离子键合
原子单位
阳极
离子
硫系化合物
电化学
化学物理
插层(化学)
相(物质)
透射电子显微镜
硫化物
材料科学
化学
化学工程
纳米技术
物理
无机化学
光电子学
物理化学
冶金
电极
工程类
量子力学
有机化学
作者
Ran Cai,Wenqi Zhang,Jinhua Zhou,Kaishuai Yang,Linfeng Sun,Le Yang,Leguan Ran,Ruiwen Shao,Toshio Fukuda,Guoqiang Tan,Haodong Liu,Jiayu Wan,Qiaobao Zhang,Lixin Dong
标识
DOI:10.1002/smtd.202200995
摘要
Abstract It is a major challenge to achieve a high‐performance anode for sodium‐ion batteries (SIBs) with high specific capacity, high rate capability, and cycling stability. Bismuth sulfide, which features a high theoretical specific capacity, tailorable morphology, and low cost, has been considered as a promising anode for SIBs. Nevertheless, due to a lack of direct atomistic observation, the detailed understanding of fundamental intercalation behavior and Bi 2 S 3 's (de)sodiation mechanisms remains unclear. Here, by employing in situ high‐resolution transmission electron microscopy, consecutive electron diffraction coupled with theoretical calculations, it is not only for the first time identified that Bi 2 S 3 exhibits specific ionic transport pathways preferred to diffuse along the (110) direction instead of the (200) plane, but also tracks their real‐time phase transformations (de)sodiation involving multi‐step crystallographic tuning. The finite‐element analysis further disclosed multi‐reaction induced deformation and the relevant stress evolution originating from the combined effect of the mechanical and electrochemical interaction. These discoveries not only deepen the understanding of fundamental science about the microscopic reaction mechanism of metal chalcogenide anodes but also provide important implications for performance optimization.
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