0000000001308956

AUTHOR

James R. Durrant

showing 9 related works from this author

Supermolecular control of charge transfer in dye-sensitized nanocrystalline TiO2 films: towards a quantitative structure-function relationship.

2005

Electron transferMaterials sciencechemistryQuantitative structurechemistry.chemical_elementCharge (physics)General ChemistryGeneral MedicinePhotochemistryCatalysisNanocrystalline materialRutheniumTitanium oxideAngewandte Chemie (International ed. in English)
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Optical sensing of cyanide using hybrid biomolecular films

2006

The selective sensing of cyanide anions in water has been studied using a hybrid biomaterial composed of a mesoporous TiO2 film of crystalline nanoparticles and the protein hemoglobin. The mesoporous structure of the film prevents protein unfolding and also stabilizes the oxidized form of the prosthetic groups. Low-levels of cyanide anions (<0.2 ppm (0.2 mgr/L)) can be detected by monitoring the changes in the optical properties of the hybrid biomolecular films upon cyanide binding to the heme groups.

biologyCyanideInorganic chemistryBiomaterialNanoparticleBioinorganic chemistryPhotochemistryCofactorInorganic Chemistrychemistry.chemical_compoundchemistryMaterials Chemistrybiology.proteinsense organsHemoglobinPhysical and Theoretical ChemistryMesoporous materialHemeInorganic Chemistry Communications
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Reversible Colorimetric Probes for Mercury Sensing

2005

The selectivity and sensitivity of two colorimetric sensors based on the ruthenium complexes N719 [bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) bis(tetrabutylammonium) bis(thiocyanate)] and N749 [(2,2':6',2' '-terpyridine-4,4',4' '-tricarboxylate)ruthenium(II) tris(tetrabutylammonium) tris(isothiocyanate)] are described. It was found that mercury ions coordinate reversibly to the sulfur atom of the dyes' NCS groups. This interaction induces a color change in the dyes at submicromolar concentrations of mercury. Furthermore, the color change of these dyes is selective for mercury(II) when compared with other ions such as lead(II), cadmium(II), zinc(II), or iron(II). The detection limit…

IronInorganic chemistrychemistry.chemical_elementBiosensing TechniquesBiochemistrySensitivity and SpecificityCatalysischemistry.chemical_compoundColloid and Surface ChemistryIsothiocyanatesOrganometallic CompoundsColoring AgentsIonsTitaniumAqueous solutionThiocyanateMolecular StructureChemistryGeneral ChemistryMercuryChemical sensorTransition metal ionsMercury (element)RutheniumZincLeadRuthenium CompoundsColorimetrySpectrophotometry UltravioletSelectivityThiocyanatesCadmium
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Tuning Charge Carrier Dynamics and Surface Passivation in Organolead Halide Perovskites with Capping Ligands and Metal Oxide Interfaces

2018

Organolead halide perovskites have emerged as exciting optoelectronic materials but a complete understanding of their photophysical properties is still lacking. Here, a morphological series of methylammonium lead bromide (MAPbBr 3 ) perovskites are studied by transient optical spectroscopies over eight orders of magnitude in timescale to investigate the effect of nanostructuring and surface states on the charge carrier dynamics. The sample preparation route and corresponding morphology changes influence the position of the optical features, recombination dynamics, excitation fluence dependence, and dramatically impact surface trap passivation. Growth of the perovskite layer in the presence …

Materials sciencePassivationOxideHalide02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsMetalchemistry.chemical_compoundChemical engineeringchemistryvisual_artOptoelectronic materialsvisual_art.visual_art_mediumCharge carrier0210 nano-technology
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State selective electron injection in non-aggregated titanium phthalocyanine sensitised nanocrystalline TiO2 films

2004

We describe a novel titanium phthalocyanine that shows no aggregation when anchored to nanocrystalline TiO2 films through its axial carboxylated ligand without the use of co-adsorbents; state selective electron injection into the TiO2 is demonstrated, resulting in efficient photocurrent generation in dye sensitised photoelectrochemical solar cells. Palomares Gil, Emilio J, epagil@alumni.uv.es

Solar cellsMaterials scienceState selectiveUNESCO::QUÍMICAchemistry.chemical_elementNanotechnologyPhotochemistry:QUÍMICA [UNESCO]Catalysischemistry.chemical_compoundElectron injectionMaterials ChemistryUNESCO::QUÍMICA::Química orgánicaElectron injectionPhotocurrentTitaniumLigand:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistryNanocrystalline materialSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryTiO2 filmsCeramics and CompositesPhthalocyanineElectron injection ; Titanium ; TiO2 films ; Solar cellsTitanium
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Solid film versus solution-phase charge-recombination dynamics of exTTF-bridge-C60 dyads.

2005

The charge-recombination dynamics of two exTTF-C 6 0 dyads (exTTF=9,10-bis(l,3-dithiol-2-ylidene)-9,10-dihydroanthracene), observed after photoinduced charge separation, are compared in solution and in the solid state. The dyads differ only in the degree of conjugation of the bridge between the donor (exTTF) and the acceptor (C 6 0 ) moieties. In solution, photoexcitation of the nonconjugated dyad C 6 0 -BN-exTTF (1) (BN=1,1'-binaphthyl) shows slower charge-recombination dynamics compared with the conjugated dyad C 6 0 -TVB-exTTF (2) (TVB = bisthienylvinylenebenzene) (lifetimes of 24 and 0.6 μs, respectively), consistent with the expected stronger electronic coupling in the conjugated dyad.…

Organic solar cellChemistryOrganic ChemistrySettore CHIM/06 - Chimica OrganicaGeneral ChemistryPhotochemistryAcceptorCatalysisDissociation (chemistry)PhotoexcitationPhotophysiscsElectron transferFullerenePhotoinduced charge separationSelf-assemblyRecombinationDonor-Acceptor ensemblesChemistry (Weinheim an der Bergstrasse, Germany)
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Acid versus base peptization of mesoporous nanocrystalline TiO2 films: functional studies in dye sensitized solar cells

2005

We report an analysis of the influence of acid/base conditions employed in the synthesis of TiO2 nanoparticles upon the performance of dye sensitised photoelectrochemical solar cells fabricated from these particles. The functional properties of the TiO2 nanoparticles in these devices are investigated by potential step chronoamperometry, transient laser spectroscopy, and photovoltaic device characterisation. We find that base peptization conditions employed in the sol–gel fabrication of the TiO2 nanoparticles result in a reduction in film electron density under negative applied bias, correlated with slower interfacial recombination losses and a higher device open circuit voltage.

Solution of Schrödinger equation for a step potentialDye-sensitized solar cellMaterials scienceFabricationChemical engineeringOpen-circuit voltageInorganic chemistryMaterials ChemistryGeneral ChemistryChronoamperometryPeptizationMesoporous materialNanocrystalline materialJournal of Materials Chemistry
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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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Data used in article 'Tuning Charge Carrier Dynamics and Surface Passivation in Organolead Halide Perovskites with Capping Ligands and Metal Oxide In…

2018

Data underlying the article &#39;Tuning Charge Carrier Dynamics and Surface Passivation in Organolead Halide Perovskites with Capping Ligands and Metal Oxide Interfaces&#39; published in Advanced Optical Materials.

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