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Dithienocarbazole- and benzothiadiazole-based donor-acceptor conjugated polymers for bulk heterojunction polymer solar cells

查看全文 作　　者：Ziqing [1,2]Rong;Yunfeng [1,2]Deng;Zhiyuan [1]Xie;Yanhou [1]Geng;Fosong [1]Wang 高影响力作者 机构地区：[1]State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry,Chinese Academy of Sciences;[2]University of Chinese Academy of Sciences高影响力机构 出　　处：《Science China Chemistry》索引2015年第58卷第2期,共7页高影响力期刊 基　　金：financially supported by the National Basic Research Program of China(2014CB643504);the National Natural Science Foundation of China(51273193);the Strategic Priority Research Program of the Chinese Academy of Sciences(XDB12010300) 摘　　要：Donor-acceptor(D-A)-conjugated polymers P(BT-C1)and P(BT-C2),with dithieno[2,3-b;7,6-b]carbazole(C1)or dithieno[3,2-b;6,7-b]carbazole(C2)as D-unit and benzothiadiazole(BT)as A-unit,were synthesized.The optical bandgaps of the polymers are similar(1.84 and 1.88 e V,respectively).The structures of donor units noticeably influence the energy levels and backbone curvature of the polymers.P(BT-C1)shows a large backbone curvature;its highest occupied molecular orbital(HOMO)energy level is 5.18 e V,whereas P(BT-C2)displays a pseudo-straight backbone and has a HOMO energy level of 5.37 e V.The hole mobilities of the polymers without thermal annealing are 1.9×10 3 and 2.7×10 3 cm2 V 1 s 1 for P(BT-C1)and P(BT-C2),respectively,as measured by organic thin-film transistors(OTFTs).Polymer solar cells using P(BT-C1)and P(BT-C2)as the donor and phenyl-C71-butyric acid methyl ester(PC71BM)as the acceptor were fabricated.Power conversion efficiencies(PCEs)of 4.9%and 5.0%were achieved for P(BT-C1)and P(BT-C2),respectively.The devices based on P(BT-C2)exhibited a higher Voc due to the deeper HOMO level of the polymer,which led to a slightly higher PCE. 关 键 词：共轭聚合物 苯并噻二唑 太阳能电池 受体 HOMO能级 异质结 Dit 有机薄膜晶体管
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