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Sample records for ag sp electrons

  1. A further insight into the mechanism of Ag + biosorption by Lactobacillus sp. strain A09

    NASA Astrophysics Data System (ADS)

    Lin, Zhongyu; Zhou, Chaohui; Wu, Jianming; Zhou, Jianzhang; Wang, Lin

    2005-04-01

    The mechanism of Ag + biosorption by resting cell of Lactobacillus sp. strain A09 has been further investigated at the molecular level using spectroscopic techniques. The values of estimated equilibrium constants, rate constants, half-life periods and apparent enthalpies of the binding reaction were calculated via the determination of Ag + adsorbed by the biomass using atomic absorption spectrophotometry (AAS). The reductive ratio of the Ag + to Ag 0 by the A09 biomass was examined by X-ray photoelectron spectroscopy (XPS). Analysis for sulfur and nitrogen atomic contents in dry powder of the biomass with EA-1110 elemental analysis (EA) showed that amino acid residues retaining the reductive property of Ag + to Ag 0 are very small quantity, whereas glucose content in the hydrolysates of the biomass analyzed by ultraviolet-visible spectrophotometry (UV-vis) indicated that the amount of reducing sugars in the biomass is much larger than 2.71%. The fourier transform infrared (FTIR) spectrophotometry on blank and silver-loaded biomass demonstrated that the chemical functional group such as the free aldehyde group of the hemiacetalic hydroxyl group from reducing sugars, i.e. the hydrolysates of the polysaccharides from the cell wall plays a leading role in serving as the electron donor for reducing the Ag + to Ag 0. This result was further supported by characterizations on the interaction of the Ag + with glucose using X-ray powder diffractometry (XRD) and FTIR spectroscopy.

  2. Electron microscope study of Sarcocystis sp

    USGS Publications Warehouse

    Zeve, V.H.; Price, D.L.; Herman, C.M.

    1966-01-01

    Sarcocystis sp. obtained from wild populations of grackles, Quiscalus quiscula (Linn.), were examined to clarify the effect of the parasite on the host. Electron micrographs are presented to show areas of muscle destruction adjacent to the parasite which appear to be mechanically produced by the parasite. The microtubules within the villus-like projections of the cyst suggest that their possible function is absorptive and/or conductive with regard to the production of a toxin or the conveyance of nutritive material to the developing cells. The proposed function of submembranous filaments and their relation to the conoid is discussed. Similarities in the ultrastructure to Toxoplasma and other protozoa tend to negate the relegation of Sarcocystis to the fungi and further emphasize its protozoan nature.

  3. A comparative study about electronic structures at rubrene/Ag and Ag/rubrene interfaces

    SciTech Connect

    Sinha, Sumona Mukherjee, M.

    2015-10-15

    The contact between the electrode and the organic semiconductor is one of the most crucial factors in determining the organic device performance. The development and production technology of different organic devices require the understanding of different types of metal/organic semiconducting thin film interfaces. Comparisons about the electronic structures at Rubrene/Ag and Ag/Rubrene interfaces have been studied using photoemission spectroscopy. The Ag on rubrene interfaces is found to show more interesting and complex natures than its counterpart. The vacuum level (VL) was shifted about 0.51 eV from push back effect for deposition of 5 Å rubrene onto Ag film whereas the electronic features of silver was only suppressed and no energy shift was resulted. While the deposition of 5 Å Ag onto rubrene film leads to the diffusion of the Ag atoms, as a cluster with quantum size effect, inside the film. Angle dependent XPS measurement indicates that diffused metal clusters were present at entire probed depth of the film. Moreover these clusters dope the uppermost surface of the rubrene film which consequences a shift of the electronic states of thick organic film towards higher binding energy. The VL was found to shift about 0.31 eV toward higher binding energy whereas the shift was around 0.21 eV for the electronic states of rubrene layer.

  4. A comparative study about electronic structures at rubrene/Ag and Ag/rubrene interfaces

    NASA Astrophysics Data System (ADS)

    Sinha, Sumona; Mukherjee, M.

    2015-10-01

    The contact between the electrode and the organic semiconductor is one of the most crucial factors in determining the organic device performance. The development and production technology of different organic devices require the understanding of different types of metal/organic semiconducting thin film interfaces. Comparisons about the electronic structures at Rubrene/Ag and Ag/Rubrene interfaces have been studied using photoemission spectroscopy. The Ag on rubrene interfaces is found to show more interesting and complex natures than its counterpart. The vacuum level (VL) was shifted about 0.51 eV from push back effect for deposition of 5 Å rubrene onto Ag film whereas the electronic features of silver was only suppressed and no energy shift was resulted. While the deposition of 5 Å Ag onto rubrene film leads to the diffusion of the Ag atoms, as a cluster with quantum size effect, inside the film. Angle dependent XPS measurement indicates that diffused metal clusters were present at entire probed depth of the film. Moreover these clusters dope the uppermost surface of the rubrene film which consequences a shift of the electronic states of thick organic film towards higher binding energy. The VL was found to shift about 0.31 eV toward higher binding energy whereas the shift was around 0.21 eV for the electronic states of rubrene layer.

  5. Superhard sp2-sp3 hybrid carbon allotropes with tunable electronic properties

    NASA Astrophysics Data System (ADS)

    Hu, Meng; Ma, Mengdong; Zhao, Zhisheng; Yu, Dongli; He, Julong

    2016-05-01

    Four sp2-sp3 hybrid carbon allotropes are proposed on the basis of first principles calculations. These four carbon allotropes are energetically more favorable than graphite under suitable pressure conditions. They can be assembled from graphite through intralayer wrinkling and interlayer buckling, which is similar to the formation of diamond from graphite. For one of the sp2-sp3 hybrid carbon allotropes, mC24, the electron diffraction patterns match these of i-carbon, which is synthesized from shock-compressed graphite (H. Hirai and K. Kondo, Science, 1991, 253, 772). The allotropes exhibit tunable electronic characteristics from metallic to semiconductive with band gaps comparable to those of silicon allotropes. They are all superhard materials with Vickers hardness values comparable to that of cubic BN. The sp2-sp3 hybrid carbon allotroes are promising materials for photovoltaic electronic devices, and abrasive and grinding tools.

  6. Investigation of the structure of a Ag/Pd/Ag( 1 1 1 ) trilayer by means of electronic spectroscopies

    NASA Astrophysics Data System (ADS)

    Dumont, J.; Ghijsen, J.; Sporken, R.

    2002-06-01

    The growth of the Ag/Pd/Ag system has been studied by X-ray photoelectron spectroscopy and low energy electron diffraction. No chemical reaction or interdiffusion was observed between the Pd and Ag layers. The growth of the Pd interlayer follows the Frank Van der Merwe mode but is not pseudomorphic on the Ag(1 1 1) substrate. The growth of the top Ag layer on the Pd interlayer is pseudomorphic and layer by layer but contains around 12% of voids.

  7. Individual and collective electronic properties of Ag nanocrystals

    SciTech Connect

    Kim, S.H.; Medeiros-Ribeiro, G.; Ohlberg, D.A.A.; Williams, R.S.; Heath, J.R.

    1999-11-25

    The authors report on the electronic transport properties of individual alkanethiol-passivated Ag nanocrystals and their superlattices. Isolated Ag particles with diameters in the range of 2.7--4.8 nm supported by a metallic substrate passivated with an organic layer show a Coulomb gap. Monolayer films of Ag particles exhibit four distinct electronic signatures, two of which have not been previously reported, depending on their structures. In two-dimensional ordered superlattices of octanethiol-capped 4.8 nm diameter nanocrystals on graphite, the strong interparticle electronic coupling produces metallic films. A disordered monolayer of dodecanethiol-capped 6.6 nm diameter nanocrystals exhibits a temperature-dependent differential conductance, which is attributed to the localized states formed by the disorder in the lattice. For two-dimensional ordered superlattices of pentanethiol- and hexanethiol-capped 2.7 nm diameter Ag particles. It was shown that the films are insulating, and individual nanocrystals maintain their individual electronic identity. Two different types of insulating films have been observed: one with electronically homogeneous nanocrystals in a close-packed lattice and the other with sublattices of electronically distinct monocrystals within a square lattice. The relationship of the Coulomb blockade and nanocrystal ordering to the electronic behavior of this class of architectonic materials are discussed.

  8. Effects of Ag and Cu ions on the microbial corrosion of 316L stainless steel in the presence of Desulfovibrio sp.

    PubMed

    Unsal, Tuba; Ilhan-Sungur, Esra; Arkan, Simge; Cansever, Nurhan

    2016-08-01

    The utilization of Ag and Cu ions to prevent both microbial corrosion and biofilm formation has recently increased. The emphasis of this study lies on the effects of Ag and Cu ions on the microbial corrosion of 316L stainless steel (SS) induced by Desulfovibrio sp. Electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization were used to analyze the corrosion behavior. The biofilm formation, corrosion products and Ag and Cu ions on the surfaces were investigated using scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDS) and elemental mapping. Through circuit modeling, EIS results were used to interpret the physicoelectric interactions between the electrode, biofilm and culture interfaces. EIS results indicated that the metabolic activity of Desulfovibrio sp. accelerated the corrosion rate of SS in both conditions with and without ions. However, due to the retardation in the growth of Desulfovibrio sp. in the presence of Ag and Cu ions, significant decrease in corrosion rate was observed in the culture with the ions. In addition, SEM and EIS analyses revealed that the presence of the ions leads to the formation on the SS of a biofilm with different structure and morphology. Elemental analysis with EDS detected mainly sulfide- and phosphorous-based corrosion products on the surfaces. PMID:27105168

  9. Effects of Ag and Cu ions on the microbial corrosion of 316L stainless steel in the presence of Desulfovibrio sp.

    PubMed

    Unsal, Tuba; Ilhan-Sungur, Esra; Arkan, Simge; Cansever, Nurhan

    2016-08-01

    The utilization of Ag and Cu ions to prevent both microbial corrosion and biofilm formation has recently increased. The emphasis of this study lies on the effects of Ag and Cu ions on the microbial corrosion of 316L stainless steel (SS) induced by Desulfovibrio sp. Electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization were used to analyze the corrosion behavior. The biofilm formation, corrosion products and Ag and Cu ions on the surfaces were investigated using scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDS) and elemental mapping. Through circuit modeling, EIS results were used to interpret the physicoelectric interactions between the electrode, biofilm and culture interfaces. EIS results indicated that the metabolic activity of Desulfovibrio sp. accelerated the corrosion rate of SS in both conditions with and without ions. However, due to the retardation in the growth of Desulfovibrio sp. in the presence of Ag and Cu ions, significant decrease in corrosion rate was observed in the culture with the ions. In addition, SEM and EIS analyses revealed that the presence of the ions leads to the formation on the SS of a biofilm with different structure and morphology. Elemental analysis with EDS detected mainly sulfide- and phosphorous-based corrosion products on the surfaces.

  10. Robust Ag nanoplate ink for flexible electronics packaging

    NASA Astrophysics Data System (ADS)

    Li, Ruo-Zhou; Hu, Anming; Bridges, Denzel; Zhang, Tong; Oakes, Ken D.; Peng, Rui; Tumuluri, Uma; Wu, Zili; Feng, Zhili

    2015-04-01

    Nanoinks are currently a topic of heightened interest with respect to low temperature bonding processes and printable electronics. We have developed an innovative polyvinylpyrrolidone (PVP)-stabilized Ag nanoplate ink amenable to very strong low temperature packaging, and investigated the relationship between bonding strength and electrical conductivity post-bonding. PVP shell plastic deformations observed in failure microcracks with the formation of PVP nanofibers, revealed bonding strength at low temperatures (<250 °C) was primarily due to adhesive bonding. It is found that, utilizing photonic sintering, ~70 °C reduction of transformation temperature from adhesive to metallic bonding was achieved compared to that of thermal sintering. A numerical simulation was developed to better understand the influences of the light-induced heat generation, which demonstrated near-infrared light can facilitate sintering. Bonding strengths of 27 MPa were achieved at room temperatures, and 29.4 MPa at 210 °C with photonic sintering. Moreover, the anisotropic resistivity was observed with different thermal dependences. These results demonstrate Ag nanoplate inks have potential for low temperature 3D interconnections in lead-free microcircuits, flexible electronic packaging, and diverse sensing applications.Nanoinks are currently a topic of heightened interest with respect to low temperature bonding processes and printable electronics. We have developed an innovative polyvinylpyrrolidone (PVP)-stabilized Ag nanoplate ink amenable to very strong low temperature packaging, and investigated the relationship between bonding strength and electrical conductivity post-bonding. PVP shell plastic deformations observed in failure microcracks with the formation of PVP nanofibers, revealed bonding strength at low temperatures (<250 °C) was primarily due to adhesive bonding. It is found that, utilizing photonic sintering, ~70 °C reduction of transformation temperature from adhesive to

  11. In situ growth of Ag nanoparticles on α-Ag2WO4 under electron irradiation: probing the physical principles

    NASA Astrophysics Data System (ADS)

    San-Miguel, Miguel A.; da Silva, Edison Z.; Zannetti, Sonia M.; Cilense, Mario; Fabbro, Maria T.; Gracia, Lourdes; Andrés, Juan; Longo, Elson

    2016-06-01

    Exploiting the plasmonic behavior of Ag nanoparticles grown on α-Ag2WO4 is a widely employed strategy to produce efficient photocatalysts, ozone sensors, and bactericides. However, a description of the atomic and electronic structure of the semiconductor sites irradiated by electrons is still not available. Such a description is of great importance to understand the mechanisms underlying these physical processes and to improve the design of silver nanoparticles to enhance their activities. Motivated by this, we studied the growth of silver nanoparticles to investigate this novel class of phenomena using both transmission electron microscopy and field emission scanning electron microscopy. A theoretical framework based on density functional theory calculations (DFT), together with experimental analysis and measurements, were developed to examine the changes in the local geometrical and electronic structure of the materials. The physical principles for the formation of Ag nanoparticles on α-Ag2WO4 by electron beam irradiation are described. Quantum mechanical calculations based on DFT show that the (001) of α-Ag2WO4 displays Ag atoms with different coordination numbers. Some of them are able to diffuse out of the surface with a very low energy barrier (less than 0.1 eV), thus, initiating the growth of metallic Ag nanostructures and leaving Ag vacancies in the bulk material. These processes increase the structural disorder of α-Ag2WO4 as well as its electrical resistance as observed in the experimental measurements.

  12. In situ growth of Ag nanoparticles on α-Ag2WO4 under electron irradiation: probing the physical principles.

    PubMed

    San-Miguel, Miguel A; da Silva, Edison Z; Zannetti, Sonia M; Cilense, Mario; Fabbro, Maria T; Gracia, Lourdes; Andrés, Juan; Longo, Elson

    2016-06-01

    Exploiting the plasmonic behavior of Ag nanoparticles grown on α-Ag2WO4 is a widely employed strategy to produce efficient photocatalysts, ozone sensors, and bactericides. However, a description of the atomic and electronic structure of the semiconductor sites irradiated by electrons is still not available. Such a description is of great importance to understand the mechanisms underlying these physical processes and to improve the design of silver nanoparticles to enhance their activities. Motivated by this, we studied the growth of silver nanoparticles to investigate this novel class of phenomena using both transmission electron microscopy and field emission scanning electron microscopy. A theoretical framework based on density functional theory calculations (DFT), together with experimental analysis and measurements, were developed to examine the changes in the local geometrical and electronic structure of the materials. The physical principles for the formation of Ag nanoparticles on α-Ag2WO4 by electron beam irradiation are described. Quantum mechanical calculations based on DFT show that the (001) of α-Ag2WO4 displays Ag atoms with different coordination numbers. Some of them are able to diffuse out of the surface with a very low energy barrier (less than 0.1 eV), thus, initiating the growth of metallic Ag nanostructures and leaving Ag vacancies in the bulk material. These processes increase the structural disorder of α-Ag2WO4 as well as its electrical resistance as observed in the experimental measurements. PMID:27114472

  13. Ag-graphene hybrid conductive ink for writing electronics.

    PubMed

    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. PMID:24406681

  14. 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.

  15. Stretchable electronics based on Ag-PDMS composites.

    PubMed

    Larmagnac, Alexandre; Eggenberger, Samuel; Janossy, Hanna; Vörös, Janos

    2014-12-01

    Patterned structures of flexible, stretchable, electrically conductive materials on soft substrates could lead to novel electronic devices with unique mechanical properties allowing them to bend, fold, stretch or conform to their environment. For the last decade, research on improving the stretchability of circuits on elastomeric substrates has made significant progresses but designing printed circuit assemblies on elastomers remains challenging. Here we present a simple, cost-effective, cleanroom-free process to produce large scale soft electronic hardware where standard surface-mounted electrical components were directly bonded onto all-elastomeric printed circuit boards, or soft PCBs. Ag-PDMS tracks were stencil printed onto a PDMS substrate and soft PCBs were made by bonding the top and bottom layers together and filling punched holes with Ag-PDMS to create vias. Silver epoxy was used to bond commercial electrical components and no mechanical failure was observed after hundreds of stretching cycles. We also demonstrate the fabrication of a stretchable clock generator.

  16. Stretchable electronics based on Ag-PDMS composites

    NASA Astrophysics Data System (ADS)

    Larmagnac, Alexandre; Eggenberger, Samuel; Janossy, Hanna; Vörös, Janos

    2014-12-01

    Patterned structures of flexible, stretchable, electrically conductive materials on soft substrates could lead to novel electronic devices with unique mechanical properties allowing them to bend, fold, stretch or conform to their environment. For the last decade, research on improving the stretchability of circuits on elastomeric substrates has made significant progresses but designing printed circuit assemblies on elastomers remains challenging. Here we present a simple, cost-effective, cleanroom-free process to produce large scale soft electronic hardware where standard surface-mounted electrical components were directly bonded onto all-elastomeric printed circuit boards, or soft PCBs. Ag-PDMS tracks were stencil printed onto a PDMS substrate and soft PCBs were made by bonding the top and bottom layers together and filling punched holes with Ag-PDMS to create vias. Silver epoxy was used to bond commercial electrical components and no mechanical failure was observed after hundreds of stretching cycles. We also demonstrate the fabrication of a stretchable clock generator.

  17. Comparison of electronic structure between monolayer silicenes on Ag (111)

    NASA Astrophysics Data System (ADS)

    Chun-Liang, Lin; Ryuichi, Arafune; Maki, Kawai; Noriaki, Takagi

    2015-08-01

    The electronic structures of monolayer silicenes (4 × 4 and ) grown on Ag (111) surface are studied by scanning tunneling spectroscopy (STS) and density functional theory (DFT) calculations. While both phases have similar electronic structures around the Fermi level, significant differences are observed in the higher energy unoccupied states. The DFT calculations show that the contributions of Si 3pz orbitals to the unoccupied states are different because of their different buckled configurations. Project supported by the Ministry of Education, Culture, Sports, Science and Technology (MEXT) through Grants-in-Aid for Scientific Research (Grant Nos. 24241040 and 25110008) and the World Premier International Research Center Initiative (WPI), MEXT, Japan.

  18. The A2Σ+-XΠi electronic transition of AgS

    NASA Astrophysics Data System (ADS)

    Gupta, Varun; Mazzotti, Fabio J.; Rice, Corey A.; Nagarajan, Ramya; Maier, John P.

    2013-04-01

    The near-infrared electronic transition of silver monosulfide, AgS was measured for the first time using mass-resolved 1+1' resonance enhanced ionization spectroscopy in the 10 000-11 000 cm-1 region. The observed vibronic bands were analysed to obtain ωe″=331.6(2) cm and ωexe″=1.3(1) cm for the ground state, and Te=10528.3(2) cm, ωe'=318.4(1) cm, ωexe'=1.4(1) cm for the excited state of 107Ag32 S. The transitions are assigned to the A2Σ+-X2Πi system based on the rotational analysis of the Ω″=3/2 spin-orbit component of the 0-0 and 1-0 vibronic bands. The rotational constants for the X2Π state were determined to be B″=0.13126(16) cm , D″=5.5(17)×10-7 cmand A″=-477(8) cm .

  19. Surface Analysis of sp2 Carbon in Ag and Al Covetic Alloys*

    NASA Astrophysics Data System (ADS)

    Jaim, H. M. Iftekhar; Cole, Daniel P.; Salamanca-Riba, Lourdes G.

    Ag, Al-6061 and Al-7075 were doped with carbon by an electrocharging assisted process where high electric current is applied to the molten metal containing particles of activated carbon. This process gives rise to epitaxial growth of graphene nanoribbons (GNR) and carbon nanostructures within the metal matrix. Alloys produced with such technique are named Covetics. Al-6061 and Al-7075 covetics have shown superior mechanical, electrical and anti-corrosion properties. The nanostructured carbon incorporation has been confirmed by XPS, Raman, and TEM studies. Here, we present detailed surface characterization of the carbon nanostructures in these new alloys. Raman and EELS mapping of carbon nanostructure were carried out to identify the nature of bonding, strain and defect characteristics. Mostly, crystalline GNR or graphene sheets were found to create networks with sp2 character, under compressive strain with high concentration of defects. AFM and KPFM showed contrast in phases and potentials for ribbon like features. Incorporation of sp2 carbon in metals is an initial step for the integration of carbon nanostructures for future applications requiring high strength and conductivity.

  20. Angle-dependent study of a direct optical transition in the sp bands of Ag(111) by one- and two-photon photoemission

    NASA Astrophysics Data System (ADS)

    Winkelmann, Aimo; Sametoglu, Vahit; Zhao, Jin; Kubo, Atsushi; Petek, Hrvoje

    2007-11-01

    We have measured angle-dependent photoemission spectra for one-photon and two-photon excitation from Ag(111). The observed dispersion of the sp -band transition of Ag(111) can be reproduced using a nearly-free-electron model for the initial and final states involved. The observed dispersion agrees with the known band structure. We illustrate how the strong refraction of low-energy electrons becomes a limiting factor to obtain quantitative band-structure information. Conversely, low-energy electrons of a well-defined direct optical interband transition can provide a sensitive probe of the inner potential. We observe asymmetric two-photon photoelectron intensity distributions with respect to detection along the surface normal. These intensity distributions can be well described by a phenomenological model which employs the Fresnel equations to calculate the electric field components of the incident radiation inside the sample. Very good agreement is found using tabulated optical constants and a momentum matrix element, which is oriented along the surface normal. In contrast, the observed intensity distribution for one-photon photoemission from Ag(111) does not fit the simple Fresnel model. We interpret this as the influence of surface photoemission. By comparison to Cu(001), we show that the expected intensity distributions of the Fresnel model for one-photon photoemission and two-photon photoemission are valid for an orientation of the momentum matrix element along the surface normal if the influence of additional effects like surface photoemission can be neglected.

  1. Robust Ag nanoplate ink for flexible electronics packaging

    DOE PAGES

    Li, Ruo -Zhou; Hu, Anming; Bridges, Denzel; Oakes, Ken D.; Peng, Rui; Tumuluri, Uma; Wu, Zili; Feng, Zhili; Zhang, Tong

    2015-03-24

    Nanoinks are currently a topic of heightened interest with respect to low temperature bonding processes and printable electronics. We have developed an innovative polyvinylpyrrolidone (PVP)-stabilized Ag nanoplate ink amenable to very strong low temperature packaging, and investigated the relationship between bonding strength and electrical conductivity post-bonding. PVP shell plastic deformations observed in failure microcracks with the formation of PVP nanofibers, revealed bonding strength at low temperatures (<250 °C) was primarily due to adhesive bonding. It is found that, utilizing photonic sintering, ~70 °C reduction of transformation temperature from adhesive to metallic bonding was achieved compared to that of thermal sintering.more » A numerical simulation was developed to better understand the influences of the light-induced heat generation, which demonstrated near-infrared light can facilitate sintering. Bonding strengths of 27 MPa were achieved at room temperatures, and 29.4 MPa at 210 °C with photonic sintering. Moreover, the anisotropic resistivity was observed with different thermal dependences. Furthermore, these results demonstrate Ag nanoplate inks have potential for low temperature 3D interconnections in lead-free microcircuits, flexible electronic packaging, and diverse sensing applications.« less

  2. Robust Ag nanoplate ink for flexible electronics packaging

    SciTech Connect

    Li, Ruo -Zhou; Hu, Anming; Bridges, Denzel; Oakes, Ken D.; Peng, Rui; Tumuluri, Uma; Wu, Zili; Feng, Zhili; Zhang, Tong

    2015-03-24

    Nanoinks are currently a topic of heightened interest with respect to low temperature bonding processes and printable electronics. We have developed an innovative polyvinylpyrrolidone (PVP)-stabilized Ag nanoplate ink amenable to very strong low temperature packaging, and investigated the relationship between bonding strength and electrical conductivity post-bonding. PVP shell plastic deformations observed in failure microcracks with the formation of PVP nanofibers, revealed bonding strength at low temperatures (<250 °C) was primarily due to adhesive bonding. It is found that, utilizing photonic sintering, ~70 °C reduction of transformation temperature from adhesive to metallic bonding was achieved compared to that of thermal sintering. A numerical simulation was developed to better understand the influences of the light-induced heat generation, which demonstrated near-infrared light can facilitate sintering. Bonding strengths of 27 MPa were achieved at room temperatures, and 29.4 MPa at 210 °C with photonic sintering. Moreover, the anisotropic resistivity was observed with different thermal dependences. Furthermore, these results demonstrate Ag nanoplate inks have potential for low temperature 3D interconnections in lead-free microcircuits, flexible electronic packaging, and diverse sensing applications.

  3. Stretchable electronics based on Ag-PDMS composites

    PubMed Central

    Larmagnac, Alexandre; Eggenberger, Samuel; Janossy, Hanna; Vörös, Janos

    2014-01-01

    Patterned structures of flexible, stretchable, electrically conductive materials on soft substrates could lead to novel electronic devices with unique mechanical properties allowing them to bend, fold, stretch or conform to their environment. For the last decade, research on improving the stretchability of circuits on elastomeric substrates has made significant progresses but designing printed circuit assemblies on elastomers remains challenging. Here we present a simple, cost-effective, cleanroom-free process to produce large scale soft electronic hardware where standard surface-mounted electrical components were directly bonded onto all-elastomeric printed circuit boards, or soft PCBs. Ag-PDMS tracks were stencil printed onto a PDMS substrate and soft PCBs were made by bonding the top and bottom layers together and filling punched holes with Ag-PDMS to create vias. Silver epoxy was used to bond commercial electrical components and no mechanical failure was observed after hundreds of stretching cycles. We also demonstrate the fabrication of a stretchable clock generator. PMID:25434843

  4. Stretchable electronics based on Ag-PDMS composites.

    PubMed

    Larmagnac, Alexandre; Eggenberger, Samuel; Janossy, Hanna; Vörös, Janos

    2014-01-01

    Patterned structures of flexible, stretchable, electrically conductive materials on soft substrates could lead to novel electronic devices with unique mechanical properties allowing them to bend, fold, stretch or conform to their environment. For the last decade, research on improving the stretchability of circuits on elastomeric substrates has made significant progresses but designing printed circuit assemblies on elastomers remains challenging. Here we present a simple, cost-effective, cleanroom-free process to produce large scale soft electronic hardware where standard surface-mounted electrical components were directly bonded onto all-elastomeric printed circuit boards, or soft PCBs. Ag-PDMS tracks were stencil printed onto a PDMS substrate and soft PCBs were made by bonding the top and bottom layers together and filling punched holes with Ag-PDMS to create vias. Silver epoxy was used to bond commercial electrical components and no mechanical failure was observed after hundreds of stretching cycles. We also demonstrate the fabrication of a stretchable clock generator. PMID:25434843

  5. Robust Ag nanoplate ink for flexible electronics packaging.

    PubMed

    Li, Ruo-Zhou; Hu, Anming; Bridges, Denzel; Zhang, Tong; Oakes, Ken D; Peng, Rui; Tumuluri, Uma; Wu, Zili; Feng, Zhili

    2015-04-28

    Nanoinks are currently a topic of heightened interest with respect to low temperature bonding processes and printable electronics. We have developed an innovative polyvinylpyrrolidone (PVP)-stabilized Ag nanoplate ink amenable to very strong low temperature packaging, and investigated the relationship between bonding strength and electrical conductivity post-bonding. PVP shell plastic deformations observed in failure microcracks with the formation of PVP nanofibers, revealed bonding strength at low temperatures (<250 °C) was primarily due to adhesive bonding. It is found that, utilizing photonic sintering, ∼ 70 °C reduction of transformation temperature from adhesive to metallic bonding was achieved compared to that of thermal sintering. A numerical simulation was developed to better understand the influences of the light-induced heat generation, which demonstrated near-infrared light can facilitate sintering. Bonding strengths of 27 MPa were achieved at room temperatures, and 29.4 MPa at 210 °C with photonic sintering. Moreover, the anisotropic resistivity was observed with different thermal dependences. These results demonstrate Ag nanoplate inks have potential for low temperature 3D interconnections in lead-free microcircuits, flexible electronic packaging, and diverse sensing applications. PMID:25824693

  6. Structural and electronic analysis of the atomic scale nucleation of Ag on α-Ag2WO4 induced by electron irradiation

    PubMed Central

    Andrés, Juan; Gracia, Lourdes; Gonzalez-Navarrete, Patricio; Longo, Valeria M.; Avansi, Waldir; Volanti, Diogo P.; Ferrer, Mateus M.; Lemos, Pablo S.; La Porta, Felipe A.; Hernandes, Antonio C.; Longo, Elson

    2014-01-01

    In this work, we utilise a combination of theory, computation and experiments to understand the early events related to the nucleation of Ag filaments on α-Ag2WO4 crystals, which is driven by an accelerated electron beam from an electron microscope under high vacuum. The growth process and the chemical composition and elemental distribution in these filaments were analysed in depth at the nanoscale level using TEM, HAADF, EDS and XPS; the structural and electronic aspects were systematically studied in using first-principles electronic structure theory within QTAIM framework. The Ag nucleation and formation on α-Ag2WO4 is a result of the order/disorder effects generated in the crystal by the electron-beam irradiation. Both experimental and theoretical results show that this behavior is associated with structural and electronic changes of the [AgO2] and [AgO4] clusters and, to a minor extent, to the [WO6] cluster; these clusters collectively represent the constituent building blocks of α-Ag2WO4. PMID:24953210

  7. Electronic structures of zigzag silicene nanoribbons with asymmetric sp2-sp3 edges

    NASA Astrophysics Data System (ADS)

    Ding, Yi; Wang, Yanli

    2013-04-01

    The nanomaterials with peculiar spintronic characteristics, such as half-metals, spin gapless semiconductors [X. L. Wang, Phys. Rev. Lett. 100, 156404 (2008)], and bipolar magnetic semiconductors [Li et al., Nanoscale 4, 5680 (2012)], play the crucial role in nano-electronics and spintronics. Here, we report the zigzag silicene nanoribbons (ZSiNRs) with asymmetric sp2-sp3 edges are bipolar magnetic semiconductors due to the incorporation of Klein and zigzag edge states. With the bipolar feature, these asymmetric ZSiNRs can be altered to half-metals with opposite conductive spin channels by p-type and n-type dopings. Moreover, the semiconducting properties can also be tailored by the strain, which makes the nanoribbons into spin gapless semiconductors or ferromagnetic metals.

  8. Phonon drag of electrons in Ag{sub 2}S

    SciTech Connect

    Aliev, S. A.; Aliev, F. F. Gasanov, Z. S.; Abdullayev, S. M.; Selim-zade, R. I.

    2010-06-15

    The temperature dependences of the heat-conductivity coefficient {chi} and the thermopower 6h of Ag{sub 2}S are investigated in the range of 4.2-300 K. It is found that the value of 6h sharply increases (6h {infinity} T{sup -3}) with decreasing T at T < 100 K and passes through a maximum at 16-18 K. The heat-conductivity coefficient passes through a maximum at {approx}30 K. The sharp increase in 6h is found to be caused by the effect of long-wavelength-phonon drag of electrons. It is shown that the shift of the 6h and {chi} peaks, as well as the temperature dependence of the phonon thermopower 6h{sub ph} {infinity} T{sup -3}, agrees with the Herring theory.

  9. The electron paramagnetic resonance spectrum of Ag2 3

    NASA Astrophysics Data System (ADS)

    van der Pol, A.; Reijersen, E. J.; de Boer, E.; Wasowicz, T.; Michalik, J.

    A highly resolved EPR spectrum of the silver trimer 109Ag2+3, present in 109Ag1-NaA zeolite, has been measured. The spectrum is characterized by an axially symmetric spin Hamiltonian having and for each of the 109Ag nuclei tMPH0037_images.

  10. Inactivation of Amphidinium sp. in ballast waters using UV/Ag-TiO2+O3 advanced oxidation treatment.

    PubMed

    Wu, Donghai; You, Hong; Zhang, Ran; Chen, Chuan; Lee, Duu-Jong

    2011-11-01

    Ballast water poses a biological threat to the world's waterways by transferring aquatic species from one body of water to another. This study investigates the use of combined ultraviolet (UV)/Ag-TiO(2)+ozone (O(3)) processes for treating ballast water using Amphidinium sp. as an indicator microorganism. Sufficient Amphidinium sp. cells in ballast waters can be inactivated using O(3) alone, UV irradiation alone (with or without an Ag-TiO(2) coating), and combined treatments. For the low inactivation ratio (<40%) regime, the effects of ozonation and photocatalysis were observed to be cumulative. The combined UV/Ag-TiO(2)+O(3) treatment produced excess hydroxyl radicals and total residual oxidants (TROs), and readily damaged cell membranes to release intracellular substances. The comparison tests revealed that the combined treatments synergistically inactivate Escherichia coli in ballast waters. However, the combined process did not synergistically inactivate Amphidinium sp. cells. Inactivating different aqua species in ballast waters needs distinct treatment methods and dosages.

  11. Electronic properties and bonding characteristics of AlN:Ag thin film nanocomposites

    SciTech Connect

    Lekka, Ch. E.; Patsalas, P.; Komninou, Ph.; Evangelakis, G. A.

    2011-03-01

    We present theoretical and experimental results on the bonding and structural characteristics of AlN:Ag thin film nanocomposites obtained by means of density functional theory (DFT) computations, high resolution transmission electron microscopy (HRTEM) observations, Auger electron spectroscopy (AES), and x-ray diffraction (XRD) measurements. From the theoretical calculations it was determined that the presence of the Ag substitutional of N or Al atoms affects the electronic density of states (EDOS) of the resulting systems. In particular, occupied energy states are introduced (between others) that lie within the energy gap of the AlN matrix due to Ag-d, Al-p (accompanied with a charge transfer from Al to Ag), Ag-p, and N-p hybridizations, respectively. The effect is predicted to be even more pronounced in the case of Ag nanoparticle inclusions affecting the EDOS of the composite system. These predictions were verified by the HRTEM images that gave unequivocal evidence for the presence and stability of Ag nanoparticles in the AlN matrix. In addition, the AES data suggested a metal-metal (Ag-Al) bonding preference, while the XRD patterns revealed that the atomic Ag dispersions in the AlN thin films results in a small elongation of the Wurtzite lattice, which is in agreement with the DFT predictions. These results may useful in tailoring the electronic response of AlN-based systems and the design of devices for various opto-electronic applications.

  12. The influence of electron confinement, quantum size effects, and film morphology on the dispersion and the damping of plasmonic modes in Ag and Au thin films

    NASA Astrophysics Data System (ADS)

    Politano, Antonio; Chiarello, Gennaro

    2015-05-01

    Plasmons are collective longitudinal modes of charge fluctuation in metal samples excited by an external electric field. Surface plasmons (SPs) are waves that propagate along the surface of a conductor. SPs find applications in magneto-optic data storage, optics, microscopy, and catalysis. The investigation of SPs in silver and gold is relevant as these materials are extensively used in plasmonics. The theoretical approach for calculating plasmon modes in noble metals is complicated by the existence of localized d electrons near the Fermi level. Nevertheless, recent calculations based on linear response theory and time-dependent local density approximation adequately describe the dispersion and damping of SPs in noble metals. Furthermore, in thin films the electronic response is influenced by electron quantum confinement. Confined electrons modify the dynamical screening processes at the film/substrate interface by introducing novel properties with potential applications. The presence of quantum well states in the Ag and Au overlayer affects both the dispersion relation of SP frequency and the damping processes of the SP. Recent calculations indicate the emergence of acoustic surface plasmons (ASP) in Ag thin films exhibiting quantum well states. The slope of the dispersion of ASP decreases with film thickness. High-resolution electron energy loss spectroscopy (HREELS) is the main experimental technique for investigating collective electronic excitations, with adequate resolution in both the energy and momentum domains to investigate surface modes. Herein we review on recent progress of research on collective electronic excitations in Ag and Au films deposited on single-crystal substrates.

  13. Chemical patterning of Ag(111): Spatially confined oxide formation induced by electron beam irradiation

    SciTech Connect

    Guenther, S.; Reichelt, R.; Wintterlin, J.; Barinov, A.; Mentes, T. O.; Nino, M. A.; Locatelli, A.

    2008-12-08

    Low energy electron irradiation of a Ag(111) surface during NO{sub 2} adsorption at 300 K induces formation of Ag oxide. Using a spatially confined electron beam, small Ag{sub 2}O spots could be grown with a sharp, {approx}100 nm wide, boundary to the nonirradiated metallic surface. Since the structure size will mainly depend on the sharpness of the irradiating electron beam, this process has the potential of a single step nanostructuring process. Temperature treatment offers an easy way to manipulate the boundary between oxide and metallic silver by steering a chemical front.

  14. Quantum Electronic Transport of Topological Surface States in β-Ag2Se Nanowire.

    PubMed

    Kim, Jihwan; Hwang, Ahreum; Lee, Sang-Hoon; Jhi, Seung-Hoon; Lee, Sunghun; Park, Yun Chang; Kim, Si-In; Kim, Hong-Seok; Doh, Yong-Joo; Kim, Jinhee; Kim, Bongsoo

    2016-04-26

    Single-crystalline β-Ag2Se nanostructures, a new class of 3D topological insulators (TIs), were synthesized using the chemical vapor transport method. The topological surface states were verified by measuring electronic transport properties including the weak antilocalization effect, Aharonov-Bohm oscillations, and Shubnikov-de Haas oscillations. First-principles band calculations revealed that the band inversion in β-Ag2Se is caused by strong spin-orbit coupling and Ag-Se bonding hybridization. These investigations provide evidence of nontrivial surface state about β-Ag2Se TIs that have anisotropic Dirac cones.

  15. Formation of Ag Nanoparticles on β-Ag2WO4 through Electron Beam Irradiation: A Synergetic Computational and Experimental Study.

    PubMed

    Roca, Roman A; Gouveia, Amanda F; Lemos, Pablo S; Gracia, Lourdes; Andrés, Juan; Longo, Elson

    2016-09-01

    In the present work, a combined theoretical and experimental study was performed on the structure, optical properties, and growth of Ag nanoparticles in metastable β-Ag2WO4 microcrystals. This material was synthesized using the precipitation method without the presence of surfactants. The structural behavior was analyzed using X-ray diffraction and Raman and infrared spectroscopy. Field-emission scanning electron microscopy revealed the presence of irregular spherical-like Ag nanoparticles on the β-Ag2WO4 microcrystals, which were induced by electron beam irradiation under high vacuum conditions. A detailed analysis of the optimized β-Ag2WO4 geometry and theoretical results enabled interpretation of both the Raman and infrared spectra and provided deeper insight into rationalizing the observed morphology. In addition, first-principles calculations, within the quantum theory of atoms in molecules framework, provided an in-depth understanding of the nucleation and early evolution of Ag nanoparticles. The Ag nucleation and formation is the result of structural and electronic changes of the [AgO6] and [AgO5] clusters as a constituent building block of β-Ag2WO4, which is consistent with Ag metallic formation. PMID:27533109

  16. Atomic structure of "multilayer silicene" grown on Ag(111): Dynamical low energy electron diffraction analysis

    NASA Astrophysics Data System (ADS)

    Kawahara, Kazuaki; Shirasawa, Tetsuroh; Lin, Chun-Liang; Nagao, Ryo; Tsukahara, Noriyuki; Takahashi, Toshio; Arafune, Ryuichi; Kawai, Maki; Takagi, Noriaki

    2016-09-01

    We have investigated the atomic structure of the "multilayer silicene" grown on the Ag(111) single crystal surface by using low energy electron diffraction (LEED) and scanning tunneling microscopy (STM). We measured the intensity of the LEED spot as a function of the incident electron energy (I-V curve) and analyzed the I-V curve using a dynamical LEED theory. We have found that the Si(111)(√{ 3} ×√{ 3})-Ag model well reproduces the I-V curve whereas the models consisting of the honeycomb structure of Si do not. The bias dependence of the STM image of multilayer silicene agrees with that of the Si(111)(√{ 3} ×√{ 3})-Ag reconstructed surface. Consequently, we have concluded that the multilayer silicene grown on Ag(111) is identical to the Si(111)(√{ 3} ×√{ 3})-Ag reconstructed structure.

  17. In situ Transmission Electron Microscopy observation of Ag nanocrystal evolution by surfactant free electron-driven synthesis

    PubMed Central

    Longo, Elson; Avansi, Waldir; Bettini, Jefferson; Andrés, Juan; Gracia, Lourdes

    2016-01-01

    The study of the interaction of electron irradiation with matter and the response of the material to the passage of electrons is a very challenging problem. However, the growth mechanism observed during nanostructural evolution appears to be a broad and promising scientific field in nanotechnology. We report the in situ TEM study of nanostructural evolution of electron-driven silver (Ag) nanocrystals through an additive-free synthetic procedure. Observations revealed the direct effect of the electron beam on the morphological evolution of Ag nanocrystals through different mechanisms, such as mass transport, site-selective coalescence, and an appropriate structural configuration after coalescence leading to a more stable configuration. A fundamental understanding of the growth and formation mechanisms of Ag nanocrystals, which interact with the electron beam, is essential to improve the nanocrystal shape-control mechanisms as well as the future design and study of nanomaterials. PMID:26979671

  18. High-performance polyimide nanocomposites with core-shell AgNWs@BN for electronic packagings

    NASA Astrophysics Data System (ADS)

    Zhou, Yongcun; Liu, Feng

    2016-08-01

    The increasing density of electronic devices underscores the need for efficient thermal management. Silver nanowires (AgNWs), as one-dimensional nanostructures, possess a high aspect ratio and intrinsic thermal conductivity. However, high electrical conductivity of AgNWs limits their application for electronic packaging. We synthesized boron nitride-coated silver nanowires (AgNWs@BN) using a flexible and fast method followed by incorporation into synthetic polyimide (PI) for enhanced thermal conductivity and dielectric properties of nanocomposites. The thinner boron nitride intermediate nanolayer on AgNWs not only alleviated the mismatch between AgNWs and PI but also enhanced their interfacial interaction. Hence, the maximum thermal conductivity of an AgNWs@BN/PI composite with a filler loading up to 20% volume was increased to 4.33 W/m K, which is an enhancement by nearly 23.3 times compared with that of the PI matrix. The relative permittivity and dielectric loss were about 9.89 and 0.015 at 1 MHz, respectively. Compared with AgNWs@SiO2/PI and Ag@BN/PI composites, boron nitride-coated core-shell structures effectively increased the thermal conductivity and reduced the permittivity of nanocomposites. The relative mechanism was studied and discussed. This study enables the identification of appropriate modifier fillers for polymer matrix nanocomposites.

  19. 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.

  20. Effect of a phase transition on the electron energy spectrum in Ag{sub 2}S

    SciTech Connect

    Aliev, F. F. Jafarov, M. B.; Tairov, B. A.; Pashaev, G. P.; Saddinova, A. A.; Kuliev, A. A.

    2008-10-15

    Temperature dependences of electrical conductivity {sigma}, Hall coefficient R, and thermopower {alpha}{sub 0} in Ag{sub 2}S are reported. It is established that at T {approx} 435 {+-} 5 K, all kinetic parameters vary drastically, which is associated with a change in parameters of the conduction band. It is shown that the dispersion law of electron energy in {beta}-Ag{sub 2}S corresponds to the Kane model.

  1. Direct in situ observation of the electron-driven synthesis of Ag filaments on α-Ag2WO4 crystals.

    PubMed

    Longo, E; Cavalcante, L S; Volanti, D P; Gouveia, A F; Longo, V M; Varela, J A; Orlandi, M O; Andrés, J

    2013-01-01

    In this letter, we report, for the first time, the real-time in situ nucleation and growth of Ag filaments on α-Ag2WO4 crystals driven by an accelerated electron beam from an electronic microscope under high vacuum. We employed several techniques to characterise the material in depth. By using these techniques combined with first-principles modelling based on density functional theory, a mechanism for the Ag filament formation followed by a subsequent growth process from the nano- to micro-scale was proposed. In general, we have shown that an accelerated electron beam from an electronic microscope under high vacuum enables in situ visualisation of Ag filaments with subnanometer resolution and offers great potential for addressing many fundamental issues in materials science, chemistry, physics and other fields of science.

  2. Immobilization of Highly Dispersed Ag Nanoparticles on Carbon Nanotubes Using Electron-Assisted Reduction for Antibacterial Performance.

    PubMed

    Yan, Xiaoliang; Li, Sha; Bao, Jiehua; Zhang, Nan; Fan, Binbin; Li, Ruifeng; Liu, Xuguang; Pan, Yun-Xiang

    2016-07-13

    Silver nanoparticles (Ag NPs) supported on certain materials have been widely used as disinfectants. Yet, to date, the antibacterial activity of the supported Ag NPs is still far below optimum. This is mainly associated with the easy aggregation of Ag NPs on the supporting materials. Herein, an electron-assisted reduction (EAR) method, which is operated at temperatures as low as room temperature and without using any reduction reagent, was employed for immobilizing highly dispersed Ag NPs on aminated-CNTs (Ag/A-CNTs). The average Ag NPs size on the EAR-prepared Ag/A-CNTs is only 3.8 nm, which is much smaller than that on the Ag/A-CNTs fabricated from the traditional thermal calcination (25.5 nm). Compared with Ag/A-CNTs fabricated from traditional thermal calcination, EAR-prepared Ag/A-CNTs shows a much better antibacterial activity to E. coli/S. aureus and antifouling performance to P. subcordiformis/T. lepidoptera. This is mainly originated from the significantly enhanced Ag(+) ion releasing rate and highly dispersed Ag NPs with small size on the EAR-prepared Ag/A-CNTs. The findings from the present work are helpful for fabricating supported Ag NPs with small size and high dispersion for efficient antibacterial process. PMID:27327238

  3. Paromomycin Derived from Streptomyces sp. AG-P 1441 Induces Resistance against Two Major Pathogens of Chili Pepper.

    PubMed

    Balaraju, Kotnala; Kim, Chang-Jin; Park, Dong-Jin; Nam, Ki-Woong; Zhang, Kecheng; Sang, Mee Kyung; Park, Kyungseok

    2016-09-28

    This is the first report that paromomycin, an antibiotic derived from Streptomyces sp. AG-P 1441 (AG-P 1441), controlled Phytophthora blight and soft rot diseases caused by Phytophthora capsici and Pectobacterium carotovorum, respectively, in chili pepper (Capsicum annum L.). Chili pepper plants treated with paromomycin by foliar spray or soil drenching 7 days prior to inoculation with P. capsici zoospores showed significant (p < 0.05) reduction in disease severity (%) when compared with untreated control plants. The disease severity of Phytophthora blight was recorded as 8% and 50% for foliar spray and soil drench, respectively, at 1.0 ppm of paromomycin, compared with untreated control, where disease severity was 83% and 100% by foliar spray and soil drench, respectively. A greater reduction of soft rot lesion areas per leaf disk was observed in treated plants using paromomycin (1.0 μg/ml) by infiltration or soil drench in comparison with untreated control plants. Paromomycin treatment did not negatively affect the growth of chili pepper. Furthermore, the treatment slightly promoted growth; this growth was supported by increased chlorophyll content in paromomycin-treated chili pepper plants. Additionally, paromomycin likely induced resistance as confirmed by the expression of pathogenesis-related (PR) genes: PR-1, β-1,3-glucanase, chitinase, PR-4, peroxidase, and PR-10, which enhanced plant defense against P. capsici in chili pepper. This finding indicates that AG-P 1441 plays a role in pathogen resistance upon the activation of defense genes, by secretion of the plant resistance elicitor, paromomycin. PMID:27291677

  4. Switching behaviour of individual Ag-TCNQ nanowires: an in situ transmission electron microscopy study.

    PubMed

    Ran, Ke; Rösner, Benedikt; Butz, Benjamin; Fink, Rainer H; Spiecker, Erdmann

    2016-10-21

    The organic semiconductor silver-tetracyanoquinodimethane (Ag-TCNQ) exhibits electrical switching and memory characteristics. Employing a scanning tunnelling microscopy setup inside a transmission electron microscope, the switching behaviour of individual Ag-TCNQ nanowires (NWs) is investigated in detail. For a large number of NWs, the switching between a high (OFF) and a low (ON) resistance state was successfully stimulated by negative bias sweeps. Fitting the experimental I-V curves with a Schottky emission function makes the switching features prominent and thus enables a direct evaluation of the switching process. A memory cycle including writing, reading and erasing features is demonstrated at an individual NW. Moreover, electronic failure mechanisms due to Joule heating are discussed. These findings have a significant impact on our understanding of the switching behaviour of Ag-TCNQ. PMID:27622904

  5. Switching behaviour of individual Ag-TCNQ nanowires: an in situ transmission electron microscopy study

    NASA Astrophysics Data System (ADS)

    Ran, Ke; Rösner, Benedikt; Butz, Benjamin; Fink, Rainer H.; Spiecker, Erdmann

    2016-10-01

    The organic semiconductor silver-tetracyanoquinodimethane (Ag-TCNQ) exhibits electrical switching and memory characteristics. Employing a scanning tunnelling microscopy setup inside a transmission electron microscope, the switching behaviour of individual Ag-TCNQ nanowires (NWs) is investigated in detail. For a large number of NWs, the switching between a high (OFF) and a low (ON) resistance state was successfully stimulated by negative bias sweeps. Fitting the experimental I-V curves with a Schottky emission function makes the switching features prominent and thus enables a direct evaluation of the switching process. A memory cycle including writing, reading and erasing features is demonstrated at an individual NW. Moreover, electronic failure mechanisms due to Joule heating are discussed. These findings have a significant impact on our understanding of the switching behaviour of Ag-TCNQ.

  6. Lateral quantization of two-dimensional electron states by embedded Ag nanocrystals.

    PubMed

    Schouteden, K; Van Haesendonck, C

    2012-02-17

    We show that quantization of image-potential state (IS) electrons above the surface of nanostructures can be experimentally achieved by Ag nanocrystals that appear as stacking-fault tetrahedrons (SFTs) at Ag(111) surfaces. By means of cryogenic scanning tunneling spectroscopy, the n=1 IS of the Ag(111) surface is revealed to split up in discrete energy levels, which is accompanied by the formation of pronounced standing wave patterns that directly reflect the eigenstates of the SFT surface. The IS confinement behavior is compared to that of the surface state electrons in the SFT surface and can be directly linked to the particle-in-a-box model. ISs provide a novel playground for investigating quantum size effects and defect-induced scattering above nanostructured surfaces.

  7. Lateral quantization of two-dimensional electron states by embedded Ag nanocrystals

    NASA Astrophysics Data System (ADS)

    Van Haesendonck, Chris; Schouteden, Koen

    2013-03-01

    We show that quantization of image-potential state (IS)electrons above the surface of nanostructures can be experimentally achieved by Ag nanocrystals that appear as stacking fault tetrahedrons (SFTs) at Ag(111) surfaces. By means of cryogenic scanning tunneling spectroscopy the n = 1 IS of the Ag(111) surface is revealed to split up in discrete energy levels, which is accompanied by the formation of pronounced standing wave patterns that directly reflect the eigenstates of the SFT surface. The IS confinement behavior is compared to that of the surface state electrons in the SFT surface and can be directly linked to the particle-in-a-box model. ISs provide a novel playground for investigating quantum size effects and defect induced scattering above nanostructured surfaces. This work has been supported by the Research Foundation - Flanders (FWO, Belgium). K.S. is a postdoctoral researcher of the FWO.

  8. Lateral Quantization of Two-Dimensional Electron States by Embedded Ag Nanocrystals

    NASA Astrophysics Data System (ADS)

    Schouteden, K.; Van Haesendonck, C.

    2012-02-01

    We show that quantization of image-potential state (IS) electrons above the surface of nanostructures can be experimentally achieved by Ag nanocrystals that appear as stacking-fault tetrahedrons (SFTs) at Ag(111) surfaces. By means of cryogenic scanning tunneling spectroscopy, the n=1 IS of the Ag(111) surface is revealed to split up in discrete energy levels, which is accompanied by the formation of pronounced standing wave patterns that directly reflect the eigenstates of the SFT surface. The IS confinement behavior is compared to that of the surface state electrons in the SFT surface and can be directly linked to the particle-in-a-box model. ISs provide a novel playground for investigating quantum size effects and defect-induced scattering above nanostructured surfaces.

  9. Switching behaviour of individual Ag-TCNQ nanowires: an in situ transmission electron microscopy study.

    PubMed

    Ran, Ke; Rösner, Benedikt; Butz, Benjamin; Fink, Rainer H; Spiecker, Erdmann

    2016-10-21

    The organic semiconductor silver-tetracyanoquinodimethane (Ag-TCNQ) exhibits electrical switching and memory characteristics. Employing a scanning tunnelling microscopy setup inside a transmission electron microscope, the switching behaviour of individual Ag-TCNQ nanowires (NWs) is investigated in detail. For a large number of NWs, the switching between a high (OFF) and a low (ON) resistance state was successfully stimulated by negative bias sweeps. Fitting the experimental I-V curves with a Schottky emission function makes the switching features prominent and thus enables a direct evaluation of the switching process. A memory cycle including writing, reading and erasing features is demonstrated at an individual NW. Moreover, electronic failure mechanisms due to Joule heating are discussed. These findings have a significant impact on our understanding of the switching behaviour of Ag-TCNQ.

  10. THE TWO-DIMENSIONAL VALENCE ELECTRONIC STRUCTURE OF A MONOLYAER OF Ag ON Cu(00l)

    SciTech Connect

    Tobin, J.G.; Robey, S.W.; Shirley, D.A.

    1985-05-01

    The metal overlayer system c(10x2)Ag/Cu(001) was studied at coverages near one monolayer with angle-resolved photoemission. The observed spectroscopic features indicate a two-dimensional d-band electronic structure that can be interpreted using a model with planar, hexagonal symmetry in which crystal field effects dominate over spin-orbit effects.

  11. Structure, dynamics, and electronic structure of liquid Ag-Se alloys investigated by ab initio simulation

    NASA Astrophysics Data System (ADS)

    Kirchhoff, F.; Holender, J. M.; Gillan, M. J.

    1996-07-01

    Ab initio molecular-dynamics simulations have been used to investigate the structure, dynamics, and electronic properties of the liquid alloy Ag1-xSex at 1350 K and at the three compositions x=0.33, 0.42, and 0.65. To provide a point of reference, calculations are also presented for the equilibrium structure and the electronic structure of the α-Ag2Se crystal. The calculations are based on density-functional theory in the local-density approximation and on the pseudopotential plane-wave method. For the solid, we find excellent agreement with experiment for the equilibrium lattice parameters and the atomic coordinates of the 12-atom orthorhombic unit cell, and we present an analysis of the electronic density of states and density distribution. The reliability of the liquid simulations is confirmed by detailed comparisons with very recent neutron-diffraction results for the partial structure factors and radial distribution functions (RDF) of the stoichiometric liquid Ag2Se. Comparison with the predictions of an empirical interaction model due to Rino et al. is also given for l-Ag2Se. The ab initio simulations show a dramatic change of the Se-Se RDF with increasing Se content. This change is due to the formation of Se clusters bound by covalent bonds, the Se-Se bond length being almost the same as in pure c-Se and l-Se. The clusters are predominantly chainlike, but for higher x there is a significant fraction of threefold coordinated Se atoms. It is shown that the equilibrium fractions of Se present as isolated atoms and in clusters can be understood on a simple charge-balance model based on an ionic interpretation. The Ag diffusion coefficient in the simulated stoichiometric liquid is consistent with experimental values measured in the high-temperature superionic solid. The Ag and Se diffusion coefficients both increase with Se content, in spite of the Se clustering. An analysis of the Se-Se bond dynamics reveals surprisingly short bond lifetimes of less than 1 ps

  12. Coaxial Ag/ZnO/Ag nanowire for highly sensitive hot-electron photodetection

    SciTech Connect

    Zhan, Yaohui; Li, Xiaofeng Wu, Kai; Wu, Shaolong; Deng, Jiajia

    2015-02-23

    Single-nanowire photodetectors (SNPDs) are mostly propelled by p-n junctions, where the detection wavelength is constrained by the band-gap width. Here, we present a simple doping-free metal/semiconductor/metal SNPD, which shows strong detection tunability without such a material constraint. The proposed hot-electron SNPD exhibits superior optical and electrical advantages, i.e., optically the coaxial design leads to a strong asymmetrical photoabsorption and results in a high unidirectional photocurrent, as desired by the hot-electron collection; electrically the hot-electrons are generated in the region very close to the barrier, facilitating the electrical transport. Rigorous calculations predict an unbiased photoresponsivity of ∼200 nA/mW.

  13. Surface electronic structure of polar NiO thin film grown on Ag(111)

    NASA Astrophysics Data System (ADS)

    Das, Jayanta; Menon, Krishnakumar S. R.

    2015-06-01

    The growth and structure of NiO thin films on top of Ag(111) substrate were studied where the formation of faceted surface was confirmed by Low Energy Electron Diffraction. The electronic structure of polar NiO(111) surface has been probed using photoemission techniques. The core energy levels and the valence band electronic structure were excited by x-ray and ultraviolet photons respectively. The modifications in physical structure and valence band electronic structure of the film under vacuum annealing have also been enlightened.

  14. Surface electronic structure of polar NiO thin film grown on Ag(111)

    SciTech Connect

    Das, Jayanta; Menon, Krishnakumar S. R.

    2015-06-24

    The growth and structure of NiO thin films on top of Ag(111) substrate were studied where the formation of faceted surface was confirmed by Low Energy Electron Diffraction. The electronic structure of polar NiO(111) surface has been probed using photoemission techniques. The core energy levels and the valence band electronic structure were excited by x-ray and ultraviolet photons respectively. The modifications in physical structure and valence band electronic structure of the film under vacuum annealing have also been enlightened.

  15. Excitation of plasmons in Ag/Fe/W structure by spin-polarized electrons

    SciTech Connect

    Samarin, Sergey N.; Kostylev, Mikhail; Williams, J. F.; Artamonov, Oleg M.; Baraban, Alexander P.; Guagliardo, Paul

    2015-09-07

    Using Spin-polarized Electron-Energy Loss Spectroscopy (SPEELS), the plasmon excitations were probed in a few atomic layers thick Ag film deposited on an Fe layer or on a single crystal of W(110). The measurements were performed at two specular geometries with either a 25° or 72° angle of incidence. On a clean Fe layer (10 atomic layers thick), Stoner excitation asymmetry was observed, as expected. Deposition of a silver film on top of the Fe layer dramatically changed the asymmetry of the SPEELS spectra. The spin-effect depends on the kinematics of the scattering: angles of incidence and detection. The spin-dependence of the plasmon excitations in the silver film on the W(110) surface and on the ferromagnetic Fe film is suggested to arise from the spin-active Ag/W or Ag/Fe interfaces.

  16. Electronic structures and optical properties for Ag-N-codoped ZnO nanotubes

    PubMed Central

    2013-01-01

    The structural and electronic/optical properties of pure and Ag-N-codoped (8,0) ZnO nanotubes have been studied using first-principles calculations in the framework of the local spin density approximation. The configurations for Zn atoms replaced by Ag atoms are p-type semiconductor materials, and the bandgap increases when N atoms are doped into ZnO nanotube configurations. The optical studies based on dielectric function and reflectivity indicate that new transition peaks in the visible light range are observed, which can be ascribed to the Ag and N doping. Furthermore, there is a red shift observed with the increase of N concentration. PMID:23981389

  17. 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.

  18. Layer-by-layer fabrication of AgCl-PANI hybrid nanocomposite films for electronic tongues.

    PubMed

    Manzoli, Alexandra; Shimizu, Flavio M; Mercante, Luiza A; Paris, Elaine C; Oliveira, Osvaldo N; Correa, Daniel S; Mattoso, Luiz H C

    2014-11-28

    The fabrication of nanostructured films with tailored properties is essential for many applications, particularly with materials such as polyaniline (PANI) whose electrical characteristics may be easily tuned. In this study we report the one-step synthesis of AgCl-PANI nanocomposites that could form layer-by-layer (LbL) films with poly(sodium 4-styrenesulfonate) (PSS) and be used for electronic tongues (e-tongues). The first AgCl-PANI layer was adsorbed on a quartz substrate according to a nucleation-and-growth mechanism explained using the Johnson-Mehl-Avrami (JMA) model, revealing a 3D film growth confirmed by atomic force microscopy (AFM) measurements for the AgCl-PANI/PSS LbL films. In contrast to conventional PANI-containing films, the AgCl-PANI/PSS LbL films deposited on interdigitated electrodes exhibited electrical resistance that was practically unaffected by changes in pH from 4 to 9, and therefore these films can be used in e-tongues for both acidic and basic media. With a sensor array made of AgCl-PANI/PSS LbL films with different numbers of bilayers, we demonstrated the suitability of the AgCl-PANI nanocomposite for an e-tongue capable of clearly discriminating the basic tastes from salt, acid and umami solutions. Significantly, the hybrid AgCl-PANI nanocomposite is promising for any application in which PANI de-doping at high pH is to be avoided.

  19. Structural and electronic properties of ultrathin picene films on the Ag(100) surface

    NASA Astrophysics Data System (ADS)

    Kelly, Simon J.; Sorescu, Dan C.; Wang, Jun; Archer, Kaye A.; Jordan, Kenneth D.; Maksymovych, Petro

    2016-10-01

    Using scanning tunneling microscopy and electronic structure calculations, we investigated the assembly and electronic properties of picene molecules on the Ag(100), Ag(111), and Cu(111) surfaces, with particular emphasis on Ag(100). In each case, picene molecules are found to lie parallel to the surface at coverages up to half a monolayer and to adopt alternating parallel and tilted orientations at full monolayer coverage. In the latter case, the arrangement of the molecules is roughly similar to that in the bulk crystal. On the metal surfaces considered, the growth mode of picene is quite different from that of its structural isomer pentacene, which forms a bilayer overlayer on top of a dense monolayer of flat-lying molecules on metal surfaces. Tunneling spectroscopy measurements provide estimates of the energies of several low-lying unfilled molecular orbitals as well as of the highest occupied molecular orbital of the absorbed picene molecules. From analysis of these results, we establish that the on-site Coulomb repulsion for picene decreases by ~ 2 eV in going from the gas phase to the full monolayer on Ag(100), bringing it close to that of the undoped bulk crystal.

  20. Electronic Topological Transition in Ag2Te at High-pressure

    PubMed Central

    Zhang, Yuhang; Li, Yan; Ma, Yanmei; Li, Yuwei; Li, Guanghui; Shao, Xuecheng; Wang, Hui; Cui, Tian; Wang, Xin; Zhu, Pinwen

    2015-01-01

    Recently, Ag2Te was experimentally confirmed to be a 3D topological insulator (TI) at ambient pressure. However, the high-pressure behaviors and properties of Ag2Te were rarely reported. Here, a pressure-induced electronic topological transition (ETT) is firstly found in Ag2Te at 1.8 GPa. Before ETT, the positive pressure coefficient of bulk band-gap, which is firstly found in TIs family, is found by both first-principle calculations and in situ high-pressure resistivity measurements. The electrical resistivity obtained at room temperature shows a maximum at 1.8 GPa, which is nearly 3.3 times to that at ambient pressure. This result indicates that the best bulk insulating character and topological nature in Ag2Te can be obtained at this pressure. Furthermore, the high-pressure structural behavior of Ag2Te has been investigated by in situ high-pressure synchrotron powder X-ray diffraction technique up to 33.0 GPa. The accurate pressure-induced phase transition sequence is firstly determined as P21/c → Cmca → Pnma. It is worth noting that the reported isostructural P21/c phase is not existed, and the reported structure of Cmca phase is corrected by CALYPSO methodology. The second high-pressure structure, a long puzzle to previous reports, is determined as Pnma phase. A pressure-induced metallization in Ag2Te is confirmed by the results of temperature-dependent resistivity measurements. PMID:26419707

  1. Theory of the electronic states and absorption spectrum of the LiCl:Ag+ impurity system

    NASA Astrophysics Data System (ADS)

    Jackson, Koblar A.; Lin, Chun C.

    1990-01-01

    The impurity absorption spectra of Ag+ and Cu+ impurities in alkali halide hosts show characteristically different features, despite the similar nature of the corresponding free ions. We use the self-interaction-corrected local-spin-density (SIC-LSD) theory to calculate the electronic structure of the ground state (4d) and the 5s and 5p excited states of the LiCl:Ag+ impurity ion. The method of linear combinations of atomic orbitals is used to determine the wave functions and energy levels. By comparing with previous calculations for LiCl:Cu+, we are able to attribute the differences in the d-->s and d-->p transitions in the ultraviolet spectra of these systems to the increased bonding between host crystal and impurity orbitals in LiCl:Ag+, due to the more extensive nature of the Ag+ 4d orbitals. A modification of the earlier SIC-LSD impurity-crystal procedure is introduced to treat the strongly mixed impurity states.

  2. Diffusion of Ag into organic semiconducting materials: a combined analytical study using transmission electron microscopy and X-ray reflectivity.

    PubMed

    Fladischer, Stefanie; Neuhold, Alfred; Kraker, Elke; Haber, Thomas; Lamprecht, Bernhard; Salzmann, Ingo; Resel, Roland; Grogger, Werner

    2012-10-24

    This study shows that the morphology of organic/metal interfaces strongly depends on process parameters and the involved materials. The interface between organic n-type blocking layer materials and the top Ag cathode within an organic photodiode was investigated. Ag was deposited on either amorphous tris-8-hydroxyquinolinato-aluminum (Alq(3)) or crystalline 4,7-diphenyl-1,10-phenanthroline (Bphen) using different deposition techniques such as electron beam deposition, ion beam sputtering, and vacuum thermal evaporation at various deposition rates. The interfaces were studied by transmission electron microscopy and X-ray reflectivity. It was found that Bphen does not show any Ag diffusion no matter which deposition technique was used, whereas the Ag diffusion into Alq(3) depends on the deposition technique and the deposition rate. The highest amount of Ag diffusion into Alq(3) occurred by using thermal vacuum deposition at low deposition rates.

  3. Diffusion of Ag into organic semiconducting materials: a combined analytical study using transmission electron microscopy and X-ray reflectivity.

    PubMed

    Fladischer, Stefanie; Neuhold, Alfred; Kraker, Elke; Haber, Thomas; Lamprecht, Bernhard; Salzmann, Ingo; Resel, Roland; Grogger, Werner

    2012-10-24

    This study shows that the morphology of organic/metal interfaces strongly depends on process parameters and the involved materials. The interface between organic n-type blocking layer materials and the top Ag cathode within an organic photodiode was investigated. Ag was deposited on either amorphous tris-8-hydroxyquinolinato-aluminum (Alq(3)) or crystalline 4,7-diphenyl-1,10-phenanthroline (Bphen) using different deposition techniques such as electron beam deposition, ion beam sputtering, and vacuum thermal evaporation at various deposition rates. The interfaces were studied by transmission electron microscopy and X-ray reflectivity. It was found that Bphen does not show any Ag diffusion no matter which deposition technique was used, whereas the Ag diffusion into Alq(3) depends on the deposition technique and the deposition rate. The highest amount of Ag diffusion into Alq(3) occurred by using thermal vacuum deposition at low deposition rates. PMID:23027799

  4. Dissociation of oxygen on Ag(100) induced by inelastic electron tunneling.

    PubMed

    Sprodowski, Carsten; Mehlhorn, Michael; Morgenstern, Karina

    2010-07-01

    Scanning tunneling microscopy (STM) is used to study the dissociation of molecular oxygen on Ag(100) induced by inelastic electron tunneling (IET) at 5 K. This dissociation is possible above 3.3 V with a yield of (3.63 ± 0.47) × 10(-9) per electron. Dissociation leads to three different types of hot atom motion: lateral motion, a cannon ball mechanism, and abstractive dissociation. Analysis of the I-t characteristics during dissociation suggests that the dissociation is proceeded by an adsorption site change. PMID:21386462

  5. Ag on Pt(111): Changes in Electronic and CO Adsorption Properties upon PtAg/Pt(111) Monolayer Surface Alloy Formation.

    PubMed

    Diemant, Thomas; Schüttler, Konstantin M; Behm, R Jürgen

    2015-10-01

    The electronic and chemical (adsorption) properties of bimetallic Ag/Pt(111) surfaces and their modification upon surface alloy formation, that is, during intermixing of Ag and Pt atoms in the top atomic layer upon annealing, were studied by X-ray photoelectron spectroscopy (XPS) and, using CO as probe molecule, by temperature-programmed desorption (TPD) and infrared reflection absorption spectroscopy (IRRAS), respectively. The surface alloys are prepared by deposition of sub-monolayer Ag amounts on a Pt(111) surface at room temperature, leading to extended Ag monolayer islands on the substrate, and subsequent annealing of these surfaces. Surface alloy formation starts at ≈600-650 K, which is evidenced by core-level shifts (CLSs) of the Ag(3d5/2 ) signal. A distinct change of the CO adsorption properties is observed when going to the intermixed PtAg surface alloys. Most prominently, we find the growth of a new desorption feature at higher temperature (≈550 K) in the TPD spectra upon surface alloy formation. This goes along with a shift of the COad -related IR bands to lower wave number. Surface alloy formation is almost completed after heating to 700 K.

  6. Intraband optical conductivity sigma/omega,T/ of Cu, Ag, and Au - Contribution from electron-electron scattering

    NASA Technical Reports Server (NTRS)

    Parkins, G. R.; Lawrence, W. E.; Christy, R. W.

    1981-01-01

    The frequency and temperature dependence of the intraband optical conductivity of the noble metals Cu, Ag and Au is measured and contributions of electron-electron scattering are assessed. Optical measurements were performed at temperatures of 77, 295 and 425 K to obtain values of the Drude electron scattering rate with a linear dependence on temperature which may be attributed to electron-phonon scattering, and a quadratic dependence on photon energy, which is suggestive of electron-electron scattering but is a factor of two to three times greater than would be expected. Comparison of the optical data with dc electrical and thermal resistivity data which also show behavior attributed to electron-electron scattering reveals discrepancies of up to an order of magnitude. Other possible mechanisms for the frequency dependence, including absorptance, electron-surface plasmon interactions, a two-carrier model, and a structure dependence are considered, and it is concluded that the frequency dependence in the Drude scattering rates of the noble metals is not yet quantitatively understood

  7. Magnetic and electronic structure of Mn nanostructures on Ag(111) and Au(111)

    NASA Astrophysics Data System (ADS)

    Cardias, R.; Bezerra-Neto, M. M.; Ribeiro, M. S.; Bergman, A.; Szilva, A.; Eriksson, O.; Klautau, A. B.

    2016-01-01

    We present results of the electronic and magnetic structure of Mn nanowires adsorbed on Ag(111) and Au(111) surfaces. For finite Mn nanowires on Ag(111) and Au(111) surfaces, our ab initio results show that the large difference between the spin-orbit splitting of these two surfaces leads to completely different magnetic configurations. The magnetic ordering for Mn nanowires adsorbed on Ag(111) is governed by the strong exchange interaction between Mn adatoms. For Mn nano-chains on Au(111), the competition between Heisenberg and Dzyaloshinskii-Moriya interactions leads to a complex magnetic structure of the clusters considered here. Among the more conspicuous results we note a spin-spiral helical type for the nanowire with seven atoms, and a complex magnetic configuration incommensurate with the substrate lattice for a double-sized Mn wire. The effect of the structural relaxation is also investigated, showing sensitivity of the exchange interactions to the bond distance to the substrate. We also demonstrate that small changes in the band filling of these Mn chains results in drastically different changes of the interatomic exchange. Finally, we show that dispersion of the electronic energy spectrum is possible even in nanostructures with bounded spatial extension.

  8. Optical and electronic properties of mixed Ag-Au tetramer cations

    SciTech Connect

    Shayeghi, A. Schäfer, R.; Heard, C. J.; Johnston, R. L.

    2014-02-07

    We present experimental and theoretical studies of the optical response of mixed Ag {sub n} Au {sub 4−n}{sup +} (n=1–3) clusters in the photon energy range ℏω = 1.9–3.5 eV. Absorption spectra are recorded by a newly built longitudinal molecular beam depletion spectroscopy apparatus providing lower limits to absolute photodissociation cross sections. The experimental data are compared to optical response calculations in the framework of long-range corrected time-dependent density functional theory with initial cluster geometries obtained by the unbiased Birmingham Cluster Genetic Algorithm coupled with density functional theory. Experiments and excited state calculations shed light on the structural and electronic properties of the mixed Ag-Au tetramer cations.

