Search results for "EXCITATION"

showing 10 items of 1290 documents

Temperature and excitation energy dependence of decay processes of luminescence in Ge-doped silica

2003

We report experimental results on the time decay of photoluminescence at 4.2 eV in Ge-doped silica. This optical emission is assigned to a singlet-singlet transition between electronic states localized on an oxygen deficiency nearby a Ge atom and its radiative decay rate is in competition with an intersystem crossing mechanism that populates an excited triplet state. We investigate the dependence of the lifetime of this photoluminescence on the temperature, in the 6--295 K range, and on the excitation energy, in the ultraviolet and vacuum ultraviolet region. The mean value of the decay time decreases on increasing the temperature, in agreement with the phonon-assisted nature of the intersys…

Range (particle radiation)Materials scienceIntersystem crossingPhotoluminescenceExcited stateAtomActivation energyAtomic physicsTriplet stateExcitation
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Luminescence and vacuum ultraviolet excitation spectroscopy of samarium doped SrB4O7

2020

Abstract Sm2+ and Sm3+ co-doped SrB4O7 could be utilized in several high-level optical devices and fundamental knowledge about the optical behavior of these materials benefits the development of luminescent applications. Herein, we report luminescence and its vacuum ultraviolet (VUV) excitation spectra in samarium doped SrB4O7. Both, Sm2+ and Sm3+ luminescence centers have been examined and distinguished in the emission and the excitation spectra investigated under synchrotron radiation. The contribution of either Sm2+ or Sm3+ emission lines into the emission spectra heavily depended on the excitation energy, and strong f-f transitions of both Sm2+ and Sm3+ were detected. At 10 K, a broad i…

Range (particle radiation)Materials scienceMechanical EngineeringExcitonDopingMetals and Alloyschemistry.chemical_elementSynchrotron radiation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSamariumchemistryMechanics of MaterialsMaterials ChemistryEmission spectrumAtomic physics0210 nano-technologyLuminescenceExcitationJournal of Alloys and Compounds
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UV light energy storage and thermoluminescence in AlN ceramics

2007

AlN ceramics, untreated and subjected to oxygen ion implantation, are studied for potential application in TL dosimetry of UV light. Based on photoluminescence and thermoluminescence measurements there are shown advantages of the selection of the 480 emission band for TL signal recording instead of the previously used 400 nm band: higher intensity of the TL signal, lower fading rate of the accumulated TL signal, excitation region (270-340 nm) corresponding to UV-B range, monitoring of which is actual in UV dosimetry. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)

Range (particle radiation)Materials sciencePhotoluminescencebusiness.industryCondensed Matter PhysicsThermoluminescenceSignalvisual_artLight energyvisual_art.visual_art_mediumDosimetryOptoelectronicsCeramicbusinessExcitationphysica status solidi c
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Luminescence of γ-radiation-induced defects in α-quartz

2004

Optical transitions associated with γ-radiation-induced defects in crystalline α-quartz were investigated by photoluminescence excited by both pulsed synchrotron radiation and steady-state light. After a 10 MGy γ-dose we observed two emissions at 4.9 eV (ultraviolet band) and 2.7 eV (blue band) excitable in the range of the induced absorption band at 7.6 eV. These two luminescence bands show a different temperature dependence: the ultraviolet band becomes bright below 80 K; the blue band increases below 180 K, but drops down below 80 K. Both emissions decay in a timescale of a few ns under pulsed excitation, however the blue band could also be observed in slow recombination processes and it…

Range (particle radiation)Photoluminescencebusiness.industryChemistrySynchrotron radiationCondensed Matter Physicsmedicine.disease_causeMolecular physicsAbsorption bandExcited statemedicineOptoelectronicsGeneral Materials ScienceLuminescencebusinessExcitationUltravioletJournal of Physics: Condensed Matter
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A rotating wheel system for the detection of spontaneously fissioning nuclides from heavy ion reactions

1981

Abstract A rotating wheel system for the detection of spontaneously fissioning reaction products from heavy ion reactions was developed. In this system products recoiling from a rotating target wheel are stopped in a catcher foil stack which can be rotated at various velocities up to 80 rotations per second. All products emitted within a wide emission cone are stopped in the catcher foils and are rotated into shielded positions with stationary fission-track detectors positioned on both sides of each rotating foil. This technique allows a sensitive detection of spontaneously fissioning nuclides over a broad range of half-lives from 1 ms to about 1 d. By post-bombardment exposure of the catch…

Range (particle radiation)Physics::Instrumentation and DetectorsChemistryDetectorGeneral Engineeringlaw.inventionNuclear physicsStack (abstract data type)lawShielded cableHeavy ionNuclideAtomic physicsNuclear ExperimentFOIL methodExcitationNuclear Instruments and Methods in Physics Research
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Luminescence of ZnO nanopowders

2004

Abstract The luminescence of ZnO nanocrystals prepared by different methods was studied under pulsed electron beam excitation. It is shown that the luminescence intensity depends on the nanocrystal sintering conditions and does not depend on the nanocrystal size within the range 10–50 nm. The relative luminescence intensities for the 3.32 eV (free exciton) and ∼3.20 eV (bound exciton) bands showed a dependence on nanocrystal size. The role of the nanocrystal surface in excitonic luminescence is discussed.

