Search results for "Spectral"

showing 10 items of 3116 documents

Experimental and theoretical study of line mixing in methane spectra. III. The Q branch of the Raman ν1 band

2000

The shape of the ν1 Raman Q branch of CH4 perturbed by Ar and He at room temperature has been studied. Stimulated Raman spectroscopy (SRS) experiments have been made in the 2915–2918 cm−1 spectral region for total pressures from 0.4 to 70 atm and mixtures of ≈5% CH4 with He and Ar. Analysis of the spectra demonstrates that the shape of the Q branch is significantly influenced by line mixing and much narrower than what is predicted by the addition of individual line profiles. For the first time, a model is proposed for the calculation and analysis of the effects of collisions on the considered spectra. In this approach, the rotational part of the relaxation matrix is constructed, with no adj…

ChemistryAnalytical chemistryGeneral Physics and AstronomySemiclassical physicsSpectral linesymbols.namesakesymbolsCoherent anti-Stokes Raman spectroscopyPhysical and Theoretical ChemistryAtomic physicsRaman spectroscopySpectroscopyMixing (physics)Raman scatteringLine (formation)The Journal of Chemical Physics
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Determination of concentrations in ternary and quaternary molecular gas mixtures using femtosecond Raman spectroscopy

2002

Measurements of concentrations in gas mixtures of three and four molecular components are presented. They rely on a femtosecond time-resolved pump–probe technique based on Raman-induced polarization spectroscopy. The rotational time response of the molecular gas mixture is measured as a function of the pump–probe time delay. No selective frequency tunability is needed as the molecular rotational spectra are excited within the laser bandwidth. The results obtained from experiments performed at room temperature in N2O–CO2–N2 and N2O–CO2–O2–N2 mixtures are presented and the accuracy of the method is discussed. Copyright © 2002 John Wiley & Sons, Ltd.

ChemistryAnalytical chemistryPolarization (waves)LaserSpectral linelaw.inventionsymbols.namesakelawExcited stateFemtosecondsymbolsGeneral Materials ScienceRaman spectroscopySpectroscopyTernary operationSpectroscopyJournal of Raman Spectroscopy
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Analysis of Mn2+EPR spectral shapes for studies of the oxyfluoride glass ceramics

2011

We investigated the EPR superhyperfine structure of the Mn 2+ ion in the disordered BaF2 crystalline media which tends to crystallize in the oxyfluoride glass-ceramics material. Obtained EPR spectra reveal explicit shf structure due to Mn 2+ ion building into the BaF2 lattice showing its usefulness as a probe in orientationally disordered and amorphous structures. Two types with explicit shf structure of Mn 2+ ion characteristic EPR spectra were obtained in BaF2 powder samples characteristic with broad (type 1) and narrow (type 2) hyperfine structure lines. Spectra of the ZnF2-BaF2 oxyfluoride glass-ceramics samples revealed explicit fine structure lines.

ChemistryAnalytical chemistrySpectral linelaw.inventionAmorphous solidIonCrystallographylawLattice (order)visual_artvisual_art.visual_art_mediumCeramicElectron paramagnetic resonanceHyperfine structureIOP Conference Series: Materials Science and Engineering
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High-Resolution Spectroscopy and Structure of Osmium Tetroxide. A Benchmark Study on 192OsO4

2012

Osmium tetroxide (OsO(4)) is a heavy tetrahedral molecule that constitutes a benchmark for quantum chemistry calculations. Its favorable spin statistics (due to the zero nuclear spin of oxygen atoms) is such that only A(1) and A(2) (T(d) symmetry) rovibrational levels are allowed, leading to a dense but quite easily resolvable spectrum. We reinvestigate here the ν(1)/ν(3) stretching fundamental (940-980 cm(-1)) dyad region and perform new assignments and effective Hamiltonian parameter fits for the main isotopologue ((192)OsO(4)). We also investigate the ν(2)/ν(4) bending fundamental dyad (300-360 cm(-1)) for the first time and perform a preliminary analysis. New experimental data have been…

ChemistryAnalytical chemistryTetrahedral molecular geometry02 engineering and technologyRotational–vibrational spectroscopy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesQuantum chemistryMolecular physicsSpectral line0104 chemical sciencesInorganic Chemistrysymbols.namesakesymbolsIsotopologuePhysical and Theoretical Chemistry0210 nano-technologySpectroscopyHamiltonian (quantum mechanics)Spin (physics)Inorganic Chemistry
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Vibrations of a single adsorbed organic molecule: anharmonicity matters!

