WorldWideScience

Sample records for au ag pd

  1. Asymmetric AgPd-AuNR heterostructure with enhanced photothermal performance and SERS activity

    Science.gov (United States)

    Zhang, Han; Liu, Zeke; Kang, Xiaolin; Guo, Jun; Ma, Wanli; Cheng, Si

    2016-01-01

    Most as-reported nanostructures through galvanic replacement reactions are still symmetric hollow structures, until now. Asymmetric structures fabricated through a galvanic replacement reaction have been rarely reported. However, asymmetric heterostructures can generally lead to new intriguing properties through asymmetric synergistic coupling. Here, we report a simple synthesis of an asymmetric one-ended AgPd bimetal on Au nanorods (AuNR) by combining a galvanic replacement reaction with an Ostwald ripening process. The morphological evolution from a nanodumbbell to a dandelion structure is thoroughly investigated. The unique asymmetric AgPd-AuNR heterostructures possess the required plasmonic performance and avoid strong damping caused by the poor plasmonic metal Pd, resulting in a superior photothermal heating performance and enhanced SERS sensitivity for in situ monitoring of a catalytic reaction compared with the symmetric counterparts.Most as-reported nanostructures through galvanic replacement reactions are still symmetric hollow structures, until now. Asymmetric structures fabricated through a galvanic replacement reaction have been rarely reported. However, asymmetric heterostructures can generally lead to new intriguing properties through asymmetric synergistic coupling. Here, we report a simple synthesis of an asymmetric one-ended AgPd bimetal on Au nanorods (AuNR) by combining a galvanic replacement reaction with an Ostwald ripening process. The morphological evolution from a nanodumbbell to a dandelion structure is thoroughly investigated. The unique asymmetric AgPd-AuNR heterostructures possess the required plasmonic performance and avoid strong damping caused by the poor plasmonic metal Pd, resulting in a superior photothermal heating performance and enhanced SERS sensitivity for in situ monitoring of a catalytic reaction compared with the symmetric counterparts. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr07333b

  2. Electron-spectroscopy study of YbXCu4 (X=Ag,Au,Pd)

    International Nuclear Information System (INIS)

    We have studied the electronic structure of the heavy-electron compounds YbXCu4, with X = Ag,Au,Pd, using x-ray photoemission and bremsstrahlung isochromat spectroscopies. Consistent with other evidence of small Kondo temperatures, we find that Yb in this system is nearly trivalent and that Kondo features in the Yb 4f BIS spectra are either absent or weak

  3. 分子动力学模拟Au-Pd和Ag-Pt合金的热学和力学性质%Thermal and Mechanical Properties of Au-Pd and Ag-Pt Alloy by Molecular Dynamics Simulation

    Institute of Scientific and Technical Information of China (English)

    闫雪松; 齐新; 林平; 杨磊

    2011-01-01

    利用Finnis-Sinclair势,对金属Au、Pd、Ag、Pt和合金Au3Pd、AuPd3、Ag3Pt、AgPt3的热学和力学性质进行了分子动力学模拟.首次计算了不同温度下合金的晶格常数、结合能和弹性常数,并预测了它们的熔点.通过比较发现,Au3Pd、AuPd3和Ag3Pt这3种合金的晶格常数、结合能和弹性常数介于其组分金属之间,而AgPt3的剪切模量和熔点高于其组分hg和Pt.%With the Finnis-Sinclair potential, the thermal and mechanical properties of Au, Pd, Ag, Pt pure metals and their alloys Au3Pd, AuPd3, Ag3Pt, AgPt3 were studied by molecular dynamics simulations. Lattice constants and elastic constants of Au3Pd, AuPd3, Ag3Pt and AgPt3 at different temperatures were predicted for the first time. Melting temperatures of these alloys were calculated too. Furthermore, lattice constants, elastic constants and melting temperature of pure metals Au, Pd, Ag, and Pt were calculated for comparison. It is found that for Au3Pd,AuPd3 and Ag3Pt, lattice constants, elastic constants and melting temperatures lie between those of their two components. For AgPt3, the values of shear modulus and melting temperature are higher than those for both Ag and Pt pure metals.

  4. Beet juice utilization: Expeditious green synthesis of nobel metal nanoparticles (Ag, Au, Pt, and Pd) using microwaves

    Science.gov (United States)

    Metal nanoparticles of Ag, Au, Pt, and Pd were prepared in aqueous solutions via a rapid microwave-assisted green method using beet juice, an abundant sugar-rich agricultural produce, served as both a reducing and a capping reagent. The Ag nanoparticles with capping prepared by b...

  5. PdAgAu alloy with high resistance to corrosion by H2S

    Energy Technology Data Exchange (ETDEWEB)

    Braun, Fernando [Inst. de Investigaciones en Catalisis y Petroquimica, Santa Fe (Argentina); Miller, James B. [Carnegie Mellon Univ., Pittsburgh, PA (United States). Dept. of Chemical Engineering; National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States); Gellman, Andrew J. [Carnegie Mellon Univ., Pittsburgh, PA (United States). Dept. of Chemical Engineering; National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States); Tarditi, Ana M. [Inst. de Investigaciones en Catalisis y Petroquimica, Santa Fe (Argentina); Fleutot, Benoit [Carnegie Mellon Univ., Pittsburgh, PA (United States). Dept. of Chemical Engineering; Kondratyuk, Petro [Carnegie Mellon Univ., Pittsburgh, PA (United States). Dept. of Chemical Engineering; National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States); Cornaglia, Laura M. [Inst. de Investigaciones en Catalisis y Petroquimica, Santa Fe (Argentina)

    2012-12-01

    PdAgAu alloy films were prepared on porous stainless steel supports by sequential electroless deposition. Two specific compositions, Pd83Ag2Au15 and Pd74Ag14Au12, were studied for their sulfur tolerance. The alloys and a reference Pd foil were exposed to 1000 H2S /H2 at 623 K for periods of 3 and 30 hours. The microstructure, morphology and bulk composition of both nonexposed and H2S-exposed samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). XRD and SEM analysis revealed time-dependent growth of a bulk Pd{sub 4}S phase on the Pd foil during H2S exposure. In contrast, the PdAgAu ternary alloys displayed the same FCC structure before and after H2S exposure. In agreement with the XRD and SEM results, sulfur was not detected in the bulk of either ternary alloy samples by EDS, even after 30 hours of H2S exposure. X-ray photoelectron spectroscopy (XPS) depth profiles were acquired for both PdAgAu alloys after 3 and 30 hours of exposure to characterize sulfur contamination near their surfaces. Very low S 2p and S 2s XPS signals were observed at the top-surfaces of the PdAgAu alloys, and those signals disappeared before the etch depth reached ~ 10 nm, even for samples exposed to H2S for 30 hours. The depth profile analyses also revealed silver and gold segregation to the surface of the alloys; preferential location of Au on the alloys surface may be related to their resistance to bulk sulfide formation. In preliminary tests, a PdAgAu alloy membrane displayed higher initial H{sub 2} permeability than a similarly prepared pure Pd sample and, consistent with resistance to bulk sulfide formation, lower permeability loss in H2S than pure Pd.

  6. Thermal cyclic test for Sn-4Ag-0.5Cu solders on high P Ni/Au and Ni/Pd/Au surface finishes

    Directory of Open Access Journals (Sweden)

    M.A. Azmah Hanim

    2015-12-01

    Full Text Available In electronic packaging, the reliability of the interconnection changes with the surface finish and the type of solders being used. Thermal cycling is one method of reliability assessment. In thermal cycling experiments, the strain state is simplified by soldering together regular shaped pieces of materials with different coefficients of thermal expansion and exposing the joint to repeated fluctuations of temperature within a certain range. Thus, this study focuses on the intermetallic evolution of Sn-4Ag-0.5Cu on Ni/Au and Ni/Pd/Au surface finishes with thermal cycling up to 1000 cycles with the range of temperature varying from 10 to 80 °C. Sandwich samples were prepared by placing solder balls of Sn-4Ag-0.5Cu between two substrates of two different surface finishes: Ni/Au and Ni/Pd/Au. Optical microscope and FESEM (Field emission scanning electron microscope were used to analyze the samples. From the study, it was observed that the intermetallic changes from (Cu, Ni6Sn5 to (Ni, Cu3Sn4 after 1000 thermal cycles for Ni/Au. These changes promote the formation of cracks at the solder joint because of the different mechanical properties between Ni-Sn based intermetallic and Cu-Sn intermetallics. However, for the Ni/Pd/Au surface finishes, no cracks formed after thermal cycling up to 1000 cycles. This shows that the reliability of the solder joint is higher for Ni/Pd/Au surface finishes in this experiment. Based on these results, it can be concluded that the reliability of the Ni/Pd/Au surface finishes with Sn-4Ag-0.5Cu solders is higher within the given condition of this research.

  7. Effect of thione primers on adhesive bonding between an indirect composite material and Ag-Pd-Cu-Au alloy.

    Science.gov (United States)

    Imai, Hideyuki; Koizumi, Hiroyasu; Shimoe, Saiji; Hirata, Isao; Matsumura, Hideo; Nikawa, Hiroki

    2014-01-01

    The current study evaluated the effect of primers on the shear bond strength of an indirect composite material joined to a silverpalladium-copper-gold (Ag-Pd-Cu-Au) alloy (Castwell). Disk specimens were cast from the alloy and were air-abraded with alumina. Eight metal primers were applied to the alloy surface. A light-polymerized indirect composite material (Solidex) was bonded to the alloy. Shear bond strength was determined both before and after the application of thermocycling. Two groups primed with Metaltite (thione) and M. L. Primer (sulfide) showed the greatest post-thermocycling bond strength (8.8 and 6.5 MPa). The results of the X-ray photoelectron spectroscopic (XPS) analysis suggested that the thione monomer (MTU-6) in the Metaltite primer was strongly adsorbed onto the Ag-Pd-Cu-Au alloy surface even after repeated cleaning with acetone. The application of either the thione (MTU-6) or sulfide primer is effective for enhancing the bonding between a composite material and Ag-Pd-Cu-Au alloy.

  8. Leaching of Au, Ag, and Pd from waste printed circuit boards of mobile phone by iodide lixiviant after supercritical water pre-treatment

    International Nuclear Information System (INIS)

    Highlights: • We report a novel process for recovering Au, Ag, and Pd from waste PCBs. • The effect of SCWO on the leaching of Au, Ag, and Pd in waste PCBs was studied. • SCWO was highly efficient for enhancing the leaching of Au, Ag, and Pd. • The optimum leaching parameters for Au, Ag, and Pd in iodine–iodide were studied. - Abstract: Precious metals are the most attractive resources in waste printed circuit boards (PCBs) of mobile phones. In this work, an alternative process for recovering Au, Ag, and Pd from waste PCBs of mobile phones by supercritical water oxidation (SCWO) pre-treatment combined with iodine–iodide leaching process was developed. In the process, the waste PCBs of mobile phones were pre-treated in supercritical water, then a diluted hydrochloric acid leaching (HL) process was used to recovery the Cu, whose leaching efficiency was approximately 100%, finally the resulting residue was subjected to the iodine–iodide leaching process for recovering the Au, Ag, and Pd. Experimental results indicated that SCWO pre-treatment temperature, time, and pressure had significant influence on the Au, Ag, and Pd leaching from (SCWO + HL)-treated waste PCBs. The optimal SCWO pre-treatment conditions were 420 °C and 60 min for Au and Pd, and 410 °C and 30 min for Ag. The optimum dissolution parameters for Au, Pd, and Ag in (SCWO + HL)-treated PCBs with iodine–iodide system were leaching time of 120 min (90 min for Ag), iodine/iodide mole ratio of 1:5 (1:6 for Ag), solid-to-liquid ratio (S/L) of 1:10 g/mL (1:8 g/mL for Ag), and pH of 9, respectively. It is believed that the process developed in this study is environment friendly for the recovery of Au, Ag, and Pd from waste PCBs of mobile phones by SCWO pre-treatment combined with iodine–iodide leaching process

  9. Leaching of Au, Ag, and Pd from waste printed circuit boards of mobile phone by iodide lixiviant after supercritical water pre-treatment

    Energy Technology Data Exchange (ETDEWEB)

    Xiu, Fu-Rong, E-mail: xiu_chem@hotmail.com [College of Ecological Environment and Urban Construction, Fujian University of Technology, Fuzhou 350108 (China); Qi, Yingying [College of Ecological Environment and Urban Construction, Fujian University of Technology, Fuzhou 350108 (China); Zhang, Fu-Shen [Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China)

    2015-07-15

    Highlights: • We report a novel process for recovering Au, Ag, and Pd from waste PCBs. • The effect of SCWO on the leaching of Au, Ag, and Pd in waste PCBs was studied. • SCWO was highly efficient for enhancing the leaching of Au, Ag, and Pd. • The optimum leaching parameters for Au, Ag, and Pd in iodine–iodide were studied. - Abstract: Precious metals are the most attractive resources in waste printed circuit boards (PCBs) of mobile phones. In this work, an alternative process for recovering Au, Ag, and Pd from waste PCBs of mobile phones by supercritical water oxidation (SCWO) pre-treatment combined with iodine–iodide leaching process was developed. In the process, the waste PCBs of mobile phones were pre-treated in supercritical water, then a diluted hydrochloric acid leaching (HL) process was used to recovery the Cu, whose leaching efficiency was approximately 100%, finally the resulting residue was subjected to the iodine–iodide leaching process for recovering the Au, Ag, and Pd. Experimental results indicated that SCWO pre-treatment temperature, time, and pressure had significant influence on the Au, Ag, and Pd leaching from (SCWO + HL)-treated waste PCBs. The optimal SCWO pre-treatment conditions were 420 °C and 60 min for Au and Pd, and 410 °C and 30 min for Ag. The optimum dissolution parameters for Au, Pd, and Ag in (SCWO + HL)-treated PCBs with iodine–iodide system were leaching time of 120 min (90 min for Ag), iodine/iodide mole ratio of 1:5 (1:6 for Ag), solid-to-liquid ratio (S/L) of 1:10 g/mL (1:8 g/mL for Ag), and pH of 9, respectively. It is believed that the process developed in this study is environment friendly for the recovery of Au, Ag, and Pd from waste PCBs of mobile phones by SCWO pre-treatment combined with iodine–iodide leaching process.

  10. Self-consistent linear-muffin-tin-orbitals coherent-potential technique for bulk and surface calculations: Cu-Ni, Ag-Pd, and Au-Pt random alloys

    DEFF Research Database (Denmark)

    Abrikosov, I. A.; Skriver, Hans Lomholt

    1993-01-01

    energies and work functions for three fcc-based alloys (Cu-Ni, Ag-Pd, and Au-Pt) over the complete concentration range. The calculated mixing enthalpies for the Ag-Pd and Au-Pt systems agrees with experimental values, and the calculated concentration dependence of the lattice parameters agrees...

  11. Structure and properties of EuTSb (T = Cu, Pd, Ag, Pt, Au) and YbIrSb

    Energy Technology Data Exchange (ETDEWEB)

    Mishra, Trinath; Schellenberg, Inga; Eul, Matthias; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

    2011-07-01

    The equiatomic antimonides EuTSb (T = Cu, Pd, Ag, Pt, Au) and YbIrSb were synthesized from the elements in sealed tantalum tubes in an induction furnace. The samples were investigated by powder X-ray diffraction and the structures were refined on the basis of single crystal X-ray diffractometer data: ZrBeSi type, P6{sub 3}/mmc, a = 450.7(5), c = 853.2(7) pm, wR2 = 0.032, 273 F{sup 2} values, 8 variables for EuCuSb, a = 474.9(1), c = 829.4(3) pm, wR2 = 0.028, 166 F{sup 2} values, 8 variables for EuAgSb, a = 467.1(2), c = 848.8(3) pm, wR2 = 0.042, 162 F{sup 2} values, 8 variables for EuAuSb, and TiNiSi type, space group Pnma, a = 762.5(3), b = 469.1(1), c = 792.1(1) pm, wR2 = 0.046, 670 F{sup 2} values, 20 variables for EuPdSb, and a = 700.7(1), b = 444.68(8), c = 781.3(1) pm, wR2 = 0.075, 592 F{sup 2} values, 20 variables for YbIrSb. The structures are ordered superstructure variants of the aristotype AlB{sub 2}3 with planar T{sub 3}Sb{sub 3} hexagons in EuTSb (T = Cu, Ag, Au) and puckered T{sub 3}Sb{sub 3} hexagons in EuTSb (T = Pd, Pt) and YbIrSb. TiNiSi type EuPtSb was characterized via powder data: a = 759.8(3), b = 465.4(3), c = 791.4(3) pm. Temperature dependent magnetic susceptibility measurements indicate antiferromagnetic ordering for all compounds. The samples were additionally characterized by {sup 121}Sb and {sup 151}Eu Moessbauer spectra. (orig.)

  12. Distribution of Precious Metals (Ag, Au, Pd, Pt, and Rh) Between Copper Matte and Iron Silicate Slag

    Science.gov (United States)

    Avarmaa, Katri; Johto, Hannu; Taskinen, Pekka

    2016-02-01

    The distributions of precious metals (Ag, Au, Pd, Pt, and Rh) between copper matte and silica-saturated iron silicate slag were determined at 1523 K to 1623 K (1250 °C to 1350 °C), in controlled CO-CO2-SO2-Ar gas mixtures. The experiments were done in silica crucibles and a fixed partial pressure of sulfur dioxide for matte grades of 55, 65, and 75 wt pct Cu. High-temperature equilibration/quenching/electron probe X-ray microanalysis technique was used to obtain compositions of the equilibrated matte and slag. The technique was applied for the first time to the distributions of precious metals in simulated flash smelting conditions. The resolution of electron probe microanalysis became critical as the detection limits were insufficient to measure reliably the precious metals concentrations (except silver) in the slag. The distribution coefficient of silver, L m/s[Ag] = [wt pctAg in matte]/(wt pctAg in slag), was found to be between 200 and 300, which agrees well with the latest studies in the literature. For other precious metals, the minimum values of distribution coefficients were determined according to the detection limits in the slag. The values obtained were for gold and platinum >250, for palladium >1000, and for rhodium >900. The distribution coefficients of palladium, although locating above distribution coefficient of the detection limit, formed a clear dependency with a good repeatability as a function of the matte grade. It increased along with matte grade and was approximately 1000 at 50 pct Cu and 2000 to 3000 at 70 pct Cu. The precious metals replace metal in the matte structure and they are present as sulfides in the copper matte.

  13. DFT study of Hg adsorption on M-substituted Pd(1 1 1) and PdM/γ-Al2O3(1 1 0) (M = Au, Ag, Cu) surfaces

    Science.gov (United States)

    Wang, Jiancheng; Yu, Huafeng; Geng, Lu; Liu, Jianwen; Han, Lina; Chang, Liping; Feng, Gang; Ling, Lixia

    2015-11-01

    The adsorption of Hgn (n = 1-3) on the Au-, Ag-, Cu-substituted Pd(1 1 1) surfaces as well as the PdM/γ-Al2O3(1 1 0) (M = Au, Ag, Cu) surfaces has been investigated using spin-polarized density functional theory calculations. It is found that M-substituted Pd(1 1 1) surfaces show as good Hg adsorption capacity as the perfect Pd(1 1 1) at low Hg coverage, while the Hg adsorption capacity is only slightly weakened at high Hg coverage. On the basis of stepwise adsorption energies analysis, it is concluded that M-substituted Pd(1 1 1) surfaces can contribute to the binding of Hg atom on the surfaces at high Hg coverage. The electronic properties of the second metal atoms are the main factor contributes to the Hg adsorption capacity. Gas phase Pd2 shows better Hg adsorption capacity than Pd2/γ-Al2O3, while PdM/γ-Al2O3 can adsorb Hg more efficiently than bare PdM clusters. It suggests that the γ-Al2O3 support can enhance the activity of PdM for Hg adsorption and reduces the activity of Pd2. It is also found that Pd is the main active composition responsible for the interaction of mercury with the surface for PdM/γ-Al2O3 sorbent. Taking Hg adsorption capacity and economic costs into account, Cu addition is a comparatively good candidate for Hg capture.

  14. Copper-based alloys, crystallographic and crystallochemical parameters of alloys in binary systems Cu-Me (Me=Co, Rh, Ir, Cu, Ag, Au, Ni, Pd, Pt)

    Energy Technology Data Exchange (ETDEWEB)

    Porobova, Svetlana, E-mail: porobova.sveta@yandex.ru; Loskutov, Oleg, E-mail: lom58@mail.ru [Tomsk State University of Architecture and Building, Russia, Tomsk, 2 Solyanaya sq, Tomsk, 634003 (Russian Federation); Markova, Tat’jana, E-mail: patriot-rf@mail.ru [Siberian State Industrial University. 42 Kirov St., Novokuznetsk, 654007 (Russian Federation); Klopotov, Vladimir, E-mail: vdklopotov@mail.ru [Research Tomsk Polytechnic University, 30 Lenin Ave., Tomsk, 634050 (Russian Federation); Klopotov, Anatoliy, E-mail: klopotovaa@tsuab.ru [Tomsk State University of Architecture and Building, Russia, Tomsk, 2 Solyanaya sq, Tomsk, 634003 (Russian Federation); National Research Tomsk State University, 36, Lenin Ave., Tomsk, 634050 (Russian Federation); Vlasov, Viktor, E-mail: vik@tsuab.ru [Tomsk State University of Architecture and Building, Russia, Tomsk, 2 Solyanaya sq, Tomsk, 634003 (Russian Federation); Research Tomsk Polytechnic University, 30 Lenin Ave., Tomsk, 634050 (Russian Federation)

    2016-01-15

    The article presents the results of the analysis of phase equilibrium of ordered phases in binary systems based on copper Cu- Me (where Me - Co, Rh, Ir, Ag, Au, Ni, Pd, Pt) to find correlations of crystallochemical and crystallographic factors. It is established that the packing index in disordered solid solutions in binary systems based on copper is close to the value of 0.74 against the background of an insignificant deviation of atomic volumes from the Zen’s law.

  15. Copper-based alloys, crystallographic and crystallochemical parameters of alloys in binary systems Cu-Me (Me=Co, Rh, Ir, Cu, Ag, Au, Ni, Pd, Pt)

    Science.gov (United States)

    Porobova, Svetlana; Markova, Tat'jana; Klopotov, Vladimir; Klopotov, Anatoliy; Loskutov, Oleg; Vlasov, Viktor

    2016-01-01

    The article presents the results of the analysis of phase equilibrium of ordered phases in binary systems based on copper Cu- Me (where Me - Co, Rh, Ir, Ag, Au, Ni, Pd, Pt) to find correlations of crystallochemical and crystallographic factors. It is established that the packing index in disordered solid solutions in binary systems based on copper is close to the value of 0.74 against the background of an insignificant deviation of atomic volumes from the Zen's law.

  16. Adsorption of Pd, Pt, Cu, Ag, and Au monomers on NiAl(110) surface: a comparative study from DFT calculations.

    Science.gov (United States)

    San-Miguel, Miguel A; Amorim, Edgard P M; da Silva, E Z

    2014-08-01

    First principles calculations based on periodic density functional theory (DFT) have been used to investigate the structural, energetic and electronic properties of different transition metal atoms (Pd, Pt, Cu, Ag, and Au) on the NiAl(110) surface at low coverages (0.08 and 0.25 monolayer). All adatoms prefer to adsorb on 4-fold coordinated sites interacting with two Al and two Ni atoms and forming polar and covalent bonds, respectively. The calculated negative work function changes are explained by the effect of positive surface image created after adsorption, which induces the polarization of the negatively charged adsorbates. Consequently, for metals with similar electronegativity as Ni (Ag and Cu), this polarization effect becomes more significant and leads to larger negative work function changes, but the charge transferred is small. PMID:24219765

  17. Self-consistent linear-muffin-tin-orbitals coherent-potential technique for bulk and surface calculations: Cu-Ni, Ag-Pd, and Au-Pt random alloys

    OpenAIRE

    Abrikosov, I. A.; Skriver, Hans Lomholt

    1993-01-01

    We present an efficient technique for calculating surface properties of random alloys based on the coherent-potential approximation within a tight-binding linear-muffin-tin-orbitals basis. The technique has been applied in the calculation of bulk thermodynamic properties as well as (001) surface energies and work functions for three fcc-based alloys (Cu-Ni, Ag-Pd, and Au-Pt) over the complete concentration range. The calculated mixing enthalpies for the Ag-Pd and Au-Pt systems agrees with exp...

  18. Adsorption properties of Ag(I), Au(III), Pd(II) and Pt(IV) ions on commercial 717 anion-exchange resin

    Institute of Scientific and Technical Information of China (English)

    LIU Peng; LIU Guang-feng; CHEN Da-lin; CHENG Shao-yi; TANG Ning

    2009-01-01

    The adsorption properties of the four precious metal ions (Ag(Ⅰ),Au(Ⅲ),Pd(Ⅱ) and Pt(Ⅳ)) on the commercial Cl--form 717 strongly basic anion-exchange resin were studied in detail.The effects of the contact time,solution acidity,and concentrations of Cl~- and Pb~(2+) ions on the adsorption properties were studied by the batch method.Then,the column method was conducted under the optimized adsorption conditions (pH=3.0).The effects of the sample loading flow rate and the length-to-diameter ratios of the columns were investigated.The precious metal ions adsorbed could not be eluted completely after the saturated adsorption because the precious metal ions were found to be reduced to their metallic states during the adsorption process.So,it is recommended that the commercial Cl~--form 717 strongly basic anion-exchange resin should be decomposed directly to recovery the precious metals after the saturated adsorption.

  19. Influence of the noble metals (Pd, Au, Ag) in the thermoluminescent signal induced by radiation in the ZrO2

    International Nuclear Information System (INIS)

    When increasing the use of the ionizing and non ionizing radiations (for example, gamma and ultraviolet radiation) in different areas of the science and technology, there is necessary to apply more accurate safety measures and to avoid over-exposures that could put in risk the life of workers that manipulate radiation sources, patient that are exposed to this under some medical treatment, as well as materials that undergo intentionally to radiation. Also, the UV radiation that arrives to the earth can cause some damages, to the one to weaken the protector layer of ozone the UV radiation increases that arrives to the earth surface being able to affect the alive beings and the materials. By this so much the development of new materials able to take a census of in a more accurate way, fields of gamma and UV radiation is becoming necessary. In this sense, this work presents the obtained results when quantifying radiation fields, through the analysis in the thermoluminescent behavior (TL) induced by the gamma and UV radiation in the zirconium dioxide synthesized by the sol gel method and doped with nanoparticles of Pd, Au and Ag. It is necessary to mention that in reported works in this respect its mention that the zircon has good thermoluminescent sensitivity induced by these radiation types, however it has shown high thermoluminescent instability that is translated in an important lost of the information after the irradiation. For that through the incorporation of the metallic nanoparticles it was intended to stabilize the TL behavior of zircon. The results showed that the doped zircon has a high sensitivity to the gamma and UV radiation. These also show that the ionizing and non ionizing radiation induce a thermoluminescent curve consisting of two TL peaks with maxima located around 65 C and 145 C and that the intensity is increased with the dose, following a lineal behavior in certain interval of dose exposure that is influenced by the presence of the nanoparticles

  20. Propiedades de aleaciones Ag-Pd para usos odontológicos

    OpenAIRE

    Basualto, J.; Barceló, C.; Gaete, A.

    1996-01-01

    In this search for economically alternative alloys for odontological uses, three complex Ag-Pd alloys, Ag-Pd-Au-Cu type, are studied: two experimental alloys and one commercial product. Chemical and mechanical properties were obtained for these alloys and a comparative analysis of these results was made. The cost, important factor, is established in relation to the materials cost of the commercial product. Vickers hardness values obtained from Ag-Pd alloys with different heat treatments allow...

  1. Casting of MOD inlay using rings with holes on both sides: 12∼18 wt%Au-20∼26Pd-14.48∼26.48Cu-40Ag-1.5Zn-0.02Ir alloys.

    Science.gov (United States)

    Ohkuma, Kazuo; Kazama, Miku; Ogura, Hideo

    2012-01-01

    Using a casting ring with openings on both sides and a water-absorbent polymer, heterogeneity is maintained in a single casting and a precise MOD inlay can be produced. We produced 9 different kinds of gold-silver-palladium (Au-Ag-Pd) alloys by changing the ratio of palladium, gold, and copper and investing them, and changing parameters such as the angulation of the casting ring openings and the water:powder ratios to produce MOD inlay castings. We measured the expansion and shrinkage percentage of the castings in both the buccolingual and mesiodistal directions. From this experiment, we learned that precise MOD inlay castings can be produced using rings with 240° openings when invested in a thick mix having a standard water:powder ratio or using rings with 200° openings when invested in a thick mix having a water:powder ratio for a 12 wt%Au-20∼26Pd-20.48∼26.48Cu-40Ag-1.5Zn-0.02Ir alloyes.

  2. LaMgX and CeMgX (X = Ga, In, Tl, Pd, Ag, Pt, Au) with ZrNiAl type structure - A systematic view on electronic structure and chemical bonding

    Science.gov (United States)

    Matar, Samir F.; Etourneau, Jean; Pöttgen, Rainer

    2015-05-01

    The intermetallic magnesium compounds LaMgX and CeMgX (X = Ga, In, Tl, Pd, Ag, Pt, Au) crystallize with the hexagonal ZrNiAl type structure, space group P 6 bar 2 m , with full Mg-X ordering. From density functional theory calculations carried out exemplarily on four representative compounds: LaMgX and CeMgX with X = Ga, Pd, significant differences were traced out as to the magnetism arising only for the Ce series leading to identify CeMgGa as an antiferromagnet in its ground state, in agreement with experiment. The bulk module magnitudes show the trend of harder transition metal based ternaries and the cohesive energies favor the X = Pd compounds versus X = Ga ones. Such features were clarified by examining the properties of chemical bonding which exhibit more directional bonds thanks to the Pd d states. Rationalizing the trends of charge transfers, negatively charged triel and transition element atoms are observed. The resulting chemical pictures assign these compounds as gallides and palladides.

  3. Influence of the noble metals (Pd, Au, Ag) in the thermoluminescent signal induced by radiation in the ZrO{sub 2}; Influencia de los metales nobles (Pd, Au, Ag) en la senal termoluminiscente inducida por la radiacion en la ZrO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Villa S, G

    2006-07-01

    When increasing the use of the ionizing and non ionizing radiations (for example, gamma and ultraviolet radiation) in different areas of the science and technology, there is necessary to apply more accurate safety measures and to avoid over-exposures that could put in risk the life of workers that manipulate radiation sources, patient that are exposed to this under some medical treatment, as well as materials that undergo intentionally to radiation. Also, the UV radiation that arrives to the earth can cause some damages, to the one to weaken the protector layer of ozone the UV radiation increases that arrives to the earth surface being able to affect the alive beings and the materials. By this so much the development of new materials able to take a census of in a more accurate way, fields of gamma and UV radiation is becoming necessary. In this sense, this work presents the obtained results when quantifying radiation fields, through the analysis in the thermoluminescent behavior (TL) induced by the gamma and UV radiation in the zirconium dioxide synthesized by the sol gel method and doped with nanoparticles of Pd, Au and Ag. It is necessary to mention that in reported works in this respect its mention that the zircon has good thermoluminescent sensitivity induced by these radiation types, however it has shown high thermoluminescent instability that is translated in an important lost of the information after the irradiation. For that through the incorporation of the metallic nanoparticles it was intended to stabilize the TL behavior of zircon. The results showed that the doped zircon has a high sensitivity to the gamma and UV radiation. These also show that the ionizing and non ionizing radiation induce a thermoluminescent curve consisting of two TL peaks with maxima located around 65 C and 145 C and that the intensity is increased with the dose, following a lineal behavior in certain interval of dose exposure that is influenced by the presence of the nanoparticles

  4. Hollow Au@Pd and Au@Pt core-shell nanoparticles as electrocatalysts for ethanol oxidation reactions

    KAUST Repository

    Song, HyonMin

    2012-09-27

    Hybrid alloys among gold, palladium and platinum become a new category of catalysts primarily due to their enhanced catalytic effects. Enhancement means not only their effectiveness, but also their uniqueness as catalysts for the reactions that individual metals may not catalyze. Here, preparation of hollow Au@Pd and Au@Pt core-shell nanoparticles (NPs) and their use as electrocatalysts are reported. Galvanic displacement with Ag NPs is used to obtain hollow NPs, and higher reduction potential of Au compared to Ag, Pd, and Pt helps to produce hollow Au cores first, followed by Pd or Pt shell growth. Continuous and highly crystalline shell growth was observed in Au@Pd core-shell NPs, but the sporadic and porous-like structure was observed in Au@Pt core-shell NPs. Along with hollow core-shell NPs, hollow porous Pt and hollow Au NPs are also prepared from Ag seed NPs. Twin boundaries which are typically observed in large size (>20 nm) Au NPs were not observed in hollow Au NPs. This absence is believed to be due to the role of the hollows, which significantly reduce the strain energy of edges where the two lattice planes meet. In ethanol oxidation reactions in alkaline medium, hollow Au@Pd core-shell NPs show highest current density in forward scan. Hollow Au@Pt core-shell NPs maintain better catalytic activities than metallic Pt, which is thought to be due to the better crystallinity of Pt shells as well as the alloy effect of Au cores. © 2012 The Royal Society of Chemistry.

  5. Electrical properties of thin-film structures formed by pulsed laser deposition of Au, Ag, Cu, Pd, Pt, W, Zr metals on n-6H-SiC crystal

    International Nuclear Information System (INIS)

    Diode structures with ideality factors of 1.28-2.14 and potential barriers from 0.58 to 0.62 eV on the semiconductor side were formed by pulsed laser deposition of Au, Ag, Cu, Pd, Pt, W, and Zr metal films on n-6H-SiC crystal without epitaxial layer preparation. A high density of surface acceptor and donor states was formed at the metal-semiconductor interface during deposition of the laser-induced atomic flux, which violated the correlation between the potential barrier height and metal work function. The barrier heights determined from characteristic currents and capacitance measurements were in quite good agreement. For the used low-resistance semiconductor and contact elements, the sizes of majority carrier (electron) depletion regions were determined as 26-60 nm.

  6. Strain distributions of confined Au/Ag and Ag/Au nanoparticles

    Institute of Scientific and Technical Information of China (English)

    黄红华; 章英; 刘晓山; 骆兴芳; 袁彩雷; 叶双莉

    2015-01-01

    The strain distributions of Au/Ag and Ag/Au nanoparticles confined in the Al2O3 matrix with different core sizes are investigated by using the finite element method, respectively. The simulation results clearly indicate that the compressive strains exerted on the Au/Ag and Ag/Au nanoparticles can be induced by the Al2O3 matrix. Moreover, it can be found that the strain gradient existing in a Au/Ag nanoparticle is much larger than that in a Ag/Au nanoparticle, which could be due to the larger Young’s modulus of Au than that of Ag. With the core size increasing, the strain gradient existing in the Au/Ag nanoparticle becomes larger, while the strain gradient existing in the Ag/Au nanoparticle keeps constant. These different strain distributions may have significant infl uences on the structures and morphologies of the Au/Ag and Ag/Au nanoparticles, leading to the different physical properties for potential applications.

  7. Au, Ag and Au:Ag colloidal nanoparticles synthesized by pulsed laser ablation as SERS substrates

    Directory of Open Access Journals (Sweden)

    M. Vinod

    2014-12-01

    Full Text Available Chemically pure colloidal suspensions of gold and silver nanoparticles were synthesized using pulsed laser ablation. The dependence of laser fluence on the surface plasmon characteristics of the nanoparticles was investigated. Au:Ag colloidal suspensions were prepared by mixing highly monodisperse Au and Ag nanocolloids. The plasmon band of these mixtures was found to be highly sensitive to Au:Ag concentration ratio and wavelength of the laser beam used in the ablation process. The Au:Ag mixture consists of almost spherical shaped nanostructures with a tendency to join with adjacent ones. The surface enhanced Raman scattering activity of the Au, Ag and Au:Ag colloidal suspensions was tested using crystal violet as probe molecules. Enhancement in Raman signal obtained with Au:Ag substrates was found to be promising and strongly depends on its plasmon characteristics.

  8. Au, Ag and Au:Ag colloidal nanoparticles synthesized by pulsed laser ablation as SERS substrates

    Institute of Scientific and Technical Information of China (English)

    M. Vinod; K.G.Gopchandran

    2014-01-01

    Chemically pure colloidal suspensions of gold and silver nanoparticles were synthesized using pulsed laser ablation. The dependence of laser fluence on the surface plasmon characteristics of the nanoparticles was investigated. Au:Ag colloidal suspensions were prepared by mixing highly monodisperse Au and Ag nanocolloids. The plasmon band of these mixtures was found to be highly sensitive to Au:Ag concentration ratio and wavelength of the laser beam used in the ablation process. The Au:Ag mixture consists of almost spherical shaped nanostructures with a tendency to join with adjacent ones. The surface enhanced Raman scattering activity of the Au, Ag and Au:Ag colloidal suspensions was tested using crystal violet as probe molecules. Enhancement in Raman signal obtained with Au:Ag substrates was found to be promising and strongly depends on its plasmon characteristics.

  9. Development of highly transparent Pd-coated Ag nanowire electrode for display and catalysis applications

    International Nuclear Information System (INIS)

    Highlights: • Highly uniform thin-layer coating of Pd onto Ag nanowire surface was accomplished. • A transparent electrode of Pd-coated Ag nanowire was uniformly deposited on flexible substrate. • 95% of optical transmittance and 175 Ω/sq sheet resistance were obtained. • Extremely low haze of 1.9% and high oxidation stability proved an efficient transparent electrode. • This electrode can be used as Pd-catalyst for synthesis reactions and fuel cell electrode applications. - Abstract: Ag nanowire transparent electrode has excellent transmittance (90%) and sheet resistance (20 Ω/sq), yet there are slight drawbacks such as optical haze and chemical instability against aerial oxidation. Chemical stability of Ag nanowires needs to be improved in order for it to be suitable for electrode applications. In our recent article, we demonstrated that coating Ag nanowires with a thin layer of Au through galvanic exchange reactions enhances the chemical stability of Ag nanowire films highly and also helps to obtain lower haze. In this study, coating of a thin Pd layer has been applied successfully onto the surface of Ag nanowires. A mild Pd complex oxidant [Pd(en)2](NO3)2 was prepared in order to oxidize Ag atoms partially on the surface via galvanic displacement. The mild galvanic exchange allowed for a thin layer (1–2 nm) of Pd coating on the Ag nanowires with minimal truncation of the nanowire, where the average length and the diameter were 12.5 μm and 59 nm, respectively. The Pd-coated Ag nanowires were suspended in methanol and then electrostatically sprayed on flexible polycarbonate substrates. It has been revealed that average total transmittance remain around 95% within visible spectrum region (400–800 nm) whereas sheet resistance rises up to 175 Ω/sq. To the best of our knowledge, for the first time in the literature, Pd coating was employed on Ag nanowires in order to design transparent electrodes for high transparency and strong chemical resistivity

  10. Development of highly transparent Pd-coated Ag nanowire electrode for display and catalysis applications

    Energy Technology Data Exchange (ETDEWEB)

    Canlier, Ali, E-mail: ali.canlier@agu.edu.tr [Department of Materials Science and Nanotechnology Engineering, Abdullah Gul University, P.O. Box 38080, Kayseri (Turkey); Ucak, Umit Volkan, E-mail: sirvolkan@gmail.com [Department of Materials Science and Nanotechnology Engineering, Abdullah Gul University, P.O. Box 38080, Kayseri (Turkey); Graduate School of Energy, Environment, Water, and Sustainability (EEWS), Korea Advanced Institute of Science and Technology (KAIST), P.O. Box 305-701, Daejeon (Korea, Republic of); Usta, Hakan, E-mail: husta38@gmail.com [Department of Materials Science and Nanotechnology Engineering, Abdullah Gul University, P.O. Box 38080, Kayseri (Turkey); Cho, Changsoon, E-mail: cscho@kaist.ac.kr [Graduate School of Energy, Environment, Water, and Sustainability (EEWS), Korea Advanced Institute of Science and Technology (KAIST), P.O. Box 305-701, Daejeon (Korea, Republic of); Lee, Jung-Yong, E-mail: jungyong.lee@kaist.ac.kr [Graduate School of Energy, Environment, Water, and Sustainability (EEWS), Korea Advanced Institute of Science and Technology (KAIST), P.O. Box 305-701, Daejeon (Korea, Republic of); Sen, Unal, E-mail: senunal@gmail.com [Department of Mechanical Engineering, Abdullah Gul University, P.O. Box 38080, Kayseri (Turkey); Citir, Murat, E-mail: muratcitir@gmail.com [Department of Chemical Engineering, Abdullah Gul University, P.O. Box 38080, Kayseri (Turkey)

    2015-09-30

    Highlights: • Highly uniform thin-layer coating of Pd onto Ag nanowire surface was accomplished. • A transparent electrode of Pd-coated Ag nanowire was uniformly deposited on flexible substrate. • 95% of optical transmittance and 175 Ω/sq sheet resistance were obtained. • Extremely low haze of 1.9% and high oxidation stability proved an efficient transparent electrode. • This electrode can be used as Pd-catalyst for synthesis reactions and fuel cell electrode applications. - Abstract: Ag nanowire transparent electrode has excellent transmittance (90%) and sheet resistance (20 Ω/sq), yet there are slight drawbacks such as optical haze and chemical instability against aerial oxidation. Chemical stability of Ag nanowires needs to be improved in order for it to be suitable for electrode applications. In our recent article, we demonstrated that coating Ag nanowires with a thin layer of Au through galvanic exchange reactions enhances the chemical stability of Ag nanowire films highly and also helps to obtain lower haze. In this study, coating of a thin Pd layer has been applied successfully onto the surface of Ag nanowires. A mild Pd complex oxidant [Pd(en){sub 2}](NO{sub 3}){sub 2} was prepared in order to oxidize Ag atoms partially on the surface via galvanic displacement. The mild galvanic exchange allowed for a thin layer (1–2 nm) of Pd coating on the Ag nanowires with minimal truncation of the nanowire, where the average length and the diameter were 12.5 μm and 59 nm, respectively. The Pd-coated Ag nanowires were suspended in methanol and then electrostatically sprayed on flexible polycarbonate substrates. It has been revealed that average total transmittance remain around 95% within visible spectrum region (400–800 nm) whereas sheet resistance rises up to 175 Ω/sq. To the best of our knowledge, for the first time in the literature, Pd coating was employed on Ag nanowires in order to design transparent electrodes for high transparency and strong

  11. Partial phase diagram of Pd-Ag-Ru-Gd quaternary system

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    On the basis of the Ag-Pd-Gd, Ag-Ru-Gd and Pd-Ru-Gd ternary systems, the partial phase diagram of Pd-Ag-Ru-Gd(Gd<25% atom fraction) quaternary system has been studied by means of X-ray diffraction analysis, differential thermal analysis, electron probe microanalysis and optical microscopy.The 700℃ isothermal sections of the Ag-Pd-5Ru-Gd, Ag-Pd-20Ru-Gd and Ag-Pd-50Ru-Gd (Gd≤25%atom fraction) phase diagrams were determined respectively. And the 700℃ isothermal section of the PdAg-Ru-Gd (Gd≤25% atom fraction) quaternary system phase diagram was finally irferred. The section consists of four single-phase regions: solid solution Pd(Ag), (Ru), Pd3Gd and Ag51 Gd14; five two-phase regions: Pd(Ag) + (Ru), Pd(Ag) + Ag51 Gd14 , (Ru) + Ag51 Gd14 , Pd(Ag) + Pd3Gd and (Ru) +Pd3Gd; three three-phase regions: Pd(Ag) + Pd3Gd+ (Ru), Pd(Ag) + Ag51Gd14 + (Ru) and (Ru) +Ag51Gd14 + Pd3Gd; one four-phase region Pd(Ag) + (Ru) + Ag51Gd14 + Pd3Gd. No new quaternary intermetallic phase is found.

  12. Monodispersed bimetallic PdAg nanoparticles with twinned structures: Formation and enhancement for the methanol oxidation

    OpenAIRE

    Zhen Yin; Yining Zhang; Kai Chen; Jing Li; Wenjing Li; Pei Tang; Huabo Zhao; Qingjun Zhu; Xinhe Bao; Ding Ma

    2014-01-01

    Monodispersed bimetallic PdAg nanoparticles can be fabricated through the emulsion-assisted ethylene glycol (EG) ternary system. Different compositions of bimetallic PdAg nanoparticles, Pd80Ag20, Pd65Ag35 and Pd46Ag54 can be obtained via adjusting the reaction parameters. For the formation process of the bimetallic PdAg nanoparticles, there have two-stage growth processes: firstly, nucleation and growth of the primary nanoclusters; secondly, formation of the secondary nanoparticles with the s...

  13. Hydrogen evolution on Au(111) covered with submonolayers of Pd

    DEFF Research Database (Denmark)

    Björketun, Mårten; Karlberg, Gustav; Rossmeisl, Jan;

    2011-01-01

    . The energetics of adsorption and desorption of hydrogen on/from different types of sites on the Pd-Au(111) surface are assessed by means of density functional theory calculations combined with thermodynamic modeling. Based on the density functional and Monte Carlo data, the hydrogen evolution activity......A theoretical investigation of electrochemical hydrogen evolution on Au(111) covered with submonolayers of Pd is presented. The size and shape of monoatomically high Pd islands formed on the Au(111) surface are determined using Monte Carlo simulations, for Pd coverages varying from 0.02 to 0.95 ML...... line defects for Pd island formation and hydrogen evolution are discussed. It is argued, with support from theoretical data, that this kind of defects is likely to be responsible for a dramatic increase in activity observed experimentally [ChemPhysChem 7, 985 (2006); Electrochim. Acta 52, 5548 (2007...

  14. Structure and Mobility of Metal Clusters in MOFs: Au, Pd, and AuPd Clusters in MOF-74

    DEFF Research Database (Denmark)

    Vilhelmsen, Lasse; Walton, Krista S.; Sholl, David S.

    2012-01-01

    Understanding the adsorption and mobility of metal–organic framework (MOF)-supported metal nanoclusters is critical to the development of these catalytic materials. We present the first theoretical investigation of Au-, Pd-, and AuPd-supported clusters in a MOF, namely MOF-74. We combine density...... functional theory (DFT) calculations with a genetic algorithm (GA) to reliably predict the structure of the adsorbed clusters. This approach allows comparison of hundreds of adsorbed configurations for each cluster. From the investigation of Au8, Pd8, and Au4Pd4 we find that the organic part of the MOF...... is just as important for nanocluster adsorption as open Zn or Mg metal sites. Using the large number of clusters generated by the GA, we developed a systematic method for predicting the mobility of adsorbed clusters. Through the investigation of diffusion paths a relationship between the cluster...

  15. Optical absorption engineering in stacked plasmonic Au-SiO₂-Pd nanoantennas.

    Science.gov (United States)

    Wadell, Carl; Antosiewicz, Tomasz J; Langhammer, Christoph

    2012-09-12

    The nonradiative decay of a localized surface plasmon through absorption of a captured photon and excitation of an energetic electron-hole pair is a potentially very effective way to enhance chemical reactions on metal nanoparticle surfaces, so far limited to Ag (and Au). Here we explore the possibility of efficient and spectrally widely tunable optical absorption engineering based on heterometallic optical nanoantennas. They consist of an optimized antenna element made of Au (or Ag) and a catalytically active second metallic element separated by a thin SiO(2) layer. Specifically, we find that stacked Au-SiO(2)-Pd nanodisk antennas exhibit pronounced local absorption enhancement in the catalytic Pd particle. The effect is caused by efficient power transfer from the Au disk, exhibiting a narrow low-loss resonance and acting as an antenna collecting photons, to the Pd disk due to strong coupling between the two. The Pd element thus acts as receiver that efficiently dissipates energy into electron-hole pairs owing to efficient coupling to intra and interband transitions. In fact, the energy transfer is found to be so effective that the absorption efficiency at a given wavelength can be enhanced up to 6 to 9 times, and the total absorption integrated over a wide spectral range (400-900 nm) up to 2-fold, depending on the antenna dimensions. This finding suggests a novel route toward highly efficient plasmon-enhanced catalysis on widely selectable catalytic metal particle surfaces not limited to the "classic" plasmonic metals Au and Ag. PMID:22916998

  16. Fabricating a Homogeneously Alloyed AuAg Shell on Au Nanorods to Achieve Strong, Stable, and Tunable Surface Plasmon Resonances

    KAUST Repository

    Huang, Jianfeng

    2015-08-13

    Colloidal metal nanocrystals with strong, stable, and tunable localized surface plasmon resonances (SPRs) can be useful in a corrosive environment for many applications including field-enhanced spectroscopies, plasmon-mediated catalysis, etc. Here, a new synthetic strategy is reported that enables the epitaxial growth of a homogeneously alloyed AuAg shell on Au nanorod seeds, circumventing the phase segregation of Au and Ag encountered in conventional synthesis. The resulting core–shell structured bimetallic nanorods (AuNR@AuAg) have well-mixed Au and Ag atoms in their shell without discernible domains. This degree of mixing allows AuNR@AuAg to combine the high stability of Au with the superior plasmonic activity of Ag, thus outperforming seemingly similar nanostructures with monometallic shells (e.g., Ag-coated Au NRs (AuNR@Ag) and Au-coated Au NRs (AuNR@Au)). AuNR@AuAg is comparable to AuNR@Ag in plasmonic activity, but that it is markedly more stable toward oxidative treatment. Specifically, AuNR@AuAg and AuNR@Ag exhibit similarly strong signals in surface-enhanced Raman spectroscopy that are some 30-fold higher than that of AuNR@Au. When incubated with a H2O2 solution (0.5 m), the plasmonic activity of AuNR@Ag immediately and severely decayed, whereas AuNR@AuAg retained its activity intact. Moreover, the longitudinal SPR frequency of AuNR@AuAg can be tuned throughout the red wavelengths (≈620–690 nm) by controlling the thickness of the AuAg alloy shell. The synthetic strategy is versatile to fabricate AuAg alloyed shells on different shaped Au, with prospects for new possibilities in the synthesis and application of plasmonic nanocrystals.

  17. Alumina supported model Pd Ag catalysts: A combined STM, XPS, TPD and IRAS study

    Science.gov (United States)

    Khan, N. A.; Uhl, A.; Shaikhutdinov, S.; Freund, H.-J.

    2006-05-01

    The bimetallic Pd-Ag model catalysts were prepared by physical vapor deposition on thin alumina films. The morphology and structure of the Pd-Ag particles were studied by STM, XPS, and by TPD and IRAS of CO. The results showed the formation of true alloy particles with Ag segregated at the surface. The addition of Ag first suppresses the most strongly bonded CO on threefold hollow sites of Pd. With further increasing Ag coverage, only isolated Pd atoms surrounded by Ag atoms are likely present on the surface. The results on CO adsorption suggest that the model Pd-Ag system mimics the structure of the real Pd-Ag catalysts.

  18. Hydrogen adsorption on bimetallic PdAu(111) surface alloys

    DEFF Research Database (Denmark)

    Takehiro, Naoki; Liu, Ping; Bergbreiter, Andreas;

    2014-01-01

    The adsorption of hydrogen on structurally well defined PdAu-Pd(111) monolayer surface alloys was investigated in a combined experimental and theoretical study, aiming at a quantitative understanding of the adsorption and desorption properties of individual PdAu nanostructures. Combining...... the structural information obtained by high resolution scanning tunneling microscopy (STM), in particular on the abundance of specific adsorption ensembles at different Pd surface concentrations, with information on the adsorption properties derived from temperature programmed desorption (TPD) spectroscopy...... and high resolution electron energy loss spectroscopy (HREELS) provides conclusions on the minimum ensemble size for dissociative adsorption of hydrogen and on the adsorption energies on different sites active for adsorption. Density functional theory (DFT) based calculations give detailed insight...

  19. Component conversion from pure Au nanorods to multiblock Ag-Au-Ag nanorods assisted by Pt nanoframe templates

    Science.gov (United States)

    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

  20. Selective Hydrogenation of Acetylene over Pd, Au, and PdAu Supported Nanoparticles

    Science.gov (United States)

    Walker, Michael P.

    The removal of trace amounts of acetylene in ethylene streams is a high-volume industrial process that must possess high selectivity of alkyne hydrogenation over hydrogenation of alkenes. Current technology uses metallic nanoparticles, typically palladium or platinum, for acetylene removal. However, problems arise due to the deactivation of the catalysts at high temperatures as well as low selectivities at high conversions. Pore expanded MCM-41 is synthesized via a two-step strategy in which MCM-41 was prepared via cetyltrimethylammonium bromide (CTMABr) followed by the hydrothermal treatment with N,N-dimethyldecylamine (DMDA). This material was washed with ethanol to remove DMDA, or calcined to remove both surfactants. PE-MCM-41 based materials were impregnated with palladium, gold, and palladium-gold nanoparticles. The removal of DMDA had an effect on both the conversion and selectivity, in which they were found to drop significantly. However, by using the bimetallic PdAu catalysts, higher selectivity could be achieved due to increased electron density.

  1. Hysteresis-free nanoplasmonic pd-au alloy hydrogen sensors

    DEFF Research Database (Denmark)

    Wadell, Carl; Nugroho, Ferry Anggoro Ardy; Lidström, Emil;

    2015-01-01

    The recent market introduction of hydrogen fuel cell cars and the prospect of a hydrogen economy have drastically accelerated the need for safe and accurate detection of hydrogen. In this Letter, we investigate the use of arrays of nanofabricated Pd-Au alloy nanoparticles as plasmonic optical...

  2. Ordered phase formation and diffusion composition path in Cu3Au/Pd couple

    International Nuclear Information System (INIS)

    EDX-TEM technique, IKL-ALCHEMI and Monte Carlo simulation were employed to reveal the relation between diffusion composition path and the ordered structures in Cu3Au/Pd diffusion couple annealed at 573 K. A Cu3Au layer including Pd, a CuAu layer including Pd, a CuPd layer and a Pd layer including Cu existed in sequence between Cu3Au and Pd. The Au concentration increased by up-hill diffusion from the Cu3Au layer to the CuAu layer, whereas Au scarcely diffused from the CuAu into the CuPd layer. The diffusion composition path deviated from the Cu3Au-Pd line in the Cu-Au-Pd Gibbs triangle and exhibited an 'S-shaped' curve through the CuAu and CuPd existence regions. The atomic configurations in the L10-type phase were highly ordered and consistent with the equilibrium state. In the Monte Carlo simulation, diffusion couples were virtually produced. The diffusion composition paths, Fourier power spectra and Warren-Cowley parameters were estimated in this way. The strong ordering interactions of the Cu-Au pair and Cu-Pd pair in the first nearest neighbor and the high activation barrier for migration of Au reproduced experimental results

  3. Manipulating the optical properties of symmetrically branched Au/Pd nanocrystals through interior design.

    Science.gov (United States)

    DeSantis, Christopher J; Skrabalak, Sara E

    2014-05-25

    Au/Pd octopods with hollow, cubic interiors and Oh symmetry were synthesized for the first time by etching core@shell Pd@Au/Pd octopods to selectively remove their Pd interiors. Integration of multiple architectural features - in this case branching symmetry, composition, and interior design - into one nanostructure provides design strategies to new plasmonic colloids.

  4. An optical fiber hydrogen sensor with Pd/Ag film

    Institute of Scientific and Technical Information of China (English)

    CUI Lu-jun; CHEN You-ping; ZHANG Gang

    2009-01-01

    A 20 nanometer palladium-silver (Pd/Ag) ultra-thin film was used for hydrogen gas sensing. The atomic ratio of Pd: Ag was 3:1, the thin film was evaporated on the optical glass, the Pd/Ag alloy could increase the life and provide the stability of the sensing film. The artificial neutral network was used for processing the data collected from the optical fiber bundle hydro-gen sensor, which could enhance the measuring accuracy, at the same time, the intrinsic and extrinsic influences were eliminated mainly. Experimental results and numerical simulation show the training method available, a linear precision of 0.1% for the optical hydrogen sensor is achieved.

  5. Sodium citrate assisted facile synthesis of AuPd alloy networks for ethanol electrooxidation with high activity and durability

    Science.gov (United States)

    Zhai, Yanling; Zhu, Zhijun; Lu, Xiaolin; Zhou, H. Susan

    2016-10-01

    The direct ethanol fuel cell is an emerging energy conversion device for which palladium is considered as the one of the most effective components for anode catalyst, however, its widespread application has been still limited by the activity and durability of the anode catalyst. In this work, AuPd alloy networks (NWs) are synthesized using H2PdCl4 and HAuCl4 as precursors reduced by NaBH4 in the presence of sodium citrate (SC). The results reveal that SC plays significant role in network structure, resulting in the enhanced electrocatalytic activity of the catalyst. This self-supported AuPd NWs catalyst exhibits much higher electrochemical catalytic activity than commercial Pd/C catalyst toward ethanol electrooxidation in alkaline solution. Significantly, AuPd NWs catalyst shows extremely high durability at the beginning of the chronoamperometry test, and as high as 49% of the mass current density (1.41 A/mgPd) remains after 4000 s current-time test at -0.3 V (vs. Ag/AgCl) in N2-saturated KOH-ethanol solution. This strategy provides a facile method for the preparation of alloy networks with high electrochemical activity, and can be potentially expanded to a variety of electrochemical applications.

  6. PdAu/C catalysts prepared by plasma sputtering for the electro-oxidation of glycerol

    OpenAIRE

    Mougenot, Mathieu; Caillard, Amaël; Simoes, Mario; Baranton, Steve; Coutanceau, Christophe; Brault, Pascal

    2011-01-01

    Co-sputtered Pd0.7Au0.3 catalyst and alternate sputtered Pd0.35Au0.3Pd0.35 and Au0.15Pd0.7Au0.15 materials were prepared by plasma deposition of Au and Pd atoms on a carbon diffusion layer. Atomic composition and metal loadings were evaluated from EDX and RBS, respectively. The low amount of metal deposited and the resulting low metallic film thickness made TEM and XRD characterizations difficult to perform, therefore, catalyst microstructures and surface compositions were determined from ele...

  7. Synthesis of Pt, Pd, Pt/Ag and Pd/Ag nanoparticles by microwave-polyol method

    Indian Academy of Sciences (India)

    Kirti Patel; Sudhir Kapoor; Devilal Purshottam Dave; Tulsi Mukherjee

    2005-07-01

    Pt, Pd, Pt-Ag and Pd-Ag bimetallic nanoparticles were synthesized in ethylene glycol and glycerol using the microwave technique in the presence of a stabilizer poly(N-vinylpyrrolidone) (PVP). It has been observed that PVP is capable of complexing and stabilizing nanoparticles. Mixed clusters were formed by simultaneous reduction of the metal ions. The clusters were characterized using UV-Vis spectra, XRD and dynamic light scattering. To understand the mechanism of formation of mixed nanoparticles, several experimental parameters such as in situ irradiation of mixed metal salts and mixing of individual sols were attempted.

  8. Propiedades de aleaciones Ag-Pd para usos odontológicos

    Directory of Open Access Journals (Sweden)

    Basualto, J.

    1996-10-01

    Full Text Available In this search for economically alternative alloys for odontological uses, three complex Ag-Pd alloys, Ag-Pd-Au-Cu type, are studied: two experimental alloys and one commercial product. Chemical and mechanical properties were obtained for these alloys and a comparative analysis of these results was made. The cost, important factor, is established in relation to the materials cost of the commercial product. Vickers hardness values obtained from Ag-Pd alloys with different heat treatments allow to show their versatility in relation to restorative uses and to classify them according to standard practice. Electrochemical and tarnish behavior were obtained that allow to compare the trends. It is concluded that chemical properties are acceptable, when they are compared with odontological alloys of reference. Experimental alloys A1 y A2 were installed in mouth, over a year ago, with satisfactory results until now, which validate previous laboratory predictions.

    En la búsqueda de aleaciones para usos odontológicos, económicamente alternativas, se trabaja con tres aleaciones Ag-Pd complejas, del tipo Ag-Pd-Au-Cu-Otros, dos aleaciones experimentales y un producto comercial. Se determinan las propiedades mecánicas y químicas de estas aleaciones y se hace un análisis comparativo de los resultados. El costo, factor importante, se establece con relación a los materiales del producto comercial. Se determina la dureza Vickers de las aleaciones Ag-Pd con diversos tratamientos térmicos, lo que permite mostrar su versatilidad en cuanto a usos restauradores y clasificarlas según norma. Se determina su comportamiento electroquímico y la resistencia a la pigmentación, lo que permite comparar las tendencias exhibidas. Se concluye que las propiedades químicas son aceptables cuando se compara con aleaciones odontológicas de referencia. Se instalaron en boca aleaciones experimentales A1 y A2, hace más de un año, con resultados satisfactorios hasta

  9. Compositional changes of Pd-Au bimetallic nanoclusters upon hydrogenation

    OpenAIRE

    Di Vece, M; Bals, S.; Verbeeck, J.; Lievens, P.; van Tendeloo, G.

    2009-01-01

    Changes in the size distribution and composition of bimetallic Pd-Au nanoclusters have been observed after hydrogen exposure. This effect is caused by hydrogen-induced Ostwald ripening whereby the hydrogen reduces the binding energy of the cluster atoms leading to their detachment from the cluster. The composition changes due to a difference in mobility of the detached palladium and gold atoms on the surface. Fast palladium atoms contribute to the formation of larger nanoclusters, while the s...

  10. Au/Pd core-shell nanoparticles with varied hollow Au cores for enhanced formic acid oxidation

    Science.gov (United States)

    Hsu, Chiajen; Huang, Chienwen; Hao, Yaowu; Liu, Fuqiang

    2013-03-01

    A facile method has been developed to synthesize Au/Pd core-shell nanoparticles via galvanic replacement of Cu by Pd on hollow Au nanospheres. The unique nanoparticles were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, ultraviolet-visible spectroscopy, and electrochemical measurements. When the concentration of the Au solution was decreased, grain size of the polycrystalline hollow Au nanospheres was reduced, and the structures became highly porous. After the Pd shell formed on these Au nanospheres, the morphology and structure of the Au/Pd nanoparticles varied and hence significantly affected the catalytic properties. The Au/Pd nanoparticles synthesized with reduced Au concentrations showed higher formic acid oxidation activity (0.93 mA cm-2 at 0.3 V) than the commercial Pd black (0.85 mA cm-2 at 0.3 V), suggesting a promising candidate as fuel cell catalysts. In addition, the Au/Pd nanoparticles displayed lower CO-stripping potential, improved stability, and higher durability compared to the Pd black due to their unique core-shell structures tuned by Au core morphologies.

  11. Highly Active Carbon Supported Pd-Ag Nanofacets Catalysts for Hydrogen Production from HCOOH.

    Science.gov (United States)

    Wang, Wenhui; He, Ting; Liu, Xuehua; He, Weina; Cong, Hengjiang; Shen, Yangbin; Yan, Liuming; Zhang, Xuetong; Zhang, Jinping; Zhou, Xiaochun

    2016-08-17

    Hydrogen is regarded as a future sustainable and clean energy carrier. Formic acid is a safe and sustainable hydrogen storage medium with many advantages, including high hydrogen content, nontoxicity, and low cost. In this work, a series of highly active catalysts for hydrogen production from formic acid are successfully synthesized by controllably depositing Pd onto Ag nanoplates with different Ag nanofacets, such as Ag{111}, Ag{100}, and the nanofacet on hexagonal close packing Ag crystal (Ag{hcp}). Then, the Pd-Ag nanoplate catalysts are supported on Vulcan XC-72 carbon black to prevent the aggregation of the catalysts. The research reveals that the high activity is attributed to the formation of Pd-Ag alloy nanofacets, such as Pd-Ag{111}, Pd-Ag{100}, and Pd-Ag{hcp}. The activity order of these Pd-decorated Ag nanofacets is Pd-Ag{hcp} > Pd-Ag{111} > Pd-Ag{100}. Particularly, the activity of Pd-Ag{hcp} is up to an extremely high value, i.e., TOF{hcp} = 19 000 ± 1630 h(-1) at 90 °C (lower limit value), which is more than 800 times higher than our previous quasi-spherical Pd-Ag alloy nanocatalyst. The initial activity of Pd-Ag{hcp} even reaches (3.13 ± 0.19) × 10(6) h(-1) at 90 °C. This research not only presents highly active catalysts for hydrogen generation but also shows that the facet on the hcp Ag crystal can act as a potentially highly active catalyst. PMID:27454194

  12. Enhanced optical responses of Au@Pd core/shell nanobars.

    Science.gov (United States)

    Zhang, Ke; Xiang, Yanjuan; Wu, Xiaochun; Feng, Lili; He, Weiwei; Liu, Jianbo; Zhou, Weiya; Xie, Sishen

    2009-01-20

    A Pd nanoshell was epitaxially grown on a Au nanorod (NR) via simple seed-mediated growth. Compared with the cylindrical shape of the Au NR, the Au core/Pd shell (Au@Pd) nanorods change to a rectangular shape due to the disappearance of {110} facets. The Au NRs exhibit a strong longitudinal surface plasmon resonance (LSPR). As Pd is deposited, damping and broadening occur to the LSPR band. Interestingly, the LSPR band maximum first shows a small red-shift (ca. 40 nm) which then is followed by a blue-shift as the amount of Pd is increased. A thickness-dependent LSPR feature of the Pd shell is believed to contribute to the shift. At a thinner Pd thickness, the Au@Pd nanobars exhibit a well-defined LSPR band in the visible and near-infrared region, which demonstrates a higher dielectric sensitivity than that of the corresponding Au NRs. It thus opens up the potential of Pd nanostructures for SPR-based sensing. Investigations on the surface-enhanced Raman scattering (SERS) indicate that the SERS activities of the Au@Pd nanobars at thicknesses smaller than 2.5 nm mainly originate from the Au cores; thus, the SERS activities can be improved by tuning the aspect ratio of the Au core and/or the Pd shell thickness. PMID:19090666

  13. Thermodynamic description of Au-Ag-Si ternary system

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Based on the available experimental information, the Ag-Si binary system was thermodynamically assessed using the CALPHAD method. The solution phases, including liquid, fcc-Al and diamond-A4, were modeled as substitutional solutions, of which the excess Gibbs energies were expressed by Redlich-Kister polynomial functions. Combined with previous assessment of the Ag-Au and Au-Si binary systems, thermodynamic description of the Au-Ag-Si ternary system was performed to reproduce the reported phase equilibria. Thermodynamic properties of liquid alloys, liquidus projection and several vertical and isothermal sections of this ternary system were calculated, which are in reasonable agreement with the reported experimental data.

  14. Controlled Synthesis of Au@AgAu Yolk-Shell Cuboctahedra with Well-Defined Facets.

    Science.gov (United States)

    Londono-Calderon, Alejandra; Bahena, Daniel; Yacaman, Miguel J

    2016-08-01

    The synthesis of Au@AgAu yolk-shell cuboctahedra nanoparticles formed by galvanic replacement in a seed-mediated method is described. Initially, single-crystal Au seeds are used for the formation of Au@Ag core-shell nanocubes, which serve as the template material for the deposition of an external Au layer. The well-controlled synthesis yields the formation of cuboctahedra nanoparticles with smooth inner and outer Au/Ag surfaces. The deposition/oxidation process is described to understand the formation of cuboctahedra and octahedra nanoparticles. The Au core maintains the initial morphology of the seed and remains static at the center of the yolk-shell because of residual Ag. Structural analysis of the shell indicates intrinsic stacking faults (SFs) near the surface. Energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) compositional analysis show an Au-Ag nonordered alloy forming the shell. The three-dimensional structure of the nanoparticles presented open facets on the [111] as observed by electron tomography SIRT reconstruction over a stack of high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) images. The geometrical model was validated by analyzing the direction of streaks in coherent nanobeam diffraction (NBD). The catalytic activity was evaluated using a model reaction based on the reduction of 4-nitrophenol (4-NTP) by NaBH4 in the presence of Au@AgAu yolk-shell nanoparticles. PMID:27385583

  15. Fermi Surfaces of Surface States on Si(111) + Ag, Au

    OpenAIRE

    Crain, J. N.; Altmann, K. N.; Bromberger, Ch.; Himpsel, F. J.

    2002-01-01

    Metallic surface states on semiconducting substrates provide an opportunity to study low-dimensional electrons decoupled from the bulk. Angle resolved photoemission is used to determine the Fermi surface, group velocity, and effective mass for surface states on Si(111)sqrt3xsqrt3-Ag, Si(111)sqrt3x sqrt3-Au, and Si(111)sqrt21xsqrt21-(Ag+Au). For Si(111)sqrt3xsqrt3-Ag the Fermi surface consists of small electron pockets populated by electrons from a few percent excess Ag. For Si(111)sqrt21xsqrt...

  16. Adsorption of atomic oxygen on PdAg/Pd(111) surface alloys and coadsorption of CO

    Energy Technology Data Exchange (ETDEWEB)

    Farkas, Arnold P. [Institute of Surface Chemistry and Catalysis, Ulm University, D-89069 Ulm (Germany); Reaction Kinetics Research Group, University of Szeged, Chemical Research Center of the Hungarian Academy of Sciences, H-6720 Szeged (Hungary); Bansmann, Joachim; Diemant, Thomas; Behm, R. Juergen [Institute of Surface Chemistry and Catalysis, Ulm University, D-89069 Ulm (Germany)

    2011-07-01

    The interaction of dissociated oxygen with structurally well-defined PdAg/Pd(111) surface alloys and the coadsorption of CO was studied by high resolution electron energy loss spectroscopy (HREELS) and temperature-programmed desorption (TPD). After oxygen saturation of the non-modified Pd(111) surface at RT, we observed the formation of a prominent peak in the HREEL spectra at 60 meV corresponding to the perpendicular vibration of oxygen atoms adsorbed in threefold hollow sites. Deposition of small Ag amounts does not change the signal intensity of this peak; it decreases only above 20% Ag. Beyond this Ag content, the peak intensity steeply declines and disappears at around 55-60% Ag. CO coadsorption on the oxygen pre-covered surfaces at 120 K leads to the formation of additional features in HREELS. For a surface alloy with 29% Ag, three loss features due to CO adsorption in on-top, bridge, and threefold-hollow sites can be discriminated already after the lowest CO exposure. Annealing of the co-adsorbed layer to 200 K triggers a decrease of the oxygen concentration due to CO{sub 2} formation. These findings are corroborated by TPD spectra of the CO desorption and CO{sub 2} production.

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

    Science.gov (United States)

    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

  18. Photoreduction of Ag{sup +} in Ag/Ag{sub 2}S/Au memristor

    Energy Technology Data Exchange (ETDEWEB)

    Mou, N.I.; Tabib-Azar, M., E-mail: azar.m@utah.edu

    2015-06-15

    Highlights: • The effect of illumination on the operating voltages and switching speed of Ag/Ag{sub 2}S/Au memristors is studied • Illumination decreased the average switching time from high to low resistance states by ∼19% and decreased the turn-off voltages dramatically from −0.8 V to −0.25 V. • Photo-induced reduction of silver in Ag{sub 2}S may be used in three dimensional optical memories that can be electronically read and reset. • Illumination changed sulfur's valency and modified its oxidation/reduction potential. - Abstract: 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/Ag{sub 2}S/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 Ag{sub 2}S may be used in three dimensional optical memories that can be electronically read and reset.

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

    Energy Technology Data Exchange (ETDEWEB)

    Boomi, Pandi [Department of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630 003, Tamil Nadu (India); Prabu, Halliah Gurumallesh, E-mail: hgprabu2010@gmail.com [Department of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630 003, Tamil Nadu (India); Manisankar, Paramasivam [Department of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630 003, Tamil Nadu (India); Ravikumar, Sundaram [Department of Oceanography and Coastal Area Studies, School of Marine Sciences, Alagappa University, Thondi Campus 623 409, Tamil Nadu (India)

    2014-05-01

    Graphical abstract: - Highlights: • New method of synthesizing PANI-Ag-Au nanocomposite. • Surface Plasmon resonance and formation of composite at nano level were analyzed. • HR-TEM study revealed uniform distribution of nanoparticles. • PANI-Ag-Au nanocomposite exhibited good antibacterial activity. - Abstract: 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.

  20. Fermi surfaces of surface states on Si(111)-Ag, Au

    Science.gov (United States)

    Crain, J. N.; Altmann, K. N.; Bromberger, C.; Himpsel, F. J.

    2002-11-01

    Metallic surface states on semiconducting substrates provide an opportunity to study low-dimensional electrons decoupled from the bulk. Angle resolved photoemission is used to determine the Fermi surface, group velocity, and effective mass for surface states on Si(111)(3)×(3)-Ag, Si(111)(3)×(3)-Au, and Si(111)(21)×(21)-(Ag+Au). For Si(111)(3)×(3)-Ag the Fermi surface consists of small electron pockets populated by electrons from a few % excess Ag. For Si(111)(21)×(21)-(Ag+Au) the pockets increase their size corresponding to a filling by three electrons per unit cell. The (21)×(21) superlattice leads to an intricate surface umklapp pattern and to minigaps of 110 meV, giving an interaction potential of 55 meV for the (21)×(21) superlattice.

  1. Wetting of Au and Ag particles on monocrystalline graphite substrates

    Institute of Scientific and Technical Information of China (English)

    Joonho Lee; Toshihiro Tanaka; Kazufumi Seo; Nobumitsu Hirai; Jung-Goo Lee; Hirotaro Mori

    2006-01-01

    The wetting behavior of Au and Ag particles on a monocrystalline graphite substrate was investigated using the microscopic sessile drop method under a purified Ar atmosphere at 1300 K. The measured contact angles of the liquid Au and Ag on monocrystalline graphite substrates of (0001) face were 129° and 124°, respectively. It is believed that the interaction at the interface is dominated by the physical bonding (van der Waal's interaction).

  2. Synthesis of ultrathin face-centered-cubic Au@Pt and Au@Pd core-shell nanoplates from hexagonal-close-packed Au square sheets

    KAUST Repository

    Fan, Zhanxi

    2015-03-17

    The synthesis of ultrathin face-centered-cubic (fcc) Au@Pt rhombic nanoplates is reported through the epitaxial growth of Pt on hexagonal-close-packed (hcp) Au square sheets (AuSSs). The Pt-layer growth results in a hcp-to-fcc phase transformation of the AuSSs under ambient conditions. Interestingly, the obtained fcc Au@Pt rhombic nanoplates demonstrate a unique (101)f orientation with the same atomic arrangement extending from the Au core to the Pt shell. Importantly, this method can be extended to the epitaxial growth of Pd on hcp AuSSs, resulting in the unprecedented formation of fcc Au@Pd rhombic nanoplates with (101)f orientation. Additionally, a small amount of fcc (100)f-oriented Au@Pt and Au@Pd square nanoplates are obtained with the Au@Pt and Au@Pd rhombic nanoplates, respectively. We believe that these findings will shed new light on the synthesis of novel noble bimetallic nanostructures. Phase change: Ultrathin Au@Pt and Au@Pd core-shell nanoplates were prepared from Au square sheets. A phase transformation from hexagonal close-packed (hcp) to face-centered cubic (fcc) is observed upon coating the hcp Au square sheets with Pt or Pd under ambient conditions. The prepared fcc Au@Pt and Au@Pd rhombic nanoplates demonstrate unique (101)f orientation (picture shows a typical fcc Au@Pt rhombic nanoplate). © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Hydrodechlorination Catalysis of Pd-on-Au Nanoparticles Varies with Particle Size

    Energy Technology Data Exchange (ETDEWEB)

    Pretzer, Lori A.; Song, Hyun J.; Fang, Yu-Lun; Zhao, Zhun; Guo, Neng; Wu, Tianpin; Arslan, Ilke; Miller, Jeffrey T.; Wong, Michael S.

    2013-02-01

    The dependence of bimetallic PdAu catalytic activity on the relative ratios of Pd and Au has been theoretically predicted and experimentally observed for a number of reactions. Trichloroethene (TCE), a common carcinogenic solvent that is difficult to remove from contaminated groundwater in many industrialized nations, can be chemically degraded especially rapidly with Au nanoparticles partially coated with Pd ("Pd-on-Au NPs"). These NPs catalyze the room-temperature water-phase TCE hydrodechlorination (HDC) reaction with activities that follow a volcano-shape dependence on Pd surface coverage. The effect of particle size is not known, though. Pd-on-Au NPs synthesized with 3, 7, and 10 nm Au NPs and Pd surface coverages between 0 and 150% were studied in detail. Volcano-shape dependence on Au particle size and Pd surface coverage was observed, with 7 nm Au NPs with a Pd coverage of 60-70% having the highest TCE HDC activity. Extended x-ray absorption fine-structure spectroscopy (EXAFS) revealed the correlation was strongest between catalytic activity and the presence of non-oxidized Pd ensembles of ~2-3 atoms in contact with ~8-10 Au atoms. Isolated Pd atoms and Pd ensembles were visualized for the first time through aberration-corrected scanning transmission electron microscopy (STEM). This study provides the most direct evidence yet for Pd-on-Au NPs containing 2-dimensional Pd ensembles as the active sites for TCE HDC and likely for other chemical reactions. A portion of the research was performed using EMSL, a national scientific user facility sponsored by the Department of Energy's Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory. This research was supported by the Laboratory Directed Research and Development program at Pacific Northwest National Laboratory. The Pacific Northwest National Laboratory is operated by Battelle for the US Department of Energy.

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

    Science.gov (United States)

    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.

  5. A combined experimental and computational study of AuPd nanoparticles

    Science.gov (United States)

    Bruma, Alina

    The thesis is focused on the investigation of structural properties of AuPd nanoparticles via theoretical and experimental studies. For the first system, the 98-atom AuPd nanoclusters, a theoretical analysis has been employed to study the energetics and segregation effects and to assess how typical is the Leary Tetrahedron (LT). Although this motif is the most stable at the empirical level, it loses stability at the DFT level against FCC or Marks Decahedron. The second system is the Au24Pd1 nanoclusters. Theoretically, by performing a search at the DFT level using Basin Hopping Monte Carlo, we identified pyramidal cage structures as putative global minima, where Pd sits in the core and Au occupies surface positions. The Lowdin analysis emphasized charge transfer between Pd and Au, explaining the enhanced catalytic activity with respect to Au25 clusters. Experimentally, STEM has been employed for the structural characterization of Au24Pd1 clusters supported on Multiwall Carbon Nanotubes. Whenever possible, we have tried to link the experimental analysis to the theoretical findings. The third system has been the evaporated AuPd nanoparticles. We observed that the annealing process led to the formation of L12 ordered phases as well as layered and core-shell structures. This study aimed to bring an insight on the segregation and energetics effects of AuPd nanoparticles with potential applications in nanocatalysis.

  6. Bimetallic Au-decorated Pd catalyst for the liquid phase hydrodechlorination of 2,4-dichlorophenol

    Science.gov (United States)

    Zhou, Juan; Chen, Huan; Chen, Quanyuan; Huang, Zhaolu

    2016-11-01

    Monometallic and bimetallic Pd-Au catalysts supported on multi-walled carbon nanotubes (CNTs) with varied Au cooperation amounts were prepared using the complexing-reduction method in the presence of tetrahydrofuran (THF). The liquid phase catalytic hydrodechlorination (HDC) of 2,4-dichlorophenol (2,4-DCP) was investigated over these bimetallic catalysts. The catalysts were characterized by N2 adsorption-desorption isotherms, X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, and H2 chemisorption. Characterization results showed that the co-reduction of Pd and Au mainly formed alloy-like structure. The bimetallic catalysts had smaller metal particles and larger numbers of exposed active site than that of monometallic catalysts. In addition, compared with Pd(1.7)/CNTs and Au(0.4)/CNTs, the binding energies of Pd 3d5/2 shifted to higher positions while that of Au 4f7/2 had negative shifts in the Pd-Au bimetallic catalysts, which can be ascribed to the electrons transferred from metal Pd to Au and the cationization of Pd particles was enhanced. Accordingly, the bimetallic Pd-Au particles with different Au contents in the catalysts exhibited varied synergistic effects for the catalytic HDC of 2,4-DCP, with Pd(1.8)Au(0.4)/CNTs having the highest catalytic activity. For the bimetallic catalysts, a disproportional increase of turnover frequency (TOF) was observed with increasing Au content due to the enhanced cationization of Pd particles. Moreover, the dechlorination of 2,4-DCP over the supported monometallic and bimetallic catalysts proceeded via both the stepwise and concerted pathway, and the concerted pathway became predominant with Au decoration amount in the catalyst.

