Search results for "ultrafast"

showing 10 items of 170 documents

X‐ray and pulsed electron beam excited luminescence and optical absorption in KTaO 3 crystals

2005

Pulsed electron beam excited time-resolved transient absorption and luminescence have been studied in nominally pure and Li-doped KTaO3 single crystals. It is found that under electron beam excitation in nominally pure KTaO3 the absorption bands peaks at ∼0.8 eV, ∼1.1 eV and 1.7 eV whereas in KTaO3:Li at ∼1.1 eV and ∼1.7 eV. The transient absorption decay varies over the spectrum thus revealing several short-lived centers. The main luminescence peak is centred at ∼2.7 eV in all KTaO3 specimens. Luminescence decay kinetics observed for the two bands slightly differ indicating different kinds of excited states are involved. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)

PhotoluminescenceAbsorption spectroscopyChemistryExcited stateUltrafast laser spectroscopyX-rayEmission spectrumAtomic physicsLuminescenceAbsorption (electromagnetic radiation)physica status solidi (c)
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Ultrafast Relaxation Dynamics of Osmium−Polypyridine Complexes in Solution

2013

We present steady-state absorption and emission spectroscopy and femtosecond broadband photoluminescence up-conversion spectroscopy studies of the electronic relaxation of Os(dmbp)(3) (Os1) and Os(bpy)(2)(dpp) (Os2) in ethanol, where dmbp is 4,4'-dimethyl-2,2'-biypridine, bpy is 2,2'-biypridine, and dpp is 2,3-dipyridyl pyrazine. In both cases, the steady-state phosphorescence is due to the lowest (MLCT)-M-3 state, whose quantum yield we estimate to be <= 5.0 x 10(-3). For Os1, the steady-state phosphorescence lifetime is 25 ns. In both complexes, the photoluminescence excitation spectra map the absorption spectrum, pointing to an excitation wavelength-independent quantum yield. The ultrafa…

PhotoluminescenceAbsorption spectroscopyChemistryQuantum yieldPhotochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyIntersystem crossingPhotoluminescence excitationSinglet statePhysical and Theoretical ChemistryTriplet statePhosphorescenceultrafast metal complex fluorescence upconversion osmium
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Carbon Nanodots: A Review—From the Current Understanding of the Fundamental Photophysics to the Full Control of the Optical Response

2018

Carbon dots (CDs) are an emerging family of nanosystems displaying a range of fascinating properties. Broadly speaking, they can be described as small, surface-functionalized carbonaceous nanoparticles characterized by an intense and tunable fluorescence, a marked sensitivity to the environment and a range of interesting photochemical properties. CDs are currently the subject of very intense research, motivated by their possible applications in many fields, including bioimaging, solar energy harvesting, nanosensing, light-emitting devices and photocatalyis. This review covers the latest advancements in the field of CDs, with a focus on the fundamental understanding of their key photophysica…

PhotoluminescenceMaterials science530 PhysicsultrafastphotophysicNanoparticleNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesElectronic stateslcsh:QD241-441lcsh:Organic chemistryCarbon nanodotscarbon dots540 Chemistryfemtosecondcarbon dotphotophysicsphotochemistrynanocarbonSettore FIS/01 - Fisica SperimentaleGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciencesSolar energy harvestingFemtosecondfluorescence0210 nano-technologyUltrashort pulse
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Effect of Halogen Ions on the Photocycle of Fluorescent Carbon Nanodots

2019

Carbon dots (C-dots) are well-known for their strong sensitivity to the environment, which reflects on intensity and shape changes of their fluorescence, induced by various interacting ions and molecules in solution. Although these interactions have been extensively studied in the last few years, especially in view of their possible sensing applications, the existing works have mostly focused on the quenching of C-dot fluorescence induced by metal cations. In fact, these latter easily bind to C-dots surfaces, which are negatively charged in most cases, promoting an electron transfer from the surface to them. Much less is known from the literature on the effect induced on C-dots by prototypi…

Photoluminescencequenchingfluorescence quenching02 engineering and technology010402 general chemistryPhotochemistryultrafast transient absorption01 natural sciencesIonlcsh:QD241-441lcsh:Organic chemistrycarbon nanodotheavy atom effectPhysics::Atomic and Molecular ClustersMoleculecarbon nanodotsQuenching (fluorescence)ChemistrySettore FIS/01 - Fisica SperimentaleGeneral Medicine021001 nanoscience & nanotechnologyFluorescence0104 chemical sciencesIntersystem crossingHalogenAbsorption (chemistry)0210 nano-technologyC
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Size-And Wavelength-Dependent Two-Photon Absorption Cross-Section of CsPbBr3 Perovskite Quantum Dots

2017

All-inorganic colloidal perovskite quantum dots (QDs) based on cesium, lead, and halide have recently emerged as promising light emitting materials. CsPbBr3 QDs have also been demonstrated as stable two-photon-pumped lasing medium. However, the reported two photon absorption (TPA) cross sections for these QDs differ by an order of magnitude. Here we present an in-depth study of the TPA properties of CsPbBr3 QDs with mean size ranging from 4.6 to 11.4 nm. By using femtosecond transient absorption (TA) spectroscopy we found that TPA cross section is proportional to the linear one photon absorption. The TPA cross section follows a power law dependence on QDs size with exponent 3.3 +- 0.2. The …

