Search results for "Polymer solar cell"

showing 10 items of 43 documents

Ab initio modeling of excitonic and charge-transfer states in organic semiconductors: the PTB1/PCBM low band gap system.

2013

A detailed quantum chemical simulation of the excitonic and charge-transfer (CT) states of a bulk heterojunction model containing poly(thieno[3,4-b]thiophene benzodithiophene) (PTB1)/[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) is reported. The largest molecular model contains two stacked PTB1 trimer chains interacting with C60 positioned on top of and lateral to the (PTB1)3 stack. The calculations were performed using the algebraic diagrammatic construction method to second order (ADC(2)). One main result of the calculations is that the CT states are located below the bright inter-chain excitonic state, directly accessible via internal conversion processes. The other important aspects…

Chemistrybusiness.industryBand gapAb initioTrimerCharge (physics)General ChemistryInternal conversion (chemistry)BiochemistryMolecular physicsCatalysisPolymer solar cellOrganic semiconductorDelocalized electronColloid and Surface ChemistryOptoelectronicsbusinessJournal of the American Chemical Society
researchProduct

Organoboron Polymers for Photovoltaic Bulk Heterojunctions

2010

We report on the application of three-coordinate organoboron polymers, inherently strong electron acceptors, in flexible photovoltaic (PV) cells. Poly[(1,4-divinylenephenylene)(2,4,6-triisopropylphenylborane)] (PDB) has been blended with poly(3-hexylthiophene-2,5-diyl) (P3HT) to form a thin film bulk heterojunction (BHJ) on PET/ITO substrates. Morphology may be modulated to give a high percentage of domains (10-20 nm in size) allowing exciton separation. The photoelectric properties of the BHJs in devices with aluminium back electrodes were imaged by light beam induced current (LBIC) and light beam induced voltage (LBIV) techniques. Open circuit voltages, short circuit currents and overall …

Conductive polymerMaterials sciencePolymers and PlasticsOrganic solar cellOpen-circuit voltagebusiness.industryOrganic ChemistryHeterojunctionPhotoelectric effectPolymer solar cellPolymer chemistryMaterials ChemistryOptoelectronicsThin filmbusinessShort circuitMacromolecular Rapid Communications
researchProduct

Ester-functionalized poly(3-alkylthiophene) copolymers : synthesis, physicochemical characterization and performance in bulk heterojunction organic s…

2013

Abstract The introduction of functional moieties in the donor polymer (side chains) offers a potential pathway toward selective modification of the nanomorphology of conjugated polymer:fullerene active layer blends applied in bulk heterojunction organic photovoltaics, pursuing morphology control and solar cell stability. For this purpose, two types of poly(3-alkylthiophene) random copolymers, incorporating different amounts (10/30/50%) of ester-functionalized side chains, were efficiently synthesized using the Rieke method. The solar cell performance of the functionalized copolymers was evaluated and compared to the pristine P3HT:PCBM system. It was observed that the physicochemical and opt…

Conductive polymerchemistry.chemical_classificationMaterials scienceOrganic solar cellfullerenesGeneral ChemistryPolymerCondensed Matter PhysicsPolymer solar cellbulk heterojunction solar cellsElectronic Optical and Magnetic Materialslaw.inventionBiomaterialschemistry.chemical_compoundchemistrylawSolar cellPolymer chemistryMaterials ChemistryCopolymerSide chainPolythiopheneorganic photovoltaicsElectrical and Electronic Engineeringconductive polymers
researchProduct

Role of photoactive layer morphology in high fill factor all-polymer bulk heterojunction solar cells

2011

We report on the realization of all-polymer solar cells based on blends of poly(3-hexylthiophene-2,5-diyl) (P3HT) as a donor and poly{[N,N'-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5'-(2,2'-bithiophene)} (P(NDI2OD-T2)) as an acceptor. High fill factors are demonstrated for the first time in this class of devices suggesting high dissociation efficiency for the bounded electron-hole pairs and balanced electron and hole mobility along the thin films. The use of the high-mobility n-type P(NDI2OD-T2) polymer enables us to overcome one of the problems limiting the efficiency of all-polymer solar cells, resulting in fill factors comparable with those reported for …

