADS)

    Chen, Wei-Min; Zhang, Li-Jun; Du, Yong; Huang, Bai-Yun

    2014-04-01

    The recently developed Arrhenius formula for the modified Sutherland equation was employed to calculate the self- and impurity diffusivities in liquid Sn, Ag, and In. The reliability of the calculated self- and impurity diffusivities was validated by comparing the presently calculated results with critically reviewed literature data. Based on reliable tracer and chemical diffusivities available in literature, the atomic mobility parameters in Sn-Ag and Sn-In melts were then evaluated with the aid of the available thermodynamic description for the liquid phase. Comprehensive comparisons showed that most of the measured and theoretical diffusivities in Sn-Ag and Sn-In melts can be reasonably reproduced by the currently obtained atomic mobilities. Moreover, the atomic mobilities were further verified by comparing the model-predicted concentration profiles with the measured ones in various liquid Sn-In diffusion couples. In addition, a simulation of Ag dissolution into liquid Sn-Ag solder during a reflow process was performed via the presently obtained atomic mobilities in the Sn-Ag melt.

  18. Instantly AgNPs deposition through facile solventless technique for poly-functional cotton fabrics.

    PubMed

    Emam, Hossam E; Saleh, N H; Nagy, Khaled S; Zahran, M K

    2016-03-01

    Nowadays, functional clothes are employed for human body protection in addition to be fashionable clothes. Hence functionalization of clothes increases the attention of scientists and business. In the current study, poly-functional cotton fabric was carried out by instantly deposition of AgNPs using two solventless techniques namely; sorption and padding. Sorption technique was exhibited extremely high efficiency than padding one by ca. 10 times. By using the same concentrations of AgNO3, Ag content was ranged 69.3-6094.8 mg/kg and 33.8-609.3 mg/kg for sorption and padding, respectively. After AgNPs deposition, fabrics color was turned to gray-reddish yellow. By applying 5912.3 mgAg/kg fabric, bacterial reduction and UPF value were reached 99% and 12.59. Bacterial reduction and UPF were lessened to 90% and 10.19 after 20 washings. These findings proved that the direct AgNPs deposition into cotton using solventless/sorption technique is applicable in manufacturing of antibacterial/UV resistant fabrics with acquired decorative color.

  19. AG-041R, a gastrin/CCK-B antagonist, stimulates chondrocyte proliferation and metabolism in vitro.

    PubMed

    Ochi, M; Kawasaki, K; Kataoka, H; Uchio, Y; Nishi, H

    2001-05-25

    A newly synthesized compound, AG-041R, 3R-1-(2,2Diethoxyethyl)-3-((4methylphenyl) amino-carbonylmethyl)-3-((4methylphenyl)ureido-indoline-2-one), is a cholecyctokinin-B/gastrin receptor antagonist, but unexpectedly magnified cartilage formation in vivo. Indeed, AG-041R is a potentially effective reagent for the repair of articular cartilage defects. To clarify its effects on chondrocytes, we studied the proliferation, matrix formation, and gene expression of rabbit primary chondrocytes cultured in type I collagen gel composites with AG-041R. Both proliferation and glycosaminoglycan synthesis were stimulated with 1 microM AG-041R, but suppressed with 10 microM. The ratio of the amounts of two chondroitin sulfate isomers, chondroitin-6-sulfate to chondroitin-4-sulfate (an indicator of cartilage maturation), increased with 1 microM but decreased with 10 microM AG-041R. Gene expression analysis showed there was no change in the relative expression levels of chondrocyte markers, Type II collagen and Aggrecan, and osteoblast and adipocyte markers, Type I collagen and PPARgamma, respectively. These findings suggest that adequate concentrations of AG-041R stimulate proliferation of chondrocytes in the matrix, without changing their differentiated characteristics.

  20. Cu/Ag-based bifunctional nanoparticles obtained by one-pot laser-assisted galvanic replacement

    NASA Astrophysics Data System (ADS)

    Giorgetti, Emilia; Marsili, Paolo; Canton, Patrizia; Muniz-Miranda, Maurizio; Caporali, Stefano; Giammanco, Francesco

    2013-01-01

    We have prepared, for the first time, stable and uncapped Ag/Cu-based bifunctional nanoparticles (NPs) (BFNPs) in water, by combining ps laser ablation in liquid environment and galvanic replacement. The particles were obtained in a single step by 1,064 nm irradiation of a Cu target in water solutions of AgNO3 or AgNO2. Under proper salt concentration and irradiation conditions, the laser beam activates formation of deep orange colloids, which are positively charged and stable for weeks. High resolution transmission electron microscopy (HRTEM) analysis showed a predominance of composite crystalline nanostructures with size in the 1-15 nm range and consisting of fcc Ag and fcc Cu (or its oxides). While CuO tenorite crystalline phase was detected by HRTEM, X-ray photoelectron spectroscopy analysis permitted to observe also the Cu(I) oxidation state of Cu, being the Cu(I)/Cu(II) ratio different in the samples obtained in AgNO3 or AgNO2 baths. Functionalization with organic ligands and subsequent Raman tests demonstrated the SERS activity of the BFNPs and the existence of different complexing surface sites.

  1. Highly Reproducible Ag NPs/CNT-Intercalated GO Membranes for Enrichment and SERS Detection of Antibiotics.

    PubMed

    Qu, Lu Lu; Liu, Ying-Ya; Liu, Ming-Kai; Yang, Guo-Hai; Li, Da-Wei; Li, Hai-Tao

    2016-10-05

    The increasing pollution of aquatic environments by antibiotics makes it necessary to develop efficient enrichment and sensitive detection methods for environmental antibiotics monitoring. In this work, silver nanoparticles and carbon nanotube-intercalated graphene oxide laminar membranes (Ag NPs/CNT-GO membranes) were successfully prepared for enrichment and surface-enhanced Raman scattering (SERS) detection of antibiotics. The prepared Ag NPs/CNT-GO membranes exhibited a high enrichment ability because of the π-π stacking and electrostatic interactions of GO toward antibiotic molecules, which enhanced the sensitivity of SERS measurements and enabled the antibiotics to be determined at sub-nM concentrations. In addition, the nanochannels created by the intercalation of CNTs into GO layers resulted in an 8-fold enhancement in the water permeance of Ag NPs/CNT-GO membranes compared to that of pure GO membranes. More importantly, the Ag NPs/CNT-GO membranes exhibited high reproducibility and long-term stability. The spot-to-spot variation in SERS intensity was less than 15%, and the SERS performance was maintained for at least 70 days. The Ag NPs/CNT-GO membranes were also used for SERS detection of antibiotics in real samples; the results showed that the characteristic peaks of antibiotics were obviously recognizable. Thus, the sensitive SERS detection of antibiotics based on Ag NPs/CNT-GO offers great potential for practical applications in environmental analysis.

  2. Transparent Conductive ITO/Ag/ITO Electrode Deposited at Room Temperature for Organic Solar Cells

    NASA Astrophysics Data System (ADS)

    Kim, Jun Ho; Kang, Tae-Woon; Kwon, Sung-Nam; Na, Seok-In; Yoo, Young-Zo; Im, Hyeong-Seop; Seong, Tae-Yeon

    2017-01-01

    We investigated the optical and electrical properties of room-temperature-deposited indium-tin-oxide (ITO)/Ag (19 nm)/ITO multilayer films as a function of ITO layer thickness. The optical and electrical properties of the ITO/Ag/ITO films were compared with those of high-temperature-deposited ITO-only films for use as an anode in organic solar cells (OSCs). The ITO/Ag/ITO multilayer films had sheet resistances in the range 5.40-5.78 Ω/sq, while the ITO-only film showed 14.18 Ω/sq. The carrier concentration of the ITO/Ag/ITO films gradually decreased from 2.01 × 1022 to 7.20 × 1021 cm-3 as the ITO thickness increased from 17 nm to 83 nm. At 530 nm, the transmittance of the ITO/Ag/ITO (50 nm/19 nm/50 nm) films was 90%, while that of the ITO-only film gave 96.5%. The multilayer film had a smooth surface with a root mean square (RMS) roughness of 0.49 nm. Poly (3-hexylthiophene) (P3HT):[6,6]-phenyl-C61 butyric acid methylester (PCBM) bulk heterojunction (BHJ)-based OSCs fabricated with the ITO/Ag/ITO (50 nm/19 nm/50 nm) film showed a power conversion efficiency (PCE) (2.84%) comparable to that of OSCs with a conventional ITO-only anode (3.48%).

  3. Evaluation of genotoxic effect of silver nanoparticles (Ag-Nps) in vitro and in vivo

    NASA Astrophysics Data System (ADS)

    Tavares, Priscila; Balbinot, Fernanda; de Oliveira, Hugo Martins; Fagundes, Gabriela Elibio; Venâncio, Mireli; Ronconi, João Vitor Vieira; Merlini, Aline; Streck, Emílio L.; da Silva Paula, Marcos Marques; de Andrade, Vanessa Moraes

    2012-03-01

    Silver nanoparticles (Ag-NPs) are the most prominent nanoproducts. Due to their antimicrobial activity, they have been incorporated in different materials, such as catheters, clothes, electric home appliance, and many others. The genotoxicity of Ag-NPs (5-45 nm), in different concentrations and times of exposure, was evaluated by the comet assay in in vitro and in vivo conditions, respectively, using human peripheral blood and Swiss mice. The results showed the genotoxic effect of Ag-NPs in vitro , in all the doses tested in the initial hour of exposure, possibly through the reactive oxygen species generation. Nevertheless, the values for this damage decrease with time, indicating that the DNA may have been restored by the repair system. In the in vivo conditions, we found no genotoxicity of Ag-NPs in any hour of exposure and any dose investigated, which can be attributed to the activation of a cellular antioxidant network and the hydrophobic nature of Ag-NPs. Now, it is absolutely necessary to investigate the role of Ag-NPs in different cell lines in vivo.

  4. Microstructure evolution during annealing of an SPD- processed supersaturated Cu - 3 at.% Ag alloy

    NASA Astrophysics Data System (ADS)

    Gubicza, J.; Hegedüs, Z.; Lábár, J. L.; Subramanya Sarma, V.; Kauffmann, A.; Freudenberger, J.

    2014-08-01

    Supersaturated Cu - 3 at.% Ag alloy was processed by rolling at liquid nitrogen temperature and subsequent annealing at 623 K up to 20 min. It was found that after annealing, an inhomogeneous solute atom distribution developed, since the Ag particles with small size and/or large specific interfacial energy were dissolved due to the Gibbs-Thomson effect. In the region where the solute concentration increased, a high dislocation density was retained in the Cu matrix even after annealing, while in the region where the Ag solute content did not increase, the dislocation density decreased by more than one order of magnitude. Therefore, in the cryorolled and annealed samples, heterogeneous microstructures were developed where both the dislocation density and the solute concentration varied considerably.

  5. Inhibition of bacterial surface colonization by immobilized silver nanoparticles depends critically on the planktonic bacterial concentration.

    PubMed

    Wirth, Stacy M; Bertuccio, Alex J; Cao, Feng; Lowry, Gregory V; Tilton, Robert D

    2016-04-01

    Immobilization of antimicrobial silver nanoparticles (AgNPs) on surfaces has been proposed as a method to inhibit biofouling or as a possible route by which incidental releases of AgNPs may interfere with biofilms in the natural environment or in wastewater treatment. This study addresses the ability of planktonic Pseudomonas fluorescens bacteria to colonize surfaces with pre-adsorbed AgNPs. The ability of the AgNP-coated surfaces to inhibit colonization was controlled by the dissolved silver in the system, with a strong dependence on the initial planktonic cell concentration in the suspension, i.e., a strong inoculum effect. This dependence was attributed to a decrease in dissolved silver ion bioavailability and toxicity caused by its binding to cells and/or cell byproducts. Therefore, when the initial cell concentration was high (∼1×10(7)CFU/mL), an excess of silver binding capacity removed most of the free silver and allowed both planktonic growth and surface colonization directly on the AgNP-coated surface. When the initial cell concentration was low (∼1×10(5)CFU/mL), 100% killing of the planktonic cell inoculum occurred and prevented colonization. When an intermediate initial inoculum concentration (∼1×10(6)CFU/mL) was sufficiently large to prevent 100% killing of planktonic cells, even with 99.97% initial killing, the planktonic population recovered and bacteria colonized the AgNP-coated surface. In some conditions, colonization of AgNP-coated surfaces was enhanced relative to silver-free controls, and the bacteria demonstrated a preferential attachment to AgNP-coated, rather than bare, surface regions. The degree to which the bacterial concentration dictates whether or not surface-immobilized AgNPs can inhibit colonization has significant implications both for the design of antimicrobial surfaces and for the potential environmental impacts of AgNPs.

  6. Fluorescent DNA-bound Ag nanoclusters

    NASA Astrophysics Data System (ADS)

    O'Neill, Patrick; Velazquez, Lourdes; Weirich, Kim; Fygenson, Deborah

    2009-03-01

    Few-atom fluorescent Ag nanoclusters self-assemble on short, synthetic DNA strands, and exhibit sequence and structure dependent fluorescence ranging from the blue to the near infrared. Here we report UV excitation as a ubiquitous feature of these emitters. Each emitter thus has two excitation peaks: a visible peak which is cluster-dependent, and a UV peak which has the same wavelength for all DNA-bound Ag clusters. This UV peak corresponds to resonant absorbance by the DNA bases, and produces the same emission spectra as visible excitation, suggesting energy transfer from the DNA bases to the Ag cluster. We make use of this UV excitation to image the emitters in unstained polyacrylamide gels, and show that electrophoresis can be used to create a pure solution of green DNA:Ag11 clusters from an inhomogeneous red solution of DNA:Ag>12 clusters.

  7. Direct electrospinning of Ag/polyvinylpyrrolidone nanocables

    NASA Astrophysics Data System (ADS)

    Song, Jie; Chen, Menglin; Olesen, Mikkel Buster; Wang, Chenxuan; Havelund, Rasmus; Li, Qiang; Xie, Erqing; Yang, Rong; Bøggild, Peter; Wang, Chen; Besenbacher, Flemming; Dong, Mingdong

    2011-12-01

    Core-sheath silver nanowire/polyvinylpyrrolidone (AgNW/PVP) nanocables have been fabricated via an efficient single-spinneret electrospinning method. The core-sheath structure is revealed by combining several characterization methods. A possible formation mechanism of the AgNW/PVP nanocable involving a strong stretching during the electrospinning process is proposed. Further, electrical measurements were performed on AgNW/PVP nanocables as well as bare AgNWs, which indicated the nanocables became insulating due to the isolation of highly conductive AgNWs by insulating PVP sheath. Therefore, the described fabrication method holds potential for the fabrication of low-cost metal/polymer composite materials for nanoelectronic applications in general.

  8. Promotion of Ag/H-BEA by Mn for lean NO reduction with propane at low temperature.

    PubMed

    Pan, Hua; Su, Qingfa; Chen, Jie; Ye, Qing; Liu, Yiting; Shi, Yao

    2009-12-15

    Effects of adding manganese to Ag/H-BEA for selective catalytic reduction of NO(x) with propane (C(3)H(8)-SCR) were investigated under a lean-burn condition. Mn addition significantly promotes the catalytic performance of Ag/H-BEA below 673 K. A Ag-Mn/H-BEA catalyst with equal metal weight of 3 wt % has the highest activity for C(3)H(8)-SCR among samples with a different bimetal loading. Manganese is mainly present in the 3+ and 4+ oxidation states in Ag-Mn/H-BEA catalysts. The major contributions of manganese suggested by the data presented in this paper are to catalyze the NO oxidation and stabilize silver in a dispersed Ag(+) state. The presence of silver enforces the transformation of a certain amount of Mn(3+) ions to Mn(4+) ions. The activity of Ag-Mn/H-BEA decreases slightly at low SO(2) concentrations (0-200 ppm) but decreases significantly at high SO(2) concentrations (400-800 ppm). In the presence of 10% H(2)O and 200 ppm SO(2), the inhibition of C(3)H(8)-SCR below 673 K is more significant than that at high temperature above 673 K. Ag-Mn/H-BEA is a promising catalyst for the removal of NO(x) from diesel engine exhaust.

  9. Surface-enhanced Raman scattering studies of the reduction of p-nitroaniline catalyzed by a nanonized Ag porous-glass hybrid composite

    NASA Astrophysics Data System (ADS)

    Huang, Genin Gary; Sou, Nga-Lai; Hung, Mei-Jou

    2016-09-01

    Nanonized noble metal composites have been known for their excellent catalytic properties. However, the mechanism and intermediates formed on the surfaces of nanocatalysts during catalysis are speculated with mostly insufficient evidence. In this study, to obtain further understanding of the roles of noble metal nanocatalysts in a catalytic reaction, surface-enhanced Raman scattering (SERS) was used to monitor the surfaces of silver (Ag) nanocatalysts. Furthermore, UV-Vis spectrometry was used to trace the concentration variations of reactants and products in bulk solutions, thereby correlating the variations of the Ag nanocatalyst surfaces with those in the bulk solutions. Nanonized Ag porous-glass hybrid composites were prepared by reducing naked Ag nanoparticles on porous-glass filter plates and were used as catalysts for nitroanilines reduction. The complete process was monitored using SERS and UV-Vis spectrometry simultaneously. The results indicated that the reactant and product molecules adsorbed on the Ag nanocatalysts can reach equilibrium, and the equilibrium is affected by the reaction conditions, including reducing agent concentration, pH of the reaction system, and temperature. In addition, the reduction of reactants in the bulk solutions is also related to the behavior of Ag nanocatalyst surfaces. Furthermore, Ag nanocatalysts can act as electron relays even if their surfaces are occupied by reactants and products. Analyzing the collected SERS and UV-Vis spectra can provide a new insight into Ag nanoparticle catalysis, and the role of Ag nanocatalysts can be further comprehended.

  10. Surface-enhanced Raman scattering studies of the reduction of p-nitroaniline catalyzed by a nanonized Ag porous-glass hybrid composite.

    PubMed

    Huang, Genin Gary; Sou, Nga-Lai; Hung, Mei-Jou

    2016-09-05

    Nanonized noble metal composites have been known for their excellent catalytic properties. However, the mechanism and intermediates formed on the surfaces of nanocatalysts during catalysis are speculated with mostly insufficient evidence. In this study, to obtain further understanding of the roles of noble metal nanocatalysts in a catalytic reaction, surface-enhanced Raman scattering (SERS) was used to monitor the surfaces of silver (Ag) nanocatalysts. Furthermore, UV-Vis spectrometry was used to trace the concentration variations of reactants and products in bulk solutions, thereby correlating the variations of the Ag nanocatalyst surfaces with those in the bulk solutions. Nanonized Ag porous-glass hybrid composites were prepared by reducing naked Ag nanoparticles on porous-glass filter plates and were used as catalysts for nitroanilines reduction. The complete process was monitored using SERS and UV-Vis spectrometry simultaneously. The results indicated that the reactant and product molecules adsorbed on the Ag nanocatalysts can reach equilibrium, and the equilibrium is affected by the reaction conditions, including reducing agent concentration, pH of the reaction system, and temperature. In addition, the reduction of reactants in the bulk solutions is also related to the behavior of Ag nanocatalyst surfaces. Furthermore, Ag nanocatalysts can act as electron relays even if their surfaces are occupied by reactants and products. Analyzing the collected SERS and UV-Vis spectra can provide a new insight into Ag nanoparticle catalysis, and the role of Ag nanocatalysts can be further comprehended.

  11. Raman gas sensing of modified Ag nanoparticle SERS

    NASA Astrophysics Data System (ADS)

    Myoung, NoSoung; Yoo, Hyung Keun; Hwang, In-Wook

    2014-03-01

    Recent progress in modified Surface Enhanced Raman Scattering (SERS) using Ag nanoparticles makes them promising optical technique for direct gas sensing of interest. However, SERS has been shown to provide sub ppb level detection of the compounds in the vapor phase. The major problem with the sensitivity scaling-up was in the development of fabrication technology for stability and reproducibility of SERS substrates. We report an optimization of 1-propanethiol coated multiple Ag nanoparticle layers on SiO2 substrate as well as new records of real-time, simultaneous vapor phase detection of toluene and 1-2 dichlorobenzene by the radiation of fiber optic coupled 785 nm diode laser and spectrograph. Multiple depositions of Ag NPs were loaded on SiO2 and soaked in 1-propanethiol solution for 24 hours to modify the surface into hydrophobic due to the characteristics of vapor phase of our interests. Raman bands at 1003 cm-1 and 1130 cm-1 for toluene and 12DCB, respectively were compared to 1089 cm-1 and each gas concentration in 1000 mL flask were calculated as a function of each vapor phase ratio. The saturation of toluene and 12DCB were limited only by 800 ppm and the detectable range was 0.6-800 ppm.

  12. Point defects in epitaxial silicene on Ag(111) surfaces

    NASA Astrophysics Data System (ADS)

    Liu, Hongsheng; Feng, Haifeng; Du, Yi; Chen, Jian; Wu, Kehui; Zhao, Jijun

    2016-06-01

    Silicene, a counterpart of graphene, has achieved rapid development due to its exotic electronic properties and excellent compatibility with the mature silicon-based semiconductor technology. Its low room-temperature mobility of ˜100 cm2 V-1 s-1, however, inhibits device applications such as in field-effect transistors. Generally, defects and grain boundaries would act as scattering centers and thus reduce the carrier mobility. In this paper, the morphologies of various point defects in epitaxial silicene on Ag(111) surfaces have been systematically investigated using first-principles calculations combined with experimental scanning tunneling microscope (STM) observations. The STM signatures for various defects in epitaxial silicene on Ag(111) surface are identified. In particular, the formation energies of point defects in Ag(111)-supported silicene sheets show an interesting dependence on the superstructures, which, in turn, may have implications for controlling the defect density during the synthesis of silicene. Through estimating the concentrations of various point defects in different silicene superstructures, the mystery of the defective appearance of \\sqrt{13}× \\sqrt{13} and 2\\sqrt{3}× 2\\sqrt{3} silicene in experiments is revealed, and 4 × 4 silicene sheet is thought to be the most suitable structure for future device applications.

  13. Antibacterial biodegradable Mg-Ag alloys.

    PubMed

    Tie, D; Feyerabend, F; Müller, W D; Schade, R; Liefeith, K; Kainer, K U; Willumeit, R

    2013-06-16

    The use of magnesium alloys as degradable metals for biomedical applications is a topic of ongoing research and the demand for multifunctional materials is increasing. Hence, binary Mg-Ag alloys were designed as implant materials to combine the favourable properties of magnesium with the well-known antibacterial property of silver. In this study, three Mg-Ag alloys, Mg2Ag, Mg4Ag and Mg6Ag that contain 1.87 %, 3.82 % and 6.00 % silver by weight, respectively, were cast and processed with solution (T4) and aging (T6) heat treatment. The metallurgical analysis and phase identification showed that all alloys contained Mg4Ag as the dominant β phase. After heat treatment, the mechanical properties of all Mg-Ag alloys were significantly improved and the corrosion rate was also significantly reduced, due to presence of silver. Mg(OH)₂ and MgO present the main magnesium corrosion products, while AgCl was found as the corresponding primary silver corrosion product. Immersion tests, under cell culture conditions, demonstrated that the silver content did not significantly shift the pH and magnesium ion release. In vitro tests, with both primary osteoblasts and cell lines (MG63, RAW 264.7), revealed that Mg-Ag alloys show negligible cytotoxicity and sound cytocompatibility. Antibacterial assays, performed in a dynamic bioreactor system, proved that the alloys reduce the viability of two common pathogenic bacteria, Staphylococcus aureus (DSMZ 20231) and Staphylococcus epidermidis (DSMZ 3269), and the results showed that the killing rate of the alloys against tested bacteria exceeded 90%. In summary, biodegradable Mg-Ag alloys are cytocompatible materials with adjustable mechanical and corrosion properties and show promising antibacterial activity, which indicates their potential as antibacterial biodegradable implant materials.

