Search results for "Laser Spectroscopy"

showing 10 items of 151 documents

Electromagnetic moments of scandium isotopes and $N=28$ isotones in the distinctive $0f_{7/2}$ orbit

2022

The electric quadrupole moment of $^{49}$Sc was measured by collinear laser spectroscopy at CERN-ISOLDE to be $Q_{\rm s}=-0.159(8)$ $e$b, and a nearly tenfold improvement in precision was reached for the electromagnetic moments of $^{47,49}$Sc. The single-particle behavior and nucleon-nucleon correlations are investigated with the electromagnetic moments of $Z=21$ isotopes and $N=28$ isotones as valence neutrons and protons fill the distinctive $0f_{7/2}$ orbit, respectively, located between magic numbers, 20 and 28. The experimental data are interpreted with shell-model calculations using an effective interaction, and ab-initio valence-space in-medium similarity renormalization group calcu…

Nuclear and High Energy PhysicsNuclear Theorynucl-thCollinear laser spectroscopyNuclear TheoryFOS: Physical sciencesAstronomy & Astrophysicsnucl-exComputer Science::Digital LibrariesPhysics Particles & FieldsElectromagnetic momentsNuclear Theory (nucl-th)Nuclear Physics - ExperimentNuclear Experiment (nucl-ex)Nuclear ExperimentNuclear ExperimentisotoopitScience & TechnologyPhysicsNUCLEAR MOMENTSQUADRUPOLE-MOMENTSPhysics NuclearNucleon-nucleon correlationNuclear Physics - TheoryPhysical SciencesSHELL-MODELCOLLECTIVITYPräzisionsexperimente - Abteilung BlaumydinfysiikkaskandiumAb-initio calculation
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Relaxation of electronic excitations in strontium titanate

2002

The transient absorption spectra and kinetics were studied for undoped, lead doped and high purity SrTiO 3 single crystals. The pulsed electron beam induced transient absorption is studied in all crystals. The strong absorption at 0.8 v eV was observed only in high purity SrTiO 3 . This absorption is suggested to arise from intrinsic electron polaron. The bound electron polarons are likely responsible for absorption band at 1.4 v eV. The main luminescence band under excitation pulse is observed at 2.75 v eV. The luminescence decay is faster than that of transient absorption.

Nuclear and High Energy PhysicsRadiationAbsorption spectroscopyChemistryDopingAnalytical chemistryCondensed Matter PhysicsPolaronMolecular physicschemistry.chemical_compoundAbsorption bandUltrafast laser spectroscopyStrontium titanateGeneral Materials ScienceLuminescenceAbsorption (electromagnetic radiation)Radiation Effects and Defects in Solids
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The experimental observation of the potential barrier for self-trapped exciton decay into F-H pair in KCl-Na crystals

1995

Abstract The optical absorption induced by the electron pulse irradiation of Na+ doped KCl has been measured. Transient optical absorption band of FA centers was observed at 80 K (LNT). The temperature dependence of FA center formation was studied. It is proposed that the obtained activation energy originates from the potential barrier between the STE perturbed by the cation impurity and the nearest neighbour FA-H pair. The mechanism of the suppression of the defect formation by the monovalent cation impurity in alkali halide crystals is discussed.

Nuclear and High Energy PhysicsRadiationAbsorption spectroscopyChemistryExcitonAnalytical chemistryActivation energyCondensed Matter PhysicsImpurityAbsorption bandUltrafast laser spectroscopyPhysics::Atomic and Molecular ClustersRectangular potential barrierGeneral Materials ScienceAbsorption (chemistry)Atomic physicsRadiation Effects and Defects in Solids
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Transient color centers in GGG crystals

2002

Electron pulse induced absorption and their decay kinetics have been investigated in samples of GGG crystals with different starting absorption spectra. It is shown that for all samples there appears a wide transient absorption (TA) band with two maxima in the region 14,000-17,000 v cm m 1 and 22,000-26,000 v cm m 1 . TA decay kinetics measurements in 14,000 v cm m 1 and 22,000 v cm m 1 are two-exponential (with half-time order several tens and several hundreds ns). Analyzing the obtained results, we can suppose that low and high energy TA bands are connected with the F + (or O m ) and F transient color centers (TCC) respectively.

Nuclear and High Energy PhysicsRadiationAbsorption spectroscopyChemistrybusiness.industryKineticsAnalytical chemistryElectronRadiationCondensed Matter PhysicsOpticsElectron pulseUltrafast laser spectroscopyGeneral Materials ScienceTransient (oscillation)businessAbsorption (electromagnetic radiation)Radiation Effects and Defects in Solids
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Time-resolved spectroscopy of ZnWO4

2001

The luminescence spectra of ZnWO 4 excited by a pulsed electron beam, pulsed nitrogen laser and X-ray are studied. The luminescence decay kinetics are compared with transient absorption relaxation kinetics. Broad band transient absorption spectra are observed and it is shown that the slow decay component (∼14 μs at RT) of the transient absorption matches well with the luminescence decay therefore this absorption is due to the excited state absorption of the luminescence center.

Nuclear and High Energy PhysicsRadiationAbsorption spectroscopyCondensed Matter::OtherChemistryRelaxation (NMR)Physics::OpticsCondensed Matter PhysicsExcited stateUltrafast laser spectroscopyGeneral Materials ScienceNitrogen laserAtomic physicsTime-resolved spectroscopyAbsorption (electromagnetic radiation)LuminescenceRadiation Effects and Defects in Solids
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Induced optical absorption and ITS relaxation in LiNbO3

1999

Abstract Electron pulse induced absorption spectra and their decay kinetics have been investigated in LiNbO3 crystals with various Li/Nb ratios rasnging from congruent to stoichiometric composition. It is shown that the absorption spectra, the optical density and the decay kinetics depend on the Li/Nb ratio. The rising front of the induced absorption is too fast to be resolved. The room temperature decay, characterized by the half-lifetime Δt, is faster in the stoichiometric crystal (∼ 750 ns) than in the congrruent crystal (∼ 3.5 μs).