  7. A simple approach for facile synthesis of Ag, anisotropic Au and bimetallic (Ag/Au) nanoparticles using cruciferous vegetable extracts

    Energy Technology Data Exchange (ETDEWEB)

    Jacob, Jasmine; Mukherjee, Tulsi; Kapoor, Sudhir, E-mail: sudhirk@barc.gov.in

    2012-10-01

    We present a simple and straightforward approach for the synthesis and stabilization of relatively monodisperse Ag, Au and bimetallic (Ag/Au) nanoparticles by using cruciferous vegetable (green/red) extracts by simply adjusting the pH environment in the aqueous medium. The vegetable extracts act both as reducing and capping agents. The monometallic and bimetallic nanoparticles of Ag and Au so obtained were characterized by UV-visible spectroscopy, X-ray diffraction (XRD), dynamic light scattering (DLS) and transmission electron microscopy (TEM). It is shown that red cabbage extract can be used for the preparation of anisotropic Au nanoparticles. The formation of Au anisotropic nanoparticles was found to depend on a number of environmental factors, such as the pH of the reaction medium, reaction time, and initial reactant concentrations. Additionally, it is shown that these extract-stabilized Au and Ag nanoparticles can be used as a seed for preparation of bimetallic Au/Ag nanoparticles. For bimetallic alloy nanoparticles the absorption peak was observed between the two maxima of the corresponding metallic particles. The surface plasmon absorption maxima for bimetallic nanoparticles changed linearly with increasing Au mole ratio content in various alloy compositions. It has been shown that the formation of hollow Au spheres depends on the experimental conditions. - Graphical abstract: TEM image of gold nanoparticles at pH 3.27 formed by red cabbage extract. Highlights: Black-Right-Pointing-Pointer First report on the reactivity of the extracts toward metal ions using a spectrophotometric technique. Black-Right-Pointing-Pointer Red cabbage extract has better reducing properties than green cabbage extract. Black-Right-Pointing-Pointer Red cabbage extract can reduce metal ions at any pH. Black-Right-Pointing-Pointer Reduction of metal ions can have important consequences in the study of soil chemistry.

  8. A simple approach for facile synthesis of Ag, anisotropic Au and bimetallic (Ag/Au) nanoparticles using cruciferous vegetable extracts

    International Nuclear Information System (INIS)

    We present a simple and straightforward approach for the synthesis and stabilization of relatively monodisperse Ag, Au and bimetallic (Ag/Au) nanoparticles by using cruciferous vegetable (green/red) extracts by simply adjusting the pH environment in the aqueous medium. The vegetable extracts act both as reducing and capping agents. The monometallic and bimetallic nanoparticles of Ag and Au so obtained were characterized by UV–visible spectroscopy, X-ray diffraction (XRD), dynamic light scattering (DLS) and transmission electron microscopy (TEM). It is shown that red cabbage extract can be used for the preparation of anisotropic Au nanoparticles. The formation of Au anisotropic nanoparticles was found to depend on a number of environmental factors, such as the pH of the reaction medium, reaction time, and initial reactant concentrations. Additionally, it is shown that these extract-stabilized Au and Ag nanoparticles can be used as a seed for preparation of bimetallic Au/Ag nanoparticles. For bimetallic alloy nanoparticles the absorption peak was observed between the two maxima of the corresponding metallic particles. The surface plasmon absorption maxima for bimetallic nanoparticles changed linearly with increasing Au mole ratio content in various alloy compositions. It has been shown that the formation of hollow Au spheres depends on the experimental conditions. - Graphical abstract: TEM image of gold nanoparticles at pH 3.27 formed by red cabbage extract. Highlights: ► First report on the reactivity of the extracts toward metal ions using a spectrophotometric technique. ► Red cabbage extract has better reducing properties than green cabbage extract. ► Red cabbage extract can reduce metal ions at any pH. ► Reduction of metal ions can have important consequences in the study of soil chemistry.

  9. Effect of electromigration on interfacial reaction in Ni/Sn3.0Ag0.5Cu/Au/Pd/Ni-P flip chip solder joints%电迁移对Ni/Sn3.0Ag0.5Cu/Au/Pd/Ni—P倒装焊点界面反应的影响

    Institute of Scientific and Technical Information of China (English)

    黄明亮; 陈雷达; 周少明; 赵宁

    2012-01-01

    本文研究了150℃,1.0×104A/cm2条件下电迁移对Ni/Sn3.0Ag0.5Cu/Au/Pd/Ni-P倒装焊点界面反应的影响.回流后在solder/Ni和solder/NiP的界面上均形成(Cu,Ni)6Sn5类型金属间化合物.时效过程中两端界面化合物都随时间延长而增厚,且化合物类型都由(Cu,Ni)6Sn5转变为(Ni,Cu)3Sn4.电迁移过程中电子的流动方向对Ni—P层的消耗起着决定性作用.当电子从基板端流向芯片端时,电迁移促进了Ni—P层的消耗,600h后阴极端Ni-P层全部转变为Ni2SnP层.阴极界面处由于Ni2SnP层的存在,使界面Cu-Sn—Ni三元金属间化合物发生电迁移脱落溶解,而且由于Ni2SnP层与Cu焊盘的结合力较差,在Ni2SnP/Cu界面处会形成裂纹.当电子从芯片端流向基板端时,阳极端Ni—P层并没有发生明显的消耗.电流拥挤效应导致了阴极芯片端Ni层和Cu焊盘均发生了局部快速溶解,溶解到钎料中的Cu和Ni原子沿电子运动的方向往阳极运动并在钎料中形成了大量的化合物颗粒.电迁移过程中(Au,Pd,Ni)Sn4的聚集具有方向性,即(Au,Pd,Ni)Sn4因电流作用而在阳极界面处聚集.%The effect of electromigration (EM) on the interracial reaction in the Ni/Sn3.0Ag0.5Cu/Au/Pd/Ni-P flip chip solder joint is investigated under a current density of 1.0 ×104 A/cm2 at 150℃. The (Cu,Ni)6Sn5 intermetallic compounds (IMCs) form at both solder/Ni and solder/Ni-P interfaces in the as-reflowed state. During aging at 150℃, the (Cu,Ni)6Sn5 interfacial IMCs grow thicker and transform into (Ni,Cu)3Sn4 type after 200 h at solder/Ni interface and 600 h at solder/Ni-P interface, respectively. During EM, the current direction plays an important role in Ni-P layer consumption. When electrons flow from Ni-P to Ni, EM enhances the consumption of Ni-P, i.e., the Ni-P s completely consumed and transforms into Ni2SnP after EM for 600 h. There is

  10. Ti/Pd/Ag Contacts to n-Type GaAs for High Current Density Devices

    Science.gov (United States)

    Huo, Pengyun; Rey-Stolle, Ignacio

    2016-06-01

    The metallization stack Ti/Pd/Ag on n-type Si has been readily used in solar cells due to its low metal/semiconductor specific contact resistance, very high sheet conductance, bondability, long-term durability, and cost-effectiveness. In this study, the use of Ti/Pd/Ag metallization on n-type GaAs is examined, targeting electronic devices that need to handle high current densities and with grid-like contacts with limited surface coverage (i.e., solar cells, lasers, or light emitting diodes). Ti/Pd/Ag (50 nm/50 nm/1000 nm) metal layers were deposited on n-type GaAs by electron beam evaporation and the contact quality was assessed for different doping levels (from 1.3 × 1018 cm-3 to 1.6 × 1019 cm-3) and annealing temperatures (from 300°C to 750°C). The metal/semiconductor specific contact resistance, metal resistivity, and the morphology of the contacts were studied. The results show that samples doped in the range of 1018 cm-3 had Schottky-like I- V characteristics and only samples doped 1.6 × 1019 cm-3 exhibited ohmic behavior even before annealing. For the ohmic contacts, increasing annealing temperature causes a decrease in the specific contact resistance ( ρ c,Ti/Pd/Ag ~ 5 × 10-4 Ω cm2). In regard to the metal resistivity, Ti/Pd/Ag metallization presents a very good metal conductivity for samples treated below 500°C ( ρ M,Ti/Pd/Ag ~ 2.3 × 10-6 Ω cm); however, for samples treated at 750°C, metal resistivity is strongly degraded due to morphological degradation and contamination in the silver overlayer. As compared to the classic AuGe/Ni/Au metal system, the Ti/Pd/Ag system shows higher metal/semiconductor specific contact resistance and one order of magnitude lower metal resistivity.

  11. One step electrochemical synthesis of bimetallic PdAu supported on nafion–graphene ribbon film for ethanol electrooxidation

    Energy Technology Data Exchange (ETDEWEB)

    Shendage, Suresh S., E-mail: sureshsshendage@gmail.com; Singh, Abilash S.; Nagarkar, Jayashree M., E-mail: jm.nagarkar@ictmumbai.edu.in

    2015-10-15

    Highlights: • Electrochemical deposition of bimetallic PdAu NPs. • Highly loaded PdAu NPs are obtained. • Nafion–graphene supported PdAu NPs shows good activity for ethanol electrooxidation. - Abstract: A nafion–graphene ribbon (Nf–GR) supported bimetallic PdAu nanoparticles (PdAu/Nf–GR) catalyst was prepared by electrochemical codeposition of Pd and Au at constant potential. The prepared catalyst was characterized by scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDAX), transmission electron microscopy (TEM) and X-ray diffraction analysis (XRD). The average particle size of PdAu nanoparticles (NPs) determined from XRD was 3.5 nm. The electrocatalytic activity of the PdAu/Nf–GR catalyst was examined by cyclic voltametry. It was observed that the as prepared catalyst showed efficient activity and good stability for ethanol electrooxidation in alkaline medium.

  12. Synthesis, Annealing and Performance of Pd-Au Asymmetric Composite Membranes for Hydrogen Purification

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Yi Hua [Worcester Polytechnic Institute; Chen, Chao-Huang [Worcester Polytechnic Institute; Catalano, Jacopo [Worcester Polytechnic Institute; Guazzone, Federico [Worcester Polytechnic Institute; Payzant, E Andrew [ORNL

    2013-01-01

    Composite asymmetric Pd-Au membranes, based on porous Inconel and Hastelloy tubular supports, were prepared by means of electroless deposition and galvanic displacement techniques and tested, before and after Au deposition, in pure H2 atmosphere. The final membranes, with Au average bulk composition up to 16.7 wt%, were 9 15 m thick and showed, for the entire duration of characterization, H2/He ideal selectivity in excess of 900. The annealing of the as-prepared membranes was conducted through the coating and diffusion mechanism in He and H2 atmospheres at 500 C. The annealing conditions were chosen after non-isothermal and isothermal HT-XRD studies on coupons synthetized with similar preparation methods. After the formation of the Pd-Au layer, the membranes showed steady flux and a stable Au gradient on the membrane top layer. Comparisons between permeance for Pd/Au and pure Pd membranes indicated that the membranes with an Au average bulk composition of 4.5 and 5.4 wt% had an enhancement, up to 20%, of the H2 permeability in the temperature range 250 450 C with respect to pure Pd membranes. On the other hand, the membrane having the highest Au composition, 16.7 wt%, even though characterized by a lower H2 permeability (77% of pure Pd) had a rather high surface Au composition (approximately 46 wt%), which might provide good H2S poisoning tolerance.

  13. Dependence of SERS enhancement on the chemical composition and structure of Ag/Au hybrid nanoparticles.

    Science.gov (United States)

    Chaffin, Elise; O'Connor, Ryan T; Barr, James; Huang, Xiaohua; Wang, Yongmei

    2016-08-01

    Noble metal nanoparticles (NPs) such as silver (Ag) and gold (Au) have unique plasmonic properties that give rise to surface enhanced Raman scattering (SERS). Generally, Ag NPs have much stronger plasmonic properties and, hence, provide stronger SERS signals than Au NPs. However, Ag NPs lack the chemical stability and biocompatibility of comparable Au NPs and typically exhibit the most intense plasmonic resonance at wavelengths much shorter than the optimal spectral region for many biomedical applications. To overcome these issues, various experimental efforts have been devoted to the synthesis of Ag/Au hybrid NPs for the purpose of SERS detections. However, a complete understanding on how the SERS enhancement depends on the chemical composition and structure of these nanoparticles has not been achieved. In this study, Mie theory and the discrete dipole approximation have been used to calculate the plasmonic spectra and near-field electromagnetic enhancements of Ag/Au hybrid NPs. In particular, we discuss how the electromagnetic enhancement depends on the mole fraction of Au in Ag/Au alloy NPs and how one may use extinction spectra to distinguish between Ag/Au alloyed NPs and Ag-Au core-shell NPs. We also show that for incident laser wavelengths between ∼410 nm and 520 nm, Ag/Au alloyed NPs provide better electromagnetic enhancement than pure Ag, pure Au, or Ag-Au core-shell structured NPs. Finally, we show that silica-core Ag/Au alloy shelled NPs provide even better performance than pure Ag/Au alloy or pure solid Ag and pure solid Au NPs. The theoretical results presented will be beneficial to the experimental efforts in optimizing the design of Ag/Au hybrid NPs for SERS-based detection methods.

  14. Solid phase metallurgy strategy to sub-5 nm Au-Pd and Ni-Pd bimetallic nanoparticles with controlled redox properties.

    Science.gov (United States)

    Tang, Yu; Xu, Shaodan; Dai, Yihu; Yan, Xiaoqing; Li, Renhong; Xiao, Liping; Fan, Jie

    2014-01-01

    A solid phase metallurgy strategy is applied to synthesize Au-Pd and Ni-Pd bimetallic nanoparticles (BMNPs) with a tight sub-5 nm particle size distribution. The near-surface elemental composition and redox properties of Au-Pd BMNPs can be well tailored, which leads to an optimized catalytic performance in n-hexane combustion.

  15. One-step facile synthesis of carbon-supported PdAu nanoparticles and their electrochemical property and stability

    International Nuclear Information System (INIS)

    Graphical abstract: Well-crystallized PdAu alloy nanoparticles with the average size of 2–5 nm supported on Ketjen Black (KB) were successfully fabricated from the metal wire electrodes via a one-step solution plasma process in water at atmospheric pressure. Multi-scan cyclic voltammetry showed they have better electrochemical stability in alkaline than in acidic solution. - Highlights: • Carbon-supported PdAu nanoparticles were fabricated by a solution plasma technique. • As-obtained PdAu nanoparticles were confirmed to be alloy. • PdAu nanoparticles have good electrochemical activities and stabilities. • PdAu nanoparticles in alkaline have better stability than that in acidic solution. - Abstract: Well-crystallized PdAu nanoparticles supported on Ketjen Black (KB) were successfully fabricated when both Pd and Au wires were served as the electrode pair by a solution plasma technique at atmospheric pressure. The synthesis of PdAu nanoparticles was almost simultaneous with their dispersion on KB. As-obtained PdAu nanoparticles were confirmed to be alloy by ultraviolet–visible spectrophotometer, transmission electron microscopy (TEM) and energy dispersive X-ray analysis (EDX) of each particle. PdAu nanoparticles with the average diameter of 2–5 nm were equably distributed on KB. PdAu nanoparticles showed good electrocatalytic activity both in acidic and alkaline solution corresponding to their obvious oxidation and reduction features. PdAu nanoparticles have improved electrochemical stability compared with the electrochemical properties of Pd and Au nanoparticles mixture after long time multi-scan cyclic voltammetry. Multi-scan cyclic voltammetry also presented the PdAu nanoparticles in alkaline solution have better stability than that in acidic solution. Thus as-obtained PdAu alloy nanoparticles would become a promising electrocatalysts for fuel cells or Li-air batteries. This novel process showed its potential applications in designing optimization of

  16. One-step facile synthesis of carbon-supported PdAu nanoparticles and their electrochemical property and stability

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Xiulan, E-mail: whoxiulan@163.com [College of Materials Science and Engineering, Nanjing Tech University (China); Shi, Junjun; Zhang, Jianbo [College of Materials Science and Engineering, Nanjing Tech University (China); Tang, Weiping [Shanghai Institute of Space Power Sources, Shanghai (China); Zhu, Haikui; Shen, Xiaodong [College of Materials Science and Engineering, Nanjing Tech University (China); Saito, Nagahiro [Department of Materials, Physics and Energy Engineering, Graduate School of Engineering, Nagoya University (Japan)

    2015-01-15

    Graphical abstract: Well-crystallized PdAu alloy nanoparticles with the average size of 2–5 nm supported on Ketjen Black (KB) were successfully fabricated from the metal wire electrodes via a one-step solution plasma process in water at atmospheric pressure. Multi-scan cyclic voltammetry showed they have better electrochemical stability in alkaline than in acidic solution. - Highlights: • Carbon-supported PdAu nanoparticles were fabricated by a solution plasma technique. • As-obtained PdAu nanoparticles were confirmed to be alloy. • PdAu nanoparticles have good electrochemical activities and stabilities. • PdAu nanoparticles in alkaline have better stability than that in acidic solution. - Abstract: Well-crystallized PdAu nanoparticles supported on Ketjen Black (KB) were successfully fabricated when both Pd and Au wires were served as the electrode pair by a solution plasma technique at atmospheric pressure. The synthesis of PdAu nanoparticles was almost simultaneous with their dispersion on KB. As-obtained PdAu nanoparticles were confirmed to be alloy by ultraviolet–visible spectrophotometer, transmission electron microscopy (TEM) and energy dispersive X-ray analysis (EDX) of each particle. PdAu nanoparticles with the average diameter of 2–5 nm were equably distributed on KB. PdAu nanoparticles showed good electrocatalytic activity both in acidic and alkaline solution corresponding to their obvious oxidation and reduction features. PdAu nanoparticles have improved electrochemical stability compared with the electrochemical properties of Pd and Au nanoparticles mixture after long time multi-scan cyclic voltammetry. Multi-scan cyclic voltammetry also presented the PdAu nanoparticles in alkaline solution have better stability than that in acidic solution. Thus as-obtained PdAu alloy nanoparticles would become a promising electrocatalysts for fuel cells or Li-air batteries. This novel process showed its potential applications in designing optimization of

  17. Monodispersed bimetallic PdAg nanoparticles with twinned structures: Formation and enhancement for the methanol oxidation

    Science.gov (United States)

    Yin, Zhen; Zhang, Yining; Chen, Kai; Li, Jing; Li, Wenjing; Tang, Pei; Zhao, Huabo; Zhu, Qingjun; Bao, Xinhe; Ma, Ding

    2014-03-01

    Monodispersed bimetallic PdAg nanoparticles can be fabricated through the emulsion-assisted ethylene glycol (EG) ternary system. Different compositions of bimetallic PdAg nanoparticles, Pd80Ag20, Pd65Ag35 and Pd46Ag54 can be obtained via adjusting the reaction parameters. For the formation process of the bimetallic PdAg nanoparticles, there have two-stage growth processes: firstly, nucleation and growth of the primary nanoclusters; secondly, formation of the secondary nanoparticles with the size-selection and relax process via the coalescence or aggregation of the primary nanoclusters. The as-prepared PdAg can be supported on the carbon black without any post-treatment, which exhibited high electro-oxidation activity towards methanol oxidation under alkaline media. More importantly, carbon-supported Pd80Ag20 nanoparticles reveal distinctly superior activities for the methanol oxidation, even if compared with commercial Pt/C electro-catalyst. It is concluded that the enhanced activity is dependant on the unique twinning structure with heterogeneous phase due to the dominating coalescence growth in EG ternary system.

  18. Pd-Au bimetallic catalysts: understanding alloy effects from planar models and (supported) nanoparticles.

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Feng; Goodman, Wayne D.

    2012-12-21

    Pd-Au bimetallic catalysts often display enhanced catalytic activities and selectivities compared with Pd-alone catalysts. This enhancement is often caused by two alloy effects, i.e., ensemble and ligand effects. The ensemble effect is dilution of surface Pd by Au. With increasing surface Au coverages, contiguous Pd ensembles disappear and isolated Pd ensembles form. For certain reactions, for example vinyl acetate synthesis, this effect is responsible for reaction rate enhancement via the formation of highly active surface sites, e.g., isolated Pd pairs. The disappearance of contiguous Pd ensembles also switches off side reactions catalyzed by these sites. This explains selectivity increase of certain reactions, for example direct H2O2 synthesis. The ligand effect is electronic perturbation of Au to Pd. By direct charge transfer or affecting bond length, the ligand effect causes the Pd d band to be more filled and the d-band center away from the Fermi level. Both changes make Pd more "atomic like" therefore binding reactants and products weaker. For certain reactions, this eliminates the so-called "self poisoning" and enhances activity/selectivity.

  19. Results from experiment E917 for Au + Au collisions at the AGS

    International Nuclear Information System (INIS)

    The effects of baryon stopping and its resulting energy deposition on the dynamics of Au + Au collisions at 6, 8 and 10.8 GeV/nucleon are explored with recent results from the AGS experiment E917. Current analyses of stopping, collective flow signals and HBT parameters are presented. Strangeness and anti-baryon production is examined using the yields of anti-lambdas and anti-protons

  20. Interference removals on Pd, Ru and Au with ICP-QQQ-MS in PGE RM

    Science.gov (United States)

    Nadeem Hussain Bokhari, Syed; Meisel, Thomas; Walkner, Christoph

    2015-04-01

    Gold and platinum group elements (PGE) are essential industrial precious metals with high world demand due to their unique properties. Struggle for natural exploration of PGE is on great pace and recycling from industrial wastes, electronics and catalytic convertor is on the rise for PGE supply chain. Along with these developments it is becoming more challenging for analytical chemists to determine gold and PGE out of complex matrix which causes severe interferences. The current state of art is online analysis coupled with chromatographic separation of interferences. The ICP-QQQ-MS Agilent 8800 has the capability of using multi tunes and mass shifts. We aim to remove interferences on Pd+ (for direct and isotope dilution analysis) Au+ and Ru+ in lieu of chemical separations. YO+, SrOH+, ZnAr+, NiAr+, ZrO+, CuAr+, MoO+ , Ru+and Cd+ are expected interferences on Pd+ while Au+ is interfered by TaO+, HfOH+, GdAr+ and 102Ru+ ,104Ru+ by 102Pd+ ,104Pd+ etc. Initial test were performed on pure solutions of 1mg/l (interfering elements): 1 ng/l (Pd, Ru & Au) respectively. The outcomes of initial tests were applied on PGE reference material (RM) WMG-1 and SARM-7 (digested with Na2O2 sintering). The results obtained show that YO+, SrOH+ interfere (104Pd,105Pd), 104 Ru+ on (104Pd), ZnAr+ has slight interference on (104Pd and106Pd), ZrO+, NiAr+, CuAr+ interferences are negligible, MoO+ has severe interference on (108Pd, 110Pd) and that Cd+ has severe isobaric interference on (106Pd,108Pd, 110Pd). These interference have been removed by formation of Pd(NH3)3+complex. The TaO+, HfOH+ and GdAr+ interferences on Au+ are best removed by formation of Au(NH3)+ and Au(NH3)2+ complexes. 102Pd+,104Pd+interference on 102Ru+ ,104Ru+ can be removed by formation of Ru(NH3)4+ and RuO+ compounds. The results obtained comply with certified values of RM. The developed method is being tested on low concentration PGE reference materials. References: Sugiyama, N. " Removal of complex spectral

  1. Phase Equilibria in System Pd-Au-Sn and Pd-Cu-Sn at 800℃ and 500℃

    Institute of Scientific and Technical Information of China (English)

    KABANOVA E. G.; KAREVA M. A.; KUZNETSOV V. N.; VASEKIN V. V.

    2012-01-01

    Alloys of Pd-Au-Sn and Pd-Cu-Sn systems were investigated using metallography,electron microprobe,X-ray diff action and DTA.Partial isothermal sections were plots at 800℃ and 500℃.Ternary τ-phase having tetragonal structure has been established in each systems.The region of existence of phases in equilibrium with the solid solution based on palladium.

  2. Permeability of hydrogen isotopes through Pd-Ag membrane

    International Nuclear Information System (INIS)

    This paper represents the permeabilities, diffusion coefficients and isotope effects for hydrogen and deuterium through Pd-25 wt.% Ag alloy tubes The feed gas H2 or D2 flowing into the permeation cell was preheated before it reached to the outer surface of the permeation tube made of palladium-silver alloy. Permeation time lag method could be successfully carried out with the present apparatus to measure both permeability and diffusion coefficient. The square-root pressure dependence for the permeation of hydrogen isotopes was observed. The observed systematic temperature dependence indicates that the approximation of the Arrhenius' relation was effective within this experimental conditions. Some tendency of permeation fluxes in relation to the reciprocal temperature, 1/T, was seen. The permeability ratio was larger than the square root of isotopic mass ratio, and it decreased with temperature rise. On the contrary, the diffusion coefficient ratio was much smaller than the square root of isotopic mass ratio. (Kato, T.)

  3. Strain Distribution of Au and Ag Nanoparticles Embedded in Al2O3 Thin Film

    Directory of Open Access Journals (Sweden)

    Honghua Huang

    2014-01-01

    Full Text Available Au and Ag nanoparticles embedded in amorphous Al2O3 matrix are fabricated by the pulsed laser deposition (PLD method and rapid thermal annealing (RTA technique, which are confirmed by the experimental high-resolution transmission electron microscope (HRTEM results, respectively. The strain distribution of Au and Ag nanoparticles embedded in the Al2O3 matrix is investigated by the finite-element (FE calculations. The simulation results clearly indicate that both the Au and Ag nanoparticles incur compressive strain by the Al2O3 matrix. However, the compressive strain existing on the Au nanoparticle is much weaker than that on the Ag nanoparticle. This phenomenon can be attributed to the reason that Young’s modulus of Au is larger than that of Ag. This different strain distribution of Au and Ag nanoparticles in the same host matrix may have a significant influence on the technological potential applications of the Au-Ag alloy nanoparticles.

  4. An ab-initio study of silicon adsorption on metallic surfaces (Au/Ag): Novel perspective to explore chemical bonding

    Science.gov (United States)

    Chakraborty, S.; Ghaisas, S. V.; Majumder, C.

    2012-07-01

    We report a first-principle investigation of the structure and electronic properties of small Sin (n = 1-6,9) clusters deposited on the Au(111) and Ag(111) surfaces. The calculations were performed using a plane wave based pseudopotential method under the framework of density functional theory. The results reveal the preference of Si atom to be adsorbed on the h.c.p. site of the metal (111) surfaces with strong binding energy. We study monolayer (ML) deposition as well as the cluster deposition on both the surfaces. The clusters introduce interlayer forces in the adsorbate. Based on PDOS (projected density of states) analysis it is found that Si atoms acquire charges from the Au/Ag surface. The binding energies are consistent with the known cohesive energy of Ag and Au silicides. The planar Sin cluster deposition on metal surfaces show that Au provides an adjustable surface with relatively strong Au-Si interaction while Ag-Si relatively weak interaction leading to dimerization of Si. The strong bonding with the surface atoms is a result of p-d hybridization. Some of the 3-D clusters show shape distortions after deposition on metal surfaces. This leads to internal stresses after deposition. A statistical parameter is defined over PDOS. It helps to measure the state delocalization in energy. Implications of the Si-Metal interaction on the initial stages of growth are discussed.

  5. Magnetism of CoPd self-organized alloy clusters on Au(111)

    Science.gov (United States)

    Ohresser, P.; Otero, E.; Wilhelm, F.; Rogalev, A.; Goyhenex, C.; Joly, L.; Bulou, H.; Romeo, M.; Speisser, V.; Arabski, J.; Schull, G.; Scheurer, F.

    2013-12-01

    Magnetic properties of gold-encapsulated CoxPd1-x self-organized nano-clusters on Au(111) are analyzed by x-ray magnetic circular dichroism for x = 0.5, 0.7, and 1.0. The clusters are superparamagnetic with a blocking temperature decreasing with increasing Pd concentration, due to a reduction of the out-of-plane anisotropy strength. No magnetic moment is detected on Pd in these clusters, within the detection limit, contrary to thick CoPd films. Both reduction of anisotropy and vanishing Pd moment are attributed to strain.

  6. Structured Pd-Au/Cu-fiber catalyst for gas-phase hydrogenolysis of dimethyl oxalate to ethylene glycol.

    Science.gov (United States)

    Zhang, Li; Han, Lupeng; Zhao, Guofeng; Chai, Ruijuan; Zhang, Qiaofei; Liu, Ye; Lu, Yong

    2015-07-01

    Galvanic co-deposition of 0.5 wt% Au and 0.1 wt% Pd on a microfibrous-structure using 8 μm Cu-fibers delivers a Pd-Au/Cu-fiber catalyst, which is highly active, selective and stable for the hydrogenolysis of dimethyl oxalate to ethylene glycol. Au and Pd synergistically promote the hydrogenolysis activity of Cu(+) sites, while Au also critically stabilizes Cu(+) sites to prevent deep reductive deactivation. PMID:26040855

  7. Au-Ag-Cu nano-alloys: tailoring of permittivity

    Science.gov (United States)

    Hashimoto, Yoshikazu; Seniutinas, Gediminas; Balčytis, Armandas; Juodkazis, Saulius; Nishijima, Yoshiaki

    2016-04-01

    Precious metal alloys enables new possibilities to tailor materials for specific optical functions. Here we present a systematic study of the effects of a nanoscale alloying on the permittivity of Au-Ag-Cu metals at 38 different atomic mixing ratios. The permittivity was measured and analyzed numerically by applying the Drude model. X-ray diffraction (XRD) revealed the face centered cubic lattice of the alloys. Both, optical spectra and XRD results point towards an equivalent composition-dependent electron scattering behavior. Correlation between the fundamental structural parameters of alloys and the resulting optical properties is elucidated. Plasmonic properties of the Au-Ag-Cu alloy nanoparticles were investigated by numerical simulations. Guidelines for designing plasmonic response of nano- structures and their patterns are presented from the material science perspective.

  8. The role of Pd in the transport of Ag in SiC

    Energy Technology Data Exchange (ETDEWEB)

    Olivier, E.J., E-mail: jolivier@nmmu.ac.za [Centre for High Resolution Transmission Electron Microscopy, Nelson Mandela Metropolitan University, Port Elizabeth (South Africa); Neethling, J.H. [Centre for High Resolution Transmission Electron Microscopy, Nelson Mandela Metropolitan University, Port Elizabeth (South Africa)

    2013-01-15

    This paper presents results in support of a newly proposed transport mechanism to account for the release of Ag from intact TRISO particles during HTR reactor operation. The study reveals that the migration of Ag in polycrystalline SiC can occur in association with Pd, a relatively high yield metallic fission product. The migration takes place primarily along grain boundary routes, seen in the form of distinct Pd, Ag and Si containing nodules. Pd is known to rapidly migrate to the SiC and iPyC interface within TRISO particles during operation. It has been shown to chemically corrode the SiC to form palladium silicides. These palladium silicides are found present along SiC grain boundaries in nodule like form. It is suggested that Ag penetrates these nodules together with the palladium silicide, to form a Pd, Ag and Si solution capable of migrating along SiC grain boundaries over time.

  9. The role of Pd in the transport of Ag in SiC

    International Nuclear Information System (INIS)

    This paper presents results in support of a newly proposed transport mechanism to account for the release of Ag from intact TRISO particles during HTR reactor operation. The study reveals that the migration of Ag in polycrystalline SiC can occur in association with Pd, a relatively high yield metallic fission product. The migration takes place primarily along grain boundary routes, seen in the form of distinct Pd, Ag and Si containing nodules. Pd is known to rapidly migrate to the SiC and iPyC interface within TRISO particles during operation. It has been shown to chemically corrode the SiC to form palladium silicides. These palladium silicides are found present along SiC grain boundaries in nodule like form. It is suggested that Ag penetrates these nodules together with the palladium silicide, to form a Pd, Ag and Si solution capable of migrating along SiC grain boundaries over time.

  10. Study of Ag and Au Nanoparticles Synthesized by Arc Discharge in Deionized Water

    Directory of Open Access Journals (Sweden)

    Der-Chi Tien

    2010-01-01

    Full Text Available The paper presents a study of Ag and Au nanofluids synthesized by the arc discharge method (ADM in deionized water. The metallic Ag nanoparticle (Ag0 and ionic Ag (Ag+ have played an important role in the battle against germs which are becoming more drug-resistant every year. Our study indicates that Ag nanoparticle suspension (SNPS fabricated by using ADM without added surfactants exclusively contains the metallic Ag nanoparticle and ionic Ag. Besides that, the ADM in deionized water has also been employed for the fabrication process of Au nanoparticles. The experimental results indicate that the prepared Ag nanoparticles can react with the dissolved H2CO3 in deionized water, leading to the formation of Ag2CO3. Significantly different to Ag, the prepared Au nanoparticles with their surfaces bonded by oxygen are suspended in deionized water by the formation of hydrogen bonded with the neighboring water molecules.

  11. HCOOH oxidation on thin Pd layers on Au: Self-poisoning by the subsequent reaction of the reaction product

    International Nuclear Information System (INIS)

    Highlights: ► Thin layers of Pd@Au are more active for HCOOH oxidation than pure Pd. ► Pd@Au surfaces are poisoned more rapidly than Pd black. ► Poisoning is caused by COads formed in CO2 electroreduction. -- Abstract: The oxidation of HCOOH has been investigated on thin Pd layers ranging from 1 to 17 ML equivalents electrodeposited on polycrystalline Au substrate (Pd@Au). The results are compared to those on Pd black. Potentiodynamic polarization curves suggest that on both types of catalyst HCOOH oxidizes through dehydrogenation path. The high current densities achieved on 4–17 ML Pd@Au surpass more than three times the activity of Pd black. Chronoamperometric test reveals that the Pd@Au electrodes lose their activity faster than Pd black. In the stripping experiment performed after the chronoamperometry COads is detected on all the surfaces. On the 4 ML Pd@Au, which exhibits the highest deactivation rate, the COads coverage is the largest. After the chronoamperometric test repeated in the CO2 saturated supporting electrolyte, the anodic stripping shows that COads is present on all the electrodes, again with the highest coverage on 4 ML Pd@Au. It is concluded that deactivation of Pd surfaces is caused by the COads formed in the electrochemical reduction of CO2, which is the product of HCOOH oxidation. Electronic modification of Pd by Au substrate causes stronger interactions of Pd with HCOOH and CO, which increases HCOOH oxidation rate, but also accelerates the poisoning by COads

  12. Supported Pd-Au Membrane Reactor for Hydrogen Production: Membrane Preparation, Characterization and Testing.

    Science.gov (United States)

    Iulianelli, Adolfo; Alavi, Marjan; Bagnato, Giuseppe; Liguori, Simona; Wilcox, Jennifer; Rahimpour, Mohammad Reza; Eslamlouyan, Reza; Anzelmo, Bryce; Basile, Angelo

    2016-01-01

    A supported Pd-Au (Au 7wt%) membrane was produced by electroless plating deposition. Permeation tests were performed with pure gas (H₂, H₂, N₂, CO₂, CH₄) for long time operation. After around 400 h under testing, the composite Pd-Au membrane achieved steady state condition, with an H₂/N₂ ideal selectivity of around 500 at 420 °C and 50 kPa as transmembrane pressure, remaining stable up to 1100 h under operation. Afterwards, the membrane was allocated in a membrane reactor module for methane steam reforming reaction tests. As a preliminary application, at 420 °C, 300 kPa of reaction pressure, space velocity of 4100 h(-1), 40% methane conversion and 35% hydrogen recovery were reached using a commercial Ni/Al₂O₃ catalyst. Unfortunately, a severe coke deposition affected irreversibly the composite membrane, determining the loss of the hydrogen permeation characteristics of the supported Pd-Au membrane. PMID:27171067

  13. Synthesis, Study, and Discrete Dipole Approximation Simulation of Ag-Au Bimetallic Nanostructures.

    Science.gov (United States)

    Hu, Yang; Zhang, An-Qi; Li, Hui-Jun; Qian, Dong-Jin; Chen, Meng

    2016-12-01

    Water-soluble Ag-Au bimetallic nanostructures were prepared via co-reduction and seed-mediated growth routes employing poly-(4-styrenesulfonic acid-co-maleic acid) (PSSMA) as both a reductant and a stabilizer. Ag-Au alloy nanoparticles were obtained by the co-reduction of AgNO3 and HAuCl4, while Ag-Au core-shell nanostructures were prepared through seed-mediated growth using PSSMA-Au nanoparticle seeds in a heated AgNO3 solution. The optical properties of the Ag-Au alloy and core-shell nanostructures were studied, and the growth mechanism of the bimetallic nanoparticles was investigated. Plasmon resonance bands in the range 422 to 517 nm were observed for Ag-Au alloy nanoparticles, while two plasmon resonances were found in the Ag-Au core-shell nanostructures. Furthermore, discrete dipole approximation theoretical simulation was used to assess the optical property differences between the Ag-Au alloy and core-shell nanostructures. Composition and morphology studies confirmed that the synthesized materials were Ag-Au bimetallic nanostructures. PMID:27094823

  14. Preparation and characterization of metallic supported thin Pd-Ag membranes for hydrogen separation

    OpenAIRE

    Fernandez, Ekain; Medrano, Jose Antonio; Melendez, Jon; Parco, Maria; Viviente, J.L.; van Sint Annaland, Martin; Gallucci, Fausto; Pacheco Tanaka, David A.

    2015-01-01

    This paper reports the preparation and characterization of thin-film (4-5 µm thick) Pd-Ag metallic supported membranes for high temperature applications. Various thin film membranes have been prepared by depositing a ceramic interdiffusion barrier layer prior to the simultaneous Pd-Ag electroless plating deposition. Two deposition techniques for ceramic layers (made of zirconia and alumina) have been evaluated: atmospheric plasma spraying and dip coating of a powder suspension. Initially, the...

  15. Platinum(iv) prodrug conjugated Pd@Au nanoplates for chemotherapy and photothermal therapy

    Science.gov (United States)

    Shi, Saige; Chen, Xiaolan; Wei, Jingping; Huang, Yizhuan; Weng, Jian; Zheng, Nanfeng

    2016-03-01

    Owing to the excellent near infrared (NIR) light absorption and efficient passive targeting toward tumor tissue, two-dimensional (2D) core-shell PEGylated Pd@Au nanoplates have great potential in both photothermal therapy and drug delivery systems. In this work, we successfully conjugate Pd@Au nanoplates with a platinum(iv) prodrug c,c,t-[Pt(NH3)2Cl2(O2CCH2CH2CO2H)2] to obtain a nanocomposite (Pd@Au-PEG-Pt) for combined photothermal-chemotherapy. The prepared Pd@Au-PEG-Pt nanocomposite showed excellent stability in physiological solutions and efficient Pt(iv) prodrug loading. Once injected into biological tissue, the Pt(iv) prodrug was easily reduced by physiological reductants (e.g. ascorbic acid or glutathione) into its cytotoxic and hydrophilic Pt(ii) form and released from the original nanocomposite, and the NIR laser irradiation could accelerate the release of Pt(ii) species. More importantly, Pd@Au-PEG-Pt has high tumor accumulation (29%ID per g), which makes excellent therapeutic efficiency at relatively low power density possible. The in vivo results suggested that, compared with single therapy the combined thermo-chemotherapy treatment with Pd@Au-PEG-Pt resulted in complete destruction of the tumor tissue without recurrence, while chemotherapy using Pd@Au-PEG-Pt without irradiation or photothermal treatment using Pd@Au-PEG alone did not. Our work highlights the prospects of a feasible drug delivery strategy of the Pt prodrug by using 2D Pd@Au nanoplates as drug delivery carriers for multimode cancer treatment.Owing to the excellent near infrared (NIR) light absorption and efficient passive targeting toward tumor tissue, two-dimensional (2D) core-shell PEGylated Pd@Au nanoplates have great potential in both photothermal therapy and drug delivery systems. In this work, we successfully conjugate Pd@Au nanoplates with a platinum(iv) prodrug c,c,t-[Pt(NH3)2Cl2(O2CCH2CH2CO2H)2] to obtain a nanocomposite (Pd@Au-PEG-Pt) for combined photothermal-chemotherapy. The

  16. Core-shell Au-Pd nanoparticles as cathode catalysts for microbial fuel cell applications

    Science.gov (United States)

    Yang, Gaixiu; Chen, Dong; Lv, Pengmei; Kong, Xiaoying; Sun, Yongming; Wang, Zhongming; Yuan, Zhenhong; Liu, Hui; Yang, Jun

    2016-01-01

    Bimetallic nanoparticles with core-shell structures usually display enhanced catalytic properties due to the lattice strain created between the core and shell regions. In this study, we demonstrate the application of bimetallic Au-Pd nanoparticles with an Au core and a thin Pd shell as cathode catalysts in microbial fuel cells, which represent a promising technology for wastewater treatment, while directly generating electrical energy. In specific, in comparison with the hollow structured Pt nanoparticles, a benchmark for the electrocatalysis, the bimetallic core-shell Au-Pd nanoparticles are found to have superior activity and stability for oxygen reduction reaction in a neutral condition due to the strong electronic interaction and lattice strain effect between the Au core and the Pd shell domains. The maximum power density generated in a membraneless single-chamber microbial fuel cell running on wastewater with core-shell Au-Pd as cathode catalysts is ca. 16.0 W m−3 and remains stable over 150 days, clearly illustrating the potential of core-shell nanostructures in the applications of microbial fuel cells. PMID:27734945

  17. Core-shell Au-Pd nanoparticles as cathode catalysts for microbial fuel cell applications

    Science.gov (United States)

    Yang, Gaixiu; Chen, Dong; Lv, Pengmei; Kong, Xiaoying; Sun, Yongming; Wang, Zhongming; Yuan, Zhenhong; Liu, Hui; Yang, Jun

    2016-10-01

    Bimetallic nanoparticles with core-shell structures usually display enhanced catalytic properties due to the lattice strain created between the core and shell regions. In this study, we demonstrate the application of bimetallic Au-Pd nanoparticles with an Au core and a thin Pd shell as cathode catalysts in microbial fuel cells, which represent a promising technology for wastewater treatment, while directly generating electrical energy. In specific, in comparison with the hollow structured Pt nanoparticles, a benchmark for the electrocatalysis, the bimetallic core-shell Au-Pd nanoparticles are found to have superior activity and stability for oxygen reduction reaction in a neutral condition due to the strong electronic interaction and lattice strain effect between the Au core and the Pd shell domains. The maximum power density generated in a membraneless single-chamber microbial fuel cell running on wastewater with core-shell Au-Pd as cathode catalysts is ca. 16.0 W m‑3 and remains stable over 150 days, clearly illustrating the potential of core-shell nanostructures in the applications of microbial fuel cells.

  18. Thermal diffusivity of nanofluids containing Au/Pd bimetallic nanoparticles of different compositions.

    Science.gov (United States)

    Sánchez-Ramírez, J F; Jiménez Pérez, J L; Cruz Orea, A; Gutierrez Fuentes, R; Bautista-Hernández, A; Pal, U

    2006-03-01

    Colloidal suspensions of bimetallic Au/Pd nanoparticles were prepared by simultaneous reduction of the metal ions from their corresponding chloride salts with polymer (PVP) stabilizer. Thermal properties of water containing bimetallic nanoparticles with different nominal compositions (Au/Pd = 12/1, 5/1, 1/1, 1/5) were measured using the mode mismatched dual-beam thermal lens technique to determine the effect of particle composition on the thermal diffusivity of the nanofluids. The characteristic time constant of the transient thermal lens was estimated by fitting the experimental data to the theoretical expression for transient thermal lens. The thermal diffusivity of the nanofluids (water, containing Au/Pd bimetallic nanoparticles) is seen to be strongly dependent on the composition of the particles. The maximum diffusivity was achieved for the nanoparticles with highest Au/Pd molar ratio. A possible mechanism for such high thermal diffusivity of the nanofluids with bimetallic particles is given. UV-Vis spectroscopy, TEM and high-resolution electron microscopy (HREM) techniques were used to characterize the Au/Pd bimetallic nanoparticles. PMID:16573121

  19. Synthesis of biocompatible AuAgS/Ag2S nanoclusters and their applications in photocatalysis and mercury detection

    International Nuclear Information System (INIS)

    In this paper, a facile approach for preparation of AuAgS/Ag2S nanoclusters was developed. The unique AuAgS/Ag2S nanoclusters capped with biomolecules exhibit interesting excellent optical and catalytic properties. The fluorescent AuAgS/Ag2S nanoclusters show tunable luminescence depending on the nanocluster size. The apoptosis assay demonstrated that the AuAgS/Ag2S nanoclusters showed low cytotoxicity and good biocompatibility. Therefore, the nanoclusters can be used not only as a probe for labeling cells but also for their photocatalytic activity for photodegradation of organic dye. Moreover, a highly selective and sensitive assay for detection of mercury including Hg2+ and undissociated mercury complexes was developed based on the quenching fluorescent AuAgS/Ag2S nanoclusters, which provides a promising approach for determining various forms of Hg in the mercury-based compounds in environment. These unique nanoclusters may have potential applications in biological labeling, sensing mercury, and photodegradation of various organic pollutants in waste water.Graphical Abstract

  20. Synthesis of biocompatible AuAgS/Ag{sub 2}S nanoclusters and their applications in photocatalysis and mercury detection

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Qian; Chen, Shenna; Zhang, Lingyang; Huang, Haowen, E-mail: hhwn09@163.com; Liu, Fengping [Hunan University of Science and Technology, Key Laboratory of Theoretical Organic Chemistry and Function Molecule, Ministry of Education, Hunan Provincial University Key Laboratory of QSAR/QSPR, School of Chemistry and Chemical Engineering (China); Liu, Xuanyong, E-mail: xyliu@mail.sic.ac.cn [Chinese Academy of Sciences, State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics (China)

    2014-12-15

    In this paper, a facile approach for preparation of AuAgS/Ag{sub 2}S nanoclusters was developed. The unique AuAgS/Ag{sub 2}S nanoclusters capped with biomolecules exhibit interesting excellent optical and catalytic properties. The fluorescent AuAgS/Ag{sub 2}S nanoclusters show tunable luminescence depending on the nanocluster size. The apoptosis assay demonstrated that the AuAgS/Ag{sub 2}S nanoclusters showed low cytotoxicity and good biocompatibility. Therefore, the nanoclusters can be used not only as a probe for labeling cells but also for their photocatalytic activity for photodegradation of organic dye. Moreover, a highly selective and sensitive assay for detection of mercury including Hg{sup 2+} and undissociated mercury complexes was developed based on the quenching fluorescent AuAgS/Ag{sub 2}S nanoclusters, which provides a promising approach for determining various forms of Hg in the mercury-based compounds in environment. These unique nanoclusters may have potential applications in biological labeling, sensing mercury, and photodegradation of various organic pollutants in waste water.Graphical Abstract.

  1. Enhanced plasmonic behavior of bimetallic (Ag-Au multilayered spheres

    Directory of Open Access Journals (Sweden)

    Pal Umapada

    2011-01-01

    Full Text Available Abstract In this article we study the plasmonic behavior of some stable, highly biocompatible bimetallic metal-dielectric-metal (MDM and double concentric nanoshell (DCN structures. By simply switching the material of the inner structure from Au to Ag, the intensity of their surface plasmon resonance could be increased in the optical transparency region of the human tissues up to 20 and 60 percent for the MDM and DCN, respectively, while the biocompatibility is retained. The obtained results indicate that these novel structures could be highly suitable for surface enhanced Raman scattering and photothermal cancer therapy.

  2. Site-specific growth of Au-Pd alloy horns on Au nanorods: A platform for highly sensitive monitoring of catalytic reactions by surface enhancement raman spectroscopy

    KAUST Repository

    Huang, Jianfeng

    2013-06-12

    Surface-enhanced Raman scattering (SERS) is a highly sensitive probe for molecular detection. The aim of this study was to develop an efficient platform for investigating the kinetics of catalytic reactions with SERS. To achieve this, we synthesized a novel Au-Pd bimetallic nanostructure (HIF-AuNR@AuPd) through site-specific epitaxial growth of Au-Pd alloy horns as catalytic sites at the ends of Au nanorods. Using high-resolution electron microscopy and tomography, we successfully reconstructed the complex three-dimensional morphology of HIF-AuNR@AuPd and identified that the horns are bound with high-index {11l} (0.25 < l < 0.43) facets. With an electron beam probe, we visualized the distribution of surface plasmon over the HIF-AuNR@AuPd nanorods, finding that strong longitudinal surface plasmon resonance concentrated at the rod ends. This unique crystal morphology led to the coupling of high catalytic activity with a strong SERS effect at the rod ends, making HIF-AuNR@AuPd an excellent bifunctional platform for in situ monitoring of surface catalytic reactions. Using the hydrogenation of 4-nitrothiophenol as a model reaction, we demonstrated that its first-order reaction kinetics could be accurately determined from this platform. Moreover, we clearly identified the superior catalytic activity of the rod ends relative to that of the rod bodies, owing to the different SERS activities at the two positions. In comparison with other reported Au-Pd bimetallic nanostructures, HIF-AuNR@AuPd offered both higher catalytic activity and greater detection sensitivity. © 2013 American Chemical Society.

  3. Bonding, Luminescence, Metallophilicity in Linear Au3 and Au2Ag Chains Stabilized by Rigid Diphosphanyl NHC Ligands.

    Science.gov (United States)

    Ai, Pengfei; Mauro, Matteo; Gourlaouen, Christophe; Carrara, Serena; De Cola, Luisa; Tobon, Yeny; Giovanella, Umberto; Botta, Chiara; Danopoulos, Andreas A; Braunstein, Pierre

    2016-09-01

    The heterofunctional and rigid ligand N,N'-diphosphanyl-imidazol-2-ylidene (PCNHCP; P = P(t-Bu)2), through its phosphorus and two N-heterocyclic carbene (NHC) donors, stabilizes trinuclear chain complexes, with either Au3 or AgAu2 cores, and dinuclear Au2 complexes. The two oppositely situated PCNHCP (L) ligands that "sandwich" the metal chain can support linear and rigid structures, as found in the known tricationic Au(I) complex [Au3(μ3-PCNHCP,κP,κCNHC,κP)2](OTf)3 (OTf = CF3SO3; [Au3L2](OTf)3; Chem. Commun. 2014, 50, 103-105) now also obtained by transmetalation from [Ag3(μ3-PCNHCP,κP,κCNHC,κP)2](OTf)3 ([Ag3L2](OTf)3), or in the mixed-metal tricationic [Au2Ag(μ3-PCNHCP,κP,κCNHC,κP)2](OTf)3 ([Au2AgL2](OTf)3). The latter was obtained stepwise by the addition of AgOTf to the digold(I) complex [Au2(μ2-PCNHCP,κP,κCNHC)2](OTf)2 ([Au2L2](OTf)2). The latter contains two dangling P donors and displays fluxional behavior in solution, and the Au···Au separation of 2.8320(6) Å in the solid state is consistent with metallophilic interactions. In the solvento complex [Au3Cl2(tht)(μ3-PCNHCP,κP,κCNHC,κP)](OTf)·MeCN ([Au3Cl2(tht)L](OTf)·MeCN), which contains only one L and one tht ligand (tht = tetrahydrothiophene), the metal chain is bent (148.94(2)°), and the longer Au···Au separation (2.9710(4) Å) is in line with relaxation of the rigidity due to a more "open" structure. Similar features were observed in [Au3Cl2(SMe2)L](OTf)·2MeCN. A detailed study of the emission properties of [Au3L2](OTf)3, [Au3Cl2(tht)L](OTf)·MeCN, [Au2L2](OTf)2, and [Au2AgL2](OTf)3 was performed by means of steady state and time-resolved photophysical techniques. The complex [Au3L2](OTf)3 displays a bright (photoluminescence quantum yield = 80%) and narrow emission band centered at 446 nm with a relatively small Stokes' shift and long-lived excited-state lifetime on the microsecond timescale, both in solution and in the solid state. In line with the very narrow emission

  4. First principles investigation of the activity of thin film Pt, Pd and Au surface alloys for oxygen reduction

    DEFF Research Database (Denmark)

    Tripkovic, Vladimir; Hansen, Heine Anton; Rossmeisl, Jan;

    2015-01-01

    . This is particularly challenging for alloys containing Au due to a high propensity of Au to segregate to the surface. We also show that once Au is on the surface it will diffuse to defect sites, explaining why small amounts of Au retard dissolution of Pt nanoparticles. For the PtPd thin films there is no pronounced...

  5. Sensitive voltammetric determination of vanillin with an AuPd nanoparticles-graphene composite modified electrode.

    Science.gov (United States)

    Shang, Lei; Zhao, Faqiong; Zeng, Baizhao

    2014-05-15

    In this work, graphene oxide was reduced to graphene with an endogenous reducing agent from dimethylformamide, and then AuPd alloy nanoparticles were electrodeposited on the graphene film. The obtained AuPd-graphene hybrid film was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction and voltammetry. The electrochemical behavior of vanillin was studied using the AuPd-graphene hybrid based electrode. It presented high electrocatalytic activity and vanillin could produce a sensitive oxidation peak at it. Under the optimal conditions, the peak current was linear to the concentration of vanillin in the ranges of 0.1-7 and 10-40 μM. The sensitivities were 1.60 and 0.170 mA mM(-1) cm(-2), respectively; the detection limit was 20 nM. The electrode was successfully applied to the detection of vanillin in vanilla bean, vanilla tea and biscuit samples.

  6. Hydrogen sensing with optical microfibers coated with Pd/Au nanoparticles

    Science.gov (United States)

    Monzón-Hernández, David; Luna-Moreno, Donato; Martínez-Escobar, Dalia; Villatoro, Joel

    2010-10-01

    Optical microfibers decorated with PdAu nanoparticles are proposed for fast hydrogen sensing. The microfibers were obtained by simply tapering conventional telecommunications fiber down to dimensions comparable to the wavelength of the guided light. A few millimeters of the microfiber were coated with a PdAu layer in island form by depositing the layer at low evaporation rate (0.1 Å/s). Then the islands were grown with a thermal annealing process until composite nanoparticles were formed. The PdAu nanoparticles deposited on the optical microfibers experience optical and physical changes when they exposed to hydrogen. This gives rise to reversible transmission changes with an unusual pulsed like behavior which is attributed to scattering of the guided light. The devices are promising for detecting low concentrations of hydrogen (up to 8%) at room temperature with response and recovery times on the order of seconds.

  7. Investigation of the Phase Equilibria of Sn-Cu-Au Ternary and Ag-Sn-Cu-Au Quaternary Systems and Interfacial Reactions in Sn-Cu/Au Couples

    Science.gov (United States)

    Yen, Yee-Wen; Jao, Chien-Chung; Hsiao, Hsien-Ming; Lin, Chung-Yung; Lee, Chiapyng

    2007-02-01

    The phase equilibria of the Sn-Cu-Au ternary, Ag-Sn-Cu-Au quaternary systems and interfacial reactions between Sn-Cu alloys and Au were experimentally investigated at specific temperatures in this study. The experimental results indicated that there existed three ternary intermetallic compounds (IMCs) and a complete solid solubility between AuSn and Cu6Sn5 phases in the Sn-Cu-Au ternary system at 200°C. No quaternary IMC was found in the isoplethal section of the Ag-Sn-Cu-Au quaternary system. Three IMCs, AuSn, AuSn2, and AuSn4, were found in all couples. The same three IMCs and (Au,Cu)Sn/(Cu,Au)6Sn5 phases were found in all Sn-Cu/Au couples. The thickness of these reaction layers increased with increasing temperature and time. The mechanism of IMC growth can be described by using the parabolic law. In addition, when the reaction time was extended and the Cu content of the alloy was increased, the AuSn4 phase disappeared gradually. The (Au, Cu)Sn and (Cu,Au)6Sn5 layers played roles as diffusion barriers against Sn in Sn-Cu/Au reaction couple systems.

  8. Cu-Ag sulfides as indicators of pre-porphyritic epithermal Au-Ag deposits in Northeastern Russia

    Science.gov (United States)

    Savva, N. E.; Sidorov, A. A.; Volkov, A. V.

    2016-08-01

    Au-Ag mineralization of the Olcha and Teploe epithermal deposits underwent thermal metamorphism due to porphyritic intrusions. The presence of Bi-bearing galena and matildite in the ores (Teploe), Cu-Te-bearing naumannite (Olcha), the occurrence of middle- and high-temperature facies of metasomatic rocks (epidote and actinolite), and temperature formation conditions are related, firstly, to the influence of granitoids on the ore process, which supplied not only Cu and Mo, but also Bi, Te, and, secondly, to the heating of host rocks containing pre-porphyritic epithermal Au-Ag mineralization. The abundance of Cu-Ag sulfides and Cu-acanthite resulted from the enrichment of later mineral phases in Cu and Ag under the substance redistribution with the formation of Ag-acanthite ores. The data considered in the paper are of practical importance for regional forecasting of metallogenic constructions, exploration, and evaluation of the epithermal Au-Ag deposits.

  9. Novel PdAgCu ternary alloy: Hydrogen permeation and surface properties

    Energy Technology Data Exchange (ETDEWEB)

    Tarditi, Ana M.; Braun, Fernando [Instituto de Investigaciones en Catalisis y Petroquimica (FIQ, UNL-CONICET), Santiago del Estero 2829, 3000 Santa Fe (Argentina); Cornaglia, Laura M., E-mail: lmcornag@fiq.unl.edu.ar [Instituto de Investigaciones en Catalisis y Petroquimica (FIQ, UNL-CONICET), Santiago del Estero 2829, 3000 Santa Fe (Argentina)

    2011-05-15

    Dense PdAgCu ternary alloy composite membranes were synthesized by the sequential electroless plating of Pd, Ag and Cu on top of both disk and tubular porous stainless steel substrates. X-ray diffraction and scanning electron microscopy were employed to study the structure and morphology of the tested samples. The hydrogen permeation performance of these membranes was investigated over a 350-450 deg. C temperature range and a trans-membrane pressure up to 100 kPa. After annealing at 500 deg. C in hydrogen stream followed by permeation experiments, the alloy layer presented a FCC crystalline phase with a bulk concentration of 68% Pd, 7% Ag and 25% Cu as revealed by EDS. The PdAgCu tubular membrane was found to be stable during more than 300 h on hydrogen stream. The permeabilities of the PdAgCu ternary alloy samples were higher than the permeabilities of the PdCu alloy membranes with a FCC phase. The co-segregation of silver and copper to the membrane surface was observed after hydrogen permeation experiments at high temperature as determined by XPS.

  10. Adsorption of Au and Pd on Ruthenium-Supported Bilayer Silica

    OpenAIRE

    Büchner, C.; L. Lichtenstein; Stuckenholz, S.; Heyde, M; Ringleb, F.; Sterrer, M.; Kaden, W.; Giordano, L; G. Pacchioni; H. Freund

    2014-01-01

    Adsorption of Au and Pd over bilayer SiO2/Ru has been investigated using scanning-probe microscopy, X-ray photoemission spectroscopy (XPS), and density functional theory (DFT). Low temperature (∼5 K) atomic force (AFM) and scanning tunneling microscopy (STM) measurements reveal the presence of small adsorption features after exposing the samples to small doses of either metal. In the case of Pd, we note a homogeneous distribution of adsorbates across the entire surface, which consists of both...

  11. Polarization-sensitive photocurrent in the resistive Ag/Pd films

    Science.gov (United States)

    Saushin, A. S.; Zonov, R. G.; Mikheev, K. G.; Shamshetdinov, R. R.; Mikheev, G. M.

    2016-08-01

    We report on the observation of helicity dependent photocurrent of the 20 μm thick silver-palladium (Ag/Pd) films manufactured by the thick-film technology. The transverse photocurrent is observed at oblique incidence of laser radiation with different wavelengths in the spectral range of 266 - 2100 nm. At the wavelength range of 532 - 2100 nm the polarity of the transverse photocurrent is positive (negative) for the left- (right-) circular polarized beam. We show that action of high temperature on the films in vacuum results in the decrease of longitudinal photocurrent due to the reduction of PdO content. The photon drag effect is suggested to be the origin of the polarization-sensitive photocurrent in the Ag/Pd films. The obtained results show that the Ag/Pd resistive films may be of interest for polarization- sensitive measurements.

  12. Band-Structure Effects in the High-Field Magnetization of Pd and Dilute Pd-Rh and Pd-Ag Alloys

    DEFF Research Database (Denmark)

    Andersen, O. Krogh

    1970-01-01

    [Single Bond]Ag alloys. A van Hove singularity near the Fermi level of the 7% Rh[Single Bond]Pd alloy has a profound effect on DeltaB. Our results are consistent with the measurements of Foner and McNiff, but detailed comparison is difficult since DeltaB is of the same order as the experimental uncertainty...

  13. Final Technical Report: First Principles Investigations for the Ensemble Effects of PdAu and PtAu Bimetallic Nanocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Ruqian Wu

    2012-05-18

    Bimetallic surfaces with tunable chemical properties have attracted broad attention in recent years due to their ample potential for heterogeneous catalysis applications. The local chemical properties of constituents are strongly altered from their parent metals by 'ligand effect', a term encompassing the influences of charge transfer, orbital rehybridization and lattice strain. In comparison to the aforementioned, the 'ensemble effect' associated with particular arrangements of the active constituents have received much less attention, despite their notable importance towards the determination of reactivity and selectivity of bimetallic catalysts. We performed theoretical studies for understanding the ensemble effects on bimetallic catalysis: (i) simulations for the formation of different ensembles on PdAu and PtAu nanoclusters; (ii) studies of the size, shape, and substrate dependence of their electronic properties; and (iii) simulations for model reactions such as CO oxidation, methanol, ethylene and water dehydrogenation on PdAu and PtAu nanoclusters. In close collaboration with leading experimental groups, our theoretical research elucidated the fundamentals of Au based bimetallic nanocatalysts.

  14. Vibrational properties at the ordered metallic surface alloy system Au(110)-1×2-Pd

    Science.gov (United States)

    Kheffache, Sedik; Chadli, Rabah; Khater, Antoine

    2016-06-01

    We present a calculation for the vibrational properties of the ordered surface alloy Au(110)-1×2-Pd on a crystalline substrate of Au. The surface phonon dispersion curves and the local vibrations densities of states (LDOS) are calculated in the harmonic approximation for the system, using the phase field matching theory (PFMT) method and associated real space Green’s functions. In particular, it is shown that the surface alloy presents optic vibrational modes above the Au bulk bands, along the directions of high-symmetry ΓX¯, XS¯, SY¯ and Y Γ¯ of the corresponding two-dimensional Brillouin zone. Measurements of the surface phonon dispersion branches can hence be made by different techniques such as helium atom scattering (HAS) to compare with. The calculated LDOS for Au and Pd atomic sites in the four top surface atomic layers span a wider range of frequencies than those for the individual Au(110) or Pd(110) metallic surfaces. These LDOS provide a spectral signature for the progressive transition from the surface dynamics to that of the Au crystal bulk. Knowledge of these LDOS for the surface alloy can also serve as an input for modeling the diffusion and reaction rates of chemical species at its surface.

  15. Sulfur Tolerant Pd/Cu and Pd/Au Alloy Membranes for H2 Separation with High Pressure CO2 for Sequestration

    Energy Technology Data Exchange (ETDEWEB)

    Yi Hua Ma; Natalie Pomerantz; Chao-Huang Chen

    2008-09-30

    The effect of H{sub 2}S poisoning on Pd, Pd/Cu, and Pd/Au alloy composite membranes prepared by the electroless deposition method on porous Inconel supports was investigated to provide a fundamental understanding of the durability and preparation of sulfur tolerant membranes. X-ray photoelectron spectroscopy (XPS) studies showed that the exposure of pure Pd to 50 ppm H{sub 2}S/H{sub 2} mixtures caused bulk sulfide formation at lower temperatures and surface sulfide formation at higher temperatures. Lower temperatures, longer exposure times, and higher H{sub 2}S concentrations resulted in a higher degree of sulfidation. In a Pd membrane, the bulk sulfide formation caused a drastic irrecoverable H{sub 2} permeance decline and an irreparable loss in selectivity. Pd/Cu and Pd/Au alloy membranes exhibited permeance declines due to surface sulfide formation upon exposure to 50 ppm H{sub 2}S/H{sub 2} gas mixtures. However in contrast to the pure Pd membrane, the permeances of the Pd/Cu and Pd/Au alloy membranes were mostly recovered in pure H{sub 2} and the selectivity of the Pd alloy layers remained essentially intact throughout the characterization in H{sub 2}, He and H{sub 2}S/H{sub 2} mixtures which lasted several thousand hours. The amount of irreversible sulfur poisoning decreased with increasing temperature due to the exothermicity of H{sub 2}S adsorption. Longer exposure times increased the amount of irreversible poisoning of the Pd/Cu membrane but not the Pd/Au membrane. Pd/Au coupon studies of the galvanic displacement method showed that higher Au{sup 3+} concentrations, lower pH values, higher bath temperatures and stirring the bath at a rate of 200 rpm yielded faster displacement rates, more uniform depositions, and a higher Au content within the layers. While 400 C was found to be sufficient to form a Pd/Au alloy on the surface, high temperature X-ray diffraction (HTXRD) studies showed that even after annealing between 500-600 C, the Pd/Cu alloys could have

  16. One-step synthesis of PtPdAu ternary alloy nanoparticles on graphene with superior methanol electrooxidation activity

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Yuzhen; Gu Yonge; Lin Shaoxiong; Wei Jinping; Wang Zaihua [Department of Chemistry, Lanzhou University, Lanzhou 730000 (China); Wang Chunming, E-mail: wangcm@lzu.edu.cn [Department of Chemistry, Lanzhou University, Lanzhou 730000 (China); Du Yongling; Ye Weichun [Department of Chemistry, Lanzhou University, Lanzhou 730000 (China)

    2011-10-01

    Highlights: > PtPdAu nanoparticles were synthesized on graphene sheets via chemical reduction method. > The prepared PtPdAu nanoparticles were ternary alloy with fcc structure. > The catalyst exhibited superior catalytic activity and stability for MOR in alkaline. - Abstract: Well-dispersed PtPdAu ternary alloy nanoparticles were synthesized on graphene sheets via a simple one-step chemical reduction method in ethylene glycol (EG) and water system, in which EG served as both reductive and dispersing agent. The electrocatalytic activity of PtPdAu/G was tested by methanol oxidation reaction (MOR). The catalyst was further characterized by transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD), which indicated that the as-synthesized PtPdAu nanoparticles with alloy structures were successfully dispersed on the graphene sheets. Electrocatalytic properties of the catalyst for MOR in alkaline have been investigated by cyclic voltammetry (CV), chronoamperometry and Tafel curves. The electrocatalytic activity and stability of PtPdAu/G were superior to PtPd/G, PtAu/G and Pt/G. In addition, the anodic peak current on PtPdAu/G catalyst was proportional to the concentration of methanol in the range of 0.05-1.00 M. This study implies that the prepared catalyst have great potential applications in fuel cells.

  17. Ethanol electro-oxidation in alkaline medium using Pd/MWCNT and PdAuSn/MWCNT electrocatalysts prepared by electron beam irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Geraldes, Adriana Napoleao; Silva, Dionisio Furtunato da; Andrade e Silva, Leonardo Gondin de; Spinace, Estevam Vitorio; Oliveira Neto, Almir, E-mail: drinager@ig.com.br, E-mail: dfsilva@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Santos, Mauro Coelho dos [Universidade Federal do ABC (LEMN/CCNH/UFABC), Santo Andre, SP (Brazil)

    2015-07-01

    Environmental problems and the world growing demand for energy has mobilized the scientific community in finding of clean and renewable energy sources. In this context, fuel cells appear as appropriate technology for generating electricity through alcohols electro-oxidation. Multi Wall Carbon Nanotubes (MWCNT)-supported Pd and trimetallic PdAuSn (Pd:Au:Sn 50:10:40 atomic ratio) electrocatalysts were prepared using electron beam irradiation. The obtained materials were characterized by VC, Chronoamperometry, EDX, TEM and XRD. The catalytic activities of electrocatalysts toward ethanol electro-oxidation were evaluated in alkaline medium in a single alkaline direct ethanol fuel cell (ADEFC) in a range temperature 60 to 90 deg C. The best performances were obtained at 85 deg C: 33 mW.cm{sup -2} and 31 mW.cm{sup -2} for Pd/ MWCNT and PdAuSn/MWCNT electrocatalysts, respectively. X-ray diffractograms of electrocatalysts showed the presence of Pd-rich (fcc) and Au-rich (fcc) phases. Cyclic voltammetry and chronoamperometry experiments showed that PdAuSn/MWCNT electrocatalyst demonstrated similar activity toward ethanol electro-oxidation at room temperature, compared to electrocatalyst Pd/MWCNT. (author)

  18. Electrochemical synthesis of reduced graphene sheet-AuPd alloy nanoparticle composites for enzymatic biosensing.

    Science.gov (United States)

    Yang, Jiang; Deng, Shengyuan; Lei, Jianping; Ju, Huangxian; Gunasekaran, Sundaram

    2011-11-15

    A simple, fast, green and controllable approach was developed for electrochemical synthesis of a novel nanocomposite of electrochemically reduced graphene oxide (ERGO) and gold-palladium (1:1) bimetallic nanoparticles (AuPdNPs), without the aid of any reducing reagent. The electrochemical reduction efficiently removed oxygen-containing groups in ERGO, which was then modified with homogeneously dispersed AuPdNPs in a good size distribution. ERGO-AuPdNPs nanocomposite showed excellent biocompatibility, enhanced electron transfer kinetics and large electroactive surface area, and were highly sensitive and stable towards oxygen reduction. A biosensor was constructed by immobilizing glucose oxidase as a model enzyme on the nanocomposites for glucose detection through oxygen consumption during the enzymatic reaction. The biosensor had a detection limit of 6.9μM, a linear range up to 3.5mM and a sensitivity of 266.6μAmM(-1)cm(-2). It exhibited acceptable reproducibility and good accuracy with negligible interferences from common oxidizable interfering species. These characteristics make ERGO-AuPdNPs nanocomposite highly suitable for oxidase-based biosensing. PMID:21903376

  19. Nanoscale electrical characteristics of metal (Au, Pd)-graphene-metal (Cu) contacts

    Science.gov (United States)

    Ruffino, F.; Meli, G.; Grimaldi, M. G.

    2016-01-01

    Free-standing graphene presents exceptional physical properties (as a high carrier mobility) making it the ideal candidate for the next generation nanoelectronics. However, when graphene layers are inserted in real electronics devices, metal contacting is required. The metal-graphene interaction significantly affects the graphene electrical properties, drastically changing its behavior with respect to the free-standing configuration. So, this work presents an experimental study on the nanoscale electric characteristics of metal/graphene/metal contacts. In particular, starting from single-layer graphene grown on Cu foil we deposited on the graphene surface two different metal films (Au or Pd) and the Au/graphene/Cu and Pd/graphene/Cu current-voltage characteristics are acquired, on the nanometric scale, by the conductive atomic force microscopy. Both systems presented a current voltage rectifying behavior. However, the Au/graphene/Cu system conducts significantly at negative applied bias (graphene behaves as a p-type semiconductor in a meta/semiconductor contact), while in the Pd/graphene/Cu at positive applied bias (graphene behaves as a n-type semiconductor in a metal/semiconductor contact). This difference is discussed on the basis of the band energy diagram at the metal/graphene interface and the modification of the graphene Fermi level due to the Au/graphene or Pd/graphene interaction.

  20. Volcano-like behavior of Au-Pd core-shell nanoparticles in the selective oxidation of alcohols.

    Science.gov (United States)

    Silva, Tiago A G; Teixeira-Neto, Erico; López, Núria; Rossi, Liane M

    2014-01-01

    Gold-palladium (AuPd) nanoparticles have shown significantly enhanced activity relative to monometallic Au and Pd catalysts. Knowledge of composition and metal domain distributions is crucial to understanding activity and selectivity, but these parameters are difficult to ascertain in catalytic experiments that have primarily been devoted to equimolar nanoparticles. Here, we report AuPd nanoparticles of varying Au:Pd molar ratios that were prepared by a seed growth method. The selective oxidation of benzyl alcohol was used as a model reaction to study catalytic activity and selectivity changes that occurred after varying the composition of Pd in bimetallic catalysts. We observed a remarkable increase in catalytic conversion when using a 10:1 Au:Pd molar ratio. This composition corresponds to the amount of Pd necessary to cover the existing Au cores with a monolayer of Pd as a full-shell cluster. The key to increased catalytic activity derives from the balance between the number of active sites and the ease of product desorption. According to density functional theory calculations, both parameters are extremely sensitive to the Pd content resulting in the volcano-like activity observed. PMID:25042537

  1. Highly energetic nonequilibrium microstructure fabricated by ion beam manipulation in the Ag-Pd system

    CERN Document Server

    Li, Z C

    2003-01-01

    An artificial ordered layered structure of high energy was obtained by a form of ion beam manipulation, namely interface-assisted ion beam mixing, of appropriately designed nano-sized Ag-Pd multilayered films, in which the interfacial free energy elevated the Ag-Pd multilayered films to near to the corresponding highly energetic state. Diffraction analysis suggested that the ordered layered structure consisted of two overlapped face-centred-cubic lattices with lattice constants smaller than those of both pure Ag and pure Pd. The growth mechanism was also discussed in terms of a dynamic atomic collision, followed by a relaxation lasting for an extremely short time, involved in the irradiation process.

  2. Preparation and characterization of Pd-Ag alloy composite membrane with magnetron sputtering

    Institute of Scientific and Technical Information of China (English)

    赵宏宾[1; 熊国兴[2; N.Stroh[3; H.Brunner[4

    1999-01-01

    A Pd-Ag (24 wt%) alloy composite membrane was prepared by the magnetron sputtering. A γ-Al2O3 membrane was synthesized by the sol-gel method and used as substrate of the Pd-Ag alloy film. The process parameters of the magnetron sputtering were optimized as a function of the compactness of the Pd-Ag alloy film. The best membrane with a thickness of 1 μm was produced with a sputtering pressure of 2.7 Pa and a substrate temperature of 400℃. The membrane had an H2/N2 permselectivity of 51.5--1000 and an H2 permeation rate of 0.036--1.17×10-5cm3/cm2·s· Pa, depending on operating conditions.

  3. Promotion of Phenol Photodecomposition over TiO2 Using Au, Pd, and AuPd Nanoparticles

    DEFF Research Database (Denmark)

    Su, Ren; Tiruvalam, Ramchandra; He, Qian;

    2012-01-01

    using phenol as a probe molecule. A different phenol degradation pathway was observed when using M/TiO2 catalysts as compared to pristine TiO2.We propose a mechanism to illustrate how the noble metal nanoparticles enhance the efficiency of phenol decomposition based on photoreduction of p......Pd decorated TiO2 materials exhibit excellent long-term photoactivity, in which ∼90% of the phenol can be fully decomposed to CO2 in each cycle....

  4. Solvent and stabilizer free growth of Ag and Pd nanoparticles using metallic salts/cyclotriphosphazenes mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Díaz Valenzuela, C. [Departamento de Química, Facultad de Química, Universidad de Chile, La Palmeras 3425, Nuñoa, Casilla 653, Santiago de Chile (Chile); Valenzuela, M.L., E-mail: mlvalenzuela@unab.cl [Universidad Andres Bello, Departamento de Ciencias Química, Facultad de Ciencias Exactas, Av. Republica 275, Santiago (Chile); Caceres, S.; Diaz, R. [Departamento de Química, Facultad de Química, Universidad de Chile, La Palmeras 3425, Nuñoa, Casilla 653, Santiago de Chile (Chile); O' Dwyer, C. [Applied Nanoscience Group, Department of Chemistry, University College Cork, Cork (Ireland); Micro and Nanoelectronics Centre, Tyndall National Institute, Lee Maltings, Cork (Ireland)

    2013-12-16

    Cyclotriphosphazene is used as a sacrificial solid-state template to synthesize a range of Ag and Pd nanoparticles with diverse geometries by thermal treatment using MLn/N{sub 3}P{sub 3}(O{sub 2}C{sub 12}H{sub 8}){sub 3} mixtures. The Pd and Ag nanoparticles are synthesized by solid-state pyrolysis of AgPPh{sub 3}[CF{sub 3}SO{sub 3}]/N{sub 3}P{sub 3}(O{sub 2}C{sub 12}H{sub 8}){sub 3} and PdCl{sub 2}/N{sub 3}P{sub 3}(O{sub 2}C{sub 12}H{sub 8}){sub 3} mixtures with molar relationships of 1:1, 1:5 and 1:10 respectively, in air and at 800 °C. The morphology of the as-prepared nanoparticles is found to depend on the molar ratio of the precursor mixture, the preparation method and of the nature of the metal. Ag and Pd, microcrystals were thermally grown on Si from the respective 1:1 precursors while that metal foams were grown from 1:5 ratios precursors on SiO{sub 2} wafers. High resolution transmission electron microscopy investigations reveal in most cases small crystals of Pd. HRSTEM measurements indicate that the formation of the Pd and Ag nanoparticles occurs through a phase demixing and dewetting mechanism. This approach has potential to be a useful and facile method to prepare metallic nanoparticles without requiring solutions or surfactants for application in electronic, catalytic and sensor materials and devices. - Highlights: • Pyrolysis MLn/N{sub 3}P{sub 3}(O{sub 2}C{sub 12}H{sub 8}){sub 3} mixtures under air, give Pd and Ag nanoparticles. • AgPPh{sub 3}[CF{sub 3}SO{sub 3}] and PdCl{sub 2} in molar ratios 1:1 and 1:5 were used. • Metal foams were obtained from 1:5 ratios when deposited on SiO{sub 2.} • Using crucible supporting in 1:1 metal/trimer <2 nm Pd nanoparticles were obtained. • The probable mechanism involves a dewetting, nucleation and ripening crystallization.

  5. Facile synthesis of PdAgTe nanowires with superior electrocatalytic activity

    Science.gov (United States)

    Hong, Wei; Wang, Jin; Wang, Erkang

    2014-12-01

    In this work, ultrathin Te nanowires (NWs) with high-aspect-ratio are prepared by a simple hydrothermal method. By using Te NWs as the sacrificial template, we demonstrate a facile and efficient method for the synthesis of PdAgTe NWs with high-quality through the partly galvanic replacement between Te NWs and the corresponding noble metal salts precursors in an aqueous solution. The compositions of PdAgTe NWs can be tuned by simply altering the concentration of the precursors. After cyclic voltammetry treatment, multi-component PdAgTe NW with a highly active and stable surface can be obtained. The structure and composition of the as-prepared nanomaterials are analyzed by transmission electron microscope, X-ray diffraction, energy dispersive X-ray spectroscopy, inductively coupled plasma-mass spectroscopy and X-ray photoelectron spectroscopy. Electrochemical catalytic measurement results prove that the as synthesized PdAgTe NWs present superior catalytic activity toward ethanol electrooxidation in alkaline solution than the commercial Pd/C catalyst, which making them can be used as effective catalysts for the direct ethanol fuel cells.

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

    Science.gov (United States)

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

    2016-01-01

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

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

    Science.gov (United States)

    Zhang, Chao; Chen, Mei; Wang, Guizhen; Fang, Wei; Ye, Chen; Hu, Hanhua; Fa, Zhenzong; Yi, Jiu; Liao, Wan-Qing

    2016-01-01

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

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

    Directory of Open Access Journals (Sweden)

    Chao Zhang

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

  9. Bimetallic Au/Pd catalyzed aerobic oxidation of alcohols in the poly(ethylene glycol)/CO2 system

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Bimetallic Au/Pd nanoparticles were prepared and used to catalyze oxidation of alcohols in the poly(ethylene glycol) (PEG)/CO2 biphasic system using O2 as the oxidant without adding any base.The catalytic activity of Au/Pd bimetal with different mole ratios was studied using benzyl alcohol as the substrate.It was found that bimetallic Au/Pd nanoparticles with Au:Pd=1:3.5 had higher catalytic activity than monometallic Au,Pd and the bimetallic Au/Pd nanoparticles with other molar ratios.The effect of CO2 pressure on the oxidation of benzyl alcohol and 1-phenylethanol in PEG/CO2 was investigated.It was demonstrated that CO2 pressure could be used to tune the conversion and selectivity of the reactions effectively.α,β-Unsaturated alcohols were also studied and found to be more reactive than benzyl alcohol and 1-phenylethanol.Recycling experiments showed that the Au/Pd/PEG/CO2 catalytic system could be recycled at least four times without reducing the activity.In addition,the catalytic system is clean and the products can be separated easily.

