Search results for "LASER SPECTROSCOPY"

showing 10 items of 151 documents

Energy transfer in LH2 of Rhodospirillum Molischianum, studied by subpicosecond spectroscopy and configuration interaction exciton calculations.

2001

Two color transient absorption measurements were performed on a LH2 complex from Rhodospirillum molischianum by using several excitation wavelengths (790, 800, 810, and 830 nm) and probing in the spectral region from 790 to 870 nm at room temperature. The observed energy transfer time of ∼1.0 ps from B800 to B850 at room temperature is longer than the corresponding rates in Rhodopseudomonas acidophila and Rhodobacter sphaeroides. We observed variations (0.9-1.2 ps) of B800-850 energy transfer times at different B800 excitation wavelengths, the fastest time (0.9 ps) was obtained with 800 nm excitation. At 830 nm excitation the energy transfer to the B850 ring takes place within 0.5 ps. The m…

/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energybiologyChemistryExcitonConfiguration interactionbiology.organism_classificationSpectral lineSurfaces Coatings and FilmsRhodobacter sphaeroidesUltrafast laser spectroscopyMaterials ChemistrySDG 7 - Affordable and Clean EnergyPhysical and Theoretical ChemistryAtomic physicsAbsorption (electromagnetic radiation)SpectroscopyExcitation
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Injection and ultrafast regeneration in dye-sensitized solar cells

2014

Injection of an electron from the excited dye molecule to the semiconductor is the initial charge separation step in dye-sensitized solar cells (DSC's). Though the dynamics of the forward injection process has been widely studied, the results reported so far are controversial, especially for complete DSC's. In this work, the electron injection in titanium dioxide (TiO2) films sensitized with ruthenium bipyridyl dyes N3 and N719 was studied both in neat solvent and in a typical iodide/triiodide (I-/I3 -) DSC electrolyte. Transient absorption (TA) spectroscopy was used to monitor both the formation of the oxidized dye and the arrival of injected electrons to the conduction band of TiO2. Emiss…

/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energyta221Analytical chemistrychemistry.chemical_elementElectrolyteNanosecondPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsRutheniumDye-sensitized solar cellchemistry.chemical_compoundGeneral EnergychemistryPicosecondTitanium dioxideUltrafast laser spectroscopySDG 7 - Affordable and Clean EnergyPhysical and Theoretical ChemistryTriiodideta116
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Time-resolved photoisomerization of 1,1′-di-tert-butylstilbene and 1,1′-dicyanostilbene

2016

Abstract Photoisomerization of 1,1′-di-tert-butylstilbene ( 3 ) and 1,1′-dicyanostilbene ( 4 ) is monitored with stationary and broadband transient absorption spectroscopy. The electron affinity of the substituents correlates with the shift of the absorption band. The weak extinction of 3 complicates data interpretation, but comparison with earlier measured 1,1′-dimethylstilbene ( 1 ) and 1,1′-diethylstilbene ( 2 ) helps to assign transient spectra and relaxation paths. For 3 a long-lived perpendicular state P is observed with lifetime τ P  = 134 ps in acetonitrile. For 4 τ P  = 2.1 ps in acetonitrile and 27 ps in n-hexane, the difference indicating a substantial dipole moment (∼3D) of the …

010304 chemical physicsPhotoisomerizationChemistryRelaxation (NMR)Analytical chemistryGeneral Physics and Astronomy010402 general chemistry01 natural sciences0104 chemical sciencesDipolechemistry.chemical_compoundAbsorption bandElectron affinity0103 physical sciencesUltrafast laser spectroscopyPhysical and Theoretical ChemistrySpectroscopyAcetonitrileChemical Physics Letters
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Bowl-shape electron donors with absorptions in the visible range of the solar spectrum and their supramolecular assemblies with C 60

