10,868 research outputs found
Polarization dependence of the light coupling to surface plasmons in an Ag nanoparticle & Ag nanowire system
No full textPolarization dependence of the coupling of excitation light to surface plasmon polaritons (SPPs) was investigated in a Ag nanoparticle-nanowire waveguide system (a Ag nanoparticle attached to a Ag nanowire). It was found that under the illumination of excitation light on the nanoparticle-nanowire junction, the coupling efficiency of light to SPPs depends on the polarization of the excitation light. Theoretical simulations revealed that it is the local near-field coupling between the nanoparticle and the nanowire that enhances the incident light to excite the nanowire SPPs. Because the shapes of the Ag nanoparticles differ, the local field intensity, and thus the excitement of the nanowire SPPs, vary with the polarization of the excitation light.Physics, MultidisciplinarySCI(E)EI中国科技核心期刊(ISTIC)中国科学引文数据库(CSCD)[email protected]
Effects of shell thickness on the thermal stability of Cu-Ag core-shell nanoparticles: A molecular dynamics study
No full textCu-Ag core-shell (CS) nanoparticle (NP) is considered as a cost-effective alternative material to nano silver sintering material in die attachment application. To further reduce the cost, the thickness of the Ag shell can be adjusted. Whereas the shell thickness will also affect the thermal stability of the Cu-Ag CSNPs. In this study, molecular dynamics simulation was applied to study the thickness effect on the thermal behavior of Cu-Ag CSNPs. The melting points of CSNPs and Pure NPs can be determined by the evolutions of Potential Energy (PE), and the Lindemann index (LI) of the system. The results indicated that the melting points of CS NPs were lower than monometallic NP and the melting point of CS NP is influenced by the size of the Cu core and the number of lattice mismatches. Moreover, the distribution of atoms’ LI showed that the premelting point is independent of shell thickness. However, the fraction of atoms that occurred premelting is increased with the decrease of the shell thickness. Otherwise, we also simulated the sintering process of double CS NPs with equal size.Green Open Access added to TU Delft Institutional Repository 'You share, we take care!' - Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.Electronic Components, Technology and Material
Voltammetric Detection of Urea on an Ag-Modified Zeolite- Expanded Graphite-Epoxy Composite Electrode
No full textIn this paper, a modified expanded graphite composite electrode based on natural zeolitic volcanic tuff modified with silver (EG-Ag-Z-Epoxy) was developed. Cyclic voltammetry measurements revealed a reasonably fast electron transfer and a good stability of the electrode in 0.1 M NaOH supporting electrolyte. This modified electrode exhibited moderate electrocatalytic effect towards urea oxidation, allowing its determination in aqueous solution. The linear dependence of the current versus urea concentration was reached using square-wave voltammetry in the concentrations range of urea between 0.2 to 1.4 mM, with a relatively low limit of detection of 0.05 mM. A moderate enhancement of electroanalytical sensitivity for the determination of urea at EG-Ag-Z-Epoxy electrode was reached by applying a chemical preconcentration step prior to voltammetric/amperometric quantification.ChemE/Chemical EngineeringApplied Science
Ore mineralogy and trace element (re)distribution at the metamorphosed Lappberget Zn-Pb-Ag-(Cu-Au) deposit, Garpenberg, Sweden
No full textQualitative and quantitative mineralogical and textural investigations were undertaken for the different sulfide minerals in the 1.89 Ga Lappberget deposit, with a focus on sphalerite and pyrite. Three sphalerite types were identified and associated with: (1) main massive sulfide mineralization, (2) Fe-Mn skarn ore, and (3) Ag-rich fissure veins. Sphalerite-1 contained a relatively higher amount of trace elements (Fe, Co, Ge, Cu, Sn, and Au) but is lower in Mn/Fe, Ga, and Hg compared to sphalerite-2. Evidence of tectono-metamorphic modification of sulfides is observed throughout the deposit, such as the formation of growth twins and deformation twins in sulfides, the development of high-angled triple-point junctions in recrystallized pyrite and sphalerite, and the formation of â??ball oreâ?? or â??durchbewegungâ?? textures within mineralized shear zones. The recrystallization of pyrite and galena may have led to the re-distribution of fluid-mobile elements (As, Cu, Zn, Pb, Ag, and Au), some of which were deposited in discordant Ag-rich fissure veins peripheral to the main massive sulfide lenses. Trace element signatures of sulfides in Lappberget are compatible with the other metamorphosed and deformed, subseafloor volcanogenic carbonate replacement (SVALS)-type deposits in the Bergslagen mining district. © 2021 The Author(s)</p
