Search results for "Time-resolved"

showing 10 items of 70 documents

Luminescence properties of KNbO3 crystals

1997

Thermostimulated luminescence, X-ray-induced luminescence, photostimulated luminescence as well as the time-resolved luminescence and absorption after pulsed electron beam irradiation were studied in KNbO3 crystals at 80–400 K. A correlation between defects causing the luminescence and blue-light-induced IR absorption effects supressing the second harmonic generation efficiency in KNbO3 is discussed.

Materials scienceIr absorptionOptically stimulated luminescencebusiness.industryPhotostimulated luminescenceBiophysicsSecond-harmonic generationGeneral ChemistryCondensed Matter PhysicsBiochemistryAtomic and Molecular Physics and OpticsElectron beam irradiationOptoelectronicsTime-resolved spectroscopyLuminescencebusinessAbsorption (electromagnetic radiation)Journal of Luminescence
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Selective excitation of up-conversion luminescence by Yb3+–Er3+ energy transfer in glass and crystalline phase of oxyfluoride glass ceramics

2010

Up-conversion luminescence of oxyfluoride glass and glass ceramics containing LaF3 crystallites doped with Yb 3+ and Er 3+ was investigated at low temperature. Excitation of Yb 3+ in the IR region revealed the fast and the slow components of Er 3+ up-conversion luminescence originating from both glass and crystalline phases. The temporal differences of the both kinds of the luminescence allowed reconstructing the excitation spectra of the up-conversion luminescence related to the glass and crystalline phases in the glass ceramics. 2010 Elsevier B.V. All rights reserved.

Materials scienceOrganic ChemistryDopingAnalytical chemistryAtomic and Molecular Physics and OpticsPhoton upconversionElectronic Optical and Magnetic MaterialsInorganic Chemistryvisual_artPhase (matter)visual_art.visual_art_mediumCeramicCrystalliteElectrical and Electronic EngineeringPhysical and Theoretical ChemistryTime-resolved spectroscopyLuminescenceSpectroscopyExcitationOptical Materials
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Time-resolved cathodoluminescence spectroscopy of YAG and YAG:Ce3+ phosphors

2019

Abstract The phosphor powders, both undoped and Ce3+ doped with different concentration Y3Al5O12 (YAG), were synthesized by the solid-state reaction method with addition of BaF2 flux. SEM and XRD characterization of the samples were performed. The spectral and luminescence decay kinetic characteristics under the electron beam irradiation with nano- and picoseconds pulse duration and the electron energies of 250 keV and 55 keV were studied, respectively. Two bands in the cathodoluminescence spectrum of YAG:Ce3+ phosphors were observed with maxima at 2.19 ± 0.05 and 2.4 eV. The intensity ratio of these two bands depends on the electron energy and the duration of the excitation pulse. Instead,…

Materials scienceOrganic ChemistryDopingAnalytical chemistrychemistry.chemical_elementPulse durationCathodoluminescencePhosphor02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsInorganic ChemistryCeriumchemistryElectrical and Electronic EngineeringPhysical and Theoretical ChemistryTime-resolved spectroscopy0210 nano-technologyLuminescenceSpectroscopySpectroscopyOptical Materials
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Differentiation of natural and synthetic gem-quality diamonds by luminescence properties

2003

Abstract Laser-excited time-resolved and UV-excited static photoluminescence (PL) as well as cathodoluminescence (CL) techniques were applied to identify the origin of diamonds. Samples represented natural faced and rough diamonds from diamond market and different kimberlites as well as the most common high pressure–high temperature (HPHT) and as-grown synthetic diamonds. The time-resolved PL spectra of natural and synthetic diamonds display clear mutual differences. The static PL and CL spectra of natural diamonds revealed emission bands caused by complex nitrogen–vacancy (N–V)-aggregates whereas the bands of synthetic diamonds reflect simple N–V-aggregates and nickel-containing defects. T…

Materials sciencePhotoluminescenceSynthetic diamondOrganic ChemistryAnalytical chemistryDiamondMineralogyCathodoluminescenceengineering.materialCrystallographic defectAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic Materialslaw.inventionInorganic ChemistrylawengineeringElectrical and Electronic EngineeringPhysical and Theoretical ChemistryTime-resolved spectroscopyLuminescenceKimberliteSpectroscopyOptical Materials
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Transient photoresponse and incident power dependence of high-efficiency germanium quantum dot photodetectors

2012

We report a systematic study of time-resolved and power-dependent photoresponse in high-efficiency germanium quantum dot photodetectors (Ge-QD PDs), with internal quantum efficiencies greater than 100 over a broad wavelength, reverse bias, and incident power range. Turn-on and turn-off response times (τ on and τ off) are shown to depend on series resistance, bias, optical power, and thickness (W QD) of the Ge-QD layer, with measured τ off values down to ∼40 ns. Two different photoconduction regimes are observed at low and high reverse bias, with a transition around -3 V. A transient current overshoot phenomenon is also observed, which depends on bias and illumination power. © 2012 American …

Materials sciencePhotoresponseReverse biaGeneral Physics and Astronomychemistry.chemical_elementPhotodetectorGermaniumOptical powerPhotoconductionTime-resolvedSettore ING-INF/01 - ElettronicaSeries resistanceOpticsElectrical resistance and conductancePhotodetectorOptical powerEquivalent series resistanceSystematic studybusiness.industryPhotoconductivityInternal quantum efficiencyQuantum-dot photodetectorPhotonWavelengthSemiconductor quantum dots GermaniumchemistryQuantum dotTransient current Electric resistanceOptoelectronicsIncident powerbusiness
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Luminescent silicon nanocrystals produced by near-infrared nanosecond pulsed laser ablation in water

2014

Abstract We report the investigation of luminescent nanoparticles produced by ns pulsed Nd:YAG laser ablation of silicon in water. Combined characterization by AFM and IR techniques proves that these nanoparticles have a mean size of ∼3 nm and a core–shell structure consisting of a Si-nanocrystal surrounded by an oxide layer. Time resolved luminescence spectra evidence visible and UV emissions; a band around 1.9 eV originates from Si-nanocrystals, while two bands centered at 2.7 eV and 4.4 eV are associated with oxygen deficient centers in the SiO 2 shell.

