Publications

6,096 articles found

5061

Role of water vapour in the interaction of SnO2 gas sensors with CO and CH4

Ionescu, R; Vancu, A; Moise, C; Tomescu, A

DEC 14 1999, SENSORS AND ACTUATORS B-CHEMICAL, 61, 42

DOI: 10.1016/S0925-4005(99)00277-4

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New aspects of the influence of water vapour in the interaction of SnO2 gas sensors with different reducing gases are evidenced by an original experimental method. This consists in measuring the conductance transients during and after rapid transitions from dry into humid air containing identical concentrations of methane and CO, respectively. The results indicate that while methane and water compete in reacting with one type of oxygen ions on the surface, CO reacts mainly with another type of surface oxygen, almost insensitive to water. (C) 1999 Elsevier Science S.A. All rights reserved.

5062

Increased sensor sensitivities obtained by polymer-coated quartz microbalances

Oprea, A; Henkel, K; Oehmgen, R; Appel, G; Schmeisser, D; Lauer, H; Hausmann, P

DEC 1 1999, MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS, 8-9, 512

DOI: 10.1016/S0928-4931(99)00065-X

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Polymer-coated quartz microbalances were produced and studied. They exhibited high sensitivities for heavy noncyclical hydrocarbons and CO2 concentration measurements. Detection limit of 1 ppm CO2 and 10 ppm Shellsol (Shell solvent containing: 28.7% C10H22; 66.4% C11H24; 5% C12H26) are obtained and reported. The time constants of the absorption and desorption processes were investigated also. A diffusion-free behaviour was observed and related to the porosity of the layer. Collateral AFM (atomic force microscopy) analysis of the polymer structure was performed. We explain big values of the absorption-desorption time constant for CO2 and small values for CnH2n+2 mixtures in connection with the peculiarities of the chemical reaction involved by the sensing mechanisms. (C) 1999 Elsevier Science S.A. All rights reserved.

5063

Jahn-Teller configurations in natural spinels

Kuncser, V; Russo, U; Graziani, R; Della Giusta, A; Palade, P; Bulinski, M; Filoti, G

DEC 1999, PHYSICS AND CHEMISTRY OF MINERALS, 27, 102

DOI: 10.1007/s002690050245

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The local configurations and related hyperfine interactions of the tetrahedrally coordinated Fe2+ in two natural spinels were investigated. A special fitting procedure of the Mossbauer spectra is proposed in order to cover the involved mechanisms over the whole temperature range. The behavior of the quadrupole splitting vs temperature was successfully explained in terms of the split of the electronic 3d ground state doublet under a non-cooperative Jahn-Teller effect also providing estimates of the splitting energy for each configuration.

5064

Interfacial chemical effect evidenced on SERS spectra of polyaniline thin films deposited on rough metallic supports

Baibarac, M; Mihut, L; Louarn, G; Mevellec, JY; Wery, J; Lefrant, S; Baltog, I

DEC 1999, JOURNAL OF RAMAN SPECTROSCOPY, 30, 1113

DOI: 10.1002/(SICI)1097-4555(199912)30:12<1105::AID-JRS507>3.0.CO;2-3

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Surface-enhanced Raman scattering (SERS) has proved to be an effective technique for studying the structural properties of conducting polymer thin films. The enhancement process has a twofold origin, electromagnetic and chemical, The electromagnetic enhancement, which is the dominant mechanism in SERS generation, consists in the excitation of localized and delocalized surface plasmons (SPs) in the metallic support of the thin film, The Raman emission of the adsorbed molecules on the metal surface (the most efficient being Ag, Au and Cu) is due to the intense evanescent electromagnetic field located at the interface between the metal and the surrounding medium. The second enhancing mechanism for SERS is of chemical origin, involving the formation of new chemical bonds between the molecules and the metal surface, with the polarizability thus becoming considerably higher than that of the free molecules. This mechanism is as a rule accompanied by a metal-molecule or molecule-metal charge transfer, which partly accounts for the success of the SERS studies on conducting polymers. Unfortunately, these studies have revealed that the chemical effects at the polymer-metal interface varied substantially depending on the various types of polymer and metallic support. In this context, polyaniline containing two different entities (a reduced and an oxidized state) in its repeating units exhibits specific alterations in its SERS spectra depending on the type of metallic support. This paper presents new results concerning the structure of emeraldine-base and emeraldine-salt polyaniline thin films deposited on rough Ag and Au supports. The effect on the SERS spectra of the polymer-metal and polymer-ambient interface chemical reactions is also described. The presence of an interface compound depending on the oxidizing properties of the metallic support has a strong influence on the SERS spectra, no matter how the PAN films were deposited on the support (whether by solvent evaporation or by an electrochemical process, i.e. cyclic voltammetry). When an emeraldine base is doped with HSO4- ions, it turns into an emeraldine salt, which exhibits a disordered state in its macromolecular chain, leading to a modified profile of the similar to 1162 cm(-1) Raman line which is associated with the C-H bond of the quinoid ring. The Lorentzian profile is altered by the addition of a Gaussian profile component. For a rough Ag support, the SERS spectra show that the transformation of emeraldine base films into emeraldine salt films is a reversible process, Copyright (C) 1999 John Wiley & Sons, Ltd.