Ore mineralogy and trace element (re)distribution at the metamorphosed Lappberget Zn-Pb-Ag-(Cu-Au) deposit, Garpenberg, Sweden
No full textQualitative and quantitative mineralogical and textural investigations were undertaken for the different sulfide minerals in the 1.89 Ga Lappberget deposit, with a focus on sphalerite and pyrite. Three sphalerite types were identified and associated with: (1) main massive sulfide mineralization, (2) Fe-Mn skarn ore, and (3) Ag-rich fissure veins. Sphalerite-1 contained a relatively higher amount of trace elements (Fe, Co, Ge, Cu, Sn, and Au) but is lower in Mn/Fe, Ga, and Hg compared to sphalerite-2. Evidence of tectono-metamorphic modification of sulfides is observed throughout the deposit, such as the formation of growth twins and deformation twins in sulfides, the development of high-angled triple-point junctions in recrystallized pyrite and sphalerite, and the formation of â??ball oreâ?? or â??durchbewegungâ?? textures within mineralized shear zones. The recrystallization of pyrite and galena may have led to the re-distribution of fluid-mobile elements (As, Cu, Zn, Pb, Ag, and Au), some of which were deposited in discordant Ag-rich fissure veins peripheral to the main massive sulfide lenses. Trace element signatures of sulfides in Lappberget are compatible with the other metamorphosed and deformed, subseafloor volcanogenic carbonate replacement (SVALS)-type deposits in the Bergslagen mining district. © 2021 The Author(s)</p
A comparative study in CCl4 reaction on Ag/Si(111) surfaces: PEEM and PES investigations
No full textA comparative study in CCl4 reaction on Ag/Si(111) surfaces: PEEM and PES investigations
Yunxi Yao, Qiang Fu, Xinhe Bao
State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, P.R. China
We report a comparative study in the reactivity of bulk Ag(111), monolayer Ag film on Si(111), and Si(111)-77 surfaces via X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectroscopy (UPS), photoemission electron microscopy (PEEM), and scanning tunneling microscopy (STM). The monolayer Ag film grown on Si(111), which is known as √3×√3-Ag-Si surface structure, was obtained by depositing one monolayer Ag on the Si(111)-77 surface at 550 K. The most simple halogen methane, CCl4, was chosen as the probe molecule to study the surface reactivity of the bulk Ag(111) surface, the monolayer Ag film, and the Si(111) surface. XPS and UPS data indicate that the monolayer Ag film presents unique reactivity to CCl4 in comparison to the other two surfaces. For the PEEM study, a dedicated sample consisting of bulk Ag particles supported on the monolayer Ag film was prepared as shown in the schematics in Fig. 1. In situ PEEM imaging of the surface reaction in presence of CCl4 shows a gradual change in the grey intensity from bright to totally dark on the Ag particles but little change on the √3×√3-Ag-Si surface. The grey intensity decrease is due to local work function increase from the dissociated Cl atoms. The experiments suggest that monolayer Ag is inert toward dissociation of CCl4 compared to the Ag(111) and Si(111) surface. It has proposed that the confinement of 5sp electron of Ag atoms in the √3×√3-Ag-Si surface, which is delocalized in the bulk Ag(111) surface, is decisive to the different reactivity.
Figure 1: (a) Schematic representation of the √3×√3-Ag-Si surface supported Ag islands; (b) PEEM image of the Ag islands/√3×√3-Ag-Si sample before CCl4 exposure. Field of view (FoV) is 27 μm; (c) PEEM image shows the same area in (b) but after 24 L (5.2×10-9 mbar × 6000 s) CCl4 exposure; (d) the work function change (ΔΦ) of the Ag(111) and √3×√3-Ag-Si surfaces when exposed to different amount of CCl4 at RT, measured from PES results.
References:
[1] Y.X. Yao, X. Liu, Q. Fu, W.X. Li, D.L. Tan, X.H. Bao, ChemPhysChem 2008, 9: 975-979.