  9. Influence of electron beam irradiation on structural and optical properties of α-Ag2WO4 nanoparticles.

    PubMed

    A, Sreedevi; K P, Priyanka; K K, Babitha; S, Ganesh; Varghese, T

    2016-09-01

    The influence of 8MeV electron beam irradiation on the structural and optical properties of silver tungstate (α-Ag2WO4) nanoparticles synthesized by chemical precipitation method was investigated. The dose dependent effect of electron irradiation was investigated by various characterization techniques such as, X-ray diffraction, scanning electron microscopy, UV-vis absorption spectroscopy, photoluminescence and Raman spectroscopy. Systematic studies confirm that electron beam irradiation induces non-stoichiometry, defects and particle size variation on α-Ag2WO4, which in turn results changes in optical band gap, photoluminescence spectra and Raman bands.

  10. Generation of attosecond electron packets via conical surface plasmon electron acceleration

    NASA Astrophysics Data System (ADS)

    Greig, S. R.; Elezzabi, A. Y.

    2016-01-01

    We present a method for the generation of high kinetic energy attosecond electron packets via magnetostatic and aperture filtering of conical surface plasmon (SP) accelerated electrons. The conical SP waves are excited by coupling an ultrafast radially polarized laser beam to a conical silica lens coated with an Ag film. Electromagnetic and particle tracking models are employed to characterize the ultrafast electron packets.

  11. Transmission electron microscopy investigation of Ag diffusion mechanisms in β-SiC

    NASA Astrophysics Data System (ADS)

    Coward, Robert A.; Winkler, Christopher R.; Hanson, William A.; Jablonski, Michael L.; Taheri, Mitra L.

    2015-02-01

    β-Silicon carbide (β-SiC) acts as the main layer for metallic fission product retention in tristructural-isotropic (TRISO) fuel particles. It is critical to track these fission products in the β-SiC layer to provide a baseline understanding of safe fuel operation for next generation nuclear reactors. In this study, the microstructural evolution of the β-SiC layer is examined through the comparison of as-implanted and annealed samples up to 1600 °C using high resolution transmission electron microscopy (HRTEM). Faceted voids were observed in annealed samples but not in the as-implanted samples, suggesting the possibility that a void mediated fission product transport mechanism due to the change in microstructure of the β-SiC layer at elevated temperatures plays a role in the diffusion of metallic species through the β-SiC cladding layer. It should be noted, however, that Ag implantation at room temperature is not an ideal method to study Ag diffusion in TRISO fuel particles. Ultimately, Ag implantation should be performed above the critical temperature for which amorphization will not occur to better correlate to conditions in a Generation IV reactor and to see if void formation occurs.

  12. Ab initio calculation of structural stability, electronic and optical properties of Ag{sub 2}Se

    SciTech Connect

    Rameshkumar, S.; Jayalakshmi, V.; Jaiganesh, G.; Palanivel, B.

    2015-06-24

    The structural stability, electronic and optical properties of Ag{sub 2}Se compound is studied using ab initio packages. Ag{sub 2}Se is found to crystallize in orthorhombic structure with two different space groups i.e. P2{sub 1}2{sub 1}2{sub 1} (No. 19) and P222{sub 1} (No. 17). For this compound in these two space groups, the total energy has been computed as a function of volume. Our calculated results suggest that the P2{sub 1}2{sub 1}2{sub 1}–phase is more stable than that of the P222{sub 1}–phase. The band structure calculation show that Ag{sub 2}Se is semimetallic with an overlap of about 0.014 eV in P2{sub 1}2{sub 1}2{sub 1}–phase whereas is metallic in nature in P222{sub 1}–phase. Moreover, the optical properties including the dielectric function, energy loss spectrum are obtained and analysed.

  13. Structural and electronic properties of graphene nanoflakes on Au(111) and Ag(111)

    PubMed Central

    Tesch, Julia; Leicht, Philipp; Blumenschein, Felix; Gragnaniello, Luca; Fonin, Mikhail; Marsoner Steinkasserer, Lukas Eugen; Paulus, Beate; Voloshina, Elena; Dedkov, Yuriy

    2016-01-01

    We investigate the electronic properties of graphene nanoflakes on Ag(111) and Au(111) surfaces by means of scanning tunneling microscopy and spectroscopy as well as density functional theory calculations. Quasiparticle interference mapping allows for the clear distinction of substrate-derived contributions in scattering and those originating from graphene nanoflakes. Our analysis shows that the parabolic dispersion of Au(111) and Ag(111) surface states remains unchanged with the band minimum shifted to higher energies for the regions of the metal surface covered by graphene, reflecting a rather weak interaction between graphene and the metal surface. The analysis of graphene-related scattering on single nanoflakes yields a linear dispersion relation E(k), with a slight p-doping for graphene/Au(111) and a larger n-doping for graphene/Ag(111). The obtained experimental data (doping level, band dispersions around EF, and Fermi velocity) are very well reproduced within DFT-D2/D3 approaches, which provide a detailed insight into the site-specific interaction between graphene and the underlying substrate. PMID:27002297

  14. Electron transport in carbon wires in contact with Ag electrodes: a detailed first principles investigation.

    PubMed

    Bonardi, Paolo; Achilli, Simona; Tantardini, Gian Franco; Martinazzo, Rocco

    2015-07-28

    The structure and electronic properties of carbon atom chains Cn in contact with Ag electrodes are investigated in detail with first principles means. The ideal Ag(100) surface is used as a model for binding, and electron transport through the chains is studied as a function of their length, applied bias voltage, presence of capping atoms (Si, S) and adsorption site. It is found that the metal-molecule bond largely influences electronic coupling to the leads. Without capping atoms the quality of the electric contact improves when increasing the carbon atom coordination number to the metal (1, 2 and 4 for adsorption on a top, bridge and hollow position, respectively) and this finding translates almost unchanged in more realistic tip-like contacts which present one, two or four metal atoms at the contact. Current-voltage characteristics show Ohmic behaviour over a wide range of bias voltages and the resulting conductances change only weakly when increasing the wire length. The effect of a capping species is typically drastic, and either largely reduces (S) or largely increases (Si) the coupling of the wire to the electrodes. Comparison of our findings with recent experimental results highlights the limits of the adopted approach, which can be traced back to the known gap problem of density-functional-theory. PMID:26106869

  15. Electronic evidence of asymmetry in the Si(111)(3)×(3)-Ag structure

    NASA Astrophysics Data System (ADS)

    Matsuda, Iwao; Morikawa, Harumo; Liu, Canhua; Ohuchi, Satoru; Hasegawa, Shuji; Okuda, Taichi; Kinoshita, Toyohiko; Ottaviani, Carlo; Cricenti, Antonio; D'Angelo, Marie; Soukiassian, Patrick; Le Lay, Guy

    2003-08-01

    Our photoemission spectroscopy results clearly demonstrate that symmetry breakdown in atomic arrangement brings about a lift of degeneracy in electronic states, leading to settle a long-standing controversy on a surface superstructure. We provide unambiguous evidences that Si(111)(3)×(3)-Ag has the inequivalent triangle structure (IET), excluding a long-lived honeycomb-chained triangle model. We also give critical experimental proof that the surface exhibits a disorder-order phase transition by cooling; the thermally fluctuating IET structure is frozen.

  16. Structural, elastic, electronic, and thermodynamic properties of MgAgSb investigated by density functional theory

    NASA Astrophysics Data System (ADS)

    Wang, Jun-Fei; Fu, Xiao-Nan; Zhang, Xiao-Dong; Wang, Jun-Tao; Li, Xiao-Dong; Jiang, Zhen-Yi

    2016-08-01

    The structural, elastic, electronic, and thermodynamic properties of thermoelectric material MgAgSb in γ,β,α phases are studied with first-principles calculations based on density functional theory. The optimized lattice constants accord well with the experimental data. According to the calculated total energy of the three phases, the phase transition order is determined from α to γ phase with cooling, which is in agreement with the experimental result. The physical properties such as elastic constants, bulk modulus, shear modulus, Young’s modulus, Poisson’s ratio, and anisotropy factor are also discussed and analyzed, which indicates that the three structures are mechanically stable and each has a ductile feature. The Debye temperature is deduced from the elastic properties. The total density of states (TDOS) and partial density of states (PDOS) of the three phases are investigated. The TDOS results show that the γ phase is most stable with a pseudogap near the Fermi level, and the PDOS analysis indicates that the conduction band of the three phases is composed mostly of Mg-3s, Ag-4d, and Sb-5p. In addition, the changes of the free energy, entropy, specific heat, thermal expansion of γ-MgAgSb with temperature are obtained successfully. The obtained results above are important parameters for further experimental and theoretical tuning of doped MgAgSb as a thermoelectric material at high temperature. Project supported by the National Natural Science Foundation of China (Grant No. 11504088), the Fund from Henan University of Technology, China (Grant Nos. 2014YWQN08 and 2013JCYJ12), the Natural Science Fund from the Henan Provincial Education Department, China (Grant No. 16A140027), the Natural Science Foundation of Shaanxi Province of China (Grant Nos. 2013JQ1018 and 15JK1759), and the Science Foundation of Northwest University of China (Grant No. 14NW23).

  17. Structural, elastic, electronic, and thermodynamic properties of MgAgSb investigated by density functional theory

    NASA Astrophysics Data System (ADS)

    Wang, Jun-Fei; Fu, Xiao-Nan; Zhang, Xiao-Dong; Wang, Jun-Tao; Li, Xiao-Dong; Jiang, Zhen-Yi

    2016-08-01

    The structural, elastic, electronic, and thermodynamic properties of thermoelectric material MgAgSb in γ,β,α phases are studied with first-principles calculations based on density functional theory. The optimized lattice constants accord well with the experimental data. According to the calculated total energy of the three phases, the phase transition order is determined from α to γ phase with cooling, which is in agreement with the experimental result. The physical properties such as elastic constants, bulk modulus, shear modulus, Young’s modulus, Poisson’s ratio, and anisotropy factor are also discussed and analyzed, which indicates that the three structures are mechanically stable and each has a ductile feature. The Debye temperature is deduced from the elastic properties. The total density of states (TDOS) and partial density of states (PDOS) of the three phases are investigated. The TDOS results show that the γ phase is most stable with a pseudogap near the Fermi level, and the PDOS analysis indicates that the conduction band of the three phases is composed mostly of Mg-3s, Ag-4d, and Sb-5p. In addition, the changes of the free energy, entropy, specific heat, thermal expansion of γ-MgAgSb with temperature are obtained successfully. The obtained results above are important parameters for further experimental and theoretical tuning of doped MgAgSb as a thermoelectric material at high temperature. Project supported by the National Natural Science Foundation of China (Grant No. 11504088), the Fund from Henan University of Technology, China (Grant Nos. 2014YWQN08 and 2013JCYJ12), the Natural Science Fund from the Henan Provincial Education Department, China (Grant No. 16A140027), the Natural Science Foundation of Shaanxi Province of China (Grant Nos. 2013JQ1018 and 15JK1759), and the Science Foundation of Northwest University of China (Grant No. 14NW23).

  18. Ag(I)-Catalyzed C-H Activation: The Role of the Ag(I) Salt in Pd/Ag-Mediated C-H Arylation of Electron-Deficient Arenes.

    PubMed

    Whitaker, Daniel; Burés, Jordi; Larrosa, Igor

    2016-07-13

    The use of stoichiometric Ag(I)-salts as additives in Pd-catalyzed C-H functionalization reactions is widespread. It is commonly proposed that this additive acts as an oxidant or as a halide scavenger promoting Pd-catalyst turnover. We demonstrate that, contrary to current proposals, phosphine ligated Ag(I)-carboxylates can efficiently carry out C-H activation on electron-deficient arenes. We show through a combination of stoichiometric and kinetic studies that a (PPh3)Ag-carboxylate is responsible for the C-H activation step in the Pd-catalyzed arylation of Cr(CO)3-complexed fluorobenzene. Furthermore, the reaction rate is controlled by the rate of Ag(I)-C-H activation, leading to an order zero on the Pd-catalyst. H/D scrambling studies indicate that this Ag(I) complex can carry out C-H activation on a variety of aromatic compounds traditionally used in Pd/Ag-mediated C-H functionalization methodologies. PMID:27303956

  19. Understanding the formation and growth of Ag nanoparticles on silver chromate induced by electron irradiation in electron microscope: A combined experimental and theoretical study

    NASA Astrophysics Data System (ADS)

    Fabbro, Maria T.; Gracia, Lourdes; Silva, Gabriela S.; Santos, Luís P. S.; Andrés, Juan; Cordoncillo, Eloisa; Longo, E.

    2016-07-01

    Ag2CrO4 microcrystals were synthesized using the co-precipitation method. These microcrystals were characterized through X-ray diffraction (XRD) with Rietveld analysis, field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) with energy-dispersive spectroscopy (EDS), micro-Raman (MR). XRD patterns and Rietveld refinement data showed that the material exhibits an orthorhombic structure without any deleterious phases. FE-SEM and TEM micrographs revealed the morphology and the growth of Ag nanoparticles on Ag2CrO4 microcrystals during electron beam irradiation. These events were directly monitored in real-time. Their optical properties were investigated using ultraviolet-visible (UV-vis) diffuse reflectance spectroscopy that allowed the calculation of the optical band gap energy. Theoretical analyses based on the density functional theory level indicate that the incorporation of electrons is responsible for structural modifications and formation of defects on the [AgO6] and [AgO4] clusters, generating ideal conditions for the growth of Ag nanoparticles.

  20. Thermal evaporated hyperbranched Ag nanostructure as an effective secondary-electron trapping surface coating

    NASA Astrophysics Data System (ADS)

    He, Y. N.; Peng, W. B.; Cui, W. Z.; Ye, M.; Zhao, X. L.; Wang, D.; Hu, T. C.; Wang, R.; Li, Y.

    2016-02-01

    We study secondary electron yield (SEY) suppression of silver using a hyperbranched nanostructure obtained by thermal evaporation. First, we perform thermal evaporation at different residual gas pressures for studying the influence of pressure on surface morphologies. A self-assembled hyperbranched Ag nanostructure has been achieved at 100 Pa. Then, we further investigate the detailed formation process of the self-assembled hyperbranched Ag nanostructure qualitatively and find it to be dominated by "screening effect". Finally, we study the obvious SEY suppression effect of this special structure. We show that 100 Pa is the best process condition within our experimental scope from the SEY suppression point of view. It exhibits maximum SEY (δmax) of ˜0.9. We also show that the combining of this nanostructure with the micro-porous surface we developed before can further improve its SEY suppression effect which leading to a δmax of ˜0.8. We propose a novel 2D rectangular-hemisphere hybrid trap model to perform numerical simulation of secondary electron dynamics for interpretation of the experimental results. In total, this work provides guidance to controllable preparation of low SEY metallic surfaces for potential applications in particle accelerators, RF microwave components and satellite systems.

  1. Benzene derivatives adsorbed to the Ag(111) surface: Binding sites and electronic structure

    SciTech Connect

    Miller, Daniel P.; Tymińska, Nina; Zurek, Eva; Simpson, Scott

    2015-03-14

    Dispersion corrected Density Functional Theory calculations were employed to study the adsorption of benzenes derivatized with functional groups encompassing a large region of the activated/deactivated spectrum to the Ag(111) surface. Benzenes substituted with weak activating or deactivating groups, such as methyl and fluoro, do not have a strong preference for adsorbing to a particular site on the substrate, with the corrugations in the potential energy surface being similar to those of benzene. Strong activating (N(CH{sub 3}){sub 2}) and deactivating (NO{sub 2}) groups, on the other hand, possess a distinct site preference. The nitrogen in the former prefers to lie above a silver atom (top site), but in the latter a hollow hexagonal-closed-packed (H{sub hcp}) site of the Ag(111) surface is favored instead. Benzenes derivatized with classic activating groups donate electron density from their highest occupied molecular orbital to the surface, and those functionalized with deactivating groups withdraw electron density from the surface into orbitals that are unoccupied in the gas phase. For benzenes functionalized with two substituents, the groups that are strongly activating or deactivating control the site preference and the other groups assume sites that are, to a large degree, dictated by their positions on the benzene ring. The relative stabilities of the ortho, meta, and para positional isomers of disubstituted benzenes can, in some cases, be modified by adsorption to the surface.

  2. Low temperature sintering of Ag nanoparticles/graphene composites for paper based writing electronics

    NASA Astrophysics Data System (ADS)

    Wang, Fuliang; Zhu, Haixin; He, Hu

    2016-10-01

    With the great demand in the applications of flexible electronics, the methods leading to improvements in the electrical and mechanical performance have been widely investigated. In this work, we firstly prepared a hybrid composite ink using Ag nanoparticles and graphene. Then, a hot-press sintering process was deployed to obtain the desired electrical tracks which could be applied in flexible electronics. We have systematically investigated the effects of sintering time, pressure and temperature, as well as the different percentage of weight (wt%) of graphene for the electrical and mechanical performance of sintered electrical tracks. We achieved reasonably low electrical resistivity at low sintering temperature (120 °C). Specifically, the resistivity reaches 6.19  ×  10-8 Ω · m which is just 3.87 times higher than the value of bulk silver. Additionally, the prepared hybrid composite ink obtained better electrical reliability against bending test comparing with Ag nanoparticle ink. Finally, the optimal wt% of graphene and potential effect to the electrical and mechanical performance were also investigated.

  3. Draft Genome Sequence of a Tetrabromobisphenol A–Degrading Strain, Ochrobactrum sp. T, Isolated from an Electronic Waste Recycling Site

    PubMed Central

    Liang, Zhishu; Li, Guiying; Zhang, Guoxia; Das, Ranjit

    2016-01-01

    Ochrobactrum sp. T was previously isolated from a sludge sample collected from an electronic waste recycling site and characterized as a unique tetrabromobisphenol A (TBBPA)–degrading bacterium. Here, the draft genome sequence (3.9 Mb) of Ochrobactrum sp. T is reported to provide insights into its diversity and its TBBPA biodegradation mechanism in polluted environments. PMID:27445374

  4. Electronic structures of efficient MBiO3 (M = Li, Na, K, Ag) photocatalyst

    NASA Astrophysics Data System (ADS)

    Wen-Liu, Zhou; Zong-Yan, Zhao

    2016-03-01

    In order to deepen the understanding of the relationship between fundamental properties (including: microstructure and composition) and photocatalytic performance, four bismuthate compounds, including: LiBiO3, NaBiO3, KBiO3, and AgBiO3, are regarded as research examples in the present work, because they have particular crystal structures and similar compositions. Using density functional theory calculations, their structural, electronic, and optical properties are investigated and compared systematically. First of all, the calculated results of crystal structures and optical properties are in agreement with available published experimental data. Based on the calculated results, it is found that the tunneled or layered micro-structural properties lead to the stronger interaction between bismuth and oxygen, and the weaker interaction between alkaline-earth metal and [BiO6] octahedron, resulting in the feature of multi-band gaps in the cases of LiBiO3, NaBiO3, and KBiO3. This conclusion is supported by the case of AgBiO3, in which the feature of multi-band gaps disappears, due to the stronger interaction between the noble metal and [BiO6] octahedron. These properties have significant advantages in the photocatalytic performance: absorbing low energy photons, rapidly transferring energy carriers. Furthermore, the features of electronic structures of bismuthate compounds are well reflected by the absorption spectra, which could be confirmed by experimental measurements in practice. Combined with the calculated results, it could be considered that the crystal structures and compositions of the photocatalyst determine the electronic structures and optical properties, and subsequently determine the corresponding photocatalytic performance. Thus, a novel Bi-based photocatalyst driven by visible-light could be designed by utilizing specific compositions to form favorable electronic structures or specific micro-structures to form a beneficial channel for energy carriers

  5. Molecular cloning, characterization and enzymatic properties of a novel βeta-agarase from a marine isolate Psudoalteromonas SP. AG52

    PubMed Central

    Oh, Chulhong; Nikapitiya, Chamilani; Lee, Youngdeuk; Whang, Ilson; Kang, Do-Hyung; Heo, Soo-Jin; Choi, Young-Ung; Lee, Jehee

    2010-01-01

    An agar-degrading Pseudoalteromonas sp. AG52 bacterial strain was identified from the red seaweed Gelidium amansii collected from Jeju Island, Korea. A β-agarase gene which has 96.8% nucleotide identity to Aeromonas β-agarase was cloned from this strain, and was designated as agaA. The coding region is 870 bp, encoding 290 amino acids and possesses characteristic features of the glycoside hydrolase family (GHF)-16. The predicted molecular mass of the mature protein was 32 kDa. The recombinant β-agarase (rAgaA) was overexpressed in Escherichia coli and purified as a fusion protein. The optimal temperature and pH for activity were 55 °C and 5.5, respectively. The enzyme had a specific activity of 105.1 and 79.5 unit/mg toward agar and agarose, respectively. The pattern of agar hydrolysis demonstrated that the enzyme is an endo-type β-agarase, producing neoagarohexaose and neoagarotetraose as the final main products. Since, Pseudoalteromonas sp. AG52 encodes an agaA gene, which has greater identity to Aeromonas β-agarase, the enzyme could be considered as novel, with its unique bio chemical characteristics. Altogether, the purified rAgaA has potential for use in industrial applications such as development of cosmetics and pharmaceuticals. PMID:24031567

  6. Ion-modulated nonlinear electronic transport in carbon nanotube bundle/RbAg4I5 thin film composite nanostructures

    NASA Astrophysics Data System (ADS)

    Sun, Jia-Lin; Zhang, Wei; Wei, Jinquan; Gu, Bingfu

    2014-01-01

    We have explored the ion-modulated electronic transport properties of mixed ionic-electronic conductor (MIEC) composite nanostructures made of superionic conductor RbAg4I5 films and carbon nanotube (CNT) bundle spiderwebs. Our experimental and theoretical studies indicate that the formation of ion-electron bound states (IEBSs) leads to strong ion-electron interference effect and interesting electronic transport of CNT, such as nonlinear current-voltage (I-V) characteristics and novel temperature dependence of the current. With increasing temperature, the hybrid nanostructures show rich phases with different dependence of current on temperature, which is related to the structural phase transition of RbAg4I5 and the transition of dissociation of IEBSs. The ion-modulation of the electric conductivity in such MIEC composite nanostructures with great tunability has been used to design new ionic-electronic composite nano-devices with function like field effect transistor.

  7. Preparation, characterization, and photocatalytic activity of porous AgBr@Ag and AgBrI@Ag plasmonic photocatalysts

    NASA Astrophysics Data System (ADS)

    Yang, Fan; Tian, Baozhu; Zhang, Jinlong; Xiong, Tianqing; Wang, Tingting

    2014-02-01

    Porous AgBr@Ag and AgBrI@Ag plasmonic photocatalysts were synthesized by a multistep route, including a dealloying method to prepare porous Ag, a transformation from Ag to AgBr and AgBrI, and a photo-reduction process to form Ag nanoparticles on the surface of AgBr and AgBrI. It was found that the porous structure kept unchanged during Ag was transferred into AgBr, AgBrI, AgBr@Ag, and AgBrI@Ag. Both porous AgBr@Ag and porous AgBrI@Ag showed much higher visible-light photocatalytic activity than cubic AgBr@Ag for the degradation of methyl orange, which is because the interconnected pore channels not only provide more reactive sites but also favor the transportation of photo-generated electrons and holes. For AgBrI@Ag, AgBrI solid solution formed at the interface of AgBr and AgI, and the phase junction can effectively separate the photo-generated electrons and holes, favorable to the improvement of photocatalytic activity. The optimal I content for obtaining the highest activity is ∼10 at.%.

  8. Electronic Reconstruction of α-Ag2WO4 Nanorods for Visible-Light Photocatalysis.

    PubMed

    Lin, Zhaoyong; Li, Jiling; Zheng, Zhaoqiang; Yan, Jiahao; Liu, Pu; Wang, Chengxin; Yang, Guowei

    2015-07-28

    α-Ag2WO4 (AWO) has been studied extensively due to its H2 evolution and organic pollution degradation ability under the irradiation of UV light. However, the band gap of AWO is theoretically calculated to be 3.55 eV, resulting in its sluggish reaction to visible light. Herein, we demonstrated that, by using the electronic reconstruction of AWO nanorods upon a unique process of laser irradiation in liquid, these nanorods performed good visible-light photocatalytic organics degradation and H2 evolution. Using commercial AWO powders as the starting materials, we achieved the electronic reconstruction of AWO by a recrystallization of the starting powders upon laser irradiation in liquid and synthesized AWO nanorods. Due to the weak bond energy of AWO and the far from thermodynamic equilibrium process created by laser irradiation in liquid, abundant cluster distortions, especially [WO6] cluster distortions, are introduced into the crystal lattice, the defect density increases by a factor of 2.75, and uneven intermediate energy levels are inset into the band gap, resulting in a 0.44 eV decrease of the band gap, which modified the AWO itself by electronic reconstruction to be sensitive to visible light without the addition of others. Further, the first-principles calculation was carried out to clarify the electronic reconstruction of AWO, and the theoretical results confirmed the deduction based on the experimental measurements.

  9. Structural stability and electronic properties of AgInS2 under pressure

    NASA Astrophysics Data System (ADS)

    Dongho Nguimdo, G. M.; Manyali, George S.; Abdusalam, Mahmud; Joubert, Daniel P.

    2016-04-01

    We employ state-of-the-art ab initio density functional theory techniques to investigate the structural, dynamical, mechanical stability and electronic properties of the ternary AgInS2 compounds under pressure. Using cohesive energy and enthalpy, we found that from the six potential phases explored, the chalcopyrite and the orthorhombic structures were very competitive as zero pressure phases. A pressure-induced phase transition occurs around 1.78 GPa from the low pressure chalcopyrite phase to a rhombohedral RH-AgInS2 phase. The pressure phase transition around 1.78 GPa is accompanied by notable changes in the volume and bulk modulus. The calculations of the phonon dispersions and elastic constants at different pressures showed that the chalcopyrite and the orthorhombic structures remained stable at all the selected pressure (0, 1.78 and 2.5 GPa), where detailed calculations were performed, while the rhombohedral structure is only stable from the transition pressure 1.78 GPa. Pressure effect on the bandgap is minimal due to the small range of pressure considered in this study. The meta-GGA MBJ functional predicts bandgaps which are in good agreement with available experimental values.

  10. Quantum mechanical investigation of CO, NO and HCN adsorption on Ag8 nanoclusters; (structural, electronic and topological properties)

    NASA Astrophysics Data System (ADS)

    Akbarzadeh, Hadi; Torbatian, Zahra; Javad Hashemifar, S.

    2012-02-01

    We used DFT-GW method to study pure Ag8 nanocluster and CO, NO, HCN adsorption on it. The pure Ag8 stabilizes in Td structure and the behavior of binding energy is consistent with the total charge density at bond points while bond length exhibits a behavior similar to the mean bond charge. Adsorption of CO, NO and HCN molecules on different atomic sites of Ag8 were studied and it was found that all these molecules, mainly due to electron donation, prefer to be adsorbed by LUMO orbital. This finding is in qualitative agreement with the experimental observation of the enhanced binding of CO molecule on positively charged silver atoms, compared with the neutral and negatively charged samples [J. Phys. Chem. A 2006, 110, 7167-7172]. Our calculation shows no significant charge transfer during NO adsorption on Ag8. The CO, NO and HCN adsorbed nanoclusters as well as cationic and anionic samples do not stabilize in Td structure. This charge induced geometry transition is related to the high (low) value of LUMO (HOMO) state in Td structure which indicates high energy cost of electron donation (acceptation) in this isomer. The topological analysis of electron density clarify that the adsorption energy of molecules on Ag8 is consistent with the value of the charge density at the topological bond point between molecule and nanocluster.

  11. Unusual surface and edge morphologies, sp2 to sp3 hybridized transformation and electronic damage after Ar+ ion irradiation of few-layer graphene surfaces.

    PubMed

    Al-Harthi, Salim Hamood; Elzain, Mohammed; Al-Barwani, Muataz; Kora'a, Amal; Hysen, Thomas; Myint, Myo Tay Zar; Anantharaman, Maliemadom Ramaswamy

    2012-01-01

    Roughness and defects induced on few-layer graphene (FLG) irradiated by Ar+ ions at different energies were investigated using X-ray photoemission spectroscopy (XPS) and atomic force microscopy techniques. The results provide direct experimental evidence of ripple formation, sp2 to sp3 hybridized carbon transformation, electronic damage, Ar+ implantation, unusual defects and edge reconstructions in FLG, which depend on the irradiation energy. In addition, shadowing effects similar to those found in oblique-angle growth of thin films were seen. Reliable quantification of the transition from the sp2-bonding to sp3-hybridized state as a result of Ar+ ion irradiation is achieved from the deconvolution of the XPS C (1s) peak. Although the ion irradiation effect is demonstrated through the shape of the derivative of the Auger transition C KVV spectra, we show that the D parameter values obtained from these spectra which are normally used in the literature fail to account for the sp2 to sp3 hybridization transition. In contrast to what is known, it is revealed that using ion irradiation at large FLG sample tilt angles can lead to edge reconstructions. Furthermore, FLG irradiation by low energy of 0.25 keV can be a plausible way of peeling graphene layers without the need of Joule heating reported previously. PMID:22901368

  12. Structural transformation of hydrogen-adsorbed Si(111)-√3×√3-Ag surfaces induced by electron-stimulated desorption

    NASA Astrophysics Data System (ADS)

    Watanabe, Heiji; Ichikawa, Masakazu

    1997-07-01

    Atomic hydrogen irradiated Si(111)-√3×√3-Ag surfaces, which involve nanometer size Ag clusters and hydrogen terminated regions, are studied by combined surface analysis with ultrahigh-vacuum scanning electron microscopy (UHV-SEM), scanning reflection electron microscopy (SREM), microprobe reflection high-energy electron diffration (μ-RHEED) and Auger electron spectroscopy (AES). Electron beam irradiation onto this surface results in disappearance of the Ag clusters, and subsequent low-temperature annealing at 275°C transforms the surface to the original √3×√3-Ag structure. Hydrogen removal from the Si surface induced by electron-stimulated desorption (ESD) and surface diffusion of Ag atoms on the bare regions by low-temperature annealing explain this structural transformation.

  13. Atomic and electronic structures evolution of the narrow band gap semiconductor Ag2Se under high pressure

    NASA Astrophysics Data System (ADS)

    Naumov, P.; Barkalov, O.; Mirhosseini, H.; Felser, C.; Medvedev, S. A.

    2016-09-01

    Non-trivial electronic properties of silver telluride and other chalcogenides, such as the presence of a topological insulator state, electronic topological transitions, metallization, and the possible emergence of superconductivity under pressure have attracted attention in recent years. In this work, we studied the electronic properties of silver selenide (Ag2Se). We performed direct current electrical resistivity measurements, in situ Raman spectroscopy, and synchrotron x-ray diffraction accompanied by ab initio calculations to explore pressure-induced changes to the atomic and electronic structure of Ag2Se. The temperature dependence of the electrical resistivity was measured up to 30 GPa in the 4–300 K temperature interval. Resistivity data showed an unusual increase in the thermal energy gap of phase I, which is a semiconductor under ambient conditions. Recently, a similar effect was reported for the 3D topological insulator Bi2Se3. Raman spectroscopy studies revealed lattice instability in phase I indicated by the softening of observed vibrational modes with pressure. Our hybrid functional band structure calculations predicted that phase I of Ag2Se would be a narrow band gap semiconductor, in accordance with experimental results. At a pressure of ~7.5 GPa, Ag2Se underwent a structural transition to phase II with an orthorhombic Pnma structure. The temperature dependence of the resistivity of Ag2Se phase II demonstrated its metallic character. Ag2Se phase III, which is stable above 16.5 GPa, is also metallic according to the resistivity data. No indication of the superconducting transition is found above 4 K in the studied pressure range.

  14. Atomic and electronic structures evolution of the narrow band gap semiconductor Ag2Se under high pressure.

    PubMed

    Naumov, P; Barkalov, O; Mirhosseini, H; Felser, C; Medvedev, S A

    2016-09-28

    Non-trivial electronic properties of silver telluride and other chalcogenides, such as the presence of a topological insulator state, electronic topological transitions, metallization, and the possible emergence of superconductivity under pressure have attracted attention in recent years. In this work, we studied the electronic properties of silver selenide (Ag2Se). We performed direct current electrical resistivity measurements, in situ Raman spectroscopy, and synchrotron x-ray diffraction accompanied by ab initio calculations to explore pressure-induced changes to the atomic and electronic structure of Ag2Se. The temperature dependence of the electrical resistivity was measured up to 30 GPa in the 4-300 K temperature interval. Resistivity data showed an unusual increase in the thermal energy gap of phase I, which is a semiconductor under ambient conditions. Recently, a similar effect was reported for the 3D topological insulator Bi2Se3. Raman spectroscopy studies revealed lattice instability in phase I indicated by the softening of observed vibrational modes with pressure. Our hybrid functional band structure calculations predicted that phase I of Ag2Se would be a narrow band gap semiconductor, in accordance with experimental results. At a pressure of ~7.5 GPa, Ag2Se underwent a structural transition to phase II with an orthorhombic Pnma structure. The temperature dependence of the resistivity of Ag2Se phase II demonstrated its metallic character. Ag2Se phase III, which is stable above 16.5 GPa, is also metallic according to the resistivity data. No indication of the superconducting transition is found above 4 K in the studied pressure range. PMID:27439023

  15. Atomic and electronic structures evolution of the narrow band gap semiconductor Ag2Se under high pressure

    NASA Astrophysics Data System (ADS)

    Naumov, P.; Barkalov, O.; Mirhosseini, H.; Felser, C.; Medvedev, S. A.

    2016-09-01

    Non-trivial electronic properties of silver telluride and other chalcogenides, such as the presence of a topological insulator state, electronic topological transitions, metallization, and the possible emergence of superconductivity under pressure have attracted attention in recent years. In this work, we studied the electronic properties of silver selenide (Ag2Se). We performed direct current electrical resistivity measurements, in situ Raman spectroscopy, and synchrotron x-ray diffraction accompanied by ab initio calculations to explore pressure-induced changes to the atomic and electronic structure of Ag2Se. The temperature dependence of the electrical resistivity was measured up to 30 GPa in the 4-300 K temperature interval. Resistivity data showed an unusual increase in the thermal energy gap of phase I, which is a semiconductor under ambient conditions. Recently, a similar effect was reported for the 3D topological insulator Bi2Se3. Raman spectroscopy studies revealed lattice instability in phase I indicated by the softening of observed vibrational modes with pressure. Our hybrid functional band structure calculations predicted that phase I of Ag2Se would be a narrow band gap semiconductor, in accordance with experimental results. At a pressure of ~7.5 GPa, Ag2Se underwent a structural transition to phase II with an orthorhombic Pnma structure. The temperature dependence of the resistivity of Ag2Se phase II demonstrated its metallic character. Ag2Se phase III, which is stable above 16.5 GPa, is also metallic according to the resistivity data. No indication of the superconducting transition is found above 4 K in the studied pressure range.

  16. Structural and electronic properties of V2O3 ultrathin film on Ag(001): LEED and photoemission study

    NASA Astrophysics Data System (ADS)

    Kundu, Asish K.; Menon, Krishnakumar S. R.

    2016-05-01

    V2O3 ultrathin films were grown on Ag(001) substrate by reactive evaporation of vanadium (V) metal in presence of oxygen and their structural and electronic properties were studied by Low Energy Electron Diffraction (LEED), X-ray Photo Electron Spectroscopy (XPS) and Angle Resolved Photoemission Spectroscopic (ARPES) techniques, respectively. On top of square symmetry substrate Ag(001), hexagonal surface of V2O3 (0001) is stabilized in the form of two domain structure, rotated by 30°(or 90°)to each other, has been observed by LEED. Rather than epitaxial flat monolayer, formation of well-ordered V2O3 (0001) island has been confirmed from the LEED and the Photoemission Spectroscopic (PES) study. Stoichiometry of the grown film was confirmed by the XPS study. Evolution of valance band electronic structure of V2O3 (0001) surface has been studied as a function of film thickness by ARPES.

  17. Photoconductivities from band states and a dissipative electron dynamics: Si(111) without and with adsorbed Ag clusters.

    PubMed

    Vazhappilly, Tijo; Hembree, Robert H; Micha, David A

    2016-01-14

    A new general computational procedure is presented to obtain photoconductivities starting from atomic structures, combining ab initio electronic energy band states with populations from density matrix theory, and implemented for a specific set of materials based on Si crystalline slabs and their nanostructured surfaces without and with adsorbed Ag clusters. The procedure accounts for charge mobility in semiconductors in photoexcited states, and specifically electron and hole photomobilities at Si(111) surfaces with and without adsorbed Ag clusters using ab initio energy bands and orbitals generated from a generalized gradient functional, however with excited energy levels modified to provide correct bandgaps. Photoexcited state populations for each band and carrier type were generated using steady state solution of a reduced density matrix which includes dissipative medium effects. The present calculations provide photoexcited electronic populations and photoinduced mobilities resulting from applied electric fields and obtained from the change of driven electron energies with their electronic momentum. Extensive results for Si slabs with 8 layers, without and with adsorbed Ag clusters, show that the metal adsorbates lead to substantial increases in the photomobility and photoconductivity of electrons and holes. PMID:26772554

  18. Effect of exogenous electron shuttles on growth and fermentative metabolism in Clostridium sp. BC1

    SciTech Connect

    Yarlagadda V. N.; Francis A.; Gupta, A.; Dodge, C. J.

    2012-03-01

    In this study, the influence exogenous electron shuttles on the growth and glucose fermentative metabolism of Clostridium sp. BC1 was investigated. Bicarbonate addition to mineral salts (MS) medium accelerated growth and glucose fermentation which shifted acidogenesis (acetic- and butyric-acids) towards solventogenesis (ethanol and butanol). Addition of ferrihydrite, anthraquinone disulfonate, and nicotinamide adenine dinucleotide in bicarbonate to growing culture showed no significant influence on fermentative metabolism. In contrast, methyl viologen (MV) enhanced ethanol- and butanol-production by 28- and 12-fold, respectively with concomitant decrease in hydrogen, acetic- and butyric-acids compared to MS medium. The results show that MV addition affects hydrogenase activity with a significant reduction in hydrogen production and a shift in the direction of electron flow towards enhanced production of ethanol and butanol.

  19. Electronic structure and conductivity of nanocomposite metal (Au,Ag,Cu,Mo)-containing amorphous carbon films

    SciTech Connect

    Endrino, Jose L.; Horwat, David; Gago, Raul; Andersson, Joakim; Liu, Y.S.; Guo, Jinghua; Anders, Andre

    2008-05-14

    In this work, we study the influence of the incorporation of different metals (Me = Au, Ag, Cu, Mo) on the electronic structure of amorphous carbon (a-C:Me) films. The films were produced at room temperature using a novel pulsed dual-cathode arc deposition technique. Compositional analysis was performed with secondary neutral mass spectroscopy whereas X-ray diffraction was used to identify the formation of metal nanoclusters in the carbon matrix. The metal content incorporated in the nanocomposite films induces a drastic increase in the conductivity, in parallel with a decrease in the band gap corrected from Urbach energy. The electronic structure as a function of the Me content has been monitored by x-ray absorption near edge structure (XANES) at the C K-edge. XANES showed that the C host matrix has a dominant graphitic character and that it is not affected significantly by the incorporation of metal impurities, except for the case of Mo, where the modifications in the lineshape spectra indicated the formation of a carbide phase. Subtle modifications of the spectral lineshape are discussed in terms of nanocomposite formation.

  20. The structural and electronic properties of cubic AgMO3 (M=Nb, Ta) by first principles calculations

    NASA Astrophysics Data System (ADS)

    Prasad, K. Ganga; Niranjan, Manish K.; Asthana, Saket

    2016-05-01

    We report the electronic structure of the AgMO3(M=Nb, Ta) within the frame work of density functional theory and calculations are performed within the generalized gradient approximation (GGA) by using ultrasoft pseudopotentials. The calculated equilibrium lattice parameters and volumes are extracted from fitting of Birch third order equation of state and which are reasonable agreement with the available experimental results. The density of states,band structure of Ag(Nb,Ta)O3 reveals that the valance bands mostly occupied with O-2p and O-2s states and whereas conduction band occupied with Nb (Ta) 4d(5d) states including less contribution from Ag 5s states.

  1. Ultrafast electronic response of Ag(111) and Cu(111) surfaces: From early excitonic transients to saturated image potential

    NASA Astrophysics Data System (ADS)

    Silkin, V. M.; Lazić, P.; Došlić, N.; Petek, H.; Gumhalter, B.

    2015-10-01

    We investigate the evolution of attosecond to femtosecond screening and emergent potentials that govern the dynamics and energetics of electrons and holes excited in the various stages of multiphoton photoemission processes and control the photoelectron yield in recently reported experiments [X. Cui, C. Wang, A. Argondizzo, S. Garrett-Roe, B. Gumhalter, and H. Petek, Nat. Phys. 10, 505 (2014), 10.1038/nphys2981]. The study is focused on the dynamical screening of holes created in preexistent quasi-two-dimensional Shockley state bands on Ag(111) and Cu(111) surfaces and of electrons excited to the intermediate and emerging screened states. Using the formalism of self-consistent electronic response, we analyze first the effects of screening on the dynamics of photoexcited electrons and holes and then of the Coulomb correlated photoexcited pair. Special attention is paid to the correlated primary electron-hole states, which commence as transient surface excitons and develop in the course of screening into uncorrelated electrons and holes propagating in the image potential and surface state bands, respectively. The obtained results enable to establish a consistent picture of transient electron dynamics at Ag(111) and Cu(111) surfaces that are becoming accessible by the time-, energy-, and momentum-resolved pump-probe multiphoton photoelectron spectroscopies.

  2. Enhancing photocatalysis in SrTiO3 by using Ag nanoparticles: A two-step excitation model for surface plasmon-enhanced photocatalysis.

    PubMed

    Ma, Lei; Sun, Tao; Cai, Hua; Zhou, Zhi-Quan; Sun, Jian; Lu, Ming

    2015-08-28

    Surface plasmon (SP)-enhanced ultraviolet and visible photocatalytic activities of SrTiO3 (STO) are observed after incorporating Ag nanoparticles (Ag-NPs) on STO surfaces. A two-step excitation model is proposed to explain the SP-enhanced photocatalysis. The point of the model is that an electron at the valence band of STO is first excited onto the Fermi level of Ag-NP by the SP field generated on the Ag-NP, and then injected into the conduction band of STO from the SP band, leaving a hole at the valence band of STO. A full redox catalytic reaction at the surface of STO is then available. For Ag-NP incorporated STO, up-converted and inter-band photoluminescence emissions of STO are observed, and nonlinear evolutions of photocatalytic activity with illumination light powers are found. Furthermore, near infrared photocatalysis is detected. These results support the proposed model.

  3. Enhancing photocatalysis in SrTiO{sub 3} by using Ag nanoparticles: A two-step excitation model for surface plasmon-enhanced photocatalysis

    SciTech Connect

    Ma, Lei; Sun, Tao; Cai, Hua; Zhou, Zhi-Quan; Sun, Jian E-mail: minglu55@fudan.edu.cn; Lu, Ming E-mail: minglu55@fudan.edu.cn

    2015-08-28

    Surface plasmon (SP)-enhanced ultraviolet and visible photocatalytic activities of SrTiO{sub 3} (STO) are observed after incorporating Ag nanoparticles (Ag-NPs) on STO surfaces. A two-step excitation model is proposed to explain the SP-enhanced photocatalysis. The point of the model is that an electron at the valence band of STO is first excited onto the Fermi level of Ag-NP by the SP field generated on the Ag-NP, and then injected into the conduction band of STO from the SP band, leaving a hole at the valence band of STO. A full redox catalytic reaction at the surface of STO is then available. For Ag-NP incorporated STO, up-converted and inter-band photoluminescence emissions of STO are observed, and nonlinear evolutions of photocatalytic activity with illumination light powers are found. Furthermore, near infrared photocatalysis is detected. These results support the proposed model.

  4. 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.

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

    PubMed

    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

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

    NASA Astrophysics Data System (ADS)

    Wang, Fuliang; Mao, Peng; He, Hu

    2016-02-01

    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.

  7. Structural and electronic features of binary Li2S-P2S5 glasses

    NASA Astrophysics Data System (ADS)

    Ohara, Koji; Mitsui, Akio; Mori, Masahiro; Onodera, Yohei; Shiotani, Shinya; Koyama, Yukinori; Orikasa, Yuki; Murakami, Miwa; Shimoda, Keiji; Mori, Kazuhiro; Fukunaga, Toshiharu; Arai, Hajime; Uchimoto, Yoshiharu; Ogumi, Zempachi

    2016-02-01

    The atomic and electronic structures of binary Li2S-P2S5 glasses used as solid electrolytes are modeled by a combination of density functional theory (DFT) and reverse Monte Carlo (RMC) simulation using synchrotron X-ray diffraction, neutron diffraction, and Raman spectroscopy data. The ratio of PSx polyhedral anions based on the Raman spectroscopic results is reflected in the glassy structures of the 67Li2S-33P2S5, 70Li2S-30P2S5, and 75Li2S-25P2S5 glasses, and the plausible structures represent the lithium ion distributions around them. It is found that the edge sharing between PSx and LiSy polyhedra increases at a high Li2S content, and the free volume around PSx polyhedra decreases. It is conjectured that Li+ ions around the face of PSx polyhedra are clearly affected by the polarization of anions. The electronic structure of the DFT/RMC model suggests that the electron transfer between the P ion and the bridging sulfur (BS) ion weakens the positive charge of the P ion in the P2S7 anions. The P2S7 anions of the weak electrostatic repulsion would causes it to more strongly attract Li+ ions than the PS4 and P2S6 anions, and suppress the lithium ionic conduction. Thus, the control of the edge sharing between PSx and LiSy polyhedra without the electron transfer between the P ion and the BS ion is expected to facilitate lithium ionic conduction in the above solid electrolytes.

  8. Structural and electronic features of binary Li2S-P2S5 glasses

    PubMed Central

    Ohara, Koji; Mitsui, Akio; Mori, Masahiro; Onodera, Yohei; Shiotani, Shinya; Koyama, Yukinori; Orikasa, Yuki; Murakami, Miwa; Shimoda, Keiji; Mori, Kazuhiro; Fukunaga, Toshiharu; Arai, Hajime; Uchimoto, Yoshiharu; Ogumi, Zempachi

    2016-01-01

    The atomic and electronic structures of binary Li2S-P2S5 glasses used as solid electrolytes are modeled by a combination of density functional theory (DFT) and reverse Monte Carlo (RMC) simulation using synchrotron X-ray diffraction, neutron diffraction, and Raman spectroscopy data. The ratio of PSx polyhedral anions based on the Raman spectroscopic results is reflected in the glassy structures of the 67Li2S-33P2S5, 70Li2S-30P2S5, and 75Li2S-25P2S5 glasses, and the plausible structures represent the lithium ion distributions around them. It is found that the edge sharing between PSx and LiSy polyhedra increases at a high Li2S content, and the free volume around PSx polyhedra decreases. It is conjectured that Li+ ions around the face of PSx polyhedra are clearly affected by the polarization of anions. The electronic structure of the DFT/RMC model suggests that the electron transfer between the P ion and the bridging sulfur (BS) ion weakens the positive charge of the P ion in the P2S7 anions. The P2S7 anions of the weak electrostatic repulsion would causes it to more strongly attract Li+ ions than the PS4 and P2S6 anions, and suppress the lithium ionic conduction. Thus, the control of the edge sharing between PSx and LiSy polyhedra without the electron transfer between the P ion and the BS ion is expected to facilitate lithium ionic conduction in the above solid electrolytes. PMID:26892385

  9. Isolation of a Diborane(6) Dication: Formation and Cleavage of an Electron-Precise B(sp(3))-B(sp(3)) Bond.

    PubMed

    Kong, Lingbing; Lu, Wei; Li, Yongxin; Ganguly, Rakesh; Kinjo, Rei

    2016-07-13

    One-electron oxidation of organoboron L2PhB: 1 (L = oxazol-2-ylidene) afforded a dicationic diborane(6) species [L2PhB-BPhL2]·2X (X = OTf, BF4, AlCl4) 3, representing a new strategy to construct a B(sp(3))-B(sp(3)) covalent bond. Each boron atom in 3 is in the formal oxidation state +II, and tetracoordinate with a Ph group and two oxazol-2-ylidenes. The cyclic voltammetry of 3 shows irreversible reduction and oxidation. Indeed, two-electron reduction of 3 with potassium graphite (KC8) afforded 1, making a fully reversible 1 ↔ 3 redox system, whereas two-electron oxidation with AuCl produced a boronium [L2PhBCl]OTf 4. Moreover, the reactions of 3 with isonitrile derivatives RNC: under heating conditions gave a cyano-substituted boronium [L2PhBCN]BF4 5 and a 2-boranyl-indole derivative 6, depending on the substituent R. The proposed reaction mechanism involves a borinylium radical 1(•+) which is generated via a homolytic cleavage of the B-B bond of 3. PMID:27309118

  10. The nature of the Ag-staining of nucleolus organizer regions. Electron- and light-microscopic studies on human cells in interphase, mitosis, and meiosis.

    PubMed

    Schwarzacher, H G; Mikelsaar, A V; Schnedl, W

    1978-01-01

    Electron micrographs reveal that the Ag-stainable substance is located on the outside of NOR's or around them but not in the chromosomes themselves. In association figures, the Ag-positive material lies between the acrocentric chromosomes. Light-microscopic studies show that the Ag stainability of the nucleolus in interphase is correlated with the function of the NOR, as seen from inactive and activated lymphocytes. Much more Ag-positive material is seen in prophase than in meta- and anaphase. It starts to increase again in late telophase. In male meiosis the NOR's remain Ag-positive until pachytene. First and second metaphase figures are negative. Experiments using RNase, TCA, and trypsin indicate that the Ag-stainable substance is an acidic protein. The precipitation of Ag granules in interphase nuclei seen in the electron microscope is greatest over the fibrillar component of the nucleolus. The most likely interpretation is that the Ag-stainable material is a component of ribonucleic protein accumulating around active NOR's. In mitosis some of this material remains at the NOR's. In first meiosis it is completely removed before diakinesis. PMID:77208

  11. Evidence for hybrid surface metallic band in (4 × 4) silicene on Ag(111)

    SciTech Connect

    Tsoutsou, D. Xenogiannopoulou, E.; Golias, E.; Tsipas, P.; Dimoulas, A.

    2013-12-02

    The electronic band structure of monolayer (4 × 4) silicene on Ag(111) is imaged by angle resolved photoelectron spectroscopy. A dominant hybrid surface metallic band is observed to be located near the bulk Ag sp-band which is also faintly visible. The two-dimensional character of the hybrid band has been distinguished against the bulk character of the Ag(111) sp-band by means of photon energy dependence experiments. The surface band exhibits a steep linear dispersion around the K{sup ¯}{sub Ag} point and has a saddle point near the M{sup ¯}{sub Ag} point of Ag(111) resembling the π-band dispersion in graphene.

  12. Generation of attosecond electron packets via conical surface plasmon electron acceleration

    PubMed Central

    Greig, S. R.; Elezzabi, A. Y.

    2016-01-01

    We present a method for the generation of high kinetic energy attosecond electron packets via magnetostatic and aperture filtering of conical surface plasmon (SP) accelerated electrons. The conical SP waves are excited by coupling an ultrafast radially polarized laser beam to a conical silica lens coated with an Ag film. Electromagnetic and particle tracking models are employed to characterize the ultrafast electron packets. PMID:26764129

  13. Trimethylamine oxide respiration in Proteus sp. strain NTHC153: electron transfer-dependent phosphorylation and L-serine transport.

    PubMed Central

    Stenberg, E; Styrvold, O B; Strøm, A R

    1982-01-01

    Cells of Proteus sp. strains NTHC153 grown anaerobically with glucose and trimethylamine oxide (TMAO) were converted to spheroplasts by the penicillin method. The spheroplasts were lysed by osmotic shock, and the membrane vesicles were purified by sucrose gradient centrifugation. Vesicles energized electron transfer from formate to TMAO displayed active anaerobic transport of serine. An anaerobic cell-free extract of Proteus sp. disrupted in a French pressure cell reduced TMAO with formate and NADH with the concomitant formation of organic phosphate. The net P/2e- ratios determined were 0.1 and 0.3, respectively. The NADH- and TMAO-dependent phosphorylation was sensitive to uncouplers of oxidative phosphorylation (protonophores), and the formate- and TMAO-dependent serine transport was sensitive to ionophores and protonophores. We conclude that TMAO reduction in Proteus sp. fulfills the essential features of anaerobic respiration. PMID:6798018

  14. Light and electron microscope observations on Nephroselmis gaoae sp. nov. (Prasinophyceae)

    NASA Astrophysics Data System (ADS)

    Tseng, C. K.; Jiao-Fen, Chen; Zhe-Fu, Zhang; Hui-Qi, Zhang

    1994-09-01

    Nephroselmis gaoae sp. nov. is described on the basis of light and electron microscope observations of cultured material originally collected and isolated from seawater of Jiaozhou Bay, Qingdao, China. The periplasts on the cell body and flagella are covered by five types of scales, two types on the flagella and three on the body. Among these, the morphology and the number of spines of large stellate body scales differ remarkably from those of previously described species of Nephroselmis. Apart from these, the unusual fine structure of the eyespot (stigma) is very characteristic. As in the other species of Nephroselmis, the eyespot lies immediately under the two-membraned chloroplast envelope; unlike the others, however, it is not composed of a number of osmiophilic globules, but consists of about 14 curved rod-shaped osmiophilic bodies arranged loosely and randomly. This feature distinguishes the present new species not only from the other species of Nephroselmis but also from the other motile algal species, the eyespots structure of which had been previously described.

  15. Relation between transport and thermodynamic properties in liquid sp-electron metals near freezing.

    PubMed

    Alonso, J A; March, N H

    1999-10-01

    Classical statistical mechanics based on assumed pair potentials leads, for liquid metals, to an approximate relation between shear viscosity eta, surface tension sigma, and thermal velocity vT defined as (kBT/M)(1/2), with M the ionic mass. Theory predicts for the dimensionless grouping sigma/etav(T) evaluated at the melting temperature Tm a single value 15 / 16; liquid sp-electron metals exhibit, however, a scatter from around 0.7 to 2.3. Therefore, an alternative grouping sigma/etav(s), with v(s) the velocity of sound, is considered here in detail, first using experimental data and second using both theoretical and semiempirical arguments. The scatter of sigma/etav(s) at Tm is less than for the earlier grouping, and also insight can be gained as to various physical factors determining sigma/etav(s). In essence, this quantity is proportional to the product of two factors, both dimensionless, namely, the surface thickness L measured in units of the mean interionic separation, and the square root of the energy Mv(2)s, measured in units of the thermal energy kBTm. Theoretical estimates are made of both of these factors, in fair accord with the experimental data. PMID:11970248

  16. Effect of electron donors on the fractionation of sulfur isotopes by a marine Desulfovibrio sp.

    NASA Astrophysics Data System (ADS)

    Sim, Min Sub; Ono, Shuhei; Donovan, Katie; Templer, Stefanie P.; Bosak, Tanja

    2011-08-01

    Sulfur isotope effects produced by microbial dissimilatory sulfate reduction are used to reconstruct the coupled cycling of carbon and sulfur through geologic time, to constrain the evolution of sulfur-based metabolisms, and to track the oxygenation of Earth's surface. In this study, we investigate how the coupling of carbon and sulfur metabolisms in batch and continuous cultures of a recently isolated marine sulfate reducing bacterium DMSS-1, a Desulfovibrio sp ., influences the fractionation of sulfur isotopes. DMSS-1 grown in batch culture on seven different electron donors (ethanol, glycerol, fructose, glucose, lactate, malate and pyruvate) fractionates 34S/ 32S ratio from 6‰ to 44‰, demonstrating that the fractionations by an actively growing culture of a single incomplete oxidizing sulfate reducing microbe can span almost the entire range of previously reported values in defined cultures. The magnitude of isotope effect correlates well with cell specific sulfate reduction rates (from 0.7 to 26.1 fmol/cell/day). DMSS-1 grown on lactate in continuous culture produces a larger isotope effect (21-37‰) than the lactate-grown batch culture (6‰), indicating that the isotope effect also depends on the supply rate of the electron donor and microbial growth rate. The largest isotope effect in continuous culture is accompanied by measurable changes in cell length and cellular yield that suggest starvation. The use of multiple sulfur isotopes in the model of metabolic fluxes of sulfur shows that the loss of sulfate from the cell and the intracellular reoxidation of reduced sulfur species contribute to the increase in isotope effects in a correlated manner. Isotope fractionations produced during sulfate reduction in the pure culture of DMSS-1 expand the previously reported range of triple sulfur isotope effects ( 32S, 33S, and 34S) by marine sulfate reducing bacteria, implying that microbial sulfur disproportionation may have a smaller 33S isotopic fingerprint

  17. Electronic structure and optical properties of Ag{sub 3}PO{sub 4} photocatalyst calculated by hybrid density functional method

    SciTech Connect

    Liu, J. J.; Fu, X. L.; Chen, S. F.; Zhu, Y. F.

    2011-11-07

    The electronic structure and optical properties of Ag{sub 3}PO{sub 4} were studied by hybrid density functional theory. The results indicated that the band gap is 2.43 eV, which agrees well with the experimental value of 2.45 eV. The conduction bands of Ag{sub 3}PO{sub 4} are mainly attributable to Ag 5s and 5p states, while the valence bands are dominated by O 2p and Ag 4d states. The highest valence band edge potential was 2.67 V (vs. normal hydrogen electrode), which has enough driving force for photocatalytic water oxidation and pollutants degradation. The optical absorption spectrum showed that Ag{sub 3}PO{sub 4} is a visible light response photocatalyst.

  18. Optical properties and electronic band structure of AgGaTe2 chalcopyrite semiconductor.

    PubMed

    Arai, Shinya; Ozaki, Shunji; Adachi, Sadao

    2010-02-10

    The optical properties of AgGaTe(2) chalcopyrite semiconductor are studied by optical absorption, spectroscopic ellipsometry (SE), and thermoreflectance (TR) spectroscopy. Optical absorption spectra suggest that AgGaTe(2) is a direct-gap semiconductor having a bandgap of approximately 1.2 eV at T=300 K. The pseudodielectric-function spectra of AgGaTe(2) are determined by SE in the range between E=1.2 and 5.2 eV for both states of polarization. These spectra reveal distinct structures at energies of the critical points in the Brillouin zone. The TR spectra are also measured in the E=1.0-5.3 eV ranges at T=20 K-300 K. The spin-orbit and crystal-field splitting parameters of AgGaTe(2) are determined to be Delta(so)=0.70 eV and Delta(cr)=-0.23 eV, respectively.

  19. 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

  20. Electronic structure, transport, and phonons of SrAgChF (Ch = S,Se,Te): Bulk superlattice thermoelectrics

    DOE PAGES

    Gudelli, Vijay Kumar; Kanchana, V.; Vaitheeswaran, G.; Singh, David J.; Svane, Axel; Christensen, Niels Egede; Mahanti, Subhendra D.

    2015-07-15

    Here, we report calculations of the electronic structure, vibrational properties, and transport for the p-type semiconductors, SrAgChF (Ch = S, Se, and Te). We find soft phonons with low frequency optical branches intersecting the acoustic modes below 50 cm–1, indicative of a material with low thermal conductivity. The bands at and near the valence-band maxima are highly two-dimensional, which leads to high thermopowers even at high carrier concentrations, which is a combination that suggests good thermoelectric performance. These materials may be regarded as bulk realizations of superlattice thermoelectrics.

  1. Atom probe tomography and transmission electron microscopy characterisation of precipitation in an Al-Cu-Li-Mg-Ag alloy.

    PubMed

    Gault, B; de Geuser, F; Bourgeois, L; Gabble, B M; Ringer, S P; Muddle, B C

    2011-05-01

    State-of-the art atom probe tomography (APT) combined with transmission electron microscopy (TEM) were used to investigate the microstructure at different stages of the ageing process of an alloy of composition (at%) Al-1.68%Cu-4.62%Li-0.33%Mg-0.1%Ag. These alloys were shown to exhibit a complex microstructure of T(1) plates and several metastable phases, including θ' and S. We will highlight the early stages of clustering, precipitate interactions and possible solute segregation at the matrix/precipitate interfaces and detail the chemical composition of the different phases.

  2. Microstructural investigation of the oxidation behavior of Cu in Ag-coated Cu films using a focused ion beam transmission electron microscopy technique

    NASA Astrophysics Data System (ADS)

    Kim, Ji Hwan; Lee, Jong-Hyun

    2016-06-01

    With the aim of elucidating a detailed mechanism for the oxidation behavior in submicron Cu particles coated with a thin Ag layer, the dewetting of Ag and the oxidation behavior of Cu in Ag-coated Cu films upon heating were investigated with a focused ion beam transmission electron microscopy technique. A slight dewetting of the Ag layer began at approximately 200 °C and aggregates of Cu2O particles were formed on the Ag layer, indicating that the initial Cu2O phase was formed on the thin Ag layer. Voids were formed in the Cu layer because of Cu atoms diffusing through the thin Ag layer to be oxidized in the upper Cu2O aggregates. After being heated to 250 °C, the Ag layer became more irregular, and in some regions, it disappeared because of intensive dewetting. The number and average size of the voids also increased. At 300 °C, a hollow structure with a Cu2O shell was formed. Pillar-like structures of unoxidized Cu and large voids were found under the Cu2O layer.

  3. Epitaxial Ag(001) grown on MgO(001) and TiN(001): Twinning, surface morphology, and electron surface scattering

    SciTech Connect

    Chawla, J. S.; Gall, D.

    2012-02-15

    Epitaxial Ag(001) layers were deposited on MgO(001) in order to study electron surface scattering. X-ray reflection indicates 3D layer nucleation with a high rms surface roughness of 1.0 nm for a layer thickness d = 3.5 nm. X-ray diffraction shows that {l_brace}111{r_brace} twins form at d < 11 nm, followed by 2nd generation twinning for 11 nm < d < 120 nm. Increasing the growth temperature from 25 to 150 deg. C suppresses 2nd generation twinning and reduces the twin density by 2 orders of magnitude. In situ deposition of epitaxial 2.5-nm-thick TiN(001) underlayers prior to Ag deposition results in twin-free single-crystal Ag(001) with 10 x smoother surfaces for d = 3.5 nm. This is attributed to a better wetting on the higher energy TiN(001) than MgO(001) surface, resulting in the absence of 3D nuclei with exposed {l_brace}111{r_brace} facets, which facilitate twin nucleation. The twinned Ag/MgO layers have a higher resistivity {rho} than the single crystal Ag/TiN layers at both 298 and 77 K, due to electron scattering at grain and twin boundaries. The {rho} for single-crystal Ag layers increases with decreasing d, which is well explained with known surface scattering models and provides specularity parameters for the Ag-vacuum and the Ag-air interfaces of p = 0.8 {+-} 0.1 and 0.4 {+-} 0.1, respectively. A comparison with corresponding epitaxial Cu(001) layers shows that {rho}{sub Ag} < {rho}{sub Cu} for d > 50 nm, consistent with known bulk values. However, {rho}{sub Ag} > {rho}{sub Cu} for d < 40 nm. This is attributed to the larger electron mean free path for electron-phonon scattering and a correspondingly higher resistivity contribution from surface scattering in Ag than Cu. In contrast, air exposure causes {rho}{sub Ag} < {rho}{sub Cu} for all d, due to diffuse scattering at the oxidized Cu surface and the correspondingly higher Cu resistivity.

  4. The effect of Ag adsorption on the structural, electronic, and optical properties of the ZnO (10 1 ̅ 0) surface: A first-principles study

    NASA Astrophysics Data System (ADS)

    Lahmer, M. A.

    2016-09-01

    The effect of the Ag adsorption on the structural, electronic and optical properties of the clean ZnO(10 1 ̅ 0) surface was investigated using the first principles method. The obtained results show that adsorbed Ag atoms transfer charge to the surface which results in a charge accumulation in near-surface region accompanied with a decrease of the work function. On the other hand, our results show that the adsorption of Ag atoms leads also to the new optical absorption peaks in the visible region which could improve ZnO photocatalytical properties.

  5. Microalgae associated Brevundimonas sp. MSK 4 as the nano particle synthesizing unit to produce antimicrobial silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Rajamanickam, Karthic; Sudha, S. S.; Francis, Mebin; Sowmya, T.; Rengaramanujam, J.; Sivalingam, Periyasamy; Prabakar, Kandasamy

    2013-09-01

    The biosynthesis of silver nanoparticles and its antimicrobial property was studied using bacteria isolated from Spirulina products. Isolated bacteria were identified as Bacillus sp. MSK 1 (JX495945), Staphylococcus sp. MSK 2 (JX495946), Bacillus sp. MSK 3 (JX495947) and Brevundimonas sp. MSK 4 (JX495948). Silver nanoparticles (AgNPs) were synthesized using bacterial culture filtrate with AgNO3. The initial syntheses of Ag nanoparticles were characterized by UV-vis spectrophotometer (by measuring the color change to intense brown). Fourier Transform Infrared Spectroscopy (FTIR) study showed evidence that proteins are possible reducing agents and Energy-dispersive X-ray (EDX) study showing the metal silver as major signal. The structure of AgNPs was determined by Scanning electron microscopy (SEM) and X-ray diffraction (XRD). Synthesized Ag nanoparticles with an average size of 40-65 nm have antimicrobial property against human pathogens like Proteus vulgaris, Salmonella typhi, Vibrio cholera, Streptococcus sp., Bacillus subtilis, Staphylococcus aureus, and Escherichia coli. Among the isolates Brevundimonas sp. MSK 4 alone showed good activity in both synthesis of AgNPs and antimicrobial activity. This work demonstrates the possible use of biological synthesized silver nanoparticles to combat the drug resistant problem.

  6. [Anaerobic reduction of humus/Fe (III) and electron transport mechanism of Fontibacter sp. SgZ-2].

    PubMed

    Ma, Chen; Yang, Gui-qin; Lu, Qin; Zhou, Shun-gui

    2014-09-01

    Humus and Fe(III) respiration are important extracellular respiration metabolism. Electron transport pathway is the key issue of extracellular respiration. To understand the electron transport properties and the environmental behavior of a novel Fe(III)- reducing bacterium, Fontibacter sp. SgZ-2, capacities of anaerobic humus/Fe(III) reduction and electron transport mechanisms with four electron acceptors were investigated in this study. The results of anaerobic batch experiments indicated that strain SgZ-2 had the ability to reduce humus analog [ 9,10-anthraquinone-2,6-disulfonic acid (AQDS) and 9,10-anthraquinone-2-sulfonic acid (AQS)], humic acids (HA), soluble Fe(III) (Fe-EDTA and Fe-citrate) and Fe(III) oxides [hydrous ferric oxide (HFO)]. Fermentative sugars (glucose and sucrose) were the most effective electron donors in the humus/Fe(III) reduction by strain SgZ-2. Additionally, differences of electron carrier participating in the process of electron transport with different electron acceptors (i. e. , oxygen, AQS, Fe-EDTA and HFO) were investigated using respiratory inhibitors. The results suggested that similar respiratory chain components were involved in the reducing process of oxygen and Fe-EDTA, including dehydrogenase, quinones and cytochromes b-c. In comparison, only dehydrogenase was found to participate in the reduction of AQS and HFO. In conclusion, different electron transport pathways may be employed by strain SgZ-2 between insoluble and soluble electron acceptors or among soluble electron acceptors. Preliminary models of electron transport pathway with four electron acceptors were proposed for strain SgZ-2, and the study of electron transport mechanism was explored to the genus Fontibacter. All the results from this study are expected to help understand the electron transport properties and the environmental behavior of the genus Fontibacter.

  7. Illustration of high-active Ag2CrO4 photocatalyst from the first-principle calculation of electronic structures and carrier effective mass

    NASA Astrophysics Data System (ADS)

    Zhang, Jinfeng; Yu, Weilai; Liu, Jianjun; Liu, Baoshun

    2015-12-01

    Although Ag2CrO4 has been frequently studied as a highly active photocatalytic material under visible light irradiation in recent years, we are still less-known on its detailed mechanism. Also, it is difficult to illustrate this issue just from the experimental discussion. Contrarily, theoretical investigation can deepen our understanding on its photocatalytic mechanism from the electronic level. In this work, the crystal structures, band structures, density of states, and chemical bonding for Ag2CrO4 were studied by the first-principles calculation based on the density functional theory. The calculation results indicate that Ag2CrO4 has an indirect band gap of ca. 1.42 eV, a deep position of valence band edge and a strong optical absorption coefficient, implying that Ag2CrO4 has strong oxidation ability and high photocatalytic activity for decomposing organic pollutant under visible light irradiation. Moreover, our calculation also indicates that Ag2CrO4 has small effective mass of electrons and holes, and great effective mass difference between hole and electron, which can respectively facilitate the migration and separation of electrons and holes, and finally improve the photocatalytic performance.

  8. Ion-modulated nonlinear electronic transport in carbon nanotube bundle/RbAg{sub 4}I{sub 5} thin film composite nanostructures

    SciTech Connect

    Sun, Jia-Lin; Zhang, Wei; Wei, Jinquan; Gu, Bingfu

    2014-01-28

    We have explored the ion-modulated electronic transport properties of mixed ionic-electronic conductor (MIEC) composite nanostructures made of superionic conductor RbAg{sub 4}I{sub 5} films and carbon nanotube (CNT) bundle spiderwebs. Our experimental and theoretical studies indicate that the formation of ion-electron bound states (IEBSs) leads to strong ion-electron interference effect and interesting electronic transport of CNT, such as nonlinear current-voltage (I–V) characteristics and novel temperature dependence of the current. With increasing temperature, the hybrid nanostructures show rich phases with different dependence of current on temperature, which is related to the structural phase transition of RbAg{sub 4}I{sub 5} and the transition of dissociation of IEBSs. The ion-modulation of the electric conductivity in such MIEC composite nanostructures with great tunability has been used to design new ionic-electronic composite nano-devices with function like field effect transistor.

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

    NASA Astrophysics Data System (ADS)

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

    2014-04-01

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

  10. Electronic structure and photoelectrical properties of Ag2In2SiSe6 and Ag2In2GeSe6

    NASA Astrophysics Data System (ADS)

    Khyzhun, O. Y.; Myronchuk, G. L.; Zamuruyeva, O. V.; Parasyuk, O. V.

    2014-12-01

    High-quality Ag2In2SiSe6 and Ag2In2GeSe6 single crystals have been successfully grown by the vertical Bridgman-Stockbarger method and the horizontal gradient freeze technique, respectively. For pristine and Ar+ ion-irradiated surfaces of the single crystals under study, X-ray photoelectron core-level and valence-band spectra have been measured. Results of these studies allow for concluding that the Ag2In2SiSe6 and Ag2In2GeSe6 single crystal surfaces are sensitive with respect to Ar+ ion-irradiation. In particular, Ar+ ion-bombardment with energy of 3.0 keV during 5 min at an ion current density of 14 μA/cm2 has induced some modification in top surface layers leading to an increase of content of In atoms in the layers. Comparison on a common energy scale of the X-ray emission Se Kβ2 bands representing energy distribution of the Se 4p states and the X-ray photoelectron valence-band spectra reveal that the main contribution of the valence Se p states occur in the upper portion of the valence band, with also their significant contributions in other valence band regions of the Ag2In2SiSe6 and Ag2In2GeSe6 single crystals. In addition, for the single crystals under consideration, temperature dependences of specific dark conductivity and spectral distributions of photoconductivity have been explored. It has been established that the Ag2In2SiSe6 and Ag2In2GeSe6 single crystals are high-resistance semiconductors with value of the specific electrical conductivity σ ≈ 1.67 × 10-9 Ω-1 сm-1 (at Т = 300 K). The both compounds are materials with p-type conductivity.

  11. Single-Electron Transmetalation via Photoredox/Nickel Dual Catalysis: Unlocking a New Paradigm for sp(3)-sp(2) Cross-Coupling.

    PubMed

    Tellis, John C; Kelly, Christopher B; Primer, David N; Jouffroy, Matthieu; Patel, Niki R; Molander, Gary A

    2016-07-19

    The important role of transition metal-catalyzed cross-coupling in expanding the frontiers of accessible chemical territory is unquestionable. Despite empowering chemists with Herculean capabilities in complex molecule construction, contemporary protocols are not without their Achilles' heel: Csp(3)-Csp(2)/sp(3) coupling. The underlying challenge in sp(3) cross-couplings is 2-fold: (i) methods employing conventional, bench-stable precursors are universally reliant on extreme reaction conditions because of the high activation barrier of transmetalation; (ii) circumvention of this barrier invariably relies on use of more reactive precursors, thereby sacrificing functional group tolerance, operational simplicity, and broad applicability. Despite the ubiquity of this problem, the nature of the transmetalation step has remained unchanged from the seminal reports of Negishi, Suzuki, Kumada, and Stille, thus suggesting that the challenges in Csp(3)-Csp(2)/sp(3) coupling result from inherent mechanistic constraints in the traditional cross-coupling paradigm. Rather than submitting to the limitations of this conventional approach, we envisioned that a process rooted in single-electron reactivity could furnish the same key metalated intermediate posited in two-electron transmetalation, while demonstrating entirely complementary reactivity patterns. Inspired by literature reports on the susceptibility of organoboron reagents toward photochemical, single-electron oxidative fragmentation, realization of a conceptually novel open shell transmetalation framework was achieved in the facile coupling of benzylic trifluoroborates with aryl halides via cooperative visible-light activated photoredox and Ni cross-coupling catalysis. Following this seminal study, we disclosed a suite of protocols for the cross-coupling of secondary alkyl, α-alkoxy, α-amino, and α-trifluoromethylbenzyltrifluoroborates. Furthermore, the selective cross-coupling of Csp(3) organoboron moieties in the

  12. The effect of Ag diffusion on properties of YBa 2Cu 3O 7- x thin films produced by electron beam deposition techniques

    NASA Astrophysics Data System (ADS)

    Görür, O.; Küçükömeroğlu, T.; Terzioğlu, C.; Varilci, A.; Altunbaş, M.

