卤化物
钙钛矿(结构)
碘化物
带隙
溴化物
半导体
超快激光光谱学
材料科学
吸收(声学)
混合(物理)
相(物质)
Crystal(编程语言)
化学
化学物理
无机化学
光谱学
结晶学
光电子学
有机化学
复合材料
量子力学
物理
计算机科学
程序设计语言
作者
Eline M. Hutter,Loreta A. Muscarella,Francesca Wittmann,Jan Versluis,Lucie McGovern,Huib J. Bakker,Young-Won Woo,Young‐Kwang Jung,Aron Walsh,Bruno Ehrler
标识
DOI:10.1016/j.xcrp.2020.100120
摘要
Mixing iodide and bromide in halide perovskite semiconductors is an effective strategy to tune their bandgap, therefore mixed-halide perovskites hold great promise for color-tunable LEDs and tandem solar cells. However, the bandgap of mixed-halide perovskites is unstable under (sun-)light, since the halides segregate into domains of different bandgaps. Using pressure-dependent ultrafast transient absorption spectroscopy, we show that high external pressure increases the range of thermodynamically stable halide mixing ratios. Chemical pressure, by inserting a smaller cation, has the same effect, which means that any iodide-to-bromide ratio can be thermodynamically stabilized by tuning the crystal volume and compressibility. We interpret this stabilization by an alteration of the Helmholtz free energy via the largely overlooked PdeltaV term.
科研通智能强力驱动
Strongly Powered by AbleSci AI