  10. The effect of CNTs on structures and catalytic properties of AuPd clusters for H2O2 synthesis.

    Science.gov (United States)

    Yang, Hua-feng; Xie, Peng-yang; Yu, Hui-you; Li, Xiao-nian; Wang, Jian-guo

    2012-12-28

    The structures and catalytic properties of AuPd clusters supported on carbon nanotubes (CNTs) for H(2)O(2) synthesis have been investigated by means of density functional theory calculations. Firstly, the structures of AuPd clusters are strongly influenced by CNTs, in which the bottom layers are mainly composed of Pd and the top layers are a mix of Au and Pd due to the stronger binding of Pd than Au on CNTs. Especially, it is found that O(2) adsorption on the Pd/CNTs interfacial sites is much weaker than that on the only Pd sites, which is in contrast to transition metal oxide (for example TiO(2), Al(2)O(3), CeO(2)) supported metal clusters. Furthermore, Pd ensembles on the interfacial sites have far superior catalytic properties for H(2)O(2) formation than those away from CNT supports due to the changes in electronic structures caused by the CNTs. Therefore, our study provides a physical insight into the enhanced role of carbon supports in H(2)O(2) synthesis over supported AuPd catalysts. PMID:23032860

  11. Growth of various Au Ag nanocomposites from gold seeds in amino acid solutions

    Science.gov (United States)

    Huang, Yu-Fen; Lin, Yang-Wei; Chang, Huan-Tsung

    2006-10-01

    In this paper, we describe an easy procedure for the preparation of differently shaped and sized Au-Ag nanocomposites from gold nanorod (AuNR) seeds in various amino acid solutions—arginine (Arg), cysteine (Cys), glycine (Gly), glutamate (Glu), glutamine (Gln), histidine (His), lysine (Lys), and methionine (Met), respectively—at values of pH ranging from 8.0 to 11.5. Our results suggest that the pH, the nature of the amino acid, and its concentration all have significant impact on the preparation of Au-Ag nanocomposites; these factors exhibit their effects mainly through control over the reducing ability of ascorbate and/or its recognition capability, as well as through control over the surface charges of the amino acids on the AuNRs. Depending on the value of pH, we were able to prepare I-shaped, dumbbell-shaped, and/or sphere-shaped Au-Ag nanocomposites in 0.1 M solutions of Arg, Gly, Glu, Gln, Lys, and Met. In His solutions at pH 8.0 and 9.0, we obtained peanut-shaped Au-Ag nanocomposites. Corn-shaped Au-Ag nanocomposites were prepared in 0.1 M Met solutions (pH 9.0 and 10.0). By controlling the Lys concentration at pH 10.0, we synthesized pearl-necklace-shaped Au-Ag nanoparticles and Au-Ag wires. Based on the TEM images, we conclude that this simple and reproducible synthetic approach allows preparation of high-quality (>87%, beside>77% in His solutions) Au-Ag nanocomposites with various shapes and sizes under different conditions.

  12. Growth of various Au-Ag nanocomposites from gold seeds in amino acid solutions

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Y-F [Department of Chemistry, National Taiwan University, 1, Section 4, Roosevelt Road, Taipei, Taiwan (China); Lin, Y-W [Department of Chemistry, National Taiwan University, 1, Section 4, Roosevelt Road, Taipei, Taiwan (China); Chang, H-T [Department of Chemistry, National Taiwan University, 1, Section 4, Roosevelt Road, Taipei, Taiwan (China)

    2006-10-14

    In this paper, we describe an easy procedure for the preparation of differently shaped and sized Au-Ag nanocomposites from gold nanorod (AuNR) seeds in various amino acid solutions-arginine (Arg), cysteine (Cys), glycine (Gly), glutamate (Glu), glutamine (Gln), histidine (His), lysine (Lys), and methionine (Met), respectively-at values of pH ranging from 8.0 to 11.5. Our results suggest that the pH, the nature of the amino acid, and its concentration all have significant impact on the preparation of Au-Ag nanocomposites; these factors exhibit their effects mainly through control over the reducing ability of ascorbate and/or its recognition capability, as well as through control over the surface charges of the amino acids on the AuNRs. Depending on the value of pH, we were able to prepare I-shaped, dumbbell-shaped, and/or sphere-shaped Au-Ag nanocomposites in 0.1 M solutions of Arg, Gly, Glu, Gln, Lys, and Met. In His solutions at pH 8.0 and 9.0, we obtained peanut-shaped Au-Ag nanocomposites. Corn-shaped Au-Ag nanocomposites were prepared in 0.1 M Met solutions (pH 9.0 and 10.0). By controlling the Lys concentration at pH 10.0, we synthesized pearl-necklace-shaped Au-Ag nanoparticles and Au-Ag wires. Based on the TEM images, we conclude that this simple and reproducible synthetic approach allows preparation of high-quality (>87%, beside>77% in His solutions) Au-Ag nanocomposites with various shapes and sizes under different conditions.

  13. The bifurcation point of the oxygen reduction reaction on Au-Pd nanoalloys.

    Science.gov (United States)

    Staszak-Jirkovský, Jakub; Ahlberg, Elisabet; Panas, Itai; Schiffrin, David J

    2016-07-01

    The oxygen reduction reaction is of major importance in energy conversion and storage. Controlling electrocatalytic activity and its selectivity remains a challenge of modern electrochemistry. Here, first principles calculations and analysis of experimental data unravel the mechanism of this reaction on Au-Pd nanoalloys in acid media. A mechanistic model is proposed from comparison of the electrocatalysis of oxygen and hydrogen peroxide reduction on different Au-Pd ensembles. A H2O production channel on contiguous Pd sites proceeding through intermediates different from H2O2 and OOH(σ) adsorbate is identified as the bifurcation point for the two reaction pathway alternatives to yield either H2O or H2O2. H2O2 is a leaving group, albeit reduction of H2O2 to H2O can occur by electrocatalytic HO-OH dissociation that is affected by the presence of adsorbed OOH(σ). Similarities and differences between electrochemical and direct synthesis from H2 + O2 reaction on Au-Pd nanoalloys are discussed. PMID:27089504

  14. Supported Pd-Au Membrane Reactor for Hydrogen Production: Membrane Preparation, Characterization and Testing

    Directory of Open Access Journals (Sweden)

    Adolfo Iulianelli

    2016-05-01

    Full Text Available A supported Pd-Au (Au 7wt% membrane was produced by electroless plating deposition. Permeation tests were performed with pure gas (H2, H2, N2, CO2, CH4 for long time operation. After around 400 h under testing, the composite Pd-Au membrane achieved steady state condition, with an H2/N2 ideal selectivity of around 500 at 420 °C and 50 kPa as transmembrane pressure, remaining stable up to 1100 h under operation. Afterwards, the membrane was allocated in a membrane reactor module for methane steam reforming reaction tests. As a preliminary application, at 420 °C, 300 kPa of reaction pressure, space velocity of 4100 h−1, 40% methane conversion and 35% hydrogen recovery were reached using a commercial Ni/Al2O3 catalyst. Unfortunately, a severe coke deposition affected irreversibly the composite membrane, determining the loss of the hydrogen permeation characteristics of the supported Pd-Au membrane.

  15. Atomic simulation of amorphization and crystallization of Ag50 Au50 alloy during rapid solidification

    Institute of Scientific and Technical Information of China (English)

    王丽; 杨华; 张均艳; 边秀房; 衣粟

    2002-01-01

    By means of constant temperature and constant pressure molecular dynamic simulation technique, a series of simulations of the glass transition and crystallization processes of Ag50Au50 were performed. The atoms interact via EAM potential function. Pair correlation functions of liquid Ag50Au50 during different cooling rates and temperatures were simulated to reveal the structural features of liquid, super-cooled liquid, glass state and crystal. The thermodynamics and kinetics of structure transition of Ag50Au50 during cooling processes were performed.

  16. Differential flow of protons in Au+Au collisions at AGS energies

    Energy Technology Data Exchange (ETDEWEB)

    Sahu, P.K. E-mail: pradip@iopb.res.in; Cassing, W

    2002-12-30

    We study the proton sideward and elliptic differential flow for Au+Au collisions at AGS energies (2-8 A GeV) in a microscopic relativistic transport model that includes all baryon resonances up to a mass of 2 GeV as well as string degrees of freedom for the higher hadronic excitations. In order to explore the sensitivity of the various differential flows to the nuclear equation of state (EoS) we use three different parameterizations of the scalar and vector mean-fields, i.e., NL2 (soft), NL23 (medium) and NL3 (hard), with their momentum dependence fitted to the experimental Schroedinger equivalent potential (at normal nuclear matter density {rho}{sub 0}) up to kinetic energies of 1 GeV. We calculate the excitation function of sideward and elliptic flow within these parameter sets for Au+Au collisions and compare with the recent data from the E895 Collaboration as a function of rapidity, impact parameter and transverse momentum, respectively. We find that the best description of the differential data is provided by a rather 'stiff' EoS at 2 A GeV (NL3) while at higher bombarding energies (4-8 A GeV) a 'medium' EoS leads to the lowest {chi}{sup 2} with respect to the data. However, the differences in the transverse and elliptic flows (from the different parameter sets) become of minor significance at 4-8 A GeV. We attribute this insensitivity to a similar reduction of the vector potential in all models and to the dominance of string degrees of freedom at these bombarding energies.

  17. H{sub 2} reduction of surface oxides on Pd-based membrane model systems – The case of Pd(1 0 0) and Pd{sub 75}Ag{sub 25}(1 0 0)

    Energy Technology Data Exchange (ETDEWEB)

    Fernandes, V.R. [Department of Physics, Norwegian University of Science and Technology, NO-7491 Trondheim (Norway); Gustafson, J. [Division of Synchrotron Radiation Research, Lund University, Box 117, SE-221 00 Lund (Sweden); Farstad, M.H.; Walle, L.E. [Department of Physics, Norwegian University of Science and Technology, NO-7491 Trondheim (Norway); Blomberg, S.; Lundgren, E. [Division of Synchrotron Radiation Research, Lund University, Box 117, SE-221 00 Lund (Sweden); Venvik, H.J. [Department of Chemical Engineering, Norwegian University of Science and Technology, NO-7491 Trondheim (Norway); Borg, A., E-mail: anne.borg@ntnu.no [Department of Physics, Norwegian University of Science and Technology, NO-7491 Trondheim (Norway)

    2014-09-15

    Highlights: • H{sub 2} reduction of the surface oxide is significantly slower for Pd{sub 75}Ag{sub 25}(1 0 0) compared to Pd(1 0 0). • The reduction behavior shows complex temperature dependence, not well described by Avrami kinetics. • Oxygen spillover effects during the surface oxide reduction are observed for Pd(1 0 0). • For Pd(1 0 0) the observed reduction rate is rather independent of temperature. • For Pd{sub 75}Ag{sub 25}(1 0 0) the reduction rate displays a non-monotonic variation with temperature. - Abstract: Reduction of the (√(5)×√(5))R27° surface oxide on Pd(1 0 0) and Pd{sub 75}Ag{sub 25}(1 0 0) surfaces by H{sub 2} has been studied using high-resolution photoelectron spectroscopy in situ at H{sub 2} pressures 5 × 10{sup −9} mbar and 5 × 10{sup −8} mbar and selected temperatures in the range 30 °C to 170 °C. The reduction is slower on Pd{sub 75}Ag{sub 25}(1 0 0) compared to Pd(1 0 0) for all temperatures and pressures investigated. For Pd(1 0 0), the surface oxide reduction rate is rather independent of temperature, while for Pd{sub 75}Ag{sub 25}(1 0 0) a non-monotonic variation is observed. As indicated by kinetic analysis, the complex reduction behavior is not well described by Avrami kinetics. Oxygen spillover effects contribute to this picture for Pd(1 0 0), while surface compositional effects appear to dominate the performance for Pd{sub 75}Ag{sub 25}(1 0 0). These findings may have implications for understanding the oxidation, reduction and hydrogen transport properties of Pd–Ag membranes.

  18. DFT study of selective hydrogenation of acetylene to ethylene on Pd doping Ag nanoclusters

    Science.gov (United States)

    Liu, D.

    2016-11-01

    Recently, it has been reported that the reaction selectivity of catalytic hydrogenation of acetylene to ethylene can be significantly enhanced via the approach of Pd mono-atomic catalysis [Pei et al. ACS Catal. 5 (2015) 3717-3725]. To explain the catalytic mechanism of this binary alloy catalyst, C2H2 hydrogenation reactions on Pd doping Ag nanoclusters are studied using density functional theory simulations. The simulation results indicate that H2 and C2H2 can simultaneously bind with a single Pd doping atom no matter it is on vertex and edge sites of Ag clusters. The following H2 dissociation and C2H2 hydrogenation are not difficult since the corresponding reaction barrier values are no more than 0.58 eV. The generated C2H4 molecule can not be further hydrogenated since it locates on the top of Pd doping atom, which is the only adsorption site for H2. On two Pd doping atoms at contiguous sites of Ag clusters, C2H4 hydrogenation reactions can be carried out since there are enough sites for co-adsorption of H2 and C2H4.

  19. Characterization and electrocatalytic properties of sonochemical synthesized PdAg nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Godinez-Garcia, Andres, E-mail: agodinez@qro.cinvestav.mx [Depto. Materiales, Centro de Investigacion y de Estudios Avanzados del IPN, Libramiento norponiente 2000, Fracc. Real de Juriquilla, C.P. 76230 Santiago de Queretaro, Qro. (Mexico); Perez-Robles, Juan Francisco [Depto. Materiales, Centro de Investigacion y de Estudios Avanzados del IPN, Libramiento norponiente 2000, Fracc. Real de Juriquilla, C.P. 76230 Santiago de Queretaro, Qro. (Mexico); Martinez-Tejada, Hader Vladimir [Grupo de Energia y Termodinamica, Universidad Pontificia Bolivariana, Medellin, Antioquia C.P. 050031 (Colombia); Solorza-Feria, Omar [Depto. Quimica, CINVESTAV-IPN, Av. IPN 2508, A. P. 14-740, 07360 D.F. Mexico (Mexico)

    2012-06-15

    High intensity ultrasound was used in the synthesis of PdAg nanoparticles. PdAg nanoparticles were characterized by X-ray diffraction (XRD), atomic force microscopy (AFM), energy dispersive spectroscopy (EDS), scanning transmission electron microscopy (STEM) and high-resolution transmission electron microscopy (HRTEM). Catalytic properties for oxygen reduction reaction (ORR) were determined by electrochemical techniques of cyclic voltammetry (CV) and thin-film rotating disk electrode (TF-RDE). Finally the electrocatalyst was tested as a cathode in a single polymer electrolyte membrane fuel cell (PEMFC). Sonochemical synthesis (SS) decreased the overpotential required for the ORR and increased the double-layer capacitance (DLC) respect to the sodium borohydride reduction method due to a better distribution on vulcan carbon support. The electrocatalytic activity of the nanometric bimetallic electrocatalyst for the ORR in acid media showed a favorable multielectron charge transfer process (n = 4e{sup -}) to water formation. The performance of the membrane electrode assembly (MEA) prepared with dispersed PdAg/C as a cathode catalyst in a single PEMFC is lower in comparison to platinum. - Highlights: Black-Right-Pointing-Pointer Sonochemical synthesized PdAg nanoparticles supported on carbon were produced. Black-Right-Pointing-Pointer The material showed catalytic properties for the oxygen reduction reaction (ORR). Black-Right-Pointing-Pointer The ORR favored the pathway to water formation.

  20. Spectroscopic Characterization of Stability and Interaction of Pd-Ag Complexes

    Directory of Open Access Journals (Sweden)

    Sharad V. Lande

    2014-01-01

    Full Text Available Colloidal metal nanoparticles are of great interest because of their use as catalysts, photocatalysts, adsorbents, and sensors as well as their application in optical, electronic, and magnetic devices. Supported bimetallic systems represent a large part of heterogeneous catalysts which have been used in various reactions important in the chemical, petrochemical, and oil industry. Pd-Ag bimetallic nanocatalysts have become vitally important in some of the petrochemical industry’s processes like hydrogenation of C2–C5 olefins. A heat-treatment method for the preparation of well-stable Pd-Ag complexes is demonstrated using water, concentrated HCl and concentrated nitric acid as media. The stability and interaction of Pd-Ag complexes were characterized by UV-vis absorption spectroscopy. Pd-Ag bimetallic nanoparticles of spherical cubic and octahedral shape in the range of average particle size of 20–60 nm have been prepared and characterized by transmission electron microscopy (TEM.

  1. Ore mineralogy of the Serra Pelada Au-Pd-Pt deposit, Carajás, Brazil and implications for ore-forming processes

    Science.gov (United States)

    Berni, Gabriel V.; Heinrich, Christoph A.; Lobato, Lydia M.; Wall, Vic

    2016-08-01

    Serra Pelada is a world-class hydrothermal Au-Pd-Pt deposit located at the eastern border of the Amazon craton, northern Brazil. The rocks at Serra Pelada have experienced intense tropical weathering for about 70 Ma, but drill core samples preserve the primary mineralogy and hydrothermal alteration features, with extreme grades of Au, Pd and Pt individually reaching hundreds of parts per million (ppm) by weight. Mineralization at Serra Pelada occurs in hydrothermally altered metasiltstones and dolomitic metasandstones at the hinge zone of a recumbent syncline, comprising zones of hematite, chlorite-carbon, argillic, and siliceous alteration. The main hydrothermal gangue minerals are quartz, kaolinite, sericite, amesite, hematite, monazite, florencite and variable amounts of highly reflective carbonaceous matter. Hydrothermal carbon input is evident from precipitated carbon occurring along crenulation planes and veinlets associated with the precious metals. Ore and accessory minerals include a variety of sulphide, selenide, arsenide, sulphate and oxide minerals, including gold with variable metal contents, palladian gold, fischesserite, sudovikovite, sperrylite, selenian braggite, isomertieite, mertieite-II and secondary Au-Pt-Pd alloys. The composition of fischesserite varies from the ideal formula (Ag3AuSe2) towards a more Ag-rich composition, indicating a disordered solid solution form that is stable only above 260 °C, consistent with the high thermal maturity of associated carbonaceous matter approaching graphite. Primary ore and gangue minerals at Serra Pelada comprise a suite of elements that are best transported in oxidising conditions and precipitated upon reduction. This suggests that fluid mixing between a highly oxidised (metal carrier) and a reduced fluid was a key process for high-grade noble metal precipitation at Serra Pelada.

  2. In vitro cytotoxicity of Ag-Pd-Cu-based casting alloys.

    Science.gov (United States)

    Niemi, L; Hensten-Pettersen, A

    1985-01-01

    The cytotoxicity and its correlation to alloy composition, structure, corrosion, as well as galvanic coupling was studied with 12 Ag-Pd-Cu-type alloys, one conventional type III gold alloy and pure Ag, Cu, and Pd. The agar overlay cell culture technique was used. Single phase binary CuPd alloys were only slightly cytotoxic below a Cu content of 30 wt%. The tested multiphase alloys were all toxic, but no correlation between toxicity and Cu content could be observed. Solid solution annealing increased the cytotoxicity of a multiphase alloy. Exposure of a single phase alloy to an artificial saliva for 1 week prior to the test decreased its cytotoxicity significantly. Galvanic coupling of the alloys through an outer copper wire decreased their cytotoxicity.

  3. The adsorption and reaction of vinyl acetate on Au/Pd(100) alloy surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Li, Zhenjun [Pacific Northwest National Laboratory (PNNL); Calaza, Florencia C [ORNL; Tysoe, Wilfred [University of Wisconsin, Milwaukee

    2012-01-01

    The surface chemistry of vinyl acetate monomer (VAM) is studied on Au/Pd(100) alloys as a function of alloy composition using temperature-programmed desorption and reflection adsorption infrared spectroscopy. VAM adsorbs weakly on isolated palladium sites on the alloy with a heat of adsorption of ~55 kJ/mol, with the plane of the VAM adsorbed close to parallel to the surface. The majority of the VAM adsorbed on isolated sites desorbs molecularly with only a small portion decomposing. At lower gold coverages (below ~0.5 ML of gold), where palladium palladium bridge sites are present, VAM binds to the surface in a distorted geometry via a rehybridized vinyl group. A larger proportion of this VAM decomposes and this reaction is initiated by C\\O bond scission in the VAM to form adsorbed acetate and vinyl species. The implication of this surface chemistry for VAM synthesis on Au/Pd(100) alloys is discussed.

  4. Fungal biomolecules assisted biosynthesis of Au-Ag alloy nanoparticles and evaluation of their catalytic property.

    Science.gov (United States)

    Tripathi, Ravi Mani; Gupta, Rohit Kumar; Bhadwal, Akhshay Singh; Singh, Priti; Shrivastav, Archana; Shrivastav, B R

    2015-08-01

    The catalytic reduction of methylene blue was studied using biosynthesised gold-silver (Au-Ag) alloy nanoparticles (NPs). The fungal biomass of Trichoderma harzianum was used as a reducing and stabilising agent in the synthesis of Au-Ag alloy NPs. The synthesised NPs were well characterised by UV-vis spectroscopy, dynamic light scattering, X-ray diffraction, transmission electron microscopy, energy dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy. The plausible synthesis mechanism involved in the formation of Au-Ag alloy NPs was also discussed with diagrammatic representation. A series of experiments was performed to investigate the catalytic activity of the as-prepared Au-Ag alloy NPs and found that the alloy NPs show excellent catalytic activity. PMID:26224346

  5. Enthalpies of mixing of the liquid phase in the ternary system Ag-Au-Bi

    Energy Technology Data Exchange (ETDEWEB)

    Zoro, E. [Laboratoire de Chimie Physique Minerale et Bioinorganique, EA401, Fac. Pharm., Universite de Paris XI, 5 rue JB Clement, 92296 Chatenay Malabry (France) and Laboratoire de Physico-Chimie de l' Etat Solide, UMR 8648, Bat 410-415, 91405 Orsay Cedex (France)]. E-mail: zoroe@netcourrier.com; Boa, D. [Laboratoire de Thermodynamique et de Physico-Chimie du Milieu, Universite d' Abobo-Adjame, UFR-SFA, 02 BP801 Abidjan 02, Cote d' Ivoire, Africa (Ivory Coast); Servant, C. [Laboratoire de Physico-Chimie de l' Etat Solide, UMR 8648, Bat 410-415, 91405 Orsay Cedex (France); Legendre, B. [Laboratoire de Chimie Physique Minerale et Bioinorganique, EA401, Fac. Pharm., Universite de Paris XI, 5 rue JB Clement, 92296 Chatenay Malabry (France)

    2005-08-02

    The enthalpies of mixing of the liquid phase of the Ag-Au-Bi ternary alloys along the sections Ag {sub x}Bi{sub 1-x}-Au (x = 0.11, 0.10 and 0.24) and Au {sub x}Bi{sub 1-x}-Ag (x = 0.11 and 0.27) have been determined at 673 and 773 K. We used a SETARAM devised heat flow calorimeter of Tian-Calvet type. The values obtained are almost compatible with estimations from Scientific Group of Thermodata Europe (SGTE) binary database without adding ternary thermodynamic excess parameters. However, slight discrepancies are observed. The result of this study is useful tools for the Ag-Au-Bi ternary system thermodynamic computer optimization in process by the authors.

  6. Pd-Au Electrocatalysts for Hydrogen Evolution Reaction at Neutral pH

    OpenAIRE

    Elitsa Chorbadzhiyska; Mario Mitov; Georgi Hristov; Nina Dimcheva; Lori Nalbandian; Antigoni Evdou; Yolina Hubenova

    2014-01-01

    Pd-Au codeposits with different ratio of both metals were electrodeposited on carbon felt, characterized by scanning electron microscopy, and investigated as electrocatalysts towards hydrogen evolution reaction in neutral phosphate buffer solution. The quantities of the produced hydrogen gas with different electrocatalysts, estimated from data obtained by chronoamperometry, were confirmed by mass spectrometry analysis. The highest hydrogen evolution rate was achieved with the electrocatalysts...

  7. Phospholipid Encapsulated AuNR@Ag/Au Nanosphere SERS Tags with Environmental Stimulus Responsive Signal Property.

    Science.gov (United States)

    Su, Xueming; Wang, Yunqing; Wang, Wenhai; Sun, Kaoxiang; Chen, Lingxin

    2016-04-27

    Surface-enhanced Raman scattering (SERS) tags draw much attention due to the ultrasensitivity and multiplex labeling capability. Recently, a new kind of SERS tags was rationally designed by encapsulating metal nanoparticles with phospholipid bilayers, showing great potential in theranostics. The lipid bilayer coating confers biocompatibility and versatility to changing surface chemistry of the tag; however, its "soft" feature may influence SERS signal stability, which is rarely investigated. Herein, we prepared phospholipid-coated AuNR@Ag/Au nanosphere SERS tags by using three different kinds of Raman reporters, i.e., thio-containing 4-nitrothiophenol (NT), nitrogen-containing hydrophobic chromophore cyanine 7 monoacid (Cy7), and alkyl chain-chromophore conjugate 1,1'-dioctadecyl-3,3,3',3'-tetramethylindodicarbocyanine (DiD). It was found that signal responses were different upon additional stimulation which the tags may encounter in theranostic applications including the presence of detergent Triton X-100, lipid membrane, and photothermal treatment. Living-cell imaging also showed signal changing distinction. The different SERS signal performances were attributed to the different Raman reporter releasing behaviors from the tags. This work revealed that Raman reporter structure determined signal stability of lipid-coated SERS tags, providing guidance for the design of stimulus responsive tags. Moreover, it also implied the potential of SERS technique for real time drug release study of lipid based nanomedicine. PMID:27052206

  8. Experimental study of the phase diagram of the Ag-Au-Sb ternary system

    Energy Technology Data Exchange (ETDEWEB)

    Zoro, E. [Laboratoire de Chimie des Materiaux Inorganiques, Universite de Cocody, UFR-SSMT, 22 BP 582 Abidjan 22 (Ivory Coast) and Laboratoire de Physico-Chimie de l' Etat Solide, UMR 8648 Bat 410-415, 91405 Orsay Cedex (France); Laboratoire de Chimie Physique Minerale et Bioinorganique, EA401, Fac. Pharm., Universite de Paris-Sud XI, 5, rue JB Clement 92296 Chatenay Malabry (France); Servant, C. [Laboratoire de Physico-Chimie de l' Etat Solide, UMR 8648 Bat 410-415, 91405 Orsay Cedex (France)]. E-mail: colette.servant@lpces.u-psud.fr; Legendre, B. [Laboratoire de Chimie Physique Minerale et Bioinorganique, EA401, Fac. Pharm., Universite de Paris-Sud XI, 5, rue JB Clement 92296 Chatenay Malabry (France)

    2006-12-21

    The phase diagram of the Ag-Au-Sb ternary system has been assessed using X-ray diffraction analysis, electron-probe micro-analysis and differential scanning calorimetry. Four isopletic sections were studied: 80, 70 and 10 at.% Ag and 10 at.% Au. Three ternary invariant reactions were noted. This study is part of an international program, COST 531, about lead-free soldering materials.

  9. A comparison study of oxygen reduction on the supported Pt, Pd, Au monolayer on WC(0001)

    Science.gov (United States)

    Zhang, Xilin; Lu, Zhansheng; Yang, Zongxian

    2016-07-01

    Using the first principles methods, the geometric and electronic structures of the metal monolayers supported on WC(0001) surfaces (MML/WC(0001) (M = Pt, Pd, and Au)) and their catalytic activity toward the oxygen reduction reaction (ORR) were comparatively studied. Both the kinetics and the density of states results demonstrated that the direct dissociation of O2 on all three MML/WC(0001) surfaces are almost impossible. Yet the barriers of the formation and dissociation of OOH on AuML/WC(0001) are much smaller than those on the PtML/WC(0001) and the PdML/WC(0001) surfaces, implying that the AuML/WC(0001) exhibits the highest catalytic activity for ORR via a combination of 2e- hydrogenation of O2 and 4e- dissociation of OOH. The rate-limiting step barrier of 0.83 eV for the hydrogenation of OH forming H2O is also comparable to that on the traditional Pt-based catalysts. The deactivation mechanism of PtML/WC(0001) and the performance of PdML/WC(0001) for ORR were identified. The present study is conductive to designing new efficient catalyst without using of the precious Pt for efficiently promoting ORR.

  10. Hollow raspberry-like PdAg alloy nanospheres: High electrocatalytic activity for ethanol oxidation in alkaline media

    Science.gov (United States)

    Peng, Cheng; Hu, Yongli; Liu, Mingrui; Zheng, Yixiong

    2015-03-01

    Palladium-silver (PdAg) alloy nanospheres with unique structure were prepared using a one-pot procedure based on the galvanic replacement reaction. Their electrocatalytic activity for ethanol oxidation in alkaline media was evaluated. The morphology and crystal structure of the samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD). Electrochemical characterization techniques, including cyclic voltammetry (CV) and chronoamperometry (CA) measurements were used to analyze the electrochemical performance of the PdAg alloy nanospheres. The SEM and TEM images showed that the PdAg alloy nanospheres exhibit a hierarchical nanostructure with hollow interiors and porous walls. Compared to the commercial Pd/C catalyst, the as-prepared PdAg alloy nanospheres exhibit superior electrocatalytic activity and stability towards ethanol electro-oxidation in alkaline media, showing its potential as a new non-Pt electro-catalyst for direct alcohol fuel cells (DAFCs).

  11. Resonance Scattering Detection of Trace Hg2+ Using Aptamer-modified AuPd Nanoalloy Probe as Catalyst

    Institute of Scientific and Technical Information of China (English)

    刘庆业; 范燕燕; 梁爱惠; 蒋治良

    2011-01-01

    The 5 nm AuPd nanoalloy in mole ratio of Au:Pd=32 : 1 was prepared, using sodium citrate as the stabilizing agent and NaBH4 as the reductant. The AuPd nanoalloy was modified by the aptamer to prepare an aptamer- AuPd (AptAuPd) probe for resonance scattering (RS) detection of 5.(Y-1250 nmol/L Hg2+. The AptAuPd-Hg2+ aptamer reaction solution was filtrated by membrane, and the AptAuPd in the filtrate exhibited strong catalytic ef- fect on the slow NiP particle reaction between NiCI2 and NaHzPO2, and the NiP particles showed a RS peak at 508 nm. The RS intensity decreased when Hg2+ concentration increased. The decreased RS intensity was linear to Hg2+ concentration in the range of 0.5--1250 nmol/L. The RS assays were used to determine Hg2+ in real samples, with good results.

  12. Wearout Reliability and Intermetallic Compound Diffusion Kinetics of Au and PdCu Wires Used in Nanoscale Device Packaging

    Directory of Open Access Journals (Sweden)

    C. L. Gan

    2013-01-01

    Full Text Available Wearout reliability and diffusion kinetics of Au and Pd-coated Cu (PdCu ball bonds are useful technical information for Cu wire deployment in nanoscale semiconductor device packaging. This paper discusses the HAST (with bias and UHAST (unbiased HAST wearout reliability performance of Au and PdCu wires used in fine pitch BGA packages. In-depth failure analysis has been carried out to identify the failure mechanism under various wearout conditions. Intermetallic compound (IMC diffusion constants and apparent activation energies (Eaa of both wire types were investigated after high temperature storage life test (HTSL. Au bonds were identified to have faster IMC formation, compared to slower IMC growth of PdCu. PdCu wire was found to exhibit equivalent or better wearout reliability margin compared to conventional Au wire bonds. Failure mechanisms of Au, Cu ball bonds post-HAST and UHAST tests are been proposed, and both Au and PdCu IMC diffusion kinetics and their characteristics are discussed in this paper.

  13. Nanocrystalline Pd alloy films coated by electroless deposition.

    Science.gov (United States)

    Strukov, G V; Strukova, G K; Batov, I E; Sakharov, M K; Kudrenko, E A; Mazilkin, A A

    2011-10-01

    The structures of palladium and palladium alloys thin films deposited from organic electrolytes onto metallic substrates by electroless plating method have been investigated. The coatings are dense, pore-free 0.005-1 microm thick films with high adhesive strength to the substrate surface. EDX, XRD, SEM and TEM methods were used to determine the composition and structure of alloy coatings of the following binary systems: Pd-Au, Pd-Ag, Pd-Ni, Pd-Pb, and ternary system Pd-Au-Ni. The coatings of Pd-Au, Pd-Ag and Pd-Ni have a solid solution structure, whereas Pd-Pb is intermetallic compound. It has been found that the deposited films consist of nanocrystalline grains with sizes in the range of 11-35 nm. Scanning and transmission electron microscopy investigations reveal the existence of clusters formed by nanocrystalline grains. The origin for the formation of nanocrystalline structures of coating films is discussed. PMID:22400291

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

    Science.gov (United States)

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

    2012-10-01

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

  15. Capability of defective graphene-supported Pd13 and Ag13 particles for mercury adsorption

    Science.gov (United States)

    Meeprasert, Jittima; Junkaew, Anchalee; Rungnim, Chompoonut; Kunaseth, Manaschai; Kungwan, Nawee; Promarak, Vinich; Namuangruk, Supawadee

    2016-02-01

    Reactivity of single-vacancy defective graphene (DG) and DG-supported Pdn and Agn (n = 1, 13) for mercury (Hg0) adsorption has been studied using density functional theory calculation. The results show that Pdn binds defective site of DG much stronger than the Agn, while metal nanocluster binds DG stronger than single metal atom. Metal clustering affects the adsorption ability of Pd composite while that of Ag is comparatively less. The binding strength of -8.49 eV was found for Pd13 binding on DG surface, indicating its high stability. Analyses of structure, energy, partial density of states, and d-band center (ɛd) revealed that the adsorbed metal atom or cluster enhances the reactivity of DG toward Hg adsorption. In addition, the Hg adsorption ability of Mn-DG composite is found to be related to the ɛd of the deposited Mn, in which the closer ɛd of Mn to the Fermi level correspond to the higher adsorption strength of Hg on Mn-DG composite. The order of Hg adsorption strength on Mn-DG composite are as follows: Pd13 (-1.68 eV) >> Ag13 (-0.67 eV) ∼ Ag1 (-0.69 eV) > Pd1 (-0.62 eV). Pd13-DG composite is therefore more efficient sorbent for Hg0 removal in terms of high stability and high adsorption reactivity compared to the Ag13. Further design of highly efficient carbon based sorbents should be focused on tailoring the ɛd of deposited metals.

  16. Phytosynthesis of stable Au, Ag and Au-Ag alloy nanoparticles using J. Sambac leaves extract, and their enhanced antimicrobial activity in presence of organic antimicrobials

    Science.gov (United States)

    Yallappa, S.; Manjanna, J.; Dhananjaya, B. L.

    2015-02-01

    A green chemistry approach for the synthesis of Au, Ag and Au-Ag alloy nanoparticles (NPs) using the corresponding metal precursors and Jasminum sambac leaves extract as both reducing and capping media, under microwave irradiation, is reported. During the formation, as expected, the reaction mixture shows marginal decrease in pH and an increase in solution potential. The formation of NPs is evident from their surface plasmon resonance (SPR) peak observed at ∼555 nm for Au, ∼435 nm for Ag and ∼510 nm for Au-Ag alloy. The XRD pattern shows fcc structure while the FTIR spectra indicate the presence of plant residues adsorbed on these NPs. Such a bio-capping of NPs is characterized by their weight loss, ∼35% due to thermal degradation of biomass, as observed in TG analysis. The colloidal dispersion of NPs is stable for about 6 weeks. The near spherical shape of NPs (ϕ20-50 nm) is observed by FE-SEM/TEM images and EDAX gives the expected elemental composition. Furthermore, these NPs showed enhanced antimicrobial activity (∼1-4-fold increase in zone of inhibition) in combination with antimicrobials against test strains. Thus, the phytosynthesized NPs could be used as effective growth inhibitors for various microorganisms.

  17. Biosynthesis and stabilization of Au and Au–Ag alloy nanoparticles by fungus, Fusarium semitectum

    Directory of Open Access Journals (Sweden)

    Balaji Dasaratrao Sawle, Basavaraja Salimath, Raghunandan Deshpande, Mahesh Dhondojirao Bedre, Belawadi Krishnamurthy Prabhakar and Abbaraju Venkataraman

    2008-01-01

    Full Text Available Crystallized and spherical-shaped Au and Au–Ag alloy nanoparticles have been synthesized and stabilized using a fungus, F . semitectum in an aqueous system. Aqueous solutions of chloroaurate ions for Au and chloroaurate and Ag+ ions (1 : 1 ratio for Au–Ag alloy were treated with an extracellular filtrate of F . semitectum biomass for the formation of Au nanoparticles (AuNP and Au–Ag alloy nanoparticles (Au–AgNP. Analysis of the feasibility of the biosynthesized nanoparticles and core–shell alloy nanoparticles from fungal strains is particularly significant. The resultant colloidal suspensions are highly stable for many weeks. The obtained Au and Au–Ag alloy nanoparticles were characterized by the surface plasmon resonance (SPR peaks using a UV-vis spectrophotometer, and the structure, morphology and size were determined by Fourier transform infrared spectroscopy (FTIR, x-ray diffraction (XRD, and transmission electron microscopy (TEM. Possible optoelectronics and medical applications of these nanoparticles are envisaged.

  18. Study of thermal diffusivity of nanofluids with bimetallic nanoparticles with Au(core)/Ag(shell) structure

    Science.gov (United States)

    Gutierrez Fuentes, R.; Pescador Rojas, J. A.; Jiménez-Pérez, J. L.; Sanchez Ramirez, J. F.; Cruz-Orea, A.; Mendoza-Alvarez, J. G.

    2008-11-01

    The thermal diffusivity of Au/Ag nanoparticles with core/shell structure, at different compositions (Au/Ag = 3/1, 1/1, 1/3, 1/6), was measured by using the mismatched mode of the dual-beam thermal lens (TL) technique. This study determines the effect of the bimetallic composition on the thermal diffusivity of the nanofluids. In these results we find a lineal increment of the nanofluid it thermal diffusivity when the Ag shell thickness is increased. Our results show that the nanoparticle structure is an important parameter to improve the heat transport in composites and nanofluids. These results could have importance for applications in therapies and photothermal deliberation of drugs. Complementary measurements with UV-vis spectroscopy and TEM, were used to characterize the Au(core)/Ag(shell) nanoparticles.

  19. Study of thermal diffusivity of nanofluids with bimetallic nanoparticles with Au(core)/Ag(shell) structure

    Energy Technology Data Exchange (ETDEWEB)

    Gutierrez Fuentes, R.; Pescador Rojas, J.A. [CICATA-IPN, Legaria 694, Mexico 11500, D.F. (Mexico); Jimenez-Perez, J.L. [CICATA-IPN, Legaria 694, Mexico 11500, D.F. (Mexico)], E-mail: jimenezp@fis.cinvestav.mx; Sanchez Ramirez, J.F. [CICATA-IPN, Legaria 694, Mexico 11500, D.F. (Mexico); Departamento de Fisica, CINVESTAV-IPN, A.P. 14-740, Mexico 07360, D.F. (Mexico); Cruz-Orea, A.; Mendoza-Alvarez, J.G. [Departamento de Fisica, CINVESTAV-IPN, A.P. 14-740, Mexico 07360, D.F. (Mexico)

    2008-11-30

    The thermal diffusivity of Au/Ag nanoparticles with core/shell structure, at different compositions (Au/Ag = 3/1, 1/1, 1/3, 1/6), was measured by using the mismatched mode of the dual-beam thermal lens (TL) technique. This study determines the effect of the bimetallic composition on the thermal diffusivity of the nanofluids. In these results we find a lineal increment of the nanofluid it thermal diffusivity when the Ag shell thickness is increased. Our results show that the nanoparticle structure is an important parameter to improve the heat transport in composites and nanofluids. These results could have importance for applications in therapies and photothermal deliberation of drugs. Complementary measurements with UV-vis spectroscopy and TEM, were used to characterize the Au(core)/Ag(shell) nanoparticles.

  20. Electrical conductivity dependence of thin metallic films of Au and Pd as a top electrode in capacitor applications

    International Nuclear Information System (INIS)

    Electrical conductivity dependence of thin metallic films of Au and Pd over the different perovskites was investigated. It is found from electrical properties that crystallographic growth orientation of Au and Pd thin layers attained from X-ray diffraction results indicate the slop of current (I)-voltage (V) plots. Besides, surface morphology and topography was considered using Field Emission Scanning Electron Microscopy and Atomic Force Microscopy, respectively. Obtained results showed the Stranski-Krastanov growth of the Pd and Au. Indeed, diminishing of the root-mean-square roughness of Pd/BiMnO3/SrTiO3 following by Au deposition should be concerned due to growth of Au onto the crack-like parts of the substrate. These crack-like parts appeared due to parasitic phases of the Bi-Mn-O system mainly Mn3O4 (l 0 l) and Mn3O4 (0 0 4 l). The different response in the electrical properties of heterostructures suggests that electrical conductance of the Au and Pd thin metallic films have the crystallographic orientation dependence. Furthermore, polycrystallinity of the thin metallic films are desired in electrode applications due to increase the conductivity of the metallic layers.

  1. Isolation of atomically precise mixed ligand shell PdAu24 clusters

    Science.gov (United States)

    Sels, Annelies; Barrabés, Noelia; Knoppe, Stefan; Bürgi, Thomas

    2016-05-01

    Exposure of PdAu24(2-PET)18 (2-PET: 2-phenylethylthiolate) to BINAS (1,1-binaphthyl-2,2-dithiol) leads to species of composition PdAu24(2-PET)18-2x(BINAS)x due to ligand exchange reactions. The BINAS adsorbs in a specific mode that bridges the apex and one core site of two adjacent S(R)-Au-S(R)-Au-S(R) units. Species with different compositions of the ligand shell can be separated by HPLC. Furthermore, site isomers can be separated. For the cluster with exactly one BINAS in its ligand shell only one isomer is expected due to the symmetry of the cluster, which is confirmed by High-Performance Liquid Chromatography (HPLC). Addition of a second BINAS to the ligand shell leads to several isomers. In total six distinguishable isomers are possible for PdAu24(2-PET)14(BINAS)2 including two pairs of enantiomers concerning the adsorption pattern. At least four distinctive isomers are separated by HPLC. Calculations indicate that one of the six possibilities is energetically disfavoured. Interestingly, diastereomers, which have an enantiomeric relationship concerning the adsorption pattern of chiral BINAS, have significantly different stabilities. The relative intensity of the observed peaks in the HPLC does not reflect the statistical weight of the different isomers. This shows, as supported by the calculations, that the first adsorbed BINAS molecule influences the adsorption of the second incoming BINAS ligand. In addition, experiments with the corresponding Pt doped gold cluster reveal qualitatively the same behaviour, however with slightly different relative abundances of the corresponding isomers. This finding points towards the influence of electronic effects on the isomer distribution. Even for clusters containing more than two BINAS ligands a limited number of isomers were found, which is in contrast to the corresponding situation for monothiols, where the number of possible isomers is much larger.Exposure of PdAu24(2-PET)18 (2-PET: 2-phenylethylthiolate) to BINAS (1

  2. Plasmonic-induced inhibition and enhancement of the electrocatalytic activity of Pd-Au hetero-nanoraspberries for ethanol oxidation

    Science.gov (United States)

    Wang, Qiyu; Zheng, Weitao; Chen, Hong; Zhang, Bingsen; Su, Dangsheng; Cui, Xiaoqiang

    2016-06-01

    Plasmonic modulation of the catalytic performances of metallic nanostructures shows great potential in the development of novel materials for catalysis. In addition to the challenges of devising new catalysts with high activity while maintaining controllable plasmonic properties, the mechanisms underlying the enhancement of the activity by surface plasmon resonance (SPR) are still under exploration. Here, we design a Pd-Au bimetallic hetero structure and use the well-defined SPR property of the core Au NPs to tune its surface electro catalytic activity. The hot electrons are transferred into the Pd nanopetals from the Au core with visible-light irradiation, resulting in an enhancement of the electrocatalytic oxidation of ethanol on Au concurrent with an inhibition on Pd. The anti-poisoning and stability of the as-prepared heterostructures is also enhanced by visible-light irradiation.

  3. Hollow Ag-Pd core–shell nanotubes as highly active catalysts for the electro-oxidation of formic acid

    International Nuclear Information System (INIS)

    Ag nanowires are prepared as templates by a polyol reduction process. Then Ag nanotubes coated with a thin layer of Pd are synthesized through sequential reduction accompanied with the galvanic displacement reaction. The products show a hollow core–shell nanotubular structure, as demonstrated by detailed characterizations. The Ag-Pd can significantly improve the electrocatalytic activity towards the electro-oxidation of formic acid and enhance the stability of the Pd component. It is proposed that the enhanced electrochemically active surface area and modulated electron structure of Pd by Ag are responsible for the improvement of electrocatalytic activity and durability. The results obtained in this work are different from those previous reports, in which alloy walls with hollow interiors are usually formed. This work provides a new and simple method for synthesizing novel bimetallic core–shell structure with a hollow interior, which can be applied as high-performance catalysts for the electro-oxidation of formic acid. (paper)

  4. AuPd CATALYTIC NANOPARTICLE SIZE EFFECT ON THE FORMATION OF AMORPHOUS SILICON NANOWIRES

    Institute of Scientific and Technical Information of China (English)

    LIU ZU-QIN; SUN LIAN-FENG; TANG DONG-SHENG; ZHOU WEI-YA; LI YU-BAO; Zou XIAO-PING

    2000-01-01

    Amorphous silicon (a-Si) nanowires have been prepared on SiO2/Si substrates by AuPd nanoparticles / silane reaction method. Field-emission scanning electron microscopy and transmission electron microscopy were used to characterize the samples. The typical a-Si nanowires we obtained are of a uniform diameter about 20 nm and length up to several micrometers. The growth mechanism of the nanowires seems to be the vapor-liquid-solid mechanism. The catalytic particle size effect on the formation of the nanowires and the cause of forming amorphous state Si nanowires are discussed.

  5. Selective Oxidation of Raw Glycerol Using Supported AuPd Nanoparticles

    Directory of Open Access Journals (Sweden)

    Carine E. Chan-Thaw

    2015-02-01

    Full Text Available Bimetallic AuPd supported on different carbonaceous materials and TiO2 was tested in the liquid phase oxidation of commercial grade and raw glycerol. The latter was directly obtained from the base-catalyzed transesterification of edible rapeseed oil using KOH. The best catalytic results were obtained using activated carbon and nitrogen-functionalized carbon nanofibers as supports. In fact, the catalysts were more active using pure glycerol instead of the one obtained from rapeseed, where strong deactivation phenomena were present. Fourier transform infrared (FT-IR and TEM were utilized to investigate the possible reasons for the observed loss of activity.

  6. Hydrogen adsorption on bimetallic PdAu(111) surface alloys:minimum adsorption ensemble, ligand and ensemble effects, and ensemble confinement

    OpenAIRE

    Takehiro, Naoki; Liu, Ping; Bergbreiter, Andreas; K. Nørskov, Jens; Behm, R. Juergen

    2014-01-01

    The adsorption of hydrogen on structurally well defined PdAu-Pd(111) monolayer surface alloys was investigated in a combined experimental and theoretical study, aiming at a quantitative understanding of the adsorption and desorption properties of individual PdAu nanostructures. Combining the structural information obtained by high resolution scanning tunneling microscopy (STM), in particular on the abundance of specific adsorption ensembles at different Pd surface concentrations, with informa...

  7. Highly sensitive electrochemical determination of Sunset Yellow based on the ultrafine Au-Pd and reduced graphene oxide nanocomposites.

    Science.gov (United States)

    Wang, Jin; Yang, Beibei; Zhang, Ke; Bin, Duan; Shiraishi, Yukihide; Yang, Ping; Du, Yukou

    2016-11-01

    A sensitive and novel electrochemical sensor with Au-Pd and reduced graphene oxide (RGO) nanocomposites modified glassy carbon electrode (Au-Pd-RGO/GCE) was successfully fabricated by one-step synthesis method for the detection of Sunset Yellow. The as-prepared composites were uniformly dispersed on the surface of electrode with an average diameter of approximately 3.44nm, and the ultrafine nanoparticles effectively enhanced the electrochemical active surface area of GCE. The modified electrode had been characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction and electrochemical tests. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) results showed high stability and outstanding electrocatalytic activity of Au-Pd-RGO/GCE for the detection of SY with low detection limits (1.5 nM, S/N=3) and wide concentration ranges (0.686-331.686μM). The Au-Pd-RGO/GCE was further applied to detect SY in real samples with good recovery. Herein, the fabricated Au-Pd-RGO/GCE showed excellent sensitivity, stability and repeatability for the detection of SY and will be a promising application in electrochemical sensor. PMID:27475710

  8. Core-shell Au/Ag nanoparticles embedded in silicate sol-gel network for sensor application towards hydrogen peroxide

    Indian Academy of Sciences (India)

    Shanmugam Manivannan; Ramasamy Ramaraj

    2009-09-01

    The electrocatalytic activity of core-shell Au100-Ag ( = 15, 27, 46, and 60) bimetallic nanoparticles embedded in methyl functionalized silicate MTMOS network towards the reduction of hydrogen peroxide was investigated by using cyclic voltammetry and chronoamperometric techniques. Core-shell Au/Ag bimetallic nanoparticles were characterized by absorption spectra and HRTEM. The MTMOS silicate sol-gel embedded Au73Ag27 core-shell nanoparticles modified electrode showed better synergistic electrocatalytic effect towards the reduction of hydrogen peroxide when compared to monometal MTMOS-Aunps and MTMOS-Agnps modified electrodes. These modified electrodes were studied without immobilizing any enzyme in the MTMOS sol-gel matrix. The present study highlights the influence of molar composition of Ag nanoparticles in the Au/Ag bimetallic composition towards the electrocatalytic reduction and sensing of hydrogen peroxide in comparison to monometal Au and Ag nanoparticles.

  9. Developing an aqueous approach for synthesizing Au and M@Au (M = Pd, CuPt) hybrid nanostars with plasmonic properties

    CERN Document Server

    Du, Jingshan; Xiong, Yalin; Lin, Zhuoqing; Zhang, Hui; Yang, Deren

    2014-01-01

    Anisotropic Au nanoparticles show unique localized surface plasmon resonance (LSPR) properties, which make it attractive in optical, sensing, and biomedical applications. In this contribution, we report a general and facile strategy towards aqueous synthesis of Au and M@Au (M = Pd, CuPt) hybrid nanostars by reducing HAuCl4 with ethanolamine in the presence of cetyltrimethylammonium bromide (CTAB). According to electron microscopic observation and spectral monitoring, we found that the layered epitaxial growth mode (i.e., Frank-van der Merwe mechanism) contributes to the enlargement of the core, while, the random attachment of Au nanoclusters onto the cores accounts for the formation of the branches. Both of them are indispensable for the formation of the nanostars. The LSPR properties of the Au nanoparticles have been well investigated with morphology control via precursor amount and growth temperature. The Au nanostars showed improved surface-enhanced Raman spectroscopy (SERS) performance for rhodamine 6G du...

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

    Science.gov (United States)

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

    2015-09-01

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

  11. Critical Factors Controlling Pd and Pt Potential in Porphyry Cu–Au Deposits: Evidence from the Balkan Peninsula

    Directory of Open Access Journals (Sweden)

    Demetrios G. Eliopoulos

    2014-03-01

    Full Text Available Porphyry Cu–Au–Pd±Pt deposits are significant Au resources, but their Pd and Pt potential is still unknown. Elevated Pd, Pt (hundreds of ppb and Au contents are associated with typical stockwork magnetite-bornite-chalcopyrite assemblages, at the central parts of certain porphyry deposits. Unexpected high grade Cu–(Pd+Pt (up to 6 ppm mineralization with high Pd/Pt ratios at the Elatsite porphyry deposit, which is found in a spatial association with the Chelopech epithermal deposit (Bulgaria and the Skouries porphyry deposit, may have formed during late stages of an evolved hydrothermal system. Estimated Pd, Pt and Au potential for porphyry deposits is consistent with literature model calculations demonstrating the capacity of aqueous vapor and brine to scavenge sufficient quantities of Pt and Pd, and could contribute to the global platinum-group element (PGE production. Critical requirements controlling potential of porphyry deposits may be from the metals contained in magma (metasomatized asthenospheric mantle wedge as indicated by significant Cr, Co, Ni and Re contents. The Cr content may be an indicator for the mantle input.

  12. Polar Kerr spectroscopic magneto-optics in Au/Co-Ag/Ag granular thin films on glass: Experiments and simulation

    Energy Technology Data Exchange (ETDEWEB)

    Borcia, I.D. [Faculty of Physics, Alexandru Ioan Cuza University, 6600 Iasi (Romania); Beauvillain, P. [Institut d' Electronique Fondamentale, Universite Paris-Sud, UMR CNRS 8622, 91405 Orsay Cedex (France)]. E-mail: Pierre.Beauvillain@ief.u-psud.fr; Bartenlian, B. [Institut d' Electronique Fondamentale, Universite Paris-Sud, UMR CNRS 8622, 91405 Orsay Cedex (France); Gogol, P. [Institut d' Electronique Fondamentale, Universite Paris-Sud, UMR CNRS 8622, 91405 Orsay Cedex (France); Megy, R. [Institut d' Electronique Fondamentale, Universite Paris-Sud, UMR CNRS 8622, 91405 Orsay Cedex (France)

    2006-06-15

    In Au/Co-Ag/Ag granular thin films, linear polar magneto-optical Kerr spectra were measured in the 250-800 nm wavelength range. These experimental spectra were compared to magneto-optical (MO) simulations using an optical multilayer model based on matrix formalism. MO simulations using homogenous layers of uniform thickness led to a great difference of amplitude and shape between the measured and simulated curves. Atomic force microscopy and scanning electron microscopy images were used to estimate the granular structure of the samples and determine the mean diameter and height, respectively of the Ag and Ag-Co islands of each layer. Using this granular structure in our MO simulations, a reasonable agreement between the simulations and MO experiments was obtained for both the Kerr rotation and ellipticity spectra.

  13. Development of Au-Ag nanowire mesh fabrication by UV-induced approach

    Energy Technology Data Exchange (ETDEWEB)

    Saggar, Siddhartha [Laboratory for Molecular Photonics and Electronics, Department of Physics, National Institute of Technology, Calicut, Kerala, India and School of Nanoscience and Technology, National Institute of Technology, Calicut, Kerala (India); Predeep, Padmanabhan, E-mail: predeep@nitc.ac.in

    2014-10-15

    In an attempt to overcome the limitations of the presently prevailing transparent conducting electrode (TCE) - indium tin oxide (ITO) - many materials have been considered for replacing ITO. Recently, a novel method has been reported for the synthesis of Au-Ag nanowire (NW) mesh, and tested successfully for organic-light-emitting-diodes (OLEDs). It employs UV-induced reduction of gold- and silver- precursors to form Au-Ag NW mesh. In this report, Au-Ag NW mesh thin films are synthesized on glass substrates with an objective for use as facing-electrode for Organic Photovoltaics. Various issues and factors affecting the fabrication-process have been improved, and are also discussed here. The electrode showed good transmitivity, of around 95% (excluding that of glass substrate). The advantage of the technique is its simple processing method and cost-effectiveness.

  14. Hollow Ag@Pd core-shell nanotubes as highly active catalysts for the electro-oxidation of formic acid

    DEFF Research Database (Denmark)

    Jiang, Yuanyuan; Lu, Yizhong; Han, Dongxue;

    2012-01-01

    Ag nanowires are prepared as templates by a polyol reduction process. Then Ag nanotubes coated with a thin layer of Pd are synthesized through sequential reduction accompanied with the galvanic displacement reaction. The products show a hollow core-shell nanotubular structure, as demonstrated...

  15. Dissociative adsorption of water on Au/MgO/Ag(001) from first principles calculations

    Science.gov (United States)

    Nevalaita, J.; Häkkinen, H.; Honkala, K.

    2015-10-01

    The molecular and dissociative adsorption of water on a Ag-supported 1 ML, 2 ML and 3 ML-a six atomic layer-thick MgO films with a single Au adatom is investigated using density functional theory calculations. The obtained results are compared to a bulk MgO(001) surface with an Au atom. On thin films the negatively charged Au strengthens the binding of the polar water molecule due to the attractive Au-H interaction. The adsorption energy trends of OH and H with respect to the film thickness depend on an adsorption site. In the case OH or H binds atop Au on MgO/Ag(001), the adsorption becomes more exothermic with the increasing film thickness, while the reverse trend is seen when the adsorption takes place on bare MgO/Ag(001). This behavior can be explained by different bonding mechanisms identified with the Bader analysis. Interestingly, we find that the rumpling of the MgO film and the MgO-Ag interface distance correlate with the charge transfer over the thin film and the interface charge, respectively. Moreover, we employ a modified Born-Haber-cycle to analyze the effect of film thickness to the adsorption energy of isolated Au and OH species on MgO/Ag(001). The analysis shows that the attractive Coulomb interaction between the negatively charged adsorbate and the positive MgO-Ag-interface does not completely account for the weaker binding with increasing film thickness. The redox energy associated with the charge transfer from the interface to the adsorbate is more exothermic with the increasing film thickness and partly compensates the decrease in the attractive Coulomb interaction.

  16. Nanometer sized electrodes fabricated by electromigration of Au and Pd nanowires

    Science.gov (United States)

    Vlad, Alexandru; Faniel, Sébastien; Hackens, Benoît; Bayot, Vincent; Melinte, Sorin

    2008-03-01

    Electromigration-driven metallic nanowire failure is presented. Here, Au and Pd nanowires patterned by electron-beam lithography were electrically stressed up to their breaking point. Feedback control and simple voltage sweep techniques have been successfully used to form nanometer-sized gaps. We observe a material- and geometry-dependent behavior. The Au nanowires showed a Joule-induced reversible resistance increase with the applied voltage up to the breaking point. In contrast, Pd nanowires presented an anomalous resistance decrease close to their failure point. This was associated to the melting and agglomeration of metallic grains within the electrically stressed nanowires. The SEM images acquired at intermediate stages of electromigration agree with the electrical data findings. The influence of the nanowire geometry upon the morphology of fabricated nanoelectrodes is considered. Beside the morphological characterization of our break junctions, we also measured their current-voltage characteristics. We observed single electron tunneling effects, probably due to the presence of metallic clusters formed close to the nanoelectrodes during the electromigration. Our results are consistent with recent findings on Coulomb blockade phenomena in electromigrated gold break junctions.

  17. Topological description of mechanical behavior of Cu, Ag and Au: A first-principle study

    Directory of Open Access Journals (Sweden)

    M Saghayezhian

    2011-12-01

    Full Text Available  Mechanical properties and stress-strain curves of Cu, Ag and Au single crystals are calculated using ab initio methods. Elastic and Plastic regions are scrutinized. Yield stress and slope of these curves can shed light on brittlenesss and ductility of these metals that prove Cu, despite its high ultimate tensile strength, is less ductile than Au and Ag. Analysis of topology of charge density along with stress-strain curves shows that the elastic-plastic transition accompanies topological transition and for these metals, both transitions occur in the same strain. Some charactristics of critical point, especially bond points, are inspected.

  18. Characterizing the economic value of an epithermal Au-Ag ore with Laser Induced Breakdown Spectroscopy (LIBS)

    NARCIS (Netherlands)

    Dalm, M.; Buxton, M.W.N.

    2016-01-01

    LIBS was applied to 19 Au-Ag ore samples to investigate if this technique can be used to distinguish between economic and sub-economic ore either by direct detection of these elements or by using other elements as indicators. However, the Au and Ag grades of the samples are below the detection limit

  19. Synthesis and characterization of PdAg as a catalyst for oxygen reduction reaction in acid medium; Sintesis y caracterizacion de PdAg como catalizador para la reaccion de reduccion de oxigeno en medio acido

    Energy Technology Data Exchange (ETDEWEB)

    Martinez-Casillas, D. C.; Vazquez-Huerta, G.; Solorza-Feria, O. [Centro de Investigacion y de Estudios Avanzados del IPN, Mexico D.F. (Mexico)]. E-mail: dcmartinez@cinvestav.mx

    2009-09-15

    This work presents the synthesis of the binary compound PdAg and the electrochemical characterization for oxygen reduction reaction (ORR) in acid medium. The catalyst is obtained from the reduction of Pd(NO{sub 3}){sub 2}·2H{sub 2}O and AgNO{sub 3} with NaBH{sub 4} in THF. The synthesized compound was physically characterized with transmission electron microscopy (TEM), sweep electron microscopy (SEM) and x-ray diffraction (XRD) of powder. Electrochemical studies were conducted to determine the catalytic activity and intrinsic properties of the PdAg material for the ORR in acid medium using cyclic voltamperometry (CV), rotary disc electrode (RDE) and electrochemical impedance spectroscopy (EIS) in a solution of H{sub 2}SO{sub 4} 0.5 M at 25 degrees Celsius. The electrochemical current-potential responses were compared to those of palladium and platinum. The kinetic results showed an increase in the performance of the bimetallic electrocatalyst containing Ag as compared to pure Pd, but less than that obtained with nanometric Pt. The Tafel slopes obtained are roughly120 mV dec-1, similar to that reported for Pt and Pd and for other Ru-based electrocatalysts. [Spanish] En este trabajo se presentan la sintesis del compuesto binario PdAg y su caracterizacion electroquimica para la reaccion de reduccion de oxigeno (RRO) en medio acido. El catalizador se obtuvo a partir de la reduccion de Pd(NO{sub 3}){sub 2}·2H{sub 2}O y AgNO{sub 3} con NaBH{sub 4} en THF. El compuesto sintetizado se caracterizo fisicamente por microscopia electronica de transmision (MET), microscopia electronica de barrido (MEB) y difraccion de rayos X (DRX) de polvos. Se realizaron estudios electroquimicos para determinar la actividad catalitica y las propiedades intrinsecas del material de PdAg para la reaccion de reduccion de oxigeno (RRO) en medio acido, utilizando las tecnicas de voltamperometria ciclica (VC), electrodo disco rotatorio (EDR) y espectroscopia de impedancia electroquimica (EIE), en

  20. Transparent ITO/Ag-Pd-Cu/ITO multilayer cathode use in inverted organic solar cells

    Directory of Open Access Journals (Sweden)

    Hyo-Joong Kim

    2015-10-01

    Full Text Available The characteristics of transparent ITO/Ag-Pd-Cu (APC/ITO multilayer cathodes were investigated for use in inverted organic solar cells (IOSCs. The insertion of an APC interlayer into the ITO film effectively led to crystallization of the top ITO layer, unlike that in the Ag interlayer, and resulted in a low sheet resistance of 6.55 Ohm/square and a high optical transmittance of 84.14% without post annealing. In addition, the alloying of the Pd and Cu elements into Ag prevented agglomeration and oxidization of the metal interlayer and led to more stable ITO/APC/ITO films under ambient conditions. The microstructure and interfacial structure of the transparent ITO/APC/ITO cathode in the IOSCs were examined in detail by synchrotron X-ray scattering and high resolution transmission electron microscopy. Furthermore, we suggested a possible mechanism to explain the lower PCE of the IOSCs with an ITO/APC/ITO cathode than that of a reference IOSC with a crystalline ITO cathode using the external quantum efficiency of the IOSCs.

  1. Transparent ITO/Ag-Pd-Cu/ITO multilayer cathode use in inverted organic solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Hyo-Joong; Kim, Han-Ki, E-mail: imdlhkkim@khu.ac.kr [Department of Advanced Materials Engineering for Information and Electronics, Kyung Hee University, 1 Seocheon-dong, Yongin-si, Gyeonggi-do 446-701 (Korea, Republic of); Lee, Hyun Hwi [Pohang Accelerator Laboratory, POSTECH, Jigokro-127beon-gil, Nam-gu, Pohang 790-784 (Korea, Republic of); Kal, Jinha; Hahn, Jungseok [Future Technology Research Group, Kolon Central Research Park, 154 Mabukro, Giheung-ku, Yongin-si, Kyunggi-do, 16910 (Korea, Republic of)

    2015-10-15

    The characteristics of transparent ITO/Ag-Pd-Cu (APC)/ITO multilayer cathodes were investigated for use in inverted organic solar cells (IOSCs). The insertion of an APC interlayer into the ITO film effectively led to crystallization of the top ITO layer, unlike that in the Ag interlayer, and resulted in a low sheet resistance of 6.55 Ohm/square and a high optical transmittance of 84.14% without post annealing. In addition, the alloying of the Pd and Cu elements into Ag prevented agglomeration and oxidization of the metal interlayer and led to more stable ITO/APC/ITO films under ambient conditions. The microstructure and interfacial structure of the transparent ITO/APC/ITO cathode in the IOSCs were examined in detail by synchrotron X-ray scattering and high resolution transmission electron microscopy. Furthermore, we suggested a possible mechanism to explain the lower PCE of the IOSCs with an ITO/APC/ITO cathode than that of a reference IOSC with a crystalline ITO cathode using the external quantum efficiency of the IOSCs.

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

    Directory of Open Access Journals (Sweden)

    Pogacean F

    2014-02-01

    Full Text Available Florina Pogacean,1 Alexandru R Biris,2 Maria Coros,1 Mihaela Diana Lazar,1 Fumiya Watanabe,3 Ganesh K Kannarpady,3 Said A Farha Al Said,4 Alexandru S Biris,3 Stela Pruneanu1 1Department of Isotopic Physics and Technology, 2Department of Mass Spectrometry, Chromatography, and Applied Physics, National Institute for Research and Development of Isotopic and Molecular Technologies, Cluj-Napoca, Romania; 3Center for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, Arkansas, USA; 4Department of Physics, College of Science, King Abdulaziz University, Jeddah, Saudi Arabia Abstract: In this paper, we present a novel approach for the electrochemical detection of S-captopril based on graphene AuAg nanostructures used to modify an Au electrode. Multi-layer graphene (Gr sheets decorated with embedded bimetallic AuAg nanoparticles were successfully synthesized catalytically with methane as the carbon source. The two catalytic systems contained 1.0 wt% Ag and 1.0 wt% Au, while the second had a larger concentration of metals (1.5 wt% Ag and 1.5 wt% Au and was used for the synthesis of the Gr-AuAg-1 and Gr-AuAg-1.5 multicomponent samples. High-resolution transmission electron microscopy analysis indicated the presence of graphene flakes that had regular shapes (square or rectangular and dimensions in the tens to hundreds of nanometers. We found that the size of the embedded AuAg nanoparticles varied between 5 and 100 nm, with the majority being smaller than 20 nm. Advanced scanning transmission electron microscopy studies indicated a bimetallic characteristic of the metallic clusters. The resulting Gr-AuAg-1 and Gr-AuAg-1.5 samples were used to modify the surface of commonly used Au substrates and subsequently employed for the direct electrochemical oxidation of S-captopril. By comparing the differential pulse voltammograms recorded with the two modified electrodes at various concentrations of captopril, the peak current

  3. PdM (M = Pt, Au) bimetallic alloy nanowires with enhanced electrocatalytic activity for electro-oxidation of small molecules

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Chengzhou; Guo, Shaojun; Dong, Shaojun [State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, 130022 (China)

    2012-05-02

    A facile and general method has been developed to synthesize well-defined PdPt and PdAu alloy nanowires, which exhibit significantly enhanced activity towards small molecules, such as ethanol, methanol, and glucose electro-oxidation in an alkaline medium. Considering the important role of one-dimensional alloy nanowires in electrocatalytic systems, the present Pd-based alloy nanostructures could offer a promising new class of advanced electrocatalysts for direct alcohol fuel cells and electrochemical sensors. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  4. Structural and magnetic phase transitions in CeCu6 -xTx (T =Ag ,Pd )

    Science.gov (United States)

    Poudel, L.; de la Cruz, C.; Payzant, E. A.; May, A. F.; Koehler, M.; Garlea, V. O.; Taylor, A. E.; Parker, D. S.; Cao, H. B.; McGuire, M. A.; Tian, W.; Matsuda, M.; Jeen, H.; Lee, H. N.; Hong, T.; Calder, S.; Zhou, H. D.; Lumsden, M. D.; Keppens, V.; Mandrus, D.; Christianson, A. D.

    2015-12-01

    The structural and the magnetic properties of CeCu6 -xAgx (0 ≤x ≤0.85 ) and CeCu6 -xPdx (0 ≤x ≤0.4 ) have been studied using neutron diffraction, resonant ultrasound spectroscopy (RUS), x-ray diffraction measurements, and first principles calculations. The structural and magnetic phase diagrams of CeCu6 -xAgx and CeCu6 -xPdx as a function of Ag/Pd composition are reported. The end member, CeCu6, undergoes a structural phase transition from an orthorhombic (P n m a ) to a monoclinic (P 21/c ) phase at 240 K. In CeCu6 -xAgx , the structural phase transition temperature (Ts) decreases linearly with Ag concentration and extrapolates to zero at xS ≈0.1 . The structural transition in CeCu6 -xPdx remains unperturbed with Pd substitution within the range of our study. The lattice constant b slightly decreases with Ag/Pd doping, whereas a and c increase with an overall increase in the unit cell volume. Both systems, CeCu6 -xAgx and CeCu6 -xPdx , exhibit a magnetic quantum critical point (QCP), at x ≈0.2 and x ≈0.05 , respectively. Near the QCP, long range antiferromagnetic ordering takes place at an incommensurate wave vector (δ10 δ2), where δ1˜0.62 ,δ2˜0.25 ,x =0.125 for CeCu6 -xPdx and δ1˜0.64 ,δ2˜0.3 ,x =0.3 for CeCu6 -xAgx . The magnetic structure consists of an amplitude modulation of the Ce moments which are aligned along the c axis of the orthorhombic unit cell.

  5. Surface characterization of Pd/Ag23 wt% membranes after different thermal treatments

    International Nuclear Information System (INIS)

    Hydrogen permeation measurements of 1.5-10 μm thick Pd/Ag23 wt% membranes before and after thermal treatments at 300 deg. C in air (both sides) or in the temperature range 300-450 deg. C in N2 (feed side) and Ar (permeate side) were performed. Accompanying changes in surface topography and chemical composition were subsequently investigated by atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and Auger electron spectroscopy (AES) depth profiling. For a 2 μm thick membrane, the surface roughness increased for all annealing temperatures applied, while a temperature of 450 deg. C was required for an increase in roughness of both membrane surfaces to occur for the 5 μm membrane. The thickest membrane, of 10 μm, showed changed surface roughness on one side of the membrane only and a slight decrease in hydrogen permeance after all heat treatments in N2/Ar. X-ray photoelectron spectroscopy investigations performed after treatment and subsequent permeation measurements revealed segregation of silver to the membrane surfaces for all annealing temperatures applied. In comparison, heat treatment at 300 deg. C in air resulted in significantly increased hydrogen permeance accompanied by increasing surface roughness. Upon exposure to oxygen, Pd segregates to the surface to form a 2-3 nm thick oxide layer (PdO), with more complex segregation behavior after subsequent reduction and permeance measurements in pure hydrogen. The available permeance data for the Pd/Ag23 wt% membranes after heat treatment in air at 300 deg. C is found to depend linearly on the inverse membrane thickness, implying bulk limited hydrogen permeation for thicknesses down to 1.5-2.0 μm.

  6. Water-dispersable hybrid Au-Pd nanoparticles as catalysts in ethanol oxidation, aqueous phase Suzuki-Miyaura and Heck reactions

    KAUST Repository

    Song, HyonMin

    2012-01-01

    The catalytic activities of water-dispersable Au@Pd core-shell nanoparticles (NPs) and Au-Pd alloy NPs were examined. There is growing interest in Au-Pd hybridized NPs in a supported matrix or non-supported forms as catalysts in various reactions that are not limited to conventional Pd-related reactions. Four different Au@Pd core-shell NPs in this study were prepared at room temperature with help from the emulsion phase surrounding the Au core NPs. Au-Pd alloy NPs were prepared over 90 °C, and underwent phase transfer to aqueous medium for their catalytic use. Au@Pd core-shell NPs show catalytic activity in ethanol oxidation reactions as electrocatalysts, and both core-shell and alloy NPs are good to excellent catalysts in various Suzuki-Miyaura and Heck reactions as heterogeneous catalysts. Specifically, Au@Pd core-shell NPs with sharp branched arms show the highest yield in the reactions tested in this study. A relatively small amount (0.25 mol%) was used throughout the catalytic reactions. © 2012 The Royal Society of Chemistry.

  7. Mg-AI Mixed Oxides Supported Bimetallic Au-Pd Nanoparticles with Superior Catalytic Properties in Aerobic Oxidation of Benzyl Alcohol and Glycerol

    Institute of Scientific and Technical Information of China (English)

    王亮; 张伟; 曾尚景; 苏党生; 孟祥举; 肖丰收

    2012-01-01

    Nano-sized Au and Pd catalysts are favorable for oxidations with molecular oxygen, and the preparation of this kind of nanoparticles with high catalytic activities is strongly desirable. We report a successful synthesis of bimetal- lic Au-Pd nanoparticles with rich edge and comer sites on unique support of Mg-AI mixed oxides (Au-Pd/MAO), which are favorable for producing metal nanoparticles with high degree of coordinative unsaturation of metal atoms The systematic microscopic characterizations confirm the bimetallic Au-Pd nanoparticles are present as Au-Pd alloy The irregular shape of the bimetallic nanoparticles are directly observed in HRTEM images. As we expected, Au-Pd/MAO gives very excellent catalytic performances in the aerobic oxidation of benzyl alcohol and glycerol. For example, Au-Pd/MAO shows very high TOF of 91000 h i at 433 K with molecular oxygen at air pressure in solvent-free oxidation of benzyl alcohol; this catalyst also shows relatively high selectivity for tartronic acid (TA- RAC, 36.6%) at high conversion (98.5%) in aerobic oxidation of glycerol. The superior catalytic properties of Au-Pd/MAO would be potentially important tbr production of fine chemicals.

  8. Collagen-chitosan scaffold modified with Au and Ag nanoparticles: Synthesis and structure

    Science.gov (United States)

    Rubina, M. S.; Kamitov, E. E.; Zubavichus, Ya. V.; Peters, G. S.; Naumkin, A. V.; Suzer, S.; Vasil'kov, A. Yu.

    2016-03-01

    Nowadays, the dermal biomimetic scaffolds are widely used in regenerative medicine. Collagen-chitosan scaffold one of these materials possesses antibacterial activity, good compatibility with living tissues and has been already used as a wound-healing material. In this article, collagen-chitosan scaffolds modified with Ag and Au nanoparticles have been synthesized using novel method - the metal-vapor synthesis. The nanocomposite materials are characterized by XPS, TEM, SEM and synchrotron radiation-based X-ray techniques. According to XRD data, the mean size of the nanoparticles (NPs) is 10.5 nm and 20.2 nm in Au-Collagen-Chitosan (Au-CollCh) and Ag-Collagen-Chitosan (Ag-CollCh) scaffolds, respectively in fair agreement with the TEM data. SAXS analysis of the composites reveals an asymmetric size distribution peaked at 10 nm for Au-CollCh and 25 nm for Ag-CollCh indicative of particle's aggregation. According to SEM data, the metal-carrying scaffolds have layered structure and the nanoparticles are rather uniformly distributed on the surface material. XPS data indicate that the metallic nanoparticles are in their unoxidized/neutral states and dominantly stabilized within the chitosan-rich domains.

  9. Onset of Intense Surface Enhanced Raman Scattering and Aggregation in the Au@Ag System

    Directory of Open Access Journals (Sweden)

    Priya Bhatia

    2015-01-01

    Full Text Available Gold core/silver shell (Au@Ag nanoparticles of ~37 ± 5 nm diameter generate intense SERS (λEX=785 nm responses in solution when they interact with the SERS labels rhodamine 6G (R6G, 4-mercaptopyridine (MPY, and 4-mercaptobenzoic acid (MBA. Herein the relationship between SERS intensity, aggregation, and adsorption phenomenon isobserved by titrating Au@Ag with the above labels. As the labels adsorb to the Au@Ag, they drive aggregation as evidenced by the creation of NIR extinction peaks, and the magnitude of this NIR extinction (measured at 830 nm correlates very closely to magnitude of the intense SERS signals. The label MBA is an exception since it does not trigger aggregation nor does it result in intense SERS; rather intense SERS is recovered only after MBA coated Au@Ag is aggregated with KCl. An “inner filter” model is introduced and applied to compensate for solution extinction when the exciting laser radiation is significantly attenuated. This model permits a summary of the SERS responses in the form of plots of SERS intensity versus the aggregate absorption at 830 nm, which shows the excellent correlation between intense SERS and LSPR bands extinction.

  10. Evolution of a defect structure of Pd-Ag alloys during tritium exposure

    Energy Technology Data Exchange (ETDEWEB)

    Tebus, V. E-mail: tebus@bochvar.ru; Rivkis, L.; Dmitrievskaia, E.; Arutunova, G.; Golikov, I.; Ryazantseva, N.; Filin, V.; Kapychev, V.; Bulkin, V

    2002-12-01

    Pd-Ag alloys, a material for palladium diffuser of the ITER fuel clean-up system, were investigated after long-term usage exposition in tritium. Nucleation and evolution of the alloy structure defects as a result of a radiogenic helium-3 accumulation have been examined using electron microscopy, positron annihilation and X-ray analysis. The types of helium containing defects and their characteristics were determined. The early stage of helium bubbles forming was observed. It was shown that the simple defect concentration decreased slowly and helium-3 bubble sizes and concentration increased during the tritium exposure.

  11. Preparation of Ag{sub core}/Au{sub shell} bimetallic nanoparticles from physical mixtures of Au clusters and Ag ions under dark conditions and their catalytic activity for aerobic glucose oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Haijun, E-mail: zhanghaijun@wust.edu.cn [College of Materials and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei Province 430081 (China); Toshima, Naoki; Takasaki, Kanako [Department of Applied Chemistry, Tokyo University of Science Yamaguchi, SanyoOnoda-shi, Yamaguchi 756-0884 (Japan); Okumura, Mitsutaka [Department of Chemistry, Graduate School of Science, Osaka University, Machikaneyama, Toyonaka, Osaka 560-0043 (Japan)

    2014-02-15

    Graphical abstract: The synthesis, characterization and catalytic activities for glucose oxidation of AgAu bimetallic nanoparticles (BNPs) with size of less than 2 nm are reported. The catalytic activity of Ag{sub 10}Au{sub 90} BNPs was about two times higher than that of Au NPs, even the BNPs have a larger particle size than that of Au NPs. -- Highlights: • Ag{sub core}/Au{sub shell} BNPs with size of less than 2.0 nm were prepared. • No any reducing reagents and lights were used for the preparation of the BNPs. • The catalytic activity of the BNPs is about two times higher than that of Au NPs. -- Abstract: AgAu bimetallic nanoparticles (BNPs), one of the most extensively studied bimetallic systems in the literatures, could have various structures and compositions depending on their preparation conditions. In the present work, catalytically highly active PVP-protected Ag{sub core}/Au{sub shell} BNPs of about 2.5 nm in diameter were fabricated from physical mixtures of aqueous dispersions of Au nanoparticles and Ag{sup +} ions under dark conditions without using any reducing agents. The prepared Ag{sub core}/Au{sub shell} BNP colloidal catalysts, which possessed a high activity for aerobic glucose oxidation, were characterized by Ultraviolet–visible spectrophotometry (UV–Vis), Inductive coupled plasma emission spectrometer (ICP), Transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and Energy disperse spectroscopy (EDS) in High-resolution scanning transmission electron microscopy (HR-STEM). The highest activity (11,360 mol-glucose h{sup −1} mol-metal{sup −1}) was observed for the BNPs with the Ag/Au atomic ratio of 1/9, the TOF value of which is about two times higher than that of Au nanoparticles with the particle size of 1.3 nm. The enhanced catalytic activity of the prepared Ag{sub core}/Au{sub shell} BNPs compared to Au NPs can be ascribed to the presence of negatively charged Au atoms resulted from electron donations

  12. Dendrite characteristics in directionally solidified Pb-8 pct Au and Pb-3 pct Pd alloys

    Science.gov (United States)

    Tewari, S. N.

