Search results for "EXCITATION"

showing 10 items of 1290 documents

Excitation modes for fourier transform-ion cyclotron resonance mass spectrometry.

1992

AbstractVarious geometric configurations for the excitation of coherent ion motion in Fourier transform-ion cyclotron resonance mass spectrometry (FT-ICR/MS) are analyzed (in some cases for the first time) with unified notation. The instantaneous power absorption, F·v, in which v is ion velocity and F the force produced by the applied excitation electric field (harmonic, single frequency, on-resonance, in-phase), is time averaged and then set equal to the time rate of change of ion total (cyclotron + magnetron + trapping) energy, to yield a differential equation that is readily solved for the (time-dependent) amplitude of each of the various ion motions. The standard FT-ICR excitation (name…

ChemistryCyclotronAnalytical chemistryCyclotron resonanceMass spectrometryFourier transform ion cyclotron resonanceIonlaw.inventionAmplitudeStructural BiologylawPhysics::Plasma PhysicsAtomic physicsSpectroscopyIon cyclotron resonanceExcitationJournal of the American Society for Mass Spectrometry
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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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Oxygen influence on luminescence properties of rare-earth doped NaLaF 4

2016

Abstract Luminescence properties of erbium and europium doped NaLaF4 with different oxygen content have been studied. Vacuum ultraviolet (VUV) excitation luminescence spectroscopy technique has been applied by using synchrotron radiation excitation. It was found that oxygen impurity leads to significant degradation of Er3+ or Eu3+ emission under VUV excitation. The intensive O2−–Er3+ charge transfer excitation band has been detected from oxygen abundant NaLaF4 in the 150–165 nm spectral range. This band reveals a competing absorption mechanism in oxygen containing NaLaF4. It is clearly demonstrated that one reason for the Er3+ emission degradation in oxygen abundant NaLaF4 is strong suppres…

ChemistryDopingBiophysicsAnalytical chemistrychemistry.chemical_element02 engineering and technologyGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsPhotochemistry01 natural sciencesBiochemistryOxygenAtomic and Molecular Physics and OpticsIonAbsorption band0103 physical sciences010306 general physics0210 nano-technologySpectroscopyLuminescenceEuropiumExcitationJournal of Luminescence
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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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Excitation of Nucleobases from a Computational Perspective I: Reaction Paths

2013

The main intrinsic photochemical events in nucleobases can be described on theoretical grounds within the realm of non-adiabatic computational photochemistry. From a static standpoint, the photochemical reaction path approach (PRPA), through the computation of the respective minimum energy path (MEP), can be regarded as the most suitable strategy in order to explore the electronically excited isolated nucleobases. Unfortunately, the PRPA does not appear widely in the studies reported in the last decade. The main ultrafast decay observed experimentally for the gas-phase excited nucleobases is related to the computed barrierless MEPs from the bright excited state connecting the initial Franck…

ChemistryExcited stateElectronConical intersectionGround stateInternal conversion (chemistry)Quantum chemistryMolecular physicsExcitationNucleobase
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Self-trapped exciton luminescence in crystalline α-quartz under two-photon laser excitation

2003

Abstract The luminescence of pure crystalline α-quartz is studied under pulsed ArF laser excitation. The luminescence parameters obtained correspond well with those of self-trapped excitons (STEs) in α-quartz, indicating that the excitation process is two-photon. The efficiency of two-photon excitation is of the same order of magnitude as the one-photon excitation of sodium salicylate. The STE luminescence decay kinetics and their temperature dependence under photoexcitation were recorded with higher accuracy than previously. Changes in the decay kinetics with temperature are explained by the splitting of the STE triplet state in zero magnetic field and are analyzed with the assumption of t…

ChemistryExcitonRelaxation (NMR)Spin–lattice relaxationPhysics::OpticsGeneral ChemistryCondensed Matter PhysicsPhotoexcitationCondensed Matter::Materials ScienceTwo-photon excitation microscopyPhysics::Atomic and Molecular ClustersMaterials ChemistryTriplet stateAtomic physicsLuminescenceExcitationSolid State Communications
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Molecular Stark-effect spectroscopy of Prodan and Laurdan in different solvents and electric dipole moments in their equilibrated ground and Franck–C…

2007

Abstract The results from electrooptical absorption measurements (EOAM) on the ground and excited Franck–Condon state dipole moments of Prodan and Laurdan in 1,4-dioxane and cyclohexane are presented. The ground and excited Franck–Condon state electric dipole moments as well as the respective transition moment of both probes are parallel. The electric dipole moments of Prodan and Laurdan in the ground state in cyclohexane and 1,4-dioxane have values within the range (15.7–16.5) × 10 −30  C m. On optical excitation the dipole moments increase by (42.1–49.5) × 10 −30  C m. The obtained results are compared with the values of the dipole moments of Prodan and Laurdan determined by other methods.

ChemistryGeneral Chemical EngineeringTransition dipole momentGeneral Physics and AstronomyGeneral ChemistryPhotochemistrysymbols.namesakeDipolechemistry.chemical_compoundStark effectExcited statesymbolsAtomic physicsSpectroscopyGround stateLaurdanExcitationJournal of Photochemistry and Photobiology A: Chemistry
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Theoretical Study of the Twisted Intramolecular Charge Transfer in 1-Phenylpyrrole

2000

Ab initio results for the electronic spectra of 1-phenylpyrrole are presented. Vertical, emission, and nonvertical excitation energies have been computed using multiconfigurational second-order per...

ChemistryIntramolecular forceAb initioCharge (physics)Physics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsExcitationSpectral lineThe Journal of Physical Chemistry A
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Vibrational effects in Na2( , v′)+Na(3p3/2) associative ionization

1999

Abstract Associative ionizing Na2( A 1 Σ + u , v′)+Na(3p3/2) collisions have been studied in a single supersonic beam with respect to the influence of the initial vibrational excitation of the molecules on the reaction efficiency. An enhancement of trimer ion yield of nearly one order of magnitude has been observed as the vibrational excitation increases from v′=0 to v′=14.

ChemistryIonizationGeneral Physics and AstronomyMoleculeSupersonic speedTrimerPhysical and Theoretical ChemistryAtomic physicsOrder of magnitudeBeam (structure)ExcitationIonizing radiationChemical Physics Letters
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Atomic Radiative Lifetimes Measured by Pulsed Laser Spectroscopy in the Uv/Vuv Spectral Region

1998

Abstract Experimental lifetime measurements on free atoms and ions performed by using pulsed laser excitation in the ultraviolet and vacuum-ultraviolet spectral regions are presented. Different methods of laser pulse generation, atomization and light detection are described. A short summary of results obtained is also given. Future possibilities in determination of lifetimes and transition probabilities in the short wavelengths region are discussed.

ChemistryLasermedicine.disease_causeIonlaw.inventionPulse (physics)WavelengthlawmedicineRadiative transferPhysics::Atomic PhysicsAtomic physicsSpectroscopyExcitationUltraviolet
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