  14. An ultrasensitive, uniform and large-area surface-enhanced Raman scattering substrate based on Ag or Ag/Au nanoparticles decorated Si nanocone arrays

    NASA Astrophysics Data System (ADS)

    Zhang, P. P.; Gao, J.; Sun, X. H.

    2015-01-01

    Large-area and highly ordered Si nanocone arrays decorated with Ag or Au/Ag nanoparticles have been fabricated via a mask-free lithography with reaction ion etching, followed by metal deposition process. Ultrasensitive surface enhanced Raman scattering signals with an enhancement factor of 1012 were achieved even at the concentration of the Rhodamine 6G as low as 10-15 M. The surface-enhanced Raman spectroscopy (SERS) substrate was also applied on the detection of Sudan I dye and the Raman signals were substantially enhanced as well. The stability of the SERS substrate can be significantly improved by covering Ag nanoparticles with Au thin layer, which maintain a high SERS performance even after one month storage. This nanofabrication process appears to be a feasible approach to prepare uniform and reproducible SERS-active substrates with high sensitivity and stability for practical SERS applications.

  15. Photo- and thermo-chemical transformation of AgCl and Ag2S in environmental matrices and its implication.

    PubMed

    Yin, Yongguang; Xu, Wei; Tan, Zhiqiang; Li, Yanbin; Wang, Weidong; Guo, Xiaoru; Yu, Sujuan; Liu, Jingfu; Jiang, Guibin

    2017-01-01

    AgCl and Ag2S prevalently exist in the environment as minerals and/or the chlorination and sulfidation products of ionic silver and elemental silver nanoparticles (AgNPs). In this work, we investigated the chemical transformation of AgCl and Ag2S under simulated sunlight (in water) and incineration (in sludge and simulated municipal solid waste, SMSW). In the presence of natural organic matter, AgCl in river water was observed to be transformed into AgNPs under simulated sunlight, while photo-reduction of Ag2S could not take place under the same experimental conditions. During the course of incineration, pure Ag2S was transformed into elemental silver while AgCl remained stable; however, both Ag2S in sludge and AgCl in SMSW can be transformed to elemental silver under incineration, evident by the results of X-ray absorption spectroscopy and scanning electron microscopy measurements. Incineration temperature played an important role in the transformation of Ag2S and AgCl into elemental silver. These results suggest that chemical transformations of Ag2S and AgCl into elemental silver could be a possible source of naturally occurring or unintentionally produced AgNPs, affecting the fate, transport, bioavailability and toxicity of silver. Therefore, it is necessary to include the contributions of this transformation process when assessing the risk of ionic silver/AgNPs and the utilization and management of incineration residues.

  16. Formation of AgGaS2 nano-pyramids from Ag2S nanospheres through intermediate Ag2S-AgGaS2 heterostructures and AgGaS2 sensitized Mn2+ emission.

    PubMed

    Huang, Feng; Zhou, Jiangcong; Xu, Ju; Wang, Yuansheng

    2014-02-21

    A one-pot solution synthesis of monodisperse AgGaS2 nanocrystals with uniform pyramid-like shape is realized for the first time, in which an interesting phase and shape evolution from monodisperse Ag2S nanospheres to pure AgGaS2 nano-pyramids through an intermediate stage of Ag2S-AgGaS2 heterostructures, is revealed. Evidently, upon introducing Mn(2+) ions into the reaction system, they are incorporated into AgGaS2 nano-pyramids which act as efficient sensitization matrixes for the red emission of Mn(2+) d-d transition under blue excitation. Benefiting from their non-toxicity and facile fabrication, Mn:AgGaS2 nanocrystals may find potential applications in some fields such as blue chip excited LEDs and bio-labeling.

  17. Dielectric Barrier Discharge (DBD) Plasma Assisted Synthesis of Ag2O Nanomaterials and Ag2O/RuO2 Nanocomposites

    PubMed Central

    Ananth, Antony; Mok, Young Sun

    2016-01-01

    Silver oxide, ruthenium oxide nanomaterials and its composites are widely used in a variety of applications. Plasma-mediated synthesis is one of the emerging technologies to prepare nanomaterials with desired physicochemical properties. In this study, dielectric barrier discharge (DBD) plasma was used to synthesize Ag2O and Ag2O/RuO2 nanocomposite materials. The prepared materials showed good crystallinity. The surface morphology of the Ag2O exhibited “garland-like” features, and it changed to “flower-like” and “leaf-like” at different NaOH concentrations. The Ag2O/RuO2 composite showed mixed structures of aggregated Ag2O and sheet-like RuO2. Mechanisms governing the material’s growth under atmospheric pressure plasma were proposed. Chemical analysis was performed using Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Thermogravimetric analysis (TGA) showed the thermal decomposition behavior and the oxygen release pattern. PMID:28344299

  18. All-thiol-stabilized Ag44 and Au12Ag32 nanoparticles with single-crystal structures.

    PubMed

    Yang, Huayan; Wang, Yu; Huang, Huaqi; Gell, Lars; Lehtovaara, Lauri; Malola, Sami; Häkkinen, Hannu; Zheng, Nanfeng

    2013-01-01

    Noble metal nanoparticles stabilized by organic ligands are important for applications in assembly, site-specific bioconjugate labelling and sensing, drug delivery and medical therapy, molecular recognition and molecular electronics, and catalysis. Here we report crystal structures and theoretical analysis of three Ag44(SR)30 and three Au12Ag32(SR)30 intermetallic nanoclusters stabilized with fluorinated arylthiols (SR=SPhF, SPhF2 or SPhCF3). The nanocluster forms a Keplerate solid of concentric icosahedral and dodecahedral atom shells, protected by six Ag2(SR)5 units. Positive counterions in the crystal indicate a high negative charge of 4(-) per nanoparticle, and density functional theory calculations explain the stability as an 18-electron superatom shell closure in the metal core. Highly featured optical absorption spectra in the ultraviolet-visible region are analysed using time-dependent density functional perturbation theory. This work forms a basis for further understanding, engineering and controlling of stability as well as electronic and optical properties of these novel nanomaterials.

  19. 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.

  20. A plasmonic ELISA for the naked-eye detection of chromium ions in water samples.

    PubMed

    Yao, Cuize; Yu, Shiting; Li, Xiuqing; Wu, Ze; Liang, Jiajie; Fu, Qiangqiang; Xiao, Wei; Jiang, Tianjiu; Tang, Yong

    2017-02-01

    Here, we describe the development of a triangular silver nanoprism (AgNPR) etching-based plasmonic ELISA for the colorimetric determination of Cr(III) levels in environmental water samples. This involved the creation of a novel signal generation system (substrate reaction solution) for a competitive ELISA in which hydrogen peroxide (H2O2) is used to etch triangular AgNPRs, inducing a change in color. This is achieved by controlling the H2O2 concentration that remains after degradation by catalase, which is conjugated to the secondary antibody of the ELISA. Because the degree of color change and the shift in the absorption spectrum of the substrate reaction solution are closely correlated with the Cr(III) concentration, this plasmonic ELISA can be used not only for the quantification of Cr(III) concentrations ranging from 3.13 to 50 ng/mL, with a limit of detection (LOD) of 3.13 ng/mL, but also for the visual detection (indicated by a color change from blue to mauve) of Cr(III) with a sensitivity of 6.25 ng/mL by the naked eye. Therefore, the plasmonic ELISA developed in this work represents a new strategy for heavy metal ion detection and has high potential applicability in resource-constrained areas. Graphical Abstract Schematic diagram of triangular silver nanoprism etching-based signal generation system.

  1. Electron spin resonance and thermoluminescence studies in CaSO4: Dy,Ag phosphor

    NASA Astrophysics Data System (ADS)

    Dhabekar, Bhushan; Menon, Sanjeev; Kumar, Rajesh; Gundu Rao, T. K.; Bhatt, B. C.; Lakshmanan, A. R.

    2005-09-01

    The defect centres formed in the thermoluminescence (TL) phosphor CaSO4 : Dy,Ag are studied using the technique of electron spin resonance (ESR). The Ag co-doped phosphor exhibits three glow peaks around 130°C, 220°C and 375°C, in contrast to the two glow peaks observed in the CaSO4 : Dy phosphor at 130°C and 220°C, at gamma ray dose of 1 Gy when the TL measurements were carried out in the spectral region 300-650 nm. ESR studies show that the additional peak at 375°C correlates with a Ag2+ centre formed owing to γ-irradiation and observable below -170°C. The Ag2+ centre is characterized by an axial g-tensor with principal values g|| = 2.38 and gbottom = 2.41. ESR studies further indicate that the precursor to a centre observable at low temperature (-170°C) appears to act as the recombination centre for the TL peak at 375°C; this radical is characterized by the g-values g|| = 2.0023 and gbottom = 2.0038 and is assigned to the SO_{3}^{-} radical. It is observed that there is more incorporation of Ag in the CaSO4 : Dy system as compared with that in the pure CaSO4 system. The variation of Ag2 + ESR intensity with Ag concentration as well as with dose in the range 0.3-120 kGy is studied. The Ag2 + ESR signal and TL saturate at 2 × 104 Gy, but the intensity of the SO_{3}^{-} radical continues to increase up to the studied dose of 1.2 × 105 Gy. The intensity of the SO_{3}^{-} radical decreases with Ag concentration in CaSO4 : Dy,Ag, in agreement with the TL model proposed in this work.

  2. Synthesis, kinetics and photocatalytic study of "ultra-small" Ag-NPs obtained by a green chemistry method using an extract of Rosa 'Andeli' double delight petals.

    PubMed

    Suárez-Cerda, Javier; Alonso-Nuñez, Gabriel; Espinoza-Gómez, Heriberto; Flores-López, Lucía Z

    2015-11-15

    This paper reports the effect of different concentrations of Rosa 'Andeli' double delight petals aqueous extract (PERA) in the synthesis of silver nanoparticles (Ag-NPs), using an easy green chemistry method. Its kinetics study and photocatalytic activity were also evaluated. The Ag-NPs were obtained using an aqueous silver nitrate solution (AgNO3) with 9.66% w/v, 7.25% w/v, and 4.20% w/v PERA as both reducing-stabilizing agent. The formation of the Ag-NPs was demonstrated by analysis of UV-vis spectroscopy, scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS) and transmission electron microscopy (TEM). TEM analysis shows spherical nanoparticles in shape and size between ∼0.5 and 1.4nm. A comparative study was done to determine which concentration was the best reducing-stabilizing agent, and we found out that "ultra-small" nanoparticles (0.5-1.1nm) were obtained with 9.66% w/v of PERA. The size of the Ag-NPs depends on the concentration of PERA and Ag(I). The reaction of formation of "ultra-small" Ag-NPs, proved to be first order for metallic precursor (silver) and second order for reducing-stabilizing agent (PERA). The Ag-NPs showed photocatalytic activity, in degradation of commercial dye with an efficiency of 95%.

  3. Endogenous Hydrogen Sulfide Enhances Cell Proliferation of Human Gastric Cancer AGS Cells.

    PubMed

    Sekiguchi, Fumiko; Sekimoto, Teruki; Ogura, Ayaka; Kawabata, Atsufumi

    2016-01-01

    Hydrogen sulfide (H2S), the third gasotransmitter, is endogenously generated by certain H2S synthesizing enzymes, including cystathionine-γ-lyase (CSE) and cystathionine-β-synthase (CBS) from L-cysteine in the mammalian body. Several studies have shown that endogenous and exogenous H2S affects the proliferation of cancer cells, although the effects of H2S appear to vary with cell type, being either promotive or suppressive. In the present study, we determined whether endogenously formed H2S regulates proliferation in human gastric cancer AGS cells. CSE, but not CBS, was expressed in AGS cells. CSE inhibitors, DL-propargylglycine (PPG) and β-cyano-L-alanine (BCA), significantly suppressed the proliferation of AGS cells in a concentration-dependent manner. CSE inhibitors did not increase lactate dehydrogenase (LDH) release in the same concentration range. The inhibitory effects of PPG and BCA on cell proliferation were reversed by repetitive application of NaHS, a donor of H2S. Interestingly, nuclear condensation and fragmentation were detected in AGS cells treated with PPG or BCA. These results suggest that endogenous H2S produced by CSE may contribute to the proliferation of gastric cancer AGS cells, most probably through anti-apoptotic actions.

  4. AgS2O6CF3: the first trifluoromethylsulfonylsulfate(VI).

    PubMed

    Malinowski, Przemysław J; Derzsi, Mariana; Grochala, Wojciech

    2013-08-07

    We describe the synthetic route towards a novel class of salts, trifluoromethylsulfonylsulfates, as exemplified by the silver(I) derivative (AgS2O6CF3). Formation proceeds via direct reaction between a triflate precursor, AgSO3CF3, and SO3. The title compound crystallizes in the P2(1)/c unit cell with a = 5.15746(14) Å, b = 25.8563(9) Å, c = 5.53970(14) Å and β = 101.1749(19)°. The structure is layered with the puckered [AgS2O6] 2D sheets; the terminal CF3 groups are separated by the van der Waals gap, as seen also for related metal triflates. The compound is very fragile thermally and it decomposes endothermally to AgSO3CF3 with concomitant evolution of SO3 even at 65 °C or upon grinding in an agate mortar; thus it may serve as a solid store of--otherwise volatile and corrosive--SO3. The IR and Raman spectra of AgS2O6CF3 have been tentatively assigned based on similarities to those of related Ag2S2O7 and AgSO3CF3 and phonon calculations. Synthesis and properties of KS2O6CF3 are also briefly described.

  5. Study of antibacterial activity of Ag and Ag2CO3 nanoparticles stabilized over montmorillonite

    NASA Astrophysics Data System (ADS)

    Sohrabnezhad, Sh.; Pourahmad, A.; Mehdipour Moghaddam, M. J.; Sadeghi, A.

    2015-02-01

    Silver carbonate and silver nanoparticles (NPs) over of stabilizer montmorillonite (MMT) have been synthesized in aqueous and polyol solvent, respectively. Dispersions of silver nanoparticles have been prepared by the reduction of silver nitrate over of MMT in presence and absence of Na2CO3 compound in ethylene glycol. It was observed that montmorillonite was capable of stabilizing formed Ag nanoparticles through the reduction of Ag+ ions in ethylene glycol. Na2CO3 was used as carbonate source in synthesis of Ag2CO3 NPs in water solvent and also for controlling of Ag nanoparticles size in ethylene glycol medium. The samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and ultraviolet-visible diffuse reflectance spectroscopy (DRS). The TEM images showed that Ag NPs size in presence Na2CO3 salts was smaller than without that. The results indicated intercalation of Ag and Ag2CO3 nanoparticles into the montmorillonite clay layers. The diffuse reflectance spectra exhibited a strong surface plasmon resonance (SPR) adsorption peak in the visible region, resulting from Ag nanoparticles. The antibacterial testing results showed that the Ag2CO3-MMT nanocomposite exhibited an antibacterial activity higher than Ag-MMT sample against Escherichia coli.

  6. Focused-ion-beam-fabricated Au nanorods coupled with Ag nanoparticles used as surface-enhanced Raman scattering-active substrate for analyzing trace melamine constituents in solution.

    PubMed

    Sivashanmugan, Kundan; Liao, Jiunn-Der; Liu, Bernard Haochih; Yao, Chih-Kai

    2013-10-24

    A well-ordered Au-nanorod array with a controlled tip ring diameter (Au_NRsd) was fabricated using the focused ion beam method. Au_NRsd was then coupled with Ag nanoparticles (Ag NPs) to bridge the gaps among Au nanorods. The effect of surface-enhanced Raman scattering (SERS) on Au_NRsd and Ag NPs/Au_NRsd was particularly verified using crystal violet (CV) as the molecular probe. Raman intensity obtained from a characteristic peak of CV on Au_NRsd was estimated by an enhancement factor of ≈10(7) in magnitude, which increased ≈10(12) in magnitude for that on Ag NPs/Au_NRsd. A highly SERS-active Ag NPs/Au_NRsd was furthermore applied for the detection of melamine (MEL) at very low concentrations. Raman-active peaks of MEL (10(-3) to 10(-12)M) in water or milk solution upon Au_NRsd or Ag NPs/Au_NRsd were well distinguished. The peaks at 680 and 702 cm(-1) for MEL molecules were found suitable to be used as the index for sensing low-concentration MEL in a varied solution, while that at 1051 cm(-1) was practical to interpret MEL molecules in water or milk solution bonded with Au (i.e., Au_NRsd) or Ag (i.e., Ag NPs/Au_NRsd) surface. At the interface of Ag NPs/Au_NRsd and MEL molecules in milk solution, a laser-induced electromagnetic field or hotspot effect was produced and competent to sense low-concentration MEL molecules interacting with Ag and Au surfaces. Accordingly, Ag NPs/Au_NRsd is very promising to be used as a fast and sensitive tool for screening MEL in complex matrices such as adulteration in e.g., food and pharmaceutical products.

  7. Effects on the optical properties and conductivity of Ag-N co-doped ZnO

    NASA Astrophysics Data System (ADS)

    Xu, Zhenchao; Hou, Qingyu; Qu, Lingfeng

    2017-01-01

    Nowadays, the studies of the effects on the optical bandgap, absorption spectrum, and electrical properties of Ag-N co-doped ZnO have been extensively investigated. However, Ag and N atoms in doped systems are randomly doped, and the asymmetric structure of ZnO is yet to be explored. In this paper, the geometric structure, stability, density of states, absorption spectra and conductivity of pure and Ag-N co-doped Zn1‑xAgxO1‑xNx(x=0.03125, 0.0417 and 0.0625) in different orientations are calculated by using plane-wave ultrasoft pseudopotential on the basis of density functional theory with GGA+U method. Results show that the volume, equivalent total energy and formation energy of the doped system increase as the concentration of Ag-N co-doped Zn1‑xAgxO1‑xNx increases at the same doping mode. The doped systems also become unstable, and difficulty in doping. At the same concentration of Ag-N co-doped Zn1‑xAgxO1‑xNx, the systems with Ag-N along the c-axis orientation is unstable, and doping is difficult. The optical bandgap of Ag-N co-doped systems is narrower than that of the pure ZnO. At the same doping mode, the optical bandgap of the systems with Ag-N perpendicular to the c-axis orientation becomes narrow as the concentration of Ag-N co-doped Zn1‑xAgxO1‑xNx increases. The absorption spectra of the doped systems exhibit a red shift, and this red shift becomes increasingly significant as the concentration of Ag-N co-doped Zn1‑xAgxO1‑xNx increases. Under the same condition, the relative hole concentrations of the doped systems increases, the hole effective mass in valence band maximum decreases, the hole mobility decreases, the ionization energy decreases, Bohr radius increases, the conductance increases and the conductivity become better. Our results may be used as a basis for the designing and preparation of new optical and electrical materials for Ag-N co-doped ZnO applied in low temperature end of temperature difference battery.

  8. Hierarchically plasmonic photocatalysts of Ag/AgCl nanocrystals coupled with single-crystalline WO3 nanoplates

    NASA Astrophysics Data System (ADS)

    Chen, Deliang; Li, Tao; Chen, Qianqian; Gao, Jiabing; Fan, Bingbing; Li, Jian; Li, Xinjian; Zhang, Rui; Sun, Jing; Gao, Lian

    2012-08-01

    The hierarchical photocatalysts of Ag/AgCl@plate-WO3 have been synthesized by anchoring Ag/AgCl nanocrystals on the surfaces of single-crystalline WO3 nanoplates that were obtained via an intercalation and topochemical approach. The heterogeneous precipitation process of the PVP-Ag+-WO3 suspensions with a Cl- solution added drop-wise was developed to synthesize AgCl@WO3 composites, which were then photoreduced to form Ag/AgCl@WO3 nanostructures in situ. WO3 nanocrystals with various shapes (i.e., nanoplates, nanorods, and nanoparticles) were used as the substrates to synthesize Ag/AgCl@WO3 photocatalysts, and the effects of the WO3 contents and photoreduction times on their visible-light-driven photocatalytic performance were investigated. The techniques of TEM, SEM, XPS, EDS, XRD, N2 adsorption-desorption and UV-vis DR spectra were used to characterize the compositions, phases and microstructures of the samples. The RhB aqueous solutions were used as the model system to estimate the photocatalytic performance of the as-obtained Ag/AgCl@WO3 nanostructures under visible light (λ >= 420 nm) and sunlight. The results indicated that the hierarchical Ag/AgCl@plate-WO3 photocatalyst has a higher photodegradation rate than Ag/AgCl, AgCl, AgCl@WO3 and TiO2 (P25). The contents and morphologies of the WO3 substrates in the Ag/AgCl@plate-WO3 photocatalysts have important effects on their photocatalytic performance. The related mechanisms for the enhancement in visible-light-driven photodegradation of RhB molecules were analyzed.The hierarchical photocatalysts of Ag/AgCl@plate-WO3 have been synthesized by anchoring Ag/AgCl nanocrystals on the surfaces of single-crystalline WO3 nanoplates that were obtained via an intercalation and topochemical approach. The heterogeneous precipitation process of the PVP-Ag+-WO3 suspensions with a Cl- solution added drop-wise was developed to synthesize AgCl@WO3 composites, which were then photoreduced to form Ag/AgCl@WO3 nanostructures in

  9. SERS detection of low-concentration adenine by a patterned silver structure immersion plated on a silicon nanoporous pillar array.

    PubMed

    Feng, Fei; Zhi, Gang; Jia, He Shun; Cheng, Liang; Tian, Yong Tao; Li, Xin Jian

    2009-07-22

    A patterned Ag structure was grown on a Si nanoporous pillar array (Si-NPA) by an immersion plating method, and its surface-enhanced Raman scattering (SERS) activity toward adenine was studied. It was shown that two kinds of Ag structures were grown on Si-NPA, a continuous film covering the Si-NPA substrate and composed of Ag nanocrystallites (nc-Ag), and a quasi-regular, interconnected network composed of loop-chains of sub-micron Ag crystallites surrounding the porous Si pillars. The SERS detection of low-concentration adenine solution was performed by using Ag/Si-NPA as active substrates, in which significantly enhanced Raman signals were observed. The SERS enhancement was attributed to the active spacing sites formed between the Ag particles and the nc-Ag which met the optimal size for causing a SERS effect. Based on the measured SERS spectra, the adsorption mode of adenine molecules on Ag particles was deduced. These results indicated that Ag/Si-NPA might be a promising active substrate for SERS detection of low-concentration bio-molecules.

  10. The AGS with four helical magnets

    SciTech Connect

    Tsoupas, N.; Huang, H.; MacKay, W.W.; Roser, T.; Trbojevic, D.

    2010-02-25

    The idea of using multiple partial helical magnets was applied successfully to the AGS synchrotron, to preserve the proton beam polarization. In this paper we explore in details the idea of using four helical magnets placed symmetrically in the AGS ring. This modification provides many advantages over the present setup of the AGS that uses two partial helical magnets. First, it provides a larger 'spin tune gap' for the placement of the vertical betatron tune of the AGS during acceleration, second, the vertical spin direction during the beam injection and extraction is closer to vertical, third, the symmetric placement of the snakes allows for a better control of the AGS optics, and for reduced values of the beta and eta functions, especially near injection, fourth, the optical properties of the helical magnets also favor the placement of the horizontal betatron tune in the 'spin tune gap', thus eliminating the horizontal spin resonances. In this paper we provide results on the spin tune and on the optics of the AGS with four partial helical magnets, and we compare these results with the present setup of the AGS that uses two partial helical magnets.