DYNAMICSElectron mobilityMaterials scienceFullerenePHOTOVOLTAIC DEVICESLIGHT-INTENSITY DEPENDENCEBLENDSPolymer solar cellPhotoactive layerMaterials ChemistryThin filmSettore CHIM/02 - Chimica FisicaOpen-circuit voltagebusiness.industryORIGINPOLY(3-HEXYLTHIOPHENE)General ChemistryHybrid solar cellAcceptorTRANSPORTOPEN-CIRCUIT VOLTAGEsolar cells bulk heterojunctions devices organic electronicsTRANSISTORSOptoelectronicsbusinessCONJUGATED POLYMERS
researchProduct

Simultaneous determination of carrier lifetime and electron density-of-states in P3HT:PCBM organic solar cells under illumination by impedance spectr…

2010

We report new insights into recombination kinetics in poly(3-hexylthiophene):methanofullerene (P3HT:PCBM) bulk heterojunction (BHJ) solar cells, based on simultaneous determination of the density of states (DOS), internal recombination resistance, and carrier lifetime, at different steady states, by impedance spectroscopy. A set of measurements at open circuit under illumination was performed aiming to better understand the limitations to the photovoltage, which in this class of solar cells remains far below the theoretical limit which is the difference between the LUMO level of PCBM and the HOMO of P3HT (∼1.1 eV). Recombination kinetics follows a bimolecular law, being the recombination ti…

Electron densityOrganic solar cellRenewable Energy Sustainability and the EnvironmentChemistryBulk heterojunctionFermi levelAnalytical chemistryCharge densityImpedance spectroscopyCarrier lifetimeMolecular physicsPolymer solar cellSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialssymbols.namesakeOrganic solar cellsymbolsDensity of statesHOMO/LUMOLifetime
researchProduct

Template-assisted fabrication of free-standing nanorod arrays of a hole-conducting cross-linked triphenylamine derivative: toward ordered bulk-hetero…

2009

Free-standing nanorod arrays of a thermally cross-linked semiconducting triphenylamine were fabricated on conductive ITO/glass substrates via an anodic aluminum oxide (AAO) template-assisted approach. By using a solution wetting method combined with a subsequent thermal imprinting step to fill the nanoporous structure of the template with a cross-linkable triphenylamine derivative, a polymeric replication of the AAO was obtained after thermal curing and selective removal of the template. To obtain well-aligned and free-standing nanorod arrays, aggregation and collapse of the nanorods were prevented by optimizing their aspect ratio and applying a freeze-drying technique to remove the aqueous…

FabricationMaterials scienceOrganic solar cellNanoporousbusiness.industryGeneral EngineeringGeneral Physics and AstronomyNanotechnologyTriphenylaminePolymer solar cellchemistry.chemical_compoundchemistryOptoelectronicsGeneral Materials ScienceNanorodWettingbusinessCuring (chemistry)ACS nano
researchProduct

Carbazole-based green and blue-BODIPY dyads and triads as donors for bulk heterojunction organic solar cells.

2020

Two BODIPY derivatives with one (B2) and two (B3) carbazole moieties were synthesized and applied as electron-donor materials in organic photovoltaic cells (OPV). Their optical and electrochemical properties were systematically investigated. These BODIPY dyes exhibit excellent solubility in organic solvents and present high molar extinction coefficients (1.37–1.48 × 105 M−1 cm−1) in solutions with absorption maxima at 586 nm for mono-styryl groups and at 672 nm for di-styryl groups. The introduction of the styryl moieties results in a large bathochromic shift and a significant decrease in the HOMO–LUMO energy-gaps. The BODIPY dyes show relatively low HOMO energies ranging from −4.99 to −5.1…

Inorganic Chemistrychemistry.chemical_compoundMaterials sciencechemistryOrganic solar cellCarbazoleBathochromic shiftMolecular orbitalCyclic voltammetryBODIPYPhotochemistryAcceptorPolymer solar cellDalton transactions (Cambridge, England : 2003)
researchProduct