    2005-01-01

    Superconducting YBa 2Cu 3O 7- x thin films were prepared on pure MgO and Ag/MgO substrates (without and with Ag buffer layer) using an electron beam evaporation technique. The effects of isothermal annealing temperature and Ag diffusion on the crystalline structure and some superconducting properties were investigated by X-ray diffraction, scanning electron microscopy, critical temperature, critical current density and room temperature resistivity measurements. The optimum annealing conditions causing a high degree of preferential orientation with the c-axis perpendicular to the substrates were found to be the isothermal annealing at 930 °C for 5 h. Annealing of films on Ag/MgO substrates is accompanied by Ag diffusion from the buffer layer into YBCO films. The higher rate of crystallization of the YBCO films, the higher degree of c-axis orientation, the higher dense surface morphology, the increased lattice parameter c (by ≈0.1%), the reduced room temperature resistivity (2-3 times), the slightly enchanced critical temperature ( Tc = 92 K at R = 0) and the critical current density ( Jc = 4.2 × 10 5 A/cm 2 at 77 K) were observed for the Ag-doped films (on Ag/MgO substrates) in comparison with those for the undoped films (on MgO substrates). The temperature dependence of the Ag diffusion coefficient in YBCO films in the range 600-800 °C was described by the relation D = 1.9 × 10 -6 exp(-0.73 eV/kT).

  13. Electron structure of AgCl nanocrystal with silver ion adsorbed on atomic-rough surface and quantum transitions

    NASA Astrophysics Data System (ADS)

    Timoshenko, Yury K.; Shunina, Valentina A.

    2009-08-01

    Adsorption was considered as on the atomically-rough surface (near the step and step fracture) as on the smooth surface. The electron structure of AgCl nanocrystals with the adsorbed silver ion were calculated by semiempirical tight-binding method relying on a self-consistent approach for the effective charges and dipole moments of the ions and in frame of DFT method B3LYP/HW. The quantum transitions were investigated in semiempirical approach. Visualization of the wave functions was performed for the localized states. Basing on the obtained data a conclusion is specically made that one can expect an enhancement of photoelectron localization with a decrease of the anions number in the substrate nearest to the adsorbed ion. It means that the most ecient trapping of photoelectron should occur under adsorption on a smooth surface rather than near the steps and their fractures as it was assumed previously. Also probabilities of quantum transitions for AgCl : J nanocrystal with the adsorbed silver ion were been discussed. This work is a continuation of paper [1].

  14. Angular dependence of L X-rays emission for Ag by 10 keV electron-impact

    NASA Astrophysics Data System (ADS)

    Wang, Xing; Xu, Zhongfeng; Zhang, Ying; Ma, Chao; Zhu, Chengwei

    2016-08-01

    The characteristic X-ray intensities of Ag-Lα, Lβ1, Lβ2 and Lγ1 are measured in electron-impact ionization at energy of 10 keV. The emission angle in this work ranges from 0° to 20° at interval of 5°. The angular dependence of L X-ray intensity ratios has been investigated for Lα / Lβ1, Lβ2 / Lβ1 and Lγ1 / Lβ1. It is found from the experimental results that the emissions of Lβ1, Lβ2 and Lγ1 X-rays are spatially isotropic, while the Lα X-rays exhibit anisotropic emission. Consequently, the alignment behavior of vacancy states is discussed with thorough analysis of vacancy transfer process.

  15. Ag K-shell ionization by electron impact: New cross-section measurements between 50 and 100 keV and review of previous experimental data

    NASA Astrophysics Data System (ADS)

    Vanin, V. R.; Manso Guevara, M. V.; Maidana, N. L.; Martins, M. N.; Fernández-Varea, J. M.

    2016-02-01

    We report the measurement of Ag K-shell ionization cross-section by electron impact in the range 50-100 keV and review the experimental data found in the literature. The sample consisted in a thin film of Ag evaporated on a thin C backing. The x-ray spectra generated by electron bombardment in the São Paulo Microtron were observed with a planar HPGe detector. The ratios between characteristic and bremsstrahlung x-ray yields were transformed to ionization cross sections with the help of theoretical atomic-field bremsstrahlung cross sections. The measured cross sections are compared with existing experimental values and calculations based on the semi-relativistic distorted-wave Born approximation. According to our experiment, the ratio of Ag Kβ to Kα x-ray intensities is 0.2018(24).

  16. Structural and electronic properties of polar MnO ultrathin film grown on Ag(111)

    NASA Astrophysics Data System (ADS)

    Kundu, Asish K.; Menon, Krishnakumar S. R.

    2016-05-01

    Surface electronic structure of ultrathin polar MnO film was studied by Low-energy Electron Diffraction (LEED) and Photoemission Spectroscopic (PES) techniques. Epitaxial monolayer to facet formation with increasing film thickness has been observed by LEED. Our LEED result shows p(2x2) surface reconstruction along with facet formation, stabilize the polar MnO(111) surface. The core levels and the valence band electronic structure of MnO films have been studied as a function of film thickness using X-ray and ultraviolet photoelectron spectroscopy techniques.

  17. Measurements of L-shell X-ray production cross-sections of Ag and Sb by low-energy electron impact

    NASA Astrophysics Data System (ADS)

    Zhao, J. L.; An, Z.; Zhu, J. J.; Tan, W. J.; Liu, M. T.

    2016-05-01

    The total L-shell X-ray production cross-sections of Ag and Sb elements were measured by detecting the characteristic X-rays induced by the electron impact in the energy range of 6-28 keV. In this experiment, the thin films with thick aluminum substrates were used as the targets, and the experimental setup was improved. The influence of multiple scattering of electrons penetrating the targets films, electrons reflected from the thick aluminum substrates and bremsstrahlung photons produced when incident electrons impacted the targets were corrected by using the Monte Carlo method. The experimental results determined in this paper were compared with some theoretical models and other available experimental data in the literature. It was shown that the L-shell X-ray production cross-sections of Ag and Sb elements measured in this paper were in good agreement with the theoretical predictions within the uncertainties.

  18. Influence of Carbon Sources and Electron Shuttles on Ferric Iron Reduction by Cellulomonas sp. Strain ES6

    SciTech Connect

    Dr Robin Gerlach; Erin K. Field; Sridhar Viamajala; Brent M. Peyton; William A. Apel; Al B. Cunningham

    2011-09-01

    Microbially reduced iron minerals can reductively transform a variety of contaminants including heavy metals, radionuclides, chlorinated aliphatics, and nitroaromatics. A number of Cellulomonas spp. strains, including strain ES6, isolated from aquifer samples obtained at the U.S. Department of Energy's Hanford site in Washington, have been shown to be capable of reducing Cr(VI), TNT, natural organic matter, and soluble ferric iron [Fe(III)]. This research investigated the ability of Cellulomonas sp. strain ES6 to reduce solid phase and dissolved Fe(III) utilizing different carbon sources and various electron shuttling compounds. Results suggest that Fe(III) reduction by and growth of strain ES6 was dependent upon the type of electron donor, the form of iron present, and the presence of synthetic or natural organic matter, such as anthraquinone-2,6-disulfonate (AQDS) or humic substances. This research suggests that Cellulomonas sp. strain ES6 could play a significant role in metal reduction in the Hanford subsurface and that the choice of carbon source and organic matter addition can allow for independent control of growth and iron reduction activity.

  19. Influence of carbon sources and electron shuttles on ferric iron reduction by Cellulomonas sp. strain ES6.

    PubMed

    Gerlach, Robin; Field, Erin K; Viamajala, Sridhar; Peyton, Brent M; Apel, William A; Cunningham, Al B

    2011-09-01

    Microbially reduced iron minerals can reductively transform a variety of contaminants including heavy metals, radionuclides, chlorinated aliphatics, and nitroaromatics. A number of Cellulomonas spp. strains, including strain ES6, isolated from aquifer samples obtained at the U.S. Department of Energy's Hanford site in Washington, have been shown to be capable of reducing Cr(VI), TNT, natural organic matter, and soluble ferric iron [Fe(III)]. This research investigated the ability of Cellulomonas sp. strain ES6 to reduce solid phase and dissolved Fe(III) utilizing different carbon sources and various electron shuttling compounds. Results suggest that Fe(III) reduction by and growth of strain ES6 was dependent upon the type of electron donor, the form of iron present, and the presence of synthetic or natural organic matter, such as anthraquinone-2,6-disulfonate (AQDS) or humic substances. This research suggests that Cellulomonas sp. strain ES6 could play a significant role in metal reduction in the Hanford subsurface and that the choice of carbon source and organic matter addition can allow for independent control of growth and iron reduction activity.

  20. Humic analog AQDS and AQS as an electron mediator can enhance chromate reduction by Bacillus sp. strain 3C3.

    PubMed

    Hong, Yiguo; Wu, Peng; Li, Wenru; Gu, Jiguang; Duan, Shunshan

    2012-03-01

    Humus as an electron mediator is recognized as an effective strategy to improve the biological transformation and degradation of toxic substances, yet the action of humus in microbial detoxification of chromate is still unknown. In this study, a humus-reducing strain 3C(3) was isolated from mangrove sediment. Based on the analyses of morphology, physiobiochemical characteristics, and 16S rRNA gene sequence, this strain was identified Bacillus sp. Strain 3C(3) can effectively reduce humic analog anthraquinone-2,6-disulfonate (AQDS) and anthraquinone-2-sulfonate (AQS) with lactate, formate, or glucose as electron donors. When the cells were killed by incubation at 95°C for 30 min or an electron donor was absent, the humic reduction did not occur, showing that the humic reduction was a biochemical process. However, strain 3C(3) had low capability of chromate reduction under anaerobic conditions, despite of having strong tolerance of the toxic metal. But in the presence of humic substances AQDS or AQS, we found that chromate reduction by strain 3C(3) was enhanced greatly. Because strain 3C(3) is an effective humus-reducing bacterium, it is proposed that humic substances could serve as electron mediator to interact with chromate and accelerate chromate reduction. Our results suggest that chromate contaminations can be detoxified by adding humic analog (low to 0.1 mM) as an electron mediator in the microbial incubation.

  1. Wearable Electricity Generators Fabricated Utilizing Transparent Electronic Textiles Based on Polyester/Ag Nanowires/Graphene Core-Shell Nanocomposites.

    PubMed

    Wu, Chaoxing; Kim, Tae Whan; Li, Fushan; Guo, Tailiang

    2016-07-26

    The technological realization of wearable triboelectric generators is attractive because of their promising applications in wearable self-powered intelligent systems. However, the low electrical conductivity, the low electrical stability, and the low compatibility of current electronic textiles (e-textiles) and clothing restrict the comfortable and aesthetic integration of wearable generators into human clothing. Here, we present high-performance, transparent, smart e-textiles that employ commercial textiles coated with silver nanowire/graphene sheets fabricated by using a scalable, environmentally friendly, full-solution process. The smart e-textiles show superb and stable conduction of below 20 Ω/square as well as excellent flexibility, stretchability, foldability, and washability. In addition, wearable electricity-generating textiles, in which the e-textiles act as electrodes as well as wearable substrates, are presented. Because of the high compatibility of smart e-textiles and clothing, the electricity-generating textiles can be easily integrated into a glove to harvest the mechanical energy induced by the motion of the fingers. The effective output power generated by a single generator due to that motion reached as high as 7 nW/cm(2). The successful demonstration of the electricity-generating glove suggests a promising future for polyester/Ag nanowire/graphene core-shell nanocomposite-based smart e-textiles for real wearable electronic systems and self-powered clothing.

  2. Wearable Electricity Generators Fabricated Utilizing Transparent Electronic Textiles Based on Polyester/Ag Nanowires/Graphene Core-Shell Nanocomposites.

    PubMed

    Wu, Chaoxing; Kim, Tae Whan; Li, Fushan; Guo, Tailiang

    2016-07-26

    The technological realization of wearable triboelectric generators is attractive because of their promising applications in wearable self-powered intelligent systems. However, the low electrical conductivity, the low electrical stability, and the low compatibility of current electronic textiles (e-textiles) and clothing restrict the comfortable and aesthetic integration of wearable generators into human clothing. Here, we present high-performance, transparent, smart e-textiles that employ commercial textiles coated with silver nanowire/graphene sheets fabricated by using a scalable, environmentally friendly, full-solution process. The smart e-textiles show superb and stable conduction of below 20 Ω/square as well as excellent flexibility, stretchability, foldability, and washability. In addition, wearable electricity-generating textiles, in which the e-textiles act as electrodes as well as wearable substrates, are presented. Because of the high compatibility of smart e-textiles and clothing, the electricity-generating textiles can be easily integrated into a glove to harvest the mechanical energy induced by the motion of the fingers. The effective output power generated by a single generator due to that motion reached as high as 7 nW/cm(2). The successful demonstration of the electricity-generating glove suggests a promising future for polyester/Ag nanowire/graphene core-shell nanocomposite-based smart e-textiles for real wearable electronic systems and self-powered clothing. PMID:27284809

  3. Surface reconstruction of titania with g-C3N4 and Ag for promoting efficient electrons migration and enhanced visible light photocatalysis

    NASA Astrophysics Data System (ADS)

    Leong, Kah Hon; Liu, Sze Ling; Sim, Lan Ching; Saravanan, Pichiah; Jang, Min; Ibrahim, Shaliza

    2015-12-01

    The developments of heterogeneous photocatalysts are one among the competent reconstruction approach to enrich the visible light responsiveness of conventional TiO2. In the present work the TiO2 was reconstructed with graphitic carbon nitride (g-C3N4) and silver (Ag) to form a ternary (g-C3N4)-Ag/TiO2. The graphitic carbon nitride an intriguing material was prepared through a facile pyrolysis by using urea as a precursor. The silver (Ag) that plays a role as electron-conduction mobiliser in the ternary was synthesised through solar mediated photodeposition method. The synthesised ternary composite characteristics were thoroughly investigated through various physical and chemical analyses. The presence of g-C3N4 in the ternary photocatalysts promoted the formation of interface between the Ag/TiO2 and g-C3N4 and stimulated the electron transfer between them. These electrons migration acknowledged by the synergic effect prolonged the lifetime of charge carriers. The g-C3N4 also significantly tuned the energy band of conventional TiO2. The prepared ternary exhibited significantly high visible light photocatalytic performance by degrading Amoxicillin (AMX) a poor photosensitising pollutant at highest rate.

  4. Understanding nanostructures in thermoelectric materials: an electron microscopy study of AgPb{sub 18}SbSe{sub 20} crystals.

    SciTech Connect

    Lioutas, C. B.; Frangis, N.; Todorov, I.; Chung, D. Y.; Kanatzidis, M. G.; Materials Science Division; Aristotle Univ. Thessaloniki; Northwestern Univ.

    2010-01-01

    The characterization and understanding of the presence of nanostructuring in bulk thermoelectric materials requires real space atomic level information. We report electron diffraction and high-resolution transmission electron microscopy studies of crystals of the system AgPb{sub 18}SbSe{sub 20} (=18PbSe + AgSbSe{sub 2}) which reveal that this system is nanostructured rather than a solid solution. Nanocrystals of varying sizes are found, endotaxially grown in the matrix of PbSe (phase A), and consist of two phases, a cubic one (phase B) and a tetragonal one (phase C). Well-defined coherent interfaces between the phases in the same nanocrystals are observed. On the basis of the results of combined electron crystallography techniques, we propose reasonable structural models for the phases B and C. There are significant differences in the nanostructuring chemistry between AgPb{sub 18}SbSe{sub 20} and the telluride analog AgPb{sub 18}SbTe{sub 20} (LAST-18).

  5. FLAVODIIRON2 and FLAVODIIRON4 proteins mediate an oxygen-dependent alternative electron flow in Synechocystis sp. PCC 6803 under CO2-limited conditions.

    PubMed

    Shimakawa, Ginga; Shaku, Keiichiro; Nishi, Akiko; Hayashi, Ryosuke; Yamamoto, Hiroshi; Sakamoto, Katsuhiko; Makino, Amane; Miyake, Chikahiro

    2015-02-01

    This study aims to elucidate the molecular mechanism of an alternative electron flow (AEF) functioning under suppressed (CO2-limited) photosynthesis in the cyanobacterium Synechocystis sp. PCC 6803. Photosynthetic linear electron flow, evaluated as the quantum yield of photosystem II [Y(II)], reaches a maximum shortly after the onset of actinic illumination. Thereafter, Y(II) transiently decreases concomitantly with a decrease in the photosynthetic oxygen evolution rate and then recovers to a rate that is close to the initial maximum. These results show that CO2 limitation suppresses photosynthesis and induces AEF. In contrast to the wild type, Synechocystis sp. PCC 6803 mutants deficient in the genes encoding FLAVODIIRON2 (FLV2) and FLV4 proteins show no recovery of Y(II) after prolonged illumination. However, Synechocystis sp. PCC 6803 mutants deficient in genes encoding proteins functioning in photorespiration show AEF activity similar to the wild type. In contrast to Synechocystis sp. PCC 6803, the cyanobacterium Synechococcus elongatus PCC 7942 has no FLV proteins with high homology to FLV2 and FLV4 in Synechocystis sp. PCC 6803. This lack of FLV2/4 may explain why AEF is not induced under CO2-limited photosynthesis in S. elongatus PCC 7942. As the glutathione S-transferase fusion protein overexpressed in Escherichia coli exhibits NADH-dependent oxygen reduction to water, we suggest that FLV2 and FLV4 mediate oxygen-dependent AEF in Synechocystis sp. PCC 6803 when electron acceptors such as CO2 are not available. PMID:25540330

  6. Texture analysis of monofilamentary, Ag-sheathed (Pb,Bi) 2Sr 2Ca 2Cu 3O x tapes by electron backscatter diffraction (EBSD)

    NASA Astrophysics Data System (ADS)

    Koblischka-Veneva, A.; Koblischka, M. R.; Qu, T.; Han, Z.; Mücklich, F.

    2008-02-01

    Using automated orientation imaging, the grain orientations and texture of monofilamentary, Ag-sheathed (Pb,Bi) 2Sr 2Ca 2Cu 3O x (Bi-2223) tape is analysed in detail by means of electron backscatter diffraction (EBSD). The achieved high image quality of the Kikuchi patterns enables multi-phase scans including Bi-2223, Bi 2Sr 2CaCu 2O x, Bi 2Sr 2CuO x, (Sr,Ca) 14Cu 24O 41 and Ag to be performed. Two areas are selected for the EBSD analysis, one close to the silver sheath, the other located in the center of the sample. The grain orientation maps are presented for each phase separately allowing a new insight into the microtexture of Ag-sheathed Bi-2223 tapes. Furthermore, the EBSD analysis provides the possibility for a misorientation angle analysis within each individual phase.

  7. Freeze-dried PVP-Ag+ precursors to novel AgBr/AgCl-Ag hybrid nanocrystals for visible-light-driven photodegradation of organic pollutants

    NASA Astrophysics Data System (ADS)

    Chen, Deliang; Chen, Qianqian; Zhang, Wenjie; Ge, Lianfang; Shao, Gang; Fan, Bingbing; Lu, Hongxia; Zhang, Rui; Yang, Daoyuan; Shao, Guosheng

    2015-04-01

    AgBr/AgCl-Ag nanocrystals with various molar Br-to-Ag ratios (RBr/Ag = 0, 1/3, 1/2, 2/3, 1) and different photoreduction times (0-20 min) were synthesized via stepwise liquid-solid reactions using the freeze-dried PVP-Ag+ hybrid as the Ag source, followed by a photoreduction reaction. The AgBr/AgCl-Ag7.5(1:2) nanocrystals obtained take on a spherical morphology with a particle-size range of 58 ± 15 nm. The photocatalytic performance of AgBr/AgCl-Ag nanocrystals was evaluated by photodegrading organic dyes, 4-chlorophenol and isopropanol under artificial visible light (λ ⩾ 420 nm, 100 mW cm-2). For the decomposition of rhodamine B, the AgBr/AgCl-Ag7.5(1:2) nanocrystals has a photodegradation rate of ∼0.87 min-1, ∼159 times higher than that (∼0.0054 min-1) of TiO2 (P25), whereas the AgCl-Ag and AgBr-Ag nanocrystals have photodegradation rates of 0.35 min-1 and 0.45 min-1, respectively. The efficient separation of photogenerated electron-hole pairs in the ternary system consisting of AgBr, AgCl and Ag species plays a key role in the enhancement of photocatalytic performance.

  8. The crystal and electronic structures of the Li{sub 2-x}Ag{sub 1+x}In{sub 3} (x=0.05) indide

    SciTech Connect

    Chumak, Ihor; Pavlyuk, Volodymyr; Pauly, Hermann; Ehrenberg, Helmut

    2013-01-15

    The crystal structure of Li{sub 2-x}Ag{sub 1+x}In{sub 3} (x=0.05) has been determined on a single crystal synthesized from the elements in a tantalum crucible. The compound crystallizes in orthorhombic space group Pmma (a=9.325 (3) A, b=3.198 (1) A, c=8.043 (3) A at 296 K) with 12 atoms per unit cell and represents a new structure type. The structure of Li{sub 2-x}Ag{sub 1+x}In{sub 3} is closely related to the LaCoAl{sub 4} structure and belongs to the structural family, the representative members of which may be derived from the hexagonal AlB{sub 2} structure type by a combination of internal deformation and substitution. The strong In-In interaction and close to zero electrons concentration around Li and Ag atoms, calculated by LTMO, allow to suggest high mobility of lithium atoms located within the channels formed by the strongly waved [-In-In-] polyanionic chains. - Graphical abstract: The crystal structure of Li{sub 2-x}Ag{sub 1+x}In{sub 3} (x=0.05) indide. Highlights: Black-Right-Pointing-Pointer The crystal structure of Li{sub 2-x}Ag{sub 1+x}In{sub 3} has been determined on a single crystal. Black-Right-Pointing-Pointer A detailed crystal chemical analysis of Li{sub 2-x}Ag{sub 1+x}In{sub 3} was performed. Black-Right-Pointing-Pointer The electronic structure of the title compound was calculated.

  9. Structural and electronic properties of small bimetallic Ag-Cu clusters

    NASA Astrophysics Data System (ADS)

    Kilimis, D. A.; Papageorgiou, D. G.

    2010-01-01

    The structural and electronic properties of small gas-phase AgmCun clusters with m+n=2-5 atoms are investigated using spin-polarized density functional theory. The LANL2DZ effective core potential and the corresponding basis set are employed while the performance of several exchange-correlation functionals is assessed. For a given cluster size all possible compositions are subject to optimization using a variety of initial structures. The geometry, binding energy, relative stability, ionization potential, electron affinity and HOMO-LUMO gap are reported for the lowest energy structure of every cluster size and composition. The results show that planar structures are favored, triangular for trimers, rhombic for tetramers and trapezoidal for pentamers. Moreover, for tetramers and pentamers we found that silver atoms demonstrate a clear tendency to occupy edge positions. The calculation of electronic properties indicates that although all exchange-correlation functionals predict the same trends, the choice of method is crucial concerning the final quantitative results.

  10. Photoinduced electron transfer of DNA/Ag nanoclusters modulated by G-quadruplex/hemin complex for the construction of versatile biosensors.

    PubMed

    Zhang, Libing; Zhu, Jinbo; Guo, Shaojun; Li, Tao; Li, Jing; Wang, Erkang

    2013-02-20

    Photoinduced electron transfer (PET) has been observed for the first time between DNA/Ag fluorescent nanoclusters (NCs) and G-quadruplex/hemin complexes, accompanied by a decrease in the fluorescence of the DNA/Ag NCs. In this PET process, a parallel G-quadruplex and the sensing sequences are blocked by a duplex. The specific combination of targets with the sensing sequence triggers the release of the G-quadruplex and allows it to fold properly and bind hemin to form a stable G-quadruplex/hemin complex. The complex proves favorable for PET because it makes the G-quadruplex bind hemin tightly, which promotes the electron transfer from the DNA/Ag NCs to the hemin Fe(III) center, thus resulting in a decrease in the fluorescence intensity of the DNA/Ag NCs. This novel PET system enables the specific and versatile detection of target biomolecules such as DNA and ATP with high sensitivity based on the choices of different target sequences.

  11. Resonance Raman scattering of butadiene: Vibronic activity of a bu mode demonstrates the presence of a 1Ag symmetry excited electronic state at low energy

    NASA Astrophysics Data System (ADS)

    Chadwick, Richard R.; Zgierski, Marek Z.; Hudson, Bruce S.

    1991-11-01

    Resonance Raman spectra of buta-1,3-diene-d0 and buta-1,3-diene-1,1,4,4-d4 have been obtained with ultraviolet excitation from 239.5 to 199.9 nm. Activity of the first overtone of mode 24, the bu symmetry CCC chain deformation mode, is observed with excitation energy below the origin of the 1 1Bu state. This vibronic activity of a nontotally symmetric mode is shown to be evidence of resonance with the 2 1Ag state of butadiene. A quantitative analysis of the ratio of intensities of 2ν24 to ν9, the ag symmetry CCC chain deformation mode, demonstrates that enhancement of 2ν24 cannot be due to resonance with the 1 1Bu state. The resonance enhancement behavior of this overtone band also shows that it is of vibronic origin rather than Franck-Condon allowed. The intensity pattern seen for the modes of bu symmetry is fully consistent with the results of a quantitative calculation of vibronic activity for the eight bu symmetry modes. The 2 1Ag electronic state is estimated to be ca. 0.25 eV below the 1 1Bu electronic state. Overtones of out-of-plane C-H bending and CH2 twisting modes are seen with excitation radiation near the peak of the transition to the 2 1Ag state, indicating that the 2 1Ag state of butadiene has appreciably lower resistance to deformation along out-of-plane coordinates than does the ground electronic state. This is consistent with the expectations of semiempirical calculations.

  12. [Chromate reduction by Pseudomonas sp. str. 10 in the presence of some heavy metals and alternative electron acceptors].

    PubMed

    Smirnova, G F; Podgorskiĭ, V S

    2013-01-01

    Pseudomonas sp. str. 10 reduces chromate with a rate of 0.54 mg / L.h. The availability of Cd2+ and Zn2+ in the medium has no noticeable effect on the rate or slightly increases it. The presence of nickel and copper in the ionic form in the medium resulted in a decrease of chromate reduction rate 2.4 and 4.2 times, respectively. Change of these metals into hydroxide form significantly lowers their negative influence. Iron (III) both in ionic and hydroxide form inhibits the reduction of chromate by Pseudomonas sp. 10. Joint presence of all studied metals decreases their negative impact on chromate reduction, therefore these metals may be neutralized together without a significant lowering of the process efficacy on condition that copper-containing drain will be cleaned separately. The presence of alternative acceptors of electrons inhibited the reduction of chromate. Sulfate and oxyanions of chlorine - chlorate and perchlorate have the highest inhibitory effect on chromate reduction. PMID:24006778

  13. Permanent Draft Genome Sequence of Frankia sp. Strain ACN1ag, a Nitrogen-Fixing Actinobacterium Isolated from the Root Nodules of Alnus glutinosa.

    PubMed

    Swanson, Erik; Oshone, Rediet; Simpson, Stephen; Morris, Krystalynne; Abebe-Akele, Feseha; Thomas, W Kelley; Tisa, Louis S

    2015-01-01

    Frankia strain ACN1(ag) is a member of Frankia lineage Ia, which are able to re-infect plants of the Betulaceae and Myricaceae families. Here, we report a 7.5-Mbp draft genome sequence with a G+C content of 72.35% and 5,687 candidate protein-encoding genes. PMID:26679592

  14. Permanent Draft Genome Sequence of Frankia sp. Strain ACN1ag, a Nitrogen-Fixing Actinobacterium Isolated from the Root Nodules of Alnus glutinosa

    PubMed Central

    Swanson, Erik; Oshone, Rediet; Simpson, Stephen; Morris, Krystalynne; Abebe-Akele, Feseha; Thomas, W. Kelley

    2015-01-01

    Frankia strain ACN1ag is a member of Frankia lineage Ia, which are able to re-infect plants of the Betulaceae and Myricaceae families. Here, we report a 7.5-Mbp draft genome sequence with a G+C content of 72.35% and 5,687 candidate protein-encoding genes. PMID:26679592

  15. Quantitative description of short-range order and its influence on the electronic structure in Ag-Pd alloys

    NASA Astrophysics Data System (ADS)

    Hoffmann, M.; Marmodoro, A.; Ernst, A.; Hergert, W.; Dahl, J.; Lång, J.; Laukkanen, P.; Punkkinen, M. P. J.; Kokko, K.

    2016-08-01

    We investigate the effect of short-range order (SRO) on the electronic structure in alloys from the theoretical point of view using density of states (DOS) data. In particular, the interaction between the atoms at different lattice sites is affected by chemical disorder, which in turn is reflected in the fine structure of the DOS and, hence, in the outcome of spectroscopic measurements. We aim at quantifying the degree of potential SRO with a proper parameter. The theoretical modeling is done with the Korringa–Kohn–Rostoker Green’s function method. Therein, the extended multi-sublattice non-local coherent potential approximation is used to include SRO. As a model system, we use the binary solid solution Ag c Pd1‑c at three representative concentrations c  =  0.25, 0.5 and 0.75. The degree of SRO is varied from local ordering to local segregation through an intermediate completely uncorrelated state. We observe some pronounced features, which change over the whole energy range of the valence bands as a function of SRO in the alloy. These spectral variations should be traceable in modern photoemission experiments.

  16. Quantitative description of short-range order and its influence on the electronic structure in Ag-Pd alloys

    NASA Astrophysics Data System (ADS)

    Hoffmann, M.; Marmodoro, A.; Ernst, A.; Hergert, W.; Dahl, J.; Lång, J.; Laukkanen, P.; Punkkinen, M. P. J.; Kokko, K.

    2016-08-01

    We investigate the effect of short-range order (SRO) on the electronic structure in alloys from the theoretical point of view using density of states (DOS) data. In particular, the interaction between the atoms at different lattice sites is affected by chemical disorder, which in turn is reflected in the fine structure of the DOS and, hence, in the outcome of spectroscopic measurements. We aim at quantifying the degree of potential SRO with a proper parameter. The theoretical modeling is done with the Korringa-Kohn-Rostoker Green’s function method. Therein, the extended multi-sublattice non-local coherent potential approximation is used to include SRO. As a model system, we use the binary solid solution Ag c Pd1-c at three representative concentrations c  =  0.25, 0.5 and 0.75. The degree of SRO is varied from local ordering to local segregation through an intermediate completely uncorrelated state. We observe some pronounced features, which change over the whole energy range of the valence bands as a function of SRO in the alloy. These spectral variations should be traceable in modern photoemission experiments.

  17. High resolution electron microscopy of Ag-clusters in crystalline and non-crystalline morphologies grown inside superfluid helium nanodroplets

    SciTech Connect

    Volk, Alexander; Thaler, Philipp; Koch, Markus; Ernst, Wolfgang E.; Fisslthaler, Evelin; Grogger, Werner

    2013-06-07

    We present a first investigation of structural properties of Ag clusters with a diameter of up to 5.5 nm grown inside superfluid helium nanodroplets (He{sub N}) and deposited on an amorphous C surface. With high resolution transmission electron microscope images we are able to show that in addition to the crystalline face centered cubic (fcc) structure, noncrystalline icosahedral (Ih), and decahedral (Dh) morphologies are grown. Relative abundances (56% fcc, 31% Dh, and 13% Ih) as well as the size distribution of each morphology (mean diameters d{sub fcc}=2.62(5) nm, d{sub Dh}=3.34(7) nm, and d{sub Ih}=3.93(2) nm) do not reflect the situation expected from pure energetic considerations, where small Ihs should be followed by medium sized Dhs and large fccs. Instead, kinetic factors seem to play an important role in the formation of these structures, as it appears to be the case for clusters formed by inert gas aggregation. Considering the low temperatures (0.37 K) and extremely high cooling rates, we discuss basic ideas that might lead to a qualitative picture of the cluster formation process inside He{sub N}.

  18. High resolution electron microscopy of Ag-clusters in crystalline and non-crystalline morphologies grown inside superfluid helium nanodroplets.

    PubMed

    Volk, Alexander; Thaler, Philipp; Koch, Markus; Fisslthaler, Evelin; Grogger, Werner; Ernst, Wolfgang E

    2013-06-01

    We present a first investigation of structural properties of Ag clusters with a diameter of up to 5.5 nm grown inside superfluid helium nanodroplets (He(N)) and deposited on an amorphous C surface. With high resolution transmission electron microscope images we are able to show that in addition to the crystalline face centered cubic (fcc) structure, noncrystalline icosahedral (Ih), and decahedral (Dh) morphologies are grown. Relative abundances (56% fcc, 31% Dh, and 13% Ih) as well as the size distribution of each morphology (mean diameters d(fcc)=2.62(5) nm, d(Dh)=3.34(7) nm, and d(Ih)=3.93(2) nm) do not reflect the situation expected from pure energetic considerations, where small Ihs should be followed by medium sized Dhs and large fccs. Instead, kinetic factors seem to play an important role in the formation of these structures, as it appears to be the case for clusters formed by inert gas aggregation. Considering the low temperatures (0.37 K) and extremely high cooling rates, we discuss basic ideas that might lead to a qualitative picture of the cluster formation process inside He(N). PMID:23758376

  19. The instability of silicene on Ag(111)

    SciTech Connect

    Acun, A.; Poelsema, B.; Zandvliet, H. J. W.; Gastel, R. van

    2013-12-23

    We have used low energy electron microscopy to directly visualize the formation and stability of silicene layers on a Ag(111) substrate. Theoretical calculations call into question the stability of this graphene-like analog of silicon. We find that silicene layers are intrinsically unstable against the formation of an “sp{sup 3}-like” hybridized, bulk-like silicon structure. The irreversible formation of this bulk-like structure is triggered by thermal Si adatoms that are created by the silicene layer itself. To add injury to insult, this same instability prevents the formation of a fully closed silicene layer or a thicker bilayer, rendering the future large-scale fabrication of silicene layers on Ag substrates unlikely.

  20. Scanning tunnelling spectroscopy and Raman spectroscopy of monolayer silicene on Ag(111)

    NASA Astrophysics Data System (ADS)

    Díaz Álvarez, A.; Zhu, T.; Nys, J. P.; Berthe, M.; Empis, M.; Schreiber, J.; Grandidier, B.; Xu, T.

    2016-11-01

    Low temperature scanning tunnelling spectroscopy and Raman spectroscopy were used to study the electronic and vibrational properties of silicene formed on the Ag(111) surface for coverage up to one monolayer in the temperature range 230-250 °C. The tunnelling spectra reveal the strong contribution of silver states in the measured density of states around the Fermi level. The Raman spectra are found to evolve as a function of the submonolayer coverages, giving rise at one monolayer coverage to peaks that are characteristic of chemical bonds with distorted sp3 hybrid orbitals. Such properties account for the electronic transparency of the silicene/Ag(111) interface.

  1. Hexavalent chromium reduction by Cellulomonas sp. strain ES6: the influence of carbon source, iron minerals, and electron shuttling compounds.

    PubMed

    Field, Erin K; Gerlach, Robin; Viamajala, Sridhar; Jennings, Laura K; Peyton, Brent M; Apel, William A

    2013-06-01

    The reduction of hexavalent chromium, Cr(VI), to trivalent chromium, Cr(III), can be an important aspect of remediation processes at contaminated sites. Cellulomonas species are found at several Cr(VI) contaminated and uncontaminated locations at the Department of Energy site in Hanford, Washington. Members of this genus have demonstrated the ability to effectively reduce Cr(VI) to Cr(III) fermentatively and therefore play a potential role in Cr(VI) remediation at this site. Batch studies were conducted with Cellulomonas sp. strain ES6 to assess the influence of various carbon sources, iron minerals, and electron shuttling compounds on Cr(VI) reduction rates as these chemical species are likely to be present in, or added to, the environment during in situ bioremediation. Results indicated that the type of carbon source as well as the type of electron shuttle present influenced Cr(VI) reduction rates. Molasses stimulated Cr(VI) reduction more effectively than pure sucrose, presumably due to presence of more easily utilizable sugars, electron shuttling compounds or compounds with direct Cr(VI) reduction capabilities. Cr(VI) reduction rates increased with increasing concentration of anthraquinone-2,6-disulfonate (AQDS) regardless of the carbon source. The presence of iron minerals and their concentrations did not significantly influence Cr(VI) reduction rates. However, strain ES6 or AQDS could directly reduce surface-associated Fe(III) to Fe(II), which was capable of reducing Cr(VI) at a near instantaneous rate. These results suggest the rate limiting step in these systems was the transfer of electrons from strain ES6 to the intermediate or terminal electron acceptor whether that was Cr(VI), Fe(III), or AQDS.

  2. Influence of Carbon Sources and Electron Shuttles on Ferric Iron Reduction by Cellulomonas sp. Strain ES6

    SciTech Connect

    Erin K. Field; Robin Gerlach; Sridhar Viamajala; Laura K. Jennings; Alfred B. Cunningham; Brent M. Peyton; William A. Apel

    2011-09-01

    The reduction of hexavalent chromium, Cr(VI), to trivalent chromium, Cr(III), can be an important aspect of remediation processes at Department of Energy (DOE) and other contaminated sites. Cellulomonas species are found at several Cr(VI) contaminated and uncontaminated locations at the DOE site in Hanford, Washington. Members of this genus have demonstrated the ability to effectively reduce Cr(VI) to Cr(III) fermentatively and therefore play a potential role in hexavalent chromium remediation at this site. Batch studies were conducted with Cellulomonas sp. strain ES6 to assess the influence of various carbon sources, iron minerals, and electron shuttling compounds on Cr(VI) reduction. These chemical species are likely to be present in these terrestrial environments during in situ bioremediation. Results indicated that there were a number of interactions between these compounds that influenced Cr(VI) reduction rates. The type of carbon source as well as the type of electron shuttle present influenced Cr(VI) reduction rates. When an electron shuttle, such as anthraquinone-2,6-disulfonate (AQDS), was present in the system, reduction rates increased significantly. Biologically reduced AQDS (AHDS) reduced Cr(VI) almost instantaneously. The presence of iron minerals and their concentrations did not significantly influence Cr(VI) reduction rates. However, strain ES6 or AQDS could directly reduce surface-associated Fe(III) to Fe(II) which was capable of reducing Cr(VI) at a near instantaneous rate. These results suggest the rate limiting step in these systems is the transfer of electrons from strain ES6 to the intermediate or terminal electron acceptor whether that is Cr(VI), Fe(III), or AQDS.

  3. Exploring the benefits of electron tomography to characterize the precise morphology of core-shell Au@Ag nanoparticles and its implications on their plasmonic properties.

    PubMed

    Hernández-Garrido, J C; Moreno, M S; Ducati, C; Pérez, L A; Midgley, P A; Coronado, E A

    2014-11-01

    In the design and engineering of functional core-shell nanostructures, material characterization at small length scales remains one of the major challenges. Here we show how electron tomography in high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) mode can be applied successfully to perform nano-metrological characterization of Au@Ag core-shell nanostructures. This work stresses the benefits of HAADF-STEM tomography and its use as a novel and rigorous tool for understanding the physical-chemical properties of complex 3D core-shell nanostructures. The reconstructed Au@Ag core-shell architecture was used as an input for discrete dipole approximation (DDA)-based electrodynamics simulations of the optical properties of the nanostructures. The implications of localized surface plasmon spectroscopy as well as Raman-enhanced spectroscopy are analysed.

  4. Valence State Driven Site Preference in the Quaternary Compound Ca5MgAgGe5: An Electron-Deficient Phase with Optimized Bonding

    SciTech Connect

    Ponou, Simeon; Lidin, Sven; Zhang, Yuemei; Miller, Gordon J.

    2014-04-18

    The quaternary phase Ca5Mg0.95Ag1.05(1)Ge5 (3) was synthesized by high-temperature solid-state techniques, and its crystal structure was determined by single-crystal diffraction methods in the orthorhombic space group Pnma – Wyckoff sequence c12 with a = 23.1481(4) Å, b = 4.4736(1) Å, c = 11.0128(2) Å, V = 1140.43(4) Å3, Z = 4. The crystal structure can be described as linear intergrowths of slabs cut from the CaGe (CrB-type) and the CaMGe (TiNiSi-type; M = Mg, Ag) structures. Hence, 3 is a hettotype of the hitherto missing n = 3 member of the structure series with the general formula R2+nT2X2+n, previously described with n = 1, 2, and 4. The member with n = 3 was predicted in the space group Cmcm – Wyckoff sequence f5c2. The experimental space group Pnma (in the nonstandard setting Pmcn) corresponds to a klassengleiche symmetry reduction of index two of the predicted space group Cmcm. This transition originates from the switching of one Ge and one Ag position in the TiNiSi-related slab, a process that triggers an uncoupling of each of the five 8f sites in Cmcm into two 4c sites in Pnma. The Mg/Ag site preference was investigated using VASP calculations and revealed a remarkable example of an intermetallic compound for which the electrostatic valency principle is a critical structure-directing force. The compound is deficient by one valence electron according to the Zintl concept, but LMTO electronic structure calculations indicate electronic stabilization and overall bonding optimization in the polyanionic network. Other stability factors beyond the Zintl concept that may account for the electronic stabilization are discussed.

  5. Tuning near-gap electronic structure, interface charge transfer and visible light response of hybrid doped graphene and Ag3PO4 composite: Dopant effects

    PubMed Central

    He, Chao-Ni; Huang, Wei-Qing; Xu, Liang; Yang, Yin-Cai; Zhou, Bing-Xin; Huang, Gui-Fang; Peng, P.; Liu, Wu-Ming

    2016-01-01

    The enhanced photocatalytic performance of doped graphene (GR)/semiconductor nanocomposites have recently been widely observed, but an understanding of the underlying mechanisms behind it is still out of reach. As a model system to study the dopant effects, we investigate the electronic structures and optical properties of doped GR/Ag3PO4 nanocomposites using the first-principles calculations, demonstrating that the band gap, near-gap electronic structure and interface charge transfer of the doped GR/Ag3PO4(100) composite can be tuned by the dopants. Interestingly, the doping atom and C atoms bonded to dopant become active sites for photocatalysis because they are positively or negatively charged due to the charge redistribution caused by interaction. The dopants can enhance the visible light absorption and photoinduced electron transfer. We propose that the N atom may be one of the most appropriate dopants for the GR/Ag3PO4 photocatalyst. This work can rationalize the available experimental results about N-doped GR-semiconductor composites, and enriches our understanding on the dopant effects in the doped GR-based composites for developing high-performance photocatalysts. PMID:26923338

  6. An efficient photocatalyst for degradation of various organic dyes: Ag@Ag2MoO4-AgBr composite.

    PubMed

    Bai, Yu-Yang; Lu, Yi; Liu, Jin-Ku

    2016-04-15

    The Ag2MoO4-AgBr composite was prepared by a facile in-situ anion-exchange method, then the Ag nanoparticles were coated on this composite through photodeposition route to form a novel Ag@Ag2MoO4-AgBr composite. The in-situ Br(-) replacement in a crystal lattice node position of Ag2MoO4 crystal allows for overcoming the resistance of electron transition effectively. Meanwhile silver nano-particles on the surface of Ag@Ag2MoO4-AgBr composite could act as electron traps to intensify the photogeneration electron-hole separation and the subsequent transfer of the trapped electron to the adsorbed O2 as an electron acceptor. As an efficient visible light catalyst, the Ag@Ag2MoO4-AgBr composite exhibited superior photocatalytic activity for the degradation of various organic dyes. The experimental results demonstrated superior photocatalytic rate of Ag@Ag2MoO4-AgBr composite compared to pure AgBr and Ag2MoO4 crystals (37.6% and 348.4% enhancement respectively). The Ag@Ag2MoO4-AgBr composite cloud degraded Rhodamin B, bromophenol blue, and amino black 10b completed in 7min. PMID:26775100

  7. An efficient photocatalyst for degradation of various organic dyes: Ag@Ag2MoO4-AgBr composite.

    PubMed

    Bai, Yu-Yang; Lu, Yi; Liu, Jin-Ku

    2016-04-15

    The Ag2MoO4-AgBr composite was prepared by a facile in-situ anion-exchange method, then the Ag nanoparticles were coated on this composite through photodeposition route to form a novel Ag@Ag2MoO4-AgBr composite. The in-situ Br(-) replacement in a crystal lattice node position of Ag2MoO4 crystal allows for overcoming the resistance of electron transition effectively. Meanwhile silver nano-particles on the surface of Ag@Ag2MoO4-AgBr composite could act as electron traps to intensify the photogeneration electron-hole separation and the subsequent transfer of the trapped electron to the adsorbed O2 as an electron acceptor. As an efficient visible light catalyst, the Ag@Ag2MoO4-AgBr composite exhibited superior photocatalytic activity for the degradation of various organic dyes. The experimental results demonstrated superior photocatalytic rate of Ag@Ag2MoO4-AgBr composite compared to pure AgBr and Ag2MoO4 crystals (37.6% and 348.4% enhancement respectively). The Ag@Ag2MoO4-AgBr composite cloud degraded Rhodamin B, bromophenol blue, and amino black 10b completed in 7min.

  8. Electrode as sole electrons donor for enhancing decolorization of azo dye by an isolated Pseudomonas sp. WYZ-2.

    PubMed

    Wang, You-zhao; Wang, Ai-jie; Zhou, Ai-juan; Liu, Wen-zong; Huang, Li-ping; Xu, Mei-ying; Tao, Hu-chun

    2014-01-01

    Pseudomonas sp. WYZ-2 was isolated from a biocathode which accelerating azo dye decolorization. When the electrode was polarized at -0.8 V (vs. SCE), WYZ-2 could exist on electrode, because the current of working electrode stabilized at -0.35 mA from -0.13 mA after inoculation. Moreover, cyclic voltammetry scanned an unidentified redox-active molecule which involved in the electron charge transfer potentially. On azo dye decolorization experiments by WYZ-2 modified electrode, electrochemical tests also indicated that the catalytic ability of WYZ-2 modified electrode was improved because charge transfer resistance decreased to 255 Ω from 720 Ω, azo dye reduction potential was shifted to -0.78 V from -0.89 V, and the maximum decolorization efficiency of azo dye was increased to 93.4% from 53.2%, comparing with unmodified electrode. Although numerous studies on azo dye decolorization employed biological agents, electrochemical activity bacteria accelerate the decolorization process using electrode as sole electron source has seldom been reported.

  9. Electrode as sole electrons donor for enhancing decolorization of azo dye by an isolated Pseudomonas sp. WYZ-2.

    PubMed

    Wang, You-zhao; Wang, Ai-jie; Zhou, Ai-juan; Liu, Wen-zong; Huang, Li-ping; Xu, Mei-ying; Tao, Hu-chun

    2014-01-01

    Pseudomonas sp. WYZ-2 was isolated from a biocathode which accelerating azo dye decolorization. When the electrode was polarized at -0.8 V (vs. SCE), WYZ-2 could exist on electrode, because the current of working electrode stabilized at -0.35 mA from -0.13 mA after inoculation. Moreover, cyclic voltammetry scanned an unidentified redox-active molecule which involved in the electron charge transfer potentially. On azo dye decolorization experiments by WYZ-2 modified electrode, electrochemical tests also indicated that the catalytic ability of WYZ-2 modified electrode was improved because charge transfer resistance decreased to 255 Ω from 720 Ω, azo dye reduction potential was shifted to -0.78 V from -0.89 V, and the maximum decolorization efficiency of azo dye was increased to 93.4% from 53.2%, comparing with unmodified electrode. Although numerous studies on azo dye decolorization employed biological agents, electrochemical activity bacteria accelerate the decolorization process using electrode as sole electron source has seldom been reported. PMID:24314602

  10. Hybrid two-dimensional electronic systems and other applications of sp-2 bonded light elements

    NASA Astrophysics Data System (ADS)

    Kessler, Brian Maxwell

    The field-effect is a cornerstone of modern technology lying at the heart of transistors in consumer electronics. Experimentally, it allows one to continuously vary the carrier concentration in a material while studying its properties. The recent isolation of graphene, the first truly two-dimensional crystal, allows application of the field effect to a much wider range of physical situations. In the first part of the thesis, we investigate hybrid materials formed by coupling metals to the two-dimensional electron gas (2DEG) in graphene. We couple superconducting materials to the graphene sheet by cluster deposition. This material displays a superconducting phase whose properties are tuned by the carrier density via the field effect. The transition temperature is well-described by Berezinskii-Kosterlitz-Thouless vortex unbinding. The ground state properties show interesting effects due to the distribution of cluster spacings. Observations related to other hybrid electronic systems including ferromagnets and normal metals are presented. The second part of this thesis involves energy applications of light element materials. The mechanisms affecting coating of carbon nanotubes using atomic layer deposition is developed and applied to photovoltaic systems. The gas adsorption properties of activated boron nitride are investigated and the relative influence of surface area and hydrogen binding affinity is elaborated. The third part of this thesis explores electromechanical properties of suspended graphene membranes. We investigate buckling and strain in exfoliated graphene membranes as well as their deformation under an applied gate potential.

  11. Electron beam assisted synthesis of silver nanoparticle in chitosan stabilizer: Preparation, stability and inhibition of building fungi studies

    NASA Astrophysics Data System (ADS)

    Jannoo, Kanokwan; Teerapatsakul, Churapa; Punyanut, Adisak; Pasanphan, Wanvimol

    2015-07-01

    Silver nanoparticles (AgNPs) in chitosan (CS) stabilizer were successfully synthesized using electron beam irradiation. The effects of irradiation dose, molecular weight (MW) of CS stabilizer, concentration of AgNO3 precursor and addition of tert-butanol on AgNPs production were studied. The stability of the AgNPs under different temperatures and storage times were also investigated. The AgNPs formation in CS was observed using UV-vis, FT-IR and XRD. The characteristic surface plasmon resonance (SPR) of the obtained AgNPs was around 418 nm. The CS stabilizer and its MW, AgNO3 precursor and irradiation doses are important parameters for the synthesis of AgNPs. The optimum addition of 20% v/v tert-butanol could assist the formation of AgNPs. The AgNPs in CS stabilizer were stable over a period of one year when the samples were kept at 5 °C. The AgNPs observed from TEM images were spherical with an average particle size in the range of 5-20 nm depending on the irradiation doses. The AgNPs in CS solution effectively inhibited the growth of several fungi, i.e., Curvularia lunata, Trichoderma sp., Penicillium sp. and Aspergillus niger, which commonly found on the building surface.

  12. Proton-assisted two-electron transfer in natural variants of tetraheme cytochromes from Desulfomicrobium Sp.

    PubMed

    Correia, Ilídio J; Paquete, Catarina M; Coelho, Ana; Almeida, Claudia C; Catarino, Teresa; Louro, Ricardo O; Frazão, Carlos; Saraiva, Lígia M; Carrondo, Maria Arménia; Turner, David L; Xavier, António V

    2004-12-10

    The tetraheme cytochrome c3 isolated from Desulfomicrobium baculatum (DSM 1743)(Dsmb) was cloned, and the sequence analysis showed that this cytochrome differs in just three amino acid residues from the cytochrome c3 isolated from Desulfomicrobium norvegicum (Dsmn): (DsmnXXDsmb) Thr-37 --> Ser, Val-45 --> Ala, and Phe-88 --> Tyr. X-ray crystallography was used to determine the structure of cytochrome c3 from Dsmb, showing that it is very similar to the published structure of cytochrome c3 from Dsmn. A detailed thermodynamic and kinetic characterization of these two tetraheme cytochromes c3 was performed by using NMR and visible spectroscopy. The results obtained show that the network of cooperativities between the redox and protonic centers is consistent with a synergetic process to stimulate the hydrogen uptake activity of hydrogenase. This is achieved by increasing the affinity of the cytochrome for protons through binding electrons and, reciprocally, by favoring a concerted two-electron transfer assisted by the binding of proton(s). The data were analyzed within the framework of the differences in the primary and tertiary structures of the two proteins, showing that residue 88, close to heme I, is the main cause for the differences in the microscopic thermodynamic parameters obtained for these two cytochromes c3. This comparison reveals how replacement of a single amino acid can tune the functional properties of energy-transducing proteins, so that they can be optimized to suit the bioenergetic constraints of specific habitats.

  13. Local atomic structure inheritance in Ag{sub 50}Sn{sub 50} melt

    SciTech Connect

    Bai, Yanwen; Bian, Xiufang Qin, Jingyu; Hu, Lina; Yang, Jianfei; Zhang, Kai; Zhao, Xiaolin; Yang, Chuncheng; Zhang, Shuo; Huang, Yuying

    2014-01-28

    Local structure inheritance signatures were observed during the alloying process of the Ag{sub 50}Sn{sub 50} melt, using high-temperature X-ray diffraction and ab initio molecular dynamics simulations. The coordination number N{sub m} around Ag atom is similar in the alloy and in pure Ag melts (N{sub m} ∼ 10), while, during the alloying process, the local structure around Sn atoms rearranges. Sn-Sn covalent bonds were substituted by Ag-Sn chemical bonds, and the total coordination number around Sn increases by about 70% as compared with those in the pure Sn melt. Changes in the electronic structure of the alloy have been studied by Ag and Sn K-edge X-ray absorption spectroscopy, as well as by calculations of the partial density of states. We propose that a leading mechanism for local structure inheritance in Ag{sub 50}Sn{sub 50} is due to s-p dehybridization of Sn and to the interplay between Sn-s and Ag-d electrons.

  14. Electron transport in carbon nanotube/RbAg{sub 4}I{sub 5} film composite nanostructures modulated by optical field

    SciTech Connect

    Zhang, Guowei; Zhu, Jia-Lin; Wei, Jinquan; Zhang, Wei E-mail: jlsun@tsinghua.edu.cn; Sun, Jia-Lin E-mail: jlsun@tsinghua.edu.cn

    2014-06-16

    We explore the transport properties of mixed ionic-electronic conductors made of carbon nanotube/RbAg{sub 4}I{sub 5} film composite nanostructures in the presence of optical fields. The formation of ion-electron bound states (IEBSs) due to Coulomb interactions results in significant conductance decrease. The wavelength-dependent and power-dependent dynamic responses show that the effect of photo-induced dissociation of IEBSs is pronounced in the visible region and negligible in near-infrared region. Our results lead to a deeper understanding of the impact of ion-electron interactions (IEIs) on transport and are expected to open up a way for designing new-type photodetectors based on IEIs.

  15. Crystal and electronic structures and high-pressure behavior of AgSO4, a unique narrow band gap antiferromagnetic semiconductor: LDA(+U) picture.

    PubMed

    Derzsi, Mariana; Stasiewicz, Juliusz; Grochala, Wojciech

    2011-09-01

    We demonstrate that DFT calculations performed with the local density approximation (LDA) allow for significantly better reproduction of lattice constants, the unit cell volume and the density of Ag(II)SO(4) than those done with generalized gradient approximation (GGA). The LDA+U scheme, which accounts for electronic correlation effects, enables the accurate prediction of the magnetic superexchange constant of this strongly correlated material and its band gap at the Fermi level. The character of the band gap places the compound on the borderline between a Mott insulator and a charge transfer insulator. The size of the band gap (0.82 eV) indicates that AgSO(4) is a ferrimagnetic semiconductor, and possibly an attractive material for spintronics. A bulk modulus of 27.0 GPa and a compressibility of 0.037 GPa(-1) were determined for AgSO(4) from the third-order Birch-Murnaghan isothermal equation of state up to 20 GPa. Several polymorphic types compete with the ambient pressure P-1 phase as the external pressure is increased. The P-1 phase is predicted to resist pressure-induced metallization up to at least 20 GPa.

  16. Structural, mechanical, electronic and thermal properties of KZnF3 and AgZnF3 Perovskites: FP-(L)APW+lo calculations

    NASA Astrophysics Data System (ADS)

    Hiadsi, S.; Bouafia, H.; Sahli, B.; Abidri, B.; Bouaza, A.; Akriche, A.

    2016-08-01

    This study presents a theoretical prediction of the structural, mechanical, electronic and thermal properties of the zinc-based Perovskites (AgZnF3 and KZnF3) within the framework of Density Functional Theory (DFT) using All-electron self consistent Full Potential Augmented Plane Waves plus local orbital FP-(L)APW + lo method. To make our work comparable and reliable, several functional were used for the exchange-correlation potential. Also, this study intends to provide a basis and an improvement for updating either the values already predicted by other previous work (by using obsolete functional) or to predict them for the first time. GGA-PBE and GGA-PBEsol were used to predict the structural properties of AgZnF3 and KZnF3 Perovskites such as lattice parameter, bulk modulus and its pressure derivative and the cohesive energy. For these properties, the found values are in very good agreement; also those found by GGA-PBEsol are closer to other available previous and experimental results. The electronic properties of these materials are investigated and compared to provide a consolidated prediction by using the modified Becke Johnson potential TB-mBJ with other functional; the values found by this potential are closer to the available proven results and show that these materials exhibit an indirect gap from R to Γ point. The charge densities plot for [110] direction and QTAIM (Quantum Theory of Atoms in Molecules) theory indicate that ionic character is predominate for (K, Ag, Zn)sbnd F bonds. Finally, the effect of temperature and pressure on the unit cell volume, the heat capacity CV and entropy were studied using the quasi-harmonic Debye model.

  17. Electronic structure, transport, and phonons of SrAgChF (Ch = S,Se,Te): Bulk superlattice thermoelectrics

    SciTech Connect

    Gudelli, Vijay Kumar; Kanchana, V.; Vaitheeswaran, G.; Singh, David J.; Svane, Axel; Christensen, Niels Egede; Mahanti, Subhendra D.

    2015-07-15

    Here, we report calculations of the electronic structure, vibrational properties, and transport for the p-type semiconductors, SrAgChF (Ch = S, Se, and Te). We find soft phonons with low frequency optical branches intersecting the acoustic modes below 50 cm–1, indicative of a material with low thermal conductivity. The bands at and near the valence-band maxima are highly two-dimensional, which leads to high thermopowers even at high carrier concentrations, which is a combination that suggests good thermoelectric performance. These materials may be regarded as bulk realizations of superlattice thermoelectrics.

  18. Electronic structures of an epitaxial graphene monolayer on SiC(0001) after metal intercalation (metal = Al, Ag, Au, Pt, and Pd): A first-principles study

    NASA Astrophysics Data System (ADS)

    Hsu, Chia-Hsiu; Lin, Wen-Huan; Ozolins, Vidvuds; Chuang, Feng-Chuan

    2012-02-01

    The atomic structures and electronic properties of metal-intercalated (metal = Al, Ag, Au, Pt, and Pd) graphene monolayers on SiC(0001) were investigated using first-principles calculations. The unique Dirac cone of graphene near the K point reappeared as the graphite layer was intercalated by these metals at a coverage of 3/8 ML. Furthermore, our results show that metal intercalation leads to n-type doping of graphene. The bands contributed from graphene exhibit small splitting after intercalation, whereas the bands contributed from the intercalated metal layer have significant Rashba spin-orbit splittings in all cases except Al.

  19. Draft Genome Sequence of Bacillus sp. GZT, a 2,4,6-Tribromophenol-Degrading Strain Isolated from the River Sludge of an Electronic Waste-Dismantling Region

    PubMed Central

    Liang, Zhishu; Li, Guiying; Das, Ranjit

    2016-01-01

    Here, we report the draft genome sequence of Bacillus sp. strain GZT, a 2,4,6-tribromophenol (TBP)-degrading bacterium previously isolated from an electronic waste-dismantling region. The draft genome sequence is 5.18 Mb and has a G+C content of 35.1%. This is the first genome report of a brominated flame retardant-degrading strain. PMID:27257197

  20. Weak ferromagnetic behavior, crystal structure, and electronic studies of novel [Cu(II)(Br)(PhCO 2)(Sp)] (Sp=(-)-sparteine) complex

    NASA Astrophysics Data System (ADS)

    Reyes-Ortega, Yasmi; Alcántara-Flores, José Luis; Hernández-Galindo, María del Carmen; Gutiérrez-Pérez, René; Ramírez-Rosales, Daniel; Bernès, Sylvain; Cabrera-Vivas, Blanca Martha; Durán-Hernández, Alejandro; Zamorano-Ulloa, Rafael

    2006-05-01

    Complex [Cu(II)(Br)(PhCO 2)(Sp)] 1 is obtained starting from copper(0), (-)-sparteine (sp) and benzoyl bromide. 1 Crystallizes in the monoclinic space group P2 1 with a=14.8857(11), b=8.9257(9), c=17.4456(14) Å, β=111.689(5)°, and Z=4. The UV-vis spectrum is characteristic of Cu(II) complexes with tetragonally distorted square pyramidal geometry. The far IR spectrum of 1 shows characteristic vibrations of Cu-Br (239 cm -1), Cu-N (437 cm -1) and Cu-O (466 cm -1) bonds. The 1H NMR broad chemical shifts of 1 integrated for a total of 31 protons and are typical of Cu(II) complexes. ESR spectra of polycrystalline 1 at 77 and 300 K show axial spectra with areas in the ratio A77/ A300=4.02, suggesting a very weak Cu-Cu ferromagnetic interaction. Complex 1-doped with Zn(II) gives hfs with hyperfine interaction constant value A∥=112.45×10 -4 cm -1. The magnetization vs temperature data in the 2-299 K range, show that cupric ion pairs interact through a small antiferromagnetic Heisenberg exchange energy— JS1· S2 with a ground singlet state S=0, separated by J=-1.3 cm -1 from the excited triplet state S=1. The sign of the very weak interchange interaction constant, J, does not agree with the ESR spectra areas ratio of 1 at 77 and 300 K, which is a more accurate quantification of the weak ferromagnetic interaction Cu-Cu through the space.

  1. Excitons in AgI-BASED-GLASSES and -

    NASA Astrophysics Data System (ADS)

    Fujishiro, Fumito; Mochizuki, Shosuke

    2007-01-01

    We summarize our recent optical studies on different pristine AgI films, different AgI-based glasses and different AgI-oxide fine particle composites. The exciton spectra of these specimens give useful information about the ionic and electronic structures at the AgI/glass and AgI/oxide particle interfaces.

  2. Electronic properties of GeTe and Ag- or Sb-substituted GeTe studied by low-temperature Te125 NMR

    DOE PAGES

    Cui, J.; Levin, E. M.; Lee, Y.; Furukawa, Y.

    2016-08-18

    We have carried out 125Te nuclear magnetic resonance (NMR) in a wide temperature range of 1.5–300 K to investigate the electronic properties of Ge50 Te50, Ag2 Ge48Te50 , and Sb2 Ge48 Te50 from a microscopic point of view. From the temperature dependence of the NMR shift (K) and nuclear spin lattice relaxation rate (1/T1), we found that two bands contribute to the physical properties of the materials. One band overlaps the Fermi level providing the metallic state where no strong electron correlations are revealed by Korringa analysis. The other band is separated from the Fermi level by an energy gapmore » of Eg/kB ~67 K, which gives rise to semiconductorlike properties. First-principles calculation reveals that the metallic band originates from the Ge vacancy while the semiconductorlike band is related to the fine structure of the density of states near the Fermi level. We find low-temperature Te125 NMR data for the materials studied here clearly show that Ag substitution increases hole concentration while Sb substitution decreases it.« less

  3. Electronic properties of GeTe and Ag- or Sb-substituted GeTe studied by low-temperature 125Te NMR

    NASA Astrophysics Data System (ADS)

    Cui, J.; Levin, E. M.; Lee, Y.; Furukawa, Y.

    2016-08-01

    We have carried out 125Te nuclear magnetic resonance (NMR) in a wide temperature range of 1.5-300 K to investigate the electronic properties of Ge50Te50 ,Ag2Ge48Te50 , and Sb2Ge48Te50 from a microscopic point of view. From the temperature dependence of the NMR shift (K ) and nuclear spin lattice relaxation rate (1 /T1 ), we found that two bands contribute to the physical properties of the materials. One band overlaps the Fermi level providing the metallic state where no strong electron correlations are revealed by Korringa analysis. The other band is separated from the Fermi level by an energy gap of Eg/kB˜67 K, which gives rise to semiconductorlike properties. First-principles calculation reveals that the metallic band originates from the Ge vacancy while the semiconductorlike band is related to the fine structure of the density of states near the Fermi level. Low-temperature 125Te NMR data for the materials studied here clearly show that Ag substitution increases hole concentration while Sb substitution decreases it.

  4. Superatomic S(2) silver clusters stabilized by a thiolate-phosphine monolayer: insight into electronic and optical properties of Ag14(SC6H3F2)12(PPh3)8 and Ag16(SC6H3F2)14(DPPE)4.

    PubMed

    Gell, Lars; Lehtovaara, Lauri; Häkkinen, Hannu

    2014-09-18

    The electronic structure of two recently crystallographically solved, thiolate-phosphine protected silver clusters Ag14 and Ag16 are analyzed via density functional theory (DFT) and their optical excitations are analyzed from time-dependent DFT perturbation theory. Both clusters can be characterized as having the S(2) free-electron configuration in the metal core, which is the first time such a configuration is confirmed for structurally known ligand-protected noble metal clusters. However, their different core shapes and ligand layer induce significantly different optical spectra. Performance of gradient-corrected DFT functionals is discussed and it is shown that the asymptotically correct Leeuwen-Baerends LB94 functional reproduces the optical spectrum of Ag14 in a good agreement with experiment. Choice of the functional becomes important for clusters where the optical transitions are dominated by the electron-rich ligand layer.

  5. Electron Affinities, Fluoride Affinities, and Heats of Formation of the Second Row Transition Metal Hexafluorides: MF6 (M = Mo, Tc, Ru, Rh, Pd, Ag)

    SciTech Connect

    Craciun, Raluca; Long, Rebecca T.; Dixon, David A.; Christe, Karl O.

    2010-07-22

    High-level electronic structure calculations were used to evaluate reliable, self-consistent thermochemical data sets for the second row transition metal hexafluorides. The electron affinities, heats of formation, first (MF{sub 6} {yields} MF{sub 5} + F) and average M-F bond dissociation energies, and fluoride affinities of MF{sub 6} (MF{sub 6} + F{sup -} {yields} MF{sub 7}{sup -}) and MF{sub 5} (MF{sub 5} + F{sup -} {yields} MF{sub 6}{sup -}) were calculated. The electron affinities are higher than those of the corresponding third row hexafluorides, making them stronger one-electron oxidizers. The calculated electron affinities, in good agreement with the available experimental values, are 4.23 eV for MoF{sub 6}, 5.89 eV for TcF{sub 6}, 7.01 eV for RuF{sub 6}, 6.80 eV for RhF{sub 6}, 7.95 eV for PdF{sub 6}, and 8.89 eV for AgF{sub 6}. The corresponding pentafluorides are also very strong Lewis acids, although their acidities on the pF{sup -} scale are about one unit lower than those of the third row pentafluorides. The performance of a wide range of DFT exchange-correlation functionals was benchmarked by comparing them to our more accurate CCSD(T) results.

  6. Angular distribution of bremsstrahlung produced by electrons with initial energies in the range from 10 to 20 keV incident on thick Ag

    NASA Astrophysics Data System (ADS)

    Gonzales, Daniel; Cavness, Brandon; Williams, Scott

    2012-03-01

    Experimental results are presented comparing the intensities of the thick-target bremsstrahlung produced by electrons with initial energies ranging from 10 to 20 keV incident on Ag, measured at forward angles in the range of 0 to 55 degrees. When the data are corrected for attenuation due to photon absorption within the target, the results indicate that the detected radiation is distributed anisotropically only at photon energies k that are approximately equal to the initial energy of the incident electrons E0. The results of our experiments suggest that, as k/E0->0, the detected radiation essentially becomes isotropic due primarily to the scattering of electrons within the target. Comparison to the theory of Kissel et al. [At. Data Nucl. Data Tables 28, 381 (1983)] suggests that the angular distribution of bremsstrahlung emitted by electrons incident on thick targets is similar to the angular distribution of bremsstrahlung emitted by electrons incident on free-atom targets only when k/E0 1. The experimental data also are in approximate agreement with the angular distribution predictions of the Monte Carlo program PENELOPE.

  7. Mono- and bis-furanone derivatives from the endolichenic fungus Peziza sp.

    PubMed

    Zhang, Kun; Ren, Jinwei; Ge, Mei; Li, Li; Guo, Liangdong; Chen, Daijie; Che, Yongsheng

    2014-01-01

    Seven new mono- and bis-furanones, pezizolides A-G (1-7), have been isolated from the crude extract of the endolichenic fungus Peziza sp. inhabiting the lichen Xanthoparmelia sp. The structures of the new compounds were elucidated mainly by NMR and MS methods. The absolute configuration of 1-4 was assigned by the application of CD exciton chirality method, and 1 was further supported by electronic circular dichroism (ECD) calculations, whereas that of 5 was deduced by Snatzke's method following the relative configuration analysis of its acetonide. The cytotoxity and antimicrobial activity of compounds 1-7 were tested.

  8. Development of Sn-Ag-Cu-X Solders for Electronic Assembly by Micro-Alloying with Al

    SciTech Connect

    Boesenberg, Adam; Anderson, Iver; Harringa, Joel

    2012-03-10

    Of Pb-free solder choices, an array of solder alloys based on the Sn-Ag-Cu (SAC) ternary eutectic (T eut = 217°C) composition have emerged with potential for broad use, including ball grid array (BGA) joints that cool slowly. This work investigated minor substitutional additions of Al (<0.25 wt.%) to Sn-3.5Ag-0.95Cu (SAC3595) solders to promote more consistent solder joint microstructures and to avoid deleterious product phases, e.g., Ag3Sn “blades,” for BGA cooling rates, since such Al additions to SAC had already demonstrated excellent thermal aging stability. Consistent with past work, blade formation was suppressed for increased Al content (>0.05Al), but the suppression effect faded for >0.20Al. Undercooling suppression did not correlate specifically with blade suppression since it became significant at 0.10Al and increased continuously with greater Al to 0.25Al. Surprisingly, an intermediate range of Al content (0.10 wt.% to 0.20 wt.% Al) promoted formation of significant populations of 2-μm to 5-μm faceted Cu-Al particles, identified as Cu33Al17, that clustered at the top of the solder joint matrix and exhibited extraordinary hardness. Clustering of Cu33Al17 was attributed to its buoyancy, from a lower density than Sn liquid, and its early position in the nucleation sequence within the solder matrix, permitting unrestricted migration to the top interface. Joint microstructures and implications for the full nucleation sequence for these SAC + Al solder joints are discussed, along with possible benefits from the clustered particles for improved thermal cycling resistance.

  9. 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. PMID:27236845

  10. Ab initio studies of structural, electronic, optical, elastic and thermal properties of silver gallium dichalcogenides (AgGaX{sub 2}: X = S, Se, Te)

    SciTech Connect

    Sharma, Sheetal; Verma, A.S.; Jindal, V.K.

    2014-05-01

    Graphical abstract: - Highlights: • FP-LAPW method has been used to compute the solid state properties of AgGaX{sub 2} (X = S, Se, Te). • Electronic and optical properties reported with recently developed mBJ potential. • Thermal expansion, heat capacity, Debye temperature, entropy and Grüneisen parameter were evaluated. • Hardness was calculated for the first time at different temperature and pressure. - Abstract: We have performed ab initio calculations for the structural, electronic, optical, elastic and thermal properties of the silver gallium dichalcogenides (AgGaX{sub 2}: X = S, Se, Te). In this study, we have used the accurate full potential linearized augmented plane wave (FP-LAPW) method to find the equilibrium structural parameters and to compute the six elastic constants (C{sub 11}, C{sub 12}, C{sub 13}, C{sub 33}, C{sub 44} and C{sub 66}). We have reported electronic and optical properties with the recently developed density functional theory of Tran and Blaha, and this theory is used along with the Wu-Cohen generalized gradient approximation (WC-GGA) for the exchange-correlation potential. Furthermore, optical features such as dielectric functions, refractive indices, extinction coefficient, optical reflectivity, absorption coefficients and optical conductivities were calculated for photon energies up to 40 eV. The thermodynamical properties such as thermal expansion, heat capacity, debye temperature, entropy, Grüneisen parameter and bulk modulus were calculated employing the quasi-harmonic Debye model at different temperatures (0–900 K) and pressures (0–8 GPa) and the silent results were interpreted. Hardness of the materials was calculated for the first time at different temperatures and pressures.

  11. Quantum mechanics capacitance molecular mechanics modeling of core-electron binding energies of methanol and methyl nitrite on Ag(111) surface.

    PubMed

    Löytynoja, T; Li, X; Jänkälä, K; Rinkevicius, Z; Ågren, H

    2016-07-14

    We study a newly devised quantum mechanics capacitance molecular mechanics (QMCMM) method for the calculation of core-electron binding energies in the case of molecules adsorbed on metal surfaces. This yet untested methodology is applied to systems with monolayer of methanol/methyl nitrite on an Ag(111) surface at 100 K temperature. It was found out that the studied C, N, and O 1s core-hole energies converge very slowly as a function of the radius of the metallic cluster, which was ascribed to build up of positive charge on the edge of the Ag slab. Further analysis revealed that an extrapolation process can be used to obtain binding energies that deviated less than 0.5 eV against experiments, except in the case of methanol O 1s where the difference was as large as 1.8 eV. Additional QM-cluster calculations suggest that the latter error can be connected to the lack of charge transfer over the QM-CMM boundary. Thus, the results indicate that the QMCMM and QM-cluster methods can complement each other in a holistic picture of molecule-adsorbate core-ionization studies, where all types of intermolecular interactions are considered.