Materials scienceSiliconCore–shellmedicine.medical_treatmentOxideAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_elementNanoparticleSpectral lineAtomic force microscopychemistry.chemical_compoundmedicineSi nanocrystalLaser ablationLaser ablation;Si nanocrystal;Silica;Core–shell;Time-resolved luminescence;Atomic force microscopy;Micro-Raman;IR absorptionNear-infrared spectroscopyTime-resolved luminescenceSilicaSurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsAblationLaser ablationSurfaces Coatings and FilmsMicro-RamanchemistryLuminescenceIR absorption
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Visible luminescence peculiar to sintered silica nanoparticles: Spectral and decay properties

2015

We report that the sintering at 1000 degrees C of silica nanoparticles (an average diameter of 14 nm) produces a transparent sample that exhibits a bright visible emission under UV excitation. The use of time resolved luminescence spectroscopy and a tunable laser source allows us to single out three contributions centered at 1.96 eV, 2.41 eV and 3.43 eV. The excitation spectra of these emissions evidence bell shaped bands consistent with transitions between localized defects' states. For each emission we study the intensity and the lifetime in the temperature range from 300 K down to 10 K, thus evidencing the competition between radiative and non-radiative processes in the optical cycle of …

Materials scienceSintering Silica nanoparticles Time-resolved Luminescence Defect stateBiophysicsAnalytical chemistryNanoparticleSinteringGeneral ChemistryAtmospheric temperature rangeCondensed Matter PhysicsBiochemistryMolecular physicsAtomic and Molecular Physics and OpticsRadiative transferLuminescenceSpectroscopyTunable laserExcitation
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Femtosecond Raman time-resolved molecular spectroscopy

2004

Abstract The applicability of several femtosecond time resolved non-linear coherent techniques such as Raman induced polarization spectroscopy (RIPS), degenerate four-wave mixing (DFWM) and coherent anti-Stokes Raman spectroscopy (CARS) for molecular spectroscopy is presented. All methods rely on the initial coherent excitation of molecular states producing wavepackets, whose time evolution is then measured. In the case of RIPS and DFWM only pure rotational transitions are involved, whereas in CARS vibrational states can be excited. First the methodology of concentration and temperature measurements using RIPS in gas mixtures involving N2, CO2, O2, and N2O is shown. In addition some applica…

Materials sciencebusiness.industryGeneral EngineeringTime evolutionEnergy Engineering and Power TechnologyMolecular physicssymbols.namesakeOpticsExcited stateFemtosecondsymbolsCoherent anti-Stokes Raman spectroscopyTime-resolved spectroscopyRaman spectroscopybusinessSpectroscopyExcitationComptes Rendus Physique
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Characterization of used mineral oil condition by spectroscopic techniques

2004

Optical absorption, fluorescence, and quantitative 13C NMR spectroscopy have been used to study the degradation of mineral gearbox oil. Samples of used oil were collected from field service. Measured absorption, fluorescence, and quantitative 13C NMR spectra of used oils show characteristic changes from the spectra of a fresh oil sample. A clearly observable, approximately 20-nm blueshift of the fluorescence emission occurs during the early stages of oil use and correlates with changes in intensity of some specific 13C NMR resonance lines. These changes correlate with oil age because of the connection between the blueshift and breaking of the larger conjugated hydrocarbons of oil as a resul…

Materials sciencebusiness.industryMaterials Science (miscellaneous)Analytical chemistryCarbon-13 NMRFluorescenceIndustrial and Manufacturing EngineeringFluorescence spectroscopyBlueshiftOpticsNuclear magnetic resonancemedicinesense organsBusiness and International ManagementTime-resolved spectroscopybusinessSpectroscopyMineral oilAbsorption (electromagnetic radiation)medicine.drugApplied Optics
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Laser-induced time-resolved luminescence in analysis of rare earth elements in apatite and calcite

2021

Laser-induced time-resolved luminescence was used to study rare earth element (REE) containing natural apatite and calcite minerals. The luminescence from 400 nm to 700 nm in the minerals was analyzed with excitation ranges 210–340 nm and 405–535 nm. As an outcome, several useful excitation wavelengths to detect one or more REE from apatite and calcite are reported. The feasibility of selected excitations in e.g. avoiding the disturbance of intense Mn2+ luminescence band, results was demonstrated with a non-gated detector. peerReviewed

Materials sciencespektroskopiaBiophysicsAnalytical chemistryrare earth elements02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryApatitetime-resolved spectroscopylaw.inventionchemistry.chemical_compoundlawkalsiittimineraalitalkuaineanalyysiCalciteRare-earth elementluminesenssiGeneral Chemistrymineralsharvinaiset maametallit021001 nanoscience & nanotechnologyCondensed Matter PhysicsLaserAtomic and Molecular Physics and Optics0104 chemical sciencesWavelengthapatiittichemistryvisual_artapatiteTime resolved luminescencevisual_art.visual_art_mediumlaser-induced luminescence0210 nano-technologyLuminescencecalciteExcitation
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