    1986-01-01

    An investigation of Pb-8 pct Au and Pb-3 pct Pd alloy specimens which have been partially directionally solidified and then quenched is performed in order to characterize their dendritic microstructural details and solute composition profiles. A controlled sectioning technique is employed to measure dendrite tip radii. It is found that most of the observed behavior is predicted quite well by a modification of the Burden and Hunt (1974) model proposed by Laxmanan (1984), in addition to the models based on the marginal stability approach. Results indicate that quantitative comparison of the primary arm spacing measurements can not form the basis of distinguishing among the various dendrite growth models in a positive temperature gradient.

  13. The adsorption of ethylene on Au/Pd(100) alloy surfaces

    Science.gov (United States)

    Li, Zhenjun; Thuening, Theodore; Tysoe, Wilfred T.

    2016-04-01

    The surface chemistry of ethylene is explored on model Au/Pd(100) alloy surfaces using a combination of temperature-programmed desorption and reflection-absorption infrared spectroscopy. The heat of adsorption of ethylene on the model alloy surface is found to increase monotonically with increasing palladium coverage in the alloy, from ~ 33 kJ/mol for a completely gold-covered surface to ~ 80 kJ/mol as the gold coverage decreases to zero. A large change in heat of adsorption is found for palladium coverages between 0 and ~ 0.35 monolayers, where previous studies have shown that the surface comprises exclusively isolated palladium sites. The heat of adsorption changes more slowly for higher palladium coverages, when palladium-palladium bridge sites appear. Vinyl species are identified for palladium coverages above ~ 0.8 ML from a vibrational mode at ~ 1120 cm- 1, which disappears when the sample is heated to ~ 250 K, due to vinyl decomposition.

  14. Effect of the Pd-Au thin film thickness uniformity on the performance of an optical fiber hydrogen sensor

    Energy Technology Data Exchange (ETDEWEB)

    Luna-Moreno, Donato [Centro de Investigaciones en Optica A. C., Loma del Bosque 115, Leon GTO, 37150 (Mexico)]. E-mail: dluna@cio.mx; Monzon-Hernandez, David [Centro de Investigaciones en Optica A. C., Loma del Bosque 115, Leon GTO, 37150 (Mexico)

    2007-08-31

    Thin alloy film of Pd and Au, formed by simultaneous electron-beam and thermal evaporation techniques, respectively, is used in the design of an optical fiber hydrogen sensor. The sensor consists of a multimode fiber (MMF) in which a short section of single mode fiber (SMF), coated with the Pd-Au thin film, is inserted. Due to core diameter mismatch, the SMF cladding guides light, allowing the interaction between the sensing layer and the guided light. When the sensor is exposed to hydrogen, the Pd-Au layer refractive index diminishes and causes attenuation changes on the transmitted light. Several samples with different layer thickness uniformity were fabricated and tested in a very simple experimental set-up. We have observed that the sensor signal change is dependant on layer thickness uniformity, since the effective interaction length between the evanescent field and the sensing layer is increased. By contrast, such uniformity practically has no influence on the time response of the sensor. The resulting Pd-Au film can detect 4% hydrogen with a response time of 15 s.

  15. Shape-controlled synthesis of Au@Pd core-shell nanoparticles and their corresponding electrochemical properties

    KAUST Repository

    Song, HyonMin

    2012-01-01

    The shape-controlled synthesis of Au@Pd core-shell nanoparticles (NPs) was successfully achieved through the emulsion phase generated during the phase transfer from organic to aqueous medium. Contrary to conventional epitaxial growth for obtaining core-shell structures, this method does not require high temperatures and does not have shape restrictions. © 2012 The Royal Society of Chemistry.

  16. Synthesis and characterization of Pt, Au or Pd clusters deposited titania-modified mesoporous silicate MCM-41

    International Nuclear Information System (INIS)

    Nanosized metal clusters Pt, Au and Pd were deposited in the mesopore of titania-modified MCM-41 by the photocatalytic reduction method under the mild conditions. The resulting Pt-, Au- or Pd-deposited titania-modified MCM-41 were characterized by using XRD, nitrogen adsorption-desorption isotherms, X-ray photoelectron spectroscopy (XPS), TEM and diffuse reflectance UV-Vis spectroscopy. The results showed that Pt(IV), Au(III) or Pd(II) was reduced to metallic Pt, Au or Pd efficiently on the surface of titania, which modified over the inner surface of mesopore of the MCM-41 after the UV light irradiation for 4 h, and the metal nanoparticles deposited in the channels of the titania-modified MCM-41. The BET surface areas and pore volumes of the metal deposited samples decreased due to the noble metal clusters in the mesopore. The UV absorption spectra of titania-modified MCM-41 broadened and changed the UV absorption in the range of 190-300 nm after loading the metal clusters

  17. Amphiphilic hollow porous shell encapsulated Au@Pd bimetal nanoparticles for aerobic oxidation of alcohols in water

    KAUST Repository

    Zou, Houbing

    2015-01-01

    © The Royal Society of Chemistry 2015. This work describes the design, synthesis and analysis of an amphiphilic hollow mesoporous shell encapsulating catalytically active Au@Pd bimetal nanoparticles. The particles exhibited excellent catalytic activity and stability in the aerobic oxidation of primary and secondary alcohols to their corresponding aldehydes or ketones in water when using air as an oxidizing agent under atmospheric pressure.

  18. Change of Work Function of Pd, Ag, K on Al(001) as a Function of External Electric Field

    Institute of Scientific and Technical Information of China (English)

    侯柱峰; 黄美纯; 朱梓忠; 黄荣彬; 郑兰荪

    2001-01-01

    We present a local density functional calculation of the effect of an external electric field on the work function change of Pd and Ag adsorption on an Al(001) surface. The adsorption of K has also been considered for comparison. We found that the work functions for all the systems increased linearly when the strength of the external electric field was increased. Since the polarized electrons at the interstitial regions between the adsorbate and substrate for Pd/Al(001) and Ag/Al(001) react to the external electric field differently, the subtle differences between Pd/Al(001) and Ag/Al(001) bondings has been characterized through the comparison of the slopes of the work function change versus electric field.

  19. Photochemical synthesis of bimetallic Au-Ag nanoparticles with "core-shell" type structure by seed mediated catalytic growth

    Institute of Scientific and Technical Information of China (English)

    DONG Shou-an; TANG Chun

    2005-01-01

    The colloidal Au core/Ag shell structure composite nanoparticles were synthesized in PEG-acetone solution by photochemical route. The monodispersed Au nanoparticles with average diameter of 3.9 nm were used as growth seeds. The optical property of colloids and the sizes of composite nanoparticles were characterized when the molar ratio of Au to Ag ranges from 4 : 1 to 1 : 4. The results show that a composite nanoparticle structure similar to strawberry shape is formed at the molar ratio of Au to Ag from 4 : 1 to 1 : 1; the composite nanoparticles consisting of a core of Au and shell of Ag were generated at the 1: 4 molar ratio, having a striking feature of forming interconnected network structure.

  20. Compensation effect in H 2 permeation kinetics of PdAg membranes

    KAUST Repository

    Zeng, Gaofeng

    2012-08-30

    Knowledge about the (inter)dependence of permeation kinetic parameters on the stoichiometry of H 2-selective alloys is still rudimentary, although uncovering the underlying systematic correlations will greatly facilitate current efforts into the design of novel high-performance H 2 separation membranes. Permeation measurements with carefully engineered, 2-7 μm thick supported Pd 100-xAg x membranes reveal that the activation energy and pre-exponential factor of H 2 permeation laws vary systematically with alloy composition, and both kinetic parameters are strongly correlated for x ≤ 50. We show that this permeation kinetic compensation effect corresponds well with similar correlations in the hydrogen solution thermodynamics and diffusion kinetics of PdAg alloys that govern H 2 permeation rates. This effect enables the consistent description of permeation characteristics over wide temperature and alloy stoichiometry ranges, whereas hydrogen solution thermodynamics may play a role, too, as a yet unrecognized source of kinetic compensation in, for example, H 2-involving reactions over metal catalysts or hydrogenation/ dehydrogenation of hydrogen storage materials. © 2012 American Chemical Society.

  1. Electromotive force measurements in liquid Ag-In-Pd lead-free alloys

    Institute of Scientific and Technical Information of China (English)

    Grzegorz Garzel; Leszek A. Zabdyr

    2006-01-01

    Emf technique was employed to determine indium activities in the liquid Ag-In-Pd alloys using galvanic cellswith yttria-stabilised-zirconia as solid electrolyte according to the scheme: kanthal/rhenium, Ag-In-Pd, In2O3 | YSZ | Ni, NiO, Pt. Composition and temperature measurement ranges were limited, because of very steep liquidus surface; 35 compositions for XPd up to 0.3 were investigated and at temperatures from near-liquidus up to 1700 K. High temperature experiments required special moly furnace to be constructed with unique automatic gas supply system for furnace winding protective atmosphere. Emf readings were taken and recorded by automatic data acquisition system. Linear dependence of emf on temperature was observed for all compositions investigated, and results were approximated by straight line equations. Then In activities were calculated using well-known relations and taking into account correction for thermoelectric power between kanthal and platinum. Results are to be used along with other existing data to perform assessment of the ternary system under accord.

  2. Magnetic properties of ZnS doped with noble metals (X = Ru, Rh, Pd, and Ag)

    Science.gov (United States)

    Tan, Zhiyun; Xiao, Wenzhi; Wang, Lingling; Yang, Youchang

    2012-12-01

    Density functional theory calculations are carried out to study the electronic structures and magnetic properties in zinc-blende structure ZnS doped with nonmagnetic noble metals (X = Ru, Rh, Pd, and Ag). Results show robust magnetic ground states for X-doped ZnS. The total magnetic moments are about 2.0, 3.0, and 2.0 μB per supercell for the Ru-, Rh-, and Pd-doped ZnS, respectively. As the atomic number of X element increases, the local magnetic moment tends toward delocalize and the hybridization between X-4d and S-3p states become stronger. This trend is strongly related to the difference in electronegativity between the substitutional X and the cation in the ZnS host. For Ag-doped ZnS, both non-spin- and spin-polarized calculations yield nearly equal total energy. The substitution of Zn in ZnS parent material by the nonmagnetic 4d transition-metals may lead to half-metallic ferromagnetism which stems from the hybridization between X-4d and S-3p states and could be attributed to a double-exchange mechanism. Curie temperature values are estimated using mean-field approximation.

  3. In situ biosynthesis of Ag, Au and bimetallic nanoparticles using Piper pedicellatum C.DC: green chemistry approach.

    Science.gov (United States)

    Tamuly, Chandan; Hazarika, Moushumi; Borah, Sarat Ch; Das, Manash R; Boruah, Manas P

    2013-02-01

    The synthesis of Ag, Au and Ag-Au bimetallic nanoparticles using Piper pedicellatum C.DC leaf extract is demonstrated here. The rapid formation of stable Ag and Au nanoparticles has been found using P. pedicellatum C.DC leaf extract in aqueous medium at normal atmospheric condition. Competitive reduction of Ag(+) and Au(3+) ions present simultaneously in solution during exposure to P. pedicellatum C.DC leaf extract leads to the synthesis of bimetallic Ag-Au nanoparticles in solution. Transmission electron microscopy (TEM) analysis revealed that the Ag nanoparticles predominantly form spherical in shape with the size range of 2.0±0.5-30.0±1.2 nm. In case of Au nanoparticles, the particles are spherical in shape along with few triangular, hexagonal and pentagonal shaped nanoparticles also observed. X-ray diffraction (XRD) studies revealed that the nanoparticles were face centered cubic (fcc) in shape. Fourier transform infrared spectroscopy (FTIR) showed nanoparticles were capped with plant compounds. The chemical constituents, viz. catechin, gallic acid, courmaric acid and protocatechuic acid of the leaf extract were identified which may act as a reducing, stabilizing and capping agent. The expected reaction mechanism in the formation of Ag and Au nanoparticles is also reported.

  4. In situ biosynthesis of Ag, Au and bimetallic nanoparticles using Piper pedicellatum C.DC: green chemistry approach.

    Science.gov (United States)

    Tamuly, Chandan; Hazarika, Moushumi; Borah, Sarat Ch; Das, Manash R; Boruah, Manas P

    2013-02-01

    The synthesis of Ag, Au and Ag-Au bimetallic nanoparticles using Piper pedicellatum C.DC leaf extract is demonstrated here. The rapid formation of stable Ag and Au nanoparticles has been found using P. pedicellatum C.DC leaf extract in aqueous medium at normal atmospheric condition. Competitive reduction of Ag(+) and Au(3+) ions present simultaneously in solution during exposure to P. pedicellatum C.DC leaf extract leads to the synthesis of bimetallic Ag-Au nanoparticles in solution. Transmission electron microscopy (TEM) analysis revealed that the Ag nanoparticles predominantly form spherical in shape with the size range of 2.0±0.5-30.0±1.2 nm. In case of Au nanoparticles, the particles are spherical in shape along with few triangular, hexagonal and pentagonal shaped nanoparticles also observed. X-ray diffraction (XRD) studies revealed that the nanoparticles were face centered cubic (fcc) in shape. Fourier transform infrared spectroscopy (FTIR) showed nanoparticles were capped with plant compounds. The chemical constituents, viz. catechin, gallic acid, courmaric acid and protocatechuic acid of the leaf extract were identified which may act as a reducing, stabilizing and capping agent. The expected reaction mechanism in the formation of Ag and Au nanoparticles is also reported. PMID:23107941

  5. Hydroquinone-assisted synthesis of branched au-ag nanoparticles with polydopamine coating as highly efficient photothermal agents.

    Science.gov (United States)

    Li, Jing; Wang, Wenjing; Zhao, Liang; Rong, Li; Lan, Shijie; Sun, Hongchen; Zhang, Hao; Yang, Bai

    2015-06-01

    Despite the success of galvanic replacement in preparing hollow nanostructures with diversified morphologies via the replacement reaction between sacrificial metal nanoparticles (NPs) seeds and less active metal ions, limited advances are made for producing branched alloy nanostructures. In this paper, we report an extended galvanic replacement for preparing branched Au-Ag NPs with Au-rich core and Ag branches using hydroquinone (HQ) as the reductant. In the presence of HQ, the preformed Ag seeds are replaceable by Au and, in turn, supply the growth of Ag branches. By altering the feed ratio of Ag seeds, HAuCl4, and HQ, the size and morphology of the NPs are tunable. Accordingly, the surface plasmon resonance absorption is tuned to near-infrared (NIR) region, making the branched NPs as potential materials in photothermal therapy. The branched NPs are further coated with polydopamine (PDA) shell via dopamine polymerization at room temperature. In comparison with bare NPs, PDA-coated branched Au-Ag (Au-Ag@PDA) NPs exhibit improved stability, biocompatibility, and photothermal performance. In vitro experiments indicate that the branched Au-Ag@PDA NPs are competitive agents for photothermal ablation of cancer cells.

  6. Longitudinal Flow from 2-8 AGeV Au+Au Collisions at the Brookhaven AGS

    CERN Document Server

    Klay, J L; Alexander, J M; Anderson, M; Best, D; Brady, F P; Case, T; Caskey, W; Cebra, D; Chance, J L; Chung, P; Cole, B; Crowe, K; Das, A C; Draper, J E; Gilkes, M L; Gushue, S; Heffner, M; Hirsch, A S; Hjort, E L; Huo, L; Justice, M; Kaplan, M; Keane, D; Kintner, J C; Krofcheck, D; Lacey, R A; Law, C; Lauret, J; Lisa, M A; Liu, H; Liu, Y M; McGrath, R; Milosevich, Z; Odyniec, Grazyna Janina; Olson, D L; Panitkin, S Y; Pinkenburg, C H; Porile, N T; Rai, G; Ritter, H G; Romero, J L; Scharenberg, R P; Schröder, L; Srivastava, B; Stone, N T B; Symons, T J M; Wang, S; Wells, R; Whitfield, J; Wienold, T; Witt, R; Wood, L; Zhang Wei Ning

    2002-01-01

    Longitudinal flow extracted from the rapidity density distributions of protons from Au + Au collisions measured by the E895 Collaboration in the energy range from 2 to 8 AGeV at the Brookhaven AGS is presented. The almost 4pi coverage provided by the EOS Time Projection Chamber allows reconstruction of proton transverse mass spectra over a broad range of rapidities. The asymptotic slope of each mt-m0 spectrum provides a temperature with which to calculate an expected dN/dy using a thermal model which includes collective longitudinal flow. This expected dN/dy is fit to the data to extract the longitudinal flow. The results show an approximately linear increase in the longitudinal flow velocity, beta*gamma_{L}, as a function of the logarithm of beam energy.

  7. Structural features and high quasi-static strain rate sensitivity of Au{sub 49}Cu{sub 26.9}Ag{sub 5.5}Pd{sub 2.3}Si{sub 16.3} bulk metallic glass

    Energy Technology Data Exchange (ETDEWEB)

    Ketov, S. V.; Chen, N.; Inoue, A.; Louzguine-Luzgin, D. V. [WPI Advanced Institute for Materials Research, Tohoku University, 2-1-1, Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Caron, A. [Institute of Micro- and Nanomaterials, University of Ulm, 89081 Ulm (Germany)

    2012-12-10

    Here we report on the formation of a crystalline Au-based solid solution surface layer on solidification, which is responsible for yellow color of the Au-based bulk metallic glass (BMG) samples. The structure of the BMG alloy was studied by X-ray diffractometry, scanning electron microscopy, and transmission electron microscopy. The deformation behavior of these Au-based BMG samples on heating was studied at temperatures above T{sub g} at different strain rates.

  8. Calculation of Elastic Constants of Ag/Pd Superlattice Thin Films by Molecular Dynamics with Many-Body Potentials

    Institute of Scientific and Technical Information of China (English)

    GAO Ning; LAI Wen-Sheng

    2006-01-01

    @@ The calculation of elastic constants of Ag/Pd superlattice thin films by molecular dynamics simulations with many-body potentials is presented. It reveals that the elastic constants C11 and C55 increase with decreasing modulation wavelength A of the films, which is consistent with experiments. However, the change of C11 and C55 with A is found to be around the values determined by a rule of mixture using bulk elastic constants of metals.No supermodulus effect is observed and it is due to cancellation between enhanced and reduced contributions to elastic constants from Ag and Pd layers subjected to compressive and tensile strains, respectively.

  9. Evolution of the quantum well states in Ag layers on Au(111)

    Energy Technology Data Exchange (ETDEWEB)

    Nuber, Andreas; Bendounan, Azzedine [Universitaet Wuerzburg, Experimentelle Physik II, Am Hubland, 97074 Wuerzburg (Germany); Huang, Li [Surface Physics Laboratory, Dept. of Physics, Fudan Univ (China); Oak Ridge National Lab., TN (United States). Materials Science and Technology Div.; Gong, Xingao [Surface Physics Laboratory, Dept. of Physics, Fudan Univ (China); Zhang, Zhenyu [Oak Ridge National Lab., TN (United States). Materials Science and Technology Div.

    2007-07-01

    Electronic quantum well states (QWS) confined in ultrathin films are of great scientific interest. Outside the substrate energy gap the confinement is supressed. They can couple with substrate states and form quantum well resonances (QWR). We present systematic studies on epitaxial layer-by-layer growing Ag films up to 45 ML on Au(111) using angular resolved photoelectron spectroscopy (ARUPS) ({delta}E=3 meV,{delta}{theta}=0.3 ). Our data in combination with density functional theory show the transition from QWR to QWS. We investigated the localization of the states in terms of their center-of-charge, peak position and lineshape. In contrast to comparable systems like Ag/W(110) QWS in Ag/Au(111) are formed not before a thickness of {approx}8 ML. The center-of-charge and the peak position are localized within the Ag overlayer and Au energy gap, respectively, at the same film thickness and hence can be used as criteria for the formation of QWS. Further investigations on their lineshape close to the substrate gap edge allow access to further many-body characteristics of the QWS.

  10. Blood surface-enhanced Raman spectroscopy based on Ag and Au nanoparticles for nasopharyngeal cancer detection

    Science.gov (United States)

    Lin, Duo; Ge, Xiaosong; Lin, Xueliang; Chen, Guannan; Chen, Rong

    2016-05-01

    This study aims to evaluate and compare the utility of blood surface-enhanced Raman spectroscopy (SERS) based on Au or Ag nanoparticles (NPs), respectively, for detection of nasopharyngeal cancer (NPC). A rapid home-made Raman system was employed for SERS measurement, and high quality SERS spectra can be recorded from blood plasma samples belonging to 60 healthy volunteers and 100 NPC patients, using both metallic NPs. The spectral differences under Ag-SERS measurement between the normal and cancer groups are more significant than Au-SERS. Principal component analysis combined with linear discriminant analysis (PCA-LDA) was used for differentiating the two blood groups with a diagnostic sensitivity and specificity of 90% and 95%, respectively, using Ag-SERS method, which has almost a 20% improvement in diagnostic specificity in comparison to Au-SERS. This exploratory study demonstrates that blood SERS based on Ag NPs is capable of achieving a better diagnostic performance for NPC detection, and has promising potential for improving NPC screening.

  11. Fe-Au and Fe-Ag composites as candidates for biodegradable stent materials.

    Science.gov (United States)

    Huang, Tao; Cheng, Jian; Bian, Dong; Zheng, Yufeng

    2016-02-01

    In this study, Fe-Ag and Fe-Au composites were fabricated by powder metallurgy using spark plasma sintering. Their microstructures, mechanical properties, and biocorrosion behavior were investigated by using optical microscopy, X-ray diffraction, environment scanning electronic microscopy, compressive test, electrochemical measurements, and immersion tests. Microstructure characterization indicated that the as-sintered iron-based materials obtained much finer grains than that of as-cast pure iron. Phase analysis showed that the Fe-Ag composites were composed of α-Fe and pure Ag phases, and Fe-Au composites consisted of α-Fe and Au phases. Compressive test showed that the improved mechanical strengths were obtained in as-sintered iron-based materials, among which the Fe-5 wt %Ag exhibited the best mechanical properties. The electrochemical and immersion tests revealed that the addition of Ag and Au could increase the corrosion rate of the iron matrix and change the corrosion mode into more uniform one. Based on the results of cytotoxicity evaluation, it was found that all the experimental material extracts performed no significant toxicity on the L-929 cells and EA. hy-926 cells, whereas a considerable inhibition on the proliferation of vascular smooth muscle cells was observed. The hemocompatibility tests showed that the hemolysis of all the experimental materials was within the range of 5%, which is the criteria value of biomaterials with good hemocomaptibility. The amount of platelet adhered on the surface of as-sintered iron-based materials was lower than that of as-cast pure iron, and the morphology of platelets kept smoothly spherical on the surface of all the experimental materials. PMID:25727071

  12. A general and high-yield galvanic displacement approach to Au-M (M = Au, Pd, and Pt) core-shell nanostructures with porous shells and enhanced electrocatalytic performances.

    Science.gov (United States)

    Kuai, Long; Geng, Baoyou; Wang, Shaozhen; Sang, Yan

    2012-07-23

    In this work, we utilize the galvanic displacement synthesis and make it a general and efficient method for the preparation of Au-M (M = Au, Pd, and Pt) core-shell nanostructures with porous shells, which consist of multilayer nanoparticles. The method is generally applicable to the preparation of Au-Au, Au-Pd, and Au-Pt core-shell nanostructures with typical porous shells. Moreover, the Au-Au isomeric core-shell nanostructure is reported for the first time. The lower oxidation states of Au(I), Pd(II), and Pt(II) are supposed to contribute to the formation of porous core-shell nanostructures instead of yolk-shell nanostructures. The electrocatalytic ethanol oxidation and oxygen reduction reaction (ORR) performance of porous Au-Pd core-shell nanostructures are assessed as a typical example for the investigation of the advantages of the obtained core-shell nanostructures. As expected, the Au-Pd core-shell nanostructure indeed exhibits a significantly reduced overpotential (the peak potential is shifted in the positive direction by 44 mV and 32 mV), a much improved CO tolerance (I(f)/I(b) is 3.6 and 1.63 times higher), and an enhanced catalytic stability in comparison with Pd nanoparticles and Pt/C catalysts. Thus, porous Au-M (M = Au, Pd, and Pt) core-shell nanostructures may provide many opportunities in the fields of organic catalysis, direct alcohol fuel cells, surface-enhanced Raman scattering, and so forth.

  13. A green method to prepare Pd-Ag nanoparticles supported on reduced graphene oxide and their electrochemical catalysis of methanol and ethanol oxidation

    Science.gov (United States)

    Li, Lingzhi; Chen, Mingxi; Huang, Guanbo; Yang, Nian; Zhang, Li; Wang, Huan; Liu, Yu; Wang, Wei; Gao, Jianping

    2014-10-01

    Bimetallic palladium-silver nanoparticles (NPs) supported on reduced oxide graphene (RGO) with different Pd/Ag ratios (Pd-Ag/RGO) were prepared by an easy green method which did not use any additional reducing agents or a dispersing agent. During the process, simultaneous redox reactions between AgNO3, K2PdCl4 and graphene oxide (GO) led to bimetallic Pd-Ag NPs. The morphology and composition of the Pd-Ag/RGO were characterized by transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, thermogravimetric analysis and Raman spectroscopy. Cyclic voltammetry and chronoamperometry were used to investigate the electrochemical activities and stabilities of these Pd-Ag/RGO catalysts for the electro-oxidation of methanol and ethanol in alkaline media. Among the different Pd/Ag ratios, the Pd-Ag (1:1)/RGO had the best catalytic activities and stability. So it is a promising catalyst for direct alcohol fuel cell applications.

  14. An intermetallic Au24Ag20 superatom nanocluster stabilized by labile ligands.

    Science.gov (United States)

    Wang, Yu; Su, Haifeng; Xu, Chaofa; Li, Gang; Gell, Lars; Lin, Shuichao; Tang, Zichao; Häkkinen, Hannu; Zheng, Nanfeng

    2015-04-01

    An intermetallic nanocluster containing 44 metal atoms, Au24Ag20(2-SPy)4(PhC≡C)20Cl2, was successfully synthesized and structurally characterized by single-crystal analysis and density funtional theory computations. The 44 metal atoms in the cluster are arranged as a concentric three-shell Au12@Ag20@Au12 Keplerate structure having a high symmetry. For the first time, the co-presence of three different types of anionic ligands (i.e., phenylalkynyl, 2-pyridylthiolate, and chloride) was revealed on the surface of metal nanoclusters. Similar to thiolates, alkynyls bind linearly to surface Au atoms using their σ-bonds, leading to the formation of two types of surface staple units (PhC≡C-Au-L, L = PhC≡C(-) or 2-pyridylthiolate) on the cluster. The co-presence of three different surface ligands allows the site-specific surface and functional modification of the cluster. The lability of PhC≡C(-) ligands on the cluster was demonstrated, making it possible to keep the metal core intact while removing partial surface capping. Moreover, it was found that ligand exchange on the cluster occurs easily to offer various derivatives with the same metal core but different surface functionality and thus different solubility.

  15. Influence of water on the properties of an Au/Mpy/Pd metal/molecule/metal junction

    Directory of Open Access Journals (Sweden)

    Jan Kučera

    2011-07-01

    Full Text Available The geometric and electronic structure of the metal–molecule interface in metal/molecule/metal junctions is of great interest since it affects the functionality of such units in possible nanoelectronic devices. We have investigated the interaction between water and a palladium monolayer of a Au(111/4-mercaptopyridine/Pd junction by means of DFT calculations. A relatively strong bond between water and the palladium monolayer of the Au/Mpy/Pd complex is observed via a one-fold bond between the oxygen atom of the water molecule and a Pd atom. An isolated H2O molecule adsorbs preferentially in a flat-lying geometry on top of a palladium atom that is at the same time also bound to the nitrogen atom of a Mpy molecule of the underlying self-assembled monolayer. The electronic structure of these Pd atoms is considerably modified which is reflected in a reduced local density of states at the Fermi energy. At higher coverages, water can be arranged in a hexagonal ice-like bilayer structure in analogy to water on bulk metal surfaces, but with a much stronger binding which is dominated by O–Pd bonds.

  16. OPTIMIZATION IN THE RECOVERY OF Au AND Ag VIA CYANIDATION OF FOUNDRY IN SLAG

    Directory of Open Access Journals (Sweden)

    Natalia Hidalgo

    2014-03-01

    Full Text Available This work aim was to recover and improvethe extraction of gold and silvercontained in the slag smelting, using the same metallurgical processes as in gold ores.The slag was concentrated in a centrifuge type Knelson, obtaining a(C1 concentrate and a (T1 tail. In order to optimize the recovery, an intensive T1 leaching was conducted. The variables used were: particle size, NaCN concentration (2000 to 4000 g/cm3 and aeration, with the residence time of 120 minutes. It is concluded that the recovery of Au, using gravity concentration (Knelson centrifuge is 83.6%, with Ag recovery of 52.5%. Au recovery is optimized to 90.4% by means of leaching tail centrifugal separation and 45.6% of Ag. The optimal conditions are: 4000 g/cm3of NaCN and artificial aeration, size [-14 # - # +35], in a lapse of 98 hours.

  17. Effects of Ag + and Au 3+ ion implantation of lithium niobate

    Science.gov (United States)

    Amolo, G. O.; Comins, J. D.; Naidoo, S. R.; Connell, S. H.; Witcomb, M. J.; Derry, T. E.

    2006-09-01

    The optical effects of implantation of lithium niobate crystals with 100 keV Ag + and 8 MeV Au 3+ ions with fluences of 1 × 10 17 ions/cm 2 have been investigated. Metal nanoparticle formation has been studied as a function of annealing temperature, and the resulting optical extinction curves have been simulated by the Mie theory in the small particle limit. Transmission electron microscopy (TEM) has provided direct evidence for the MNP sizes allowing comparison with the calculated results. A TEM study of an X-cut sample implanted with Ag + ions show that the implanted region is partially amorphised. The differences in the temperature of Au colloid development in X- and Y-cut faces of the lithium niobate crystal are attributed to restoration of crystallinity as a result of annealing.

  18. Double Detection of Mycotoxins Based on SERS Labels Embedded Ag@Au Core-Shell Nanoparticles.

    Science.gov (United States)

    Zhao, Yuan; Yang, Yaxin; Luo, Yaodong; Yang, Xuan; Li, Manli; Song, Qijun

    2015-10-01

    A sensitive surface-enhanced Raman scattering (SERS) signal dependent double detection of mycotoxins is achieved for the first time, without the aid of nucleic acid amplification strategies. SERS labels embedded Ag@Au core-shell (CS) nanoparticles (NPs) as novel SERS tags are successfully prepared through a galvanic replacement-free deposition. SERS tags produce stable and quantitative SERS signal, emerging from the plasmonic coupling at the junction of Ag core and Au shell. SERS tags engineered Raman aptasensors are developed for the double detection of ochratoxin A (OTA) and aflatoxin B1 (AFB1) in maize meal. The limits of detection (LODs) are as low as 0.006 ng/mL for OTA and 0.03 ng/mL for AFB1. The developed protocol can be extended to a large set of different SERS tags for the sensitive detection of multiple targets that possess different lengths of aptamers.

  19. Focused-ion-beam-fabricated Au nanorods coupled with Ag nanoparticles used as surface-enhanced Raman scattering-active substrate for analyzing trace melamine constituents in solution

    International Nuclear Information System (INIS)

    Graphical abstract: -- Highlights: •Well-ordered Au-nanorod array with a controlled tip ring diameter (AuNRsd) is made by focused ion beam. •AuNRsd coupled with Ag nanoparticles (Ag NPs/AuNRsd) is competent to sense target molecules in a solution. •Ag NPs/AuNRsd SERS active substrate can detect a single molecule of crystal violet. •Ag NPs/AuNRsd as a SERS-active substrate can distinguish melamine contaminants at low concentrations (e.g., 10−12 M). -- Abstract: A well-ordered Au-nanorod array with a controlled tip ring diameter (AuNRsd) was fabricated using the focused ion beam method. AuNRsd was then coupled with Ag nanoparticles (Ag NPs) to bridge the gaps among Au nanorods. The effect of surface-enhanced Raman scattering (SERS) on AuNRsd and Ag NPs/AuNRsd was particularly verified using crystal violet (CV) as the molecular probe. Raman intensity obtained from a characteristic peak of CV on AuNRsd was estimated by an enhancement factor of ≈107 in magnitude, which increased ≈1012 in magnitude for that on Ag NPs/AuNRsd. A highly SERS-active Ag NPs/AuNRsd was furthermore applied for the detection of melamine (MEL) at very low concentrations. Raman-active peaks of MEL (10−3 to 10−12 M) in water or milk solution upon AuNRsd or Ag NPs/AuNRsd were well distinguished. The peaks at 680 and 702 cm−1 for MEL molecules were found suitable to be used as the index for sensing low-concentration MEL in a varied solution, while that at 1051 cm−1 was practical to interpret MEL molecules in water or milk solution bonded with Au (i.e., AuNRsd) or Ag (i.e., Ag NPs/AuNRsd) surface. At the interface of Ag NPs/AuNRsd and MEL molecules in milk solution, a laser-induced electromagnetic field or hotspot effect was produced and competent to sense low-concentration MEL molecules interacting with Ag and Au surfaces. Accordingly, Ag NPs/AuNRsd is very promising to be used as a fast and sensitive tool for screening MEL in complex matrices such as adulteration in e.g., food

  20. Fabrication of AgAu alloy-TiO2 core-shell nanoparticles and their photocatalytic properties

    Science.gov (United States)

    Zhang, Xiao-yu; Yuan, Shu-long; Yuan, Yu-zhen; Li, Xue

    2015-01-01

    In this paper, for improving the photocatalytic efficiency of titania (TiO2) nanoparticles (NPs), AgAu alloy-TiO2 core-shell NPs are fabricated via a sol-gel (SG) process in the presence of AgAu alloy NPs with block copolymer shells as templates. The photocatalytic activities of the AgAu-TiO2 NPs on the photodecomposition of methylene blue (MB) are investigated. The AgAu-TiO2 composite NPs coated with 5.0% titania related to block copolymers show higher photocatalytic activity than the other samples in which the titania contents are larger than 5.0%. The results indicate that the increase of the thickness of the TiO2 shell leads to the decrease of the photocatalytic activity.

  1. Structural properties of Au and Ag nanoclusters embedded in MgO

    NARCIS (Netherlands)

    Fedorov, A.V.; Veen, A. van; Falub, C.V.; Eijt, S.W.H.; Kooi, B.J.; Hosson, J.Th.M. De; Hibma, T.; Zimmerman, R.L.

    2002-01-01

    Gold and silver nanoclusters embedded in MgO were created by means of ion implantation of 1.0 MeV Au or 600 keV Ag ions to a dose of 10^16 cm–2 into single crystals of MgO(100) and subsequent annealing at 1473 K for a period of 22 h. The structural properties of the nanoclusters were characterised b

  2. New apparatus for DTA at 2000 bar: thermodynamic studies on Au, Ag, Al and HTSC oxides

    OpenAIRE

    Garnier, V.; Giannini, E.; Hugi, S.; Seeber, B.; Flukiger, R.

    2004-01-01

    A new DTA (Differential Thermal Analysis) device was designed and installed in a Hot Isostatic Pressure (HIP) furnace in order to perform high-pressure thermodynamic investigations up to 2 kbar and 1200C. Thermal analysis can be carried out in inert or oxidising atmosphere up to p(O2) = 400 bar. The calibration of the DTA apparatus under pressure was successfully performed using the melting temperature (Tm) of pure metals (Au, Ag and Al) as standard calibration references. The thermal propert...

  3. Chemisorption of atomic and molecular oxygen on Au and Ag cluster anions : discrimination of different isomers

    OpenAIRE

    Kim, Young Dok; Ganteför, Gerd; Sun, Qiang; Jena, Purusottam

    2004-01-01

    Structures of coinage metal clusters reacted with atomic and molecular oxygen were studied using Ultraviolet Photoelectron Spectroscopy and Density Functional Theory calculations. We show that O2 partially dissociates on Ag-2, and this dissociative chemisorption is a kinetically hindered step. For Au4O-2, in addition to the previously observed molecularly adsorbed oxygen, we are now able to synthesize a second isomer using atomic oxygen reagents, in which oxygen adsorbs dissociatively. We dem...

  4. Calculating model of mass action concentrations for Ag-Au-Cu melts

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Based on phase diagrams and measured activities, the calculating model of mass action concentrations for heterogeneous melts Ag-Au-Cu was formulated. Calculated results agree with the improved results of recent research work.showing that the model formulated can reflect the structural characteristics of these melts. In this model, without the help of any empirical parameters, only three equilibrium constants are used, hence it is simple, lear, and favorable to the simplification of calculation.

  5. Electrospun polyacrylonitrile nanofibers supported Ag/Pd nanoparticles for hydrogen generation from the hydrolysis of ammonia borane

    Science.gov (United States)

    Tong, Yan; Lu, Xiaofeng; Sun, Weining; Nie, Guangdi; Yang, Liu; Wang, Ce

    2014-09-01

    A high-performance hydrogen generation system based on the electrospun polyacrylonitrile (PAN)/Ag/Pd composite nanofibers, which were prepared by microwave reducing the electrospun PAN/AgNO3 nanofibers and followed by a replacement reaction has been demonstrated. The morphology of the as-prepared PAN/Ag/Pd composite nanofibers and the metal nanoparticles on the fibers were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), high resolution TEM (HRTEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) measurements. It has been demonstrated that the obtained PAN/Ag/Pd composite nanofibers possess fine morphology and high catalytic activities for H2 generation from aqueous solution of ammonia borane (NH3BH3, AB). The H2 generation test exhibited that the catalyst had excellent catalytic activity (with turnover frequency (TOF) of 377.2 mol H2 h-1 (mol Pd)-1), good recycle stability and easy-separation from the reaction system. This new kind of nanofibers possesses great potential application for the new clean energy development.

  6. A green approach to ethyl acetate: Quantitative conversion of ethanol through direct dehydrogenation in a Pd-Ag membrane reactor

    KAUST Repository

    Zeng, Gaofeng

    2012-11-07

    Pincers do the trick: The conversion of ethanol to ethyl acetate and hydrogen was achieved using a pincer-Ru catalyst in a Pd-Ag membrane reactor. Near quantitative conversions and yields could be achieved without the need for acid or base promoters or hydrogen acceptors (see scheme). © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Electron configuration and charge state of electrically active Cu, Ag and Au ions in ZnSe

    International Nuclear Information System (INIS)

    The Hall effect, electrical conductivity and electron mobility are investigated at temperatures between 55 and 500 K in n-ZnSe crystals doped with Cu, Ag or Au. The presence of a small amount of Cu atoms leads to an inversion of the sign of the Hall coefficient at temperatures above 300 K. Anomalous temperature dependence of the electron mobility is observed in the samples with low Cu concentration (Zn+ (d10) and CuZn2+ (d9), and two acceptor levels near the valence band. Silver and gold exist in single-charged states AgZn+ and AuZn+ with d10 electron configuration forming single energy levels near the valence band. Au atoms form mainly interstitial Aui donors at low doping concentrations and substitutional AuZn and AuZn-based acceptors at high doping concentrations. Time stimulation of the amphoteric properties of Ag is discussed

  8. Highly Stretchable and Transparent Supercapacitor by Ag-Au Core-Shell Nanowire Network with High Electrochemical Stability.

    Science.gov (United States)

    Lee, Habeom; Hong, Sukjoon; Lee, Jinhwan; Suh, Young Duk; Kwon, Jinhyeong; Moon, Hyunjin; Kim, Hyeonseok; Yeo, Junyeob; Ko, Seung Hwan

    2016-06-22

    Stretchable and transparent electronics have steadily attracted huge attention in wearable devices. Although Ag nanowire is the one of the most promising candidates for transparent and stretchable electronics, its electrochemical instability has forbidden its application to the development of electrochemical energy devices such as supercapacitors. Here, we introduce a highly stretchable and transparent supercapacitor based on electrochemically stable Ag-Au core-shell nanowire percolation network electrode. We developed a simple solution process to synthesize the Ag-Au core-shell nanowire with excellent electrical conductivity as well as greatly enhanced chemical and electrochemical stabilities compared to pristine Ag nanowire. The proposed core-shell nanowire-based supercapacitor still possesses fine optical transmittance and outstanding mechanical stability up to 60% strain. The Ag-Au core-shell nanowire can be a strong candidate for future wearable electrochemical energy devices. PMID:27285849

  9. Effect of Refractive Index of Substrate on Fabrication and Optical Properties of Hybrid Au-Ag Triangular Nanoparticle Arrays

    OpenAIRE

    Jing Liu; Yushan Chen; Haoyuan Cai; Xiaoyi Chen; Changwei Li; Cheng-Fu Yang

    2015-01-01

    In this study, the nanosphere lithography (NSL) method was used to fabricate hybrid Au-Ag triangular periodic nanoparticle arrays. The Au-Ag triangular periodic arrays were grown on different substrates, and the effect of the refractive index of substrates on fabrication and optical properties was systematically investigated. At first, the optical spectrum was simulated by the discrete dipole approximation (DDA) numerical method as a function of refractive indexes of substrates and mediums. S...

  10. Coalescence of heteroclusters Au767 and Ag767:a molecular-dynamics study

    Institute of Scientific and Technical Information of China (English)

    Li Guo-Jian; Wang Qiang; Li Hu-Tian; Wang Kai; He Ji-Cheng

    2008-01-01

    This paper studies the coalescence of heteroclusters Au767 and Ag767 by using molecular dynamics with the embedded atom method,where layer atomic energy is employed to describe the potential energy variation of per atom in different layers along radial direction.The results show that the coalescence is driven by releasing the atomic energy of the coalesced zone.The deformation,which is induced by substitutional and vacancy diffusion during the coalescence,makes the coalesced cluster disorder.If the summation of the thermal energy and the released atomic energy is large enough to keep the disorder state,the clusters form a metastable liquid droplet;otherwise,the clusters coalesce into a solid cluster when the coalesced cluster reaches the equilibrium state,and the coalesced cluster experiences liquid to solid ordering changes during the coalescence of a solid Au767 with a liquid Ag767 and a liquid Au767 with a liquid Ag767.The centre of figure of the cluster system is shifted during the coalescence process,and higher coalescence temperature causes larger shift degree.

  11. New isotopic evidence bearing on bonanza (Au-Ag) epithermal ore-forming processes

    Science.gov (United States)

    Saunders, James A.; Mathur, Ryan; Kamenov, George D.; Shimizu, Toru; Brueseke, Matthew E.

    2016-01-01

    New Cu, S, and Pb isotope data provide evidence for a magmatic source of metal(loid)s and sulfur in epithermal Au-Ag deposits even though their ore-forming solutions are composed primarily of heated meteoric (ground) waters. The apparent isotopic discrepancy between ore metals and ore-forming solutions, and even between the ore and associated gangue minerals, indicates two different sources of epithermal ore-forming constituents: (1) a shallow geothermal system that not only provides the bulk of water for the ore-forming solutions but also major chemical constituents leached from host rocks (silica, aluminum, potassium, sodium, calcium) to make gangue minerals and (2) metals and metalloids (As, Te, Sb, etc.) and sulfur (±Se) derived from deeper magma bodies. Isotopic data are consistent with either vapor-phase transport of metal(loids) and sulfur and their subsequent absorption by shallow geothermal waters or formation of metallic (Au, Ag, Cu phases) nanoparticles at depth from magmatic fluids prior to encountering the geothermal system. The latter is most consistent with ore textures that indicate physical transport and aggregation of nanoparticles were significant ore-forming processes. The recognition that epithermal Au-Ag ores form in tectonic settings that produce magmas capable of releasing metal-rich fluids necessary to form these deposits can refine exploration strategies that previously often have focused on locating fossil geothermal systems.

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

    Science.gov (United States)

    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

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

    Science.gov (United States)

    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.

  14. Redox-Robust Pentamethylferrocene Polymers and Supramolecular Polymers, and Controlled Self-Assembly of Pentamethylferricenium Polymer-Embedded Ag, AgI, and Au Nanoparticles.

    Science.gov (United States)

    Gu, Haibin; Ciganda, Roberto; Castel, Patricia; Vax, Amélie; Gregurec, Danijela; Irigoyen, Joseba; Moya, Sergio; Salmon, Lionel; Zhao, Pengxiang; Ruiz, Jaime; Hernández, Ricardo; Astruc, Didier

    2015-12-01

    We report the first pentamethylferrocene (PMF) polymers and the redox chemistry of their robust polycationic pentamethylferricenium (PMFium) analogues. The PMF polymers were synthesized by ring-opening metathesis polymerization (ROMP) of a PMF-containing norbornene derivative by using the third-generation Grubbs ruthenium metathesis catalyst. Cyclic voltammetry studies allowed us to determine confidently the number of monomer units in the polymers through the Bard-Anson method. Stoichiometric oxidation by using ferricenium hexafluorophosphate quantitatively and instantaneously provided fully stable (even in aerobic solutions) blue d(5) Fe(III) metallopolymers. Alternatively, oxidation of the PMF-containing polymers was conducted by reactions with Ag(I) or Au(III) , to give PMFium polymer-embedded Ag and Au nanoparticles (NPs). In the presence of I2 , oxidation by using Ag(I) gave polymer-embedded Ag/AgI NPs and AgNPs at the surface of AgI NPs. Oxidation by using Au(III) also produced an Au(I) intermediate that was trapped and characterized. Engineered single-electron transfer reactions of these redox-robust nanomaterial precursors appear to be a new way to control their formation, size, and environment in a supramolecular way.

  15. Novel electrochemical redox-active species: one-step synthesis of polyaniline derivative-Au/Pd and its application for multiplexed immunoassay

    Science.gov (United States)

    Wang, Liyuan; Feng, Feng; Ma, Zhanfang

    2015-11-01

    Electrochemical redox-active species play crucial role in electrochemically multiplexed immunoassays. A one-pot method for synthesizing four kinds of new electrochemical redox-active species was reported using HAuCl4 and Na2PdCl4 as dual oxidating agents and aniline derivatives as monomers. The synthesized polyaniline derivative-Au/Pd composites, namely poly(N-methyl-o-benzenediamine)-Au/Pd, poly(N-phenyl-o-phenylenediamine)-Au/Pd, poly(N-phenyl-p-phenylenediamine)-Au/Pd and poly(3,3’,5,5’-tetramethylbenzidine)-Au/Pd, exhibited electrochemical redox activity at -0.65 V, -0.3 V, 0.12 V, and 0.5 V, respectively. Meanwhile, these composites showed high H2O2 electrocatalytic activity because of the presence of Au/Pd. The as-prepared composites were used as electrochemical immunoprobes in simultaneous detection of four tumor biomarkers (carcinoembryonic antigen (CEA), carbohydrate antigen 19-9 (CA199), carbohydrate antigen 72-4 (CA724), and alpha fetoprotein (AFP)). This immunoassay shed light on potential applications in simultaneous gastric cancer (related biomarkers: CEA, CA199, CA724) and liver cancer diagnosis (related biomarkers: CEA, CA199, AFP). The present strategy to the synthesize redox species could be easily extended to other polymers such as polypyrrole derivatives and polythiophene derivatives. This would be of great significance in the electrochemical detection of more analytes.

  16. Synthesis of multifunctional Ag@Au@phenol formaldehyde resin particles loaded with folic acids for photothermal therapy.

    Science.gov (United States)

    Yang, Ping; Xu, Qi-Zhi; Jin, Sheng-Yu; Lu, Yang; Zhao, Yang; Yu, Shu-Hong

    2012-07-23

    Multifunctional Ag@Au@ phenol formaldehyde resin (PFR) particles loaded with folic acids (FA) have been designed for killing tumor cells through photothermy conversion under the irradiation of near-infrared (NIR) light. Possessing the virtue of good fluorescence, low toxicity, and good targeting, the nanocomposite consists of an Ag core, an Au layer, a PFR shell, and folic acids on the PFR shell. The Ag@PFR core-shell structure can be prepared with a simple hydrothermal method after preheating. We then filled the PFR shell with a layer of Au by heating and modified the shell with polyelectrolyte to change its surface charge state. To capture tumor cells actively, FA molecules were attached onto the surface of the Ag@Au@PFR particles in the presence of 1-ethyl-3-(3-dimethly aminopropyl) carbodiimide (EDAC) and N-hydroxysuccinimide (NHS). Owing to the excellent property of Au NPs and Ag NPs as photothermal conversion agents, the Ag@Au@ PFR@FA particles can be utilized to kill tumor cells when exposed to NIR light.

  17. SERS-active Ag, Au and Ag–Au alloy nanoparticles obtained by laser ablation in liquids for sensing methylene blue

    Energy Technology Data Exchange (ETDEWEB)

    Olea-Mejía, Oscar, E-mail: oleaoscar@yahoo.com.mx [Centro Conjunto de Investigación en Química Sustentable UAEM-UNAM, Universidad Autónoma del Estado de México, km 14.5 Carretera Toluca-Atlacomulco, San Cayetano 50200, México (Mexico); Fernández-Mondragón, Mariana; Rodríguez-de la Concha, Gabriela [Centro Conjunto de Investigación en Química Sustentable UAEM-UNAM, Universidad Autónoma del Estado de México, km 14.5 Carretera Toluca-Atlacomulco, San Cayetano 50200, México (Mexico); Camacho-López, Marco [Laboratorio de Investigación y Desarrollo de Materiales Avanzados, Universidad Autónoma del Estado de México, Km 14.5 Carretera Toluca-Atlacomulco, San Cayetano 50925, México (Mexico)

    2015-09-01

    Highlights: • We synthesized Ag/Au nanoparticles by laser ablation in liquids. • We characterized such particles by UV–vis, TEM and EDS/STEM. • The SERS effect was studied for the obtained nanoparticles. • Pure silver nanoparticles showed the highest SERS signals. • We can sense methylene blue at a concentration of 10{sup −10} mole/L. - Abstract: We have synthesized Ag–Au nanoparticles by laser ablation in liquids using five different targets: 100% Ag, 80%Ag/20%Au, 50%Ag/50%Au, 20%Ag/80%Au and 100% Au (weight percentages). We used ethanol and methylene blue solutions in ethanol as the liquid media. The nanoparticles were mostly spherical with diameters 15, 19, 18, 23 and 11 nm, respectively. When alloyed targets were used, the resulting nanoparticles were completely alloyed forming solid solutions as evidenced by UV–vis Spectroscopy and Scanning Transmission Electron Microscopy. The obtained nanoparticles were employed to study the SERS effect of the methylene blue molecule. All the samples showed good SERS activity, however the ones composed of pure silver showed the greatest Raman signal enhancement. Finally, pure Ag nanoparticles were used for sensing methylene blue at different concentrations. While almost no signal can be discerned from the Raman spectrum when no particles are used at a concentration of methylene blue of 1 × 10{sup −2} M (∼3000 ppm), when Ag nanoparticles are used one can observe the characteristic peak of the molecule at concentrations as low as 1 × 10{sup −10} M (∼3 × 10{sup −5} ppm)

  18. Fabrication a new modified electrochemical sensor based on Au-Pd bimetallic nanoparticle decorated graphene for citalopram determination.

    Science.gov (United States)

    Daneshvar, Leili; Rounaghi, Gholam Hossein; Es'haghi, Zarrin; Chamsaz, Mahmoud; Tarahomi, Somayeh

    2016-12-01

    This paper proposes a simple approach for sensing of citalopram (CTL) using gold-palladium bimetallic nanoparticles (Au-PdNPs) decorated graphene modified gold electrode. Au-PdNPs were deposited at the surface of a graphene modified gold electrode with simple electrodeposition method. The morphology and the electrochemical properties of the modified electrode were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), energy dispersion spectroscopy (EDS), electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV) and square wave voltammetry (SWV). The novel sensor exhibited an excellent catalytic activity towards the oxidation of CTL. The oxidation peak current of CTL, was linear in the range of 0.5-50μM with a detection limit 0.049μM with respect to concentration of citalopram. The proposed sensor was successfully applied for determination of CTL tablet and human plasma samples with satisfactory results. PMID:27612758

  19. Fabrication a new modified electrochemical sensor based on Au-Pd bimetallic nanoparticle decorated graphene for citalopram determination.

    Science.gov (United States)

    Daneshvar, Leili; Rounaghi, Gholam Hossein; Es'haghi, Zarrin; Chamsaz, Mahmoud; Tarahomi, Somayeh

    2016-12-01

    This paper proposes a simple approach for sensing of citalopram (CTL) using gold-palladium bimetallic nanoparticles (Au-PdNPs) decorated graphene modified gold electrode. Au-PdNPs were deposited at the surface of a graphene modified gold electrode with simple electrodeposition method. The morphology and the electrochemical properties of the modified electrode were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), energy dispersion spectroscopy (EDS), electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV) and square wave voltammetry (SWV). The novel sensor exhibited an excellent catalytic activity towards the oxidation of CTL. The oxidation peak current of CTL, was linear in the range of 0.5-50μM with a detection limit 0.049μM with respect to concentration of citalopram. The proposed sensor was successfully applied for determination of CTL tablet and human plasma samples with satisfactory results.

  20. Particle growth mechanisms in Ag-ZrO2 and Au-ZrO2 granular films obtained by pulsed laser deposition

    International Nuclear Information System (INIS)

    Thin films consisting of Ag and Au nanoparticles embedded in amorphous ZrO2 matrix were grown by pulsed laser deposition in a wide range of metal volume concentrations in the dielectric regime (0.08AgAuc(Ag)∼0.28 and xc(Au)∼0.52)

  1. All-thiol-stabilized Ag44 and Au12Ag32 nanoparticles with single-crystal structures.

    Science.gov (United States)

    Yang, Huayan; Wang, Yu; Huang, Huaqi; Gell, Lars; Lehtovaara, Lauri; Malola, Sami; Häkkinen, Hannu; Zheng, Nanfeng

    2013-01-01

    Noble metal nanoparticles stabilized by organic ligands are important for applications in assembly, site-specific bioconjugate labelling and sensing, drug delivery and medical therapy, molecular recognition and molecular electronics, and catalysis. Here we report crystal structures and theoretical analysis of three Ag44(SR)30 and three Au12Ag32(SR)30 intermetallic nanoclusters stabilized with fluorinated arylthiols (SR=SPhF, SPhF2 or SPhCF3). The nanocluster forms a Keplerate solid of concentric icosahedral and dodecahedral atom shells, protected by six Ag2(SR)5 units. Positive counterions in the crystal indicate a high negative charge of 4(-) per nanoparticle, and density functional theory calculations explain the stability as an 18-electron superatom shell closure in the metal core. Highly featured optical absorption spectra in the ultraviolet-visible region are analysed using time-dependent density functional perturbation theory. This work forms a basis for further understanding, engineering and controlling of stability as well as electronic and optical properties of these novel nanomaterials.

  2. Electrochemical Glucose Oxidation Using Glassy Carbon Electrodes Modified with Au-Ag Nanoparticles: Influence of Ag Content

    Directory of Open Access Journals (Sweden)

    Nancy Gabriela García-Morales

    2015-01-01

    Full Text Available This paper describes the application of glassy carbon modified electrodes bearing Aux-Agy nanoparticles to catalyze the electrochemical oxidation of glucose. In particular, the paper shows the influence of the Ag content on this oxidation process. A simple method was applied to prepare the nanoparticles, which were characterized by transmission electron microscopy, Ultraviolet-Visible spectroscopy, X-ray diffraction spectroscopy, and cyclic voltammetry. These nanoparticles were used to modify glassy carbon electrodes. The effectiveness of these electrodes for electrochemical glucose oxidation was evaluated. The modified glassy carbon electrodes are highly sensitive to glucose oxidation in alkaline media, which could be attributed to the presence of Aux-Agy nanoparticles on the electrode surface. The voltammetric results suggest that the glucose oxidation speed is controlled by the glucose diffusion to the electrode surface. These results also show that the catalytic activity of the electrodes depends on the Ag content of the nanoparticles. Best results were obtained for the Au80-Ag20 nanoparticles modified electrode. This electrode could be used for Gluconic acid (GA production.

  3. Fermi surface study of ScAu{sub 2}(Al, In) and ScPd{sub 2}(Sn, Pb) compounds

    Energy Technology Data Exchange (ETDEWEB)

    Reddy, P. V. Sreenivasa; Kanchana, V., E-mail: kanchana@iith.ac.in [Department of Physics, Indian Institute of Technology Hyderabad, Ordnance Factory Estate, Yeddumailaram-502205, Telangana (India); Vaitheeswaran, G. [Advanced Centre of Research in High Energy Materials (ACRHEM), University of Hyderabad, Prof. C. R. Rao Road, Gachibowli, Hyderabad-500046 (India)

    2015-06-24

    A detailed study on the electronic structure and Fermi surface (FS) of superconducting Heusler compounds ScAu{sub 2}(Al, In) and ScPd{sub 2}(Sn, Pb) has been carried out using first principles electronic structure calculations. The spin orbit coupling is found to play a major role in understanding the band structure and FS. Analysis of the data shows the importance of spin orbit coupling effect in the above compounds. The bands which cross Fermi level (EF) are found to be dominated by the Sc d{sub t2g}-states. The calculated total density of states are in good agreement with the experimentally reported value for ScPd{sub 2}Sn. Under compression we find a change in the Fermi surface topology of ScPd{sub 2}Sn at V/V{sub 0} = 0.95 (pressure of≈15 GPa), which is explained using the band structure calculations.

  4. Fermi surface study of ScAu2(Al, In) and ScPd2(Sn, Pb) compounds

    International Nuclear Information System (INIS)

    A detailed study on the electronic structure and Fermi surface (FS) of superconducting Heusler compounds ScAu2(Al, In) and ScPd2(Sn, Pb) has been carried out using first principles electronic structure calculations. The spin orbit coupling is found to play a major role in understanding the band structure and FS. Analysis of the data shows the importance of spin orbit coupling effect in the above compounds. The bands which cross Fermi level (EF) are found to be dominated by the Sc dt2g-states. The calculated total density of states are in good agreement with the experimentally reported value for ScPd2Sn. Under compression we find a change in the Fermi surface topology of ScPd2Sn at V/V0 = 0.95 (pressure of≈15 GPa), which is explained using the band structure calculations

  5. Ionic liquid assisted synthesis of nano Pd-Au particles and application for the detection of epinephrine, dopamine and uric acid

    Energy Technology Data Exchange (ETDEWEB)

    Tsai, Tsung-Hsuan; Thiagarajan, Soundappan; Chen Shenming, E-mail: smchen78@ms15.hinet.net; Cheng Chingyi

    2012-01-31

    Nano Pd-Au particles have been electrochemically fabricated utilizing ionic liquid as green electrolyte (1-Butyl-3-methylimidazolium tetrafluoroborate). Nano Pd-Au particles modified glassy carbon electrode (GCE) and indium tin oxide coated glass electrodes were examined using atomic force microscopy, field emission scanning electron microscope and X-ray diffraction studies. Electrodeposited nano Pd-Au particles' average diameter was found as 33 nm. Nano Pd-Au particle modified GCE was electrochemically active and stable in various pH solutions. The proposed nano particle modified GCE reduces the over potential and shows the well defined oxidation peaks for the detection of epinephrine and simultaneous determination of dopamine and uric acid (in pH 7.0 phosphate buffer solution) using cyclic voltammetry and differential pulse voltammetry.

  6. Green Synthesis of Ag and Pd Nanospheres, Nanowires, and Nanorods Using Vitamin B2: Catalytic Polymerisation of Aniline and Pyrrole

    Directory of Open Access Journals (Sweden)

    Mallikarjuna N. Nadagouda

    2008-01-01

    Full Text Available For the first time, we report green chemistry approach using vitamin B2 in the synthesis of silver (Ag and palladium (Pd, nanospheres, nanowires, and nanorods at room temperature without using any harmful reducing agents, such as sodium borohydride (NaBH4 or hydroxylamine hydrochloride and any special capping or dispersing agent. Vitamin B2 was used as reducing agent as well as capping agent due to its high-water solubility, biodegradability, and low-toxicity compared with other reducing agents. The average particle size of nanoprticle was found to be Ag (average size 6.1±0.1 nm and Pd (average size 4.1±0.1 nm nanoparticles in ethylene glycol and Ag (average size 5.9±0.1 nm, and average size 6.1±0.1 nanoparticles in acetic acid and NMP, respectively. The formation of noble multiple shape nanostructures and their self assembly were dependent on the solvent employed for the preparation. When water was used as solvent media, Ag and Pd nanoparticles started to self-assemble into rod-like structures and in isopropanol Ag and Pd nanoparticles yielded wire-like structures with a thickness in the range of 10 to 20 nm and several hundred microns in length. In acetone and acetonitrile medium, the Ag and Pd nanoparticles are self-assembled into a regular pattern making nanorod structures with thicknesses ranging from 100 to 200 nm and lengths of a few microns. The so-synthesized nanostructures were characterized using scanning electron microscopy (SEM, transmission electron microscopy (TEM, energy dispersive X-ray (EDX analysis, and UV spectroscopy. The ensuing Ag and Pd nanoparticles catalyzed the reactions of aniline and pyrrole to generate polyaniline and polypyrrole nanofibers and may find various technological and biological applications. This single-step greener approach is general and can be extended to other noble metals and transition metal oxides.

  7. Facile synthesis of Au-Pd core-shell nanocrystals with systematic shape evolution and tunable size for plasmonic property examination.

    Science.gov (United States)

    Chiu, Chun-Ya; Yang, Min-Yi; Lin, Fan-Cheng; Huang, Jer-Shing; Huang, Michael H

    2014-07-01

    A facile synthetic method has been developed for the formation of Au-Pd core-shell nanocrystals in aqueous solution in just 0.5-2 h at 50 °C with systematic shape evolution from cubic to truncated cubic, cuboctahedral, truncated octahedral, and octahedral structures using octahedral gold cores. By adjusting the amounts of H2PdCl4, ascorbic acid, and sometimes surfactants and gold cores added, the particle morphology can be finely tuned, and Pd shells with ultrathin thicknesses have been achieved. Gold cores of three different sizes (35, 45, and 74 nm in opposite corner distance) were used to obtain a full range of particle sizes and shapes for a most complete examination of their plasmonic properties. Visual observations made during particle synthesis reveal that Au-Pd cubes are formed at a faster rate than that for the growth of octahedra. For the smaller cubes, cuboctahedra, and truncated octahedra prepared using 35 and 45 nm gold cores, the surface plasmon resonance (SPR) absorption band from the gold cores can be seen only when the Pd shell thickness is just 1 nm at the thinnest points of the particles. For small-sized Au-Pd octahedra, this band is observable at a Pd shell thickness of around 5 nm. For larger Au-Pd nanocrystals synthesized from 74 nm gold cores, the Au SPR band is more recognizable for all particle shapes, although octahedra still exhibit the most obvious band. The band shifts slightly to the red going from cubes to octahedra. Simulation spectra have been performed, and they roughly match with the experimental spectra. Au-Pd octahedra with two different core sizes and shell thicknesses have been used for hydrogen sensing by comparing their UV-vis spectra before and after hydrogen incorporation forming PdH. The results show that the shell thickness is more important in producing a larger spectral red-shift after hydrogen absorption.

  8. Polymer monolithic capillary microextraction on-line coupled with inductively coupled plasma-mass spectrometry for the determination of trace Au and Pd in biological samples

    International Nuclear Information System (INIS)

    A novel method based on on-line polymer monolithic capillary microextraction (CME)-inductively coupled plasma mass spectrometry (ICP-MS) was developed for the determination of trace Au and Pd in biological samples. For this purpose, poly(glycidyl methacrylate-ethylene dimethacrylate) monolith was prepared and functionalized with mercapto groups. The prepared monolith exhibited good selectivity to Au and Pd, and good resistance to strong acid with a long life span. Factors affecting the extraction efficiency of CME, such as sample acidity, sample flow rate, eluent conditions and coexisting ion interference were investigated in detail. Under the optimal conditions, the limits of detection (LODs, 3σ) were 5.9 ng L−1 for Au and 8.3 ng L−1 for Pd, and the relative standard deviations (RSDs, c = 50 ng L−1, n = 7) were 6.5% for Au and 1.1% for Pd, respectively. The developed method was successfully applied to the determination of Au and Pd in human urine and serum samples with the recovery in the range of 84–118% for spiked samples. The developed on-line polymer monolithic CME-ICP-MS method has the advantages of rapidity, simplicity, low sample/reagent consumption, high sensitivity and is suitable for the determination of trace Au and Pd in biological samples with limited amount available and complex matrix. - Highlights: • An on-line CME-ICP-MS method was developed for Au and Pd analysis in human fluids. • Poly(GMA-EDMA-SH) monolith exhibited good selectivity for Au/Pd and acid-resistance. • The method is rapid, simple, and sensitive with low sample/reagents consumption

  9. Bimetallic Ag-Pd nanoparticles-decorated graphene oxide: a fascinating three-dimensional nanohybrid as an efficient electrochemical sensing platform for vanillin determination

    International Nuclear Information System (INIS)

    Highlights: • A 3D Ag-Pd/GO nanohybrid was fabricated via a green and in situ chemical route. • Ag-Pd/GO shows excellent electro-catalytic properties for the oxidation of vanillin. • The 3D hybrid-based sensor shows excellent performances for the vanillin detection. • This proposed method was successfully used to detect vanillin in children’s snacks. - Abstract: In this work, a fascinating hybrid based on Ag-Pd bimetallic nanoparticles-decorated graphene oxide (Ag-Pd/GO) has been successfully synthesized by a green and in situ chemical reduction strategy. The resultant hybrid was particularly characterized by scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, ultraviolet-visible spectroscopy and electrochemical techniques. The morphological results illustrate that Ag-Pd nanoparticles in microspheric appearances are highly dispersed and embedded on the GO layers, resulting in a rough surface and three-dimensional (3D) microstructure with a high Ag-Pd content in the matrix. The as-synthesized 3D Ag-Pd/GO hybrid displays distinctly enhanced electrocatalytic activity for the vanillin oxidation in comparison with that of the monometal-decorated GO, revealing a synergistic effect of the matrix GO and the doped bimetallic Ag-Pd. Therefore, the Ag-Pd/GO composite can be used as an enhanced electrochemical sensing platform for the sensitive determination of vanillin, and the fabricated sensor displays a wide detection range of 0.02–45 μmol dm−3, low detection limit of 5 nmol dm−3 and satisfactory recoveries between 98.8 % and 103.5 %. All the results demonstrate that the 3D hybrids integrated graphene with bimetallic nanoparticles are promising candidates for the development of high-performance electrochemical sensors

  10. Au and Pd nanoparticles supported on CeO{sub 2}, TiO{sub 2}, and Mn{sub 2}O{sub 3} oxides

    Energy Technology Data Exchange (ETDEWEB)

    Nascente, P.A.P., E-mail: nascente@ufscar.br [Federal University of Sao Carlos, Department of Materials Engineering, Sao Carlos, SP (Brazil); Maluf, S.S.; Afonso, C.R.M. [Federal University of Sao Carlos, Department of Materials Engineering, Sao Carlos, SP (Brazil); Landers, R. [State University of Campinas, Institute of Physics, Department of Applied Physics, Campinas, SP (Brazil); Pinheiro, A.N.; Leite, E.R. [Federal University of Sao Carlos, Department of Chemistry, Sao Carlos, SP (Brazil)

    2014-10-01

    Highlights: • CeO{sub 2}, TiO{sub 2}, and Mn{sub 2}O{sub 3} supported Au and Pd nanoparticles. • Additions of 0.5 wt% of Au and Pd onto CeO{sub 2}, TiO{sub 2}, and Mn{sub 2}O{sub 3} supports. • Characterization by XRD, XPS, EDS, TEM, HRTEM, STEM, and EFTEM. - Abstract: Gold and palladium nanoparticles were incorporated on CeO{sub 2}, TiO{sub 2}, and Mn{sub 2}O{sub 3} supports prepared by a sol–gel method. The samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), high resolution TEM (HRTEM), scanning TEM (STEM) in high angle annular dark field mode (HAADF), and energy filtered TEM (EFTEM) using electron energy loss spectroscopy (EELS). The XRD diffractograms presented sharp and intense peaks indicating that the samples are highly crystalline, but it did not detected any peak corresponding to Au or Pd phases. This indicates that the Au and Pd NPs were incorporated into the structures of the oxides. It was not possible to obtain an Au 4f spectrum for Au/Mn{sub 2}O{sub 3} due to an overlap with the Mn 3p spectrum. The XPS Au 4f spectra for Au/CeO{sub 2} and Au/TiO{sub 2} present negative chemical shifts that could be attributed to particle-size-related properties. The XPS Pd 3d spectra indicate that for both CeO{sub 2} and TiO{sub 2} substrates, the Pd NPs were in the metallic state, while for the Mn{sub 2}O{sub 3} substrate, the Pd NPs were oxidized. The HRTEM results show the formation of nanocrystalline oxides having particles sizes between 50 and 200 nm. TEM micrographs show that the addition of Au caused the formation of Au clusters in between the CeO{sub 2} NPS, formation of Au NPs for the TiO{sub 2} support, and homogeneous distribution of Au clusters for the Mn{sub 2}O{sub 3} support. The addition of Pd yielded a homogeneous dispersion throughout the CeO{sub 2} and TiO{sub 2}, but caused the formation of Pd clusters for the Mn{sub 2}O

  11. Phonons, nature of bonding, and their relation to anomalous thermal expansion behavior of M2O (M = Au, Ag, Cu)

    Science.gov (United States)

    Gupta, M. K.; Mittal, R.; Chaplot, S. L.; Rols, S.

    2014-03-01

    We report a comparative study of the dynamics of Cu2O, Ag2O, and Au2O (i.e., M2O with M = Au, Ag, and Cu) using first principle calculations based on the density functional theory. Here, for the first time, we show that the nature of chemical bonding and open space in the unit cell are directly related to the magnitude of thermal expansion coefficient. A good match between the calculated phonon density of states and that derived from inelastic neutron scattering measurements is obtained for Cu2O and Ag2O. The calculated thermal expansions of Ag2O and Cu2O are negative, in agreement with available experimental data, while it is found to be positive for Au2O. We identify the low energy phonon modes responsible for this anomalous thermal expansion. We further calculate the charge density in the three compounds and find that the magnitude of the ionic character of the Ag2O, Cu2O, and Au2O crystals is in decreasing order, with an Au-O bond of covalent nature strongly rigidifying the Au4O tetrahedral units. The nature of the chemical bonding is also found to be an important ingredient to understand the large shift of the phonon frequencies of these solids with pressure and temperature. In particular, the quartic component of the anharmonic term in the crystal potential is able to account for the temperature dependence of the phonon modes.

  12. Preparation of Au and Ag nanoparticles using Artemisia annua and their in vitro antibacterial and tyrosinase inhibitory activities

    Energy Technology Data Exchange (ETDEWEB)

    Basavegowda, Nagaraj; Idhayadhulla, Akber; Lee, Yong Rok, E-mail: yrlee@yu.ac.kr

    2014-10-01

    This work describes a plant-mediated approach to the preparation of metal nanoparticles using leaf extract of Artemisia annua (A. annua), an ethno-medicinal plant widely found in Asia, which was used as reducing and stabilizing agent. A. annua is used in traditional Chinese medicine to alleviate fever. Au and Ag nanoparticles were prepared using a one-step aqueous method at room temperature without any toxic chemicals. The formation of Au and Ag nanoparticles was monitored by UV–vis spectroscopy. Synthesized nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX), Fourier transform infrared (FT-IR) spectroscopy, and thermogravimetric analysis (TGA). TEM analysis of Au nanoparticles showed that they had triangular and spherical shapes with sizes ranging from 15 to 40 nm. The silver nanoparticles were predominantly spherical and uniformly sized (30–50 nm). The Au and Ag nanoparticles produced showed significant tyrosinase inhibitory and antibacterial effects. These results suggest that the synthesized nanoparticles provide good alternatives in varied medical and industrial applications. - Highlights: • Au and Ag nanoparticles were synthesized using Artemisia annua leaf aqueous extract. • Nanoparticles were characterized by UV–vis spectroscopy, FT-IR, TEM, EDX, XRD, and TGA. • Au and Ag nanoparticles were of size 25 and 30 nm respectively, in spherical forms. • Nanoparticles showed significant tyrosinase inhibitory and antibacterial activities.

  13. Enzyme-free hydrogen peroxide sensor based on Au@Ag@C core-double shell nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yancai, E-mail: liyancai@mnnu.edu.cn [College of Chemistry & Environment, Minnan Normal University, Zhangzhou 363000 (China); Fujian Province Key Laboratory of Modern Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou 363000 (China); Zhang, Yayun; Zhong, Yanmei [College of Chemistry & Environment, Minnan Normal University, Zhangzhou 363000 (China); Li, Shunxing [College of Chemistry & Environment, Minnan Normal University, Zhangzhou 363000 (China); Fujian Province Key Laboratory of Modern Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou 363000 (China)

    2015-08-30

    Graphical abstract: - Highlights: • A facile method was designed to synthesize Au@Ag@C core-double shell nanocomposites. • Carbon nanomaterials at the outermost layer could protect Au and Ag nanoparticles from oxidation and aggregation. • The Au@Ag@C core-double shell nanocomposites showed high sensitivity and selectivity to electrocatalytic reduction of hydrogen peroxide. • The hydrogen peroxide sensor has a wide linear range of 5.0 μM to 4.75 mM and a limit of detection as low as 0.14 μM. - Abstract: The well-designed Au@Ag@C core-double shell nanocomposites were synthesized via a facile method, and were used to fabricate an enzyme-free amperometric hydrogen peroxide (H{sub 2}O{sub 2}) sensor. The size, shape, elementary composition and structure of the nanocomposites were characterized by transmission electron microscope (TEM), energy-dispersed spectrum (EDS) and X-ray diffraction (XRD). The outermost layer of the nanocomposites was amorphous carbon, the second layer was Ag and the core was Au. The Au@Ag@C core-double shell nanocomposites exhibit attractive activity for electrocatalytic reduction of H{sub 2}O{sub 2} according to the electrochemical experiments. It also demonstrates the H{sub 2}O{sub 2} sensor possess well performance with a wide linear range of 5.0 μM to 4.75 mM and a limit of detection (LOD) as low as 0.14 μM (S/N = 3). Furthermore, the interference from the common interfering species, such as glucose, ascorbic acid, dopamine and uric acid can be effectively avoided. In a word, the Au@Ag@C nanocomposites are promising candidates for enzyme-free H{sub 2}O{sub 2} sensor.

  14. Physico-chemical and antimicrobial properties of co-sputtered Ag-Au/PTFE nanocomposite coatings

    Energy Technology Data Exchange (ETDEWEB)

    Zaporojtchenko, V [Chair for Multicomponent Materials, Technische Fakultaet der CAU, Kaiserstrasse 2, D-24143 Kiel (Germany); Podschun, R [Institute for Infection Medicine, University Hospital SH, Campus Kiel (Germany); Schuermann, U [Chair for Multicomponent Materials, Technische Fakultaet der CAU, Kaiserstrasse 2, D-24143 Kiel (Germany); Kulkarni, A [Chair for Multicomponent Materials, Technische Fakultaet der CAU, Kaiserstrasse 2, D-24143 Kiel (Germany); Faupel, F [Chair for Multicomponent Materials, Technische Fakultaet der CAU, Kaiserstrasse 2, D-24143 Kiel (Germany)

    2006-10-14

    In this work, we used co-sputtering of noble metals together with polytetrafluorethylene (PTFE) as a method for producing antibacterial metal/polymer nanocomposite coatings, where the precious metals are only incorporated in a thin surface layer. Moreover, they are finely dispersed as nanoparticles, thus saving additional material and providing a very large effective surface for metal ion release. Nanocomposite films with thickness between 100 and 300 nm were prepared with a wide range of metal filling between 10 and 40%. The antimicrobial effect of the nanocomposite coatings was evaluated by means of two different assays. The bactericidal activity due to silver release from the surface was determined by a modification of conventional disc diffusion methods. Inhibition of bacterial growth on the coated surface was investigated through a modified proliferation assay. Staphylococcus aureus and S. epidermidis were used as test bacteria, as these species commonly cause infections associated with medical polymer devices. The antibacterial efficiency of the coatings against different bacteria was demonstrated at extremely small noble metal consumption: Au: {approx}1 mg m{sup -2} and Ag: {approx}0.1 g m{sup -2}. The maximum ability for having an antibacterial effect was shown by the Ag-Au/PTFE nanocomposite, followed by the Ag/PTFE nanocomposite.

  15. Modification of the electronic properties of Au/molecule/Pd junctions by adsorbed hydrogen: a DFT study

    Energy Technology Data Exchange (ETDEWEB)

    Kucera, Jan; Gross, Axel [Institut fuer Theoretische Chemie, Universitaet Ulm, D-89069 Ulm (Germany)

    2011-07-01

    Metal-molecule-metal contacts assembled from a Pd monolayer deposited on a Au-supported self-assembled monolayer (SAM) of 4-mercaptopyridine or 4-aminothiophenol were recently achieved by means of an electrochemical approach. Subsequent photoelectron spectroscopy showed a strongly reduced Pd density of states (DOS) at the Fermi energy. This phenomenon is still not fully comprehended, however, its understanding is crucial for the use of the sandwich design as a platform for future nanoelectronics. Periodic density functional theory (DFT) calculation revealed that the dehydrogenation of the amino group and the subsequent strong bonding of the remaining nitrogen atom to the Pd layer could explain the observed modification of the DOS. We have now extended this study in order to clarify the role of hydrogen atoms for the electronic properties of the Pd layers. In equilibrium, these layers should always show a considerable hydrogen coverage in an aqueous environment. Our calculations demonstrate that indeed the adsorbed hydrogen atoms significantly modify the electronic structure of the Pd layers.

  16. Digestive ripening facilitated atomic diffusion at nanosize regime: Case of AuIn2 and Ag3In intermetallic nanoparticles

    International Nuclear Information System (INIS)

    Highlights: • A digestive ripening facilitated interatomic diffusion process is presented. • Nearly monodisperse AuIn2 and Ag3In intermetallic nanoparticles were synthesized. • Optimization of reaction temperature facilitates interatomic transfer. • Presence of excess ligand plays a crucial role in the digestive ripening process. - Abstract: Monodisperse colloidal gold–indium (AuIn2) intermetallic nanoparticles have been synthesized from Au and In colloids using the digestive ripening process. Formation of the intermetallic proceeds via digestive ripening facilitated atomic diffusion of Au and In atoms from the Au and In nanoparticles followed simultaneously by their growth in the solution. Optimization of the reaction temperature was found to be crucial for the formation of AuIn2 intermetallic from gold and indium nanoparticles. Transmission electron microscopy revealed the presence of nearly monodisperse nanoparticles of Au and AuIn2 with particle size distribution of 3.7 ± 1.0 nm and 5.0 ± 1.6 nm, respectively. UV–visible spectral studies brought out the absence of SPR band in pure AuIn2 intermetallic nanoparticles. Optical study and electron microscopy, in combination with powder X-ray diffraction established phase pure AuIn2 intermetallic nanoparticles unambiguously. The potential of such an unprecedented approach has been further exploited in the synthesis of Ag3In intermetallic nanoparticles with the dimension of less than 10 nm

  17. Antibacterial Activity of Partially Oxidized Ag/Au Nanoparticles against the Oral Pathogen Porphyromonas gingivalis W83

    Directory of Open Access Journals (Sweden)

    Megan S. Holden

    2016-01-01

    Full Text Available Advances in nanotechnology provide opportunities for the prevention and treatment of periodontal disease. While physicochemical properties of Ag containing nanoparticles (NPs are known to influence the magnitude of their toxicity, it is thought that nanosilver can be made less toxic to eukaryotes by passivation of the NPs with a benign metal. Moreover, the addition of other noble metals to silver nanoparticles, in the alloy formulation, is known to alter the silver dissolution behavior. Thus, we synthesized glutathione capped Ag/Au alloy bimetallic nanoparticles (NPs via the galvanic replacement reaction between maltose coated Ag NPs and chloroauric acid (HAuCl4 in 5% aqueous triblock F127 copolymer solution. We then compared the antibacterial activity of the Ag/Au NPs to pure Ag NPs on Porphyromonas gingivalis W83, a key pathogen in the development of periodontal disease. Only partially oxidized glutathione capped Ag and Ag/Au (Au : Ag ≈ 0.2 NPs inhibited the planktonic growth of P. gingivalis W83. This effect was enhanced in the presence of hydrogen peroxide, which simulates the oxidative stress environment in the periodontal pocket during chronic inflammation.

