Side-chain engineering of high-efficiency conjugated polymer photovoltaic materials

被引:343
作者
Zhang, Zhi-Guo [1 ]
Li, Yongfang [1 ,2 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, CAS Key Lab Organ Solids, Beijing 100190, Peoples R China
[2] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Lab Adv Optoelect Mat, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
polymer solar cells; conjugated polymers; side-chain engineering; photovoltaic materials; 2D-conjugated polymers; HETEROJUNCTION SOLAR-CELLS; OPEN-CIRCUIT-VOLTAGE; MOLECULAR-ENERGY LEVEL; POWER CONVERSION EFFICIENCY; DITHIOPHENE-BASED POLYMERS; ACCEPTOR GROUPS SYNTHESIS; BROAD ABSORPTION; SEMICONDUCTING POLYMERS; BAND-GAP; SUBSTITUTED BENZODITHIOPHENE;
D O I
10.1007/s11426-014-5260-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In recent years, conjugated polymers have attracted great attention in the application as photovoltaic donor materials in polymer solar cells (PSCs). Broad absorption, lower-energy bandgap, higher hole mobility, relatively lower HOMO energy levels, and higher solubility are important for the conjugated polymer donor materials to achieve high photovoltaic performance. Side-chain engineering plays a very important role in optimizing the physicochemical properties of the conjugated polymers. In this article, we review recent progress on the side-chain engineering of conjugated polymer donor materials, including the optimization of flexible side-chains for balancing solubility and intermolecular packing (aggregation), electron-withdrawing substituents for lowering HOMO energy levels, and two-dimension (2D)-conjugated polymers with conjugated side-chains for broadening absorption and enhancing hole mobility. After the molecular structural optimization by side-chain engineering, the 2D-conjugated polymers based on benzodithiophene units demonstrated the best photovoltaic performance, with power-conversion efficiency higher than 9%.
引用
收藏
页码:192 / 209
页数:18
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