Search results for "surfaces"

showing 10 items of 2837 documents

Ab Initio Calculations of the Transfer and Aggregation of F Centers in CaF2

2012

The F center and R center in CaF2 crystals have been studied by using density functional theory (DFT) with a hybrid B3PW description of exchange and correlation. Our calculations show that the F-center diffusion barrier is equal to 1.67 eV. During the F-center transfer, the trapped electron is more delocalized than that in the regular F-center case, and the gap between defect level and CB in the α-spin state decreases. The surface F-center investigation shows the trend of F centers to locate near the surface. The association energy calculations of R centers indicate stable aggregations of isolated F centers. During the F-center aggregation, a considerable covalency forms between two neighbo…

Electron pairValence (chemistry)Diffusion barrierChemistrychemistry.chemical_elementElectronSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDelocalized electronGeneral EnergyAb initio quantum chemistry methodsFluorineDensity functional theoryPhysical and Theoretical ChemistryAtomic physicsThe Journal of Physical Chemistry C
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Electron Transfer from the Singlet and Triplet Excited States of Ru(dcbpy)2(NCS)2into Nanocrystalline TiO2Thin Films

2002

Time-resolved absorption spectroscopy was used to study the femtosecond and picosecond time scale electron injection from the excited singlet and triplet states of Ru(dcbpY)(2)(NCS)(2) (RuN3) into titanium dioxide (TiO2) nanocrystalline particle film in acetonitrile. The fastest resolved time constant of similar to30 fs was shown to reflect a sum of two parallel ultrafast processes, nonergodic electron transfer (ET) from the initially excited singlet state of RuN3 to the conduction band of TiO2 and intersystem crossing (ISC). The branching ratio of 1.5 between the two competing processes gives rate constants of 1/50 fs(-1) for ET and 1/75 fs(-1) for ISC. Following the ultrafast processes, a…

Electron transferIntersystem crossingAbsorption spectroscopyChemistryExcited statePicosecondSinglet fissionMaterials ChemistrySinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet stateSurfaces Coatings and FilmsThe Journal of Physical Chemistry B
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First-principles calculations for SrTiO3() surface structure

2002

As a continuation of our recent abinitio calculations of SrTiO 3(1 0 0) surface relaxation for the two different terminations (SrO and TiO2) [Phys. Rev. B 64 (2001) 23417], we analyze here their electronic structures (band structure, density of states, and the electronic density redistribution with emphasis on the covalency effects). We compare results of abinitio Hartree–Fock method with electron correlation corrections and density functional theory with different exchange-correlation functionals, including hybrid (B3PW, B3LYP) exchange techniques. Our results are also compared with previous abinitio plane-wave local density approximation calculations and experiments when availab le. Consi…

Electronic correlationChemistrySurfaces and InterfacesElectronic structureCondensed Matter PhysicsMolecular physicsSurfaces Coatings and FilmsAb initio quantum chemistry methodsComputational chemistryMaterials ChemistryDensity of statesDensity functional theoryLocal-density approximationElectronic band structureElectronic densitySurface Science
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Heterovalent BiIII/PbII ionic substitution in one-dimensional trimethylsulfoxonium halide pseudo-perovskites (X = I, Br)

2021

We report on the synthesis and characterization of novel lead and bismuth hybrid (organic-inorganic) iodide and bromide pseudo-perovskites (ABX3) containing the trimethylsulfoxonium cation (CH3)3SO+ (TMSO) in the A site, Pb/Bi in the B site, and Br or I as X anions. All of these compounds are isomorphic and crystallize in the orthorhombic Pnma space group. Lead-based pseudo-perovskites consist of one-dimensional (1D) chains of face-sharing [PbX6] octahedra, while in the bismuth-based ones, the chains of [BiX6] are interrupted, with one vacancy every third site, leading to a zero-dimensional (0D) local structure based on separated [Bi2I9]3- dimers. Five solid solutions for the iodide with di…

Electronic structureMaterials scienceBand gapHalideIonic bondingchemistry.chemical_elementElectronic structurePositive ionPerovskiteIonBismuthPhysical and Theoretical ChemistryPerovskite (structure)Design for testabilityX ray powder diffractionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsEnergy gapCrystallographyGeneral EnergychemistryDensity functional theoryorganic-inorganic materialDensity functional theoryDefectBismuth
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Graph-based analysis of ethylene glycol decomposition on a palladium cluster

2017

The ethylene glycol, CH2OH-CH2OH, decomposition mechanism, occurring on a subnanometric palladium cluster shaped by 12 atoms, was investigated by means of density functional theory. Different reaction routes were identified leading to H2 and CO. The whole reaction network was analyzed, framing the results within the graph theory. The possible decomposition pathways were discussed and compared, allowing one to draw a whole picture of all the parallel, possibly competitive, routes that starting from CH2OH-CH2OH originate H2 and CO.

