期刊
ENERGY & ENVIRONMENTAL SCIENCE
卷 12, 期 11, 页码 3328-3337出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ee01890e
关键词
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资金
- NSFC [51573076, 21801124]
- Shenzhen Basic Research Fund [JCYJ20170817105905899]
- Shenzhen Peacock Plan Project [KQTD20140630110339343]
- Shenzhen Key Lab funding [ZDSYS201505291525382]
- Shen Zhen Technology and Innovation Commission [JCYJ20170413173814007, JCYJ20170818113905024]
- Hong Kong Research Grants Council (Research Impact Fund) [R602118, 16305915, 16322416, 606012, 16303917]
- Hong Kong Innovation and Technology Commission [ITC-CNERC14SC01, ITS/471/18]
- HKUST president's office [FP201]
- Center for Computational Science and Engineering of SUSTech
Thiophene and its derivatives have been extensively used in organic electronics, particularly in the field of polymer solar cells (PSCs). Significant research efforts have been dedicated to modifying thiophene-based units by attaching electron-donating or withdrawing groups to tune the energy levels of conjugated materials. Herein, we report the design and synthesis of a novel thiophene derivative, FE-T, featuring a monothiophene functionalized with both an electron-withdrawing fluorine atom (F) and an ester group (E). The FE-T unit possesses distinctive advantages of both F and E groups, the synergistic effects of which enable significant downshifting of the energy levels and enhanced aggregation/crystallinity of the resulting organic materials. Shown in this work are a series of polymers obtained by incorporating the FE-T unit into a PM6 polymer to fine-tune the energetics and morphology of this high-performance PSC material. The optimal polymer in the series shows a downshifted HOMO and an improved morphology, leading to a high PCE of 16.4% with a small energy loss (0.53 eV) enabled by the reduced non-radiative energy loss (0.23 eV), which are among the best values reported for non-fullerene PSCs to date. This work shows that the FE-T unit is a promising building block to construct donor polymers for high-performance organic photovoltaic cells.
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