  11. Tm:YLF Pumped Ho:YAG and Ho:LuAG Lasers

    NASA Technical Reports Server (NTRS)

    Barnes, Norman P.; Reichle, Donald J.; Walsh, Brian M.; Axenson, Theresa J.

    2004-01-01

    Room temperature Ho:YAG and Ho:LuAG lasers pumped by a Tm:YLF laser demonstrated a 3.4 mJ threshold and 0.41 slope efficiency, incident optical to laser output energy. Results for numerous rod lengths, Ho concentrations, and output mirror reflectivities are presented.

  12. Ag-Incorporated Organic-Inorganic Perovskite Films and Planar Heterojunction Solar Cells.

    PubMed

    Chen, Qi; Chen, Lei; Ye, Fengye; Zhao, Ting; Tang, Feng; Rajagopal, Adharsh; Jiang, Zheng; Jiang, Shenlong; Jen, Alex K-Y; Xie, Yi; Cai, Jinhua; Chen, Liwei

    2017-04-06

    Controlled doping for adjustable material polarity and charge carrier concentration is the basis of semiconductor materials and devices, and it is much more difficult to achieve in ionic semiconductors (e.g., ZnO and GaN) than in covalent semiconductors (e.g., Si and Ge), due to the high intrinsic defect density in ionic semiconductors. The organic-inorganic perovskite material, which is frenetically being researched for applications in solar cells and beyond, is also an ionic semiconductor. Here we present the Ag-incorporated organic-inorganic perovskite films and planar heterojunction solar cells. Partial substitution of Pb(2+) by Ag(+) leads to improved film morphology, crystallinity, and carrier dynamics as well as shifted Fermi level and reduced electron concentration. Consequently, in planar heterojunction photovoltaic devices with inverted stacking structure, Ag incorporation results in an enhancement of the power conversion efficiency from 16.0% to 18.4% in MAPbI3 based devices and from 11.2% to 15.4% in MAPbI3-xClx based devices. Our work implies that Ag incorporation is a feasible route to adjust carrier concentrations in solution-processed perovskite materials in spite of the high concentration of intrinsic defects.

  13. Distribution of Ag in Cu-sulfides in Kupferschiefer deposit, SW Poland

    NASA Astrophysics Data System (ADS)

    Kozub, Gabriela A.

    2014-05-01

    The Cu-Ag Kupferschiefer deposit located at the Fore-Sudetic Monocline (SW Poland) is a world class deposit of stratabound type. The Cu-Ag mineralization in the deposit occurs in the Permian sedimentary rocks (Rotliegend and Zechstein) in three lithological types of ore: the dolomite, the black shale and the sandstone. Silver, next to copper, is the most important element in the Kupferschiefer deposit (Salamon 1979; Piestrzyński 2007; Pieczonka 2011). Although occurrence of the Ag-minerals such as native silver, silver amalgams, stromeyerite, jalpaite and mckinstryite, silver is mainly present in the deposit due to isomorphic substitutions in Cu-minerals such as chalcocite, bornite, tennantite, covellite and chalcopyrite. The aim of the study was to define distribution of silver in Cu-minerals and correlate occurrence of Ag-enriched Cu-sulfides with native silver and silver amalgams. Identification of minerals and textural observation were performed using field emission scanning electron microscope. Analyzes of chemical composition of Cu-sulfides were performed utilizing electron microprobe. Silver concentration in Cu sulfides ranges from 0.1 to 10.4 wt.% in chalcocite, 0.2-15.8 wt.% in bornite, 0.1-2.9 wt.% in tennantite, 0.05-0.3 wt.% in chalcopyrite and ca. 0.4 wt.% in covellite. In general, distribution of silver in Cu-minerals is irregular, as indicated by high variations of Ag concentration in each mineral. Content of Ag in Cu-sulphides, in samples where native silver and silver amalgams are not found, is lower than in samples, where native silver and silver amalgams are noted. The chemical analyzes of Ag-bearing Cu-minerals indicate decrease of Cu content in minerals with high Ag concentration. In such case, decrease of Fe content is also noted in bornite. Lack of micro-inclusions of the native silver or silver amalgams in the Cu-minerals indicates that presence of Ag is mainly related to the isomorphic substitutions. This is in agreement with previous

  14. Surface- and tip-enhanced Raman scattering of bradykinin onto the colloidal suspended Ag surface.

    PubMed

    Swiech, D; Ozaki, Y; Kim, Y; Proniewicz, E

    2015-07-14

    In this paper, surface- (SERS) and tip-enhanced Raman scattering (TERS) techniques were used to determine the adsorption mode of bradykinin (BK), a small peptide implicated in, for example, carcinoma growth, onto colloidal suspended Ag surfaces under various environmental conditions, including: peptide concentrations (10(-5)-10(-7) M), excitation wavelengths (514.5 and 785.0 nm), and pH of aqueous sol solutions (from pH = 3 to pH = 11). The metal surface plasmon and rheology of the colloidal suspended Ag surface were explored by ultraviolet-visible (UV-Vis) spectroscopy and atomic force/scanning electron microscopy (AFM/SEM). The SERS results indicated that the peptide concentration of 10(-5) M was the optimal peptide concentration for monolayer colloidal coverage. The Phe(5/8) and Arg(9) residues of BK generally participated in the interactions with colloidal suspended Ag surfaces. The amide group appeared to be arranged in the same manner to the Ag surface in the pH range of 3 to 11. At acidic pH of the solution (pH = 3 to 5), the BK -COO(-) terminal group binds to the Ag surface as a bidentate (at pH = 3) or monodentate (at pH = 5) chelating ligand. At pH = 11, the imino group of Arg(9), probably due to its -C[double bond, length as m-dash]N(⊕)H2 protonation state, was not involved in the interaction with Ag. The reduction in the solution alkalinity (pH = 9) produced the deprotonation of the -C=N(⊕)H2 group followed by group rearrangement in a way favoring the interaction between the lone electron pair on N and Ag. The TERS studies confirmed the proposed, on the basis of SERS, behavior of BK onto the colloidal suspended Ag at pH = 7 and showed that in different points of the colloidal suspended Ag surface the same peptide fragments approximately having the same orientations with respect to this surface interact with it.

  15. Ion-exchange synthesis of Ag/Ag2S/Ag3CuS2 ternary hollow microspheres with efficient visible-light photocatalytic activity.

    PubMed

    Xing, Chaosheng; Zhang, Yuan; Wu, Zhudong; Jiang, Deli; Chen, Min

    2014-02-21

    Ternary Ag/Ag2S/Ag3CuS2 hollow microspheres were synthesized via an in situ ion-exchange method using Cu7S4 hollow submicrospheres as the template. The as-obtained Ag/Ag2S/Ag3CuS2 composite exhibited a well-defined uniform hollow microsphere morphology with an average diameter of about 1.3 μm. The photocatalytic property of the as-prepared Ag/Ag2S/Ag3CuS2 hollow microsphere composite was investigated by the decomposition of methyl orange (MO) under visible light irradiation (λ > 420 nm). It was shown that the photocatalytic activity of the Ag/Ag2S/Ag3CuS2 hollow microsphere was higher than those of Ag/Ag2S, Cu2O, Cu7S4 and P25 for the photodegradation of MO under visible light irradiation. Radical scavenger experiments demonstrated that superoxide radicals and holes were the main reactive species for MO degradation.

  16. Agent planning in AgScala

    NASA Astrophysics Data System (ADS)

    Tošić, Saša; Mitrović, Dejan; Ivanović, Mirjana

    2013-10-01

    Agent-oriented programming languages are designed to simplify the development of software agents, especially those that exhibit complex, intelligent behavior. This paper presents recent improvements of AgScala, an agent-oriented programming language based on Scala. AgScala includes declarative constructs for managing beliefs, actions and goals of intelligent agents. Combined with object-oriented and functional programming paradigms offered by Scala, it aims to be an efficient framework for developing both purely reactive, and more complex, deliberate agents. Instead of the Prolog back-end used initially, the new version of AgScala relies on Agent Planning Package, a more advanced system for automated planning and reasoning.

  17. SPIN MATCHING FROM AGS TO RHIC.

    SciTech Connect

    MACKAY,W.W.; TSOUPAS,N.

    2002-11-06

    With a partial Siberian snake in the AGS and transport lines with interspersed horizontal and vertical bends, the incoming spin direction at the injection points of both the collider rings is not likely to match the ideal vertical stable spin direction of RHIC which has two full helical Siberian snakes per ring. In this paper we examine the matching of a polarized beam transferred from the AGS into RHIC. The present 5% partial solenoidal snake as well as a proposed 20% superconducting helical are considered for the AGS. Solutions with retuned snakes in RHIC to better match the incoming beam have been found.

  18. Ozone decomposition on Ag/SiO2 and Ag/clinoptilolite catalysts at ambient temperature.

    PubMed

    Nikolov, Penko; Genov, Krassimir; Konova, Petya; Milenova, Katya; Batakliev, Todor; Georgiev, Vladimir; Kumar, Narendra; Sarker, Dipak K; Pishev, Dimitar; Rakovsky, Slavcho

    2010-12-15

    Silver modified zeolite (Bulgarian natural clinoptilolite) and Ag/silica catalysts were synthesized by ion exchange and incipient wet impregnation method respectively and characterized by different techniques. DC arc-AES was used for Ag detection. XRD spectra show that Ag is loaded over the surface of the SiO(2) sample and that after the ion-exchange process the HEU type structure of clinoptilolite is retained. UV-VIS (specific reflection at 310 nm) and IR (band at 695 cm(-1)) spectroscopy analysis proved that silver is loaded as a T-atom into zeolite channels as Ag(+), instead of Na(+), Ca(2+), or K(+) ions, existing in the natural clinoptilolite form. The samples Ag/SiO(2) and Ag-clinoptilolite were tested as catalysts for decomposition of gas phase ozone. Very high catalytic activity (up to 99%) was observed and at the same time the catalysts remained active over time at room temperature.

  19. Control and performance of the AGS and AGS Booster Main Magnet Power Supplies

    SciTech Connect

    Reece, R.K.; Casella, R.; Culwick, B.; Geller, J.; Marneris, I.; Sandberg, J.; Soukas, A.; Zhang, S.Y.

    1993-01-01

    Techniques for precision control of the main magnet power supplies for the AGS and AGS Booster synchrotron will be discussed. Both synchrotrons are designed to operate in a Pulse-to-Pulse Modulation (PPM) environment with a Supercycle Generator defining and distributing global timing events for the AGS Facility. Details of modelling, real-time feedback and feedforward systems, generation and distribution of real time field data, operational parameters and an overview of performance for both machines are included.

  20. Control and performance of the AGS and AGS Booster Main Magnet Power Supplies

    SciTech Connect

    Reece, R.K.; Casella, R.; Culwick, B.; Geller, J.; Marneris, I.; Sandberg, J.; Soukas, A.; Zhang, S.Y.

    1993-06-01

    Techniques for precision control of the main magnet power supplies for the AGS and AGS Booster synchrotron will be discussed. Both synchrotrons are designed to operate in a Pulse-to-Pulse Modulation (PPM) environment with a Supercycle Generator defining and distributing global timing events for the AGS Facility. Details of modelling, real-time feedback and feedforward systems, generation and distribution of real time field data, operational parameters and an overview of performance for both machines are included.

  1. 1,4-Benzodiazepine drugs adsorption on the Ag colloidal surface

    NASA Astrophysics Data System (ADS)

    Cîntã, S.; Iliescu, T.; Astilean, S.; David, L.; Cozar, O.; Kiefer, W.

    1999-05-01

    The adsorption behaviour in the SERS complex of diazepam (7-chloro-1-methyl-5-phenyl-3-dihydro-1,4-benzodiazepin-2-one) and nitrazepam (1,3-dihydro-7-nitro-5-phenyl-1,4-benzodiazepin-2-one) with the Ag colloidal particles is reported and discussed. In both cases, the CN bond vibration of the 1,4-benzodiazepine is strongly affected by adsorption and enhanced. The SERS system of Ag colloid with diazepam or nitrazepam allow the recognition of the drug sample at concentration of 10 -7 mol l -1.

  2. Enhancement of electric field and Raman scattering by Ag coated Ni nanotips

    NASA Astrophysics Data System (ADS)

    Ye, Dexian; Mutisya, Stephen; Bertino, Massimo

    2011-08-01

    Localization and enhancement of electric field by Ag-coated vertical Ni nanotip arrays were studied by using finite-different time domain calculations. With the 30 nm thick Ag coating, the nanotips can localize and enhance the electric field to more than 103 times under the excitation of TE-polarized light with a 532 nm wavelength. Nanotip-enhanced Raman scattering of cytochrome-c protein was demonstrated in a confocal Raman microscope. Significant enhancement of Raman spectrum was achieved at 1 × 10-9 mol/l concentration of the proteins.

  3. Effects of Ag on the Kirkendall void formation of Sn-xAg/Cu solder joints

    NASA Astrophysics Data System (ADS)

    Kim, Sunghwan; Yu, Jin

    2010-10-01

    Binary Sn-Ag solders with varying amounts of Ag (0.5, 2.0, and 3.5 wt %) were reacted with Cu under bump metallurgy (UBM) which was electroplated with bis-sodium sulfopropyl-disulfide additive, and the characteristics of Kirkendall void formation at the solder joints were investigated. The results indicate that the propensity to form Kirkendall voids at the solder joint decreased with the Ag content. Subsequent Auger electron spectroscopy analyses showed that Ag dissolved in the Cu UBM reduced the segregation of S to the Cu3Sn/Cu interface, which suppressed the nucleation of Kirkendall voids at the interface.

  4. Nanoporous Ag prepared from the melt-spun Cu-Ag alloys

    NASA Astrophysics Data System (ADS)

    Li, Guijing; Song, Xiaoping; Sun, Zhanbo; Yang, Shengchun; Ding, Bingjun; Yang, Sen; Yang, Zhimao; Wang, Fei

    2011-07-01

    Nanoporous Ag ribbons with different morphology and porosity were achieved by the electrochemical corrosion of the melt-spun Cu-Ag alloys. The Cu-rich phase in the alloys was removed, resulting in the formation of the nanopores distributed across the whole ribbon. It is found that the structures, morphology and porosity of the nanoporous Ag ribbons were dependent on the microstructures of the parent alloys. The most of ligaments presented a rod-like shape due to the formation of pseudoeutectic microstructure in the melt-spun Cu 55Ag 45 and Cu 70Ag 30 alloys. For nanoporous Ag prepared from Cu 85Ag 15 alloys, the ligaments were camber-like because of the appearance of the divorced microstructures. Especially, a novel bamboo-grove-like structure could be observed at the cross-section of the nanoporous Ag ribbons. The experiment reveals that nanoporous Ag ribbons exhibited excellent enhancement of surface-enhanced Raman scattering (SERS) effect, but a slight difference existed due to the discrepancy of their morphology.

  5. Maximizing the photo catalytic and photo response properties of multimodal plasmonic Ag/WO3-x heterostructure nanorods by variation of the Ag size

    NASA Astrophysics Data System (ADS)

    Ghosh, Sirshendu; Saha, Manas; Paul, Sumana; de, S. K.

    2015-10-01

    High quality nearly monodisperse colloidal WO3-x nanorods with an aspect ratio ~18 were synthesized using the thermal decomposition technique. The effects of a capping agent and an activating agent on the nanorod aspect ratio have been studied. Excess carrier concentration due to large oxygen vacancy and smaller width of the nanorods compared to the Bohr exciton radius gives rise to an increase of the band gap. Shape anisotropy in nanorods results in two plasmonic absorbance bands at about 890 nm and 5900 nm corresponding to short axis and long axis plasmon modes. The short axis mode reveals an excellent plasmonic sensitivity of ~345 nm per refractive index. A plasmonic photocatalysis process based on WO3-x nanorods has been developed to synthesize Ag/WO3-x heterostructures consisting of multiple Ag dots with ~2 nm size, randomly decorated on the surface of the WO3-x nanorods. Long time irradiation leads to an increase in the size (5 nm) of Ag nanocrystals concomitant with decrease in the number of Ag nanocrystals attached per WO3-x nanorod. Plasmonic photocatalysis followed by thermal annealing produces only one Ag nanocrystal of size ~10 nm on each WO3-x nanorod. Red shifting and broadening of plasmon bands of Ag nanocrystals and WO3-x nanorods confirm the formation of heterostructures between the metal and semiconductor. Detailed transmission electron micrograph analysis indicates the epitaxial growth of Ag nanocrystals onto WO3-x nanorods. A high photocurrent gain of about 4000 is observed for Ag (10 nm)/WO3-x heterostructures. The photodegradation rate for Rhodamine-B and methylene blue is maximum for Ag (10 nm)/WO3-x heterostructures due to efficient electron transfer from WO3-x nanorods to Ag nanocrystals. Metal plasmon-semiconductor exciton coupling, prominent plasmon absorbance of metal nanoparticles, and formation of an epitaxial interface are found to be the important factors to achieve the maximum photocatalytic activity and fabrication of a high speed

  6. Lesson 3: Attorney General (AG) Certification

    EPA Pesticide Factsheets

    The AG Certification is a letter confirming legal authority to implement the electronic reporting covered by the application and enforce the affected programs using the electronic documents received under those programs.

  7. Near-infrared electrogenerated chemiluminescence of ultrasmall Ag2Se quantum dots for the detection of dopamine.

    PubMed

    Cui, Ran; Gu, Yi-Ping; Bao, Lei; Zhao, Jing-Ya; Qi, Bao-Ping; Zhang, Zhi-Ling; Xie, Zhi-Xiong; Pang, Dai-Wen

    2012-11-06

    The near-infrared (NIR) electrogenerated chemiluminescence (ECL) of water-dispersed Ag(2)Se quantum dots (QDs) with ultrasmall size was presented for the first time. The Ag(2)Se QDs have shown a strong and efficient cathodic ECL signal with K(2)S(2)O(8) as coreactant on the glassy carbon electrode (GCE) in aqueous solution. The ECL spectrum exhibited a peak at 695 nm, consistent with the peak in photoluminescence (PL) spectrum of the Ag(2)Se QDs solution, indicating that the Ag(2)Se QDs had no deep surface traps. Dopamine was chosen as a model analyte to study the potential of Ag(2)Se QDs in the ECL analytical application. The ECL signal of Ag(2)Se QDs can also be used for the detection of the dopamine concentration in the practical drug (dopamine hydrochloride injection) containing several adjuvants such as edetate disodium, sodium bisulfite, sodium chloride and so on. The Ag(2)Se QDs could be a promising candidate emitter of ECL biosensors in the future due to their fantastic features, such as ultrasmall size, low toxicity, good water solubility, and near infrared (NIR) fluorescent emission.

  8. The Lumipulse G HBsAg-Quant assay for screening and quantification of the hepatitis B surface antigen.

    PubMed

    Yang, Ruifeng; Song, Guangjun; Guan, Wenli; Wang, Qian; Liu, Yan; Wei, Lai

    2016-02-01

    Qualitative HBsAg assay is used to screen HBV infection for decades. The utility of quantitative assay is also rejuvenated recently. We aimed to evaluate and compare the performance of a novel ultra-sensitive and quantitative assay, the Lumipulse assay, with the Architect and Elecsys assays. As screening methods, specificity was compared using 2043 consecutive clinical routine samples. As quantitative assays, precision and accuracy were assessed. Sera from 112 treatment-naïve chronic hepatitis B patients, four patients undergoing antiviral therapy and one patient with acute infection were tested to compare the correlations. Samples with concurrent HBsAg/anti-HBs were also quantified. The Lumipulse assay precisely quantified ultra-low level of HBsAg (0.004 IU/mL). It identified additional 0.98% (20/2043) clinical samples with trance amount of HBsAg. Three assays displayed excellent linear correlations irrespective of genotypes and S-gene mutations (R(2)>0.95, P<0.0001), while minor quantitative biases existed. The Lumipulse assay did not yield higher HBsAg concentrations in samples with concomitant anti-HBs. Compared with other assays, the Lumipulse assay is sensitive and specific for detecting HBsAg. The interpretation of the extremely low-level results, however, is challenging. Quantitative HBsAg results by different assays are highly correlated, but they should be interpreted interchangeably only after conversion to eliminate the biases.

  9. One-pot green fabrication and antibacterial activity of thermally stable corn-like CNC/Ag nanocomposites

    NASA Astrophysics Data System (ADS)

    Yu, Hou-Yong; Qin, Zong-Yi; Sun, Bin; Yan, Chen Feng; Yao, Ju-Ming

    2014-01-01

    Corn-like cellulose nanocrystals/silver (CNC/Ag) nanocomposites were prepared by formic acid/hydrochloric acid hydrolysis of commercial microcrystalline cellulose (MCC), and redox reaction with silver ammonia aqueous solution (Ag(NH3)2(OH)) in one-pot green synthesis, in which the preparation and modification of CNCs were performed simultaneously and the resultant modified CNCs could be as reducing, stabilizing and supporting agents for silver nanoparticles. The influences of the Ag+ ion concentrations on the morphology, microstructure, and properties of the CNC/Ag nanocomposites were investigated. It is found that corn-like CNC/Ag nanocomposites containing Ag nanoparticles with diameter of about 20-40 nm were obtained. Compared to the MCCs, high crystallinity of 88.5 % and the maximum degradation temperature ( T max) of 364.5 °C can be achieved. Moreover, the CNC/Ag nanocomposites showed strong antibacterial activity against both Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus. Furthermore, such nanocomposites can act as bifunctional nanofillers to improve thermal stability, mechanical property, and antibacterial activity of commercial poly(3-hydroxybutyrate-co-3-hydroxyvalerate) and poly(lactic acid).

  10. ZnO-Ag core shell nanocomposite formed by green method using essential oil of wild ginger and their bactericidal and cytotoxic effects

    NASA Astrophysics Data System (ADS)

    Azizi, Susan; Mohamad, Rosfarizan; Rahim, Raha Abdul; Moghaddam, Amin Boroumand; Moniri, Mona; Ariff, Arbakariya; Saad, Wan Zuhainis; Namvab, Farideh

    2016-10-01

    In this paper, a novel green method for fabrication of zinc oxide-silver (ZnO-Ag) core-shell nanocomposite using essential oil of ginger (EO-G) is reported. The EO-G played two significant roles in the synthesis process: it could act as a reaction media for the formation of ZnO and reduce Ag+ to Ag0. The bioformed ZnO-Ag nanocomposite was compared with pure biosynthesized ZnO-NPs and characterized by UV-vis spectroscopy, TEM, EDX, XRD and FTIR. The characterization results confirmed that Ag-NPs had been embedded in ZnO hexagonal nanoparticles. Six Gram positive and negative pathogens were used to investigate the antibacterial effects of these samples. Ag-doping improves the bactericidal activity of ZnO-NPs. In vitro cytotoxicity studies on Vero cells, a dose dependent toxicity with non-toxic effect of concentration below 100 μg/mL was shown for ZnO-Ag nanocomposite. The biosynthesized ZnO-Ag nanocomposites were found to be comparable to those obtained from the conventional methods using hazardous materials which can be an excellent alternative for the synthesis of ZnO-Ag using biomass.

  11. Failure of the Hume-Rothery stabilization mechanism in the Ag5Li8 gamma-brass studied by first-principles FLAPW electronic structure calculations

    NASA Astrophysics Data System (ADS)

    Mizutani, U.; Asahi, R.; Sato, H.; Noritake, T.; Takeuchi, T.

