High-Entropy Design for 2D Halide Perovskite

被引:1
|
作者
Song, Yan [1 ]
Lan, Shun [1 ]
Yang, Bingbing [1 ,2 ]
Zheng, Yunpeng [1 ]
Zhou, Zhifang [1 ]
Nan, Ce-Wen [1 ]
Lin, Yuan-Hua [1 ]
机构
[1] Tsinghua Univ, Sch Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
[2] Chinese Acad Sci, Inst Solid State Phys, Key Lab Mat Phys, Hefei 230031, Peoples R China
基金
中国国家自然科学基金;
关键词
LIGHT-EMISSION; NANOCRYSTALS; EFFICIENT; CATIONS; BLUE;
D O I
10.1021/jacs.4c01882
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hybrid halide perovskites are good candidates for a range of functional materials such as optical electronic and photovoltaic devices due to their tunable band gaps, long carrier diffusion lengths, and solution processability. However, the instability in moisture/air, the toxicity of lead, and rigorous reaction setup or complex postprocessing have long been the bottlenecks for practical application. Herein, we present a simultaneous configurational entropy design at A-sites, B-sites, and X-sites in the typical (CHA)(2)PbBr4 two-dimensional (2D) hybrid perovskite. Our results demonstrate that the high-entropy effect favors the stabilization of the hybrid perovskite phase and facilitates a simple crystallization process without precise control of the cooling rate to prepare regular crystals. Moreover, high-entropy 2D perovskite crystals exhibit tunable energy band gaps, broadband emission, and a long carrier lifetime. Meanwhile, the high-entropy composition almost maintains the initial crystal structure in deionized water for 18 h while the original (CHA)(2)PbBr4 crystal mostly decomposes, suggesting obviously improved humidity stability. This work offers a facile approach to synthesize humidity-stable hybrid perovskites under mild conditions, accelerating relevant preparation of optoelectronics and light-emitting devices and facilitating the ultimate commercialization of halide perovskite.
引用
收藏
页码:19748 / 19755
页数:8
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