Mixed-Halide Double Perovskite Cs2AgBiX6 (X=Br, I) with Tunable Optical Properties via Anion Exchange

被引:28
|
作者
Wu, Hua [1 ]
Erbing, Axel [2 ]
Johansson, Malin B. [1 ]
Wang, Junxin [3 ,4 ]
Kamal, Chinnathambi [2 ,5 ]
Odelius, Michael [2 ]
Johansson, Erik M. J. [1 ]
机构
[1] Uppsala Univ, Angstrom Lab, Dept Chem, Inst Phys Chem, S-75120 Uppsala, Sweden
[2] Stockholm Univ, Dept Phys, AlbaNova Univ Ctr, S-10691 Stockholm, Sweden
[3] Uppsala Univ, Dept Mat Sci & Engn, Angstrom Lab, S-75103 Uppsala, Sweden
[4] Univ Oxford, Dept Chem, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England
[5] Raja Ramanna Ctr Adv Technol, Theory & Simulat Lab, HRDS, Indore 452013, India
基金
瑞典研究理事会;
关键词
bandgap engineering; density functional calculations; ion exchange; lead-free double perovskites; solar cells; ORGANOMETAL TRIHALIDE PEROVSKITE; SOLAR-CELLS; COLLOIDAL NANOCRYSTALS; PHASE SEGREGATION; BAND-GAPS; EFFICIENCY; FORMAMIDINIUM; SUBSTITUTION; CONVERSION; IODIDE;
D O I
10.1002/cssc.202101146
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lead-free double perovskites, A(2)M(+)M(' 3+)X(6), are considered as promising alternatives to lead-halide perovskites, in optoelectronics applications. Although iodide (I) and bromide (Br) mixing is a versatile tool for bandgap tuning in lead perovskites, similar mixed I/Br double perovskite films have not been reported in double perovskites, which may be due to the large activation energy for ion migration. In this work, mixed Br/I double perovskites were realized utilizing an anion exchange method starting from Cs2AgBiBr6 solid thin-films with large grain-size. The optical and structural properties were studied experimentally and theoretically. Importantly, the halide exchange mechanism was investigated. Hydroiodic acid was the key factor to facilitate the halide exchange reaction, through a dissolution-recrystallization process. In addition, the common organic iodide salts could successfully perform halide-exchange while retaining high mixed-halide phase stability and strong light absorption capability.
引用
收藏
页码:4507 / 4515
页数:9
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