摘要
P3HT stands out from numerous polymer donors owing to the merits of low cost and high scalability of synthesis. However, the photovoltaic performance of P3HT-based blends lags significantly behind the state-of-the-art systems, especially for all-polymer solar cells (APSCs) that generally show efficiency of around 3%–4% due to the lack of matched polymer acceptors. Herein, a polymer acceptor, named IDTBTC8-CN, was designed and synthesized with indacenodithiophene (IDT) and mono-cyano (CN)-substituted benzothiadiazole (BT-CN) as building blocks. Introducing a CN group endowed the polymer with decreased bandgap, and apparent n-type charge transport character despite the relatively high energy levels. Additionally, IDTBTC8-CN showed largely improved miscibility with P3HT, compared with that of BT-based control polymer IDTBTC8. The high miscibility between P3HT and IDTBTC8-CN as well as the amorphous aggregation behavior of IDTBTC8-CN enabled a broad manipulation room for the blend film to acquire favorable morphology. Eventually, a champion efficiency of 8.30% was achieved, in sharp contrast to that of the IDTBTC8-based system (1.21%). Such efficiency is a new record for P3HT-based APSCs reported so far. Moreover, P3HT:IDTBTC8-CN blend film also exhibited excellent mechanical robustness. This study implies the guidance of molecular design of the polymer acceptors and morphology control for P3HT-based APSCs. [Figure not available: see fulltext.]
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 216-227 |
| 页数 | 12 |
| 期刊 | Science China Chemistry |
| 卷 | 66 |
| 期 | 1 |
| DOI | |
| 出版状态 | 已出版 - 1月 2023 |
| 已对外发布 | 是 |
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