Functional organic cation induced 3D-to-0D phase transformation and surface reconstruction of CsPbI3 inorganic perovskite

被引:18
作者
Chen, Yuetian [1 ]
Wang, Xingtao [1 ]
Wang, Yao [1 ]
Liu, Xiaomin [1 ]
Miao, Yanfeng [1 ]
Zhao, Yixin [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Frontiers Sci Ctr Transformat Mol, Sch Environm Sci & Engn, Shanghai 200240, Peoples R China
[2] Shanghai Noncarbon Energy Convers & Utilizat Inst, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
In-situ phase transformation; Secondary growth; CsPbI3 inorganic perovskite; Zero-dimension perovskite; Inorganic perovskite solar cell; SOLAR-CELLS; NANOCRYSTALS;
D O I
10.1016/j.scib.2023.03.029
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Efficiency and stability are the main research focuses for perovskite solar cells. Inorganic perovskites like CsPbI3 possess higher chemical stability than those with organic A-site cations, while they also exhibit higher defect density. Nonetheless, it is highly challenging to induce orderly secondary arrangement or reconstruction of inorganic perovskites with reduced defects because of their unique chemical properties. In this work, in-situ three-dimension-to-zero-dimension (3D-to-0D) phase transformation and surface reconstruction on CsPbI3 film is achieved as induced by a functional organic cation, benzyldode- cyldimethylammonium (BDA), a process of which that is similar to phase-transfer catalysis. With the help of BDABr salt treatment, 0D Cs4PbI6 perovskites are secondarily formed along CsPbI3 grain boundaries with Cs-related cationic defects passivated, yielding structures of higher stability. The BDA-CsPbI3 films exhibit reduced non-radiative recombination and promoted charge transfer, leading to inorganic per- ovskite solar cells with a high power conversion efficiency of 20.63% and good operational stability.(c) 2023 Science China Press. Published by Elsevier B.V. and Science China Press. All rights reserved.
引用
收藏
页码:706 / 712
页数:7
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