Search results for "TRIPLE"

showing 10 items of 506 documents

The high-pressure, high-temperature phase diagram of cerium

2020

Abstract We present an experimental study of the high-pressure, high-temperature behaviour of cerium up to ∼22 GPa and 820 K using angle-dispersive x-ray diffraction and external resistive heating. Studies above 820 K were prevented by chemical reactions between the samples and the diamond anvils of the pressure cells. We unambiguously measure the stability region of the orthorhombic oC4 phase and find it reaches its apex at 7.1 GPa and 650 K. We locate the α-cF4–oC4–tI2 triple point at 6.1 GPa and 640 K, 1 GPa below the location of the apex of the oC4 phase, and 1–2 GPa lower than previously reported. We find the α-cF4 → tI2 phase boundary to have a positive gradient of 280 K (GPa)−1, less…

Phase boundaryMaterials scienceTriple pointThermodynamicsDiamondchemistry.chemical_element02 engineering and technologyengineering.material021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesCeriumchemistryPhase (matter)0103 physical sciencesX-ray crystallographyengineeringGeneral Materials ScienceOrthorhombic crystal system010306 general physics0210 nano-technologyPhase diagramJournal of Physics: Condensed Matter
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Bis-Sulfone- and Bis-Sulfoxide-Spirobifluorenes: Polar Acceptor Hosts with Tunable Solubilities for Blue-Phosphorescent Light-Emitting Devices

2016

Bis-sulfone- and bis-sulfoxide-spirobifluorenes are a promising class of high-triplet-energy electron-acceptor hosts for blue phosphorescent light-emitting devices. The molecular design and synthetic route are simple and facilitate tailoring of the solubilities of the host materials without lowering the high-energy triplet state. The syntheses and characterization (including single-crystal structures) of four electron-accepting hosts are reported; the trend in their reduction potentials is consistent with the electron-withdrawing nature of the sulfone or sulfoxide substituents. Emission maxima of 421–432 nm overlap with the MLCT absorption of the sky-blue emitter bis(4,6-difluorophenyl-pyri…

Phosphine oxidechemistry.chemical_classificationOrganic ChemistrySulfoxide02 engineering and technologyElectron acceptor010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesAcceptor0104 chemical sciencesSulfonechemistry.chemical_compoundchemistryOLEDPhysical and Theoretical ChemistryTriplet state0210 nano-technologyPhosphorescenceEuropean Journal of Organic Chemistry
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Ab initio study on the low-lying excited states of retinal

1997

Ab initio results for the electronic spectrum of all-trans-retinal and its truncated model 3-methyl-all-trans (10-s-cis)-2,4,6,8,10-undecapentaen-1-al are presented. The study includes geometry determination of the ground state. Vertical excitation energies have been computed using multiconfigurational second-order perturbation theory through the CASPT2 formalism. The lowest singlet excited state in gas phase is predicted to be of nπ∗ character. The lowest triplet state corresponds, however, to a ππ∗ state. The most intense feature of the spectrum is due to the strongly dipole-allowed ππ∗ transition, in accordance with the observed maximum in the one-photon spectra. The vertical excitation …

PhotochemistryChemistryExcited statesAb initioGeneral Physics and AstronomyPerturbation theoryTriplet stateSpectral lineGround statesUNESCO::FÍSICA::Química físicaAb initio quantum chemistry methodsExcited stateOrganic compoundsSolvent effectsTwo-photon spectraIsomerisationAb initio calculationsSinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet state:FÍSICA::Química física [UNESCO]Ground stateExcitationOrganic compounds ; Excited states ; Ab initio calculations ; Perturbation theory ; Triplet state ; Solvent effects ; Isomerisation ; Ground states ; Two-photon spectra ; Photochemistry
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Intramolecular Interactions in the Triplet Excited States of Benzophenone–Thymine Dyads

2005

Time-resolved and product studies on the synthesized dyads 1 and 2 have provided evidence that the benzophenone-to-thymine orientation strongly influences intramolecular photophysical and photochemical processes. The prevailing reaction mechanism has been established as a Paterno-Büchi cycloaddition to give oxetanes 3-6; however, the ability of benzophenone to achieve a formal hydrogen abstraction from the methyl group of thymidine has also been evidenced by the formation of photoproducts 7 and 8. These processes have been observed only in the case of the cisoid dyad 1. Adiabatic photochemical cycloreversion of the oxetane ring is achieved upon direct photolysis to give the starting dyad 1 …

PhotochemistryOrganic ChemistryGeneral ChemistryOxetaneHydrogen atom abstractionPhotochemistryCatalysisCycloadditionBenzophenoneschemistry.chemical_compoundchemistryEthers CyclicExcited stateIntramolecular forceBenzophenoneTriplet stateThymineThymidineMethyl groupChemistry - A European Journal
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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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Luminescence-detected EPR of oxygen-fluorine vacancy complexes in CaF2