  12. Quantum mechanics capacitance molecular mechanics modeling of core-electron binding energies of methanol and methyl nitrite on Ag(111) surface

    NASA Astrophysics Data System (ADS)

    Löytynoja, T.; Li, X.; Jänkälä, K.; Rinkevicius, Z.; Ågren, H.

    2016-07-01

    We study a newly devised quantum mechanics capacitance molecular mechanics (QMCMM) method for the calculation of core-electron binding energies in the case of molecules adsorbed on metal surfaces. This yet untested methodology is applied to systems with monolayer of methanol/methyl nitrite on an Ag(111) surface at 100 K temperature. It was found out that the studied C, N, and O 1s core-hole energies converge very slowly as a function of the radius of the metallic cluster, which was ascribed to build up of positive charge on the edge of the Ag slab. Further analysis revealed that an extrapolation process can be used to obtain binding energies that deviated less than 0.5 eV against experiments, except in the case of methanol O 1s where the difference was as large as 1.8 eV. Additional QM-cluster calculations suggest that the latter error can be connected to the lack of charge transfer over the QM-CMM boundary. Thus, the results indicate that the QMCMM and QM-cluster methods can complement each other in a holistic picture of molecule-adsorbate core-ionization studies, where all types of intermolecular interactions are considered.

  13. Quantum mechanics capacitance molecular mechanics modeling of core-electron binding energies of methanol and methyl nitrite on Ag(111) surface.

    PubMed

    Löytynoja, T; Li, X; Jänkälä, K; Rinkevicius, Z; Ågren, H

    2016-07-14

    We study a newly devised quantum mechanics capacitance molecular mechanics (QMCMM) method for the calculation of core-electron binding energies in the case of molecules adsorbed on metal surfaces. This yet untested methodology is applied to systems with monolayer of methanol/methyl nitrite on an Ag(111) surface at 100 K temperature. It was found out that the studied C, N, and O 1s core-hole energies converge very slowly as a function of the radius of the metallic cluster, which was ascribed to build up of positive charge on the edge of the Ag slab. Further analysis revealed that an extrapolation process can be used to obtain binding energies that deviated less than 0.5 eV against experiments, except in the case of methanol O 1s where the difference was as large as 1.8 eV. Additional QM-cluster calculations suggest that the latter error can be connected to the lack of charge transfer over the QM-CMM boundary. Thus, the results indicate that the QMCMM and QM-cluster methods can complement each other in a holistic picture of molecule-adsorbate core-ionization studies, where all types of intermolecular interactions are considered. PMID:27421423

  14. Study of grain boundary properties in Ag-clad Bi2Sr2Ca2Cu3Ox tapes by multi-phase electron backscatter diffraction analysis

    NASA Astrophysics Data System (ADS)

    Koblischka-Veneva, A.; Koblischka, M. R.

    2008-01-01

    The properties of grain boundaries within Ag-clad (Pb,Bi)2Sr2Ca2Cu3Ox (Bi-2223) tapes are studied by means of electron backscatter diffraction (EBSD). The achieved high image quality of the Kikuchi patterns enables multi-phase EBSD scans including Bi-2223, Bi2Sr2CaCu2Ox (Bi-2212), Bi2Sr2CuOx (Bi-2201), (Sr,Ca)14Cu24O41 and Ag to be performed. For the EBSD scans a maximum spatial resolution of 30 nm was reached enabling a detailed orientation analysis. The nature of the grain boundaries is discussed on the base of the EBSD data. While the main orientation of the tape is in [0 0 1] direction, a large number of misorientations is detected. These misorientations are visualized using crystal direction (CD) maps. Furthermore, EBSD enables the spatially resolved mapping of the misorientation angles within each phase separately. The influence of these grain boundaries on the current transport properties is discussed.

  15. Deviations from one-electron behavior in the Ag and Pd M4,5-VV Auger spectra of AgcPd1-c alloys

    NASA Astrophysics Data System (ADS)

    Mariot, J.-M.; Hague, C. F.; Dufour, G.

    1981-04-01

    A systematic investigation of the Ag and Pd M4,5-VV Auger spectra in the pure metals and in the AgcPd1-c(0.1<=c<=0.9) alloys is presented. The shape of the Auger spectra is discussed in relation to the values of the effective Coulomb interaction Ueff between the two holes present in the final state of the Auger transition and of the width W of the one-electron local densities of states as obtained from Lβ2,15 soft-x-ray emission bands. The Auger spectra of Ag in the metal and the alloys have a pronounced quasiatomic character, as can be expected from the Ueff2W ratio which is found to be close to unity. The Auger spectrum of pure Pd (Ueff2W~0.4) can be explained in terms of an atomic model in which strong band effects are present. For alloys with low-Pd content where Pd forms an impurity state, it is shown that final states other than the localized [4d2] two-hole state have to be invoked to explain the line shape.

  16. Laser-based synthesis of core Ag-shell AgI nanoparticles

    NASA Astrophysics Data System (ADS)

    Tan, Hua; Fan, Wai Yip

    2005-05-01

    A laser-controlled synthesis of silver iodide (AgI) nanoparticles with isolable AgI shell-Ag core stable intermediates is achieved via molecular iodine photodissociation in the presence of pure Ag nanoparticles dispersed in water. Ag nanoparticles were introduced into the solution containing sodium dodecylsulphate surfactants and iodine by ablating a piece of silver foil with a 532 nm pulsed Nd-YAG laser. Transmission electron microscopy images showed that different AgI shell-Ag core sizes could be achieved by controlling the photolysis of I 2 in solution. These nanoparticles were also found to catalyse an atom-economy Grignard-Barbier organic reaction.

  17. A comparative study of the effects of Ag2S films prepared by MPD and HRTD methods on the performance of polymer solar cells

    NASA Astrophysics Data System (ADS)

    Zhai, Yong; Li, Fumin; Ling, Lanyun; Chen, Chong

    2016-10-01

    In this work, the Ag2S nanocrystalline thin films are deposited on ITO glass via molecular precursor decomposition (MPD) method and newly developed HRTD method for organic solar cells (ITO/Ag2S/P3HT:PCBM/MoO3/Au) as an electron selective layer and a light absorption material. The surface morphology, structure characterization, and optical property of the Ag2S films prepared by these two methods were compared and the effect of the prepared Ag2S film on the device performance is investigated. It is found that the Ag2S films prepared by HRTD method have lower roughness and better uniformity than the corresponding films prepared by the MPD method. In addition, a more effective and rapid transporting ability for the electrons and holes in the ITO/Ag2S(HRTD, n)/P3HT:PCBM/MoO3/Au cells is found, which reduces the charge recombination, and thus, improves the device performance. The highest efficiency of 3.21% achieved for the ITO/Ag2S(HRTD, 50)/P3HT:PCBM/MoO3/Au cell is 93% higher than that of the ITO/Ag2S(MPD, 2)/P3HT:PCBM/MoO3/Au cell.

  18. Visible-light-driven photocatalysts Ag/AgCl dispersed on mesoporous Al2O3 with enhanced photocatalytic performance.

    PubMed

    Feng, Zhouzhou; Yu, Jiajie; Sun, Dongping; Wang, Tianhe

    2016-10-15

    In this paper, Ag/AgCl and Ag/AgCl/Al2O3 photocatalysts were synthesized via a precipitation reaction between NaCl and CH3COOAg or Ag(NH3)2NO3, wherein Ag/AgCl was immobilized into mesoporous Al2O3 medium. The Ag/AgCl-based nanostructures were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) spectra, and so on. The photocatalysts displayed excellent photocatalytic activity for the degradations of methyl orange (MO) and methylene blue (MB) pollutants under visible light irradiation. The Ag/AgCl(CH3COOAg)/Al2O3 sample exhibited the best photocatalytic performance, degrading 99% MO after 9min of irradiation, which was 1.1 times, 1.22 times and 1.65 times higher than that of Ag/AgCl(Ag(NH3)2NO3)/Al2O3, Ag/AgCl(CH3COOAg) and Ag/AgCl(Ag(NH3)2NO3) photocatalyst, respectively. Meanwhile, Ag/AgCl(CH3COOAg)/Al2O3 also showed excellent capability of MB degradation. Compared to the data reported for Ag/AgCl/TiO2, the Ag/AgCl/Al2O3 prepared in this work exhibited a good performance for the degradation of methyl orange (MO). The results suggest that the dispersion of Ag/AgCl on mesoporous Al2O3 strongly affected their photocatalytic activities. O2(-), OH radicals and Cl(0) atoms are main active species during photocatalysis. PMID:27442145

  19. Anion effects on electronic structure and electrodynamic properties of the Mott insulator κ -(BEDT-TTF ) 2Ag2(CN) 3

    NASA Astrophysics Data System (ADS)

    Pinterić, M.; Lazić, P.; Pustogow, A.; Ivek, T.; Kuveždić, M.; Milat, O.; Gumhalter, B.; Basletić, M.; Čulo, M.; Korin-Hamzić, B.; Löhle, A.; Hübner, R.; Sanz Alonso, M.; Hiramatsu, T.; Yoshida, Y.; Saito, G.; Dressel, M.; Tomić, S.

    2016-10-01

    The Mott insulator κ -(BEDT-TTF ) 2Ag2(CN) 3 forms a highly-frustrated triangular lattice of S =1 /2 dimers with a possible quantum-spin-liquid state. Our experimental and numerical studies reveal the emergence of a slight charge imbalance between crystallographically inequivalent sites, relaxor dielectric response, and hopping dc transport. In a broader perspective we conclude that the universal properties of strongly-correlated charge-transfer salts with spin liquid state are an anion-supported valence band and cyanide-induced quasidegenerate electronic configurations in the relaxed state. The generic low-energy excitations are caused by charged domain walls rather than by fluctuating electric dipoles. They give rise to glassy dynamics characteristic of dimerized Mott insulators, including the sibling compound κ -(BEDT-TTF)2Cu2 (CN )3.

  20. Role of layer packing for the electronic properties of the organic superconductor (BEDT-TTF ) 2Ag (CF3)4(TCE )

    NASA Astrophysics Data System (ADS)

    Altmeyer, Michaela; Valentí, Roser; Jeschke, Harald O.

    2015-06-01

    The charge-transfer compound (BEDT-TTF ) 2Ag (CF3)4(TCE ) crystallizes in three polymorphs with different alternating layers: While a phase with a κ packing motif has a low superconducting transition temperature of Tc=2.6 K , two phases with higher Tc of 9.5 and 11 K are multilayered structures consisting of α' and κ layers. We investigate these three systems within density functional theory and find that the α' layer shows different degrees of charge order for the two κ -α' systems and directly influences the electronic behavior of the conducting κ layer. We discuss the origin of the distinct behavior of the three polymorphs and propose a minimal tight-binding Hamiltonian for the description of these systems based on projective molecular Wannier functions.

  1. Theoretical study of the structures and electron affinities of the dimers and trimers of the group IB metals (Cu, Ag, and Au)

    NASA Technical Reports Server (NTRS)

    Bauschlicher, Charles W., Jr.; Langhoff, Stephen R.; Partridge, Harry

    1989-01-01

    The molecular structure of both the neutral and negatively charged diatomic and triatomic systems containing the Cu, Ag, and Au metals are determined from ab initio calculations. For the neutral triatomic systems, the lowest energy structure is found to be triangular. The relative stability of the 2A1 and 2B2 structures can be predicted simply by knowing the constituent diatomic bond distances and atomic electron affinities (EAs). The lowest energy structure is linear for all of the negative ions. For anionic clusters containing Au, the Au atom(s) preferentially occupy the terminal position(s). The EAs of the heteronuclear systems can be predicted relatively accurately from a weighted average of the corresponding homonuclear systems. Although the theoretical EAs are systematically too small, accurate predictions for the EAs of the triatomics are obtained by uniformly scaling the ab initio results using the accurate experimental EA values available for the atoms and homonuclear diatomics.

  2. Selective photochemical synthesis of Ag nanoparticles on position-controlled ZnO nanorods for the enhancement of yellow-green light emission

    NASA Astrophysics Data System (ADS)

    Park, Hyeong-Ho; Zhang, Xin; Lee, Keun Woo; Sohn, Ahrum; Kim, Dong-Wook; Kim, Joondong; Song, Jin-Won; Choi, Young Su; Lee, Hee Kwan; Jung, Sang Hyun; Lee, In-Geun; Cho, Young-Dae; Shin, Hyun-Beom; Sung, Ho Kun; Park, Kyung Ho; Kang, Ho Kwan; Park, Won-Kyu; Park, Hyung-Ho

    2015-12-01

    A novel technique for the selective photochemical synthesis of silver (Ag) nanoparticles (NPs) on ZnO nanorod arrays is established by combining ultraviolet-assisted nanoimprint lithography (UV-NIL) for the definition of growth sites, hydrothermal reaction for the position-controlled growth of ZnO nanorods, and photochemical reduction for the decoration of Ag NPs on the ZnO nanorods. During photochemical reduction, the size distribution and loading of Ag NPs on ZnO nanorods can be tuned by varying the UV-irradiation time. The photochemical reduction is hypothesized to facilitate the adsorbed citrate ions on the surface of ZnO, allowing Ag ions to preferentially form Ag NPs on ZnO nanorods. The ratio of visible emission to ultraviolet (UV) emission for the Ag NP-decorated ZnO nanorod arrays, synthesized for 30 min, is 20.5 times that for the ZnO nanorod arrays without Ag NPs. The enhancement of the visible emission is believed to associate with the surface plasmon (SP) effect of Ag NPs. The Ag NP-decorated ZnO nanorod arrays show significant SP-induced enhancement of yellow-green light emission, which could be useful in optoelectronic applications. The technique developed here requires low processing temperatures (120 °C and lower) and no high-vacuum deposition tools, suitable for applications such as flexible electronics.A novel technique for the selective photochemical synthesis of silver (Ag) nanoparticles (NPs) on ZnO nanorod arrays is established by combining ultraviolet-assisted nanoimprint lithography (UV-NIL) for the definition of growth sites, hydrothermal reaction for the position-controlled growth of ZnO nanorods, and photochemical reduction for the decoration of Ag NPs on the ZnO nanorods. During photochemical reduction, the size distribution and loading of Ag NPs on ZnO nanorods can be tuned by varying the UV-irradiation time. The photochemical reduction is hypothesized to facilitate the adsorbed citrate ions on the surface of ZnO, allowing Ag ions to

  3. All-metal electride molecules CuAg@Ca7M (M = Be, Mg, and Ca) with multi-excess electrons and all-metal polyanions: molecular structures and bonding modes as well as large infrared nonlinear optical responses.

    PubMed

    He, Hui-Min; Li, Ying; Sun, Wei-Ming; Wang, Jia-Jun; Wu, Di; Zhong, Rong-Lin; Zhou, Zhong-Jun; Li, Zhi-Ru

    2016-02-14

    All-metal electride molecules, CuAg@Ca7M (M = Be, Mg and Ca), have been designed and researched in theory for the first time. In these molecules, a pull-push electron relay occurs. Unusually, the all-metal polyanions of fourfold negatively charged [Cu-Ag-Be/Mg](4-) and [Cu-Ag](4-) with 4 extra electrons gained from Ca atoms push the remaining valence electrons of the Ca atoms forming the multi-excess electrons (Ne = 10/12). Therefore, these molecules can be described as salt-like [(Ca(2+))7(CuAgM)(4-)] + 10e(-) (M = Be and Mg) and [(Ca(2+))8(CuAg)(4-)] + 12e(-). In these salt-like molecules, there are extraordinary covalent bonding modes, which include 2c-2e/3c-2e σ-bonding in the polyanions and the Ca(2+) cations sharing the diffuse multi-excess electrons. For an intriguing nonlinear optical (NLO) response, these all-metal electride molecules display large electronic first hyperpolarizabilities (β0), thus a new class of NLO molecules, all-metal electride NLO molecules, emerge. Moreover, it is also found that manipulating the atomic number and position of M is a new strategy to enhance β0. As a result, CuAg@Ca7Mg(1) exhibits a considerable β0 (1.43 × 10(4) au), which is 16 times the β0 sum of two isolated CuAg and Ca7Mg(1) subunits, and this deeply reveals the fundamental origin of the considerable β0, namely, the multi-excess electrons generated by the subunit interaction. These all-metal electride molecules have the infrared (IR) transparent region of 1.3-6 μm, and hence are new IR NLO molecules. In addition the electronic contribution, β0, the large effects of vibrations on the static first hyperpolarizabilities of these all-metal electride molecules are also estimated. Thus, this study opens the new research field of all-metal electride IR NLO molecules.

  4. All-metal electride molecules CuAg@Ca7M (M = Be, Mg, and Ca) with multi-excess electrons and all-metal polyanions: molecular structures and bonding modes as well as large infrared nonlinear optical responses.

    PubMed

    He, Hui-Min; Li, Ying; Sun, Wei-Ming; Wang, Jia-Jun; Wu, Di; Zhong, Rong-Lin; Zhou, Zhong-Jun; Li, Zhi-Ru

    2016-02-14

    All-metal electride molecules, CuAg@Ca7M (M = Be, Mg and Ca), have been designed and researched in theory for the first time. In these molecules, a pull-push electron relay occurs. Unusually, the all-metal polyanions of fourfold negatively charged [Cu-Ag-Be/Mg](4-) and [Cu-Ag](4-) with 4 extra electrons gained from Ca atoms push the remaining valence electrons of the Ca atoms forming the multi-excess electrons (Ne = 10/12). Therefore, these molecules can be described as salt-like [(Ca(2+))7(CuAgM)(4-)] + 10e(-) (M = Be and Mg) and [(Ca(2+))8(CuAg)(4-)] + 12e(-). In these salt-like molecules, there are extraordinary covalent bonding modes, which include 2c-2e/3c-2e σ-bonding in the polyanions and the Ca(2+) cations sharing the diffuse multi-excess electrons. For an intriguing nonlinear optical (NLO) response, these all-metal electride molecules display large electronic first hyperpolarizabilities (β0), thus a new class of NLO molecules, all-metal electride NLO molecules, emerge. Moreover, it is also found that manipulating the atomic number and position of M is a new strategy to enhance β0. As a result, CuAg@Ca7Mg(1) exhibits a considerable β0 (1.43 × 10(4) au), which is 16 times the β0 sum of two isolated CuAg and Ca7Mg(1) subunits, and this deeply reveals the fundamental origin of the considerable β0, namely, the multi-excess electrons generated by the subunit interaction. These all-metal electride molecules have the infrared (IR) transparent region of 1.3-6 μm, and hence are new IR NLO molecules. In addition the electronic contribution, β0, the large effects of vibrations on the static first hyperpolarizabilities of these all-metal electride molecules are also estimated. Thus, this study opens the new research field of all-metal electride IR NLO molecules. PMID:26740006

  5. 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.

  6. 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.

  7. FesM, a membrane iron-sulfur protein, is required for cyclic electron flow around photosystem I and photoheterotrophic growth of the cyanobacterium Synechococcus sp. PCC 7002.

    PubMed

    Xu, Dongyi; Liu, Xianwei; Zhao, Jiao; Zhao, Jindong

    2005-07-01

    While it is known that cyclic electron flow around photosystem I is an important pathway of photosynthetic electron transfer for converting light energy to chemical energy, some components of cyclic electron flow remain to be revealed. Here, we show that fesM, encoding a novel membrane iron-sulfur protein, is essential to cyclic electron flow in the cyanobacterium Synechococcus sp. PCC 7002. The FesM protein is predicted to have a cAMP-binding domain, an NtrC-like domain, a redox sensor motif, and an iron-sulfur (4Fe-4S) motif. Deletion of fesM (fesM-D) led to an inability for Synechococcus cells to grow in the presences of glycerol and 3-(3,4-dichlorophenyl)-1,1-dimethylurea. Photoheterotrophic growth was restored by a complete fesM gene present on a replicable plasmid. A mutant fesM gene encoding a truncated FesM protein lacking the cAMP domain failed to restore the phenotype, suggesting this domain is important to the function of FesM. Measurements of reduction of P700(+) and the redox state of interphotosystem electron carriers showed that cells had a slower rate of respiratory electron donation to the interphotosystem electron transport chain, and cyclic electron flow around photosystem I in fesM-D was impaired, suggesting that FesM is a critical protein for respiratory and cyclic electron flow. Phosphatase fusion analysis showed that FesM contains nine membrane-spanning helices, and all functional domains of FesM are located on the cytoplasmic face of the thylakoid membranes.

  8. Investigation into anomalous total secondary electron yield for micro-porous Ag surface under oblique incidence conditions

    NASA Astrophysics Data System (ADS)

    Ye, M.; He, Y. N.; Hu, S. G.; Yang, J.; Wang, R.; Hu, T. C.; Peng, W. B.; Cui, W. Z.

    2013-09-01

    We study the dependence of total secondary electron yield (SEY) of micro-porous silver surface on incident angle of primary electron. First, we produce regular and random micro-porous surfaces on silver plated aluminium samples by photolithography pattern process and direct chemical etching method, respectively. Second, we study the dependence of the SEY characteristics of these surfaces on the primary electron incident angle from 0° to 60°. The experimental results show that micro-porous surface with large porosity can suppress SEY effectively either for normal incidence or oblique incidence. The maximum SEY of the directly chemical etched sample can reach a 45% reduction relative to the original flat sample. We also show the anomalous experimental phenomenon that the SEY of directly chemical etched sample with large porosity does not increase with incident angle. Third, we explain the complicated SEY dependence on incident angle qualitatively by the secondary electron trapping effect in micro-pores as well as the Monte Carlo simulation based on phenomenological model of secondary electron emission. Finally, we suggest a third order polynomial formula to describe the SEY dependence on incident angle which will be useful in particle simulation. In total, we demonstrate that micro-porous surface with large porosity is effective in SEY suppression under both normal and oblique incidence and thus the proposed direct chemical etching method is prospective in related areas such as multipactor improvement.

  9. 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.

  10. Molecular functionalization of silicene/Ag(111) by covalent bonds: a DFT study.

    PubMed

    Stephan, Régis; Hanf, Marie-Christine; Sonnet, Philippe

    2015-06-14

    Among the 2D crystals, silicene, which forms sp(2)-sp(3) bonds, is expected to present a higher reactivity than graphene, characterized by sp(2) bonds only. However, silicene functionalization, in particular with organic molecules, remains an open question. By means of density functional theory, we study the adsorption of benzene, a model organic molecule, on (3 × 3) silicene on the (4 × 4) Ag(111) surface. Our calculations show that the dispersion interactions must be taken into account in order to describe this system properly. The adsorption energy is calculated by means of the semi-empirical dispersion-corrected density functional theory (DFT-D2) and the optB86b-vdW density functional. The charge density and electron localization function maps indicate that the molecule is chemisorbed on the silicene surface by means of two Si-C covalent bonds. In agreement with charge density difference calculations, two C-C double bonds are formed in the benzene molecule, which adopts a butterfly configuration. The silicene lattice is slightly deformed upon benzene adsorption, but the Si-Si distance remains the same as in bare silicene/Ag(111). Bader analysis shows a charge transfer from top Si atoms to both molecules and Ag substrates. Finally, we show that the covalent functionalization of silicene is possible.

  11. Modification of photosynthetic electron transport and amino acid levels by overexpression of a circadian-related histidine kinase hik8 in Synechocystis sp. PCC 6803

    PubMed Central

    Kuwahara, Ayuko; Arisaka, Satomi; Takeya, Masahiro; Iijima, Hiroko; Hirai, Masami Yokota; Osanai, Takashi

    2015-01-01

    Cyanobacteria perform oxygenic photosynthesis, and the maintenance of photosynthetic electron transport chains is indispensable to their survival in various environmental conditions. Photosynthetic electron transport in cyanobacteria can be studied through genetic analysis because of the natural competence of cyanobacteria. We here show that a strain overexpressing hik8, a histidine kinase gene related to the circadian clock, exhibits an altered photosynthetic electron transport chain in the unicellular cyanobacterium Synechocystis sp. PCC 6803. Respiratory activity was down-regulated under nitrogen-replete conditions. Photosynthetic activity was slightly lower in the hik8-overexpressing strain than in the wild-type after nitrogen depletion, and the values of photosynthetic parameters were altered by hik8 overexpression under nitrogen-replete and nitrogen-depleted conditions. Transcripts of genes encoding Photosystem I and II were increased by hik8 overexpression under nitrogen-replete conditions. Nitrogen starvation triggers increase in amino acids but the magnitude of the increase in several amino acids was diminished by hik8 overexpression. These genetic data indicate that Hik8 regulates the photosynthetic electron transport, which in turn alters primary metabolism during nitrogen starvation in this cyanobacterium. PMID:26539179

  12. Electronic structure and thermoelectric properties of p-type Ag-doped Mg₂Sn and Mg₂Sn{sub 1-x}Si{sub x} (x=0.05, 0.1)

    SciTech Connect

    Kim, Sunphil; Jin, Hyungyu; Wiendlocha, Bartlomiej; Tobola, Janusz; Heremans, Joseph P.

    2014-10-21

    An experimental and theoretical study of p-type Ag-doped Mg₂Sn and Mg₂Sn{sub 1-x}Si{sub x} (x=0.05, 0.1) is presented. Band structure calculations show that behavior of Ag in Mg₂Sn depends on the site it occupies. Based on Bloch spectral functions and density of states calculations, we show that if Ag substitutes for Sn, it is likely to form a resonant level; if it substitutes for Mg, a rigid-band-like behavior is observed. In both cases, the doped system should exhibit p-type conductivity. Experimentally, thermoelectric, thermomagnetic, and galvanomagnetic properties are investigated of p-type Mg₂Sn{sub 1–x}Si{sub x} (x=0, 0.05, 0.1) samples synthesized by a co-melting method in sealed crucibles. Ag effectively dopes the samples p-type, and thermoelectric power factors in excess of 20μW cm⁻¹K⁻² are observed in optimally doped samples. From the measured Seebeck coefficient, Nernst coefficient, and mobility, we find that the combination of acoustic phonon scattering, optical phonon scattering and defect scattering results in an energy-independent scattering rate. No resonant-like increase in thermopower is observed, which correlates well with electronic structure calculations assuming the location of Ag on Mg site.

  13. Photostimulated Luminescence and Dynamics of AgI and Ag Nanoclusters in Zeolites

    SciTech Connect

    Chen, Wei; Joly, Alan G.; Roark, Joel

    2002-06-15

    The photoluminescence and photostimulated luminescence of Ag and AgI nanoclusters formed in zeolite-Y are studied using fluorescence spectroscopy. The photoluminescence spectra of AgI nanoclusters show emission from both AgI and Ag nanoclusters, while the in the photostimulated luminescence, only the emission of Ag clusters is observed. While the photoluminescence from both Ag and AgI particles displays both sub-nanosecond and microsecond lifetimes, the emission from photostimulated luminescence shows very short, picosecond lifetimes. A model which ascribes the photostimulated luminescence to recombination of electrons trapped in the zeolite with Ag in close proximity to the trap site is proposed. The appearance of strong photostimulated luminescence with short decays in these systems demonstrates that nanoparticles have potential for digital storage and medical radiology applications.

  14. Regulation of pepc gene expression in Anabaena sp. PCC 7120 and its effects on cyclic electron flow around photosystem I and tolerances to environmental stresses.

    PubMed

    Jia, Xiao-Hui; Zhang, Peng-Peng; Shi, Ding-Ji; Mi, Hua-Ling; Zhu, Jia-Cheng; Huang, Xi-Wen; He, Pei-Min

    2015-05-01

    Since pepc gene encoding phosphoenolpyruvate carboxylase (PEPCase) has been cloned from Anabaena sp. PCC 7120 and other cyanobacteria, the effects of pepc gene expression on photosynthesis have not been reported yet. In this study, we constructed mutants containing either upregulated (forward) or downregulated (reverse) pepc gene in Anabaena sp. PCC 7120. Results from real-time quantitative polymerase chain reaction (RT-qPCR), Western blot and enzymatic analysis showed that PEPCase activity was significantly reduced in the reverse mutant compared with the wild type, and that of the forward mutant was obviously increased. Interestingly, the net photosynthesis in both the reverse mutant and the forward mutant were higher than that of the wild type, but dark respiration was decreased only in the reverse mutant. The absorbance changes of P700 upon saturation pulse showed the photosystem I (PSI) activity was inhibited, as reflected by Y(I), and Y(NA) was elevated, and dark reduction of P700(+) was stimulated, indicating enhanced cyclic electron flow (CEF) around PSI in the reverse mutant. Additionally, the reverse mutant photosynthesis was higher than that of the wild type in low temperature, low and high pH, and high salinity, and this implies increased tolerance in the reverse mutant through downregulated pepc gene.

  15. Enhancing UV-emissions through optical and electronic dual-function tuning of Ag nanoparticles hybridized with n-ZnO nanorods/p-GaN heterojunction light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Yao, Yung-Chi; Yang, Zu-Po; Hwang, Jung-Min; Chuang, Yi-Lun; Lin, Chia-Ching; Haung, Jing-Yu; Chou, Chun-Yang; Sheu, Jinn-Kong; Tsai, Meng-Tsan; Lee, Ya-Ju

    2016-02-01

    near-band-edge (NBE) emission (ZnO, λ = 380 nm) of our hybridized structure is increased almost 1.5-2 times and can be further modified in a controlled manner by varying the surface morphology of the surrounding medium of the Ag NPs. The improved light-output power is mainly attributed to the LSP resonance between the NBE emission of ZnO NRs and LSPs in Ag NPs. We also observed different behaviors in the electroluminescence (EL) spectra as the injection current increases for the treatment and reference LEDs. This observation might be attributed to the modification of the energy band diagram for introducing Ag NPs at the interface between n-ZnO NRs and p-GaN. Our results pave the way for developing advanced nanostructured LED devices with high luminescence efficiency in the UV emission regime. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr08561f

  16. An X-ray Absorption Spectroscopy Study of the Cathodic Discharge of Ag2VO2PO4: Geometric and Electronic Structure Characterization of Intermediate Phases and Mechanistic Insights

    SciTech Connect

    C Patridge; C Jaye; T Abtew; B Ravel; D Fischer; A Marschilok; P Zhang; K Takeuchi; E Takeuchi; S Baneerjee

    2011-12-31

    Bimetallic phosphorus oxides have emerged as attractive candidates for use as cathode materials in the next generation of lithium-based batteries owing to the operation of multielectron transfer processes and thermochemical stabilities conferred by the incorporation of phosphate groups. In particular silver vanadium phosphorus oxide, Ag{sub 2}VO{sub 2}PO{sub 4}, shows a much desired in situ conductivity enhancement upon discharge resulting in inherently high power capability with minimal conductive additives needed. However, the amorphization of Ag{sub 2}VO{sub 2}PO{sub 4} during electrochemical discharge precludes the use of standard diffraction tools to monitor changes in the local electronic and geometric structure. Here, we have utilized a combination of V K-, V L-, Ag K-, and O K-edge X-ray absorption fine structure spectroscopy to determine the local vanadium and silver oxidation states, local coordination geometry, and stoichiometry for Ag{sub 2}VO{sub 2}PO{sub 4} samples with varying extents of electrochemical lithiation. Soft X-ray V L- and O K-edge measurements provide a detailed orbital-specific picture of changes in vanadium electronic structure upon discharge.

  17. In situ heating transmission electron microscopy observation of nanoeutectic lamellar structure in Sn-Ag-Cu alloy on Au under-bump metallization.

    PubMed

    Seo, Jong-Hyun; Yoon, Sang-Won; Kim, Kyou-Hyun; Chang, Hye-Jung; Lee, Kon-Bae; Seong, Tae-Yeon; Fleury, Eric; Ahn, Jae-Pyoung

    2013-08-01

    We investigated the microstructural evolution of Sn(96.4)Ag(2.8)Cu(0.8) solder through in situ heating transmission electron microscopy observations. As-soldered bump consisted of seven layers, containing the nanoeutectic lamella structure of AuSn and Au₅Sn phases, and the polygonal grains of AuSn₂ and AuSn₄, on Au-plated Cu bond pads. Here, we found that there are two nanoeutectic lamellar layers with lamella spacing of 40 and 250 nm. By in situ heating above 140°C, the nanoeutectic lamella of AuSn and Au₅Sn was decomposed with structural degradation by sphering and coarsening processes of the lamellar interface. At the third layer neighboring to the lamella layer, on the other hand, Au₅Sn particles with a zig-zag shape in AuSn matrix became spherical and were finally dissipated in order to minimize the interface energy between two phases. In the other layers except both lamella layers, polycrystal grains of AuSn₂ and AuSn₄ grew by normal grain growth during in situ heating. The high interface energy of nanoeutectic lamella and polygonal nanograins, which are formed by rapid solidification, acted as a principal driving force on the microstructural change during the in situ heating. PMID:23920173

  18. In situ heating transmission electron microscopy observation of nanoeutectic lamellar structure in Sn-Ag-Cu alloy on Au under-bump metallization.

    PubMed

    Seo, Jong-Hyun; Yoon, Sang-Won; Kim, Kyou-Hyun; Chang, Hye-Jung; Lee, Kon-Bae; Seong, Tae-Yeon; Fleury, Eric; Ahn, Jae-Pyoung

    2013-08-01

    We investigated the microstructural evolution of Sn(96.4)Ag(2.8)Cu(0.8) solder through in situ heating transmission electron microscopy observations. As-soldered bump consisted of seven layers, containing the nanoeutectic lamella structure of AuSn and Au₅Sn phases, and the polygonal grains of AuSn₂ and AuSn₄, on Au-plated Cu bond pads. Here, we found that there are two nanoeutectic lamellar layers with lamella spacing of 40 and 250 nm. By in situ heating above 140°C, the nanoeutectic lamella of AuSn and Au₅Sn was decomposed with structural degradation by sphering and coarsening processes of the lamellar interface. At the third layer neighboring to the lamella layer, on the other hand, Au₅Sn particles with a zig-zag shape in AuSn matrix became spherical and were finally dissipated in order to minimize the interface energy between two phases. In the other layers except both lamella layers, polycrystal grains of AuSn₂ and AuSn₄ grew by normal grain growth during in situ heating. The high interface energy of nanoeutectic lamella and polygonal nanograins, which are formed by rapid solidification, acted as a principal driving force on the microstructural change during the in situ heating.

  19. 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.

  20. Comparison of denitrification between Paracoccus sp. and Diaphorobacter sp.

    PubMed

    Chakravarthy, Srinandan S; Pande, Samay; Kapoor, Ashish; Nerurkar, Anuradha S

    2011-09-01

    Denitrification was compared between Paracoccus sp. and Diaphorobacter sp. in this study, both of which were isolated from activated sludge of a denitrifying reactor. Denitrification of both isolates showed contrasting patterns, where Diaphorobacter sp. showed accumulation of nitrite in the medium while Paracoccus sp. showed no accumulation. The nitrate reduction rate was 1.5 times more than the nitrite reduction in Diaphorobacter sp., as analyzed by the resting state denitrification kinetics. Increasing the nitrate concentration in the medium increased the nitrite accumulation in Diaphorobacter sp., but not in Paracoccus sp., indicating a branched electron transfer during denitrification. Diaphorobacter sp. was unable to denitrify efficiently at high nitrate concentrations from 1 M, but Paracoccus sp. could denitrify even up to 2 M nitrate. Paracoccus sp. was found to be an efficient denitrifier with insignificant amounts of nitrite accumulation, and it could also denitrify high amounts of nitrate up to 2 M. Efficient denitrification without accumulation of intermediates like nitrite is desirable in the removal of high nitrates from wastewaters. Paracoccus sp. is shown to suffice this demand and could be a potential organism to remove high nitrates effectively. PMID:21509603

  1. PSI Mehler reaction is the main alternative photosynthetic electron pathway in Symbiodinium sp., symbiotic dinoflagellates of cnidarians.

    PubMed

    Roberty, Stéphane; Bailleul, Benjamin; Berne, Nicolas; Franck, Fabrice; Cardol, Pierre

    2014-10-01

    Photosynthetic organisms have developed various photoprotective mechanisms to cope with exposure to high light intensities. In photosynthetic dinoflagellates that live in symbiosis with cnidarians, the nature and relative amplitude of these regulatory mechanisms are a matter of debate. In our study, the amplitude of photosynthetic alternative electron flows (AEF) to oxygen (chlororespiration, Mehler reaction), the mitochondrial respiration and the Photosystem I (PSI) cyclic electron flow were investigated in strains belonging to three clades (A1, B1 and F1) of Symbiodinium. Cultured Symbiodinium strains were maintained under identical environmental conditions, and measurements of oxygen evolution, fluorescence emission and absorption changes at specific wavelengths were used to evaluate PSI and PSII electron transfer rates (ETR). A light- and O2 -dependent ETR was observed in all strains. This electron transfer chain involves PSII and PSI and is insensitive to inhibitors of mitochondrial activity and carbon fixation. We demonstrate that in all strains, the Mehler reaction responsible for photoreduction of oxygen by the PSI under high light, is the main AEF at the onset and at the steady state of photosynthesis. This sustained photosynthetic AEF under high light intensities acts as a photoprotective mechanism and leads to an increase of the ATP/NADPH ratio.

  2. PSI Mehler reaction is the main alternative photosynthetic electron pathway in Symbiodinium sp., symbiotic dinoflagellates of cnidarians.

    PubMed

    Roberty, Stéphane; Bailleul, Benjamin; Berne, Nicolas; Franck, Fabrice; Cardol, Pierre

    2014-10-01

    Photosynthetic organisms have developed various photoprotective mechanisms to cope with exposure to high light intensities. In photosynthetic dinoflagellates that live in symbiosis with cnidarians, the nature and relative amplitude of these regulatory mechanisms are a matter of debate. In our study, the amplitude of photosynthetic alternative electron flows (AEF) to oxygen (chlororespiration, Mehler reaction), the mitochondrial respiration and the Photosystem I (PSI) cyclic electron flow were investigated in strains belonging to three clades (A1, B1 and F1) of Symbiodinium. Cultured Symbiodinium strains were maintained under identical environmental conditions, and measurements of oxygen evolution, fluorescence emission and absorption changes at specific wavelengths were used to evaluate PSI and PSII electron transfer rates (ETR). A light- and O2 -dependent ETR was observed in all strains. This electron transfer chain involves PSII and PSI and is insensitive to inhibitors of mitochondrial activity and carbon fixation. We demonstrate that in all strains, the Mehler reaction responsible for photoreduction of oxygen by the PSI under high light, is the main AEF at the onset and at the steady state of photosynthesis. This sustained photosynthetic AEF under high light intensities acts as a photoprotective mechanism and leads to an increase of the ATP/NADPH ratio. PMID:24975027

  3. Ab initio study of the structural, electronic and elastic properties of AgSbTe2, AgSbSe2, Pr3AlC, Ce3AlC, Ce3AlN, La3AlC and La3AlN compounds

    NASA Astrophysics Data System (ADS)

    Berri, S.; Maouche, D.; Medkour, Y.

    2012-09-01

    In this paper, we study the structural, electronic and elastic properties of the ternary AgSbTe2, AgSbSe2, Pr3AlC, Ce3AlC, Ce3AlN, La3AlC and La3AlN compounds using the full-potential linearized augmented plane wave (FP-LAPW) scheme and the pseudopotential plane wave (PP-PW) scheme in the frame of generalized gradient approximation (GGA). Results are given for the lattice parameters, bulk modulus, and its pressure derivative. The calculated lattice parameters are in good agreement with experimental results. We have determined the full set of first-order elastic constants, shear modulus, Young's modulus and Poisson's ratio of these compounds. Also, we have presented the results of the band structure, densities of states, it is found that this compounds metallic behavior, and a negative gap Г→R for Pr3AlC. The analysis charge densities show that bonding is of covalent-ionic and ionic nature for AgSbSe2 and AgSbTe2 compounds.

  4. Study on antibacterial activity of chemically synthesized PANI-Ag-Au nanocomposite

    NASA Astrophysics Data System (ADS)

    Boomi, Pandi; Prabu, Halliah Gurumallesh; Manisankar, Paramasivam; Ravikumar, Sundaram

    2014-05-01

    Pristine polyaniline (PANI), PANI-Ag, PANI-Au and PANI-Ag-Au nanocomposites have been successfully synthesized by chemical oxidative polymerization method using aniline as monomer, ammonium persulphate as oxidant and metal (Ag, Au and Ag-Au) colloids. UV-Vis analysis exhibited surface Plasmon resonances of Ag, Au, Ag-Au nanoparticles. FT-IR spectra revealed the shift in peak position of N-H stretching. X-ray diffraction (XRD) results confirm the presence of Ag, Au and Au-Ag nanoparticles. HR-TEM images show nanosizes of Ag, Au, Ag-Au and the incorporation of such nanoparticles into the PANI matrix. Pristine PANI, PANI-Ag, PANI-Au and PANI-Ag-Au nanocomposites were tested for antibacterial activity by agar well diffusion method. PANI-Ag-Au nanocomposite exhibited higher antibacterial activity against both gram-positive [Streptococcus sp. (MTCC 890), Staphylococcus sp. (MTCC 96)] and gram-negative bacteria [Escherichia coli (MTCC 1671) and Klebsiella sp. (MTCC 7407)] when compared with PANI-Ag nanocomposite, PANI-Au nanocomposite and pristine PANI. The novelty of this study is the polymer-bimetal synthesis and its antibacterial potential.

  5. Study of structural modification of PVA by incorporating Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Saini, Isha; Sharma, Annu; Rozra, Jyoti; Aggarwal, Sanjeev; Dhiman, Rajnish; Sharma, Pawan K.

    2016-05-01

    Nanocomposites of PVA with Ag nanoparticles dispersed in it were synthesized using solution casting method. The morphology and size distribution of Ag nanoparticles embedded in PVA matrix were obtained by transmission electron microscopy (TEM) and Field emission scanning electron microscopy (FE-SEM). Raman spectroscopy was used to examine structural changes taking place inside polyvinyl alcohol (PVA) matrix due to incorporation of Ag nanoparticle. Raman analysis indicates that Ag nanoparticles interact with PVA through H-bonding.

  6. Experimental study of single-electron detachment for Cu{sup −}, Ag{sup −}, Au{sup −}, Co{sup −}, and Ir{sup −} in collisions with Kr and Xe

    SciTech Connect

    Ye, Jingru; Zhao, Zilong; Zhu, Yiyang; Li, Junqin; Zhang, Xuemei

    2014-09-15

    The single electron detachment (SED) cross sections for Cu{sup −}, Ag{sup −}, Au{sup −}, Co{sup −}, and Ir{sup −} in collisions with Kr and Xe in the energy range of 10keV≤E≤30keV are measured by using the growth rate method in our experiments. The SED cross sections increase as the incident velocity increases. These data are compared with other available experimental data for the corresponding negative ions colliding with Ar. The affinities of the negative ions and the mass relation between the projectile and the target seem important in the electron detachment process.

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

    NASA Astrophysics Data System (ADS)

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

    2014-03-01

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

  8. Ag/AgBr/TiO2 visible light photocatalyst for destruction of azodyes and bacteria.

    PubMed

    Hu, Chun; Lan, Yongqing; Qu, Jiuhui; Hu, Xuexiang; Wang, Aimin

    2006-03-01

    Ag/AgBr/TiO2 was prepared by the deposition-precipitation method and was found to be a novel visible light driven photocatalyst. The catalyst showed high efficiency for the degradation of nonbiodegradable azodyes and the killing of Escherichia coli under visible light irradiation (lambda>420 nm). The catalyst activity was maintained effectively after successive cyclic experiments under UV or visible light irradiation without the destruction of AgBr. On the basis of the characterization of X-ray diffraction, X-ray photoelectron spectroscopy, and Auger electron spectroscopy, the surface Ag species mainly exist as Ag0 in the structure of all samples before and after reaction, and Ag0 species scavenged hVB+ and then trapped eCB- in the process of photocatalytic reaction, inhibiting the decomposition of AgBr. The studies of ESR and H2O2 formation revealed that *OH and O2*- were formed in visible light irradiated aqueous Ag/AgBr/TiO2 suspension, while there was no reactive oxygen species in the visible light irradiated Ag0/TiO2 system. The results indicate that AgBr is the main photoactive species for the destruction of azodyes and bacteria under visible light. In addition, the bactericidal efficiency and killing mechanism of Ag/AgBr/TiO2 under visible light irradiation are illustrated and discussed. PMID:16509698

  9. AGS II

    SciTech Connect

    Palmer, R.B.

    1984-01-01

    Interest in rare K decays, neutrino oscillations and other fields have generated an increasing demand for running, and improved intensity and duty cycle, at the AGS. Current projects include acceleration of polarized protons and light ions (up to mass 32). Future plans are for a booster to increase intensity and allow heavy ions (up to mass 200), and a stretcher to give 100% duty cycle. A later upgrade could yield an average current of 32 ..mu.. amps. 6 figures, 2 tables.

  10. Screened-exchange density functional theory description of the electronic structure and phase stability of the chalcopyrite materials AgInSe2 and AuInSe2

    NASA Astrophysics Data System (ADS)

    Kim, Namhoon; Martin, Pamela Peña; Rockett, Angus A.; Ertekin, Elif

    2016-04-01

    We present a systematic assessment of the structural properties, the electronic density of states, the charge densities, and the phase stabilities of AgInSe2 and AuInSe2 using screened-exchange hybrid density functional theory, and compare their properties to those of CuInSe2. For AgInSe2, hybrid density functional theory properly captures several experimentally measured properties, including the increase in the band gap and the change in the direction of the lattice distortion parameter u in comparison to CuInSe2. While the electronic properties of AuInSe2 have not yet been experimentally characterized, we predict it to be a small gap (≈0.15 eV) semiconductor. We also present the phase stability of AgInSe2 and AuInSe2 according to screened-exchange density functional theory, and compare the results to predictions from conventional density functional theory, results tabulated from several online materials data repositories, and experiment (when available). In comparison to conventional density functional theory, the hybrid functional predicts phase stabilities of AgInSe2 in better agreement with experiment: discrepancies in the calculated formation enthalpies are reduced by approximately a factor of 3, from ≈0.20 eV/atom to ≈0.07 eV/atom, similar to the improvement observed for CuInSe2. We further predict that AuInSe2 is not a stable phase, and can only be present under nonequilibrium conditions.

  11. Cytochrome P450-catalyzed dealkylation of atrazine by Rhodococcus sp. strain NI86/21 involves hydrogen atom transfer rather than single electron transfer.

    PubMed

    Meyer, Armin H; Dybala-Defratyka, Agnieszka; Alaimo, Peter J; Geronimo, Inacrist; Sanchez, Ariana D; Cramer, Christopher J; Elsner, Martin

    2014-08-28

    Cytochrome P450 enzymes are responsible for a multitude of natural transformation reactions. For oxidative N-dealkylation, single electron (SET) and hydrogen atom abstraction (HAT) have been debated as underlying mechanisms. Combined evidence from (i) product distribution and (ii) isotope effects indicate that HAT, rather than SET, initiates N-dealkylation of atrazine to desethyl- and desisopropylatrazine by the microorganism Rhodococcus sp. strain NI86/21. (i) Product analysis revealed a non-selective oxidation at both the αC and βC-atom of the alkyl chain, which is expected for a radical reaction, but not SET. (ii) Normal (13)C and (15)N as well as pronounced (2)H isotope effects (εcarbon: -4.0‰ ± 0.2‰; εnitrogen: -1.4‰ ± 0.3‰, KIEH: 3.6 ± 0.8) agree qualitatively with calculated values for HAT, whereas inverse (13)C and (15)N isotope effects are predicted for SET. Analogous results are observed with the Fe(iv)[double bond, length as m-dash]O model system [5,10,15,20-tetrakis(pentafluorophenyl)porphyrin-iron(iii)-chloride + NaIO4], but not with permanganate. These results emphasize the relevance of the HAT mechanism for N-dealkylation by P450.

  12. Effect of surfactant-induced cell surface modifications on electron transport system and catechol 1,2-dioxygenase activities and phenanthrene biodegradation by Citrobacter sp. SA01.

    PubMed

    Li, Feng; Zhu, Lizhong

    2012-11-01

    In order to better understand how surfactants affect biodegradation of hydrophobic organic compounds (HOCs), Tween 80 and sodium dodecyl benzene sulfonate (SDBS), were selected to investigate effects on cell surface hydrophobicity (CSH), electron transport system (ETS) activities and phenanthrene biodegradation by Citrobacter sp. SA01. Tween 80 and SDBS increased CSH by 19.8-25.2%, ETS activities by 352.1-376.0μmol/gmin, catechol 1,2-dioxygenase (C12) activities by 50.8-52.7U/L, and phenanthrene biodegradation by 8.9-17.2% separately in the presence of 50mg/L of surfactants as compared to in their absence. Lipopolysaccharide (LPS) release was 334.7μg/mg in the presence of both surfactants whereas in their absence only 8.6-44.4μg/mg of LPS was released. Thus, enhanced LPS release probably increased ETS and C12 activities as well as phenanthrene biodegradation by increasing CSH. The results demonstrate that surfactant-enhanced CSH provides a simple, yet effective strategy for field applications of surfactant-enhanced bioremediation of HOCs.

  13. Use of Fe(III) as an electron acceptor to recover previously uncultured hyperthermophiles: isolation and characterization of Geothermobacterium ferrireducens gen. nov., sp. nov.

    PubMed

    Kashefi, Kazem; Holmes, Dawn E; Reysenbach, Anna-Louise; Lovley, Derek R

    2002-04-01

    It has recently been recognized that the ability to use Fe(III) as a terminal electron acceptor is a highly conserved characteristic in hyperthermophilic microorganisms. This suggests that it may be possible to recover as-yet-uncultured hyperthermophiles in pure culture if Fe(III) is used as an electron acceptor. As part of a study of the microbial diversity of the Obsidian Pool area in Yellowstone National Park, Wyo., hot sediment samples were used as the inoculum for enrichment cultures in media containing hydrogen as the sole electron donor and poorly crystalline Fe(III) oxide as the electron acceptor. A pure culture was recovered on solidified, Fe(III) oxide medium. The isolate, designated FW-1a, is a hyperthermophilic anaerobe that grows exclusively by coupling hydrogen oxidation to the reduction of poorly crystalline Fe(III) oxide. Organic carbon is not required for growth. Magnetite is the end product of Fe(III) oxide reduction under the culture conditions evaluated. The cells are rod shaped, about 0.5 microm by 1.0 to 1.2 microm, and motile and have a single flagellum. Strain FW-1a grows at circumneutral pH, at freshwater salinities, and at temperatures of between 65 and 100 degrees C with an optimum of 85 to 90 degrees C. To our knowledge this is the highest temperature optimum of any organism in the Bacteria. Analysis of the 16S ribosomal DNA (rDNA) sequence of strain FW-1a places it within the Bacteria, most closely related to abundant but uncultured microorganisms whose 16S rDNA sequences have been previously recovered from Obsidian Pool and a terrestrial hot spring in Iceland. While previous studies inferred that the uncultured microorganisms with these 16S rDNA sequences were sulfate-reducing organisms, the physiology of the strain FW-1a, which does not reduce sulfate, indicates that these organisms are just as likely to be Fe(III) reducers. These results further demonstrate that Fe(III) may be helpful for recovering as-yet-uncultured microorganisms

  14. Use of Fe(III) as an electron acceptor to recover previously uncultured hyperthermophiles: isolation and characterization of Geothermobacterium ferrireducens gen. nov., sp. nov.

    PubMed

    Kashefi, Kazem; Holmes, Dawn E; Reysenbach, Anna-Louise; Lovley, Derek R

    2002-04-01

    It has recently been recognized that the ability to use Fe(III) as a terminal electron acceptor is a highly conserved characteristic in hyperthermophilic microorganisms. This suggests that it may be possible to recover as-yet-uncultured hyperthermophiles in pure culture if Fe(III) is used as an electron acceptor. As part of a study of the microbial diversity of the Obsidian Pool area in Yellowstone National Park, Wyo., hot sediment samples were used as the inoculum for enrichment cultures in media containing hydrogen as the sole electron donor and poorly crystalline Fe(III) oxide as the electron acceptor. A pure culture was recovered on solidified, Fe(III) oxide medium. The isolate, designated FW-1a, is a hyperthermophilic anaerobe that grows exclusively by coupling hydrogen oxidation to the reduction of poorly crystalline Fe(III) oxide. Organic carbon is not required for growth. Magnetite is the end product of Fe(III) oxide reduction under the culture conditions evaluated. The cells are rod shaped, about 0.5 microm by 1.0 to 1.2 microm, and motile and have a single flagellum. Strain FW-1a grows at circumneutral pH, at freshwater salinities, and at temperatures of between 65 and 100 degrees C with an optimum of 85 to 90 degrees C. To our knowledge this is the highest temperature optimum of any organism in the Bacteria. Analysis of the 16S ribosomal DNA (rDNA) sequence of strain FW-1a places it within the Bacteria, most closely related to abundant but uncultured microorganisms whose 16S rDNA sequences have been previously recovered from Obsidian Pool and a terrestrial hot spring in Iceland. While previous studies inferred that the uncultured microorganisms with these 16S rDNA sequences were sulfate-reducing organisms, the physiology of the strain FW-1a, which does not reduce sulfate, indicates that these organisms are just as likely to be Fe(III) reducers. These results further demonstrate that Fe(III) may be helpful for recovering as-yet-uncultured microorganisms

  15. High resolution electron microscopy study of a high Cu variant of Weldalite (tm) 049 and a high strength Al-Cu-Ag-Mg-Zr alloy

    NASA Technical Reports Server (NTRS)

    Herring, R. A.; Gayle, Frank W.; Pickens, Joseph R.

    1991-01-01

    Weldalite (trademark) 049 is an Al-Cu-Li-Ag-Mg alloy that is strengthened in artificially aged tempers primarily by very thin plate-like precipitates lying on the set of (111) matrix planes. This precipitate might be expected to be the T(sub 1) phase, Al2CuLi, which has been observed in Al-Cu-Li alloys. However, in several ways this precipitate is similar to the omega phase which also appears as the set of (111) planes plates and is found in Al-Cu-Ag-Mg alloys. The study was undertaken to identify the set of (111) planes precipitate or precipitates in Weldalite (trademark) 049 in the T8 (stretched and artificially aged) temper, and to determine whether T(sub 1), omega, or some other phase is primarily responsible for the high strength (i.e., 700 MPa tensile strength) in this Al-Cu-Li-Ag-Mg alloy.

  16. 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.

  17. 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.

  18. Enhanced thermoelectric performance of CdO : Ag nanocomposites.

    PubMed

    Gao, Linjie; Wang, Shufang; Liu, Ran; Zha, Xinyu; Sun, Niefeng; Wang, Shujie; Wang, Jianglong; Fu, Guangsheng

    2016-07-26

    CdO : Ag nanocomposites with metallic Ag nanoparticles embedded in the polycrystalline CdO matrix were synthesized by the solid-state reaction method. The addition of Ag led to increased grain boundaries of CdO and created numerous CdO/Ag interfaces. By incorporating Ag into the CdO matrix, the power factor was increased which was probably due to the carrier energy filtering effect induced by the enhanced energy-dependent scattering of electrons. In addition, reduced thermal conductivity was also achieved by stronger phonon scattering from grain boundaries, CdO/Ag interfaces and Ag nanoparticles. These concomitant effects resulted in enhanced ZT values for all CdO : Ag nanocomposites, demonstrating that the strategy of introducing metallic Ag nanoparticles into the CdO host was very effective in optimizing the thermoelectric performance. PMID:27411573

  19. New insight into daylight photocatalysis of AgBr@Ag: synergistic effect between semiconductor photocatalysis and plasmonic photocatalysis.

    PubMed

    Jiang, Jing; Li, Hao; Zhang, Lizhi

    2012-05-14

    Noble metal nanoparticles (NPs) are often used as electron scavengers in conventional semiconductor photocatalysis to suppress electron-hole (e(-)-h(+) ) recombination and promote interfacial charge transfer, and thus enhance photocatalytic activity of semiconductors. In this contribution, it is demonstrated that noble metal NPs such as Ag NPs function as visible-light harvesting and electron-generating centers during the daylight photocatalysis of AgBr@Ag. Novel Ag plasmonic photocatalysis could cooperate with the conventional AgBr semiconductor photocatalysis to enhance the overall daylight activity of AgBr@Ag greatly because of an interesting synergistic effect. After a systematic investigation of the daylight photocatalysis mechanism of AgBr@Ag, the synergistic effect was attributed to surface plasmon resonance induced local electric field enhancement on Ag, which can accelerate the generation of e(-)-h(+) pairs in AgBr, so that more electrons are produced in the conduction band of AgBr under daylight irradiation. This study provides new insight into the photocatalytic mechanism of noble metal/semiconductor systems as well as the design and fabrication of novel plasmonic photocatalysts.

  20. Biosynthesis and characterisation of silver nanoparticles using Sphingomonas paucimobilis sp. BDS1.

    PubMed

    Gou, Yujun; Zhang, Feng; Zhu, Xiaoyan; Li, Xiangqian

    2015-04-01

    Sphingomonas is a novel and abundant microbial resource for biodegradation of aromatic compounds. It has great potential in environment protection and industrial production. The use of microorganisms for the synthesis of nanoparticles is in the limelight of modern nanotechnology, since it is cost effective, non-toxic and friendly to the ever-overwhelmed environment. In this paper, the biosynthesis of silver nanoparticles (AgNPs) using Sphingomonas paucimobilis sp. BDS1 under ambient conditions was investigated for the first time. Biosynthesised AgNPs were characterised with powder ultraviolet-visible spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy and energy dispersive X-ray spectroscopy. The overall results revealed that well-dispersed face centred cubic spherical AgNPs in the range of 50-80 nm were produced on the surface of Sphingomonas paucimobilis sp. BDS1, after challenging pure wet biomass with silver nitrate solution. This suggests that the capture of silver ions may be a complex process of physical and chemical adsorption and the proteins on the surface of the bacteria may play the role of reduction and stabilising agent with regard to the result of FTIR.

  1. Electron

    NASA Astrophysics Data System (ADS)

    Springford, Michael

    1997-03-01

    1. J. J. Thomson and the discovery of the electron A. B. P. Pippard; 2. The isolated electron W. N. Cottingham; 3. The relativistic electron D. I. Olive; 4. The electron glue B. L. Gyorffy; 5. The electron fluid P. Coleman; 6. The magnetic electron G. G. Lonzarich; 7. The paired electron A. J. Leggett; 8. The heavy electron M. Springford; 9. The coherent electron Y. Imry and M. Peskin; 10. The composite electron R. Nicholas; 11. The electron in the cosmos M. S. Longair.

  2. Electron

    NASA Astrophysics Data System (ADS)

    Springford, Michael

    2008-12-01

    1. J. J. Thomson and the discovery of the electron A. B. P. Pippard; 2. The isolated electron W. N. Cottingham; 3. The relativistic electron D. I. Olive; 4. The electron glue B. L. Gyorffy; 5. The electron fluid P. Coleman; 6. The magnetic electron G. G. Lonzarich; 7. The paired electron A. J. Leggett; 8. The heavy electron M. Springford; 9. The coherent electron Y. Imry and M. Peskin; 10. The composite electron R. Nicholas; 11. The electron in the cosmos M. S. Longair.

  3. Raman chemical imaging of the rhizosphere bacterium Pantoea sp. YR343 and its co-culture with Arabidopsis thaliana

    DOE PAGES

    Polisetti, Sneha; Bible, Amber N.; Morrell-Falvey, Jennifer L.; Bohn, Paul W.

    2016-02-29

    Chemical imaging of plant-bacteria co-cultures renders it possible to characterize bacterial populations and behaviors and their interactions with proximal organisms, under conditions closest to the environment in the rhizosphere. Here Raman micro-spectroscopy and confocal Raman imaging are used as minimally invasive probes to study the rhizosphere bacterial isolate, Pantoea sp. YR343, and its co-culture with model plant Arabidopsis thaliana by combining enhanced Raman spectroscopies with electron microscopy and principal component analysis (PCA). The presence of carotenoid pigments in the wild type Pantoea sp. YR343 was characterized using resonance Raman scattering, which was also used to confirm successful disruption of themore » crtB gene in an engineered carotenoid mutant strain. Other components of the Pantoea sp. YR343 cells were imaged in the presence of resonantly enhanced pigments using a combination of surface enhanced Raman imaging and PCA. Pantoea sp. YR343 cells decorated with Ag colloid synthesized ex situ gave spectra dominated by carotenoid scattering, whereas colloids synthesized in situ produced spectral signatures characteristic of flavins in the cell membrane. Scanning electron microscopy (SEM) of whole cells and transmission electron microscopy (TEM) images of thinly sliced cross-sections were used to assess structural integrity of the coated cells and to establish the origin of spectral signatures based on the position of Ag nanoparticles in the cells. Finally, raman imaging was also used to characterize senescent green Arabidopsis thaliana plant roots inoculated with Pantoea sp. YR343, and PCA was used to distinguish spectral contributions from plant and bacterial cells, thereby establishing the potential of Raman imaging to visualize the distribution of rhizobacteria on plant roots.« less

  4. Raman chemical imaging of the rhizosphere bacterium Pantoea sp. YR343 and its co-culture with Arabidopsis thaliana.

    PubMed

    Polisetti, Sneha; Bible, Amber N; Morrell-Falvey, Jennifer L; Bohn, Paul W

    2016-04-01

    Chemical imaging of plant-bacteria co-cultures makes it possible to characterize bacterial populations and behaviors and their interactions with proximal organisms, under conditions closest to the environment in the rhizosphere. Here Raman micro-spectroscopy and confocal Raman imaging are used as minimally invasive probes to study the rhizosphere bacterial isolate, Pantoea sp. YR343, and its co-culture with model plant Arabidopsis thaliana by combining enhanced Raman spectroscopies with electron microscopy and principal component analysis (PCA). The presence of carotenoid pigments in the wild type Pantoea sp. YR343 was characterized using resonance Raman scattering, which was also used to confirm successful disruption of the crtB gene in an engineered carotenoid mutant strain. Other components of the Pantoea sp. YR343 cells were imaged in the presence of resonantly enhanced pigments using a combination of surface enhanced Raman imaging and PCA. Pantoea sp. YR343 cells decorated with Ag colloid synthesized ex situ gave spectra dominated by carotenoid scattering, whereas colloids synthesized in situ produced spectral signatures characteristic of flavins in the cell membrane. Scanning electron microscopy (SEM) of whole cells and transmission electron microscopy (TEM) images of thinly sliced cross-sections were used to assess structural integrity of the coated cells and to establish the origin of spectral signatures based on the position of Ag nanoparticles in the cells. Raman imaging was also used to characterize senescent green Arabidopsis thaliana plant roots inoculated with Pantoea sp. YR343, and PCA was used to distinguish spectral contributions from plant and bacterial cells, thereby establishing the potential of Raman imaging to visualize the distribution of rhizobacteria on plant roots. PMID:26948490

  5. New frontiers in water purification: highly stable amphopolycarboxyglycinate-stabilized Ag-AgCl nanocomposite and its newly discovered potential

    NASA Astrophysics Data System (ADS)

    Krutyakov, Yurii A.; Zherebin, Pavel M.; Kudrinskiy, Alexey A.; Zubavichus, Yan V.; Presniakov, Mikhail Yu; Yapryntsev, Alexey D.; Karabtseva, Anastasia V.; Mikhaylov, Dmitry M.; Lisichkin, Georgii V.

    2016-09-01

    A simple synthetic procedure for high-stable dispersions of porous composite Ag/AgCl nanoparticles stabilized with amphoteric surfactant sodium tallow amphopolycarboxyglycinate has been proposed for the first time. The prepared samples were characterized by UV-vis spectroscopy, x-ray powder diffraction (XRD), x-ray photoelectron spectroscopy, small area electron diffraction (SAED), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and electron probe micro-analysis. In addition, measurements (carried out at the Kurchatov synchrotron radiation source stations) of the Ag K-edge extended x-ray absorption fine structure (EXAFS) and x-ray absorption near edge structure (XANES) spectra and XRD of the prepared nanoparticles have been performed. The obtained results suggest that small-sized Ag clusters are homogeneously distributed in the mass of the AgCl nanoparticle (~80 nm) formed during the synthesis. The Ag/AgCl dispersion demonstrates photocatalytic activity (with respect to methyl orange) and high bactericidal activity against E. coli. This activity is superior to the activity of both Ag and AgCl nanoparticles stabilized by the same surfactant. Thus, porous composite Ag/AgCl nanoparticles can be used as a multifunctional agent that is able to remove both pollutants and bacterium from water.

  6. The synthesis, activity, stability and the charge transfer identification of Ag:AgBr/γ-Al2O3 photocatalyst for organic pollutant decomposition in water

    NASA Astrophysics Data System (ADS)

    Huang, Shan; Si, Zhichun; Weng, Duan

    2015-12-01

    Highly stable Ag:AgBr/γ-Al2O3 photo-catalyst was obtained by dispersing AgBr sol on hollow γ-Al2O3 microsphere. Metallic Ag nanoparticles were in situ generated on AgBr crystals by a photo-reduction method. The activity of catalyst was characterized by MO and phenol decomposition. The light irradiation response, the life times of the photo-induced charges, and the charge separation and transition were determined by the UV-vis diffuse reflection spectra, open circuit voltage decay spectra and transient photocurrent responses. The as-prepared Ag:AgBr/γ-Al2O3 catalyst can response to visible light irradiation. Charge separation was clarified to correlate with electrons transferring from Ag to AgBr surface and the consequent reaction with ads-O2 to generate rad O2- species. It was found that the rad O2- rather than rad OH played a dominant role in the photocatalytic oxidation of MO and phenol in water. However, the electrons trended to transfer from AgBr to Ag intrinsically without light irradiation. Therefore, the electron transfer between Ag and AgBr reaching the dynamic equilibrium was the key factor for obtaining a high stable Ag/AgBr catalyst which can be obtained by optimizing the Ag:AgBr ratio. Loading amount of Ag:AgBr on γ-Al2O3 was optimized to 30 wt.% and the metallic Ag content was stabilized at 9 wt.% of Ag:AgBr catalyst.

  7. 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. PMID:27450302

  8. 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.

  9. Anomalous evolution of interfaces in Fe/Ag magnetic multilayer

    NASA Astrophysics Data System (ADS)

    Sharma, Gagan; Gupta, Ranjeeta; Kumar, Dileep; Gupta, Ajay

    2013-12-01

    Interfaces greatly influence the magnetic properties of multilayer nanostructures. In the present work, the x-ray standing wave (XSW) technique along with conversion electron Mössbauer spectroscopy have been used to study the evolution of interfaces in Fe/Ag system as a function of thermal annealing. The XSW technique has sufficient depth resolution so as to determine the concentration profiles of Fe across the two interfaces, namely Fe-on-Ag and Ag-on-Fe independently. In as-deposited Ag/Fe/Ag trilayer, Fe-on-Ag interface has a substantially higher roughness of 1.3 nm as compared to 0.9 nm of Ag-on-Fe interface. It is shown that the observed difference in the roughness of the two interfaces is due to a substantial intermixing between Fe and Ag occurring preferentially at Fe-on-Ag interface. With thermal annealing, the two interfaces exhibit opposite behaviour; while Fe-on-Ag interface exhibits an initial sharpening, Ag-on-Fe interface exhibits a monotonous broadening. Two competing processes occur at the interfaces, (i) interface sharpening as a result of de-mixing, driven by a large positive heat of mixing between Fe and Ag and (ii) increase in topological roughness due to increased thermal agitation. This results in a non-monotonous variation in the roughness of Fe-on-Ag interface. At sufficiently high temperature the layered structure is completely destroyed, leading to formation of Fe and Ag nanoparticles.

  10. Surface and electronic structure of 6H-SiC(0001)-(3 × 3) surfaces and ultrathin Ag films on Si(111) and Si(001)

    NASA Astrophysics Data System (ADS)

    Gasparov, V. A.

    2011-10-01

    Surface topographic (LEED, STM) and spectroscopic (ARUPS, XPS, STS) studies have been performed on Si-terminated 6H-SiC(0001)-(3 × 3) surfaces and Ag superstructures and ultrathin films on Si(001) and Si(111) surfaces, using a scanning tunneling microscope (STM) in ultrahigh vacuum. Our results confirm that 2D epitaxial metal growth is favored on Si(001) at low temperatures and a solid, two-domain Ag(111) film has been achieved at coverages as low as 10 ML. The films reveal a morphology with 3-dimensional features and with a well defined honeycomb structure in between. An atomically flat Si(111)/Ag -(√3 ×√3 )R30∘ surface has been modified by use of a scanning tunneling microscope (STM) in ultrahigh vacuum (UHV). High quality 6H-SiC(0001)-(3 × 3) and Si(111)/-Ag(√3 ×√3 )R30∘ upper structures have been prepared and studied by means of ARUPS, XPS and LEED. The local density of states proportional to the spectrum of normalized differential conductivity (dI/dV)/(I/V) vs V reveals distinct bands of empty (-0.6 eV) and filled (0.65 eV) sites separated by 1.2 eV, for both areas. The results support the use of a Mott-Hubbard-type model for calculating the density of states of 6H-SiC(0001)-(3 × 3) surfaces with a Hubbard gap of 1 eV.

  11. Photoreduction of Ag+ in Ag/Ag2S/Au memristor

    NASA Astrophysics Data System (ADS)

    Mou, N. I.; Tabib-Azar, M.

    2015-06-01

    Silver halides and chalcogenides are excellent memristor materials that have been extensively used in the past as photosensitive layers in photography. Here we examine the effect of illumination on the operating voltages and switching speed of Ag/Ag2S/Au memristors using a green laser (473-523 nm). Our results indicate that illumination decreases the average switching time from high to low resistance states by ∼19% and decreases the turn-off voltages dramatically from -0.8 V to -0.25 V that we attribute to the change in sulfur valency and a photo-induced change in its oxidation/reduction potential. Photo-induced reduction of silver in Ag2S may be used in three dimensional optical memories that can be electronically read and reset.

  12. Crystallization kinetics of {alpha}-AgI in AgI-based silver orthoborate glasses

    SciTech Connect

    Taniguchi, Akihiro; Tatsumisago, Masahiro; Minami, Tsutomu

    1995-02-01

    Kinetics for nucleation and growth of {alpha}-AgI crystals in AgI-based silver orthoborate glasses, in which only {alpha}-AgI crystals were found to crystallize in the heating process of the glasses, were studied by isothermal and nonisothermal measurements using differential scanning calorimetry and by observations of the microstructure of the glasses using scanning electron microscopy. The values of both n and m, dependent on the crystallization mechanism, were found to be 3, indicating that a constant number of nuclei of {alpha}-AgI precipitated in a glass matrix grew three-dimensionally. The preannealing of the glasses at temperatures between glass transition and crystallization did not affect the DSC isothermal curves in the crystal growth process, which suggested that the number of {alpha}-AgI nuclei would have been saturated in the glass when the glasses were prepared by quenching the AgI-based melts.

  13. Ag induced electromagnetic interference shielding of Ag-graphite/PVDF flexible nanocomposites thinfilms

    NASA Astrophysics Data System (ADS)

    Kumaran, R.; Alagar, M.; Dinesh Kumar, S.; Subramanian, V.; Dinakaran, K.

    2015-09-01

    We report Ag nanoparticle induced Electromagnetic Interference (EMI) shielding in a flexible composite films of Ag nanoparticles incorporated graphite/poly-vinylidene difluoride (PVDF). PVDF nanocomposite thin-films were synthesized by intercalating Ag in Graphite (GIC) followed by dispersing GIC in PVDF. The X-ray diffraction analysis and the high-resolution transmission electron microscope clearly dictate the microstructure of silver nanoparticles in graphite intercalated composite of PVDF matrix. The conductivity values of nanocomposites are increased upto 2.5 times when compared to neat PVDF having a value of 2.70 S/cm at 1 MHz. The presence of Ag broadly enhanced the dielectric constant and lowers the dielectric loss of PVDF matrix proportional to Ag content. The EMI shielding effectiveness of the composites is 29.1 dB at 12.4 GHz for the sample having 5 wt. % Ag and 10 wt. % graphite in PVDF.

  14. 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.

  15. Biosynthesis, characterization and antimicrobial activity of silver nanoparticles by Streptomyces sp. SS2.

    PubMed

    Mohanta, Yugal Kishore; Behera, Sujit Kumar

    2014-11-01

    In the present study the microbial biosynthesis of silver nanoparticles (AgNPs) by secondary metabolites of Streptomyces sp. SS2 in an eco-friendly approach has been reported. The Streptomyces sp. SS2 was isolated from the soil sediment of Similipal Biosphere Reserve. The identification of this strain was determined by phenotypical characteristics (morphological and biochemical) and molecular characterization method using 16 s rDNA sequencing. The morphological study was also done by high-resolution scanning electron microscopy. The preliminary characterization of biosynthesized silver nanoparticle was carried out using UV-Vis spectrum analysis, which showed an absorption peak at 420 nm corresponding to plasmon absorption of silver. The average size and charge (zeta potential) of the particles were found to be 67.95 ± 18.52 nm and -17.7 ± 5.30 mV, respectively. The functional groups were identified by FTIR studies and their morphology (round and spherical shape) was determined by scanning electron microscopy. The synthesized AgNPs exhibited excellent antibacterial activity against Escherichia coli (MTCC 1089), Bacillus subtilis (MTCC 7164), Staphylococcus epidermis (MTCC 3615), Vibrio cholerae (MTCC 3904) and Staphylococcus aureus (MTCC 1144). These biotechnological approaches of synthesis of nanoparticles can direct a new path in biomaterial sciences and enrich biomedical applications. PMID:24842223

  16. Exposure-dependent Ag+ release from silver nanoparticles and its complexation in AgS2 sites in primary murine macrophages

    NASA Astrophysics Data System (ADS)

    Veronesi, G.; Aude-Garcia, C.; Kieffer, I.; Gallon, T.; Delangle, P.; Herlin-Boime, N.; Rabilloud, T.; Carrière, M.

