材料科学
阴极
电池(电)
离子
辐照
位错
化学物理
透射电子显微镜
微观结构
电化学
纳米技术
光电子学
复合材料
化学
电极
物理化学
物理
功率(物理)
有机化学
核物理学
量子力学
作者
Muhammad Mominur Rahman,Wei‐Ying Chen,Linqin Mu,Zhengrui Xu,Ziqi Xiao,Meimei Li,Xian-Ming Bai,Feng Lin
标识
DOI:10.1038/s41467-020-18345-4
摘要
Abstract Understanding defect evolution and structural transformations constitutes a prominent research frontier for ultimately controlling the electrochemical properties of advanced battery materials. Herein, for the first time, we utilize in situ high-energy Kr ion irradiation with transmission electron microscopy to monitor how defects and microstructures evolve in Na- and Li-layered cathodes with 3d transition metals. Our experimental and theoretical analyses reveal that Li-layered cathodes are more resistant to radiation-induced structural transformations, such as amorphization than Na-layered cathodes. The underlying mechanism is the facile formation of Li-transition metal antisite defects in Li-layered cathodes. The quantitative mathematical analysis of the dynamic bright-field imaging shows that defect clusters preferentially align along the Na/Li ion diffusion channels ( a-b planes), which is likely governed by the formation of dislocation loops. Our study provides critical insights into designing battery materials for extreme irradiation environments and understanding fundamental defect dynamics in layered oxides.
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