PhotonSDG 16 - PeaceExcitonAnalytical chemistryPhysics::Opticsquantum dots02 engineering and technology010402 general chemistry01 natural sciencesTwo-photon absorptionMolecular physicsCsPbBr3 Perovskite Quantum DotsCondensed Matter::Materials ScienceUltrafast laser spectroscopyGeneral Materials SciencePhysical and Theoretical ChemistrySpectroscopyAbsorption (electromagnetic radiation)Perovskite (structure)ta114ChemistrySDG 16 - Peace Justice and Strong Institutions021001 nanoscience & nanotechnologyCondensed Matter::Mesoscopic Systems and Quantum Hall Effect/dk/atira/pure/sustainabledevelopmentgoals/peace_justice_and_strong_institutionsJustice and Strong Institutions0104 chemical sciencesQuantum dot0210 nano-technology
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Relaxation processes of point defects in vitreous silica from femtosecond to nanoseconds

2008

We studied ultrafast relaxation of localized excited states at Ge-related oxygen deficient centers in silica using femtosecond transient-absorption spectroscopy. The relaxation dynamics exhibits a biexponential decay, which we ascribe to the departure from the Frank-Condon region of the first excited singlet state in 240 fs, followed by cooling in ∼10 ps. At later times, a nonexponential relaxation spanning up to 40 ns occurs, which is fitted with an inhomogeneous distribution of nonradiative relaxation rates, following a chi-square distribution with one degree of freedom. This reveals several analogies with phenomena such as neutron reactions, quantum dot blinking, or intramolecular vibrat…

Physics and Astronomy (miscellaneous)Chemistrypoint defectSilicaNanosecondExcited state (localized; relaxation processes of point defects in vitreous silica from femtosecond to nanoseconds); Excited singlet state; Localized electronic state; Point defects; Vibrational relaxation (relaxation processes of point defects in vitreous silica from femtosecond to nanoseconds); Optical absorption (transient; relaxation processes of point defects in vitreous silica from femtosecond to nanoseconds)Crystallographic defectSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)ultrafast spectroscopyNuclear magnetic resonanceQuantum dotExcited stateFemtosecondVibrational energy relaxationNeutronrelaxation point defect vitreous silica nanosecondPhysics::Chemical PhysicsAtomic physicsSpectroscopyApplied Physics Letters
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Strong Exciton-Coherent Phonon Coupling in Single-Layer MoS2

2020

Broadband transient absorption with sub-20fs temporal resolution, supported by ab-initio calculations, quantitatively provides the strength of exciton-coherent phonon coupling in 1L-MoS2, showing a resonant profile around the C exciton.

PhysicsCouplingPhononExcitonCondensed Matter::Mesoscopic Systems and Quantum Hall EffectMolecular physicsPhoton countingCondensed Matter::Materials Sciencesymbols.namesakeTemporal resolutionUltrafast laser spectroscopysymbolsRaman spectroscopyRaman scatteringThe 22nd International Conference on Ultrafast Phenomena 2020
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Transient absorption of polarons in KNbO3

2002

Abstract Transient absorption spectra have been measured in a number of undoped KNbO 3 crystals following two kinds of electronic excitation: two-photon absorption of 200 fs laser pulses and 10 ns pulsed electron beam. A band peaking at 0.8 eV and broad, poorly resolved absorption in the range 1.3–3.3 eV were observed. Based on similarity to the 1 eV band in LiNbO 3 previously identified as the intrinsic electron polaron (electron self-localized on niobium in the regular lattice site), we suggest that the transient absorption band at 0.8 eV in KNbO 3 is also associated with the intrinsic electron polaron.

PhysicsNuclear and High Energy PhysicsExtended X-ray absorption fine structureElectronPolaronLaserSpectral linelaw.inventionlawUltrafast laser spectroscopyAtomic physicsAbsorption (electromagnetic radiation)InstrumentationExcitationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Optical investigations of TlBr detector crystals

2004

Shift of fundamental absorption edge, the position of main luminescence bands, the luminescence decay and transient absorption spectra in three TlBr crystals were studied. The γ-quanta detector made from TlBr crystals with similar transient absorption and luminescence parameters shows similar detector properties. The iodine impurity in TlBr was detected by optical methods. The role of impurities and crystal defects in γ-quanta detectors manufactured is discussed.

PhysicsNuclear and High Energy PhysicsPhysics::Instrumentation and Detectorsbusiness.industryDetectorPhysics::OpticsCrystallographic defectSpectral lineSemiconductor detectorAbsorption edgeImpurityCondensed Matter::SuperconductivityUltrafast laser spectroscopyOptoelectronicsHigh Energy Physics::ExperimentLuminescencebusinessInstrumentationNuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
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Ultrafast and Energy-Efficient Quenching of Spin Order: Antiferromagnetism Beats Ferromagnetism

2017

By comparing femtosecond laser pulse induced ferro- and antiferromagnetic dynamics in one and the same material - metallic dysprosium - we show both to behave fundamentally different. Antiferromagnetic order is considerably faster and much more efficiently manipulated by optical excitation than its ferromagnetic counterpart. We assign the fast and extremely efficient process in the antiferromagnet to an interatomic transfer of angular momentum within the spin system. Our findings do not only reveal this angular momentum transfer channel effective in antiferromagnets and other magnetic structures with non-parallel spin alignment, they also point out a possible route towards energy-efficient …

PhysicsQuenchingCondensed Matter - Materials ScienceAngular momentumCondensed Matter - Mesoscale and Nanoscale PhysicsCondensed matter physicsInstitut für Physik und AstronomieGeneral Physics and AstronomyMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciences02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesFerromagnetismUltrafast magnetic dynamics antiferromagnetic dynamics interatomic spin transfer0103 physical sciencesFemtosecondMesoscale and Nanoscale Physics (cond-mat.mes-hall)AntiferromagnetismCondensed Matter::Strongly Correlated Electrons010306 general physics0210 nano-technologyUltrashort pulseExcitationSpin-½
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