作者
Yang Bai,Zijian Huang,Xiao Zhang,Jiuzhou Lu,Xiuxiu Niu,Ziwen He,Cheng Zhu,Mengqi Xiao,Qizhen Song,Xueyuan Wei,Chenyue Wang,Zhenhua Cui,Jing Dou,Yihua Chen,Fengtao Pei,Huachao Zai,Wei Wang,Tinglu Song,Pengfei An,Jing Zhang,Juncai Dong,Yiming Li,Jiangjian Shi,Haibo Jin,Pengwan Chen,Yuchao Sun,Yujing Li,Haining Chen,Zhongming Wei,Huanping Zhou,Qi Chen
摘要
The mixtures of cations and anions used in hybrid halide perovskites for high-performance solar cells often undergo element and phase segregation, which limits device lifetime. We adapted Schelling's model of segregation to study individual cation migration and found that the initial film inhomogeneity accelerates materials degradation. We fabricated perovskite films (FA1-xCsxPbI3; where FA is formamidinium) through the addition of selenophene, which led to homogeneous cation distribution that retarded cation aggregation during materials processing and device operation. The resultant devices achieved enhanced efficiency and retained >91% of their initial efficiency after 3190 hours at the maximum power point under 1 sun illumination. We also observe prolonged operational lifetime in devices with initially homogeneous FACsPb(Br0.13I0.87)3 absorbers.