A-Site Cation Segregation in Alloyed Perovskite Solar Cells

被引:1
作者
Ding, Zijin [1 ]
Yang, Hao [1 ]
Li, Saisai [1 ]
Wang, Di [1 ]
Jiang, Yuanzhi [1 ]
Yuan, Mingjian [1 ,2 ]
机构
[1] Nankai Univ, Coll Chem, Frontiers Sci Ctr New Organ Matter,Minist Educ, State Key Lab Adv Chem Power Sources,Key Lab Adv E, Tianjin 300071, Peoples R China
[2] Haihe Lab Sustainable Chem Transformat, Tianjin 300051, Peoples R China
来源
ACS PHOTONICS | 2024年
基金
中国国家自然科学基金;
关键词
A-site alloyed perovskite; cation segregation; ion migration; spatially resolved characterizations; crystallization pathways; operational stability; PHOTOINDUCED HALIDE SEGREGATION; SUPPRESSED ION MIGRATION; LEAD IODIDE PEROVSKITE; PHASE SEGREGATION; EFFICIENT; FORMAMIDINIUM; PASSIVATION; PERFORMANCE; STABILITY; IMPACT;
D O I
10.1021/acsphotonics.4c01330
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Organic-inorganic lead halide perovskites have emerged as a dominant candidate for third-generation photovoltaics technologies. Further improvement of both the photovoltaic power conversion efficiency and the long-term operational stability is crucial for the deployment of this technology. However, within the perovskite layer, the labile nature of the A-site alloyed composition can initiate cation segregation during crystallization and device operation, which potentially leads to device failure and hinders commercialization. In this Review, we provide a mechanistic overview of the underlying origins of cation segregation and summarize the characterization techniques and the implications of cation segregation on perovskite films and devices. By assessing the nature and effect of cation segregation, we further discuss the ongoing studies for mitigating the segregation, including the modified crystallization process, optimized thin-film fabrication, suppressed cation migration, and monitor external stress conditions. Finally, we outline challenges and potential methods in constructing homogeneous A-site alloyed perovskites for photovoltaic applications.
引用
收藏
页码:5061 / 5083
页数:23
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