Search results for "Electronics"

showing 10 items of 4340 documents

Adhesion trends and growth mode of ultra-thin copper films on MgO

2004

Ab initio simulations are performed for Cu atoms adsorbed on the perfect MgO(001) substrate, with an ordered metal coverage varied from 1 monolayer (ML), i.e. almost single atoms, up t o1M L. As trong dependence of the adhesion energy and the sub-monolayer film distance from the substrate on the surface coverage and adsorbate positions (Mg 2+ or O 2− )i s discussed. The nature of interfacial bonding at all coverages is physisorption .W hen increasing Cu atomic fraction, a decrease of the substrate-induced polarization of adatoms accompanied by an increase of both in-plane metallic bonding and the interfacial distance has been found. Combining results of ab initio calculations with thermodyn…

ChemistryAb initioAnalytical chemistrychemistry.chemical_elementSubstrate (electronics)Condensed Matter PhysicsCopperTransition metalPhysisorptionAb initio quantum chemistry methodsComputational chemistryMonolayerGeneral Materials ScienceMetallic bondingJournal of Physics: Condensed Matter
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Metal film growth on regular and defective MgO(001) surface: A comparative ab initio simulation and thermodynamic study

2006

Abstract In order to understand the difference in metallic film growth modes on perfect and defective oxide substrates, we have combined ab initio B3LYP periodic calculations on the slab models of the corresponding Me/MgO(0 0 1) interfaces (Me = Ag, Cu) with thermodynamic theory of solid solutions. For a defectless magnesia surface, we confirm the experimentally observed submonolayer growth of 3D metallic islands (Ag possesses a higher trend than Cu). Formation of Fs centers (neutral O vacancies) on the substrate markedly enhances metal atom adsorption as compared to physisorption over regular sites on a defect-free substrate. For the first time, we predict that the presence of these surfac…

ChemistryAb initioOxideSurfaces and InterfacesSubstrate (electronics)Condensed Matter PhysicsSurfaces Coatings and FilmsMetalchemistry.chemical_compoundAdsorptionPhysisorptionComputational chemistryAb initio quantum chemistry methodsvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical chemistrySolid solutionSurface Science
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Laser cleaning of oxide iron layer : efficiency enhancement due to electrochemical induced absorptivity change

1999

Laser cleaning experiments exhibited a higher cleaning efficiency of the laser cleaning upon application of electrochemical potential on an oxidised iron surface. The objective of this study is to clarify the role of such an electrochemical control on cleaning efficiency. Therefore a study by optical spectrometry at normal incidence in the relevant conditions was performed. From these measurements the optical parameters n and k were deduced. While n is mainly not affected, k changes for a factor of 10 upon application of an electrochemical potential. These results explain the differences in laser cleaning efficiency due to the modified absorption length.

ChemistryAnalytical chemistryAttenuation lengthOxideGeneral ChemistryMolar absorptivityLaserElectrochemistryMass spectrometrylaw.inventionchemistry.chemical_compoundlawGeneral Materials Scienceddc:530pacs:78.20.CiLayer (electronics)pacs:81.65.Cfpacs:81.65.MqElectrochemical potential
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Ab initio modeling of copper adhesion on regular BaTiO3(001) surfaces

2005

Ab initio calculations have been performed for copper adsorption on a regular, defect-free TiO"2- and BaO-terminated (001) surfaces of a cubic BaTiO"3, using a posteriori HF-CC method as implemented into the CRYSTAL-03 computer code. To clarify the nature of the interfacial bonding, we use slab models of the Cu/BaTiO"3(001) interfaces with different one-side substrate coverages, varied from 1/8 monolayer (ML) up to 1/2 ML, over both TiO"2- and BaO-terminated surfaces. TiO"2 termination has been found to be energetically more favorable for the adsorption of copper atoms. In agreement with previous experimental and theoretical data, our calculations indicate essential contribution of atomic p…

ChemistryBinding energyAb initiochemistry.chemical_elementSubstrate (electronics)Electronic structureCondensed Matter PhysicsCopperAtomic and Molecular Physics and OpticsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAdsorptionAb initio quantum chemistry methodsChemical physicsMonolayerElectrical and Electronic EngineeringAtomic physicsMicroelectronic Engineering
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Study of interface diffusion of Ti and TiN PVD layers by Bremsstrahlung-induced AES

1992

The influence of heat treatment in ultrahigh vacuum (UHV) on Ti and TiN layers coated by physical vapour deposition (PVD) has been studied by AES, XPS and bremsstrahlung-induced AES. It could be concluded that up to 500 o C (1 h) the Ti layer does not change significantly. At the TiN/steel substrate interface, however, a counter-diffusion of nitrogen and adventitious oxygen takes place, resulting in partial nitridation of the steel substrate and oxidation of the coating

