摘要
A novel p-type organic semiconductor (p-OS), P2TBR, based on a non-fused ring structure of thiophene-benzene-thiophene (TBT) as the core and 2D-conjugated benzodithiophene (BDT) units as π spacers and 3-ethylrhodanines as terminal groups, was synthesized and used as the donor material for all-small-molecule organic solar cells (SM-OSCs). P2TBR shows strong absorption, a low-lying HOMO energy level, high hole mobility and good thermal stability. The optimized P2TBR:IDIC film exhibits face-on and edge-on co-existent texture and three dimensional (3D) charge pathway, which is far better than the face-on orientated blend film without any treatment. As a result, a notable power conversion efficiency (PCE) of 11.5% and a satisfactory fill factor (FF) of 70.1% are achieved. This efficiency is the highest PCE for non-fullerene SM-OSCs reported in the literature so far. Overall, the results indicate that P2TBR is a promising candidate p-OS donor material for use in SM-OSCs, and the molecular design strategy for P2TBR provides the possibility that the simple-structured and easy to chemically modify non-fused unit can also be used as a building block in high performance p-OS donors.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 3682-3690 |
| 页数 | 9 |
| 期刊 | Journal of Materials Chemistry A |
| 卷 | 7 |
| 期 | 8 |
| DOI | |
| 出版状态 | 已出版 - 2019 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 7 经济适用的清洁能源
学术指纹
探究 'A small molecule donor containing a non-fused ring core for all-small-molecule organic solar cells with high efficiency over 11%' 的科研主题。它们共同构成独一无二的指纹。引用此
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