    2008-07-01

    The first-principles FLAPW (full potential linearized augmented plane wave) electronic structure calculations were performed for the Ag5Li8 gamma-brass, which contains 52 atoms in a unit cell and has been known for many years as one of the most structurally complex alloy phases. The calculations were also made for its neighboring phase AgLi B2 compound. The main objective in the present work is to examine if the Ag5Li8 gamma-brass is stabilized at the particular electrons per atom ratio e/a = 21/13 in the same way as some other gamma-brasses like Cu5Zn8 and Cu9Al4, obeying the Hume-Rothery electron concentration rule. For this purpose, the e/a value for the Ag5Li8 gamma-brass as well as the AgLi B2 compound was first determined by means of the FLAPW-Fourier method we have developed. It proved that both the gamma-brass and the B2 compound possess an e/a value equal to unity instead of 21/13. Moreover, we could demonstrate why the Hume-Rothery stabilization mechanism fails for the Ag5Li8 gamma-brass and proposed a new stability mechanism, in which the unique gamma-brass structure can effectively lower the band-structure energy by forming heavily populated bonding states near the bottom of the Ag-4d band.

  12. AgRISTARS documents tracking list report

    NASA Technical Reports Server (NTRS)

    Hawkins, J. L.

    1982-01-01

    A quarterly listing of those documents and related publications that have been issued and placed in the AgRISTARS tracking system is presented. The Tracking List Report provides a catalog, by project, of technical publications arranged by type of document and gives the reference AgRISTARS document numbers, title and date of publication, the issuing organization, and the National Technical Information Service reference number.

  13. BNL AGS - a context for kaon factories

    SciTech Connect

    Littenberg, L.S.

    1983-05-01

    Figure 1 shows the Brookhaven site with the AGS-CBA complex highlighted. In this photograph the AGS is dwarfed by CBA and indeed during the past few years future plans for particle physics at BNL have been dominated by this enormous project. However, very recently interest in future physics use of the AGS has undergone a strong revival. Indeed, since the beginning of this year, two projects for augmenting the AGS have been proposed. Such projects could keep the AGS viable as a research machine for many years to come. In general such schemes will also improve the performance and increase the versatility of the CBA, and so are doubly valuable. It should be kept in mind that in spite of the fact the AGS has been perhaps the most fruitful machine in the history of high energy physics, its full capacities have never been exploited. Even without improvements at least one generation of rare K decay experiments beyond those currently launched seems feasible. Beyond that a major effort at any of the experiments discussed above could take it to the point where it would be limited by intrinsic physics background. To pursue a full program of physics at this level one would want to increase the intensity of the AGS as described. A ten-fold increase in K flux would remove such experiments from the category of all-out technological assaults and render them manageable by reasonably small groups of physicists. In addition, certain other, cleaner experiments, e.g., K/sub L//sup 0/ ..-->.. e/sup +/e/sup -/ or e/sup +/e/sup -/..pi../sup 0/, could be pushed to limits unobtainable at the present AGS. The increased flux would also be welcomed by the neutrino and hypernuclear physics programs. Even experiments which do not at present require higher fluxes would benefit through the availability of purer beams and cleaner conditions.

  14. 20% PARTIAL SIBERIAN SNAKE IN THE AGS.

    SciTech Connect

    Huang, H; Bai, M; Brown, K A; Glenn, W; Luccio, A U; Mackay, W W; Montag, C; Ptitsyn, V; Roser, T; Tsoupas, N; Zeno, K; Ranjbar, V; Spinka, H; Underwood, D

    2002-11-06

    An 11.4% partial Siberian snake was used to successfully accelerate polarized proton through a strong intrinsic depolarizing spin resonance in the AGS. No noticeable depolarization was observed. This opens up the possibility of using a 20% to 30% partial Siberian snake in the AGS to overcome all weak and strong depolarizing spin resonances. Some design and operation issues of the new partial Siberian snake are discussed.

  15. AGS polarized proton operation in run 8.

    SciTech Connect

    Huang,H.; Ahrens, L.; Bai, M.; Brown, K.A.; Gardner, C.; Glenn, J.W.; Lin, F.; Luccio, A.U.; MacKay, W.W.; Roser, T.; Tepikian, S.; Tsoupas, N.; Yip, K.; Zeno, K.

    2008-06-23

    Dual partial snake scheme has been used for the Brookhaven AGS (Alternating Gradient Synchrotron) polarized proton operation for several years. It has provided polarized proton beams with 1.5 x 10{sup 11} intensity and 65% polarization for RHIC spin program. There is still residual polarization loss. Several schemes such as putting horizontal tune into the spin tune gap, and injection-on-the-fly were tested in the AGS to mitigate the loss. This paper presents the experiment results and analysis.

  16. Dealloying-driven synthesis and characterization of AgCl/Ag/TiO2 nanocomposites with enhanced photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Wang, Tongyang; Wang, Yan; Zhao, Zhengfeng; Zhang, Lanxiang; Huang, Shifeng

    2017-03-01

    The combination of dealloying with acid treatment was used to fabricate mesoporous anatase TiO2 with high specific surface area of 233 m2/g. Using anatase TiO2 as a matrix, a photoreduction strategy was developed to synthesize AgCl/Ag/TiO2 nanocomposites with different Ti/Ag molar ratios. The morphology and properties of AgCl/Ag/TiO2 nanocomposites were investigated by X-ray diffraction, field emission scanning electron microscopy and transmission electron microscopy. The AgCl/Ag/TiO2 nanocomposites showed an enhanced photocatalytic activity for the degradation of methyl orange solution under visible light irradiation. The optimum Ti/Ag molar ratio in the AgCl/Ag/TiO2 nanocomposites was shown to be 6:1, which was attributed to its high specific surface area of 207 m2/g and the surface plasmon resonance effect.

  17. A visible-light-driven core-shell like Ag2S@Ag2CO3 composite photocatalyst with high performance in pollutants degradation.

    PubMed

    Yu, Changlin; Wei, Longfu; Zhou, Wanqin; Dionysiou, Dionysios D; Zhu, Lihua; Shu, Qing; Liu, Hong

    2016-08-01

    A series of Ag2S-Ag2CO3 (4%, 8%, 16%, 32% and 40% Ag2S), Ag2CO3@Ag2S (32%Ag2S) and Ag2S@Ag2CO3 (32%Ag2S) composite photocatalysts were fabricated by coprecipitation or successive precipitation reaction. The obtained catalysts were analyzed by N2 physical adsorption, powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, UV-vis diffuse reflectance spectroscopy and photocurrent test. Under visible light irradiation, the influences of Ag2S content and core-shell property on photocatalytic activity and stability were evaluated in studies focused on the degradation of methyl orange (MO) dye, phenol, and bisphenol A. Results showed that excellent photocatalytic performance was obtained over Ag2S/Ag2CO3 composite photocatalysts with respect to Ag2S and Ag2CO3. With optimal content of Ag2S (32 wt%), the Ag2S-Ag2CO3 showed the highest photocatalytic degradation efficiency. Moreover, the structured property of Ag2S/Ag2CO3 greatly influenced the activity. Compared with Ag2S-Ag2CO3 and Ag2CO3@Ag2S, core-shell like Ag2S@Ag2CO3 demonstrated the highest activity and stability. The main reason for the boosting of photocatalytic performance was due to the formation of Ag2S/Ag2CO3 well contacted interface and unique electron structures. Ag2S/Ag2CO3 interface could significantly increase the separation efficiency of the photo-generated electrons (e(-)) and holes (h(+)), and production of OH radicals. More importantly, the low solubility of Ag2S shell could effectively protect the core of Ag2CO3, which further guarantees the stability of Ag2CO3.

  18. Structure and morphology controllable synthesis of Ag/carbon hybrid with ionic liquid as soft-template and their catalytic properties

    SciTech Connect

    Wu Shuying; Ding Yunsheng Zhang Xiaomin; Tang Haiou; Chen Long; Li Boxuan

    2008-09-15

    Ag/carbon hybrids were fabricated by the redox of glucose and silver nitrate (AgNO{sub 3}) in the presence of imidazolium ionic liquid ([C{sub 14}mim]BF{sub 4}) under hydrothermal condition. Monodisperse carbon hollow sub-microspheres encapsulating Ag nanoparticles and Ag/carbon cables were selectively prepared by varying the concentration of ionic liquid. Other reaction parameters, such as reaction temperature, reaction time and the mole ratio of silver nitrate to glucose, play important roles in controlling the structures of the products. The products were characterized by XRD, TEM (HRTEM), SEM, energy-dispersive X-ray spectroscopy (EDX), FTIR spectroscopy and a Raman spectrometer. The possible formation mechanism was proposed. The catalytic property of the hybrid in the oxidation of 1-butanol by H{sub 2}O{sub 2} was also investigated. - Graphical abstract: Monodisperse carbon hollow nanospheres encapsulating Ag nanoparticles and Ag/carbon nanocables were selectively prepared with ionic liquids as the soft-template. The controllable synthesis of Ag/C nano-hybrids was realized by varying the concentration of ionic liquids, reaction temperature, reaction time and the mole ratio of silver nitrate to glucose. The catalysis of Ag/C nano-hybrid in the oxidation of 1-butanol by H{sub 2}O{sub 2} was also investigated.

  19. Supersensitive and selective detection of picric acid explosive by fluorescent Ag nanoclusters.

    PubMed

    Zhang, Jian Rong; Yue, Yuan Yuan; Luo, Hong Qun; Li, Nian Bing

    2016-02-07

    Picric acid (PA) explosive is a hazard to public safety and health, so the sensitive and selective detection of PA is very important. In the present work, polyethyleneimine stabilized Ag nanoclusters were successfully used for the sensitive and selective quantification of PA on the basis of fluorescence quenching. The quenching efficiency of Ag nanoclusters is proportional to the concentration of PA and the logarithm of PA concentration over two different concentration ranges (1.0 nM-1 μM for the former and 0.25-20 μM for the latter), thus the proposed quantitative strategy for PA provides a wide linear range of 1.0 nM-20 μM. The detection limit based on 3σ/K is 0.1 nM. The quenching mechanism of Ag nanoclusters by PA is discussed in detail. The results indicate that the selective detection of PA over other nitroaromatics including 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (2,4-DNT), p-nitrotoluene (p-NT), m-dinitrobenzene (m-DNB), and nitrobenzene (NB), is due to the electron transfer and energy transfer between PA and polyethyleneimine-capped Ag nanoclusters. In addition, the experimental data obtained for the analysis of artificial samples show that the proposed PA sensor is potentially applicable in the determination of trace PA explosive in real samples.

  20. Preparation of graphene–Ag composites and their application for electrochemical detection of chloride

    SciTech Connect

    Yu, Mei; Liu, Pengrui; Zhang, Shilu; Liu, Jianhua; An, Junwei; Li, Songmei

    2012-11-15

    Highlights: ► Graphene–Ag composites were prepared in situ using ascorbic acid as green reducing agent. ► The morphology of Ag particles was irregular sheet and Ag particles homogeneously distributed on the graphene matrix. ► The surface-enhanced Raman scattering enhancement factor of D band is 5.85 for composites. ► The composites exhibited good sensitivity for the detection of chloride ions. -- Abstract: Graphene–Ag composites were prepared in situ using ascorbic acid as green reducing agent. The composites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected-area electronic diffraction (SAED), and Raman spectrometer. It was showed that Ag particles homogeneously distributed on the graphene matrix. The morphology of Ag particles was irregular sheet with (1 1 1) basal plane. The surface-enhanced Raman scattering (SERS) enhancement factor of D band is 5.85 for composites. The application of the composites for electrochemical detection of chloride was studied by cyclic voltammetry. The composites exhibited good sensitivity for the detection of chloride ions. The maximum peak current of cyclic voltammetry curve in 5 mM KCl was 0.80 mA. In the range of 500 μM to 50 mM for Cl{sup −}, the current response was proportional and linear to the Cl{sup −} concentration. The sensitivity to the detection for Cl{sup −} was 0.059 (mA/mM) and the detection limit was 61 μM for Cl{sup −}. It indicates graphene–Ag composites would be a competitive material for detection of halide.

  1. Ag-NP@Ge-nanotaper/Si-micropillar ordered arrays as ultrasensitive and uniform surface enhanced Raman scattering substrates

    NASA Astrophysics Data System (ADS)

    Liu, Jing; Meng, Guowen; Li, Zhongbo; Huang, Zhulin; Li, Xiangdong

    2015-10-01

    Surface-enhanced Raman scattering (SERS) is considered to be an excellent candidate for analytical detection schemes, because of its molecular specificity, rapid response and high sensitivity. Here, SERS-substrates of Ag-nanoparticle (Ag-NP) decorated Ge-nanotapers grafted on hexagonally ordered Si-micropillar (denoted as Ag-NP@Ge-nanotaper/Si-micropillar) arrays are fabricated via a combinatorial process of two-step etching to achieve hexagonal Si-micropillar arrays, chemical vapor deposition of flocky Ge-nanotapers on each Si-micropillar and decoration of Ag-NPs onto the Ge-nanotapers through galvanic displacement. With high density three-dimensional (3D) ``hot spots'' created from the large quantities of the neighboring Ag-NPs and large-scale uniform morphology, the hierarchical Ag-NP@Ge-nanotaper/Si-micropillar arrays exhibit strong and reproducible SERS activity. Using our hierarchical 3D SERS-substrates, both methyl parathion (a commonly used pesticide) and PCB-2 (one congener of highly toxic polychlorinated biphenyls) with concentrations down to 10-7 M and 10-5 M have been detected respectively, showing great potential in SERS-based rapid trace-level detection of toxic organic pollutants in the environment.Surface-enhanced Raman scattering (SERS) is considered to be an excellent candidate for analytical detection schemes, because of its molecular specificity, rapid response and high sensitivity. Here, SERS-substrates of Ag-nanoparticle (Ag-NP) decorated Ge-nanotapers grafted on hexagonally ordered Si-micropillar (denoted as Ag-NP@Ge-nanotaper/Si-micropillar) arrays are fabricated via a combinatorial process of two-step etching to achieve hexagonal Si-micropillar arrays, chemical vapor deposition of flocky Ge-nanotapers on each Si-micropillar and decoration of Ag-NPs onto the Ge-nanotapers through galvanic displacement. With high density three-dimensional (3D) ``hot spots'' created from the large quantities of the neighboring Ag-NPs and large-scale uniform

  2. Fabrication of nanoporous silver by de-alloying Cu-Zr-Ag amorphous alloys

    NASA Astrophysics Data System (ADS)

    Wang, Hui; Xiao, Shang-gang; Zhang, Tao

    2016-07-01

    Nanoporous silver (NPS) with a ligament size ranging from 15 to 40 nm was fabricated by de-alloying (Cu50Zr50)100- x Ag x ( x = 10at%, 20at%, 30at%, and 40at%) amorphous ribbons in a mixed aqueous solution of hydrofluoric (HF) acid and nitric acid under free corrosion conditions. Nanoporous silver ligaments and pore sizes were able to be fine-tuned through tailoring the chemical composition, corrosion conditions, and de-alloying time. The ligament size increases with an increase in Ag content and de-alloying time, but decreases with an increase in HF concentration. This phenomenon may be attributed to the dissolution of Zr/Cu and the diffusion, aggregation, nucleation, and recrystallization of Ag, leading to an oriented attachment of adjacent nanocrystals as revealed by TEM analysis.

  3. Preparation and structural properties of pure and codoped (Mg, Ag) ZnO nanoparticles

    NASA Astrophysics Data System (ADS)

    Reddy, B. Sankara; Reddy, S. Venkatramana; Reddy, N. Koteeswara

    2013-06-01

    Pure and co-doped (Mg, Ag) ZnO nanoparticles (Zn0.90Mg0.05Ag0.05O) are synthesized by chemical co-precipitation method in the presence of capping agent Polyethylene glycol 600 (PEG 600) and annealed at 500°C in air ambient for 1h. The XRD measurements reveals that the pure and co-doped ZnO samples have hexagonal structure without any change and the size of ZnO nanoparicles were decreased from 17 nm to 13 nm. FESEM images indicates that they are flake like structures of the ZnO and co-doped ZnO samples and ED AX spectra reveals that the successful doping concentration of Mg and Ag. From the TEM results, the size of the ZnO nanoparticles which are in good agreement with the XRD results.

  4. Morphologically manipulated Ag/ZnO nanostructures as surface enhanced Raman scattering probes for explosives detection

    NASA Astrophysics Data System (ADS)

    Shaik, Ummar Pasha; Hamad, Syed; Ahamad Mohiddon, Md.; Soma, Venugopal Rao; Ghanashyam Krishna, M.

    2016-03-01

    The detection of secondary explosive molecules (e.g., ANTA, FOX-7, and CL-20) using Ag decorated ZnO nanostructures as surface enhanced Raman scattering (SERS) probes is demonstrated. ZnO nanostructures were grown on borosilicate glass substrates by rapid thermal oxidation of metallic Zn films at 500 °C. The oxide nanostructures, including nanosheets and nanowires, emerged over the surface of the Zn film leaving behind the metal residue. We demonstrate that SERS measurements with concentrations as low as 10 μM, of the three explosive molecules ANTA, FOX-7, and CL-20 over ZnO/Ag nanostructures, resulted in enhancement factors of ˜107, ˜107, and ˜104, respectively. These measurements validate the high sensitivity of detection of explosive molecules using Ag decorated ZnO nanostructures as SERS substrates. The Zn metal residue and conditions of annealing play an important role in determining the detection sensitivity.

  5. Preparation and thermoelectric properties of sulfur doped Ag2Te nanoparticles via solvothermal methods.

    PubMed

    Zhou, Wenwen; Zhao, Weiyun; Lu, Ziyang; Zhu, Jixin; Fan, Shufen; Ma, Jan; Hng, Huey Hoon; Yan, Qingyu

    2012-07-07

    In this work, n-type Ag(2)Te nanoparticles are prepared by a solvothermal approach with uniform and controllable sizes, e.g. 5-15 nm. The usage of dodecanethiol during the synthesis effectively introduces sulfur doping into the sample, which optimizes the charge carrier concentration of the nanoparticles to >1 × 10(20) cm(-3). This allows us to achieve the desired electrical resistivities of <5 × 10(-6)Ω m. It is demonstrated that Ag(2)Te particles prepared by this solvothermal process can exhibit high ZT values, e.g. 15 nm Ag(2)Te nanoparticles with effective sulphur doping show a maximum ZT value of ~0.62 at 550 K.

  6. Preparation of a novel silk microfiber covered by AgCl nanoparticles with antimicrobial activity.

    PubMed

    Xie, Qifan; Xu, Zongpu; Hu, Binhui; He, Xiuling; Zhu, Liangjun

    2017-03-01

    We prepared silk fibroin microfibers in which silver chloride (AgCl) nanoparticles were dispersed, by sequential dipping of microfibers obtained using alkaline hydrolysis in alternating solutions of silver nitrate and potassium chloride. Scanning and transmission electron microscopy showed an increase in nanoparticle size and quantity with increase in dipping cycles and solution concentration, but ultrasound irradiation did not affect nanoparticle formation. The presence of cubic AgCl crystals was confirmed by energy dispersive X-ray spectroscopy and X-ray diffractometry. Differential scanning calorimetry and Fourier transform infrared spectroscopy revealed that the nanoparticles do not affect the microfiber properties. The growth of Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria was inhibited by microfiber covered with AgCl nanoparticles. This antimicrobial activity allows to use microfiber as a reinforced or surface additive biomaterial. Microsc. Res. Tech. 80:272-279, 2017. © 2016 Wiley Periodicals, Inc.

  7. 3D Ag/ZnO hybrids for sensitive surface-enhanced Raman scattering detection

    NASA Astrophysics Data System (ADS)

    Huang, Chenyue; Xu, Chunxiang; Lu, Junfeng; Li, Zhaohui; Tian, Zhengshan

    2016-03-01

    To combine the surface plasma resonance of metal and local field enhancement in metal/semiconductor interface, Ag nanoparticles (NPs) were assembled on a ZnO nanorod array which was grown by hydrothermally on carbon fibers. The construction of dimensional (3D) Surface-Enhanced Raman Scattering (SERS) substrate is used for the sensitive detection of organic pollutants with the advantages such as facile synthesis, short detection time and low cost. The hybrid substrate was manifested a high sensitivity to phenol red at a lower concentration of 1 × 10-9 M and a higher enhancement factor of 3.18 × 109. Moreover, the ZnO nanostructures decorated with Ag NPs were demonstrated self-cleaning function under UV irradiation via photocatalytic degradation of the analytic molecules. The fabrication process of the materials and sensors, optimization of the SERS behaviors for different sized Ag NPs, the mechanism of SERS and recovery were presented with a detailed discussion.

  8. Surface-enhanced Raman scattering from 4-aminothiophenol molecules embedded inside Ag coated gold nanorods

    NASA Astrophysics Data System (ADS)

    Khlebtsov, Boris N.

    2016-04-01

    Here we report on the preparation of uniform Au@Ag core/shell nanorods with a controllable Ag shell thickness. 4- aminothiophenol molecules, used as the Raman reporters, were placed between the Au core and the Ag shell. The dependence of Raman intensity on the inside/surface location of the reporter molecules was studied. The interior molecules showed a strong and uniform Raman intensity, at least an order of magnitude higher than that of the molecules on the nanoparticle surface. In contrast to usual surface-functionalized Raman tags, aggregation and clustering of nanoparticles with embedded molecules decreased the SERS signal. The findings from this study provide the basis for a novel technique of low analyte concentration detection based on high SERS response inside the core/shell metal nanostructures.

  9. High Visible Photoelectrochemical Activity of Ag Nanoparticle-Sandwiched CdS/Ag/ZnO Nanorods.

    PubMed

    Yang, Xu; Li, Hui; Zhang, Wu; Sun, Mingxuan; Li, Lequn; Xu, Ning; Wu, Jiada; Sun, Jian

    2017-01-11

    We report on the sensitizing of CdS-coated ZnO (CdS/ZnO) nanorods (NRs) by Ag nanoparticles (NPs) embedded between the CdS coating and the ZnO nanorod and the improved optical and photoelectrochemical properties of the Ag NP-sandwiched nanostructure CdS/Ag/ZnO NRs. The CdS/Ag/ZnO NRs were fabricated by growing Ag NPs on hydrothermally grown ZnO NRs and subsequently depositing CdS coatings followed by subsequent N2 annealing. The structure of the fabricated CdS/Ag/ZnO NRs was characterized by field-emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and Raman backscattering, revealing that the ZnO NRs and the CdS coatings are both structured with hexagonal wurtzite and the Ag NPs contact well with ZnO and CdS. Optical properties were evaluated by measuring optical absorption and photoluminescence, showing that the Ag NPs behave well as sensitizers for optical property improvement and the CdS/Ag/ZnO NRs exhibit better photoresponse in a wide spectral region than CdS/ZnO because of plasmon-enhanced absorption due to the embedment of Ag NPs. The Ag NPs also serve as electron relays from CdS to ZnO, facilitating electron transfer from the CdS coatings to the ZnO NRs. The excellent photoresponse and efficient electron transfer make the CdS/Ag/ZnO NRs highly photoelectrochemically active. The CdS/Ag/ZnO NRs fabricated on indium-tin oxide present much better photoelectrochemical performance as photoanodes working in the visible region than CdS/ZnO NRs without Ag NPs. Under visible illumination, a maximum optical-to-chemical conversion efficiency of 3.13% is obtained for CdS/Ag/ZnO NR photoanodes against 1.35% for CdS/ZnO NR photoanodes.