ChemistryDiffusionAnalytical chemistrychemistry.chemical_elementSurfaces and InterfacesGeneral ChemistrySubstrate (electronics)engineering.materialCondensed Matter PhysicsOxygenNitrogenSurfaces Coatings and FilmsCoatingX-ray photoelectron spectroscopyChemical engineeringMaterials ChemistryengineeringTinLayer (electronics)Surface and Interface Analysis
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Operational Mechanism of Conjugated Polyelectrolytes

2014

Conjugated polyelectrolytes (CPEs) are versatile materials used in a range of organic optoelectronic applications. Because of their ionic/electronic nature, characterizing these materials is nontrivial, and their operational mechanism is not fully understood. In this work we use a methodology that combines constant-voltage-driven current-density transient measurements with fast current vs voltage scans to allow decoupling of ionic and electronic phenomena. This technique is applied to diodes prepared with cationic CPEs having different charge-compensating anions. Our results indicate that the operational mechanism of these devices is governed by electrochemical doping of the CPE. On the bas…

ChemistryDopingIonic bondingNanotechnologyGeneral ChemistryBiochemistryConjugated PolyelectrolytesCatalysisIonColloid and Surface ChemistryDepletion regionDecoupling (electronics)DiodeVoltageJournal of the American Chemical Society
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Atmospheric compensation in Fourier transform infrared (FT-IR) spectra of clinical samples.

2013

A new method is proposed for the elimination of the spectral contribution of two atmospheric gases (CO2 and H2O) in Fourier transform infrared (FT-IR) spectra of clinical samples. The algorithm is based on the measurement of reference spectra of H2O followed by an automatic calculation of the spectral contribution of the above-mentioned gases to the sample spectra. Then this contribution is compensated by spectral subtraction. Attenuated total reflectance FT-IR spectra of serum and urine samples in the presence of atmospheric gases were corrected and compared with spectra obtained with an N2 purge. Visual inspection of the spectra as well as calculated noise levels confirmed that the metho…

ChemistryInfraredbusiness.industryAnalytical chemistryInfrared spectroscopyNoise (electronics)Spectral lineChemometricssymbols.namesakeOpticsFourier transformAttenuated total reflectionsymbolsFourier transform infrared spectroscopybusinessInstrumentationSpectroscopyApplied spectroscopy
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Adsorption of 3d Transition Elements on a TiO2(110) Surface.

2008

International audience; A first-principles study on the adsorption of 3d transition metal atoms on a stoichiometric TiO2(110) surface is reported. For all 3d elements except Cu, the most stable on-surface adsorption site is a site where the adatom binds to two twofold and one threefold surface oxygen atoms. For Ti, V, and Cr, however, a subsurface site, where the adatom substitutes a sixfold Ti atom, is more stable. The adatoms are oxidized in all cases. The charge transfer to the substrate is larger for the substitutional site than for the on-surface adsorption sites and decreases with atomic number along the 3d series. The relative stabilities of the adsorption sites are discussed in term…

ChemistryInorganic chemistry02 engineering and technologySubstrate (electronics)021001 nanoscience & nanotechnology01 natural sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsElectronegativityA-siteCrystallographyGeneral EnergyAdsorptionTransition metal0103 physical sciencesAtomAtomic numberPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyStoichiometry
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Probing optical and magnetic properties via subtle stereoelectronic effects in mononuclear DyIII-complexes

2021

Tapping into the secondary coordination environment of mononuclear DyIII-complexes leads to drastic changes in luminescence and magnetism. Visualization of effects induced by stereoelectronics on the opto-magnetic properties was achieved through subtle modifications in the ligand framework.

ChemistryMagnetismLigandMetals and Alloys02 engineering and technologyGeneral Chemistryequipment and supplies010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyMaterials ChemistryCeramics and Composites0210 nano-technologyLuminescencehuman activitiesStereoelectronicsChemical Communications
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Redox switching of the antiferromagnetic coupling in permethylated dicopper(ii) paracyclophanes

2012

A unique magnetic electroswitching behavior has been observed in an oxamato-based permethylated dicopper(II) paracyclophane; upon reversible one-electron oxidation of the double tetramethyl-substituted p-phenylenediamidate bridging skeleton, the spin alignment of the two Cu(II) ions (S(Cu) = ½) changes from antiparallel (OFF) to parallel (ON) in the resulting dicopper(II) π-radical cation species.

ChemistryMetals and AlloysGeneral ChemistryPhotochemistryRedoxCatalysisAntiferromagnetic couplingSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCrystallographyMaterials ChemistryCeramics and CompositesAntiparallel (electronics)Chemical Communications
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