Range (particle radiation)RadiationMaterials scienceNanocrystalExcitonAnalytical chemistrySinteringElectronLuminescenceInstrumentationSpectral lineExcitationRadiation Measurements
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The influence of internal degrees of freedom on the unimolecular decay of the molecule–cluster compound Au8+CH3OH

2002

Time-resolved photodissociation measurements of the sequential reaction Au8+CH3OH→Au8+→Au7+ and the direct reaction Au8+→Au7+ have been performed for several excitation energies. The production rates and yields of the final state Au7+ in the sequential process are strongly influenced by the excitation energy deposited into the evaporated methanol molecule during the initial fragmentation step. Both the rate constants and yields can be fitted with a single parameter, the cluster–methanol binding energy.

Reaction rate constantFragmentation (mass spectrometry)ChemistryBinding energyPhotodissociationDegrees of freedom (physics and chemistry)General Physics and AstronomyPhysical chemistryMoleculePhysical and Theoretical ChemistryAtomic physicsExcitationIonThe Journal of Chemical Physics
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Lineshapes and optical selectivity in high-resolution double-resonance ionization mass spectrometry

1999

Abstract Lineshapes expected in high-resolution double-resonance ionization spectroscopy are calculated using the density matrix formalism, integrated over experimentally realistic conditions including atomic velocity and angular distributions as well as laser intensity profiles. The results of these calculations are compared with experimental measurements on the system 4s2 1S0 → 4s4p 1P1 → 4s4d 1D1 → ion for calcium. The measurements of lineshape, with a dynamic range of >106, reveal and confirm subtle effects predicted by theory. These include the shape, position and intensity of the laser-induced structure in the spectra and the simultaneous presence of coherent and incoherent excitation…

Resolution (mass spectrometry)ChemistryAnalytical chemistryMass spectrometryMolecular physicsAtomic and Molecular Physics and OpticsSpectral lineAnalytical ChemistryIonIonizationMass spectrumPhysics::Atomic PhysicsSpectroscopyInstrumentationSpectroscopyExcitationSpectrochimica Acta Part B: Atomic Spectroscopy
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Computational determination of the dominant triplet population mechanism in photoexcited benzophenone

2014

In benzophenone, intersystem crossing occurs efficiently between the S-1(n pi(star)) state and the T-1 state of dominant n pi(star) character, leading to excited triplet states after photoexcitation. The transition mechanism between S-1(n pi(star)) and T-1 is still a matter of debate, despite several experimental studies. Quantum mechanical calculations have been performed in order to assess the relative efficiencies of previously proposed mechanisms, in particular, the direct S-1 -> T-1 and indirect S-1 -> T-2(pi pi(star)) -> T-1 ones. Multiconfigurational wave function based methods are used to discuss the nature of the relevant states and also to determine minimum energy paths a…

STATE DIPOLE-MOMENTSPopulationMechanistic organic photochemistryEXCITED BENZOPHENONEGeneral Physics and AstronomyGAS-PHASEABSORPTION-SPECTROSCOPYchemistry.chemical_compoundORGANIC-PHOTOCHEMISTRYMOLECULAR WAVE-FUNCTIONSBenzophenonePhysical and Theoretical ChemistryeducationWave functioneducation.field_of_studyROW ATOMSChemistryCONICAL INTERSECTIONSPhotoexcitation[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryIntersystem crossingExcited state2ND-ORDER PERTURBATION-THEORYANO BASIS-SETSAtomic physicsPhosphorescence
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Time-dependent ground-state correlations in heavy ion scattering

1982

Using a time-dependent generator-coordinate method, we derive a theory for time-dependent collective ground-state correlations which account for some quantum fluctuations about a TDHF trajectory. This theory is particularly suited for evaluating spreading widths of collective one-body operators. As an application we study head-on collision of heavy ions in a one-dimensional model. As one of the prominent results we find a substantial enhancement of the spreading width of the internal excitation energy due to the correlations.

ScatteringChemistryQuantum electrodynamicsTrajectoryGround stateCollisionQuantum fluctuationEnergy (signal processing)ExcitationIon
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