卤化物
化学物理
晶界
纳米尺度
离子
有机半导体
材料科学
金属卤化物
钙钛矿(结构)
纳米技术
化学
无机化学
光电子学
结晶学
有机化学
微观结构
作者
Jing Liang,Lei Miao,Jie Pang,Xing‐Hua Xia,Jian Li
标识
DOI:10.1002/anie.202410557
摘要
The performance and stability of organic metal halide perovskite (OMHP) optoelectronic devices have been associated with ion migration. Understanding of nanoscale resolved organic cation migration mechanism would facilitate structure engineering and commercialization of OMHP. Here, we report a three‐dimensional approach for in situ nanoscale infrared imaging of organic ion migration behavior in OMHPs, enabling to distinguish migrations along grain boundary and in crystal lattice. Our results reveal that organic cation migration along OMHP film surface and grain boundaries (GBs) occurs at lower biases than in crystal lattice. We visualize the transition of organic cation migration channels from GBs to volume upon increasing electric field. The temporal resolved results demonstrate the fast MA+ migration kinetics at GBs, which is comparable to diffusivity of halide ions. Our findings help understand the role of organic cations in the performance of OMHP devices, and the proposed approach holds broad applicability for revealing migration mechanisms of organic ions in OMHPs based optoelectronic devices.
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