    2015-04-01

    the fraction of Ag+ ions released from the AgNPs under a given exposure condition and highlights their complexation with thiolate groups; the ab initio modelling of the extended spectra allows measuring the Ag-S bond length in cellulo. Dissolution rates depend on the exposure scenario, chronicity leading to higher Ag+ release than acute exposure; Ag-S bond lengths are 2.41 +/- 0.03 Å and 2.38 +/- 0.01 Å in acute and chronic exposure respectively, compatible with digonal AgS2 coordination. Glutathione is identified as the most likely putative ligand for Ag+. The proposed method offers a scope for the investigation of metallic nanoparticle dissolution and recombination in cellular models. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr00353a

  17. Desorption of Ag from Grain Boundaries in Ag Film on Br and H-Passivated Si(111) Surfaces

    SciTech Connect

    Roy, Anupam; Batabyal, R.; Mahato, J. C.; Dev, B. N.; Sundaravel, B.

    2011-07-15

    Growth of Ag film on Br- and H-passivated Si(111) surfaces was examined by Rutherford backscattering spectrometry (RBS), scanning electron microscopy (SEM) and photoemission electron microscopy (PEEM) techniques. The phenomenon of thermal grooving was observed after annealing at higher temperatures. Hierarchical desorption of Ag from the grain boundaries produce a fractal structure of Ag-depleted regions. Hierarchical desorption may be used for nanopatterning of the layer.

  18. Effect of Ag+ and PO43‑ ratios on the microstructure and photocatalytic activity of Ag3PO4

    NASA Astrophysics Data System (ADS)

    Qin, Jiaqian; Zhang, Xinyu; Yang, Chengwu; Song, Aijun; Zhang, Bing; Rajendran, Saravanan; Ma, Mingzhen; Liu, Riping

    2016-09-01

    In this work, the catalyst silver phosphate (Ag3PO4) with different initial ratios of Ag+ and PO43‑ in aqueous solution was synthesized by a simple precipitation method from AgNO3 and NH4H2PO4 which were used as the precursor. After that, the prepared samples were characterized by different techniques such as field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), UV-visible diffuse reflectance spectroscopy (UV-DRS) and decomposition evolution of rhodamine B (RhB) solution. The results indicate that the initial ratios of Ag+/PO43‑ in aqueous solution can modify the morphology and also it can significantly affect the photocatalytic performance. During photocatalytic process, the rich Ag+ ion Ag3PO4 can form the surface plasmon resonance (SPR) of Ag nanoparticles, which inhibit the reduction of Ag3PO4 resulting in higher photocatalytic activity and stability.

  19. Highly efficient and stable Ag-AgBr/TiO2 composites for destruction of Escherichia coli under visible light irradiation.

    PubMed

    Wang, Xiaoping; Lim, Teik-Thye

    2013-08-01

    A series of Ag-AgBr/TiO2 composites were prepared by a sol-gel method followed by photoreduction. Effect of Ag-AgBr content on the physicochemical properties and antibacterial activities of the Ag-AgBr/TiO2 composites was investigated. These composites showed intrinsic antibacterial activities against Escherichia coli (E. coli) in the dark attributed to the Ag nanoparticles dispersed in the composites. Under visible light irradiation, inactivation of E. coli over these Ag-AgBr/TiO2 composites was attributed to both their photocatalytic disinfection activities and intrinsic antibacterial properties. The Ag-AgBr/TiO2 with an optimum Ti/Ag atomic ratio of 10 exhibited superior visible-light photocatalytic activities for ibuprofen degradation and mineralization as compared to the other Ag-AgBr/TiO2 composites and also Ag-AgBr/P25, Ag/TiO2 and TiO2. It is probably because of the coexistence of two visible-light active components (AgBr and Ag nanoparticles) and the most effective separation of photogenerated electrons and holes in this photocatalyst. Correspondingly, the photocatalyst achieved a much higher efficiency of E. coli destruction than Ag-AgBr/P25 and TiO2. E. coli was almost completely inactivated (7-log reduction) within 60 min by the photocatalyst with a rather low dosage of 0.05 g L(-1) under white LED irradiation. Furthermore, the Ag-AgBr/TiO2 showed high stability for photocatalytic destruction of E. coli and the dark repair and photoreactivation did not occur after the photocatalytic process. Finally, the action spectrum of this photocatalyst for E. coli inactivation and the influence of several inorganic ions present in surface water were also investigated.

  20. The electronic spectrum of AgBr 2: Ab initio benchmark vs. DFT calculations on the lowest ligand-field states including spin-orbit effects

    NASA Astrophysics Data System (ADS)

    Santoyo-Castillo, I.; Ramírez-Solís, A.

    2010-10-01

    The X 2Π g, 2Σ g+ and 2Δ g states of AgBr 2 have been studied through benchmark ab initio CASSCF + Averaged Coupled Pair Functional (ACPF) and DFT calculations using especially developed valence basis sets to study the transition energies, geometries, vibrational frequencies, Mulliken charges and spin densities. The spin-orbit (SO) effects were included through the effective hamiltonian formalism using the |ΛSΣ> ACPF energies as diagonal elements. At the ACPF level, the ground state is 2Π g, in contradiction with ligand-field theory and Hartree-Fock results. The ACPF adiabatic excitation energies of the 2Σ g+ and 2Δ g states are 3825 and 20 152 cm -1, respectively. The inclusion of the SO effects leads to a pure Ω = 3/2 ( 2Π g) ground state, a Ω = 1/2 (97% 2Π g + 3% 2Σ g+) A state, a Ω = 1/2 (3% 2Π g + 97% 2Σ g+) B state, a Ω = 5/2 ( 2Δ g) C state and a Ω = 3/2 (99% 2Δ g) D state. The B97, B3LYP and PBE0 functionals, which were shown to yield accurate transition energies for CuCl 2, overestimate the X 2Π g- 2Σ g+ T e by around 25% but provide a qualitative energetic ordering in agreement with CASSCF and ACPF results. The nature of the bonding in the X 2Π g ground state is different from that of AgCl 2 since the Mulliken charge on the metal is 0.95 while the spin density is only 0.39. DFT strongly delocalizes the spin density providing even smaller values of around 0.13 on Ag not only for the ground state, but also for the 2Σ g+ state.

  1. Enhanced thermal stability of Ag nanorods through capping

    SciTech Connect

    Bachenheimer, Lou; Elliott, Paul; Stagon, Stephen; Huang, Hanchen

    2014-11-24

    Ag nanorods may serve as sensors in the detection of trace amounts of chemical agents, even single molecules, through surface enhanced Raman spectroscopy (SERS). However, thermal coarsening of Ag nanorods near room temperature limits their applications. This letter proposes the use of a thin oxide capping layer to enhance the thermal stability of Ag nanorods beyond 100 °C. Using electron microscopy characterization and SERS tests, the authors show that the proposed method is effective in stabilizing both morphology and sensitivity of Ag nanorods. The results of this work extend the applicability of Ag nanorods as chemical sensors to higher temperatures.

  2. Bonding characteristics of the. sqrt. 3-script. sqrt. 3 Ag/Si interface identified by the energy dependence of the photoionization cross section

    SciTech Connect

    Yeh, J.; Bertness, K.A.; Cao, R.; Hwang, J.; Lindau, I.

    1987-02-15

    Synchrotron-radiation photoemission of the metal-semiconductor interface has a unique advantage in identifying the bonding characteristics of the rehybridized orbitals between the metal and the semiconductor. By varying the photon energy and measuring the magnitude of the photoionization cross section, the bonding peak at the metal-semiconductor interface can be identified as being formed with or without hybridization with the metal's d orbitals. The latter case is clearly illustrated by the annealed Ag/Si(111) interface. A sharp structure at 3.8 eV below the Fermi level grows as a result of annealing of the Ag/Si(111) interface. This structure is also accompanied by the formation of the ..sqrt..3 x ..sqrt..3 (R30/sup 0/) low-energy electron diffraction pattern and the narrowing of the Ag 4d band signal. Since the so-called Cooper-minimum effect is not observed for this annealing-induced peak, it is concluded that the structure does not have 4d-orbital characteristics within the regime of the theory of linear combination of atomic orbitals. This is the direct evidence to show that the Ag 4d band does not hybridize with the substrate Si sp/sup 3/ orbitals in forming Ag: Si bonds after high-temperature annealing. Judging from the photoionization cross-section variation, it can instead be inferred that the sharp structure has mostly Ag 5s or 5p and Si sp characteristics. The methodology shown here can be extended to other metal-semiconductor interfaces and can provide information on the bonding formation of the metal atoms and the semiconductor substrate.

  3. Bonding characteristics of the √3°√3 Ag/Si interface identified by the energy dependence of the photoionization cross section

    NASA Astrophysics Data System (ADS)

    Yeh, J.-J.; Bertness, K. A.; Cao, R.; Hwang, J.; Lindau, I.

    1987-02-01

    Synchrotron-radiation photoemission of the metal-semiconductor interface has a unique advantage in identifying the bonding characteristics of the rehybridized orbitals between the metal and the semiconductor. By varying the photon energy and measuring the magnitude of the photoionization cross section, the bonding peak at the metal-semiconductor interface can be identified as being formed with or without hybridization with the metal's d orbitals. The latter case is clearly illustrated by the annealed Ag/Si(111) interface. A sharp structure at 3.8 eV below the Fermi level grows as a result of annealing of the Ag/Si(111) interface. This structure is also accompanied by the formation of the √3 × √3 (R30°) low-energy electron diffraction pattern and the narrowing of the Ag 4d band signal. Since the so-called Cooper-minimum effect is not observed for this annealing-induced peak, it is concluded that the structure does not have 4d-orbital characteristics within the regime of the theory of linear combination of atomic orbitals. This is the direct evidence to show that the Ag 4d band does not hybridize with the substrate Si sp3 orbitals in forming Ag-Si bonds after high-temperature annealing. Judging from the photoionization cross-section variation, it can instead be inferred that the sharp structure has mostly Ag 5s or 5p and Si sp characteristics. The methodology shown here can be extended to other metal-semiconductor interfaces and can provide information on the bonding formation of the metal atoms and the semiconductor substrate. This is important in discussing metal-semiconductor interfaces but difficult to obtain unambiguously with other techniques and in theoretical predictions.

  4. Ag/AgBr/g-C{sub 3}N{sub 4}: A highly efficient and stable composite photocatalyst for degradation of organic contaminants under visible light

    SciTech Connect

    Cao, Jing; Zhao, Yijie; Lin, Haili; Xu, Benyan; Chen, Shifu

    2013-10-15

    Graphical abstract: Ag/AgBr/g-C{sub 3}N{sub 4} composite photocatalysts displayed excellent photocatalytic activities on the degradation of methyl orange (MO) under visible light. The improved photocatalytic performance and stability of Ag/AgBr/g-C{sub 3}N{sub 4} originated from the synergetic effects of AgBr/g-C{sub 3}N{sub 4} interface and metallic Ag nanoparticles. ·O{sub 2}−, one of the reactive species, was responsible for the photodegradation of MO compared to H+ and ·OH. - Highlights: • Novel Ag/AgBr/g-C{sub 3}N{sub 4} composite photocatalyst was reported. • Ag/AgBr/g-C{sub 3}N{sub 4} had novel energy band combination between AgBr and g-C{sub 3}N{sub 4}. • Synergetic effects of AgBr/g-C{sub 3}N{sub 4} interface and metallic Ag nanoparticles. • Electron trapping role of metallic Ag dominated the stability of Ag/AgBr/g-C{sub 3}N{sub 4}. - Abstract: Novel Ag/AgBr/g-C{sub 3}N{sub 4} composite photocatalysts were constructed via deposition–precipitation method and extensively characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM) and UV–vis diffuse reflectance spectroscopy (DRS). Under visible light (λ > 420 nm), Ag/AgBr/g-C{sub 3}N{sub 4} composite photocatalysts displayed much higher photocatalytic activities than those of Ag/AgBr and g-C{sub 3}N{sub 4} for degradation of methyl orange (MO). 50% Ag/AgBr/g-C{sub 3}N{sub 4} presented the best photocatalytic performance, which was mainly attributed to the synergistic effects of AgBr/g-C{sub 3}N{sub 4} interface and the in situ metallic Ag nanoparticles for efficiently separating electron–hole pairs. Furthermore, Ag/AgBr/g-C{sub 3}N{sub 4} remained good photocatalytic activity through 5 times of cycle experiments. Additionally, the radical scavengers experiment indicated that ·O{sub 2}{sup −} was the main reactive species for the MO degradation under visible light.

  5. Enhanced Raman scattering and photocatalytic activity of Ag/ZnO heterojunction nanocrystals.

    PubMed

    Chen, Chongqi; Zheng, Yuanhui; Zhan, Yingying; Lin, Xingyi; Zheng, Qi; Wei, Kemei

    2011-10-01

    In this work, we study the enhancement of Raman signals and photocatalytic activity of Ag/ZnO heterojunctions with an Ag content of 1 at.%, which were synthesized by photochemical deposition of Ag nanoparticles onto pre-synthesized ZnO nanorods. A strong interaction between Ag and ZnO nanocrystals were evidenced by XPS and UV-vis spectroscopy. The binding energy of Ag nanoparticles shifts toward lower energy compared to that of pure Ag nanoparticles, revealing that electrons transfer from Ag to the ZnO nanocrystals. The red shift of the plasmon absorption peak of Ag nanoparticles in Ag/ZnO heterojunctions further confirms the strong interaction between the two components. This strong interaction, arising from the coupling between Ag and ZnO nanocrystals, is responsible for the enhancement of Raman signals and photocatalytic activity of the Ag/ZnO heterojunctions. PMID:21847472

  6. Uncovering the Key Role of the Fermi Level of the Electron Mediator in a Z-Scheme Photocatalyst by Detecting the Charge Transfer Process of WO3-metal-gC3N4 (Metal = Cu, Ag, Au).

    PubMed

    Li, Houfen; Yu, Hongtao; Quan, Xie; Chen, Shuo; Zhang, Yaobin

    2016-01-27

    Z-scheme photocatalytic system shows superiority in degradation of refractory pollutants and water splitting due to the high redox capacities caused by its unique charge transfer behaviors. As a key component of Z-scheme system, the electron mediator plays an important role in charge carrier migration. According to the energy band theory, we believe the interfacial energy band bendings facilitate the electron transfer via Z-scheme mechanism when the Fermi level of electron mediator is between the Fermi levels of Photosystem II (PS II) and Photosystem I (PS I), whereas charge transfer is inhibited in other cases as energy band barriers would form at the semiconductor-metal interfaces. Here, this inference was verified by the increased hydroxyl radical generation and improved photocurrent on WO3-Cu-gC3N4 (with the desired Fermi level structure), which were not observed on either WO3-Ag-gC3N4 or WO3-Au-gC3N4. Finally, photocatalytic degradation rate of 4-nonylphenol on WO3-Cu-gC3N4 was proved to be as high as 11.6 times than that of WO3-gC3N4, further demonstrating the necessity of a suitable electron mediator in Z-scheme system. This study provides scientific basis for rational construction of Z-scheme photocatalytic system.

  7. Facile synthesis of ternary Ag/AgBr-Ag2CO3 hybrids with enhanced photocatalytic removal of elemental mercury driven by visible light.

    PubMed

    Zhang, Anchao; Zhang, Lixiang; Lu, Hao; Chen, Guoyan; Liu, Zhichao; Xiang, Jun; Sun, Lushi

    2016-08-15

    A novel technique for photocatalytic removal of elemental mercury (Hg(0)) using visible-light-driven Ag/AgBr-Ag2CO3 hybrids was proposed. The ternary Ag/AgBr-Ag2CO3 hybrids were synthesized by a simple modified co-precipitation method and characterized by N2 adsorption-desorption, scanning electron microscope (SEM), X-ray diffraction (XRD), UV-vis diffused reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS) and electron spin resonance (ESR) techniques. The effects of AgBr content, fluorescent lamp (FSL) irradiation, solution temperature, SO2 and NO on Hg(0) removal were investigated in detail. Furthermore, a possible reaction mechanism for higher Hg(0) removal was proposed, and the simultaneous removal of Hg(0), SO2 and NO was studied. The results showed that a high efficiency of Hg(0) removal was obtained by using Ag/AgBr-Ag2CO3 hybrids under fluorescent lamp irradiation. The AgBr content, FSL irradiation, solution temperature, and SO2 all exhibited significant effects on Hg(0) removal, while NO had slight effect on Hg(0) removal. The addition of Ca(OH)2 demonstrated a little impact on Hg(0) removal and could significantly improve the SO2-resistance performance of Ag/AgBr(0.7)-Ag2CO3 hybrid. The characterization results exhibited that hydroxyl radical (OH), superoxide radical (O2(-)), hole (h(+)), and Br(0), were reactive species responsible for removing Hg(0), and the h(+) played a key role in Hg(0) removal. PMID:27135702

  8. Temperature dependent effects during Ag deposition on Cu(110)

    SciTech Connect

    Taylor, T.N.; Muenchausen, R.E.; Hoffbauer, M.A.; Denier van der Gon, A.W.; van der Veen, J.F.; FOM-Instituut voor Atoom-en Molecuulfysica, Amsterdam )

    1989-01-01

    The composition, structure, and morphology of ultrathin films grown by Ag deposition on Cu(110) were monitored as a function of temperature using low-energy electron diffraction (LEED), Auger electron spectroscopy (AES), and medium energy ion scattering (MEIS). Aligned backscattering measurements with 150 keV He ions indicate that the Ag resides on top of the Cu and there is no significant surface compound formation. Measurements with LEED show that the Ag is initially confined to the substrate troughs. Further deposition forces the Ag out of the troughs and results in a split c(2 {times} 4) LEED pattern, which is characteristic of a distorted Ag(111) monolayer template. As verified by both AES and MEIS measurements, postmonolayer deposition of Ag on Cu(110) at 300K leads to a pronounced 3-dimensional clustering. Ion blocking analysis of the Ag clusters show that the crystallites have a (110)-like growth orientation, implying that the Ag monolayer template undergoes a rearrangement. These data are confirmed by low temperature LEED results in the absence of clusters, which indicate that Ag multilayers grow from a Ag--Cu interface where the Ag is captured in the troughs. Changes observed in the film structure and morphology are consistent with a film growth mechanism that is driven by overlayer strain response to the substrate corrugation. 16 refs., 4 figs.

  9. Optimization and Characterization of Silver Nanoparticle by Endophytic Fungi Penicillium sp. Isolated from Curcuma longa (Turmeric) and Application Studies against MDR E. coli and S. aureus

    PubMed Central

    Singh, Dattu; Rathod, Vandana; Ninganagouda, Shivaraj; Hiremath, Jyothi; Singh, Ashish Kumar; Mathew, Jasmine

    2014-01-01

    Development of ecofriendly and reliable processes for the synthesis of nanoparticles has attracted considerable interest in nanotechnology because of its tremendous impetus in modulating metals into nanosize to their potential use for human benefits. In this study an endophytic fungus, Penicillium sp., isolated from healthy leaves of Curcuma longa (turmeric) was subjected to extracellular biosynthesis of silver nanoparticles (AgNps) and their activity against MDR E. coli and S. aureus. The biosynthesized AgNps optimization was studied and characterized by UV-visible spectroscopy, Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM). Then produced AgNps were tested against MDR E. coli and S. aureus. The endophytic fungus Penicillium sp. from healthy leaves of C. longa (turmeric) was found to be a good producer of AgNps. Parametric optimization showed maximum absorbance of 420–425 nm at pH-7, 25°C with 1 mM AgNO3 concentration and 15–20 g of wet biomass. Further TEM revealed the formation of spherical, well-dispersed nanoparticles with size ranging between 25 and 30 nm and FTIR shows the bands at 1644 and 1538 cm−1 corresponding to the binding vibrations of amide I and II bands of proteins, respectively. Antibacterial activity against MDR E. coli and S. aureus showed good results showing maximum zone of inhibition of 17 mm and 16 mm, respectively, at 80 µL of AgNps. PMID:24639625

  10. Optimization and Characterization of Silver Nanoparticle by Endophytic Fungi Penicillium sp. Isolated from Curcuma longa (Turmeric) and Application Studies against MDR E. coli and S. aureus.

    PubMed

    Singh, Dattu; Rathod, Vandana; Ninganagouda, Shivaraj; Hiremath, Jyothi; Singh, Ashish Kumar; Mathew, Jasmine

    2014-01-01

    Development of ecofriendly and reliable processes for the synthesis of nanoparticles has attracted considerable interest in nanotechnology because of its tremendous impetus in modulating metals into nanosize to their potential use for human benefits. In this study an endophytic fungus, Penicillium sp., isolated from healthy leaves of Curcuma longa (turmeric) was subjected to extracellular biosynthesis of silver nanoparticles (AgNps) and their activity against MDR E. coli and S. aureus. The biosynthesized AgNps optimization was studied and characterized by UV-visible spectroscopy, Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM). Then produced AgNps were tested against MDR E. coli and S. aureus. The endophytic fungus Penicillium sp. from healthy leaves of C. longa (turmeric) was found to be a good producer of AgNps. Parametric optimization showed maximum absorbance of 420-425 nm at pH-7, 25°C with 1 mM AgNO3 concentration and 15-20 g of wet biomass. Further TEM revealed the formation of spherical, well-dispersed nanoparticles with size ranging between 25 and 30 nm and FTIR shows the bands at 1644 and 1538 cm(-1) corresponding to the binding vibrations of amide I and II bands of proteins, respectively. Antibacterial activity against MDR E. coli and S. aureus showed good results showing maximum zone of inhibition of 17 mm and 16 mm, respectively, at 80 µL of AgNps.

  11. Decoupling optical and electronic optimization of organic solar cells using high-performance temperature-stable TiO{sub 2}/Ag/TiO{sub 2} electrodes

    SciTech Connect

    Kim, Kwang-Dae; Pfadler, Thomas; Zimmermann, Eugen; Feng, Yuyi; Weickert, Jonas Schmidt-Mende, Lukas; Dorman, James A.

    2015-10-01

    An electrode structured with a TiO{sub 2}/Ag/TiO{sub 2} (TAT) multilayer as indium tin oxide (ITO) replacement with a superior thermal stability has been successfully fabricated. This electrode allows to directly tune the optical cavity mode towards maximized photocurrent generation by varying the thickness of the layers in the sandwich structure. This enables tailored optimization of the transparent electrode for different organic thin film photovoltaics without alteration of their electro-optical properties. Organic photovoltaic featuring our TAT multilayer shows an improvement of ∼12% over the ITO reference and allows power conversion efficiencies (PCEs) up to 8.7% in PTB7:PC{sub 71}BM devices.

  12. Regional vertical total electron content (VTEC) modeling together with satellite and receiver differential code biases (DCBs) using semi-parametric multivariate adaptive regression B-splines (SP-BMARS)

    NASA Astrophysics Data System (ADS)

    Durmaz, Murat; Karslioglu, Mahmut Onur

    2015-04-01

    There are various global and regional methods that have been proposed for the modeling of ionospheric vertical total electron content (VTEC). Global distribution of VTEC is usually modeled by spherical harmonic expansions, while tensor products of compactly supported univariate B-splines can be used for regional modeling. In these empirical parametric models, the coefficients of the basis functions as well as differential code biases (DCBs) of satellites and receivers can be treated as unknown parameters which can be estimated from geometry-free linear combinations of global positioning system observables. In this work we propose a new semi-parametric multivariate adaptive regression B-splines (SP-BMARS) method for the regional modeling of VTEC together with satellite and receiver DCBs, where the parametric part of the model is related to the DCBs as fixed parameters and the non-parametric part adaptively models the spatio-temporal distribution of VTEC. The latter is based on multivariate adaptive regression B-splines which is a non-parametric modeling technique making use of compactly supported B-spline basis functions that are generated from the observations automatically. This algorithm takes advantage of an adaptive scale-by-scale model building strategy that searches for best-fitting B-splines to the data at each scale. The VTEC maps generated from the proposed method are compared numerically and visually with the global ionosphere maps (GIMs) which are provided by the Center for Orbit Determination in Europe (CODE). The VTEC values from SP-BMARS and CODE GIMs are also compared with VTEC values obtained through calibration using local ionospheric model. The estimated satellite and receiver DCBs from the SP-BMARS model are compared with the CODE distributed DCBs. The results show that the SP-BMARS algorithm can be used to estimate satellite and receiver DCBs while adaptively and flexibly modeling the daily regional VTEC.

  13. Ag@Ag8W4O16 nanoroasted rice beads with photocatalytic, antibacterial and anticancer activity.

    PubMed

    Selvamani, Muthamizh; Krishnamoorthy, Giribabu; Ramadoss, Manigandan; Sivakumar, Praveen Kumar; Settu, Munusamy; Ranganathan, Suresh; Vengidusamy, Narayanan

    2016-03-01

    Increasing resistance of pathogens and cancer cell line towards antibiotics and anticancer agents has caused serious health problems in the past decades. Due to these problems in recent years, researchers have tried to combine nanotechnology with material science to have intrinsic antimicrobial and anticancer activity. The metals and metal oxides were investigated with respect to their antimicrobial and anticancer effects towards bacteria and cancer cell line. In the present work metal@metal tungstate (Ag@Ag8W4O16 nanoroasted rice beads) is investigated for antibacterial activity against Escherichia coli and Staphylococcus aureus using Mueller-Hinton broth and the anticancer activity against B16F10 cell line was studied. Silver decorated silver tungstate (Ag@Ag8W4O16) was synthesized by the microwave irradiation method using Cetyl Trimethyl Ammonium Bromide (CTAB). Ag@Ag8W4O16 was characterized by using various spectroscopic techniques. The phase and crystalline nature were analyzed by using XRD. The morphological analysis was carried out using Field Emission Scanning Electron Microscopy (FE-SEM), and High Resolution Transmission Electron Microscopy (HR-TEM). Further, Fourier Transform Infrared Spectroscopy (FT-IR) and Raman spectral analysis were carried out in order to ascertain the presence of functional groups in Ag@Ag8W4O16. The optical property was investigated using Diffuse Reflectance Ultraviolet-Visible Spectroscopy (DRS-UV-Vis) and the band gap was found to be 3.08eV. Surface area of the synthesized Ag@Ag8W4O16 wasanalyzed by BET analysis and Ag@Ag8W4O16 was utilized for the degradation of organic dyes methylene blue and rhodamine B. The morphology of the Ag@Ag8W4O16 resembles roasted rice beads with breath and length in nm range. The oxidation state of tungsten (W) and silver (Ag) was investigated using X-ray photoelectron spectroscopy (XPS).

  14. Reducing Strength Prevailing at Root Surface of Plants Promotes Reduction of Ag+ and Generation of Ag0/Ag2O Nanoparticles Exogenously in Aqueous Phase

    PubMed Central

    Pardha-Saradhi, Peddisetty; Yamal, Gupta; Peddisetty, Tanuj; Sharmila, Peddisetty; Nagar, Shilpi; Singh, Jyoti; Nagarajan, Rajamani; Rao, Kottapalli S.

    2014-01-01

    Potential of root system of plants from wide range of families to effectively reduce membrane impermeable ferricyanide to ferrocyanide and blue coloured 2,6-dichlorophenol indophenol (DCPIP) to colourless DCPIPH2 both under non-sterile and sterile conditions, revealed prevalence of immense reducing strength at root surface. As generation of silver nanoparticles (NPs) from Ag+ involves reduction, present investigations were carried to evaluate if reducing strength prevailing at surface of root system can be exploited for reduction of Ag+ and exogenous generation of silver-NPs. Root system of intact plants of 16 species from 11 diverse families of angiosperms turned clear colorless AgNO3 solutions, turbid brown. Absorption spectra of these turbid brown solutions showed silver-NPs specific surface plasmon resonance peak. Transmission electron microscope coupled with energy dispersive X-ray confirmed the presence of distinct NPs in the range of 5–50 nm containing Ag. Selected area electron diffraction and powder X-ray diffraction patterns of the silver NPs showed Bragg reflections, characteristic of crystalline face-centered cubic structure of Ag0 and cubic structure of Ag2O. Root system of intact plants raised under sterile conditions also generated Ag0/Ag2O-NPs under strict sterile conditions in a manner similar to that recorded under non-sterile conditions. This revealed the inbuilt potential of root system to generate Ag0/Ag2O-NPs independent of any microorganism. Roots of intact plants reduced triphenyltetrazolium to triphenylformazon and impermeable ferricyanide to ferrocyanide, suggesting involvement of plasma membrane bound dehydrogenases in reduction of Ag+ and formation of Ag0/Ag2O-NPs. Root enzyme extract reduced triphenyltetrazolium to triphenylformazon and Ag+ to Ag0 in presence of NADH, clearly establishing potential of dehydrogenases to reduce Ag+ to Ag0, which generate Ag0/Ag2O-NPs. Findings presented in this manuscript put forth a novel, simple

  15. 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.

  16. Synthesis, characterization and optical properties of low nuclearity liganded silver clusters: Ag31(SG)19 and Ag15(SG)11.

    PubMed

    Bertorelle, Franck; Hamouda, Ramzi; Rayane, Driss; Broyer, Michel; Antoine, Rodolphe; Dugourd, Philippe; Gell, Lars; Kulesza, Alexander; Mitrić, Roland; Bonačić-Koutecký, Vlasta

    2013-06-21

    We report a simple synthesis of silver:glutathione (Ag:SG) clusters using a cyclic reduction under oxidative conditions. Two syntheses are described which lead to solutions containing well-defined Ag31(SG)19 and Ag15(SG)11 clusters that have been characterized by mass spectrometry. The optical properties of silver:glutathione (Ag:SG) cluster solutions have been investigated experimentally. In particular, the solution containing Ag15(SG)11 clusters shows a bright and photostable emission. For Ag31(SG)19 and Ag15(SG)11 clusters, the comparison of experimental findings with DFT and TDDFT calculations allowed us to reveal the structural and electronic properties of such low nuclearity liganded silver clusters.

  17. New isomeric state in {sup 116}Ag

    SciTech Connect

    Batchelder, J.C.; Carter, H.K.; Spejewski, E.H.; Bingham, C.R.; Fong, D.; Hamilton, J.H.; Hwang, J.K.; Ramayya, A.V.; Garrett, P.E.; Hartley, D.J.; Krolas, W.; Kulp, W.D.; Wood, J.L.; Larochelle, Y.; Tantawy, M.N.; Piechaczek, A.

    2005-10-01

    A new isomer in {sup 116}Ag with a half-life of 20(1) s has been discovered through the use of conversion electron, {beta}, and {gamma} spectroscopy of on-line mass-separated radioactivities at the Holifield Radioactive Ion Beam Facility at ORNL. The observed electron peaks at 22.5, 44.42, and 47.33 keV were interpreted as the K,L, and M conversion electron lines resulting from a 47.9-keV E3 transition associated with the decay of a second isomeric level in {sup 116}Ag. A new level structure of {sup 116}Ag is proposed, with the levels identified as the 0{sup -} ground-state and isomers at 47.9 and 128.8 keV having spin/parities of 3{sup +} and 6{sup -} respectively.

  18. Ab inito study of Ag-related defects in ZnO

    NASA Astrophysics Data System (ADS)

    Wan, Qixin; Xiong, Zhihua; Li, Dongmei; Liu, Guodong

    2008-12-01

    Using first-principles calculations, we investigated the structure and electronic properties of Ag-related defects in ZnO. The calculation results indicate that AgZn behaves as acceptor. Simultaneously, by comparing the formation energy and electronic structure of Ag-related defects in ZnO, Oi-AgZn behaves as acceptor in Ag-doped ZnO and it is better to gain p-type ZnO. However, Hi-AgZn complex has the lowest formation energy. Thus, the formation of the other point defects is greatly suppressed by the formation of Hi in Ag-doped ZnO. Moreover, the H atoms can be easily dissociated from hydrogen-passivated complexes by post-annealing at moderate temperatures, thus, codoping Ag with H may be a good method to achieve p-type in Ag-doped ZnO.

  19. Novel visible-light-responsive Ag/AgCl@MIL-101 hybrid materials with synergistic photocatalytic activity.

    PubMed

    Gao, Shutao; Feng, Tao; Feng, Cheng; Shang, Ningzhao; Wang, Chun

    2016-03-15

    In this paper, a novel visible-light responsive photocatalyst of Ag/AgCl@MIL-101 was synthesized via vapor diffusion-photoreduction strategy. The as-prepared composite material was characterized using X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, ultraviolet-visible diffuse reflection spectra and X-ray photoelectron spectroscopy. Due to the synergistic effect between Ag/AgCl and MIL-101, the composite photocatalyst exhibited an enhanced and stable photoactivity for the degradation of Rhodamine B under visible light irradiation. The relationship between the photocatalytic activity and the structure of Ag/AgCl@MIL-101 hybrid material was discussed and the possible reaction mechanism was proposed.

  20. Isomorphism and solid solutions among Ag- and Au-selenides

    NASA Astrophysics Data System (ADS)

    Palyanova, Galina A.; Seryotkin, Yurii V.; Kokh, Konstantin A.; Bakakin, Vladimir V.

    2016-09-01

    Au-Ag selenides were synthesized by heating stoichiometric mixtures of elementary substances of initial compositions Ag2-xAuxSe with a step of x=0.25 (0≤x≤2) to 1050 °C and annealing at 500 °C. Scanning electron microscopy, optical microscopy, electron microprobe analysis and X-ray powder diffraction methods have been applied to study synthesized samples. Results of studies of synthesized products revealed the existence of three solid solutions with limited isomorphism Ag↔Au: naumannite Ag2Se - Ag1.94Au0.06Se, fischesserite Ag3AuSe2 - Ag3.2Au0.8Se2 and gold selenide AuSe - Au0.94Ag0.06Se. Solid solutions and AgAuSe phases were added to the phase diagram of Ag-Au-Se system. Crystal-chemical interpretation of Ag-Au isomorphism in selenides was made on the basis of structural features of fischesserite, naumannite, and AuSe.

  1. Ag(+)-mediated assembly of 5'-guanosine monophosphate.

    PubMed

    Loo, Kristine; Degtyareva, Natalya; Park, Jihae; Sengupta, Bidisha; Reddish, Michaeal; Rogers, Christopher C; Bryant, Andrea; Petty, Jeffrey T

    2010-04-01

    Polymorphic forms of nucleic acids provide platforms for new nanomaterials, and transition metal cations give access to alternative arrangements of nucleobases by coordinating with electron-rich functional groups. Interaction of Ag(+) with 5'-guanosine monophosphate (5'-GMP) is considered in this work. Ag(+) promotes nucleotide stacking and aggregation, as indicated by the increased viscosity of 5'-GMP solutions with Ag(+), magnification of the circular dichroism response of guanine by Ag(+), and exothermic reactions between Ag(+) and guanine derivatives. Isothermal titration calorimetry studies show that the reaction is favored starting at 10 microM 5'-GMP. Utilizing the exothermic heat change associated with reaction of Ag(+) with 5'-GMP, local structure within the aggregate was assessed. On the basis of the salt dependence of the reaction and comparison with the corresponding nucleoside, the dianionic phosphate of 5'-GMP is one binding site for Ag(+), although this electrostatic interaction is not a dominant contribution to the overall heat change. Another binding site is the N7 on the nucleobase, as determined via studies with 7-deazaguanosine. Besides this binding site, Ag(+) also associates with the O6, as earlier studies deduced from the shift in the carbonyl stretching frequency associated with adduct formation. With these two binding sites on the nucleobase, the empirical stoichiometry of approximately 1 Ag(+):nucleobase derived from the calorimetry studies indicates that Ag(+) coordinates two nucleobases. The proposed structural model is a Ag(+)-mediated guanine dimer within a base stacked aggregate. PMID:20205377

  2. Metallurgical characterization of experimental Ag-based soldering alloys

    PubMed Central

    Ntasi, Argyro; Al Jabbari, Youssef S.; Silikas, Nick; Al Taweel, Sara M.; Zinelis, Spiros

    2014-01-01

    Aim To characterize microstructure, hardness and thermal properties of experimental Ag-based soldering alloys for dental applications. Materials and methods Ag12Ga (AgGa) and Ag10Ga5Sn (AgGaSn) were fabricated by induction melting. Six samples were prepared for each alloy and microstructure, hardness and their melting range were determined by, scanning electron microscopy, energy dispersive X-ray (EDX) microanalysis, X-ray diffraction (XRD), Vickers hardness testing and differential scanning calorimetry (DSC). Results Both alloys demonstrated a gross dendritic microstructure while according to XRD results both materials consisted predominately of a Ag-rich face centered cubic phase The hardness of AgGa (61 ± 2) was statistically lower than that of AgGaSn (84 ± 2) while the alloys tested showed similar melting range of 627–762 °C for AgGa and 631–756 °C for AgGaSn. Conclusion The experimental alloys tested demonstrated similar microstructures and melting ranges. Ga and Sn might be used as alternative to Cu and Zn to modify the selected properties of Ag based soldering alloys. PMID:25382945

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

    NASA Astrophysics Data System (ADS)

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

    2015-03-01

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

  4. Plasmon-assisted degradation of methylene blue with Ag/AgCl/montmorillonite nanocomposite under visible light

    NASA Astrophysics Data System (ADS)

    Sohrabnezhad, Sh.; Zanjanchi, M. A.; Razavi, M.

    2014-09-01

    Metal-semiconductor compounds, such as Ag/AgX (X = Cl, Br, I), enable visible light absorption and separation of photogenerated electron-hole through surface plasmon resonance (SPR) effect. However, the electron-hole generated and separated by light are vulnerable in Ag/AgX phase because of the occurrence of secondary recombined. In order to more effectively utilize the SPR photocatalytic effect, nanoparticles are located in a matrix. In this article, Ag/AgCl nanoparticles were synthesized in montmorillonite (MMT) matrix using dispersion method and light irradiation. The structure, composition and optical properties of such material were investigated by transmission electron microscopy (TEM), UV-visible diffuse reflectance spectroscopy (UV-Vis DRS), X-ray diffraction (XRD) and FTIR. Powder X-ray diffraction showed intercalation of Ag/AgCl nanoparticles into the clay layers. The as-prepared plasmonic photocatalyst exhibited an enhanced and stable photoactivity for the degradation of methylene blue (MB) under visible light. The high activity was attributed to the surface plasmon resonance (SPR) exhibited by Ag nanoparticles on the surface of AgCl. The detection of reactive species by radical scavengers displays that rad O2- and rad OH- are the main reactive species for the degradation of MB under visible light irradiation. The studies showed that 20 min illumination under visible light can complete degradation of methylene blue (MB), and indicate a high stability of photocatalytic degradation. The mechanism of separation of the photo-generated electrons and holes at the Ag/AgCl-MMT nanocomposite was discussed.

  5. Nano Ag@AgBr surface-sensitized Bi2WO6 photocatalyst: oil-in-water synthesis and enhanced photocatalytic degradation

    NASA Astrophysics Data System (ADS)

    Lin, Shuanglong; Liu, Li; Hu, Jinshan; Liang, Yinghua; Cui, Wenquan

    2015-01-01

    Nano Ag@AgBr decorated on the surface of flower-like Bi2WO6 (hereafter designated Ag@AgBr/Bi2WO6) were prepared via a facile oil-in-water self-assembly method. The photocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (DRS), etc. The characterization results indicated that nano Ag@AgBr was observed to be evenly dispersed on the surface of Bi2WO6, and was approximately 20 nm in size. Ag@AgBr/Bi2WO6 composites exhibited excellent UV-vis absorption, due to quantum dimension effect of Ag@AgBr, the surface plasmonic resonance (SPR) of Ag nanoparticles and the special flower-like structure of Bi2WO6. The photoelectrochemical measurement verified that the suitable band potential of Ag@AgBr and Bi2WO6 and the existence of metal Ag resulted in the high efficiency in charge separation of the composite. The photocatalytic activities of the Ag@AgBr/Bi2WO6 samples were examined under visible-light irradiation for the degradation of methylene blue (MB). The composite presented excellent photocatalytic activity due to the synergetic effect of Bi2WO6, AgBr, and Ag nanoparticles. The Ag@AgBr(20 wt.%)/Bi2WO6 sample exhibited the best photocatalytic activity, degrading 95.03% MB after irradiation for 2 h, which was respectively 1.29 times and 1.28 times higher than that of Ag@AgBr and Bi2WO6 photocatalyst. Meanwhile, phenol and salicylic acid were degraded to further prove the degradation ability of Ag@AgBr/Bi2WO6. Additionally, studies performed using radical scavengers indicated that O2-•, •OH and Br0 acted as the main reactive species. Based on above, a photocatalytic mechanism for organics degradation over Ag@AgBr/Bi2WO6 was proposed.

  6. Fabrication of Sn-3.5Ag Eutectic Alloy Powder by Annealing Sub-Micrometer Sn@Ag Powder Prepared by Citric Acid-Assisted Ag Immersion Plating.

    PubMed

    Chee, Sang-Soo; Choi, Eun Byeol; Lee, Jong-Hyun

    2015-11-01

    A Sn-3.5Ag eutectic alloy powder has been developed by chemically synthesizing sub-micrometer Sn@Ag powder at room temperature. This synthesis was achieved by first obtaining a sub-micrometer Sn powder for the core using a modified variant of the polyol method, and then coating this with a uniformly thin and continuous Ag layer through immersion plating in 5.20 mM citric acid. The citric acid was found to play multiple roles in the Ag coating process, acting as a chelating agent, a reducing agent and a stabilizer to ensure coating uniformity; and as such, the amount used has an immense influence on the coating quality of the Ag shells. It was later verified by transmission electron microscopy and X-ray diffraction analysis that the coated Ag layer transfers to the Sn core via diffusion to form an Ag3Sn phase at room temperature. Differential scanning calorimetry also revealed that the synthesized Sn@Ag powder is nearly transformed into Sn-3.5Ag eutectic alloy powder upon annealing three times at a temperature of up to 250 degrees C, as evidenced by a single melting peak at 220.5 degrees C. It was inferred from this that Sn-3.5Ag eutectic alloy powder can be successfully prepared through the synthesis of core Sn powders by a modified polyol method, immersion plating using citric acid, and annealing, in that order.

  7. Antibacterial Ag/a-C nanocomposite coatings: The influence of nano-galvanic a-C and Ag couples on Ag ionization rates

    NASA Astrophysics Data System (ADS)

    Manninen, N. K.; Calderon, S.; Carvalho, I.; Henriques, M.; Cavaleiro, A.; Carvalho, S.

    2016-07-01

    Biofilm formation has been pointed as a major concern in different industrial applications, namely on biomedical implants and surgical instruments, which has prompted the development of new strategies for production of efficient antimicrobial surfaces. In this work, nano-galvanic couples were created to enhance the antibacterial properties of silver, by embedding it into amorphous carbon (a-C) matrix. The developed Ag/a-C nanocomposite coatings, deposited by magnetron sputtering, revealed an outstanding antibacterial activity against Staphylococcus epidermidis, promoting a total reduction in biofilm formation with no bacteria counts in all dilution. The open circuit potential (OCP) tests in 0.9% NaCl confirmed that a-C shows a positive OCP value, in contrast to Ag coating, thus enhancing the ionization of biocidal Ag+ due to the nano-galvanic couple activation. This result was confirmed by the inductively coupled plasma-optical emission spectroscopy (ICP-OES), which revealed a higher Ag ionization rate in the nanocomposite coating in comparison with the Ag coating. The surface of Ag/a-C and Ag coatings immersed in 0.9% NaCl were monitored by scanning electron microscopy (SEM) over a period of 24 h, being found that the Ag ionization determined by ICP-OES was accompanied by an Ag nanoparticles coalescence and agglomeration in Ag/a-C coating.

  8. EXAFS Studies of Bimetallic Ag-Pt and Ag-Pd Nanorods

    SciTech Connect

    Lahiri, D.; Chattopadhyay, S.; Bunker, B.A.; Doudna, C.M.; Bertino, M.F.; Blum, F.; Tokuhiro, A.; Terry, J.

    2008-10-30

    Nanoparticles of Ag-Pt and Ag-Pd with high aspect ratios were synthesized using a radiolysis method. Gamma rays at dose rates below 0.5 kGy/h were used for irradiation. The nanoparticles were characterized by transmission electron microscopy (TEM), optical absorption spectroscopy and x-ray Absorption Fine Structure (XAFS) spectroscopy. Bright field micrographs show that Ag-Pt nanowires are composed of large particles with diameters ranging from 20-30 nm and joined by filaments of diameter between 2-5 nm. The Ag-Pd nanowires have diameters of 20-25 nm and lengths of 1.5 {micro}m. For XAFS measurements, the Pt L3 edge (11.564 keV), Ag K-edge (25.514 keV) and Pd K-edge (24.350 keV) were excited to determine the local structure around the respective atoms in the cluster. The Ag-Pt particles were found to possess a distinct core-shell structure with Pt in the core surrounded by Ag shell, with no indication of alloy formation. However, nanorods of Ag-Pd have formed an alloy for all the alloy compositions.

  9. Plasmonic modification of electron-longitudinal-optical phonon coupling in Ag-nanoparticle embedded InGaN/GaN quantum wells

    SciTech Connect

    Llopis, Antonio; Neogi, Arup; Pereira, Sérgio M. S.; Watson, Ian M.

    2014-09-01

    Surface plasmon enhanced GaN and InGaN quantum wells (QWs) show promise for use as room-temperature light emitters. The effectiveness of the plasmon enhancement, however, is limited by the strong electron/hole and longitudinal optical phonon coupling found in the III-V nitrides. The electron-phonon coupling within semiconductor QWs has been modified using silver nanoparticles embedded within the QWs. Direct evidence is provided for this change via confocal Raman spectroscopy of the samples. This evidence is augmented by Angle-dependent photoluminescence experiments which show the alteration of the electron-phonon coupling strength through measurement of the emitted phonon replicas. Together these demonstrate a direct modification of carrier-phonon interactions within the system, opening up the possibility of controlling the coupling strength to produce high-efficiency room-temperature light emitters.

  10. Fluoride-induced reduction of Ag(I) cation leading to formation of silver mirrors and luminescent Ag-nanoparticles.

    PubMed

    Maity, Krishnendu; Panda, Dillip K; Lochner, Eric; Saha, Sourav

    2015-03-01

    In aprotic solvents, Lewis basic F(-) anion reduces Lewis acidic Ag(I) cation to Ag(0), forming metallic silver mirrors on the inner surfaces of reaction vessels and luminescent Ag-nanoparticles (AgNPs) in supernatant solutions, which emit blue light upon UV irradiation. The F(-)-induced formation of silver mirrors and AgNPs was confirmed through X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), fluorescence spectroscopy, and mass spectrometry, whereas the Ag(I)-induced oxidation of F(-) to Ḟ radical, followed by its conversion to HF2(-) via H-abstraction and H-bonding, was evident from (19)F NMR spectroscopy. This redox reaction is deactivated in water, as the reducing power of hydrated F(-) diminishes drastically. Less Lewis basic Cl(-), Br(-), and I(-) ions do not reduce Ag(I) to Ag(0), instead they can only form Ag(I) halide precipitates irrespective of protic or aprotic solvents. The Ag-coated surfaces, luminescent AgNPs, and Ḟ radicals produced by this unprecedented redox reaction could be exploited as electrodes, light-emitting materials, and radical initiators, respectively.

  11. Microstructure, mechanical properties, bio-corrosion properties and antibacterial properties of Ti-Ag sintered alloys.

    PubMed

    Chen, Mian; Zhang, Erlin; Zhang, Lan

    2016-05-01

    In this research, Ag element was selected as an antibacterial agent to develop an antibacterial Ti-Ag alloy by a powder metallurgy. The microstructure, phase constitution, mechanical properties, corrosion resistance and antibacterial properties of the Ti-Ag sintered alloys have been systematically studied by X-ray diffraction (XRD), scanning electron microscope (SEM), compressive test, electrochemical measurements and antibacterial test. The effects of the Ag powder size and the Ag content on the antibacterial property and mechanical property as well as the anticorrosion property have been investigated. The microstructure results have shown that Ti-Ag phase, residual pure Ag and Ti were the mainly phases in Ti-Ag(S75) sintered alloy while Ti2Ag was synthesized in Ti-Ag(S10) sintered alloy. The mechanical test indicated that Ti-Ag sintered alloy showed a much higher hardness and the compressive yield strength than cp-Ti but the mechanical properties were slightly reduced with the increase of Ag content. Electrochemical results showed that Ag powder size had a significant effect on the corrosion resistance of Ti-Ag sintered alloy. Ag content increased the corrosion resistance in a dose dependent way under a homogeneous microstructure. Antibacterial tests have demonstrated that antibacterial Ti-Ag alloy was successfully prepared. It was also shown that the Ag powder particle size and the Ag content influenced the antibacterial activity seriously. The reduction in the Ag powder size was benefit to the improvement in the antibacterial property and the Ag content has to be at least 3wt.% in order to obtain a strong and stable antibacterial activity against Staphylococcus aureus bacteria. The bacterial mechanism was thought to be related to the Ti2Ag and its distribution. PMID:26952433

  12. Microstructure, mechanical properties, bio-corrosion properties and antibacterial properties of Ti-Ag sintered alloys.

    PubMed

    Chen, Mian; Zhang, Erlin; Zhang, Lan

    2016-05-01

    In this research, Ag element was selected as an antibacterial agent to develop an antibacterial Ti-Ag alloy by a powder metallurgy. The microstructure, phase constitution, mechanical properties, corrosion resistance and antibacterial properties of the Ti-Ag sintered alloys have been systematically studied by X-ray diffraction (XRD), scanning electron microscope (SEM), compressive test, electrochemical measurements and antibacterial test. The effects of the Ag powder size and the Ag content on the antibacterial property and mechanical property as well as the anticorrosion property have been investigated. The microstructure results have shown that Ti-Ag phase, residual pure Ag and Ti were the mainly phases in Ti-Ag(S75) sintered alloy while Ti2Ag was synthesized in Ti-Ag(S10) sintered alloy. The mechanical test indicated that Ti-Ag sintered alloy showed a much higher hardness and the compressive yield strength than cp-Ti but the mechanical properties were slightly reduced with the increase of Ag content. Electrochemical results showed that Ag powder size had a significant effect on the corrosion resistance of Ti-Ag sintered alloy. Ag content increased the corrosion resistance in a dose dependent way under a homogeneous microstructure. Antibacterial tests have demonstrated that antibacterial Ti-Ag alloy was successfully prepared. It was also shown that the Ag powder particle size and the Ag content influenced the antibacterial activity seriously. The reduction in the Ag powder size was benefit to the improvement in the antibacterial property and the Ag content has to be at least 3wt.% in order to obtain a strong and stable antibacterial activity against Staphylococcus aureus bacteria. The bacterial mechanism was thought to be related to the Ti2Ag and its distribution.

  13. Ag surface diffusion and out-of-bulk segregation in CrN-Ag nano-composite coatings.

    PubMed

    Incerti, L; Rota, A; Ballestrazzi, A; Gualtieri, E; Valeri, S

    2011-10-01

    CrN-Ag nanocomposite coatings are deposited on Si(100) wafers and 20MnCr5 steel disks in a mixed Ar+N2 atmosphere by reactive magnetron sputtering. Structure, composition and morphology were investigated by Scanning Electron Microscopy (SEM), Auger Electron Spectroscopy (AES), X-ray Photoemission Spectroscopy (XPS), X-ray Diffraction (XRD) and Focused Ion Beam (FIB) cross sectional analysis. The as deposited film matrix is mainly composed by CrN phase (78%), but a relevant part (28%) is composed by Cr2N. Ag agglomerates in the CrN matrix forming elongated grains 200-400 nm wide and 50-100 nm high, which extends on the top of CrN columns. At the surface Ag aggregates into two different structures: large tetrahedral crystalline clusters, with typical dimension ranging from 200 to 500 nm, and smaller Ag nanoparticles with diameter of 15-25 nm. The annealing in N2 atmosphere up to 500 degrees C does not affect size and distribution of the Ag grains in the sub-surface region, while it induces a size increase of the bigger Ag clusters on the surface, mainly related to Ag surface diffusion and clusters coalescence. Annealing at higher temperature leads to an evident Ag out-of-bulk segregation, generating Ag depleted voids in the near-surface region, and further increasing of the Ag clusters size at the surface. Tribological tests on as deposited CrN-Ag film reveal a coefficient of friction against a steel ball reduced with respect to CrN film, probably related to the presence of Ag which acts as solid lubricant, but the coating is removed after a very short sliding distance. The poor mechanical properties of the realized Ag-based coatings are confirmed by lower hardness and Young modulus values with respect to pure CrN.

  14. Bimetallic Ag-Au nanoparticles: Extracting meaningful optical constants from the surface-plasmon extinction spectrum

    NASA Astrophysics Data System (ADS)

    Moskovits, M.; Srnova-Sloufova, I.; Vlckova, B.

    2002-06-01

    We report an approach for extracting the optical constants of bimetallic Ag-Au nanoparticles from the measured surface-plasmon (SP) extinction spectra. The dielectric function of the metal is expressed as an analytic function of the wavelength in which the interband (and all other non-Drude) contributions to the dielectric function are represented by a sum of Lorentz functions. This expression is then used to fit the experimental extinction spectra to appropriate functions based on Mie theory. Three Lorentz functions (plus a Drude term) were found to be sufficient to reproduce the dielectric functions of Ag and Au [P. B. Johnson and R. W. Christy, Phys. Rev. B 6, 4370 (1972)] over the entire 0.6-6.5 eV range reported. With functions of this type, an excellent multiparameter fit of the measured extinction spectrum of colloidal Ag was obtained. Extinction spectra of a series of (Ag)Au hydrosols, prepared by reducing a gold precursor in the presence of previously synthesized silver seed particles with Au mole fractions ranging from 0.1 to 0.8, were measured. The extinction spectra show a single band (attributed to the surface plasmon) for all of the colloids produced, suggesting alloy formation. Transmission electron microscopy (TEM) images, however, indicate clear core-shell contrast for nanoparticles with Au mole fractions 0.4 and higher. With a presumed particle structure consisting of Ag core and Ag/Au alloy shell, very good fits were obtained for all of the measured extinction spectra by using a fitting strategy that restricted the number of parameters allowed to vary freely in the aforementioned dielectric function. The values of the dielectric function of the presumed shells were extracted in this manner as a function of wavelength. For particles with Au mole fraction 0.1-0.3, the results suggest an incompletely formed shell. For particles with higher Au mole fractions, the dielectric function of the shell gradually approaches that of Au. Overall, the results

  15. Molecular dynamics study of nanojoining between axially positioned Ag nanowires

    NASA Astrophysics Data System (ADS)

    Cui, Jianlei; Theogene, Barayavuga; Wang, Xuewen; Mei, Xuesong; Wang, Wenjun; Wang, Kedian

    2016-08-01

    The miniaturization of electronics devices into nanometer scale is indispensable for next-generation semiconductor technology. Ag nanowires (Ag NWs) are considered to be the promising candidates for future electronic circuit owing to the excellent electrical and thermal properties. The nanojoining of axially positioned Ag NWs was performed by molecular dynamics simulation. Through the detailed atomic evolution during the nanojoining, the results indicate that the temperature and the distance between Ag NWs in axial direction have a great impact on nanojoining effect. When the nanojoining temperature is relatively high, the atoms are disordered and the atomic queues become to distort with strong thermodynamic properties and weak effect of metal bonds. At the relatively low temperature, the Ag NWs can be well connected with good junction quality and their own morphology, which is similar to the cold welding without fusion, while the distance between Ag NWs should be controlled for interaction and diffusion of interfacial atoms at nanowires head. When the Ag NWs are placed on Si and SiO2 substrate, because the atomic species and lattice structure of substrate material can differently affect the motions of Ag atoms through the interactive force between the atoms, the nanojoining quality of Ag NWs on Si substrate is better than that on the SiO2 substrate. So, for getting effective and reliable nanojoining without nanosolders and other materials, the temperature, distance and substrate surface should be reasonably controlled and selected, providing helpful theoretical guidance for experiment and application of nanojoining.

  16. Double dumbbell shaped AgNi alloy by pulsed electrodeposition

    SciTech Connect

    Dhanapal, K.; Vasumathi, M.; Santhi, Kalavathy; Narayanan, V. Stephen, A.

    2014-01-28

    Silver-Nickel is the well-known thermally immiscible system that makes them quite complex for the formation of alloy. This kind of alloy can be attained from electrodeposition method. In the present work, AgNi alloy was synthesized by pulsed electrodeposition in a single bath two electrode system with the use of anodic alumina membrane. The prepared AgNi alloy and pure Ag were characterized with X-ray Diffraction (XRD) for structural confirmation, Scanning Electron Microscopy (SEM) for morphological, and magnetic properties by Vibrating Sample Magnetometer, respectively. The X-ray Diffraction study shows the formation of cubic structure for pure Ag. SEM analysis reveals the double dumbbell morphology for AgNi alloy and spherically agglomeration for pure silver. Hysteresis behaviour from VSM measurement indicates that the AgNi alloy have good ferro-magnetic properties.

  17. Hydrogen in Ag-doped ZnO: theoretical calculations.

    PubMed

    He, H Y; Hu, J; Pan, B C

    2009-05-28

    Based on density functional theory calculations, we systematically investigate the behaviors of a H atom in Ag-doped ZnO involving the preference sites, diffusion behaviors, the electronic structures, and vibrational properties. We find that a H atom can migrate to the doped Ag to form a Ag-H complex by overcoming energy barriers of 0.3-1.0 eV. The lowest-energy site for H location is the bond center of a Ag-O in the basal plane. Moreover, H can migrate between this site and its equivalent sites with energy cost of less than 0.5 eV. In contrast, dissociation of such a Ag-H complex needs energy of about 1.1-1.3 eV. This implies that the Ag-H complexes can commonly exist in the Ag-doped ZnO, which have a negative effect on the desirable p-type carrier concentrations of Ag-doped ZnO. In addition, based on the frozen phonon calculation, the vibrational properties of ZnO with a Ag-H complex are predicted. Some new vibrational modes associated with the Ag-H complex present in the vibrational spectrum of the system.

  18. Light scattering by adsorbates at Ag particles: Quantum-mechanical approach for energy transfer induced interfacial optical processes involving surface plasmons, multipoles, and electron-hole pairs

    NASA Astrophysics Data System (ADS)

    Pettinger, B.

    1986-12-01

    A quantum-mechanical approach for surface-enhanced optical processes is given, which may solve an old controversy regarding the surface enhancement mechanisms: The present formalism contains three terms: The first is equivalent to the classically derived electromagnetic enhancement; the second represents a loss term due to a competitive dipole-multipole and dipole-electron-hole pair coupling; and the third reveals an additional energy transfer induced gain for excitable molecules. Thus, the total pure surface enhancement can be much greater for ``colored'' species than for transparent ones.

  19. 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)

  20. 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.

  1. High Resolution PDF Measurements on Ag Nanoparticles

    SciTech Connect

    Rocha, Tulio C. R.; Martin, Chris; Kycia, Stefan; Zanchet, Daniela

    2009-01-29

    The quantitative analysis of structural defects in Ag nanoparticles was addressed in this work. We performed atomic scale structural characterization by a combination of x-ray diffraction (XRD) using the Pair Distribution Function analysis (PDF) and High Resolution Transmission Electron Microscopy (HRTEM). The XRD measurements were performed using an innovative instrumentation setup to provide high resolution PDF patterns.

  2. Contact Resistance of Ti-Si-C-Ag and Ti-Si-C-Ag-Pd Nanocomposite Coatings

    NASA Astrophysics Data System (ADS)

    Sarius, N. G.; Lauridsen, J.; Lewin, E.; Jansson, U.; Högberg, H.; Öberg, Å.; Sarova, G.; Staperfeld, G.; Leisner, P.; Eklund, P.; Hultman, L.

    2012-03-01

    Ti-Si-C-Ag-Pd and Ti-Si-C-Ag nanocomposite coatings were deposited by direct-current magnetron sputtering on Cu substrates with an electroplated Ni layer. Analytical electron microscopy, x-ray diffraction, and x-ray photoelectron spectroscopy show that the nanocomposites consist of TiC, Ag:Pd, and amorphous SiC. The contact resistance of these coatings against a spherical Au-Co surface was measured for applied contact forces up to 5 N. Ti-Si-C-Ag-Pd coatings with Ag:Pd top coating had ~10 times lower contact resistance at contact forces below 1 N (~10 mΩ at ~0.1 N), and 2 to 3 times lower for contact forces around 5 N (<1 mΩ at 5 N), compared with the Ti-Si-C-Ag coating.

  3. Microstructural characterization of Ag-sheathed Tl-Ba-Ca-Cu-O and Bi-Sr-Ca-Cu-O superconducting tapes by analytical electron microscopy

    SciTech Connect

    Hu, J.G.; Miller, D.J.; Goretta, K.C.; Poeppel, R.B.

    1992-09-01

    The microstructures of Tl(1223) and Pb-doped Bi(2223) silver tapes produced by the powder-in-tube (PM) method have been examined by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive spectrometry (EDS). The Tl tapes annealed below the melting point exhibited fine grains and a high density of pores while tapes subjected to partial melting prior to solid state annealing were fully dense with large grains. However, these tapes also showed an increase in the size and density of impurity particles, particularly CaO and a Ba-Cu rich phase. Silver powders added to the precursors tended to promote the growth of Tl(1223) at lower temperatures but also interfered with the development of texture by providing nucleation sites of random orientations. In contrast, the Bi(2223) tape exhibited a high degree of texture and alignment. The incorporation of silver within the superconducting phase was found to be negligible for both the Tl(1223) and Bi(2223) tapes.

  4. 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.

  5. Recyclable and visible light sensitive Ag-AgBr/TiO2: Surface adsorption and photodegradation of MO

    NASA Astrophysics Data System (ADS)

    Liu, Xinxin; Zhang, Dong; Guo, Biao; Qu, Yue; Tian, Ge; Yue, Huijuan; Feng, Shouhua

    2015-10-01

    A range of highly efficient nanoheterojunction structured Ag-AgBr/TiO2 photocatalysts have been synthesized by CTAB-assisted method and characterized by X-ray diffraction (XRD), focused ion beam scanning electron microscopy (FIB-SEM), energy-dispersive spectroscopy (EDS), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS) and photoluminescence (PL). The results demonstrated that Ag-AgBr nanoparticles were successfully deposited on the surface of anatase TiO2 hierarchical spheres. The remarkable adsorptive removal of methyl orange (MO) by the uncalcined samples was investigated before evaluating its photocatalytic ability. All the calcined three-component catalysts possessed excellent photocatalytic activities for degrading MO under visible light, in which, 162.4% Ag-AgBr/TiO2 exhibited highest efficiency. The greatly enhanced activity can be attributed to the well combination of surface plasmons photocatalyst Ag-AgBr and TiO2, which can simultaneously inhibit the photo-generated electrons and holes recombination. The nanoheterojunctions architecture catalyst also showed high stability even after five consecutive cycles. Meanwhile, the possible mechanism and interpretation of the photocatalytic process were also proposed.

  6. Preparation, characterization and photocatalytic activity of visible-light-driven plasmonic Ag/AgBr/ZnFe{sub 2}O{sub 4} nanocomposites

    SciTech Connect

    Li, Xiaojuan Tang, Duanlian; Tang, Fan; Zhu, Yunyan; He, Changfa; Liu, Minghua Lin, Chunxiang; Liu, Yifan

    2014-08-15

    Highlights: • A plasmonic Ag/AgBr/ZnFe{sub 2}O{sub 4} photocatalyst has been successfully synthesized. • Ag/AgBr/ZnFe{sub 2}O{sub 4} nanocomposites exhibit high visible light photocatalytic activity. • Ag/AgBr/ZnFe{sub 2}O{sub 4} photocatalyst is stable and magnetically separable. - Abstract: A visible-light-driven plasmonic Ag/AgBr/ZnFe{sub 2}O{sub 4} nanocomposite has been successfully synthesized via a deposition–precipitation and photoreduction through a novel one-pot process. X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy and UV–vis diffuse reflectance spectroscopy were employed to investigate the crystal structure, chemical composition, morphology, and optical properties of the as-prepared nanocomposites. The photocatalytic activities of the nanocomposites were evaluated by photodegradation of Rhodamine B (RhB) and phenol under visible light. The results demonstrated that the obtained Ag/AgBr/ZnFe{sub 2}O{sub 4} nanocomposites exhibited higher photocatalytic activity as compared to pure ZnFe{sub 2}O{sub 4}. In addition, the sample photoreduced for 20 min and calcined at 500 °C achieved the highest photocatalytic activity. Furthermore, the Ag/AgBr/ZnFe{sub 2}O{sub 4} nanocomposite has high stability under visible light irradiation and could be conveniently separated by using an external magnetic field.

  7. A special conjugated model around sp3 carbon atoms: density functional theory study on the homoaromatic electron delocalization and applications of benzo-fused tetra(triptycene)porphyrins.

    PubMed

    Qi, Dongdong; Zhang, Lijuan; Zhao, Luyang; Cai, Xue; Jiang, Jianzhuang

    2012-06-01

    The three-unit homoaromatic electron-delocalizing nature of the benzo-fused tetra(triptycene)porphyrins (TTPs) with a three-dimensional conjugated model is clarified using density functional theory studies. Due to the electron delocalization, the unidirectional photon-induced current of this kind of TTP molecular skeleton with a highest efficiency of about 90% in the range between 350 and 500 nm gives them great potential as efficient solar antenna collectors. In addition, their active triptycene cups fused at the central porphyrin core render possible potential application in host-guest chemistry.

  8. Ag/Ag2SO3 plasmonic catalysts with high activity and stability for CO2 reduction with water vapor under visible light.

    PubMed

    Wang, Da; Yu, Yan; Zhang, Zhipeng; Fang, Huiying; Chen, Jianmeng; He, Zhiqiao; Song, Shuang

    2016-09-01

    The conversion of CO2 into useful raw materials for fuels and chemicals by solar energy is described using a plasmonic photocatalyst comprised of Ag supported on Ag2SO3 (Ag/Ag2SO3) fabricated by a facile solid-state ion-exchange method and subsequent reduction with hydrazine hydrate. The optimum molar ratio of Ag(0)/Ag(+) was 5 %. Visible light irradiation (>400 nm) of the Ag/Ag2SO3 powder in the presence of CO2 and water vapor led to the formation of CH4 and CO with a quantum yield of 0.126 %, and an energy returned on energy invested of 0.156 %. The Ag/Ag2SO3 retained high catalytic activity after ten successive experimental cycles. The catalysts were characterized using X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy with energy-dispersive X-ray analysis, UV/Vis absorption spectroscopy, and Brunauer-Emmett-Teller analyses, as well as photocurrent action spectroscopy. It is proposed that the photocatalytic activity of the catalysts is initiated by energy conversion from incident photons to localized surface plasmon resonance oscillations of silver nanoparticles. This plasmonic energy is transferred to the Ag2SO3 by direct electron transfer and/or resonant energy transfer, causing the separation of photogenerated electron/hole pairs. PMID:27282369

  9. Effect of trace metals and electron shuttle on simultaneous reduction of reactive black-5 azo dye and hexavalent chromium in liquid medium by Pseudomonas sp.

    PubMed

    Mahmood, Shahid; Khalid, Azeem; Arshad, Muhammad; Ahmad, Riaz

    2015-11-01

    This study demonstrates the role of electron shuttles and trace metals in the biotransformation of azo dye reactive black-5 and hexavalent chromium (CrVI) that are released simultaneously in tannery effluent. Previously isolated bacterial strain Pseudomonas putida KI was used for the simultaneous reduction of the dye (100 mg L(-1)) and CrVI (2 mg L(-1)) in a mineral salts medium (MSM). Among various trace metals, only Cu(II) had a stimulating effect on the bacterial-mediated reduction process. Application of electron shuttles such as hydroquinone and uric acid at a low concentration (1mM) had a positive effect on the reduction process and caused simultaneous reduction of 100% dye and 97% CrVI in 12-18 h. Mannitol, EDTA and sodium benzoate at all concentrations (ranging from 1 to 9 mM) showed an inhibitory effect on the reduction of reactive black-5 and CrVI. An inverse linear relationship between the velocity of reaction (V) and the concentration [S] of electron shuttles was observed. The results imply that both types and concentration of an electron shuttle and trace metals can affect the simultaneous reduction of reactive black-5 and CrVI.

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

    NASA Astrophysics Data System (ADS)

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

    2016-03-01

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

  11. In situ ion exchange synthesis of strongly coupled Ag@AgCl/g-C₃N₄ porous nanosheets as plasmonic photocatalyst for highly efficient visible-light photocatalysis.

    PubMed

    Zhang, Shouwei; Li, Jiaxing; Wang, Xiangke; Huang, Yongshun; Zeng, Meiyi; Xu, Jinzhang

    2014-12-24

    A novel efficient Ag@AgCl/g-C3N4 plasmonic photocatalyst was synthesized by a rational in situ ion exchange approach between exfoliated g-C3N4 nanosheets with porous 2D morphology and AgNO3. The as-prepared Ag@AgCl-9/g-C3N4 plasmonic photocatalyst exhibited excellent photocatalytic performance under visible light irradiation for rhodamine B degradation with a rate constant of 0.1954 min(-1), which is ∼41.6 and ∼16.8 times higher than those of the g-C3N4 (∼0.0047 min(-1)) and Ag/AgCl (∼0.0116 min(-1)), respectively. The degradation of methylene blue, methyl orange, and colorless phenol further confirmed the broad spectrum photocatalytic degradation abilities of Ag@AgCl-9/g-C3N4. These results suggested that an integration of the synergetic effect of suitable size plasmonic Ag@AgCl and strong coupling effect between the Ag@AgCl nanoparticles and the exfoliated porous g-C3N4 nanosheets was superior for visible-light-responsive and fast separation of photogenerated electron-hole pairs, thus significantly improving the photocatalytic efficiency. This work may provide a novel concept for the rational design of stable and high performance g-C3N4-based plasmonic photocatalysts for unique photochemical reaction.

  12. Sarcocystis acanthocolubri sp. n. infecting three lizard species of the genus Acanthodactylus and the problem of host specificity. Light and electron microscopic study.

    PubMed

    Morsy, Kareem; Bashtar, Abdel-Rahman; Abdel-Ghaffar, Fathy; Mehlhorn, Heinz; Al Quraishy, Saleh; Al-Ghamdi, Ali; Koura, Eglal; Maher, Sherein

    2012-01-01

    In the present investigation, macroscopic sarcocysts of Sarcocystis acanthocolubri were observed in muscles of 42 (4.3%) out of 975 Acanthodactylus sp. lizards collected from different geographical areas in Egypt. The infection rate was 6.4% in Acanthodactylus boskianus, 2.1% in Acanthodactylus sculentus, and 5% in Acanthodactylus paradalis. The highest infection rate was recorded in the lizards captured from Baltem (10% in A. boskianus and 8% in A. paradalis). The infection rate was usually higher in females (7.4%) than in males (3.8%). Moreover, the highest infection rate was recorded in summer (7.53%), autumn (3.57%), and spring (3.11%), and the lowest was recorded in winter (0.91%). Also, old animals had higher infection rates (10.8%) than young ones (0-2.7%). Macrocysts measured 0.95 × 10.12 mm. Both macroscopic and microscopic sarcocysts were enclosed only by a primary cyst wall, which had many finger-like, stalkless, and non-branched protrusions giving it a striated appearance. The primary cyst wall measured 3.9 μm. A dark granulated ground substance was found directly underneath the protrusions and is extended interiorly dividing the cyst cavity into many compartments containing the parasites (metrocytes and merozoites). Metrocytes were found directly under the ground substance and usually multiply asexually by endodyogeny producing two merozoites from each metrocyte. Both metrocytes and merozoites had the apical complex structures characteristic to the genus Sarcocystis. Transmission experiments with three snake species indicated that the snake Spalerosophis diadema is the proper final host belonging to the family Colubridae. The prepatent period was 16 days, while the patent period was 35 days. The results obtained from the present investigation revealed that this is a new species which was named Sarcocystis acanthocolubri. PMID:21710348

  13. Photoemission from Shockley surface state on Ag(111)

    NASA Astrophysics Data System (ADS)

    Karkare, Siddharth; Wan, Weishi; Feng, Jun; Padmore, Howard

    We present measurements of quantum yield and transverse momentum distributions of electrons emitted from the Shockley surface state on Ag(111) surface using near threshold photons. Our measurements shed light on the validity of the conservation of transverse momentum during photoemission when the kinetic energy of electrons is less than 0.1 eV. We also develop a one-step photoemission model that quantitatively explains photoemission from single crystal metal surfaces. This model accurately calculates the dependence of the electron yield on the angle of incidence and the polarization of incident light (vectorial photoelectric effect). We show excellent agreement between the measured and calculated photoemission properties of the Ag(111) surface. Our measurements show that Ag(111) surface can act as an excellent electron source for several applications like Free Electron Lasers and Ultra-fast Electron Diffraction.