2010

Vibrational spectroscopy is a powerful tool to identify molecules and to characterise their chemical state. Inelastic electron tunnelling spectroscopy (IETS) combined with scanning tunnelling microscopy (STM) allows the application of vibrational analysis to a single molecule. Up to now, IETS was restricted to small species due to the complexity of vibration spectra for larger molecules. We extend the horizon of IETS for both experiment and theory by measuring the STM-IETS spectra of mercaptopyridine adsorbed on the (111) surface of gold and comparing it to theoretical spectra. Such complex spectra with more than 20 lines can be reliably determined and computed leading to completely new ins…

ChemistryAnharmonicityGeneral Physics and AstronomyInfrared spectroscopySelf-assembled monolayerElectronic structureSpectral linesymbols.namesakeComputational chemistryChemical physicssymbolsMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryRaman spectroscopyQuantum tunnellingPhysical chemistry chemical physics : PCCP
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Dithionite bleaching of thermomechanical pulp: factors having effects on bleaching efficiency

2000

The efficiency of dithionite bleaching of Norway spruce (Picea abies) thermomechanical pulp was studied by applying various multivariate data analysis techniques to analytical data (temperature, pH, ion chromatographic and energy-dispersive X-ray fluorescence data). In addition, modeling the residual sulfur content of bleached pulp by means of diffuse reflectance UV-vis spectral data from laboratory-scale bleaching experiments was attempted. The results indicated that this lignin-preserving bleaching process could be evaluated by means of the analytical data using either PCR or PLS models. These models also indicated that wavelengths below 400 nm should not be used in measuring the pulp bri…

ChemistryApplied MathematicsPulp (paper)Ion chromatographyOrthogonal signal correctionAnalytical chemistryengineering.materialDithioniteAnalytical Chemistrychemistry.chemical_compoundengineeringSulfur contentDiffuse reflectionSpectral dataJournal of Chemometrics
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Tieftemperatur-Remissionsspektren oktaedrisch koordinierter Cu2+ -Ionen im Ligandenfeldbereich / Low temperature reflectance spectra of octahedrally …

1973

Abstract The ligand field reflectance spectra of octahedrally coordinated Cu2+-ions in different host lattices and at different temperature (300 °K - 4 °K) are critically compared. Especially the band shifts with decreasing temperature are analysed with respect to transitions from a dynamical to a static Jahn-Teller effect (macroscopic Jahn -Teller distortion of the lattice). In addition the square planar coordination of Cu2+ is discussed and alternative descriptions in the crystal field formalism and the angular overlap model are given.

ChemistryCu2 ionsAnalytical chemistryGeneral Physics and AstronomyPhysical and Theoretical ChemistryReflectivityMathematical PhysicsSpectral lineZeitschrift für Naturforschung A
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The Triplet Excimer of Naphthalene: A Model System for Triplet−Triplet Interactions and Its Spectral Properties

2011

Basic concepts of triplet excimer formation and triplet−triplet interactions between molecules with conjugated π-systems are investigated by means of ab initio quantum chemical calculations, employing the second-order coupled-cluster method CC2 and the second-order propagator method ADC(2). The naphthalene dimer turns out to be a very fruitful model system for which weak and strong electronic coupling can be identified depending on the mutual arrangement of the monomer moieties. From geometry optimizations in the excited state, we determine binding energies, including solvent effects, and transient absorption spectra. The most stable T1 conformation turns out to be a face-to-face arrangemen…

ChemistryDimerBinding energyIntermolecular forceAb initioPhotochemistryExcimerSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergyChemical physicsExcited statePhysical and Theoretical ChemistrySolvent effectsThe Journal of Physical Chemistry C
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Recombination processes in rare-earth doped MAl2O4(M = Ca, Sr) persistent phosphors investigated by optically-detected magnetic resonance

2007

Single crystalline MAl 2 O 4 (M = Ca and Sr) persistent phosphors, which are nominally pure or additionally doped with Eu and Nd or Dy, respectively, were investigated for their recombination luminescence (RL) and microwave-induced changes in the RL at low temperatures. The analysis of the optically-detected electron paramagnetic resonance (EPR) spectra, recorded after ultraviolet excitation at 4.2 K, shows that intrinsic donor and acceptor centres are involved in the recombination process. Spectral dependent RL-EPR measurements on undoped CaAl 2 O 4 (CAO) and SrAl 2 O 4 (SAO) show that we deal with only one donor but at least two different acceptors. The g value of the donor is 1.99 in CAO…

ChemistryDopingAnalytical chemistryPhosphorSurfaces and InterfacesCondensed Matter PhysicsAcceptorSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionlawMaterials ChemistryElectrical and Electronic EngineeringLuminescenceElectron paramagnetic resonanceRecombinationExcitationNuclear chemistryphysica status solidi (a)
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Intrinsic luminescence and energy transfer processes in pure and doped YVO 4 crystals

2007

Luminescence properties of nominally pure and neodymium doped YVO4 single crystals have been studied by means of time-resolved luminescence spectroscopy technique. It was detected that, besides the main well-known blue excitonic emission band near 2.8 eV, an additional UV emission band at ∼3.1 eV appears in the spectra of intrinsic luminescence at low temperatures (∼80 K) for all crystals studied. Decay time of the UV band is much faster in comparison with the blue one and the UV band is quenched at temperatures above 150 K. Origin of the UV emission band is discussed. A significant rise front was observed in the relaxation kinetics of Nd3+ emission under band-to-band excitation. The time c…

ChemistryDopingchemistry.chemical_elementAstrophysics::Cosmology and Extragalactic AstrophysicsAtmospheric temperature rangeCondensed Matter PhysicsMolecular physicsNeodymiumSpectral lineIonAtomic physicsLuminescenceSpectroscopyAstrophysics::Galaxy AstrophysicsExcitationphysica status solidi c
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