2012

We describe the synthesis, electronic, optical and photophysical properties of a family of three electron-donor bowl-shaped organic molecules that absorb light in the whole range of the visible spectrum (up to 800 nm in one case), and associate C60 in solution with binding constants in the range of 104–102 M−1 as measured from both UV-vis and fluorescence titrations in several solvents. These molecules are π-extended derivatives of tetrathiafulvalene, based on a truxene core to which two or three units of dithiole are covalently attached. The inclusion of the bulky dithiole groups is responsible for their bowl-shape geometry, which allows them to associate with C60, and their electron-donor…

010405 organic chemistrySupramolecular chemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesPhotoexcitationchemistry.chemical_compoundchemistryIntramolecular forceUltrafast laser spectroscopyDensity functional theoryAbsorption (chemistry)TetrathiafulvaleneVisible spectrum
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Regioselective Hydrogenation of a 60-Carbon Nanographene Molecule toward a Circumbiphenyl Core.

2019

Regioselective peripheral hydrogenation of a nanographene molecule with 60 contiguous sp2 carbons provides unprecedented access to peralkylated circumbiphenyl (1). Conversion to the circumbiphenyl core structure was unambiguously validated by MALDI-TOF mass spectrometry, NMR, FT-IR, and Raman spectroscopy. UV–vis absorption spectra and DFT calculations demonstrated the significant change of the optoelectronic properties upon peripheral hydrogenation. Stimulated emission from 1, observed via ultrafast transient absorption measurements, indicates potential as an optical gain material.

Absorption spectroscopyChemistryCommunicationChemistry (all)RegioselectivityGeneral Chemistry010402 general chemistryMass spectrometryPhotochemistryCatalysis; Chemistry (all); Biochemistry; Colloid and Surface Chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCatalysissymbols.namesakeColloid and Surface ChemistryUltrafast laser spectroscopysymbolsMoleculeStimulated emissionRaman spectroscopyJournal of the American Chemical Society
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Opportunities and limitations of in-gas-cell laser spectroscopy of the heaviest elements with RADRIS

2022

International audience; The radiation detection resonance ionization spectroscopy (RADRIS) technique enables laser spectroscopic investigations of the heaviest elements which are produced in atom-at-a-time quantities from fusion-evaporation reactions. To achieve a high efficiency, laser spectroscopy is performed in a buffer-gas environment used to thermalize and stop the high-energy evaporation residues behind the velocity filter SHIP. The required cyclic measurement procedure in combination with the applied filament collection for neutralization as well as confinement of the stopped ions and subsequent pulse-heat desorption constrains the applicability of the technique. Here, some of these…

Actinidesactinideslaser spectroscopygas celltutkimusmenetelmätSuper heavy elements[PHYS.PHYS.PHYS-INS-DET]Physics [physics]/Physics [physics]/Instrumentation and Detectors [physics.ins-det]Laser spectroscopy[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]laserspektroskopiasuper heavy elementsGas cell
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Nitroanilines as Quenchers of Pyrene Fluorescence

2012

The quenching of pyrene and 1‐methylpyrene fluorescence by nitroanilines (NAs), such as 2‐, 3‐, and 4‐nitroaniline (2‐NA, 3‐NA, and 4‐NA, respectively), 4‐methyl‐3‐nitroaniline (4‐M‐3‐NA), 2‐methyl‐4‐nitroaniline (2‐M‐4‐NA), and 4‐methyl‐3,5‐dinitroaniline (4‐M‐3,5‐DNA), are studied in toluene and 1,4‐dioxane. Steady‐state fluorescence data show the higher efficiency of the 4‐NAs as quenchers and fit with a sphere‐of‐action model. This suggests a 4‐NA tendency of being in close proximity to the fluorophore, which could be connected with their high polarity/hyperpolarizability. In addition, emission and excitation spectra evidence the formation of emissive pyrene—NA ground‐state complexes in…

