钝化
钙钛矿(结构)
材料科学
能量转换效率
晶界
吡啶
结晶
热稳定性
化学工程
纳米技术
光电子学
复合材料
图层(电子)
有机化学
化学
工程类
微观结构
作者
Sheng Fu,Xiaodong Li,Li Wan,Yulei Wu,Wenxiao Zhang,Yueming Wang,Qinye Bao,Junfeng Fang
标识
DOI:10.1002/aenm.201901852
摘要
Abstract Stability has become the main obstacle for the commercialization of perovskite solar cells (PSCs) despite the impressive power conversion efficiency (PCE). Poor crystallization and ion migration of perovskite are the major origins of its degradation under working condition. Here, high‐performance PSCs incorporated with pyridine‐2‐carboxylic lead salt (PbPyA 2 ) are fabricated. The pyridine and carboxyl groups on PbPyA 2 can not only control crystallization but also passivate grain boundaries (GBs), which result in the high‐quality perovskite film with larger grains and fewer defects. In addition, the strong interaction among the hydrophobic PbPyA 2 molecules and perovskite GBs acts as barriers to ion migration and component volatilization when exposed to external stresses. Consequently, superior optoelectronic perovskite films with improved thermal and moisture stability are obtained. The resulting device shows a champion efficiency of 19.96% with negligible hysteresis. Furthermore, thermal (90 °C) and moisture (RH 40–60%) stability are improved threefold, maintaining 80% of initial efficiency after aging for 480 h. More importantly, the doped device exhibits extraordinary improvement of operational stability and remains 93% of initial efficiency under maximum power point (MPP) tracking for 540 h.
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