材料科学
光伏系统
接受者
有机太阳能电池
带隙
光电子学
电气工程
复合材料
物理
聚合物
凝聚态物理
工程类
作者
Tao Zhang,Cunbin An,Ye Xu,Pengqing Bi,Zhihao Chen,Jingwen Wang,Ni Yang,Yi Yang,Bowei Xu,Huifeng Yao,Xiaotao Hao,Shaoqing Zhang,Jianhui Hou
标识
DOI:10.1002/adma.202207009
摘要
Abstract The correlation between molecular structure and photovoltaic performance is lagging for constructing high‐performance indoor organic photovoltaic (OPV) cells. Herein, this relationship is investigated in depth by employing two medium‐bandgap nonfullerene acceptors (NFAs). The newly synthesized NFA of FTCCBr exhibits a similar bandgap and molecular energy level, but a much stronger dipole moment and larger average electrostatic potential (ESP) compared with ITCC. After blending with the polymer donor PB2, the PB2:ITCC and PB2:FTCCBr blends exhibit favorable bulk‐heterojunction morphologies and the same driving force, but the PB2:FTCCBr blend exhibits a large ESP difference. In OPV cells, the PB2:ITCC‐based device produces a power conversion efficiency (PCE) of 11.0%, whereas the PB2:FTCCBr‐based device gives an excellent PCE of 14.8% with an open‐circuit voltage ( V OC ) of 1.05 V, which is the highest value among OPV cells with V OC values above 1.0 V. When both acceptor‐based devices work under a 1000 lux of 3000 K light‐emitting diode, the PB2:ITCC‐based 1 cm 2 device yields a good PCE of 25.4%; in contrast, the PB2:FTCCBr‐based 1 cm 2 device outputs a record PCE of 30.2%. These results suggest that a large ESP offset in photovoltaic materials is important for achieving high‐performance OPV cells.
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