Electronic Optical and Magnetic MaterialGraph basedSurfaces Coatings and Filmchemistry.chemical_elementGraph theory02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundEnergy (all)General EnergychemistryComputational chemistryOrganic chemistryDensity functional theoryPhysical and Theoretical Chemistry0210 nano-technologyEthylene glycolPalladium
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New Quasi-Atomic Nanoheterostructures: Superatoms and Excitonic Quasi-Molecules

2016

In this review, the state-of-the-art of research of artificial atoms (superatoms or quasi-atomic nanoheterostructures) and more complex nanostructures based on them—synthetic molecules is discussed, a new model of an artificial atom, which satisfactorily explains its electronic properties, is proposed, and the prospects for development of the new scientific trend are mentioned. В этом обзоре обсуждается современное состояние исследований искусственных атомов (сверхатомов или квазиатомных наногетероструктур) и более сложных наноструктур на их основе — синтетических молекул, предложена новая модель искусственного атома, удовлетворительно объясняющая его электронные свойства, а также указаны п…

Electronic Optical and Magnetic MaterialMaterials Science (miscellaneous)Excitonic quasi-moleculeQuantum dotSuperatomNanoheterostructureCeramics and CompositeEnergy spectrumElectronHoleSettore FIS/03 - Fisica Della MateriaSurfaces Coatings and Films
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Biomimetic oxidation of pyrene and related aromatic hydrocarbons. Unexpected electron accepting abilities of pyrenequinones

2014

We present a mild catalytic method to oxidize PAHs and, in particular, pyrene. The pyrenediones are much better electron acceptors than benzoquinone in the gas phase and present similar accepting abilities in solution.

ElectronsElectronPhotochemistryHydrocarbons AromaticCatalysisGas phaseCatalysischemistry.chemical_compoundBiomimeticsMaterials ChemistryOrganic chemistryElectrodeschemistry.chemical_classificationPyrenesMetals and AlloysQuinonesOxidation reductionGeneral ChemistryElectron acceptorBenzoquinoneSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesPyreneOxidation-ReductionCatalytic method
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Ettringite surface chemistry: Interplay of electrostatic and ion specificity

2011

International audience; This paper presents a detailed experimental study combined with Monte Carlo (MC) simulations within the primitive model of the physical chemistry at the ettringite-water interface over a wide range of pH and bulk conditions for which ettringite exists thanks to its solubility in aqueous solutions. Ettringite, which is an important phase in hydrated cement-based systems, bears a permanent and positive structural charge. In contrast with previous studies, electrokinetic measurements together with the careful chemical analysis of the equilibrium solutions of the dispersions have brought strong support to designate sulfate as being the ion determining the potential. Simu…

ElectrophoresisEttringiteSurface PropertiesStatic Electricity02 engineering and technology010402 general chemistryEttringite01 natural sciencesMonte Carlo simulationsIonBiomaterialschemistry.chemical_compoundElectrokinetic phenomenaColloid and Surface ChemistryPhase (matter)Computer SimulationSulfateSolubilityIonsMineralsAqueous solutionSulfatesChemistryAdsorption potentialWaterHydrogen-Ion Concentration021001 nanoscience & nanotechnologyElectrostaticsSulfate0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Models ChemicalChemical physicsPhysical chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyMonte Carlo MethodJournal of Colloid and Interface Science
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Electrophoretic flow behaviour and mobility of colloidal fluids and crystals.

2007

We report on measurements of the electrophoretic mobility mu of charged colloidal spheres in the deionized state, where the suspensions show fluid or crystalline order. In the fluid state, parabolic flow profiles are observed due to electro-osmotic solvent flow. In the crystalline state, complex flow profiles occur due to additional crystal cohesion. The mobility mu then may inferred from the flow velocity averaged over the complete cell cross section as performed in our home built super-heterodyne Doppler velocimeter. For two particle species of 68 and 122 nm diameter we measured mu as a function of particle concentration. Starting from a plateau value at low concentration, mu decreases ap…

ElectrophoresisPhase transitionPolymersStatic ElectricityAnalytical chemistryMolecular physicsEffective nuclear chargeIonColloidMotionColloid and Surface ChemistrySuspensionsColloidsPhysical and Theoretical ChemistryParticle SizeChemistryWaterSurfaces and InterfacesGeneral MedicineColloidal crystalElectrophoresisFlow velocityAcrylatesPolystyrenesParticle sizeCrystallizationRheologyBiotechnologyColloids and surfaces. B, Biointerfaces
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Prediction of friction and heat flow in machining incorporating thermophysical properties of the coating–chip interface

2004

Abstract This paper deals with an experimental and analytical investigation into the thermodynamically activated effects influencing the behaviour of the multi-layered coated tool rake face during orthogonal cutting of ferromagnetic and paramagnetic steels. Temperature measurements on the tool rake face using a thermocouple-based technique and identification of the contact zone by means of computer image processing were carried out. New methodology for assessing friction and the amount of thermal energy generated when machining with a coated tool insert with natural and restricted contact coupled with a metallic chip, using thermophysical properties of the sliding materials is developed in …

Engineering drawingMaterials sciencebusiness.industrySurfaces and Interfacesengineering.materialCondensed Matter PhysicsTemperature measurementSurfaces Coatings and FilmsMachiningCoatingHeat fluxMechanics of MaterialsThermocoupleHeat transferMaterials ChemistryengineeringComposite materialbusinessMaterial propertiesThermal energyWear
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