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Molecular Design and Photovoltaic Performances of Organic Dyes Containing Triphenylamine for Dye-Sensitized Solar Cell

Title
Molecular Design and Photovoltaic Performances of Organic Dyes Containing Triphenylamine for Dye-Sensitized Solar Cell
Author(s)
Jung, Mi RanJo, Hyo JeongYang, Hyun SikKim, HyojeongKang, Jin KyuKim, Dae HwanAhn, Kwang-SoonKim, Jae Hong
DGIST Authors
Kang, Jin KyuKim, Dae Hwan
Issued Date
2011
Type
Article
Article Type
Article; Proceedings Paper
Subject
Active AreaChromophoresConversion EfficiencyDye-Sensitized Solar CellDye-Sensitized Solar Cells (DSCs)Electron AcceptorFill-FactorImpedance AnalysisLife-TimesMolecular DesignNano-Structured MaterialsOpen Circuit Photo VoltageOrganic DyeOrganic PhotosensitizersPhoto-AnodePhotoelectrochemical CellsPhotonicsPhotosensitizersPhotovoltaic EffectsPhotovoltaic PerformancePhotovoltaic PerformancesPhotovoltaic PropertyPower Conversion EfficienciesRecombination KineticsSolar CellsSolar Power GenerationTiOTitanium DioxideTriphenyl AminesTriphenylamine Chromophores
ISSN
1542-1406
Abstract
Organic dyes containing multi-acceptors/anchors in a chromophore were synthesized for use in a dye-sensitized solar cell. The photovoltaic properties of organic dyes composed of different acceptor in their chromophores were measured to identify the effects on the DSSC performance. The organic dye, 4 containing multi-cyanoacrylic acid as the electron acceptor showed a power conversion efficiency of 4.7% under AM 1.5 illumination (100mWcm-2) in an photo active area of 0.24cm2, short circuit current density of 12.9mAcm-2, open circuit photo voltage of 0.62V and a fill-factor of 60%. The retarded recombination kinetics from TiO2 electrode to electrolyte enhanced the electron life time of organic dye, 4 in the photoanode in DSSC that was well confirmed with the impedance analysis.
URI
http://hdl.handle.net/20.500.11750/5402
DOI
10.1080/15421406.2011.564102
Publisher
Taylor and Francis Ltd.
Related Researcher
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Appears in Collections:
Convergence Research Center for Solar Energy 1. Journal Articles

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