Search results for "Time-resolved"

showing 10 items of 70 documents

Application of time-resolved spectroscopy to concentration measurements in gas mixtures

2001

1296-2147; Concentration measurements using femtosecond Raman Induced Polarization Spectroscopy (RIPS) are performed in binary gas mixtures CO2-N2 and CO2-N2O at room temperature. The principle of these measurements is based on the nonlinear rotational time response of each molecular component of the mixture, The general form of this molecular response is a series of periodic transients with a period related to the rotational constant Be The relative strength of the individual responses allows an accurate determination of the concentration. Two techniques are presented using either two pulses (one pump and one probe) or three pulses (two pumps and one probe). (C) 2001 Academie des sciences/…

DYNAMICSmolecular concentrationMaterials scienceAnalytical chemistryGeneral Physics and Astronomy01 natural sciencesInduced polarizationsymbols.namesakeINDUCED POLARIZATION SPECTROSCOPYfemtosecond laser0103 physical sciencesMOLECULE010306 general physicsSpectroscopyPOPULATIONINTERFERENCE010304 chemical physicsTriatomic moleculeFEMTOSECONDDiatomic moleculeINVERSE RAMAN-SPECTROSCOPYROTATIONAL COHERENCEFemtosecondsymbolsCO2Rotational spectroscopyTime-resolved spectroscopyRaman spectroscopystimulated Raman effect
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Concentration measurements in molecular gas mixtures with a two-pump pulse femtosecond polarization spectroscopy technique

2001

0021-9606; Recently, we have demonstrated the ability of the Raman-induced polarization spectroscopy (RIPS) technique to accurately determine concentration or polarizability anisotropy ratio in low-pressure binary molecular mixtures [E. Hertz, B. Lavorel, O. Faucher, and R. Chaux, J. Chem. Phys. 113, 6629 (2000)]. It has been also pointed out that macroscopic interference, occurring when two revivals associated to different molecules time overlap, can be used to achieve measurements with picosecond time resolution. The applicability of the technique is intrinsically limited to a concentration range where the signals of both molecules are of the same magnitude. In this paper, a two-pump puls…

INTERFERENCEDYNAMICS010304 chemical physicsChemistrybusiness.industryGeneral Physics and AstronomyPulse sequenceTRANSITIONSPolarization (waves)01 natural sciencesMolecular physicsROTATIONAL COHERENCEOpticsPolarizabilityPicosecond0103 physical sciencesFemtosecondCO2Physical and Theoretical ChemistryTime-resolved spectroscopy010306 general physicsSpectroscopyAnisotropybusinessPOPULATION
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Photoluminescence study of terbium-exchanged ultrastable Y zeolites: Number of species, photoluminescence decays and decay-associated spectra

2008

Terbium-exchanged ultrastable Y (USY) zeolites were investigated by using time-resolved photoluminescence spectroscopy techniques and methods. To determine the distribution of terbium species in USY zeolites together with their photoluminescence properties, several analysis methods for the time-resolved luminescence spectra were used such as the area normalization of time-resolved photoluminescence spectra, singular value decomposition, global nonlinear least squares, and the maximum entropy. Except for a questionable long lifetime, small contribution of a terbium species with lifetime of 1.9¿2.1 ms, all the experimental and analysis results converged to a two terbium species distribution w…

LanthanidePhotoluminescenceSilylationAnalytical chemistryFísicaGeneral Physics and Astronomychemistry.chemical_elementTerbiumQuímica analíticaCiència dels materialsSpectral linechemistryNon-linear least squaresInstitut für ChemieTime-resolved spectroscopySpectroscopy
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Nano-Oxides produced by ns laser ablation in liquids

2014

Laser ablation in liquids was successfully applied to produce nanosized oxides from Si, Ti and Zn targets. The obtained colloidal solutions of nanoparticles were investigated by complementary techniques: AFM, IR and Raman spectroscopies; optical absorption and time resolved photoluminescence. The results demonstrate the production of SiO2, TiO2 and ZnO. The absorption and emission properties of these material have been also investigated and appear to be promising for optical applications.

Lases ablation nanosized oxides IR spectroscopy Atomic Force Microscopy time-resolved luminescence
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Mixed complexes of alkaline earth uranyl cabonates: A laser-induced time-resolved fluorescence spectroscopic study

2008

The interaction of the alkaline earth ions Mg2+, Sr2+ and Ba2+ with the uranyl tricarbonate complex has been studied by time resolved laser-induced fluorescence spectroscopy. In contrast to the non-luminescent uranyl tricarbonate complex the formed products show slight luminescence properties. These have been used to determine the stoichiometry and complex stabilities of the formed compounds. As the alkaline earth elements are located in an outer shell of the complex the influence of the type of the alkaline earth element on the stability constant is not very drastic. Therefore all obtained data were averaged in order to derive an common stability constant for the described complexes. These…

LuminescenceLightAnalytical chemistryCarbonateschemistry.chemical_elementFluorescence spectroscopyAnalytical ChemistryPhosphatesuraniumchemistry.chemical_compoundAlkaline earth elementscarbonatecomplex formationluminescenceMagnesiumInstrumentationSpectroscopyIonsAlkaline earth metalModels StatisticalTemperatureBariumHydrogen-Ion ConcentrationUranylAtomic and Molecular Physics and OpticsCarbonSpectrometry FluorescencechemistryStability constants of complexesBariumStrontiumUraniumTime-resolved spectroscopyLuminescenceStoichiometry
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Structural and luminescence properties of amorphous SiO2 nanoparticles

