A crystal capping layer for formation of black-phase FAPbI <sub>3</sub> perovskite in humid air

Yu Zou(Peking University), Wenjin Yu(Peking University), Haoqing Guo(Peking University), Qizhi Li(Peking University), Xiangdong Li(Peking University), Liang Li(Peking University), Yueli Liu(Peking University), Hantao Wang(Peking University), Zhenyu Tang(Peking University), Shuang Yang(Peking University), Yanrun Chen(Beijing Institute of Technology), Bo Qu(Peking University), Yunan Gao(Peking University), Zhijian Chen(Peking University), Shufeng Wang(Peking University), Dongdong Zhang(Tsinghua University), Yihua Chen(Beijing Institute of Technology), Qi Chen(Beijing Institute of Technology), Shaik M. Zakeeruddin(École Polytechnique Fédérale de Lausanne), Y. Y. Peng(Peking University), Huanping Zhou(Peking University), Qihuang Gong(Peking University), Mingyang Wei(École Polytechnique Fédérale de Lausanne), Michaël Grätzel(École Polytechnique Fédérale de Lausanne), Lixin Xiao(Peking University)
Science
July 11, 2024
Cited by 197

Abstract

Black-phase formamidinium lead iodide (α-FAPbI 3 ) perovskites are the desired phase for photovoltaic applications, but water can trigger formation of photoinactive impurity phases such as δ-FAPbI 3 . We show that the classic solvent system for perovskite fabrication exacerbates this reproducibility challenge. The conventional coordinative solvent dimethyl sulfoxide (DMSO) promoted δ-FAPbI 3 formation under high relative humidity (RH) conditions because of its hygroscopic nature. We introduced chlorine-containing organic molecules to form a capping layer that blocked moisture penetration while preserving DMSO-based complexes to regulate crystal growth. We report power conversion efficiencies of &gt;24.5% for perovskite solar cells fabricated across an RH range of 20 to 60%, and 23.4% at 80% RH. The unencapsulated device retained 96% of its initial performance in air (with 40 to 60% RH) after 500-hour maximum power point operation.


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