成核
锡
结晶
钙钛矿(结构)
化学工程
材料科学
化学
结晶学
有机化学
冶金
工程类
作者
Huan Rao,Yang Su,Gengling Liu,Hongbo Zhou,Jia Yang,Wangping Sheng,Yang Zhong,Licheng Tan,Yiwang Chen
标识
DOI:10.1002/anie.202306712
摘要
Abstract The classic solvent system can't sufficiently separate one‐dimensional edge‐sharing SnI 2 crystals in solution, which severely restricts the fabrication of high‐quality tin‐based perovskite film. Herein, a strong Lewis base (hexamethylphosphoramide, HMPA) has been introduced to coordinate Sn 2+ to modulate solvation behaviours on perovskite precursor and regulate crystallization kinetics. The large molecular volume of HMPA and stronger bind energy of SnI 2 ⋅ 2HMPA (−0.595 eV vs −0.118 eV for SnI 2 ⋅ 2DMSO) change the solvation structure of SnI 2 from edge‐sharing cluster to monodisperse adduct, which contributes to uniform nucleation sites and prolongs crystal growth process. Delightfully, a fully‐covered perovskite film is formed on the large‐area substrate and tin‐based perovskite solar cells processed with HMPA exhibit an excellent efficiency of 13.46 %. This research provides novel insights and directions for the solution preparation of smooth and uniform large‐area tin‐based perovskite film.
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