Search results for "Spectroscopy"

showing 10 items of 10293 documents

Atomic and electronic structure of the corundum (0001) surface: comparison with surface spectroscopies

1997

Abstract The electronic structure and geometry of the Al-terminated corundum (0001) surface were studied using a slab model within the ab-initio Hartree-Fock technique. The distance between the top Al plane and the next O basal plane is found to be considerably reduced on relaxation (by 0.57 A, i.e. by 68% of the corresponding interlayer distance in the bulk). An interpretation of experimental photoelectron spectra (UPS He I) and metastable impact electron spectra (MIES) is given using the calculated total density of states of the slab and the projections to the atoms, atomic orbitals, and He 1s floating atomic orbital at different positions above the surface. Calculated projected densities…

ChemistrySurfaces and InterfacesElectronic structureCondensed Matter PhysicsElectron spectroscopySpectral lineSurfaces Coatings and FilmsAtomic orbitalX-ray photoelectron spectroscopyMetastabilityPhysics::Atomic and Molecular ClustersMaterials ChemistryDensity of statesRelaxation (physics)Physics::Atomic PhysicsAtomic physicsSurface Science
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Synthesis and Crystal Structure of Ln3(OH)(CrO4)4 · 3.5H2O (Ln = Pr, Nd) and Ln2(OH)2(CrO4)2 (Ln = Tb, Gd): Thermal Behavior and Infrared Spectra of …

1993

Abstract Crystal structures of Ln 2 (OH) 2 (CrO 4 ) 2 ( Ln = Gd, Tb) and Ln 3 (OH)(CrO 4 ) 4 · 3.5H 2 O ( Ln = Pr, Nd) were determined by a conventional single-crystal X-ray diffraction technique. Crystals of Ln 2 (OH) 2 (CrO 4 ) 2 ( Ln = Gd, Tb) are monoclinic, space group P 2 1 / c (no. 14) with lattice parameters a = 8.2454(4) A, b = 11.3834(5) A, C = 12.1420(8) A, and β = 136,590(5)°, Z = 4, D x = 4.92 mg · m -3 for Gd 2 (OH) 2 (CrO 4 ) 2 and a = 8.214(1) A, b = 11.348(1) A, c = 12.094(2) A, and β = 136.59(1)°, Z = 4, D x = 5.01 Mg · m -3 for Tb 2 (OH) 2 (CrO 4 ) 2 . Crystals of Ln 3 (OH)(CrO 4 )) 4 · 3.5H 2 O ( Ln = Pr, Nd) are monoclinic, space group C 2/ c (No. 15) with lattice param…

ChemistryThermal decompositionInfrared spectroscopyCrystal structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsSquare antiprismInorganic ChemistryCrystallographyMaterials ChemistryCeramics and CompositesMoleculePhysical and Theoretical ChemistryThermal analysisHydrateMonoclinic crystal systemNuclear chemistryJournal of Solid State Chemistry
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Modelling of the cation motions in complex system: case of Na-mordenites

2002

Abstract Semi-empirical inter-atomic potentials and Monte Carlo algorithms are proposed to predict the evolution of the interaction energy between sodium ions and a mordenite type aluminosilicate network as a function of Si/Al ratio. This result is favourably compared with the activation energy barriers for Na + `jumps' responsible for the polarization change, measured by thermally stimulated current (TSC) spectroscopy, for Na-mordenites characterized by Si/Al ratios ranged from 5.5 to 12. Finally, we propose a possible mechanism for the cation motions, which involves activation barriers within the same order of magnitude than those measured by TSC.

ChemistryThermodynamicsInteratomic potentialActivation energyInteraction energyCondensed Matter PhysicsMordeniteElectronic Optical and Magnetic MaterialsIonComputational chemistryAluminosilicateMaterials ChemistryCeramics and CompositesSpectroscopyOrder of magnitudeJournal of Non-Crystalline Solids
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Ionic transport and heat capacity of glass-forming metalnitrate mixtures

1997

Abstract Ionic transport of the glass-forming metalnitrate mixtures [Ca(NO 3 ) 2 ] 0.44 [KNO 3 ] 0.56 (MKN), and [Mg(NO 3 ) 2 ] 0.44 [NaNO 3 ] 0.56 (MNN) was investigated near the glass transition using broadband spectroscopy of the complex conductivity to 300 MHz. The real part of the conductivity exhibits a transition from frequency independent to power law behavior as found in most ionic conductors. At high frequencies the frequency exponent approaches unity and becomes larger at low temperatures. In the real part of the dielectric constant, a relaxation step could be observed in CRN. A detailed evaluation of the results within the modulus formalism is presented. The imaginary part of t…

ChemistryThermodynamicsIonic bondingDielectricConductivityCondensed Matter Physics530Power lawHeat capacityElectronic Optical and Magnetic MaterialsNano-Materials ChemistryCeramics and CompositesSpectroscopyGlass transitionJournal of Non-Crystalline Solids
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Ultrafast Electronic and Vibrational Energy Relaxation of Fe(acetylacetonate)3 in Solution

2007

Transient mid-infrared spectroscopy is used to probe the dynamics initiated by excitation of ligand-to-metal (400 nm) and metal-to-ligand (345 nm) charge transfer states of FeIII complexed with acetylacetonate (Fe(acac)3, where acac stands for deprotonated anion of acetylacetone) in solution. Transient spectra in the 1500-1600 cm-1 range show two broad absorptions red-shifted from the bleach of the nu(CO) (approximately 1575 cm-1) and nu(C=C) (approximately 1525 cm-1) ground state absorptions. Bleach recovery kinetics has a time constant of 12-19 ps in chloroform and tetrachloroethylene and it decreases by 30-40% in a 10% mixture of methanol in tetrachloroethylene. The transient absorptions…

