Search results for "transition"

showing 10 items of 3988 documents

Structural relaxation in a molten salt probed by time-dependent dc conductivity measurements

1998

Abstract Time-dependent dc conductivity was measured after cooling steps of about 2 K in the glass transformation range of 2Ca(NO 3 ) 2 -3RbNO 3 . The shape and time scale of the structural relaxation function was thus monitored for times 60 s t 6 s. The time scale could be compared with results from scanning calorimetry measurements and good agreement was found. From the heat capacity data and from the solid state conductivity the expected liquid state conductivity relaxation time was calculated using several models. The good compatibility of these calculations with the experimental results provides evidence that near the calorimetric glass transition the mobile ions perform concerted moti…

ChemistryDc conductivityRelaxation (NMR)Analytical chemistryThermodynamicsCalorimetryConductivityCondensed Matter Physics530Heat capacityElectronic Optical and Magnetic MaterialsIonMaterials ChemistryCeramics and CompositesMolten saltGlass transitionJournal of Non-Crystalline Solids
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Size Dependence of Tracer Diffusion in Supercooled Liquids

1996

We have determined by forced Rayleigh scattering the diffusion coefficients D of several photochromic tracers with van der Waals radii between 0.38 and 8 nm (the largest ones being photolabeled polystyrene micronetworks) in 10 glass-forming liquids at temperatures between the glass temperature Tg and ∼1.2Tg. The results were analyzed in terms of power law plots, D(T) ∝ T/η(T)ξ, where η is the solvent shear viscosity, and temperature shifts, D(T) ∝ T/η(T + ΔT). The shift ΔT was related with the width of the rotational correlation time distribution via the time−temperature superposition principle.

ChemistryDiffusionGeneral EngineeringThermodynamicsPower lawPhysics::Fluid DynamicsCondensed Matter::Soft Condensed Mattersymbols.namesakeSuperposition principlechemistry.chemical_compoundsymbolsVan der Waals radiusPolystyrenePhysical and Theoretical ChemistrySupercoolingGlass transitionRotational correlation timeThe Journal of Physical Chemistry
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Spectroscopic signatures of the carbon buckyonions C60@C180 and C60@C240: a dispersion-corrected DFT study

2013

We have investigated, using dispersion corrected DFT methods, the structure and the spectroscopic properties of carbon buckyonions C-60@C-180 and C-60@C-240. C-60, C-180 and C-240 showed a noticeable variation of their geometries in C-60@C-180 and C-60@C-240, upon encapsulation. Inclusion of the dispersion correction term in the calculations has a significant effect on the geometry. C-60@C-180 has a large positive interaction energy, while for C-60@C-240 a negative value is found indicating that only C-240 can easily accommodate C-60. In both cases dispersion interactions strongly contribute to the stabilization of the complexes. Vibrational frequencies, electronic transitions and NMR prope…

ChemistryDispersion Correctionfullerenes; computational chemistryAnalytical chemistryfullerenesGeneral Physics and AstronomyPositive interactioncomputational chemistryDFTEncapsulated buckyonionSpectroscopic.Atomic electron transitionChemical physicsPhysical and Theoretical ChemistrySettore CHIM/02 - Chimica Fisica
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Theoretical Study on the Structures and Electronic Spectra of TCNE2−

2006

Investigations into the charge-separated states and electron-transfer transitions in tetracyanoethylene (TCNE) compiles have recently generated much interest. In this work we present theoretical calculations showing that the most stable structure of the dianion TCNE 2- has D 2d symmetry in vacuum as well as in the solvents dichloromethane and cicetonitrile. By means of the coupled cluster linear response, we compute the vertical electronic spectrum in both the gas phase and solution. The theoreitcal results, are compared to the experimental data and good agreement is achieved.

ChemistryElectronic structureTetracyanoethyleneMolecular physicsAtomic and Molecular Physics and OpticsMolecular electronic transitionSpectral lineSymmetry (physics)chemistry.chemical_compoundCoupled clusterComputational chemistryAb initio quantum chemistry methodsPhysical and Theoretical ChemistrySolvent effectsChemPhysChem
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Electro-optical and laser spectrofluorimetry study of coumarins 7 and 30: evidence for the existence of the close-lying electronic states and conform…

1997

Our experiments and calculations reveal a set of anomalous and interesting properties of coumarin 7 (CU7) and coumarin 30 (CU30) in solution. The spectral dependence of electro-optical coefficients and, consequently, dipole moments indicates that the absorption band is a superposition of several (at least two) electronic transitions. Probably, there are two close-lying π,π* singlet electronic excited states which contribute to the first absorption band. The calculations using the MM2 program show that both dyes in the ground state have two stable plane anti conformers. From time-resolved spectrofluorimetric measurements we obtained evidence for the existence of conformers in paraffin oil so…

ChemistryGeneral Chemical EngineeringAnalytical chemistryGeneral Physics and AstronomyGeneral ChemistryMolecular physicsDipoleAtomic electron transitionAbsorption bandExcited stateSinglet stateAbsorption (chemistry)Ground stateConformational isomerismJournal of Photochemistry and Photobiology A: Chemistry
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Molecular Stark-effect spectroscopy of Prodan and Laurdan in different solvents and electric dipole moments in their equilibrated ground and Franck–C…

