成核
结晶
钙钛矿(结构)
卤化物
材料科学
锡
化学工程
动力学
化学物理
化学
无机化学
冶金
有机化学
物理
量子力学
工程类
作者
Xiangyue Meng,Yunfei Li,Yi-Zhi Qu,Haining Chen,Nan Jiang,Minghua Li,Ding‐Jiang Xue,Jin‐Song Hu,Hui Huang,Shihe Yang
标识
DOI:10.1002/anie.202012280
摘要
Abstract Tin halide perovskites are rising as promising materials for lead‐free perovskite solar cells (PSCs). However, the crystallization rate of tin halide perovskites is much faster than the lead‐based analogs, leading to more rampant trap states and lower efficiency. Here, we disclose a key finding to modulate the crystallization kinetics of FASnI 3 through a non‐classical nucleation mechanism based on pre‐nucleation clusters (PNCs). By introducing piperazine dihydriodide to tune the colloidal chemistry of the FASnI 3 perovskite precursor solution, stable clusters could be readily formed in the solution before nucleation. These pre‐nucleation clusters act as intermediate phase and thus can reduce the energy barrier for the perovskite nucleation, resulting in a high‐quality perovskite film with lower defect density. This PNCs‐based method has led to a conspicuous photovoltaic performance improvement for FASnI 3 ‐based PSCs, delivering an impressive efficiency of 11.39 % plus improved stability.
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