ChemistryVibrational energy relaxationAnalytical chemistryCharge (physics)Transient (oscillation)Physical and Theoretical ChemistrySpectroscopyUltrashort pulseExcitationThe Journal of Physical Chemistry A
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Anharmonic vibrational frequency calculations for solvated molecules in the B3LYP Kohn–Sham basis set limit

2012

Abstract The solvent dependence of harmonic and anharmonic vibrational wavenumbers of water, formaldehyde and formamide was studied using the B3LYP method. The results obtained with the hierarchy of Jensen's polarization-consistent basis sets were fitted with two-parameter formula toward the B3LYP Kohn–Sham complete basis set (CBS) limit. Anharmonic corrections have been obtained by a second order perturbation treatment (VPT2) and vibrational configuration interaction (VCI) method. The solvent environment was treated according to the self-consistent reaction field polarizable continuum model (SCRF PCM) approach.

ChemistryVibrational partition functionMolecular vibrationAnharmonicityPhysics::Atomic and Molecular ClustersKohn–Sham equationsPhysics::Chemical PhysicsSolvent effectsConfiguration interactionAtomic physicsPolarizable continuum modelSpectroscopyBasis setVibrational Spectroscopy
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Assessing air quality inside vehicles and at filling stations by monitoring benzene, toluene, ethylbenzene and xylenes with the use of semipermeable …

2007

BTEX (benzene, toluene, ethylbenzene, and xylenes) were used as target molecules to evaluate the quality of air inside motor vehicles and near filling stations, using semipermeable membrane devices (SPMDs) as low-cost passive sampling devices. A direct, fast, simple methodology based on the use of headspace-gas chromatography-mass spectrometry detection (HS-GC-MS) was developed for BTEX determinations, without any sample pre-treatment. SPMDs (25.4 cm2 surface, filled with 100 microL triolein) were employed as static samplers. After the selected deployment time, the SPMDs were heated inside a HS vial at 150 degrees C for 20 min and BTEX compounds were determined by GC-MS in selected ion moni…

ChemistryXyleneAnalytical chemistryBTEXBiochemistryEthylbenzeneTolueneAnalytical Chemistrychemistry.chemical_compoundEnvironmental ChemistrySemipermeable membraneGasolineBenzeneAir quality indexSpectroscopyAnalytica Chimica Acta
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Recyclable Catalyst Reservoir: Oxidation of Alcohols Mediated by Noncovalently Supported Bis(imidazolium)-Tagged 2,2,6,6-Tetramethylpiperidine 1-Oxyl

2013

Bis(imidazolium)-tagged 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO) catalysts were adsorbed on different supports such as silica gel, silica gel modified with highly cross-linked polymeric imidazolium networks, and highly cross-linked polymeric imidazolium networks entrapping magnetic particles. These systems provided a convenient tool for the oxidation of both primary and secondary alcohols working as recyclable reservoirs for the bis(imidazolium)-tagged TEMPO catalysts. By using EPR spectroscopy it was demonstrated that the catalyst was released as the corresponding oxoammonium salt in the solution during the recycling step, thus promoting the oxidative process in a homogeneous fashion. …

ChemistryalcoholoxidationOrganic ChemistryketoneALCOHOLSSettore CHIM/06 - Chimica OrganicaRecyclable catalystCatalysisaldehydelaw.inventionInorganic Chemistry2 2 6 6 tetramethylpiperidine 1 oxyllawAlcohol oxidationKETONESOrganic chemistryPhysical and Theoretical Chemistrysupported catalystsElectron paramagnetic resonanceEPR spectroscopy
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Nanoelectron spectroscopy for chemical analysis: a novel energy filter for imaging x-ray photoemission spectroscopy

2005

An ovel instrument for imaging ESCA is described. It is based on a tandem arrangement of two hemispherical energy analysers used as an imaging energy filter. The main spherical aberration (α 2 -term) of the analyser is corrected by the antisymmetry of the tandem configuration. The kinetic energy range useable for imaging extends up to 1.6 keV; this is compatible with Mg and Al Kα laboratory x-ray sources. First experiments on the chemical surface composition of a Cu0.98Bi0.02 polycrystal, a GaAs/AlGaAs heterostructure and Ag crystallites on Si(111) have been performed using synchrotron radiation. The results reveal an energy resolutio no f190 meV and a lateral resolution (edge resolution) o…

Chemistrybusiness.industryAnalyserBremsstrahlungAnalytical chemistrySynchrotron radiationCondensed Matter PhysicsKinetic energyElectron spectroscopySpherical aberrationOpticsX-ray photoelectron spectroscopyGeneral Materials ScienceSpectroscopybusinessJournal of Physics: Condensed Matter
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Direct observation of the electroadsorptive effect on ultrathin films for microsensor and catalytic-surface control.

2013

Microchemical sensors and catalytic reactors make use of gases during adsorption in specific ways on selected materials. Fine-tuning is normally achieved by morphological control and material doping. The latter relates surface properties to the electronic structure of the bulk, and this suggests the possibility of electronic control. Although unusual for catalytic surfaces, such phenomena are sometimes reported for microsensors, but with little understanding of the underlying mechanisms. Herein, direct observation of the electroadsorptive effect by a combination of X-ray photoelectron spectroscopy and conductivity analysis on nanometre-thick semiconductor films on buried control electrodes …

Chemistrybusiness.industryDopingNanotechnologyElectronic structureConductivityAtomic and Molecular Physics and OpticsAdsorptionSemiconductorX-ray photoelectron spectroscopyElectrodePhysical and Theoretical ChemistryThin filmbusinessChemphyschem : a European journal of chemical physics and physical chemistry
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