  14. Plasmon-enhanced photocatalytic properties of nano Ag@AgBr on single-crystalline octahedral Cu2O (1 1 1) microcrystals composite photocatalyst

    NASA Astrophysics Data System (ADS)

    Liu, Li; Lin, Shuanglong; Hu, Jinshan; Liang, Yinghua; Cui, Wenquan

    2015-03-01

    A new composite photocatalyst Ag@AgBr/Cu2O was prepared by loading Ag@AgBr on (1 1 1) facts of octahedral Cu2O substrate via a facile precipitation in situ photoreduction method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), ultraviolet-visible diffuse reflectance spectroscopy (UV-vis), nitrogen sorption and the photoelectrochemical measurements. The results show that Ag@AgBr nanoparticles are well-dispersed on Cu2O nanoparticles with narrow size distributions and controllable sizes from 10 to 30 nm. TEM results of the as-synthesized Ag@AgBr/Cu2O nanocomposite revealed that Ag@AgBr nanoparticles were attached to the surface of octahedral Cu2O. Photocatalytic degradation of methylene blue (MB) was carried out to evaluate the photocatalytic activity of Ag@AgBr/Cu2O under visible-light irradiation. The Ag@AgBr/Cu2O composite showed stronger visible light absorption capacity and higher photocatalytic activity than pure Cu2O. The Ag@AgBr (15 wt.%)/Cu2O sample presented the best photocatalytic activity, degrading 93.28% MB after irradiation for 90 min, due to their high surface area (18.499 m2 g-1), the Crystal effect of Cu2O and surface plasmon resonance of Ag NPs. Meanwhile, phenol was degraded to further prove the degradation ability of Ag@AgBr/Cu2O. In addition, the quenching effect was examined in the photocatalytic reaction process of MB. Active h+, Br0 and the resulting rad O2- played the major roles for the dye degradation, while rad OH was verified to be insignificant. Based on the experimental results, a photocatalytic mechanism for organics degradation over Ag@AgBr/Cu2O photocatalysts was proposed. The electronic interactions were systematically studied and confirmed by the photoelectrochemical measurements.

  15. Enhancing UV-emissions through optical and electronic dual-function tuning of Ag nanoparticles hybridized with n-ZnO nanorods/p-GaN heterojunction light-emitting diodes.

    PubMed

    Yao, Yung-Chi; Yang, Zu-Po; Hwang, Jung-Min; Chuang, Yi-Lun; Lin, Chia-Ching; Haung, Jing-Yu; Chou, Chun-Yang; Sheu, Jinn-Kong; Tsai, Meng-Tsan; Lee, Ya-Ju

    2016-02-28

    ZnO nanorods (NRs) and Ag nanoparticles (NPs) are known to enhance the luminescence of light-emitting diodes (LEDs) through the high directionality of waveguide mode transmission and efficient energy transfer of localized surface plasmon (LSP) resonances, respectively. In this work, we have demonstrated Ag NP-incorporated n-ZnO NRs/p-GaN heterojunctions by facilely hydrothermally growing ZnO NRs on Ag NP-covered GaN, in which the Ag NPs were introduced and randomly distributed on the p-GaN surface to excite the LSP resonances. Compared with the reference LED, the light-output power of the near-band-edge (NBE) emission (ZnO, λ = 380 nm) of our hybridized structure is increased almost 1.5-2 times and can be further modified in a controlled manner by varying the surface morphology of the surrounding medium of the Ag NPs. The improved light-output power is mainly attributed to the LSP resonance between the NBE emission of ZnO NRs and LSPs in Ag NPs. We also observed different behaviors in the electroluminescence (EL) spectra as the injection current increases for the treatment and reference LEDs. This observation might be attributed to the modification of the energy band diagram for introducing Ag NPs at the interface between n-ZnO NRs and p-GaN. Our results pave the way for developing advanced nanostructured LED devices with high luminescence efficiency in the UV emission regime.

  16. 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.

  17. Stability of Ag nanoparticles dispersed in amphiphilic organic matrix

    NASA Astrophysics Data System (ADS)

    Suvorova, Elena I.; Klechkovskaya, Vera V.; Kopeikin, Victor V.; Buffat, Philippe A.

    2005-02-01

    Nano- and thin-film technologies based on novel systems associating metals particles to polymer matrix open a broad range of different applications. Such composites were found to be more efficient and safe, for instance, in biomedical needs. The Ag/poly(N-vinyl-2-pyrrolidone) (Ag/PVP) composite investigated in the present work is a new bactericide mean applied in complicated cases of infected burns and purulent wounds. High-resolution transmission electron microscopy (HRTEM) and X-ray energy-dispersive (EDS) microanalysis were used to bring chemical and structural information in a study of the properties and stability of thin-film nanocomposite whih consisted of Ag nanoparticles dispersed in water-soluble organic matrix poly(N-vinyl-2-pyrrolidone). The nanostructural investigation of Ag/PVP composite by HRTEM and EDS exposed to SO 2 and H 2S from the atmosphere and some traces of S-containing substances explains the limited stability of this system by a structural modification associated with a phase change and formation of Ag 2S and Ag 2SO 3. However, formation of the hardly water-soluble Ag 2S and Ag 2SO 3 salts may play an important role in the suppression of bacterial growth. On the one hand, silver could block S-H groups in vital proteins and conduced to their destruction, in that way revealing the antibacterial power. On the other hand, antiseptic properties of Ag consist in binding the products of the protein decay.

  18. Synthesis, characterization and optical properties of low nuclearity liganded silver clusters: Ag31(SG)19 and Ag15(SG)11

    NASA Astrophysics Data System (ADS)

    Bertorelle, Franck; Hamouda, Ramzi; Rayane, Driss; Broyer, Michel; Antoine, Rodolphe; Dugourd, Philippe; Gell, Lars; Kulesza, Alexander; MitrićPresent Address: Institut Für Physikalische Und Theoretische Chemie, Julius-Maximilians Universität Würzburg, Emil-Fischer-Straße 42, 97074 Würzburg, Germany, Roland; Bonačić-Koutecký, Vlasta

    2013-05-01

    We report a simple synthesis of silver:glutathione (Ag:SG) clusters using a cyclic reduction under oxidative conditions. Two syntheses are described which lead to solutions containing well-defined Ag31(SG)19 and Ag15(SG)11 clusters that have been characterized by mass spectrometry. The optical properties of silver:glutathione (Ag:SG) cluster solutions have been investigated experimentally. In particular, the solution containing Ag15(SG)11 clusters shows a bright and photostable emission. For Ag31(SG)19 and Ag15(SG)11 clusters, the comparison of experimental findings with DFT and TDDFT calculations allowed us to reveal the structural and electronic properties of such low nuclearity liganded silver clusters.We report a simple synthesis of silver:glutathione (Ag:SG) clusters using a cyclic reduction under oxidative conditions. Two syntheses are described which lead to solutions containing well-defined Ag31(SG)19 and Ag15(SG)11 clusters that have been characterized by mass spectrometry. The optical properties of silver:glutathione (Ag:SG) cluster solutions have been investigated experimentally. In particular, the solution containing Ag15(SG)11 clusters shows a bright and photostable emission. For Ag31(SG)19 and Ag15(SG)11 clusters, the comparison of experimental findings with DFT and TDDFT calculations allowed us to reveal the structural and electronic properties of such low nuclearity liganded silver clusters. Electronic supplementary information (ESI) available: Optimal settings for the MS instrument; schematic diagrams for syntheses A and B; ESI mass spectra of silver clusters from ``synthesis A'' in different solvent mixtures, at different pH values and with different synthesis protocols; excitation and emission spectra of clusters from ``synthesis B'' in water and of the separated band after PAGE separation; lifetime measurements of silver clusters from a solution of ``synthesis B'' in water; the structure and absorption spectrum of the two lowest-energy isomers

  19. Environmentally friendly microwave ionic liquids synthesis of hybrids from cellulose and AgX (X=Cl, Br).

    PubMed

    Dong, Yan-Yan; He, Jing; Sun, Shao-Long; Ma, Ming-Guo; Fu, Lian-Hua; Sun, Run-Cang

    2013-10-15

    The purpose of this article was to explore an environmentally friendly strategy to synthesis of biomass-based hybrids. Herein, microwave-assisted ionic liquids method was applied to fabricate the hybrids from cellulose and AgX (X=Cl, Br) using cellulose and AgNO3. The ionic liquids act simultaneously as a solvent, a microwave absorber, and a reactant. Ionic liquids provided Cl(-) or Br(-) to the synthesis of AgCl or AgBr crystals; thus no additional reactant is needed. The products are characterized by X-ray powder diffraction (XRD), Fourier transform infrared spectrometry (FTIR), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and differential thermal analysis (DTA). The cellulose-Ag/AgCl hybrid and cellulose-Ag/AgBr hybrid were also obtained by using cellulose-AgCl and cellulose-AgBr hybrids as precursors. This environmentally friendly microwave-assisted ionic liquids method is beneficial to the hybrids with high dispersion.

  20. Adsorption of sulfur on Ag(100)

    SciTech Connect

    Russell, Selena M.; Shen, Mingmin; Liu, Da-Jiang; Thiel, Patricia A.

    2010-12-17

    We have used scanning tunneling microscopy and density Functional theory to investigate the structures formed by sulfur on Ag(100). As indicated by previous low-energy electron diffraction studies, the main phases have unit cells of p(2 x 2) and ({radical}17 x {radical}17)R14{sup o}. We show that the latter is a reconstruction. The favored structural model is one in which 5 Ag atoms are missing from the (100) surface plane per unit cell. The ejected Ag atoms combine with sulfur to form islands of the reconstructed phase on the terraces. The ({radical}17 x {radical}17)R14{sup o} phase coexists with the p(2 x 2), at sulfur coverages slightly above 0.25 monolayers. In addition, chain-like structures are observed in STM, both at room temperature (where they are dynamic) and below (where they are not). These results are compared with relevant literature for copper surfaces.

  1. 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.

  2. Temperature dependence of exciton-surface plasmon polariton coupling in Ag, Au, and Al films on In{sub x}Ga{sub 1−x}N/GaN quantum wells studied with time-resolved cathodoluminescence

    SciTech Connect

    Estrin, Y.; Rich, D. H.; Keller, S.; DenBaars, S. P.

    2015-01-28

    The optical properties and coupling of excitons to surface plasmon polaritons (SPPs) in Ag, Au, and Al-coated In{sub x}Ga{sub 1−x}N/GaN multiple and single quantum wells (SQWs) were probed with time-resolved cathodoluminescence. Excitons were generated in the metal coated SQWs by injecting a pulsed high-energy electron beam through the thin metal films. The Purcell enhancement factor (F{sub p}) was obtained by direct measurement of changes in the temperature-dependent radiative lifetime caused by the SQW exciton-SPP coupling. Three chosen plasmonic metals of Al, Ag, and Au facilitate an interesting comparison of the exciton-SPP coupling for energy ranges in which the SP energy is greater than, approximately equal to, and less than the excitonic transition energy for the InGaN/GaN QW emitter. A modeling of the temperature dependence of the Purcell enhancement factor, F{sub p}, included the effects of ohmic losses of the metals and changes in the dielectric properties due to the temperature dependence of (i) the intraband behavior in the Drude model and (ii) the interband critical point transition energies which involve the d-bands of Au and Ag. We show that an inclusion of both intraband and interband effects is essential when calculating the ω vs k SPP dispersion relation, plasmon density of states (DOS), and the dependence of F{sub p} on frequency and temperature. Moreover, the “back bending” in the SPP dispersion relation when including ohmic losses can cause a finite DOS above ω{sub sp} and lead to a measurable F{sub p} in a limited energy range above ω{sub sp}, which can potentially be exploited in plasmonic devices utilizing Ag and Au.

  3. Impedance studies of the cell Ag/AgI/Ag beta alumina/AgI/Ag. Technical report No. 15, August 1987-August 1988

    SciTech Connect

    Breiter, M.W.; Drstak, H.; Maly-Schreiber, M.

    1988-07-01

    The construction of the cell Ag/AgI/Ag beta alumina/AgI/Ag is described. The impedance of this cell was measured between .001 and 10000 Hz at temperatures between 20 and 550 C. At temperatures below 100 C the cell impedance is determined to a large extent by the bulk resistance of the AgI layer and to a smaller extent by the impedance of the interface Ag/Agi. At temperatures between 160 and 350 C the impedance is controlled by the bulk resistance of the Ag beta alumina and an impedance due to contact problems between Ag and AgI. The bulk resistance of the beta' alumina becomes predominant between 350 and 550 C. A hindrance due to the transfer of silver ions from AgI to Ag beta' alumina was not observable in the whole temperature range.

  4. Spherical and sheetlike Ag/AgCl nanostructures: interesting photocatalysts with unusual facet-dependent yet substrate-sensitive reactivity.

    PubMed

    Shen, Yunfan; Chen, Penglei; Xiao, Dan; Chen, Chuncheng; Zhu, Mingshan; Li, Tiesheng; Ma, Wangong; Liu, Minghua

    2015-01-13

    We herein report that spherical and sheetlike Ag/AgCl nanostructures could be controllably synthesized by means of chemical reactions between AgNO3 and cetyltrimethylammonium chloride (CTAC) surfactant. In this synthesis system, AgNO3 works as the silver source, while CTAC serves not only as the chlorine source but also as the directing reagent for a controllable nanofabrication. We show that compared to the spherical Ag/AgCl nanostructures, the sheetlike counterparts, wherein the AgCl nanospecies are predominantly enriched with {111} facets, could exhibit superior catalytic performances toward the photodegradation of methyl orange. Interestingly, we further demonstrate that when 4-chlorophenol or phenol is used as the substrate, the sheetlike Ag/AgCl nanostructures exhibit inferior catalytic reactivity, whereas the spherical counterparts display superior catalytic performances comparatively. Our results disclose new insights on the facet-dependent catalytic performances with regard to a facet-selective but substrate-sensitive photoinduced electron-hole separation.

  5. Size distributions of chemically synthesized Ag nanocrystals

    NASA Astrophysics Data System (ADS)

    Thøgersen, Annett; Bonsak, Jack; Fosli, Carl Huseby; Muntingh, Georg

    2011-08-01

    Silver nanocrystals made by a chemical reduction of silver salts (AgNO3) by sodium borohydride (NaBH4) were studied using transmission electron microscopy and light scattering simulations. For various AgNO3/NaBH4 molar ratios, the size distributions of the nanocrystals were found to be approximately log-normal. In addition, a linear relation was found between the mean nanocrystal size and the molar ratio. In order to relate the size distribution of Ag nanocrystals of the various molar ratios to the scattering properties of Ag nanocrystals in solar cell devices, light scattering simulations of Ag nanocrystals in Si, SiO2, SiN, and Al2O3 matrices were carried out using MiePlot. These light scattering spectra for the individual nanocrystal sizes were combined into light scattering spectra for the fitted size distributions. The evolution of these scattering spectra with respect to an increasing mean nanocrystal size was then studied. From these findings, it is possible to find the molar ratio for which the corresponding nanocrystal size distribution has maximum scattering at a particular wavelength in the desired matrix.

  6. Component conversion from pure Au nanorods to multiblock Ag-Au-Ag nanorods assisted by Pt nanoframe templates

    NASA Astrophysics Data System (ADS)

    Lee, Sangji; Jang, Hee-Jeong; Jang, Ho Young; Kim, Seong Kyu; Park, Sungho

    2016-06-01

    We developed a new method for synthesizing multiblock Ag-Au-Ag nanorods using Pt nanoframes that had been deposited on the edges of Au nanorod seeds. As a function of Au etching time, the length of the Au nanorod decreased symmetrically starting from the two ends, leading to the formation of empty inner space at the ends. Subsequent reduction of Ag ions could be selectively performed in the inner space confined by Pt nanoframes and the resulting Ag-Au-Ag nanorods exhibited characteristic LSPR modes originating from each block component (in a transverse direction) and SPR coupling (in a longitudinal direction). The high quality of the resulting multiblock nanorods enabled observation of the longitudinal quadrupole mode that was induced by Ag-Au SPR coupling in a long axis. The mode exhibited high sensitivity in accordance with the change in the surrounding media, demonstrating great potential for sensor applications.We developed a new method for synthesizing multiblock Ag-Au-Ag nanorods using Pt nanoframes that had been deposited on the edges of Au nanorod seeds. As a function of Au etching time, the length of the Au nanorod decreased symmetrically starting from the two ends, leading to the formation of empty inner space at the ends. Subsequent reduction of Ag ions could be selectively performed in the inner space confined by Pt nanoframes and the resulting Ag-Au-Ag nanorods exhibited characteristic LSPR modes originating from each block component (in a transverse direction) and SPR coupling (in a longitudinal direction). The high quality of the resulting multiblock nanorods enabled observation of the longitudinal quadrupole mode that was induced by Ag-Au SPR coupling in a long axis. The mode exhibited high sensitivity in accordance with the change in the surrounding media, demonstrating great potential for sensor applications. Electronic supplementary information (ESI) available. See DOI: 10.1039/c6nr03484e

  7. Low SP1 Expression Differentially Affects Intestinal-Type Compared with Diffuse-Type Gastric Adenocarcinoma

    PubMed Central

    Oh, Ensel; Erkin, Özgür Cem; Jung, Hun Soon; Cho, Mi-Hyun; Kwon, Mi Jeong; Chae, Seoung Wan; Kim, Seok-Hyung; Wang, Li-Hui; Park, Min-Jeong; Lee, Su-Yeon; Yang, Ho Bin; Jia, Lina; Choi, Yoon-La; Shin, Young Kee

    2013-01-01

    Specificity protein 1 (SP1) is an essential transcription factor that regulates multiple cancer-related genes. Because aberrant expression of SP1 is related to cancer development and progression, we focused on SP1 expression in gastric carcinoma and its correlation with disease outcomes. Although patient survival decreased as SP1 expression increased (P<0.05) in diffuse-type gastric cancer, the lack of SP1 expression in intestinal-type gastric cancer was significantly correlated with poor survival (P<0.05). The knockdown of SP1 in a high SP1-expressing intestinal-type gastric cell line, MKN28, increased migration and invasion but decreased proliferation. Microarray data in SP1 siRNA-transfected MKN28 revealed that the genes inhibiting migration were downregulated, whereas the genes negatively facilitating proliferation were increased. However, both migration and invasion were decreased by forced SP1 expression in a low SP1-expressing intestinal-type gastric cell line, AGS. Unlike the intestinal-type, in a high SP1-expressing diffuse-type gastric cell line, SNU484, migration and invasion were decreased by SP1 siRNA. In contrast to previous studies that did not identify differences between the 2 histological types, our results reveal that low expression of SP1 is involved in cancer progression and metastasis and differentially affects intestinal-type compared with diffuse-type gastric adenocarcinoma. PMID:23437057

  8. In situ assembly of well-dispersed Ag nanoparticles (AgNPs) on electrospun carbon nanofibers (CNFs) for catalytic reduction of 4-nitrophenol.

    PubMed

    Zhang, Peng; Shao, Changlu; Zhang, Zhenyi; Zhang, Mingyi; Mu, Jingbo; Guo, Zengcai; Liu, Yichun

    2011-08-01

    Carbon nanofibers/silver nanoparticles (CNFs/AgNPs) composite nanofibers were fabricated by two steps consisting of the preparation of the CNFs by electrospinning and the hydrothermal growth of the AgNPs on the CNFs. The as-prepared nanofibers were characterized by scanning electron microscopy, energy dispersive spectroscopy, transmission electron microscopy, X-ray diffraction, resonant Raman spectra, thermal gravimetric and differential thermal analysis, and X-ray photoelectron spectroscopy, respectively. The results indicated that not only were AgNPs (25-50 nm) successfully grown on the CNFs but also the AgNPs were distributed without aggregation on the CNFs. Further more, by adjusting the parameters in hydrothermal processing, the content of silver supported on the CNFs could be easily controlled. The catalytic activities of the CNFs/AgNPs composite nanofibers to the reduction of 4-nitrophenol (4-NP) with NaBH(4) were tracked by UV-visible spectroscopy. It was suggested that the CNFs/AgNPs composite nanofibers exhibited high catalytic activity in the reduction of 4-NP, which might be attributed to the high surface areas of AgNPs and synergistic effect on delivery of electrons between CNFs and AgNPs. And, the catalytic efficiency was enhanced with the increasing of the content of silver on the CNFs/AgNPs composite nanofibers. Notably, the CNFs/AgNPs composite nanofibers could be easily recycled due to their one-dimensional nanostructural property.

  9. Transparent Conductive AGZO/Ag/AGZO Multilayers on PET Substrate by Roll-to-Roll Sputtering.

    PubMed

    Kim, Taehoon; Park, Kwangwon; Kim, Jongsu

    2016-02-01

    Indium-free Al and Ga-codoped ZnO (AGZO) multilayer films with nanoscale Ag interlayer were deposited by dual target roll-to-roll RF for AGZO and DC sputtering systems for Ag at room temperature for a large scale. The thicknesses of AGZO/Ag/AGZO multilayer were optimized by changing the roll speed: 0.15/1.1/0.15 m/min for AGZO/Ag/AGZO multilayers, respectively. The optimum thicknesses of AGZO/Ag/AGZO multilayer are 9.21, 8.32 and 8.04 nm, respectively. Optimized AGZO/Ag/AGZO multilayer films showed an excellent transparency (84% at 550 nm) and a low sheet resistance (9.2 omega/sq.) on PET substrates for opto-electronic applications. The effects of nanoscale Ag interlayer on optical and electrical properties of AGZO/Ag/AGZO multilayer films were discussed.

  10. Synthesis of Cu core Ag shell nanoparticles using chemical reduction method

    NASA Astrophysics Data System (ADS)

    Chinh Trinh, Dung; Dung Dang, Thi My; Khanh Huynh, Kim; Fribourg-Blanc, Eric; Chien Dang, Mau

    2015-01-01

    A simple chemical reduction method is used to prepare colloidal bimetallic Cu-Ag core-shell (Cu@Ag) nanoparticles. Polyvinyl pyrrolidone (PVP) was used as capping agent, and ascorbic acid (C6H8O6) and sodium borohydride (NaBH4) were used as reducing agents. The obtained Cu@Ag nanoparticles were characterized by powder x-ray diffraction (XRD), transmission electron microscopy (TEM) and UV-vis spectrophotometry. The influence of [Ag]/[Cu] molar ratios on the formation of Ag coatings on the Cu particles was investigated. From the TEM results we found that the ratio [Ag+]/[Cu2+] = 0.2 is the best for the stability of Cu@Ag nanoparticles with an average size of 22 nm. It is also found out that adding ammonium hydroxide (NH4OH) makes the obtained Cu@Ag nanoparticles more stable over time when pure deionized water is used as solvent.

  11. Transparent Conductive AGZO/Ag/AGZO Multilayers on PET Substrate by Roll-to-Roll Sputtering.

    PubMed

    Kim, Taehoon; Park, Kwangwon; Kim, Jongsu

    2016-02-01

    Indium-free Al and Ga-codoped ZnO (AGZO) multilayer films with nanoscale Ag interlayer were deposited by dual target roll-to-roll RF for AGZO and DC sputtering systems for Ag at room temperature for a large scale. The thicknesses of AGZO/Ag/AGZO multilayer were optimized by changing the roll speed: 0.15/1.1/0.15 m/min for AGZO/Ag/AGZO multilayers, respectively. The optimum thicknesses of AGZO/Ag/AGZO multilayer are 9.21, 8.32 and 8.04 nm, respectively. Optimized AGZO/Ag/AGZO multilayer films showed an excellent transparency (84% at 550 nm) and a low sheet resistance (9.2 omega/sq.) on PET substrates for opto-electronic applications. The effects of nanoscale Ag interlayer on optical and electrical properties of AGZO/Ag/AGZO multilayer films were discussed. PMID:27433648

  12. Microstructure and thermal conduction properties of Al{sub 2}O{sub 3}-Ag composites

    SciTech Connect

    Liu, D.M.; Tuan, W.H.

    1996-02-01

    Microstructure and thermal conduction properties involving thermal diffusivity and conductivity of composite, Al{sub 2}O{sub 3}-Ag, were investigated. The Ag particles observed in the composites were spread sporadically throughout the composite with inclusion size increasing with Ag content, rather than forming a network of thin film foil. Thermal conductivity of the composite increased with Ag content and followed composite theory prediction with a negligible influence of interfacial contact resistance. The temperature dependence of the thermal conductivity became less pronounced with increasing Ag content reflecting the nature of electron contribution in Ag rather than the typical phonon contribution in polycrystalline Al{sub 2}O{sub 3}. The lower composite conductivity at higher Ag contents as compared to theoretical predictions is due primarily to the residual pore phase, associated with the cavity formation for the composite containing 10 vol.% Ag.

  13. Stabilizing subnanometer Ag(0) nanoclusters by thiolate and diphosphine ligands and their crystal structures

    NASA Astrophysics Data System (ADS)

    Yang, Huayan; Wang, Yu; Zheng, Nanfeng

    2013-03-01

    The combined use of thiolate and diphosphine as surface ligands helps to stabilize subnanometer Ag(0) nanoclusters, resulting in the successful crystallization of two Ag(0)-containing nanoclusters (Ag16 and Ag32) for X-ray single crystal analysis. Both clusters have core-shell structures with Ag86+ and Ag2212+ as their cores, which are not simply either fragments of face-centered cubic metals or their five-fold twinned counterparts. The clusters display UV-Vis absorption spectra consisting of molecule-like optical transitions.The combined use of thiolate and diphosphine as surface ligands helps to stabilize subnanometer Ag(0) nanoclusters, resulting in the successful crystallization of two Ag(0)-containing nanoclusters (Ag16 and Ag32) for X-ray single crystal analysis. Both clusters have core-shell structures with Ag86+ and Ag2212+ as their cores, which are not simply either fragments of face-centered cubic metals or their five-fold twinned counterparts. The clusters display UV-Vis absorption spectra consisting of molecule-like optical transitions. Electronic supplementary information (ESI) available: Experimental details, more pictures of the structure and XPS spectra of the clusters. CCDC 916463 and 916464. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c3nr34328f

  14. The Effect of Ag and Ag+N Ion Implantation on Cell Attachment Properties

    SciTech Connect

    Urkac, Emel Sokullu; Oztarhan, Ahmet; Gurhan, Ismet Deliloglu; Iz, Sultan Gulce; Tihminlioglu, Funda; Oks, Efim; Nikolaev, Alexey; Ila, Daryush

    2009-03-10

    Implanted biomedical prosthetic devices are intended to perform safely, reliably and effectively in the human body thus the materials used for orthopedic devices should have good biocompatibility. Ultra High Molecular Weight Poly Ethylene (UHMWPE) has been commonly used for total hip joint replacement because of its very good properties. In this work, UHMWPE samples were Ag and Ag+N ion implanted by using the Metal-Vapor Vacuum Arc (MEVVA) ion implantation technique. Samples were implanted with a fluency of 1017 ion/cm2 and extraction voltage of 30 kV. Rutherford Backscattering Spectrometry (RBS) was used for surface studies. RBS showed the presence of Ag and N on the surface. Cell attachment properties investigated with model cell lines (L929 mouse fibroblasts) to demonstrate that the effect of Ag and Ag+N ion implantation can favorably influence the surface of UHMWPE for biomedical applications. Scanning electron microscopy (SEM) was used to demonstrate the cell attachment on the surface. Study has shown that Ag+N ion implantation represents more effective cell attachment properties on the UHMWPE surfaces.

  15. Ag induced electromagnetic interference shielding of Ag-graphite/PVDF flexible nanocomposites thinfilms

    SciTech Connect

    Kumaran, R.; Alagar, M.; Dinesh Kumar, S.; Subramanian, V.; Dinakaran, K.

    2015-09-14

    We report Ag nanoparticle induced Electromagnetic Interference (EMI) shielding in a flexible composite films of Ag nanoparticles incorporated graphite/poly-vinylidene difluoride (PVDF). PVDF nanocomposite thin-films were synthesized by intercalating Ag in Graphite (GIC) followed by dispersing GIC in PVDF. The X-ray diffraction analysis and the high-resolution transmission electron microscope clearly dictate the microstructure of silver nanoparticles in graphite intercalated composite of PVDF matrix. The conductivity values of nanocomposites are increased upto 2.5 times when compared to neat PVDF having a value of 2.70 S/cm at 1 MHz. The presence of Ag broadly enhanced the dielectric constant and lowers the dielectric loss of PVDF matrix proportional to Ag content. The EMI shielding effectiveness of the composites is 29.1 dB at 12.4 GHz for the sample having 5 wt. % Ag and 10 wt. % graphite in PVDF.

  16. The Effect of Ag and Ag+N Ion Implantation on Cell Attachment Properties

    NASA Astrophysics Data System (ADS)

    Urkac, Emel Sokullu; Oztarhan, Ahmet; Tihminlioglu, Funda; Gurhan, Ismet Deliloglu; Iz, Sultan Gulce; Oks, Efim; Nikolaev, Alexey; Ila, Daryush

    2009-03-01

    Implanted biomedical prosthetic devices are intended to perform safely, reliably and effectively in the human body thus the materials used for orthopedic devices should have good biocompatibility. Ultra High Molecular Weight Poly Ethylene (UHMWPE) has been commonly used for total hip joint replacement because of its very good properties. In this work, UHMWPE samples were Ag and Ag+N ion implanted by using the Metal-Vapor Vacuum Arc (MEVVA) ion implantation technique. Samples were implanted with a fluency of 1017 ion/cm2 and extraction voltage of 30 kV. Rutherford Backscattering Spectrometry (RBS) was used for surface studies. RBS showed the presence of Ag and N on the surface. Cell attachment properties investigated with model cell lines (L929 mouse fibroblasts) to demonstrate that the effect of Ag and Ag+N ion implantation can favorably influence the surface of UHMWPE for biomedical applications. Scanning electron microscopy (SEM) was used to demonstrate the cell attachment on the surface. Study has shown that Ag+N ion implantation represents more effective cell attachment properties on the UHMWPE surfaces.

  17. Surface-enhanced Raman scattering from AgNP-graphene-AgNP sandwiched nanostructures

    NASA Astrophysics Data System (ADS)

    Wu, Jian; Xu, Yijun; Xu, Pengyu; Pan, Zhenghui; Chen, Sheng; Shen, Qishen; Zhan, Li; Zhang, Yuegang; Ni, Weihai

    2015-10-01

    We developed a facile approach toward hybrid AgNP-graphene-AgNP sandwiched structures using self-organized monolayered AgNPs from wet chemical synthesis for the optimized enhancement of the Raman response of monolayer graphene. We demonstrate that the Raman scattering of graphene can be enhanced 530 fold in the hybrid structure. The Raman enhancement is sensitively dependent on the hybrid structure, incident angle, and excitation wavelength. A systematic simulation is performed, which well explains the enhancement mechanism. Our study indicates that the enhancement resulted from the plasmonic coupling between the AgNPs on the opposite sides of graphene. Our approach towards ideal substrates offers great potential to produce a ``hot surface'' for enhancing the Raman response of two-dimensional materials.We developed a facile approach toward hybrid AgNP-graphene-AgNP sandwiched structures using self-organized monolayered AgNPs from wet chemical synthesis for the optimized enhancement of the Raman response of monolayer graphene. We demonstrate that the Raman scattering of graphene can be enhanced 530 fold in the hybrid structure. The Raman enhancement is sensitively dependent on the hybrid structure, incident angle, and excitation wavelength. A systematic simulation is performed, which well explains the enhancement mechanism. Our study indicates that the enhancement resulted from the plasmonic coupling between the AgNPs on the opposite sides of graphene. Our approach towards ideal substrates offers great potential to produce a ``hot surface'' for enhancing the Raman response of two-dimensional materials. Electronic supplementary information (ESI) available: Additional SEM images, electric field enhancement profiles, Raman scattering spectra, and structure-dependent peak ratios. See DOI: 10.1039/c5nr04500b

  18. Formation of AgFeO2, α-FeOOH, and Ag2O from mixed Fe(NO3)3-AgNO3 solutions at high pH

    NASA Astrophysics Data System (ADS)

    Krehula, Stjepko; Musić, Svetozar

    2013-07-01

    Precipitation of ternary oxide silver ferrite (AgFeO2), iron oxyhydroxide goethite (α-FeOOH) and silver(I) oxide (Ag2O) from mixed Fe(NO3)3-AgNO3 solutions in a whole [Ag+]:[Fe3+] concentration ratio range at high pH was investigated using X-ray powder diffraction (XRD), 57Fe Mössbauer, FT-IR and UV-Vis-NIR spectroscopies and field emission scanning electron microscopy (FE-SEM). Strong alkalis organic tetramethylammonium hydroxide (TMAH) or inorganic NaOH were used as precipitating agents. Monodispersed lath-like α-FeOOH particles were formed from a pure Fe(NO3)3 solution. The presence of Ag+ ions influenced the formation of the delafossite-type ternary oxide AgFeO2 beside α-FeOOH. The positions of XRD and Mössbauer lines did not suggest any significant incorporation of Ag+ ions into the α-FeOOH structure. AgFeO2 was formed in the precipitation system with the equimolar initial [Ag+]:[Fe3+] concentration ratio. The size and shape of AgFeO2 particles, as well as their structural polytype (2H or 3R), were dependent on reaction temperature, aging time and alkali used. In systems with an excess of Ag+ ions mixtures of AgFeO2 and Ag2O were formed. Single phase Ag2O precipitated from a pure AgNO3 solution.

  19. Effect of Axial Torsion on sp Carbon Atomic Wires

    NASA Astrophysics Data System (ADS)

    Ravagnan, Luca; Manini, Nicola; Cinquanta, Eugenio; Onida, Giovanni; Sangalli, Davide; Motta, Carlo; Devetta, Michele; Bordoni, Andrea; Piseri, Paolo; Milani, Paolo

    2009-06-01

    Ab initio calculations within density-functional theory combined with experimental Raman spectra on cluster-beam deposited pure-carbon films provide a consistent picture of sp-carbon chains stabilized by sp3 or sp2 terminations, the latter being sensitive to torsional strain. This unexplored effect promises many exciting applications since it allows one to modify the conductive states near the Fermi level and to switch on and off the on-chain π-electron magnetism.

  20. Room temperature synthesis and photocatalytic property of AgO/Ag{sub 2}Mo{sub 2}O{sub 7} heterojunction nanowires

    SciTech Connect

    Hashim, Muhammad; Hu, Chenguo; Wang, Xue; Wan, Buyong; Xu, Jing

    2012-11-15

    Graphical abstract: The AgO nanoparticles are attached on the surface of the Ag{sub 2}Mo{sub 2}O{sub 7} nanowires to form a heterojunction structure. The AgO nanoparticles start embedding into the nanowires with increasing reaction temperature or time. Highlights: ► AgO/Ag{sub 2}Mo{sub 2}O{sub 7} heterojunction NWs were synthesized at room temperature for the first time. ► AgO particles embed into the Ag{sub 2}Mo{sub 2}O{sub 7} NWs with increase in reaction time and temperature. ► The heterojunction NWs display much better photocatalytic activity than the none-heterojunction NWs. ► The catalytic mechanism was proposed. -- Abstract: AgO/Ag{sub 2}Mo{sub 2}O{sub 7} heterojunction nanowires were synthesized at temperatures of 25 °C, 50 °C, 80 °C, and 110 °C, under magnetic stirring in solution reaction. The catalytic activity of AgO/Ag{sub 2}Mo{sub 2}O{sub 7} nanowires was evaluated by the degradation of Rhodmine B dye under the irradiation of the simulated sunlight. The synthesized samples were characterized by X-ray diffractometer, energy dispersive spectrometry, X-ray photoelectron spectrometer, scanning electron microscopy, and transmission electron microscopy. The results show that the AgO nanoparticles are attached on the surface of the Ag{sub 2}Mo{sub 2}O{sub 7} nanowires to form a heterojunction structure. The length of the nanowires is up to 10 μm and the size of the AgO nanoparticles is 10–20 nm. The length of nanowires increases with increasing reaction time and temperature while the AgO particles are gradually embedded into the nanowires. The photocatalytic activity is greatly improved for the AgO/Ag{sub 2}Mo{sub 2}O{sub 7} heterojunction nanowires compared with that of the pure Ag{sub 2}Mo{sub 2}O{sub 7} nanowires, indicating a remarkable role of AgO particles on the Ag{sub 2}Mo{sub 2}O{sub 7} nanowires in the photodegradation.

  1. Guided ion beam and theoretical studies of the reaction of Ag{sup +} with CS{sub 2}: Gas-phase thermochemistry of AgS{sup +} and AgCS{sup +} and insight into spin-forbidden reactions

    SciTech Connect

    Armentrout, P. B.; Kretzschmar, Ilona

    2010-01-14

    The gas-phase reactivity of the atomic transition metal cation, Ag{sup +}, with CS{sub 2} is investigated using guided-ion beam mass spectrometry. Endothermic reactions forming AgS{sup +} and AgCS{sup +} are observed but are quite inefficient. This observation is largely attributed to the stability of the closed shell Ag{sup +}({sup 1}S,4d{sup 10}) ground state, but is also influenced by the fact that the reactions producing ground state AgS{sup +} and AgCS{sup +} products are both spin forbidden. Analysis of the kinetic energy dependence of the cross sections for formation of these two products yields the 0 K bond energies of D{sub 0}(Ag{sup +}-S)=1.40{+-}0.12 eV and D{sub 0}(Ag{sup +}-CS)=1.98{+-}0.14 eV. Quantum chemical calculations are used to investigate the electronic structure of the two product ions as well as the potential energy surfaces for reaction. The primary mechanism involves oxidative addition of a CS bond to the metal cation followed by simple Ag-S or Ag-CS bond cleavage. Crossing points between the singlet and triplet surfaces are located near the transition states for bond activation. Comparison with analogous work on other late second-row transition metal cations indicates that the location of the crossing points bears directly on the efficiency of these spin-forbidden processes.

  2. Herringbone and triangular patterns of dislocations in Ag, Au, and AgAu alloy films on Ru(0001).

    SciTech Connect

    Thayer, Gayle Echo; de la Figuera, Juan; Bartelt, Norman Charles; Carter, C. Barrington; Hwang, R. Q.; Thurmer, Konrad; Ling, W. L.; Hamilton, John C.; McCarty, Kevin F.

    2008-10-01

    We have studied the dislocation structures that occur in films of Ag, Au, and Ag{sub 0.5}Au{sub 0.5} alloy on a Ru(0001) substrate. Monolayer (ML) films form herringbone phases while films two or more layers thick contain triangular patterns of dislocations. We use scanning tunneling microscopy (STM) and low-energy electron diffraction (LEED) to determine how the film composition affects the structure and periodicity of these ordered structures. One layer of Ag forms two different herringbone phases depending on the exact Ag coverage and temperature. Low-energy electron microscopy (LEEM) establishes that a reversible, first-order phase transition occurs between these two phases at a certain temperature. We critically compare our 1 ML Ag structures to conflicting results from an X-ray scattering study [H. Zajonz et al., Phys. Rev. B 67 (2003) 155417]. Unlike Ag, the herringbone phases of Au and AgAu alloy are independent of the exact film coverage. For two layer films in all three systems, none of the dislocations in the triangular networks thread into the second film layer. In all three systems, the in-plane atomic spacing of the second film layer is nearly the same as in the bulk. Film composition does, however, affect the details of the two layer structures. Ag and Au films form interconnected networks of dislocations, which we refer to as 'trigons.' In 2 ML AgAu alloy, the dislocations form a different triangular network that shares features of both trigon and moire structures. Yet another well-ordered structure, with square symmetry, forms at the boundaries of translational trigon domains in 2 ML Ag films but not in Au films.

  3. Extracellular biosynthesis of silver nanoparticle using Streptomyces sp. 09 PBT 005 and its antibacterial and cytotoxic properties

    NASA Astrophysics Data System (ADS)

    Saravana Kumar, P.; Balachandran, C.; Duraipandiyan, V.; Ramasamy, D.; Ignacimuthu, S.; Al-Dhabi, Naif Abdullah

    2015-02-01

    The application of microorganisms for the synthesis of nanoparticles as an eco-friendly and promising approach is welcome due to its non-toxicity and simplicity. The aim of this study was to synthesize silver nanoparticle using Streptomyces sp. (09 PBT 005). 09 PBT 005 was isolated from the soil sample of the agriculture field in Vengodu, Thiruvannamalai district, Tamil Nadu, India. 09 PBT 005 was subjected to molecular characterization by 16S rRNA sequence analysis. It was found that 09 PBT 005 belonged to Streptomyces sp. The isolate Streptomyces sp. 09 PBT 005 was inoculated in fermentation medium and incubated at 30 ºC for 12 days in different pH conditions. The 0.02 molar concentration showed good antibacterial activity against Gram-positive and Gram-negative bacteria at pH-7. The synthesis of silver nanoparticles was investigated by UV-Vis spectroscopy, scanning electron microscopy and Fourier Transform Infrared analysis. The synthesized AgNPs sizes were found to be in the dimensions ranging between 198 and 595 nm. The cytotoxicity of the synthesized nanoparticles was studied against A549 adenocarcinoma lung cancer cell line. It showed 83.23 % activity at 100 μl with IC 50 value of 50 μl. This method will be useful in the biosynthesis of nanoparticles.

  4. Communication: UV photoionization of cytosine catalyzed by Ag+

    NASA Astrophysics Data System (ADS)

    Taccone, Martín I.; Féraud, Geraldine; Berdakin, Matías; Dedonder-Lardeux, Claude; Jouvet, Christophe; Pino, Gustavo A.

    2015-07-01

    The photo-induced damages of DNA in interaction with metal cations, which are found in various environments, still remain to be characterized. In this paper, we show how the complexation of a DNA base (cytosine (Cyt)) with a metal cation (Ag+) changes its electronic properties. By means of UV photofragment spectroscopy of cold ions, it was found that the photoexcitation of the CytAg+ complex at low energy (315-282) nm efficiently leads to ionized cytosine (Cyt+) as the single product. This occurs through a charge transfer state in which an electron from the p orbital of Cyt is promoted to Ag+, as confirmed by ab initio calculations at the TD-DFT/B3LYP and RI-ADC(2) theory level using the SV(P) basis set. The low ionization energy of Cyt in the presence of Ag+ could have important implications as point mutation of DNA upon sunlight exposition.

  5. Communication: UV photoionization of cytosine catalyzed by Ag(+).

    PubMed

    Taccone, Martín I; Féraud, Geraldine; Berdakin, Matías; Dedonder-Lardeux, Claude; Jouvet, Christophe; Pino, Gustavo A

    2015-07-28

    The photo-induced damages of DNA in interaction with metal cations, which are found in various environments, still remain to be characterized. In this paper, we show how the complexation of a DNA base (cytosine (Cyt)) with a metal cation (Ag(+)) changes its electronic properties. By means of UV photofragment spectroscopy of cold ions, it was found that the photoexcitation of the CytAg(+) complex at low energy (315-282) nm efficiently leads to ionized cytosine (Cyt(+)) as the single product. This occurs through a charge transfer state in which an electron from the p orbital of Cyt is promoted to Ag(+), as confirmed by ab initio calculations at the TD-DFT/B3LYP and RI-ADC(2) theory level using the SV(P) basis set. The low ionization energy of Cyt in the presence of Ag(+) could have important implications as point mutation of DNA upon sunlight exposition.

  6. Mechanism of coercivity enhancement by Ag addition in FePt-C granular films for heat assisted magnetic recording media

    SciTech Connect

    Varaprasad, B. S. D. Ch. S.; Takahashi, Y. K. Wang, J.; Hono, K.; Ina, T.; Nakamura, T.; Ueno, W.; Nitta, K.; Uruga, T.

    2014-06-02

    We investigated the Ag distribution in a FePtAg-C granular film that is under consideration for a heat assisted magnetic recording medium by aberration-corrected scanning transmission electron microscope-energy dispersive X-ray spectroscopy and X-ray absorption fine structure. Ag is rejected from the core of FePt grains during the deposition, forming Ag-enriched shell surrounding L1{sub 0}-ordered FePt grains. Since Ag has no solubility in both Fe and Pt, the rejection of Ag induces atomic diffusions thereby enhancing the kinetics of the L1{sub 0}-order in the FePt grains.

  7. Alkalilimnicola ehrlichii sp. nov., a novel, arsenite-oxidizing haloalkaliphilic gammaproteobacterium capable of chemoautotrophic or heterotrophic growth with nitrate or oxygen as the electron acceptor

    USGS Publications Warehouse

    Hoeft, S.E.; Blum, J.S.; Stolz, J.F.; Tabita, F.R.; Witte, B.; King, G.M.; Santini, J.M.; Oremland, R.S.

    2007-01-01

    A facultative chemoautotrophic bacterium, strain MLHE-1T, was isolated from Mono Lake, an alkaline hypersaline soda lake in California, USA. Cells of strain MLHE-1T were Gram-negative, short motile rods that grew with inorganic electron donors (arsenite, hydrogen, sulfide or thiosulfate) coupled with the reduction of nitrate to nitrite. No aerobic growth was attained with arsenite or sulfide, but hydrogen sustained both aerobic and anaerobic growth. No growth occurred when nitrite or nitrous oxide was substituted for nitrate. Heterotrophic growth was observed under aerobic and anaerobic (nitrate) conditions. Cells of strain MLHE-1T could oxidize but not grow on CO, while CH4 neither supported growth nor was it oxidized. When grown chemoautotrophically, strain MLHE-1T assimilated inorganic carbon via the Calvin-Benson-Bassham reductive pentose phosphate pathway, with the activity of ribulose 1,5-bisphosphate carboxylase (RuBisCO) functioning optimally at 0.1 M NaCl and at pH 7.3. Strain MLHE-1T grew over broad ranges of pH (7.3-10.0; optimum, 9.3), salinity (115-190 g l-1; optimum 30 g l-1) and temperature (113-40 ??C; optimum, 30 ??C). Phylogenetic analysis of 16S rRNA gene sequences placed strain MLHE-1T in the class Gammaproteobacteria (family Ectothiorhodospiraceae) and most closely related to Alkalispirillum mobile (98.5%) and Alkalilimnicola halodurans (98.6%), although none of these three haloalkaliphilic micro-organisms were capable of photoautotrophic growth and only strain MLHE-1T was able to oxidize As(III). On the basis of physiological characteristics and DNA-DNA hybridization data, it is suggested that strain MLHE-1T represents a novel species within the genus Alkalilimnicola for which the name Alkalilimnicola ehrlichii is proposed. The type strain is MLHE-1T (=DSM 17681T =ATCC BAA-1101T). Aspects of the annotated full genome of Alkalilimnicola ehrlichii are discussed in the light of its physiology. ?? 2007 IUMS.

  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. A Systematic Search for Structures, Stabilities, Electronic and Magnetic Properties of Silicon Doped Silver Clusters: Comparison with Pure Silver Clusters

    NASA Astrophysics Data System (ADS)

    Zhao, Ya-Ru; Zhang, Hai-Rong; Zhang, Mei-Guang; Zheng, Bao-Bing; Kuang, Xiao-Yu

    2013-05-01

    The geometric structures, stabilities, electronic and magnetic properties of silicon doped silver clusters AgnSi (n = 1 - 9) have been systematically investigated by using meta-generalized gradient approximation (meta-GGA) exchange correlation Tao-Perdew-Staroverov-Scuseria (TPSS) functional. Due to the sp3 hybridization, the lowest energy structures of doped clusters favour the threedimensional structure. The silicon atom prefers to be located at the surface of the host silver clusters. The isomers that correspond to high coordination numbers of the Si-Ag bonds are found to be more stable. By analyzing the relative stabilities, the results show that the quadrangular bipyramid Ag4Si structure is the most stable geometry for the AgnSi clusters. Meanwhile, the fragmentation energies, second-order difference of energies, difference of highest occupied and lowest unoccupied molecular orbital (HOMO-LUMO gaps), and total magnetic moments exhibit pronounced even-odd alternations. The largest hardness difference (2:24 eV) exists between the clusters Ag4Si and Ag5, which illustrates that the corresponding Ag4Si cluster has dramatically enhanced chemical stability.

  10. Kinetics-controlled growth of bimetallic RhAg on Au nanorods and their catalytic properties

    NASA Astrophysics Data System (ADS)

    Ye, Wei; Guo, Xia; Xie, Fang; Zhu, Rui; Zhao, Qing; Yang, Jian

    2014-03-01

    Controlled growth of hybrid metallic nanocomposites for a desirable structure in a combination of selected components is highly important for their applications. Herein, the controllable growth of RhAg on the gold nanorods is achieved from the dumbbell-like RhAg-tipped nanorods to the brushy RhAg-coated nanorods, or the rod-like Au@Ag-Rh nanorattles. These different growth modes of RhAg on the gold nanorods are correlated with the reducing kinetics of RhCl3 and AgNO3. In view of the promising catalytic properties of Rh, the gold nanorods modified by RhAg in different structures are examined as catalysts for the oxidation of o-phenylenediamine. It is found that brushy RhAg-coated nanorods present a higher catalytic efficiency than dumbbell-like RhAg-tipped nanorods and rod-like Au@Ag-Rh nanorattles. These results would benefit the overgrowth control on the one-dimensional metallic nanorods and the rational design of new generation heterogeneous catalysts and optical devices.Controlled growth of hybrid metallic nanocomposites for a desirable structure in a combination of selected components is highly important for their applications. Herein, the controllable growth of RhAg on the gold nanorods is achieved from the dumbbell-like RhAg-tipped nanorods to the brushy RhAg-coated nanorods, or the rod-like Au@Ag-Rh nanorattles. These different growth modes of RhAg on the gold nanorods are correlated with the reducing kinetics of RhCl3 and AgNO3. In view of the promising catalytic properties of Rh, the gold nanorods modified by RhAg in different structures are examined as catalysts for the oxidation of o-phenylenediamine. It is found that brushy RhAg-coated nanorods present a higher catalytic efficiency than dumbbell-like RhAg-tipped nanorods and rod-like Au@Ag-Rh nanorattles. These results would benefit the overgrowth control on the one-dimensional metallic nanorods and the rational design of new generation heterogeneous catalysts and optical devices. Electronic

  11. Coating stainless steel plates with Ag/TiO2 for chlorpyrifos decontamination

    NASA Astrophysics Data System (ADS)

    Abdel Fattah, Wafa I.; Gobara, Mohammed M.; El-Hotaby, Walid; Mostafa, Sherif F. M.; Ali, Ghareib W.

    2016-05-01

    Spray coatings of either nanosilver (Ag), titanium (TiO2) or nanosilver titanium (Ag/TiO2) on stainless steel substrates prepared by sol-gel process were successfully achieved. The efficiency of the Ag/TiO2 coat onto 316 stainless steel surface towards cloropyrifos degradation as a chemical warfare agent (CWA) was proved. The crystalline structure and morphological characterization, as well as surface roughness measurements, were assessed. X-ray diffraction results proved the crystalline TiO2 anatase phase. The uniform distribution of Ag along with TiO2 nanoparticles was evidenced through transmission electron microscopy and scanning electron microscopy mapping. The hydrophilic nature of individual Ag, TiO2 and Ag/TiO2 coats was proved by contact angle measurements. The loading of Ag nanoparticles influenced positively the Ag/TiO2 coats surface roughness. The photocatalytic cloropyrifos degradation achieved about 50% within one-hour post UV treatment proving, therefore, the promising Ag/TiO2 continued decontamination efficiency. In conclusion, tuning the physical and morphological properties of TiO2 coated on stainless steel surface could be significantly enhanced by Ag nanoparticles incorporation. The developed Ag/TiO2 coat could be conveniently applied as CWA decontaminant.

  12. Coating stainless steel plates with Ag/TiO2 for chlorpyrifos decontamination

    NASA Astrophysics Data System (ADS)

    Abdel Fattah, Wafa I.; Gobara, Mohammed M.; El-Hotaby, Walid; Mostafa, Sherif F. M.; Ali, Ghareib W.

    2016-05-01

    Spray coatings of either nanosilver (Ag), titanium (TiO2) or nanosilver titanium (Ag/TiO2) on stainless steel substrates prepared by sol–gel process were successfully achieved. The efficiency of the Ag/TiO2 coat onto 316 stainless steel surface towards cloropyrifos degradation as a chemical warfare agent (CWA) was proved. The crystalline structure and morphological characterization, as well as surface roughness measurements, were assessed. X-ray diffraction results proved the crystalline TiO2 anatase phase. The uniform distribution of Ag along with TiO2 nanoparticles was evidenced through transmission electron microscopy and scanning electron microscopy mapping. The hydrophilic nature of individual Ag, TiO2 and Ag/TiO2 coats was proved by contact angle measurements. The loading of Ag nanoparticles influenced positively the Ag/TiO2 coats surface roughness. The photocatalytic cloropyrifos degradation achieved about 50% within one-hour post UV treatment proving, therefore, the promising Ag/TiO2 continued decontamination efficiency. In conclusion, tuning the physical and morphological properties of TiO2 coated on stainless steel surface could be significantly enhanced by Ag nanoparticles incorporation. The developed Ag/TiO2 coat could be conveniently applied as CWA decontaminant.

  13. Fabrication, characterization and photocatalytic properties of Ag/AgI/BiOI heteronanostructures supported on rectorite via a cation-exchange method

    SciTech Connect

    Chen, Yunfang; Fang, Jianzhang; Lu, Shaoyou; Wu, Yan; Chen, Dazhi; Huang, Liyan; Xu, Weicheng; Zhu, Ximiao; Fang, Zhanqiang

    2015-04-15

    Highlights: • Ag/AgI/BiOI-rectorite was prepared by twice cation-exchange process. • Ag/AgI/BiOI-rectorite photocatalyst possessed SPR and adsorption capacity. • Ag/AgI/BiOI-rectorite exhibited highly photocatalytic activity. • Trapped holes and ·O{sub 2}{sup −} were formed active species in the photocatalytic system. - Abstract: In this work, a new plasmonic photocatalyst Ag/AgI/BiOI-rectorite was prepared via a cation exchange process. The photocatalyst had been characterized by X-ray powder diffraction (XRD), Raman spectra, nitrogen sorption (BET), field-emission scanning electron microscope (FE-SEM), X-ray photoelectron spectroscopy (XPS) and UV–vis diffuse reflectance spectroscopy (DRS). The photocatalytic activity, which was evaluated by degradation of rhodamine B (RhB) and bisphenol A (BPA) under visible light irradiation, was enhanced significantly by loading Ag/AgI/BiOI nanoparticles onto rectorite. The photogenerated holes and superoxide radical (·O{sub 2}{sup −}) were both formed as active species for the photocatalytic reactions under visible light irradiation. The existence of metallic Ag particles, which possess the surface plasmon resonance effect, acted as an indispensable role in the photocatalytic reaction.

  14. Asymmetrical Precipitation of Ag3Sn Intermetallic Compounds Induced by Thermomigration of Ag in Pb-Free Microbumps During Solid-State Aging

    NASA Astrophysics Data System (ADS)

    Su, Yu-Ping; Wu, Chun-Sen; Ouyang, Fan-Yi

    2016-01-01

    Three-dimensional integrated circuit technology has become a major trend in electronics packaging in the microelectronics industry. To effectively remove heat from stacked integrated circuitry, a temperature gradient must be established across the chips. Furthermore, because of the trend toward higher device current density, Joule heating is more serious and temperature gradients across soldered joints are expected to increase. In this study we used heat-sink and heat-source devices to establish a temperature gradient across SnAg microbumps to investigate the thermomigration behavior of Ag in SnAg solder. Compared with isothermal conditions, small Ag3Sn particles near the hot end were dissolved and redistributed toward the cold end under a temperature gradient. The results indicated that temperature gradient-induced movement of Ag atoms occurred from the hot side toward the cold side, and asymmetrical precipitation of Ag3Sn resulted. The mechanism of growth of the intermetallic compound (IMC) Ag3Sn, caused by thermomigration of Ag, is discussed. The rate of growth Ag3Sn IMC at the cold side was found to increase linearly with solid-aging time under a temperature gradient. To understand the force driving Ag diffusion under the temperature gradient, the molar heat of transport ( Q*) of Ag in Sn was calculated as +13.34 kJ/mole.

  15. New frontiers in water purification: highly stable amphopolycarboxyglycinate-stabilized Ag–AgCl nanocomposite and its newly discovered potential

    NASA Astrophysics Data System (ADS)

    Krutyakov, Yurii A.; Zherebin, Pavel M.; Kudrinskiy, Alexey A.; Zubavichus, Yan V.; Presniakov, Mikhail Yu; Yapryntsev, Alexey D.; Karabtseva, Anastasia V.; Mikhaylov, Dmitry M.; Lisichkin, Georgii V.

    2016-09-01

    A simple synthetic procedure for high-stable dispersions of porous composite Ag/AgCl nanoparticles stabilized with amphoteric surfactant sodium tallow amphopolycarboxyglycinate has been proposed for the first time. The prepared samples were characterized by UV–vis spectroscopy, x-ray powder diffraction (XRD), x-ray photoelectron spectroscopy, small area electron diffraction (SAED), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and electron probe micro-analysis. In addition, measurements (carried out at the Kurchatov synchrotron radiation source stations) of the Ag K-edge extended x-ray absorption fine structure (EXAFS) and x-ray absorption near edge structure (XANES) spectra and XRD of the prepared nanoparticles have been performed. The obtained results suggest that small-sized Ag clusters are homogeneously distributed in the mass of the AgCl nanoparticle (~80 nm) formed during the synthesis. The Ag/AgCl dispersion demonstrates photocatalytic activity (with respect to methyl orange) and high bactericidal activity against E. coli. This activity is superior to the activity of both Ag and AgCl nanoparticles stabilized by the same surfactant. Thus, porous composite Ag/AgCl nanoparticles can be used as a multifunctional agent that is able to remove both pollutants and bacterium from water.

  16. Morphology, dimension, and composition dependence of thermodynamically preferred atomic arrangements in Ag-Pt nanoalloys.

    PubMed

    Deng, Lei; Deng, Huiqiu; Xiao, Shifang; Tang, Jianfeng; Hu, Wangyu

    2013-01-01

    The present article is on Metropolis Monte Carlo simulations coupled with semiempirical potentials to obtain the thermodynamically preferred configurations of Ag-Pt nanoalloys. The effects of particle size, morphology or alloy composition on the surface segregation and the chemical ordering patterns were investigated. Surface segregation of Ag is observed in all Ag-Pt nanoalloys. Such segregation develops quickly as the increase of particle sizes or global Ag composition. Generally, Ag surface enrichment is more apparent for more open particles except for large sized icosahedron (ICO) nanoalloys. The most energetically favorable chemical ordering patterns gradually evolve from Pt-core/Ag-shell to onion-like structures when the global Ag composition increases. Due to the site preference of Ag segregation, the presence of partly alloyed facets and Ag blocked vertices or edges at low global Ag compositions can modify the electronic and geometric structures on the nanoalloys' surface. The coupling between Pt and Ag sites is a topic of particular interest for catalysis. The detailed atomistic understanding of atomic arrangements in Ag-Pt nanoalloys is essential to intelligently design robust and active nanocatalysts with a low cost. PMID:24015590

  17. Calculations of stopping powers of 100 eV-30 keV electrons in 31 elemental solids

    SciTech Connect

    Tanuma, S.; Powell, C. J.; Penn, D. R.

    2008-03-15

    We present calculated electron stopping powers (SPs) for 31 elemental solids (Li, Be, glassy C, graphite, diamond, Na, Mg, K, Sc, Ti, V, Fe, Y, Zr, Nb, Mo, Ru, Rh, In, Sn, Cs, Gd, Tb, Dy, Hf, Ta, W, Re, Os, Ir, and Bi). These SPs were determined with an algorithm previously used for the calculation of electron inelastic mean free paths and from energy-loss functions (ELFs) derived from experimental optical data. The SP calculations were made for electron energies between 100 eV and 30 keV and supplement our earlier SP calculations for ten additional solids (Al, Si, Cr, Ni, Cu, Ge, Pd, Ag, Pt, and Au). Plots of SP versus atomic number for the group of 41 solids show clear trends. Multiple peaks and shoulders are seen that result from the contributions of valence-electron and various inner-shell excitations. Satisfactory agreement was found between the calculated SPs and values from the relativistic Bethe SP equation with recommended values of the mean excitation energy (MEE) for energies above 10 keV. We determined effective MEEs versus maximum excitation energy from the ELFs for each solid. Plots of effective MEE versus atomic number showed the relative contributions of valence-electron and different core-electron excitations to the MEE. For a maximum excitation energy of 30 keV, our effective MEEs agreed well for Be, graphite, Na, Al, and Si with recommended MEEs; a difference for Li was attributed to sample oxidation in the SP measurements for the recommended MEE. Substantially different effective MEEs were found for the three carbon allotropes (graphite, diamond, and glassy C)

  18. Atomic oxygen flux determined by mixed-phase Ag/Ag2O deposition

    SciTech Connect

    Kaspar, Tiffany C.; Droubay, Timothy C.; Chambers, Scott A.

    2010-11-01

    The flux of atomic oxygen generated in a electron cyclotron resonance (ECR) microwave plasma source was quantified by two different methods. The commonly applied approach of monitoring the frequency change of a silver-coated quartz crystal microbalance (QCM) deposition rate monitor as the silver is oxidized was found to underestimate the atomic oxygen flux by an order of magnitude compared to a more direct deposition approach. In the mixed-phase Ag/Ag2O deposition method, silver films were deposited in the presence of the plasma such that the films were partially oxidized to Ag2O; x-ray photoelectron spectroscopy (XPS) was utilized for quantification of the oxidized fraction. The inaccuracy of the QCM oxidation method was tentatively attributed to efficient catalytic recombination of O atoms on the silver surface.

  19. Ag Division States Philosophy

    ERIC Educational Resources Information Center

    American Vocational Journal, 1976

    1976-01-01

    The discussion which took place during the American Vocational Association's (AVA) Agriculture Division meeting at the 1975 AVA Convention is summarized, and the statement of vo-ag education philosophy (including 13 key concepts), which was passed during the convention, is presented. (AJ)

  20. Formation and properties of hyaluronan/nano Ag and hyaluronan-lecithin/nano Ag films.

    PubMed

    Khachatryan, Gohar; Khachatryan, Karen; Grzyb, Jacek; Fiedorowicz, Maciej

    2016-10-20

    A facile and environmentally friendly method of the preparation of silver nanoparticles embedded in hyaluronan (Hyal/Ag) and hyaluronan-lecithin (Hyal-L/Ag) matrix was developed. Thin, elastic foils were prepared from gels by an in situ synthesis of Ag in an aqueous solution of sodium hyaluronate (Hyal), using aq. d-(+)-xylose solution as a reducing agent. The gels were applied to a clean, smooth, defatted Teflon surface and left for drying in the air. The dry foils were stored in a closed container. UV-vis spectroscopy, transmission electron microscopy (TEM) and Fourier transform infrared (FTIR) spectra confirmed formation of about 10nm ball-shaped Ag nanoparticles situated within the polysaccharide template. Thermal properties of the composites were characterized involving differential scanning calorimetry (DSC) and thermogravimetric (TGA) analyses, whereas molecular weights of polysaccharide chains of the matrix were estimated with the size exclusion chromatography coupled with multiangle laser light scattering and refractometric detectors (HPSEC-MALLS-RI). An increase in the molecular weight of the hyaluronate after generation of Ag nanoparticles was observed. The foils showed specific properties. The study confirmed that silver nanoparticles can be successfully prepared with environmentally friendly method, using hyaluronan as a stabilizing template. Hyaluronan and hyaluronan-lecithin matrices provide nanocrystals uniform in size and shape. The composites demonstrated a bacteriostatic activity. PMID:27474588

  1. Semitransparent inverted polymer solar cells employing a sol-gel-derived TiO2 electron-selective layer on FTO and MoO3/Ag/MoO3 transparent electrode

    PubMed Central

    2014-01-01

    We report a new semitransparent inverted polymer solar cell (PSC) with a structure of glass/FTO/nc-TiO2/P3HT:PCBM/MoO3/Ag/MoO3. Because high-temperature annealing which decreased the conductivity of indium tin oxide (ITO) must be handled in the process of preparation of nanocrystalline titanium oxide (nc-TiO2), we replace glass/ITO with a glass/fluorine-doped tin oxide (FTO) substrate to improve the device performance. The experimental results show that the replacing FTO substrate enhances light transmittance between 400 and 600 nm and does not change sheet resistance after annealing treatment. The dependence of device performances on resistivity, light transmittance, and thickness of the MoO3/Ag/MoO3 film was investigated. High power conversion efficiency (PCE) was achieved for FTO substrate inverted PSCs, which showed about 75% increase compared to our previously reported ITO substrate device at different thicknesses of the MoO3/Ag/MoO3 transparent electrode films illuminated from the FTO side (bottom side) and about 150% increase illuminated from the MoO3/Ag/MoO3 side (top side). PMID:25332693

  2. Crystal structures and electronic properties for the over-lithiated and Li–Ag substituted phases of Li{sub 9}V{sub 3}(P{sub 2}O{sub 7}){sub 3}(PO{sub 4}){sub 2} insertion electrode system

    SciTech Connect

    Onoda, Masashige Inagaki, Makoto; Saito, Hiroaki

    2014-11-15

    For the Li{sub 9}V{sub 3}(P{sub 2}O{sub 7}){sub 3}(PO{sub 4}){sub 2} insertion electrode system with a multiple-electron reaction, the over-lithiated phase Li{sub x}V{sub 3}(P{sub 2}O{sub 7}){sub 3}(PO{sub 4}){sub 2} with 9Ag substituted phase Li{sub 9−y}Ag{sub y}V{sub 3}(P{sub 2}O{sub 7}){sub 3}(PO{sub 4}){sub 2} with 0electronic properties are explored through measurements of X-ray diffraction with a four-circle diffractometer, electrochemistry, electrical resistivity, and magnetization. Both the structures are isomorphous to that of Li{sub 9}V{sub 3}(P{sub 2}O{sub 7}){sub 3}(PO{sub 4}){sub 2} which has (VP2{sub 2}O{sub 7}){sub 3}(P1O{sub 4}){sub 2} layers in the ab-plane built up of VO{sub 6} octahedra sharing corners with P1O{sub 4} tetrahedra and P2{sub 2}O{sub 7} groups. In Li{sub x}V{sub 3}(P{sub 2}O{sub 7}){sub 3}(PO{sub 4}){sub 2}, the over-inserted Li4 ion surrounded by three oxygens in a planar triangular arrangement resides with a significantly large thermal parameter in the tunnels formed by the stacking of the layers and in between the octahedral Li1 sites, leading to a linear chain of Li ions with the distance 3.40 Å parallel to the direction of diffusion pathways. In Li{sub 9−y}Ag{sub y}V{sub 3}(P{sub 2}O{sub 7}){sub 3}(PO{sub 4}){sub 2}, where the Li1 site is substituted by Ag, the reduction of the electron hopping and the electrostatic potential for V ions are revealed in comparison with those of unsubstituted parent, which may account for the increase of mean voltage in the Li ion battery. - Highlights: • Li{sub x}V{sub 3}(P{sub 2}O{sub 7}){sub 3}(PO{sub 4}){sub 2} (x>9) and Li{sub 9−y}Ag{sub y}V{sub 3}(P{sub 2}O{sub 7}){sub 3}(PO{sub 4}){sub 2} (0electronic properties are clarified. • In Li{sub x}V{sub 3}(P{sub 2}O{sub 7}){sub 3}(PO{sub 4}){sub 2}, the over-inserted Li4 ion resides in between the Li

  3. Facile Preparation of Ag/NiO Composite Nanosheets and Their Antibacterial Activity

    NASA Astrophysics Data System (ADS)

    Shi, Cui-E.; Pan, Lu; Wang, Cheng-Run; He, Yi; Wu, Yong-Feng; Xue, Sai-Sai

    2016-01-01

    Sheet-like precursors of NiO and Ag/NiO with different Ag contents were synthesized by a facile and easily controlled hydrothermal method. The NiO and Ag/NiO composite nanosheets were prepared by calcination of the corresponding precursors at 400°C for 3 h. The as-synthesized samples were characterized by thermogravimetric analysis, x-ray diffraction, transmission electron microscopy, and scanning electron microscopy. The antibacterial activity of NiO and Ag/NiO composites to several gram-positive and gram-negative bacteria was examined. Results showed that NiO nanosheets hardly exhibited antibacterial activity; however, Ag/NiO composites displayed higher activity even with low Ag content.

  4. Self-healing of cracks in Ag joining layer for die-attachment in power devices

    NASA Astrophysics Data System (ADS)

    Chen, Chuantong; Nagao, Shijo; Suganuma, Katsuaki; Jiu, Jinting; Zhang, Hao; Sugahara, Tohru; Iwashige, Tomohito; Sugiura, Kazuhiko; Tsuruta, Kazuhiro

    2016-08-01

    Sintered silver (Ag) joining has attracted significant interest in power devices modules for its ability to form stable joints with a porous interconnection layer. A function for the self-healing of cracks in sintered porous Ag interlayers at high temperatures is discovered and reported here. A crack which was prepared on a Ag joining layer was closed after heating at 200 °C in air. The tensile strength of pre-cracked Ag joining layer specimens recovers to the value of non-cracked specimens after heating treatment. Transmission electron microscopy (TEM) was used to probe the self-healing mechanism. TEM images and electron diffraction patterns show that a large quantity of Ag nanoparticles formed at the gap with the size less than 10 nm, which bridges the crack in the self-healing process. This discovery provides additional motivation for the application of Ag as an interconnection material for power devices at high temperature.

  5. The role of Mott-Schottky heterojunctions in Ag-Ag8SnS6 as counter electrodes in dye-sensitized solar cells.

    PubMed

    He, Qingquan; Huang, Shoushuang; Wang, Cheng; Qiao, Qiquan; Liang, Na; Xu, Miao; Chen, Wenlong; Zai, Jiantao; Qian, Xuefeng

    2015-03-01

    Well-defined uniform pyramidal Ag-Ag8SnS6 heterodimers are prepared via a one-pot method. A plausible formation mechanism for the unique structures based on a seed-growth process and an etching effect due to oleylamine is proposed. The formed metal-semiconductor Mott-Schottky heterojunction promotes electron transfer from semiconducting Ag8 SnS6 to metallic Ag, which catalyzes the reduction of I3 (-) to I(-). When used as counter electrode in dye-sensitized solar cells, the heterodimers show comparable performance to platinum.

  6. 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.

  7. 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.

  8. Destabilization of Ag nanoislands on Ag(100) by adsorbed sulfur

    SciTech Connect

    Shen, Mingmin; Russell, Selena M.; Liu, Da-Jiang; Thiel, Patricia A.

    2011-10-17

    Sulfur accelerates coarsening of Ag nanoislands on Ag(100) at 300 K, and this effect is enhanced with increasing sulfur coverage over a range spanning a few hundredths of a monolayer, to nearly 0.25 monolayers. We propose that acceleration of coarsening in this system is tied to the formation of AgS{sub 2} clusters primarily at step edges. These clusters can transport Ag more efficiently than can Ag adatoms (due to a lower diffusion barrier and comparable formation energy). The mobility of isolated sulfur on Ag(100) is very low so that formation of the complex is kinetically limited at low sulfur coverages, and thus enhancement is minimal. However, higher sulfur coverages force the population of sites adjacent to step edges, so that formation of the cluster is no longer limited by diffusion of sulfur across terraces. Sulfur exerts a much weaker effect on the rate of coarsening on Ag(100) than it does on Ag(111). This is consistent with theory, which shows that the difference between the total energy barrier for coarsening with and without sulfur is also much smaller on Ag(100) than on Ag(111).

  9. Activity and stability studies of titanates and titanate-carbon nanotubes supported Ag anode catalysts for direct methanol fuel cell

    NASA Astrophysics Data System (ADS)

    Mohamed, Mohamed Mokhtar; Khairy, M.; Eid, Salah

    2016-02-01

    Titanate-SWCNT; synthesized via exploiting the interaction between TiO2 anatase with oxygen functionalized SWCNT, supported Ag nanoparticles and Ag/titanate are characterized using XRD, TEM-EDX-SAED, N2 adsorption, Photoluminescence, Raman and FTIR spectroscopy. These samples are tested for methanol electrooxidation via using cyclic voltammetry (CV) and impedance measurements. It is shown that Ag/titanate nanotubes exhibited superior electrocatalytic performance for methanol oxidation (4.2 mA cm-2) than titanate-SWCNT, Ag/titanate-SWCNT and titanate. This study reveals the existence of a strong metal-support interaction in Ag/titanate as explored via formation of Ti-O-Ag bond at 896 cm-1 and increasing surface area and pore volume (103 m2 g-1, 0.21 cm3 g-1) compared to Ag/titanate-SWCNT (71 m2 g-1, 0.175 cm3 g-1) that suffers perturbation and defects following incorporation of SWCNT and Ag. Embedding Ag preferably in SWCNT rather than titanate in Ag/titanate-SWCNT disturbs the electron transfer compared to Ag/titanate. Charge transfer resistance depicted from Nyquist impedance plots is found in the order of titanate > Ag/titanate-SWCNT > titanate-SWCNT > Ag/titanate. Accordingly, Ag/titanate indicates a slower current degradation over time compared to rest of catalysts. Conductivity measurements indicate that it follows the order Ag/titanate > Ag/titanate-SWCNT > titanate > titanate-SWCNT declaring that SWCNT affects seriously the conductivity of Ag(titanate) due to perturbations caused in titanate and sinking of electrons committed by Ago through SWCNT.

  10. Spin polarization and additional magneto-optical activity of nonmagnetic layers in Fe/Ag CMF

    NASA Astrophysics Data System (ADS)

    Xu, Y. B.; Zhai, H. R.; Lu, M.; Jin, Q. Y.; Miao, Y. Z.

