Search results for " laser spectroscopy"

showing 10 items of 113 documents

High-resolution laser system for the S3-Low Energy Branch

2022

International audience; In this paper we present the first high-resolution laser spectroscopy results obtained at the GISELE laser laboratory of the GANIL-SPIRAL2 facility, in preparation for the first experiments with the S$^3$-Low Energy Branch. Studies of neutron-deficient radioactive isotopes of erbium and tin represent the first physics cases to be studied at S$^3$. The measured isotope-shift and hyperfine structure data are presented for stable isotopes of these elements. The erbium isotopes were studied using the $4f^{12}6s^2$$^3H_6 \rightarrow 4f^{12}(^3 H)6s6p$$J = 5$ atomic transition (415 nm) and the tin isotopes were studied by the $5s^25p^2 (^3P_0) \rightarrow 5s^25p6s (^3P_1)$…

Resonance ionization laser spectroscopyNuclear and High Energy PhysicsIsotope shiftAtomic Physics (physics.atom-ph)FOS: Physical sciencesHyperfine structureNuclear Experiment (nucl-ex)[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]Nuclear ground state propertiesNuclear ExperimentInstrumentation[PHYS.PHYS.PHYS-GEN-PH]Physics [physics]/Physics [physics]/General Physics [physics.gen-ph]Physics - Atomic Physics
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The origin of slow electron recombination processes in dye-sensitized solar cells with alumina barrier coatings

2004

We investigate the effect of a thin alumina coating of nanocrystalline TiO2 films on recombination dynamics of dye-sensitized solar cells. Both coated and uncoated cells were measured by a combination of techniques: transient absorption spectroscopy, electrochemical impedance spectroscopy, and open-circuit voltage decay. It is found that the alumina barrier reduces the recombination of photoinjected electrons to both dye cations and the oxidized redox couple. It is proposed that this observed retardation can be attributed primarily to two effects: almost complete passivation of surface trap states in TiO2 that are able to inject electrons to acceptor species, and slowing down by a factor of…

Solar cellsCharge injectionPassivationAbsorption spectroscopyIon recombinationThin filmsAluminaAnalytical chemistryGeneral Physics and AstronomyPhotochemistryTime resolved spectraTitanium compounds ; Alumina ; Nanostructured materials ; Semiconductor materials ; Thin films ; Solar cells ; Ion recombination ; Dyes ; Charge exchange ; Charge transfer states ; Charge injection ; Electrochemical impedance spectroscopy ; Time resolved spectraSemiconductor materials:FÍSICA [UNESCO]Ultrafast laser spectroscopyCharge exchangeThin filmSpectroscopyDyesQCChemistryUNESCO::FÍSICANanostructured materialsAcceptorDielectric spectroscopyDye-sensitized solar cellTACharge transfer statesTitanium compoundsElectrochemical impedance spectroscopy
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Do fluorescence and transient absorption probe the same intramolecular charge transfer state of 4-(dimethylamino)benzonitrile?

2009

International audience; We present here the results of time-resolved absorption and emission experiments for 4-(dimethylamino)benzonitrile in solution, which suggest that the fluorescent intramolecular charge transfer (ICT) state may differ from the twisted ICT (TICT) state observed in transient absorption.

Time Factorstime resolved spectraGeneral Physics and Astronomyvisible spectra010402 general chemistryPhotochemistry01 natural sciencesTime resolved spectraSpectral lineFluorescencechemistry.chemical_compoundspectrochemical analysisOrganic compoundsUltrafast laser spectroscopyNitrilesCharge exchangePhysical and Theoretical ChemistryVisible spectra:FÍSICA::Química física [UNESCO]Fluorescent DyesSpectrochemical analysis010405 organic chemistryChemistrycharge exchangeFluorescenceUNESCO::FÍSICA::Química física0104 chemical sciences3. Good health[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryBenzonitrileIntramolecular forceCharge exchange ; Fluorescence ; Organic compounds ; Spectrochemical analysis ; Time resolved spectra ; Visible spectraAbsorption (chemistry)Time-resolved spectroscopyLuminescenceorganic compoundsThe Journal of chemical physics
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Ultrafast excitation dynamics of low energy pigments in reconstituted peripheral light-harvesting complexes of photosystem I

2000

AbstractUltrafast dynamics of a reconstituted Lhca4 subunit from the peripheral LHCI-730 antenna of photosystem I of higher plants were probed by femtosecond absorption spectroscopy at 77 K. Intramonomeric energy transfer from chlorophyll (Chl) b to Chl a and energy equilibration between Chl a molecules observed on the subpicosecond time scale are largely similar to subpicosecond energy equilibration processes within LHCII monomers. However, a 5 ps equilibration process in Lhca4 involves unique low energy Chls in LHCI absorbing at 705 nm. These pigments localize the excitation both in the Lhca4 subunit and in LHCI-730 heterodimers. An additional 30–50 ps equilibration process involving red …

Time-resolved spectroscopyPhotosystem I0106 biological sciencesAbsorption spectroscopyPhotosynthetic Reaction Center Complex ProteinsLight-Harvesting Protein ComplexesBiophysicsPhotochemistryPhotosystem I01 natural sciences7. Clean energyBiochemistryFluorescence spectroscopyLight-harvesting complexExcitation energy transfer03 medical and health scienceschemistry.chemical_compoundStructural BiologyUltrafast laser spectroscopyGeneticsMolecular BiologyPlant Proteins030304 developmental biology0303 health sciencesPhotosystem I Protein ComplexSpectrophotometry AtomicPigments BiologicalCell BiologyPlantsLHCI-730 heterodimerEnergy TransferchemistryAntennaChlorophyllPicosecondChlorophyll Binding ProteinsLight-harvesting complexTime-resolved spectroscopyDimerization010606 plant biology & botanyFEBS Letters
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Subpicosecond Laser Spectroscopy of Blue-Light-Induced Absorption in KNbO3 and LiNbO3

2000

Pulses of 427-nm light from am amplified Ti:sapphire frequency-doubled laser are absorbed in two-photon band-gap excitations of KNbO3 and LiNbO3. Induced absorption spectra measured in the visible and recently extended in the infrared have been recorded as a function of delay from 0 to 250 ps after two-photon blue excitation. Samples include stoichiometric as well as congruent LiNbO3. Comparison is made to transient absorption in the nanosecond and longer time range induced by electron pulses of~10 ns width and 270 keV energy. Parts of the absorption can be attributed to bound and free polarons, including the intrinsic electron polaron.