5065

Two-time electron-LO-phonon quantum kinetics and the generalized Kadanoff-Baym approximation

Gartner, P; Banyai, L; Haug, H

NOV 15 1999, PHYSICAL REVIEW B, 60, 14241

DOI: 10.1103/PhysRevB.60.14234

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We solve numerically the time-dependent self-consistent random phase approximation Dyson equations for a system of electrons and holes of a direct gap semiconductor excited by an ultrashort laser pulse interacting with LO phonons in equilibrium. Special care is devoted to the proper treatment of the prehistory of the system by including the polaron effects. We show that for weak Frohlich coupling (alpha=0.1), the generalized Kadanoff-Baym relationship, which enables a one-time formulation, is excellently verified while for intermediate coupling(alpha=1) the deviations become important. [S0163-1829(99)03943-0].

5066

Low metal loading Ru-MCM-41 stereocontrolled hydrogenation of prostaglandin intermediates

Coman, S; Florea, M; Cocu, F; Parvulescu, VI; Jacobs, PA; Danumah, C; Kaliaguine, S

NOV 7 1999

DOI: 10.1039/a907119i

5067

XTEM study of Al doped TiO2 anatase epitaxial films deposited on MgO by pulsed laser deposition

Teodorescu, VS; Blanchin, MG; Garapon, C; Champeaux, C

NOV 1999, JOURNAL OF MATERIALS SCIENCE, 34, 5476

DOI: 10.1023/A:1004796008417

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Al doped TiO2 anatase films epitaxially grown by Pulsed Laser Deposition (PLD) on MgO single crystal substrates have been studied by cross-section transmission electron microscopy. The main structural features of such films are the columnar morphology of the anatase grains and the formation of a spinel buffer layer at the TiO2/MgO interface. The spinel layer is Al rich and displays a steep gradient in Mg composition. Correlation between the microstructure and the optical properties of the films is presented also. (C) 1999 Kluwer Academic Publishers.

5068

Evidence for metal-C(60) interface interaction from Raman spectroscopy

Manaila, R; Belu-Marian, A; Macovei, D; Brehm, G; Marian, DT; Baltog, I

NOV 1999, JOURNAL OF RAMAN SPECTROSCOPY, 30, 1025

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Thin Cu-C(60) films were prepared by vacuum co-deposition and investigated by Raman spectroscopy. Evidence was found for alteration of the intramolecular vibrational modes of C(60) due to the presence of Cu and also for activation of silent modes. The effects were attributed to the interaction at the interface between the metal and fullerene and to the related formation of interstitial metallic ions. This hypothesis is supported by structural evidence derived from x-ray diffraction and EXAFS, Copyright (C) 1999 John Wiley & Sons, Ltd.

5069

Spectroscopical study of amorphous AsSe : Sn films

Iovu, MS; Syrbu, NN; Shutov, SD; Vasiliev, IA; Rebeja, S; Colomeico, E; Popescu, M; Sava, F

OCT 16 1999, PHYSICA STATUS SOLIDI A-APPLIED RESEARCH, 175, 622

DOI: 10.1002/(SICI)1521-396X(199910)175:2<615::AID-PSSA615>3.0.CO;2-N

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The effect of tin impurities on optical spectra of thermally deposited AsSe films doped with Sn (1 to 10 at%) was studied in a wide energy interval from 0.8 to 6.2 eV by combination of reflection, absorption, photoresponse and photocapacitance spectroscopies. Most changes have been detected at the fundamental absorption edge over which a correlation between the band tail width and optical gap is demonstrated for various tin concentrations. The tin induced absorption band associated with a localized energy level at about 1.6 eV in the gap was revealed. Distinct variations in the reflectivity spectra of the fundamental absorption region suggest a tin assistance in the formation of the valence band states of the material.

5070

Design of semiconductor heterostructures with preset electron reflectance by inverse scattering techniques

Bessis, D; Mezincescu, GA

OCT 1999, MICROELECTRONICS JOURNAL, 30, 974

DOI: 10.1016/S0026-2692(99)00059-2

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We present the application of the inverse scattering method to the design of semiconductor heterostructures having a preset dependence of the (conduction) electrons' reflectance on the energy. The electron dynamics are described by either the effective mass Schrodinger equation or by the (variable mass) BenDaniel and Duke equations. The problem of phase (re)construction for the complex transmission and reflection coefficients is solved by a combination of Pade approximation techniques, obtaining reference solutions with simple analytic properties. Reflectance-preserving transformations allow bound state and reflection resonance management. The inverse scattering problem for the Schrodinger equation is solved using an algebraic approach due to Sabatier. This solution can be mapped unitarily onto a family of BenDaniel and Duke type equations. The boundary value problem for the nonlinear equation which determines the mapping is discussed in some detail. The chemical concentration profile of heterostructures whose self consistent potential yields the desired reflectance is solved completely in the case of Schrodinger dynamics and approximately for BenDaniel and Duke dynamics. The Appendix contains a brief digest of results from the scattering and inverse scattering theory for the one-dimensional Schrodinger equation which is used in the article. (C) 1999 Elsevier Science Ltd. All rights reserved.