  18. Novel PdAgCu ternary alloy as promising materials for hydrogen separation membranes: Synthesis and characterization

    Science.gov (United States)

    Tarditi, Ana M.; Cornaglia, Laura M.

    2011-01-01

    The use of the sequential electroless plating method allowed us to obtain the PdAgCu ternary alloy on top of dense stainless steel (SS) 316 L disks. The XRD analysis indicated that initially the nucleation of the two phases of the alloy (FCC and BCC) takes place, but the FCC/BCC ratio increases with the annealing time at 500 °C in H 2 stream. After 162 h, the film contained only the FCC phase, which presents promising properties to be applied in the synthesis of hydrogen selective membranes. SEM cross-section results showed that a dense, continuous, defect-free film was deposited on top of the SS support, and the EDS data indicated that no significant gradient was present on the thickness of the film. XPS and LEIS allowed us to determine that Cu and Ag surface segregation takes place after annealing up to 500 °C/5 days. In the top-most surface layer, Ag enrichment takes place as determined by ARXPS experiments which can be the result of the lower surface tension of Ag compared to that of Cu and Pd. Increasing the annealing temperature results in an increase of the Ag surface segregation while the Cu concentration in the top-most surface layer decreases.

  19. The Optical Nonlinearity of Au and Ag Nanoparticle Prepared by the Γ-Radiation Method

    Directory of Open Access Journals (Sweden)

    Esmaeil Shahriari

    2010-01-01

    Full Text Available Problem statement: The third order nonlinear optical properties of metal nanoparticles have been of interest in physical chemistry, medical diagnostics and optical devices. Gold colloidal nanoparticles are responsible for the brilliant reds seen in stained glass windows and silver particles are typically yellow. The purpose of the study was to determine the nonlinear refraction and absorption coefficient of the Au and Ag nanoparticles in PVP solution. Approach: The samples were prepared by Γ-radiation method and the nonlinear optical properties of the composites were investigated using a single beam Z-scan technique with a beam power of 40 mW and operated at wavelength of 532 nm. The measurements were carried out for both Open and closed aperture Z-scan arrangements. Results: For both Au/PVP and Ag/PVP samples the results exhibited reverse saturable absorption. The closed aperture Z-scan of the nano-fluid samples revealed self-defocusing effect while the open aperture Z-scan of the samples show a reversible saturable absorption. Conclusion: The Z-scan measurement showed that silver and gold nano-fluid prepared by gamma radiation exhibited large thermal nonlinear refractive index n2 as -8.78×10-7 and -2.478×10-6 cm2/W, respectively. We have also investigated nonlinear absorption of these samples and we found a large value of nonlinear absorption for Ag nanoparticle and a weak absorption for Au nanoparticle. In conclusion, the experimental result shows a good nonlinear refractive index at low laser power in which encouraging for possible applications in nonlinear optical devices.

  20. Comparison between the fragmentation processes in central Pb + Ag and Pb + Au collisions

    Energy Technology Data Exchange (ETDEWEB)

    Jouault, B.; Royer, G.; Sebille, F.; Haddad, F.; Lecolley, J.F.

    1996-12-31

    The fragmentation processes of a medium mass system and of a very massive one formed in central collisions are compared within the Landau-Vlasov model taking into account both the isospin dependence and the two-body residual interactions. The simulations predict the formation of a roughly ellipsoidal source in the central Pb + Ag reactions while, for the Pb + Au system, the fragmentation occurs from an hollow source, the configuration of which being intermediate between bubble-like and toroidal shapes. This difference shapes explain and allow to reproduce semi-quantitatively the two different profiles of the experimental kinetic energy spectra. (authors).

  1. Green-chemistry Compatible Approach to TiO2-supported PdAu Bimetallic Nanoparticles for Solvent-free 1-Phenylethanol Oxidation under Mild Conditions

    Institute of Scientific and Technical Information of China (English)

    Jian-Bing Chang; Chang-Hai Liu; Jie Liu; Yu-Yan Zhou; Xu Gao; Sui-Dong Wang

    2015-01-01

    TiO2-supported PdAu bimetallic nanoparticles (NPs) with small size and good dispersity were prepared by the room-temperature ionic liquid-assisted bimetal sputtering, which is simple, environmentally friendly, and free of additives and byproducts. Pd/Au atomic ratio can be tuned by controlling the sputtering conditions simply. High catalytic activity was found in PdAu–NPs–TiO2 hybrids for solvent-free selective oxidation of 1-phenylethanol using O2 as the oxidant at the low temperature of 50 °C and low pressure of 1 atm. It was found that Pd/Au ratio strongly affected the catalytical activity, and the highest conversion of about 35%and turnover frequency of about 421 h-1 were achieved at 1:1 of Pd/Au atomic ratio. The synergistic effect in PdAu NPs was also discussed based on the comprehensive characterization results. The present approach may offer an alternative platform for future development of green-chemistry compatible bimetallic nanocatalysts.

  2. Preparation and Characterization of Au/Pd Modified-TiO2 Photocatalysts for Phenol and Toluene Degradation under Visible Light—The Effect of Calcination Temperature

    Directory of Open Access Journals (Sweden)

    Anna Cybula

    2014-01-01

    Full Text Available Rutile loaded with Au/Pd nanoparticles was prepared using a water-in-oil microemulsion system of water/AOT/cyclohexane followed by calcination. The effect of calcination temperature (from 350 to 700°C on the structure of Au/Pd nanoparticles deposited at rutile matrix and the photocatalytic properties of Au/Pd-TiO2 was investigated in two model reactions (toluene degradation in gas phase and phenol degradation in aqueous phase. Toluene was irradiated over Au/Pd-TiO2 using light emitting diodes (LEDs, λmax⁡ = 415 nm. The sample 0.5 mol% Pd/TiO2 exhibited the highest activity under visible light irradiation in gas and aqueous phase reaction among all photocatalysts calcined at 350°C, while the sample modified only with gold nanoparticles showed the lowest activity. The Au/Pd-TiO2 sample calcinated at 350°C possesses the highest photocatalytic activity when degrading phenol under visible light, which is 14 times higher than that of the one calcinated at 450°C. It was observed that increasing temperature from 350 to 700°C during calcination step caused segregation of metals and finally resulted in photoactivity drop.

  3. Localized surface plasmon resonance-based hybrid Au-Ag nanoparticles for detection of Staphylococcus aureus enterotoxin B

    Science.gov (United States)

    Zhu, Shaoli; Du, ChunLei; Fu, Yongqi

    2009-09-01

    A triangular hybrid Au-Ag nanoparticles array was proposed for the purpose of biosensing in this paper. Constructing the hybrid nanoparticles, an Au thin film is capped on the Ag nanoparticles which are attached on glass substrate. The hybrid nanoparticles array was designed by means of finite-difference and time-domain (FDTD) algorithm-based computational numerical calculation and optimization. Sensitivity of refractive index of the hybrid nanoparticles array was obtained by the computational calculation and experimental detection. Moreover, the hybrid nanoparticles array can prevent oxidation of the pure Ag nanoparticles from atmosphere environment because the Au protective layer was deposited on top of the Ag nanoparticles so as to isolate the Ag particles from the atmosphere. We presented a novel surface covalent link method between the localized surface plasmon resonance (LSPR) effect-based biosensors with hybrid nanoparticles array and the detected target molecules. The generated surface plasmon wave from the array carries the biological interaction message into the corresponding spectra. Staphylococcus aureus enterotoxin B (SEB), a small protein toxin was directly detected at nanogramme per milliliter level using the triangular hybrid Au-Ag nanoparticles. Hence one more option for the SEB detection is provided by this way.

  4. Nucleation-mediated synthesis and enhanced catalytic properties of Au-Pd bimetallic tripods and bipyramids with twinned structures and high-energy facets

    Science.gov (United States)

    Zhang, Lei; Chen, Qiaoli; Wang, Xue; Jiang, Zhiyuan

    2016-01-01

    The Au-Pd alloy has been proved to be an excellent catalyst in many applications, such as the electro-oxidation of formic acid, CO oxidation and oxidation of alcohols to aldehydes. However, most of the research has been focused on the shape-controlled Au-Pd alloy NCs with a single-crystal structure. Due to the existence of high-energy atoms on the twin defects, twinned structures usually will further increase their catalytic activities. It is necessary to develop a method to prepare the Au-Pd alloy with twinned structures and investigate their catalytic properties. Herein, we successfully synthesized Au-Pd alloy tripods and bipyramids with twinned structures by the cooperation of cetyltrimethyl ammonium chloride (CTAC) and cetyltrimethyl ammonium bromide (CTAB). The tripods contain one twin plane, while the bipyramids consist of a fivefold-twinned structure. In addition, the tripods and bipyramids are both exposed by high-energy facets. We proposed that the tripods and bipyramids are evolved from bipyramid seeds and fivefold twinned seeds, respectively. The as-prepared Au-Pd tripods and bipyramids performed better activity for electrocatalytic oxidation of formic acid compared to the cubic Au-Pd nanoparticles.The Au-Pd alloy has been proved to be an excellent catalyst in many applications, such as the electro-oxidation of formic acid, CO oxidation and oxidation of alcohols to aldehydes. However, most of the research has been focused on the shape-controlled Au-Pd alloy NCs with a single-crystal structure. Due to the existence of high-energy atoms on the twin defects, twinned structures usually will further increase their catalytic activities. It is necessary to develop a method to prepare the Au-Pd alloy with twinned structures and investigate their catalytic properties. Herein, we successfully synthesized Au-Pd alloy tripods and bipyramids with twinned structures by the cooperation of cetyltrimethyl ammonium chloride (CTAC) and cetyltrimethyl ammonium bromide (CTAB

  5. Green Synthesis of Ag and Pd Nanospheres, Nanowires, and Nanorods Using Vitamin B2: Catalytic Polymerisation of Aniline and Pyrrole

    OpenAIRE

    Mallikarjuna N. Nadagouda; Varma, Rajender S.

    2008-01-01

    For the first time, we report green chemistry approach using vitamin B2 in the synthesis of silver (Ag) and palladium (Pd), nanospheres, nanowires, and nanorods at room temperature without using any harmful reducing agents, such as sodium borohydride (NaBH4) or hydroxylamine hydrochloride and any special capping or dispersing agent. Vitamin B2 was used as reducing agent as well as capping agent due to its high-water solubility, biodegradability, and low-toxicity compared with other reducing a...

  6. Total oxidation of VOCs on Pd and/or Au supported on TiO2/ZrO2 followed by ''operando'' Drift

    International Nuclear Information System (INIS)

    Catalytic performances of nano-structured meso-porous TiO2-ZrO2 mixed oxides impregnated by Pd and/or Au were studied in toluene total oxidation in a fixed bed micro-reactor and with 'operando' DRIFT. Meso-porous TiO2-ZrO2 mixed oxides with various Ti:Zr mole ratio of 80/20, 50/50 and 20/80, high surface areas were synthesised using a mixture of zirconium prop-oxide and titanium iso-prop-oxide as Zr and Ti sources and also CTMABr as surfactant. The new supports are impregnated by 0.5 or 1.5 wt% of palladium and 1 wt% of gold using impregnation and Deposition-Precipitation methods. The catalytic activity for the nano-structured meso-porous TiO2-ZrO2 mixed oxides varies depending on the molar ratio of Ti:Zr and also for all series of the studied catalysts impregnated by Pd and/or Au, when the gold is loaded firstly the activity in toluene complete oxidation is higher than when Pd was deposited firstly (PdAu/TZ ≥ 1.5Pd/TZ ≥ AuPd/TZ ≥ Pd/TZ ≥ Au/TZ ≥ TZ). The highest activity of PdAu/TZ (80/20) can be related to the higher acid sites density of the support and also to the presence of a synergetic effect between palladium and gold. 'Operando' DRIFT allowed following the VOCs oxidation but also suggesting an interaction between the adsorbed molecule and the catalyst which decreases when the activity for oxidation reaction increases. (authors)

  7. Study on deposition technique and properties of Pd/Ag alloy film sensor supported on ceramic substrate

    Science.gov (United States)

    Geng, Z. T.; He, Q.; Jin, C. G.

    2016-07-01

    Developing high-quality hydrogen sensitive material is the core part of hydrogen sensor, whose performance is determined by the sensitive response, reproducibility and recovery of hydrogen material etc. In order to overcome the defects of hydrogen embrittlement in previous hydrogen sensor which were based on the pure palladium, sliver as the second component added to the palladium was studied. Using photochemical etching technology to produce a bent metal mask, the mask is put on the ceramic substrate. Firstly, the thin film of Ta2O5 as a transition layer grew on the ceramic substrate. Then, a series of Pd/Ag alloy film sensors were prepared, and each performance characterization of Pd/Ag alloy film was studied. Testing results indicated that the thin film had a good linear output performance at 0∼⃒30% hydrogen concentration range, and demonstrates a high responsiveness and good repeatability. With temperature increasing, the strength of the responsive signal of the Pd/Ag alloy film decreases and its responsive time was also shortened.

  8. Catalytic Conversion of Short-Chain Alcohols on Atomically Dispersed Au and Pd Supported on Nanoscale Metal Oxides

    Science.gov (United States)

    Wang, Chongyang

    dehydrogenation of ethanol. Bare ZnZrOx activate ethanol conversion in the range of 280-300°C and produce undesired ethylene as product of ethanol dehydration, whereas, addition of small amount of gold (metals for selective alcohol conversion reactions. In summary, this thesis work has investigated two noble metals Au and Pd from Group IB and Group VIII, respectively, for methanol and ethanol alcohol reforming reactions employing a novel ZnZrOx composite oxide as a platform catalyst support. Comprehensive study of Au catalyst has deepened our understanding of atomically dispersed Au anchored on various supports through oxygen bonds as the active sites for alcohol reforming reactions, and showed the support effect to be indirect, serving as the carrier and stabilizer of the gold species. For Pd, the Zn species of the composite oxide is necessary to modify the Pd catalyst and the PdZn alloy gives it the desired Au-like properties. Full characterization of the catalysts used here by ICP, XPS, XRD, FTIR and STEM imaging was conducted throughout the thesis to identify the stable species and correlate the catalyst performance with its composition and morphology. Surface acidity titration by isopropanol temperature-programmed desorption/mass spectrometry (IPA-TPD/MS) and pyridine-IR adsorption/desorption was conducted in parallel to temperature-programmed surface reaction (TPSR) studies and products from isothermal steady-state reactions were monitored online by mass spectrometry.

  9. Molecular dynamics simulation of joining process of Ag-Au nanowires and mechanical properties of the hybrid nanojoint

    Directory of Open Access Journals (Sweden)

    Su Ding

    2015-05-01

    Full Text Available The nanojoining process of Ag-Au hybrid nanowires at 800K was comprehensively studied by virtue of molecular dynamics (MD simulation. Three kinds of configurations including end-to-end, T-like and X-like were built in the simulation aiming to understand the nanojoining mechanism. The detailed dynamic evolution of atoms, crystal structure transformation and defects development during the nanojoining processes were performed. The results indicate that there are two stages in the nanojoining process of Ag-Au nanowires which are atom diffusion and new bonds formation. Temperature is a key parameter affecting both stages ascribed to the energy supply and the optimum temperature for Ag-Au nanojoint with diameter of 4.08 nm has been discussed. The mechanical properties of the nanojoint were examined with simulation of tensile test on the end-to-end joint. It was revealed that the nanojoint was strong enough to resist fracture at the joining area.

  10. Ohmic contacts of Au and Ag metals to n-type GdN thin films

    Directory of Open Access Journals (Sweden)

    Felicia Ullstad

    2015-05-01

    Full Text Available The rare-earth nitrides appear as attractive alternatives to dilute ferromagnetic semiconductors for spintronics device applications. Most of them combine the properties of the ferromagnet and the semiconductor, an exceedingly rare combination. In this work we have grown n-type polycrystalline semiconducting GdN layers between pre-deposited contacts made of Cr/Au and Cr/Ag. The resistivity of the GdN layers ranges from 4.4×10-4 Ωcm to 3.1×10-2 Ωcm depending on the nitrogen pressure during the growth. The electrical properties of metal/n-type GdN/metal planar junctions are investigated as a function of the temperature. The current voltage characteristics of the junctions were linear for temperatures ranging from 300 K down to 5 K, suggesting an ohmic contact between the Au or Ag metal and the n-type GdN layer.

  11. Propagation Characteristics of Surface Plasmon Waves on Au, Ag and Al at Optical Wavelengths

    Directory of Open Access Journals (Sweden)

    Reshmi Maity

    2011-01-01

    Full Text Available In this paper the propagation characteristics of Surface Plasmon Waves (SPWs which exists on noble metals like gold (Au, silver (Ag and aluminium (Al due to the formation of Surface Plasmon Polaritons (SPPs, have been evaluated theoretically and simulated with the help of MATLAB programming language. The variation of the propagation constant, the attenuation coefficient and penetration depth inside the metal and the dielectric has been evaluated. The variations of the spot size width with the propagating wavelength also have been determined for the metals. It has been found that highly conducting metals Au and Ag provide a strong confinement to the SPWs than Al at optical frequencies as the spot size width of the former is found to be nearly 10 µm less than that of the later. The comparative study reveals that metal having higher conductivity can support a more confined SPW, having a lower penetration depth than metals of lower conductivity at terahertz frequencies when its dielectric constant assumes a negative value.

  12. Interatomic interactions and thermodynamic parameters in dilute solid solutions of the Ag-Au system

    Science.gov (United States)

    Bogdanov, V. I.; Bol'shov, L. A.; Korneichuk, E. A.; Popov, V. A.; Korneichuk, S. K.; Badanin, D. A.

    2015-07-01

    The thermodynamic parameters of interaction and the enthalpy parameters are of fundamental importance in the theory of solutions, i.e., the coefficients of the expansion of partial excess thermodynamic functions into series in terms of the concentrations of the dissolved components. In the approximation of pairwise interactions between the impurity atoms in the solution, the above parameters can be computed using the methods of the density-functional theory in the electron theory of alloys. As an example, the substitutional solid solutions of Au in Ag have been chosen, which are formed by atoms of the components with close chemical properties, in which the deformation interactions should be small, and in which there is no need to take into account the complex magnetic contributions to the pair potentials. The total energy of the dilute solution of Au in Ag and the contributions from the chemical and strain-induced interactions to the potentials of pairwise interactions are calculated up to the seventh coordination shell. Quite satisfactory agreement with the thermodynamic parameters obtained from the experimental data has been obtained.

  13. Intercluster Reactions between Au25(SR)18 and Ag44(SR)30.

    Science.gov (United States)

    Krishnadas, K R; Ghosh, Atanu; Baksi, Ananya; Chakraborty, Indranath; Natarajan, Ganapati; Pradeep, Thalappil

    2016-01-13

    We present the first example of intercluster reactions between atomically precise, monolayer protected noble metal clusters using Au25(SR)18 and Ag44(SR)30 (RS- = alkyl/aryl thiolate) as model compounds. These clusters undergo spontaneous reaction in solution at ambient conditions. Mass spectrometric measurements both by electrospray ionization and matrix assisted laser desorption ionization show that the reaction occurs through the exchange of metal atoms and protecting ligands of the clusters. Intercluster alloying is demonstrated to be a much more facile method for heteroatom doping into Au25(SR)18, as observed by doping up to 20 Ag atoms. We investigated the thermodynamic feasibility of the reaction using DFT calculations and a tentative mechanism has been presented. Metal core-thiolate interfaces in these clusters play a crucial role in inducing these reactions and also affect rates of these reactions. We hope that our work will help accelerate activities in this area to establish chemistry of monolayer protected clusters. PMID:26677722

  14. Au@Ag/Au nanoparticles assembled with activatable aptamer probes as smart ``nano-doctors'' for image-guided cancer thermotherapy

    Science.gov (United States)

    Shi, Hui; Ye, Xiaosheng; He, Xiaoxiao; Wang, Kemin; Cui, Wensi; He, Dinggeng; Li, Duo; Jia, Xuekun

    2014-07-01

    Although nanomaterial-based theranostics have increased positive expectations from cancer treatment, it remains challenging to develop in vivo ``nano-doctors'' that provide high-contrast image-guided site-specific therapy. Here we designed an activatable theranostic nanoprobe (ATNP) via self-assembly of activatable aptamer probes (AAPs) on Au@Ag/Au nanoparticles (NPs). As both quenchers and heaters, novel Au@Ag/Au NPs were prepared, showing excellent fluorescence quenching and more effective near-infrared photothermal therapy than Au nanorods. The AAP comprised a thiolated aptamer and a fluorophore-labeled complementary DNA; thus, the ATNP with quenched fluorescence in the free state could realize signal activation through target binding-induced conformational change of the AAP, and then achieve on-demand treatment under image-guided irradiation. By using S6 aptamer as the model, in vitro and in vivo studies of A549 lung cancer verified that the ATNP greatly improved imaging contrast and specific destruction, suggesting a robust and versatile theranostic strategy for personalized medicine in future.Although nanomaterial-based theranostics have increased positive expectations from cancer treatment, it remains challenging to develop in vivo ``nano-doctors'' that provide high-contrast image-guided site-specific therapy. Here we designed an activatable theranostic nanoprobe (ATNP) via self-assembly of activatable aptamer probes (AAPs) on Au@Ag/Au nanoparticles (NPs). As both quenchers and heaters, novel Au@Ag/Au NPs were prepared, showing excellent fluorescence quenching and more effective near-infrared photothermal therapy than Au nanorods. The AAP comprised a thiolated aptamer and a fluorophore-labeled complementary DNA; thus, the ATNP with quenched fluorescence in the free state could realize signal activation through target binding-induced conformational change of the AAP, and then achieve on-demand treatment under image-guided irradiation. By using S6 aptamer as

  15. Effects of Binary Mixture of Yb2O3-La2O3 on Pd/Ag Co-Deposition by Electroless Plating

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The binary mixture of Yb2O3-La2O3 was used as an additive to improve the traditional electroless plating for Pd-Ag co-deposition on the inside surface of a porous ceramic tube. The main attention were paid to investigating the effects of Yb2O3-La2O3 on Pd-Ag co-deposition rate, plating temperature, Ag content in film and Pd/Ag reduction potentials. The experimental results show that the co-deposition rate is increased by 63%, the plating temperature is decreased by 10~20 ℃ for obtaining the same co-deposition rate and the Ag content in film basically remains unchangeable when Yb2O3-La2O3 is added into the traditional electroless plating solution. The experiment also shows that Pd/Ag reduction potentials basically remain unchangeable with the binary rare earths based on the electrochemical mathematical models An inorganic composite membrane with alloy film of 76.8(mol)% Pd-23.2(mol)% Ag and the thickness of 7.7 μm on the porous ceramic tube was prepared and the permeation fluxes of hydrogen and nitrogen through the membrane are 8.65×10-3 and 1.92×10-6 m3·m-2·s-1 at 350 ℃ and 0.3 MPa respectively.

  16. [Au]/[Pd] Multicatalytic Processes: Direct One-Pot Access to Benzo[ c ]chromenes and Benzo[ b ]furans

    KAUST Repository

    Oonishi, Yoshihiro

    2014-08-28

    A new synthetic protocol that combines the advantages offered by eco-friendly solvent-free reactions and sequential transformations is reported. This strategy offers straightforward access to benzo[c]chromenes and benzo[b]furans from commercially available starting materials. This two-step, one-pot strategy consists of an Au-catalyzed hydrophenoxylation process followed by Pd-catalyzed C-H activation or Mizoroki-Heck reactions. The selectivity of the process towards C-H activation or Mizoroki-Heck reaction can be easily tuned. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. Integration of Methane Steam Reforming and Water Gas Shift Reaction in a Pd/Au/Pd-Based Catalytic Membrane Reactor for Process Intensification.

    Science.gov (United States)

    Castro-Dominguez, Bernardo; Mardilovich, Ivan P; Ma, Liang-Chih; Ma, Rui; Dixon, Anthony G; Kazantzis, Nikolaos K; Ma, Yi Hua

    2016-09-19

    Palladium-based catalytic membrane reactors (CMRs) effectively remove H₂ to induce higher conversions in methane steam reforming (MSR) and water-gas-shift reactions (WGS). Within such a context, this work evaluates the technical performance of a novel CMR, which utilizes two catalysts in series, rather than one. In the process system under consideration, the first catalyst, confined within the shell side of the reactor, reforms methane with water yielding H₂, CO and CO₂. After reforming is completed, a second catalyst, positioned in series, reacts with CO and water through the WGS reaction yielding pure H₂O, CO₂ and H₂. A tubular composite asymmetric Pd/Au/Pd membrane is situated throughout the reactor to continuously remove the produced H₂ and induce higher methane and CO conversions while yielding ultrapure H₂ and compressed CO₂ ready for dehydration. Experimental results involving (i) a conventional packed bed reactor packed (PBR) for MSR, (ii) a PBR with five layers of two catalysts in series and (iii) a CMR with two layers of two catalysts in series are comparatively assessed and thoroughly characterized. Furthermore, a comprehensive 2D computational fluid dynamics (CFD) model was developed to explore further the features of the proposed configuration. The reaction was studied at different process intensification-relevant conditions, such as space velocities, temperatures, pressures and initial feed gas composition. Finally, it is demonstrated that the above CMR module, which was operated for 600 h, displays quite high H₂ permeance and purity, high CH₄ conversion levels and reduced CO yields.

  18. Integration of Methane Steam Reforming and Water Gas Shift Reaction in a Pd/Au/Pd-Based Catalytic Membrane Reactor for Process Intensification.

    Science.gov (United States)

    Castro-Dominguez, Bernardo; Mardilovich, Ivan P; Ma, Liang-Chih; Ma, Rui; Dixon, Anthony G; Kazantzis, Nikolaos K; Ma, Yi Hua

    2016-01-01

    Palladium-based catalytic membrane reactors (CMRs) effectively remove H₂ to induce higher conversions in methane steam reforming (MSR) and water-gas-shift reactions (WGS). Within such a context, this work evaluates the technical performance of a novel CMR, which utilizes two catalysts in series, rather than one. In the process system under consideration, the first catalyst, confined within the shell side of the reactor, reforms methane with water yielding H₂, CO and CO₂. After reforming is completed, a second catalyst, positioned in series, reacts with CO and water through the WGS reaction yielding pure H₂O, CO₂ and H₂. A tubular composite asymmetric Pd/Au/Pd membrane is situated throughout the reactor to continuously remove the produced H₂ and induce higher methane and CO conversions while yielding ultrapure H₂ and compressed CO₂ ready for dehydration. Experimental results involving (i) a conventional packed bed reactor packed (PBR) for MSR, (ii) a PBR with five layers of two catalysts in series and (iii) a CMR with two layers of two catalysts in series are comparatively assessed and thoroughly characterized. Furthermore, a comprehensive 2D computational fluid dynamics (CFD) model was developed to explore further the features of the proposed configuration. The reaction was studied at different process intensification-relevant conditions, such as space velocities, temperatures, pressures and initial feed gas composition. Finally, it is demonstrated that the above CMR module, which was operated for 600 h, displays quite high H₂ permeance and purity, high CH₄ conversion levels and reduced CO yields. PMID:27657143

  19. Facile synthesis and intraparticle self-catalytic oxidation of dextran-coated hollow Au-Ag nanoshell and its application for chemo-thermotherapy.

    Science.gov (United States)

    Jang, Hongje; Kim, Young-Kwan; Huh, Hyun; Min, Dal-Hee

    2014-01-28

    Galvanic replacement reaction is a useful method to prepare various hollow nanostructures. We developed fast and facile preparation of biocompatible and structurally robust hollow Au-Ag nanostructures by using dextran-coated Ag nanoparticles. Oxidation of the surface dextran alcohols was enabled by catalytic activity of the core Au-Ag nanostructure, introducing carbonyl groups that are useful for further bioconjugation. Subsequent doxorubicin (Dox) conjugation via Schiff base formation was achieved, giving high payload of approximately 35 000 Dox per particle. Near-infrared-mediated photothermal conversion showed high efficacy of the Dox-loaded Au-Ag nanoshell as a combinational chemo-thermotherapy to treat cancer cells.

  20. Role of different Pd/Pt ensembles in determining CO chemisorption on Au-based bimetallic alloys: A first-principles study

    Energy Technology Data Exchange (ETDEWEB)

    Ham, Hyung Chul, E-mail: hchahm@kist.re.kr [Department of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712 (United States); Fuel Cell Research Center, Korea Institute of Science and Technology, Seoul (Korea, Republic of); Manogaran, Dhivya [Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin, TX 78712 (United States); Hwang, Gyeong S., E-mail: gshwang@che.utexas.edu [Department of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712 (United States); Han, Jonghee; Kim, Hyoung-Juhn; Nam, Suk Woo; Lim, Tae Hoon [Fuel Cell Research Center, Korea Institute of Science and Technology, Seoul (Korea, Republic of)

    2015-03-30

    Graphical abstract: - Highlights: • Pd ensembles greatly reduce CO adsorption energy as compared to Pt ensembles. • The steeper potential energy surface of CO adsorption in Pd(1 1 1) than in Pt(1 1 1). • Switch of binding site preference in ensembles is key to determining CO adsorption. • Opposite electronic (ligand) effect in Pd and Pt ensemble. - Abstract: Using spin-polarized density functional calculations, we investigate the role of different Pd/Pt ensembles in determining CO chemisorption on Au-based bimetallic alloys through a study of the energetics, charge transfer, geometric and electronic structures of CO on various Pd/Pt ensembles (monomer/dimer/trimer/tetramer). We find that the effect of Pd ensembles on the reduction of CO chemisorption energy is much larger than the Pt ensemble case. In particular, small-sized Pd ensembles like monomer show a substantial reduction of CO chemisorption energy compared to the pure Pd (1 1 1) surface, while there are no significant size and shape effects of Pt ensembles on CO chemisorption energy. This is related to two factors: (1) the steeper potential energy surface (PES) of CO in Pd (1 1 1) than in Pt (1 1 1), indicating that the effect of switch of binding site preference on CO chemisorption energy is much larger in Pd ensembles than in Pt ensembles, and (2) down-shift of d-band in Pd ensembles/up-shift of d-band in Pt ensembles as compared to the corresponding pure Pd (1 1 1)/Pt (1 1 1) surfaces, suggesting more reduced activity of Pd ensembles toward CO adsorption than the Pt ensemble case. We also present the different bonding mechanism of CO on Pd/Pt ensembles by the analysis of orbital resolved density of state.

  1. Role of different Pd/Pt ensembles in determining CO chemisorption on Au-based bimetallic alloys: A first-principles study

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Pd ensembles greatly reduce CO adsorption energy as compared to Pt ensembles. • The steeper potential energy surface of CO adsorption in Pd(1 1 1) than in Pt(1 1 1). • Switch of binding site preference in ensembles is key to determining CO adsorption. • Opposite electronic (ligand) effect in Pd and Pt ensemble. - Abstract: Using spin-polarized density functional calculations, we investigate the role of different Pd/Pt ensembles in determining CO chemisorption on Au-based bimetallic alloys through a study of the energetics, charge transfer, geometric and electronic structures of CO on various Pd/Pt ensembles (monomer/dimer/trimer/tetramer). We find that the effect of Pd ensembles on the reduction of CO chemisorption energy is much larger than the Pt ensemble case. In particular, small-sized Pd ensembles like monomer show a substantial reduction of CO chemisorption energy compared to the pure Pd (1 1 1) surface, while there are no significant size and shape effects of Pt ensembles on CO chemisorption energy. This is related to two factors: (1) the steeper potential energy surface (PES) of CO in Pd (1 1 1) than in Pt (1 1 1), indicating that the effect of switch of binding site preference on CO chemisorption energy is much larger in Pd ensembles than in Pt ensembles, and (2) down-shift of d-band in Pd ensembles/up-shift of d-band in Pt ensembles as compared to the corresponding pure Pd (1 1 1)/Pt (1 1 1) surfaces, suggesting more reduced activity of Pd ensembles toward CO adsorption than the Pt ensemble case. We also present the different bonding mechanism of CO on Pd/Pt ensembles by the analysis of orbital resolved density of state

  2. Facile Synthesis of Ag Nanorods with No Plasmon Resonance Peak in the Visible Region by Using Pd Decahedra of 16 nm in Size as Seeds.

    Science.gov (United States)

    Luo, Ming; Huang, Hongwen; Choi, Sang-Il; Zhang, Chao; da Silva, Robson Rosa; Peng, Hsin-Chieh; Li, Zhi-Yuan; Liu, Jingyue; He, Zhike; Xia, Younan

    2015-10-27

    This article describes a seed-mediated approach to the synthesis of Ag nanorods with thin diameters and tunable aspect ratios. The success of this method is built upon our recent progress in the synthesis of Pd decahedra as uniform samples, together with controllable sizes. When used as a seed, the Pd decahedron could direct the deposition of Ag atoms along the 5-fold axis to generate a nanorod, with its diameter being determined by the lateral dimension of the seed. We were able to generate Ag nanorods with uniform diameters down to 20 nm. Under the conditions we used for growth, symmetry breaking occurred as the Ag atoms were only deposited along one side of the Pd decahedral seed to generate a Ag nanorod with the Pd seed being positioned at one of its two ends. We also systematically investigated the localized surface plasmon resonance (LSPR) properties of the Ag nanorods. With the transverse mode kept below 400 nm, the longitudinal mode could be readily tuned from the visible to the near-infrared region by varying the aspect ratio. As an important demonstration, we obtained Ag nanorods with no LSPR peak in the visible spectrum (400-800 nm), which are attractive for applications related to the fabrication of touchscreen displays, solar films, and energy-saving smart windows. PMID:26372854

  3. Sonochemical synthesis of a PdAg/C electrocatalyst for oxygen reduction reaction; Sintesis sonoquimica de un electrocatalizador de PdAg/C para la reaccion de reduccion de oxigeno

    Energy Technology Data Exchange (ETDEWEB)

    Godinez-Garcia, A.; Perez-Robles, J.F. [Centro de Investigacion y de Estudios Avanzados del IPN. Santiago de Queretaro, Queretaro (Mexico)]. E-mail: jperez@qro.cinvestav.mx; Solorza-Feria, O. [CINVESTAV-IPN, Mexico, D.F. (Mexico)

    2009-09-15

    The synthesis and characterization of nanocatalysts for fuel cells has been a primary line of research for the purpose of obtaining less expensive electrocatalysts with better activity. A large variety of methods exist to synthesize useful nanoparticles as electrocatalysts. Each method generates particles with a different surface morphology and, therefore, the catalytic activity usually varies depending on which is used in the synthesis. In this work, PdAg/C electrocatalysts are synthesized with high-intensity ultrasonic irradiation and compared to those obtained using a conventional method such as reduction by NaBH{sub 4}. The study of this technique is of interest because it produces highly dispersed carbon-supported nanoparticles with very clean surfaces. Each electrocatalyst was evaluated for its oxygen reduction reaction (ORR) in acid medium with cyclic voltamperometry (CV) and rotating disc electrode (RDE). The electrocatalyst was characterized with x-ray diffraction and transmission electron microscopy (TEM). The physical characterization reveals that the electrocatalyst is composed of nanometric bimetallic aggregates. An important characteristic of the PdAg/C alloy obtained using ultrasound is better activity than that obtained by reduction with NaBH{sub 4}. [Spanish] La sintesis y caracterizacion de nanocatalizadores para celdas de combustible ha sido una de las principales lineas de investigacion, con el objetivo de obtener electrocatalizadores mas baratos y con una mejor actividad. Existen una gran variedad de metodos para sintetizar nanoparticulas utiles como electrocatalizadores, cada metodo genera particulas con una morfologia superficial diferente por lo que la actividad catalitica suele variar dependiendo de cual se utilice en la sintesis. En este trabajo se sintetizan electrocatalizadores de PdAg/C con irradiacion ultrasonica de alta intensidad y se comparan con las obtenidas con un metodo convencional como es la reduccion por NaBH{sub 4}. Esta

  4. Fast and facile preparation of CTAB based gels and their applications in Au and Ag nanoparticles synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Upadhyay, Ravi Kant, E-mail: rkupadhyay85@gmail.com [Department of Chemistry, School of Natural Sciences, Shiv Nadar University, Gautam Budh Nagar, 201314 Uttar Pradesh (India); Soin, Navneet, E-mail: n.soin@bolton.ac.uk [Knowledge Centre for Materials Chemistry (KCMC), Institute for Materials Research and Innovation (IMRI), University of Bolton, Deane Road, Bolton BL3 5AB (United Kingdom); Saha, Susmita, E-mail: ssaha@bose.res.in [Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700 098 (India); Barman, Anjan, E-mail: abarman@bose.res.in [Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block JD, Sector III, Salt Lake, Kolkata 700 098 (India); Sinha Roy, Susanta, E-mail: susanta.roy@snu.edu.in [Department of Physics, School of Natural Sciences, Shiv Nadar University, Gautam Budh Nagar, 201314 Uttar Pradesh (India)

    2015-04-15

    We have demonstrated that the gel-like mesophase of Cetyltrimethylammonium bromide (CTAB) can be synthesized by judicial adjustment of water to surfactant molar ratio (W{sub 0}), without using any additional salts, gelating agents or co-surfactants. Gel formation was found to be highly dependent on the water to surfactant molar ratio (W{sub 0}), with the lowest value of W{sub 0} (41.5) resulting in rapid gel formation. Environmental scanning electron microscope (ESEM) analysis revealed that the gel was comprised of interconnected cylindrical structures. The presence of hydrogen bonding in the gel-like mesophase was confirmed by Fourier Transform Infrared spectroscopy (FTIR) analysis. Rheology measurements revealed that all the gel samples were highly viscoelastic in nature. Furthermore, Au and Ag containing CTAB gels were explored as precursors for the preparation of spherical Gold (Au) and Silver (Ag) nanoparticles using Sodium borohydride (NaBH{sub 4}) as reducing agent. The effects of NaBH{sub 4} concentration on the particle size and morphology of the Au and Ag nanoparticles have also been studied. - Highlights: • A facile synthesis of CTAB based gel-like mesophase is reported. • CTAB gels were obtained by adjusting water to surfactant molar ratio (W{sub 0}). • FTIR analysis revealed that hydrogen bonding plays a key role in gel formation. • Au, Ag nanoparticles were synthesized by using CTAB gel and NaBH{sub 4}.

  5. Chitosan nanocomposite films based on Ag-NP and Au-NP biosynthesis by Bacillus Subtilis as packaging materials.

    Science.gov (United States)

    Youssef, Ahmed M; Abdel-Aziz, Mohamed S; El-Sayed, Samah M

    2014-08-01

    Chitosan-silver (CS-Ag) and Chitosan-gold (CS-Au) nanocomposites films were synthesized by a simple chemical method. A local bacterial isolate identified as Bacillus subtilis ss subtilis was found to be capable to synthesize both silver nanoparticles (Ag-NP) and gold nanoparticles (Au-NP) from silver nitrate (AgNO3) and chloroauric acid (AuCl(4-)) solutions, respectively. The biosynthesis of both Ag-NP and Au-NP characterize using UV/vis spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD), and then added to chitosan by different ratios (0.5, 1 and 2%). The prepared chitosan nanocomposites films were characterize using UV, XRD, SEM and TEM. Moreover, the antibacterial activity of the prepared films was evaluated against gram positive (Staphylococcus aureus) and gram negative bacteria (Pseudomonas aerugenosa), fungi (Aspergillus niger) and yeast (Candida albicans). Therefore, these materials can be potential used as antimicrobial agents in packaging applications.

  6. Experimental and theoretical study of the adsorption of fumaramide [2]rotaxane on Au(111) and Ag(111) surfaces

    NARCIS (Netherlands)

    Mendoza, S.M.; Whelan, C.M.; Jalkanen, J.-P.; Zerbetto, F.; Gatti, F.; Kay, E.R.; Leigh, D.A.; Lubomska, Monika; Rudolf, Petra

    2005-01-01

    Thin films of fumaramide [2] rotaxane, a mechanically interlocked molecule composed of a macrocycle and a thread in a "bead and thread" configuration, were prepared by vapor deposition on both Ag(111) and Au(111) substrates. X-ray photoelectron spectroscopy (XPS) and high-resolution electron-energy-

  7. Effects of plasmon excitation on photocatalytic activity of Ag/TiO 2 and Au/TiO2 nanocomposites

    DEFF Research Database (Denmark)

    Sellappan, Raja; González-Posada, Fernando; Chakarov, Dinko;

    2013-01-01

    Model nanocomposite photocatalysts consisting of undoped TiO2 films with optically active Ag or Au nanoparticles (NPs) were designed, fabricated, and examined to address the role of plasmon excitations in their performance. Different composition configurations were tested in which the NPs were ei...

  8. Fast and facile preparation of CTAB based gels and their applications in Au and Ag nanoparticles synthesis

    International Nuclear Information System (INIS)

    We have demonstrated that the gel-like mesophase of Cetyltrimethylammonium bromide (CTAB) can be synthesized by judicial adjustment of water to surfactant molar ratio (W0), without using any additional salts, gelating agents or co-surfactants. Gel formation was found to be highly dependent on the water to surfactant molar ratio (W0), with the lowest value of W0 (41.5) resulting in rapid gel formation. Environmental scanning electron microscope (ESEM) analysis revealed that the gel was comprised of interconnected cylindrical structures. The presence of hydrogen bonding in the gel-like mesophase was confirmed by Fourier Transform Infrared spectroscopy (FTIR) analysis. Rheology measurements revealed that all the gel samples were highly viscoelastic in nature. Furthermore, Au and Ag containing CTAB gels were explored as precursors for the preparation of spherical Gold (Au) and Silver (Ag) nanoparticles using Sodium borohydride (NaBH4) as reducing agent. The effects of NaBH4 concentration on the particle size and morphology of the Au and Ag nanoparticles have also been studied. - Highlights: • A facile synthesis of CTAB based gel-like mesophase is reported. • CTAB gels were obtained by adjusting water to surfactant molar ratio (W0). • FTIR analysis revealed that hydrogen bonding plays a key role in gel formation. • Au, Ag nanoparticles were synthesized by using CTAB gel and NaBH4

  9. Effect of alloying on the electronic structure and magnetic properties of Fe, Co and Ni with Au and Ag

    Indian Academy of Sciences (India)

    Ashish Bhattacharjee; Mesbahuddin Ahmed; Abhijit Mookerjee; Amal Halder

    2003-01-01

    We use the self-consistent, augmented space recursion technique to study the electronic structure and magnetic properties of alloys of the transition metals, Fe, Co and Ni with the noble metals, Ag and Au. We analyse the effect of local environment and the hybridization between the constituent bands on the electronic and magnetic properties.

  10. Tailor-made Au-Ag core–shell nanoparticle 2D arrays on protein-coated graphene oxide with assembly enhanced antibacterial activity

    International Nuclear Information System (INIS)

    Water-dispersible two-dimensional (2D) assemblies of Au-Ag core–shell nanoparticles are obtained through a highly selective electroless silver deposition on pre-assembled gold nanoparticles on bovine serum albumin (BSA)-coated graphene oxide (BSA-GO). While neither BSA-GO nor AuNP-decorated BSA-GO shows any antibacterial ability, the silver-coated GO-Au nanosheets (namely GO-Au-Ag) exhibit an enhanced antibacterial activity against Gram-negative Escherichia coli (E. coli) bacteria, superior to unassembled Au-Ag nanoparticles and even ionic Ag. Such an improvement may be attributed to the increased local concentration of silver nanoparticles around a bacterium and a polyvalent interaction with the bacterial surface. In addition, the colloidal stability of this novel nano-antimicrobial against the formation of random nanoparticle aggregates guarantees a minimized activity loss of the Au-Ag nanoparticles. The antibacterial efficacy of GO-Au-Ag is less sensitive to the existence of Cl−, in comparison with silver ions, providing another advantage for wound dressing applications. Our research unambiguously reveals a strong and very specific interaction between the GO-Au-Ag nanoassembly and E. coli, which could be an important clue toward a rational design, synthesis and assembly of innovative and highly active antibacterial nanomaterials. (paper)

  11. Electrical characterization of the organic semiconductor Ag/CuPc/Au Schottky diode

    Institute of Scientific and Technical Information of China (English)

    Mutabar Shah; M. H. Sayyad; Kh. S. Karimov

    2011-01-01

    This paper reports on the fabrication and investigation of a surface-type organic semiconductor copper phthalocyanine (CuPc) based diode. A thin film of CuPc of thickness 100 nm was thermally sublimed onto a glass substrate with preliminary deposited metallic electrodes to form a surface-type Ag/CuPc/Au Schottky diode. The current-voltage characteristics were measured at room temperature under dark conditions. The barrier height was calculated as 1.05 eV. The values of mobility and conductivity was found to be 1.74 x l0-9 cm2/(V.s) and 5.5 x 10-6 Ω-1. cm-1, respectively. At low voltages the device showed ohmic conduction and the space charge limited current conduction mechanisms were dominated at higher voltages.

  12. Tunable Au-Ag nanobowl arrays for size-selective plasmonic biosensing.

    Science.gov (United States)

    Jana, Debrina; Lehnhoff, Emily; Bruzas, Ian; Robinson, Jendai; Lum, William; Sagle, Laura

    2016-08-01

    Selectivity is often a major obstacle for localized surface plasmon resonance-based biosensing in complex biological solutions. An additional degree of selectivity can be achieved through the incorporation of shape complementarity on the nanoparticle surface. Here, we report the versatile fabrication of substrate-bound Au-Ag nanobowl arrays through the galvanic ion replacement of silver nanodisk arrays. Both localized surface plasmon resonance (LSPR) and surface enhanced Raman spectroscopy (SERS) were carried out to detect the binding of analytes of varying size to the nanobowl arrays. Large increases in the LSPR and SERS response were measured for analytes that were small enough to enter the nanobowls, compared to those too large to come into contact with the interior of the nanobowls. This size-selective sensing should prove useful in both size determination and differentiation of large analytes in biological solutions, such as viruses, fungi, and bacterial cells.

  13. Direct laser planting of hybrid Au-Ag/C nanostructures - nanoparticles, flakes and flowers

    CERN Document Server

    Manshina, Alina; Bashouti, Muhammad; Povolotskiy, Alexey; Petrov, Yuriy; Koshevoy, Igor; Christiansen, Silke; Tunik, Sergey; Leuchs, Gerd

    2015-01-01

    We demonstrate a new approach for forming hybrid metal/carbonaceous nanostructures in a controlled direct laser planting process. Au-Ag nanoclusters in amorphous or crystalline carbonaceous matrices are formed with different morphology: nanoparticles, nanoflakes, and nanoflowers. In contrast to other generation techniques our approach is simple, involving only a single laser-induced process transforming supramolecular complexes dissolved in solvent such as acetone, acetophenone, or dichloroethane into hybrid nanostructures in the laser-affected area of the substrate. The morphology of the hybrid nanostructures can be steered by controlling the deposition parameters, the composition of the liquid phase and the type of substrate, amorphous or crystalline. The carbonaceous phase of the hybrid nanostructures consists of hydrogenated amorphous carbon in the case of nanoparticles and of crystalline orthorhombic graphite of nanoscale thickness in the case of flakes and flowers. To the best of our knowledge this is t...

  14. Electrochemical sensor for detection of hydrazine based on Au@Pd core–shell nanoparticles supported on amino-functionalized TiO2 nanotubes

    International Nuclear Information System (INIS)

    In this paper, we reported a simple strategy for synthesizing well-defined TiO2NTs–Au@Pd hybrid nanostructures with prior TiO2 nanotube functionalization (F-TiO2NTs). TiO2NTs with larger surface area (BET surface area is 184.9 m2 g−1) were synthesized by hydrothermal method, and the NTs are anatase phase with a range of 2–3 μm in length and 30–50 nm in diameter after calcined at 400 °C for 3 h. 3-Aminopropyl-trimethoxysilane (APTMS) as a coupling agent was reacted with the surface hydroxyl groups as anchoring sites for flower-shaped bimetallic Au@Pd nanostructures, self-assembling amine functionality on the surface of TiO2NTs. Note that two faces at the interface between F-TiO2NTs with (004) plane and Au@Pd nanostructures with (111) one of cubic Au and Pd nanoparticles are compatible, benefiting to the charge transfer between two components due to their crystalline coordination. The results showed that as-prepared F-TiO2NTs–Au@Pd hybrid nanostructures modified glassy carbon electrode (GCE) exhibits high electrocatalytic activity toward hydrazine (N2H4) at low potential and a linear response from 0.06 to 700 μM with the detection limit for N2H4 was found to be 1.2 × 10−8 M (S/N = 3). Based on scan rate effect during the hydrazine oxidation, it indicates that the number of electrons transferred in the rate-limiting step is 1, and a transfer coefficient (α) is estimated as 0.73. The self-assembled F-TiO2NTs–Au@Pd hybrid nanostructures as enhanced materials present excellent electrocatalytic activity, fast response, highly sensitive and have a promising application potential in nonenzymatic sensing. - Highlights: • Flower Au@Pd nanoparticles -TiO2 nanotubes (NTs) hybrid nanostructures were prepared by a self-assembled technique. • (004) plane of TiO2NTs and (111) one of Au@Pd nanoparticles at the interface are compatible. • The electrochemical sensor exhibits high activity toward hydrazine (N2H4)

  15. Optimization of Pt and Pd Displacement Process of Au Reduced Solution

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    The question existed in the displacement of platinum and palladium from Au reduced solution was analyzed. The process optimization scheme was put forward and adopted to practice and has achieved a good result.

  16. Focused-ion-beam-fabricated Au nanorods coupled with Ag nanoparticles used as surface-enhanced Raman scattering-active substrate for analyzing trace melamine constituents in solution

    Energy Technology Data Exchange (ETDEWEB)

    Sivashanmugan, Kundan [Department of Materials Science and Engineering, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Liao, Jiunn-Der, E-mail: jdliao@mail.ncku.edu.tw [Department of Materials Science and Engineering, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Center for Micro/Nano Science and Technology, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Liu, Bernard Haochih; Yao, Chih-Kai [Department of Materials Science and Engineering, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China)

    2013-10-24

    Graphical abstract: -- Highlights: •Well-ordered Au-nanorod array with a controlled tip ring diameter (Au{sub N}Rs{sub d}) is made by focused ion beam. •Au{sub N}Rs{sub d} coupled with Ag nanoparticles (Ag NPs/Au{sub N}Rs{sub d}) is competent to sense target molecules in a solution. •Ag NPs/Au{sub N}Rs{sub d} SERS active substrate can detect a single molecule of crystal violet. •Ag NPs/Au{sub N}Rs{sub d} as a SERS-active substrate can distinguish melamine contaminants at low concentrations (e.g., 10{sup −12} M). -- Abstract: A well-ordered Au-nanorod array with a controlled tip ring diameter (Au{sub N}Rs{sub d}) was fabricated using the focused ion beam method. Au{sub N}Rs{sub d} was then coupled with Ag nanoparticles (Ag NPs) to bridge the gaps among Au nanorods. The effect of surface-enhanced Raman scattering (SERS) on Au{sub N}Rs{sub d} and Ag NPs/Au{sub N}Rs{sub d} was particularly verified using crystal violet (CV) as the molecular probe. Raman intensity obtained from a characteristic peak of CV on Au{sub N}Rs{sub d} was estimated by an enhancement factor of ≈10{sup 7} in magnitude, which increased ≈10{sup 12} in magnitude for that on Ag NPs/Au{sub N}Rs{sub d}. A highly SERS-active Ag NPs/Au{sub N}Rs{sub d} was furthermore applied for the detection of melamine (MEL) at very low concentrations. Raman-active peaks of MEL (10{sup −3} to 10{sup −12} M) in water or milk solution upon Au{sub N}Rs{sub d} or Ag NPs/Au{sub N}Rs{sub d} were well distinguished. The peaks at 680 and 702 cm{sup −1} for MEL molecules were found suitable to be used as the index for sensing low-concentration MEL in a varied solution, while that at 1051 cm{sup −1} was practical to interpret MEL molecules in water or milk solution bonded with Au (i.e., Au{sub N}Rs{sub d}) or Ag (i.e., Ag NPs/Au{sub N}Rs{sub d}) surface. At the interface of Ag NPs/Au{sub N}Rs{sub d} and MEL molecules in milk solution, a laser-induced electromagnetic field or hotspot effect was produced and

  17. Electrochemical and surface studies on the passivity of a dental Pd-based casting alloy in alkaline sulphide solution

    International Nuclear Information System (INIS)

    The corrosion and tarnish behavior of a dental casting Pd-25Ag-18Cu-12Au alloy in 0.1% Na2S solution at 37 deg. C was investigated using potentiodynamic polarization and spectrocolorimetric techniques. The surface film was characterized by X-ray photoelectron spectroscopy (XPS). This alloy exhibited markedly higher resistance to corrosion and tarnish than did the Ag-20Pd-18Cu-12Au alloy in current clinical use. XPS spectra indicated the presence of a thin sulphide film composed of PdS. It was found that the PdS film is very protective and is responsible for the passivity of the Pd-25Ag-18Cu-12Au alloy in 0.1% Na2S solution

  18. Studies of the AgM5N45N4.5 spectrum of disordered Ag0.5Pd0.5 alloy by Auger photoelectron coincidence spectroscopy (APECS)

    International Nuclear Information System (INIS)

    Full text: The Auger electron emission process from solids is very complex, with a range of intrinsic processes producing intensity in final spectra. These processes can include the basic Auger process, initial- and final-states, shake-up/off and Coster-Kronig (CK) processes. Auger Photoelectron Coincidence Spectroscopy (APECS) is a technique to detect the Auger electron only when the 'initial' photoelectron also is detected. By counting those Auger electrons that arrive in coincidence with a photoelectron of certain binding energy, the initial state is uniquely determined, thus controlling the magnitude of various satellites of the Auger spectrum. AxPd1-x is a disordered alloy. XPS spectra indicated that the FWHM of Ag 3d5/2 increases from 0.56 eV in pure Ag to 0.77 eV in Ag0.5Pd0.5. The disorder broadening of the Ag 3d core line in AgPd is due to the spread of local potentials in the atomic cores arising from the effects of charge transfer. In this study, an effect of disorder broadening of the core level photoelectron line on the Ag MVV Auger spectra in random substituted Ag0.5Pd0.5 alloy has been investigated by APECS. Data were collected for the AgM5V45V45 Auger line in coincidence with Ag 3d photoelectron lines. It is shown that the broadening of the AgM5V45V45 line is directly associated with the presence of disorder broadening of the Ag 3d5/2 photoelectron line

  19. Brazing of zirconia to titanium using Ag-Cu and Au-Ni filler alloys

    Directory of Open Access Journals (Sweden)

    Jean S. Pimenta

    2013-12-01

    Full Text Available Advanced ceramic is usually joined to metal by the well-known direct brazing process, where costly active filler alloys can be considered a limitation. Brazing using active-metal-free filler alloy as insert between the joint components is an attempt to overcome it. The active metal diffusion from the titanium member through the bulk of molten filler to the ceramic was responsible to produce an active filler alloy in loco and promote reduction of the zirconium oxide to improve wetting on the ceramic surface. Unalloyed titanium was joined in a high-vacuum furnace (<3x10-5 mbar to yttria-tetragonal zirconia polycristals (Y-TZP and zirconia partially stabilized with magnesia (Mg-PSZ, where commercial fillers Ag-28Cu and Au-18Ni with respective thermal cycles were evaluated. Helium gas leak detection test was performed at the ceramic/metal interface at room temperature; samples from reliable vacuum tight joints were examined by microstructural analysis techniques and energy dispersive X-ray analysis at the joint cross-section. Tight joints were produced with eutectic Ag-Cu filler, revealing an intermetallic layer and a dark reaction layer near the ceramic surface; titanium diffusion was efficient for superficial chemical interactions between individual components. Brazing joints were also tested using three-point flexure testing.

  20. Synthesis and Optical Properties of Au-Ag Alloy Nanoclusters with Controlled Composition

    Directory of Open Access Journals (Sweden)

    J. F. Sánchez-Ramírez

    2008-01-01

    Full Text Available Colloidal solid-solution-like Au-Ag alloy nanoclusters of different compositions were synthesized through citrate reduction of mixed metal ions of low concentrations, without using any other protective or capping agents. Optical absorption of the alloy nanoclusters was studied both theoretically and experimentally. The position of the surface plasmon resonance (SPR absorption band of the nanoclusters could be tuned from 419 nm to 521 nm through the variation of their composition. Considering effective dielectric constant of the alloy, optical absorption spectra for the nanoclusters were calculated using Mie theory, and compared with the experimentally obtained spectra. Theoretically obtained optical spectra well resembled the experimental spectra when the true size distribution of the nanoparticles was considered. High-resolution transmission electron microscopy (HREM, high-angle annular dark field (HAADF imaging, and energy dispersive spectroscopy (EDS revealed the true alloy nature of the nanoparticles with nominal composition being preserved. The synthesis technique can be extended to other bimetallic alloy nanoclusters containing Ag.

  1. Investigation of nanostructured Pd-Ag/n-ZnO thin film based Schottky junction for methane sensing

    Science.gov (United States)

    Roy, S.; Das, S.; Sarkar, C. K.

    2016-07-01

    Undoped nanocrystalline n-type ZnO thin film was deposited by chemical deposition technique on a thermally oxidized p-Si (~5 Ω cm resistivity and orientation) substrate. Formation of stable zinc oxide thin film was confirmed by two-dimensional X-Ray Diffraction (XRD) and EDX analysis. The average crystallite size of the ZnO sample was evaluated as ~50 nm. The surface was characterized by Field Emission Scanning Electron Microscopy (FESEM) and Atomic Force Microscopy (AFM) that confirm the formation of nanocrystalline (grain size ~50 nm) ZnO thin film with surface roughness of ~100 nm. Good conversion of precursor into ZnO thin film in the chemical deposition method was evident by Fourier Transform Infrared Spectroscopy (FTIR). A small peak at 479 cm-1was observed in the FTIR spectrum confirming the formation of quartzite structure of the ZnO. The band gap (~3.44 eV) of the material was calculated from the optical absorption spectroscopy. To prepare Pd-Ag/n-ZnO Schottky junction, Pd-Ag contacts were taken by electron beam evaporation method. I-V characteristics of the junction were studied at different temperatures in inert and reducing ambient (N2 and N2 + CH4) with turn on voltage of around 0.2 V. The parameters like ideality factor ( η), saturation current ( I 0), series resistance ( Rs), and barrier height ( Φ BO) of the junction were calculated in the temperature range 50-200 °C in N2 as well as in 1 % CH4 + N2 ambient. It was observed that the ideality factor decreases in the temperature range 50-200 °C ( η = 12.34 at 50 °C and η = 1.52 at 200 °C) in N2 ambient and η = 1.18 in N2 +CH4 ambient at 200 °C. Schottky Barrier Height ( Φ BO) of the Pd-Ag/n-ZnO junction was found to increase with temperature. A close observation of Pd-Ag/n-ZnO junction in the presence of methane was performed to appreciate its application as methane sensor. The sensing mechanism was illustrated by a simplified energy band diagram.

  2. Integration of Methane Steam Reforming and Water Gas Shift Reaction in a Pd/Au/Pd-Based Catalytic Membrane Reactor for Process Intensification

    Science.gov (United States)

    Castro-Dominguez, Bernardo; Mardilovich, Ivan P.; Ma, Liang-Chih; Ma, Rui; Dixon, Anthony G.; Kazantzis, Nikolaos K.; Ma, Yi Hua

    2016-01-01

    Palladium-based catalytic membrane reactors (CMRs) effectively remove H2 to induce higher conversions in methane steam reforming (MSR) and water-gas-shift reactions (WGS). Within such a context, this work evaluates the technical performance of a novel CMR, which utilizes two catalysts in series, rather than one. In the process system under consideration, the first catalyst, confined within the shell side of the reactor, reforms methane with water yielding H2, CO and CO2. After reforming is completed, a second catalyst, positioned in series, reacts with CO and water through the WGS reaction yielding pure H2O, CO2 and H2. A tubular composite asymmetric Pd/Au/Pd membrane is situated throughout the reactor to continuously remove the produced H2 and induce higher methane and CO conversions while yielding ultrapure H2 and compressed CO2 ready for dehydration. Experimental results involving (i) a conventional packed bed reactor packed (PBR) for MSR, (ii) a PBR with five layers of two catalysts in series and (iii) a CMR with two layers of two catalysts in series are comparatively assessed and thoroughly characterized. Furthermore, a comprehensive 2D computational fluid dynamics (CFD) model was developed to explore further the features of the proposed configuration. The reaction was studied at different process intensification-relevant conditions, such as space velocities, temperatures, pressures and initial feed gas composition. Finally, it is demonstrated that the above CMR module, which was operated for 600 h, displays quite high H2 permeance and purity, high CH4 conversion levels and reduced CO yields. PMID:27657143

  3. Optimised photocatalytic hydrogen production using core–shell AuPd promoters with controlled shell thickness

    DEFF Research Database (Denmark)

    Jones, Wilm; Su, Ren; Wells, Peter;

    2014-01-01

    of these materials towards the reforming of alcohols for hydrogen production. The core–shell structured Au–Pd bimetallic nanoparticle supported on TiO2 has being of interest as it exhibited extremely high quantum efficiencies for hydrogen production. However, the effect of shell composition and thickness...

  4. Rapid Synthesis of Highly Monodisperse Au x Ag 1− x Alloy Nanoparticles via a Half-Seeding Approach

    KAUST Repository

    Chng, Ting Ting

    2011-05-03

    Gold-silver alloy AuxAg1-x is an important class of functional materials promising new applications across a wide array of technological fields. In this paper, we report a fast and facile synthetic protocol for preparation of highly monodisperse AuxAg1-x alloy nanoparticles in the size range of 3-6 nm. The precursors employed in this work are M(I)-alkanethiolates (M = Au and Ag), which can be easily prepared by mixing common chemicals such as HAuCl4 or AgNO3 with alkanethiols at room temperature. In this half-seeding approach, one of the M(I)-alkanethiolates is first heated and reduced in oleylamine solvent, and freshly formed metal clusters will then act as premature seeds on which both the first and second metals (from M(I)-alkanethiolates, M = Au and Ag) can grow accordingly without additional nucleation and thus achieve high monodispersity for product alloy nanoparticles. Unlike in other prevailing methods, both Au and Ag elements present in these solid precursors are in the same monovalent state and have identical supramolecular structures, which may lead to a more homogeneous reduction and complete interdiffusion at elevated reaction temperatures. When the M(I)-alkanethiolates are reduced to metallic forms, the detached alkanethiolate ligands will serve as capping agent to control the growth. More importantly, composition, particle size, and optical properties of AuxAg1-x alloy nanoparticles can be conveniently tuned with this approach. The optical limiting properties of the prepared particles have also been investigated at 532 and 1064 nm using 7 ns laser pulses, which reveals that the as-prepared alloy nanoparticles exhibit outstanding broadband optical limiting properties with low thresholds. © 2011 American Chemical Society.

  5. Organic-Inorganic Hybrid Nanoparticles for Bacterial Inhibition: Synthesis and Characterization of Doped and Undoped ONPs with Ag/Au NPs

    Directory of Open Access Journals (Sweden)

    Carlos Alberto Huerta Aguilar

    2015-04-01

    Full Text Available Organic nanoparticles (ONPs of lipoic acid and its doped derivatives ONPs/Ag and ONPs/Au were prepared and characterized by UV-Visible, EDS, and TEM analysis. The antibacterial properties of the ONPs ONPs/Ag and ONPs/Au were tested against bacterial strains (Staphylococcus aureus, Bacillus cereus, Escherichia coli and Salmonella typhi. Minimal Inhibitory Concentration (MIC and bacterial growth inhibition tests show that ONPs/Ag are more effective in limiting bacterial growth than other NPs, particularly, for Gram positive than for Gram-negative ones. The order of bacterial cell growth inhibition was ONPs/Ag > ONPs > ONPs/Au. The morphology of the cell membrane for the treated bacteria was analyzed by SEM. The nature of bond formation of LA with Ag or Au was analyzed by molecular orbital and density of state (DOS using DFT.

  6. Bi-SERS sensing and enhancement by Au-Ag bimetallic non-alloyed nanoparticles on amorphous and crystalline silicon substrate.

    Science.gov (United States)

    Tan, Chee Leong; Lee, Soo Kyung; Lee, Yong Tak

    2015-03-01

    We have demonstrated Au-Ag bimetallic non-alloy nanoparticles (BNNPs) on thin a-Si film and c-Si substrate for high SERS enhancement, low cost, high sensitivity and reproducible SERS substrate with bi-SERS sensing properties where two different SERS peak for Au NPs and Ag NPs are observed on single SERS substrate. The isolated Au-Ag bimetallic NPs, with uniform size and spacing distribution, are suitable for uniform high density hotspot SERS enhancement. The SERS enhancement factor of Au-Ag BNNPs is 2.9 times higher compared to Ag NPs on similar substrates due to the increase of the localized surface plasmon resonance effect. However there is a decrement of SERS peak intensity at specific wavenumbers when the surrounding refractive index increases due to out-phase hybridization of Au NPs. The distinct changes of the two different SERS peaks on single Au-Ag BNNPs SERS substrate due to Au and Ag NPs independently show possible application for bi-molecular sensing. PMID:25836846

  7. Influence of silver on the glycerol electro-oxidation over AuAg/C catalysts in alkaline medium: a cyclic voltammetry and in situ FTIR spectroscopy study

    International Nuclear Information System (INIS)

    In the present work, we investigated the influence of silver on the glycerol electro-oxidation over carbon-supported AuAg catalysts by cyclic voltammetry and in situ FTIR spectroscopy. We observed that the presence of Ag in the bimetallic materials provided a more efficient catalyst in terms of the ability to electro-oxidize glycerol at relatively low potentials. On the other hand, the bimetallic catalysts were found to be less promising than the Au/C catalyst with respect to the reaction rate. Ag addition influenced the mechanism of glycerol electro-oxidation, favoring the C-C-C bond breaking, as evidenced by the selective formation of formic acid on the bimetallic catalysts. The impact of Ag on the glycerol electro-oxidation over AuAg/C may be driven by electronic modifications and Ag segregation on the catalysts surface

  8. Ultrasensitive electrochemical sensor for Hg(2+) by using hybridization chain reaction coupled with Ag@Au core-shell nanoparticles.

    Science.gov (United States)

    Li, Zongbing; Miao, Xiangmin; Xing, Ke; Peng, Xue; Zhu, Aihua; Ling, Liansheng

    2016-06-15

    A novel electrochemical biosensor for Hg(2+) detection was reported by using DNA-based hybridization chain reaction (HCR) coupled with positively charged Ag@Au core-shell nanoparticles ((+)Ag@Au CSNPs) amplification. To construct the sensor, capture probe (CP ) was firstly immobilized onto the surface of glass carbon electrode (GCE). In the presence of Hg(2+), the sandwiched complex can be formed between the immobilized CP on the electrode surface and the detection probe (DP) modified on the gold nanoparticles (AuNPs) based on T-Hg(2+)-T coordination chemistry. The carried DP then opened two ferrocene (Fc) modified hairpin DNA (H1 and H2) in sequence and propagated the happen of HCR to form a nicked double-helix. Numerous Fc molecules were formed on the neighboring probe and produced an obvious electrochemical signal. Moreover, (+)Ag@Au CSNPs were assembly onto such dsDNA polymers as electrochemical signal enhancer. Under optimal conditions, such sensor presents good electrochemical responses for Hg(2+) detection with a detection limit of 3.6 pM. Importantly, the methodology has high selectivity for Hg(2+) detection. PMID:26852203

  9. Synthesis and photo physical properties of Au - Ag (core - shell) nanoparticles disperse in poly vinyl alcohol matrix

    International Nuclear Information System (INIS)

    Synthesis of core - shell (Au - Ag) nanoparticle with varying silver composition has been carried out in aqueous poly vinyl alcohol (PVA) matrix. Core gold nanoparticle (∼15 nm) has been synthesized through seed-mediated growth process. Synthesis of silver shell with increasing thickness (∼1–5 nm) has been done by reducing Ag+ over the gold sol in the presence of mild reducing ascorbic acid. Characterization of Au - Ag nanoparticles has been done by UV–Vis, High resolution transmission electron microscope (HRTEM) and energy dispersive X-ray (EDX) spectroscopic study. The blue shift of surface plasmon resonance (SPR) band with increasing mole fraction of silver has been interpreted due to dampening of core, i.e. Au SPR by Ag. The dependence of nonlinear optical response of spherical core - shell nanoparticles has been investigated as a function of relative composition of each metal. Simulation of SPR extinction spectra based on quasi-static theory is done. A comparison of our experimental and the simulated extinction spectra using quasi-static theory of nanoshell suggests that our synthesized bimetallic particles have core - shell structure rather than bimetallic alloy particles.

  10. One-step Solution Processing of Ag, Au and Pd@MXene Hybrids for SERS.

    Science.gov (United States)

    Satheeshkumar, Elumalai; Makaryan, Taron; Melikyan, Armen; Minassian, Hayk; Gogotsi, Yury; Yoshimura, Masahiro

    2016-01-01

    We report on one-step hybridization of silver, gold and palladium nanoparticles from solution onto exfoliated two-dimensional (2D) Ti3C2 titanium carbide (MXene) nanosheets. The produced hybrid materials can be used as substrates for surface-enhanced Raman spectroscopy (SERS). An approximate analytical approach is also developed for the calculation of the surface plasmon resonance (SPR) frequency of nanoparticles immersed in a medium, near the interface of two dielectric media with different dielectric constants. We obtained a good match with the experimental data for SPR wavelengths, 440 nm and 558 nm, respectively for silver and gold nanoparticles. In the case of palladium, our calculated SPR wavelength for the planar geometry was 160 nm, demonstrating that non-spherical palladium nanoparticles coupled with 2D MXene yield a broad, significanlty red-shifted SPR band with a peak at 230 nm. We propose a possible mechanism of the plasmonic hybridization of nanoparticles with MXene. The as-prepared noble metal nanoparticles on MXene show a highly sensitive SERS detection of methylene blue (MB) with calculated enhancement factors on the order of 10(5). These findings open a pathway for extending visible-range SERS applications of novel 2D hybrid materials in sensors, catalysis, and biomedical applications. PMID:27557838

  11. One-step Solution Processing of Ag, Au and Pd@MXene Hybrids for SERS

    Science.gov (United States)

    Satheeshkumar, Elumalai; Makaryan, Taron; Melikyan, Armen; Minassian, Hayk; Gogotsi, Yury; Yoshimura, Masahiro

    2016-08-01

    We report on one-step hybridization of silver, gold and palladium nanoparticles from solution onto exfoliated two-dimensional (2D) Ti3C2 titanium carbide (MXene) nanosheets. The produced hybrid materials can be used as substrates for surface-enhanced Raman spectroscopy (SERS). An approximate analytical approach is also developed for the calculation of the surface plasmon resonance (SPR) frequency of nanoparticles immersed in a medium, near the interface of two dielectric media with different dielectric constants. We obtained a good match with the experimental data for SPR wavelengths, 440 nm and 558 nm, respectively for silver and gold nanoparticles. In the case of palladium, our calculated SPR wavelength for the planar geometry was 160 nm, demonstrating that non-spherical palladium nanoparticles coupled with 2D MXene yield a broad, significanlty red-shifted SPR band with a peak at 230 nm. We propose a possible mechanism of the plasmonic hybridization of nanoparticles with MXene. The as-prepared noble metal nanoparticles on MXene show a highly sensitive SERS detection of methylene blue (MB) with calculated enhancement factors on the order of 105. These findings open a pathway for extending visible-range SERS applications of novel 2D hybrid materials in sensors, catalysis, and biomedical applications.

  12. Ultrasensitive electrochemical aptasensor for the detection of thrombin based on dual signal amplification strategy of Au@GS and DNA-CoPd NPs conjugates.

    Science.gov (United States)

    Wang, Yaoguang; Zhang, Yong; Yan, Tao; Fan, Dawei; Du, Bin; Ma, Hongmin; Wei, Qin

    2016-06-15

    In this work, an ultrasensitive electrochemical aptasensor for the detection of thrombin was developed based on Au nanoparticles decorated graphene sheet (Au@GS) and CoPd binary nanoparticles (CoPd NPs). A sulfydryl-labeled thrombin capture probe (Apt1) and a biotin-labeled thrombin reporter probe (Apt2) were designed to achieve a sandwich-type strategy. Au@GS was used as a sensing platform for the facile immobilization of Apt1 through Au-S bond, forming a sensing interface for thrombin. The specific recognition of thrombin induced the attachment of Apt2-CoPd NPs to the electrode. The labeled CoPd NPs showed good catalytic properties toward the reduction of H2O2, resulting in an amperometric signal. The amperometric response was correlated to the thrombin concentration in sample solutions. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) confirmed the successful fabrication of the aptasensor. A linear response to thrombin in the range of 0.01-2.00 ng mL(-1) with a low detection limit (5 pg mL(-1)) was achieved. The proposed aptasensor showed good selectivity, good reproducibility and acceptable stability. This proposed strategy may find many potential applications in the detection of other biomolecules.

  13. Room temperature hydrogen generation from hydrolysis of ammonia-borane over an efficient NiAgPd/C catalyst

    KAUST Repository

    Hu, Lei

    2014-12-01

    NiAgPd nanoparticles are successfully synthesized by in-situ reduction of Ni, Ag and Pd salts on the surface of carbon. Their catalytic activity was examined in ammonia borane (NH3BH3) hydrolysis to generate hydrogen gas. This nanomaterial exhibits a higher catalytic activity than those of monometallic and bimetallic counterparts and a stoichiometric amount of hydrogen was produced at a high generation rate. Hydrogen production rates were investigated in different concentrations of NH3BH3 solutions, including in the borates saturated solution, showing little influence of the concentrations on the reaction rates. The hydrogen production rate can reach 3.6-3.8 mol H2 molcat -1 min-1 at room temperature (21 °C). The activation energy and TOF value are 38.36 kJ/mol and 93.8 mol H2 molcat -1 min-1, respectively, comparable to those of Pt based catalysts. This nanomaterial catalyst also exhibits excellent chemical stability, and no significant morphology change was observed from TEM after the reaction. Using this catalyst for continuously hydrogen generation, the hydrogen production rate can be kept after generating 6.2 L hydrogen with over 10,000 turnovers and a TOF value of 90.3 mol H2 molcat -1 min-1.

  14. Development of Pd-Ag Compostie Membrane for Separation of Hydrogen at Elevated Temperature

    Energy Technology Data Exchange (ETDEWEB)

    Shamsuddin Ilias

    2009-02-28

    Pd-based membrane reactor offers the possibility of combining reaction and separation in a single operation at high temperatures to overcome the equilibrium limitations experienced in conventional reactor configurations. In this project to develop a defect-free and hermally-stable Pd-film on microporous stainless steel (MPSS) support for H2-separation and membrane reactor applications, the electroless plating process was revisited with an aim to improve the membrane morphology. Specifically, this study includes; (a) an improvement f activation step using Pulse Laser Deposition (PLD), (b) development of a novel surfactant induced electroless plating (SIEP) for depositing robust Pd-film on microporous support, and (c) application of Pd-membrane as membrane reactor in steam methanol reforming (SMR) reactions.

  15. Sensitive electrochemical sensors for simultaneous determination of ascorbic acid, dopamine, and uric acid based on Au@Pd-reduced graphene oxide nanocomposites

    Science.gov (United States)

    Jiang, Jingjing; Du, Xuezhong

    2014-09-01

    Sensitive electrochemical sensors were fabricated with reduced graphene oxide-supported Au@Pd (Au@Pd-RGO) nanocomposites by one-step synthesis for individual and simultaneous determination of ascorbic acid (AA), dopamine (DA), and uric acid (UA) with low detection limits and wide concentration ranges. From the Au@Pd-RGO-modified electrodes, well-separated oxidation peaks and enhanced peak currents of AA, DA, and UA were observed owing to the superior conductivity of RGO and the excellent catalytic activity of Au@Pd nanoparticles. For individual detection, the linear responses of AA, DA, and UA were in the concentration ranges of 0.1-1000, 0.01-100, and 0.02-500 μM with detection limits of 0.02, 0.002, and 0.005 μM (S/N = 3), respectively. For simultaneous detection by synchronous change of the concentrations of AA, DA, and UA, the linear response ranges were 1-800, 0.1-100, and 0.1-350 μM with detection limits of 0.28, 0.024, and 0.02 μM (S/N = 3), respectively. The fabricated sensors were further applied to the detection of AA, DA, and UA in urine samples. The Au@Pd-RGO nanocomposites have promising applications in highly sensitive and selective electrochemical sensing.Sensitive electrochemical sensors were fabricated with reduced graphene oxide-supported Au@Pd (Au@Pd-RGO) nanocomposites by one-step synthesis for individual and simultaneous determination of ascorbic acid (AA), dopamine (DA), and uric acid (UA) with low detection limits and wide concentration ranges. From the Au@Pd-RGO-modified electrodes, well-separated oxidation peaks and enhanced peak currents of AA, DA, and UA were observed owing to the superior conductivity of RGO and the excellent catalytic activity of Au@Pd nanoparticles. For individual detection, the linear responses of AA, DA, and UA were in the concentration ranges of 0.1-1000, 0.01-100, and 0.02-500 μM with detection limits of 0.02, 0.002, and 0.005 μM (S/N = 3), respectively. For simultaneous detection by synchronous change of the

  16. Sensitive determination of dopamine in the presence of uric acid and ascorbic acid using TiO2 nanotubes modified with Pd, Pt and Au nanoparticles.

    Science.gov (United States)

    Mahshid, Sara; Li, Chengcheng; Mahshid, Sahar Sadat; Askari, Masoud; Dolati, Abolghasem; Yang, Lixia; Luo, Shenglian; Cai, Qingyun

    2011-06-01

    A simple modified TiO(2) nanotubes electrode was fabricated by electrodeposition of Pd, Pt and Au nanoparticles. The TiO(2) nanotubes electrode was prepared using the anodizing method, followed by modifying Pd nanoparticles onto the tubes surface, offering a uniform conductive surface for electrodeposition of Pt and Au. The performance of the modified electrode was characterized by cyclic voltammetry and differential pulse voltammetry methods. The Au/Pt/Pd/TiO(2) NTs modified electrode represented a high sensitivity towards individual detection of dopamine as well as simultaneous detection of dopamine and uric acid using 0.1 M phosphate buffer solution (pH 7.00) as the base solution. In both case, electro-oxidation peak currents of dopamine were linearly related to accumulated concentration over a wide concentration range of 5.0 × 10(-8) to 3.0 × 10(-5) M. However in the same range of dopamine concentration, the sensitivity had a significant loss at Pt/Pd/TiO(2) NTs electrode, suggesting the necessity for Au nanoparticles in modified electrode. The limit of the detection was determined as 3 × 10(-8) M for dopamine at signal-to-noise ratio equal to 3. Furthermore, the Au/Pt/Pd/TiO(2) NTs modified electrode was able to distinguish the oxidation response of dopamine, uric acid and ascorbic acid in mixture solution of different acidity. It was shown that the modified electrode possessed a very good reproducibility and long-term stability. The method was also successfully applied for determination of DA in human urine samples with satisfactory results. PMID:21494708

  17. Surface plasmon dispersion engineering via double-metallic AU/AG layers for nitride light-emitting diodes

    Science.gov (United States)

    Tansu, Nelson; Zhao, Hongping; Zhang, Jing; Liu, Guangyu

    2014-04-01

    A double-metallic deposition process is used whereby adjacent layers of different metals are deposited on a substrate. The surface plasmon frequency of a base layer of a first metal is tuned by the surface plasmon frequency of a second layer of a second metal formed thereon. The amount of tuning is dependent upon the thickness of the metallic layers, and thus tuning can be achieved by varying the thicknesses of one or both of the metallic layers. In a preferred embodiment directed to enhanced LED technology in the green spectrum regime, a double-metallic Au/Ag layer comprising a base layer of gold (Au) followed by a second layer of silver (Ag) formed thereon is deposited on top of InGaN/GaN quantum wells (QWs) on a sapphire/GaN substrate.

