异质结
材料科学
纳米线
钙钛矿(结构)
外延
光电子学
卤化物
光伏
相变
带隙
二极管
半导体
离子键合
离子
相(物质)
纳米技术
无机化学
凝聚态物理
结晶学
化学
光伏系统
图层(电子)
有机化学
物理
生物
生态学
作者
Jing Li,Jiao Xu,Yanan Bao,Jianliang Li,Hengshan Wang,Chengyu He,Meiqi An,Huayi Tang,Zhiguang Sun,Yurui Fang,Shuang Liang,Yiming Yang
标识
DOI:10.1002/adma.202109867
摘要
Anion-exchange in halide perovskites provides a unique pathway of bandgap engineering for fabricating heterojunctions in low-cost photovoltaics and optoelectronics. However, it remains challenging to achieve robust and sharp perovskite heterojunctions, due to the spontaneous anion interdiffusion across the heterojunction in 3D perovskites. Here, it is shown that the anionic behavior in 1D perovskites is fundamentally different, that the anion exchange can readily drive an indirect-to-direct bandgap phase transition in CsPbI3 nanowires (NWs) and greatly lower the phase transition temperature. In addition, the heterojunction created by phase transition is epitaxial in nature, and its chemical composition can be precisely controlled upon postannealing. Further study of the phase transition dynamics reveals a threshold-dominating anion exchange mechanism in these 1D NWs rather than the gradient-dominating mechanism in 3D systems. The results provide important insights into the ionic behavior in halide perovskites, which is beneficial for applications in solar cells, light-emitting diodes (LEDs), and other semiconductor devices.
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