Analytical chemistryHyperpolarizabilityPhotochemistryFluorescenceFluorescence spectroscopyAbsorptionDioxaneschemistry.chemical_compoundFOTOQUIMICAANILINASUltrafast laser spectroscopySinglet statePhysical and Theoretical ChemistryFluorescent DyesAniline CompoundsPyrenesQuenching (fluorescence)ChemistryOtras Ciencias QuímicasCiencias QuímicasFluorescenceAtomic and Molecular Physics and OpticsPIRENODESACTIVACIONEnergy TransferExcited statePyreneCIENCIAS NATURALES Y EXACTASTolueneChemPhysChem
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Transient and stable color centers in pure and Cu-doped LiNbO3

2003

The present work is devoted to investigation of stable and transient color centers that are induced by radiation and temperature in pure and Cu-doped LiNbO 3 single crystals. The transient changes of absorption of the crystals induced by pulsed electron beam (E=0.25 MeV) are studied in 0-5000 ns time range, as well as stable changes of absorption induced by reducing annealing and irradiation with γ-quanta, high energy electrons or fast reactor neutrons.

Annealing (metallurgy)Chemistrybusiness.industryDopingAnalytical chemistryGeneral ChemistryElectronRadiationCondensed Matter PhysicsFerroelectricityOpticsUltrafast laser spectroscopyCathode rayGeneral Materials ScienceIrradiationbusinessCrystal Research and Technology
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Electron Transfer from Organic Aminophenyl Acid Sensitizers to Titanium Dioxide Nanoparticle Films

2009

Electron transfer from three conjugated amino-phenyl acid dyes to titanium and aluminum oxide nanocrystalline films was studied by using transient absorption spectroscopy with sub 20 fs time-resolution over the visible spectral region. All the dyes attached to TiO2 showed long-lived ground state bleach signals indicative of formation of new species. Global analysis of the transient kinetics of the dyes on TiO2 revealed stimulated emission decays of about 40 fs and less than 300 fs assigned to electron injection. The same dyes on Al2O3 substrates displayed long stimulated emission decays (ns) suggesting that electron transfer is blocked in this high band gap semiconductor. For two of the dye…

Band gapConjugated systemPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundElectron transferGeneral EnergychemistryTitanium dioxideUltrafast laser spectroscopyDensity functional theoryStimulated emissionPhysical and Theoretical ChemistrySpectroscopyThe Journal of Physical Chemistry C
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Evidence of a sudden increase in the nuclear size of proton-rich silver-96

2021

Understanding the evolution of the nuclear charge radius is one of the long-standing challenges for nuclear theory. Recently, density functional theory calculations utilizing Fayans functionals have successfully reproduced the charge radii of a variety of exotic isotopes. However, difficulties in the isotope production have hindered testing these models in the immediate region of the nuclear chart below the heaviest self-conjugate doubly-magic nucleus 100Sn, where the near-equal number of protons (Z) and neutrons (N) lead to enhanced neutron-proton pairing. Here, we present an optical excursion into this region by crossing the N = 50 magic neutron number in the silver isotopic chain with th…

CHARGE RADIIEFFICIENCYProtonScienceSYMMETRYNuclear TheoryGeneral Physics and AstronomyIONIZATION SPECTROSCOPY[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologyEffective nuclear chargeArticleNuclear physicsCharge radiusMOMENTS0103 physical sciencesexperimental nuclear physicsNeutronNuclear Physics - ExperimentPhysics::Atomic PhysicsBETA-DECAYExperimental nuclear physics010306 general physicsLASER SPECTROSCOPYNuclear ExperimentPhysicsRESONANCE IONIZATIONisotoopitMultidisciplinaryScience & TechnologyIsotope010308 nuclear & particles physicsQGeneral ChemistryRadiusION-SOURCEMultidisciplinary SciencesTheoretical nuclear physicsNeutron numbertheoretical nuclear physicsScience & Technology - Other TopicsISOTOPESDensity functional theoryydinfysiikka
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