Search results for "Fullerene derivatives"

showing 5 items of 5 documents

Fullerene polymers: synthesis and properties

2007

chemistry.chemical_classificationFullerene derivativesFullereneChemical engineeringFullereneChemistryNanotechnologyGeneral ChemistryGeneral MedicinePolymerSettore CHIM/06 - Chimica Organicapolymers
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Polymer solar cells with novel fullerene-based acceptor

2004

Abstract Alternative acceptor materials are possible candidates to improve the optical absorption and/or the open circuit voltage of polymer–fullerene solar cells. We studied a novel fullerene-type acceptor, DPM-12, for application in polymer–fullerene bulk heterojunction photovoltaic devices. Though DPM-12 has the identical redox potentials as methanofullerene PCBM, surprisingly high open circuit voltages in the range V OC =0.95 V were measured for OC 1 C 10 -PPV:DPM-12-based samples. The potential for photovoltaic application was studied by means of photovoltaic characterization of solar cells including current–voltage measurements and external quantum yield spectroscopy. Further studies …

Organic solar cellbusiness.industryChemistryPhotovoltaic systemMetals and AlloysSettore CHIM/06 - Chimica OrganicaSurfaces and InterfacesPhotovoltaic effectHybrid solar cellAcceptorPolymer solar cellSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionlawPhotovoltaicsfullerene derivativessolar cellsSolar cellMaterials ChemistryOptoelectronicsOrganic chemistrybusinessThin Solid Films
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Mimicking photosynthesis: covalent [60]fullerene-based donor–acceptor ensembles

2004

Abstract Within the context of exploring photophysical properties of [60]fullerene-based donor–acceptor ensembles, we highlight in this contribution an approach towards the synthesis of a novel series of donor-bridge-acceptor, C 60 –wire– ex TTF , ensembles that incorporate p -phenylenevinylene oligomers, in which the conjugation length has been systematically increased, as bridges that connect π-extended tetrathiafulvalenes (exTTF) (electron donor) with [60]fullerene (electron acceptor). This molecular design allows probing the effects of distance and rate, at which electron transfer processes occur, as well as the molecular-wire behavior of the oligo-PPV fragments.

chemistry.chemical_classificationFullereneChemistryMechanical EngineeringMetals and AlloysContext (language use)Electron donorSettore CHIM/06 - Chimica OrganicaElectron acceptorCondensed Matter PhysicsPhotochemistryPhotoinduced electron transferElectronic Optical and Magnetic MaterialsMolecular wireElectron transferchemistry.chemical_compoundFullerene derivativesMechanics of MaterialsMaterials ChemistryTetrathiafulvaleneSynthetic Metals
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Electronic communication through pi-conjugated wires in covalently linked porphyrin/C60 ensembles

2005

Novel photo- and electroactive triads, in which pi-conjugated p-phenylenevinylene oligomers (oPPVs) of different length are connected to a photoexcited-state electron donor (i.e., zinc tetraphenylporphyrin) and an electron acceptor (i.e., C(60)), were designed, synthesized, and tested as electron-transfer model systems. A detailed physicochemical investigation, concentrating mainly on long-range charge separation and charge recombination and kinetics, revealed small attenuation factors beta of 0.03+/-0.005 A(-1). Energy matching between the HOMO levels of C(60) and oPPVs emerged as a key parameter for supporting molecular-wire-like behavior: It favors rapid and efficient electron or hole in…

chemistry.chemical_classificationFullereneOrganic ChemistryElectron donorGeneral ChemistrySettore CHIM/06 - Chimica OrganicaElectron acceptorConjugated systemPhotochemistryPorphyrinCatalysisElectron transferMolecular wirechemistry.chemical_compoundchemistryCovalent bondFullerene derivatives
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Design, synthesis and photovoltaic properties of [60]fullerene based molecular materials

2005

Abstract The possibility to use new organic semiconductor materials, in place of silicon wafers, in the fabrication of photovoltaic devices on substrates offer the prospect of lower manufacturing costs, particularly for large area applications. Thus, one of the most promising areas in fullerene research involves its potential application, mixed with conjugated polymers, in mimicking photosynthesis and in the related solar energy conversion. The tendency to phase segregation in blends of C60 derivatives and conjugated polymers has to be optimized to improve both charge photogeneration and transport in photovoltaic devices. In order to optimize device performances, a great deal of work has be…

chemistry.chemical_classificationFullereneFabricationMaterials scienceOrganic solar cellPhotovoltaic systemphotovoltaic devicesBioengineeringNanotechnologyPolymerSettore CHIM/06 - Chimica OrganicaConjugated systemBiomaterialsOrganic semiconductorchemistryMechanics of Materialsfullerene derivativesWafer
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