2009

In several CaF2 single crystals grown by the Bridgman method and doped with CaO or in addition with SrF2 or NaF a luminescence band between 470 nm and 600 nm could be excited at 212 nm, its peak wavelength depending on the doping. With photo-luminescence (PL) detected EPR five spin triplet centres were identified. Their axial fine structure constants D varied from 87 mT to 690 mT whereby the most intense spectra had the smallest D value. Theoretical calculations of the fine structure tensors and superhyperfine interactions show that the most intense and probable triplet centre consists of a pair of an OF– on a F– site next to a nearest neighbour F– vacancy which, compared to the well-known …

PhotoluminescenceChemistryCondensed Matter PhysicsSpectral lineElectronic Optical and Magnetic Materialslaw.inventionlawVacancy defectExcited stateMetastabilityTriplet stateAtomic physicsLuminescenceElectron paramagnetic resonancephysica status solidi (b)
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Optically detected magnetic resonance investigation of oxygen luminescence centres in BaF2

2002

The structure of two oxygen-related luminescence centres in oxygen-doped BaF2 was investigated by means of photoluminescence (PL) and photoluminescence-detected electron paramagnetic resonance (PL-EPR). One of the oxygen-related luminescences peaking at 2.83 eV is associated with an excited triplet state (S = 1) of an oxygen–vacancy complex with the z-axis of the fine-structure tensor parallel to the 110 direction. This complex can be described as an oxygen on a fluorine lattice site with a next-nearest fluorine vacancy along the 110 direction. The luminescence at 2.25 eV is also associated with a triplet state. Its PL-EPR spectrum is probably due to oxygen–vacancy complexes with a nearest …

PhotoluminescenceChemistryCrystal structureCondensed Matter PhysicsCrystallographic defectMolecular physicslaw.inventionNuclear magnetic resonancelawVacancy defectExcited stateGeneral Materials ScienceTriplet stateLuminescenceElectron paramagnetic resonanceJournal of Physics: Condensed Matter
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Optically detected magnetic resonance investigation of a luminescent oxygen–vacancy complex in Mn-doped LiBaF3

2006

The structure of an oxygen-related luminescence centre in manganese-doped LiBaF 3 was investigated by means of photoluminescence (PL) and PL-detected electron paramagnetic resonance. At 20 K an oxygen-related complex shows two luminescence bands peaking at about 430 and 475 nm, when excited at 220 nm. These bands can be attributed to an excited triplet state (S = 1) of an oxygen-vacancy complex with the z axis of the fine structure tensor parallel to the (110) direction. This complex is believed to be next to a Mn 2+ impurity on a Ba 2+ site and can be described as an oxygen on a fluorine lattice site with a nearest fluorine vacancy along the (110) direction.

PhotoluminescenceChemistryDopingCondensed Matter Physicslaw.inventionCrystallographyNuclear magnetic resonanceImpuritylawVacancy defectExcited stateGeneral Materials ScienceTriplet stateLuminescenceElectron paramagnetic resonanceJournal of Physics: Condensed Matter
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Role of diffusing molecular hydrogen on relaxation processes in Ge-doped glass

2007

Temperature dependencies of steady-state and time-resolved photoluminescence (PL) from triplet state at 3.1 eV and singlet state at 4.2 eV ascribed to the twofold-coordinated Ge have been measured in unloaded and H2-loaded Ge-doped silica samples under 5.0 eV excitation in the 10–310 K range. Experimental evidences indicate that diffusing molecular hydrogen (H2) depopulates by a collisional mechanism the triplet state, decreasing both its lifetime of about 14% and the associated triplet PL intensity, whereas those of the singlet are insensitive to the presence of H2.

PhotoluminescenceChemistryDopingRelaxation (NMR)Condensed Matter PhysicsPhotochemistryMolecular physicsElectronic Optical and Magnetic MaterialsHydrogen in glassOptical spectroscopyLuminescenceGermanatesSinglet fissionMaterials ChemistryCeramics and CompositesSinglet stateTriplet stateSpectroscopyExcitationJournal of Non-Crystalline Solids
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Temperature dependence of luminescence decay in Sn-doped silica

2005

We report an experimental study on the temperature dependence, in the range 18-300 K, of the decay kinetics of the emission at 4.1 eV from the first excited electronic state of oxygen deficient centers in a 2000 ppm Sn-doped sol-gel silica. At low temperature, this luminescence decays exponentially with a lifetime of 8.4 ns, whereas, on increasing the temperature, the time decay decreases and cannot be fitted with an exponential function. These results are expected if there is a competition between the radiative and the thermally activated intersystem-crossing decay channels toward the associated triplet state. The comparison with previous data in pure oxygen-deficient and Ge-doped silica g…

PhotoluminescenceChemistrypoint defectDopingActivation energyCondensed Matter PhysicsCrystallographic defectElectronic Optical and Magnetic MaterialsExponential growthsilicatinExcited stateluminescenceMaterials ChemistryCeramics and CompositesAtomic physicsTriplet stateLuminescenceJournal of Non-Crystalline Solids
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