  18. Synthesis of Ag-Au bimetallic film at liquid-liquid interface and its application in vapor sensing

    Energy Technology Data Exchange (ETDEWEB)

    Pasricha, Renu, E-mail: pasrichar@mail.nplindia.ernet.i [Material Characterization Division, National Physical Laboratory, New Delhi-110012 (India); Gupta, Shweta [Material Characterization Division, National Physical Laboratory, New Delhi-110012 (India); Sastry, M. [Tata Chemical Innovation Center, Anmol Pride, Baner Road, Pune-45 (India); Singh, Nahar; Gupta, Prabhat [Material Characterization Division, National Physical Laboratory, New Delhi-110012 (India)

    2010-11-30

    We demonstrate a novel process for preparing densely packed film of silver nanoparticles at the liquid-liquid interface followed by a transmetallation reaction with gold ion to yield a film of bimetallic nanoparticles. Films of assembled silver as well as Ag-Au bimetallic were characterized by UV-vis-spectroscopy, transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) analysis. I-V measurement shows linear behavior for both the films with ca. five orders of magnitude drop in resistance for the Ag-Au bimetallic film. Temperature dependent I-V measurement revealed a semiconductor to metal transition after transmetallation reaction. The films where checked for their potential application in chemical vapor sensing to ammonia vapors.

  19. Broadband light absorption enhancement in dye-sensitized solar cells with Au-Ag alloy popcorn nanoparticles

    Science.gov (United States)

    Xu, Qi; Liu, Fang; Liu, Yuxiang; Cui, Kaiyu; Feng, Xue; Zhang, Wei; Huang, Yidong

    2013-07-01

    In this paper, we present an investigation on the use of Au-Ag alloy popcorn-shaped nanoparticles (NPs) to realise the broadband optical absorption enhancement of dye-sensitized solar cells (DSCs). Both simulation and experimental results indicate that compared with regular plasmonic NPs, such as nano-spheres, irregular popcorn-shaped alloy NPs exhibit absorption enhancement over a broad wavelength range due to the excitation of localized surface plasmons (LSPs) at different wavelengths. The power conversion efficiency (PCE) of DSCs is enhanced by 16% from 5.26% to 6.09% by incorporating 2.38 wt% Au-Ag alloy popcorn NPs. Moreover, by adding a scattering layer on the exterior of the counter electrode, the popcorn NPs demonstrate an even stronger ability to increase the PCE by 32% from 5.94% to 7.85%, which results from the more efficient excitation of the LSP mode on the popcorn NPs.

  20. Fano effect in the angle-integrated valence band photoemission of the noble metals Cu, Ag, and Au

    International Nuclear Information System (INIS)

    Results of a combined experimental and theoretical investigation on the Fano-effect in the angle-integrated valence band photoemission of the noble metals are presented. In line with the fact that the Fano-effect is caused by the spin-orbit-coupling, the observed spin polarization of the photocurrent was found to be the more pronounced the higher the atomic number of the element investigated. The ratio of the normalized spin difference curves, however, agreed only for Cu and Ag with the ratio of the corresponding spin-orbit coupling strength parameters. The deviation from this expected behavior in the case of Au could be explained by the properties of individual d-p- and d-f-contributions to the total spin difference curves, that were found to be quite different for Au compared to Cu and Ag

  1. Fluid inclusion chemistry of adularia-sericite epithermal Au-Ag deposits of the southern Hauraki Goldfield, New Zealand

    Science.gov (United States)

    Simpson, Mark P.; Strmic Palinkas, Sabina; Mauk, Jeffrey L.; Bodnar, Robert J.

    2015-01-01

    Microthermometry, laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), and Raman spectroscopy have been used to determine the temperature, apparent salinity, and composition of individual fluid inclusions in adularia-sericite Au-Ag epithermal veins from the Karangahake, Martha, Favona, and Waitekauri deposits, southern Hauraki goldfield, New Zealand. Quartz veins contain colloform to crustiform bands that alternate with coarse-grained quartz and amethyst. The ore mineralization occurs only in colloform to crustiform bands.

  2. Broadband light absorption enhancement in dye-sensitized solar cells with Au-Ag alloy popcorn nanoparticles

    OpenAIRE

    Qi Xu; Fang Liu; Yuxiang Liu; Kaiyu Cui; Xue Feng; , Wei Zhang; Yidong Huang

    2013-01-01

    In this paper, we present an investigation on the use of Au-Ag alloy popcorn-shaped nanoparticles (NPs) to realise the broadband optical absorption enhancement of dye-sensitized solar cells (DSCs). Both simulation and experimental results indicate that compared with regular plasmonic NPs, such as nano-spheres, irregular popcorn-shaped alloy NPs exhibit absorption enhancement over a broad wavelength range due to the excitation of localized surface plasmons (LSPs) at different wavelengths. The ...

  3. Stopping Power of Be, Al, Cu, Ag, Pt, and Au for 5-12-MeV Protons and Deuterons

    DEFF Research Database (Denmark)

    Andersen, H.H.; Hanke, C.; Sørensen, H.;

    1967-01-01

    Recent measurements on stopping power of aluminum have been continued with the stopping materials Be, Cu, Ag, Pt, and Au. The method of measuring stopping powers utilizing a thermometric compensation technique working at liquid-helium temperature has been used. Results are obtained with a standard...... deviation of 0.3%, and agree with other published experimental results and with Bichsel's tabulated values within their stated errors....

  4. A label-free amperometric immunosensor for detection of zearalenone based on trimetallic Au-core/AgPt-shell nanorattles and mesoporous carbon

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Lei; Chao, Yingjun; Cao, Wei, E-mail: chm_caow@ujn.edu.cn; Wang, Yulan; Luo, Chuannan; Pang, Xuehui; Fan, Dawei; Wei, Qin, E-mail: sdjndxwq@163.com

    2014-10-17

    Highlights: • Au@AgPt nanorattles have special structure of Au-core and imperfect AgPt-shell. • Au@AgPt are proposed for the first time applied in electrochemical immunosensor. • Substrate materials MC/Au@AgPt possess excellent conductivity and high surface area. • The proposed immunosensor exhibits a low detection limit of 1.7 pg mL{sup −1}. - Abstract: A novel label-free amperometric immunosensor is proposed for the ultrasensitive detection of zearalenone (ZEN) based on mesoporous carbon (MC) and trimetallic nanorattles (core/shell particles with movable cores encapsulated in the shells). The nanorattles are composed of special Au-core and imperfect AgPt-shell structure (Au@AgPt). The Au@AgPt nanorattles are loaded onto the MC by physical adsorption. The structure of the Au@AgPt nanorattles was characterized by using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Energy dispersive X-ray spectroscopy (EDS) confirmed the composition of the synthesized nanorattles. Compared with monometallic and bimetallic nanoparticles (NPs), Au@AgPt nanorattles show a higher electron transfer rate due to the synergistic effect of the Au, Ag and Pt NPs. MC further improves the sensitivity of the immunosensor because of its extraordinarily large specific surface area, suitable pore arrangement and outstanding conductivity. The large specific surface area of MC and MC@Au@AgPt were characterized by the BET method. ZEN antibodies are immobilized onto the nanorattles via Ag–NH{sub 2} bonds and Pt–NH{sub 2} bonds. Cyclic voltammetry and square wave voltammetry were used to characterize the recognizability of ZEN. Under optimum experimental conditions, the proposed immunosensor exhibited a low detection limit (1.7 pg mL{sup −1}), a wide linear range (from 0.005 to 15 ng mL{sup −1}) as well as good stability, reproducibility and selectivity. The sensor can be used in clinical analysis.

  5. Formation of Cu, Ag and Au nanofiims under the influence of hydrogen atoms

    Directory of Open Access Journals (Sweden)

    Zhavzharov E. L.

    2015-12-01

    Full Text Available Due to their electrical properties, thin metallic films are widely used in modern micro- and nanoelectronics. These properties allow solving fundamental problems of surface and solid state physics. Up-to-date methods of producing thin films involve high vacuum or multi-stage processes, which calls for complicated equipment. The authors propose an alternative method of producing thin metallic films using atomic hydrogen. Exothermal reaction of atoms recombination in a molecule (about 4.5 eV / recombination act initiated on the solid surface by atomic hydrogen may stimulate local heating, spraying and surface atoms transfer. We investigated the process of atomic hydrogen treatment of Cu, Ag and Au metal films, obtained by thermal vacuum evaporation. There are two methods of obtaining nanofilms using atomic hydrogen treatment: sputtering and vapor-phase epitaxy. In the first method, a film is formed by reducing the thickness of the starting film. This method allows obtaining a film as thick as the monolayer. In the second method, a nanofilm is formed by deposition of metal atoms from the vapor phase. This method allows obtaining a film thickness from monolayer to ~10 nm. These methods allow creating nanofilms with controlled parameters and metal thickness. Such films would be technologically pure and have good adhesion.

  6. Dihydrogen bond interactions as a result of H2 cleavage at Cu, Ag and Au centres.

    Science.gov (United States)

    Grabowski, Sławomir J; Ruipérez, Fernando

    2016-05-14

    A quantum chemical study of H2 activation at fluorides of coinage metals, MF (M = Cu, Ag and Au), and its splitting was performed. The following reaction path was analyzed: FMH2→ FHHM → HMFH, where both the molecular complexes and the corresponding transition states have been characterized at the CCSD(T)/aug-cc-pVQZ//MP2/aug-cc-pVQZ level of theory. Further single-point CASSCF/CASPT2 calculations, including spin-orbit coupling effects, were also performed to analyze the role of non-dynamic correlation. The scalar relativistic effects are included via aug-cc-pVQZ-PP basis sets used for the metals. The dihydrogen-bonded copper (FHHCu) and silver (FHHAg) complexes are observed as a result of H2 cleavage, while the corresponding FHHAu gold complex is not found but the HAuHF arrangement is observed, instead. The energetic and geometrical parameters of the complexes have been analyzed and both the Quantum Theory of Atoms in Molecules approach and the Natural Bond Orbitals method were additionally applied to analyze the intermolecular interactions. PMID:27101741

  7. Characterization of Ag and Au nanoparticles created by nanosecond pulsed laser ablation in double distilled water

    Energy Technology Data Exchange (ETDEWEB)

    Nikolov, A.S., E-mail: anastas_nikolov@abv.bg [Institute of Electronics, Bulgarian Academy of Sciences, Tzarigradsko shousse 72, Sofia 1784 (Bulgaria); Nedyalkov, N.N.; Nikov, R.G.; Atanasov, P.A. [Institute of Electronics, Bulgarian Academy of Sciences, Tzarigradsko shousse 72, Sofia 1784 (Bulgaria); Alexandrov, M.T. [Institute of Experimental Pathology and Parasitology, Bulgarian Academy of Sciences, G. Bonchev Street, bl. 25, Sofia 1113 (Bulgaria)

    2011-04-01

    Pulsed laser ablation of Ag and Au targets, immersed in double-distilled water is used to synthesize metallic nanoparticles (NPs). The targets are irradiated for 20 min by laser pulses at different wavelengths-the fundamental and the second harmonic (SHG) ({lambda} = 1064 and 532 nm, respectively) of a Nd:YAG laser system. The ablation process is performed at a repetition rate of 10 Hz and with pulse duration of 15 ns. Two boundary values of the laser fluence for each wavelength under the experimental conditions chosen were used-it varied from several J/cm{sup 2} to tens of J/cm{sup 2}. Only as-prepared samples were measured not later than two hours after fabrication. The NPs shape and size distribution were evaluated from transmission electron microscopy (TEM) images. The suspensions obtained were investigated by optical transmission spectroscopy in the near UV and in the visible region in order to get information about these parameters. Spherical shape of the NPs at the low laser fluence and appearance of aggregation and building of nanowires at the SHG and high laser fluence was seen. Dependence of the mean particle size at the SHG on the laser fluence was established. Comments on the results obtained have been also presented.

  8. Characterization of Ag and Au nanoparticles created by nanosecond pulsed laser ablation in double distilled water

    International Nuclear Information System (INIS)

    Pulsed laser ablation of Ag and Au targets, immersed in double-distilled water is used to synthesize metallic nanoparticles (NPs). The targets are irradiated for 20 min by laser pulses at different wavelengths-the fundamental and the second harmonic (SHG) (λ = 1064 and 532 nm, respectively) of a Nd:YAG laser system. The ablation process is performed at a repetition rate of 10 Hz and with pulse duration of 15 ns. Two boundary values of the laser fluence for each wavelength under the experimental conditions chosen were used-it varied from several J/cm2 to tens of J/cm2. Only as-prepared samples were measured not later than two hours after fabrication. The NPs shape and size distribution were evaluated from transmission electron microscopy (TEM) images. The suspensions obtained were investigated by optical transmission spectroscopy in the near UV and in the visible region in order to get information about these parameters. Spherical shape of the NPs at the low laser fluence and appearance of aggregation and building of nanowires at the SHG and high laser fluence was seen. Dependence of the mean particle size at the SHG on the laser fluence was established. Comments on the results obtained have been also presented.

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

    Energy Technology Data Exchange (ETDEWEB)

    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.

  10. The solvent effect on the electrocatalytic cleavage of carbon-halogen bonds on Ag and Au

    International Nuclear Information System (INIS)

    In recent years it has been shown in detail how the electrocatalytic cleavage of carbon-halogen bonds is modulated by (a) the stepwise or concerted nature of the dissociative electron-transfer mechanism, which is influenced by the nature of the electrode surface, the type of halogen atom and the molecular structure of RX as a whole, and (b) the double-layer structure (as a function of the nature and bulkiness of the supporting electrolyte ions). In order to both complete and support the interpretative scheme thus developed, this work is focused on the solvent role. When one compares aprotic with protic organic solvents after appropriate intersolvental normalization, interesting peculiarities emerge, especially concerning protic media. Solvent proticity deeply affects both the reaction mechanism (on both non-catalytic and catalytic electrodes) and the extent of the catalytic effects. These items are discussed on the basis of a complete investigation carried out with a carefully controlled experimental protocol on two chloride and bromide couples, one aromatic and one aliphatic, representative of stepwise and concerted mechanisms, respectively, in four aprotic and four protic solvents, on both non−catalytic GC and catalytic Ag and Au electrodes. The results are discussed in the framework of a recently developed interpretative scheme of the carbon-halogen cleavage mechanism

  11. New constraints on the origin of the Skaergaard intrusion Cu-Pd-Au mineralization: Insights from high-resolution X-ray computed tomography

    Science.gov (United States)

    Godel, Bélinda; Rudashevsky, Nikolay S.; Nielsen, Troels F. D.; Barnes, Stephen J.; Rudashevsky, Vladimir N.

    2014-03-01

    This contribution presents the first detailed three-dimensional (3D) in situ analysis of samples from the Platinova Reef using high-resolution X-ray computed tomography (HRXCT) and 3D image processing and quantification coupled with microscopic and mineralogical investigations. Our HRXCT analyses reveal the complex textural relationships between Cu-rich sulfides (bulk composition close to bornite), skaergaardite (PdCu), Au-rich phases, silicates and Fe-Ti oxides and provide unequivocal textural evidences, not observed previously. The association in 3D between Cu-rich sulfide globules, PdCu alloy and ilmenite is inconsistent with a hydrothermal origin of the Cu-Pd mineralization. In contrast, our results combined with phase diagrams strongly support a primary magmatic origin for the Cu-Pd mineralization where Cu and Pd-rich, Fe-poor sulfide liquid represents a cumulus phase that forms by in-situ nucleation. These sulfide droplets and attached skaergaardite grains were trapped during the formation and crystallization of the Fe-Ti oxides. Subsequent, post-cumulus processes led to the partial to total dissolution of the sulfide not entirely enclosed by the Fe-Ti oxides (i.e., not protected from reaction) leading to the observed variability in Cu and Pd composition at the aggregate (sulfide + PdCu) scale and to the occurrence of free PdCu alloys. In contrast to the PdCu alloy, gold-bearing minerals are never observed entirely enclosed within the Fe-Ti oxide. Two hypotheses can be envisaged for the formation of the gold enriched layer in the upper part of the section. Gold may have either precipitated from high-temperature late magmatic Cl-rich fluids. Alternatively, gold may have been enriched during fractional crystallization after sulfide had been suppressed from the liquidus after the Pd layer crystallized and then deposited along redox barriers.

  12. Bio-mimetic Nanostructure Self-assembled from Au@Ag Heterogeneous Nanorods and Phage Fusion Proteins for Targeted Tumor Optical Detection and Photothermal Therapy

    OpenAIRE

    Fei Wang; Pei Liu; Lin Sun; Cuncheng Li; Valery. A. Petrenko; Aihua Liu

    2014-01-01

    Nanomaterials with near-infrared (NIR) absorption have been widely studied in cancer detection and photothermal therapy (PTT), while it remains a great challenge in targeting tumor efficiently with minimal side effects. Herein we report a novel multifunctional phage-mimetic nanostructure, which was prepared by layer-by-layer self-assembly of Au@Ag heterogenous nanorods (NRs) with rhodamine 6G, and specific pVIII fusion proteins. Au@Ag NRs, first being applied for PTT, exhibited excellent stab...

  13. Surface Plasmons and Optical Properties of TiO2/X(X = Au and Ag) Nanostructure Thin Films

    Science.gov (United States)

    Zolanvari, A.; Sadeghi, H.; Norouzi, R.; Ranjgar, A.

    2013-09-01

    TiO2/X(X = Au and Ag) nanolayers are fabricated by depositing TiO2 films using rf magnetron sputtering on thin quartz substrates embedded with Au and Ag nanoparticles. Enhancement of light absorption of the nanostructural layers is observed. These plasmonic and non-plasmonic materials are ordered in geometric arrangements with dimensions that are fractions of the wavelength of light. The light absorption enhancement of synthesized structure in comparison to TiO2 is originated from near-field enhancement caused by the plasmonic effect of metallic nanoparticles, which can be demonstrated by the optical absorption spectra. We show that plasmon modes can exist for the infrared region of the optical spectrum. Also, we analyze the optical properties of the metal-insulator films, in order to clarify the role of metal inclusions in the TiO2 dielectric matrix. Optical band gaps of the nanolayer films are calculated by using Tauc's relation, and the n values of optical band gaps with the variation composition are found from 1.80 to 3.69 eV. Band gap narrowing and absorption in the visible spectral region induced by the incorporation of TiO2/X(X=Au and Ag) nanolayers enable the design of nanostructured thin films to be achieved for photocatalysts and solar energy converters.

  14. Effect of Refractive Index of Substrate on Fabrication and Optical Properties of Hybrid Au-Ag Triangular Nanoparticle Arrays

    Directory of Open Access Journals (Sweden)

    Jing Liu

    2015-05-01

    Full Text Available In this study, the nanosphere lithography (NSL method was used to fabricate hybrid Au-Ag triangular periodic nanoparticle arrays. The Au-Ag triangular periodic arrays were grown on different substrates, and the effect of the refractive index of substrates on fabrication and optical properties was systematically investigated. At first, the optical spectrum was simulated by the discrete dipole approximation (DDA numerical method as a function of refractive indexes of substrates and mediums. Simulation results showed that as the substrates had the refractive indexes of 1.43 (quartz and 1.68 (SF5 glass, the nanoparticle arrays would have better refractive index sensitivity (RIS and figure of merit (FOM. Simulation results also showed that the peak wavelength of the extinction spectra had a red shift when the medium’s refractive index n increased. The experimental results also demonstrated that when refractive indexes of substrates were 1.43 and 1.68, the nanoparticle arrays and substrate had better adhesive ability. Meanwhile, we found the nanoparticles formed a large-scale monolayer array with the hexagonally close-packed structure. Finally, the hybrid Au-Ag triangular nanoparticle arrays were fabricated on quartz and SF5 glass substrates and their experiment extinction spectra were compared with the simulated results.

  15. Influences of Ag and Au Additions on Structure and Tensile Strength of Sn-5Sb Lead Free Solder Alloy

    Institute of Scientific and Technical Information of China (English)

    A.A.El-Daly; Y.Swilem; A.E.Hammad

    2008-01-01

    It is important,for electronic application,to decrease the melting point of Sn-5Sb solder alloy because it is relatively high as compared with the most popular eutectic Pb-Sn solder alloy.Adding Au or Ag can decrease the onset melting temperature (233℃) of this alloy to 203.5℃ and 216℃,respectively.The results indicate that the Sn-5Sb-1.5Au alloy has very good ultimate tensile strength (UTS),ductility,and fusion heat,which are better than both those of the Sn-5Sb-3.5Ag and Sn-5Sb alloys.The formation of intermetallic compounds (IMCs) AuSn4 and Ag3Sn enhanced the microstructure stability,while retained the formation of SbSn precipitates in the solidification microstructure,thus significantly improved the strength and ductility.For all alloys,both UTS and yield stress (σy) increase with increasing strain rate and decrease with increasing temperature in tensile tests,but changes of ductility are generally small with inconsistent trends.

  16. Origin and shape evolution of core-shell nanoparticles in Au-Pd: from few atoms to high Miller index facets

    Energy Technology Data Exchange (ETDEWEB)

    Bhattarai, Nabraj; Casillas, Gilberto; Khanal, Subarna; Velazquez Salazar, J. Jesus; Ponce, Arturo; Jose-Yacaman, Miguel, E-mail: miguel.yacaman@utsa.edu [University of Texas at San Antonio, Department of Physics and Astronomy (United States)

    2013-06-15

    Au-Pd core-shell nanocubes and triangular nanoparticles were systematically synthesized from a few Pd layers up to fully grown morphologies by a modified seed-mediated growth method. The shape evolution of Au-Pd core-shell nanoparticles from single crystal and singly twinned seed to final concave nanocube and triangular plates are presented at atomic level by Cs-corrected scanning transmission electron microscopy (STEM). The growth mechanism of both morphologies was studied throughout different sizes. It was found that the concave nanocubes grew from octahedral Au seeds due to fast growth along Left-Pointing-Angle-Bracket 111 Right-Pointing-Angle-Bracket directions; while the triangular nanoparticles grew from singly twinned Au seeds, growing twice as fast in Left-Pointing-Angle-Bracket 110 Right-Pointing-Angle-Bracket directions along the twin boundary; compared to the Left-Pointing-Angle-Bracket 111 Right-Pointing-Angle-Bracket direction perpendicular to the twin boundary. Both the concave nanocubes and triangular nanoparticles presented high index facet (HIF) surfaces that will increase the catalytic activity of different reactions.

  17. Microwave-assisted synthesis of photoluminescent glutathione-capped Au/Ag nanoclusters: A unique sensor-on-a-nanoparticle for metal ions, anions, and small molecules

    Institute of Scientific and Technical Information of China (English)

    Jia Zhang[1; Yue Yuan[1; Yu Wang[2; Fanfei Sun[2; Gaolin Liang[1; Zheng Jiang[2; Shu-Hong Yu[1,3

    2015-01-01

    Even though great advances have been achieved in the synthesis of luminescent metal nanoclusters, it is still challenging to develop metal nanoclusters with high quantum efficiency as well as multiple sensing functionalities. Here, we demonstrate the rapid preparation of glutathione-capped Au/Ag nanoclusters (GS-Au/Ag NCs) using microwave irradiation and their unique sensing capacities. Compared to bare GS-Au NCs, the doped Au/Ag NCs possess an enhanced quantum yield (7.8% compared to 2.2% for GS-Au NCs). Several characterization techniques were used to elucidate the atomic composition, particulate character, and electronic structure of the fabricated NCs. According to the X-ray photoelectron spectroscopy (XPS) and X-ray absorption near-edge structure (XANES) spectra, a significant amount of Au exists in the oxidized state as Au(I), and the Ag atoms are positively charged. In contrast to those nanoclusters that detect only one analyte, the GS-Au/Ag NCs can be used as a versatile sensor for metal ions, anions, and small molecules. In this manner, the NCs can be regarded as a unique sensor-on-a-nanoparticle.

  18. Traces of Z2 vortices in CuCrO2, AgCrO2, and PdCrO2

    International Nuclear Information System (INIS)

    The spin-spin relaxation of the two-dimensional triangular lattice antiferromagnets CuCrO2, AgCrO2, and PdCrO2 is investigated by electron spin resonance spectroscopy. The data proof excellent agreement with very recent predictions for the Z2-vortex ordering scenario in triangular Heisenberg antiferromagnets derived by Okubo and Kawamura. (author)

  19. Symmetry character of collective states in 104Pd populated in the EC-β+ decay of 104Ag

    International Nuclear Information System (INIS)

    The states of 104Pd, populated in the EC-β+ decay of the ground (Jπ=5+) and metastable (Jπ=2+) states of 104Ag, have been investigated in the framework of the proton-neutron interacting boson model, extending a previous analysis to take into account the newly appeared experimental data. All positive-parity states up to an excitation energy of 3 MeV and spin in the range J=1-6, fed by more than 0.3% in the decay of the parent nucleus, have been considered. As a result, strong evidence has been found for interpreting most of these states as states of collective nature having a quite pure full- or mixed-symmetry character and, in particular, for identifying the 1+ level at 2276 keV as the lowest 1+ mixed-symmetry state. (orig.)

  20. 乙烯基乙酸酯合成钯-金催化剂中金的助催化作用%Promotional Effects of Au in Pd-Au Catalysts for Vinyl Acetate Synthesis

    Institute of Scientific and Technical Information of China (English)

    陈明树; D. W. GOODMAN

    2008-01-01

    硅胶负载的钯-金双金属催化剂是乙烯乙酰氧基化制乙烯基乙酸酯(VA)的高选择性催化剂,本文应用平面和负载纳米颗粒模型催化剂体系研究金的助催化作用,应用低能离子散射谱、低能电子衍射、 X射线光电子能谱、反射红外吸收光谱及程序升温脱附等技术表征这些模型催化剂. 结果表明,金的主要助催化作用是隔离催化剂表面的催化活性钯原子,形成孤立的钯活性中心,从而大大抑制或消除反应物和/或产物在毗邻多原子钯中心上的深度分解,提高VA合成的选择性及活性. 同时由于形成了孤立的钯原子活性中心,反应副产物或中间物之一的一氧化碳吸附较弱,避免了催化剂表面的一氧化碳中毒,进而提高催化活性.%Silica supported Pd-Au bimetallic catalysts are highly selective for the acetoxylation of ethylene to vinyl acetate (VA). In this study we have used model catalysts consisting of planer surfaces and supported nanoparticles to investigate the promotional effects of Au in Pd-Au bimetallic catalysts. Low energy ion scattering spectroscopy, low energy electron diffraction, X-ray photoelectron spectroscopy, infrared reflection adsorption spectroscopy, and temperature-programmed desorption et al, were used to characterize the model systems. The catalytic performance for acetoxylation of ethylene to VA was examined for these model surfaces. In this paper, we summarize the current understanding of the promotional effects of Au in Pd-Au bimetallic catalysts for VA synthesis. The key results are that Au atoms break contiguous Pd atom ensembles at the surface into isolated Pd monomers. The absence of contiguous Pd sites significantly reduces the formation of combustion by-products and suppresses the poison effects of CO, thus enhancing the VA formation selectivity and activity.

  1. The mechanism of N-Ag bonding determined tunability of surface-enhanced Raman scattering of pyridine on MAg (M = Cu, Ag, Au) diatomic clusters.

    Science.gov (United States)

    Chen, Lei; Gao, Yang; Xu, Haoran; Wang, Zhigang; Li, Zhengqiang; Zhang, Rui-Qin

    2014-10-14

    Binary coinage metal clusters can show a significantly different enhancement in surface-enhanced Raman scattering (SERS) from that of pure element clusters, owing to their tunable surface plasmon resonance energies affected by the composition and atomic ordering. Yet, the tunability by composition requires a deep understanding in order to further optimize the SERS-based detection technique. Here, to fill this deficiency, we conducted detailed analyses of the SERS of pyridine adsorbed through N-Ag bonding on the homonuclear diatomic metal cluster Ag2 and heteronuclear diatomic metal clusters of AuAg and CuAg, as well as the involved charge transfer under an intracluster excitation, based on calculations using time-dependent density functional theory with a short-time approximation for the Raman cross-section. We find that although the SERS enhancements for all complexes can reach the order of 10(3)-10(4), the corresponding wavelengths used for SERS excitation are significantly different. Our molecular orbital analysis reveals that the complexes based on heteronuclear metal clusters can produce varied electronic transitions owing to the polarization between different metal atoms, which tune the SERS enhancements with altered optical properties. Our analyses are expected to provide a theoretical basis for exploring the multi-composition SERS substrates applicable for single molecular detection, nanostructure characterization, and biological molecular identification. PMID:25157565

  2. Ag and Au nanoparticles for SERS substrates produced by pulsed laser ablation

    Energy Technology Data Exchange (ETDEWEB)

    Agarwal, N.R.; Castiglioni, C.; Lucotti, A. [DCMIC, Politecnico di Milano, Milano (Italy); Fazio, E.; Neri, F. [Dip. Fisica della Materia e Ingegneria Elettronica, Universita di Messina, Messina (Italy); Trusso, S. [CNR- Istituto per i Processi Chimico-Fisici, Messina (Italy); Santo, N. [Centro Interdipartimentale Microscopia Avanzata, Universita degli Studi di Milano, Milano (Italy); Ossi, P.M. [Dip. Energia, Politecnico di Milano, Milano (Italy)

    2011-08-15

    A method for the growth of films consisting of Nanoparticles (NP) of Ag and Au is presented. Nanostructured films were obtained by means of nanosecond pulsed laser ablation of a metallic target in presence of a controlled Ar atmosphere. The morphology of these films from island structures to isolated nanoparticles, measured by SEM, depends on the varying gas pressure (10-100 Pa) and on the number of laser pulses (500-30000), keeping other deposition parameters such as the target to substrate distance, incidence angle, laser wavelength, laser fluence constant. Fast imaging of the plasma, performed using a intensified and gateable CCD camera at different time delays with respect to the arrival of the laser pulse, allows revelation of the propagation regime of the ablation plume and inference of plasma initial velocity. This data along with the measured average ablated mass per pulse were taken as inputs to a model to estimate the average size of NPs grown in the expanding plume. The theoretical NP sizes were compared with sizes measured from TEM images. These images indicate narrow gradients of NP sizes. Hence strict control of growth parameters aids fine tuning of NP size that is essential for many applications, including Surface Enhanced Raman Spectroscopy (SERS) active substrates. UV-Visible Spectroscopy helped in determination of appropriate laser wavelength for resonant excitation of the localized surface plasmon. SERS Spectra obtained with increasingly lower concentrations of reference dye Rhodamin 6G (Rh6G) and medical drug Apomorphine, are discussed as a perspective of application to biomedical sensors. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  3. Sensitive Glycoprotein Sandwich Assays by the Synergistic Effect of In Situ Generation of Raman Probes and Plasmonic Coupling of Ag Core-Au Satellite Nanostructures.

    Science.gov (United States)

    Bi, Xiaoshuang; Li, Xueyuan; Chen, Dong; Du, Xuezhong

    2016-05-01

    Sensitive surface-enhanced Raman scattering (SERS) assays of glycoproteins have been proposed using p-aminothiophenol (PATP)-embedded Ag core-Au satellite nanostructures modified with p-mercaptophenylboronic acid (PMBA) and the self-assembled monolayer of PMBA on a smooth gold-coated wafer. The apparent Raman probe PATP on the surfaces of the Ag cores underwent a photodimerization to generate 4,4'-dimercaptoazobenzene (DMAB) in situ upon excitation of laser, and the in situ generated DMAB acted as the actual Raman probe with considerably strong SERS signals, which was further enhanced by the plasmonic coupling of the Ag core-Au satellite nanostructures due to the synergistic effect. The sandwich assays of glycoproteins showed high sensitivity and excellent selectivity against nonglycoproteins. The Ag core-Au satellite SERS nanostructures can be used for highly sensitive SERS assays of other analytes.

  4. Genesis of Middle Miocene Yellowstone hotspot-related bonanza epithermal Au-Ag deposits, Northern Great Basin, USA

    Science.gov (United States)

    Saunders, J. A.; Unger, D. L.; Kamenov, G. D.; Fayek, M.; Hames, W. E.; Utterback, W. C.

    2008-09-01

    Epithermal deposits with bonanza Au-Ag veins in the northern Great Basin (NGB) are spatially and temporally associated with Middle Miocene bimodal volcanism that was related to a mantle plume that has now migrated to the Yellowstone National Park area. The Au-Ag deposits formed between 16.5 and 14 Ma, but exhibit different mineralogical compositions, the latter due to the nature of the country rocks hosting the deposits. Where host rocks were primarily of meta-sedimentary or granitic origin, adularia-rich gold mineralization formed. Where glassy rhyolitic country rocks host veins, colloidal silica textures and precious metal-colloid aggregation textures resulted. Where basalts are the country rocks, clay-rich mineralization (with silica minerals, adularia, and carbonate) developed. Oxygen isotope data from quartz (originally amorphous silica and gels) from super-high-grade banded ores from the Sleeper deposit show that ore-forming solutions had δ 18O values up to 10‰ heavier than mid-Miocene meteoric water. The geochemical signature of the ores (including their Se-rich nature) is interpreted here to reflect a mantle source for the “epithermal suite” elements (Au, Ag, Se, Te, As, Sb, Hg) and that signature is preserved to shallow crustal levels because of the similar volatility and aqueous geochemical behavior of the “epithermal suite” elements. A mantle source for the gold in the deposits is further supported by the Pb isotopic signature of the gold ores. Apparently the host rocks control the mineralization style and gangue mineralogy of ores. However, all deposits are considered to have derived precious metals and metalloids from mafic magmas related to the initial emergence of the Yellowstone hotspot. Basalt-derived volatiles and metal(loid)s are inferred to have been absorbed by meteoric-water-dominated geothermal systems heated by shallow rhyolitic magma chambers. Episodic discharge of volatiles and metal(loid)s from deep basaltic magmas mixed with

  5. Invoking Direct Exciton-Plasmon Interactions by Catalytic Ag Deposition on Au Nanoparticles: Photoelectrochemical Bioanalysis with High Efficiency.

    Science.gov (United States)

    Ma, Zheng-Yuan; Xu, Fei; Qin, Yu; Zhao, Wei-Wei; Xu, Jing-Juan; Chen, Hong-Yuan

    2016-04-19

    In this work, direct exciton-plasmon interactions (EPI) between CdS quantum dots (QDs) and Ag nanoparticles (NPs) were invoked ingeniously by catalytic Ag deposition on Au NPs for the stimulation of high efficient damping effect toward the excitonic responses in CdS QDs, on the basis of which a novel photoelectrochemical (PEC) bioanalytical format was achieved for sensitive microRNA detection. Specifically, upon the configurational change from the hairpin probe DNA to the "Y"-shaped ternary conjugate consisting of the original probe DNA, assistant DNA, and the target microRNA, the alkaline phosphatase (ALP) catalytic chemistry would then trigger the transition of the interparticle interplay from the CdS QDs-Au NPs to the CdS QDs-Ag NPs systems for the microRNA detection due to the dependence of the photocurrent quenching on the target concentration. This work not only provided a unique method for EPI generation among the PEC nanosystems but also offered a versatile and general protocol for future PEC bioanalysis development. PMID:27023112

  6. Magnetic properties and exchange bias effects in nanocluster assembled films of equiatomic Fe-X (X=Pd, Pt, and Au) synthesized by inert gas phase condensation

    Energy Technology Data Exchange (ETDEWEB)

    Bansal, Chandrahas [Institute for Nanotechnology, Forschungszentrum Karlsruhe (Germany); University of Hyderabad, Hyderabad (India); Mishra, Ajay Kumar; Hahn, Horst [Institute for Nanotechnology, Forschungszentrum Karlsruhe (Germany)

    2008-07-01

    Nanocluster assembled films of equiatomic Fe-Pd, Fe-Pt, and Fe-Au alloys were synthesized using a UHV nanocluster film deposition system (model NANODEP60 from Oxford Applied Research, UK). The films were nanoporous and consisted of agglomerates of small size nanoclusters of diameters 4 to 5 nanometers. The M(T) data in zero-field-cooled (ZFC) and field-cooled (FC) states revealed a blocking temperature of 33 K, 35 K, and 41 K for the Fe-Pt, Fe-Pd, and Fe-Au cluster films. Besides this, there was a paramagnetic response at lower temperatures both in the ZFC and FC states showing that there was a partial oxidation of the clusters even in the as-prepared films although they were deposited at base pressures of 10-8 torr. The defect states in the oxide shell gave rise to these moments that remained uncoupled to the antiferromagnetic lattice. A exchange bias of about 1 KOe was observed in all the three alloys with the lowest value for Fe-Au and the highest value for Fe-Pd cluster films.

  7. Ultrasensitive electrochemical immunoassay for surface array protein, a Bacillus anthracis biomarker using Au-Pd nanocrystals loaded on boron-nitride nanosheets as catalytic labels.

    Science.gov (United States)

    Sharma, Mukesh Kumar; Narayanan, J; Pardasani, Deepak; Srivastava, Divesh N; Upadhyay, Sanjay; Goel, Ajay Kumar

    2016-06-15

    Bacillus anthracis, the causative agent of anthrax, is a well known bioterrorism agent. The determination of surface array protein (Sap), a unique biomarker for B. anthracis can offer an opportunity for specific detection of B. anthracis in culture broth. In this study, we designed a new catalytic bionanolabel and fabricated a novel electrochemical immunosensor for ultrasensitive detection of B. anthracis Sap antigen. Bimetallic gold-palladium nanoparticles were in-situ grown on poly (diallyldimethylammonium chloride) functionalized boron nitride nanosheets (Au-Pd NPs@BNNSs) and conjugated with the mouse anti-B. anthracis Sap antibodies (Ab2); named Au-Pd NPs@BNNSs/Ab2. The resulting Au-Pd NPs@BNNSs/Ab2 bionanolabel demonstrated high catalytic activity towards reduction of 4-nitrophenol. The sensitivity of the electrochemical immunosensor along with redox cycling of 4-aminophenol to 4-quinoneimine was improved to a great extent. Under optimal conditions, the proposed immunosensor exhibited a wide working range from 5 pg/mL to 100 ng/mL with a minimum detection limit of 1 pg/mL B. anthracis Sap antigen. The practical applicability of the immunosensor was demonstrated by specific detection of Sap secreted by the B. anthracis in culture broth just after 1h of growth. These labels open a new direction for the ultrasensitive detection of different biological warfare agents and their markers in different matrices. PMID:26874112

  8. Comparative Study on The Photocatalytic Hydrogen Production from Methanol over Cu-, Pd-, Co- and Au-Loaded TiO2

    Directory of Open Access Journals (Sweden)

    Udani P.P.C.

    2015-09-01

    Full Text Available Photocatalytic hydrogen production from a methanol-water solution was investigated in a semi-continuous reactor over different metal-loaded TiO2 catalysts under UltraViolet (UV light irradiation. The catalysts were mainly prepared by the incipient wetness impregnation method by varying the metal weight ratio in the range of 1-10 wt%. The effects of metal loading and H2 pre-treatment on the photocatalytic activity were investigated. In addition, the activity of the catalysts was also compared with a reference Au-TiO2 catalyst from the World Gold Council (WGC. The photocatalysts were characterized by using X-Ray Diffraction (XRD and N2 physisorption before and after the activity measurements. The photocatalytic activity decreased in the order of Pd > Au > Cu > Co in the comparative study of Cu-TiO2, Co-TiO2, Au-TiO2 and Pd-TiO2. Optimum hydrogen evolution was achieved with 5 wt% Pd-TiO2 and 5 wt% Cu-TiO2.

  9. Electrical and structural properties of (Pd/Au) Schottky contact to as grown and rapid thermally annealed GaN grown by MBE

    Science.gov (United States)

    Nirwal, Varun Singh; Singh, Joginder; Gautam, Khyati; Peta, Koteswara Rao

    2016-05-01

    We studied effect of thermally annealed GaN surface on the electrical and structural properties of (Pd/Au) Schottky contact to Ga-polar GaN grown by molecular beam epitaxy on Si substrate. Current voltage (I-V) measurement was used to study electrical properties while X-ray diffraction (XRD) measurement was used to study structural properties. The Schottky barrier height calculated using I-V characteristics was 0.59 eV for (Pd/Au) Schottky contact on as grown GaN, which increased to 0.73 eV for the Schottky contact fabricated on 700 °C annealed GaN film. The reverse bias leakage current at -1 V was also significantly reduced from 6.42×10-5 A to 7.31×10-7 A after annealing. The value of series resistance (Rs) was extracted from Cheung method and the value of Rs decreased from 373 Ω to 172 Ω after annealing. XRD results revealed the formation of gallide phases at the interface of (Pd/Au) and GaN for annealed sample, which could be the reason for improvement in the electrical properties of Schottky contact after annealing.

  10. Target-specific near-IR induced drug release and photothermal therapy with accumulated Au/Ag hollow nanoshells on pulmonary cancer cell membranes.

    Science.gov (United States)

    Noh, Mi Suk; Lee, Somin; Kang, Homan; Yang, Jin-Kyoung; Lee, Hyunmi; Hwang, Doyk; Lee, Jong Woo; Jeong, Sinyoung; Jang, Yoonjeong; Jun, Bong-Hyun; Jeong, Dae Hong; Kim, Seong Keun; Lee, Yoon-Sik; Cho, Myung-Haing

    2015-03-01

    Au/Ag hollow nanoshells (AuHNSs) were developed as multifunctional therapeutic agents for effective, targeted, photothermally induced drug delivery under near-infrared (NIR) light. AuHNSs were synthesized by galvanic replacement reaction. We further conjugated antibodies against the epidermal growth factor receptor (EGFR) to the PEGylated AuHNS, followed by loading with the antitumor drug doxorubicin (AuHNS-EGFR-DOX) for lung cancer treatment. AuHNSs showed similar photothermal efficiency to gold nanorods under optimized NIR laser power. The targeting of AuHNS-EGFR-DOX was confirmed by light-scattering images of A549 cells, and doxorubicin release from the AuHNSs was evaluated under low pH and NIR-irradiated conditions. Multifunctional AuHNS-EGFR-DOX induced photothermal ablation of the targeted lung cancer cells and rapid doxorubicin release following irradiation with NIR laser. Furthermore, we evaluated the effectiveness of AuHNS-EGFR-DOX drug delivery by comparing two drug delivery methods: receptor-mediated endocytosis and cell-surface targeting. Accumulation of the AuHNS-EGFR-DOX on the cell surfaces by targeting EGFR turned out to be more effective for lung cancer treatments than uptake of AuHNS-EGFR-DOX. Taken together, our data suggest a new and optimal method of NIR-induced drug release via the accumulation of targeted AuHNS-EGFR-DOX on cancer cell membranes.

  11. Digestive ripening facilitated atomic diffusion at nanosize regime: Case of AuIn{sub 2} and Ag{sub 3}In intermetallic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Arora, Neha [Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560 012 (India); Jagirdar, Balaji R., E-mail: jagirdar@ipc.iisc.ernet.in [Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560 012 (India); Klabunde, Kenneth J. [Department of Chemistry, Kansas State University, Manhattan, KS 66506 (United States)

    2014-10-15

    Highlights: • A digestive ripening facilitated interatomic diffusion process is presented. • Nearly monodisperse AuIn{sub 2} and Ag{sub 3}In intermetallic nanoparticles were synthesized. • Optimization of reaction temperature facilitates interatomic transfer. • Presence of excess ligand plays a crucial role in the digestive ripening process. - Abstract: Monodisperse colloidal gold–indium (AuIn{sub 2}) intermetallic nanoparticles have been synthesized from Au and In colloids using the digestive ripening process. Formation of the intermetallic proceeds via digestive ripening facilitated atomic diffusion of Au and In atoms from the Au and In nanoparticles followed simultaneously by their growth in the solution. Optimization of the reaction temperature was found to be crucial for the formation of AuIn{sub 2} intermetallic from gold and indium nanoparticles. Transmission electron microscopy revealed the presence of nearly monodisperse nanoparticles of Au and AuIn{sub 2} with particle size distribution of 3.7 ± 1.0 nm and 5.0 ± 1.6 nm, respectively. UV–visible spectral studies brought out the absence of SPR band in pure AuIn{sub 2} intermetallic nanoparticles. Optical study and electron microscopy, in combination with powder X-ray diffraction established phase pure AuIn{sub 2} intermetallic nanoparticles unambiguously. The potential of such an unprecedented approach has been further exploited in the synthesis of Ag{sub 3}In intermetallic nanoparticles with the dimension of less than 10 nm.

  12. The effect of intermetallic compound evolution on the fracture behavior of Au stud bumps joined with Sn-3.5Ag solder

    Science.gov (United States)

    Lee, Young-Kyu; Ko, Yong-Ho; Kim, Jun-Ki; Lee, Chang-Woo; Yoo, Sehoon

    2013-01-01

    The microstructure and joint properties of Au stud bumps joined with Sn-3.5Ag solder were investigated as functions of flip chip bonding temperature and aging time. Au stud bumps were bonded on solder-onpad (SOP) at bonding temperature of 260°C and 300°C for 10 s, respectively. Aging treatment was carried out at 150°C for 100 h, 300 h, and 500 h, respectively. After flip chip bonding, intermetallic compounds (IMCs) of AuSn, AuSn2, and AuSn4 were formed at the interface between the Au stud bump and Sn-3.5Ag solder. At a bonding temperature of 300°C, AuSn2 IMC clusters, which were surrounded by AuSn4 IMCs, were observed in the Sn-3.5Ag solder bump. After flip chip bonding, bonding strength was approximately 220.5mN/bump. As aging time increased, the bonding strength decreased. After 100 h of aging treatment, the bonding strength of the joint bonded at 300°C was lower than that bonded at 260°C due to the fast growth rate of the AuSn2 IMCs. The main failure modes were interface fractures between the AuSn2 IMCs and AuSn4 IMCs, fractures through the AuSn2 IMCs and pad lift. Initial joint microstructures after flip chip bonding strongly affected the bonding strengths of aged samples.

  13. Theoretical study of PTCDA adsorbed on the coinage metal surfaces, Ag(111), Au(111) and Cu(111)

    Energy Technology Data Exchange (ETDEWEB)

    Romaner, L; Nabok, D; Puschnig, P; Ambrosch-Draxl, C [Chair of Atomistic Modelling and Design of Materials, University of Leoben, Franz-Josef-Strasse 18, A-8700 Leoben (Austria); Zojer, E [Institute of Solid State Physics, Graz University of Technology, Petersgasse 16, A-8010 Graz (Austria)], E-mail: lorenz.romaner@unileoben.ac.at

    2009-05-15

    A thorough understanding of the adsorption of molecules on metallic surfaces is a crucial prerequisite for the development and improvement of functionalized materials. A prominent representative within the class of {pi}-conjugated molecules is 3,4,9,10-perylene-tetracarboxylic acid dianhydride (PTCDA) which, adsorbed on the Ag(111), Au(111) or Cu(111) surfaces, shows characteristic trends for work-function modification, alignment of molecular levels with the substrate Fermi energy and binding distances. We carried out density functional theory (DFT) calculations to investigate to what extent these trends can be rationalized on a theoretical basis. We used different density functionals (DF) including a fully non-local van der Waals (vdW) DF capable of describing dispersion interactions. We show that, rather independent of the DF, the calculations yield level alignments and work-function modifications consistent with ultra-violet photoelectron spectroscopy when the monolayer is placed onto the surfaces at the experimental distances (as determined from x-ray standing wave experiments). The lowest unoccupied molecular orbital is occupied on the Ag and Cu surfaces, whereas it remains unoccupied on the Au surface. Simultaneously, the work function increases for Ag but decreases for Cu and Au. Adsorption distances and energies, on the other hand, depend very sensitively on the choice of the DF. While calculations in the local density approximation bind the monolayer consistently with the experimental trends, the generalized gradient approximation in several flavors fails to reproduce realistic distances and energies. Calculations employing the vdW-DF reveal that substantial bonding contributions arise from dispersive interactions. They yield reasonable binding energies but larger binding distances than the experiments.

  14. Theoretical study of PTCDA adsorbed on the coinage metal surfaces, Ag(111), Au(111) and Cu(111)

    International Nuclear Information System (INIS)

    A thorough understanding of the adsorption of molecules on metallic surfaces is a crucial prerequisite for the development and improvement of functionalized materials. A prominent representative within the class of π-conjugated molecules is 3,4,9,10-perylene-tetracarboxylic acid dianhydride (PTCDA) which, adsorbed on the Ag(111), Au(111) or Cu(111) surfaces, shows characteristic trends for work-function modification, alignment of molecular levels with the substrate Fermi energy and binding distances. We carried out density functional theory (DFT) calculations to investigate to what extent these trends can be rationalized on a theoretical basis. We used different density functionals (DF) including a fully non-local van der Waals (vdW) DF capable of describing dispersion interactions. We show that, rather independent of the DF, the calculations yield level alignments and work-function modifications consistent with ultra-violet photoelectron spectroscopy when the monolayer is placed onto the surfaces at the experimental distances (as determined from x-ray standing wave experiments). The lowest unoccupied molecular orbital is occupied on the Ag and Cu surfaces, whereas it remains unoccupied on the Au surface. Simultaneously, the work function increases for Ag but decreases for Cu and Au. Adsorption distances and energies, on the other hand, depend very sensitively on the choice of the DF. While calculations in the local density approximation bind the monolayer consistently with the experimental trends, the generalized gradient approximation in several flavors fails to reproduce realistic distances and energies. Calculations employing the vdW-DF reveal that substantial bonding contributions arise from dispersive interactions. They yield reasonable binding energies but larger binding distances than the experiments.

  15. Growth behavior and field emission property of ZnO nanowire arrays on Au and Ag films

    Directory of Open Access Journals (Sweden)

    Sung Hyun Kim

    2013-09-01

    Full Text Available We propose a facile method to control the growth and areal density of zinc-oxide (ZnO nanowire arrays using gold or silver films deposited on aluminum-doped ZnO (AZO layers coated on glass substrates. Nanowires exceeding 5 μm in length grew on both the glass/AZO-layer and on the glass/AZO-layer/Au-film where the areal array density was controlled primarily by changing the annealing temperature. In contrast, the nanowire arrays grew only on the AZO surface but not on the Ag film owing to the formation of an Ag-oxide layer. We fabricated field emitter devices with density controlled ZnO nanowire arrays and low turn-on electric field of ∼6 V/μm and a field enhancement factor of up to 1188 were obtained with density controlled ZnO nanowire arrays.

  16. Multifragmentation in the 4.8-GeV 3He+ natAg, 197Au reactions

    International Nuclear Information System (INIS)

    Multifragmentation of natAg and 197Au nuclei induced by a 4.8-GeV 3He ions has been studied with the Indiana Silicon Sphere 4π detector array. Rapidity and moving source analyses are consistent with thermal emission from a source in approximate kinetic equilibrium. For the most dissipative collisions, the spectral Coulomb peaks are broadened to very low energies, indicative of emission from an extended nuclear system. Predictions of a model with an intranuclear cascade and an expanding, emitting source compare well with experimental multiplicity distributions and the evolution of fragment spectral shapes

  17. Multifragmentation in the 4.8-GeV {sup 3}He+ {sup nat}Ag, {sup 197}Au reactions

    Energy Technology Data Exchange (ETDEWEB)

    Kwiatkowski, K.; Morley, K.B.; Foxford, E.R.; Bracken, D.S.; Viola, V.E.; Yoder, N.R.; Legrain, R.; Pollacco, E.C.; Volant, C.; Friedman, W.A.; Korteling, R.G.; Brzychczyk, J.; Breuer, H. [Department of Chemistry and Physics and IUCF, Indiana University, Bloomington, Indiana 47405 (United States)]|[Commissariat a l`Energie Atomique DAPNIA/Service de Physique des Particles, Centre d`Etudes de Saclay, 91191 Gif-sur-Yvette Cedex (France)]|[Department of Chemistry, Simon Fraser University, Burnaby, British Columbia, Canada V5A 1SG (Canada)]|[Department of Physics, University of Wisconsin, Madison, Wisconsin 53706 (United States)]|[Institute of Physics, Jagiellonian University, 30-059 Krakow (Poland)]|[Department of Physics, University of Maryland, College Park, Maryland 20742 (United States)

    1995-05-08

    Multifragmentation of {sup nat}Ag and {sup 197}Au nuclei induced by a 4.8-GeV {sup 3}He ions has been studied with the Indiana Silicon Sphere 4{pi} detector array. Rapidity and moving source analyses are consistent with thermal emission from a source in approximate kinetic equilibrium. For the most dissipative collisions, the spectral Coulomb peaks are broadened to very low energies, indicative of emission from an extended nuclear system. Predictions of a model with an intranuclear cascade and an expanding, emitting source compare well with experimental multiplicity distributions and the evolution of fragment spectral shapes.

  18. Dopant-induced 2D-3D transition in small Au-containing clusters: DFT-global optimisation of 8-atom Au-Ag nanoalloys.

    Science.gov (United States)

    Heiles, Sven; Logsdail, Andrew J; Schäfer, Rolf; Johnston, Roy L

    2012-02-21

    A genetic algorithm (GA) coupled with density functional theory (DFT) calculations is used to perform global optimisations for all compositions of 8-atom Au-Ag bimetallic clusters. The performance of this novel GA-DFT approach for bimetallic nanoparticles is tested for structures reported in the literature. New global minimum structures for various compositions are predicted and the 2D-3D transition is located. Results are explained with the aid of an analysis of the electronic density of states. The chemical ordering of the predicted lowest energy isomers are explained via a detailed analysis of the charge separation and mixing energies of the bimetallic clusters. Finally, dielectric properties are computed and the composition and dimensionality dependence of the electronic polarizability and dipole moment is discussed, enabling predictions to be made for future electric beam deflection experiments.

  19. ⁶⁴Cu-Doped PdCu@Au Tripods: A Multifunctional Nanomaterial for Positron Emission Tomography and Image-Guided Photothermal Cancer Treatment.

    Science.gov (United States)

    Pang, Bo; Zhao, Yongfeng; Luehmann, Hannah; Yang, Xuan; Detering, Lisa; You, Meng; Zhang, Chao; Zhang, Lei; Li, Zhi-Yuan; Ren, Qiushi; Liu, Yongjian; Xia, Younan

    2016-03-22

    This article reports a facile synthesis of radiolabeled PdCu@Au core-shell tripods for use in positron emission tomography (PET) and image-guided photothermal cancer treatment by directly incorporating radioactive (64)Cu atoms into the crystal lattice. The tripod had a unique morphology determined by the PdCu tripod that served as a template for the coating of Au shell, in addition to well-controlled specific activity and physical dimensions. The Au shell provided the nanostructure with strong absorption in the near-infrared region and effectively prevented the Cu and (64)Cu atoms in the core from oxidization and dissolution. When conjugated with D-Ala1-peptide T-amide (DAPTA), the core-shell tripods showed great enhancement in targeting the C-C chemokine receptor 5 (CCR5), a newly identified theranostic target up-regulated in triple negative breast cancer (TNBC). Specifically, the CCR5-targeted tripods with an arm length of about 45 nm showed 2- and 6-fold increase in tumor-to-blood and tumor-to-muscle uptake ratios, respectively, relative to their nontargeted counterpart in an orthotopic mouse 4T1 TNBC model at 24 h postinjection. The targeting specificity was further validated via a competitive receptor blocking study. We also demonstrated the use of these targeted, radioactive tripods for effective photothermal treatment in the 4T1 tumor model as guided by PET imaging. The efficacy of treatment was confirmed by the significant reduction in tumor metabolic activity revealed through the use of (18)F-fluorodeoxyglucose PET/CT imaging. Taken together, we believe that the (64)Cu-doped PdCu@Au tripods could serve as a multifunctional platform for both PET imaging and image-guided photothermal cancer therapy.

  20. ⁶⁴Cu-Doped PdCu@Au Tripods: A Multifunctional Nanomaterial for Positron Emission Tomography and Image-Guided Photothermal Cancer Treatment.

    Science.gov (United States)

    Pang, Bo; Zhao, Yongfeng; Luehmann, Hannah; Yang, Xuan; Detering, Lisa; You, Meng; Zhang, Chao; Zhang, Lei; Li, Zhi-Yuan; Ren, Qiushi; Liu, Yongjian; Xia, Younan

    2016-03-22

    This article reports a facile synthesis of radiolabeled PdCu@Au core-shell tripods for use in positron emission tomography (PET) and image-guided photothermal cancer treatment by directly incorporating radioactive (64)Cu atoms into the crystal lattice. The tripod had a unique morphology determined by the PdCu tripod that served as a template for the coating of Au shell, in addition to well-controlled specific activity and physical dimensions. The Au shell provided the nanostructure with strong absorption in the near-infrared region and effectively prevented the Cu and (64)Cu atoms in the core from oxidization and dissolution. When conjugated with D-Ala1-peptide T-amide (DAPTA), the core-shell tripods showed great enhancement in targeting the C-C chemokine receptor 5 (CCR5), a newly identified theranostic target up-regulated in triple negative breast cancer (TNBC). Specifically, the CCR5-targeted tripods with an arm length of about 45 nm showed 2- and 6-fold increase in tumor-to-blood and tumor-to-muscle uptake ratios, respectively, relative to their nontargeted counterpart in an orthotopic mouse 4T1 TNBC model at 24 h postinjection. The targeting specificity was further validated via a competitive receptor blocking study. We also demonstrated the use of these targeted, radioactive tripods for effective photothermal treatment in the 4T1 tumor model as guided by PET imaging. The efficacy of treatment was confirmed by the significant reduction in tumor metabolic activity revealed through the use of (18)F-fluorodeoxyglucose PET/CT imaging. Taken together, we believe that the (64)Cu-doped PdCu@Au tripods could serve as a multifunctional platform for both PET imaging and image-guided photothermal cancer therapy. PMID:26824412

  1. Excitation function of squared speed-of-sound extracted from (net-)proton rapidity spectra in Au-Au and Pb-Pb collisions over an energy range from AGS to RHIC

    CERN Document Server

    Gao, Li-Na; Sun, Yan; Sun, Zhu; Lacey, Roy A

    2016-01-01

    Experimental results of the rapidity distributions of protons and net-protons (protons minus antiprotons) emitted in gold-gold (Au-Au) and lead-lead (Pb-Pb) collisions, measured by a few collaborations at the alternating gradient synchrotron (AGS), super proton synchrotron (SPS), and relativistic heavy ion collider (RHIC), are described by a revised Landau hydrodynamic model. The values of squared speed-of-sound parameter $c^2_s$ are then extracted from the rapidity distribution widths of (net-)protons. The excitation function of $c^2_s$ of the interacting system in Au-Au and Pb-Pb collisions over an energy range from AGS to RHIC is obtained to show a local minimum or softest point in the equation of state (EoS) at the center-of-mass energy per nucleon pair $\\sqrt{s_{NN}}=8.8$ GeV which confirms our previous result.

  2. Changes in the microbiological and chemical characteristics of white bread during storage in paper packages modified with Ag/TiO2-SiO2, Ag/N-TiO2 or Au/TiO2.

    Science.gov (United States)

    Peter, Anca; Mihaly-Cozmuta, Leonard; Mihaly-Cozmuta, Anca; Nicula, Camelia; Ziemkowska, Wanda; Basiak, Dariusz; Danciu, Virginia; Vulpoi, Adriana; Baia, Lucian; Falup, Anca; Craciun, Grigore; Ciric, Alexandru; Begea, Mihaela; Kiss, Claudia; Vatuiu, Daniela

    2016-04-15

    Microbiological and chemical characteristics of white bread during storage in paper-packages modified with Ag/TiO2-SiO2, Ag/N-TiO2 or Au/TiO2 were investigated. The whiteness and the water retention of the modified packages were slightly superior to those exhibited by the reference sample, as the color of the composite was lighter. The water retention was very good especially for the Ag/TiO2-SiO2-paper. These improvements can be associated with the high specific surface area and with the low agglomeration tendency of Ag nanoparticles in comparison with the Au ones. The preservation activity of the composites for the bread storage is positively influenced by photoactivity and presence of nano-Ag. Packages Ag/TiO2-SiO2-paper and Ag/N-TiO2-paper can find their applicability for extending the shelf life of bread by 2 days as compared with the unmodified paper-package. No influence of the Au/TiO2 on the extending the shelf life of bread was observed. PMID:26617018

  3. Changes in the microbiological and chemical characteristics of white bread during storage in paper packages modified with Ag/TiO2-SiO2, Ag/N-TiO2 or Au/TiO2.

    Science.gov (United States)

    Peter, Anca; Mihaly-Cozmuta, Leonard; Mihaly-Cozmuta, Anca; Nicula, Camelia; Ziemkowska, Wanda; Basiak, Dariusz; Danciu, Virginia; Vulpoi, Adriana; Baia, Lucian; Falup, Anca; Craciun, Grigore; Ciric, Alexandru; Begea, Mihaela; Kiss, Claudia; Vatuiu, Daniela

    2016-04-15

    Microbiological and chemical characteristics of white bread during storage in paper-packages modified with Ag/TiO2-SiO2, Ag/N-TiO2 or Au/TiO2 were investigated. The whiteness and the water retention of the modified packages were slightly superior to those exhibited by the reference sample, as the color of the composite was lighter. The water retention was very good especially for the Ag/TiO2-SiO2-paper. These improvements can be associated with the high specific surface area and with the low agglomeration tendency of Ag nanoparticles in comparison with the Au ones. The preservation activity of the composites for the bread storage is positively influenced by photoactivity and presence of nano-Ag. Packages Ag/TiO2-SiO2-paper and Ag/N-TiO2-paper can find their applicability for extending the shelf life of bread by 2 days as compared with the unmodified paper-package. No influence of the Au/TiO2 on the extending the shelf life of bread was observed.

  4. Environmentally benign synthesis of amides and ureas via catalytic dehydrogenation coupling of volatile alcohols and amines in a Pd-Ag membrane reactor

    KAUST Repository

    Chen, Tao

    2016-05-31

    In this study, we report the direct synthesis of amides and ureas via the catalytic dehydrogenation of volatile alcohols and amines using the Milstein catalyst in a Pd-Ag/ceramic membrane reactor. A series of amides and ureas, which could not be synthesized in an open system by catalytic dehydrogenation coupling, were obtained in moderate to high yields via catalytic dehydrogenation of volatile alcohols and amines. This process could be monitored by the hydrogen produced. Compared to the traditional method of condensation, this catalytic system avoids the stoichiometric pre-activation or in situ activation of reagents, and is a much cleaner process with high atom economy. This methodology, only possible by employing the Pd-Ag/ceramic membrane reactor, not only provides a new environmentally benign synthetic approach of amides and ureas, but is also a potential method for hydrogen storage.

  5. Enhancement of chitosan-graphene oxide SPR sensor with a multi-metallic layers of Au-Ag-Au nanostructure for lead(II) ion detection

    Science.gov (United States)

    Kamaruddin, Nur Hasiba; Bakar, Ahmad Ashrif A.; Yaacob, Mohd Hanif; Mahdi, Mohd Adzir; Zan, Mohd Saiful Dzulkefly; Shaari, Sahbudin

    2016-01-01

    We demonstrate the enhancement of surface plasmon resonance (SPR) technique by implementing a multi-metallic layers of Au-Ag-Au nanostructure in the chitosan-graphene oxide (CS-GO) SPR sensor for lead(II) ion detection. The performance of the sensor is analyzed via SPR measurements, from which the sensitivity, signal-to-noise ratio and repeatability are determined. The nanostructure layers are characterized using field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), X-ray diffraction (XRD), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). We showed that the proposed structure has increased the shift in the SPR angle up to 3.5° within the range of 0.1-1 ppm due to the enhanced evanescent field at the sensing layer-analyte interface. This sensor also exhibits great repeatability which benefits from the stable multi-metallic nanostructure. The SNR value of 0.92 for 5 ppm lead(II) ion solution and reasonable linearity range up to that concentration shows that the tri-metallic CS-GO SPR sensor gives a good response towards the lead(II) ion solution. The CS-GO SPR sensor is also sensitive to at least a 10-5 change in the refractive index. The results prove that our proposed tri-metallic CS-GO SPR sensor demonstrates a strong performance and reliability for lead(II) ion detection in accordance with the standardized lead safety level for wastewater.

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

    Science.gov (United States)

    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. PMID:27269809

  7. Interface controlled growth of nanostructures in discontinuous Ag and Au thin films fabricated by ion beam sputter deposition for plasmonic applications

    Indian Academy of Sciences (India)

    R Brahma; M Ghanashyam Krishna

    2012-08-01

    The growth of discontinuous thin films of Ag and Au by low energy ion beam sputter deposition is reported. The study focuses on the role of the film–substrate in determining the shape and size of nanostructures achieved in such films. Ag films were deposited using Ar ion energy of 150 eV while the Au films were deposited with Ar ion energies of 250–450 eV. Three types of interfaces were investigated in this study. The first set of film–substrate interfaces consisted of Ag and Au films grown on borosilicate glass and carbon coated Cu grids used as substrates. The second set of films was metallic bilayers in which one of the metals (Ag or Au) was grown on a continuous film of the other metal (Au or Ag). The third set of interfaces comprised of discontinuous Ag and Au films deposited on different dielectrics such as SiO2, TiO2 and ZrO2. In each case, a rich variety of nanostructures including self organized arrays of nanoparticles, nanoclusters and nanoneedles have been achieved. The role of the film–substrate interface is discussed within the framework of existing theories of thin film nucleation and growth. Interfacial nanostructuring of thin films is demonstrated to be a viable technique to realize a variety of nanostructures. The use of interfacial nanostructuring for plasmonic applications is demonstrated. It is shown that the surface Plasmon resonance of the metal nanostructures can be tuned over a wide range of wavelengths from 400 to 700 nm by controlling the film–substrate interface.

  8. Magneto-optical Properties of (Pt/Co/X/IZO (X = Ta, Au, Pt, Ru and Ag Structures for Magneto-optical Spatial Light Modulators

    Directory of Open Access Journals (Sweden)

    Ishibashi T.

    2013-01-01

    Full Text Available Magneto-optical properties of Si sub./(Ta/Cu2/(Pt/Co multilayer/X/indium zinc oxide (IZO (X = Ta, Au, Pt, Ru, and Ag are studied. Kerr rotations, reflectivities and figures of merit of the structures are compared with those of (Ta/Cu2/(Pt/Co multilayer/X (X = Ta, Au, Pt, Ru, and Ag with IZO layers calculated by the virtual optical constant method. Two peaks caused by interference are confirmed in both of those spectra, and the Kerr rotation of the samples with Ta, Au, and Pt capping layer reached 1.2 degrees at approximately 2.7 eV. The sample with Au capping layer gave the highest figure of merit.

  9. Total oxidation of VOCs on Pd and/or Au supported on TiO{sub 2}/ZrO{sub 2} followed by ''operando'' Drift

    Energy Technology Data Exchange (ETDEWEB)

    Hosseini, M.; Siffert, St.; Cousin, R.; Aboukais, A. [Universite du Littoral-Cote d' Opale, Lab. de Catalyse et Environnement, E.A. 2598, 59 - Dunkerque (France); Hadj-Sadok, Z.; Bao-Lian, Su [Namur Univ., Lab. de Chimie des Materiaux Inorganiques, Namur (Belgium)

    2009-06-15

    Catalytic performances of nano-structured meso-porous TiO{sub 2}-ZrO{sub 2} mixed oxides impregnated by Pd and/or Au were studied in toluene total oxidation in a fixed bed micro-reactor and with 'operando' DRIFT. Meso-porous TiO{sub 2}-ZrO{sub 2} mixed oxides with various Ti:Zr mole ratio of 80/20, 50/50 and 20/80, high surface areas were synthesised using a mixture of zirconium prop-oxide and titanium iso-prop-oxide as Zr and Ti sources and also CTMABr as surfactant. The new supports are impregnated by 0.5 or 1.5 wt% of palladium and 1 wt% of gold using impregnation and Deposition-Precipitation methods. The catalytic activity for the nano-structured meso-porous TiO{sub 2}-ZrO{sub 2} mixed oxides varies depending on the molar ratio of Ti:Zr and also for all series of the studied catalysts impregnated by Pd and/or Au, when the gold is loaded firstly the activity in toluene complete oxidation is higher than when Pd was deposited firstly (PdAu/TZ {>=} 1.5Pd/TZ {>=} AuPd/TZ {>=} Pd/TZ {>=} Au/TZ {>=} TZ). The highest activity of PdAu/TZ (80/20) can be related to the higher acid sites density of the support and also to the presence of a synergetic effect between palladium and gold. 'Operando' DRIFT allowed following the VOCs oxidation but also suggesting an interaction between the adsorbed molecule and the catalyst which decreases when the activity for oxidation reaction increases. (authors)

  10. Highly sensitive colorimetric detection of glucose in a serum based on DNA-embeded Au@Ag core-shell nanoparticles

    Science.gov (United States)

    Kang, Fei; Hou, Xiangshu; Xu, Kun

    2015-10-01

    Glucose is a key energy substance in diverse biology and closely related to the life activities of the organism. To develop a simple and sensitive method for glucose detection is extremely urgent but still remains a key challenge. Herein, we report a colorimetric glucose sensor in a homogeneous system based on DNA-embedded core-shell Au@Ag nanoparticles. In this assay, a glucose substrate was first catalytically oxidized by glucose oxidase to produce H2O2 which would further oxidize and gradually etch the outer silver shell of Au@Ag nanoparticles. Afterwards, the solution color changed from yellow to red and the surface plasmon resonance (SPR) band of Au@Ag nanoparticles declined and red-shifted from 430 to 516 nm. Compared with previous silver-based glucose colorimetric detection strategies, the distinctive SPR band change is superior to the color variation, which is critical to the high sensitivity of this assay. Benefiting from the outstanding optical property, robust stability and well-dispersion of the core-shell Au@AgNPs hybrid, this colorimetric assay obtained a detection limit of glucose as low as 10 nM, which is at least a 10-fold improvement over other AgNPs-based procedures. Moreover, this optical biosensor was successfully employed to the determination of glucose in fetal bovine serum.

  11. A simple approach to uniform PdAg alloy membranes: Comparative study of conventional and silver concentration-controlled co-plating

    KAUST Repository

    Zeng, Gaofeng

    2014-03-01

    An Ag-controlled co-plating method was developed for the preparation of palladium/silver alloy membranes on porous tubular alumina supports. By controlling the feed rate of Ag to the Pd bath, the concentration of the silver in the plating bath was restricted during the course of plating. As a result, preferential deposition of silver at the beginning was suppressed and uniform dispersion of silver inside the membrane with silver composition in the desired range was achieved. Ultrathin (∼2.5 μm) PdAg alloy membranes with uniform silver composition of ∼25% were successfully obtained. The membrane showed a hydrogen permeance of 0.88 mol m-2 s-1 and pure-gas H2/N2 selectivity of 2140 at 823 K with ΔP = 100 kPa. Only one hydride phase existed in the studied temperature range from 373 to 823 K with ΔPH=100kPa. Direct comparisons with the conventional simply-mixed co-plating method showed that membranes made by the novel Ag-controlled co-plating method had much more uniform silver distribution, smoother surface, denser membrane structure, higher utilization rate of metal sources, and shorter alloying time. © 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

  12. Kinetics of Silver Dissolution in Nitric Acid from Ag-Au0.04-Cu0.10 and Ag-Cu0.23 Scraps

    Institute of Scientific and Technical Information of China (English)

    S.K.Sadrnezhaad; E.Ahmadi; M.Mozammel

    2006-01-01

    Kinetics of dissolution of silver present in precious metal scraps in HNO3 was studied in temperature range of 26~85℃. Dissolution rate of silver was much faster than that of copper at all temperatures. Effects of particle size, stirring speed, acid concentration and temperature on the rate of dissolving of silver were evaluated.Dissolution rate decreases with particle size and increases with temperature. Dissolving was accelerated with acid concentrations less than 10 mol/L. Concentrations greater than 10 mol/L resulted in slowing down of the dissolution rate. Shrinking core model with internal diffusion equation t/τ=1-3(1-x)2/3+2(1-x)could be used to explain the mechanism of the reaction. Silver extraction resulted in activation energies of 33.95 k J/mol for Ag-Au0.04-Cu0.10 and 68.87 k J/mol for Ag-Cu0.23 particles. Inter-diffusion of silver and nitrate ions through the porous region of the insoluble alloying layer was the main resistance to the dissolving process. Results were tangible for applications in recycling of the material from electronic silver-bearing scraps, dental alloys,jewelry, silverware and anodic slime precious metal recovery.

  13. Preparation and thermal treatment of Pd/Ag composite membrane on a porous α-alumina tube by sequential electroless plating technique for H2 separation

    Institute of Scientific and Technical Information of China (English)

    E.Navaei Alvar; M.Reza Golmohammadi; M.Rezaei; H.Navaei Alvar; A.Mardanloo; S.Habibzad Nouhian; M.Didari

    2008-01-01

    Pd/Ag/α-Al2O3 composite membranes were prepared by sequential electroless plating technique. The prepared membranes were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spec-troscopy, and inductively coupled plasma atomic emission spectroscopy techniques (ICP-AES). Effects of annealing time, Ag content, and air treatment on the hydrogen permeation flux and morphology of the alloys were investigated. The results of the investigation showed that the prepared type of tube had a good potential as substrate for membrane preparation. In addition, a uniform defect-free alloy was prepared by annealing at 550 ℃ in H2 atmosphere. The permeation results showed an increase in H2 permeation flux by increasing the Ag content and the annealing time. In addition, the air treatment of the prepared membranes at 400 ℃ for 1 h changed the morphology of the alloy and substantially enhanced the hydrogen flux.

  14. Research on the performance of AuPdPt-WC/C as a composite catalyst on cathode reaction of DMFC%AuPdPt-WC/C复合材料作为直接甲醇燃料电池阴极催化剂的性能研究

    Institute of Scientific and Technical Information of China (English)

    郑仓晟; 聂明; 李庆; 王宏煜; 袁宇; 刘晓卫; 杜胜娟; 刘其阳; 王孝益

    2015-01-01

    本实验以碳化钨(WC)增强的AuPdPt-WC/C复合催化剂作为直接甲醇燃料电池(DMFC)的阴极催化剂,选取了各组元比例,温度为变量,测试了其作为 DMFC催化剂的性能。首先,采用了间歇微波加热法(IHM)制备了纳米级的碳化钨(WC)颗粒,并采用还原法和真空干燥法制备了 AuPdPt-WC/C 复合催化剂,控制 Au、Pd、Pt的比例,制备了两组催化剂。通过循环伏安扫描,线性伏安扫描等手段进行电化学测试,表征其氧还原的性能。结果显示,复合催化剂具有高于传统 Pt/C催化剂的性能,并且与实验条件息息相关。%Our research mainly focuses on the preparation and characterization of tungsten carbide (WC) enhanced AuPdPt-WC/C composite catalyst of the cathode oxygen reduction reaction of direct methanol fuel cells (DMFC). By using intermittent mi-crowave heating method, we firstly synthesized nano tungsten carbide particle, then we prepared two AuPdPt-WC/C catalyst of different composition through reduction method and vacuum drying method. For characterization, we controlled composition and temperature as variable and used cyclic voltammetry and linear sweep voltammetry for electrochemistry test. The results indicated that the composite catalyst has a better performance than common single Pt catalyst and its performance is influenced by operating conditions.

  15. CO Sensing Performance of a Micro Thermoelectric Gas Sensor with AuPtPd/SnO₂ Catalyst and Effects of a Double Catalyst Structure with Pt/α-Al₂O₃.

    Science.gov (United States)

    Goto, Tomoyo; Itoh, Toshio; Akamatsu, Takafumi; Shin, Woosuck

    2015-12-15

    The CO sensing properties of a micro thermoelectric gas sensor (micro-TGS) with a double AuPtPd/SnO₂ and Pt/α-Al₂O₃ catalyst were investigated. While several nanometer sized Pt and Pd particles were uniformly dispersed on SnO₂, the Au particles were aggregated as particles measuring >10 nm in diameter. In situ diffuse reflectance Fourier transform Infrared spectroscopy (DRIFT) analysis of the catalyst showed a CO adsorption peak on Pt and Pd, but no clear peak corresponding to the interaction between CO and Au was detected. Up to 200 °C, CO combustion was more temperature dependent than that of H₂, while H₂ combustion was activated by repeated exposure to H₂ gas during the periodic gas test. Selective CO sensing of the micro-TGS against H₂ was attempted using a double catalyst structure with 0.3-30 wt% Pt/α-Al₂O₃ as a counterpart combustion catalyst. The sensor output of the micro-TGS decreased with increasing Pt content in the Pt/α-Al₂O₃ catalyst, by cancelling out the combustion heat from the AuPtPd/SnO₂ catalyst. In addition, the AuPtPd/SnO₂ and 0.3 wt% Pt/α-Al₂O₃ double catalyst sensor showed good and selective CO detection. We therefore demonstrated that our micro-TGS with double catalyst structure is useful for controlling the gas selectivity of CO against H₂.

  16. The crystal structures of jaguéite, Cu2Pd3Se4, and chrisstanleyite, Ag2Pd3Se4

    DEFF Research Database (Denmark)

    Topa, Dan; Makovicky, Emil; Balic Zunic, Tonci

    2006-01-01

    The crystal structure of jaguéite, ideally Cu2Pd3Se4, monoclinic, a 5.672(5), b 9.909(9), c 6.264(6) Å, ß 115.40(2)º, space group P21/c, has been solved by direct methods and refi ned to an R1 index of 5.52% for 956 unique refl ections measured with MoK X-radiation on a P-4 Bruker diffractometer...... equipped with a CCD area-detector. The crystal structure of chrisstanleyite, ideally Ag2Pd3Se4, monoclinic a 5.676(2), b 10.342(4), c 6.341(2) Å, ß 114.996(4)º, space group P21/c, has been solved by direct methods and refi ned to an R1 index of 8.3% for 1203 unique refl ections measured with MoK X...

  17. Applicability of near-infrared hyperspectral imagery (NIR-HI) for sensor based sorting of an epithermal Au-Ag ore

    NARCIS (Netherlands)

    Dalm, M.; Buxton, M.W.N.; Van Ruitenbeek, F.J.A.

    2015-01-01

    In the presented study test work was performed with near-infrared hyperspectral imagery (NIR-HI) on 36 ore samples from a South-American epithermal Au-Ag mine. The aim of the test work was to investigate if NIR-HI provides information about the alteration mineralogy of samples that can be used to pr

  18. {sup 3}He induced reactions on {sup nat}Ag and {sup 197}Au at 1.8, 3.6 and 4.8 GeV

    Energy Technology Data Exchange (ETDEWEB)

    Brzychczyk, J. [CEA Centre d`Etudes de Saclay, 91 - Gif-sur-Yvette (France). Dept. d`Astrophysique, de la Physique des Particules, de la Physique Nucleaire et de l`Instrumentation Associee]|[Jagiellonian Univ., Krakow (Poland). Inst. of Physics; Pollacco, E.C.; Volant, C.; Legrain, R. [CEA Centre d`Etudes de Saclay, 91 - Gif-sur-Yvette (France). Dept. d`Astrophysique, de la Physique des Particules, de la Physique Nucleaire et de l`Instrumentation Associee; Kwiatkowski, K.; Morley, K.B.; Renshaw-Foxford, E.; Bracken, D.S.; Viola, V.E.; Yoder, N.R. [Indiana Univ., Bloomington, IN (United States). Dept. of Chemistry] [and others

    1995-03-01

    The {sup 3}He induced reactions on Ag and Au are studied using a large solid angle and low energy threshold detector array. The data show consistency with intranuclear cascade and expanding emitting source description. Charge moment analysis is presented. (author). 18 refs., 8 figs.

