All-conjugated donor–acceptor graft/block copolymers as single active components and surfactants in all-polymer solar cells

被引:0
作者
Jin Wang
Chien Lu
Tomoya Higashihara
Wen-Chang Chen
机构
[1] Chinese Academy of Sciences,Suzhou Institute of Nano
[2] National Taiwan University,Tech and Nano
[3] Yamagata University,Bionics
来源
Microsystem Technologies | 2017年 / 23卷
关键词
Poly(3-hexylthiophene); Poly(naphthalene diimide); Block copolymer; Polymer solar cells;
D O I
暂无
中图分类号
学科分类号
摘要
In this work, we report the synthesis of all-conjugated donor–acceptor (D–A) graft/block copolymers via an externally-initiated Kumada catalyst-transfer polycondensation (KCTP) method. In the first step, end-functional electron acceptor blocks, poly(naphthalene diimide)s (PNDIs), were prepared via the Stille coupling polycondensation. Then, P3HT blocks were polymerized via KCTP initiated by the Ni(COD)2-activated PNDI complexes. Therefore, a series of D–A graft copolymers and ABA-type (P3HTs were initiated from both ends of PNDI) triblock copolymers were successfully synthesized. The polymers were used to fabricate polymer thin film transistors and the results indicated that all the polymers exhibited moderate charge mobilities ranging from 10−4 to 10−3 cm2 V−1 s−1, and they could be further improved by thermal annealing. Finally, all-polymer solar cells were fabricated by using the block copolymers as the single active components or as surfactants. A power conversion efficiency (PCE) of 0.22 % with open circuit voltage (Voc) = 0.55 V, short circuit current density (Jsc) = 0.64 mA/cm2, and fill factor (FF) = 0.62 was recorded by using the donor–acceptor all-conjugated block copolymer as acceptor, and a PCE of 2.28 % with Voc = 0.61 V, Jsc = 7.00 mA/cm2, and FF = 0.54 was obtained when PNDI was used as a surfactant.
引用
收藏
页码:1183 / 1189
页数:6
相关论文
共 183 条
  • [1] Benten H(2016)High-performance ternary blend all-polymer solar cells with complementary absorption bands from visible to near-infrared wavelengths Energy Environ Sci 9 135-140
  • [2] Nishida T(2013)Dithiazolyl-benzothiadiazole-containing polymer acceptors: synthesis, characterization, and all-polymer solar cells Polym Chem 4 5228-5236
  • [3] Mori D(2013)Tuning the frontier molecular orbital energy levels of n-type conjugated copolymers by using angular-shaped naphthalene tetracarboxylic diimides, and their use in all-polymer solar cells with high open-circuit voltages J Polym Sci Part A Polym Chem 51 1999-2005
  • [4] Xu H(2013)Polymer donor-polymer acceptor (all-polymer) solar cells Mater Today 16 123-132
  • [5] Ohkita H(2016)Sequentially different AB diblock and ABA triblock copolymers as P3HT:PCBM interfacial compatibilizers for bulk-heterojunction photovoltaics ACS Appl Mater Interfaces 8 5484-5492
  • [6] Ito S(2013)Synthesis of new n-type isoindigo copolymers Polym Chem 4 1836-1841
  • [7] Cao Y(2013)Poly(3-hexylthiophene- Polym Chem 4 2053-2061
  • [8] Lei T(2005)-benzothiadiazole) (THBT) as an electron-accepting polymer for normal and inverted type all-polymer solar cells Macromolecules 38 8649-8656
  • [9] Yuan J(2011)Experimental evidence for the quasi-“living” nature of the grignard metathesis method for the synthesis of regioregular poly(3-alkylthiophenes) Macromolecules 44 2678-2684
  • [10] Wang JY(2014)Poly(3-hexylthiophene)-block-poly(pyridinium phenylene)s: block polymers of p- and n-type semiconductors ACS Maro Lett 3 1009-1014