堆积
富勒烯
有机太阳能电池
接受者
材料科学
光伏系统
聚合物太阳能电池
能量转换效率
光电子学
分子
有机半导体
化学物理
太阳能电池
光伏
带隙
纳米技术
化学工程
活动层
光化学
化学
有机化学
聚合物
物理
复合材料
生物
凝聚态物理
生态学
作者
Linglong Ye,Kangkang Weng,Jinqiu Xu,Xiaoyan Du,Sreelakshmi Chandrabose,Kai Chen,Jiadong Zhou,Guangchao Han,Songting Tan,Zengqi Xie,Yuanping Yi,Ning Li,Feng Liu,Justin M. Hodgkiss,Christoph J. Brabec,Yanming Sun
标识
DOI:10.1038/s41467-020-19853-z
摘要
Abstract In non-fullerene organic solar cells, the long-range structure ordering induced by end-group π–π stacking of fused-ring non-fullerene acceptors is considered as the critical factor in realizing efficient charge transport and high power conversion efficiency. Here, we demonstrate that side-chain engineering of non-fullerene acceptors could drive the fused-ring backbone assembly from a π–π stacking mode to an intermixed packing mode, and to a non-stacking mode to refine its solid-state properties. Different from the above-mentioned understanding, we find that close atom contacts in a non-stacking mode can form efficient charge transport pathway through close side atom interactions. The intermixed solid-state packing motif in active layers could enable organic solar cells with superior efficiency and reduced non-radiative recombination loss compared with devices based on molecules with the classic end-group π–π stacking mode. Our observations open a new avenue in material design that endows better photovoltaic performance.
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