  19. Tuning the ground state of the Kondo lattice in UT Bi2 (T = Ag, Au) single crystals

    Science.gov (United States)

    Rosa, Priscila; Luo, Yongkang; Pagliuso, Pascoal; Bauer, Eric; Thompson, Joe; Fisk, Zachary

    2015-03-01

    Motivated by the interesting magnetic anisotropy found in the Ce-based heavy fermion family Ce TX2 (T = transition metal, X = pnictogen), here we study the novel U-based parent compounds U TBi2 (T = Ag, Au) by combining magnetization, electrical resistivity, and heat-capacity measurements. The single crystals, synthesized by the self-flux method, also crystallize in the tetragonal HfCuSi2-type structure (space group P4/nmm). Interestingly, although UAgBi2 is a low- γ antiferromagnet below TN = 181 K, UAuBi2 is a moderately heavy uniaxial ferromagnet below Tc = 22 K. Nevertheless, both compounds display the easy-magnetization direction along the c-axis and a large magnetocrystalline anisotropy. Our results point out to an incoherent Kondo behaviour in the paramagnetic state and an intricate competition between crystal field effects and two anisotropic exchange interactions, which lead to the remarkable difference in the observed ground states.

  20. Ultrasensitive SERS detection of VEGF based on a self-assembled Ag ornamented-AU pyramid superstructure.

    Science.gov (United States)

    Zhao, Sen; Ma, Wei; Xu, Liguang; Wu, Xiaoling; Kuang, Hua; Wang, Libing; Xu, Chuanlai

    2015-06-15

    For the first time, we demonstrated the fabrication of silver nanoparticle ornamented-gold nanoparticle pyramids (Ag-Au Pys) using an aptamer-based self-assembly process and investigated their surface-enhanced Raman scattering (SERS) properties in the detection of vascular endothelial growth factor (VEGF). Under optimized conditions, the SERS signal was negatively related to VEGF concentration over the range 0.01-1.0 fM and the limit of detection (LOD) was as low as 22.6 aM. The matrix effect and the specificity of this developed method were further examined, and the results showed that the superstructure sensor was ultrasensitive and highly selective. This developed aptamer-based SERS detection method suggests that it may be a promising strategy for a variety of sensing applications.

  1. Spin and orbital magnetism of coinage metal trimers (Cu3, Ag3, Au3: A relativistic density functional theory study

    Directory of Open Access Journals (Sweden)

    Mahdi Afshar

    2013-11-01

    Full Text Available We have demonstrated electronic structure and magnetic properties of Cu3, Ag3 and Au3 trimers using a full potential local orbital method in the framework of relativistic density functional theory. We have also shown that the non-relativistic generalized gradient approximation for the exchange-correlation energy functional gives reliable magnetic properties in coinage metal trimers compared to experiment. In addition we have indicated that the spin-orbit coupling changes the structure and magnetic properties of gold trimer while the structure and magnetic properties of copper and silver trimers are marginally affected. A significant orbital moment of 0.21μB was found for most stable geometry of the gold trimer whereas orbital magnetism is almost quenched in the copper and silver trimers.

  2. Energy reflection coefficents for 5-10 keV He ions incident on Au, Ag and Cu

    International Nuclear Information System (INIS)

    The calorimetric deuterium-film method was used for measurements of the energy reflection coefficient γ for normal incidence of 5-10 keV He ions on Cu, Ag and Au. A theoretical calculation of β by means of transport theory gives fair agreement with the experimental results. The experimental data for all three materials lie on a single curve, if depicted as a function of the reduced entry epsilon, γ varies from 0.14 to 0.04 with epsilon varying from 0.2 to 1.6. The calculated data do not show similar behaviour, and the position of each curve depends on the specific beam-target combination. Both the experimental and theoretical results for the He ions are in acceptable agreement with other experimental and theoretical results. For He ions, the experimental γ-values are 20-30% above the values for hydrogen ions for the same value of epsilon. (Auth.)

  3. Self-standing corrugated Ag and Au-nanorods for plasmonic applications

    DEFF Research Database (Denmark)

    Habouti, S.; Mátéfi-Tempfli, M.; Solterbeck, C.-H.;

    2011-01-01

    of the NR arrays as substrates for molecular detection using Raman scattering and Rhodamine 6G (R6G) as a model dye strongly depends on noble metal. R6G concentrations down to 1 pM are detected on the corrugated arrays yielding an effective enhancement factor (EF) of approximately 2 × 10 for Ag...

  4. Synthesis, spectroscopic, thermal and anticancer studies of metal-antibiotic chelations: Ca(II), Fe(III), Pd(II) and Au(III) chloramphenicol complexes

    Science.gov (United States)

    Al-Khodir, Fatima A. I.; Refat, Moamen S.

    2016-09-01

    Four Ca(II), Fe(III), Pd(II) and Au(III) complexes of chloramphenicol drug have been synthesized and well characterized using elemental analyses, (infrared, electronic, and 1H-NMR) spectra, magnetic susceptibility measurement, and thermal analyses. Infrared spectral data show that the chloramphenicol drug coordinated to Ca(II), Pd(II) and Au(III) metal ions through two hydroxyl groups with 1:1 or 1:2 M ratios, but Fe(III) ions chelated towards chloramphenicol drug via the oxygen and nitrogen atoms of amide group with 1:2 ratio based on presence of keto↔enol form. The X-ray powder diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscopy (TEM) techniques were used to identify the nano-size particles of both iron(III) and gold(III) chloramphenicol complexes. The antimicrobial assessments of the chloramphenicol complexes were scanned and collected the results against of some kind of bacteria and fungi. The cytotoxic activity of the gold(III) complex was tested against the human colon carcinoma (HCT-116) and human hepatocellular carcinoma (HepG-2) tumor cell lines.

  5. 4{pi} studies of the 1.8-4.8 GeV {sup 3}He+{sup nat}Ag, {sup 197}Au reactions. I. Energy deposition

    Energy Technology Data Exchange (ETDEWEB)

    Morley, K.B.; Kwiatkowski, K.; Bracken, D.S.; Renshaw Foxford, E. [Indiana Univ., Bloomington, IN (United States). Dept. of Chemistry; Legrain, R.; Pollacco, E.C.; Volant, C. [CEA Centre d`Etudes de Saclay, 91 - Gif-sur-Yvette (France). Dept. d`Astrophysique, de la Physique des Particules, de la Physique Nucleaire et de l`Instrumentation Associee; Korteling, R.G. [Simon Fraser Univ., Burnaby, BC (Canada). Dept. of Chemistry; Breuer, H. [Maryland Univ., College Park, MD (United States). Dept. of Physics; Brzychczyk, J. [Jagellonian Univ., Krakow (Poland). Inst. of Physics

    1996-01-01

    The 4{pi} detector ISiS has been used to measure light-charged particles and intermediate-mass-fragments emitted in the 1.8-4.8 GeV {sup 3}He+{sup nat}Ag, {sup 197}Au reactions. Ejectile multiplicity and total event kinetic energy distribution scale systematically with projectile energy and target mass, except for the {sup nat}Ag target at 3.6 and 4.8 GeV. For this system, a saturation in deposition energy is indicated by the data, suggesting the upper projectile energy for stopping has been reached. Maximum deposition energies of {approx}950 MeV for the {sup nat}Ag target and {approx}1600 MeV for the {sup 197}Au target are inferred from the data. Comparison of the experimental distributions with intranuclear cascade predictions shows qualitative agreement. (author). Submitted to Physical Review, C (US); 46 refs.

  6. Changes in the real structure and magnetoresistance of Co90Fe10/Cu and Co90Fe10/Cu85Ag10Au5 multilayers after annealing

    International Nuclear Information System (INIS)

    Annealing of the (1.1 nm Co90Fe10/2.2 nm Cu)x20 and (1.1 nm Co90Fe10/2.2 nm Cu85Ag10Au5)x20 multilayers at 235 deg. C improved their magnetoresistance as compared to the virgin samples. Annealing at higher temperatures resulted in degradation of the magnetoresistance effect. This observation raised the motivation of a detailed structural study using small-angle X-ray scattering, wide-angle X-ray diffraction, electron diffraction and transmission electron microscopy with the aim to link the structural changes in the system to the changes in the magnetoresistance. The structure studies have shown that the maximum of the magnetoresistance observed after annealing at 235 deg. C is related to the separation of Co90Fe10 and Cu, which are partly intermixed at interfaces after the deposition process. The decay of the GMR effect at higher annealing temperatures is caused by an increase of the interface roughness, which led in the Co90Fe10/Cu multilayers to occurrence of non-continuous interfaces and to short-circuiting of magnetic layers. In the Cu85Ag10Au5 multilayers, the combination of small-angle X-ray scattering and wide-angle X-ray diffraction has shown that Cu85Ag10Au5 did not form an alloy with the nominal composition: Only a part of Au and Ag was dissolved in the copper structure; the remainder of Ag and Au formed precipitates

  7. Relativistic and correlated all-electron calculations on the ground and excited states of AgH and AuH

    Science.gov (United States)

    Witek, Henryk A.; Nakijima, Takahito; Hirao, Kimihiko

    2000-11-01

    We report relativistic all-electron multireference based perturbation calculations on the low-lying excited states of gold and silver hydrides. For AuH, we consider all molecular states dissociating to the Au(2S)+H(2S) and Au(2D)+H(2S) atomic limits, and for AgH, the states corresponding to the Ag(2S)+H(2S), Ag(2P)+H(2S), and Ag(2D)+H(2S) dissociation channels. Spin-free relativistic effects and the correlation effects are treated on the same footing through the relativistic scheme of eliminating small components (RESC). Spin-orbit effects are included perturbatively. The calculated potential energy curves for AgH are the first reported in the literature. The computed spectroscopic properties agree well with experimental findings; however, the assignment of states does not correspond to our calculations. Therefore, we give a reinterpretation of the experimentally observed C 1Π, a 3Π, B 1Σ+, b(3Δ1)1, D 1Π, c13Π1, and c0(3Π0) states. A labeling suggested by us is a1, C0+, b0-, c2, B3Π0+, d3Π1, e1, f1 and g1, respectively. The spin-orbit states corresponding to Ag(2D)+H(2S) have not well defined the Λ and S quantum numbers, and therefore, they probably correspond to Hund's coupling case c. For AuH, we present a comparison of the calculated potential energy curves and spectroscopic parameters with the previous configuration interaction study and the experiment.

  8. Nano-Crystal Formation and Growth from High-Fluence Ion Implantation of Au, Ag or Cu in Silica

    Science.gov (United States)

    Ila, D.; Baglin, J. E. E.; Zimmerman, R. L.

    The linear and non-linear optical properties of silica may be tailored by the introduction of a random distribution of nanocrystallites of an immiscible metal within a near-surface region. The size, size distribution, and spatial distribution of these crystallites must be controllable in order to optimize the functional properties for device applications. In this paper, we present a novel fabrication technique that offers such control. Energetic metal ions are implanted in silica at room temperature. Subsequent heat treatment leads to diffusion of the implanted atoms, nucleation and growth of metal crystallites, and Ostwald ripening of the resulting clusters. We have observed the kinetics and effective activation energies describing the multiple processes involved, for the cases of Au, Ag or Cu implanted at MeV energies, at various fluences, and then annealed at fixed temperatures in the range 500 °C-1000 °C. Effective activation energies found for nanocrystal nucleation and growth at temperatures below 800 °C (e.g. 64 meV for Ag) are replaced above this temperature range by much higher activation energies (e.g. 400 meV for Ag). We may attribute this to the depletion of un-attached mobile metal atoms (so that ripening of clusters will be limited by energy barriers for escape of such mobile atoms from small crystallites), and/or the annealing of implant-caused stress in the silica structure at high temperatures, that creates new channels for thermal diffusion of metal atoms within the silica host.

  9. Magnetic behaviour of Ce(Pd{sub 1-x}M{sub x}) compounds (M=Rh, Ni and Ag) within the LDA approximation

    Energy Technology Data Exchange (ETDEWEB)

    Vildosola, V.L.; Llois, A.M. E-mail: llois@cnea.gov.ar; Weissmann, M.; Sereni, J.G

    2001-10-01

    Ce intermetallic compounds have been intensively studied in the last few decades due to the large variety of behaviours they exhibit. In particular, two ways of demagnetizing Ce have been experimentally tried within the ferromagnetic systems Ce(Pd{sub 1-x}M{sub x}), namely through electronic concentration variations (M=Rh) and volume reductions (M=Ni). On the other hand, when Pd is substituted by Ag, a transformation from a ferromagnetic to an antiferromagnetic ground state has been observed. In this work, we analyse the evolution of the magnetism of Ce in the above-mentioned family of compounds by calculating the spin contribution to magnetism that results from spin polarised LDA calculations.

  10. Factors determining the structure of Au, Ag and Cr thin layers deposited on alkaline halogen substrates

    International Nuclear Information System (INIS)

    Metal thin layer deposited on dielectric substrates, in general, and on alkaline halogen substrates, in particular, have been thoroughly studied in order to make clear the phenomenology of the formation and development processes, to set out fundamental factors in determining their structure and to determine optimum conditions for the obtaining of monocrystal thin layers or metastable structured thin layers in view of their practical applications. Starting from a systematic programme of experimental investigations, an attempt has been made to investigate the influence of substrate composition, of defects within alkaline halogen substrates and of deposition conditions on the orientated formation and development of Au layer and on the formation of metastable Cr-delta structures in the case of thin Cr layers. A systematic study on the influence of deposition conditions and on alkaline halogen substrates with colloidal centres is carried out in view of elaborating a method for the development of monocrystal Au layers for ''channeling targets''. A correlation between characteristic parameters which define the atomic theory of nucleation including deposition conditions and material parameters, Au parameters for the case of epitaxial layers deposited on KBr, KCl and NaCl substrates has been attempted. (author)

  11. Energy Parameters of Interfacial Layers in Composite Systems: Graphene – (Si, Cu, Fe, Co, Au, Ag, Al, Ru, Hf, Pb and Semiconductor (Si,Ge – (Fe, Co, Cu, Al, Au, Cr, W, Pb

    Directory of Open Access Journals (Sweden)

    B.P. Koman

    2015-12-01

    Full Text Available On the basis of the non-equilibrium thermodynamics relations and the surface physics phenomena we calculate adhesion and energy parameters to characterize the interfacial interactions in graphene – (Si, Cu, Fe, Co, Au, Ag, Al, Ru, Hf, Pb and semiconductor (Si, Ge – (Fe, Co, Cu, Al, Au, Cr, W, Pb systems. We analyze trends of the interfacial energy, interfacial tension, work of adhesion and the energy of adhesive bonds on the contacting element’s atomic number in the periodic table and on the electronegativity difference of interacting elements. Thus, this work provides theoretical basis for the development of new composite materials.

  12. TiO2纳米管负载Ag、Au、Pt纳米粒子的微波合成与表征%Microwave Synthesis and Characterization of Ag, Au, Pt Nanoparticles Supported on TiO2 Nanotubes

    Institute of Scientific and Technical Information of China (English)

    包华辉; 徐铸德; 殷好勇; 郑遗凡; 陈卫祥

    2005-01-01

    TiO2 nanotubes were prepared under normal pressure at a temperature of 120℃. Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were prepared by microwave assisted heating polyol process. TEM images showed that microwave prepared Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were small and well dispersed on the surface of the TiO2 nanotubes. UV-Vis absorption spectra showed that the absorbance of Ag/TiO2 nanotubes and Au/TiO2 nanotubes in the visible light range increased greatly compared to the single titania nanotubes.

  13. Using Geomodelling and Geophysical Inversion to Evaluate the Geological Controls on Low-Sulphidation Epithermal Au-Ag mineralisation in the Drummond and Bowen Basins, Australia

    Science.gov (United States)

    Feltrin, Leonardo; Baker, Timothy; Oliver, Nick; Scott, Margaretha; Wilkinson, Kate; Fitzell, Melanie; Dixon, Owen; Bertelli, Martina

    2008-05-01

    We present a 3D geological model that integrates different datasets and incorporates geophysical inversion of airborne gravimetric and magnetic surveys of the northern part of the Drummond and Bowen basins. These basins are known for their endowment of low-sulphidation, epithermal Au-Ag mineralisation. The objective of this computer based reconstruction is to empirically evaluate the key controlling variables that contributed to the spatial localization of 147 Palaeozoic and Mesozoic shallow hydrothermal gold systems, found predominantly in veins and breccia hosted in basal volcanics and volcaniclastic intervals developed in a back-arc rift environment. The model provides a three-dimensional, regional scale (100,000 km2) perspective on the spatial associations between geology, structure, magmatism and known mineral occurrences, representing a 3D framework for precious-metals exploration. Results of 3D visualisation of geological and geophysical data suggest that magmatic intrusions, and correlative volcanic centres localized most of the major deposits and also controlled the arrangement of clusters of uneconomic Au-Ag occurrences. The empirical modelling supports a model for the genesis of low-sulphidation epithermal Au-Ag mineralisation that favours a strong spatial association with shallow felsic to intermediate magmatic intrusions, similarly to that proposed for high-sulphidation systems. Geophysical inversion estimates for the depth of magmatic bodies suggest also that they may have controlled the efficiency of the hydrothermal, mineralising systems-shallow intrusions tend to be associated with greater tonnages of Au-Ag and are spatially associated with the larger clusters of occurrences. However, the composition of magmatic intrusions (mafic, intermediate, felsic) may have been important in regulating the amount of available bisulphide in the volatile phase, exerting a control on Au grade/tonnage independent of the depth of emplacement of intrusions.

  14. 碱性溶液中铂、钯和金析氧性能比较%Performance comparison of oxygen evolution reaction for Pt/C,Pd/C and Au/C in alkaline medium

    Institute of Scientific and Technical Information of China (English)

    徐常威; 梁杰聪; 王静

    2015-01-01

    Activity and stability of oxygen evolution reaction (OER)for Pt/C,Pd /C and Au /C have been com-pared in 0.1 mol·L -1 KOH solution.The activity order of OER is Pd /C >Pt/C >Au /C and the stability order of OER is Pd /C >Au /C >Pt/C.The Pd /C gives the best OER stability,which is in agreement with that the Pd /C gives the best OER activity.Au /C gives a better stability than Pt/C,although it gives a worse activity than Pt/C.%比较研究了 Pt/C、Pd /C 和 Au/C 在0.1 mol·L -1 KOH 水溶液中的析氧催化活性和稳定性.3种催化剂的析氧催化活性的顺序:Pd /C >Pt/C >Au/C,析氧催化稳定性的顺序:Pd/C >Au/C >Pt/C.Pd/C 析氧稳定性最好,这和其最高的析氧催化活性一致.Au/C 虽然析氧催化活性比 Pt/C 低,但其析氧催化稳定性比 Pt/C 高.

  15. Room temperature biogenic synthesis of multiple nanoparticles (Ag, Pd, Fe, Rh, Ni, Ru, Pt, Co, and Li) by Pseudomonas aeruginosa SM1

    Energy Technology Data Exchange (ETDEWEB)

    Srivastava, Sarvesh Kumar; Constanti, Magda, E-mail: magdalena.constanti@urv.cat [Universitat Rovira i Virgili, Departament d' Enginyeria Quimica (Spain)

    2012-03-15

    Room temperature biosynthesis of Ag, Pd, Fe, Rh, Ni, Ru, Pt, Co, and Li nanoparticles was achieved using Pseudomonas aeruginosa SM1 without the addition of growth media, electron donors, stabilizing agents, preparation of cell/cell-free extract or temperature, and pH adjustments. The resulting nanoparticles were characterized by Transmission electron microscopy and X-ray diffraction. It was observed that P. aeruginosa SM1 is capable of producing both intracellular (Co and Li) and extracellular (Ag, Pd, Fe, Rh, Ni, Ru, and Pt) nanoparticles in both crystalline and amorphous state. The FT-IR spectra clearly showed the presence of primary and secondary amines which may be responsible for the reduction and subsequent stabilization of the resulting extracellular nanoparticles which were obtained as a one-step process. This suggests toward an unknown 'selection mechanism' that reduces certain metal ions and allows others to enter the cell membrane. Finally, in this first of its kind study, single strain of bacteria was used to produce several different mono-metallic nanoparticles.

  16. Room temperature biogenic synthesis of multiple nanoparticles (Ag, Pd, Fe, Rh, Ni, Ru, Pt, Co, and Li) by Pseudomonas aeruginosa SM1

    International Nuclear Information System (INIS)

    Room temperature biosynthesis of Ag, Pd, Fe, Rh, Ni, Ru, Pt, Co, and Li nanoparticles was achieved using Pseudomonas aeruginosa SM1 without the addition of growth media, electron donors, stabilizing agents, preparation of cell/cell-free extract or temperature, and pH adjustments. The resulting nanoparticles were characterized by Transmission electron microscopy and X-ray diffraction. It was observed that P. aeruginosa SM1 is capable of producing both intracellular (Co and Li) and extracellular (Ag, Pd, Fe, Rh, Ni, Ru, and Pt) nanoparticles in both crystalline and amorphous state. The FT-IR spectra clearly showed the presence of primary and secondary amines which may be responsible for the reduction and subsequent stabilization of the resulting extracellular nanoparticles which were obtained as a one-step process. This suggests toward an unknown “selection mechanism” that reduces certain metal ions and allows others to enter the cell membrane. Finally, in this first of its kind study, single strain of bacteria was used to produce several different mono-metallic nanoparticles.

  17. Effect of Silicon on Activity Coefficients of Siderophile Elements (P, Au, Pd, As, Ge, Sb, and In) in Liquid Fe, with Application to Core Formation

    Science.gov (United States)

    Righter, K.; Pando, K.; Danielson, L. R.; Humayun, M.; Righter, M.; Lapen, T.; Boujibar, A.

    2016-01-01

    Earth's core contains approximately 10 percent light elements that are likely a combination of S, C, Si, and O, with Si possibly being the most abundant. Si dissolved into Fe liquids can have a large effect on the magnitude of the activity coefficient of siderophile elements (SE) in Fe liquids, and thus the partitioning behavior of those elements between core and mantle. The effect of Si can be small such as for Ni and Co, or large such as for Mo, Ge, Sb, As. The effect of Si on many siderophile elements is unknown yet could be an important, and as yet unquantified, influence on the core-mantle partitioning of SE. Here we report new experiments designed to quantify the effect of Si on the partitioning of P, Au, Pd, and many other SE between metal and silicate melt. The results will be applied to Earth, for which we have excellent constraints on the mantle siderophile element concentrations.

  18. Au-Pd/reduced graphene oxide composite as a new sensing layer for electrochemical determination of ascorbic acid, acetaminophen and tyrosine.

    Science.gov (United States)

    Tadayon, Fariba; Vahed, Saba; Bagheri, Hasan

    2016-11-01

    An Au-Pd/reduced graphene oxide composite was employed as a novel electrode material for the sensitive and simultaneous determination of ascorbic acid, acetaminophen and tyrosine. The electrochemical response characteristics of the modified electrode toward the analytes were investigated by differential pulse voltammetry and cyclic voltammetry. The responses of the electrochemical sensor for the target analytes were found to be improved significantly in comparison with those obtained using a conventional carbon paste electrode (CPE) and reduced graphene oxide/CPE. The experimental conditions for simultaneous determination of these species have been established. Ternary mixtures of analytes can be determined in the ranges of 0.03-9.50μM. Under optimal conditions, the limits of detection were 15.7, 7.6 and 11.1nM for ascorbic acid, acetaminophen, and tyrosine, respectively. The method was applied successfully to determine the analytes in urine, serum and pharmaceutical samples simultaneously. PMID:27524083

  19. Reduced graphene oxide nanosheets decorated with Au-Pd bimetallic alloy nanoparticles towards efficient photocatalytic degradation of phenolic compounds in water

    Science.gov (United States)

    Darabdhara, Gitashree; Boruah, Purna K.; Borthakur, Priyakshree; Hussain, Najrul; Das, Manash R.; Ahamad, Tansir; Alshehri, Saad M.; Malgras, Victor; Wu, Kevin C.-W.; Yamauchi, Yusuke

    2016-04-01

    Reduced graphene oxide nanosheets decorated with Au-Pd bimetallic alloy nanoparticles are successfully prepared via a chemical approach consisting of reducing the metal precursors using ascorbic acid as reductant at an elevated temperature. The prepared nanocomposite is employed as a photocatalyst for the degradation of organic contaminants such as phenol, 2-chlorophenol (2-CP), and 2-nitrophenol (2-NP). The complete degradation of phenol is achieved after 300 min under natural sunlight irradiation whereas the degradation of 2-CP and 2-NP is completed after 180 min. The activity of the photocatalyst is evaluated considering several parameters such as the initial phenol concentration, the photocatalyst loading, and the pH of the solution. The degradation kinetics of all the compounds is carefully studied and found to follow a linear Langmuir-Hinshelwood model. Furthermore, the reusability of the photocatalyst is successfully achieved up to five cycles and the catalyst exhibits an excellent stability.Reduced graphene oxide nanosheets decorated with Au-Pd bimetallic alloy nanoparticles are successfully prepared via a chemical approach consisting of reducing the metal precursors using ascorbic acid as reductant at an elevated temperature. The prepared nanocomposite is employed as a photocatalyst for the degradation of organic contaminants such as phenol, 2-chlorophenol (2-CP), and 2-nitrophenol (2-NP). The complete degradation of phenol is achieved after 300 min under natural sunlight irradiation whereas the degradation of 2-CP and 2-NP is completed after 180 min. The activity of the photocatalyst is evaluated considering several parameters such as the initial phenol concentration, the photocatalyst loading, and the pH of the solution. The degradation kinetics of all the compounds is carefully studied and found to follow a linear Langmuir-Hinshelwood model. Furthermore, the reusability of the photocatalyst is successfully achieved up to five cycles and the catalyst

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

    Science.gov (United States)

    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.

  1. Optimized core-shell Au@Ag nanoparticles for label-free Raman determination of trace Rhodamine B with cancer risk in food product.

    Science.gov (United States)

    Wang, Hui; Guo, Xiaoyu; Fu, Shuyue; Yang, Tianxi; Wen, Ying; Yang, Haifeng

    2015-12-01

    A simple and reliable method based on surface-enhanced Raman scattering (SERS) with a portable Raman system is described for sensitive determination of trace levels of Rhodamine B (RB) in hot sauce samples. The sodium salt of phytic acid (IP6) stabilized Au@Ag core-shell bimetallic nanoparticles are constructed and used as SERS substrate, yielding high Raman enhancement of RB. The limit of detection for RB in water is 5 nM (2 ppb), which is below China Exit and Entry Inspection and Quarantine Bureau's tolerance level of 5 ppb. Also, the proposed easy assay of IP6-Au@Ag NPs combining with portable Raman system could be applied for on-site monitoring RB in hot sauce. PMID:26041175

  2. The Controlled Single-Step Synthesis of Ag/TiO2 and Au/TiO2 by Ultrasonic Spray Pyrolysis (USP)

    Science.gov (United States)

    Bogovic, J.; Rudolf, R.; Friedrich, B.

    2016-01-01

    This article reports the synthesis of Ag/TiO2 and Au/TiO2 nanoparticles by single-step ultrasonic spray pyrolysis (USP) conducted by an investigation of the process parameters and the morphological characteristics of the obtained nanostructures. The influence of the ratio in the precursor solution, physical characteristics of used components, and temperature had a large influence on the formation of different nanoparticle morphologies. The experimental investigations were performed using classic USP equipment, with variations of the process parameters. Scanning electron microscopy, transmission electron microscopy, and focused ion beam analyses were used to characterize the complex nanostructures. Based on the obtained results, the optimal process window for the formation of the different morphologies for the Ag/TiO2 and Au/TiO2 nanoparticles is determined and the possibility of synthesis of the core-shell structures in one step by USP is confirmed.

  3. Enhancement of superconducting Tc (33 K) by entrapment of FeSe in carbon coated Au-Pd17Se15 nanoparticles.

    Science.gov (United States)

    Mishra, Sukhada; Song, Kai; Ghosh, Kartik C; Nath, Manashi

    2014-03-25

    FeSe has been an interesting member of the Fe-based superconductor family ever since the discovery of superconductivity in this simple binary chalcogenide. Simplicity of composition and ease of synthesis has made FeSe, in particular, very lucrative as a test system to understand the unconventional nature of superconductivity, especially in low-dimensional models. In this article we report the synthesis of composite nanoparticles containing FeSe nanoislands entrapped within an ent-FeSe-Pd16Se15-Au nanoparticle and sharing an interface with Pd17Se15. This assembly exhibits a significant enhancement in the superconducting Tc (onset at 33 K) accompanied by a noticeable lattice compression of FeSe along the and directions. The Tc in FeSe is very sensitive to application of pressure and it has been shown that with increasing external pressure Tc can be increased almost 4-fold. In these composite nanoparticles reported here, immobilization of FeSe on the Pd17Se15 surface contributes to increasing the effect of interfacial pressure, thereby enhancing the Tc. The effect of interfacial pressure is also manifested in the contraction of the FeSe lattice (up to 3.8% in direction) as observed through extensive high-resolution TEM imaging. The confined FeSe in these nanoparticles occupied a region of approximately 15-25 nm, where lattice compression was uniform over the entire FeSe region, thereby maximizing its effect in enhancing the Tc. The nanoparticles have been synthesized by a simple catalyst-aided vapor transport reaction at 800 °C where iron acetylacetonate and Se were used as precursors. Morphology and composition of these nanoparticles have been studied in details through extensive electron microscopy. PMID:24494773

  4. Geology and mineralogy of the Au-As (Ag-Pb-Zn-Cu-Sb polymetallic deposit of Valiña-Azúmara (Lugo, NW Spain

    Directory of Open Access Journals (Sweden)

    Martínez-Abad, I.

    2015-12-01

    Full Text Available Valiña-Azúmara is a polymetallic Au-As (Ag-Pb-Zn-Cu-Sb deposit, located in the province of Lugo (NW Spain, that was mined for arsenic at the beginning of the 20th century. The mineralization is hosted in a Variscan thrust fault with a dip direction of N247-261ºE, and N-S and NE-SW Late-Variscan faults. These structures are hosted in black slates, Cambrian in age. To a lesser extent, the mineralization also occurs disseminated within narrow, weakly silicified and sericited selvages. Mineralization is divided into two hypogene stages. The first consists of quartz, calcite, rutile, sericite, arsenopyrite and pyrite. Two types of pyrite (Py-I and Py-II are defined according to their chemical and textural characteristics. Py-II occurs as overgrowth of previous Py-I crystals. Py-II is As-rich (≤1.7 wt.% and often contains traces of Te, Zn, Cu, Bi, Sb and Au. The mineralized drill core sections show a significant correlation between Au and As. This is due to Au occurring as invisible Au within the Py-II grains, with contents of up to 176 ppm. The Au/As ratios of Py-II indicate that Au was deposited as Au1+, as solid solution within the pyrite structure. The second stage of mineralization is enriched in Ag-Pb-Zn-Cu-Sb, replacing the first stage, and consists of quartz, calcite, chlorite, sphalerite, jamesonite, Ag-rich tetrahedrite, freibergite, chalcopyrite, pyrrhotite and galena. Although jamesonite shows traces of Ag, the Cu-Ag sulfosalts are the main carriers of the Ag mineralization in the deposit, with contents that vary from 13.7 to 23.9 wt.% of Ag. In the most superficial levels of the area, secondary Fe oxide and hydroxide, scorodite and anglesite developed due to the oxidation of the ore.Valiña-Azúmara es un yacimiento filoniano de Au-As (Ag-Pb-Zn-Cu-Sb situado en la provincia de Lugo (NO España, que fue explotado por arsénico a principios del siglo XX. La mineralización se encuentra encajada en un cabalgamiento Varisco de direcci

  5. Effect of Ag/Au bilayer assisted etching on the strongly enhanced photoluminescence and visible light photocatalysis by Si nanowire arrays.

    Science.gov (United States)

    Ghosh, Ramesh; Imakita, Kenji; Fujii, Minoru; Giri, P K

    2016-03-21

    We report on the strongly enhanced photoluminescence (PL) and visible light photocatalysis by arrays of vertically aligned single crystalline Si nanowires (NWs) grown by Ag/Au bilayer assisted etching. High resolution FESEM and TEM imaging reveals that the Si NWs are decorated with ultra-small size arbitrary shaped Si nanocrystals (NCs) due to the lateral etching of the NWs. A strong broad band and tunable visible to near-infrared (NIR) photoluminescence (PL) in the range 1.3-2.4 eV are observed for these Si NWs/NCs at room temperature, depending on the etching conditions. Our studies reveal that the visible-NIR PL intensity is about two orders of magnitude higher and it exhibits faster decay dynamics in the bilayer assisted etching case as compared to the Ag or Au single layer etching case. The enhanced PL in the bimetal case is attributed to the longer length and higher density of the Si NWs/NCs, surface plasmon resonance enhanced absorption by residual bimetal NPs and the enhanced radiative recombination rate. Studies on the time evolution of PL spectral features with laser exposure under ambient conditions and laser power dependence reveal that both the quantum confinement of carriers in Si NCs and the nonbridging oxygen hole defects in the SiOx layer contribute to the tunable PL. Interestingly, Si NWs grown by Ag/Au bilayer assisted etching exhibit enhanced photocatalytic degradation of methylene blue in comparison to Si NWs grown by single layer Ag or Au assisted etching. The Schottky barrier present between bimetallic NPs and nanoporous Si NWs with Si-H bonds facilitates the photocatalytic activity by efficient separation of photogenerated e-h pairs. Our results demonstrate the superiority of the Si NW array grown by bilayer assisted etching for their cutting edge applications in optoelectronics and environmental cleaning.

  6. Induced polarization imaging applied to exploration for low-sulfidation epithermal Au-Ag deposits, Seongsan mineralized district, South Korea

    Science.gov (United States)

    Han, Man-Ho; Shin, Seung Wook; Park, Samgyu; Cho, Seong-Jun; Kim, Jung-Ho

    2016-10-01

    The determination of mineralization boundaries during mineral exploration for undiscovered low-sulfidation epithermal Au-Ag deposits is a significant challenge because of the extensive survey areas required. Induced polarization (IP) imaging is an effective geophysical technique for the detection of sulfides or clay. Thus, this method is considered useful to determine the boundaries of subsurface mineralization and hydrothermal alteration associated with epithermal deposits. We used 2D and 3D IP imaging to define the silicification and mineralization boundaries of the Moisan deposit in the Seongsan mineralized district, which is geologically well-known. The boundaries of the silicification zone were defined by high resistivity values of 600 Ω-m, and those of the mineralization zone were defined by high global chargeability values of 3 mV V-1. The continuity of the high resistivity anomaly corresponded well to the silicification (quartz veins) exposed in outcrop. In addition, it is geologically reasonable that the chargeability anomaly, ⩾3 mV V-1, associated with the mineralization/hydrothermal alteration zone was concentrated at near-surface depths, and extensively surrounding the resistivity anomaly, ⩾600 Ω-m, associated with the silicification zone.

  7. High-performance ambipolar self-assembled Au/Ag nanowire based vertical quantum dot field effect transistor.

    Science.gov (United States)

    Song, Xiaoxian; Zhang, Yating; Zhang, Haiting; Yu, Yu; Cao, Mingxuan; Che, Yongli; Wang, Jianlong; Dai, Haitao; Yang, Junbo; Ding, Xin; Yao, Jianquan

    2016-10-01

    Most lateral PbSe quantum dot field effect transistors (QD FETs) show a low on current/off current (I on/I off) ratio in charge transport measurements. A new strategy to provide generally better performance is to design PbSe QD FETs with vertical architecture, in which the structure parameters can be tuned flexibly. Here, we fabricated a novel room-temperature operated vertical quantum dot field effect transistor with a channel of 580 nm, where self-assembled Au/Ag nanowires served as source transparent electrodes and PbSe quantum dots as active channels. Through investigating the electrical characterization, the ambipolar device exhibited excellent characteristics with a high I on/I off current ratio of about 1 × 10(5) and a low sub-threshold slope (0.26 V/decade) in the p-type regime. The all-solution processing vertical architecture provides a convenient way for low cost, large-area integration of the device. PMID:27578613

  8. Relativistic and Correlation Effects in CuH, AgH and AuH: Comparison of Various Relativistic Methods

    Science.gov (United States)

    Collins, Charlene L.; Dyall, Kenneth G.; Schaefer, Henry F., III

    1994-01-01

    The effects of relativity on the bond lengths, dissociation energies, and harmonic vibrational frequencies of the 1Epsilon(+) electronic ground states of the group IB hydrides CuH, AgH and AuH have been evaluated with a variety of ab initio methods. These properties were investigated with moderately-sized basis sets at the self-consistent field Hartree Fock (SCF HF) level and with second-order Moller-Plesset (MP2) perturbation theory for electron correlation. Comparisons were made between all-electron results using the nonrelativistic Hamiltonian, perturbation theory (PT) at first-order with only the one-electron non-fine structure terms of the Breit-Pauli Hamiltonian, the spin-free Douglas-Kroll (DK) transformed Dirac Hamiltonian and the untransformed Dirac Hamiltonian, and results using two sets of relativistic effective core potentials (RECPs). The expected trends of bond length decrease, dissociation energy increase and harmonic frequency increase with both relativity and correlation are found. Both sets of RECPs are shown to give good results, if accompanied by a reasonable basis set. The DK method is demonstrated to be an inexpensive, reliable approximation to the DHF method.

  9. High-performance ambipolar self-assembled Au/Ag nanowire based vertical quantum dot field effect transistor

    Science.gov (United States)

    Song, Xiaoxian; Zhang, Yating; Zhang, Haiting; Yu, Yu; Cao, Mingxuan; Che, Yongli; Wang, Jianlong; Dai, Haitao; Yang, Junbo; Ding, Xin; Yao, Jianquan

    2016-10-01

    Most lateral PbSe quantum dot field effect transistors (QD FETs) show a low on current/off current (I on/I off) ratio in charge transport measurements. A new strategy to provide generally better performance is to design PbSe QD FETs with vertical architecture, in which the structure parameters can be tuned flexibly. Here, we fabricated a novel room-temperature operated vertical quantum dot field effect transistor with a channel of 580 nm, where self-assembled Au/Ag nanowires served as source transparent electrodes and PbSe quantum dots as active channels. Through investigating the electrical characterization, the ambipolar device exhibited excellent characteristics with a high I on/I off current ratio of about 1 × 105 and a low sub-threshold slope (0.26 V/decade) in the p-type regime. The all-solution processing vertical architecture provides a convenient way for low cost, large-area integration of the device.

  10. Hemin on graphene nanosheets functionalized with flower-like MnO2 and hollow AuPd for the electrochemical sensing lead ion based on the specific DNAzyme.

    Science.gov (United States)

    Xue, Shuyan; Jing, Pei; Xu, Wenju

    2016-12-15

    Herein, integrated with DNAzyme highly specific to metal ions, hemin@reduced graphene oxide (hemin@rGO) functionalized with flower-like MnO2 and hollow AuPd (hAuPd-fMnO2-hemin@rGO) was used as electroactive probe and electrocatalyst to construct a universal platform for metal ion detection (lead ion Pb(2+) as the model). The proposed strategy with generality was mainly based on two aspects. Firstly, the designed probe not only showed high stability and excellent peroxidase-like activity originating from hemin, fMnO2 and hAuPd, but also possessed intrinsic redox performance from hemin, which resulted in the promotion of electron transfer and the enhancement of the response signal readout. Secondly, due to the introduction of Pb(2+), Pb(2+)-dependent DNAzyme bound in the electrode surface could be specifically identified and cleaved by Pb(2+), and the remained fragment (its supplementary sequence is a single-strand DNA S3) captured the nanocomposites S3-hAuPd-fMnO2-hemin@rGO by the hybridization reaction. Therefore, combined the cooperative catalysis of fMnO2, hAuPd and hemin to H2O2 reduction with highly specific interaction of Pb(2+)-dependent DNAzyme, the proposed Pb(2+) biosensor showed significant improvement of electrochemical analytical performance, which was involved in wide dynamic response in the range of 0.1pM-200nM, low detection limit of 0.034pM, high sensitivity and high specificity. This could facilitate the universal strategy to be a promising method for detection of other metal ions, only changing the corresponding DNAzyme specific to them. PMID:27498321

  11. CO Sensing Performance of a Micro Thermoelectric Gas Sensor with AuPtPd/SnO2 Catalyst and Effects of a Double Catalyst Structure with Pt/α-Al2O3

    Directory of Open Access Journals (Sweden)

    Tomoyo Goto

    2015-12-01

    Full Text Available The CO sensing properties of a micro thermoelectric gas sensor (micro-TGS with a double AuPtPd/SnO2 and Pt/α-Al2O3 catalyst were investigated. While several nanometer sized Pt and Pd particles were uniformly dispersed on SnO2, the Au particles were aggregated as particles measuring >10 nm in diameter. In situ diffuse reflectance Fourier transform Infrared spectroscopy (DRIFT analysis of the catalyst showed a CO adsorption peak on Pt and Pd, but no clear peak corresponding to the interaction between CO and Au was detected. Up to 200 °C, CO combustion was more temperature dependent than that of H2, while H2 combustion was activated by repeated exposure to H2 gas during the periodic gas test. Selective CO sensing of the micro-TGS against H2 was attempted using a double catalyst structure with 0.3–30 wt% Pt/α-Al2O3 as a counterpart combustion catalyst. The sensor output of the micro-TGS decreased with increasing Pt content in the Pt/α-Al2O3 catalyst, by cancelling out the combustion heat from the AuPtPd/SnO2 catalyst. In addition, the AuPtPd/SnO2 and 0.3 wt% Pt/α-Al2O3 double catalyst sensor showed good and selective CO detection. We therefore demonstrated that our micro-TGS with double catalyst structure is useful for controlling the gas selectivity of CO against H2.

  12. Design and Investigation of SST/nc-Si:H/M (M = Ag, Au, Ni and M/nc-Si:H/M Multifunctional Devices

    Directory of Open Access Journals (Sweden)

    A. F. Qasrawi

    2013-01-01

    Full Text Available Hydrogenated nanocrystalline Silicon thin films prepared by the very high frequency chemical vapor deposition technique (VHF-CVD on stainless steel (SST substrates are used to design Schottky point contact barriers for the purpose of solar energy conversion and passive electronic component applications. In this process, the contact performance between SST and M (M = Ag, Au, and Ni and between Ag, Au, and Ni electrodes was characterized by means of current-voltage, capacitance-voltage, and light intensity dependence of short circuit ( current and open circuit voltage ( of the contacts. Particularly, the devices ideality factors, barrier heights were evaluated by the Schottky method and compared to the Cheung's. Best Schottky device performance with lowest ideality factor suitable for electronic applications was observed in the SST/nc-Si:H/Ag structure. This device reflects a of 229 mV with an of 1.6 mA/cm2 under an illumination intensity of ~40 klux. On the other hand, the highest being 9.0 mA/cm2 and the of 53.1 mV were observed for Ni/nc-Si:H/Au structure. As these voltages represent the maximum biasing voltage for some of the designed devices, the SST/nc-Si:H/M and M/nc-Si:H/M can be regarded as multifunctional self-energy that provided electronic devices suitable for active or passive applications.

  13. A GREENER SYNTHESIS OF CORE (FE, CU)-SHELL (AU, PT, PD AND AG) NANOCRYSTALS USING AQUEOUS VITAMIN C

    Science.gov (United States)

    A greener method to fabricate the novel core (Fe and Cu)-shell (noble metals) metal nanocrystals using aqueous ascorbic acid (vitamin C) is described. Transition metal salts such as Cu and Fe were reduced using ascorbic acid, a benign naturally available antioxidant, and then add...

  14. Effects of the embedding kinetics on the surface nano-morphology of nano-grained Au and Ag films on PS and PMMA layers annealed above the glass transition temperature

    Energy Technology Data Exchange (ETDEWEB)

    Ruffino, F.; Grimaldi, M.G. [Dipartimento di Fisica ed Astronomia, Universita di Catania, Catania (Italy); MATIS IMM-CNR, Catania (Italy); Torrisi, V.; Marletta, G. [University of Catania, CSGI, Laboratory for Molecular Surface and Nanotechnology (LAMSUN), Department of Chemical Sciences, Catania (Italy)

    2012-06-15

    The morphology evolution of nano-grained Ag and Au films deposited on polystyrene (PS) and poly(methyl methacrylate) (PMMA) polymeric layers were studied, using the atomic force microscopy technique, when annealed above the polymers glass transition temperature. The main effects on the morphology changes were identified with those concerning the embedding kinetics of the Ag and Au nanoparticles in the PS or PMMA layers. The embedding process of the nanoparticles follows as a consequence of the long-range mobility of the polymeric chains above the glass transition temperature. In particular, the dependence of the nanoparticles mean height and surface density on the annealing time at various temperatures was quantified. The analyses of these behaviors allowed us: (1) to distinguish the overall embedding process in a first stage in which a thin wetting layer of the polymer coats the nanoparticles followed by a true embedding process of the nanoparticles into the polymer layer; (2) to evaluate the characteristic coating time for the Ag and Au nanoparticles in the PS and PMMA in the first stage; (3) to evaluate the characteristic embedding velocity for the Ag and Au nanoparticles in the PS and PMMA in the second stage; (4) to derive the activation energies for the embedding process of the Ag and Au nanoparticles in PS and PMMA; (5) to identify the embedding statistics of the Ag and Au nanoparticles in PS and PMMA with a ''failure'' Weibull statistics. (orig.)

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

    Science.gov (United States)

    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.

  16. Silver-rich telluride mineralization at Mount Charlotte and Au-Ag zonation in the giant Golden Mile deposit, Kalgoorlie, Western Australia

    Science.gov (United States)

    Mueller, Andreas G.; Muhling, Janet R.

    2013-03-01

    The gold deposits at Kalgoorlie in the 2.7-Ga Eastern Goldfields Province of the Yilgarn Craton, Western Australia, occur adjacent to the D2 Golden Mile Fault over a strike of 8 km within a district-scale zone marked by porphyry dykes and chloritic alteration. The late Golden Pike Fault separates the older (D2) shear zone system of the Golden Mile (1,500 t Au) in the southeast from the younger (D4) quartz vein stockworks at Mt Charlotte (126 t Au) in the northwest. Both deposits occur in the Golden Mile Dolerite sill and display inner sericite-ankerite alteration and early-stage gold-pyrite mineralization replacing the wall rocks. Late-stage tellurides account for 20 % of the total gold in the first, but for 30 g/t Au) is characterized by Au/Ag = 2.54 and As/Sb = 2.6-30, the latter ratio caused by arsenical pyrite. Golden Mile-type D2 lodes occur northwest of the Golden Pike Fault, but the Hidden Secret orebody, the only telluride bonanza mined (10,815 t at 44 g/t Au), was unusually rich in silver (Au/Ag = 0.12-0.35) due to abundant hessite. We describe another array of silver-rich D2 shear zones which are part of the Golden Mile Fault exposed on the Mt Charlotte mine 22 level. They are filled with crack-seal and pinch-and-swell quartz-carbonate veins and are surrounded by early-stage pyrite + pyrrhotite disseminated in a sericite-ankerite zone more than 6 m wide. Gold grade (0.5-0.8 g/t) varies little across the zone, but Au/Ag (0.37-2.40) and As/Sb (1.54-13.9) increase away from the veins. Late-stage telluride mineralization (23 g/t Au) sampled in one vein has a much lower Au/Ag (0.13) and As/Sb (0.48) and comprises scheelite, pyrite, native gold (830-854 fine), hessite, and minor pyrrhotite, altaite, bournonite, and boulangerite. Assuming 250-300 °C, gold-hessite compositions indicate a fluid log f Te2 of -11.5 to -10, values well below the stability of calaverite. The absence of calaverite and the dominance of hessite in the D2 lodes of the Mt Charlotte area

  17. Uranium and Sm isotope studies of the supergiant Olympic Dam Cu-Au-U-Ag deposit, South Australia

    Science.gov (United States)

    Kirchenbaur, Maria; Maas, Roland; Ehrig, Kathy; Kamenetsky, Vadim S.; Strub, Erik; Ballhaus, Chris; Münker, Carsten

    2016-05-01

    The Olympic Dam Cu-U-Au-Ag deposit in the Archean-Proterozoic Gawler Craton (South Australia) is a type example of the iron oxide-copper-gold (IOCG) spectrum of deposits and one of the largest Cu-U-Au resources known. Mineralization is hosted in a lithologically and texturally diverse, hematite-rich breccia complex developed within a granite of the 1.59 Ga Gawler Silicic Province. Emerging evidence indicates that both the breccia complex and its metal content developed over ∼1000 Ma, responding to major tectonic events, e.g., at 1300-1100, 825 and 500 Ma. However, metal sources and exact mechanism/s of ore formation remain poorly known. New high-precision 238U/235U data for a set of 40 whole rock samples representing all major lithological facies of the breccia complex show a narrow range (δ238UCRM112a = -0.56‰ to +0.04‰). At the scale of sampling, there is no correlation of δ238U with lithology, degree of alteration or U mineralogy, although ores with U > 5 wt.% have subtly higher δ238U values (-0.20‰ to 0.00) than the majority of samples (5 wt.% U, U/Sm ≫ 500) Olympic Dam ores define a neutron capture line, with correlated depletions in 149Sm (up to ∼2ε units) and excesses in 150Sm (up to ∼ 4ε units), but fission fragment contributions to Sm are below detection. These observations provide evidence for small-scale neutron-capture effects, with calculated neutron fluences of 1015 to 1016 n cm-2, similar to those observed in several Proterozoic and Phanerozoic U deposits. The apparent lack of fission fragment contributions in Olympic Dam high-grade ores can be explained with an age of U deposition, or re-deposition that is substantially younger than the initial 1.59 Ga age of the oldest IOCG-style mineralization. The results presented here thus (i) suggest uranium sources in common (likely igneous) upper crustal lithologies, (ii) support geochronological evidence for gradual addition of U in several stages over 1000 Ma at elevated temperatures of

  18. Henry's Law Constant for Hydrogen in Li/H{sub 3}BO{sub 3} solution using a Pd-Ag Sensor

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Eun-Hee; Lee, Deok-Hyun; Hur, Do-Haeng [KAERI, Daejeon (Korea, Republic of)

    2015-05-15

    The dissolved hydrogen concentration in PWRs has been controlled within the range of 25 - 50cc (STP)/kg-H{sub 2}O. It is well known that the dissolved hydrogen leads to primary water stress corrosion cracking (PWSCC), general corrosion of the primary structural materials, higher radiation fields, and deposit build up on the fuel rods in PWRs. Therefore, the optimization of the hydrogen concentration in the RCS is regarded as one of several effective approaches to manage the material integrity and reduction of the radiation sources in the primary circuit. During PWR operation, the hydrogen concentrations are controlled by varying hydrogen over pressures of a volume control tank (VCT). However, as the primary water flows from the VCT into the RCS, the temperature, system pressure, and solution chemistry in the RCS can affect the hydrogen concentration. In order to predict the content of the hydrogen partial pressure which affects the structural materials, it is needed to measure and monitor the hydrogen partial pressure accurately. In this paper, we fabricated a Pd-25wt.%Ag alloy hydrogen sensor to measure hydrogen partial pressures directly at high temperatures and high pressures. From the measured data, we determined the Henry's constants for various fields' applications. The hydrogen partial pressures were measured using a Pd-Ag hydrogen sensor in the 2 ppm Li and 1200 ppm B solution within the temperature and pressure ranges of 290 - 330 .deg. C and 2000 - 2900 psia, respectively. The Henry's constants were determined from the measured data.

  19. Henry's Law Constant for Hydrogen in Li/H3BO3 solution using a Pd-Ag Sensor

    International Nuclear Information System (INIS)

    The dissolved hydrogen concentration in PWRs has been controlled within the range of 25 - 50cc (STP)/kg-H2O. It is well known that the dissolved hydrogen leads to primary water stress corrosion cracking (PWSCC), general corrosion of the primary structural materials, higher radiation fields, and deposit build up on the fuel rods in PWRs. Therefore, the optimization of the hydrogen concentration in the RCS is regarded as one of several effective approaches to manage the material integrity and reduction of the radiation sources in the primary circuit. During PWR operation, the hydrogen concentrations are controlled by varying hydrogen over pressures of a volume control tank (VCT). However, as the primary water flows from the VCT into the RCS, the temperature, system pressure, and solution chemistry in the RCS can affect the hydrogen concentration. In order to predict the content of the hydrogen partial pressure which affects the structural materials, it is needed to measure and monitor the hydrogen partial pressure accurately. In this paper, we fabricated a Pd-25wt.%Ag alloy hydrogen sensor to measure hydrogen partial pressures directly at high temperatures and high pressures. From the measured data, we determined the Henry's constants for various fields' applications. The hydrogen partial pressures were measured using a Pd-Ag hydrogen sensor in the 2 ppm Li and 1200 ppm B solution within the temperature and pressure ranges of 290 - 330 .deg. C and 2000 - 2900 psia, respectively. The Henry's constants were determined from the measured data

  20. Nanosized Fe3O4 an efficient PCR yield enhancer-Comparative study with Au, Ag nanoparticles.

    Science.gov (United States)

    Kambli, Priyanka; Kelkar-Mane, Varsha

    2016-05-01

    Nanomaterials-assisted PCR is a promising field of nanobiotechnology that amalgamates nanomaterials into the conventional PCR system to achieve better amplification of desired product. With literature documenting the variable effects of these nanomaterials on the PCR yield and amplification; it was thought worthwhile to compare the PCR enhancing efficiency of three transition metal nanoparticles in form of stable colloidal suspensions at varying concentrations.The nanoparticles(NPs) of silver, gold and magnetite were chemically synthesized by reducing their respective salts and characterized using UV-vis spectroscopy. Their morphology was assessed using nanoparticle tracking system and AFM. The effect of these nanofluids on amplification of 800 bp prokaryotic DNA template with 30% GC content was studied using conventional thermal cycler. The reaction kinetics for all the three nanofluids yielded a Gaussian curve of amplification with varying concentrations. The ammonium salt of oleic acid coated magnetite (Fe3O4) nanoparticles at a concentration of 0.72 × 10(-2)nM and average size of 33 nm demonstrated highest amplification efficiency of 190% as compared to the citrate stabilized AgNP-25 nm (45%) and AuNP-15.19 nm (134%) using a conventional PCR system. The major reasons that allow Fe3O4 NPs outperform the other 2 transition metal NP's seem to be attributed to its heat conduction property as well as effective adsorption of PCR components onto the ammonium salt of oleic acid coated magnetite nanofluids. The data from our study offers valuable information for the application of ferrofluids as economically, efficient and effective alternative for nanomaterial-assisted PCR yield enhancers.

  1. Arsenic and heavy metal contamination and their uptake by rice crops around the Kubong Au-Ag mine, Korea

    Energy Technology Data Exchange (ETDEWEB)

    Ahn, Joo-Sung; Chon, Hyo-Taek [Seoul National University, Seoul (Korea); Son, Ah-Jeong; Kim, Kyoung-Woong [Kwangju Institute of Science and Technology, Kwangju (Korea)

    1999-04-30

    The concentrations and distributions of As and heavy metals have been investigated in the agricultural area around the abandoned Kubong Au-Ag mine in South-Choongchung Province, Korea. The characteristics of heavy metal uptake by rice crops were also assessed. Paddy soil was moderately contaminated by As, Cd and Pb, and their mean concentrations were 59.4, 1.4 and 67 mg/kg, respectively. The elevated levels of As, Cd, Pb and Zn in sediment by direct input of tailings were found as far as 4 km downstream, and tailings effluent contained up to 1,890 {mu}g/l of As and 25 {mu}g/l of Cd, showing that As and Cd in tailings as well as contaminated sediment can be easily mobilized into stream water and irrigation water. Arsenic, Cd and Pb were also enriched in rice crops and their concentration factors were high in the order of Cd>As>Pb. Translocation of As and Pb in rice stalk and leaves was limited to rice grains, but some of the rice grain samples were unsuitable for human diet, considering 3.1 mg/kg of Cd of a maximum content. Given the geographical distributions of As, Cd and Pb, and the increasing fractions of the exchangeable forms of heavy metals in paddy soils compared with those of tailings and stream sediments, it is suggested that the stream water, continuously affected by tailings and contaminated sediment, can be the most important source of the contamination in the study area. For the reclamation of this area, containment of tailings, dredging the contaminated sediment and mixing paddy soils with unpolluted soil or deep plowing will be needed. (author). 23 refs., 6 tabs., 8 figs.

  2. Nanosized Fe3O4 an efficient PCR yield enhancer-Comparative study with Au, Ag nanoparticles.

    Science.gov (United States)

    Kambli, Priyanka; Kelkar-Mane, Varsha

    2016-05-01

    Nanomaterials-assisted PCR is a promising field of nanobiotechnology that amalgamates nanomaterials into the conventional PCR system to achieve better amplification of desired product. With literature documenting the variable effects of these nanomaterials on the PCR yield and amplification; it was thought worthwhile to compare the PCR enhancing efficiency of three transition metal nanoparticles in form of stable colloidal suspensions at varying concentrations.The nanoparticles(NPs) of silver, gold and magnetite were chemically synthesized by reducing their respective salts and characterized using UV-vis spectroscopy. Their morphology was assessed using nanoparticle tracking system and AFM. The effect of these nanofluids on amplification of 800 bp prokaryotic DNA template with 30% GC content was studied using conventional thermal cycler. The reaction kinetics for all the three nanofluids yielded a Gaussian curve of amplification with varying concentrations. The ammonium salt of oleic acid coated magnetite (Fe3O4) nanoparticles at a concentration of 0.72 × 10(-2)nM and average size of 33 nm demonstrated highest amplification efficiency of 190% as compared to the citrate stabilized AgNP-25 nm (45%) and AuNP-15.19 nm (134%) using a conventional PCR system. The major reasons that allow Fe3O4 NPs outperform the other 2 transition metal NP's seem to be attributed to its heat conduction property as well as effective adsorption of PCR components onto the ammonium salt of oleic acid coated magnetite nanofluids. The data from our study offers valuable information for the application of ferrofluids as economically, efficient and effective alternative for nanomaterial-assisted PCR yield enhancers. PMID:26896662

  3. Current-induced spin polarization in transition metals and Bi/Ag bilayers observed by spin-polarized positron beam

    Science.gov (United States)

    Zhang, Hongjun; Yamamoto, Shunya; Fukaya, Yuki; Maekawa, Masaki; Li, Hui; Kawasuso, Atsuo; Seki, Takeshi; Saitoh, Eiji; Takanashi, Koki; JAEA Team; Tohoku Team

    2015-03-01

    Current-induced spin polarization (CISP) on the outermost surfaces of Au, Cu, Pt, Pd, Ta, and W films were studied by spin-polarized positron beam (SPPB). The Au and Cu surfaces showed no significant CISP. In contrast, the Pt, Pd, Ta, and W films exhibited large CISP (3 ~ 15% per charge current of 105 A/cm2) and the CISP of Ta and W were opposite to those of Pt and Pd. The sign of the CISP obeys the same rule in spin Hall effect suggesting that the spin-orbit coupling is mainly responsible for the CISP. The outermost spin poalrization of Bi/Ag/Al2O3andAg/Bi/Al2O3 (charge currents directly connected to Ag layers) were probed by SPPB. The opposite outermost spin polarization of Bi/Ag/Al2O3andAg/Bi/Al2O3 clarified the charge-to-spin conversion in Bi/Ag bilayers. Nevertheless, the magnitudes of the outermost spin polarization of Bi(0.3 ~5)/Ag(25)/Al2O3 (numbers in parentheses denote thickness in nm) and Ag(25 ~500)/Bi(8)/Al2O3 decrease exponentially with increasing Bi thickness and Ag thickness, respectively. This provides probably the first direct evidence for spin diffusion mechanism. Financial support from JSPS Kakenhi Grant 24310072.

  4. Photoelectron imaging and theoretical study on the structure and chemical binding of the mixed-ligand M(I) complexes, [HMSH]⁻ (M = Cu, Ag, and Au).

    Science.gov (United States)

    Qin, Zhengbo; Liu, Zhiling; Cong, Ran; Xie, Hua; Tang, Zichao; Fan, Hongjun

    2014-03-21

    We have reported a combined photoelectron imaging and theoretical study on gaseous mixed-ligand M(I) complexes of [HMSH](-) (M = Cu, Ag, and Au). With the aid of Franck-Condon simulations, vibrationally resolved photoelectron spectra yield accurate electron affinities of 3.269(6), 3.669(10), and 3.591(6) eV for [HCuSH], [HAgSH], and [HAuSH], respectively. And low-frequency modes are observed: 368(12) cm(-1) for [HCuSH], 286(12) cm(-1) for [HAgSH], and 327(12) cm(-1) for [HAuSH], respectively. Extensive theoretical calculations are performed to aid in the spectral assignments and the calculated values agree well with the experimental observations. Although the S and H atoms have little discrepancy in electronegativity (2.20 for H and 2.54 for S), distinct bonding properties are demonstrated between H-M and M-S bond. It is revealed that there exists significant ionic bonding between M-S in [HMSH](-) (M = Cu, Ag, and Au), while a gradual transition from ionic behavior between H-Cu in [HCuSH](-) to quite strong covalent bonding between H-Au in [HAuSH](-), supported by a variety of chemical bonding analyses.

  5. Photoelectron imaging and theoretical study on the structure and chemical binding of the mixed-ligand M(I) complexes, [HMSH]- (M = Cu, Ag, and Au)

    Science.gov (United States)

    Qin, Zhengbo; Liu, Zhiling; Cong, Ran; Xie, Hua; Tang, Zichao; Fan, Hongjun

    2014-03-01

    We have reported a combined photoelectron imaging and theoretical study on gaseous mixed-ligand M(I) complexes of [HMSH]- (M = Cu, Ag, and Au). With the aid of Franck-Condon simulations, vibrationally resolved photoelectron spectra yield accurate electron affinities of 3.269(6), 3.669(10), and 3.591(6) eV for [HCuSH], [HAgSH], and [HAuSH], respectively. And low-frequency modes are observed: 368(12) cm-1 for [HCuSH], 286(12) cm-1 for [HAgSH], and 327(12) cm-1 for [HAuSH], respectively. Extensive theoretical calculations are performed to aid in the spectral assignments and the calculated values agree well with the experimental observations. Although the S and H atoms have little discrepancy in electronegativity (2.20 for H and 2.54 for S), distinct bonding properties are demonstrated between H-M and M-S bond. It is revealed that there exists significant ionic bonding between M-S in [HMSH]- (M = Cu, Ag, and Au), while a gradual transition from ionic behavior between H-Cu in [HCuSH]- to quite strong covalent bonding between H-Au in [HAuSH]-, supported by a variety of chemical bonding analyses.

  6. Pentacene on Au(1 1 1), Ag(1 1 1) and Cu(1 1 1): From physisorption to chemisorption

    Science.gov (United States)

    Lu, Meng-Chao; Wang, Rong-Bin; Yang, Ao; Duhm, Steffen

    2016-03-01

    We measured the electronic and the molecular surface structure of pentacene deposited on the (1 1 1)-surfaces of coinage metals by means of ultraviolet photoelectron spectroscopy (UPS) and low-energy electron diffraction (LEED). Pentacene is almost flat-lying in monolayers on all three substrates and highly ordered on Au(1 1 1) and on Cu(1 1 1). On Ag(1 1 1), however, weak chemisorption leads to almost disordered monolayers, both, at room temperature and at 78 K. On Cu(1 1 1) pentacene is strongly chemisorbed and the lowest unoccupied molecular orbital becomes observable in UPS by a charge transfer from the substrate. On Ag(1 1 1) and Cu(1 1 1) multilayers adopt a tilted orientation and a high degree of crystallinity. On Au(1 1 1), most likely, also in multilayers the molecular short and long axes are parallel to the substrate, leading to a distinctively different electronic structure than on Ag(1 1 1) and Cu(1 1 1). Overall, it could be demonstrated that the substrate not only determines the geometric and electronic characteristics of molecular monolayer films but also plays a crucial role for multilayer film growth.

  7. Pentacene on Au(1 1 1), Ag(1 1 1) and Cu(1 1 1): From physisorption to chemisorption

    International Nuclear Information System (INIS)

    We measured the electronic and the molecular surface structure of pentacene deposited on the (1 1 1)-surfaces of coinage metals by means of ultraviolet photoelectron spectroscopy (UPS) and low-energy electron diffraction (LEED). Pentacene is almost flat-lying in monolayers on all three substrates and highly ordered on Au(1 1 1) and on Cu(1 1 1). On Ag(1 1 1), however, weak chemisorption leads to almost disordered monolayers, both, at room temperature and at 78 K. On Cu(1 1 1) pentacene is strongly chemisorbed and the lowest unoccupied molecular orbital becomes observable in UPS by a charge transfer from the substrate. On Ag(1 1 1) and Cu(1 1 1) multilayers adopt a tilted orientation and a high degree of crystallinity. On Au(1 1 1), most likely, also in multilayers the molecular short and long axes are parallel to the substrate, leading to a distinctively different electronic structure than on Ag(1 1 1) and Cu(1 1 1). Overall, it could be demonstrated that the substrate not only determines the geometric and electronic characteristics of molecular monolayer films but also plays a crucial role for multilayer film growth. (paper)

  8. The adsorption of CO and NO on the MoS2 monolayer doped with Au, Pt, Pd, or Ni: A first-principles study

    Science.gov (United States)

    Ma, Dongwei; Ju, Weiwei; Li, Tingxian; Zhang, Xiwei; He, Chaozheng; Ma, Benyuan; Lu, Zhansheng; Yang, Zongxian

    2016-10-01

    By performing the first-principles calculation, the adsorption of CO and NO molecules on the Au, Pt, Pd, or Ni doped MoS2 monolayer has been studied. The interaction between CO or NO with the doped MoS2 monolayer is strong and belongs to the chemisorption, as evidenced by the large adsorption energy and the short distance between the adsorbed molecules and the dopants. The charge transfer and the electronic property induced by the molecule adsorption are discussed. It is found that for both CO and NO adsorption, for all the cases charge transfer between the substrates and the adsorbed molecules has been observed. For NO, the adsorption obviously induces new impurity states in the band gap or the redistribution of the original impurity states. These can lead to the change of the transport properties of the doped MoS2 monolayer, by which the adsorbed CO or NO can be detected. The present work shows that introducing appropriate dopants may be a feasible method to improve the performance of MoS2-based gas sensors.

  9. Comparison of InP Schottky diodes based on Au or Pd sensing electrodes for NO2 and O3 sensing

    Science.gov (United States)

    Varenne, C.; Ndiaye, A.; Brunet, J.; Monier, G.; Spinelle, L.; Pauly, A.; Bideux, L.; Lauron, B.; Robert-Goumet, C.

    2012-06-01

    In previous reports, we have investigated on the influence of current transport mechanism on the sensitivity of InP Schottky and pseudo-Schottky diodes, for nitrogen dioxide detection. In this paper, the influence of the metal nature and the structure of the rectifying contact on the sensing layer are highlighted. More especially, we will focus on the behavior of these Schottky structures during and after their exposures to nitrogen dioxide (NO2) and ozone (O3). In this context, two types of structures have been studied: the simple Schottky diodes and the more elaborated structures called pseudo-Schottky. These diodes are realized with Au or Pd as metals. First, we will describe samples preparation and electrical characterization of the two types of structures. Then, we will compare sensor responses of these different structures under NO2 and O3. Finally, to better understand the action of these gases on the sensitive layer (the Schottky contact), X-rays photoelectron spectroscopy (XPS) is performed to follow the evolution of the metallic layer. The poisoning effect of active sites, which appears after NO2 and O3 expositions, is illustrated by comparative study of the active layer before and after exposure.

  10. Enhancement in the excitonic spontaneous emission rates for Si nanocrystal multi-layers covered with thin films of Au, Ag, and Al.

    Science.gov (United States)

    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.

  11. 阻断PD-1/PD-L1信号通路对负载HBsAg的树突细胞抗HBV免疫功能的影响%Effect of programmed death-1/progranuned death ligand-1 interaction on immune response of HBsAg-pulsed denddtic cells to hepatitis B virus

    Institute of Scientific and Technical Information of China (English)

    郭忠胜; 潘修成; 陈明; 杨帆; 李丽; 张言超; 李秀华

    2010-01-01

    目的 探讨阻断PD-1/PD-L1信号通路后,负载HBsAg的树突细胞(dendritic cells,DC)诱导HBV转基因小鼠免疫应答的作用特点.方法 体外诱导扩增BALB/c小鼠骨髓来源的DC,尾静脉免疫HBV转基因小鼠(其中在DC免疫前1 d腹腔注射PD-L1抗体,共3次).实验分5组进行:DC/HBsAg+PD-L1抗体组、DC/HBsAg组、Dc组、mlgG组和磷酸盐缓冲液(PBS)组,分别以流式细胞术、乳酸脱氢酶(LDH)释放法、酶联免疫吸附试验(ELISA)和荧光定量聚合酶链反应(PCR)等检测HBV转基因小鼠脾脏淋巴细胞增殖及细胞内干扰素γ(IFNγ)、特异性细胞毒性T淋巴细胞(CTL)活性及血清HBsAg、HBV DNA和丙氨酸转氨酶(ALT)水平.采用SPSS 13.0统计软件进行分析,组间比较采用ANOVA方差分析和q检验.结果免疫后第3天和第6天,DC/HBsAg+PD-L1抗体组与其他各组比较在诱导CD_3~+CD_8~+T淋巴细胞增殖及IFNγ分泌方面差异有统计学意义(细胞增殖:F值分别为25.22和39.01,P值均<0.01;IFNγ分泌:F值分别为32.35和36.98,P值均<0.01);而DC/HBsAg组与Dc组淋巴细胞增殖能力比较仅在第3天有统计学意义(t=6.79,P=0.012).特异性CTL的活性在DC/HBsAg+PD-L1抗体组明显升高.各组血清HBsAg在第6天差异有统计学意义(F=6.12,P<0.05).DC/HBsAg+PD-L1抗体组血清ALT水平与DC/HBsAg组比较在第3天无差异,与其他各组比较在第3和第6天差异有统计学意义(F值分别为19.22和14.30,P值均<0.05).各组对HBV DNA的清除能力没有差别,但DC/HBsAg+PD-L1抗体组有1只小鼠病毒载量下降1个数量级.结论封闭PD-1/PD-L1信号通路能通过提高特异性CD_3~+CD_8~+T淋巴细胞增殖及其分泌IFNγ能力,进而促进负载HBsAg的DC诱导转基因小鼠抗HBV免疫能力.%Objective To investigate the effect of programmed death(PD)-1/PD-L1 interaction on immunc response of HBsAg-pulsed dendritic cells(DCs)vaccine.Methods DCs were genermed from bone marrow cells from BALB/c mice and pulsed with HBsAg

  12. Fragment charge and energy distributions in the 1.8-4.8 GeV {sup 3}He + {sup nat}Ag, {sup 197}Au reactions

    Energy Technology Data Exchange (ETDEWEB)

    Bracken, D.S.; Foxford, E.R.; Kwiatkowski, K. [and others

    1995-10-01

    Moving source fits have been performed for IMFs as a function of observables related to collision violence in the 1.8-4.8 GeV {sup 3}He +{sup nat}Ag, {sup l97}Au reactions. The systematic behavior of the source properties and fragment charge distributions will be reviewed. The evolution of the spectral Coulomb parameters provides evidence for nuclear expansion prior to multifragmentation, suggesting a breakup density of p/p{sub o} {approximately} 1/3. The charge distributions will be examined in terms of power-law fits and moment analyses.

  13. Fragment charge and energy distributions in the 1.8-4.8 GeV 3He + natAg, 197Au reactions

    International Nuclear Information System (INIS)

    Moving source fits have been performed for IMFs as a function of observables related to collision violence in the 1.8-4.8 GeV 3He +natAg, l97Au reactions. The systematic behavior of the source properties and fragment charge distributions will be reviewed. The evolution of the spectral Coulomb parameters provides evidence for nuclear expansion prior to multifragmentation, suggesting a breakup density of p/po ∼ 1/3. The charge distributions will be examined in terms of power-law fits and moment analyses

  14. Rhenium and precious metal (Pt, Pd, and Au) abundances in porphyry Cu-Mo deposits of Central-Asian Mobile Belt%中亚造山带中斑岩铜钼矿的Re,Pt,Pd和Au含量

    Institute of Scientific and Technical Information of China (English)

    Anita N.Berzina; Alexander F.Korobeinikov

    2007-01-01

    Precious metal ( Pt, Pd and Au) and Re contents in rocks, ores and flotation concentrates of Siberian (Russia) and Mongolian porphyry Cu-Mo and Mo-Cu deposits were studied. The following deposits are discussed: Early Devonian porphyry Mo-Cu Sora deposit (Kuznetsk Alatau Mountains, Russia) and porphyry Cu-Mo Aksug deposit, (northeastern Tuva, Russia); Triassic porphyry Cu-Mo Erdenetiin Ovoo deposit (northern Mongolia). The samples analyzed include unaltered host rocks of plutons, porphyry rocks of ore-bearing series, different types of altered rocks, mineral separate analyses of molybdenite, chalcopyrite and magnetite, as well as flotation concentrates. Pt, Pd, Au and Re contents were determined using ICP/MS, AAS and inversion voltammetric analysis.PGE abundances in rocks and poorly mineralized samples span a large range from below detection limit to 65 ppb Pt and 74 ppb Pd. Re concentrations in whole rock samples range from below detection limit to 89 ppb. Molybdenite has been shown to be the major host phase for Re. The results presented show that Aksug deposit reveals elevated PGE and Au contents in ore minerals and flotation concentrates. High Pd contents in ores of the Aksug deposit are in accordance with the presence of palladium mineralization in the form of palladium telluride merenskyite ( Pd, Pt) Te2.The variety of precious metals and Re contents in the studied deposits could be caused by a complex interplay of several factors,including importance of primary metal concentrations derived from the source, transport of metals to the deposition area,physicochemical properties of the fluid (fo2, pH, fs, T, P), and depositional conditions. Higher Re contents in molybdenite and chalcopyrite separates are typical for copper-rich Aksug and Erdenetiin Ovoo deposits. Rhenium concentration in sulfides from molybdenum-rich Sora deposit is significantly lower. Highly oxidized, Cl-rich fluid style at Aksug and Erdenetiin Ovoo was favorable for high rhenium solubility and

  15. M@B9 and M@B10 molecular wheels containing planar nona-and deca-coordinate heavy group 11, 12, and 13 metals (M=Ag, Au, Cd, Hg, In, Tl)

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    A density functional and ab initio theory investigation on M@B9 and M@B10 molecular wheels containing planar nona-and deca-coordinate heavy group 11, 12 and 13 metals (M=Ag, Au, Cd, Hg, In, Ti) has been performed. These unusual clusters all prove to be true minima on the potential energy surfaces of the systems and σ+π double aromatic in nature. The first two vertical one-electron detachment energies of M@B-10 (M=Ag, Au) anions and first two ionization potentials of M@B9 (M=Ag, Au) and M@B10 (M=Cd, Hg) neutrals were calculated to aid future experiments. The cluster complexes designed in this work may expend the domain of planar hyper-coordinate elements to include heavy group 11, 12, and 13 metals and serve as interesting candidates to be targeted in experiments.

  16. Isolation and Structural Characterization of a Mackay 55-Metal-Atom Two-Shell Icosahedron of Pseudo-Ih Symmetry, Pd55L12(μ3-CO)20 (L = PR3, R = Isopropyl): Comparative Analysis with Interior Two-Shell Icosahedral Geometries in Capped Three-Shell Pd145, Pt-Centered Four-Shell Pd-Pt M165, and Four-Shell Au133 Nanoclusters.

    Science.gov (United States)

    Erickson, Jeremiah D; Mednikov, Evgueni G; Ivanov, Sergei A; Dahl, Lawrence F

    2016-02-10

    We present the first successful isolation and crystallographic characterization of a Mackay 55-metal-atom two-shell icosahedron, Pd55L12(μ3-CO)20 (L = PPr(i)3) (1). Its two-shell icosahedron of pseudo-Ih symmetry (without isopropyl substituents) enables a structural/bonding comparison with interior 55-metal-atom two-shell icosahedral geometries observed within the multi-shell capped 145-metal-atom three-shell Pd145(CO)72(PEt3)30 and 165-metal-atom four-shell Pt-centered (μ12-Pt)Pd164-xPtx(CO)72(PPh3)20 (x ≈ 7) nanoclusters, and within the recently reported four-shell Au133(SC6H4-p-Bu(t))52 nanocluster. DFT calculations carried out on a Pd55(CO)20(PH3)12 model analogue, with triisopropyl phosphine substituents replaced by H atoms, revealed a positive +0.84 e charge for the entire Pd55 core, with a highly positive second-shell Pd42 surface of +1.93 e.

  17. Isolation and Structural Characterization of a Mackay 55-Metal-Atom Two-Shell Icosahedron of Pseudo-Ih Symmetry, Pd55L12(μ3-CO)20 (L = PR3, R = Isopropyl): Comparative Analysis with Interior Two-Shell Icosahedral Geometries in Capped Three-Shell Pd145, Pt-Centered Four-Shell Pd-Pt M165, and Four-Shell Au133 Nanoclusters.

    Science.gov (United States)

    Erickson, Jeremiah D; Mednikov, Evgueni G; Ivanov, Sergei A; Dahl, Lawrence F

    2016-02-10

    We present the first successful isolation and crystallographic characterization of a Mackay 55-metal-atom two-shell icosahedron, Pd55L12(μ3-CO)20 (L = PPr(i)3) (1). Its two-shell icosahedron of pseudo-Ih symmetry (without isopropyl substituents) enables a structural/bonding comparison with interior 55-metal-atom two-shell icosahedral geometries observed within the multi-shell capped 145-metal-atom three-shell Pd145(CO)72(PEt3)30 and 165-metal-atom four-shell Pt-centered (μ12-Pt)Pd164-xPtx(CO)72(PPh3)20 (x ≈ 7) nanoclusters, and within the recently reported four-shell Au133(SC6H4-p-Bu(t))52 nanocluster. DFT calculations carried out on a Pd55(CO)20(PH3)12 model analogue, with triisopropyl phosphine substituents replaced by H atoms, revealed a positive +0.84 e charge for the entire Pd55 core, with a highly positive second-shell Pd42 surface of +1.93 e. PMID:26790717

  18. Bio-mimetic Nanostructure Self-assembled from Au@Ag Heterogeneous Nanorods and Phage Fusion Proteins for Targeted Tumor Optical Detection and Photothermal Therapy

    Science.gov (United States)

    Wang, Fei; Liu, Pei; Sun, Lin; Li, Cuncheng; Petrenko, Valery A.; Liu, Aihua

    2014-10-01

    Nanomaterials with near-infrared (NIR) absorption have been widely studied in cancer detection and photothermal therapy (PTT), while it remains a great challenge in targeting tumor efficiently with minimal side effects. Herein we report a novel multifunctional phage-mimetic nanostructure, which was prepared by layer-by-layer self-assembly of Au@Ag heterogenous nanorods (NRs) with rhodamine 6G, and specific pVIII fusion proteins. Au@Ag NRs, first being applied for PTT, exhibited excellent stability, cost-effectivity, biocompatibility and tunable NIR absorption. The fusion proteins were isolated from phage DDAGNRQP specifically selected from f8/8 landscape phage library against colorectal cancer cells in a high-throughput way. Considering the definite charge distribution and low molecular weight, phage fusion proteins were assembled on the negatively charged NR core by electrostatic interactions, exposing the N-terminus fused with DDAGNRQP peptide on the surface. The fluorescent images showed that assembled phage fusion proteins can direct the nanostructure into cancer cells. The nanostructure was more efficient than gold nanorods and silver nanotriangle-based photothermal agents and was capable of specifically ablating SW620 cells after 10 min illumination with an 808 nm laser in the light intensity of 4 W/cm2. The prepared nanostructure would become an ideal reagent for simutaneously targeted optical imaging and PTT of tumor.