    1992-08-01

    The experimental magneto-optical Kerr rotation spectra of Fe/Ag compositionally modulated films reported by Katayama et al. are studied theoretically. It is found that the free electrons of Ag are spin polarized. The magnitude of the polarization is about 1% with a direction opposite to that of Fe. The polarized Ag also gives rise to an additional magneto-optical activity as in Pt and Pd.

  11. 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.

  12. Ag/C nanoparticles as an cathode catalyst for a zinc-air battery with a flowing alkaline electrolyte

    NASA Astrophysics Data System (ADS)

    Han, Jia-Jun; Li, Ning; Zhang, Tian-Yun

    The cyclic voltammetry indicated that the oxygen reduction reaction (ORR) proceeded by the four-electron pathway mechanism on larger Ag particles (174 nm), and that the ORR proceeded by the four-electron pathway and the two-electron pathway mechanisms on finer Ag particles (4.1 nm), simultaneously. The kinetics towards ORR was measured at a rotating disk electrode (RDE) with Ag/C electrode. The number of exchanged electrons for the ORR was found to be close to four on larger Ag particles (174 nm) and close to three on finer Ag particles (4.1 nm). The zinc-air battery with Ag/C catalysts (25.9 nm) was fabricated and examined.

  13. Microstructure and tribological properties of NbN-Ag composite films by reactive magnetron sputtering

    NASA Astrophysics Data System (ADS)

    Ju, Hongbo; Xu, Junhua

    2015-11-01

    Recently, the chameleon thin films were developed with the purpose of adjusting their chemistry at self-mating interfaces in response to environmental changes at a wide temperature range. However, very few studies have focused on what state the lubricious noble metal exists in the films and the tribological properties at room temperature (RT). Composite NbN-Ag films with various Ag content (Ag/(Nb + Ag)) were deposited using reactive magnetron sputtering to investigate the crystal structure, mechanical and tribological properties. A combination of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and high resolution transmission electron microscopy (HRTEM) analyses showed that face-centered cubic (fcc) NbN, hexagonal close-packed (hcp) NbN and fcc silver coexisted in NbN-Ag films. The incorporation of soft Ag into NbN matrix led to the hardness decrease from 29.6 GPa at 0 at.% Ag to 11.3 GPa at 19.9 at.% Ag. Tribological properties of NbN-Ag films performed using dry pin-on-disc wear tests against Al2O3 depended on Ag content to a large extent. The average friction coefficient and wear rate of NbN-Ag films decreased as Ag content increased from 4.0 to 9.2 at.%. With a further increase of Ag content, the average friction coefficient further decreased, while the wear rate increased gradually. The optimal Ag content was found to be 9.2-13.5 at.%, which showed low average friction coefficient values of 0.46-0.40 and wear rate values of 1.1 × 10-8 to 1.7 × 10-8 mm3/(mm N). 3D Profiler and Raman spectroscopy measurements revealed that the lubricant tribo-film AgNbO3 detected on the surface of the wear tracks could lead to the friction coefficient curve stay constant and decrease the average friction coefficients. The decrease of wear rate was mainly attributed to the lubricant tribo-film AgNbO3 as Ag content increased from 4.0 to 9.2 at.%; with a further increase in Ag content, the wear rate increased with increasing Ag content in NbN-Ag films because a

  14. An oil-in-water self-assembly synthesis, characterization and photocatalytic properties of nano Ag@AgCl surface-sensitized K{sub 2}Ti{sub 4}O{sub 9}

    SciTech Connect

    Liang, Yinghua; Lin, Shuanglong; Liu, Li Hu, Jinshan; Cui, Wenquan

    2014-12-15

    Highlights: • The plasmatic Ag@AgCl surface-sensitized K{sub 2}Ti{sub 4}O{sub 9} composite photocatalysts. • Ag@AgCl greatly increased visible light absorption for K{sub 2}Ti{sub 4}O{sub 9}. • The photocatalysts exhibited enhanced photocatalytic dye degradation. - Abstract: Nano-sized plasmonic Ag@AgCl surface-sensitized K{sub 2}Ti{sub 4}O{sub 9} composite photocatalysts (hereafter designated as Ag@AgCl/K{sub 2}Ti{sub 4}O{sub 9}) was synthesized via a facile oil-in-water self-assembly method. The photocatalytic activity of the prepared materials for RhB (Rhodamine B) degradation was examined under visible light irradiation. The results reveal that the size of Ag@AgCl, which evenly dispersed on the surface of K{sub 2}Ti{sub 4}O{sub 9}, distributes about 20–50 nm. The UV–vis diffuse reflectance spectra indicate that Ag@AgCl/K{sub 2}Ti{sub 4}O{sub 9} samples have a significantly enhanced optical absorption in 380–700 nm. The photocatalytic activities of the Ag@AgCl/K{sub 2}Ti{sub 4}O{sub 9} samples increase first and then decrease with increasing amount of loading Ag@AgCl and the Ag@AgCl(20 wt.%)/K{sub 2}Ti{sub 4}O{sub 9} sample exhibits the best photocatalytic activity and 94.47% RhB was degraded after irradiation for 2 h. Additionally, studies performed using radical scavengers indicated that O{sub 2}·{sup −} and Cl{sup 0} acted as the main reactive species. The electronic interaction was systematically studied and confirmed by the photo-electrochemical measurements.

  15. Visible light driven Ag/Ag3PO4/AC photocatalyst with highly enhanced photodegradation of tetracycline antibiotics

    NASA Astrophysics Data System (ADS)

    Wang, Huiqin; Ye, Zhefei; Liu, Chun; Li, Jinze; Zhou, Mingjun; Guan, Qingfeng; Lv, Peng; Huo, Pengwei; Yan, Yongsheng

    2015-10-01

    Ag/Ag3PO4/active carbon (AC) composite photocatalysts were successfully synthesized using the simple deposition and photoinduced methods. The structures, morphology and photocatalytic properties of as-prepared 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 Ag/Ag3PO4/AC composite photocatalysts exhibited a conspicuously improved photocatalytic performance for tetracycline (TC) degradation. The optimal conditions of loaded dosage and photoinduced time were investigated, and the results showed that the photoinduced time played an important role in prepared processes, and also that for the loaded dosage of Ag3PO4. The DRS analysis showed that the composite photocatalysts exhibited strong absorption ability in the visible light range. The radicals trap experiments demonstrated that there were multiple active species during the degrading process of TC. The possible mechanism of improved photocatalytic activity of Ag-Ag3PO4/AC composite was also proposed.

  16. AGS preinjector improvement

    SciTech Connect

    Alessi, J.G.; Brennan, J.M.; Brown, H.N.; Brodowski, J.; Gough, R.; Kponou, A.; Prelec, K.; Staples, J.; Tanabe, J.; Witkover, R.

    1987-01-01

    In 1984, a polarized H/sup -/ source was installed to permit the acceleration of polarized protons in the AGS, using a low current, 750 keV RFQ Linear Accelerator as the preinjector. This RFQ was designed by LANL and has proved to be quite satisfactory and reliable. In order to improve the reliability and simplify maintenance of the overall AGS operations, it has been decided to replace one of the two 750 keV Cockcroft-Waltons (C-W) with an RFQ. The design of a new high current RFQ has been carried out by LBL and is also being constructed there. This paper describes the preinjector improvement project, centered around that RFQ, which is underway at BNL.

  17. Annealing behaviour of c-SiO 2 implanted layer distributed with high density Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Liu, Zhengxin; Wang, Honghong

    1997-01-01

    High volume density Ag nanoparticles embedded in c-SiO 2 matrix have been prepared by Ag ion implantation at an energy of 200 keV and a current density of about 20 μA/cm 2 to a nominal dose of 6.7 × 10 16ions/cm 2 at RT. Bright-field transmission electron microscopy (TEM) image indicates that Ag nanoparticles show two groups of sizes: the larger diameter is about 25 nm and the smaller is less than 10 nm. RBS spectra show that the distribution of implanted Ag atoms is bimodal which is associated with the two groups of nanoparticles above. Thermal stability of the implanted layer which consists of Ag nanoparticles, dissolved Ag atoms and c-SiO 2 matrix has been investigated by RBS, TEM and Raman spectroscopy. RBS spectra prove that little migration of Ag atoms is found and Ag nanoparticles are considerably stable at 300°C annealing. Though the obvious change in the distribution of Ag is observed at 400°C annealing in RBS spectra, TEM image identifies that both the larger and the smaller Ag nanoparticles still exist at relatively stable state. Following 750°C annealing, Ag atoms drastically move, and furthermore, the bimodal character of the distribution disappears. On the other hand, the amorphized SiO 2 implanted layer recrystal after 300°C, 400°C annealing.

  18. Nucleation and Growth of Bubbles in He Ion Implanted V/Ag Multilayers

    SciTech Connect

    Wei, Q. M.; Wang, Y. Q.; Nastasi, Michael; Misra, A.

    2011-11-18

    Microstructures of He ion-implanted pure Ag, pure V and polycrystalline V/Ag multilayers with individual layer thickness ranging from 1 nm to 50 nm were investigated by transmission electron microscopy (TEM). The bubbles in the Ag layer were faceted and larger than the non-faceted bubbles in the V layer under the same implantation conditions for both pure metals and multilayers. The substantially higher single defects surviving the spike phase and lower mobility of trapped He in bcc than those in fcc could account for this difference. For multilayers, the bubbles nucleate at interfaces but grow preferentially in Ag layers due to high mobility of trapped He in fcc Ag. In addition, the He concentration above which bubbles can be detected in defocused TEM images increases with decreasing layer thickness, from 0 for pure Ag to 4–5 at. % for 1 nm V/1 nm Ag multilayers. In contrast, the bubble size decreases with decreasing layer thickness, from approximately 4 nm in diameter in pure Ag to 1 nm in the 1 nm V/1 nm Ag multilayers. Elongated bubbles confined in the Ag layer by the V–Ag interfaces were observed in 1 nm multilayers. These observations show that bubble nucleation and growth can be suppressed to high He concentrations in nanoscale composites with interfaces that have high He solubility.

  19. Highly quasi-monodisperse ag nanoparticles on titania nanotubes by impregnative aqueous ion exchange.

    PubMed

    Toledo-Antonio, J A; Cortes-Jácome, M A; Angeles-Chavez, C; López-Salinas, E; Quintana, P

    2009-09-01

    Silver nanoparticles were homogenously dispersed on titania nanotubes (NT), which were prepared by alkali hydrothermal methodology and dried at 373 K. Ag(+) incorporation was done by impregnative ion exchange of aqueous silver nitrate onto NT. First, Ag(+) ions incorporate into the layers of nanotube walls, and then, upon heat treatment under N(2) at 573 and 673 K, they migrate and change into Ag(2)O and Ag(0) nanoparticles, respectively. In both cases, Ag nanoparticles are highly dispersed, decorating the nanotubes in a polka-dot pattern. The Ag particle size distribution is very narrow, being ca. 4 +/- 2 nm without any observable agglomeration. The reduction of Ag(2)O into Ag(0) octahedral nanoparticles occurs spontaneously and topotactically when annealing, without the aid of any reducing agent. The population of Ag(0) nanoparticles can be controlled by adjusting the annealing temperature. An electron charge transfer from NT support to Ag(0) nanoparticles, because of a strong interaction, is responsible for considerable visible light absorption in Ag(0) nanoparticles supported on NT.

  20. Bio-inspired sustainable and green synthesis of plasmonic Ag/AgCl nanoparticles for enhanced degradation of organic compound from aqueous phase.

    PubMed

    Devi, Th Babita; Ahmaruzzaman, M

    2016-09-01

    In the current study, we report the utilization of the biogenic potential of Benincasa hispida (ash gourd) peel extract for the synthesis of Ag embedded AgCl nanoparticles nanoparticles (Ag/AgCl NPs) without the use of any external organic solvents. The appearance of dark brown color from the pale yellow color confirmed the formation of Ag/AgCl nanoparticles which was further validated by absorbance peak using UV-visible spectroscopy. The phytochemicals (flavones) present in the B. hispida peel extract acts as a reducing/stabilizing agents. The morphology and size of the synthesized NPs were characterized by transmission electron microscope (TEM), selected area electron microscope (SAED) and high resolution transmission electron microscope (HR-TEM). FT-IR spectra of the B. hispida peel extract and after the development of nanoparticles are determined to identify the functional groups responsible for the conversion of metal ions to metal nanoparticles. The synthesized nanoparticles showed an excellent photocatalytic property in the degradation of toxic dye like malachite green oxalate under sunlight irradiation. For the first time, malachite green oxalate dye was degraded by Ag/AgCl nanoparticles under sunlight irradiation. PMID:27246560

  1. Bio-inspired sustainable and green synthesis of plasmonic Ag/AgCl nanoparticles for enhanced degradation of organic compound from aqueous phase.

    PubMed

    Devi, Th Babita; Ahmaruzzaman, M

    2016-09-01

    In the current study, we report the utilization of the biogenic potential of Benincasa hispida (ash gourd) peel extract for the synthesis of Ag embedded AgCl nanoparticles nanoparticles (Ag/AgCl NPs) without the use of any external organic solvents. The appearance of dark brown color from the pale yellow color confirmed the formation of Ag/AgCl nanoparticles which was further validated by absorbance peak using UV-visible spectroscopy. The phytochemicals (flavones) present in the B. hispida peel extract acts as a reducing/stabilizing agents. The morphology and size of the synthesized NPs were characterized by transmission electron microscope (TEM), selected area electron microscope (SAED) and high resolution transmission electron microscope (HR-TEM). FT-IR spectra of the B. hispida peel extract and after the development of nanoparticles are determined to identify the functional groups responsible for the conversion of metal ions to metal nanoparticles. The synthesized nanoparticles showed an excellent photocatalytic property in the degradation of toxic dye like malachite green oxalate under sunlight irradiation. For the first time, malachite green oxalate dye was degraded by Ag/AgCl nanoparticles under sunlight irradiation.

  2. Egg White Templated Synthesis of Ag and Au@Ag Alloy Microspheres for Surface-Enhanced Raman Spectroscopy Research.

    PubMed

    Li, Min; Zhang, Ying; Wang, Xiansong; Cui, Daxiang

    2016-01-01

    Herein, we report the green synthesis of Ag and Au@Ag microspheres by using the aqueous extracts of the egg white as well as their application as substrates for surface-enhanced Raman spectroscopy (SERS) detection. Both microspheres are prepared via the green synthesis method (room temperature, in aqueous solution and a benign reducer). The as-prepared urchin-like Ag microspheres have an average diameter of 600-800 nm, which is made up of some nanopricks with an average length of 10-40 nm. Meanwhile, the Au@Ag architectures prepared by galvanic replacement keep nearly similar size, which is also composed of some compact nanoparticles with an average diameter of about 10-40 nm. These products are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electronic microscopy (TEM), and Fourier transform infrared spectrophotometer (FTIR). The study on SERS activities is also carried out for both microspheres. It is found that Au@Ag microspheres possess much higher SERS activity than Ag microspheres. Our work may shed light on the design and synthesis of self-assembled 3D micro/nano-architectures for the use of SERS, catalysis, biosensors, nanomedicine, etc. PMID:27398550

  3. Egg White Templated Synthesis of Ag and Au@Ag Alloy Microspheres for Surface-Enhanced Raman Spectroscopy Research.

    PubMed

    Li, Min; Zhang, Ying; Wang, Xiansong; Cui, Daxiang

    2016-01-01

    Herein, we report the green synthesis of Ag and Au@Ag microspheres by using the aqueous extracts of the egg white as well as their application as substrates for surface-enhanced Raman spectroscopy (SERS) detection. Both microspheres are prepared via the green synthesis method (room temperature, in aqueous solution and a benign reducer). The as-prepared urchin-like Ag microspheres have an average diameter of 600-800 nm, which is made up of some nanopricks with an average length of 10-40 nm. Meanwhile, the Au@Ag architectures prepared by galvanic replacement keep nearly similar size, which is also composed of some compact nanoparticles with an average diameter of about 10-40 nm. These products are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electronic microscopy (TEM), and Fourier transform infrared spectrophotometer (FTIR). The study on SERS activities is also carried out for both microspheres. It is found that Au@Ag microspheres possess much higher SERS activity than Ag microspheres. Our work may shed light on the design and synthesis of self-assembled 3D micro/nano-architectures for the use of SERS, catalysis, biosensors, nanomedicine, etc.

  4. Stability of magic planar Ag clusters

    NASA Astrophysics Data System (ADS)

    Chiu, Y. P.; Ou, Y. S.; Chang, Y. R.; Wei, C. M.; Chang, C. S.; Tsong, Tien T.

    2007-03-01

    The spontaneous assembly of atoms and molecules in a system has attracted many research interests and created numerous potential applications. Utilizing the periodic pattern found on the Pb quantum islands, which are grown on the Si(111) surface, we have recently discovered that self-organized Ag planar clusters formed on these templates exhibit enhanced stability at some particular sizes [1]. Existence of the magic atom numbers in these clusters is mainly attributed to the electronic confinement effect. Here, we further explore the strength of these magic clusters subject to the temperature rise and oxygen exposure. Detailed calculations based on ab initio density functional theory have also been performed. The results help establish the relation between the physical and chemical stability of a magic Ag cluster and its size and shape. Ref:[1] Ya-Ping Chiu, Li-Wei Huang, Ching-Ming Wei, Chia-Seng Chang, and Tien-Tzou Tsong, Phys. Rev. Lett. 97, 165504 (2006).

  5. Initial geometries, interaction mechanism and high stability of silicene on Ag(111) surface.

    PubMed

    Gao, Junfeng; Zhao, Jijun

    2012-01-01

    Using ab initio methods, we have investigated the structures and stabilities of Si(N) clusters (N ≤ 24) on Ag(111) surface as the initial stage of silicene growth. Unlike the dome-shaped graphene clusters, Si clusters prefer nearly flat structures with low buckling, more stable than directly deposition of the 3D freestanding Si clusters on Ag surface. The p-d hybridization between Ag and Si is revealed as well as sp(2) characteristics in Si(N)@Ag(111). Three types of silicene superstructures on Ag(111) surface have been considered and the simulated STM images are compared with experimental observations. Molecular dynamic simulations show high thermal stability of silicene on Ag(111) surfaces, contrast to that on Rh(111). The present theoretical results constitute a comprehensive picture about the interaction mechanism of silicene on Ag(111) surface and explain the superiority of Ag substrate for silicene growth, which would be helpful for improving the experimentally epitaxial growth of silicene.

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

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

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

  7. Tyrosine-assisted preparation of Ag/ZnO nanocomposites with enhanced photocatalytic performance and synergistic antibacterial activities

    NASA Astrophysics Data System (ADS)

    Lu, Weiwei; Liu, Guosheng; Gao, Shuyan; Xing, Shantao; Wang, Jianji

    2008-11-01

    In this paper, Ag/ZnO metal-semiconductor nanocomposites were prepared through a facile one-pot hydrothermal method with the assistance of tyrosine. The synthesized samples were structurally characterized by x-ray diffraction, scanning electron microscope, transmission electron microscope and x-ray photoelectron spectroscopy. It was shown that the added tyrosine served both as a shape conductor for the formation of ZnO faceted nanorods and as a reducing agent of Ag+ ions. In the reaction process, the complexation of Ag+ with NH3 and OH- decreased the redox potential of Ag+/Ag, which prevented the formation of isolated Ag nanoparticles in solution. The prepared Ag/ZnO nanocomposites showed potential applications in photodegradation of organic dye pollutants and destruction of bacteria.

  8. Effects of Current-injection Firing with Ag Paste in a Boron Emitter

    PubMed Central

    Kim, Chanseok; Choi, Jae-Wook; Choi, Sungjin; Kim, Soomin; Park, Hyomin; Song, Hee-eun; Yoon, Sam S.; Huh, Joo-Youl; Kang, Yoonmook; Lee, Hae-Seok; Kim, Donghwan

    2016-01-01

    A high contact resistance for screen-printed contacts was observed when a conventional Ag paste was used on a boron emitter. The results of this study suggest that electron injection during firing is one of the processes that contribute to a lower contact resistance. Larger quantities of Ag precipitates formed upon electron injection into the boron emitter, which was confirmed by observing Ag crystallite or dendrite structures on the boron and by measuring the contact resistance between the boron emitter and the Ag bulk. The electron-injected sample had approximately 10000 times lower contact resistance than an untreated sample. The contact resistance of the electron-injected sample was 0.021 mΩ∙cm2 under optimal conditions, which is lower than that of conventional p-type silicon solar cells. Thus, electron injection can effectively lower contact resistance when using Ag paste in n-type silicon solar cells. During the cooling in the firing process, dissolved Ag ions in the glass layer are formed as dendrites or crystallites/particles. The dendrites are formed earlier than others via electrochemical migration under electron injection conditions. Then, crystallites and particles are formed via a silicon etching reaction. Thus, Ag ions that are not formed as dendrites will form as crystallites or particles. PMID:26861828

  9. Effects of Current-injection Firing with Ag Paste in a Boron Emitter.

    PubMed

    Kim, Chanseok; Choi, Jae-Wook; Choi, Sungjin; Kim, Soomin; Park, Hyomin; Song, Hee-eun; Yoon, Sam S; Huh, Joo-Youl; Kang, Yoonmook; Lee, Hae-Seok; Kim, Donghwan

    2016-01-01

    A high contact resistance for screen-printed contacts was observed when a conventional Ag paste was used on a boron emitter. The results of this study suggest that electron injection during firing is one of the processes that contribute to a lower contact resistance. Larger quantities of Ag precipitates formed upon electron injection into the boron emitter, which was confirmed by observing Ag crystallite or dendrite structures on the boron and by measuring the contact resistance between the boron emitter and the Ag bulk. The electron-injected sample had approximately 10000 times lower contact resistance than an untreated sample. The contact resistance of the electron-injected sample was 0.021 mΩ ∙ cm(2) under optimal conditions, which is lower than that of conventional p-type silicon solar cells. Thus, electron injection can effectively lower contact resistance when using Ag paste in n-type silicon solar cells. During the cooling in the firing process, dissolved Ag ions in the glass layer are formed as dendrites or crystallites/particles. The dendrites are formed earlier than others via electrochemical migration under electron injection conditions. Then, crystallites and particles are formed via a silicon etching reaction. Thus, Ag ions that are not formed as dendrites will form as crystallites or particles. PMID:26861828

  10. Effects of Current-injection Firing with Ag Paste in a Boron Emitter.

    PubMed

    Kim, Chanseok; Choi, Jae-Wook; Choi, Sungjin; Kim, Soomin; Park, Hyomin; Song, Hee-eun; Yoon, Sam S; Huh, Joo-Youl; Kang, Yoonmook; Lee, Hae-Seok; Kim, Donghwan

    2016-02-10

    A high contact resistance for screen-printed contacts was observed when a conventional Ag paste was used on a boron emitter. The results of this study suggest that electron injection during firing is one of the processes that contribute to a lower contact resistance. Larger quantities of Ag precipitates formed upon electron injection into the boron emitter, which was confirmed by observing Ag crystallite or dendrite structures on the boron and by measuring the contact resistance between the boron emitter and the Ag bulk. The electron-injected sample had approximately 10000 times lower contact resistance than an untreated sample. The contact resistance of the electron-injected sample was 0.021 mΩ ∙ cm(2) under optimal conditions, which is lower than that of conventional p-type silicon solar cells. Thus, electron injection can effectively lower contact resistance when using Ag paste in n-type silicon solar cells. During the cooling in the firing process, dissolved Ag ions in the glass layer are formed as dendrites or crystallites/particles. The dendrites are formed earlier than others via electrochemical migration under electron injection conditions. Then, crystallites and particles are formed via a silicon etching reaction. Thus, Ag ions that are not formed as dendrites will form as crystallites or particles.

  11. Effects of Current-injection Firing with Ag Paste in a Boron Emitter

    NASA Astrophysics Data System (ADS)

    Kim, Chanseok; Choi, Jae-Wook; Choi, Sungjin; Kim, Soomin; Park, Hyomin; Song, Hee-Eun; Yoon, Sam S.; Huh, Joo-Youl; Kang, Yoonmook; Lee, Hae-Seok; Kim, Donghwan

    2016-02-01

    A high contact resistance for screen-printed contacts was observed when a conventional Ag paste was used on a boron emitter. The results of this study suggest that electron injection during firing is one of the processes that contribute to a lower contact resistance. Larger quantities of Ag precipitates formed upon electron injection into the boron emitter, which was confirmed by observing Ag crystallite or dendrite structures on the boron and by measuring the contact resistance between the boron emitter and the Ag bulk. The electron-injected sample had approximately 10000 times lower contact resistance than an untreated sample. The contact resistance of the electron-injected sample was 0.021 mΩ•cm2 under optimal conditions, which is lower than that of conventional p-type silicon solar cells. Thus, electron injection can effectively lower contact resistance when using Ag paste in n-type silicon solar cells. During the cooling in the firing process, dissolved Ag ions in the glass layer are formed as dendrites or crystallites/particles. The dendrites are formed earlier than others via electrochemical migration under electron injection conditions. Then, crystallites and particles are formed via a silicon etching reaction. Thus, Ag ions that are not formed as dendrites will form as crystallites or particles.

  12. In-situ spectro-microscopy on organic films: Mn-Phthalocyanine on Ag(100)

    SciTech Connect

    Al-Mahboob A.; Vescovo, E.; Sadowski, J.T.

    2013-08-18

    Metal phthalocyanines are attracting significant attention, owing to their potential for applications in chemical sensors, solar cells and organic magnets. As the electronic properties of molecular films are determined by their crystallinity and molecular packing, the optimization of film quality is important for improving the performance of organic devices. Here, we present the results of in situ low-energy electron microscopy / photoemission electron microscopy (LEEM/PEEM) studies of incorporation-limited growth [1] of manganese-phthalocyanine (MnPc) on Ag(100) surfaces. MnPc thin films were grown on both, bulk Ag(100) surface and thin Ag(100)/Fe(100) films, where substrate spin-polarized electronic states can be modified through tuning the thickness of the Ag film [2]. We also discuss the electronic structure and magnetic ordering in MnPc thin films, investigated by angle- and spin-resolved photoemission spectroscopy.

  13. Self-regulated route to ternary hybrid nanocrystals of Ag-Ag2S-CdS with near-infrared photoluminescence and enhanced photothermal conversion

    NASA Astrophysics Data System (ADS)

    Zhu, Guoxing; Bao, Chunlin; Liu, Yuanjun; Shen, Xiaoping; Xi, Chunyan; Xu, Zheng; Ji, Zhenyuan

    2014-09-01

    Developing hybrid nanocrystals is a hot topic in materials science. Herein, a ternary hybrid nanocrystal, Ag-Ag2S-CdS, combining near infrared emission and photothermal conversion properties was demonstrated. The ternary Ag-Ag2S-CdS hybrid nanocrystals with cubic shape and uniform size were synthesized by a simple one-pot and one-step colloidal method. The growth process is self-regulated with the formation order of Ag2S, Ag, and CdS, sequentially. The formation of Ag originates from the partial reduction of Ag2S, while the formation of CdS is through an Ag2S catalytic mechanism based on its superionic feature. The obtained ternary hybrid nanocrystals show near infrared emission and photothermal conversion properties in a lab-on-a-particle system. Importantly, an enhanced effect is observed for the photothermal conversion, which is mainly due to the presence of heterointerfaces among the crystals. This work will not only advance the synthesis chemistry of multi-component hybrid nanocrystals but also provide a possible route for the design of advanced multi-model materials used in bio-related fields.Developing hybrid nanocrystals is a hot topic in materials science. Herein, a ternary hybrid nanocrystal, Ag-Ag2S-CdS, combining near infrared emission and photothermal conversion properties was demonstrated. The ternary Ag-Ag2S-CdS hybrid nanocrystals with cubic shape and uniform size were synthesized by a simple one-pot and one-step colloidal method. The growth process is self-regulated with the formation order of Ag2S, Ag, and CdS, sequentially. The formation of Ag originates from the partial reduction of Ag2S, while the formation of CdS is through an Ag2S catalytic mechanism based on its superionic feature. The obtained ternary hybrid nanocrystals show near infrared emission and photothermal conversion properties in a lab-on-a-particle system. Importantly, an enhanced effect is observed for the photothermal conversion, which is mainly due to the presence of

  14. Enhanced formation of silver nanoparticles in Ag+-NOM-iron(II, III) systems and antibacterial activity studies.

    PubMed

    Adegboyega, Nathaniel F; Sharma, Virender K; Siskova, Karolina M; Vecerova, Renata; Kolar, Milan; Zbořil, Radek; Gardea-Torresdey, Jorge L

    2014-03-18

    This work reports the role of iron redox pair (Fe(3+)/Fe(2+)) in the formation of naturally occurring silver nanoparticles (AgNPs) in the aquatic environment. The results showed that Fe(3+) or Fe(2+) ions in the mixtures of Ag(+) and natural organic matter enhanced the formation of AgNPs. The formation of AgNPs depended on pH and types of organic matter. Increase in pH enhanced the formation of AgNPs, and humic acids as ligands showed higher formation of AgNPs compared to fulvic acids. The observed results were described by considering the potentials of redox pairs of silver and iron species and the possible species involved in reducing silver ions to AgNPs. Dynamic light scattering and transmission electron microscopy measurements of AgNPs revealed mostly bimodal size distribution with decrease in size of AgNPs due to iron species in the reaction mixture. Minimum inhibitory concentration of AgNPs needed to inhibit the growth of various bacterial species suggested the role of surfaces of tested Gram-positive and Gram-negative bacteria. Stability study of AgNPs, formed in Ag(+)-humic acid/fulvic acids-Fe(3+) mixtures over a period of several months showed high stability of the particles with significant increase in surface plasmon resonance peak. The environmental implications of the results in terms of fate, transport, and ecotoxicity of organic-coated AgNPs are briefly presented. PMID:24524189

  15. Manifestation of surface and interface properties of Ag overlayer on Si (111)

    NASA Astrophysics Data System (ADS)

    Abdul Wasey, A. H. M.; Batabyal, R.; Dev, B. N.; Das, G. P.

    2013-02-01

    Ag/Si (111) interface has been investigated using first principles DFT approach, to establish the unique interplay between the structural and electronic properties. The interface induced properties, such as evolution of metal-induced gap states (MIGS), formation of Schottky barrier height (SBH), for this rectifying Ag/Si contact have been reported.

  16. Magnetic phase diagram in CePd 1- xAg x

    NASA Astrophysics Data System (ADS)

    Besnus, M. J.; Godart, C.; Kappler, J. P.; Sereni, J.

    1994-04-01

    Magnetic susceptibility, high field magnetization and specific heat measurements are presented on CePd 1- xAg x for 0 ≤ x ≤ 0.175. The strong effect of Pd substitution by Ag stresses the instability of the compound towards noble metals solutes or electron-like impurities.

  17. Floating compression of Ag nanowire networks for effective strain release of stretchable transparent electrodes

    NASA Astrophysics Data System (ADS)

    Pyo, Jun Beom; Kim, Byoung Soo; Park, Hyunchul; Kim, Tae Ann; Koo, Chong Min; Lee, Jonghwi; Son, Jeong Gon; Lee, Sang-Soo; Park, Jong Hyuk

    2015-10-01

    Manipulation of the configuration of Ag nanowire (NW) networks has been pursued to enhance the performance of stretchable transparent electrodes. However, it has remained challenging due to the high Young's modulus and low yield strain of Ag NWs, which lead to their mechanical failure when subjected to structural deformation. We demonstrate that floating a Ag NW network on water and subsequent in-plane compression allows convenient development of a wavy configuration in the Ag NW network, which can release the applied strain. A greatly enhanced electromechanical stability of Ag NW networks can be achieved due to their wavy configuration, while the NW networks maintain the desirable optical and electrical properties. Moreover, the produced NW networks can be transferred to a variety of substrates, offering flexibility for device fabrication. The Ag NW networks with wavy configurations are used as compliant electrodes for dielectric elastomer actuators. The study demonstrates their promising potential to provide improved performance for soft electronic devices.Manipulation of the configuration of Ag nanowire (NW) networks has been pursued to enhance the performance of stretchable transparent electrodes. However, it has remained challenging due to the high Young's modulus and low yield strain of Ag NWs, which lead to their mechanical failure when subjected to structural deformation. We demonstrate that floating a Ag NW network on water and subsequent in-plane compression allows convenient development of a wavy configuration in the Ag NW network, which can release the applied strain. A greatly enhanced electromechanical stability of Ag NW networks can be achieved due to their wavy configuration, while the NW networks maintain the desirable optical and electrical properties. Moreover, the produced NW networks can be transferred to a variety of substrates, offering flexibility for device fabrication. The Ag NW networks with wavy configurations are used as compliant

  18. Effects of Ag addition on FePt L1{sub 0} ordering transition: A direct observation of ordering transition and Ag segregation in FePtAg alloy films

    SciTech Connect

    Wang, Lei; Yu, Youxing; Gao, Tenghua

    2015-12-21

    FePt and (FePt){sub 91.2}Ag{sub 8.8} alloy films were deposited by magnetron sputtering. The average coercivity of (FePt){sub 91.2}Ag{sub 8.8} films reaches 8.51 × 10{sup 5} A/m, which is 0.63 × 10{sup 5} A/m higher than that of the corresponding FePt films. Ag addition effectively promotes the FePt L1{sub 0} ordering transition at a relatively low annealing temperature of 400 °C. The promotion mechanism was investigated by using in situ high-resolution transmission electron microscopy (HRTEM) and ex situ X-ray absorption fine structure (XAFS). The concurrence of ordering transition and Ag segregation in FePtAg alloy films was first observed by using in situ heating HRTEM. The time-resolved evolution reveals more details on the role of Ag addition in FePt low-temperature ordering. Ex situ XAFS results further confirm that Ag replaces Fe sites in the as-deposited films and segregates from FePt-Ag solid solution phase through annealing at elevated temperatures. The segregation of Ag atoms leaves vacancies in the grain. The vacancy formation is believed to accelerate the diffusion of Fe and Pt atoms, which is critical for the L1{sub 0} ordering transition.

  19. 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.

  20. 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

  1. Study of Ag transport in Cr2N0.61-7Ag nanocomposite thin film due to thermal exposition

    NASA Astrophysics Data System (ADS)

    Bílek, P.; Jurči, P.; Podgornik, B.; Jenko, D.; Hudáková, M.; Kusý, M.

    2015-12-01

    Cr2N0.61-7Ag nanocomposite coatings were deposited on substrates made of Cr-V ledeburitic tool steel Vanadis 6 using reactive magnetron sputtering at a deposition temperature of 500 °C. Investigations of as-deposited films and annealing experiments in closed-air atmosphere at temperatures of 300, 400 and 500 °C and the durations up to 24 h, followed by quantitative scanning electron microscopy, transmission electron microscopy, Auger electron spectroscopy and X-ray diffraction revealed that the films were composed of Cr2N0.61 matrix and individual silver agglomerates located along columnar crystals of the matrix. The maximal size of Ag-agglomerates was 80 nm. The surface population density of silver agglomerates increased with prolonging the annealing time up to 2 h and then decreased. The increase was more pronounced at lower annealing temperatures. This behaviour was referred to the competition between three phenomena, namely the transport of detached Ag atoms to the free surface, formation of oxide layer on the surface and sublimation of silver from the surface. At lower temperatures and/or shorter annealing times, the Ag-transport to the free surface was determined to be prevalent, thus, an increase in population density of silver agglomerates was determined. On the other hand, for higher temperatures and/or longer annealing times the population density of Ag-agglomerates rather decreased due to retarding effect of thicker oxide layer and sublimation of silver.

  2. In situ fabrication of AgI films on various substrates

    SciTech Connect

    Zheng, Z. Liu, A.R.; Wang, S.M.; Huang, B.J.; Ma, X.M.; Zhao, H.X.; Li, D.P.; Zhang, L.Z.

    2008-08-04

    A facile solution-phase chemical route is developed to directly construct silver iodide (AgI) films/crystals on various substrates including silver foil, silicon wafer and glass, etc. The resulting AgI films were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). The AgI films with different morphologies can be obtained by controlling the reaction parameters. This method is a simple and fast way for in situ deposition of AgI crystals/films on different substrates. These films may be applied in chemical sensing systems and solid-state batteries as solid electrolytes.

  3. PVP induce self-seeding process for growth of Au@Ag core@shell nanocomposites

    NASA Astrophysics Data System (ADS)

    Eisa, Wael H.; Al-Ashkar, Emad; El-Mossalamy, S. M.; Ali, Safaa S. M.

    2016-05-01

    A novel self-seeding route is developed for fabrication of metallic nanocomposites of gold (core) and silver (shell) (Au@Ag core@shell). Herein, polyvinylpyrrolidone (PVP) is used as both reducing and stabilizing agent. The surface plasmon resonance (SPR) of Au@Ag core@shell can be tuned by controlling the thickness of the Ag shell. The different growth stages of the Au@Ag core@shell have been traced by in situ UV-vis absorption spectra. Transmission electron microscopy (TEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy are used for the characterization of the prepared samples.

  4. A simple way to prepare Cupric oleate capped AgI nanoparticles

    SciTech Connect

    Song Meirong; Zhang Zhijun . E-mail: s234soow@henu.edu.cn

    2004-12-02

    Cupric oleate capped AgI (Cu(OA){sub 2}-AgI) nanoparticles were prepared by a simple method and they have good dispersibility in organic solvents. X-ray diffraction (XRD), transmission electron microscope (TEM), FTIR, X-ray photoelectron spectrometer (XPS) and ultraviolet-visible (UV-vis) spectrometer were used to characterize the Cu(OA){sub 2}-AgI nanoparticles. The results show that the mean size is about 80 nm; the modified reagent has been chemically bonded on the surface of AgI. In addition, new absorption peaks in the UV region appear.

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

    PubMed

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

    2012-11-01

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

  6. 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.

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

    NASA Astrophysics Data System (ADS)

    Som, Anirban; Pradeep, T.

    2012-07-01

    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. Electronic supplementary information (ESI) available: size distribution of Te and Ag2Te NWs, HRTEM and XRD of Te and Ag2Te NWs, EDS of Ag2Te NWs, TEM image and EDS spectra of partially silver reacted Te and the dumbbell shaped NWs, HRTEM, PXRD and solid state annealing data of partially silver reacted Te NWs, variation of diameter along the length of dumb-bell shaped NW, HRTEM images of heterojunction, TEM images and EDS spectra showing the time dependent growth of biphasic NWs, TEM images showing bending and breaking of biphasic system on further annealing, temperature dependence of the growth of biphasic NWs and tuning the length of Te and Ag2Te sections in biphasic NWs. See DOI: 10.1039/c2nr30730h

  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. Physiological effects of major up-regulated Alnus glutinosa peptides on Frankia sp. ACN14a.

    PubMed

    Carro, Lorena; Pujic, Petar; Alloisio, Nicole; Fournier, Pascale; Boubakri, Hasna; Poly, Franck; Rey, Marjolaine; Heddi, Abdelaziz; Normand, Philippe

    2016-07-01

    Alnus glutinosa has been shown previously to synthesize, in response to nodulation by Frankia sp. ACN14a, an array of peptides called Alnus symbiotic up-regulated peptides (ASUPs). In a previous study one peptide (Ag5) was shown to bind to Frankia nitrogen-fixing vesicles and to modify their porosity. Here we analyse four other ASUPs, alongside Ag5, to determine whether they have different physiological effects on in vitro grown Frankia sp. ACN14a. The five studied peptides were shown to have different effects on nitrogen fixation, respiration, growth, the release of ions and amino acids, as well as on cell clumping and cell lysis. The mRNA abundance for all five peptides was quantified in symbiotic nodules and one (Ag11) was found to be more abundant in the meristem part of the nodule. These findings point to some peptides having complementary effects on Frankia cells. PMID:27082768

  10. Enhanced photocatalytic performance of sandwiched ZnO@Ag@Cu2O nanorod films: the distinct role of Ag NPs in the visible light and UV region

    NASA Astrophysics Data System (ADS)

    Ren, Shoutian; Zhao, Guoliang; Wang, Yingying; Wang, Benyang; Wang, Qiang

    2015-03-01

    Sandwiched ZnO@Ag@Cu2O nanorod films were synthesized by successive electrodeposition, magnetron sputtering and the second electrodeposition. The as-synthesized composites were characterized by x-ray diffraction patterns, field emission scanning electron microscopy, low- and high-resolution transmission electron microscopy and a UV-vis spectrophotometer. Their photocatalytic performance was estimated by the degradation of a methyl orange solution under UV or visible-light irradiation, respectively. In the visible region, due to localized surface plasmon resonance absorption of Ag NPs, ZnO@Ag@Cu2O showed a significantly enhanced photocatalytic performance. The enhancement factor of Ag NPs on the catalytic performance of ZnO@Ag@Cu2O was estimated as a function of the Cu2O deposition time, and the corresponding enhancement mechanism was also evaluated by the monochromatic photocatalytic experiment and discrete dipole approximation simulation. In the UV region, due to the formation of a Schottky junction (e.g. Ag/ZnO, Ag/Cu2O), a limited enhanced photocatalytic performance was also realized for ZnO@Ag@Cu2O photocatalysts.

  11. Photocatalytic degradation of acid blue 74 in water using Ag-Ag2O-Zno nanostuctures anchored on graphene oxide

    NASA Astrophysics Data System (ADS)

    Umukoro, Eseoghene H.; Peleyeju, Moses G.; Ngila, Jane C.; Arotiba, Omotayo A.

    2016-01-01

    Water pollution due to industrial effluents from industries which utilize dyes in the manufacturing of their products has serious implications on aquatic lives and the general environment. Thus, there is need for the removal of dyes from wastewater before being discharged into the environment. In this study, a nanocomposite consisting of silver, silver oxide (Ag2O), zinc oxide (ZnO) and graphene oxide (GO) was synthesized, characterized and photocatalytically applied in the degradation (and possibly mineralization) of organic pollutants in water treatment process. The Ag-Ag2O-ZnO nanostructure was synthesized by a co-precipitation method and calcined at 400 °C. It was functionalized using 3-aminopropyl triethoxysilane and further anchored on carboxylated graphene oxide via the formation of an amide bond to give the Ag-Ag2O-ZnO/GO nanocomposite. The prepared nanocomposite was characterized by UV-Vis diffuse reflectance spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electronic microscopy (SEM), energy dispersive X-ray spectrometry (EDX), Fourier transformed infrared spectroscopy (FTIR), and Raman spectroscopy. The applicability of Ag-Ag2O-ZnO/GO nanocomposite as a photocatalyst was investigated in the photocatalytic degradation of acid blue 74 dye under visible light irradiation in synthetic wastewater containing the dye. The results indicated that Ag-Ag2O-ZnO/GO nanocomposite has a higher photocatalytic activity (90% removal) compared to Ag-Ag2O-ZnO (85% removal) and ZnO (75% removal) respectively and thus lends itself to application in water treatment, where the removal of organics is very important.

  12. Formation Mechanism and Characterization of Ag-Metal Chelate Polymer Prepared by a Wet Chemical Process

    NASA Astrophysics Data System (ADS)

    Huang, Chueh-Jung; Lin, Jiang-Jen; Shieu, Fuh-Sheng

    2005-08-01

    In this study, a metal chelate polymer (MCP) contained Ag(0) was prepared from commercial polyvinyl acetate (PVAc) and silver nitrate (AgNO3) by a wet chemical method using concentrate formic acid (HCOOH) as solvent. The characterization of these MCP materials, and the formation mechanism that involved in the MCP system, were studied by the analyses of Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), and field emission scanning electron microscopy (FESEM). The Ag(I) cations of silver nitrate (AgNO3) were found coordinated with polymer functional groups to form polymer-Ag(I) complexes. The XRD analysis revealed that these complexed Ag(I) ions were in-situ reduced to generate Ag(0) metal by HCOOH solvent in MCP system. The results of FTIR and NMR analyses demonstrated that there are hydrolyzed hydroxyl groups present in the MCP chains. The XPS analysis showed that the oxygen ligands that interacted with the Ag(0) were mostly contributed from the OH groups. The interaction between the reduced Ag(0) metal and the polymer chains was confirmed by transmission electron microscopy (TEM) investigation on the MCP materials.

  13. Surface Degradation of Ag/W Circuit Breaker Contacts During Standardized UL Testing

    NASA Astrophysics Data System (ADS)

    Yu, Haibo; Sun, Yu; Kesim, M. Tumerkan; Harmon, Jason; Potter, Jonathan; Alpay, S. Pamir; Aindow, Mark

    2015-09-01

    The near-surface microstructure of Ag/W contacts from 120 V, 30 A commercial circuit breakers in the as-manufactured condition and after standardized UL overload/temperature-rise, endurance, and short-circuit testing have been investigated using a combination of x-ray diffraction, scanning electron microscopy, energy-dispersive x-ray spectroscopy, focused ion beam milling, and transmission electron microscopy. The as-manufactured contacts comprised three constituents: sintered Ag/W composite particles with fine-grained Ag and coarse-grained W, coarse-grained pockets of Ag infiltrate, and a nano-crystalline surface Ag layer. There are also WO3 and Ag2O phases at the surface. After UL overload/temperature-rise testing, there is Ag loss giving a porous W-rich layer at the contact surface. In addition to binary oxides, we observe the formation of Ag2WO4. After UL endurance testing, material is swept across the surface by the breaker action giving a W-rich eroded porous surface on one side and a build-up of mixed oxides on the other. After UL short-circuit testing, a W crust forms due to melting and re-solidification of W and vaporization of Ag, and mid-plane cracks form due to the severe thermal gradients. There is a strong correlation between the observed microstructural features and the contact resistance measurements obtained from these samples.

  14. 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.

  15. [A STUDY OF THE ISOLATED BACTERIOPHAGE ΦAB-SP7 ADSORPTION ON THE CELL SURFACE OF THE AZOSPIRILLUM BRASILENSE SP7].

    PubMed

    Guliy, O I; Karavaeva, O A; Velikov, V A; Sokolov, O I; Pavily, S A; Larionova, O S; Burov, A M; Ignatov, O V

    2016-01-01

    The bacteriophage ΦAb-Sp7 was isolated from the cells of the Azospirillum brasilense Sp7. The morphology, size of the gram-negative colonies, and range of lytic activity against other strains and species of the genus Azospirillum was tested. The isolated phage DNA was examined using electrophoretic and restriction analysis, and the size of the genome were established. The electron microscopy. resuIts show that the phage (capsid) has a strand-like form. The electron microscopy study of the bacteriophage ΦAb-Sp7 adsorption on the A. brasilense Sp7 bacterial surface was performed. PMID:27145602

  16. [A STUDY OF THE ISOLATED BACTERIOPHAGE ΦAB-SP7 ADSORPTION ON THE CELL SURFACE OF THE AZOSPIRILLUM BRASILENSE SP7].

    PubMed

    Guliy, O I; Karavaeva, O A; Velikov, V A; Sokolov, O I; Pavily, S A; Larionova, O S; Burov, A M; Ignatov, O V

    2016-01-01

    The bacteriophage ΦAb-Sp7 was isolated from the cells of the Azospirillum brasilense Sp7. The morphology, size of the gram-negative colonies, and range of lytic activity against other strains and species of the genus Azospirillum was tested. The isolated phage DNA was examined using electrophoretic and restriction analysis, and the size of the genome were established. The electron microscopy. resuIts show that the phage (capsid) has a strand-like form. The electron microscopy study of the bacteriophage ΦAb-Sp7 adsorption on the A. brasilense Sp7 bacterial surface was performed.

  17. Hierarchical Ag/ZnO micro/nanostructure: Green synthesis and enhanced photocatalytic performance

    SciTech Connect

    Gao, Shuyan; Jia, Xiaoxia; Yang, Shuxia; Li, Zhengdao; Jiang, Kai

    2011-04-15

    Ag/ZnO metal-semiconductor nanocomposites with hierarchical micro/nanostructure have been prepared by the hydrothermal synthesis in the presence of bovine serum albumin (BSA). The results suggest that this biomolecule-assisted hydrothermal method is an efficient route for the fabrication of Ag/ZnO nanocomposites by using BSA both a shape controller and a reducing agent of Ag{sup +} ions. Moreover, Ag nanoparticles on the ZnO act as electron sinks, improving the separation of photogenerated electrons and holes, increasing the surface hydroxyl contents of ZnO, facilitating trapping the photoinduced electrons and holes to form more active hydroxyl radicals, and thus, enhancing the photocatalytic efficiency of ZnO. This is a good example for the organic combination of green chemistry and functional materials. -- Graphical Abstract: A green strategy is report to construct Ag/ZnO metal-semiconductor nanocomposites with hierarchical micro/nanostructure and enhanced photocatalytic activity. Display Omitted Research highlights: > Hierarchical micro/nanostructured Ag/ZnO nanocomposites have been prepared via a green route. > Ag nanoparticles improve the separation of photogenerated electrons and holes. > This facilitates trapping the photoinduced electrons and holes to form more hydroxyl radicals. Therefore, it enhances the photocatalytic efficiency of ZnO.

  18. 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.

  19. "Smart" Ag Nanostructures for Plasmon-Enhanced Spectroscopies.

    PubMed

    Li, Chao-Yu; Meng, Meng; Huang, Sheng-Chao; Li, Lei; Huang, Shao-Rong; Chen, Shu; Meng, Ling-Yan; Panneerselvam, Rajapandiyan; Zhang, San-Jun; Ren, Bin; Yang, Zhi-Lin; Li, Jian-Feng; Tian, Zhong-Qun

    2015-11-01

    Silver is an ideal candidate for surface plasmon resonance (SPR)-based applications because of its great optical cross-section in the visible region. However, the uses of Ag in plasmon-enhanced spectroscopies have been limited due to their interference via direct contact with analytes, the poor chemical stability, and the Ag(+) release phenomenon. Herein, we report a facile chemical method to prepare shell-isolated Ag nanoparticle/tip. The as-prepared nanostructures exhibit an excellent chemical stability and plasmonic property in plasmon-enhanced spectroscopies for more than one year. It also features an alternative plasmon-mediated photocatalysis pathway by smartly blocking "hot" electrons. Astonishingly, the shell-isolated Ag nanoparticles (Ag SHINs), as "smart plasmonic dusts", reveal a ∼1000-fold ensemble enhancement of rhodamine isothiocyanate (RITC) on a quartz substrate in surface-enhanced fluorescence. The presented "smart" Ag nanostructures offer a unique way for the promotion of ultrahigh sensitivity and reliability in plasmon-enhanced spectroscopies.

  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. Pressureless Bonding Using Sputtered Ag Thin Films

    NASA Astrophysics Data System (ADS)

    Oh, Chulmin; Nagao, Shijo; Suganuma, Katsuaki

    2014-12-01

    To improve the performance and reliability of power electronic devices, particularly those built around next-generation wide-bandgap semiconductors such as SiC and GaN, the bonding method used for packaging must change from soldering to solderless technology. Because traditional solders are problematic in the harsh operating conditions expected for emerging high-temperature power devices, we propose a new bonding method in this paper, namely a pressureless, low-temperature bonding process in air, using abnormal grain growth on sputtered Ag thin films to realize extremely high temperature resistance. To investigate the mechanisms of this bonding process, we characterized the microstructural changes in the Ag films over various bonding temperatures and times. We measured the bonding properties of the specimens by a die-shear strength test, as well as by x-ray diffraction measurements of the residual stress in the Ag films to show how the microstructural developments were essential to the bonding technology. Sound bonds with high die strength can be achieved only with abnormal grain growth at optimum bonding temperature and time. Pressureless bonding allows for production of reliable high-temperature power devices for a wide variety of industrial, energy, and environmental applications.

  2. Fabrication of Ag/CPs composite material, an effective strategy to improve the photocatalytic performance of coordination polymers under visible irradiation.

    PubMed

    Xu, Xinxin; Cui, Zhongping; Qi, Ji; Liu, Xiaoxia

    2013-10-01

    To enhance the photocatalytic property of coordination polymers (CPs) in the visible light region, Ag loaded coordination polymer composite materials (Ag/CPs) were synthesized successfully through a photoreduction reaction of Ag(+) on the surface of CPs. Photoluminescence (PL) was used to investigate the separation of photogenerated electron-hole pairs and the results illustrated Ag/CPs display higher quantum yields than CPs. This can be attributed to the strong interactions between Ag nanorods and coordination polymers, which lead to electron-hole pair separation between Ag nanorods and CPs. The degradation of Rhodamine B (RhB) was investigated to study the photocatalytic activities. Ag/CPs exhibited excellent photocatalytic activity in the UV and visible light region, while CPs can only decompose RhB under the irradiation of UV light. Furthermore, Ag/CPs showed outstanding stability during degradation of RhB.

  3. 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.

  4. 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.

  5. Silver delafossite nitride, AgTaN{sub 2}?

    SciTech Connect

    Miura, Akira; Lowe, Michael; Leonard, Brian M.; Subban, Chinmayee V.; Masubuchi, Yuji; Kikkawa, Shinichi; Dronskowski, Richard; Hennig, Richard G.; Abruna, Hector D.; DiSalvo, Francis J.

    2011-01-15

    A new silver nitride, AgTaN{sub 2}, was synthesized from NaTaN{sub 2} by a cation-exchange reaction, using a AgNO{sub 3}-NH{sub 4}NO{sub 3} flux at 175 {sup o}C. Its crystal structure type is delafossite (R3-bar m) with hexagonal lattice parameters of a=3.141(3) A, c=18.81(2) A, in which silver is linearly coordinated to nitrogen. Energy dispersive X-ray analysis and combustion nitrogen/oxygen analysis gave a composition with atomic ratios of Ag:Ta:N:O as 1.0:1.2(1):2.1(1):0.77(4), which is somewhat Ta rich and indicates some oxide formation. The X-ray photoelectron spectroscopy analysis showed a Ta- and O-rich surface and transmission electron microscope observation exhibited aggregates of ca. 4-5 nm-sized particles on the surface, which are probably related to the composition deviation from a AgTaN{sub 2}. The lattice parameters of stoichiometric AgTaN{sub 2} calculated by density functional theory agree with the experimental ones, but the possibility of some oxygen incorporation and/or silver deficiency is not precluded. -- Graphical abstract: A delafossite silver nitride, AgTaN{sub 2}, was synthesized from NaTaN{sub 2} by a cation-exchange reaction using a AgNO{sub 3}-NH{sub 4}NO{sub 3} flux. It contains N-Ag-N linear bonding. Display Omitted

  6. Photocatalytic performance of Ag doped SnO2 nanoparticles modified with curcumin

    NASA Astrophysics Data System (ADS)

    Vignesh, K.; Hariharan, R.; Rajarajan, M.; Suganthi, A.

    2013-07-01

    Visible light active Ag doped SnO2 nanoparticles modified with curcumin (Cur-Ag-SnO2) have been prepared by a combined precipitation and chemical impregnation route. The optical properties, phase structures and morphologies of the as-prepared nanoparticles were characterized using UV-visible diffuse reflectance spectra (UV-vis-DRS), X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). The surface area was measured by Brunauer. Emmett. Teller (B.E.T) analysis. Compared to bare SnO2, the surface modified photocatalysts (Ag-SnO2 and Cur-Ag-SnO2) showed a red shift in the visible region. The photocatalytic activity was monitored via the degradation of rose bengal (RB) dye and the results revealed that Cur-Ag-SnO2 shows better photocatalytic activity than that of Ag-SnO2 and SnO2. The superior photocatalytic activity of Cur-Ag-SnO2 could be attributed to the effective electron-hole separation by surface modification. The effect of photocatalyst concentration, initial dye concentration and electron scavenger on the photocatalytic activity was examined in detail. Furthermore, the antifungal activity of the photocatalysts and the reusability of Cur-Ag-SnO2 were tested.

  7. Hydroxyapatite supported Ag3PO4 nanoparticles with higher visible light photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Hong, Xiaoting; Wu, Xiaohui; Zhang, Qiuyun; Xiao, Mingfeng; Yang, Gelin; Qiu, Meirong; Han, Guocheng

    2012-03-01

    Hydroxyapatite supported Ag3PO4 nanocomposites have been synthesized by a wet impregnation process. UV-vis absorption spectra show a red shift of the absorption edges for the composite systems compared to pure hydroxyapatite support. The surface structure and morphology of the nanocomposites were characterized by Brunauer-Emmett-Teller (BET) apparatus, X-ray diffraction (XRD), transmission electron microscopy (TEM). The results suggest that Ag3PO4 nanoparticles (6-17 nm in diameter) are well dispersed on the hydroxyapatite support and Ag3PO4 nanoparticles density is larger for the higher Ag+ loading sample. The as-prepared nanocomposite photocatalysts showed a pronounced photocatalytic activity upon decomposition of methylene blue dye in aqueous solution under both visible light (wavelength > 400 nm) and UV-vis light irradiation. A synergic mechanism of inherent photocatalytic capability of Ag3PO4 and the accelerated electron/hole separation resulting from the photoinduced electrons captured by the slow-released Ag+ at the interface of Ag3PO4 and hydroxyapatite is proposed for the nanocomposites on the enhancement of photocatalytic performance in comparison to that of pure Ag3PO4 nanoparticles. The support of hydroxyapatite may also act as an absorbent which favors the mass transfer in heterogeneous photocatalysis reaction.

  8. Ag/TiO{sub 2} nanofiber heterostructures: Highly enhanced photocatalysts under visible light

    SciTech Connect

    Wang Yuan; Liu Lixin; Xu Liang; Meng Chuanmin; Zhu Wenjun

    2013-05-07

    Photocatalysis of TiO{sub 2} has recently drawn considerable attention, while the photoefficiency of TiO{sub 2} is limited by its large band-gap energy and usually fast electron-hole recombination. Here, we present an unconventional heterostructure of Ag nanoparticles modified TiO{sub 2} nanofibers synthesized by one-step electrospinning process, to improve the photoefficiency of TiO{sub 2} host. The efficient promotion of the visible light photocatalysis of Ag/TiO{sub 2} nanofiber heterostructures can be ascribed to the electronic excitation of Ag nanoparticles under visible light and the transfer of the electrons to TiO{sub 2} conduction band, which deeply depends on the number of Ag/TiO{sub 2} junctions and the height of Schottky barrier. The Ag/Ti molar ratio can be easily controlled by the electrospinning process and the Ag/TiO{sub 2} nanofibers with Ag/Ti molar ratio of 0.05 exhibit the highest photocatalytic activity. Simultaneously, the Ag/TiO{sub 2} nanofiber heterostructures show excellent photocatalytic stability.

  9. A density functional study of small sized silver-doped silicon clusters: Ag2Sin (n = 1-13)

    NASA Astrophysics Data System (ADS)

    Yang, Cai; Hao Jia, Song; Ma, Mao Fen; Zhang, Shuai; Lu, Cheng; Li, Gen Quan

    2015-11-01

    The structures and electronic properties for global minimum geometric structures of small-sized neutral Ag2Sin (n = 1-13) clusters have been investigated using the CALYPSO structure searching method coupled with density functional theory calculations. A great deal of low-energy geometric isomers are optimised at the B3LYP / GENECP theory level. The optimised structures suggest that the ground state Ag2Sin clusters are visibly distorted compared with the corresponding pure silicon clusters and favor a three-dimensional configuration. Starting with Ag2Si12, one Ag atom is fully encapsulated by the Si outer cages. Based on the averaged binding energy, fragmentation energy, second-order energy difference and HOMO-LUMO energy gap, it is seen that Ag2Si2 and Ag2Si5 are tested to be the most stable clusters, and the chemical stabilities of pure Sin+2 clusters can be reduced to some extent after doping two Ag atoms. Additionally, natural population and natural electronic configuration are discussed and the results reveal that charges transfer from the Ag atoms to the silicon frames and the spd hybridisations are present in all Ag2Sin clusters. Lastly, the results of natural bonds show that the Ag-Si bond in Ag2Sin clusters is dominated by small ionic character. Supplementary material in the form of one pdf file available from the Journal web page at http://dx.doi.org/10.1140/epjd/e2015-60404-1

  10. Synthesis, characterization and multifunctional properties of plasmonic Ag-TiO2 nanocomposites.

    PubMed

    Prakash, Jai; Kumar, Promod; Harris, R A; Swart, Chantel; Neethling, J H; van Vuuren, A Janse; Swart, H C

    2016-09-01

    We report on the synthesis of multifunctional Ag-TiO2 nanocomposites and their optical, physio-chemical, surface enhanced Raman scattering (SERS) and antibacterial properties. A series of Ag-TiO2 nanocomposites were synthesized by sol-gel technique and characterized by x-ray diffraction, scanning and transmission electron microscopy, energy-dispersed x-ray analysis, photoluminescence, UV-vis, x-ray photoelectron and Raman spectroscopy and Brunauer-Emmett-Teller method. The Ag nanoparticles (NPs) (7-20 nm) were found to be uniformly distributed around and strongly attached to TiO2 NPs. The novel optical responses of the nanocomposites are due to the strong electric field from the localized surface plasmon (LSP) excitation of the Ag NPs and decreased recombination of photo-induced electrons and holes at Ag-TiO2 interface providing potential materials for photocatalysis. The nanocomposites show enhancement in the SERS signals of methyl orange (MO) molecules with increasing Ag content attributed to the long-range electromagnetic enhancement from the excited LSP of the Ag NPs. To further understand the SERS activity, molecular mechanics and molecular dynamics simulations were used to study the geometries and SERS enhancement of MO adsorbed onto Ag-TiO2 respectively. Simulation results indicate that number of ligands (MO) that adsorb onto the Ag NPs as well as binding energy per ligand increases with increasing NP density and molecule-to-surface orientation is mainly flat resulting in strong bond strength between MO and Ag NP surface and enhanced SERS signals. The antimicrobial activity of the Ag-TiO2 nanocomposites was tested against the bacterium Staphylococcus aureus and enhanced antibacterial effect was observed with increasing Ag content explained by contact killing action mechanism. These results foresee promising applications of the plasmonic metal-semiconductor based nano-biocomposites for both chemical and biological samples. PMID:27456278

  11. Synthesis, characterization and multifunctional properties of plasmonic Ag-TiO2 nanocomposites

    NASA Astrophysics Data System (ADS)

    Prakash, Jai; Kumar, Promod; Harris, R. A.; Swart, Chantel; Neethling, J. H.; Janse van Vuuren, A.; Swart, H. C.

    2016-09-01

    We report on the synthesis of multifunctional Ag-TiO2 nanocomposites and their optical, physio-chemical, surface enhanced Raman scattering (SERS) and antibacterial properties. A series of Ag-TiO2 nanocomposites were synthesized by sol-gel technique and characterized by x-ray diffraction, scanning and transmission electron microscopy, energy-dispersed x-ray analysis, photoluminescence, UV-vis, x-ray photoelectron and Raman spectroscopy and Brunauer-Emmett-Teller method. The Ag nanoparticles (NPs) (7-20 nm) were found to be uniformly distributed around and strongly attached to TiO2 NPs. The novel optical responses of the nanocomposites are due to the strong electric field from the localized surface plasmon (LSP) excitation of the Ag NPs and decreased recombination of photo-induced electrons and holes at Ag-TiO2 interface providing potential materials for photocatalysis. The nanocomposites show enhancement in the SERS signals of methyl orange (MO) molecules with increasing Ag content attributed to the long-range electromagnetic enhancement from the excited LSP of the Ag NPs. To further understand the SERS activity, molecular mechanics and molecular dynamics simulations were used to study the geometries and SERS enhancement of MO adsorbed onto Ag-TiO2 respectively. Simulation results indicate that number of ligands (MO) that adsorb onto the Ag NPs as well as binding energy per ligand increases with increasing NP density and molecule-to-surface orientation is mainly flat resulting in strong bond strength between MO and Ag NP surface and enhanced SERS signals. The antimicrobial activity of the Ag-TiO2 nanocomposites was tested against the bacterium Staphylococcus aureus and enhanced antibacterial effect was observed with increasing Ag content explained by contact killing action mechanism. These results foresee promising applications of the plasmonic metal-semiconductor based nano-biocomposites for both chemical and biological samples.

  12. Synthesis, characterization and multifunctional properties of plasmonic Ag-TiO2 nanocomposites.

    PubMed

    Prakash, Jai; Kumar, Promod; Harris, R A; Swart, Chantel; Neethling, J H; van Vuuren, A Janse; Swart, H C

    2016-09-01

    We report on the synthesis of multifunctional Ag-TiO2 nanocomposites and their optical, physio-chemical, surface enhanced Raman scattering (SERS) and antibacterial properties. A series of Ag-TiO2 nanocomposites were synthesized by sol-gel technique and characterized by x-ray diffraction, scanning and transmission electron microscopy, energy-dispersed x-ray analysis, photoluminescence, UV-vis, x-ray photoelectron and Raman spectroscopy and Brunauer-Emmett-Teller method. The Ag nanoparticles (NPs) (7-20 nm) were found to be uniformly distributed around and strongly attached to TiO2 NPs. The novel optical responses of the nanocomposites are due to the strong electric field from the localized surface plasmon (LSP) excitation of the Ag NPs and decreased recombination of photo-induced electrons and holes at Ag-TiO2 interface providing potential materials for photocatalysis. The nanocomposites show enhancement in the SERS signals of methyl orange (MO) molecules with increasing Ag content attributed to the long-range electromagnetic enhancement from the excited LSP of the Ag NPs. To further understand the SERS activity, molecular mechanics and molecular dynamics simulations were used to study the geometries and SERS enhancement of MO adsorbed onto Ag-TiO2 respectively. Simulation results indicate that number of ligands (MO) that adsorb onto the Ag NPs as well as binding energy per ligand increases with increasing NP density and molecule-to-surface orientation is mainly flat resulting in strong bond strength between MO and Ag NP surface and enhanced SERS signals. The antimicrobial activity of the Ag-TiO2 nanocomposites was tested against the bacterium Staphylococcus aureus and enhanced antibacterial effect was observed with increasing Ag content explained by contact killing action mechanism. These results foresee promising applications of the plasmonic metal-semiconductor based nano-biocomposites for both chemical and biological samples.

  13. Highly luminescent material based on Alq3:Ag nanoparticles.

    PubMed

    Salah, Numan; Habib, Sami S; Khan, Zishan H

    2013-09-01

    Tris (8-hydroxyquinoline) aluminum (Alq3) is an organic semiconductor molecule, widely used as an electron transport layer, light emitting layer in organic light-emitting diodes and a host for fluorescent and phosphorescent dyes. In this work thin films of pure and silver (Ag), cupper (Cu), terbium (Tb) doped Alq3 nanoparticles were synthesized using the physical vapor condensation method. They were fabricated on glass substrates and characterized by X-ray diffraction, scanning electron microscope (SEM), energy dispersive spectroscopy, atomic force microscope (AFM), UV-visible absorption spectra and studied for their photoluminescence (PL) properties. SEM and AFM results show spherical nanoparticles with size around 70-80 nm. These nanoparticles have almost equal sizes and a homogeneous size distribution. The maximum absorption of Alq3 nanoparticles is observed at 300 nm, while the surface plasmon resonant band of Ag doped sample appears at 450 nm. The PL emission spectra of Tb, Cu and Ag doped Alq3 nanoparticles show a single broad band at around 515 nm, which is similar to that of the pure one, but with enhanced PL intensity. The sample doped with Ag at a concentration ratio of Alq3:Ag = 1:0.8 is found to have the highest PL intensity, which is around 2 times stronger than that of the pure one. This enhancement could be attributed to the surface plasmon resonance of Ag ions that might have increased the absorption and then the quantum yield. These remarkable result suggest that Alq3 nanoparticles incorporated with Ag ions might be quite useful for future nano-optoelectronic devices. PMID:23653126

  14. Localised Ag(+) vibrations at the origin of ultralow thermal conductivity in layered thermoelectric AgCrSe2.

    PubMed

    Damay, F; Petit, S; Rols, S; Braendlein, M; Daou, R; Elkaïm, E; Fauth, F; Gascoin, F; Martin, C; Maignan, A

    2016-01-01

    In materials science, the substructure approach consists in imagining complex materials in which a particular property is associated with a distinct structural feature, so as to combine different chosen physical characteristics, which otherwise have little chance to coexist. Applied to thermoelectric materials, it has been used to achieve simultaneously phonon-glass and electron-crystal properties. Mostly studied for its superionic conductivity, AgCrSe2 is a naturally layered compound, which achieves very low thermal conductivity, ~0.4 W.K(-1).m(-1) at RT (room temperature), and is considered a promising thermoelectric. The Cr atoms of the [CrSe2]∞ layer bear a spin S = 3/2, which orders below TN = 55 K. Here we report low temperature inelastic neutron scattering experiments on AgCrSe2, alongside the magnetic field evolution of its thermal and electrical transport. We observe a very low frequency mode at 3 meV, ascribed to large anharmonic displacements of the Ag(+) ions in the [Ag]∞ layer, and 2D magnetic fluctuations up to 3 TN in the chromium layer. The low thermal conductivity of AgCrSe2 is attributed to acoustic phonon scattering by a regular lattice of Ag(+) oscillating in quasi-2D potential wells. These findings highlight a new way to achieve localised phonon modes in a perfectly crystalline solid. PMID:27000414

  15. Localised Ag+ vibrations at the origin of ultralow thermal conductivity in layered thermoelectric AgCrSe2

    PubMed Central

    Damay, F.; Petit, S.; Rols, S.; Braendlein, M.; Daou, R.; Elkaïm, E.; Fauth, F.; Gascoin, F.; Martin, C.; Maignan, A.

    2016-01-01

    In materials science, the substructure approach consists in imagining complex materials in which a particular property is associated with a distinct structural feature, so as to combine different chosen physical characteristics, which otherwise have little chance to coexist. Applied to thermoelectric materials, it has been used to achieve simultaneously phonon-glass and electron-crystal properties. Mostly studied for its superionic conductivity, AgCrSe2 is a naturally layered compound, which achieves very low thermal conductivity, ~0.4 W.K−1.m−1 at RT (room temperature), and is considered a promising thermoelectric. The Cr atoms of the [CrSe2]∞ layer bear a spin S = 3/2, which orders below TN = 55 K. Here we report low temperature inelastic neutron scattering experiments on AgCrSe2, alongside the magnetic field evolution of its thermal and electrical transport. We observe a very low frequency mode at 3 meV, ascribed to large anharmonic displacements of the Ag+ ions in the [Ag]∞ layer, and 2D magnetic fluctuations up to 3 TN in the chromium layer. The low thermal conductivity of AgCrSe2 is attributed to acoustic phonon scattering by a regular lattice of Ag+ oscillating in quasi-2D potential wells. These findings highlight a new way to achieve localised phonon modes in a perfectly crystalline solid. PMID:27000414

  16. Localised Ag+ vibrations at the origin of ultralow thermal conductivity in layered thermoelectric AgCrSe2

    NASA Astrophysics Data System (ADS)

    Damay, F.; Petit, S.; Rols, S.; Braendlein, M.; Daou, R.; Elkaïm, E.; Fauth, F.; Gascoin, F.; Martin, C.; Maignan, A.

    2016-03-01

    In materials science, the substructure approach consists in imagining complex materials in which a particular property is associated with a distinct structural feature, so as to combine different chosen physical characteristics, which otherwise have little chance to coexist. Applied to thermoelectric materials, it has been used to achieve simultaneously phonon-glass and electron-crystal properties. Mostly studied for its superionic conductivity, AgCrSe2 is a naturally layered compound, which achieves very low thermal conductivity, ~0.4 W.K‑1.m‑1 at RT (room temperature), and is considered a promising thermoelectric. The Cr atoms of the [CrSe2]∞ layer bear a spin S = 3/2, which orders below TN = 55 K. Here we report low temperature inelastic neutron scattering experiments on AgCrSe2, alongside the magnetic field evolution of its thermal and electrical transport. We observe a very low frequency mode at 3 meV, ascribed to large anharmonic displacements of the Ag+ ions in the [Ag]∞ layer, and 2D magnetic fluctuations up to 3 TN in the chromium layer. The low thermal conductivity of AgCrSe2 is attributed to acoustic phonon scattering by a regular lattice of Ag+ oscillating in quasi-2D potential wells. These findings highlight a new way to achieve localised phonon modes in a perfectly crystalline solid.

