Search results for "Ultrafast"

showing 10 items of 170 documents

Few Cycle Dissipative Soliton Pulses

2006

We find a novel class of stable dissipative solitary waves with discrete velocities and few cycle temporal duration in a composite medium containing active and passive atoms.

PhysicsUltrafast opticsNonlinear optics01 natural sciencesLight scattering010309 opticsOptical pumpingDissipative solitonClassical mechanicsOptical propagationQuantum electrodynamics0103 physical sciencesAtom opticsDissipative system010306 general physicsComputingMilieux_MISCELLANEOUS
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Control of nonlinear instabilities in Bessel beams using shaped longitudinal intensity profiles

2017

International audience; We show that tailored longitudinal intensity shaping of a non-diffracting Bessel beam can strongly reduce four wave mixing induced oscillations and stabilize nonlinear propagation at ablation-level intensities

Physics[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]business.industryUltrafast opticsNonlinear optics01 natural sciencesIntensity (physics)010309 opticsNonlinear systemsymbols.namesakeFour-wave mixingOptics0103 physical sciencesInduced oscillationsBessel beamsymbolsPhysics::Accelerator Physics010306 general physicsbusinessBessel functionConference on Lasers and Electro-Optics
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Laser driven parametric amplification of xuv and soft-x-rays in neutral gases

2010

We present the first theoretical description and also experimental evidence for the amplification of XUV and soft-X-ray radiation by parametric stimulated emission in neutral gases driven by near-IR laser pulses reaching small-signal-gain up to 8000.

Physicsbusiness.industryAstrophysics::High Energy Astrophysical PhenomenaNonlinear opticsRadiationLaserMagnetic fieldlaw.inventionOpticslawExtreme ultravioletUltrafast laser spectroscopyOptoelectronicsStimulated emissionbusinessParametric statistics
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Probing ultrafast thermalization with field-free molecular alignment

2012

International audience; The rotation-translation thermalization of CO2 gas is investigated 500 ps after its preheating by a nonresonant short and intense laser pulse. The temperature of thermalization is optically determined with two additional short laser pulses enabling a field-free molecular alignment process and its probing, respectively. The measurements are performed for various intensities of the preheat pulse, leading to the observation of different temperatures which are in very good agreement with classical molecular dynamics simulations. The results can be regarded as a step towards real-time tracking of ultrafast relaxation pathways in molecular motion.

Physicscollisional dynamics010304 chemical physicsField (physics)ultrafast nonlinear optics[PHYS.PHYS.PHYS-ATOM-PH]Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph][ PHYS.PHYS.PHYS-ATOM-PH ] Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]femtosecond phenomenaRelaxation (NMR)ultrafast relaxationTracking (particle physics)Laser01 natural sciences37.10.Vz 34.50.Ez 42.50.MdAtomic and Molecular Physics and Opticslaw.inventionPulse (physics)Molecular dynamicsThermalisationlaw0103 physical sciencesAtomic physics010306 general physicsUltrashort pulsemolecular alignment
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Acceptor Concentration Dependence of Förster Resonance Energy Transfer Dynamics in Dye–Quantum Dot Complexes

2014

The dynamics of the photoinduced Forster resonance energy transfer (FRET) in a perylene diimide–quantum dot organic–inorganic hybrid system has been investigated by femtosecond time-resolved absorption spectroscopy. The bidentate binding of the dye acceptor molecules to the surface of CdSe/CdS/ZnS multishell quantum dots provides a well-defined dye-QD geometry for which the efficiency of the energy transfer reaction can be easily tuned by the acceptor concentration. In the experiments, the spectral characteristics of the chosen FRET pair facilitate a selective photoexcitation of the quantum dot donor. Moreover, the acceptor related transient absorption change that occurs solely after energy…

Physics::Biological PhysicsAbsorption spectroscopyChemistryCondensed Matter::Mesoscopic Systems and Quantum Hall EffectPhotochemistryAcceptorSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPhotoexcitationCondensed Matter::Materials Sciencechemistry.chemical_compoundGeneral EnergyFörster resonance energy transferQuantum dotChemical physicsUltrafast laser spectroscopyMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryPeryleneThe Journal of Physical Chemistry C
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Analysis of mebendazole binding to its target biomolecule by laser flash photolysis

2016

[EN] Mebendazole (MBZ) and related anticancer benzimidazoles act binding the beta-subunit of Tubulin (TU) before dimerization with alpha-TU with subsequent blocking microtubule formation. Laser flash photolysis (LFP) is a new tool to investigate drug-albumin interactions and to determine binding parameters such as affinity constant or population of binding sites. The aim of this study was to evaluate the interactions between the nonfluorescent mebendazole (MBZ) and its target biomolecule TU using this technique. Before analyzing the MBZ@TU complex it was needed to determine the photophysical properties of MBZ triplet excited state ((3)MBZ*) in different media. Hence, 3MBZ* showed a transien…

