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Metal Substrate (metal + substrate)
Selected AbstractsMicrostructural and Mechanical Investigations on Porcelain-Fused-to-Metal in Multilayer SystemADVANCED ENGINEERING MATERIALS, Issue 4 2010Adele Carradò Results on porcelain-fused-to-metal (PFM) technique of ceramic films for biomedical applications on metal substrate are reported. The coating of metallic implants with bio-ceramic films (glassy and opaque ceramic) was proposed to be a solution for combining the mechanical properties of the metallic material with the bioactive character of the ceramic layer, leading to a better integration of the entire implant. The aim of this paper is to determine a stress field distribution by a non-destructive method as high-energy synchrotron X-ray diffraction in energy dispersive in the metal and glass ceramic bulk as well as at metal,opaque ceramic interface in PFM three layers sample. Tensile stresses were found in palladium substrate and compressive state in glass ceramic coating. Moreover thermal stresses induced by PFM coating at the interfaces were calculated by analytical mathematical model, confirming that the stresses induced, due to the selection of the materials, are low. Finally, the micro-structural and chemical characteristics of glassy and opaque bio-ceramic coatings on palladium alloy substrate were investigated and no inter-diffusion area between metal and ceramic could be detected as well as non-homogeneity in the interface ceramic. [source] WDX Studies on Ceramic Diffusion Barrier Layers of Metal Supported SOECsFUEL CELLS, Issue 6 2009D. Wiedenmann Abstract Solid oxide electrolyser cells (SOECs) have great potential for efficient and economical production of hydrogen fuel. Element diffusion between the Ni-cermet electrode and the metal substrate of metal supported cells (MSC) is a known problem in fuel cell and electrolysis technology. In order to hinder this unintentional mass transport, different ceramic diffusion barrier layers (DBLs) are included in recent cell design concepts. This paper is based on wavelength dispersive X-ray fluorescence investigations of different SOEC and focuses on Fe, Cr and Ni diffusion between the metal grains of the cathode and the metal substrate. Due to the low detection limits and therefore high analytical sensitivity, wavelength dispersive electron probe microanalysis (EPMA) provides a precise method to determine element distribution, absolute element concentration and changes between the reference material and aged cells on a microstructural level by element mappings and concentration profiles. The results of this work show considerable concentration gradients in the metal grains caused by mass exchange during cell operation. Diffusion can be inhibited significantly by integrating different ceramic DBLs of doped LaCrO3 -type or doped LaMnO3 -type perovskite, either by vacuum plasma spraying (VPS) or physical vapour deposition technique (PVD). [source] Synthesis and Lasing Properties of Highly Ordered CdS Nanowire Arrays,ADVANCED FUNCTIONAL MATERIALS, Issue 9 2007L. Cao Abstract Highly ordered large-area arrays of wurtzite CdS nanowires are synthesized on Cd-foil substrates via a simple liquid reaction route using thiosemicarbazide and Cd foil as the starting materials. The CdS nanowires are single crystals growing along the [001],direction and are perpendicular to the surface of the substrate. The characteristic Raman peaks of CdS are red-shifted and show asymmetric broadening, which is ascribed to phonon confinement effects arising from the nanoscale dimensions of the nanowires. Significantly, the uniform CdS nanowire arrays can act as laser cavities in the visible-light range, leading to bandgap lasing at ca.,515,nm with obvious modes. The high density of nuclei and the preferential growth direction induce the formation of aligned CdS nanowires on the metal substrate. [source] Femtosecond dynamics of electron transfer, localization, and solvation processes at the ice,metal interfaceISRAEL JOURNAL OF CHEMISTRY, Issue 1-2 2005Uwe Bovensiepen The ultrafast dynamics of excess electrons in amorphous ice layers on single-crystal metal surfaces are investigated by femtosecond time- and angle-resolved two-photon-photoemission spectroscopy. Photoexcited electrons are injected from the metal substrate into delocalized states of the conduction band of ice and localize in the ice layer within 100 fs. Subsequently, energetic stabilization of this localized species is observed on a time scale of ,1 ps, which is attributed to electron solvation by nonadiabatic coupling to nuclear degrees of freedom of the surrounding polar molecular environment. Concomitant with this stabilization process, residual wave function overlap of the solvated electron with the metal substrate results in back-transfer by tunneling through the solvation shell. At such interfaces the correlation of electronic and molecular structure with the resulting solvation dynamics can be explored using different substrates as a template. Here we compare data on molecularly thin D2O ice layers grown on Cu(111) and Ru(001). On Ru(001) both the stabilization and back-transfer proceed about three times faster compared to Cu(111), which is attributed to different interfacial structures and the role of d-states, and projected band gaps