Lattice Compression Increases the Activation Barrier for Phase Segregation in Mixed-Halide Perovskites

被引:109
作者
Muscarella, Loreta A. [1 ]
Hutter, Eline M. [1 ,2 ]
Wittmann, Francesca [1 ]
Woo, Young Won [3 ]
Jung, Young-Kwang [3 ]
McGovern, Lucie [1 ]
Versluis, Jan [1 ]
Walsh, Aron [3 ,4 ]
Bakker, Huib J. [1 ]
Ehrler, Bruno [1 ]
机构
[1] AMOLF, Ctr Nanophoton, NL-1098 XG Amsterdam, Netherlands
[2] Univ Utrecht, Dept Chem, NL-3584 CB Utrecht, Netherlands
[3] Yonsei Univ, Dept Mat Sci & Engn, Seoul 03722, South Korea
[4] Imperial Coll London, Dept Mat, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会; 新加坡国家研究基金会;
关键词
ION MIGRATION; IODIDE; LIGHT; STABILITY;
D O I
10.1021/acsenergylett.0c01474
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
The bandgap tunability of mixed-halide perovskites makes them promising candidates for light-emitting diodes and tandem solar cells. However, illuminating mixed-halide perovskites results in the formation of segregated phases enriched in a single halide. This segregation occurs through ion migration, which is also observed in single-halide compositions, and whose control is thus essential to enhance the lifetime and stability. Using pressure-dependent transient absorption spectroscopy, we find that the formation rates of both iodide- and bromide-rich phases in MAPb(BrxI1-x)(3) reduce by 2 orders of magnitude on increasing the pressure to 0.3 GPa. We explain this reduction from a compression-induced increase of the activation energy for halide migration, which is supported by first-principle calculations. A similar mechanism occurs when the unit cell volume is reduced by incorporating a smaller cation. These findings reveal that stability with respect to halide segregation can be achieved either physically through compressive stress or chemically through compositional engineering.
引用
收藏
页码:3152 / 3158
页数:7
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