  17. Organic pollutant photodecomposition by Ag/KNbO3 nanocomposites: A combined experimental and theoretical study

    DOE PAGES

    Zhang, Tingting; Liu, Ping; Lei, Wanying; Rodriguez, J. A.; Yu, Jiaguo; Qi, Yang; Liu, Gang; Liu, Minghua

    2016-01-12

    In this study, Ag nanoparticles supported on well-defined perovskite orthorhombic KNbO3 nanowires are synthesized via facile photoreduction and systematically characterized by XRD, Raman, DRUV–vis, XPS, PL, TEM, HRTEM, and HAADF-STEM. The photoreactivity of Ag/KNbO3 nanocomposites as a function of Ag contents (0.4–2.8 wt %) is assessed toward aqueous rhodamine B degradation under UV- and visible-light, respectively. It is found that the UV-induced photoreactivity initially increases and then decreases with increasing Ag contents. At an optimal Ag content (ca. 1.7 wt %), the greatest photoreactivity is achieved under UV light, with the photocatalytic reaction rate of 1.7 wt % Ag/KNbO3 exceedingmore » that of pristine KNbO3 by a factor of ca. 13. In contrast, visible light-induced photoreactivity monotonically increases with increasing Ag contents in the range of 0.4–2.8 wt %. On the basis of the detected active species and intermediate products in the photocatalytic processes, conjugated structure cleavage and N-deethylation are revealed to be the respective predominant pathway under UV and visible-light illumination. To gain an insight into the observed photoreactivity, the electronic properties of Ag/KNbO3 have been investigated using spin-polarized DFT calculations. Herein, Ag extended adlayers (1–4 ML) on the slab models of KNbO3 (101) are employed to mimic large supported Ag nanoparticles. A Bader analysis of the electron density shows a small net charge transfer (ca. 0.1 e) from KNbO3 to Ag. The electron localization function of Ag/KNbO3 (101) illustrates that Ag adlayers with thickness larger than 2 ML are essentially metallic, and weak polarization occurs at the interface. In addition, the metallic Ag adlayers generate a continuum of Ag bandgap states, which play a key role in determining different Ag content-dependent behavior between UV and visible-light illumination.« less

  18. Investigation of surface-plasmon coupled red light emitting InGaN/GaN multi-quantum well with Ag nanostructures coated on GaN surface

    SciTech Connect

    Li, Yi; Liu, Bin E-mail: rzhang@nju.edu.cn; Zhang, Rong E-mail: rzhang@nju.edu.cn; Xie, Zili; Zhuang, Zhe; Dai, JiangPing; Tao, Tao; Zhi, Ting; Zhang, Guogang; Chen, Peng; Ren, Fangfang; Zhao, Hong; Zheng, Youdou

    2015-04-21

    Surface-plasmon (SP) coupled red light emitting InGaN/GaN multiple quantum well (MQW) structure is fabricated and investigated. The centre wavelength of 5-period InGaN/GaN MQW structure is about 620 nm. The intensity of photoluminescence (PL) for InGaN QW with naked Ag nano-structures (NS) is only slightly increased due to the oxidation of Ag NS as compared to that for the InGaN QW. However, InGaN QW with Ag NS/SiO{sub 2} structure can evidently enhance the emission efficiency due to the elimination of surface oxide layer of Ag NS. With increasing the laser excitation power, the PL intensity is enhanced by 25%–53% as compared to that for the SiO{sub 2} coating InGaN QW. The steady-state electric field distribution obtained by the three-dimensional finite-difference time-domain method is different for both structures. The proportion of the field distributed in the Ag NS for the GaN/Ag NS/SiO{sub 2} structure is smaller as compared to that for the GaN/naked Ag NS structure. As a result, the energy loss of localized SP modes for the GaN/naked Ag NS structure will be larger due to the absorption of Ag layer.

  19. 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. PMID:24457172

  20. Ag nanowire percolating network embedded in indium tin oxide nanoparticles for printable transparent conducting electrodes

    SciTech Connect

    Jeong, Jin-A; Kim, Han-Ki

    2014-02-17

    Solution-based printable transparent conducting electrodes consisting of Ag nanowire (NW) and indium tin oxide (ITO) nanoparticles (NPs) were fabricated by simple brush painting at room temperature under atmospheric ambient conditions. Effectively embedding the Ag NW percolating network into the ITO NPs provided a conduction path, led to a metallic conduction behavior of the ITO NPs/Ag NW/ITO NPs multilayer and supplied electrons into the ITO NPs. The optimized ITO NPs/Ag NW/ITO NPs multilayer showed a sheet resistance of 16.57 Ω/sq and an optical transparency of 79.50% without post annealing. Based on high resolution transmission electron microscope analysis, we investigated the microstructure and interface structure of the ITO NPs/Ag NW/ITO NPs multilayer electrodes and suggested a possible mechanism to explain the low resistivity of the multilayers.

  1. Ag44(SeR)30: A Hollow Cage Silver Cluster with Selenolate Protection.

    PubMed

    Chakraborty, Indranath; Kurashige, Wataru; Kanehira, Keita; Gell, Lars; Häkkinen, Hannu; Negishi, Yuichi; Pradeep, Thalappil

    2013-10-01

    Selenolate protected, stable and atomically precise, hollow silver cluster was synthesized using solid state as well as solution state routes. The optical absorption spectrum shows multiple and sharp features similar to the thiolated Ag44 cluster, Ag44(SR)30 whose experimental structure was reported recently. High-resolution electrospray ionization mass spectrometry (HRESI MS) shows well-defined molecular ion features with two, three, and four ions with isotopic resolution, due to Ag44(SePh)30. Additional characterization with diverse tools confirmed the composition. The closed-shell 18 electron superatom electronic structure, analogous to Ag44(SR)30 stabilizes the dodecahedral cage with a large HOMO-LUMO gap of 0.71 eV. The time-dependent density functional theory (TDDFT) prediction of the optical absorption spectrum, assuming the Ag44(SR)30 structure, matches the experimental data, confirming the structure.

  2. Synthesis of silver nanoparticles by solar irradiation of cell-free Bacillus amyloliquefaciens extracts and AgNO3.

    PubMed

    Wei, Xuetuan; Luo, Mingfang; Li, Wei; Yang, Liangrong; Liang, Xiangfeng; Xu, Lin; Kong, Peng; Liu, Huizhou

    2012-01-01

    Silver nanoparticles (AgNPs) were obtained by solar irradiation of cell-free extracts of Bacillusamyloliquefaciens and AgNO3. Light intensity, extract concentration, and NaCl addition influenced the synthesis of AgNPs. Under optimized conditions (solar intensity 70,000 lx, extract concentration 3 mg/mL, and NaCl content 2 mM), 98.23±0.06% of the Ag+ (1 mM) was reduced to AgNPs within 80 min, and the ζ-potential of AgNPs reached -70.84±0.66 mV. TEM (Transmission electron microscopy) and XRD (X-ray diffraction) analysis confirmed that circular and triangular crystalline AgNPs with mean diameter of 14.6 nm were synthesized. Since heat-inactivated extracts also mediated the formation of AgNPs, enzymatic reactions are likely not involved in AgNPs formation. A high absolute ζ-potential value of the AgNPs, possibly caused by interaction with proteins likely explains the high stability of AgNPs suspensions. AgNPs showed antimicrobial activity against Bacillussubtilis and Escherichiacoli in liquid and solid medium.

  3. H3P···AgI: generation by laser-ablation and characterization by rotational spectroscopy and ab initio calculations† †Electronic supplementary information (ESI) available: All underlying data are provided as electronic supplementary information accompanying this paper. See DOI: 10.1039/c6cp03512d Click here for additional data file. Click here for additional data file.

    PubMed Central

    Stephens, Susanna L.; Tew, David P.

    2016-01-01

    The new compound H3P···AgI has been synthesized in the gas phase by means of the reaction of laser-ablated silver metal with a pulse of gas consisting of a dilute mixture of ICF3 and PH3 in argon. Ground-state rotational spectra were detected and assigned for the two isotopologues H3P···107AgI and H3P···109AgI in their natural abundance by means of a chirped-pulse, Fourier-transform, microwave spectrometer. Both isotopologues exhibit rotational spectra of the symmetric-top type, analysis of which led to accurate values of the rotational constant B 0, the quartic centrifugal distortion constants D J and D JK, and the iodine nuclear quadrupole coupling constant χ aa(I) = eQq aa. Ab initio calculations at the explicitly-correlated level of theory CCSD(T)(F12*)/aug-cc-pVDZ confirmed that the atoms P···Ag–I lie on the C 3 axis in that order. The experimental rotational constants were interpreted to give the bond lengths r 0(P···Ag) = 2.3488(20) Å and r 0(Ag–I) = 2.5483(1) Å, in good agreement with the equilibrium lengths of 2.3387 Å and 2.5537 Å, respectively, obtained in the ab initio calculations. Measures of the strength of the interaction of PH3 and AgI (the dissociation energy D e for the process H3P···AgI = H3P + AgI and the intermolecular stretching force constant F P···Ag) are presented and are interpreted to show that the order of binding strength is H3P···HI < H3P···ICl < H3P···AgI for these metal-bonded molecules and their halogen-bonded and hydrogen-bonded analogues. PMID:27354204

  4. Enhancement in the excitonic spontaneous emission rates for Si nanocrystal multi-layers covered with thin films of Au, Ag, and Al.

    PubMed

    Estrin, Y; Rich, D H; Rozenfeld, N; Arad-Vosk, N; Ron, A; Sa'ar, A

    2015-10-30

    The enhancement in the spontaneous emission rate (SER) for Ag, Au, and Al films on multilayer Si nanocrystals (SiNCs) was probed with time-resolved cathodoluminescence (CL). The SiNCs were grown on Si(100) using plasma enhanced chemical vapor deposition. Electron-hole pairs were generated in the metal-covered SiNCs by injecting a pulsed high-energy electron beam through the thin metal films, which is found to be an ideal method of excitation for plasmonic quantum heterostructures and nanostructures that are opaque to laser or light excitation. Spatially, spectrally, and temporally resolved CL was used to measure the excitonic lifetime of the SiNCs in metal-covered and bare regions of the same samples. The observed enhancement in the SER for the metal-covered SiNCs, relative to the SER for the bare sample, is attributed to a coupling of the SiNC excitons with surface plasmon polaritons (SPPs) of the thin metal films. A maximum SER enhancement of ∼2.0, 1.4 and 1.2 was observed for the Ag, Au, and Al films, respectively, at a temperature of 55 K. The three chosen plasmonic metals of Ag, Au, and Al facilitate an interesting comparison of the exciton-SPP coupling for metal films that exhibit varying differences between the surface plasmon energy, ω(sp), and the SiNC excitonic emission energy. A modeling of the temperature dependence of the Purcell enhancement factor, Fp, was performed and included the temperature dependence of the dielectric properties of the metals. PMID:26436289

  5. Enhancement in the excitonic spontaneous emission rates for Si nanocrystal multi-layers covered with thin films of Au, Ag, and Al

    NASA Astrophysics Data System (ADS)

    Estrin, Y.; Rich, D. H.; Rozenfeld, N.; Arad-Vosk, N.; Ron, A.; Sa'ar, A.

    2015-10-01

    The enhancement in the spontaneous emission rate (SER) for Ag, Au, and Al films on multilayer Si nanocrystals (SiNCs) was probed with time-resolved cathodoluminescence (CL). The SiNCs were grown on Si(100) using plasma enhanced chemical vapor deposition. Electron-hole pairs were generated in the metal-covered SiNCs by injecting a pulsed high-energy electron beam through the thin metal films, which is found to be an ideal method of excitation for plasmonic quantum heterostructures and nanostructures that are opaque to laser or light excitation. Spatially, spectrally, and temporally resolved CL was used to measure the excitonic lifetime of the SiNCs in metal-covered and bare regions of the same samples. The observed enhancement in the SER for the metal-covered SiNCs, relative to the SER for the bare sample, is attributed to a coupling of the SiNC excitons with surface plasmon polaritons (SPPs) of the thin metal films. A maximum SER enhancement of ˜2.0, 1.4 and 1.2 was observed for the Ag, Au, and Al films, respectively, at a temperature of 55 K. The three chosen plasmonic metals of Ag, Au, and Al facilitate an interesting comparison of the exciton-SPP coupling for metal films that exhibit varying differences between the surface plasmon energy, ωsp, and the SiNC excitonic emission energy. A modeling of the temperature dependence of the Purcell enhancement factor, Fp, was performed and included the temperature dependence of the dielectric properties of the metals.

  6. Enhancement in the excitonic spontaneous emission rates for Si nanocrystal multi-layers covered with thin films of Au, Ag, and Al.

    PubMed

    Estrin, Y; Rich, D H; Rozenfeld, N; Arad-Vosk, N; Ron, A; Sa'ar, A

    2015-10-30

    The enhancement in the spontaneous emission rate (SER) for Ag, Au, and Al films on multilayer Si nanocrystals (SiNCs) was probed with time-resolved cathodoluminescence (CL). The SiNCs were grown on Si(100) using plasma enhanced chemical vapor deposition. Electron-hole pairs were generated in the metal-covered SiNCs by injecting a pulsed high-energy electron beam through the thin metal films, which is found to be an ideal method of excitation for plasmonic quantum heterostructures and nanostructures that are opaque to laser or light excitation. Spatially, spectrally, and temporally resolved CL was used to measure the excitonic lifetime of the SiNCs in metal-covered and bare regions of the same samples. The observed enhancement in the SER for the metal-covered SiNCs, relative to the SER for the bare sample, is attributed to a coupling of the SiNC excitons with surface plasmon polaritons (SPPs) of the thin metal films. A maximum SER enhancement of ∼2.0, 1.4 and 1.2 was observed for the Ag, Au, and Al films, respectively, at a temperature of 55 K. The three chosen plasmonic metals of Ag, Au, and Al facilitate an interesting comparison of the exciton-SPP coupling for metal films that exhibit varying differences between the surface plasmon energy, ω(sp), and the SiNC excitonic emission energy. A modeling of the temperature dependence of the Purcell enhancement factor, Fp, was performed and included the temperature dependence of the dielectric properties of the metals.

  7. Synthesis of spherical Ag/ZnO heterostructural composites with excellent photocatalytic activity under visible light and UV irradiation

    NASA Astrophysics Data System (ADS)

    Liu, Hairui; Hu, Yanchun; Zhang, Zhuxia; Liu, Xuguang; Jia, Husheng; Xu, Bingshe

    2015-11-01

    Ag nanoparticles (Ag-NPs) decorated ZnO microspheres (ZnO-MSs) heterostructural composites were fabricated via a two-step chemical method. The ZnO-MSs with the diameter about 700 nm was initially prepared by ultrasonic technology. Subsequently, Ag-NPs with a diameter of 20-50 nm were anchored onto the surface of the as-prepared ZnO-MSs by a microwave polyol process. The morphology, structural and optical properties of the as-synthesized materials were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and high resolution TEM (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-visible absorption spectroscopy, and photoluminescence spectroscopy. The results show that the surface plasmon absorption band of Ag/ZnO composites is distinctly broadened and the PL intensity of Ag/ZnO heterostructural composites varies with the increase of Ag loading. The photocatalytic activity of the Ag/ZnO composites were evaluated by the degradation of rhodamine B (RhB) solution under ultraviolet (UV) and visible light irradiation. The rate of degradation of the as-prepared Ag/ZnO composites was more than triple times faster than that of pure ZnO-MSs under UV light, which was ascribed to the formation of Schottky barriers in the regions between Ag-NPs and ZnO-MSs. Furthermore, Ag/ZnO composites exhibit superior photocatalytic activity over ZnO-MSs in the visible light region owing to the effective electron transfer from plasmon-excited Ag(0) nanoparticles to ZnO-MSs by strong localization of surface plasmon resonance (SPR). This can effectively decrease the recombination of electron-hole pairs, lead to a prolonged lifetime of the electron-holes pairs that promotes the degradation efficiency. The chemical stability and reusability of Ag/ZnO powders were also investigated.

  8. Annealing effect of ultrathin Ag films on Ni/Pt(111)

    SciTech Connect

    Su, C.W.; Yo, H.Y.; Chen, Y.J.; Shern, C.S.

    2005-06-15

    The epitaxial growth and alloy formation of Ag-capped layer on Ni/Pt(111) surface were investigated using Auger electron spectroscopy, ultraviolet photoelectron spectroscopy, and low-energy electron diffraction. The growth of Ag on one ML Ni/Pt(111) transforms from layer-by-layer mode into three-dimensional island mode after the growth of one atomic monolayer of Ag. The starting temperature for the alloy formation of Ni-Pt is dependent of the thickness of Ni films. The interface compositions after the high-temperature annealing were studied with the depth-profile analysis of Ar ion sputtering.

  9. Reversible modulated mid-infrared absorption of Ag/TiO{sub 2} by photoinduced interfacial charge transfer

    SciTech Connect

    Xu, S. C. E-mail: ghli@issp.ac.cn; Li, L.; Pan, S. S.; Luo, Y. Y.; Zhang, Y. X.; Li, G. H. E-mail: ghli@issp.ac.cn

    2014-10-06

    An enhanced mid-infrared absorption in Ag nanoparticles-decorated TiO{sub 2} microflowers was reported. It was found that the mid-infrared absorption of the Ag/TiO{sub 2} complex depends strongly on the content and size of Ag nanoparticles, the higher the Ag nanoparticles content, the stronger the infrared absorption. The average reflectivity in the entire mid-infrared region of the microflowers drops from 57.6% to 10.5% after Ag nanoparticles decoration. Reversible modulated mid-infrared absorption properties were found in the Ag/TiO{sub 2} complexes upon alternative illumination of visible and UV light due to the photoinduced interfacial electron transfer between TiO{sub 2} semiconductor and Ag nanoparticles.

  10. 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.

  11. Influence of size, shape and core–shell interface on surface plasmon resonance in Ag and Ag@MgO nanoparticle films deposited on Si/SiOx

    PubMed Central

    Pinotti, Daniele; Spadaro, Maria Chiara; Paolicelli, Guido; Grillo, Vincenzo; Valeri, Sergio; Pasquali, Luca; Bergamini, Luca; Corni, Stefano

    2015-01-01

    Summary Ag and Ag@MgO core–shell nanoparticles (NPs) with a diameter of d = 3–10 nm were obtained by physical synthesis methods and deposited on Si with its native ultrathin oxide layer SiOx (Si/SiOx). Scanning electron microscopy and transmission electron microscopy (TEM) images of bare Ag NPs revealed the presence of small NP aggregates caused by diffusion on the surface and agglomeration. Atomic resolution TEM gave evidence of the presence of crystalline multidomains in the NPs, which were due to aggregation and multitwinning occurring during NP growth in the nanocluster source. Co-deposition of Ag NPs and Mg atoms in an oxygen atmosphere gave rise to formation of a MgO shell matrix surrounding the Ag NPs. The behaviour of the surface plasmon resonance (SPR) excitation in surface differential reflectivity (SDR) spectra with p-polarised light was investigated for bare Ag and Ag@MgO NPs. It was shown that the presence of MgO around the Ag NPs caused a red shift of the plasmon excitation, and served to preserve its existence after prolonged (five months) exposure to air, realizing the possibility of technological applications in plasmonic devices. The Ag NP and Ag@MgO NP film features in the SDR spectra could be reproduced by classical electrodynamics simulations by treating the NP-containing layer as an effective Maxwell Garnett medium. The simulations gave results in agreement with the experiments when accounting for the experimentally observed aggregation. PMID:25821680

  12. How silicene on Ag(111) oxidizes: microscopic mechanism of the reaction of O2 with silicene

    NASA Astrophysics Data System (ADS)

    Morishita, Tetsuya; Spencer, Michelle J. S.

    2015-12-01

    We demonstrate, using first-principles molecular-dynamics simulations, that oxidation of silicene can easily take place either at low or high oxygen doses, which importantly helps clarify previous inconsistent reports on the oxidation of silicene on the Ag(111) substrate. We show that, while the energy barrier for an O2 molecule reacting with a Si atom strongly depends on the position and orientation of the molecule, the O2 molecule immediately dissociates and forms an Si-O-Si configuration once it finds a barrier-less chemisorption pathway around an outer Si atom of the silicene overlayer. A synergistic effect between the molecular dissociation and subsequent structural rearrangements is found to accelerate the oxidation process at a high oxygen dose. This effect also enhances self-organized formation of sp3-like tetrahedral configurations (consisting of Si and O atoms), which results in collapse of the two-dimensional silicene structure and its exfoliation from the substrate. We also find that the electronic properties of the silicene can be significantly altered by oxidation. The present findings suggest that low flux and low temperature of the oxygen gas are key to controlling oxidation of silicene.

  13. How silicene on Ag(111) oxidizes: microscopic mechanism of the reaction of O2 with silicene.

    PubMed

    Morishita, Tetsuya; Spencer, Michelle J S

    2015-12-03

    We demonstrate, using first-principles molecular-dynamics simulations, that oxidation of silicene can easily take place either at low or high oxygen doses, which importantly helps clarify previous inconsistent reports on the oxidation of silicene on the Ag(111) substrate. We show that, while the energy barrier for an O2 molecule reacting with a Si atom strongly depends on the position and orientation of the molecule, the O2 molecule immediately dissociates and forms an Si-O-Si configuration once it finds a barrier-less chemisorption pathway around an outer Si atom of the silicene overlayer. A synergistic effect between the molecular dissociation and subsequent structural rearrangements is found to accelerate the oxidation process at a high oxygen dose. This effect also enhances self-organized formation of sp(3)-like tetrahedral configurations (consisting of Si and O atoms), which results in collapse of the two-dimensional silicene structure and its exfoliation from the substrate. We also find that the electronic properties of the silicene can be significantly altered by oxidation. The present findings suggest that low flux and low temperature of the oxygen gas are key to controlling oxidation of silicene.

  14. How silicene on Ag(111) oxidizes: microscopic mechanism of the reaction of O2 with silicene

    PubMed Central

    Morishita, Tetsuya; Spencer, Michelle J.S.

    2015-01-01

    We demonstrate, using first-principles molecular-dynamics simulations, that oxidation of silicene can easily take place either at low or high oxygen doses, which importantly helps clarify previous inconsistent reports on the oxidation of silicene on the Ag(111) substrate. We show that, while the energy barrier for an O2 molecule reacting with a Si atom strongly depends on the position and orientation of the molecule, the O2 molecule immediately dissociates and forms an Si-O-Si configuration once it finds a barrier-less chemisorption pathway around an outer Si atom of the silicene overlayer. A synergistic effect between the molecular dissociation and subsequent structural rearrangements is found to accelerate the oxidation process at a high oxygen dose. This effect also enhances self-organized formation of sp3-like tetrahedral configurations (consisting of Si and O atoms), which results in collapse of the two-dimensional silicene structure and its exfoliation from the substrate. We also find that the electronic properties of the silicene can be significantly altered by oxidation. The present findings suggest that low flux and low temperature of the oxygen gas are key to controlling oxidation of silicene. PMID:26631577

  15. Coordination Chemistry of Diiodine and Implications for the Oxidation Capacity of the Synergistic Ag(+) /X2 (X=Cl, Br, I) System.

    PubMed

    Malinowski, Przemysław J; Himmel, Daniel; Krossing, Ingo

    2016-08-01

    The synergistic Ag(+) /X2 system (X=Cl, Br, I) is a very strong, but ill-defined oxidant-more powerful than X2 or Ag(+) alone. Intermediates for its action may include [Agm (X2 )n ](m+) complexes. Here, we report on an unexpectedly variable coordination chemistry of diiodine towards this direction: (A)Ag-I2 -Ag(A), [Ag2 (I2 )4 ](2+) (A(-) )2 and [Ag2 (I2 )6 ](2+) (A(-) )2 ⋅(I2 )x≈0.65 form by reaction of Ag(A) (A=Al(OR(F) )4 ; R(F) =C(CF3 )3 ) with diiodine (single crystal/powder XRD, Raman spectra and quantum-mechanical calculations). The molecular (A)Ag-I2 -Ag(A) is ideally set up to act as a 2 e(-) oxidant with stoichiometric formation of 2 AgI and 2 A(-) . Preliminary reactivity tests proved this (A)Ag-I2 -Ag(A) starting material to oxidize n-C5 H12 , C3 H8 , CH2 Cl2 , P4 or S8 at room temperature. A rough estimate of its electron affinity places it amongst very strong oxidizers like MF6 (M=4d metals). This suggests that (A)Ag-I2 -Ag(A) will serve as an easily in bulk accessible, well-defined, and very potent oxidant with multiple applications. PMID:27411163

  16. Formation of oxides and their role in the growth of Ag nanoplates on GaAs substrates.

    SciTech Connect

    Sun, Y.; Gosztola, D.; Lei, C.; Haasch, R.; Center for Nanoscale Materials; Univ. of Illinois

    2008-10-21

    Simple galvanic reactions between highly doped n-type GaAs wafers and a pure aqueous solution of AgNO3 at room temperature provide an easy and efficient protocol to directly deposit uniform Ag nanoplates with tunable dimensions on the GaAs substrates. The anisotropic growth of the Ag nanoplates in the absence of surfactant molecules might be partially ascribed to the codeposition of oxides of gallium and arsenic, which are revealed by extensive data from electron microscopy, X-ray photoelectron spectroscopy, and Raman spectroscopy, during the growth of the Ag nanoplates. The electron microscopic characterization shows that each Ag nanoplate has a 'necked' geometry, that is, it pins on the GaAs lattices through only a tiny neck (with sizes of <10 nm). In addition, the as-grown Ag nanoplates exhibit strong enhancement toward Raman scattering of materials on (or around) their surfaces.

  17. Study of Ag-Pd bimetallic nanoparticles modified glassy carbon electrode for detection of L-cysteine

    NASA Astrophysics Data System (ADS)

    Murugavelu, M.; Karthikeyan, B.

    2014-11-01

    Ag-Pd bimetallic nanoparticles (Ag-Pd BNPs) as an enhanced sensing material with improved electronic transmission rates in the electrochemical sensing of L-cysteine (L-cys) has been reported. The morphology of Ag-Pd BNPs was characterized with X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and cyclic voltammetry (CV). Oxidation of L-cys on Ag-Pd BNPs is investigated in detail by discussing the effect of the structure and from the electrocatalytic oxidation of L-cys. We found that the Ag-Pd BNPs exhibited high electrocatalytic activity towards L-cys oxidation in neutral condition and could be used for the development of nonenzymatic L-cys sensor. Based on the efficient catalytic ability of Ag-Pd BNPs, the fabricated biosensor exhibited a wide linear range of responses to the L-cys with the concentration detection limit of nearly down to 2 mM with fast response time.

  18. Photocatalysis using a Wide Range of the Visible Light Spectrum: Hydrogen Evolution from Doped AgGaS2.

    PubMed

    Yamato, Kohei; Iwase, Akihide; Kudo, Akihiko

    2015-09-01

    Doping of nickel into AgGaS2 yields a new absorption band, at a wavelength longer than the intrinsic absorption band of the AgGaS2 host. The doped nickel forms an electron donor level in a forbidden band of AgGaS2 . The nickel-doped AgGaS2 with rhodium co-catalyst shows photocatalytic activity for sacrificial H2 evolution under the light of up to 760 nm due to the transition from the electron donor level consisting of Ni(2+) to the conduction band of AgGaS2 . Apparent quantum yields for the sacrificial H2 evolution at 540-620 nm are about 1 %. Moreover, the nickel-doped AgGa0.75 In0.25 S2 also responds to near-IR light, up to 900 nm.

  19. Arthrobacter psychrophenolicus sp. nov., isolated from an alpine ice cave.

    PubMed

    Margesin, Rosa; Schumann, Peter; Spröer, Cathrin; Gounot, Anne-Monique

    2004-11-01

    On the basis of phenotypic, genotypic and chemotaxonomic characteristics, a novel species belonging to the genus Arthrobacter is described. A facultatively psychrophilic bacterium, strain AG31(T), was isolated from an alpine ice cave. The aerobic, Gram-positive, non-spore-forming, non-motile strain exhibited a rod-coccus growth cycle and produced a yellow pigment. Good growth and phenol biodegradation occurred at a temperature range of 1-25 degrees C. Up to 10 mM phenol was utilized as a sole carbon source. Glucose was not assimilated. Analysis of the 16S rRNA gene revealed that strain AG31(T) represents a distinct lineage within the genus Arthrobacter, being most closely related to Arthrobacter sulfureus. The level of DNA-DNA relatedness to the type strain of A. sulfureus was 29.9 %. Anteiso-C(15 : 0) was the predominant fatty acid (72 %). Strain AG31(T) exhibited A4alpha l-lys-l-Glu-type peptidoglycan and contained glucose as the only cell-wall sugar. MK-10 was the predominant menaquinone, and the polar lipid pattern consisted of phosphatidylglycerol, diphosphatidylglycerol, phosphatidylinositol and an unidentified glycolipid. Strain AG31(T) (=DSM 15454(T)=LMG 21914(T)) is assigned as the type strain of a novel Arthrobacter species, Arthrobacter psychrophenolicus sp. nov.

  20. Influence of size, shape and core-shell interface on surface plasmon resonance in Ag and Ag@MgO nanoparticle films deposited on Si/SiO x.

    PubMed

    D'Addato, Sergio; Pinotti, Daniele; Spadaro, Maria Chiara; Paolicelli, Guido; Grillo, Vincenzo; Valeri, Sergio; Pasquali, Luca; Bergamini, Luca; Corni, Stefano

    2015-01-01

    Ag and Ag@MgO core-shell nanoparticles (NPs) with a diameter of d = 3-10 nm were obtained by physical synthesis methods and deposited on Si with its native ultrathin oxide layer SiO x (Si/SiO x ). Scanning electron microscopy and transmission electron microscopy (TEM) images of bare Ag NPs revealed the presence of small NP aggregates caused by diffusion on the surface and agglomeration. Atomic resolution TEM gave evidence of the presence of crystalline multidomains in the NPs, which were due to aggregation and multitwinning occurring during NP growth in the nanocluster source. Co-deposition of Ag NPs and Mg atoms in an oxygen atmosphere gave rise to formation of a MgO shell matrix surrounding the Ag NPs. The behaviour of the surface plasmon resonance (SPR) excitation in surface differential reflectivity (SDR) spectra with p-polarised light was investigated for bare Ag and Ag@MgO NPs. It was shown that the presence of MgO around the Ag NPs caused a red shift of the plasmon excitation, and served to preserve its existence after prolonged (five months) exposure to air, realizing the possibility of technological applications in plasmonic devices. The Ag NP and Ag@MgO NP film features in the SDR spectra could be reproduced by classical electrodynamics simulations by treating the NP-containing layer as an effective Maxwell Garnett medium. The simulations gave results in agreement with the experiments when accounting for the experimentally observed aggregation.

  1. Local density of unoccupied states in ion-beam-mixed Pd-Ag alloys

    SciTech Connect

    Chae, K.H.; Jung, S.M.; Lee, Y.S.; Whang, C.N.; Jeon, Y.; Croft, M.; Sills, D.; Ansari, P.H.; Mack, K.

    1996-04-01

    X-ray absorption spectroscopy (XAS) measurements have been used to probe the electronic structure of ion-beam-mixed (IBM) Pd-Ag thin films with bulk alloys being studied for comparison. Pd {ital L}{sub 3} and Ag {ital L}{sub 3} absorption edges for pure Pd, Ag, and Pd{sub 1{minus}{ital x}}Ag{sub {ital x}} alloys are discussed. Structural information from both x-ray diffraction and the XAS fine structure oscillations are discussed. The observed decrease of the white-line feature strength, at the Pd {ital L}{sub 3} edge, indicates that the local density of unoccupied Pd 4{ital d} states declines upon alloying with Ag in a manner similar to that observed in previous bulk studies. However, while the Pd {ital d}-hole count decreases monotonically for bulk alloys, in the IBM alloys it saturates at higher levels in the Ag-rich materials. This disparity is interpreted on the basis of a modified charge transfer due to structural differences in the IBM alloys. The Ag {ital L}{sub 3} near-edge region is largely unchanged in these alloys, indicating that the charge transferred away from the Ag site is dominantly of {ital non}-{ital d} type. Our experimental results are discussed in the context of recent electronic structure calculations and of previous work on this alloy system. {copyright} {ital 1996 The American Physical Society.}

  2. Preparation and photocatalytic properties of AgI–SnO{sub 2} nano-composites

    SciTech Connect

    Wen, Biao; Wang, Xiao-Hui; Lu, Juan; Cao, Jia-Lei; Wang, Zuo-Shan

    2013-05-15

    Highlights: ► AgI–SnO{sub 2} nano-composites have been successfully synthesized. ► As-prepared AgI–SnO{sub 2} nano-composites own the excellent visible light photocatalytic activity. ► As-prepared AgI–SnO{sub 2} nano-composites own the excellent stability. - Abstract: AgI doped SnO{sub 2} nano-composites were prepared by the chemical coprecipitation method and were characterized by the X-ray diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy. Results showed that main of the I{sup −} ions remained in the AgI lattice which is highly dispersed in the system. The photo-catalytic experiments performed under visible light irradiation using methylene blue as the pollutant revealed that not only the photo-catalytic activity but also the stability of SnO{sub 2} based photocatalyst could be improved by introduction of an appropriate amount of AgI, and the result was further supported by the UV–Vis diffuse reflection spectra and the electron spin-resonance spectra. Among all of the samples, AgI–SnO{sub 2} nano-composite with 2At% AgI exhibited the best catalytic efficiency and stability.

  3. Oxygen reduction reaction on Cu-doped Ag cluster for fuel-cell cathode.

    PubMed

    Ma, Wenqiang; Chen, Fuyi; Zhang, Nan; Wu, Xiaoqiang

    2014-10-01

    The development of fuel cells as clean-energy technologies is largely limited by the prohibitive cost of the noble-metal catalysts needed for catalyzing the oxygen reduction reaction (ORR) in fuel cells. A fundamental understanding of catalyst design principle that links material structures to the catalytic activity can accelerate the search for highly active and abundant bimetallic catalysts to replace platinum. Here, we present a first-principles study of ORR on Ag12Cu cluster in alkaline environment. The adsorptions of O2, OOH, and OH on Cu-doped Ag13 are stronger than on Ag13. The d-band centers of adsorption sites show the Cu-doping makes d-electrons transferred to higher energy state, and improves O2 dissociation. ORR processes on Ag12Cu and Ag13 indicate Cu-doping can strongly promote ORR, and ORR process can be better preformed on Ag12Cu than on Ag13. For four-electron transfer, the effective reversible potential is 0.401 V/RHE on Ag12Cu in alkaline medium. PMID:25227449

  4. Enhanced Raman scattering and nonlinear conductivity in Ag-doped hollow ZnO microspheres

    NASA Astrophysics Data System (ADS)

    Tringe, Joseph W.; Levie, Harold W.; McCall, Scott K.; Teslich, Nick E.; Wall, Mark A.; Orme, Christine A.; Matthews, Manyalibo J.

    2012-10-01

    Hollow spherical ZnO particles doped with Ag were synthesized with a two-step oxidation and sublimation furnace annealing process. Ag nanoparticle precipitates, as observed by transmission electron microscopy, were present in the polycrystalline ZnO matrix at Ag concentrations below 0.02 mol%, significantly below the 0.8 mol% solubility limit for Ag in ZnO. Enhanced Raman scattering of ZnO phonon modes is observed, increasing with Ag nanoparticle concentration. A further enhancement in Raman scattering due to resonance effects was observed for LO phonons excited by 2.33-eV photons as compared with Raman scattering under 1.96-eV excitation. Room-temperature photoluminescence spectra showed both a near-band-edge emission due to free exciton transitions and a mid-gap transition due to the presence of singly ionized oxygen vacancies. ZnO:Ag particles were measured electrically in a packed column and in monolithic form, and in both cases displayed nonlinear current-voltage characteristics similar to those previously observed in sintered ZnO:Ag monoliths where Ag-enhanced disorder at grain boundaries is thought to control current transport. We demonstrate therefore that Ag simultaneously modifies the electrical and optical properties of ZnO particles through the introduction of vacancies and other defects.

  5. The IP6 micelle-stabilized small Ag cluster for synthesizing Ag-Au alloy nanoparticles and the tunable surface plasmon resonance effect

    NASA Astrophysics Data System (ADS)

    Wang, Na; Wen, Ying; Wang, Yao; Zhang, Rui; Chen, Xiyao; Ling, Bo; Huan, Shuangyan; Yang, Haifeng

    2012-04-01

    The stable small Ag seeds (size in diameter < 10 nm) were obtained in the presence of inositol hexakisphosphoric (IP6) micelles. Then Ag-Au bimetallic nanoparticles were synthesized through a replacement reaction with the rapid interdiffusion process between such small Ag seeds in nanoclusters and HAuCl4. Adjusting the dosage of HAuCl4 resulted in different products, which possessed unique surface plasmon resonances (SPR). The morphologies of the as-made nanoparticles were observed using transmission electron microscopy and field emission scanning electron microscopy and their compositions were determined by energy-dispersive x-ray spectroscopy. Among them, the Ag-Au alloy nanoparticles with the cauliflower-like structure had a suitable SPR for highly sensitive Raman detection application as a surface-enhanced Raman scattering (SERS) substrate with a long-term stability of six months.

  6. Bi2Sr2CaCu2O8 + x round wires with Ag/Al oxide dispersion strengthened sheaths: microstructure-properties relationships, enhanced mechanical behavior and reduced Cu depletion

    NASA Astrophysics Data System (ADS)

    Kajbafvala, Amir; Nachtrab, William; Wong, Terence; Schwartz, Justin

    2014-09-01

    Ag/Al alloys with various Al content (0.50 wt%, 0.75 wt%, 1.00 wt%, and 1.25 wt%) are made by powder metallurgy and used as the outer sheath material for Bi2Sr2CaCu2O8 + x (Bi2212)/Ag/AgAl multifilamentary round wires (RW). Bi2212/Ag/AgAl RW microstructural, mechanical and electrical properties are studied in various conditions, including as-drawn, after internal oxidation, and after partial melt processing (PMP). The results are compared with the behavior of a Bi2212/Ag/Ag0.20Mg wire of the same geometry. The grains in as-drawn Ag/Al alloys are found to be ˜25% smaller than those in the corresponding Ag/0.20 wt%Mg, but after PMP, the Ag/Al and Ag/0.20 wt%Mg grain sizes are comparable. Tensile tests show that Bi2212/Ag/AgAl green wires have yield strength (YS) of ˜115 MPa, nearly 65% higher than that of Bi2212/Ag/Ag0.20Mg. After PMP, the Bi2212/Ag/AgAl YS is about 35% greater than that of Bi2212/Ag/Ag0.20Mg. Furthermore, Bi2212/Ag/AgAl wires exhibit higher ultimate tensile strength and modulus and twice the elongation-to-failure. Atomic resolution high-angle annular dark-field scanning transmission electron microscopy, high resolution transmission electron microscopy and energy dispersive spectroscopy demonstrate the formation of nanosize MgO and Al2O3 precipitates via internal oxidation. Large spherical MgO precipitates are observed on the Ag grain boundaries of Ag/0.20 wt%Mg alloy, whereas the Al2O3 precipitates are distributed homogenously in the dispersion-strengthened (DS) Ag/Al alloy. Furthermore, it is found that less Cu diffused from the Bi2212 filaments in the Bi2212/Ag/Ag0.75Al wire during PMP than from the filaments in the Bi2212/Ag/Ag0.20Mg wire. These results show that DS Ag/Al alloy is a strong candidate for improved Bi2212 wire.

  7. Microwave-assisted hydrothermal synthesis of Ag2(W1 -xMox)O4 heterostructures: Nucleation of Ag, morphology, and photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Silva, M. D. P.; Gonçalves, R. F.; Nogueira, I. C.; Longo, V. M.; Mondoni, L.; Moron, M. G.; Santana, Y. V.; Longo, E.

    2016-01-01

    Ag2W1 -xMoxO4 (x = 0.0 and 0.50) powders were synthesized by the co-precipitation (drop-by-drop) method and processed using a microwave-assisted hydrothermal method. We report the real-time in situ formation and growth of Ag filaments on the Ag2W1 -xMoxO4 crystals using an accelerated electron beam under high vacuum. Various techniques were used to evaluate the influence of the network-former substitution on the structural and optical properties, including photoluminescence (PL) emission, of these materials. X-ray diffraction results confirmed the phases obtained by the synthesis methods. Raman spectroscopy revealed significant changes in local order-disorder as a function of the network-former substitution. Field-emission scanning electron microscopy was used to determine the shape as well as dimensions of the Ag2W1 -xMoxO4 heterostructures. The PL spectra showed that the PL-emission intensities of Ag2W1 -xMoxO4 were greater than those of pure Ag2WO4, probably because of the increase of intermediary energy levels within the band gap of the Ag2W1 -xMoxO4 heterostructures, as evidenced by the decrease in the band-gap values measured by ultraviolet-visible spectroscopy.

  8. Ag-plasma modification enhances bone apposition around titanium dental implants: an animal study in Labrador dogs.

    PubMed

    Qiao, Shichong; Cao, Huiliang; Zhao, Xu; Lo, Hueiwen; Zhuang, Longfei; Gu, Yingxin; Shi, Junyu; Liu, Xuanyong; Lai, Hongchang

    2015-01-01

    Dental implants with proper antibacterial ability as well as ideal osseointegration are being actively pursued. The antimicrobial ability of titanium implants can be significantly enhanced via modification with silver nanoparticles (Ag NPs). However, the high mobility of Ag NPs results in their potential cytotoxicity. The silver plasma immersion ion-implantation (Ag-PIII) technique may remedy the defect. Accordingly, Ag-PIII technique was employed in this study in an attempt to reduce the mobility of Ag NPs and enhance osseointegration of sandblasted and acid-etched (SLA) dental implants. Briefly, 48 dental implants, divided equally into one control and three test groups (further treated by Ag-PIII technique with three different implantation parameters), were inserted in the mandibles of six Labrador dogs. Scanning electron microscopy, X-ray photoelectron spectroscopy, and inductively coupled plasma optical emission spectrometry were used to investigate the surface topography, chemical states, and silver release of SLA- and Ag-PIII-treated titanium dental implants. The implant stability quotient examination, Microcomputed tomography evaluation, histological observations, and histomorphometric analysis were performed to assess the osseointegration effect in vivo. The results demonstrated that normal soft tissue healing around dental implants was observed in all the groups, whereas the implant stability quotient values in Ag-PIII groups were higher than that in the SLA group. In addition, all the Ag-PIII groups, compared to the SLA-group, exhibited enhanced new bone formation, bone mineral density, and trabecular pattern. With regard to osteogenic indicators, the implants treated with Ag-PIII for 30 minutes and 60 minutes, with the diameter of the Ag NPs ranging from 5-25 nm, were better than those treated with Ag-PIII for 90 minutes, with the Ag NPs diameter out of that range. These results suggest that Ag-PIII technique can reduce the mobility of Ag NPs and enhance

  9. Ag loaded WO3 nanoplates for efficient photocatalytic degradation of sulfanilamide and their bactericidal effect under visible light irradiation.

    PubMed

    Zhu, Wenyu; Liu, Jincheng; Yu, Shuyan; Zhou, Yan; Yan, Xiaoli

    2016-11-15

    Sulfonamides (SAs) are extensively used antibiotics and their residues in the water bodies propose potential threat to the public. In this study, degradation efficiency of sulfanilamide (SAM), which is the precursor of SAs, using WO3 nanoplates and their Ag heterogeneous as photocatalysts was investigated. WO3 nanoplates with uniform size were synthesized by a facile one step hydrothermal method. Different amount of Ag nanoparticles (Ag NPs) were loaded onto WO3 nanoplates using a photo-reduction method to generate WO3/Ag composites. The physio-chemical properties of synthesized nanomaterials were systematically characterized. Photodegradation of SAM by WO3 and WO3/Ag composites was conducted under visible light irradiation. The results show that WO3/Ag composites performed much better than pure WO3 where the highest removal rate was 96.2% in 5h. Ag as excellent antibacterial agent also endows certain antibacterial efficiency to WO3, and 100% removal efficiency against Escherichia Coli and Bacillus subtilis could be achieved in 2h under visible light irradiation for all three WO3/Ag composites synthesized. The improved performance in terms of SAM degradation and antibacterial activity of WO3/Ag can be attributed to the improved electron-hole pair separation rate where Ag NPs act as effective electron trapper during the photocatalytic process. PMID:27450332

  10. Preparation, characterization, and photocatalytic performance of pear-shaped ZnO/Ag core-shell submicrospheres

    NASA Astrophysics Data System (ADS)

    Guo, Xiao-Hua; Ma, Jian-Qi; Ge, Hong-Guang

    2013-05-01

    Pear-shaped ZnO/Ag core-shell submicrospheres with good monodispersity were prepared via a seed-mediated particle growth procedure, where metal Ag (by reducing Ag+ with Sn2+) deposited on the as-prepared ZnO submicrospheres served as seeds (nucleation sites) for further growth of Ag nanoparticles. The as-prepared samples were characterized by X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, ultraviolet-visible and photoluminescence spectra. Structure characterization demonstrates that the ZnO/Ag composites are composed of pear-shaped wurtzite ZnO submicrosphere core and Ag nanoparticles (nanoshell). Photoluminescence indicates that Ag nanoshell can effectively inhibit the recombination of the photoinduced electrons and holes of ZnO. This is responsible for the higher photocatalytic activity of the ZnO/Ag core-shell composites. The photocatalytic performance of the prepared ZnO/Ag samples for degradation of Rhodamine B was evaluated with a comparative study. The relationship between the structure of the samples and their photocatalytic performance shows that Ag deposits can significantly enhance the photocatalytic efficiency of ZnO submicrospheres.

  11. 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.

  12. Ultrafast processes in Ag and Au: A Monte Carlo study

    NASA Astrophysics Data System (ADS)

    van Hall, P. J.

    2001-03-01

    Monte Carlo simulations of ultrafast electron processes in Ag and Au have been used to analyze transient reflectivity as well as two-photon photoemission experiments. The model consisted of an electron Fermi gas coupled to longitudinal acoustic phonons. A laser pulse of finite width excited the electrons, after which the development of the distribution function was followed during 3-5 ps. In the electron-phonon coupling we used the full q dependence of the scattering together with a semirealistic phonon dispersion relation. The strength of the electron-phonon scattering is governed by the deformation potential. Its value was fixed to low-fluence transient reflection data. Also hot-phonon effects were included. For the electron-electron scattering we employed a Coulomb interaction screened according to the Thomas-Fermi prescription. We accounted for exchange effects in the total scattering probability. In a later stage we varied the screening. We analyzed a variety of data for Ag and Au. A good description of the temperature dependence of the transient reflectivity for various excitation powers could be obtained. Also the time evolution of the Fermi surface showed fair agreement with the experiment. In the case of Ag the lifetime of an electron above the Fermi sea was predicted correctly. For Au, however, it was necessary to increase the screening to obtain the correct lifetimes of electrons excited above the Fermi sea. Using this adjusted screening the description of the other experiments no longer was appropriate. Finally also the resistivity due to electron-phonon scattering was predicted quite well using the deformation potential extracted from the ultrafast reflectivity experiments.

  13. Ag nanocluster/DNA hybrids: functional modules for the detection of nitroaromatic and RDX explosives.

    PubMed

    Enkin, Natalie; Sharon, Etery; Golub, Eyal; Willner, Itamar

    2014-08-13

    Luminescent Ag nanoclusters (NCs) stabilized by nucleic acids are implemented as optical labels for the detection of the explosives picric acid, trinitrotoluene (TNT), and hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX). The sensing modules consist of two parts, a nucleic acid with the nucleic acid-stabilized Ag NCs and a nucleic acid functionalized with electron-donating units, including L-DOPA, L-tyrosine and 6-hydroxy-L-DOPA, self-assembled on a nucleic acid scaffold. The formation of donor-acceptor complexes between the nitro-substituted explosives, exhibiting electron-acceptor properties, and the electron-donating sites, associated with the sensing modules, concentrates the explosives in close proximity to the Ag NCs. This leads to the electron-transfer quenching of the luminescence of the Ag NCs by the explosive molecule. The quenching of the luminescence of the Ag NCs provides a readout signal for the sensing process. The sensitivities of the analytical platforms are controlled by the electron-donating properties of the donor substituents, and 6-hydroxy-L-DOPA was found to be the most sensitive donor. Picric acid, TNT, and RDX are analyzed with detection limits corresponding to 5.2 × 10(-12) M, 1.0 × 10(-12) M, and 3.0 × 10(-12) M, respectively, using the 6-hydroxy-L-DOPA-modified Ag NCs sensing module.

  14. Influence of sp(3)-sp(2) Carbon Nanodomains on Metal/Support Interaction, Catalyst Durability, and Catalytic Activity for the Oxygen Reduction Reaction.

    PubMed

    Campos-Roldán, Carlos A; Ramos-Sánchez, Guadalupe; Gonzalez-Huerta, Rosa G; Vargas García, Jorge R; Balbuena, Perla B; Alonso-Vante, Nicolas

    2016-09-01

    In this work, platinum nanoparticles were impregnated by two different techniques, namely the carbonyl chemical route and photodeposition, onto systematically surface-modified multiwalled carbon nanotubes. The different interactions between platinum nanoparticles with sp(2)-sp(3) carbon nanodomains were investigated. The oxidation of an adsorbed monolayer of carbon monoxide, used to probe electronic catalytic modification, suggests a selective nucleation of platinum nanoparticles onto sp(2) carbon nanodomains when photodeposition synthesis is carried out. XPS attests the catalytic center electronic modification obtained by photodeposition. DFT calculations were used to determine the interaction energy of a Pt cluster with sp(2) and sp(3) carbon surfaces as well as with oxidized ones. The interaction energy and electronic structure of the platinum cluster presents dramatic changes as a function of the support surface chemistry, which also modifies its catalytic properties evaluated by the interaction with CO. The interaction energy was calculated to be 8-fold higher on sp(3) and oxidized surfaces in comparison to sp(2) domains. Accelerated Stability Test (AST) was applied only on the electronic-modified materials to evaluate the active phase degradation and their activity toward oxygen reduction reaction (ORR). The stability of photodeposited materials is correlated with the surface chemical nature of supports indicating that platinum nanoparticles supported onto multiwalled carbon nanotubes with the highest sp(2) character show the higher stability and activity toward ORR. PMID:27494283

  15. Influence of sp(3)-sp(2) Carbon Nanodomains on Metal/Support Interaction, Catalyst Durability, and Catalytic Activity for the Oxygen Reduction Reaction.

    PubMed

    Campos-Roldán, Carlos A; Ramos-Sánchez, Guadalupe; Gonzalez-Huerta, Rosa G; Vargas García, Jorge R; Balbuena, Perla B; Alonso-Vante, Nicolas

    2016-09-01

    In this work, platinum nanoparticles were impregnated by two different techniques, namely the carbonyl chemical route and photodeposition, onto systematically surface-modified multiwalled carbon nanotubes. The different interactions between platinum nanoparticles with sp(2)-sp(3) carbon nanodomains were investigated. The oxidation of an adsorbed monolayer of carbon monoxide, used to probe electronic catalytic modification, suggests a selective nucleation of platinum nanoparticles onto sp(2) carbon nanodomains when photodeposition synthesis is carried out. XPS attests the catalytic center electronic modification obtained by photodeposition. DFT calculations were used to determine the interaction energy of a Pt cluster with sp(2) and sp(3) carbon surfaces as well as with oxidized ones. The interaction energy and electronic structure of the platinum cluster presents dramatic changes as a function of the support surface chemistry, which also modifies its catalytic properties evaluated by the interaction with CO. The interaction energy was calculated to be 8-fold higher on sp(3) and oxidized surfaces in comparison to sp(2) domains. Accelerated Stability Test (AST) was applied only on the electronic-modified materials to evaluate the active phase degradation and their activity toward oxygen reduction reaction (ORR). The stability of photodeposited materials is correlated with the surface chemical nature of supports indicating that platinum nanoparticles supported onto multiwalled carbon nanotubes with the highest sp(2) character show the higher stability and activity toward ORR.

  16. One pot synthesis of Ag nanoparticle modified ZnO microspheres in ethylene glycol medium and their enhanced photocatalytic performance

    SciTech Connect

    Tian Chungui; Li Wei; Pan Kai; Zhang Qi; Tian Guohui; Zhou Wei; Fu Honggang

    2010-11-15

    Ag nanoparticles (NPs) modified ZnO microspheres (Ag/ZnO microspheres) were prepared by a facile one pot strategy in ethylene glycol (EG) medium. The EG played two important roles in the synthesis: it could act as a reaction media for the formation of ZnO and reduce Ag{sup +} to Ag{sup 0}. A series of the characterizations indicated the successful combination of Ag NPs with ZnO microspheres. It was shown that Ag modification could greatly enhance the photocatalytic efficiency of ZnO microspheres by taking the photodegradation of Rhodamine B as a model reaction. With appropriate ratio of Ag and ZnO, Ag/ZnO microspheres showed the better photocatalytic performance than commercial Degussa P-25 TiO{sub 2}. Photoluminescence and surface photovoltage spectra demonstrated that Ag modification could effectively inhibit the recombination of the photoinduced electron and holes of ZnO. This is responsible for the higher photocatalytic activity of Ag/ZnO composites. -- Graphical abstract: A 'one-pot' strategy was developed for preparing the Ag/ZnO microspheres in ethylene glycol. The composites exhibited superior photocatalytic performance for photodegradation of Rhodamine B dye in water. Display Omitted

  17. SP-100 surety evaluation

    SciTech Connect

    Not Available

    1985-06-01

    This report describes surety evaluations conducted during GFY 1985 in support of the General Electric design for a Space Nuclear Power System - SP-100. Those surety evaluations address both safety and safeguards requirements, which are derived from OSNP-1 and supporting documents. The report includes results of neutronics (criticality) calculations performed by Los Alamos. The results have been benchmarked against independent calculations performed by General Electric with different codes. These comparisons show close agreement, and are summarized. Los Alamos has also provided specifications of explosion and fire environments, which have been used in evaluation of the GE SP-100 concept. Following the summary of key results, surety requirements are given and recommendations toward specification of requirements for later SP-100 project phases are presented. A conceptual design summary is presented. To establish a comprehensive background for surety evaluations, a reference mission profile and potential accidents for each phase of the mission are identified. The main body of the report addresses surety of the General Electric Thermoelectric Conversion design. GE has also developed a Stirling Engine concept, and performed comprehensive surety evaluations for it. These evaluations are reported.

  18. [Aspergillus insulicola Sp. Nov].

    PubMed

    de Montemayor, L; Santiago, A R

    1975-04-30

    A strain of Aspergillus sp. is described and proposed as a new species under the name "Aspergillus insulicola sp. nov." Montemayor & Santiago, 1973. This strain was isolated from soil samples taken in "Aves Island" during a scientific expedition.--Aves Island, situated at 15 degrees, 40 feet, 42 inches N and 63 degrees, 36 feet, 47 inches W, about 665 Km of the coast of Venezuela, has very special ecological conditions. Due to its smallness: 550 m long and 40 to 120 m across and to its low profile only 3 m over sea level, it is swept by the sea during the periodical storms and hurricanes in the area. It has thus a very interesting fauna and flora. We took a series of soil samples to study its mycological flora. Forty samples were inoculated by dilution method. In this first paper a species is described and proposed as a new species because of its macroscopic and microscopic characteristics, as well as by its biological properties, under the name "Aspergillus insulicola sp. nov.". In its study we have tried to follow as closely as possible the methods recommended by Kennet B. Raper & Dorothy Fenell, world authorities on the genera Aspergillus and Penicillium. The strain is being kept in USB under the number T1, and has been sent to ATCC & CBSC to be incorporated in their collections.

  19. Desorption of oxygen from alloyed Ag/Pt(111)

    SciTech Connect

    Jankowski, Maciej; Wormeester, Herbert Zandvliet, Harold J. W.; Poelsema, Bene

    2014-06-21

    We have investigated the interaction of oxygen with the Ag/Pt(111) surface alloy by thermal desorption spectroscopy (TDS). The surface alloy was formed during the deposition of sub-monolayer amounts of silver on Pt(111) at 800 K and subsequent cooling to 300 K. The low-temperature phase of the surface alloy is composed of nanometer-sized silver rich stripes, embedded within platinum-rich domains, which were characterized with spot profile analysis low energy electron diffraction. The TDS measurements show that oxygen adsorption is blocked on Ag sites: the saturation coverage of oxygen decreases with increasing Ag coverage. Also, the activation energy for desorption (E{sub des}) decreases with Ag coverage. The analysis of the desorption spectra from clean Pt(111) shows a linear decay of E{sub des} with oxygen coverage, which indicates repulsive interactions between the adsorbed oxygen atoms. In contrast, adsorption on alloyed Ag/Pt(111) leads to an attractive interaction between adsorbed oxygen atoms.

  20. Theme: The Electronic Classroom.

    ERIC Educational Resources Information Center

    Herz, Bruce; And Others

    1988-01-01

    Consists of seven articles on the use of electronics in vocational agricultural education. Topics include (1) the Ag Ed Network, (2) computer simulations, (3) video simulation, (4) classroom equipment, (4) online information systems, (5) expert systems, and (6) computer networking in California. (CH)

  1. Quasi-1D States Confined in a Self-Assembled Organic Super-Lattice of TTF-TCNQ on Ag(111)

    NASA Astrophysics Data System (ADS)

    Jeon, Seokmin; Ganesh, Panchapakesan; Sumpter, Bobby; Cerdá, Jorge Iribas; Maksymovych, Petro; CNMS Team; ICMM-CSIC Team

    2015-03-01

    Organic charge transfer complexes (CTC) have drawn much attention due to their potential applications to conducting or semiconducting organic thin films and contacts in devices. TTF-TCNQ is a historic organic CTC with one of the highest conductivity values among numerous organic conductors. As a two-component molecular material, TTF-TCNQ in a low-dimension form on a surface naturally creates monolayer super-lattices with corrugated electrostatic potential and adsorbate-induced strain. Generally this will lead to strong confinement of the surface states, although the detailed response of the surface electronic structure remains to be understood. We investigated TTF-TCNQ monolayer films grown on Ag(111), Au(111) and Ag(100) surfaces using STM/STS at 4.3 K. Confinement of sp-derived surface states was indeed ubiquitous, including spontaneous formation of quantum dots and quasi-1D bands. The small periodicity of the lattice caused a complete depopulation of the surface states, with up to 1 eV upshift of the band minimum - much stronger effect than normally observed in assemblies. This also allows us to infer the height of the confining potential using 1D Kronig-Penney model and critically assess the long-standing problem of molecule-surface charge transfer. A portion of this research was conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility.

  2. The electronic spectrum of AgCl2: Ab initio benchmark versus density-functional theory calculations on the lowest ligand-field states including spin-orbit effects

    NASA Astrophysics Data System (ADS)

    Ramírez-Solís, A.; Poteau, R.; Daudey, J. P.

    2006-01-01

    The XΠg2, Σg+2, and Δg2 states of AgCl2 have been studied through benchmark ab initio complete active space self-consistent field plus second-order complete active space multireference Möller-Plesset algorithm (CASSCF +CASPT2) and complete active space self-consistent field plus averaged coupled pair functional (CASSCF +ACPF) and density-functional theory (DFT) calculations using especially developed basis sets to study the transition energies, geometries, vibrational frequencies, Mulliken charges, and spin densities. The spin-orbit (SO) effects were included through the effective Hamiltonian formalism using the ΛSΣ ACPF energies as diagonal elements. At the ACPF level, the ground state is Πg2 in contradiction with ligand-field theory, SCF, and large CASSCF; the adiabatic excitation energies for the Σg+2 and Δg2 states are 1640 and 18230cm-1, respectively. The inclusion of the SO effects leads to a pure Ω =3/2(Πg2) ground state, a Ω =1/2 (66%Πg2 and 34%Σg+2) A state, a Ω =1/2 (34%Πg2 and 66%Σg+2) B state, a Ω =5/2(Δg2)C state, and a Ω =3/2(99%Δg2)D state. The X-A, X-B, X-C, and X-D transition energies are 485, 3715, 17 246, and 20110cm-1, respectively. The B97-2, B3LYP, and PBE0 functionals overestimate by ≈100% the XΠg2-Σg+2Te but provide a qualitative energetic ordering in good agreement with ACPF results. B3LYP with variable exchange leads to a 42% optimal Hartree-Fock exchange for transition energies but all equilibrium geometries get worsened. Asymptotic corrections to B3LYP do not provide improved values. The nature of the bonding in the XΠg2 state is very different from that of CuCl2 since the Mulliken charge on the metal is 1.1 while the spin density is only 0.35. DFT strongly delocalizes the spin density providing even smaller values of around 0.18 on Ag not only for the ground state, but also for the Σg+2 state.

  3. Synthesis of Ag(2) S-Ag nanoprisms and their use as DNA hybridization probes.

    PubMed

    Liu, Bing; Ma, Zhanfang

    2011-06-01

    A simple synthetic route to prepare Ag(2) S-Ag nanoprisms consists of the facile addition of Na(2) S to a solution of triangular Ag nanoprisms. The resulting Ag(2) S-Ag nanoparticles are more stable in solution than the original Ag nanoprisms, and two surface plasmon resonance (SPR) bands of the original Ag nanoprisms still remain. In addition, the SPR bands of the Ag(2) S-Ag nanoprisms are tunable over a wide range. The Ag(2) S-Ag nanoprisms can be directly bioconjugated via well-established stable Ag(2) S surface chemistry with readily available sulfur coupling agents. The nanoprisms are used in the hybridization of functionalized oligonucleotides, and show promise as probes for future biosensing applications. PMID:21538868

  4. 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.

  5. Evidence for improvement of critical current by Ag in YBaCuO-Ag thick films

    NASA Astrophysics Data System (ADS)

    Dwir, B.; Kellett, B.; Mieville, L.; Pavuna, D.

    1991-04-01

    The evidence is reported for enhancement of critical current density J(c) in YBa2Cu3O(7-delta) thick films with the addition of Ag, which is correlated with improvements in structural properties. An improvement of 50 percent in J(c) (up to about 500 A/sq cm at T = 4.2 K) was obtained in films made from YBCO + 60 wt pct Ag powder, fabricated by the spin-on technique on (100) SrTiO3, which is correlated with improvements in structure. The resulting films are 10 microns thick, uniform, partially textured, and show good adherence. The critical temperature Tc is improved by the addition of Ag, and a reduction in the density of microcracks and in the amount of secondary phases in the sintered films was observed. Normal-state resistivity is reduced by almost three orders of magnitude, making these films potentially useful for electronic applications in interconnects and novel hybrid circuits.

  6. Effect of Ag nanowire addition into nanoparticle paste on the conductivity of Ag patterns printed by gravure offset method.

    PubMed

    Ok, Ki-Hun; Lee, Chan-Jae; Kwak, Min-Gi; Choi, Duck-Kyun; Kim, Kwang-Seok; Jung, Seung-Boo; Kim, Jong-Woong

    2014-11-01

    This paper focuses on the effect of Ag nanowire addition into a commercial Ag nanopaste and the printability evaluation of the mixed paste by the gravure offset printing methodology. Ag nanowires were synthesized by a modified polyol method, and a small amount of them was added into a commercial metallic paste based on Ag nanoparticles of 50 nm in diameter. Two annealing temperatures were selected for comparison, and electrical conductivity was measured by four point probe method. As a result, the hybrid mixture could be printed by the gravure offset method for patterning fine lines up to 15 μm width with sharp edges and scarce spreading. The addition of the Ag nanowires was significantly efficient for enhancement of electrical conductivity of the printed lines annealed at a low temperature (150 degrees C), while the effect was somewhat diluted in case of high temperature annealing (200 degrees C). The experimental results were discussed with the conduction mechanism in the printed conductive circuits with a schematic description of the electron flows in the printed lines.

  7. Localized surface plasmon resonance effect in organic light-emitting devices with Ag islands

    NASA Astrophysics Data System (ADS)

    Shimazaki, Noritaka; Naka, Shigeki; Okada, Hiroyuki

    2014-04-01

    We report on luminescence enhancement of organic light-emitting devices (OLEDs) with silver islands (i-Ag) by a localized surface plasmon resonance (LSPR) effect. The devices were fabricated using tetraphenylporphyrin (TPP) as the red emission material, bis[N-(1-naphthyl)-N-phenyl] benzidine (α-NPD) as the blue emission and hole transport material, and 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) as the electron transport material. To clarify the position of emission enhancement by energy transfer from i-Ag, an ultrathin TPP layer located within the α-NPD layer. In the device with i-Ag and the TPP layer located over 10 nm from i-Ag, TPP emission was enhanced in comparison with the device without i-Ag. The enhancement of TPP emission was suggested to be the effect of the enhanced electric field resulting from LSPR excited by α-NPD emission.

  8. Changes in the structure and tribological property of Ag film by LEO space environment exposure

    NASA Astrophysics Data System (ADS)

    Gao, Xiaoming; Hu, Ming; Sun, Jiayi; Fu, Yanlong; Yang, Jun; Weng, Lijun; Liu, Weimin

    2014-11-01

    Ag films, deposited by arc ion plating, had been exposed for 43.5 h in real low earth orbit (LEO) space environment by a space environment exposure device (SEED) aboard the China Shenzhou-7 manned spaceship. The structure, morphology, composition and tribological property of the Ag films after the space environment exposure (SEE) were investigated using X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), X-ray photoelectron spectroscope (XPS) and ball-on-disk tribometer, respectively. Depth XPS and XRD analysis revealed that after the SEE, the surface layer of Ag films was partially oxidized to Ag2O, the cracking and flaking phenomena could be observed from the film surface by FESEM, and so the Ag films lose its metallic shine and became gray. As a result, the tribological performance was deteriorated and the high/unstable friction was obtained.

  9. 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.

  10. 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.

  11. Construction of heterostructured g-C₃N₄/Ag/TiO₂ microspheres with enhanced photocatalysis performance under visible-light irradiation.

    PubMed

    Chen, Yanfeng; Huang, Weixin; He, Donglin; Situ, Yue; Huang, Hong

    2014-08-27

    The visible-light photocatalytic performance of the heterostructured g-C3N4/Ag/TiO2 microspheres was investigated. As an electron-conduction bridge, Ag nanoparticles were photodeposited as the interlayer between g-C3N4 and the surface of TiO2 microspheres to increase visible-light absorption via the surface plasmon resonance. The interface between Ag/TiO2 and g-C3N4 facilitates the direct migration of photoinduced electrons from g-C3N4 to Ag/TiO2, which is conductive to retarding the recombination of electron-holes. The g-C3N4 (4%)/Ag/TiO2 microsphere sample shows significant photocatalytic activity, higher than the sum of g-C3N4 (1.2 mg) and Ag/TiO2 samples, or the sum of TiO2 and Ag/g-C3N4 (1.8 mg) samples. It indicates that the heterostructured combination of g-C3N4, Ag and TiO2 microspheres provides synergistic photocatalytic activity through an efficient electron transfer process.

  12. Communication: UV photoionization of cytosine catalyzed by Ag{sup +}

    SciTech Connect

    Taccone, Martín I.; Berdakin, Matías; Pino, Gustavo A.; Féraud, Geraldine; Dedonder-Lardeux, Claude; Jouvet, Christophe

    2015-07-28

    The photo-induced damages of DNA in interaction with metal cations, which are found in various environments, still remain to be characterized. In this paper, we show how the complexation of a DNA base (cytosine (Cyt)) with a metal cation (Ag{sup +}) changes its electronic properties. By means of UV photofragment spectroscopy of cold ions, it was found that the photoexcitation of the CytAg{sup +} complex at low energy (315-282) nm efficiently leads to ionized cytosine (Cyt{sup +}) as the single product. This occurs through a charge transfer state in which an electron from the p orbital of Cyt is promoted to Ag{sup +}, as confirmed by ab initio calculations at the TD-DFT/B3LYP and RI-ADC(2) theory level using the SV(P) basis set. The low ionization energy of Cyt in the presence of Ag{sup +} could have important implications as point mutation of DNA upon sunlight exposition.

  13. Effects of oxygen adsorption on the surface state of epitaxial silicene on Ag(111).

    PubMed

    Xu, Xun; Zhuang, Jincheng; Du, Yi; Feng, Haifeng; Zhang, Nian; Liu, Chen; Lei, Tao; Wang, Jiaou; Spencer, Michelle; Morishita, Tetsuya; Wang, Xiaolin; Dou, Shi Xue

    2014-12-18

    Epitaxial silicene, which is one single layer of silicon atoms packed in a honeycomb structure, demonstrates a strong interaction with the substrate that dramatically affects its electronic structure. The role of electronic coupling in the chemical reactivity between the silicene and the substrate is still unclear so far, which is of great importance for functionalization of silicene layers. Here, we report the reconstructions and hybridized electronic structures of epitaxial 4 × 4 silicene on Ag(111), which are revealed by scanning tunneling microscopy and angle-resolved photoemission spectroscopy. The hybridization between Si and Ag results in a metallic surface state, which can gradually decay due to oxygen adsorption. X-ray photoemission spectroscopy confirms the decoupling of Si-Ag bonds after oxygen treatment as well as the relatively oxygen resistance of Ag(111) surface, in contrast to 4 × 4 silicene [with respect to Ag(111)]. First-principles calculations have confirmed the evolution of the electronic structure of silicene during oxidation. It has been verified experimentally and theoretically that the high chemical activity of 4 × 4 silicene is attributable to the Si pz state, while the Ag(111) substrate exhibits relatively inert chemical behavior.

  14. Synthesis of Ag nanoplates on GaAs wafers : evidence for growth mechanism.

    SciTech Connect

    Sun, Y.; Center for Nanoscale Materials

    2010-01-21

    Direct synthesis of Ag nanoplates on GaAs wafers has been developed in our group through a simple solution/solid interfacial reaction (SSIR) strategy, in which aqueous solutions of pure AgNO{sub 3} react with the GaAs wafers at room temperature [J. Phys. Chem. C 2009, 113, 6061; 2008, 112, 8928; Chem. Mater. 2007, 19, 5845]. However, a number of questions are still not clear yet regarding the roles of different possible pathways for reducing Ag{sup +} ions in the growth of Ag nanoplates. In this article, we try to answer these remaining questions by specifically designing experiments and extracting direct evidence from systematic characterizations of different samples. It is conclusive that growth of high-quality Ag nanoplates on GaAs wafers is ascribed to the good separation between nucleation and growth steps, which are driven by two different reduction pathways. At the nucleation step, fast reduction of Ag{sup +} ions with a high concentration of surface electrons is crucial for the formation of Ag nuclei with multiple (111) twin planes parallel to each other, and remaining the environment of a high concentration of surface electrons for a period long enough is also important to develop the Ag nuclei into stable seeds. At the growth step, a hole injection process is mainly responsible for reduction of Ag{sup +} ions to enlarge the stable seeds into Ag nanoplates with controlled sizes by tuning the growth time. The paralleled multiple (111) twin planes provide a crystalline confinement to guide the growth of the seeds into nanoplates.

  15. The Effect of Ag-DOPING on the Critical Current Density of YBa2Cu3O7-δ Superconductors

    NASA Astrophysics Data System (ADS)

    Lue, Juh Tzeng; Kung, J. H.; Yen, H. H.; Chen, Y. C.; Wu, P. T.

    The superconducting state and the transition temperature Tc of the interstitially Ag-doped YBa2 Cu3 O7-δ are not changed even when the Ag concentration is increased up to 20%, whereas the substitutionally doped YBa2 Cu3-x Agx O7-δ system ceases to be superconductive when the contents x of Ag is over 1.2. Magnetic susceptibility measurement indicates that the interstitial Ag-doping yields higher diamagnetic signal and enhances the critical current density by 15 folds. Photoelectron emission and electron spin resonance spectroscopic studies elucidate that the copper ions change from diamagnetic to paramagnetic states at some doping levels.

  16. 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.

  17. ESR and TL mechanism in CaSO4 : Ag co-doped phosphors

    NASA Astrophysics Data System (ADS)

    Dhabekar, Bhushan; Menon, Sanjeev; Alagu Raja, E.; Sanaye, S. S.; Gundu Rao, T. K.; Bhatt, B. C.; Kher, R. K.

    2006-06-01

    Thermoluminescence (TL) studies have been carried out on CaSO4 : Mn, CaSO4 : Ag,Mn, CaSO4 : Ag,Nd, CaSO4 : Ag,Mn,Nd, CaSO4 : Ag,Zr and CaSO4 : Ag,Mn,Zr phosphors. It is found that TL at 360 °C in CaSO4 : Ag,Mn,Nd is about 40 times that of CaSO4 : Ag,Mn and about 170 times that of CaSO4 : Ag,Nd. This shows that the presence of an efficient luminescent centre (Mn2+) as well as a trivalent impurity (such as Nd3+ or Y3+) is important for enhancement of TL at 360 °C in the CaSO4 : Ag,Mn,Nd phosphor system. Electron spin resonance (ESR) studies show that the peak at 360 °C correlates with an Ag2+ centre formed due to γ-irradiation and observable only 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 360 °C. The low temperature centre is characterized by the g-values g|| = 2.0023 and gbottom = 2.0038 and is assigned to the SO_{3}^{ - } radical.

  18. AGS slow extracted beam improvement

    SciTech Connect

    Marneris, I.; Danowski, G.; Sandberg, J.; Soukas, A.

    1997-07-01

    The Brookhaven AGS is a strong focusing accelerator which is used to accelerate protons and various heavy ion species to an equivalent proton energy of 29 GeV. Since the late 1960`s it has been serving high energy physics (HEP - proton beam) users of both slow and fast extracted beams. The AGS fixed target program presently uses primary proton and heavy ion beams (HIP) in slowly extracted fashion over spill lengths of 1.5 to 4.0 seconds. Extraction is accomplished by flattoping the main and extraction magnets and exciting a third integer resonance in the AGS. Over the long spill times, control of the subharmonic amplitude components up to a frequency of 1 kilohertz is very crucial. One of the most critical contributions to spill modulation is due to the AGS MMPS. An active filter was developed to reduce these frequencies and it`s operation is described in a previous paper. However there are still frequency components in the 60-720 Hz sub-harmonic ripple range, modulating the spill structure due to extraction power supplies and any remaining structures on the AGS MMPS. A recent scheme is being developed to use the existing tune-trim control horizontal quadrupole magnets and power supply to further reduce these troublesome noise sources. Feedback from an external beam sensor and overcoming the limitations of the quadrupole system by lead/lag compensation techniques will be described.

  19. Highly visible light active Ag@TiO2 nanocomposites synthesized using an electrochemically active biofilm: a novel biogenic approach

    NASA Astrophysics Data System (ADS)

    Khan, M. Mansoob; Ansari, Sajid A.; Amal, M. Ikhlasul; Lee, Jintae; Cho, Moo Hwan

    2013-05-01

    Titanium dioxide (TiO2) nanoparticles were decorated with different amounts of silver nanoparticles (AgNPs) using an electrochemically active biofilm (EAB), which is a biogenic approach that leads to the formati