  19. M\\TiO₂ (M=Au, Ag) transparent aqueous sols and its application on polymeric surface antibacterial post-treatment.

    Science.gov (United States)

    Wu, Liangzhuan; Yu, Yuan; Song, Le; Zhi, Jinfang

    2015-05-15

    In this paper, we reported a simple and mild chemical method for synthesis of crystalline metal\\TiO2 (M=Au, Ag) transparent aqueous sols at low temperature (80°C). It should be found that the as-synthesized metal\\TiO2 sols could easily be coated on the flexible PET surfaces of the through the as-developed electroless-plating-like solution deposition (EPLSD) procedure. The as-prepared metal\\TiO2 sols and related flexible thin film were characterized by TEM, SEM, XRD, UV-vis, and FTIR analysis. The results showed that the Au and Ag nanoparticles can significantly improve the optical absorption properties of TiO2 due to the surface plasmon generated by the noble metal, which in turn enhanced the photo-induced antibacterial performance of the as-prepared metal\\TiO2 flexible film. Moreover, the photo-generated electrons could transfer between the metal and titanium dioxide under different irradiation (ultraviolet or visible light), which could significantly reduce the recombination of photo-induced electrons and holes, resulting in the better photo-induced antibacterial performance. Therefore, the EPLSD procedure may be used as a general polymeric surface antibacterial post-treatment procedure for preparing the metal\\TiO2 flexible film because of the noble metal enhanced antibacterial performance. PMID:25678155

  20. N2-Ar-He systematics and source of ore-forming fluid in Changkeng Au-Ag deposit, central Guangdong, China

    Institute of Scientific and Technical Information of China (English)

    孙晓明; 孙凯; 陈炳辉; 陈敬德; David; I.Norman

    1999-01-01

    Changkeng Au-Ag deposit is a newly-discovered new type precious metal deposit. N2-Ar-He systematics studies and 3He/4He and δD-δ18O composition analyses show that the ore-forming fluid of the deposit is composed mainly of formation water (sedimentary brine) but not of meteoric water, which was thought to be source of the ore-forming fluid by most previous researchers. The content of mantle-derived magmatic water in the ore-forming fluid is quite low, usually lower than 10%. According to the source of the ore-forming fluid, the Changkeng Au-Ag deposit should belong to sedimentary brine transformed deposits. From the Late Jurassic to the Early Cretaceous Period, with deposition and accumulation of thick sediments in Sanzhou Basin, the formation water in the sedimentary layers was expelled from the basin because of overburden pressure and increasing temperature. The expelled fluid moved laterally along sedimentary layers to the margin of the basin, and finally moved upward along a gently-dipping in

  1. First principles study of structural, electronic and elastic properties of group IB metal nitrides TMNx (TM = Cu, Ag and Au: x = 1, 2)

    International Nuclear Information System (INIS)

    Highlights: •Electronic, structural and elastic properties of group IB nitrides are investigated. •A pressure induced structural phase transition is predicted under high pressure. •Electronic structure reveals that these materials exhibit metallic behavior. •Computed elastic moduli obey traditional mechanical stability condition. •The Debye temperature values are computed for Group IB metal mono and di-nitrides. -- Abstract: The structural, electronic and elastic properties of group IB transition metal nitrides (TMNx: TM = Cu, Ag, Au and x = 1, 2) are investigated by first principles calculation using the Vienna ab initio simulation package. The lattice constants, cohesive energy, bulk modulus, band structures and the density of states are obtained. The calculated lattice parameters are in good agreement with the available results. The electronic structure reveals that these materials exhibit metallic behaviour. A pressure-induced structural phase transition from NaCl to CsCl phase in AgN at 6 GPa, NaCl to ZB phase in AuN at 34.2 GPa and ZB to NaCl phase in CuN at 36.2 GPa is observed. In group IB metal di-nitrides, CaF2 to AlB2 phase transition is predicted. The computed elastic constants indicate that these nitrides are mechanically stable at ambient pressure. The calculated Debye temperature values are in good agreement with experimental and other theoretical results

  2. New insights into micro/nanoscale combined probes (nanoAuger, μXPS) to characterize Ag/Au@SiO2 core-shell assemblies.

    Science.gov (United States)

    Ledeuil, J B; Uhart, A; Soulé, S; Allouche, J; Dupin, J C; Martinez, H

    2014-10-01

    This work has examined the elemental distribution and local morphology at the nanoscale of core@shell Ag/Au@SiO2 particles. The characterization of such complex metal/insulator materials becomes more efficient when using an initial cross-section method of preparation of the core@shell nanoparticles (ion milling cross polisher). The originality of this route of preparation allows one to obtain undamaged, well-defined and planar layers of cross-cut nano-objects. Once combined with high-resolution techniques of characterization (XPS, Auger and SEM), the process appears as a powerful way to minimize charging effects and enhance the outcoming electron signal (potentially affected by the topography of the material) during analysis. SEM experiments have unambiguously revealed the hollow-morphology of the metal core, while Auger spectroscopy observations showed chemical heterogeneity within the particles (as silver and gold are randomly found in the core ring). To our knowledge, this is the first time that Auger nano probe spectroscopy has been used and successfully optimized for the study of some complex metal/inorganic interfaces at such a high degree of resolution (≈12 nm). Complementarily, XPS Au 4f and Ag 3d peaks were finally detected attesting the possibility of access to the whole chemistry of such nanostructured assemblies.

  3. Pull strength evaluation of Sn-Pb solder joints made to Au-Pt-Pd and Au thick film structures on low-temperature co-fired ceramic -final report for the MC4652 crypto-coded switch (W80).

    Energy Technology Data Exchange (ETDEWEB)

    Uribe, Fernando; Vianco, Paul Thomas; Zender, Gary L.

    2006-06-01

    A study was performed that examined the microstructure and mechanical properties of 63Sn-37Pb (wt.%, Sn-Pb) solder joints made to thick film layers on low-temperature co-fired (LTCC) substrates. The thick film layers were combinations of the Dupont{trademark} 4596 (Au-Pt-Pd) conductor and Dupont{trademark} 5742 (Au) conductor, the latter having been deposited between the 4596 layer and LTCC substrate. Single (1x) and triple (3x) thicknesses of the 4596 layer were evaluated. Three footprint sizes were evaluated of the 5742 thick film. The solder joints exhibited excellent solderability of both the copper (Cu) lead and thick film surface. In all test sample configurations, the 5742 thick film prevented side wall cracking of the vias. The pull strengths were in the range of 3.4-4.0 lbs, which were only slightly lower than historical values for alumina (Al{sub 2}O{sub 3}) substrates. General (qualitative) observations: (a) The pull strength was maximized when the total number of thick film layers was between two and three. Fewer that two layers did not develop as strong of a bond at the thick film/LTCC interface; more than three layers and of increased footprint area, developed higher residual stresses at the thick film/LTCC interface and in the underlying LTCC material that weakened the joint. (b) Minimizing the area of the weaker 4596/LTCC interface (e.g., larger 5742 area) improved pull strength. Specific observations: (a) In the presence of vias and the need for the 3x 4596 thick film, the preferred 4596:5742 ratio was 1.0:0.5. (b) For those LTCC components that require the 3x 4596 layer, but do not have vias, it is preferred to refrain from using the 5742 layer. (c) In the absence of vias, the highest strength was realized with a 1x thick 5742 layer, a 1x thick 4596 layer, and a footprint ratio of 1.0:1.0.

  4. σ-Aromatic cyclic M3(+) (M = Cu, Ag, Au) clusters and their complexation with dimethyl imidazol-2-ylidene, pyridine, isoxazole, furan, noble gases and carbon monoxide.

    Science.gov (United States)

    Pan, Sudip; Saha, Ranajit; Mandal, Subhajit; Chattaraj, Pratim K

    2016-04-28

    The σ-aromaticity of M3(+) (M = Cu, Ag, Au) is analyzed and compared with that of Li3(+) and a prototype σ-aromatic system, H3(+). Ligands (L) like dimethyl imidazol-2-ylidene, pyridine, isoxazole and furan are employed to stabilize these monocationic M3(+) clusters. They all bind M3(+) with favorable interaction energy. Dimethyl imidazol-2-ylidene forms the strongest bond with M3(+) followed by pyridine, isoxazole and furan. Electrostatic contribution is considerably more than that of orbital contribution in these M-L bonds. The orbital interaction arises from both L → M σ donation and L ← M back donation. M3(+) clusters also bind noble gas atoms and carbon monoxide effectively. In general, among the studied systems Au3(+) binds a given L most strongly followed by Cu3(+) and Ag3(+). Computation of the nucleus-independent chemical shift (NICS) and its different extensions like the NICS-rate and NICS in-plane component vs. NICS out-of-plane component shows that the σ-aromaticity in L bound M3(+) increases compared to that of bare clusters. The aromaticity in pyridine, isoxazole and furan bound Au3(+) complexes is quite comparable with that in the recently synthesized Zn3(C5(CH3)5)3(+). The energy gap between the highest occupied molecular orbital and the lowest unoccupied molecular orbital also increases upon binding with L. The blue-shift and red-shift in the C-O stretching frequency of M3(CO)3(+) and M3(OC)3(+), respectively, are analyzed through reverse polarization of the σ- and π-orbitals of CO as well as the relative amount of OC → M σ donation and M → CO π back donation. The electron density analysis is also performed to gain further insight into the nature of interaction. PMID:26624276

  5. Saltwater ecotoxicology of Ag, Au, CuO, TiO2, ZnO and C60 engineered nanoparticles: An overview.

    Science.gov (United States)

    Minetto, D; Volpi Ghirardini, A; Libralato, G

    2016-01-01

    This review paper examined 529 papers reporting experimental nanoecotoxicological original data. Only 126 papers referred to saltwater environments (water column and sediment) including a huge variety of species (n=51), their relative endpoints and engineered nanoparticles (ENPs) (n=38). We tried to provide a synthetic overview of the ecotoxicological effects of ENPs from existing data, refining papers on the basis of cross-cutting selection criteria and supporting a "mind the gap" approach stressing on missing data for hazard and risk assessment. After a codified selection procedure, attention was paid to Ag, Au, CuO, TiO2, ZnO and C60 ENPs, evidencing and comparing the observed nanoecotoxicity range of effect. Several criticisms were evidenced: i) some model organisms are overexploited like microalgae and molluscs compared to annelids, echinoderms and fish; ii) underexploited model organisms: mainly bacteria and fish; iii) exposure scenario variability: high species-specific and ENP scenarios including organism life stage and way of administration/spiking of toxicants; iv) scarce comparability between results due to exposure scenario variability; v) micro- and mesocosms substantially unexplored; vi) mixture effects: few examples are available only for ENPs and traditional pollutants; mixtures of ENPs have not been investigated yet; vii) effects of ions and ENPs: nAg, nCuO and nZnO toxicity aetiology is still a matter of discussion; viii) size and morphology effects of ENPs: scarcely investigated, justified and understood. Toxicity results evidenced that: nAu>nZnO>nAg>nCuO>nTiO2>C60. PMID:27107224

  6. Pd-Ag Membrane Coupled to a Two-Zone Fluidized Bed Reactor (TZFBR for Propane Dehydrogenation on a Pt-Sn/MgAl2O4 Catalyst

    Directory of Open Access Journals (Sweden)

    Miguel Menéndez

    2013-05-01

    Full Text Available Several reactor configurations have been tested for catalytic propane dehydrogenation employing Pt-Sn/MgAl2O4 as a catalyst. Pd-Ag alloy membranes coupled to the multifunctional Two-Zone Fluidized Bed Reactor (TZFBR provide an improvement in propane conversion by hydrogen removal from the reaction bed through the inorganic membrane in addition to in situ catalyst regeneration. Twofold process intensification is thereby achieved when compared to the use of traditional fluidized bed reactors (FBR, where coke formation and thermodynamic equilibrium represent important process limitations. Experiments were carried out at 500–575 °C and with catalyst mass to molar flow of fed propane ratios between 15.1 and 35.2 g min mmol−1, employing three different reactor configurations: FBR, TZFBR and TZFBR + Membrane (TZFBR + MB. The results in the FBR showed catalyst deactivation, which was faster at high temperatures. In contrast, by employing the TZFBR with the optimum regenerative agent flow (diluted oxygen, the process activity was sustained throughout the time on stream. The TZFBR + MB showed promising results in catalytic propane dehydrogenation, displacing the reaction towards higher propylene production and giving the best results among the different reactor configurations studied. Furthermore, the results obtained in this study were better than those reported on conventional reactors.

  7. Designing and Validating Ternary Pd Alloys for Optimum Sulfur/Carbon Resistance in Hydrogen Separation and Carbon Capture Membrane Systems Using High-Throughput Combinatorial Methods

    Energy Technology Data Exchange (ETDEWEB)

    Lewis, Amanda; Zhao, Hongbin; Hopkins, Scott

    2014-09-30

    This report summarizes the work completed under the U.S. Department of Energy Project Award No.: DE-FE0001181 titled “Designing and Validating Ternary Pd Alloys for Optimum Sulfur/Carbon Resistance in Hydrogen Separation and Carbon Capture Membrane Systems Using High-Throughput Combinatorial Methods.” The project started in October 1, 2009 and was finished September 30, 2014. Pall Corporation worked with Cornell University to sputter and test palladium-based ternary alloys onto silicon wafers to examine many alloys at once. With the specialized equipment at Georgia Institute of Technology that analyzed the wafers for adsorbed carbon and sulfur species six compositions were identified to have resistance to carbon and sulfur species. These compositions were deposited on Pall AccuSep® supports by Colorado School of Mines and then tested in simulated synthetic coal gas at the Pall Corporation. Two of the six alloys were chosen for further investigations based on their performance. Alloy reproducibility and long-term testing of PdAuAg and PdZrAu provided insight to the ability to manufacture these compositions for testing. PdAuAg is the most promising alloy found in this work based on the fabrication reproducibility and resistance to carbon and sulfur. Although PdZrAu had great initial resistance to carbon and sulfur species, the alloy composition has a very narrow range that hindered testing reproducibility.

  8. Roles of phosphorous in Sn{sub 4}Ag{sub 0.5}Cu solder reaction with electrolytic Ni-Au

    Energy Technology Data Exchange (ETDEWEB)

    Key Chung, C. [Department of Materials Science and Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 10617, Taiwan (China); Assembly Test Global Materials, Intel Microelectronics Asia Ltd., B1, No. 205, Tun-Hwa North Road, Taipei 10595, Taiwan (China); Huang, T.C. [Department of Materials Science and Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 10617, Taiwan (China); Shia, R. [Assembly Test Global Materials, Intel Microelectronics Asia Ltd., B1, No. 205, Tun-Hwa North Road, Taipei 10595, Taiwan (China); Yang, T.L. [Department of Materials Science and Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 10617, Taiwan (China); Kao, C.R., E-mail: crkao@ntu.edu.tw [Department of Materials Science and Engineering, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 10617, Taiwan (China)

    2012-10-25

    Graphical abstract: The reaction of P-doped Sn{sub 4}Ag{sub 0.5}Cu solder with electrolytic Ni-Au forms a layer of nano crystallites in between (Cu,Ni){sub 6}Sn{sub 5} and (Ni,Cu){sub 3}Sn{sub 4}. This layer effectively suppresses the growth of intermetallic compound. Highlights: Black-Right-Pointing-Pointer P-doped solder changed the intermetallic compounds from chunky to planar structure. Black-Right-Pointing-Pointer P-doped solder suppressed the growth of intermetallic and tensile strain. Black-Right-Pointing-Pointer Nano crystallites were found in between (Ni,Cu){sub 6}Sn{sub 5} and (Cu,Ni){sub 3}Sn{sub 4}. Black-Right-Pointing-Pointer P-doped solder strengthened the interface initially but not multiple reflows. Black-Right-Pointing-Pointer P-doped solder increased the activation energy of intermetallic compounds. - Abstract: In this study, the interfacial reactions of different P-doped and undoped Sn{sub 4}Ag{sub 0.5}Cu solders with electrolytic Ni-Au were investigated. The solder joints were reflowed once and then subjected to two more reflow cycles. The thickness of the intermetallic compound (IMC) layer and the IMC composition were analyzed by scanning electron microscopy and transmission electron microscopy (TEM). The tensile properties of the solder joint were measured using a Dage 4000 instrument. The results showed that the P content of the solder was inversely proportional to the IMC layer thickness and maximum tensile strain. TEM observations showed that a nanocrystallite layer existed between (Ni,Cu){sub 6}Sn{sub 5} and (Cu,Ni){sub 3}Sn{sub 4}. This nanocrystallite layer was responsible for the abovementioned relationship. This layer not only suppressed the growth of the IMC layer effectively but also decreased the pull strength of the solder joint after three reflow cycles. Energy-dispersive X-ray spectra of this interfacial layer were recorded to determine the P, Ni, Cu, and Sn contents. As the P content of the P-doped Sn{sub 4}Ag{sub 0.5}Cu solder

  9. Structure and magnetism of 3d and 4d transition-metal alloys TT' (T = Mn, Fe and T' = Rh, Pd) with CuAu-I type ordered structure

    Energy Technology Data Exchange (ETDEWEB)

    Yamada, H. [Faculty of Science, Shinshu University, Asahi 3-1-1, Matsumoto 390-8621 (Japan)]. E-mail: hyamada@gipac.shinshu-u.ac.jp; Shimizu, H. [Faculty of Science, Shinshu University, Asahi 3-1-1, Matsumoto 390-8621 (Japan); Yamamoto, K. [Faculty of Science, Shinshu University, Asahi 3-1-1, Matsumoto 390-8621 (Japan); Uebayashi, K. [Faculty of Science, Shinshu University, Asahi 3-1-1, Matsumoto 390-8621 (Japan)

    2006-05-18

    First-principle band calculations of 3d and 4d transition-metal alloys FeRh, FePd, MnRh and MnPd with CuAu-I type ordered structure are carried out by a linear muffin-tin orbital method within an atomic sphere approximation, where a generalized gradient correction for exchange-correlation potential is taken into account. Total energies for paramagnetic, ferromagnetic and three kinds of antiferromagnetic states are estimated as a function of lattice constants a and c. Observed lattice constants and spin structures of these alloys are well described by the present calculations. It is shown that the paramagnetic (non-magnetic) state without local magnetic moments is not stable in CsCl-type structure for these alloys.

  10. Extracted Electronic Parameters of a Novel Ag/SnO2:In/Si/Au Schottky Diode for Solar Cell Application

    Directory of Open Access Journals (Sweden)

    Mostefa Benhaliliba

    2015-06-01

    Full Text Available The effect of indium on the characteristics of Ag / SnO2 : In / Si / Au Schottky diode (SD is studied. The electronic parameters, ideal factor, the effective barrier, flat band barrier height, the series resistance, the saturation current density of the diodes were extracted from the current voltage (I-V and capacitance voltage (C-V characteristics. The series resistance (Rs determined by Cheung method increases (508-534 Ω with In doping level while the barrier height still constant around 0.57 V. Norde approximation gives a similar barrier height values of 0.69 V but the series resistance reaches higher values of 5500 Ω.

  11. Ideal Weyl Semimetals in the Chalcopyrites CuTlSe_{2}, AgTlTe_{2}, AuTlTe_{2}, and ZnPbAs_{2}.

    Science.gov (United States)

    Ruan, Jiawei; Jian, Shao-Kai; Zhang, Dongqin; Yao, Hong; Zhang, Haijun; Zhang, Shou-Cheng; Xing, Dingyu

    2016-06-01

    Weyl semimetals are new states of matter which feature novel Fermi arcs and exotic transport phenomena. Based on first-principles calculations, we report that the chalcopyrites CuTlSe_{2}, AgTlTe_{2}, AuTlTe_{2}, and ZnPbAs_{2} are ideal Weyl semimetals, having largely separated Weyl points (∼0.05  Å^{-1}) and uncovered Fermi arcs that are amenable to experimental detections. We also construct a minimal effective model to capture the low-energy physics of this class of Weyl semimetals. Our discovery is a major step toward a perfect playground of intriguing Weyl semimetals and potential applications for low-power and high-speed electronics. PMID:27314733

  12. 4π studies of the 1.8 endash 4.8 GeV 3He+natAg, 197Au reactions. II. Multifragmentation

    International Nuclear Information System (INIS)

    Multifragmentation of natAg and 197Au nuclei induced by 1.8 endash 4.8 GeV 3He ions has been studied with the Indiana Silicon Sphere 4π detector array. Rapidity, moving source, and sphericity-coplanarity analyses are consistent with near-simultaneous emission from a source in approximate kinetic equilibrium. For the most dissipative collisions, the spectral peaks are broadened and shifted to very low energies, indicative of emission from an extended nuclear system with ρ/ρ0∼1/3. Predictions of an intranuclear cascade/expanding, emitting source model compare well with experimental multiplicity distributions and the evolution of fragment spectral shapes. copyright 1996 The American Physical Society

  13. Density Functional Theory with Modified Dispersion Correction for Metals Applied to Self-Assembled Monolayers of Thiols on Au(111

    Directory of Open Access Journals (Sweden)

    M. P. Andersson

    2013-01-01

    Full Text Available Using sound physical principles we modify the DFT-D2 atom pairwise semiempirical dispersion correction to density functional theory to work for metallic systems and in particular self-assembled monolayers of thiols on gold surfaces. We test our approximation for two functionals PBE-D and revPBE-D for lattice parameters and cohesive energies for Ni, Pd, Pt, Cu, Ag, and Au, adsorption energies of CO on (111 surfaces of Pd, Pt, Cu, Ag, and Au, and adsorption energy of benzene on Ag(111 and Au(111. Agreement with experimental data is substantially improved. We apply the method to self-assembled monolayers of alkanethiols on Au(111 and find reasonable agreement for PBE-D and revPBE-D for both physisorption of n-alkanethiols as well as dissociative chemisorption of dimethyl disulfide as an Au-adatom-dithiolate complex. By modifying the C6 coefficient for Au, we obtain quantitative agreement for physisorption and chemisorption for both PBE-D and revPBE-D using the same set of parameters. Our results confirm that inclusion of dispersion forces is crucial for any quantitative analysis of the thiol and thiolate bonds to the gold surface using quantum chemical calculations.

  14. Ni/Ag/Ti/Au与p-GaN的欧姆接触性能及光反射率%The reflectivity and ohmic contact resistivity of Ni/Ag/Ti/Au in contact with p-GaN

    Institute of Scientific and Technical Information of China (English)

    黄亚平; 刘硕; 云峰; 丁文; 王越; 王宏; 赵宇坤; 张烨; 郭茂峰; 侯洵

    2014-01-01

    The ohmic reflectivity of Ni/Ag/Ti/Au in contact with p-GaN is studied. It is found that under different thickness values of Ni, different annealing temperatures and different annealing atmospheres, the performances of Ni/Ag/Ti/Au electrode are greatly changed. The contact resistivity is measured using the transmission line model. The reflectivity of the electrode is investigated by using a spectrophotometer. The results reveal that the thinner the Ni metal layer, the higher its reflectivity is, in addition, the thickness value of Ni metal has a little influence on contact resistivity. There appears an abrupt decrease in reflectivity of electrode after annealing at a temperature higher than 400 ◦C. It is noticed that the reflectivity decreases more sharply after annealing in oxygen atmosphere than in nitrogen atmosphere. However, annealing in oxygen atmosphere is more helpful to reduce the contact resistivity. The comprehensive evaluations of the contact resistivity and reflectivity indicate that the better performances of Ni (1 nm)/Ag/Ti/Au electrode after rapid annealing in oxygen atmosphere at 400 ◦C are achieved: its contact resistance reaches 5.5 × 10-3 Ω·cm2 and reflectivity rises up to 85%at 450 nm. Light emitting diode (LED) of vertical structure is fabricated with an optimal electrode. The LED under an injection current of 350 mA can achieve the following working parameters: the working voltage is 3.2 V, the optical output power is 270 mW, and the electro-optical conversion efficiency is 24%.%研究了不同Ni厚度的Ni/Ag/Ti/Au电极在不同退火温度和退火气氛下与p-GaN之间的欧姆接触性能以及电极的光反射率的变化.采用矩形传输线模型对各电极的比接触电阻率进行测算,利用分光光度计对电极在不同波长下的反射率进行测量.结果表明, Ni金属层的厚度越小,电极的光反射率越高,而Ni层厚度对比接触电阻率的影响较小;当退火温度高于400◦C后,电极的

  15. The reflectivity and ohmic contact resistivity of Ni/Ag/Ti/Au in contact with p-GaN%Ni/Ag/Ti/Au与p-GaN的欧姆接触性能及光反射率

    Institute of Scientific and Technical Information of China (English)

    黄亚平; 刘硕; 云峰; 丁文; 王越; 王宏; 赵宇坤; 张烨; 郭茂峰; 侯洵

    2014-01-01

    The ohmic reflectivity of Ni/Ag/Ti/Au in contact with p-GaN is studied. It is found that under different thickness values of Ni, different annealing temperatures and different annealing atmospheres, the performances of Ni/Ag/Ti/Au electrode are greatly changed. The contact resistivity is measured using the transmission line model. The reflectivity of the electrode is investigated by using a spectrophotometer. The results reveal that the thinner the Ni metal layer, the higher its reflectivity is, in addition, the thickness value of Ni metal has a little influence on contact resistivity. There appears an abrupt decrease in reflectivity of electrode after annealing at a temperature higher than 400 ◦C. It is noticed that the reflectivity decreases more sharply after annealing in oxygen atmosphere than in nitrogen atmosphere. However, annealing in oxygen atmosphere is more helpful to reduce the contact resistivity. The comprehensive evaluations of the contact resistivity and reflectivity indicate that the better performances of Ni (1 nm)/Ag/Ti/Au electrode after rapid annealing in oxygen atmosphere at 400 ◦C are achieved: its contact resistance reaches 5.5 × 10-3 Ω·cm2 and reflectivity rises up to 85%at 450 nm. Light emitting diode (LED) of vertical structure is fabricated with an optimal electrode. The LED under an injection current of 350 mA can achieve the following working parameters: the working voltage is 3.2 V, the optical output power is 270 mW, and the electro-optical conversion efficiency is 24%.%研究了不同Ni厚度的Ni/Ag/Ti/Au电极在不同退火温度和退火气氛下与p-GaN之间的欧姆接触性能以及电极的光反射率的变化.采用矩形传输线模型对各电极的比接触电阻率进行测算,利用分光光度计对电极在不同波长下的反射率进行测量.结果表明, Ni金属层的厚度越小,电极的光反射率越高,而Ni层厚度对比接触电阻率的影响较小;当退火温度高于400◦C后,电极的

  16. Superior effect of Ni-substitution on the hydrogenation kinetics of Mg{sub 6}Pd{sub 1−x}TM{sub x} (TM = Ag, Cu, Ni) pseudo-binary compounds

    Energy Technology Data Exchange (ETDEWEB)

    Ponthieu, M. [MIRE-Group, Laboratorio de Física de Materiales de Interés Energético, Dpto Física de Materiales, Facultad de Ciencias, Universidad Autónoma de Madrid, 28049 Madrid (Spain); ICMPE/CNRS-UPEC, UMR 7182, 2-8 rue Henri Dunant, 94320 Thiais (France); Fernández, J.F., E-mail: josefrancisco.fernandez@uam.es [MIRE-Group, Laboratorio de Física de Materiales de Interés Energético, Dpto Física de Materiales, Facultad de Ciencias, Universidad Autónoma de Madrid, 28049 Madrid (Spain); Cuevas, F. [ICMPE/CNRS-UPEC, UMR 7182, 2-8 rue Henri Dunant, 94320 Thiais (France); Laversenne, L. [Institut Néel, CNRS, Grenoble (France); Bodega, J.; Ares, J.R.; Sánchez, C. [MIRE-Group, Laboratorio de Física de Materiales de Interés Energético, Dpto Física de Materiales, Facultad de Ciencias, Universidad Autónoma de Madrid, 28049 Madrid (Spain)

    2015-10-05

    Highlights: • Kinetics of (de)hydrogenation of Mg{sub 6}(Pd,TM) TM = Ag, Cu and Ni compared. • Faster hydrogenation kinetics for the Ni compound. • Faster H-desorption for the Ni compound due to MgH{sub 2}/Mg{sub 2}NiH{sub 4} synergy. - Abstract: In this investigation, the H-sorption kinetics of Mg{sub 6}Pd and Mg{sub 6}Pd{sub 1−x}TM{sub x} (TM = Ag, Cu, Ni) pseudo-binary compounds at the TM solubility limit have been studied by isothermal hydrogen absorption, thermal desorption spectroscopy and in situ neutron diffraction. Among all studied compounds, the fastest absorption kinetics takes place for the Ni-substituted one. The fit of the absorption curves to established model equations for solid–gas reaction shows that hydrogenation is controlled by diffusion. As for desorption, the peak temperature for the Ni-substituted compound is 90 K below that of MgH{sub 2}/Mg system and is characterised by a low activation energy of 68 kJ/molH{sub 2}. To better understand these results, neutron diffraction experiments during in situ thermal desorption of deuterated Mg{sub 6}Pd and Mg{sub 6}Pd{sub 0.25}Ni{sub 0.75} compounds were carried out. These experiments demonstrate a synergetic effect between MgH{sub 2} and Mg{sub 2}NiH{sub 4} hydrides as responsible for the remarkable kinetics of the Ni-containing compound.

  17. Production of ultrapure hydrogen in a Pd-Ag membrane reactor using Ru/La{sub 2}O{sub 3} catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Faroldi, B.; Carrara, C.; Lombardo, E.A.; Cornaglia, L.M. [Instituto de Investigaciones en Catalisis y Petroquimica (FIQ, UNL-CONICET), Santiago del Estero, 2829-3000 Santa Fe (Argentina)

    2007-03-01

    Ru catalysts supported on lanthanum oxide with different loadings were prepared by wet impregnation. These solids were characterized by laser Raman spectroscopy (LSR), XPS, XRD and TPR. The catalytic activity toward hydrogen production through the dry reforming of methane was determined in a fixed-bed reactor and a membrane reactor. The reaction rate expressed per gram of Ru decreased when the metal loading increased. In the Pd-Ag membrane reactor, when the sweep gas flow rate (SG) increased, the conversions overcame the equilibrium values and the difference between CH{sub 4} and CO{sub 2} conversions decreased. Both Ru(0.6) and Ru(1.2) catalysts were able to restore the equilibrium for the dry reforming reaction up to values of SG = 30 ml min{sup -1}; Ru(0.6) was the most effective catalyst. By employing a CO{sub 2}/CH{sub 4} 1 and a SG of 0.05 mmol s{sup -1}, both a high H{sub 2} permeation flux of 5.68 x 10{sup -7} mol s{sup -1} m{sup -2} and a hydrogen recovery of 80% were obtained. Both the TPR and the Raman spectroscopy data indicated the presence of Ru(III) strongly interacting with La. Significantly, this observation was further confirmed by the appearance of Ru(III) on the surface. When the Ru content increased, the higher Ru 3d binding energy component was proposed as arising from Ru(IV). Concerning the Ru(1.2) solid, the presence of Ru(IV) was detected by means of TPR experiments, in agreement with the high proportion of Ru(IV) on the surface. Therefore, a fraction of Ru loading was present in this solid as species with weaker metal-support interaction leading to the slight deactivation of this catalyst in the membrane reactor. (author)

  18. CO adsorption on Ni, Pd, Cu and Ag deposited on MgO, CaO, SrO and BaO: Density functional calculations

    International Nuclear Information System (INIS)

    The adsorption properties of CO molecules adsorbed on Ni, Pd, Cu and Ag atoms deposited on O2-, F and F+ sites of MgO, CaO, SrO and BaO terrace surfaces have been studied by means of density functional calculations and embedded cluster model. The examined clusters were embedded in the simulated Coulomb fields that closely approximate the Madelung fields of the host surfaces. The adsorption properties of CO have been analyzed with reference to the basicity of the oxide support, bond order conservation energy, pairwise and non-pairwise additivity, associative adsorption, electrostatic potentials, and orbital interactions. CO adsorption on an oxide support is drastically enhanced when CO is adsorbed on a metal deposited on this support. A dramatic change is found, and explained, when one compares the CO binding energy to O2- and F sites. The formation of a strong bond at the support-metal interface has a considerable consequence on the metal-CO binding energy. The binding of CO is dominated by the metal-CO pairwise additive term, and the non-additivity term increases with increasing the basicity of the support. While the classical contributions to the electrostatic interactions are quite similar for the deposited metals, they are quite dissimilar when going from defect-free to defect-containing surfaces. The adsorption properties correlate linearly with the basicity and energy gaps of the oxide support where the electrostatic potential generated by the oxide modifies the physical and chemical properties of the adsorbed metal and therefore its reactivity versus the CO adsorbate.

  19. Physical Properties of Film Alloys Based on Ferromagnetic and Noble Metals (Review. І. Film Materials Based on Fe and Ag or Au

    Directory of Open Access Journals (Sweden)

    L.V. Odnodvorets

    2016-10-01

    Full Text Available The results of analysis of literature and own data on the phase composition, electrophysical and magnetoresistive properties of granular film alloys based on Fe and Ag or Au are present. Analyzed the question about system designations of film structures, which adopted in the literature and does not meet their physical nature in its original state and after annealing. A new system of signs ordered and disordered solid solutions without and with the presence elements of granular state; quasigranular alloys, in which the role played granules of ferromagnetic island films; intermetallic and others was proposed. It is established that the electrophysical properties (temperature coefficient of resistance – TCR and strain coefficient – SC defined conductive matrix as s.s., and in nanoscale granules realized the ballistic conductivity mechanism that does not affect the value of TCR and SC. In granular film alloys s.s. Au (Fe + granules at the plastic deformation observed abnormal increase in comparison with the elastic deformation value SC (10 times at a concentration cFe  55-75 аt. %.

  20. Surface plasmon resonances of Ag-Au alloy nanoparticle films grown by sequential pulsed laser deposition at different compositions and temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Verma, Shweta, E-mail: shwetaverma@rrcat.gov.in; Rao, B. T.; Detty, A. P.; Kukreja, L. M. [Laser Materials Processing Division, Raja Ramanna Centre for Advanced Technology, Indore 452 013 (India); Ganesan, V.; Phase, D. M. [UGC-DAE Consortium for Scientific Research, Indore 452 001 (India); Rai, S. K. [Indus Synchrotons Utilization Division, Raja Ramanna Centre for Advanced Technology, Indore 452 013 (India); Bose, A.; Joshi, S. C. [Proton Linac and Superconducting Cavities Division, Raja Ramanna Centre for Advanced Technology, Indore 452 013 (India)

    2015-04-07

    We studied localized surface plasmon resonances (LSPR) at different compositions, substrate temperatures, and mass thicknesses of Ag-Au alloy nanoparticle films grown by sequential pulsed laser deposition. The LSPRs were pronounced at all compositions of the films grown at high substrate temperature of about 300 °C as compared to those grown at room temperature. The alloy formation and composition of the films were determined using X-ray photoelectron and energy dispersive spectroscopy. Films' mass thickness and compositional uniformity along the thickness were determined using X-ray reflectometry and secondary ion mass spectroscopy. Atomic force microscopic analysis revealed the formation of densely packed nanoparticles of increasing size with the number of laser ablation pulses. The LSPR wavelength red shifted with increasing either Au percentage or film mass thickness and corresponding LSPR tuning was obtained in the range of 450 to 690 nm. The alloy dielectric functions obtained from three different models were compared and the optical responses of the nanoparticle films were calculated from modified Yamaguchi effective medium theory. The tuning of LSPR was found to be due to combined effect of change in intrinsic and extrinsic parameters mainly the composition, morphology, particle-particle, and particle-substrate interactions.

  1. Adsorption of the ionic liquid [BMP][TFSA] on Au(111 and Ag(111: substrate effects on the structure formation investigated by STM

    Directory of Open Access Journals (Sweden)

    Benedikt Uhl

    2013-12-01

    Full Text Available In order to resolve substrate effects on the adlayer structure and structure formation and on the substrate–adsorbate and adsorbate–adsorbate interactions, we investigated the adsorption of thin films of the ionic liquid (IL 1-butyl-1-methylpyrrolidinium-bis(trifluoromethylsulfonylimide [BMP][TFSA] on the close-packed Ag(111 and Au(111 surfaces by scanning tunneling microscopy, under ultra high vacuum (UHV conditions in the temperature range between about 100 K and 293 K. At room temperature, highly mobile 2D liquid adsorbate phases were observed on both surfaces. At low temperatures, around 100 K, different adsorbed IL phases were found to coexist on these surfaces, both on silver and gold: a long-range ordered (‘2D crystalline’ phase and a short-range ordered (‘2D glass’ phase. Both phases exhibit different characteristics on the two surfaces. On Au(111, the surface reconstruction plays a major role in the structure formation of the 2D crystalline phase. In combination with recent density functional theory calculations, the sub-molecularly resolved STM images allow to clearly discriminate between the [BMP]+ cation and [TFSA]− anion.

  2. Fast-electron ejection from C, Ni, Ag and Au foils by 36 Ar 18 + (95 MeV/u): Measurements of absolute cross-sections

    Science.gov (United States)

    de Filippo, E.; Lanzanó, G.; Rothard, H.; Volant, C.; Aiello, S.; Anzalone, A.; Arena, N.; Geraci, M.; Giustolisi, F.; Pagano, A.

    2004-07-01

    Doubly differential electron velocity spectra induced by 36Ar18 + (95 MeV/ u) from thin target foils (C, Ni, Ag, Au) were measured at GANIL (Caen, France) by means of the ARGOS multidetector and the time-of-flight technique. The main features observed in the forward spectra are convoy electrons, binary-encounter electrons, and (for the Au target only) a high-velocity tail which we attribute to a “Fermi shuttle” acceleration mechanism. Backward spectra do not show distinct structures. The spectra allow us to determine absolute singly differential cross-sections as a function of the target material and the emission angle. The convoy electron yield increases with the target atomic number, but for C their yield is so small that our experiment is not able to detect them. Absolute doubly differential cross-sections for binary-encounter electron ejection from C targets are well described by a transport theory which is based on the relativistic electron impact approximation (EIA) for electron production and which accounts for angular deflection, energy loss and energy straggling of the transmitted electrons.

  3. A computational study on structure, stability and bonding in Noble Gas bound metal Nitrates, Sulfates and Carbonates (Metal = Cu, Ag, Au)

    Indian Academy of Sciences (India)

    MANAS GHARA; SUDIP PAN; JYOTIRMOY DEB; ANAND KUMAR; UTPAL SARKAR; PRATIM KUMAR CHATTARAJ

    2016-10-01

    A density functional theory based study is performed to investigate the noble gas (Ng = Ar-Rn) binding ability of nitrates, sulfates and carbonates of noble metal (M). Their ability to bind Ng atoms is assessed through bond dissociation energy and thermochemical parameters like dissociation enthalpy and dissociation free energy change corresponding to the dissociation of Ng bound compound producing Ngand the respective salt. The zero-point energy corrected dissociation energy values per Ng atom for the dissociation process producing Ng atom(s) and the corresponding salts range within 6.0–13.1 kcal/mol in NgCuNO₃, 3.1–9.8 kcal/mol in NgAgNO₃, 6.0–13.2 kcal/mol in NgCuSO₄, 3.2–10.1 kcal/mol in NgAgSO₄, 5.1–11.7 kcal/mol in Ng₂Cu₂SO₄, 2.5–8.6 kcal/mol in Ng₂Ag₂SO₂, 8.1–19.9 kcal/mol in Ng₂Au2SO₂, 5.7–12.4 kcal/mol in NgCuCO₃, 2.3–8.0 kcal/mol in Ng₂Ag₂CO₃ and 7.3–18.2 kcal/mol in Ng₂Au₂CO₃, with a gradual increase in moving from Ar to Rn. For a given type of system, the stability of Ng bound analogues follows the order as Au > Cu > Ag. All dissociation processes are endothermic in nature whereas they become endergonic as well in most of the cases of Kr-Rn bound analogues at 298 K. Natural population analysis along with the computation of Wiberg bond indices, and electron density analyses provide insights into the nature of the Ng-M bonds. The Ng-M bonds can be represented as partial covalent bonds as supported by the different electron density descriptors.

  4. Synthesis of Ag-Au Nanoparticles by Galvanic Replacement and Their Morphological Studies by HRTEM and Computational Modeling

    Directory of Open Access Journals (Sweden)

    Manuel Ramos

    2011-01-01

    Full Text Available Bimetallic nanoparticles are important because they possess catalytic and electronic properties with potential applications in medicine, electronics, and chemical industries. A galvanic replacement reaction synthesis has been used in this research to form bimetallic nanoparticles. The complete description of the synthesis consists of using the chemical reduction of metallic silver nitrite (AgNO3 and gold-III chloride hydrate (HAuCl salt precursors. The nanoparticles display round shapes, as revealed by high-resolution transmission electron microscope (HRTEM. In order to better understand the colloidal structure, it was necessary to employ computational models which involved the simulations of HRTEM images.

  5. On new ternary equiatomic scandium transition metal aluminum compounds ScTAl with T = Cr, Ru, Ag, Re, Pt, and Au

    Energy Technology Data Exchange (ETDEWEB)

    Radzieowski, Mathis; Janka, Oliver [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Benndorf, Christopher [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Muenster Univ. (Germany). Inst. fuer Physikalische Chemie; Haverkamp, Sandra [Muenster Univ. (Germany). Inst. fuer Physikalische Chemie; Eckert, Hellmut [Muenster Univ. (Germany). Inst. fuer Physikalische Chemie; University of Sao Paulo, Sao Carlos, SP (Brazil). Inst. of Physics

    2016-08-01

    The new equiatomic scandium transition metal aluminides ScTAl for T = Cr, Ru, Ag, Re, Pt, and Au were obtained by arc-melting of the elements followed by subsequent annealing for crystal growth. The samples were studied by powder and single crystal X-ray diffraction. The structures of three compounds were refined from single crystal X-ray diffractometer data: ScCrAl, MgZn{sub 2} type, P6{sub 3}/mmc, a = 525.77(3), c = 858.68(5) pm, R{sub 1} = 0.0188, wR{sub 2} = 0.0485, 204 F{sup 2} values, 13 variables, ScPtAl, TiNiSi type, Pnma, a = 642.83(4), b = 428.96(2), c = 754.54(5) pm, R{sub 1} = 0.0326, wR{sub 2} = 0.0458, 448 F{sup 2} values, 20 variables and ScAuAl, HfRhSn type, P anti 62c, a = 722.88(4), c = 724.15(4) pm, R{sub 1} = 0.0316, wR{sub 2} = 0.0653, 512 F{sup 2} values, 18 variables. Phase pure samples of all compounds were furthermore investigated by magnetic susceptibility measurements, and Pauli-paramagnetism but no superconductivity was observed down to 2.1 K for all of them. The local structural features and disordering phenomena have been characterized by {sup 27}Al and {sup 45}Sc magic angle spinning (MAS) and static NMR spectroscopic investigations.

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

    Science.gov (United States)

    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.

  7. 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

    Energy Technology Data Exchange (ETDEWEB)

    Estrin, Y.; Rich, D. H., E-mail: danrich@bgu.ac.il [Department of Physics and The Ilse Katz Institute for Nanoscale Science and Technology, Ben-Gurion University of the Negev, P.O.B 653, Beer-Sheva 84105 (Israel); Keller, S.; DenBaars, S. P. [Electrical and Computer Engineering and Materials Departments, University of California, Santa Barbara, California 93111 (United States)

    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.

  8. Measurement of the (n,2n) cross sections for 89Y, 93Nb, 103Rh, 107Ag, 169Tm, 175Lu and 197Au at 14.1 and 14.8 MeV incident neutron energies

    International Nuclear Information System (INIS)

    The (n,2n) cross sections for 89Y, 93Nb, 103Rh, 107Ag, 169Tm, 175Lu and 197Au have been measured at 14.1 and 14.8 MeV incident neutron energies. The samples were irradiated at the 14 MeV neutron generator of C.E. VALDUC. 27Al(n,α)24Na cross section was used for standard. The cross sections were obtained with an accuracy of about 5%

  9. van der Waals-corrected Density Functional Theory simulation of adsorption processes on noble-metal surfaces: Xe on Ag(111), Au(111), and Cu(111)

    CERN Document Server

    Silvestrelli, Pier Luigi

    2016-01-01

    The DFT/vdW-WF2s1 method based on the generation of localized Wannier functions, recently developed to include the van der Waals interactions in the Density Functional Theory and describe adsorption processes on metal surfaces by taking metal-screening effects into account, is applied to the case of the interaction of Xe with noble-metal surfaces, namely Ag(111), Au(111), and Cu(111). The study is also repeated by adopting the DFT/vdW-QHO-WF variant relying on the Quantum Harmonic Oscillator model which describes well many-body effects. Comparison of the computed equilibrium binding energies and distances, and the $C_3$ coefficients characterizing the adatom-surface van der Waals interactions, with available experimental and theoretical reference data shows that the methods perform well and elucidate the importance of properly including screening effects. The results are also compared with those obtained by other vdW-corrected DFT schemes, including PBE-D, vdW-DF, vdW-DF2, rVV10, and by the simpler Local Dens...

  10. Simultaneous enzymatic and SERS properties of bifunctional chitosan-modified popcorn-like Au-Ag nanoparticles for high sensitive detection of melamine in milk powder.

    Science.gov (United States)

    Li, Junrong; Zhang, Guannan; Wang, Lihua; Shen, Aiguo; Hu, Jiming

    2015-08-01

    In this work, we suggest a chitosan-modified popcorn-like Au-Ag nanoparticles (CSPNPs) based assay for high sensitive detection of melamine, in which CSPNPs not only provide with an intrinsic peroxidase-like activity but also act as surface enhanced Raman scattering (SERS) substrates. CSPNPs can catalyze the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) by H2O2 to the charge transfer complex (CTC), which contributes to a tremendous surface-enhanced resonant Raman scattering (SERRS) signals with 632.8 nm laser excitation. The target molecule melamine can generate an additional compound with H2O2, which means the available amount of H2O2 for the oxidation of TMB reduced. Correspondingly, the SERRS intensity of CTC is decreased. The decreased Raman intensity is proportional to the concentration of melamine over a wide range from 10 nM to 50 μM (R(2)=0.989), with a limit of detection (LOD) of 8.51 nM. Moreover, the proposed highly selective method is fully capable of rapid, separation-free detection of melamine in milk powder. PMID:26048843

  11. Quench characteristics of Ag/AuBi2223 HTS-stainless steel stack used for the hybrid current leads of the large hadron collider

    CERN Document Server

    Al-Mosawi, M K; Beduz, C; Yang, Y; Ballarino, A

    2008-01-01

    The quench characteristics of Ag/Au sheathed Bi2223 tapes have been investigated in an adiabatic condition and in a configuration similar to that used in hybrid high temperature superconducting current leads, namely the 13000A leads used for the Large Hadron Collider at CERN. A specialised rig was designed and constructed to provide a carefully controlled environment. The samples were prepared from HTS tape soldered onto a stainless steel substrate with a number of temperature sensors at various positions along the length of tape. One end of the lead (cold end) was maintained at 6K using G-M cryo-cooler whereas the temperature of the other end (warm end) can be varied and maintained at temperatures up to 100K. The thermal runaway currents (quench currents) at various warm end temperatures (in the range of 40-100K) were determined. The temperature evolutions at various locations along the tape were recorded at different top end temperatures and currents. The effect of the stainless steel mechanical reinforceme...

  12. Cohesive properties of noble metals by van der Waals-corrected density functional theory: Au, Ag, and Cu as case studies

    Science.gov (United States)

    Ambrosetti, Alberto; Silvestrelli, Pier Luigi

    2016-07-01

    The cohesive energy, equilibrium lattice constant, and bulk modulus of Au, Ag, and Cu noble metals are computed by different van der Waals (vdW)-corrected density functional theory (DFT) methods, including vdW-DF, vdW-DF2, vdW-DF-cx, rVV10, and PBE-D. Two specifically designed methods are also developed in order to effectively include dynamical screening effects: the DFT/vdW-WF2p method, based on the generation of maximally localized Wannier functions, and the RPAp scheme (in two variants), based on a single-oscillator model of the localized electron response. Comparison with results obtained without explicit inclusion of van der Waals effects, such as with the local density approximation (LDA), PBE, PBEsol, or the hybrid PBE0 functional, elucidates the importance of a suitable description of screened van der Waals interactions even in the case of strong metal bonding. Many-body effects are also quantitatively evaluated within the RPAp approach.

  13. Van Der Waals-Corrected Density Functional Theory Simulation of Adsorption Processes on Noble-Metal Surfaces: Xe on Ag(111), Au(111), and Cu(111)

    Science.gov (United States)

    Silvestrelli, Pier Luigi; Ambrosetti, Alberto

    2016-10-01

    The DFT/vdW-WF2s1 method based on the generation of localized Wannier functions, recently developed to include the van der Waals interactions in the density functional theory and describe adsorption processes on metal surfaces by taking metal-screening effects into account, is applied to the case of the interaction of Xe with noble-metal surfaces, namely Ag(111), Au(111), and Cu(111). The study is also repeated by adopting the DFT/vdW-QHO-WF variant relying on the quantum harmonic oscillator model which describes well many body effects. Comparison of the computed equilibrium binding energies and distances, and the C_3 coefficients characterizing the adatom-surface van der Waals interactions, with available experimental and theoretical reference data shows that the methods perform well and elucidates the importance of properly including screening effects. The results are also compared with those obtained by other vdW-corrected DFT schemes, including PBE-D, vdW-DF, vdW-DF2, rVV10, and by the simpler local density approximation and semi-local (PBE) generalized gradient approximation approaches.

  14. Isotopic Characteristics of Mesozoic Au-Ag Polymetallic Ore Deposits in Northern Hebei and Their Ore-Forming Materials Source

    Institute of Scientific and Technical Information of China (English)

    王宝德; 牛树银; 孙爱群; 李红阳

    2003-01-01

    It has long been a controversy about the source of ore-forming materials of Au-Agpolymetallic deposits both in metallogenic theory and in ore-searching practice. In terms of alarge wealth of the isotopic statistics data from Indosinian-Yanshanian endogenic ore deposits innorthern Hebei (generally referring to the areas along the northern part of Taihang Mountainsand northern Hebei, the same below) , it is considered that the ore-forming materials came fromthe deep interior of the Earth, which had migrated through plumes to the Earth surface while ex-perienced multi-stage evolution and then emplaced progressively in favorable structural loci toform ores. Their isotope data show that 559 sulfur isotopic data from 40 ore deposits are, for themost part, within the range of - 5‰ - 5‰, with a high degree of homogenization, indicatingthat the sulfur is derived mainly from magma; 200 lead isotope data from 37 ore deposits indi-cate that the ore-forming materials are principally of mantle source though some crust-source ma-terial was involved; 96 oxygen, hydrogen and carbon isotope data from 34 ore deposits illustratethat the ore-forming fluids are dominated by magmatic water while other sources of water wouldbe involved. It may therefore be seen that the formation of endogenic deposits has nothing to dowith the strata.

  15. Effect of reaction time and P content on mechanical strength of the interface formed between eutectic Sn-Ag solder and Au/electroless Ni(P)/Cu bond pad

    Science.gov (United States)

    Alam, M. O.; Chan, Y. C.; Tu, K. N.

    2003-09-01

    In this work, shear strengths of the solder joints for Sn-Ag eutectic alloy with the Au/electroless Ni(P)/Cu bond pad were measured for three different electroless Ni(P) layers. Sn-Ag eutectic solder alloy was kept in molten condition (240 °C) on the Au/electroless Ni(P)/Cu bond pad for different time periods ranging from 0.5 min to 180 min to render the ultimate interfacial reaction and the consecutive shear strength. After the shear test, fracture surfaces were investigated by scanning electron microscopy equipped with energy dispersed x ray. Cross-sectional studies of the interfaces were also conducted to correlate with the fracture surfaces. It was found that formation of crystalline phosphorous-rich Ni layer at the solder interface of Au/electroless Ni(P)/Cu bond pad with Sn-Ag eutectic alloy deteriorates the mechanical strength of the joints significantly. It was also noticed that such weak P-rich Ni layer appears quickly for high-P content electroless Ni(P) layer. However, when this P-rich Ni layer disappears from a prolonged reaction, the shear strength increases again.

  16. The Marianas-San Marcos vein system: characteristics of a shallow low sulfidation epithermal Au-Ag deposit in the Cerro Negro district, Deseado Massif, Patagonia, Argentina

    Science.gov (United States)

    Vidal, Conrado Permuy; Guido, Diego M.; Jovic, Sebastián M.; Bodnar, Robert J.; Moncada, Daniel; Melgarejo, Joan Carles; Hames, Willis

    2016-08-01

    The Cerro Negro district, within the Argentinian Deseado Massif province, has become one of the most significant recent epithermal discoveries, with estimated reserves plus resources of ˜6.7 Moz Au equivalent. The Marianas-San Marcos vein system contains about 70 % of the Au-Ag resources in the district. Mineralization consists of Upper Jurassic (155 Ma) epithermal Au- and Ag-rich veins of low to intermediate sulfidation style, hosted in and genetically related to Jurassic intermediate composition volcanic rocks (159-156 Ma). Veins have a complex infill history, represented by ten stages with clear crosscutting relationships that can be summarized in four main episodes: a low volume, metal-rich initial episode (E1), an extended banded quartz episode with minor mineralization (E2), a barren waning stage episode (E3), and a silver-rich late tectonic-hydrothermal episode (E4). The first three episodes are interpreted to have formed at the same time and probably from fluids of similar composition: a 290-230 °C fluid dominated by meteoric and volcanic waters (-3‰ to -0‰ δ18Owater), with <3 % NaCl equivalent salinity and with a magmatic source of sulfur (-1 to -2 ‰ δ34Swater). Metal was mainly precipitated at the beginning of vein formation (episode 1) due to a combination of boiling at ˜600 to 800 m below the paleowater table, and associated mixing/cooling processes, as evidenced by sulfide-rich bands showing crustiform-colloform quartz, adularia, and chlorite-smectite banding. During episodes 2 and 3, metal contents progressively decrease during continuing boiling conditions, and veins were filled by quartz and calcite during waning stages of the hydrothermal system, and the influx of bicarbonate waters (-6 to -8.5 ‰ δ18Owater). Hydrothermal alteration is characterized by proximal illite, adularia, and silica zone with chlorite and minor epidote, intermediate interlayered illite-smectite and a distal chlorite halo. This assemblage is in agreement with

  17. The Marianas-San Marcos vein system: characteristics of a shallow low sulfidation epithermal Au-Ag deposit in the Cerro Negro district, Deseado Massif, Patagonia, Argentina

    Science.gov (United States)

    Vidal, Conrado Permuy; Guido, Diego M.; Jovic, Sebastián M.; Bodnar, Robert J.; Moncada, Daniel; Melgarejo, Joan Carles; Hames, Willis

    2016-01-01

    The Cerro Negro district, within the Argentinian Deseado Massif province, has become one of the most significant recent epithermal discoveries, with estimated reserves plus resources of ˜6.7 Moz Au equivalent. The Marianas-San Marcos vein system contains about 70 % of the Au-Ag resources in the district. Mineralization consists of Upper Jurassic (155 Ma) epithermal Au- and Ag-rich veins of low to intermediate sulfidation style, hosted in and genetically related to Jurassic intermediate composition volcanic rocks (159-156 Ma). Veins have a complex infill history, represented by ten stages with clear crosscutting relationships that can be summarized in four main episodes: a low volume, metal-rich initial episode (E1), an extended banded quartz episode with minor mineralization (E2), a barren waning stage episode (E3), and a silver-rich late tectonic-hydrothermal episode (E4). The first three episodes are interpreted to have formed at the same time and probably from fluids of similar composition: a 290-230 °C fluid dominated by meteoric and volcanic waters (-3‰ to -0‰ δ18Owater), with <3 % NaCl equivalent salinity and with a magmatic source of sulfur (-1 to -2 ‰ δ34Swater). Metal was mainly precipitated at the beginning of vein formation (episode 1) due to a combination of boiling at ˜600 to 800 m below the paleowater table, and associated mixing/cooling processes, as evidenced by sulfide-rich bands showing crustiform-colloform quartz, adularia, and chlorite-smectite banding. During episodes 2 and 3, metal contents progressively decrease during continuing boiling conditions, and veins were filled by quartz and calcite during waning stages of the hydrothermal system, and the influx of bicarbonate waters (-6 to -8.5 ‰ δ18Owater). Hydrothermal alteration is characterized by proximal illite, adularia, and silica zone with chlorite and minor epidote, intermediate interlayered illite-smectite and a distal chlorite halo. This assemblage is in agreement with

  18. Atomic Structure of Au−Pd Bimetallic Alloyed Nanoparticles

    KAUST Repository

    Ding, Yong

    2010-09-08

    Using a two-step seed-mediated growth method, we synthesized bimetallic nanoparticles (NPs) having a gold octahedron core and a palladium epitaxial shell with controlled Pd-shell thickness. The mismatch-release mechanism between the Au core and Pd shell of the NPs was systematically investigated by high-resolution transmission electron microscopy. In the NPs coated with a single atomic layer of Pd, the strain between the surface Pd layer and the Au core is released by Shockley partial dislocations (SPDs) accompanied by the formation of stacking faults. For NPs coated with more Pd (>2 nm), the stacking faults still exist, but no SPDs are found. This may be due to the diffusion of Au atoms into the Pd shell layers to eliminate the SPDs. At the same time, a long-range ordered L11 AuPd alloy phase has been identified in the interface area, supporting the assumption of the diffusion of Au into Pd to release the interface mismatch. With increasing numbers of Pd shell layers, the shape of the Au-Pd NP changes, step by step, from truncated-octahedral to cubic. After the bimetallic NPs were annealed at 523 K for 10 min, the SPDs at the surface of the NPs coated with a single atomic layer of Pd disappeared due to diffusion of the Au atoms into the surface layer, while the stacking faults and the L11 Au-Pd alloyed structure remained. When the annealing temperature was increased to 800 K, electron diffraction patterns and diffraction contrast images revealed that the NPs became a uniform Au-Pd alloy, and most of the stacking faults disappeared as a result of the annealing. Even so, some clues still support the existence of the L11 phase, which suggests that the L11 phase is a stable, long-range ordered structure in Au-Pd bimetallic NPs. © 2010 American Chemical Society.

  19. Perpendicular magnetic anisotropy in granular multilayers of CoPd alloyed nanoparticles

    Science.gov (United States)

    Vivas, L. G.; Rubín, J.; Figueroa, A. I.; Bartolomé, F.; García, L. M.; Deranlot, C.; Petroff, F.; Ruiz, L.; González-Calbet, J. M.; Pascarelli, S.; Brookes, N. B.; Wilhelm, F.; Chorro, M.; Rogalev, A.; Bartolomé, J.

    2016-05-01

    Co-Pd multilayers obtained by Pd capping of pre-deposited Co nanoparticles on amorphous alumina are systematically studied by means of high-resolution transmission electron microscopy, x-ray diffraction, extended x-ray absorption fine structure, SQUID-based magnetometry, and x-ray magnetic circular dichroism. The films are formed by CoPd alloyed nanoparticles self-organized across the layers, with the interspace between the nanoparticles filled by the non-alloyed Pd metal. The nanoparticles show atomic arrangements compatible with short-range chemical order of L 10 strucure type. The collective magnetic behavior is that of ferromagnetically coupled particles with perpendicular magnetic anisotropy, irrespective of the amount of deposited Pd. For increasing temperature three magnetic phases are identified: hard ferromagnetic with strong coercive field, soft-ferromagnetic as in an amorphous asperomagnet, and superparamagnetic. Increasing the amount of Pd in the system leads to both magnetic hardness increment and higher transition temperatures. Magnetic total moments of 1.77(4) μB and 0.45(4) μB are found at Co and Pd sites, respectively, where the orbital moment of Co, 0.40(2) μB, is high, while that of Pd is negligible. The effective magnetic anisotropy is the largest in the capping metal series (Pd, Pt, W, Cu, Ag, Au), which is attributed to the interparticle interaction between de nanoparticles, in addition to the intraparticle anisotropy arising from hybridization between the 3 d -4 d bands associated to the Co and Pd chemical arrangement in a L 10 structure type.

  20. Evaluation of luminol chemiluminescence based on simultaneous introducing of coumarin derivatives as green fluorophores and chitosan-induced Au/Ag alloy nanoparticle as catalyst for the sensitive determination of glucose.

    Science.gov (United States)

    Chaichi, M J; Alijanpour, S O; Asghari, S; Shadlou, S

    2015-03-01

    We report herein the development of a novel chemiluminescence system based on simultaneous introducing of synthetic coumarin derivatives and chitosan-induced Au/Ag alloy NPs on the luminol CL system and suggest how it may be useful for determination of glucose. Chitosan-induced Au/Ag nanoalloys in the coumarin derivatives intensified-luminol CL system, in addition to catalyze CL reaction can make a change in the process of coumarin derivatives effect as fluorophore on the luminol CL system. This phenomenon is caused by interaction between active functional groups of coumarin derivatives and chitosan. The interaction strength depends on the coumarin derivatives' structure and their substituents. Considering the inevitable trend luminol radical and superoxide anion radical to absorption on the surface of the embedded Au/Ag nanoalloy in the chitosan matrix, it can be concluded that chitosan acts as a platform for all reagents involved in the CL reaction including coumarin derivatives, Au/Ag nanoalloy and luminol, and electron-transfer taking place on it; Placing all chemiluminescent reagents together on the chitosan network can lead to a powerful CL due to increasing rigidity of CL system. The most efficient coumarin derivative on the Au/Ag nanoalloy-fluorophore-luminol-H2O2 CL system, in relation to interaction capability with chitosan' functional groups, was selected and the CL condition in presence of it was optimized. Whereas the glucose oxidase-mediated oxidation of glucose yields gluconic acid and H2O2, under optimum condition the most efficient CL system was applied to detection of glucose due to enzymatically production of hydrogen peroxide. The linear response range of 1.5 × 10(-6)-5.0 × 10(-3) M and the detection limit (defined as the concentration that could be detected at the signal-to-noise ratio of 3) of 7.5 × 10(-7) M was found for the glucose standards. Also, the developed method was successfully applied to determination of glucose in

  1. Preparation Methods and Properties of PdCu Alloy Membrane for Hydrogen Transition

    Institute of Scientific and Technical Information of China (English)

    SUN Xiaoliang; MA Guang; LI Jin; ZHANG Ke

    2012-01-01

    Pd and Pd alloy membranes are of increasing interest for hydrogen separation and purification due to their good thermal stability,high permeability and perfect selectivity.PdCu alloy (60wt% Pd) membranes have similar hydrogen permeability compared with PdAg alloy; meanwhile,it is cheaper than PdAg alloy.Furthermore,it has been reported that PdCu membrane has better resistance to poisoning and deactivation by H2S impurity.This paper reviews the properties and manufacturing methods of PdCu alloy membrane,finally,introduced some achievement made by us on PdCu alloy membrane.

  2. Ag对Pd/CeO2催化剂上氧迁移的促进作用%Enhanced Migration of Oxygen on Ag-Modified Pd/CeO2 Catalyst

    Institute of Scientific and Technical Information of China (English)

    曲振平; 程谟杰; 石川; 黄伟新; 包信和

    2001-01-01

    @@Active migration and spillover of surface species on catalyst surface can be cri tical effects in catalytic processes. As a typical instance, the storage and rel ease of oxygen in the Pt-modified CeO2 catalysts were proposed to play a very important role in catalytic elimination of noxious pollutants[1]. It ha s been demonstrated that the active oxygen species transfer between Pt and CeO 2 under different conditions[2,3]. Numerous investigations on the proper ty of Pd in the catalysts have been carried out recently[4]. Compared wi th Pt, Pd has a strong interaction with CeO2 support. Silver is a unique eleme nt whose oxide can decompose thermally

  3. Contrasting fluids and reservoirs in the contiguous Marcona and Mina Justa iron oxide-Cu (-Ag-Au) deposits, south-central Perú

    Science.gov (United States)

    Chen, Huayong; Kyser, T. Kurtis; Clark, Alan H.

    2011-10-01

    The Marcona-Mina Justa deposit cluster, hosted by Lower Paleozoic metaclastic rocks and Middle Jurassic shallow marine andesites, incorporates the most important known magnetite mineralization in the Andes at Marcona (1.9 Gt at 55.4% Fe and 0.12% Cu) and one of the few major iron oxide-copper-gold (IOCG) deposits with economic Cu grades (346.6 Mt at 0.71% Cu, 3.8 g/t Ag and 0.03 g/t Au) at Mina Justa. The Middle Jurassic Marcona deposit is centred in Ica Department, Perú, and the Lower Cretaceous Mina Justa Cu (Ag, Au) prospect is located 3-4 km to the northeast. New fluid inclusion studies, including laser ablation time-of-flight inductively coupled plasma mass spectrometry (LA-TOF-ICPMS) analysis, integrated with sulphur, oxygen, hydrogen and carbon isotope analyses of minerals with well-defined paragenetic relationships, clarify the nature and origin of the hydrothermal fluid responsible for these contiguous but genetically contrasted deposits. At Marcona, early, sulphide-free stage M-III magnetite-biotite-calcic amphibole assemblages are inferred to have crystallized from a 700-800°C Fe oxide melt with a δ18O value from +5.2‰ to +7.7‰. Stage M-IV magnetite-phlogopite-calcic amphibole-sulphide assemblages were subsequently precipitated from 430-600°C aqueous fluids with dominantly magmatic isotopic compositions (δ34S = +0.8‰ to +5.9‰; δ18O = +9.6‰ to +12.2‰; δD = -73‰ to -43‰; and δ13C = -3.3‰). Stages M-III and M-IV account for over 95% of the magnetite mineralization at Marcona. Subsequent non-economic, lower temperature sulphide-calcite-amphibole assemblages (stage M-V) were deposited from fluids with similar δ34S (+1.8‰ to +5.0‰), δ18O (+10.1‰ to +12.5‰) and δ13C (-3.4‰), but higher δD values (average -8‰). Several groups of lower (200°C) fluids can be recognized in the main polymetallic (Cu, Zn, Pb) sulphide stage M-V and may record the involvement of modified seawater. At Mina Justa, early magnetite

  4. Nuclear fragmentation for Xe+Au and Xe+Ag systems at an energy of 44 A.MeV, formation and decay of hot nuclei

    International Nuclear Information System (INIS)

    A study of the formation and the decay of hot nuclear fragments produced in the reactions Xe+Au and Xe+Ag at an energy of 44 A.MeV is presented in this thesis. The 4π experimental setup consisted of four multidetectors -two for the detection of the fragments (Z>7; DELF and XYZT) and two for the detection of the charged particles (Z<6; MUR and TONNEAU) and allowed an analysis using ''complete events'' (80 % of the total charge and the total parallel linear momentum of the entrance channel) to be carried out. The reaction mechanism is binary with as observed at low energy an almost complete relaxation of the incident energy. The collision results in two hot fragments at the beginning of the exit channel which decay by evaporation and/or fragmentation. In addition of these two body events, we have identified a new dynamic mechanism where we detect a small fragment, called the neck, coming form the overlap of the nuclei during the interaction, in coincidence with a projectile-like fragment and a target-like fragment. For the most dissipative collisions, the deep inelastic collision have allowed an estimation of the lifetime of the hot nuclear fragments to be made. This is possible using proximity effects and fragment-fragment space-time correlations of the decay of one or two primary partners from the deep inelastic collisions. This method is seen to reach its limits in the case of the reactions studied here. (authors). 61 refs

  5. Ab initio investigation of the oxygen reduction reaction activity on noble metal (Pt, Au, Pd), Pt3M (M = Fe, Co, Ni, Cu) and Pd3M (M = Fe, Co, Ni, Cu) alloy surfaces, for Lisbnd O2 cells

    Science.gov (United States)

    Sankarasubramanian, Shrihari; Singh, Nikhilendra; Mizuno, Fuminori; Prakash, Jai

    2016-07-01

    First principles, density functional theory (DFT) modelling of the oxygen reduction reaction (ORR) on noble metal (Pt, Au, Pd), Pt3M (M = Fe, Co, Ni, Cu) and Pd3M (M = Fe, Co, Ni, Cu) alloy surfaces, was carried out. Periodic models of close-packed (111) surfaces were constructed, their geometry was optimized and the most stable geometric surface configuration was identified. The correlation between the intermediate species binding energy and the favored reaction pathway from amongst 1e-, 2e-, and 4e- mechanisms were studied by calculating the binding energies of a 1/4 monolayer of O, O2, LiO, LiO2, Li2O2, and Li2O on various sites and orientations. The reaction free energies (ΔGrxn) were calculated and used to compute the catalytic activity of the surfaces using molecular kinetics theory. Plots of the catalytic activity vs. Oxygen binding energy (EBinding (O)) showed a typical "volcano" profile. The insights gained from this study can be used to guide the choice of cathode catalysts in Lisbnd O2 cells.

  6. Ion-stimulated gas desorption yields of coated (Au, Ag, Pd) stainless steel vacuum chambers irradiated with 4.2 MeV/u lead ions

    CERN Document Server

    Mahner, E; Küchler, D; Malabaila, M; Taborelli, M

    2005-01-01

    The ion-induced desorption experiment, installed in the CERN Heavy Ion Accelerator (LINAC 3), has been used to measure molecular desorption yields for 4.2 MeV/u lead ions impacting on different accelerator-type vacuum chambers. In order to study the effect of the surface oxide layer on the gas desorption, gold-, silver-, and palladium-coated 316LN stainless steel chambers and similarly prepared samples were tested for desorption at LINAC 3 and analysed for chemical composition by X-ray Photoemission Spectroscopy (XPS). The large effective desorption yield of 2 x 10**4 molecules/ion, previously measured for uncoated, vacuum fired stainless steel, was reduced after noble metal coating by up to 2 orders of magnitude. In addition, the effectiveness of beam scrubbing with heavy ions and the consequence of a subsequent venting on the desorption yields of a beam-scrubbed vacuum chamber are described. Practical consequences for the vacuum system of the future Low Energy Ion Ring (LEIR) are discussed.

  7. Photoelectron imaging and theoretical study on the structure and chemical binding of the mixed-ligand M(I) complexes, [HMSH]{sup −} (M = Cu, Ag, and Au)

    Energy Technology Data Exchange (ETDEWEB)

    Qin, Zhengbo; Liu, Zhiling; Cong, Ran; Xie, Hua; Tang, Zichao, E-mail: zctang@dicp.ac.cn, E-mail: fanhj@dicp.ac.cn; Fan, Hongjun, E-mail: zctang@dicp.ac.cn, E-mail: fanhj@dicp.ac.cn [State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023 (China)

    2014-03-21

    We have reported a combined photoelectron imaging and theoretical study on gaseous mixed-ligand M(I) complexes of [HMSH]{sup −} (M = Cu, Ag, and Au). With the aid of Franck-Condon simulations, vibrationally resolved photoelectron spectra yield accurate electron affinities of 3.269(6), 3.669(10), and 3.591(6) eV for [HCuSH], [HAgSH], and [HAuSH], respectively. And low-frequency modes are observed: 368(12) cm{sup −1} for [HCuSH], 286(12) cm{sup −1} for [HAgSH], and 327(12) cm{sup −1} for [HAuSH], respectively. Extensive theoretical calculations are performed to aid in the spectral assignments and the calculated values agree well with the experimental observations. Although the S and H atoms have little discrepancy in electronegativity (2.20 for H and 2.54 for S), distinct bonding properties are demonstrated between H–M and M–S bond. It is revealed that there exists significant ionic bonding between M–S in [HMSH]{sup −} (M = Cu, Ag, and Au), while a gradual transition from ionic behavior between H–Cu in [HCuSH]{sup −} to quite strong covalent bonding between H–Au in [HAuSH]{sup −}, supported by a variety of chemical bonding analyses.

  8. 4{pi} studies of the 1.8{endash}4.8 GeV {sup 3}He+{sup nat}Ag, {sup 197}Au reactions. I. Energy deposition

    Energy Technology Data Exchange (ETDEWEB)

    Morley, K.B.; Kwiatkowski, K.; Bracken, D.S.; Renshaw Foxford, E.; Viola, V.E.; Woo, L.W.; Yoder, N.R. [Departments of Chemistry and Physics and Indiana University Cyclotron Facility, Indiana University, Bloomington, Indiana 47405 (United States); Legrain, R.; Pollacco, E.C.; Volant, C. [Commissariat a l`Energie Atomique, DAPNIA Service de Physique Nucleaire, C.E. Saclay, 91191 Gir-sur-Yvette Cedex (France); Korteling, R.G. [Department of Chemistry, Simon Fraser University, Burnaby, British Columbia (Canada); Breuer, H. [University of Maryland, College Park, Maryland 20742 (United States); Brzychczyk, J. [Institute of Physics, Jagiellonian University, 30-059 Krakow (Poland)

    1996-08-01

    The Indiana Silicon Sphere 4{pi} detector has been used to measure light-charged particles and intermediate-mass fragments (IMFs) emitted in the 18{endash}4.8 GeV {sup 3}He+{sup nat}Ag, {sup 197}Au reactions. Ejectile multiplicity and total event kinetic energy distributions scale systematically with projectile energy and target mass, except for the {sup nat}Ag target at 3.6 and 4.8 GeV. For this system, a saturation in deposition energy is indicated by the data, suggesting the upper projectile energy for stopping has been reached. Maximum deposition energies of {approximately}950 MeV for the {sup nat}Ag target and {approximately}1600 MeV for the {sup 197}Au target are inferred from the data. The results also demonstrate the importance of accounting for fast cascade processes in defining the excitation energy of the targetlike residue. Correlations between various observables and the average IMF multiplicity indicate that the total thermal energy and total observed charge provide useful gauges of the excitation energy of the fragmenting system. Comparison of the experimental distributions with intranuclear cascade predictions shows qualitative agreement. {copyright} {ital 1996 The American Physical Society.}

  9. 基于表面等离子体共振效应的Ag(Au)/半导体纳米复合光催化剂的研究进展%Research progress of Ag(Au)/semiconductor nanohybrid photocatalysts based on surface plasmon resonance

    Institute of Scientific and Technical Information of China (English)

    邵先坤; 郝勇敢; 刘同宣; 胡路阳; 王媛媛; 李本侠

    2016-01-01

    由具有表面等离子体共振(surface plasmon resonance,SPR)效应的贵金属(Ag、Au等)纳米粒子和半导体纳米结构组成的纳米复合光催化剂具有优异的可见光光催化活性,成为新型光催化材料的研究热点之一。本文综述了Ag(Au)/半导体纳米复合光催化剂的制备方法、基本性质以及光催化应用方面的一些重要研究进展;重点介绍了Ag(Au)等纳米粒子的表面等离子共振增强可见光催化活性的机理,以及Ag(Au)纳米粒子与不同类型半导体复合的光催化剂的光催化性能,其中所涉及的半导体包括金属氧化物、硫化物和其他一些半导体;本领域未来几年的研究热点将集中于新型高效的 Ag(Au)/半导体纳米复合光催化剂的微结构调控及其用于可见光驱动有机反应的机理研究。本文为基于SPR效应构建Ag(Au)/半导体纳米复合光催化剂的研究提供了有力的参考依据,并且指出Ag(Au)/半导体纳米复合光催化剂的研究是发展可见光高效光催化剂的重要方向。%Nanohybrid photocatalysts composed of noble metal nanoparticles (Ag,Au,etc.) with surface plasmon resonance (SPR) effect and semiconductor nanostructures have become one of the research hotspots in the field of advanced photocatalysis because of their excellent photocatalytic activity under visible light irradiation. This review summarized some significant research progress about the basic properties,preparation methods and the photocatalytic applications of the plasmonic Ag(Au)/semiconductor nanohybrid photocatalysts. We emphatically introduced the mechanism for the enhanced effect of Ag(Au) nanoparticles with SPR on visible light response photocatalytic activity,as well as the photocatalytic performance of the nanohybrid photocatalysts composed of Ag(Au) nanoparticles and different types of semiconductors,including metal oxides,metal chalcogenides and other semiconductors. The research in this

  10. Band structure of superconducting MgB sub 2 and isostructural CaGa sub 2 , AgB sub 2 , AuB sub 2 , ZrBe sub 2 and HfBe sub 2

    CERN Document Server

    Shein, I R; Ivanovskij, A L

    2001-01-01

    The analysis of the zonal structure of the MgB sub 2 mean-temperature superconductor is carried out. The MgB sub 2 quasi-two-dimensional structure is one of its important features. The comparison of the MgB sub 2 zonal structure and the ZrBe sub 2 , HfBe sub 2 and CaGa sub 2 isostructural hexagonal phases is carried out. The zonal structure calculations are accomplished through the Muffin-Tin self-coordinated full-potential linear method. The factors, responsible for the MgB sub 2 superconducting properties, are analyzed. The Ag and Au hypothetical diborides are considered

  11. Study of polymeric nanocomposites prepared by inserting graphene and / or Ag, Au and ZnO nanoparticles in a TEGDA polymer matrix, by means of the use of dielectric spectroscopy

    Directory of Open Access Journals (Sweden)

    Valeria Alzari

    2016-03-01

    Full Text Available Polymeric nanocomposites were prepared by inserting graphene and/or Ag, Au and ZnO nanoparticles in a TEGDA (tetraethyleneglycol diacrylate polymer matrix. The polymeric films were characterized in terms of their dielectric properties by electrochemical impedance spectroscopy. The impedance data were fitted by generalized relaxation functions in order to determine conductivity, dielectric response and molecular relaxation time of the nanocomposite films. In particular, a stretched exponential function, Kohlrausch-Williams-Watts function (KWW, was used to investigate polymer/graphene/metal nanocomposites.

  12. Geology of the epithermal Ag-Au Huevos Verdes vein system and San José district, Deseado massif, Patagonia, Argentina

    Science.gov (United States)

    Dietrich, Andreas; Gutierrez, Ronald; Nelson, Eric P.; Layer, Paul W.

    2012-03-01

    The San José district is located in the northwest part of the Deseado massif and hosts a number of epithermal Ag-Au quartz veins of intermediate sulfidation style, including the Huevos Verdes vein system. Veins are hosted by andesitic rocks of the Bajo Pobre Formation and locally by rhyodacitic pyroclastic rocks of the Chon Aike Formation. New 40Ar/39Ar constraints on the age of host rocks and mineralization define Late Jurassic ages of 151.3 ± 0.7 Ma to 144.7 ± 0.1 Ma for volcanic rocks of the Bajo Pobre Formation and of 147.6 ± 1.1 Ma for the Chon Aike Formation. Illite ages of the Huevos Verdes vein system of 140.8 ± 0.2 and 140.5 ± 0.3 Ma are 4 m.y. younger than the volcanic host rock unit. These age dates are among the youngest reported for Jurassic volcanism in the Deseado massif and correlate well with the regional context of magmatic and hydrothermal activity. The Huevos Verdes vein system has a strike length of 2,000 m, with several ore shoots along strike. The vein consists of a pre-ore stage and three main ore stages. Early barren quartz and chalcedony are followed by a mottled quartz stage of coarse saccharoidal quartz with irregular streaks and discontinuous bands of sulfide-rich material. The banded quartz-sulfide stage consists of sulfide-rich bands alternating with bands of quartz and bands of chlorite ± illite. Late-stage sulfide-rich veinlets are associated with kaolinite gangue. Ore minerals are argentite and electrum, together with pyrite, sphalerite, galena, chalcopyrite, minor bornite, covellite, and ruby silver. Wall rock alteration is characterized by narrow (220°C. Kaolinite occurring with the late sulfide-rich veinlet stage indicates pH 315°, whereas strike directions of <315° are predicted with an induced dextral strike-slip movement. The components of the structural model appear to be present on a regional scale and are not restricted to the San José district.

  13. Organic Gases in Fluid Inclusions of Ore Minerals and Their Constraints on Ore Genesis: A Case Study of the Changkeng Au-Ag Deposit, Guangdong, China

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The newly discovered Changkeng Au-Ag deposit is a new type of sediment-hosted precious metal deposit. Most of the previous researchers believed that the deposit was formed by meteoric water convection. By using a high vacuum quadrupole gas mass spectrometric system, nine light hydrocarbons ha