Search results for "Titanium compounds"

showing 4 items of 4 documents

Magnetic exchange interaction in a pair of orbitally degenerate ions: Magnetic anisotropy of [Ti2Cl9]−3

2001

The theory of the kinetic exchange in a pair of orbitally degenerate ions developed by the authors [J. Phys. Chem. A 102, 200 (1998)] is applied to the case of face-shared bioctahedral dimer (overall D3h-symmetry). The effective kinetic exchange Hamiltonian is found for a 2T2–2T2 system taking into account all relevant transfer pathways and charge-transfer crystal field states. The influence of different transfer integrals involved in the kinetic exchange on the energy pattern and magnetic properties of the system is examined. The role of other related interactions (trigonal crystal field, spin–orbit coupling) is also discussed in detail. Using the pseudoangular momentum representation and …

Condensed matter physicsChemistryDegenerate energy levelsGeneral Physics and AstronomyTrigonal crystal systemKinetic energyNegative ionsExchange interactions (electron)Magnetic exchangeIonUNESCO::FÍSICA::Química físicaMagnetic anisotropysymbols.namesakeTitanium compounds ; Magnetic anisotropy ; Negative ions ; Exchange interactions (electron)Quantum mechanicssymbolsTitanium compoundsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Hamiltonian (quantum mechanics)Magnetic anisotropy
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Polystyrene nanoparticle-templated hollow titania nanosphere monolayers as ordered scaffolds

2018

We report a novel multi-step method for the preparation of ordered mesoporous titania scaffolds and show an illustrative example of their application to solar cells. The method is based on (monolayer) colloidal nanosphere lithography that makes use of polystyrene nanoparticles organised at a water–air interface and subsequently transferred onto a solid substrate. A titania precursor solution (titanium(IV) isopropoxide in ethanol) is then drop-cast onto the monolayer and left to “incubate” overnight. Surprisingly, instead of the expected inverse monolayer-structure, a subsequent calcination step of the precursor yields an ordered monolayer of hollow titania nanospheres with a wall thickness …

X ray diffractionX ray photoelectron spectroscopySolar cellMonolayer structureWater-air interfaceMonolayerPhase interfaceSettore ING-INF/01NanocrystalPerovskiteNanocrystalline anatasePerovskite solar cellPolystyrene nanoparticlePower conversion efficienciePrecursor solutionNanoparticleTitanium compoundInterfaces (materials)Interfaces (materials); Monolayers; Nanocrystals; Nanoparticles; Nanospheres; Perovskite; Perovskite solar cells; Phase interfaces; Polystyrenes; Scaffolds (biology); Solar cells; Titanium compounds; Titanium dioxide; X ray diffraction; Monolayer structures; Nano Sphere Lithography; Nanocrystalline anatase; Polystyrene nanoparticles; Power conversion efficiencies; Precursor solutions; Titania nanospheres; Water-air interface; X ray photoelectron spectroscopyTitanium dioxideScaffolds (biology)Nano Sphere LithographyNanospherePolystyreneTitania nanosphere
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Stoichiometry-related Auger lineshapes in titanium oxides: Influence of valence-band profile and of Coster-Kronig processes

2004

International audience; The ability to determine the nature and the occurrence of defects is a central need of ceramic surface chemistry. In titanium oxides, the Ti-LMV Auger decays line shape is very sensitive to the titanium degree of oxidation, and has long been empirically used as a qualitative probe of the stoichiometry. In the present work, resonant Auger and resonant valence-band measurements at the Ti-L2,3 edges in TiO2, TiO2–x and metallic titanium provide a clear evidence that the evolutions of the Ti-LMV Auger line shape are due to drastic changes in the valence-band profile and in the probability of L2L3V Coster-Kronig decay processes when a fraction of titanium ions is reduced.…

PACS: 71.20.-b 32.80.Hd 77.84.Bw 82.80.Pvoxidationchemistry.chemical_element02 engineering and technologyceramics01 natural sciencesElectron spectroscopy71.20.-b; 32.80.Hd; 77.84.Bw; 82.80.PvIonAugerX-RAY-ABSORPTION; SURFACE-DEFECTS; RUTILE TIO2; Resonant AugerMetalsymbols.namesakephotoelectron spectra0103 physical sciencesRUTILE TIO2titanium010306 general physicstitanium compoundsAuger electron spectroscopyFermi levelvalence bandsResonant Auger021001 nanoscience & nanotechnologyCondensed Matter PhysicsSURFACE-DEFECTSElectronic Optical and Magnetic Materialsstoichiometrychemistryvisual_artX-RAY-ABSORPTIONsymbolsvisual_art.visual_art_mediumFermi levelspectral line breadthAuger electron spectraAtomic physics0210 nano-technologyStoichiometryTitanium
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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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