  10. Electron and Phonon Dynamics in Hexagonal Pd Nanosheets and Ag/Pd/Ag Sandwich Nanoplates.

    PubMed

    Wang, Li; Sagaguchi, Takuya; Okuhata, Tomoki; Tsuboi, Motohiro; Tamai, Naoto

    2017-02-28

    Pd and its hybrid nanostructures have attracted considerable attention over the past decade, with both catalytic and plasmonic properties. The electron and phonon properties directly govern conversion efficiencies in applications such as energy collectors and photocatalysts. We report the dynamic processes of electron-phonon coupling and coherent acoustic phonon vibration in hexagonal Pd nanosheets and Ag/Pd/Ag sandwich nanoplates using transient absorption spectroscopy. The electron-phonon coupling constant of Pd nanosheets, GPd-nanosheet (8.7 × 10(17) W/(m(3)·K)) is larger than that of the bulk GPd (5.0 × 10(17) W/(m(3)·K)). The effective coupling constant Geff of Ag/Pd/Ag nanoplates decreases with increasing Ag shell thickness, finally approaching the bulk GAg. The variation of Geff is explained in terms of reduced density of states near Fermi level of Pd nanosheets with 1.8 nm ultrathin thickness. Coherent acoustic phonon vibration in Pd nanosheets is assigned to a fundamental breathing mode, similar to the vibration of benzene. The period increases with increasing Ag shell thickness. For Ag/Pd/Ag nanoplates with 20 nm thick Ag shells, the vibrational mode is ascribed to a quasi-extensional mode. The results show that the modes of the coherent acoustic phonon vibration transform with the geometric variation of Pd nanosheets and Ag/Pd/Ag nanoplates. Our results represent an understanding of quantum-confinement related electron dynamics and bulk-like phonon kinetics in the ultrathin Pd nanosheets and their hybrid nanostructures.

  11. An Ab Initio Study of the Low-Lying Doublet States of AgO and AgS

    NASA Technical Reports Server (NTRS)

    Bauschlicher, Charles W., Jr.; Partridge, Harry; Langhoff, Stephen R.

    1990-01-01

    Spectroscopic constants (D(sub o), r(sub e), mu(sub e), T(sub e)) are determined for the doublet states of AgO and AgS below approx. = 30000/cm. Large valence basis sets are employed in conjunction with relativistic effective core potentials (RECPs). Electron correlation is included using the modified coupled-pair functional (MCPF) and multireference configuration interaction (MRCI) methods. The A(sup 2)Sigma(sup +) - X(sup 2)Pi band system is found to occur in the near infrared (approx. = 9000/cm) and to be relatively weak with a radiative lifetime of 900 microns for A(sup 2)Sigma(sup +) (upsilon = 0). The weakly bound C(sup 2)Pi state (our notation), the upper state of the blue system, is found to require high levels of theoretical treatment to determine a quantitatively accurate potential. The red system is assigned as a transition from the C(sup 2)Pi state to the previously unobserved A(sup 2)Sigma(sup +) state. Several additional transitions are identified that should be detectable experimentally. A more limited study is performed for the vertical excitation spectrum of AgS. In addition, a detailed all-electron study of the X(sup 2)Pi and A(sup 2)Sigma(sup +) states of AgO is carried out using large atomic natural orbital (ANO) basis sets. Our best calculated D(sub o) value for AgO is significantly less than the experimental value, which suggests that there may be some systematic error in the experimental determination.

  12. Green sonochemical synthesis of silver nanoparticles at varying concentrations of κ-carrageenan

    NASA Astrophysics Data System (ADS)

    Elsupikhe, Randa Fawzi; Shameli, Kamyar; Ahmad, Mansor B.; Ibrahim, Nor Azowa; Zainudin, Norhazlin

    2015-07-01

    A green sonochemical method was developed for preparing silver nanoparticles (Ag-NPs) in different concentrations of kappa carrageenan (κ-carrageenan). The κ-carrageenan was used as a natural eco-friendly stabilizer, and ultrasonic irradiation was used as a green reducing agent. The number of Ag-NPs increased with increasing κ-carrageenan concentrations. Formation of Ag/κ-carrageenan was determined by UV-visible spectroscopy where the surface plasmon absorption maximum was observed at 402 to 420 nm. The X-ray diffraction (XRD) analysis showed that the Ag-NPs are of a face-centered cubic structure. The Fourier transform infrared (FT-IR) spectrum indicated the presence of Ag-NPs in κ-carrageenan. Transmission electron microscopy (TEM) image for the highest concentration of κ-carrageenan showed the distribution of Ag-NPs with an average particle size near to 4.21 nm. Scan electron microscopy (SEM) images illustrated the spherical shape of the Ag-NPs. The use of photo irradiation provides a green and economic feature to this work.

  13. Fast, high-yield synthesis of amphiphilic Ag nanoclusters and the sensing of Hg(2+) in environmental samples.

    PubMed

    Xia, Nan; Yang, Jie; Wu, Zhikun

    2015-06-14

    We report the high-yield (74%) synthesis of Ag30(Capt)18 (abbreviated as Ag30) in a very time-saving fashion (half an hour). The cluster composition was determined by high-resolution mass spectrometry combined with TG analysis, and the structure was probed by 1D and 2D NMR. Interestingly, the nanoclusters can dissolve in water and methanol, as well as in most organic solvents such as ethanol, acetone, acetonitrile, dichloromethane and ethyl acetate with the assistance of acetic acid. Such a good solubility in a range of various polar solvents was not reported previously in nanoclusters' research and is important for applications. An important result from this work is that Ag30 can sense a low concentration of Hg(2+) in environmental samples (including lake water and soil solution), indicating that Ag30 can be a potential colorimetric probe for Hg(2+). The sensing mechanism was revealed to be related to the anti-galvanic reduction process.

  14. 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.

  15. Synthesis and characterization of Fe3O4-SiO2-AgCl photocatalyst

    NASA Astrophysics Data System (ADS)

    Husni, H. N.; Mahmed, N.; Ngee, H. L.

    2016-07-01

    Magnetite-silica-silver chloride (Fe3O4-SiO2-AgCl) coreshell particles with AgCl crystallite size of 117 nm was prepared by a wet chemistry method at ambient temperature. The magnetite-core was synthesized by using iron (II) sulfate heptahydrate (FeSO4•7H2O) and iron (III) sulfate hydrate (Fe2(SO4)3) with ammonium hydroxide (NH4OH) as the precipitating agent. The silica-shell was synthesized by using a modified Stöber process. The silver ions (Ag+) was adsorbed onto the silica surface after Söber process, followed by the addition of Cl- and polyvinylpyrrolidone (PVP) for the formation of Fe3O4-SiO2-AgCl coreshell particles. The effectiveness of the synthesized photocatalyst was investigated by monitoring the degradation of the methylene blue (MB) under sunlight for five cycles. About 90 % of the MB solution can be degraded after 2 hours. The degradation of MB solution by the Fe3O4-SiO2-AgCl particles is highly efficient for first three cycles according to the MB concentration recorded by the UV-Visible spectroscopy (UV-Vis). Nevertheless, the synthesized particles could be a promising material for photocatalytic applications.

  16. Synthesis and Complete Antimicrobial Characterization of CEOBACTER, an Ag-Based Nanocomposite

    PubMed Central

    Vasquez-Peña, M.; Raymond-Herrera, O.; Villavicencio-García, H.; Petranovskii, V.; Vazquez-Duhalt, R.; Huerta-Saquero, A.

    2016-01-01

    The antimicrobial activity of silver nanoparticles (AgNPs) is currently used as an alternative disinfectant with diverse applications, ranging from decontamination of aquatic environments to disinfection of medical devices and instrumentation. However, incorporation of AgNPs to the environment causes collateral damage that should be avoided. In this work, a novel Ag-based nanocomposite (CEOBACTER) was successfully synthetized. It showed excellent antimicrobial properties without the spread of AgNPs into the environment. The complete CEOBACTER antimicrobial characterization protocol is presented herein. It is straightforward and reproducible and could be considered for the systematic characterization of antimicrobial nanomaterials. CEOBACTER showed minimal bactericidal concentration of 3 μg/ml, bactericidal action time of 2 hours and re-use capacity of at least five times against E. coli cultures. The bactericidal mechanism is the release of Ag ions. CEOBACTER displays potent bactericidal properties, long lifetime, high stability and re-use capacity, and it does not dissolve in the solution. These characteristics point to its potential use as a bactericidal agent for decontamination of aqueous environments. PMID:27824932

  17. Antireflective disordered subwavelength structure on GaAs using spin-coated Ag ink mask.

    PubMed

    Yeo, Chan Il; Kwon, Ji Hye; Jang, Sung Jun; Lee, Yong Tak

    2012-08-13

    We present a simple, cost-effective, large scale fabrication technique for antireflective disordered subwavelength structures (d-SWSs) on GaAs substrate by Ag etch masks formed using spin-coated Ag ink and subsequent inductively coupled plasma (ICP) etching process. The antireflection characteristics of GaAs d-SWSs rely on their geometric profiles, which were controlled by adjusting the distribution of Ag etch masks via changing the concentration of Ag atoms and the sintering temperature of Ag ink as well as the ICP etching conditions. The fabricated GaAs d-SWSs drastically reduced the reflection loss compared to that of bulk GaAs (>30%) in the wavelength range of 300-870 nm. The most desirable GaAs d-SWSs for practical solar cell applications exhibited a solar-weighted reflectance (SWR) of 2.12%, which is much lower than that of bulk GaAs (38.6%), and its incident angle-dependent SWR was also investigated.

  18. Synthesis and Complete Antimicrobial Characterization of CEOBACTER, an Ag-Based Nanocomposite.

    PubMed

    Jaime-Acuña, O E; Meza-Villezcas, A; Vasquez-Peña, M; Raymond-Herrera, O; Villavicencio-García, H; Petranovskii, V; Vazquez-Duhalt, R; Huerta-Saquero, A

    2016-01-01

    The antimicrobial activity of silver nanoparticles (AgNPs) is currently used as an alternative disinfectant with diverse applications, ranging from decontamination of aquatic environments to disinfection of medical devices and instrumentation. However, incorporation of AgNPs to the environment causes collateral damage that should be avoided. In this work, a novel Ag-based nanocomposite (CEOBACTER) was successfully synthetized. It showed excellent antimicrobial properties without the spread of AgNPs into the environment. The complete CEOBACTER antimicrobial characterization protocol is presented herein. It is straightforward and reproducible and could be considered for the systematic characterization of antimicrobial nanomaterials. CEOBACTER showed minimal bactericidal concentration of 3 μg/ml, bactericidal action time of 2 hours and re-use capacity of at least five times against E. coli cultures. The bactericidal mechanism is the release of Ag ions. CEOBACTER displays potent bactericidal properties, long lifetime, high stability and re-use capacity, and it does not dissolve in the solution. These characteristics point to its potential use as a bactericidal agent for decontamination of aqueous environments.

  19. Influences of Ag-NPs doping chitosan/calcium silicate nanocomposites for optical and antibacterial activity.

    PubMed

    El-Nahrawy, Amany M; Ali, Ahmed I; Abou Hammad, Ali B; Youssef, Ahmed M

    2016-12-01

    Chitosan (CS)/calcium silicate nanocomposites pure and doped with Ag ions (1, 2mol%) were prepared via sol-gel method. The prepared CS/calcium silicate nanocomposites were investigated through X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). The XRD results, indicating that after increasing the Ag ions in the CS/calcium silicate nanocomposite the crystallinity degree increased regularly in the prepared nanocomposites accompanying to the continuously rearrangement in the internal structure of nanocomposite under the effect of inorganic nanoparticles. Correspondingly, the optical properties of the prepared nanocomposites films were measured using UV/vis spectroscopy. The reflectance increased while the energy band gap decreased from 3.96eV to 2.43eV with Ag-ions concentration. More over the transition type changed from direct into indirect by adding Ag-ions, indicate that new band between valence and conduction band were formed. In addition, the optical parameters showed an increase in refractive indices and decrease in the surface and volume energies losses with increasing Ag-ions. Correspondingly, the prepared nanocomposites exhibited good antibacterial activity against gram positive (Staphylococcus aureus), gram negative (Pseudomonas aeruginosa) bacteria and fungi (Candidia albicans). The results suggested that the prepared CS/calcium silicate nanocomposites can be a promised candidate for optical sensors applications and smart packaging materials.

  20. Durable antibacterial and UV-protective Ag/TiO2@ fabrics for sustainable biomedical application

    PubMed Central

    Li, Shuhui; Zhu, Tianxue; Huang, Jianying; Guo, Qingqing; Chen, Guoqiang; Lai, Yuekun

    2017-01-01

    A facile method was developed to endow cotton fabric with remarkable antibacterial and ultraviolet (UV)-protective properties. The flower-like TiO2 micro-nanoparticles were first deposited onto cotton fabric surface via hydrothermal deposition method. Then, the Ag NPs with a high deposition density were evenly formed onto TiO2@cotton surface by sodium hydroxide solution pretreatment and followed by in situ reduction of ANO3. This work focused on the influence of different hydrothermal reaction durations and the concentration of AgNO3 on antibacterial activity against relevant microorganisms in medicine as well as on the UV-blocking property. Ag NPs-loaded TiO2@cotton exhibited high antibacterial activity with an inhibition rate higher than 99% against Staphylococcus aureus and Escherichia coli bacteria. Moreover, the as-prepared cotton fabric coated with Ag NPs and TiO2 NPs demonstrated outstanding UV protective ability with a high ultraviolet protection factor value of 56.39. Morphological image of the cells revealed a likely loss of viability as a result of the synergistically biocidal effects of TiO2 and Ag on attached bacteria. These results demonstrate a facile and robust synthesis technology for fabricating multifunctional textiles with a promising biocidal activity against common Gram-negative and Gram-positive bacteria.

  1. A Convenient Ultraviolet Irradiation Technique for Synthesis of Antibacterial Ag-Pal Nanocomposite

    NASA Astrophysics Data System (ADS)

    Han, Shuai; Zhang, He; Kang, Lianwei; Li, Xiaoliang; Zhang, Chong; Dong, Yongjie; Qin, Shenjun

    2016-09-01

    In the present work, palygorskite (Pal) was initially subjected to an ion-exchange reaction with silver ions (Pal-Ag+). Subsequently, Ag-Pal nanocomposites were assembled by a convenient ultraviolet irradiation technique, using carbon dots (CDs) derived from wool fiber as the reducing agent. The obtained nanocomposites were characterized by powder X-ray diffraction (XRD), ultraviolet-visible (UV-vis) spectroscopy, transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy. The XRD patterns and UV-vis absorption spectra confirmed the formation of the Ag nanoparticles (NPs). Meanwhile, the TEM images showed that the Ag NPs, which exhibited sizes in the range of 3-7 nm, were located on the surface of the Pal nanofiber structures. Furthermore, the antibacterial activity of the nanocomposites was evaluated against Gram-positive ( Staphylococcus aureus) and Gram-negative ( Escherichia coli) bacteria by applying the disc diffusion method and minimum inhibitory concentration test. Owing to their good antibacterial properties, the Ag-Pal nanocomposites are considered to be a promising bactericide with great potential applications.

  2. Disinfection of water using Pt- and Ag-doped TiO2 photocatalysts.

    PubMed

    Suri, Rominder P S; Thornton, Hilary M; Muruganandham, M

    2012-01-01

    In this article we have reported heterogeneous photocatalytic disinfection using pristine and Ag- and Pt-doped nano TiO2 under near-UV light and solar light irradiation. Disinfection experiments were conducted in slurry reactors with Escherichia coli, artificial light and sunlight. The influence of various amounts of Pt and Ag loading (0.5% to 5%) on the E. coli inactivation was examined and results indicated that 5% Pt-TiO2 and 0.5% Ag-TiO2 showed the highest photocatalytic E. coli inactivation. The Pt- and Ag-doped photocatalysts were characterized using XPS and TEM analysis. The influence of experimental parameters such as various photocatalysts, photocatalyst concentration, reactor geometry effect, pH and temperature on the photocatalytic disinfection was studied. The experimental results show that sunlight or near-UV light with TiO2 photocatalyst strongly inactivates E. coli. The Ag-TiO2 photocatalyst was the most efficient photocatalyst tested for bactericidal activity. A plausible mechanism ofphotocatalysed E. coli inactivation is discussed. In conclusion, the doped nano TiO2 photocatalysts is a potential candidate for E. coli inactivation.

  3. A Convenient Ultraviolet Irradiation Technique for Synthesis of Antibacterial Ag-Pal Nanocomposite.

    PubMed

    Han, Shuai; Zhang, He; Kang, Lianwei; Li, Xiaoliang; Zhang, Chong; Dong, Yongjie; Qin, Shenjun

    2016-12-01

    In the present work, palygorskite (Pal) was initially subjected to an ion-exchange reaction with silver ions (Pal-Ag(+)). Subsequently, Ag-Pal nanocomposites were assembled by a convenient ultraviolet irradiation technique, using carbon dots (CDs) derived from wool fiber as the reducing agent. The obtained nanocomposites were characterized by powder X-ray diffraction (XRD), ultraviolet-visible (UV-vis) spectroscopy, transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy. The XRD patterns and UV-vis absorption spectra confirmed the formation of the Ag nanoparticles (NPs). Meanwhile, the TEM images showed that the Ag NPs, which exhibited sizes in the range of 3-7 nm, were located on the surface of the Pal nanofiber structures. Furthermore, the antibacterial activity of the nanocomposites was evaluated against Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacteria by applying the disc diffusion method and minimum inhibitory concentration test. Owing to their good antibacterial properties, the Ag-Pal nanocomposites are considered to be a promising bactericide with great potential applications.

  4. Safe disposal of radioactive iodide ions from solutions by Ag2O grafted sodium niobate nanofibers.

    PubMed

    Mu, Wanjun; Li, Xingliang; Liu, Guoping; Yu, Qianhong; Xie, Xiang; Wei, Hongyuan; Jian, Yuan

    2016-01-14

    Radioactive iodine isotopes are released into the environment by the nuclear industry and medical research institutions using radioactive materials, and have negative effects on organisms living within the ecosystem. Thus, safe disposal of radioactive iodine is necessary and crucial. For this reason, the uptake of iodide ions was investigated in Ag2O nanocrystal grafted sodium niobate nanofibers, which were prepared by forming a well-matched phase coherent interface between them. The resulting composite was applied as an efficient adsorbent for I(-) anions by forming an AgI precipitate, which also remained firmly attached to the substrates. Due to their one-dimensional morphology, the new adsorbents can be easily dispersed in liquids and readily separated after purification. This significantly enhances the adsorption efficiency and reduces the separation costs. The change in structure from the pristine sodium niobate to Ag2O anchored sodium niobate and to the used adsorbent was examined by using various characterization techniques. The effects of Ag(+) concentration, pH, equilibration time, ionic strength and competing ions on the iodide ion removal ability of the composite were studied. The Ag2O nanocrystal grafted sodium niobate adsorbent showed a high adsorption capacity and excellent selectivity for I(-) anions in basic solutions. Our results are useful for the further development of improved adsorbents for removing I(-) anions from basic wastewater.

  5. Ag(I)-cysteamine complex based electrochemical stripping immunoassay: ultrasensitive human IgG detection.

    PubMed

    Noh, Hui-Bog; Rahman, Md Aminur; Yang, Jee Eun; Shim, Yoon-Bo

    2011-07-15

    An ultrasensitive electrochemical immunosensor for a protein using a Ag (I)-cysteamine complex (Ag-Cys) as a label was fabricated. The low detection of a protein was based on the electrochemical stripping of Ag from the adsorbed Ag-Cys complex on the gold nanoparticles (AuNPs) conjugated human immunoglobulin G (anti-IgG) antibody (AuNPs-anti-IgG). The electrochemical immunosensor was fabricated by immobilizing anti-IgG antibody on a poly-5,2':5',2''-terthiophene-3'-carboxylic acid (polyTTCA) film grown on the glassy carbon electrode through the covalent bond formation between amine groups of anti-IgG and carboxylic acid groups of polyTTCA. The target protein, IgG was sandwiched between the anti-IgG antibody that covalently attached onto the polyTTCA layer and AuNPs-anti-IgG. Using square wave voltammetry, well defined Ag stripping voltammograms were obtained for the each target concentration. Various experimental parameters were optimized and interference effects from other proteins were checked out. The immunosensor exhibited a wide dynamic range with the detection limit of 0.4 ± 0.05 fg/mL. To evaluate the analytical reliability, the proposed immunosensor was applied to human IgG spiked serum samples and acceptable results were obtained indicating that the method can be readily extended to other bioaffinity assays of clinical or environmental significance.

  6. Ultrasensitive SERS performance in 3D "sunflower-like" nanoarrays decorated with Ag nanoparticles.

    PubMed

    Zhang, Xiaolei; Xiao, Xiangheng; Dai, Zhigao; Wu, Wei; Zhang, Xingang; Fu, Lei; Jiang, Changzhong

    2017-03-02

    Low-cost, stabilized and ultrasensitive three-dimensional (3D) hierarchical surface-enhanced Raman scattering substrates ("sunflower-like" nanoarrays decorated with Ag nanoparticles, denoted as SLNAs-Ag) have been obtained by fabricating binary colloidal crystals and then decorating with Ag nanoparticles. In order to provide a larger density of hot spots within the laser-illumination area, the silica sphere arrays were chosen as the island-type platform for the polystyrene (PS) nanosphere deposition, and the distances between the PS nanospheres were tuned by etching for different durations. Compared with conventional 2D planar systems, the as-fabricated 3D SLNAs-Ag exhibited extremely high SERS sensitivity ascribed to the larger SERS active regions. Quantitative detection of molecules with an extremely low incident laser power was achieved on the "sunflower-like" nanoarrays in which the PS nanospheres were etched for 5 minutes and decorated with Ag nanoparticles, and the corresponding analytical enhancement factor is calculated to be 2 × 10(14) with the concentration of rhodamine 6G down to 10(-15) M. Based on the achieved SERS substrates, we have further demonstrated the highly sensitive detection of molecules such as melamine for food safety inspection.

  7. Strongly visible-light responsive plasmonic shaped AgX:Ag (X = Cl, Br) nanoparticles for reduction of CO2 to methanol

    NASA Astrophysics Data System (ADS)

    An, Changhua; Wang, Jizhuang; Jiang, Wen; Zhang, Meiyu; Ming, Xijuan; Wang, Shutao; Zhang, Qinhui

    2012-08-01

    Plasmonic shaped AgX:Ag (X = Cl, Br) nanoparticles have been synthesized by a facile and versatile glycerol-mediated solution route. The as-prepared AgX:Ag nanoparticles exhibit regular shapes, i.e., cube-tetrapod-like AgCl:Ag nanoparticles and AgBr:Ag nanoplates. Compared with the pristine AgX, AgX:Ag nanocomposites display stronger absorption in the visible region due to the surface plasmon resonance of silver nanoparticles. The calculation of bandgaps and band positions indicates the as-achieved AgX:Ag nanoparticles can be used as a class of potential photocatalyst for the reduction of CO2. For example, reduction of CO2 under visible light irradiation with the assistance of the anisotropic AgX:Ag nanoparticles yields as much as 100 μmol methanol in the products. Furthermore, the AgX:Ag nanoparticles can maintain its structure and activity after 3 runs of reactions. Therefore, the present route opens an avenue to acquire plasmonic photocatalysts for conversion of CO2 into useful organic compounds.Plasmonic shaped AgX:Ag (X = Cl, Br) nanoparticles have been synthesized by a facile and versatile glycerol-mediated solution route. The as-prepared AgX:Ag nanoparticles exhibit regular shapes, i.e., cube-tetrapod-like AgCl:Ag nanoparticles and AgBr:Ag nanoplates. Compared with the pristine AgX, AgX:Ag nanocomposites display stronger absorption in the visible region due to the surface plasmon resonance of silver nanoparticles. The calculation of bandgaps and band positions indicates the as-achieved AgX:Ag nanoparticles can be used as a class of potential photocatalyst for the reduction of CO2. For example, reduction of CO2 under visible light irradiation with the assistance of the anisotropic AgX:Ag nanoparticles yields as much as 100 μmol methanol in the products. Furthermore, the AgX:Ag nanoparticles can maintain its structure and activity after 3 runs of reactions. Therefore, the present route opens an avenue to acquire plasmonic photocatalysts for conversion of CO2

  8. Decoration of crumpled rGO sheets with Ag nanoparticles by spray pyrolysis

    NASA Astrophysics Data System (ADS)

    Papailias, I.; Giannouri, M.; Trapalis, A.; Todorova, N.; Giannakopoulou, T.; Boukos, N.; Lekakou, C.

