| Literature DB >> 32472603 |
Yongqiang Shi1, Han Guo1, Jiachen Huang1, Xianhe Zhang1, Ziang Wu2, Kun Yang1, Yujie Zhang1, Kui Feng1, Han Young Woo2, Rocio Ortiz3, Ming Zhou4, Xugang Guo5.
Abstract
A distannylated electron-deficient bithiophene imide (BTI-Tin) monomer was readily synthesized and polymerized with imide-functionalized co-units via Stille coupling to afford homopolymer PBTI and copolymer P(BTI-BTI2), both featuring acceptor-acceptor backbone with high molecular weight. Benefitting from their improved electronic property and increased molecular weight, both polymers exhibited excellent unipolar n-type character in transistors with electron mobility up to 2.60 cm2 V-1 s-1. When applied as acceptor materials in all-polymer solar cells, PBTI and P(BTI-BTI2) achieved high power conversion efficiency (PCE) of 6.67% and 8.61%, respectively. The PCE (6.67%) of polymer PBTI, synthesized from the novel distannylated monomer, is substantially higher than that (0.14%) of the same polymer PBTI*, synthesized from typical dibrominated monomer. The 8.61% PCE of copolymer P(BTI-BTI2) is also substantially higher than those (< 1%) of homopolymers synthesized from dibrominated monomers. The results demonstrate the great success of BTI-Tin for facilely accessing structurally novel n-type polymers with greatly improved device performance.Entities:
Keywords: acceptor-acceptor polymers; all-polymer solar cells; n-type performance; organic thin-film transistors; stannylated bithiophene imide
Year: 2020 PMID: 32472603 DOI: 10.1002/anie.202002292
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336