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dc.contributor.authorPatra, Dhananjayaen_US
dc.contributor.authorSahu, Duryodhanen_US
dc.contributor.authorPadhy, Hariharaen_US
dc.contributor.authorKekuda, Dhananjayen_US
dc.contributor.authorChu, Chih-Weien_US
dc.contributor.authorLin, Hong-Cheuen_US
dc.date.accessioned2014-12-08T15:38:24Z-
dc.date.available2014-12-08T15:38:24Z-
dc.date.issued2010-12-01en_US
dc.identifier.issn0887-624Xen_US
dc.identifier.urihttp://dx.doi.org/10.1002/pola.24356en_US
dc.identifier.urihttp://hdl.handle.net/11536/26281-
dc.description.abstractA series of low-band-gap (LBG) donor-accepor conjugated main-chain copolymers (P1-P4) containing planar 2,7-carbazole as electron donors and bithiazole units (4,4'-dihexyl-2,2'-bithiazole and 4,4'-dihexyl-5,5'-di(thiophen-2-yl)-2,2'-bithiazole) as electron acceptors were synthesized and studied for the applications in bulk heterojunction (BHJ) solar cells. The effects of electron deficient bithiazole units on the thermal, optical, electrochemical, and photovoltaic (PV) properties of these LBG copolymers were investigated. Absorption spectra revealed that polymers P1-P4 exhibited broad absorption bands in UV and visible regions from 300 to 600 nm with optical band gaps in the range of 1.93-1.99 eV, which overlapped with the major region of the solar emission spectrum. Moreover, carbazole-based polymers P1-P4 showed low values of the highest occupied molecular orbital (HOMO) levels, which provided good air stability and high open circuit voltages (V(oc)) in the PV applications. The BHJ PV devices were fabricated using polymers P1-P4 as electron donors and (6,6)-phenyl-C(61)-butyric acid methyl ester (PC(61)BM) or (6,6)-phenyl-C(71)-butyric acid methyl ester (PC(71)BM) as electron acceptors in different weight ratios. The PV device bearing an active layer of polymer blend P4:PC(71)BM (1:1.5 w/w) showed the best power conversion efficiency value of 1.01% with a short circuit current density (J(sc)) of 4.83 mA/cm(2), a fill factor (FF) of 35%, and V(oc) - 0.60 V under 100 mW/cm(2) of AM 1.5 white-light illumination. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 5479-5489, 2010en_US
dc.language.isoen_USen_US
dc.subjectbithiazole unitsen_US
dc.subjectbulk heterojunctionen_US
dc.subjectcopolymersen_US
dc.subjectdonor-acceptoren_US
dc.titleSynthesis and Applications of 2,7-Carbazole-Based Conjugated Main-Chain Copolymers Containing Electron Deficient Bithiazole Units for Organic Solar Cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/pola.24356en_US
dc.identifier.journalJOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRYen_US
dc.citation.volume48en_US
dc.citation.issue23en_US
dc.citation.spage5479en_US
dc.citation.epage5489en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.department光電工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.contributor.departmentDepartment of Photonicsen_US
dc.identifier.wosnumberWOS:000284225500024-
dc.citation.woscount22-
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