Search results for "acceptor"

showing 10 items of 394 documents

Triphenyl group containing molecular glasses of azobenzene for photonic applications

2016

Abstract D-π-A type organic molecules have attracted considerable attention of scientists due to their potential applications in nonlinear optics and holographic data storage as light, flexible and low-cost photonic materials. To provide a better understanding on the relation between the compound chemical structure and their physical properties necessary for the mentioned purposes, eight glassy triphenyl group containing derivatives of azobenzene with incorporated 5,5-dimethylcyclohex-2-enylidene or 4H-pyran-4-ylidene structural fragments and dicyanomethylene, indene-1,3-dione and pyrimidine-2,4,6(1H,3H,5H)-trione acceptor groups have been synthesized and investigated. Thermal stability of …

Materials scienceOrganic solar cell02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundOrganic chemistryMoleculeThermal stabilityElectrical and Electronic EngineeringPhysical and Theoretical ChemistrySpectroscopyOrganic ChemistryNonlinear optics021001 nanoscience & nanotechnologyAcceptorAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsAmorphous solidAzobenzenechemistry0210 nano-technologyGlass transitionOptical Materials
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BODIPY–diketopyrrolopyrrole–porphyrin conjugate small molecules for use in bulk heterojunction solar cells

2018

Two small molecules denoted as BD-pPor and BD-tPor composed of a central BODIPY core surrounded with two DPP and two porphyrin units have been designed and synthesized. In BD-pPor and BD-tPor, porphyrins are linked to the central BODIPY by phenyl and thiophene bridges, respectively. The optical and electrochemical properties were systematically investigated in order to employ them as donors along with PC71BM as an acceptor for solution processed bulk heterojunction organic solar cells. After the optimization of the active layer, the organic solar cells based on BD-pPor and BD-tPor exhibit overall power conversion efficiencies of 6.67% and 8.98% with an energy loss of 0.63 eV and 0.50 eV. Th…

Materials scienceOrganic solar cell02 engineering and technology010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesPolymer solar cellchemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryThiopheneGeneral Materials Science[CHIM.COOR]Chemical Sciences/Coordination chemistryHOMO/LUMOComputingMilieux_MISCELLANEOUSRenewable Energy Sustainability and the Environment[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologySmall moleculeAcceptorPorphyrin0104 chemical scienceschemistryBODIPY0210 nano-technology
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A bacteriochlorin-diketopyrrolopyrrole triad as a donor for solution-processed bulk heterojunction organic solar cells

2019

We have designed an A–π–D–π–A small-molecule triad consisting of a bacteriochlorin (BC) donor central core linked with two diketopyrrolopyrrole (DPP) acceptors via ethynyl bridges (BC-DPP-1). BC-DPP-1 has a narrow optical bandgap of 1.38 eV with highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels of −4.93 eV and −3.40 eV, respectively, and it was used as an electron donor along with [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) as an acceptor for solution-processed small-molecule organic solar cells. After optimizing the weight ratio between BC-DPP-1 and PC71BM and pyridine as a solvent additive and subsequent solvent vapor annealing using THF, an …

Materials scienceOrganic solar cellBand gapPhotovoltaic systemEnergy conversion efficiencyAnalytical chemistry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology7. Clean energy01 natural sciencesAcceptorPolymer solar cell0104 chemical sciencesMaterials Chemistry0210 nano-technologyTernary operationHOMO/LUMOJournal of Materials Chemistry C
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Donor/Acceptor Heterojunction Organic Solar Cells

2020

The operation and the design of organic solar cells with donor/acceptor heterojunction structure and exciton blocking layer is outlined and results of their initial development and assessment are reported. Under halogen lamp illumination with 100 mW/cm2 incident optical power density, the devices exhibits an open circuit voltage VOC = 0.45 V, a short circuit current density JSC between 2 and 2.5 mA/cm2 with a fill factor FF &asymp

Materials scienceOrganic solar cellComputer Networks and Communicationslcsh:TK7800-836002 engineering and technology010402 general chemistrySettore ING-INF/01 - Elettronica01 natural scienceslaw.inventionorganic photovoltaicexciton blocking layerdonor/acceptor heterojuntionlawElectrical and Electronic Engineeringbusiness.industryOpen-circuit voltagelcsh:ElectronicsEnergy conversion efficiencyorganic solar cellsHeterojunction021001 nanoscience & nanotechnologyAcceptor0104 chemical sciencesHalogen lampHardware and ArchitectureControl and Systems EngineeringOrganic solar celllifetime and degradationSignal ProcessingOptoelectronicsQuantum efficiencyorganic photovoltaics0210 nano-technologybusinessShort circuitElectronics
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Ternary Organic Solar Cell with a Near‐Infrared Absorbing Selenophene–Diketopyrrolopyrrole‐Based Nonfullerene Acceptor and an Efficiency above 10%

2020

Materials scienceOrganic solar cellNear-infrared spectroscopyEnergy Engineering and Power TechnologyElectrical and Electronic EngineeringPhotochemistryTernary operationAcceptorAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsSolar RRL
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Nonfullerene Polymer Solar Cells Reaching a 9.29% Efficiency Using a BODIPY-Thiophene Backboned Donor Material

2018

A conjugated polymer donor containing BODIPY-thiophene dyads in the backbone, P(BdP-EHT), combined with a low bandgap nonfullerene acceptor (SMDPP) consisting of carbazole and diketopyrrolopyrrole units linked with a tetracyanobutadiene acceptor π-linker, was used to design bulk heterojunction polymer solar cells. After the optimization of the donor to acceptor weight ratio and solvent vapor annealing of the P(BdP-EHT):SMDPP active layer, the resulting polymer solar cell showed an overall power conversion efficiency of 9.29%, which is significantly higher than that for the polymer solar cell based on PC71BM (7.41%) processed under identical conditions. This improved power conversion efficie…