2007

Abstract The results from electrooptical absorption measurements (EOAM) on the ground and excited Franck–Condon state dipole moments of Prodan and Laurdan in 1,4-dioxane and cyclohexane are presented. The ground and excited Franck–Condon state electric dipole moments as well as the respective transition moment of both probes are parallel. The electric dipole moments of Prodan and Laurdan in the ground state in cyclohexane and 1,4-dioxane have values within the range (15.7–16.5) × 10 −30  C m. On optical excitation the dipole moments increase by (42.1–49.5) × 10 −30  C m. The obtained results are compared with the values of the dipole moments of Prodan and Laurdan determined by other methods.

ChemistryGeneral Chemical EngineeringTransition dipole momentGeneral Physics and AstronomyGeneral ChemistryPhotochemistrysymbols.namesakeDipolechemistry.chemical_compoundStark effectExcited statesymbolsAtomic physicsSpectroscopyGround stateLaurdanExcitationJournal of Photochemistry and Photobiology A: Chemistry
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Hansen theory applied to the identification of nonhazardous solvents for hybrid perovskite thin-films processing

2018

Abstract Metal-halide perovskites have become the most studied material for efficient next-generation solar cells, in part because of the possibility of depositing high quality semiconducting perovskites by simple solution-based methods. However, the majority of solvent systems implemented in literature for deposition of lead halide perovskites are hazardous to handle. Investigation of alternatives perovskite processing methods are hence key to safely upscale the perovskite photovoltaic manufacturing. In this manuscript we use the Hansen theory to find suitable nonhazardous solvents to solubilize two lead salts, PbBr2 and PbI2, used to fabricate the corresponding methylammonium (MA) lead ha…

ChemistryHalide02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences7. Clean energy0104 chemical sciencesInorganic ChemistrySolventHildebrand solubility parameterChemical engineeringMaterials ChemistryDeposition (phase transition)Lead saltPhysical and Theoretical ChemistryThin filmSolubility0210 nano-technologyPerovskite (structure)Polyhedron
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Adsorption of 3d Transition Elements on a TiO2(110) Surface.

2008

International audience; A first-principles study on the adsorption of 3d transition metal atoms on a stoichiometric TiO2(110) surface is reported. For all 3d elements except Cu, the most stable on-surface adsorption site is a site where the adatom binds to two twofold and one threefold surface oxygen atoms. For Ti, V, and Cr, however, a subsurface site, where the adatom substitutes a sixfold Ti atom, is more stable. The adatoms are oxidized in all cases. The charge transfer to the substrate is larger for the substitutional site than for the on-surface adsorption sites and decreases with atomic number along the 3d series. The relative stabilities of the adsorption sites are discussed in term…

ChemistryInorganic chemistry02 engineering and technologySubstrate (electronics)021001 nanoscience & nanotechnology01 natural sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsElectronegativityA-siteCrystallographyGeneral EnergyAdsorptionTransition metal0103 physical sciencesAtomAtomic numberPhysical and Theoretical Chemistry010306 general physics0210 nano-technologyStoichiometry
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First principles slab calculations of the regular Cu/MgO(001) interface

2004

Ab initio slab calculations are performed for the copper adhesion over magnesium ions on the perfect MgO(0 0 1) surface with 1/4 monolayer (ML), two types of 1/2 ML and 1 ML substrate coverages. Results of our calculations are compared with various experimental and theoretical data. Both small atomic polarization and charge redistribution give the dominant contributions to the physisorption bonding on a regular Cu/MgO(0 0 1) interface.

ChemistryInorganic chemistryAb initiochemistry.chemical_elementSurfaces and InterfacesCondensed Matter PhysicsMolecular physicsCopperSurfaces Coatings and FilmsPhysisorptionTransition metalAb initio quantum chemistry methodsMonolayerMaterials ChemistrySlabMagnesium ionSurface Science
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Some fundamentals of the vapor and solution growth of ZnSe and ZnO

1999

Abstract Some fundamentals of ZnSe and ZnO vapor and solution growth are investigated. Residual water present in gases or gaseous mixtures such as H 2 , Ar or H 2 +H 2 O is shown to act as a sublimation activator in the vapor-phase transport of both compounds. The processes involved in the growth by chemically activated sublimation with such gases and gas mixtures have been studied by close-spaced vapor transport (CSVT). The ZnSe growth rate is found to be constant, while in the ZnO case a high initial growth rate is followed by slower growth subsequently. Using a theoretical model, the thermodynamic constants of the transport – energies of activation, sublimation and condensation and entha…

ChemistryInorganic chemistryAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsInorganic ChemistrySolventDifferential thermal analysisActivator (phosphor)Materials ChemistryChlorineSublimation (phase transition)Growth rateStandard enthalpy change of formationPhase diagramJournal of Crystal Growth
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