*Corresponding author: Fax: +86-411-84694447, E-mail: [email protected], [email protected]
Nanospherical-lens lithographical Ag nanodisk arrays embedded in p-GaN for localized surface plasmon-enhanced blue light emitting diodes
No full textLarge-scale Ag nanodisks (NDs) arrays fabricated using nanospherical-lens lithography (NLL) are embedded in p-GaN layer of an InGaN/GaN light-emitting diode (LED) for generating localized surface plasmon (LSP) coupling with the radiating dipoles in the quantum-well (QWs). Based on the Ag NDs with the controlled surface coverage, LSP leads to the improved crystalline quality of regrowth p-GaN, increased photoluminescence (PL) intensity, reduced PL decay time, and enhanced output power of LED. Compared with the LED without Ag NDs, the optical output power at a current of 350 mA of the LSP-enhanced LEDs with Ag NDs having a distance of 20 and 35 nm to QWs is increased by 26.7% and 31.1%, respectively. The electrical characteristics and optical properties of LEDs with embedded Ag NPs are dependent on the distance of between Ag NPs and QWs region. The LED with Ag NDs array structure is also found to exhibit reduced emission divergence, compared to that without Ag NDs. (C) 2014 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 Unported License
Microstructure Analysis Based on 3D reconstruction Model and Transient Thermal Impedance Measurement of Resin-reinforced Sintered Ag layer for High power RF device
No full textResin-reinforced silver (Ag) sintering material is an effective and highly reliable solution for power electronics packaging. The hybrid material’s process parameters strongly influence its microstructure and pose a significant challenge in estimating its effective properties as a thin interconnect layer. This research demonstrates a novel 3D reconstruction methodology for the microstructural investigation of the resin-reinforced Ag sintering material from OverMolded Plastic (OMP) packages. Based on the reconstructed models with different sintering parameters (temperature and time), the fraction of Ag and Resin volume distribution, the connectivity of silver particles, and the tortuosity factors were estimated. A 99% connectivity of sintered Ag particles was achieved with various sintering conditions, such as 200°C for 2 hours, 200°C for 4 hours, and 250°C for 2 hours. However, coarsening of Ag particles was promoted when sintered at 250°C. Increasing the sintering time at 200°C had insignificant changes. The estimated tortuosity factor also indicated that sintering at 250°C provides the shortest heat transport path between the semiconductor die and the package substrate. In order to quantify the microstructural findings, the OMP packages’ thermal performance with different sintering conditions (temperature, time, and interconnect thickness) was experimentally assessed. Although the experimental measurements were less sensitive to the effective interface thermal resistances’, the measurement results show a good correlation with the microstructural analysis. Sintering the Resin-reinforced Ag sintering material at higher temperatures (250°C) seems to improve the package thermal performance, and increasing the sintering time at 200°C has a negligible effect.Green Open Access added to TU Delft Institutional Repository 'You share, we take care!' - Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.Electronic Components, Technology and Material
Ag/Bi12O17Cl2 composite: A case study of visible-light-driven plasmonic photocatalyst
No full textIn this investigation, novel Ag/Bi12O17C12 plasmonic composites with different Ag contents were constructed through a solvothermal and subsequent photoreduction route and fully characterized by a collection of analytical techniques. Spectroscopic results confirmed the presence and uniform dispersion of Ag nanoparticles on the 2D nanosheets of Bi12O17C12. The Ag content in composites exerted considerable influence on the extension of light-adsorption range and the enlargement of specific surface areas. The photocatalytic abilities of these Ag/Bi12O17C12 composites were evaluated toward the degradation of rhodamine B (RhB) and 2,4-dichlorophenol (2,4-DCP) under the visible-light irradiation. The results demonstrated that the Ag/Bi12O17C12 composites showed much higher photocatalytic efficiencies than that of pure Bi12O17C12, especially the sample with an optimal Ag content showing the best photocatalytic behavior among all tested samples. The remarkable enhancement of Ag/Bi12O17C12 photocatalytic efficiency could be mainly attributed to the efficient charge separation that was induced by the localized surface plasmon resonance effect of metallic Ag, strong visible-light adsorption and the favorable morphology with enlarged specific surface areas. Eventually, the photocatalysis mechanism over Ag/Bi12O17C12 composites was preliminarily proposed on the base of reactive species trapping experiments. (C) 2016 Elsevier B.V. All rights reserved
Maximizing Ag Utilization in High-Rate CO<sub>2</sub> Electrochemical Reduction with a Coordination Polymer-Mediated Gas Diffusion Electrode
No full textWe report the preparation and electrocatalytic performance of silver-containing gas diffusion electrodes (GDEs) derived from a silver coordination polymer (Ag-CP). Layer-by-layer growth of the Ag-CP onto porous supports was applied to control Ag loading. Subsequent electro-decomposition of the Ag-CP resulted in highly selective and efficient CO2-to-CO GDEs in aqueous CO2 electroreduction. Afterward, the metal-organic framework (MOF)-mediated approach was transferred to a gas-fed flow electrolyzer for high current density tests. The in situ formed GDE, with a low silver loading of 0.2 mg cm-2, showed a peak performance of jCO ≈ 385 mA cm-2 at around -1.0 V vs RHE and stable operation with high FECO (>96%) at jTotal = 300 mA cm-2 over a 4 h run. These results demonstrate that the MOF-mediated approach offers a facile route for manufacturing uniformly dispersed Ag catalysts for CO2 electrochemical reduction by eliminating ill-defined deposition steps (drop-casting, etc.) while allowing control of the catalyst structure through self-assembly.Accepted Author ManuscriptChemE/Catalysis EngineeringChemE/Materials for Energy Conversion and Storag
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