Well-controlled thieno[3,4-c]pyrrole-4,6-(5H)-dione based conjugated polymers for high performance organic photovoltaic cells with the power conversion efficiency exceeding 9%

被引:110
作者
Kim, Ji-Hoon [1 ,2 ]
Park, Jong Baek [1 ,2 ]
Jung, In Hwan [3 ]
Grimsdale, Andrew C. [4 ]
Yoon, Sung Cheol [3 ]
Yang, Hoichang [5 ]
Hwang, Do-Hoon [1 ,2 ]
机构
[1] Pusan Natl Univ, Dept Chem, Busan 609735, South Korea
[2] Pusan Natl Univ, Chem Inst Funct Mat, Busan 609735, South Korea
[3] Korea Res Inst Chem Technol, Adv Mat Div, Taejon 305600, South Korea
[4] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[5] Inha Univ, Optoelect Hybrids Res Ctr, Dept Appl Organ Mat Engn, Inchon 402751, South Korea
基金
新加坡国家研究基金会;
关键词
HETEROJUNCTION SOLAR-CELLS; OPEN-CIRCUIT VOLTAGE; BAND-GAP POLYMERS; MORPHOLOGY CONTROL; SEMICONDUCTING POLYMERS; BACKBONE ORIENTATION; BUILDING-BLOCK; HIGH HOLE; DIKETOPYRROLOPYRROLE; SINGLE;
D O I
10.1039/c5ee01627d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have synthesized a series of conjugated D-pi-A copolymers, PT-ttTPD and PBT-ttTPD, based on a (5-hexyltridecyl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione (ttTPD) acceptor unit in order to develop better photovoltaic polymers based on the TPD moiety: an epsilon-branched alkyl side chain on the TPD unit was coupled with 6-alkyl-thieno[3,2-b]thiophene (tt) pi-bridge molecules. The Stille polymerization of the brominated ttTPD and stannylated simple thiophene (T) finally gave a promising PT-ttTPD polymer showing well-ordered inter-chain orientation in the BHJ active layer. PT-ttTPD-based OPVs exhibited a highest power conversion efficiency (PCE) of 9.21% (V-OC = 0.86 V, J(SC) = 15.30 mA cm(-2), FF = 70%).
引用
收藏
页码:2352 / 2356
页数:5
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