甲脒
光热治疗
钙钛矿(结构)
热稳定性
材料科学
相(物质)
离子
分解
热分解
化学工程
纳米技术
无机化学
化学
工程类
有机化学
作者
Dachang Liu,Qiangqiang Zhao,Zhipeng Li,Xiuhong Sun,Bingqian Zhang,Zhipeng Shao,Chen Chen,Lianzheng Hao,Xianzhao Wang,Caiyun Gao,Yimeng Li,Xiao Wang,Guanglei Cui,Shuping Pang
出处
期刊:Solar RRL
[Wiley]
日期:2022-07-15
卷期号:6 (9)
被引量:3
标识
DOI:10.1002/solr.202200414
摘要
The degradation of the perovskite solar cells (PSCs) is closely related to phase decomposition, phase separation, and structural collapse, which mainly originates from the intrinsic ion migration under light soaking and thermal stress. Herein, the composition of perovskite materials is regulated based on its ion migration characteristics. By systematically studying the effect of A‐site cations on the ion migration and photothermal stability of organic–inorganic hybrid perovskite materials, it is found that the codoping of appropriate methylammonium (MA) and Cs cation in the formamidinium (FA)‐rich perovskite is favorable for the highly efficient and stable PSCs. The optimized triple‐cation FA 0.90 Cs 0.04 MA 0.06 PbI 3 exhibits significantly improved photothermal stability in comparison with the double‐cation and Br‐containing perovskite materials. Moreover, the optimized triple‐cation device demonstrates excellent operation stability at maximum power tracking, and maintains 87% of initial efficiency after 1800 h.
科研通智能强力驱动
Strongly Powered by AbleSci AI