Search results for "Photoinduced charge separation"

showing 5 items of 5 documents

Enhanced electronic communication through a conjugated bridge in a porphyrin-fullerene donor-acceptor couple

2021

A ZnP-2EDOTV-C60 triad, with enhanced electronic communication between terminus donor and acceptor moieties, was synthesized and studied both experimentally and theoretically. Electrochemical measurements and density functional theory calculations support that the first oxidation takes place on the 3,4-ethylenedioxythiophenevinylene (2EDOTV) bridge followed by the oxidation of the ZnP moiety at slightly higher energies. The electronic communication between the terminal electron-donor ZnP and the electron-acceptor C60 units is enhanced by the conjugated EDOTV-based spacer leading to photoinduced electron transfer over the distance >2 nm in the picosecond time domain. The involvement of the s…

Materials science010405 organic chemistry116 Chemical sciencesGeneral ChemistryConjugated system010402 general chemistryPhotochemistry01 natural sciencesPorphyrinAcceptorPhotoinduced electron transfer0104 chemical scienceschemistry.chemical_compoundElectron transferchemistryPhotoinduced charge separationMaterials ChemistryMoietyDensity functional theory
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Role of the bridge in photoinduced electron transfer in porphyrin-fullerene dyads.

2015

The role of π-conjugated molecular bridges in through-space and through-bond electron transfer is studied by comparing two porphyrin-fullerene donor-acceptor (D-A) dyads. One dyad, ZnP-Ph-C60 (ZnP = zinc porphyrin), incorporates a phenyl bridge between D and A and behaves very similarly to analogous dyads studied previously. The second dyad, ZnP-EDOTV-C60, introduces an additional 3,4-ethylenedioxythienylvinylene (EDOTV) unit into the conjugated bridge, which increases the distance between D and A, but, at the same time, provides increased electronic communication between them. Two essential outcomes that result from the introduction of the EDOTV unit in the bridge are as follows: 1) faster…

FullereneChemistryOrganic ChemistryGeneral ChemistryPhotochemistryExcimerBridge (interpersonal)PorphyrinCatalysisPhotoinduced electron transferElectron transferchemistry.chemical_compoundPhotoinduced charge separationIntramolecular forceChemistry (Weinheim an der Bergstrasse, Germany)
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Tunability by alkali metal cations of photoinduced charge separation in azacrown functionalized graphene.

2013

A modified graphene oxide containing aza-9-crown-3 ether units covalently anchored has been prepared; aqueous suspensions of this material in the presence of Li(+), Na(+) and K(+) cations exhibit enhanced electrochemical response, enhanced photoinduced charge separation and longer lifetimes, facts that can be attributed to stabilization of electrons on graphene oxide by the nearby alkali metal cation-azacrown complexes.

Materials scienceInorganic chemistryOxideEtherGraphite oxidePhotochemistryCatalysislaw.inventionchemistry.chemical_compoundQUIMICA ORGANICAlawMaterials ChemistryReductionAqueous solutionGrapheneMetals and AlloysGeneral ChemistryAlkali metalSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryPhotoinduced charge separationCovalent bondGraphite oxideCeramics and CompositesChemical communications (Cambridge, England)
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Photoinduced Charge Separation of Self-Organized Semiconducting Superstructures Composed of a Functional Polymer-TiO2 Hybrid

2013

chemistry.chemical_compoundMaterials sciencePolymers and PlasticschemistryPhotoinduced charge separationOrganic ChemistryTitanium dioxideMaterials ChemistryCopolymerNanotechnologySelf-assemblyPhysical and Theoretical ChemistryCondensed Matter PhysicsMacromolecular Chemistry and Physics
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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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