    2015-12-01

    In this work, crumpled reduced graphene oxide (rGO) nanostructures were produced using spray pyrolysis technique. Graphite oxide (GtO) prepared through a modified Hummers method was used as starting material. Water dispersions of graphene oxide (GO) were prepared and sprayed in a tube furnace at 300 °C, 500 °C and 700 °C using Argon (Ar) as carrier gas. Also, precursor dispersions with different AgNO3 concentrations were processed at the same conditions. During the treatment, the sprayed droplets underwent rapid heating and then gradual cooling until the exit of the oven, where crumpled rGO and Ag/rGO powders were collected. The prepared materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman and FT-IR spectroscopy. It was established that the crumpling of the nanosheets was slightly affected by the increase of the process temperature. Crumpled morphologies were obtained even at low temperature of 300 °C. In contrast, the degree of GO reduction was temperature dependent and increased with the increase of the temperature. The incorporation of Ag nanoparticles was evidenced by the XRD and TEM analysis with the size of the Ag nanoparticles to grow as the concentration of AgNO3 and/or the process temperature increased. SERS effect in the Raman spectra of the Ag/rGO materials was observed that reached a maximum at 500 °C. Spray pyrolysis was suggested as a simple, controllable and scalable route for the instantaneous crumpling, reduction and decoration of GO nanosheets with metal/metal oxide nanoparticles.

  9. Chloroplasts-mediated biosynthesis of nanoscale Au-Ag alloy for 2-butanone assay based on electrochemical sensor

    NASA Astrophysics Data System (ADS)

    Zhang, Yixia; Gao, Guo; Qian, Qirong; Cui, Daxiang

    2012-08-01

    We reported a one-pot, environmentally friendly method for biosynthesizing nanoscale Au-Ag alloy using chloroplasts as reducers and stabilizers. The prepared nanoscale Au-Ag alloy was characterized by UV-visible spectroscopy, X-ray diffraction (XRD) and high resolution transmission electron microscopy (HR-TEM). Fourier transform infrared spectroscopy (FTIR) analysis was further used to identify the possible biomolecules from chloroplasts that are responsible for the formation and stabilization of Au-Ag alloy. The FTIR results showed that chloroplast proteins bound to the nanoscale Au-Ag alloy through free amino groups. The bimetallic Au-Ag nanoparticles have only one plasmon band, indicating the formation of an alloy structure. HR-TEM images showed that the prepared Au-Ag alloy was spherical and 15 to 20 nm in diameter. The high crystallinity of the Au-Ag alloy was confirmed by SAED and XRD patterns. The prepared Au-Ag alloy was dispersed into multiwalled carbon nanotubes (MWNTs) to form a nanosensing film. The nanosensing film exhibited high electrocatalytic activity for 2-butanone oxidation at room temperature. The anodic peak current (Ip) has a linear relationship with the concentrations of 2-butanone over the range of 0.01% to 0.075% (v/v), when analyzed by cyclic voltammetry. The excellent electronic catalytic characteristics might be attributed to the synergistic electron transfer effects of Au-Ag alloy and MWNTs. It can reasonably be expected that this electrochemical biosensor provided a promising platform for developing a breath sensor to screen and pre-warn of early cancer, especially gastric cancer.

  10. Calibration of qualitative HBsAg assay results for quantitative HBsAg monitoring.

    PubMed

    Gunning, Hans; Adachi, Dena; Tang, Julian W

    2014-10-01

    Evidence is accumulating that quantitative hepatitis B surface antigen monitoring may be useful in managing patients with chronic HBV infection on certain treatment regimens. Based on these results with the Abbott Architect qualitative and quantitative HBsAg assays, it seems feasible to convert qualitative to quantitative HBsAg values for this purpose.

  11. Ultra-Fast Synthesis for Ag2Se and CuAgSe Thermoelectric Materials

    NASA Astrophysics Data System (ADS)

    DUAN, H. Z.; LI, Y. L.; ZHAO, K. P.; QIU, P. F.; SHI, X.; CHEN, L. D.

    2016-10-01

    Ag2Se and CuAgSe have been recently reported as promising thermoelectric materials at room temperature. The traditional melting-annealing-sintering processes are used to grow Ag2Se and CuAgSe materials with the disadvantages of high costs of energy and time. In this work, phase-pure polycrystalline Ag2Se and CuAgSe compounds were synthesized from raw elemental powders directly by manual mixing followed by spark plasma sintering (MM-SPS) in a few minutes. The influence of SPS heating rate on the phase composition, microstructure, and thermoelectric properties, including Seebeck coefficient, electrical conductivity, and thermal conductivity, were investigated. The zTs of 0.8 at 390 K and 0.6 at 450 K are obtained for Ag2Se and CuAgSe, respectively, which is comparable with the values in the materials prepared by the traditional method. Furthermore, this ultrafast sample synthesis can significantly save material synthesis time and thus has the obvious advantage for large-scale production.

  12. Facile synthesis of sunlight-driven AgCI:Ag plasmonic nanophotocatalyst.

    SciTech Connect

    An, C.; Peng, S.; Sun, Y.; Center for Nanoscale Materials; Univ. of Illinois

    2010-06-18

    Highly efficient plasmonic photocatalysts of AgCl:Ag hybrid nanoparticles are successfully synthesized via a one-pot synthetic approach involving a precipitation reaction followed by polyol reduction. The as-synthesized nanoparticles exhibit high catalytic performance under visible light and sunlight for decomposing organics, such as methylene blue.

  13. Beet Juice-Induced Green Fabrication of Plasmonic AgCl/Ag Nanoparticles

    EPA Science Inventory

    A simple, green, and fast approach (complete within 5 min) was explored for the fabrication of hybrid AgCl/Ag plasmonic nanoparticles under microwave (MW) irradiation. In this method, beet juice served as a reducing reagent, which is an abundant sugar-rich agricultural produce. I...

  14. Concentration of stable elements in food products

    SciTech Connect

    Montford, M.A.; Shank, K.E.; Hendricks, C.; Oakes, T.W.

    1980-01-01

    Food samples were taken from commercial markets and analyzed for stable element content. The concentrations of most stable elements (Ag, Al, As, Au, Ba, Br, Ca, Ce, Cl, Co, Cr, Cs, Cu, Fe, Hf, I, K, La, Mg, Mn, Mo, Na, Rb, Sb, Sc, Se, Sr, Ta, Th, Ti, V, Zn, Zr) were determined using multiple-element neutron activation analysis, while the concentrations of other elements (Cd, Hg, Ni, Pb) were determined using atomic absorption. The relevance of the concentrations found are noted in relation to other literature values. An earlier study was extended to include the determination of the concentration of stable elements in home-grown products in the vicinity of the Oak Ridge National Laboratory. Comparisons between the commercial and local food-stuff values are discussed.

  15. Ag on Si(111) from basic science to application

    SciTech Connect

    Belianinov, Aleksey

    2012-01-01

    In our work we revisit Ag and Au adsorbates on Si(111)-7x7, as well as experiment with a ternary system of Pentacene, Ag and Si(111). Of particular interest to us is the Si(111)-(√3x√3)R30°}–Ag (Ag-Si-√3 hereafter). In this thesis I systematically explore effects of Ag deposition on the Ag-Si-√3 at different temperatures, film thicknesses and deposition fluxes. The generated insight of the Ag system on the Si(111) is then applied to generate novel methods of nanostructuring and nanowire growth. I then extend our expertise to the Au system on the Ag-Si(111) to gain insight into Au-Si eutectic silicide formation. Finally we explore behavior and growth modes of an organic molecule on the Ag-Si interface.

  16. Observation of nonvolatile resistive memory switching characteristics in Ag/graphene-oxide/Ag devices.

    PubMed

    Venugopal, Gunasekaran; Kim, Sang-Jae

    2012-11-01

    In this paper, we report highly stable and bipolar resistive switching effects of Ag/Graphene oxide thinfilm/Ag devices. The graphene-oxide (GO) thinfilms were prepared on Ag/SiO2/Si substrates by spin-coating technique. The Ag/GO/Ag devices showed a steady and bipolar resistive switching characteristic. The resistance switching from low resistance state (LRS) and high resistance state (HRS) with the resistance ratio of HRS to LRS of about 10 which was attained at a voltage bias of 0.1 V. Based on the filamentary conduction model, the dominant conduction mechanism of switching effect was well explained. Our results show GO can be a promising candidate for future development of nonvolatile memory devices.

  17. Noble-metal Ag nanoparticle chains: annealing Ag/Bi superlattice nanowires in vacuum

    NASA Astrophysics Data System (ADS)

    Xu, Shao Hui; Fei, Guang Tao; You, Qiao; Gao, Xu Dong; Huo, Peng Cheng; De Zhang, Li

    2016-09-01

    One-dimensional noble-metal Ag nanoparticle chains have been prepared by electrodepositing Ag/Bi superlattice nanowires in a porous anodic alumina oxide (AAO) template and following an annealing process in vacuum. It is found that Bi, as a sacrificial metal, can be removed completely after annealing at 450 °C with a vacuum degree of 10-5 Torr. The regulation of particle size, shape and interparticle spacing of Ag NP chains has been realized by adjusting the segment length of the Ag/Bi superlattice nanowires and the annealing condition. With an extension of the annealing time, it is observed that Ag particles display the transform trend from ellipsoid to sphere. Our findings could inspire further investigation on the design and fabrication of metal nanoparticle chains.

  18. Noble-metal Ag nanoparticle chains: annealing Ag/Bi superlattice nanowires in vacuum.

    PubMed

    Xu, Shao Hui; Fei, Guang Tao; You, Qiao; Gao, Xu Dong; Huo, Peng Cheng; De Zhang, Li

    2016-09-16

    One-dimensional noble-metal Ag nanoparticle chains have been prepared by electrodepositing Ag/Bi superlattice nanowires in a porous anodic alumina oxide (AAO) template and following an annealing process in vacuum. It is found that Bi, as a sacrificial metal, can be removed completely after annealing at 450 °C with a vacuum degree of 10(-5) Torr. The regulation of particle size, shape and interparticle spacing of Ag NP chains has been realized by adjusting the segment length of the Ag/Bi superlattice nanowires and the annealing condition. With an extension of the annealing time, it is observed that Ag particles display the transform trend from ellipsoid to sphere. Our findings could inspire further investigation on the design and fabrication of metal nanoparticle chains.

  19. Synthesis and Characterization of BSA Conjugated Silver Nanoparticles (Ag/BSA Nanoparticles) and Evaluation of Biological Properties of Ag/BSA Nanoparticles and Ag/BSA Nanoparticles Loaded Poly(hydroxy butyrate valerate) PHBV Films

    NASA Astrophysics Data System (ADS)

    Ambaye, Almaz

    Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa are the etiological agents of several infectious diseases. Antibiotic resistance by these three microbes has emerged as a prevalent problem due in part to the misuse of existing antibiotics and the lack of novel antibiotics. Nanoparticles have emerged as an alternative antibacterial agents to conventional antibiotics owing to their high surface area to volume ratio and their unique chemical and physical properties. Among the nanoparticles, silver nanoparticles have gained increasing attention because silver nanoparticles exhibit antibacterial activity against a range of gram positive and gram negative bacteria. Nanoparticles of well-defined chemistry and morphology can be used in broad biomedical applications, especially in bone tissue engineering applications, where bone infection by bacteria can be acute and lethal. It is commonly noted in the literature that the activity of nanoparticles against microorganisms is dependent upon the size and concentration of the nanoparticles as well as the chemistry of stabilizing agent. To the best of our knowledge, a comprehensive study that evaluates the antibacterial activity of well characterized silver nanoparticles in particular Bovine Serum Albumin (BSA) stabilized against S. aureus and E. coli and cytotoxicity level of BSA stabilized silver nanoparticles towards osteoblast cells (MC3T3-E1) is currently lacking. Therefore, the primary objective of this study was to characterize protein conjugated silver nanoparticles prepared by chemical reduction of AgNO3 and BSA mixture. The formation of Ag/BSA nanoparticles was studied by UV-Vis spectroscopy. The molar ratio of silver to BSA in the Ag/BSA nanoparticles was established to be 27+/- 3: 1, based on Thermogravimetric Analysis and Atomic Absorption Spectroscopy. Based on atomic force microscopy, dynamic light scattering,and transmission electron microscopy(TEM) measurements, the particle size (diameter) of

  20. Acute toxicity of Ag and CuO nanoparticle suspensions against Daphnia magna: the importance of their dissolved fraction varying with preparation methods.

    PubMed

    Jo, Hun Je; Choi, Jae Woo; Lee, Sang Hyup; Hong, Seok Won

    2012-08-15

    A variety of methods to prepare nanoparticle suspensions have been employed for aquatic toxicity tests, although they can influence the dispersion property and subsequent toxicity of nanoparticles. Thus, in this study, we prepared stock suspensions of silver (Ag) and copper oxide (CuO) nanoparticles using different methods and compared their acute toxicity against Daphnia magna. The results showed that the dispersion method, filtration and initial concentration largely affected their toxicity, when the toxicity was expressed as the total concentrations of Ag and Cu. In case of Ag nanoparticles, the toxicity was also influenced by their different particle size. However, negligible differences in 24h-median effect concentration (EC(50)) values, which were calculated in terms of their dissolved concentrations, were observed. When expressing toxicity on the basis of dissolved concentrations, 24h-EC(50) values of the Ag and CuO nanoparticles were also found to be similar to those of the counterpart ionic species, i.e., Ag (as AgNO(3)) and Cu (as CuCl(2)·2H(2)O). These findings indicate that the dissolved fraction of nanoparticles largely contributes to their acute toxicity. Our results may help in establishing a useful guideline for preparing nanoparticle suspensions with reproducible toxicity.

  1. Variability in the fractionation of Cu, Ag, and Zn among cytosolic proteins in the bivalve Macoma balthica

    USGS Publications Warehouse

    Johansson, C.; Cain, Daniel J.; Luoma, Samuel N.

    1986-01-01

    Gel filtration chromatographs of cytosols from the clam Macorna balthica analysed from both field and laboratory treated specimens showed that uptake of Cu, Ag, and Zn in the metallothionein-like protein (MLP) pool follows exposure both in nature and in the laboratory. Specimens collected from San Francisco Bay over 18 mo showed strong temporal variability in the fractionation of the metals among cytosolic proteins. A marked increase in Cu, Ag, and Zn in a very low molecular weight pool occurred when concentrations were highest In the MLP pool. The correlation between total cytosollc metal and MLP-metal also appeared to approach a hyperbolic character at the highest concentrations.

  2. Improved Wetting Characteristics in TiO2–Modified Ag-CuO Air Braze Filler Metals

    SciTech Connect

    Weil, K. Scott; Kim, Jin Yong Y.; Hardy, John S.; Darsell, Jens T.

    2006-01-01

    In this paper we report on the results of a series of sessile drop experiments designed to examine the effect of TiO2 on the wetting behavior of Ag-CuO air braze filler metals. It was found that TiO2 concentrations as small as 0.5 mol% can significantly decrease the contact angle of Ag-CuO on alumina over a compositional range of 1 – 34mol% CuO. The effect appears to maximize at a copper oxide concentration of ~4 mol% CuO regardless of the titania content.

  3. Preparation of AgBr@SiO2 core@shell hybrid nanoparticles and their bactericidal activity.

    PubMed

    Li, Yuanyuan; Yang, Lisu; Zhao, Yanbao; Li, Binjie; Sun, Lei; Luo, Huajuan

    2013-04-01

    AgBr@SiO2 core@shell hybrid nanoparticles (NPs) were successfully prepared by sol-gel method. Their morphology and structure were characterized by transmission electron microscopy (TEM) and X-ray diffraction (XRD). The hybrid NPs are predominantly spherical in shape, with an average diameter of 180-200 nm, and each NP contains one inorganic core. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of the hybrid NPs were examined against Staphylococcus aureus (S. aureus), Pseudomonas aeruginosa (P. aeruginosa) and Escherichia coli (E. coli), respectively. Results indicated that the AgBr@SiO2 NPs had excellent antibacterial activity.

  4. Surface-engineered growth of AgIn₅S₈ crystals.

    PubMed

    Lai, Chia-Hung; Chiang, Ching-Yeh; Lin, Po-Chang; Yang, Kai-Yu; Hua, Chi Chung; Lee, Tai-Chou

    2013-05-01

    The growth of semiconductor crystals and thin films plays an essential role in industry and academic research. Considering the environmental damage caused by energy consumption during their fabrication, a simpler and cheaper method is desired. In fact, preparing semiconductor materials at lower temperatures using solution chemistry has potential in this research field. We found that solution chemistry, the physical and chemical properties of the substrate surface, and the phase diagram of the multicomponent compound semiconductor have a decisive influence on the crystal structure of the material. In this study, we used self-assembled monolayers (SAMs) to modify the silicon/glass substrate surface and effectively control the density of the functional groups and surface energy of the substrates. We first employed various solutions to grow octadecyltrichlorosilane (OTS), 3-mercaptopropyl-trimethoxysilane (MPS), and mixed OTS-MPS SAMs. The surface energy can be adjusted between 24.9 and 50.8 erg/cm(2). Using metal sulfide precursors in appropriate concentrations, AgIn5S8 crystals can be grown on the modified substrates without any post-thermal treatment. We can easily adjust the nucleation in order to vary the density of AgIn5S8 crystals. Our current process can achieve AgIn5S8 crystals of a maximum of 1 μm in diameter and a minimum crystal density of approximately 0.038/μm(2). One proof-of-concept experiment demonstrated that the material prepared from this low temperature process showed positive photocatalytic activity. This method for growing crystals can be applied to the green fabrication of optoelectronic materials.

  5. Facile synthesis of AgCl/polydopamine/Ag nanoparticles with in-situ laser improving Raman scattering effect

    NASA Astrophysics Data System (ADS)

    Zhang, Yan; Zhang, Wenqi; Wang, Lin; Wang, Feng; Yang, Haifeng

    2017-01-01

    We reported a simple and fast method to prepare a composite material of polydopamine (PDA) adlayer covered cubic AgCl core, which was inlaid with Ag nanoparticles (NPs), shortly named as AgCl/PDA/AgNPs. The resultant AgCl/PDA/AgNPs could be employed as surface-enhanced Raman scattering (SERS) substrate for in-situ detection and the SERS activity could be further greatly improved due to the production of more AgNPs upon laser irradiation. With 4-mercaptopyridine (4-Mpy) as the probe molecule, the enhancement factor could reach 107. Additionally, such SERS substrate shows good reproducibility with relative standard deviation of 7.32% and long term stability (after storage for 100 days under ambient condition, SERS intensity decay is less than 25%). In-situ elevating SERS activity of AgCl/PDA/AgNPs induced by laser may be beneficial to sensitive analysis in practical fields.

  6. Template synthesis of Ag/AgCl microrods and their efficient visible light-driven photocatalytic performance

    SciTech Connect

    Chen, Hua; Xiao, Liang; Huang, Jianhua

    2014-09-15

    Highlights: • Preparation ofAg/AgCl microrods by reaction of Ag{sub 2}WO{sub 4} microrods with NaCl solution. • Generation of metallic Ag is induced by the ambient light in the synthesis process. • Ag/AgCl shows excellent visible light-driven photodegradation of organic dyes. - Abstract: Ag/AgCl microrods, aggregated by nanoparticles with a diameter ranging from 100 nm to 2 μm, were prepared by an ion-exchange reaction at 80 °C between Ag{sub 2}WO{sub 4} template and NaCl solution. The existence of metallic Ag species was confirmed by XRD, DRS and XPS measurements. Ag/AgCl microrods showed excellent photocatalytic activity for the degradation of rhodamine B and methylene blue under visible light irradiation. The degradation rate constants of rhodamine B and methylene blue are 0.176 and 0.114 min{sup −1}, respectively. The cycling photodegradation experiments suggest that Ag/AgCl microds could be employed as stable plasmonic photocatalysts for the degradation of organic dyes under visible light irradiation.

  7. BiPO4 photocatalyst employing synergistic action of Ag/Ag3PO4 nanostructure and graphene nanosheets

    NASA Astrophysics Data System (ADS)

    Mohaghegh, N.; Rahimi, E.

    2016-06-01

    Graphene-supported BiPO4/Ag/Ag3PO4 photocatalyst has been fabricated by simple hydrothermal and impregnation reaction. In BiPO4/Ag/Ag3PO4 based on Reduced Graphene Oxide (RGO), this network renders numerous pathways for rapid mass transport, strong adsorption and multireflection of incident light; meanwhile, the interface between BiPO4/Ag/Ag3PO4 and RGO increases the active sites and electron transfer rate. BiPO4/Ag/Ag3PO4 based on RGO noticeably exhibited high photocatalytic activity than that of BiPO4/Ag/Ag3PO4 and P25 under visible light irradiation for cationic dye (Rhodamine B), anionic dye (methyl orange) and 4-chlorophenol (4-CP) as a neutral pollutant, which are usually difficult to be degraded over the other catalysts. This enhanced photocatalytic activity of Graphene-supported BiPO4/Ag/Ag3PO4 for all pollutants could be mainly ascribed to the reinforced charge transfer from BiPO4/Ag/Ag3PO4 to RGO, which suppresses the recombination of electron/hole pairs. Besides that, this photocatalyst can be used repetitively with a high photocatalytic activity and no apparent loss of activity occurs. The results reveal that the RGO nanosheets work as a photocatalyst promoter during the photocatalytic reaction, leading to an improved photocatalytic activity.

  8. Preparation of Ag2O/Ag2CO3/MWNTs composite photocatalysts for enhancement of ciprofloxacin degradation

    NASA Astrophysics Data System (ADS)

    Wang, Huiqin; Li, Jinze; Huo, Pengwei; Yan, Yongsheng; Guan, Qingfeng

    2016-03-01

    The Ag2O/Ag2CO3/multi-walled carbon nanotube (MWNTs) composite photocatalysts were prepared by calcination of the obtained precipitate. The structures and morphology of as-prepared composite photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), diffuse reflectance spectroscopy (DRS), photoluminescence (PL) spectroscopy, X-ray photoelectron spectroscopy (XPS). The Ag2O/Ag2CO3/MWNTs composite photocatalysts exhibit higher degradation rate of ciprofloxacin (CIP) than the pure Ag2CO3, Ag2O/Ag2CO3 and Ag2CO3/MWNTs under visible light irradiation. The amount of loaded Ag2CO3 onto MWNTs and calcined time for Ag2CO3/MWNTs were systematically investigated, and the optimal amount of loaded Ag2CO3 and calcined time of Ag2CO3/MWNTs are 150 wt% and 10 min, respectively. The highest photocatalytic degradation rate of CIP could reach 76% under optimal conditions. The active species trapping experiments were also analyzed, the results show that the holes are main contributor for the degradation processes of CIP, furthermore the electrons, rad O2- and rad OH are also crucially influenced the photocatalytic degradation processes of CIP. The possible photocatalytic processes of CIP with Ag2O/Ag2CO3/MWNTs composite photocatalyst are also proposed.

  9. In vitro antibacterial evaluation of sol-gel-derived Zn-, Ag-, and (Zn + Ag)-doped hydroxyapatite coatings against methicillin-resistant Staphylococcus aureus.