Tunable diode laser absorption spectroscopyMaterials scienceAbsorption spectroscopylawInfraredUltrafast laser spectroscopyNanosecondAtomic physicsSpectroscopyAbsorption (electromagnetic radiation)Laserlaw.invention
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Collinear laser spectroscopy of ZrII

2003

A new technique involving collinear laser spectroscopy of ion bunches has been used to study the radio-isotopes 87,87m,88,89,89m Zr.

X-ray laserMaterials scienceFar-infrared laserUltrafast laser spectroscopyLaser-induced breakdown spectroscopyTime-resolved spectroscopyAtomic physicsSpectroscopyCoherent spectroscopyIon
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Energy transfer to xanthene dyes in dansylated POPAM dendrimers

2011

Abstract Excitation energy transfer (EET) in host–guest complexes of dansylated POPAM dendrimers and xanthene dyes have been studied by transient absorption spectroscopy. EET from dansyl periphery to guests: rose bengal, eosin, or fluorescein, showed non-exponential behaviour as a result of distribution of donor–acceptor distances. Time constants range from 100 fs to 8 ps, independent of the dye and the dendrimer generation. Experiments suggested that in dendrimers binding more than one guest, EET among the guests becomes effective. Guest–host and guest–guest interactions induce non-radiative relaxation channels making excitation decays of the guests clearly faster in complexes than in solu…

XantheneEosinRelaxation (NMR)General Physics and AstronomyPhotochemistrychemistry.chemical_compoundchemistryDendrimerUltrafast laser spectroscopyRose bengalPhysical and Theoretical ChemistrySpectroscopyta116ExcitationChemical Physics Letters
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Excitation energy transfer in isolated chlorosomes from Chloroflexus aurantiacus

2009

Abstract Chlorosomes from green photosynthetic bacteria Chloroflexus aurantiacus have been studied by time-resolved femtosecond transient absorption spectroscopy. The fastest kinetics of 200–300 fs resolved, was interpreted to stem for intra-chlorosomal excitation energy transfer. Energy transfer from the antenna to the baseplate appeared as a major 9.2 ps rise component detected at the baseplate probe wavelength. Excitation energy transfer rates were evaluated for a model chlorosome. Calculated rod to rod, and rods to baseplate rate constants of 200–400 fs and 10–20 ps, respectively, are in accord with the experimental results.

biologyChemistryChloroflexus aurantiacusAnalytical chemistryGeneral Physics and AstronomyChlorosomebiology.organism_classificationMolecular physicsRodFemtosecondUltrafast laser spectroscopyPhotosynthetic bacteriaPhysical and Theoretical ChemistrySpectroscopyExcitationChemical Physics Letters
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Excitation Energy Transfer in Isolated Chlorosomes from Chlorobaculum tepidum and Prosthecochloris aestuarii

2012

Excitation energy transfer in chlorosomes from photosynthetic green sulfur bacteria, Chlorobaculum (Cba.) tepidum and Prosthecochloris (Pst.) aestuarii, have been studied at room temperature by time-resolved femtosecond transient absorption spectroscopy. Bleach rise times from 117 to 270 fs resolved for both chlorosomes reflect extremely efficient intrachlorosomal energy transfer. Bleach relaxation times, from 1 to 3 ps and 25 to 35 ps, probed at 758 nm were tentatively assigned to intrachlorosomal energy transfer based on amplitude changes of the global fits and model calculations. The anisotropy decay constant of about 1 ps resolved at 807 nm probe wavelength for the chlorosomes from Chlo…

biologyChemistryChloroflexus aurantiacusRelaxation (NMR)ChlorosomeGeneral Medicinebiology.organism_classificationPhotochemistryBiochemistryChemical physicsGreen sulfur bacteriaUltrafast laser spectroscopyFemtosecondPhysical and Theoretical ChemistrySpectroscopyExcitationPhotochemistry and Photobiology
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Effects of ligand substitution on the excited state dynamics of the Ru(dcbpy)(CO)2I2 complex

2003

Abstract Spectroscopic evidence suggest [PCCP 3 (2001) 1992] that illumination with visible light of the [trans-I-Ru(dcbpy)(CO)2I2] (dcbpy= 4,4′-dicarboxy-2,2′-bipyridine) complex in solution induces dissociation of a CO group followed by reorganization of the ligands and attachment of a solvent molecule. In the present study, we report results on excited state dynamics of this ruthenium complex and its photoproduct. Femtosecond transient absorption measurements reveal dominance of excited state absorption of the reactant and the photoproduct [cis-I-Ru(dcbpy)(CO)(Sol)I2] (Sol=ethanol or acetonitrile) in the visible spectral region. The time-resolved measurements for the reactant at 77 K ind…

chemistryExcited stateUltrafast laser spectroscopyGeneral Physics and Astronomychemistry.chemical_elementMoleculeZINDOPhysical and Theoretical ChemistryTriplet stateGround statePhotochemistryDissociation (chemistry)RutheniumChemical Physics
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