Efficient and stable Ruddlesden-Popper layered tin-based perovskite solar cells enabled by ionic liquid-bulky spacers

被引:0
|
作者
Jian Qiu [1 ]
Yuexin Lin [1 ]
Xueqin Ran [1 ]
Qi Wei [2 ]
Xingyu Gao [3 ]
Yingdong Xia [1 ]
Peter Müller-Buschbaum [4 ,5 ]
Yonghua Chen [1 ]
机构
[1] Key Laboratory of Flexible Electronics (KLOFE) & Institution of Advanced Materials (IAM),Nanjing Tech University (Nanjing Tech)
[2] Frontiers Science Center for Flexible Electronics,Xi'an Institute of Flexible Electronics (IFE) and Xi'an Institute of Biomedical Materials & Engineering,Northwestern Polytechnical University
[3] Shanghai Synchrotron Radiation Facility,Shanghai Institute of Applied Physics,Chinese Academy of Sciences
[4] Lehrstuhl für Funktionelle Materialien,Physik Department,Technische Universit?t München
[5] Heinz Maier-Leibnitz Zentrum (MLZ),Technische Universit?t München
基金
国家重点研发计划; 国家自然科学基金国际合作与交流项目;
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暂无
中图分类号
TM914.4 [太阳能电池];
学科分类号
摘要
The crucial component, bulky spacers, in two-dimensional Ruddlesden-Popper(2 DRP) layered tin(Sn) perovskites are highly limited by halide ammonium salts, leading to the insufficient control of complex crystallization process due to the limited interaction between bulky spacers and 2 DRP perovskite frameworks. Here, we report an ionic liquid-bulky spacer, butylammounium acetate(BAAc O), for constructing efficient and stable 2 DRP Sn-based perovskite solar cells(PSCs). In contrast to the traditional halide ammonium bulky spacer, butylammounium iodide(BAI), the Ac O--functional group in BAAc O has a strong interaction with formamidine ions(FA+) and Sn2+. The inter-component interaction allows the formation of controllable intermediates for the favorable growth of smooth, dense, and highly oriented perovskite films. A PSC with power conversion efficiency of 10.36%(7.16% for BAI) is achieved, which is the highest report, along with improved stability with ~90% retained after ~600 h storage in N2 atmosphere without any encapsulation.
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页码:1577 / 1585
页数:9
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