    PubMed

    Samani, S; Hossainalipour, S M; Tamizifar, M; Rezaie, H R

    2013-01-01

    Hydroxyapatite (HAp) coatings were applied using sol-gel method. Phosphor pentoxide and calcium nitrate were used as phosphorous and calcium precursors, respectively. Zinc nitrate and silver nitrate were used as substitute of calcium in HAp structure. As a base concentration, 1.5 wt %Ag and 2.5 wt %Zn were used. The weight percent of Ag was increased at 0.3 wt% and Zn content was scaled down at 0.5 wt%. Phase analysis and chemical bonds of synthesized materials were studied by XRD and FTIR. Antibacterial activity of Ag- and Zn-doped samples against methicilin-resistant Staphylococcus aureus (MRSA) were assessed by the plate-counting method. The XRD and FTIR results proved formation of HAp compound. Colony counting showed that silver and zinc ions prevent proliferation and growth of MRSA. Interestingly, co-presence of metal ions improves the antibacterial effectiveness of the coatings and the combined effect was greater than sum of the individual effects when each was administered alone. Overall, synergism between antibacterial activities of Zn(2+) and Ag(+) ions against MRSA can be suggested. Thus, cell toxicity decreases and biocompatibility increases without any decrement in antibacterial activity.

  10. Mussel-inspired green synthesis of polydopamine-Ag-AgCl composites with efficient visible-light-driven photocatalytic activity.

    PubMed

    Cai, Aijun; Wang, Xiuping; Guo, Aiying; Chang, Yongfang

    2016-09-01

    Polydopamine-Ag-AgCl composites (PDA-Ag-AgCl) were synthesized using a mussel-inspired method at room temperature, where PDA acts as a reducing agent to obtain the noble Ag nanoparticles from a precursor. The morphologies and structures of the as-prepared PDA-Ag-AgCl were characterized by several techniques including field emission scanning electron microscopy (FESEM), transmission electron microscopy (SEM), Raman spectra, and X-Ray photoelectron spectrum (XPS). The morphological observation depicts formation of nanoparticles with various micrometer size diameters and surface XPS analysis shows presence of various elements including Ag, N, Cl, and O. The enhanced absorbance of the PDA-Ag-AgCl particles in the visible light region is confirmed through UV-Vis diffuse reflectance spectra (DRS), and the charge transfer is demonstrated by photoluminescence (PL) and photocurrent response. The synthesized PDA-Ag-AgCl composites could be used as visible-light-driven photocatalysts for the degradation of Rhodamine B. The elevated photocatalytic activity is ascribed to the effective charge transfer from plasmon-excited Ag to AgCl that can improve the efficiency of the charge separation during the photocatalytic reaction. Furthermore, differences in the photocatalytic performance among the different PDA-Ag-AgCl composites are noticed that could be attributed to the Brunauer-Emmett-Teller (BET) specific surface area, which benefits to capture the visible light efficiently. The PDA-Ag-AgCl exhibits excellent stability without a significant loss in activity after 5cycles. The proposed method is low-cost and environmentally friendly, hence a promising new way to fabricate plasmon photocatalysts.

  11. Hemocompatibility evaluation of different silver nanoparticle concentrations employing a modified Chandler-loop in vitro assay on human blood.

    PubMed

    Krajewski, Stefanie; Prucek, Robert; Panacek, Ales; Avci-Adali, Meltem; Nolte, Andrea; Straub, Andreas; Zboril, Radek; Wendel, Hans P; Kvitek, Libor

    2013-07-01

    Due to their antibacterial effects, the use of silver nanoparticles (AgNPs) in a great variety of medical applications like coatings of medical devices has increased markedly in the last few years. However, blood in contact with AgNPs may induce adverse effects, thereby altering hemostatic functions. The objective of this study was to investigate the hemocompatibility of AgNPs in whole blood. Human whole blood (n=6) was treated with different AgNPs concentrations (1, 3 and 30mgl(-1)) or with saline/blank solutions as controls before being circulated in an in vitro Chandler-loop model for 60min at 37°C. Before and after circulation, various hematologic markers were investigated. Based on the hematologic parameters measured, no profound changes were observed in the groups treated with AgNP concentrations of 1 or 3mgl(-1). AgNP concentrations of 30mgl(-1) induced hemolysis of erythrocytes and α-granule secretion in platelets, increased CD11b expression on granulocytes, increased coagulation markers thrombin-antithrombin-III complex, kallikrein-like and FXIIa-like activities as well as complementing cascade activation. Overall, we provide for the first time a comprehensive evaluation including all hematologic parameters required to reliably assess the hemocompatibility of AgNPs. We strongly recommend integrating these hemocompatibility tests to preclinical test procedures prior to in vivo application of new AgNP-based therapies.

  12. Silver nanoparticle impact on bacterial growth: effect of pH, concentration, and organic matter.

    PubMed

    Fabrega, Julia; Fawcett, Shona R; Renshaw, Joanna C; Lead, Jamie R

    2009-10-01

    Silver nanoparticles (Ag NPs) are widely used as antibacterial agents. This antibacterial property carries with it a potential environmental risk once these NPs are discharged into the environment. This study investigated the impact on Pseudomonas fluorescens over a 24 h exposure of well characterized Ag NPs at pH values of 6-9, in the presence and absence of Suwannee River humic acids (SRHA). Ag NPs were characterized by size, aggregation, morphology, dissolution, and surface properties under all conditions. Solubility was low (less than 2%) for all Ag NP concentrations (2-2000 ppb) and under all conditions was less than 40 ppb (0.38 microM). SRHA caused a partial disaggregation of Ag NP aggregates by nanoscale film formation, with individual NPs stabilized by charge and entropically driven steric effects. Dissolved Ag reduced bacterial growth entirely at 2000 ppb (19 microM) under all conditions and adversely affected growth at 200 ppb (1.9 microM) under some conditions, indicating some toxicity. The Ag NPs showed similar toxicity at 2000 ppb (19 microM) in the absence of SRHA and at pH 9 only i.e. SRHA mitigated bactericidal action. Solubility and interactions with SRHA indicate that there was a specific nanoparticle effect which could not be explained by the effect of dissolved Ag.

  13. Preparation of sensitive and recyclable porous Ag/TiO2 composite films for SERS detection

    NASA Astrophysics Data System (ADS)

    Zhang, Zhengyi; Yu, Jiajie; Yang, Jingying; Lv, Xiang; Wang, Tianhe

    2015-12-01

    Porous Ag/TiO2 composite films were prepared by spin coating of titania on normal glass slides and subsequent photochemical deposition of silver nanoparticles (AgNPs). The films were characterized by XRD and FESEM to reveal micro structural and morphological differences between films obtained under varied conditions. The SERS properties of these films were investigated using aqueous crystal violet (CV) as probe molecules. The results indicate that the content of polyethylene glycol (PEG) and photo-reduction time had significant influences on both the microstructure and SERS performance of Ag/TiO2 films. The highest SERS sensitivity that allowed as low as 10-10 M aqueous CV to be detected, was achieved with the PEG/(C4H9O)4Ti molar ratio being 0.08% and with 30 min of UV irradiation. With this film a linear relationship was established through experiment between SERS intensity and CV concentration from 10-10 to 10-5 M, which could be used as a calibration curve for CV concentration measurement. In addition, the film could be reused as a SERS substrate for up to four times without significantly losing SERS sensitivity if a simple regeneration was followed. It is visualized that the Ag/TiO2 film on glass has potentials for being developed into a practical SERS substrate with high sensitivity and good reusability.

  14. Thermoelectric properties of AgSbTe₂ from first-principles calculations

    SciTech Connect

    Rezaei, Nafiseh; Akbarzadeh, Hadi; Hashemifar, S. Javad

    2014-09-14

    The structural, electronic, and transport properties of AgSbTe₂ are studied by using full-relativistic first-principles electronic structure calculation and semiclassical description of transport parameters. The results indicate that, within various exchange-correlation functionals, the cubic Fd3⁻m and trigonal R3⁻m structures of AgSbTe₂ are more stable than two other considered structures. The computed Seebeck coefficients at different values of the band gap and carrier concentration are accurately compared with the available experimental data to speculate a band gap of about 0.1–0.35 eV for AgSbTe₂ compound, in agreement with our calculated electronic structure within the hybrid HSE (Heyd-Scuseria-Ernzerhof) functional. By calculating the semiclassical Seebeck coefficient, electrical conductivity, and electronic part of thermal conductivity, we present the theoretical upper limit of the thermoelectric figure of merit of AgSbTe₂ as a function of temperature and carrier concentration.

  15. Nitrogen- Doped Graphene Quantum Dots: "Turn-off" Fluorescent Probe for Detection of Ag(+) Ions.

    PubMed

    Tabaraki, Reza; Nateghi, Ashraf

    2016-01-01

    Highly luminescent nitrogen-doped graphene quantum dots (N-GQDs) were prepared from glucose and ammonia as carbon and nitrogen sources, respectively. The N-GQDs showed a strong emission at 458 nm with excitation at 360 nm. The N-GQDs exhibited analytical potential as sensing probes for silver ions determination. Factors affecting the fluorescence sensing of Ag(+) ions such as pH, N-GQDs concentration and incubation time were studied using Box-Behnken experimental design. The optimum conditions were determined as pH 7, N-GQDs concentration 1 mg/mL and time 60 min. It suggested that N-GQDs exhibited high sensitivity and selectivity toward Ag(+). The linear range of N-GQDs and the limit of detection (LOD) were 0.2-40 μM and 168 nM, respectively. The N-GQDs-based Ag(+) ions sensor was successfully applied to the determination of Ag(+) in tap water and real river water samples.

  16. Enrichment of anodic MgO layers with Ag nanoparticles for biomedical applications.

    PubMed

    Necula, B S; Fratila-Apachitei, L E; Berkani, A; Apachitei, I; Duszczyk, J

    2009-01-01

    The growing fight against infections caused by bacteria poses new challenges for development of materials and medical devices with antimicrobial properties. Silver is a well known antimicrobial agent and has recently started to be used in nanoparticulate form, with the advantage of a high specific surface area and a continuous release of enough concentration of silver ions/radicals. The synthesis of MgO-Ag nanocomposite coatings by in situ deposition of silver nanoparticles during plasma electrolytic oxidation of a magnesium substrate is presented in this study. The process was performed in an electrolyte containing Ag nanoparticles under different oxidation conditions (i.e., current density, oxidizing time, silver nanoparticles concentration in the electrolyte). Surface morphology, phase composition and elemental composition (on the surface and across the thickness of MgO-Ag nanocomposite coatings) were assessed by scanning electron microscopy, X-ray diffraction, energy X-ray dispersive spectrometry and radio frequency glow discharge optical emission spectroscopy, respectively. The coatings were found to be porous, around 7 mum thick, consisting of a crystalline oxide matrix embedded with silver nanoparticles. The findings suggest that plasma electrolytic oxidation process has potential for the synthesis of MgO-Ag nanocomposite coatings.

  17. Influence of reactive sulfide (AVS) and supplementary food on Ag, Cd and Zn bioaccumulation in the marine polychaete Neanthes arenaceodentata

    USGS Publications Warehouse

    Lee, J.-S.; Lee, B.-G.; Yoo, H.; Koh, C.-H.; Luoma, S.N.

    2001-01-01

    A laboratory bioassay determined the relative contribution of various pathways of Ag, Cd and Zn bioaccumulation in the marine polychaete Neanthes arenaceodentata exposed to moderately contaminated sediments. Juvenile worms were exposed for 25 d to experimental sediments containing 5 different reactive sulfide (acid volatile sulfides, AVS) concentrations (1 to 30 ??mol g-1), but with constant Ag, Cd, and Zn concentrations of 0.1, 0.1 and 7 ??mol g-1, respectively. The sediments were supplemented with contaminated food (TetraMin??) containing 3 levels of Ag-Cd-Zn (uncontaminated, 1?? or 5??1 metal concentrations in the contaminated sediment). The results suggest that bioaccumulation of Ag, Cd and Zn in the worms occurred predominantly from ingestion of contaminated sediments and contaminated supplementary food. AVS or dissolved metals (in porewater and overlying water) had a minor effect on bioaccumulation of the 3 metals in most of the treatments. The contribution to uptake from the dissolved source was most important in the most oxic sediments, with maximum contributions of 8% for Ag, 30% for Cd and 20% for Zn bioaccumulation. Sediment bioassays where uncontaminated supplemental food is added could seriously underestimate metal exposures in an equilibrated system; N. arenaceodentata feeding on uncontaminated food would be exposed to 40-60% less metal than if the food source was equilibrated (as occurs in nature). Overall, the results show that pathways of metal exposure are dynamically linked in contaminated sediments and shift as external geochemical characteristics and internal biological attributes vary.

  18. One-pot synthesis of ternary Ag₂CO₃/Ag/AgCl photocatalyst in natural geothermal water with enhanced photocatalytic activity under visible light irradiation.

    PubMed

    Yao, Xiaxi; Liu, Xiaoheng

    2014-09-15

    Geothermal water is a clean, cheap and renewable resource and it is widely distributed all over the world. In this work, ternary Ag2CO3/Ag/AgCl photocatalyst has been successfully synthesized via a one-pot precipitation method in natural geothermal water at room temperature, wherein the geothermal water serves as the source of chlorine and carbonate. The results suggest that the Ag/AgCl nanoparticles are anchored on the surface of Ag2CO3 and Ag2CO3/Ag/AgCl composite shows strong absorption ability in the visible light region. The evaluation of the photocatalytic activity indicates that the as-synthesized Ag2CO3/Ag/AgCl photocatalyst exhibits higher photocatalytic performance for the degradation of methylene blue (MB) aqueous solution under visible light irradiation than one-component (Ag2CO3), two-component (Ag/AgCl, Ag2CO3/AgCl) and the mechanical mixture of Ag2CO3 and Ag/AgCl. The trapping experiments confirmed that holes (h(+)) and (•)O2(-) were the two main active species in the photocatalytic process. Finally, a possible Z-scheme photocatalytic mechanism of the charge transfer was proposed for the enhanced photocatalytic performance. This work may open up new insights into the application of cheap geothermal water resources in the word and provide new opportunities for facile fabrication of Ag/AgCl-based photocatalysts.

  19. Potential risk of acute toxicity induced by AgI cloud seeding on soil and freshwater biota.

    PubMed

    Fajardo, C; Costa, G; Ortiz, L T; Nande, M; Rodríguez-Membibre, M L; Martín, M; Sánchez-Fortún, S

    2016-11-01

    Silver iodide is one of the most common nucleating materials used in cloud seeding. Previous cloud seeding studies have concluded that AgI is not practically bioavailable in the environment but instead remains in soils and sediments such that the free Ag amounts are likely too low to induce a toxicological effect. However, none of these studies has considered the continued use of this practice on the same geographical areas and thus the potential cumulative effect of environmental AgI. The aim of this study is to assess the risk of acute toxicity caused by AgI exposure under laboratory conditions at the concentration expected in the environment after repeated treatments on selected soil and aquatic biota. To achieve the aims, the viability of soil bacteria Bacillus cereus and Pseudomonas stutzeri and the survival of the nematode Caenorhabditis elegans exposed to different silver iodide concentrations have been evaluated. Freshwater green algae Dictyosphaerium chlorelloides and cyanobacteria Microcystis aeruginosa were exposed to silver iodide in culture medium, and their cell viability and photosynthetic activity were evaluated. Additionally, BOD5 exertion and the Microtox® toxicity test were included in the battery of toxicological assays. Both tests exhibited a moderate AgI adverse effect at the highest concentration (12.5µM) tested. However, AgI concentrations below 2.5µM increased BOD5. Although no impact on the growth and survival endpoints in the soil worm C. elegans was recorded after AgI exposures, a moderate decrease in cell viability was found for both of the assessed soil bacterial strains at the studied concentrations. Comparison between the studied species showed that the cyanobacteria were more sensitive than green algae. Exposure to AgI at 0.43μM, the reference value used in monitoring environmental impact, induced a significant decrease in photosynthetic activity that is primarily associated with the respiration (80% inhibition) and, to a lesser

  20. Origin of the Order-Disorder Transition and the Associated Anomalous Change of Thermopower in AgBiS2 Nanocrystals: A Combined Experimental and Theoretical Study.

    PubMed

    Guin, Satya N; Banerjee, Swastika; Sanyal, Dirtha; Pati, Swapan K; Biswas, Kanishka

    2016-06-20

    Bulk AgBiS2 crystallizes in a trigonal crystal structure (space group, P3̅m1) at room temperature, which transforms to a cation disordered rock salt structure (space group, Fm3̅m) at ∼473 K. Surprisingly, at room temperature, a solution-grown nanocrystal of AgBiS2 crystallizes in a metastable Ag/Bi ordered cubic structure, which transforms to a thermodynamically stable disorded cubic structure at 610 K. Moreover, the order-disorder transition in nanocrystalline AgBiS2 is associated with an unusual change in thermopower. Here, we shed light on the origin of a order-disorder phase transition and the associated anomalous change of thermopower in AgBiS2 nanocrystals by using a combined experimental, density functional theory based first-principles calculation and ab initio molecular dynamics simulations. Positron-annilation spectroscopy indicates the presence of higher numbers of Ag vacancies in the nanocrystal compared to that of the bulk cubic counterpart at room temperature. Furthermore, temperature-dependent two-detector coincidence Doppler broadening spectroscopy and Doppler broadening of the annihilation radiation (S parameter) indicate that the Ag vacancy concentration increases abruptly during the order-disorder transition in nanocrystalline AgBiS2. At high temperature, a Ag atom shuttles between the vacancy and interstitial sites to form a locally disordered cation sublattice in the nanocrystal, which is facilitated by the formation of more Ag vacancies during the phase transition. This process increases the entropy of the system at higher vacancy concentration, which, in turn, results in the unusual rise in thermopower.

  1. 3D [Ag-Mg] polyanionic frameworks in the La 4Ag 10Mg 3 and La 4Ag 10.3Mg 12 new ternary compounds

    NASA Astrophysics Data System (ADS)

    Solokha, Pavlo; De Negri, Serena; Pavlyuk, Volodymyr; Eck, Bernhard; Dronskowski, Richard; Saccone, Adriana

    2010-12-01

    The crystal structures of two new ternary phases, La 4Ag 10Mg 3 and La 4Ag 10.3Mg 12, were refined from X-ray single crystal diffraction data. La 4Ag 10Mg 3 crystallizes in the Ca 4Au 10In 3 structure type, an ordered variant of the binary Zr 7Ni 10 compound: orthorhombic, Cmce, oS68, a=14.173(5), b=10.266(3), c=10.354(3) Å, Z=4, w R2=0.0826, 676 F2 values, 50 variables. La 4Ag 10.3Mg 12 represents a new structure type: orthorhombic, Cmmm, oS116-10.32, a=9.6130(3), b=24.9663(8), c=9.6333(2) Å, Z=4, w R2=0.0403, 1185 F2 values, 101 variables. The structural analysis of both compounds, highlighting a significant contraction of the Ag-Mg distances, suggests the existence of three-dimensional [Ag-Mg] networks hosting La atoms. LMTO calculations applied to La 4Ag 10Mg 3 indicate that the strongest bonds occur for Ag-Ag and Ag-Mg interactions, and confirm the presence of a 3D ∞[Ag 10Mg 3] δ- polyanionic framework balanced by positively charged La atoms.

  2. Bipolar Ag-Zn battery

    NASA Technical Reports Server (NTRS)

    Giltner, L. John

    1994-01-01

    The silver-zinc (AgZn) battery system has been unique in its ability to safely satisfy high power demand applications with low mass and volume. However, a new generation of defense, aerospace, and commercial applications will impose even higher power demands. These new power demands can be satisfied by the development of a bipolar battery design. In this configuration the power consuming, interelectrode current conductors are eliminated while the current is then conducted via the large cross-section electrode substrate. Negative and positive active materials are applied to opposite sides of a solid silver foil substrate. In addition to reducing the weight and volume required for a specified power level, the output voltage performance is also improved as follows. Reduced weight through: elimination of the plastic cell container; elimination of plate leads and intercell connector; and elimination of internal plate current collector. Increased voltage through: elimination of resistance of current collector; elimination of resistance of plate lead; and elimination of resistance of intercell connector. EPI worked previously on development of a secondary bipolar silver zinc battery. This development demonstrated the electrical capability of the system and manufacturing techniques. One difficulty with this development was mechanical problems with the seals. However, recent improvements in plastics and adhesives should eliminate the major problem of maintaining a seal around the periphery of the bipolar module. The seal problem is not as significant for a primary battery application or for a requirement for only a few discharge cycles. A second difficulty encountered was with activation (introducing electrolyte into the cell) and with venting gas from the cell without loss of electrolyte. During previous work, the following projections for energy density were made from test data for a high power system which demonstrated in excess of 50 discharge/charge cycles. Projected

  3. Bipolar Ag-Zn battery

    NASA Astrophysics Data System (ADS)

    Giltner, L. John

    1994-02-01

    The silver-zinc (AgZn) battery system has been unique in its ability to safely satisfy high power demand applications with low mass and volume. However, a new generation of defense, aerospace, and commercial applications will impose even higher power demands. These new power demands can be satisfied by the development of a bipolar battery design. In this configuration the power consuming, interelectrode current conductors are eliminated while the current is then conducted via the large cross-section electrode substrate. Negative and positive active materials are applied to opposite sides of a solid silver foil substrate. In addition to reducing the weight and volume required for a specified power level, the output voltage performance is also improved as follows. Reduced weight through: elimination of the plastic cell container; elimination of plate leads and intercell connector; and elimination of internal plate current collector. Increased voltage through: elimination of resistance of current collector; elimination of resistance of plate lead; and elimination of resistance of intercell connector. EPI worked previously on development of a secondary bipolar silver zinc battery. This development demonstrated the electrical capability of the system and manufacturing techniques. One difficulty with this development was mechanical problems with the seals. However, recent improvements in plastics and adhesives should eliminate the major problem of maintaining a seal around the periphery of the bipolar module. The seal problem is not as significant for a primary battery application or for a requirement for only a few discharge cycles. A second difficulty encountered was with activation (introducing electrolyte into the cell) and with venting gas from the cell without loss of electrolyte. During previous work, the following projections for energy density were made from test data for a high power system which demonstrated in excess of 50 discharge/charge cycles. Projected

  4. Spectrophotometry of the shell around AG Carinae

    NASA Technical Reports Server (NTRS)

    Mitra, P. Mila; Dufour, Reginald J.

    1990-01-01

    Spatially-resolved long-slit spectrophotometry are presented for two regions of the shell nebula around the P-Cygni variable star AG Carinae. The spectra cover the 3700-6800 A wavelength range. Emission-line diagnostics are used to derive extinction, electron temperatures, and densities for various positions in the nebula. The chemical abundances and ionization structure are calculated and compared with other types of planetary nebulae and shells around other luminous stars. It is found that the N/O and N/S ratios of Ag Car are high compared to solar neighborhood ISM values. The O/H depletion found for the AG Car shell approaches that found in the condensations of the Eta Car system.

