Search results for "Time Resolved"

showing 10 items of 41 documents

Luminescence properties of nonbridging oxygen hole centers at the silica surface

2009

Abstract Two variants of the surface-nonbridging oxygen hole center, ( Si–O)3Si–O• and ( Si–O)2(H–O)Si–O•, stabilized in porous films of silica nano-particles were investigated by time resolved luminescence excited in the visible and UV spectral range by a tunable laser system. Both defects emit a photoluminescence around 2.0 eV with an excitation spectrum evidencing two maxima at 2.0 and 4.8 eV, this emission decreases by a factor ∼2 on increasing the temperature from 8 up to 290 K. However, the different local structure influences the emission lineshape, the quantum yield and the decay lifetime. Such peculiarities are discussed on the basis of the symmetry properties of these defects.

PhotoluminescenceAnalytical chemistrychemistry.chemical_elementNanoparticleQuantum yieldCondensed Matter PhysicsOxygenMolecular physicsElectronic Optical and Magnetic MaterialschemistryExcited stateMaterials ChemistryCeramics and CompositesDefects Nanoparticles Luminescence Time resolved measurements SilicaLuminescenceExcitationTunable laserJournal of Non-Crystalline Solids
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Luminescence and absorption spectroscopy of Sn-related impurity centers in silica

2006

We report an experimental study on the absorption and luminescence spectra of oxygen deficient point defects in Sn-doped silica. The absorption band at 4.9 eV (B2β band) and the two related photoluminescence bands at ∼4.2 eV (singlet-singlet emission, S1 → S0) and at ∼3.2 eV (triplet-singlet emission, T1 → S0), linked by a thermally activated T1 → S1 inter-system crossing process (ISC), are studied as a function of temperature from 300 to 20 K. This approach allows us to investigate the dynamics properties of the matrix in the surroundings of the point defects and the effects of local disorder on the two relaxation processes from S1: the radiative channel to S0 and the ISC process to T1. We…

PhotoluminescenceOptical fiberLuminescenceAbsorption spectroscopyTime resolved measurementOptical spectroscopy71.55.JvMolecular physicsAbsorptionMaterials ChemistryAbsorption (electromagnetic radiation)SpectroscopyAerogelChemistryRelaxation (NMR)PACS: 78.55.QrSilicaAtmospheric temperature rangeCondensed Matter Physics81.20.FwElectronic Optical and Magnetic MaterialsAbsorption band63.50.+xCeramics and CompositesThermodynamicsDefectAtomic physicsLuminescence
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Attosecond control of dissociative ionization of O2molecules

2011

We demonstrate that dissociative ionization of O(2) can be controlled by the relative delay between an attosecond pulse train (APT) and a copropagating infrared (IR) field. Our experiments reveal a dependence of both the branching ratios between a range of electronic states and the fragment angular distributions on the extreme ultraviolet (XUV) to IR time delay. The observations go beyond adiabatic propagation of dissociative wave packets on IR-induced quasistatic potential energy curves and are understood in terms of an IR-induced coupling between electronic states in the molecular ion.

PhysicsInfraredAtom and Molecular Physics and OpticsWave packetAttosecondAstrophysics::Cosmology and Extragalactic AstrophysicsElectronic structureMolecular physicsPotential energySettore FIS/03 - Fisica Della MateriaAtomic and Molecular Physics and OpticsTime resolved fragmentationAtomic and Molecular PhysicsExtreme ultravioletIonizationPhysics::Atomic and Molecular ClustersAstrophysics::Solar and Stellar AstrophysicsAstrophysics::Earth and Planetary Astrophysicsand OpticsAtomic physicsAdiabatic processAstrophysics::Galaxy AstrophysicsPhysical Review A
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Accessing fast magnetization dynamics by XPEEM: Status and perspectives

2006

Abstract Being already well established as a versatile technique for high-resolution static magnetic domain imaging, X-ray photoemission electron microscopy (XPEEM) is now also capturing the field of time-resolved magnetic investigations. Using appropriate operation modes at synchrotron radiation sources, a time resolution of 10 ps and less can be achieved in recent magnetodynamics studies, giving access even to phenomena involving precessional processes.