2011

We report an experimental study on the photoluminescence band peaked at 2.7 eV (blue band) induced by thermal treatments in nanometric amorphous SiO 2. In particular the emission dependence on the nanometric particles size as a function of their mean diameter from 7 nm up to 40 nm is investigated. We found that the emission amplitude increases on decreasing the particle diameter, showing a strong correlation between the blue band and the nanometric nature of the particles. By Raman spectroscopy measurements it is evidenced that the SiO2 nanoparticles matrix is significantly affected by the reduction of size. Basing on the shell-like model, these findings are interpreted assuming that the de…

Materials Chemistry2506 Metals and AlloysPhotoluminescenceMaterials scienceShell (structure)Analytical chemistryNanoparticleCeramics and CompositeSilica nanoparticleCondensed Matter PhysicMolecular physicssymbols.namesakeMaterials ChemistryPoint-defectRamannanoparticelle di silice difetti di punto fotoluminescenzaElectronic Optical and Magnetic MaterialSettore FIS/01 - Fisica SperimentaleTime-resolved luminescenceCondensed Matter PhysicsCrystallographic defectElectronic Optical and Magnetic MaterialsAmorphous solidCeramics and CompositessymbolsParticle sizeRaman spectroscopyLuminescence
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Wide range excitation of visible luminescence in nanosilica

2010

The visible luminescence of nanometer-sized silica particles (7 nm mean diameter) was investigated using time resolved spectroscopy. This luminescence is characterized by a wide excitation in the visible and ultraviolet range. The emission spectrum is centred at 2.72 eV with a full width at half maximum of 0.70 eV when excited above 3.5 eV, whereas it progressively empties on the high energy side when excited below 3.5 eV. Moreover, the lifetime falls in the ns timescale and decreases on increasing the emission energy. These features are due to the exceptionally broad inhomogeneous distribution of the emitting centres peculiar to the silica nanoparticles. © 2010 Elsevier B.V. All rights res…

Materials Chemistry2506 Metals and AlloysRange (particle radiation)PhotoluminescenceMaterials scienceoptical down conversionChemistry (all)General ChemistrynanosilicaCondensed Matter PhysicCondensed Matter PhysicsA. NanostructureD. Optical propertieFull width at half maximumC. Point defectExcited stateMaterials ChemistryluminescenceSpontaneous emissionEmission spectrumAtomic physicsTime-resolved spectroscopyE. LuminescenceLuminescence
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High-Resolution Spectroscopy in Fast Atomic Beams

1977

Narrow optical resonances have been observed in fast beams of Na and Cs atoms, obtained from ion beams by charge-transfer collisions with Na, K, or Cs. Corresponding to the narrowing of the velocity distribution, occurring by acceleration, the Doppler width along the beam direction is considerably reduced [1, 2].

Materials scienceAnalytical chemistryInstrumental chemistryIonAccelerationsymbols.namesakesymbolsPhysics::Accelerator PhysicsLaser-induced breakdown spectroscopySoft X-ray emission spectroscopyTime-resolved spectroscopyAtomic physicsSpectroscopyDoppler effect
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Study of the defects in La3Ta0.5Ga5.5O14 single crystals

2016

Abstract Defects that are formed during crystal growth pose a serious obstacle for potential application of La 3 Ga 5.5 Ta 0.5 O 14 (LGT) as a laser or piezoelectric crystal. We have performed the study of the defects origin in LGT crystals grown in different atmospheres using optical, EPR and time-resolved luminescence characterization methods. The absorption bands detected in the transparency region at 290, 360 and 490 nm ( T =300 K) demonstrate different dependence on crystal annealing in vacuum and air. EPR analysis demonstrated that the defects responsible for these bands are non-paramagnetic. X-ray irradiation results in hole trapping by oxygen ions thus forming O − centers perturbed …

Materials scienceAnnealing (metallurgy)BiophysicsMineralogyCrystal growth02 engineering and technologyCrystal structure01 natural sciencesBiochemistrylaw.inventionCrystallaw0103 physical scienceslanthanum-gallium tantalateElectron paramagnetic resonanceSpectroscopyabsorption bandsdefects010302 applied physicstime-resolved luminescenceGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and OpticsCrystallographyAbsorption bandEPRpiezoelectric0210 nano-technologyLuminescenceJournal of Luminescence
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Formation and Growth of Pd Nanoparticles Inside a Highly Cross-Linked Polystyrene Support: Role of the Reducing Agent

2014

Simultaneous time-resolved SAXS and XANES techniques were employed to follow in situ the formation of Pd nanoparticles in a porous polystyrene support, using palladium acetate as a precursor and gaseous H2 or CO as reducing agents. These results, in conjunction with data obtained by diffuse reflectance UV–vis and DRIFT spectroscopy and TEM measurements, allowed unraveling of the different roles played by gaseous H2 and CO in the formation of the Pd nanoparticles. In particular, it was found that the reducing agent affects (i) the reduction rate (which is faster in the presence of CO) and (ii) the properties of the hosted nanoparticles, in terms of size (bigger with CO), morphology (spherica…

Materials scienceExtended X-ray absorption fine structureReducing agentSmall-angle X-ray scatteringchemistry.chemical_elementNanoparticlePd nanoparticles; SAXS; EXAFSSAXSXANESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistry.chemical_compoundEXAFSGeneral EnergyPd nanoparticleschemistryChemical engineeringPalladium nanoparticles time-resolved X-ray Absorption Spectroscopy Small Angle X-ray Spectroscopy Transmission Electron MicroscopyDiffuse reflectionPolystyrenePhysical and Theoretical ChemistryPalladium
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