Conjugated polymer single crystals and nanowires

被引:28
作者
Cao, Xinxiu [1 ]
Zhao, Kefeng [2 ]
Chen, Liang [2 ]
Liu, Jiangang [2 ]
Han, Yanchun [2 ]
机构
[1] Hunan Univ Sci & Technol, Sch Mat Sci & Engn, Hunan Prov Key Lab Adv Mat New Energy Storage & C, Xiangtan, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, 5625 Renmin St, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
backbone stiffness; conjugated polymer; crystallization; device application; nanowire; single crystal; FIELD-EFFECT TRANSISTORS; DIFFUSION-CONTROLLED GROWTH; HETEROJUNCTION SOLAR-CELLS; SELF-SEEDED GROWTH; CHARGE-TRANSPORT; THIN-FILMS; REGIOREGULAR POLY(3-HEXYLTHIOPHENE); FRACTIONATED CRYSTALLIZATION; MONODISPERSE POLYFLUORENES; 3-DIMENSIONAL NUCLEATION;
D O I
10.1002/pcr2.10064
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
Conjugated polymer single crystals and nanowires show advantages for the study of intrinsic charge transport in conjugated polymers and achieve high device performance. However, preparation of conjugated polymer single crystals and nanowires, especially donor-acceptor (D-A) conjugated polymers, is challenging. In this review, the structural features of conjugated polymers are first described. Then, the mechanism of conjugated polymer crystallization in terms of thermodynamic equilibrium state, nucleation, and growth is discussed. Single crystals of poly(alkylthiophene)s (P3ATs) and nanowires of both P3ATs and D-A conjugated polymers are subsequently reviewed. Growth kinetics are a key issue in growing D-A-conjugated polymer crystals. Finally, the device performance based on conjugated polymer single crystals and nanowires is summarized.
引用
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页数:18
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