有机太阳能电池
钙钛矿(结构)
接受者
能量转换效率
材料科学
异质结
工作(物理)
光电子学
瓶颈
电压
化学物理
化学
物理
结晶学
凝聚态物理
有机化学
热力学
计算机科学
嵌入式系统
量子力学
聚合物
作者
Jing Wang,Xudong Jiang,Hongbo Wu,Guitao Feng,Hanyu Wu,Junyu Li,Yuanping Yi,Xunda Feng,Zaifei Ma,Weiwei Li,Koen Vandewal,Zheng Tang
标识
DOI:10.1038/s41467-021-26995-1
摘要
The high voltage losses ([Formula: see text]), originating from inevitable electron-phonon coupling in organic materials, limit the power conversion efficiency of organic solar cells to lower values than that of inorganic or perovskite solar cells. In this work, we demonstrate that this [Formula: see text] can in fact be suppressed by controlling the spacing between the donor (D) and the acceptor (A) materials (DA spacing). We show that in typical organic solar cells, the DA spacing is generally too small, being the origin of the too-fast non-radiative decay of charge carriers ([Formula: see text]), and it can be increased by engineering the non-conjugated groups, i.e., alkyl chain spacers in single component DA systems and side chains in high-efficiency bulk-heterojunction systems. Increasing DA spacing allows us to realize significantly reduced [Formula: see text] and improved device voltage. This points out a new research direction for breaking the performance bottleneck of organic solar cells.
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