Porphyrin Antenna-Enriched BODIPY–Thiophene Copolymer for Efficient Solar Cells

2018

International audience; Low bandgap A−π–D copolymer, P(BdP-DEHT), consisting of alternating BOronDIPYrromethene (BODIPY) and thiophene units bridged by ethynyl linkers, and its porphyrin-enriched analogue, P(BdP/Por-DEHT), were prepared, and their optical and electrochemical properties were studied. P(BdP-DEHT) exhibits strong absorption in the 500–800 nm range with an optical bandgap of 1.74 eV. On the basis of cyclic voltammetry, the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels are evaluated to be −5.40 and −3.66 eV, respectively. After the anchoring of zinc(II) porphyrin on the BODIPY unit, P(BdP/Por-DEHT) displays broadened absor…

Materials scienceBand gap02 engineering and technology010402 general chemistry01 natural sciences7. Clean energyPolymer solar cellporphyrin substitutionDichlorobenzenechemistry.chemical_compoundThiopheneGeneral Materials ScienceHOMO/LUMOsolvent vapor annealing[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyPorphyrin0104 chemical sciencespower conversion efficiencyCrystallographyApiD copolymerchemistry[ CHIM.MATE ] Chemical Sciences/Material chemistryBODIPYCyclic voltammetry0210 nano-technologypolymer solar cells
researchProduct

A Very Low Band Gap Diketopyrrolopyrrole-Porphyrin Conjugated Polymer

2017

International audience; A porphyrin-diketopyrrolopyrrole-containing polymer (poly(porphyrin-diketopyrrolopyrrole) (PPDPP)) shows impressive molar absorption coefficients from lambda=300 to 1000 nm. The photophysical and structural properties of PPDPP have been studied. With PPDPP as the electron donor and [ 6,6]phenyl C-71 butyric acid methyl ester (PC71BM) as the electron acceptor, the bulk heterojunction polymer solar cell showed overall power conversion efficiencies of 4.18 and 6.44% for as-cast and two-step annealing processed PPDPP: PC71BM (1: 2) active layers, respectively. These results are quite impressive for porphyrin-containing polymers, especially when directly included in the p…

Materials scienceBand gapbuilding-blockporphyrinoidsElectron donorthin-film transistors02 engineering and technologyConjugated system010402 general chemistryPhotochemistry[ CHIM ] Chemical Sciences01 natural sciencesPolymer solar cellheterojunction solar-cellschemistry.chemical_compound[CHIM]Chemical Sciencessmall-moleculepolymerschemistry.chemical_classificationsemiconducting polymerscharge transferGeneral ChemistryPolymerChromophoreElectron acceptorside-chains021001 nanoscience & nanotechnologyPorphyrinphotovoltaic properties0104 chemical sciencesphotodynamic therapychemistryorganic photovoltaics0210 nano-technologyabsorptionperformanceconjugationChemPlusChem
researchProduct

Influence of the intermediate density-of-states occupancy on open-circuit voltage of bulk heterojunction solar cells with different fullerene accepto…

2010

Electron density of states (DOS) and recombination kinetics of bulk heterojunction solar cells consisting of a poly(3-hexylthiophene) (P3HT) donor and two fullerene acceptors, either [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) or 4,4′-dihexyloxydiphenylmethano[60]fullerene (DPM6), have been determined by means of impedance spectroscopy. The observed difference of 125 mV in the output open-circuit voltage is attributed to significant differences of the occupancy of the DOS in both fullerenes. Whereas DPM6 exhibits a full occupation of the electronic band, occupancy is restricted to the tail of the DOS in the case of PCBM-based devices, implying a higher rise of the Fermi level in the D…

Materials scienceFullereneOrganic solar cellOpen-circuit voltageFermi levelAnalytical chemistryCarrier lifetimeMolecular physicsPolymer solar cellMicrosecondsymbols.namesakeDensity of statessymbolsGeneral Materials SciencePhysical and Theoretical Chemistry
researchProduct