兴奋剂
发光
钙钛矿(结构)
光致发光
结合能
激子
卤化物
材料科学
光电效应
带隙
碱金属
量子产额
光电子学
扩散
化学物理
金属
离子
电子
晶界
密度泛函理论
分子物理学
量子效率
间质缺损
半导体
基态
晶体缺陷
载流子寿命
扩散阻挡层
动力学
作者
Ying Cao,Qikai Wang,Zhenguo Ji,Yaqi Qi,Jie Qin,Yuzhi Song,Chuan‐Kui Wang,Lili Lin,Lei Cai
标识
DOI:10.1021/acs.jpclett.5c02343
摘要
Metal halide perovskites have garnered significant attention due to their exceptional photoelectric properties. The alkali metal doping strategy has been demonstrated to effectively modulate grain size, control crystallization kinetics, and adjust band gap characteristics in perovskite. This study employs the first-principles calculations to reveal that the selection of alkali metal species and their corresponding doping methodologies exert markedly distinct influences on both the electronic properties and ion migration kinetics of CsPbBr3 perovskites. There is an increase in the effective mass of electrons and holes in most alkali-metal substitutions and in all interstitial occupancy systems, which increases the exciton binding energy and radiation rate. Meanwhile, calculations demonstrate that alkali metal interstitial occupancy suppresses halide ion migration by simultaneously extending diffusion pathways and strengthening Br- interactions, significantly increasing the migration barrier from 0.113 to 0.902 eV in the perovskite lattice. The Rb interstitial doped system exhibits high photoluminescence quantum yield (PLQY) and stability, retaining 87% of the original PLQY after heating at 300 °C for 30 min. This work offers a new method to optimize the performance of devices.
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