in the electron transfer process. [source] Direct analysis of lipids in mouse brain using electrospray droplet impact/SIMSJOURNAL OF MASS SPECTROMETRY (INCORP BIOLOGICAL MASS SPECTROMETRY), Issue 4 2010Daiki Asakawa Abstract Electrospray droplet impact (EDI)/secondary ion mass spectrometry (SIMS) is a new desorption/ionization technique for mass spectrometry in which highly charged water clusters produced from the atmospheric-pressure electrospray are accelerated in vacuum by 10 kV and impact the sample deposited on the metal substrate. EDI/SIMS was shown to enhance intact molecular ion formation dramatically compared to conventional SIMS. EDI/SIMS has been successfully applied to the analysis of mouse brain without any sample preparation. Five types of lipids, i.e. phosphatidylcholine (PC), phosphatidylserine, phosphatidylinositol (PI), galactocerebroside (GC) and sulfatide (ST), were readily detected from mouse brain section. In addition, by EDI/SIMS, six different regions of the mouse brain (cerebral cortex, corpus callosum, striatum, medulla oblongata, cerebellar cortex and cerebellar medulla) were examined. While GCs and STs were found to be rich in white matter, PIs were rich in gray matter. Copyright © 2010 John Wiley & Sons, Ltd. [source] Raman scattering study of molecules adsorbed on ZnS nanocrystalsJOURNAL OF RAMAN SPECTROSCOPY, Issue 1 2007Yanfei Wang Abstract The adsorption of 4-mercaptopyridine (4-Mpy) molecules on ZnS nanocrystals was investigated by means of Raman spectroscopy. We compared the Raman signals of 4-Mpy molecules adsorbed on ZnS nanocrystals and Ag substrate. The differences in the adsorption of 4-Mpy molecules on the semiconductor and the metal substrate were noted. The results demonstrated that adsorbed species on the semiconductor ZnS nanocrystals can be detected by Raman spectroscopy. Copyright © 2006 John Wiley & Sons, Ltd. [source] Electrodeposition study of ODN:SWCNT hybrids on gold substratesPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 6 2008Roya R. Lahiji Abstract Sonication of short single-stranded DNA (oligodeoxyribonucleotide; ODN) with Single-Walled Carbon Nanotubes (SWCNTs) greatly facilitates the dispersion of SWCNTs from entangled ropes in an aqueous solution, creating ODN:SWCNT hybrids. Electrodeposition has been investigated to determine if well-dispersed ODN:SWCNT hybrids on a metal substrate can be created. Preliminary studies indicate that electrodeposition using an Au substrate held at +0.5 V produces ODN:SWCNT hybrids that are uniformly deposited across the Au substrate. This result can be compared to samples produced by drop casting and evaporation techniques which yield a thick tangled mat of ODN:SWCNT hybrids across the substrate. The resulting electrodeposited samples were characterized using Scanning Probe Microscope (SPM) and X-ray Photoemission Spectroscopy (XPS) techniques. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Formation of endothermic carbides on iron and nickelPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 5 2004A. Wiltner Abstract The formation of endothermic carbides on Fe and Ni is studied using X-ray photoelectron spectroscopy (XPS) by deposition of carbon films from the vapor phase and subsequent annealing steps. The reaction between carbon and metal substrates is measured by shifts in the C 1s photoelectron peaks. By comparison with two elementary carbon photoelectron energies determined from carbon films on unreactive Au substrates, a carbide peak in the C 1s spectra on reactive Fe and Ni substrates is identified. The carbides formed after deposition of carbon films at room temperature are located at the interface between carbon film and metal substrate. We report on the behavior of elementary carbon films with respect to film thickness and thermal treatment leading to carbide formation and carbon diffusion into the bulk. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Adjustment and control of SERS activity of metal substrates by pressureJOURNAL OF RAMAN SPECTROSCOPY, Issue 4 2010Lixin Xia Abstract Metal pellets of silver and copper for surface-enhanced Raman scattering (SERS) spectroscopy were prepared by compression with different pressures. It was found that the SERS activity of the pellet could be controlled by pressure. Enhanced Raman scattering properties of the metal pellets in the presence of adsorbed 4-mercaptobenzoic acid (4-MBA) with excitation at 632.8 or 514 nm could be obtained by choosing proper pressure of pellatization. The SERS peak intensity of the band at ,1584 cm,1 of 4-MBA adsorbed on the metal pellets varies as a function of applied pressure, and which is about 1.2,32 times greater than when it is adsorbed on silver and copper particles. The calculated results of three-dimensional finite-difference time-domain method (3D-FDTD) are in good agreement with the experimental data. Moreover, no spurious peaks appear in the SERS spectra of the samples because no other chemicals are involved in the simple preparation process of the metal pellets, which will facilitate its use as an SERS-active substrate for analytical purposes. In summary, SERS-active metal pellets can be produced simply and cost effectively by the method reported here, and this method is expected to be utilized in the development of SERS-based analytical devices. Copyright © 2009 John Wiley & Sons, Ltd. [source] Structures of monolayers formed from different HS,(CH2)2,X thiols on gold, silver and copper: comparitive studies by surface-enhanced Raman scatteringJOURNAL OF RAMAN SPECTROSCOPY, Issue 11 2003Andrzej Kudelski Abstract Molecules of 2-aminoethanethiol (cysteamine, CYS), 2-mercaptoethanol (MET), 3-mercaptopropionic acid (MPA), sodium 2-mercaptoethanesulphonate (MES) and 1-propanethiol (PTH) were spontaneously chemisorbed on electrochemically activated silver, copper and gold surfaces. The structure of monolayers formed was studied with surface-enhanced Raman scattering (SERS). In CYS and MPA monolayers the relative surface concentration of gauche conformers was higher than in MET, PTH and MES monolayers. This is probably due to double bonding to the metal surface by a fraction of adsorbed MPA and CYS molecules (via the sulphur moiety and the terminal carboxylic or amino group). In CYS, MET, MPA and PTH monolayers the surface concentration of trans conformers is significantly higher on Ag than on Au or Cu. The structures of MES monolayers on Ag, Au and Cu are similar, with very high surface concentrations of trans conformers. Statistically, the wavenumbers of ,(C,S) bands of both gauche and trans conformers are the highest on Au, slightly lower on Ag and the lowest for Cu. However the positions of ,(C,S) bands are also sensitive to the other parameters (e.g. C,C,S,metal torsion angle, the overall ordering of the monolayer). Therefore, the wavenumbers of ,(C,S) bands are not good indicators of differences in the interaction between chemisorbed thiols and the metal substrates. Desorption measurements suggest that part of the adsorbed molecules is bonded significantly weaker than the rest. Thiolate monolayers on Cu decomposed relatively easily, forming a layer of copper sulphide. The strength of adsorbed MPA acid is similar on all substrates. Copyright © 2003 John Wiley & Sons, Ltd. [source] Formation of endothermic carbides on iron and nickelPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 5 2004A. Wiltner Abstract The formation of endothermic carbides on Fe and Ni is studied using X-ray photoelectron spectroscopy (XPS) by deposition of carbon films from the vapor phase and subsequent annealing steps. The reaction between carbon and metal substrates is measured by shifts in the C 1s photoelectron peaks. By comparison with two elementary carbon photoelectron energies determined from carbon films on unreactive Au substrates, a carbide peak in the C 1s spectra on reactive Fe and Ni substrates is identified. The carbides formed after deposition of carbon films at room temperature are located at the interface between carbon film and metal substrate. We report on the behavior of elementary carbon films with respect to film thickness and thermal treatment leading to carbide formation and carbon diffusion into the bulk. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Apo and ligand-bound structures of ModA from the archaeon Methanosarcina acetivoransACTA CRYSTALLOGRAPHICA SECTION F (ELECTRONIC), Issue 3 2010Sum Chan The trace-element oxyanion molybdate, which is required for the growth of many bacterial and archaeal species, is transported into the cell by an ATP-binding cassette (ABC) transporter superfamily uptake system called ModABC. ModABC consists of the ModA periplasmic solute-binding protein, the integral membrane-transport protein ModB and the ATP-binding and hydrolysis cassette protein ModC. In this study, X-ray crystal structures of ModA from the archaeon Methanosarcina acetivorans (MaModA) have been determined in the apoprotein conformation at 1.95 and 1.69,Å resolution and in the molybdate-bound conformation at 2.25 and 2.45,Å resolution. The overall domain structure of MaModA is similar to other ModA proteins in that it has a bilobal structure in which two mixed ,/, domains are linked by a hinge region. The apo MaModA is the first unliganded archaeal ModA structure to be determined: it exhibits a deep cleft between the two domains and confirms that upon binding ligand one domain is rotated towards the other by a hinge-bending motion, which is consistent with the `Venus flytrap' model seen for bacterial-type periplasmic binding proteins. In contrast to the bacterial ModA structures, which have tetrahedral coordination of their metal substrates, molybdate-bound MaModA employs octahedral coordination of its substrate like other archaeal ModA proteins. [source] Controlled Hydrothermal Synthesis and Growth Mechanism of Various Nanostructured Films of Copper and Silver TelluridesCHEMISTRY - A EUROPEAN JOURNAL, Issue 15 2006Lizhi Zhang Prof. Abstract Various nanostructured films of copper and silver tellurides were hydrothermally grown on the corresponding metal substrates through reactions between metal foils and tellurium powder in different media. Interesting morphologies including nanowires, nanorods, nanobelts, nanosheets, and hierarchical dendrites were obtained. The nanostructured films were characterized by using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and high-resolution TEM (HRTEM). A growth mechanism was proposed based on the characterization results. This study provides a low-temperature, solution-phase approach to grow low-dimensional, nanostructured metal tellurides with controllable morphologies. [source] | |||||||||||||