Materials scienceOrganic solar cellOpen-circuit voltageCarbazoleEnergy conversion efficiencyEnergy Engineering and Power Technology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry7. Clean energy01 natural sciencesAcceptorPolymer solar cell0104 chemical scienceschemistry.chemical_compoundchemistryMaterials ChemistryElectrochemistryChemical Engineering (miscellaneous)Electrical and Electronic Engineering0210 nano-technologyHOMO/LUMOShort circuitACS Applied Energy Materials
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New BODIPY derivatives with triarylamine and truxene substituents as donors for organic bulk heterojunction photovoltaic cells

2021

Abstract We have designed two new BODIPY derivatives, denoted as 6a and 6b, substituted with truxene moiety and triphenylamine (TPA) unit groups and have investigated their optical and electrochemical properties. Dyes 6a and 6b were employed as donor along with PC71BM or Y6 as acceptor for the fabrication of binary and ternary organic solar cells. After optimization of the binary and ternary active layers, we have achieved over all power conversion efficiency (PCE) of 11.37 % and 13.32% for 6a:PC71BM:Y6 and 6b:PC71BM:Y6 ternary organic solar cells, respectively, which are higher than the binary organic solar cells based on PC71BM or Y6 acceptor. The higher power conversion efficiency for te…

Materials scienceOrganic solar cellRenewable Energy Sustainability and the EnvironmentEnergy conversion efficiencyPhotochemistryTriphenylamineAcceptorPolymer solar cellchemistry.chemical_compoundchemistryMoietyGeneral Materials ScienceBODIPYTernary operationSolar Energy
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Synergies and compromises between charge and energy transfers in three-component organic solar cells

2020

In this paper, we developed different three-component organic heterojunction structures supported by PET/ITO substrates with the aim to study the possible synergies and/or compromises between charge transfer (CT) and energy transfer (ET) processes in organic solar cells (OSCs). As components, we employed poly(3-hexylthiophene-2,5-diyl) (P3HT; donor), [6,6]-phenyl-C61-butyric acid methyl ester (PCBM; acceptor) and poly(9,9-dioctylfluorene-alt-benzothiadiazole) (F8BT) that is known to give good ET to P3HT. At first, we observed that in a planar heterojunction (PHJ) solar cell, F8BT has to be properly located in between P3HT and PCBM to get a cascade energy level configuration allowing for a b…

Materials scienceOrganic solar cellbusiness.industryEnergy conversion efficiencyGeneral Physics and AstronomyHeterojunctionCharge (physics)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAcceptor0104 chemical scienceslaw.inventionActive layerPlanarlawSolar cellOptoelectronicsPhysical and Theoretical Chemistry0210 nano-technologybusinessorganic solar cells transparent heterojunctionPhysical Chemistry Chemical Physics
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Donor–Acceptor Interfaces by Engineered Nanoparticles Assemblies for Enhanced Efficiency in Plastic Planar Heterojunction Solar Cells

2016

Precisely positioning functionalized gold nanoparticles assemblies at planar donor-acceptor interfaces results in 14-fold enhancement of power conversion efficiency in P3HT/PCBM organic solar cells on plastic (ITO/PET) substrates. This result has been achieved by employing naphthalenethiol-capped gold nanoparticles (NT-Au-NPs) produced by laser ablation in liquid and size varied in the 10-30 nm range. Upon surface functionalization with the aromatic thiol, these particles self-assemble in submicrometer aggregates, which give increased light scattering. When these aggregates are deposited in the planar heterojunction between the donor and the acceptor systems, the localized scattering leads …

Materials sciencePHASOR APPROACHOrganic solar cellPOWER-CONVERSION EFFICIENCYNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesLight scatteringCoatings and FilmsElectronicOptical and Magnetic MaterialsPhysical and Theoretical ChemistryORGANIC PHOTOVOLTAIC DEVICESSURFACTANT-FREEScatteringbusiness.industryEnergy conversion efficiencyHeterojunctionPERFORMANCESELF-ORGANIZATION021001 nanoscience & nanotechnologyFREE GOLD NANOPARTICLESAU NANOPARTICLESAcceptor0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSurfacesEnergy (all)General EnergyColloidal goldTITANIUM-OXIDESurface modificationOptoelectronicsLASER-ABLATIONElectronic Optical and Magnetic Materials; Energy (all); Surfaces Coatings and Films; Physical and Theoretical Chemistry0210 nano-technologybusinessThe Journal of Physical Chemistry C
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Influence of an elastic stress on the conductivity of passive films

2001

Abstract The electrochemical impedance was measured over a large range of frequency and under straining condition in sodium chloride solution. The Mott-Schottky analysis, performed at high frequency, appears as very useful method to study the effect of an elastic stress on the capacitance values. The results obtained indicate that the semi-conductive properties of passive films formed on a type 316 L stainless steel (SS) are not markedly modified by an elastic stress when applied after ageing. In contrast, passive films formed in the presence of elastic stress have a higher donor and acceptor concentration than those formed in a stress-free state, suggesting that the passive film conductivi…

Materials sciencePassivationMechanical EngineeringMetallurgyElectrolyteConductivityCondensed Matter PhysicsAcceptorCapacitanceCorrosionStress (mechanics)Mechanics of MaterialsPitting corrosionGeneral Materials ScienceComposite materialMaterials Science and Engineering: A
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