Nuclear and High Energy PhysicsRadiationExtended X-ray absorption fine structureAbsorption spectroscopyChemistryLithium niobateRelaxation (NMR)Analytical chemistryPhysics::OpticsCondensed Matter PhysicsTwo-photon absorptionCrystalchemistry.chemical_compoundCondensed Matter::SuperconductivityUltrafast laser spectroscopyGeneral Materials ScienceAbsorption (electromagnetic radiation)Radiation Effects and Defects in Solids
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Pulsed electron beam excited transient absorption in SrTiO3

2002

Abstract Transient absorption (TA) spectra and optical density relaxation kinetics in SrTiO3 (STO), STO–Nb and STO–V were studied. The electron polaron free or bound at intrinsic defect is suggested to be responsible for the TA band at ∼1.4 eV observed in STO. The band peaking below 0.75 eV in STO–Nb is proposed to be from Nb4+. The electron center V3+ or electron polaron bound in the vicinity of V4+ is responsible for the absorption band at 1.0 eV in STO–V. The absorption from hole polarons is suggested to be in the range 1.8–2.3 eV. It is shown that TA in pure STO at room temperature decays due to electron–hole polaron recombination.

Nuclear and High Energy PhysicsRange (particle radiation)ChemistryAbsorption bandExcited stateUltrafast laser spectroscopyElectronAtomic physicsPolaronAbsorption (electromagnetic radiation)InstrumentationSpectral lineNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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High-resolution laser spectroscopy with the Collinear Resonance Ionisation Spectroscopy (CRIS) experiment at CERN-ISOLDE

2016

The Collinear Resonance Ionisation Spectroscopy (CRIS) experiment at CERN has achieved high-resolution resonance ionisation laser spectroscopy with a full width at half maximum linewidth of 20(1) MHz for 219;221Fr, and has measured isotopes as short lived as 5 ms with 214Fr. This development allows for greater precision in the study of hyperfine structures and isotope shifts, as well as a higher selectivity of singleisotope, even single-isomer, beams. These achievements are linked with the development of a new laser laboratory and new data-acquisition systems. publisher: Elsevier articletitle: High-resolution laser spectroscopy with the Collinear Resonance Ionisation Spectroscopy (CRIS) exp…

Nuclear and High Energy Physics[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]7. Clean energy01 natural scienceslaw.inventionLaser linewidthlawIonization0103 physical sciencesNuclear Physics - ExperimentLaser spectroscopy010306 general physicsSpectroscopyInstrumentationHyperfine structureLarge Hadron Collider010308 nuclear & particles physicsChemistryData acquisitionResonanceLaserIon beam purificationIsotope shiftFull width at half maximumHyperfine structureAtomic physicsNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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First application of the Laser Ion Source and Trap (LIST) for on-line experiments at ISOLDE

2012

The Laser Ion Source and Trap (LIST) provides a new mode of operation for the resonance ionization laser ion source (RILIS) at ISOLDE/CERN, reducing the amount of surface-ionized isobaric contaminants by up to four orders of magnitude. After the first successful on-line test at ISOLDE in 2011 the LIST was further improved in terms of efficiency, selectivity, and reliability through several off-line tests at Mainz University and at ISOLDE. In September 2012, the first on-line physics experiments to use the LIST took place at ISOLDE. The measurements of the improved LIST indicate more than a twofold increase in efficiency compared to the LIST of the 2011 run. The suppression of surface-ionize…

Nuclear and High Energy Physics[PHYS.PHYS.PHYS-ACC-PH]Physics [physics]/Physics [physics]/Accelerator Physics [physics.acc-ph]Ion trapchemistry.chemical_element01 natural sciencesIn-source laser spectroscopylaw.inventionFranciumTrap (computing)LISTlawIonization0103 physical sciences010306 general physicsInstrumentationLaser ion sourceLarge Hadron Collider[PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]010308 nuclear & particles physicsChemistryOn-line mass separatorOrders of magnitude (angular velocity)LaserIon sourceIon trapAtomic physics
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The Collinear Resonance Ionization Spectroscopy (CRIS) experimental setup at CERN-ISOLDE

2012

The CRIS setup at CERN-ISOLDE is a laser spectroscopy experiment dedicated to the high-resolution study of the spin, hyperfine structure and isotope shift of radioactive nuclei with low production rates (a few per second). It combines the Doppler-free resolution of the in-flight collinear geometry with the high detection efficiency of resonant ionisation. A recent commissioning campaign has demonstrated a 1% experimental efficiency, and as low as a 0.001% non-resonant ionisation. The current status of the experiment and its recent achievements with beams of francium isotopes are reported. The first identified systematic effects are discussed. publisher: Elsevier articletitle: The Collinear …

Nuclear and High Energy Physics[PHYS.PHYS.PHYS-ACC-PH]Physics [physics]/Physics [physics]/Accelerator Physics [physics.acc-ph]chemistry.chemical_element[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]7. Clean energy01 natural sciencesFranciumIonization0103 physical sciencesPhysics::Atomic PhysicsLaser spectroscopyNuclear Experiment010306 general physicsSpin (physics)SpectroscopyInstrumentationHyperfine structureComputingMilieux_MISCELLANEOUSLarge Hadron ColliderIsotopeRadioactive decay spectroscopy010308 nuclear & particles physicsIon beam purificationIsotope shiftchemistry13. Climate actionPhysics::Accelerator PhysicsHyperfine structureAtomic physicsRadioactive decayNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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