PopulationBiophysicsBinding constantElectron donor010402 general chemistryPhotochemistry01 natural sciencesAnticancer drugschemistry.chemical_compoundQUIMICA ORGANICAMebendazole triplet excited stateTubulinUltrafast laser spectroscopyRadiology Nuclear Medicine and imagingeducationchemistry.chemical_classificationeducation.field_of_studyRadiationPhotolysisRadiological and Ultrasound Technology010405 organic chemistryPhosphorescenceLasersPhotodissociationTemperatureLaser flash photolysisElectron acceptorBinding constant0104 chemical sciencesMebendazolechemistryExcited stateFlash photolysisThermodynamicsSpectrophotometry UltravioletProtein Binding
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Fast Photochemistry of Prototypical Phytochromes—A Species vs. Subunit Specific Comparison

2015

Phytochromes are multi-domain red light photosensor proteins, which convert red light photons to biological activity utilizing the multitude of structural and chemical reactions. The steady increase in structural information obtained from various bacteriophytochromes has increased understanding about the functional mechanism of the photochemical processes of the phytochromes. Furthermore, a number of spectroscopic studies have revealed kinetic information about the light-induced reactions. The spectroscopic changes are, however, challenging to connect with the structural changes of the chromophore and the protein environment, as the excited state properties of the chromophores are very sens…

Protein subunitDimertransient absorptionPhotochemistryBiochemistry Genetics and Molecular Biology (miscellaneous)Biochemistrychemistry.chemical_compoundtransient absorption spectroscopyHypothesis and TheoryUltrafast laser spectroscopyMoleculeexcited state dynamicslcsh:QH301-705.5Molecular BiologyProtein secondary structureta114ChemistryPhysicsta1182ChromophoreFluorescencelcsh:Biology (General)Excited statelaser spectroscopyred photosensorsfluorescenceFrontiers in Molecular Biosciences
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Luminescence and transient absorption in ZnWO4 and ZnWO4–Fe crystals

2001

Abstract The transient absorption spectra and relaxation kinetics under pulse electron beam excitation in ZnWO 4 and ZnWO 4 –Fe, as well as luminescence spectra and decay kinetics, were studied. It is shown that a fraction of transient absorption is due to luminescence center excited state. The energy transfer from intrinsic excitations to the defect or impurity states is not efficient. The role of Fe-impurities in the decay process is discussed.

RadiationAbsorption spectroscopyImpurityChemistryExcited stateRelaxation (NMR)Ultrafast laser spectroscopyAtomic physicsLuminescenceAbsorption (electromagnetic radiation)InstrumentationExcitationRadiation Measurements
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Time-resolved optical absorption in YAlO3 crystals

2004

Abstract The present work is devoted to the investigation of transient absorption (TA) induced by a pulsed electron beam (E=250 keV ) in pure and doped YAlO3 (YAP) single crystals. The nature of centers responsible for TA is discussed.

RadiationMaterials sciencebusiness.industryDopingElectronElectron beam irradiationUltrafast laser spectroscopyCathode rayComputer Science::Programming LanguagesOptoelectronicsIrradiationAtomic physicsbusinessAbsorption (electromagnetic radiation)InstrumentationRadiation Measurements
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Self-trapped exciton in Li2GeO3

1997

Abstract Self-trapped excitons (STE) are discovered in Li2GeO3 crystal. The PL band at 2.7 eV with a strong Stoke's shift is excited in the intrinsic absorption range of Li2GeO3 crystal, in which the optical gap is situated at 6 eV. The activation energy of the STE luminescence thermal quenching is not monoenergetic and is situated in the range 40–100 meV. The luminescence is strongly polarized. The decay kinetics can be characterized by τ = 0.9 ms at 45 K. At 5 K it can be approximated by fast (0.6 ms) and slow (4–2.5 ms) components. Decay kinetics is determined by triplet state of STE splits in zero magnetic field. Two different excited triplet states (centers) have the average ODMR param…

Range (particle radiation)ChemistryExcitonBiophysicsGeneral ChemistryCondensed Matter PhysicsBiochemistryAtomic and Molecular Physics and OpticsCrystalExcited stateUltrafast laser spectroscopyTriplet stateAtomic physicsAbsorption (electromagnetic radiation)LuminescenceJournal of Luminescence
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