Synthesis and photovoltaic properties of copolymers based on benzo[1,2-b:4,5-b′]dithiophene and thiazole with different conjugated side groups

Two new copolymers ( PT-Tz-DTBT and PT-Tz-DTffBT ) of benzo[1,2- b :4,5- b ′]dithiophene and thiazole ( Tz ) with different conjugated side groups 4,7-dithien-5-yl-2,1,3-benzodiathiazole ( DTBT ) and 5,6-difluoro-4,7-bis(4-hexylthiophen-2-yl)benzo[ c ][1,2,5]thiadiazole ( DTffBT ) were synthesized v...

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Bibliographic Details
Published inPolymer chemistry Vol. 4; no. 17; pp. 4737 - 4745
Main Authors Liu, Xunshan, Huang, Yuanshuai, Cao, Zhencai, Weng, Chao, Chen, Huajie, Tan, Songting
Format Journal Article
LanguageEnglish
Published 17.09.2013
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Summary:Two new copolymers ( PT-Tz-DTBT and PT-Tz-DTffBT ) of benzo[1,2- b :4,5- b ′]dithiophene and thiazole ( Tz ) with different conjugated side groups 4,7-dithien-5-yl-2,1,3-benzodiathiazole ( DTBT ) and 5,6-difluoro-4,7-bis(4-hexylthiophen-2-yl)benzo[ c ][1,2,5]thiadiazole ( DTffBT ) were synthesized via the Stille coupling polymerization and developed for polymer solar cell applications. The thermal, photophysical, electrochemical and photovoltaic properties of the copolymers were investigated. The two copolymers exhibited relatively low HOMO energy levels of −5.58 eV for PT-Tz-DTBT and −5.59 eV for PT-Tz-DTffBT , respectively. Bulk heterojunction (BHJ) solar cells with two as-synthesized copolymers as electron donors and (6,6)-phenyl-C 61 -butyric acid methyl ester (PC 61 BM) as an electron acceptor exhibit power conversion efficiencies (PCEs) of 2.63% and 3.75% for PT-Tz-DTBT and PT-Tz-DTffBT , respectively. When PC 71 BM was used as an electron acceptor, a promising PCE of 3.65% and 4.42% for PT-Tz-DTffBT was achieved by using a conventional and inverted device structure, respectively. Two copolymers with DTBT and DTffBT side chains were designed and synthesized. BHJ solar cells based on side chain polymer PT-Tz-DTffBT exhibited a high PCE of 4.42%.
ISSN:1759-9954
1759-9962
DOI:10.1039/c3py00614j