Tuning the A-site cation composition of FA perovskites for efficient and stable NiO-based p-i-n perovskite solar cells

被引:41
作者
Hu, Chen [1 ]
Bai, Yang [1 ]
Xiao, Shuang [1 ]
Zhang, Teng [1 ]
Meng, Xiangyue [1 ]
Ng, Wai Kit [2 ]
Yang, Yinglong [1 ]
Wong, Kam Sing [2 ]
Chen, Haining [3 ]
Yang, Shihe [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Dept Phys, Kowloon, Hong Kong, Peoples R China
[3] Beihang Univ, Sch Mat Sci & Engn, Beijing, Peoples R China
关键词
ELECTRON-TRANSPORTING LAYER; HIGH-PERFORMANCE; HALIDE PEROVSKITES; IODIDE; FILMS; STABILITY; DEGRADATION;
D O I
10.1039/c7ta07139f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cation mixing has proved to be effective in stabilizing the high-temperature phase of formamidinium (FA)-based perovskites, affording high-performance n-i-p perovskite solar cells (PSCs). However, optimum cation mixing is found to be inapplicable directly to NiO p-i-n PSCs due to the energy band misalignment. In the present study, we reveal the role of mixing cesium (Cs), methylammonium (MA) and formamidinium (FA) in the energy band alignments and the crystallization of perovskites in such a device structure. By tuning the composition of mixed cations, we have significantly improved the energy band alignments of perovskites in p-i-n NiO-based PSCs. The relative amount of Cs to MA cations also plays a decisive role in shaping the nature of perovskite precursors, thus impacting the quality of the resulting perovskite layer in NiO p-i-n PSCs. These insights and the associated engineering efforts led to a significantly improved power conversion efficiency of 18.6% based on the NiO p-i-n PSCs, in addition to their superior ambient stability to typical n-i-p PSCs.
引用
收藏
页码:21858 / 21865
页数:8
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