光致发光
光子
钙钛矿(结构)
卤化物
电子
激发
重吸收
谱线
Crystal(编程语言)
原子物理学
化学
材料科学
分子物理学
光电子学
光学
物理
无机化学
程序设计语言
量子力学
天文
计算机科学
结晶学
钠
有机化学
作者
Florian Staub,Irina Anusca,Doru C. Lupascu,Uwe Rau,Thomas Kirchartz
出处
期刊:JPhys materials
[IOP Publishing]
日期:2020-02-20
卷期号:3 (2): 025003-025003
被引量:40
标识
DOI:10.1088/2515-7639/ab6fd0
摘要
Explaining the time-dependent evolution of photoluminescence spectra of halide perovskite single crystals after pulsed excitation requires the consideration of a range of physical mechanisms, including electronic transport, recombination and reabsorption. The latter process of reabsorption and re-generation of electron-hole pairs from a photon created by radiative recombination in the single crystal itself is termed photon recycling and has been a highly controversial topic. We use photoluminescence experiments performed under different illumination conditions combined with numerical simulations that consider photon recycling to show which parameters affect temporal decays, spectral shifts and differences in the illumination direction. In addition, we use numerical simulations with and without photon recycling to understand the relative importance of charge-carrier transport and photon recycling. We conclude that under most relevant illumination conditions and times after the pulse, electronic transport is more important than photon recycling for the spectral behavior of the transients. However, inclusion of photon recycling is imperative for the understanding of the absolute density of electrons and holes present in the crystal during a certain time after the pulse.
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