  5. Enhanced chemiluminescence of the luminol-AgNO3 system by Ag nanoparticles.

    PubMed

    Li, Shifeng; Sun, Huimin; Wang, Dong; Hong, Jianguo; Tao, Shanjun; Yu, Haiyin; Wang, Xiuhua; Wei, Xianwen

    2012-01-01

    The oxidation reaction of luminol with AgNO(3) can produce chemiluminescence (CL) in the presence of silver nanoparticles (NPs) in alkaline solution. Based on the studies of UV-vis absorption spectra, photoluminescence (PL) spectra and CL spectra, a CL enhancement mechanism is proposed. The CL emission spectrum of the luminol-AgNO(3)-Ag NPs system indicated that the luminophore was still 3-aminophthalate. On injection of silver nanoparticles into the mixture of luminol and AgNO(3), they catalysed the reduction of AgNO(3) by luminol. The product luminol radicals reacted with the dissolved oxygen, to produce a strong CL emission. As a result, the CL intensity was substantially increased. Moreover, the influences of 18 amino acids, e.g. cystine, tyrosine and asparagine, and 25 organic compounds, including gallic acid, tannic acid and hydroquinone, on the luminol-AgNO(3)-Ag NPs CL system were studied by a flow-injection procedure, which led to an effective method for detecting these compounds.

  6. Ag/FeCo/Ag core/shell/shell magnetic nanoparticles with plasmonic imaging capability.

    PubMed

    Takahashi, Mari; Mohan, Priyank; Nakade, Akiko; Higashimine, Koichi; Mott, Derrick; Hamada, Tsutomu; Matsumura, Kazuaki; Taguchi, Tomohiko; Maenosono, Shinya

    2015-02-24

    Magnetic nanoparticles (NPs) have been used to separate various species such as bacteria, cells, and proteins. In this study, we synthesized Ag/FeCo/Ag core/shell/shell NPs designed for magnetic separation of subcellular components like intracellular vesicles. A benefit of these NPs is that their silver metal content allows plasmon scattering to be used as a tool to observe detection by the NPs easily and semipermanently. Therefore, these NPs are considered a potential alternative to existing fluorescent probes like dye molecules and colloidal quantum dots. In addition, the Ag core inside the NPs suppresses the oxidation of FeCo because of electron transfer from the Ag core to the FeCo shell, even though FeCo is typically susceptible to oxidation. The surfaces of the Ag/FeCo/Ag NPs were functionalized with ε-poly-L-lysine-based hydrophilic polymers to make them water-soluble and biocompatible. The imaging capability of the polymer-functionalized NPs induced by plasmon scattering from the Ag core was investigated. The response of the NPs to a magnetic field using liposomes as platforms and applying a magnetic field during observation by confocal laser scanning microscopy was assessed. The results of the magnetophoresis experiments of liposomes allowed us to calculate the magnetic force to which each liposome was subjected.

  7. Antifungal activity of multifunctional Fe 3O 4-Ag nanocolloids

    NASA Astrophysics Data System (ADS)

    Chudasama, Bhupendra; Vala, Anjana K.; Andhariya, Nidhi; Upadhyay, R. V.; Mehta, R. V.

    2011-05-01

    In recent years, rapid increase has been observed in the population of microbes that are resistant to conventionally used antibiotics. Antifungal drug therapy is no exception and now resistance to many of the antifungal agents in use has emerged. Therefore, there is an inevitable and urgent medical need for antibiotics with novel antimicrobial mechanisms. Aspergillus glaucus is the potential cause of fatal brain infections and hypersensitivity pneumonitis in immunocompromised patients and leads to death despite aggressive multidrug antifungal therapy. In the present article, we describe the antifungal activity of multifunctional core-shell Fe 3O 4-Ag nanocolloids against A. glaucus isolates. Controlled experiments are also carried out with Ag nanocolloids in order to understand the role of core (Fe 3O 4) in the antifungal action. The minimum inhibitory concentration (MIC) of nanocolloids is determined by the micro-dilution method. MIC of A. glaucus is 2000 μg/mL. The result is quite promising and requires further investigations in order to develop a treatment methodology against this death causing fungus in immunocompromised patients.

  8. The axisymmetric stellar wind of AG Carinae

    NASA Technical Reports Server (NTRS)

    Schulte-Ladbeck, Regina E.; Clayton, Geoffrey C.; Hillier, D. John; Harries, Tim J.; Howarth, Ian D.

    1994-01-01

    We present optical linear spectropolarimetry of the Luminous Blue Variable AG Carinae obtained after a recent visual brightness increase. The absence of He II lambda 4686 emission, together with the weakening of the He I spectrum and the appearance of Fe lines in the region around 5300 A, confirm that AG Car has started a new excursion across the HR diagram. The H alpha line profile exhibits very extended line wings that are polarized differently in both amount and position angle from either the continuum or the line core. The polarization changes across H alpha, together with variable continuum polarization, indicate the presence of intrinsic polarization. Coexistence of the line-wing polarization with extended flux-line wings evidences that both are formed by electron scattering in a dense wind. The position angle rotates across the line profiles, in a way that presently available models suggest is due to rotation and expansion of the scattering material. AG Car displays very large variations of its linear polarization with time, Delta P approximately 1.2%, indicating significant variations in envelope opacity. We find that the polarization varies along a preferred position angle of approximately 145 deg (with a scatter of +/- 10 deg) which we interpret as a symmetry axis of the stellar wind (with an ambiguity of 90 deg). This position angle is co-aligned with the major axis of the AG Car ring nebula and perpendicular to the AG Car jet. Our observations thus suggest that the axisymmetric geometry seen in the resolved circumstellar environment at various distances already exists within a few stellar radii of AG Car. From the H alpha polarization profile we deduce an interstellar polarization of Q = 0.31%, U = -1.15% at H alpha. The inferred interstellar polarization implies that the intrinsic polarization is not always of the same sign. This indicates either significant temporal changes in the envelope geometry, or it may arise from effects of multiple scattering

  9. Real-Space Microscopic Electrical Imaging of n+-p Junction Beneath Front-Side Ag Contact of Multicrystalline Si Solar Cells

    SciTech Connect

    Jiang, C. S.; Li, Z. G.; Moutinho, H. R.; Liang, L.; Ionkin, A.; Al-Jassim, M. M.

    2012-04-15

    We investigated the quality of the n+-p diffused junction beneath the front-side Ag contact of multicrystalline Si solar cells by characterizing the uniformities of electrostatic potential and doping concentration across the junction using the atomic force microscopy-based electrical imaging techniques of scanning Kelvin probe force microscopy and scanning capacitance microscopy. We found that Ag screen-printing metallization fired at the over-fire temperature significantly degrades the junction uniformity beneath the Ag contact grid, whereas metallization at the optimal- and under-fire temperatures does not cause degradation. Ag crystallites with widely distributed sizes were found at the Ag-grid/emitter-Si interface of the over-fired cell, which is associated with the junction damage beneath the Ag grid. Large crystallites protrude into Si deeper than the junction depth. However, the junction was not broken down; instead, it was reformed on the entire front of the crystallite/Si interface. We propose a mechanism of junction-quality degradation, based on emitter Si melting at the temperature around the Ag-Si eutectic point during firing, and subsequent re-crystallization with incorporation of Ag and other impurities and with formation of crystallographic defects during quenching. The effect of this junction damage on solar cell performance is discussed.

  10. Doping nano-Co3O4 surface with bigger nanosized Ag and its photocatalytic properties for visible light photodegradation of organic dyes

    NASA Astrophysics Data System (ADS)

    Chen, Guangliang; Si, Xiaolei; Yu, Jinsong; Bai, Huiyu; Zhang, Xianhui

    2015-03-01

    This paper reports the synthesis of nanosized Ag/Co3O4 composite catalysts using a silver-mirror reaction and the calibration of their catalytic activities towards methyl blue (MB) dye degradation with peroxymonosulfate (PMS) under visible light. The nanosized Ag/Co3O4 composites were characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV-vis spectroscopy. The experimental evidence indicated that the hydrothermal synthesis approach lead to the exposure of the {1 1 2} facets of the Co3O4 nanoflakes. Compared to Co3O4 nanoflakes, Co3O4 doped with Ag nanoparticle (average diameters of 10-15 nm) presented lower band gap energy and photoluminescent (PL) intensity. Meanwhile, the Ag/Co3O4 exhibited high stability and excellent dispersion property in dye solution. Experimental data suggested that 3.06 wt% Ag nanoparticle-doped Ag/Co3O4 nanocomposite catalyst possessed the highest catalytic activity towards MB degradation in aqueous solution at the tested concentration level of 15 mg/L, about 2.4 times higher than that of pure Co3O4. Complete decolorization of the 15 mg/L MB solution can be achieved by 3.06 wt% Ag-doped Ag/Co3O4 nanocomposite within 20 min of visible light irradiation.

  11. Rapid formation of Ag(n)X(X = S, Cl, PO4, C2O4) nanotubes via an acid-etching anion exchange reaction.

    PubMed

    Li, Jingjing; Yang, Wenlong; Ning, Jiqiang; Zhong, Yijun; Hu, Yong

    2014-06-07

    This work presents a rapid nanotube fabrication method for a series of silver compounds AgnX, such as Ag2S, AgCl, Ag3PO4, and Ag2C2O4, from pregrown Ag2CO3 nanorod templates. The anion exchange process involved takes place in non-aqueous solutions just at room temperature and completes within 10 minutes. An acid-etching anion exchange reaction mechanism has been proved underneath the transformation process from Ag2CO3 nanorods to AgnX nanotubes by the observation of an intermediate yolk-shell nanostructure. It has been found that the final structure of the products can be conveniently controlled by simply varying the concentration of HnX acids, and the organic solvents employed play a vital role in the formation of the nanotubes by effectively controlling the diffusion rates of different species of reacting ions. As a demonstration, the as-prepared AgCl and Ag3PO4 nanotubes exhibit enhanced photocatalytic activity and favorable recyclability for the photodegradation of rhodamine B (RhB) under visible-light irradiation.

  12. A new method for producing highly concentrated non-aqueous dispersions of silver nanoparticles and the evaluation of their bactericidal activity

    NASA Astrophysics Data System (ADS)

    da S. Oliveira, Roselaine; Bizeto, Marcos A.; Liberatore, Ana M. A.; Koh, Ivan H. J.; Camilo, Fernanda F.

    2014-11-01

    Different preparation methods of silver nanoparticles (AgNP) are well described in the literature, most of them in aqueous medium. Aqueous dispersions of AgNP normally have a limited capacity to tolerate high nanosilver concentrations. However, AgNP production in non-aqueous medium is still scarce although its exploitation for example, as coating for hydrophobic surfaces, would be of a huge importance in many technological applications. In this work, we report the chemical preparation of highly concentrated non-aqueous AgNP dispersions obtained by reduction of silver cation, from two distinct salt sources (AgNO3 and AgBF4), by 1-butanol in the presence of a biocompatible poly(ether-block-amide) copolymer, named PEBA. The highest concentration reached was around 5 mM, when it used AgBF4 as silver source and 4 % (w/w) of a PEBA solution in 1-butanol. This AgNP concentration is notably higher than the values reported in aqueous medium. The AgNP formation was attested by UV-Vis spectroscopic analysis, which showed the characteristic strong plasmon band at 420 nm. The X-ray diffraction patterns confirmed the formation of a crystalline fcc silver metallic phase with particle diameters ranging from 5 to 10 nm accordingly to transmission electron microscopy examination. It was also observed that the AgNP dimensions are dependent on the PEBA and silver salt concentrations. The AgNP dispersions presented a very high antimicrobial activity against E. coli and S. aureus microorganisms, even in low concentration, attested by the Kirby-Bauer method.

  13. Siberian Snake solenoid for the AGS

    SciTech Connect

    Ratner, L. G.

    1991-01-01

    Recent experiments at the Indiana University Cyclotron Facility (IUCF) have demonstrated that Siberian Snakes'' can be used to preserve the polarization of an accelerated polarized beam in a circular accelerator. Retrofitting full snakes into accelerators such as the Alternating Gradient Synchrotron (AGS) at Brookhaven is almost impossible due to space limitations, but a partial snake that can correct depolarization due to imperfection resonances with 1/20 to 1/30 of a full strength snake seems to present a viable option. We describe such a device for the AGS and give the design criteria in terms of simplicity of accelerator operation and level of achievable polarization. 2 refs., 5 figs., 1 tab.

  14. Facile synthesis of novel Ag/AgI/BiOI composites with highly enhanced visible light photocatalytic performances

    SciTech Connect

    Cao, Jing; Zhao, Yijie; Lin, Haili; Xu, Benyan; Chen, Shifu

    2013-10-15

    Novel Ag/AgI/BiOI composites were controllably synthesized via a facile ion-exchange followed by photoreduction strategy by using hierarchical BiOI microflower as substrate. The as-prepared Ag/AgI/BiOI composites were studied by X-ray powder diffractometer (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET) surface area analyzer and UV–vis diffuse reflectance spectroscopy (DRS). Under visible light (λ>420 nm), Ag/AgI/BiOI displayed highly enhanced photocatalytic activities for degradation of methyl orange (MO) compared to the pure hierarchical BiOI, which was mainly ascribed to the highly efficient separation of electrons and holes through the closely contacted interfaces in the Ag/AgI/BiOI ternary system. - Graphical abstract: Ag/AgI/BiOI displayed excellent photocatalytic activities for methyl orange degradation under visible light, which was mainly ascribed to the highly efficient separation of electrons and holes through Z-scheme pathway. Display Omitted - Highlights: • Novel Ag/AgI/BiOI composites were successfully synthesized. • Ag/AgI/BiOI displayed higher visible light activities than those of pure BiOI and AgI. • ·O{sub 2}{sup −} and h{sup +}, especially ·O{sub 2}{sup −}, dominated the photodegradation process of MO. • A Z-scheme pattern was adopted for Ag/AgI/BiOI activity enhancement.

  15. Ag@AgHPW as a plasmonic catalyst for visible-light photocatalytic degradation of environmentally harmful organic pollutants

    SciTech Connect

    Zhou, Wenhui; Cao, Minhua Li, Na; Su, Shuangyue; Zhao, Xinyu; Wang, Jiangqiang; Li, Xianghua; Hu, Changwen

    2013-06-01

    Graphical abstract: Ag@Ag{sub x}H{sub 3−x}PW12O40 (Ag@AgHPW) nanoparticles (NPs), a new visible-light driven plasmonic photocatalyst, are prepared by a green photoreduction strategy without the addition of any surfactant, which show a high activity and stability for the degradation of methyl blue (MB) under visible light irradiation. - Highlights: • A new visible-light driven photocatalyst Ag@Ag{sub x}H{sub 3−x}PW{sub 12}O{sub 40} was designed. • The photocatalyst shows a high activity for the degradation of methyl blue. • The high activity can be ascribed to the synergy of photoexcited AgHPW and Ag. - Abstract: Ag@Ag{sub x}H{sub 3−x}PW{sub 12}O{sub 40} (Ag@AgHPW) nanoparticles (NPs), a new visible-light driven plasmonic photocatalyst, are prepared by a green photoreduction strategy without the addition of any surfactant. They show strong absorption in the visible region because of the localized surface plasmon resonance (LSPR) of Ag NPs. This plasmonic photocatalyst shows a high activity and stability for the degradation of methyl blue (MB) under visible light irradiation, which could be attributed to the highly synergy of photoexcited Ag{sub x}H{sub 3−x}PW{sub 12}O{sub 40} (AgHPW) and plasmon-excited Ag NPs and the confinement effects at interfaces between polyoxometalates (POMs) and silver. POM anions have redox ability and high photocatalytic activity, whereas Ag NPs could effectively accelerate the separation of electrons and holes, both of which contribute to their high activity.

  16. Ag Nanowire Based Transparent Conductor for CIGS PV

    SciTech Connect

    Woods, L. M.; Wolk, J.; Smith, M.; Davande, H.; Ribelin, R. M.; Perkins, C. L.

    2011-01-01

    Coated silver nanowires (AgNW) have been considered as a replacement for transparent conducting oxides (TCOs) in CIGS based photovoltaic devices. The advantages of AgNW over TCOs are discussed, and optical and electrical characteristics of AgNWs on glass are presented. Similarly fabricated AgNWs with varying sheet resistance on CIGS devices were tested against ITO transparent conductor controls. The CIGS was produced using a roll-to-roll technique on a flexible polymer substrate. Variations in the ZnO layer resistivity that are adjacent to the AgNW layer in the CIGS device were also tested. Device results indicate similar Jsc, but a reduced FF for cells made with the AgNWs, and Voc dependence on the resistivity of the coated AgNW and ZnO window layers. FF and Voc losses associated with the use of AgNWs are discussed.

  17. Hierarchical Ag mesostructures for single particle SERS substrate

    NASA Astrophysics Data System (ADS)

    Xu, Minwei; Zhang, Yin

    2017-01-01

    Hierarchical Ag mesostructures with highly rough surface morphology have been synthesized at room temperature through a simple seed-mediated approach. Electron microscopy characterizations indicate that the obtained Ag mesostructures exhibit a textured surface morphology with the flower-like architecture. Moreover, the particle size can be tailored easily in the range of 250-500 nm. For the growth process of the hierarchical Ag mesostructures, it is believed that the self-assembly mechanism is more reasonable rather than the epitaxial overgrowth of Ag seed. The oriented attachment of nanoparticles is revealed during the formation of Ag mesostructures. Single particle surface enhanced Raman spectra (sp-SERS) of crystal violet adsorbed on the hierarchical Ag mesostructures were measured. Results reveal that the hierarchical Ag mesostructures can be highly sensitive sp-SERS substrates with good reproducibility. The average enhancement factors for individual Ag mesostructures are estimated to be about 106.

  18. Synthesis of g-C{sub 3}N{sub 4}/Ag{sub 3}PO{sub 4} heterojunction with enhanced photocatalytic performance

    SciTech Connect

    He, Peizhi; Song, Limin; Zhang, Shujuan; Wu, Xiaoqing; Wei, Qingwu

    2014-03-01

    Graphical abstract: g-C{sub 3}N{sub 4}/Ag{sub 3}PO{sub 4} heterojunction photocatalyst with visible-light response was prepared by a facile coprecipitation method. The results show that g-C{sub 3}N{sub 4}/Ag{sub 3}PO{sub 4} possesses a much higher activity for the decomposition of RhB than that of the pure Ag{sub 3}PO{sub 4} particles. The most mechanism is that g-C{sub 3}N{sub 4}/Ag{sub 3}PO{sub 4} heterojunction photocatalyst can efficiently separate the photogenerated electron–hole pairs, enhancing the photocatalytic activity of g-C{sub 3}N{sub 4}/Ag{sub 3}PO{sub 4} composites. - Highlights: • g-C{sub 3}N{sub 4}/Ag{sub 3}PO{sub 4} heterojunction showed much higher activity than that of Ag{sub 3}PO{sub 4}. • The high activity could be attributed to g-C{sub 3}N{sub 4} for modifying Ag{sub 3}PO{sub 4}. • More ·OH radicals may be significant reason to improve Ag{sub 3}PO{sub 4} activity. - Abstract: g-C{sub 3}N{sub 4}/Ag{sub 3}PO{sub 4} heterojunction photocatalyst with visible-light response was prepared by a facile coprecipitation method. The photocatalysts were characterized by X-ray powder diffraction, transmission electron microscopy, UV–vis absorption spectroscopy and Fourier transform infrared spectroscopy. The photocatalytic activities of the obtained samples were tested by using Rhodamine B (RhB) as the degradation target under visible light irradiation. g-C{sub 3}N{sub 4}/Ag{sub 3}PO{sub 4} decomposed RhB more effectively than the pure Ag{sub 3}PO{sub 4} particles did, and 2 wt.% g-C{sub 3}N{sub 4} had the highest activity. Furthermore, 2 wt.% g-C{sub 3}N{sub 4}/Ag{sub 3}PO{sub 4} degraded high-concentration RhB more potently than unmodified Ag{sub 3}PO{sub 4} did, probably because g-C{sub 3}N{sub 4}/Ag{sub 3}PO{sub 4} heterojunction photocatalyst enhanced the photocatalytic activity by efficiently separating the photogenerated electron–hole pairs.

  19. Core-shell structured Ag@C for direct electrochemistry and hydrogen peroxide biosensor applications.

    PubMed

    Mao, Shuxian; Long, Yumei; Li, Weifeng; Tu, Yifeng; Deng, Anping

    2013-10-15

    Ag@C core-shell nano-composites have been prepared by a simple one-step hydrothermal method and are further explored for protein immobilization and bio-sensing. The electrochemical behavior of immobilized horseradish peroxidase (HRP) on Ag@C modified indium-tin-oxide (ITO) electrode and its application as H₂O₂ sensor are investigated. Electrochemical and UV-vis spectroscopic measurements demonstrated that Ag@C nano-composites provide excellent matrixes for the adsorption of HRP and the entrapped HRP retains its bioactivities. It is found that on the HRP-Ag@C/ITO electrode, HRP exhibited a fast electron transfer process and good electrocatalytic reduction toward H₂O₂. Under optimum experimental conditions the biosensor linearly responds to H₂O₂ concentration in the range of 5.0×10⁻⁷-1.4×10⁻⁴ M with a detection limit of 2.0×10⁻⁷ M (S/N=3). The apparent Michaelis-Menten constant (K(app)(M)) of the biosensor is calculated to be 3.75×10⁻⁵ M, suggesting high enzymatic activity and affinity toward H₂O₂. In addition, the HRP-Ag@C/ITO bio-electrode shows good reproducibility and long-term stability. Thus, the core-shell structured Ag@C is an attractive material for application in the fabrication of biosensors due to its direct electrochemistry and functionalized surface for efficient immobilization of bio-molecules.

  20. Photo-enhanced salt-water splitting using orthorhombic Ag8SnS6 photoelectrodes in photoelectrochemical cells

    NASA Astrophysics Data System (ADS)

    Cheng, Kong-Wei; Tsai, Wei-Tseng; Wu, Yu-Hsuan

    2016-06-01

    Orthorhombic Ag8SnS6 photoelectrodes are prepared on various substrates via reactive sulfurization using the radio-frequency magnetron sputtering of silver-tin metal precursors. Evaluations of the photoelectrochemical performances of Ag8SnS6 photoelectrodes with various levels of silver content are carried out in various aqueous solutions. X-ray diffraction patterns and Hall measurements of samples after a three-stage sulfurization process show that all samples are the pure orthorhombic Ag8SnS6 phase with n-type conductivity. The energy band gaps, carrier concentrations, and mobilities of samples on glass substrates are 1.31-1.33 eV, 7.07 × 1011-8.52 × 1012 cm-3, and 74.9-368 cm2 V-1 s-1, respectively, depending on the [Ag]/[Ag+Sn] molar ratio in samples. The highest photoelectrochemical performances of orthorhombic Ag8SnS6 photoelectrodes in aqueous 0.35 M Na2S + 0.25 M K2SO3 and 0.5 M NaCl solutions are respectively 2.09 and 2.5 mA cm-2 at an applied voltages of 0.9 and 1.23 V vs. a reversible hydrogen electrode under light irradiation with a light intensity of 100 mW cm-2 from a 300-W Xe lamp.

  1. Monodisperse raspberry-like multihollow polymer/Ag nanocomposite microspheres for rapid catalytic degradation of methylene blue.

    PubMed

    Tian, Qiong; Yu, Xiaojing; Zhang, Lifeng; Yu, Demei

    2017-04-01

    Raspberry-like multihollow polymer microspheres were prepared by seeded swelling polymerization and decorated with silver nanoparticles (AgNPs) in the presence of polyvinylpyrrolidone (PVP) which acted as both reducing and stabilizing agent. Formation mechanism of the raspberry-like multihollow microsphere was discussed on the basis of water absorption of sulfonated groups in the seeded swelling polymerization. Effects of weight ratio of sodium 4-vinylbenzenesulfonate to styrene (NaSS/St) of the seed particles, the concentration of PVP and [Ag(NH3)2](+) ions on the properties of polymer/Ag nanocomposite microspheres were investigated by microscopic observation, nitrogen adsorption/desorption isotherms, UV-vis absorption spectra, X-ray diffraction patterns and thermogravimetric analysis. The results demonstrated that the raspberry-like multihollow microspheres were succes