PhysicsMagnetization dynamicsPhotoemission electron microscopyMagnetizationNuclear magnetic resonanceField (physics)Magnetic domainTime resolved spectraSynchrotron radiationTime resolutionCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsComputational physicsJournal of Magnetism and Magnetic Materials
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Structural dynamics in F1ATPase during the first reaction cycle of ATP hydrolysis

1991

Abstract The velocity of ATP hydrolysis, catalyzed by purified F 1 ATPase from Micrococcus luteus , was decelerated on decreasing the temperature. At 13′C one reaction cycle is completed after 20 s. Hydrolysis was triggered upon rapid mixing of the enzyme with ATP. During the first reaction cycle, succeeding structural alterations of the F 1 ATPase were traced by time resolved X-ray scattering. The scattering spectra obtained from consecutive intervals of 1 s, revealed the F 1 ATPase to pass a conformational state exhibiting an expanded (6%) molecular shape. The expanded state was observed between 45% and 65% of the time required to complete the reaction cycle. This pointx out a conformatio…

Reaction mechanismProtein ConformationStereochemistryATPaseBiophysicsTime resolved X-ray scatteringBiochemistryMicrococcusCatalysisF1ATPaseHydrolysisMolecular dynamicsAdenosine TriphosphateStructural BiologyATP hydrolysisGeneticsMolecular Biologychemistry.chemical_classificationbiologyHydrolysisX-RaysReaction cycleCell Biologybiology.organism_classificationKineticsProton-Translocating ATPasesEnzymechemistryDynamic structure transitionbiology.proteinMicrococcus luteusFEBS Letters
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Defect-related visible luminescence of silica nanoparticles

2013

The high photon emissivity in the visible spectral range is one of the most relevant phenomena emerging from the reduction of silica down to nanoscale; hence it is promising for the development of optical nanotechnologies (down converter, probes, display). It is well accepted that the origin of this luminescence is related to the high specific surface (~100 m2/g) that favors the formation of optically active defects at the nanosilica surface. With the aim to clarify the role of specific luminescent defects, here we report a detailed study of spectral and decay features by time-resolved photoluminescence spectra under a visible-UV tunable laser excitation. Our study is carried out on differe…

Silica nanoparticlesControlled atmosphereMaterials scienceAnalytical chemistryUv lasersilica nanoparticles time resolved luminesce surface defectssilica nanoparticles time-resolved luminescence surface defects laser irradiation effectsLuminescence spectraIrradiationCondensed Matter PhysicsPhotochemistryLuminescenceBlue band
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Vibrational properties of the surface-nonbridging oxygen in silica nanoparticles

2008

By studying the site-selective luminescence spectra of oxidized silica nanoparticles we identify the electronic and the vibrational lines associated with the surface nonbridging oxygen, $\ensuremath{\equiv}{\text{Si-O}}^{\ifmmode\bullet\else\textbullet\fi{}}$. This defect emits a zero-phonon line inhomogeneously distributed around 2.0 eV with full width at half maximum of 0.04 eV, weakly coupled with the local ${\text{Si-O}}^{\ifmmode\bullet\else\textbullet\fi{}}$ stretching mode whose frequency is measured to be $920\text{ }{\text{cm}}^{\ensuremath{-}1}$. These findings are different from those of the well-characterized defect in the bulk silica thus evidencing structural peculiarities of …

Silica nanoparticlesSurface (mathematics)Full width at half maximumMaterials sciencedefectsnanoparticles luminescence time resolved measurements silicaNanoparticleLuminescence spectraCondensed Matter PhysicsMolecular physicsMolecular electronic transitionElectronic Optical and Magnetic MaterialsNonbridging oxygenLine (formation)Physical Review B
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Time Resolved Photoluminescence Associated with Non Bridging Oxygen Hole Centers in Irradiated Silica

2007

Silica irradiation time resolved luminescence non bridging oxygen hole center
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Self-limiting and complete oxidation of silicon nanostructures produced by laser ablation in water

2016

Oxidized Silicon nanomaterials produced by 1064 nm pulsed laser ablation in deionized water are investigated. High-resolution transmission electron microscopy coupled with energy dispersive X-ray spectroscopy allows to characterize the structural and chemical properties at a sub-nanometric scale. This analysis clarifies that laser ablation induces both self-limiting and complete oxidation processes which produce polycrystalline Si surrounded by a layer of SiO2 and amorphous fully oxidized SiO2, respectively. These nanostructures exhibit a composite luminescence spectrum which is investigated by time-resolved spectroscopy with a tunable laser excitation. The origin of the observed luminescen…

Silicon nanocrystal Silica nanoparticles laser ablation Time resolved phtoluminescence High resolution transmission electron microscopy Silicon Oxidation Quantum Confinment DefectsMaterials scienceLaser ablationPhotoluminescenceSiliconSettore FIS/01 - Fisica SperimentaleAnalytical chemistryGeneral Physics and Astronomychemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAmorphous solidNanomaterialschemistry0210 nano-technologyLuminescenceSpectroscopyTunable laser
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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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