钙钛矿(结构)
能量转换效率
噻吩
钝化
材料科学
光电子学
堆积
X射线光电子能谱
离域电子
化学工程
纳米技术
化学
有机化学
图层(电子)
工程类
作者
Qian‐Qing Ge,Jiang‐Yang Shao,Jie Ding,Li‐Ye Deng,Wenke Zhou,Yao‐Xuan Chen,Jingyuan Ma,Li‐Jun Wan,Jiannian Yao,Jin‐Song Hu,Yu‐Wu Zhong
标识
DOI:10.1002/anie.201806392
摘要
A readily available small molecular hole-transporting material (HTM), OMe-TATPyr, was synthesized and tested in perovskite solar cells (PSCs). OMe-TATPyr is a two-dimensional π-conjugated molecule with a pyrene core and four phenyl-thiophene bridged triarylamine groups. It can be readily synthesized in gram scale with a low lab cost of around US$ 50 g-1 . The incorporation of the phenyl-thiophene units in OMe-TATPyr are beneficial for not only carrier transportation through improved charge delocalization and intermolecular stacking, but also potential trap passivation via Pb-S interaction as supported by depth-profiling XPS, photoluminescence, and electrochemical impedance analysis. As a result, an impressive best power conversion efficiency (PCE) of up to 20.6 % and an average PCE of 20.0 % with good stability has been achieved for mixed-cation PSCs with OMe-TATPyr with an area of 0.09 cm2 . A device with an area of 1.08 cm2 based on OMe-TATPyr demonstrates a PCE of 17.3 %.
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