Multisite-passivating molecules assisted regulation of perovskite crystallization kinetics for constructing high-efficiency and stable perovskite solar cells

被引:0
作者
Wu, Xiaofeng [1 ]
Yang, Tianshu [1 ]
Che, Yuliang [1 ]
Deng, Jidong [1 ]
Pan, Senxin [1 ]
Fu, Liming [2 ]
Zhang, Jinbao [1 ,3 ]
Xu, In [1 ,3 ]
机构
[1] Xiamen Univ, Coll Mat, Xiamen 361005, Fujian, Peoples R China
[2] Changzhou Shichuang Energy Co Ltd, Liyang 213300, Jiangsu, Peoples R China
[3] Xiamen Univ, Coll Mat, Xiamen Key Lab Elect Ceram Mat & Devices, Xiamen 361005, Fujian, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2025年 / 110卷
基金
中国国家自然科学基金;
关键词
Multi-site passivation; Crystallization modulation; Perovskite solar cells; GROWTH;
D O I
10.1016/j.jechem.2025.06.047
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Additive engineering has been widely employed to address defects-related issues in perovskite solar cells, including Pb2+ vacancy defects, halide migration, and FA+ lattice mismatch. However, due to the diversity and complexity of defect types in perovskites, traditional monofunctional additives are typically limited to passivate specific types of defects and are unable to achieve effective passivation of multiple defects simultaneously. To overcome this limitation, this work proposes a multidentate synergistic coordination strategy using a multifunctional additive, ethyl 4-aminopyrazole-5-carboxylate (EAPC), to achieve coordinated passivation of multiple defects in perovskites. Combined theoretical calculations and experimental investigations reveal that the carbonyl group (C=O) of EAPC forms strong coordination bonds with uncoordinated Pb2+, while its amino group (-NH2) couples with halide ions, and the pyrazole-ring N sites establish a hydrogen-bonding network with FA+ cations, thereby achieving triple-site synergistic passivation of Pb2+-X--FA+ defects. This synergistic effect accelerates the nucleation kinetics of perovskite while retarding its growth rate, thereby reducing the defect density and enhancing the crystallinity of the resulting perovskite films. Based on this strategy, the inverted perovskite solar cells (PSCs) achieved a champion power conversion efficiency (PCE) of 24.40 %, maintaining over 90.2 % of their initial efficiency after 1000 h of aging in a N2-glovebox environment and retaining 85.1 % of the original PCE under ambient conditions. This work pioneers a novel paradigm for synergistic defect passivation in perovskite optoelectronic devices. (c) 2025 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:50 / 60
页数:11
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