锡
材料科学
插层(化学)
电化学
相(物质)
透射电子显微镜
氧化还原
离子
电极
化学工程
过渡金属
无机化学
纳米技术
催化作用
化学
物理化学
冶金
有机化学
工程类
作者
Xiuzhen Wang,Zhenpeng Yao,Sooyeon Hwang,Lei Zhang,Maosen Fu,Shuang Li,Liqiang Mai,Qingyu Xu,Dong Su
出处
期刊:Nano Energy
[Elsevier]
日期:2021-01-01
卷期号:79: 105458-105458
被引量:12
标识
DOI:10.1016/j.nanoen.2020.105458
摘要
Tin disulfide is considered as a promising electrode material for sodium-ion batteries because of its two-dimensional layered structural characteristics allowing the intercalation of Na ions. Understanding the underlying reaction mechanisms and the decisive step of the reaction reversibility is critical for its applications. Herein, we investigate the sodiation and desodiation processes of SnS2 by employing in situ transmission electron microscopy (TEM). After the initial intercalation reaction, a rock-salt NaySnS2 phase with disordering Na and Sn cations is observed, followed with a conversion reaction and an alloying reaction. The disordering reaction occurs along < 1–10 > direction of pristine SnS2 phase which is correlated with local bonding rearrangements induced by the exchange of Sn and Na cations. In-situ TEM studies and first-principles calculations indicate that the original 2D SnS2 structure could not be recovered during desodiation. Instead, the disordered NaySnS2 phase is finally formed, which indicates that the irreversible disordering transition is the determining step of irreversible cycling. This work probes the structural evolution of sodiation, providing a fundamental understanding of the electrochemical properties of metal sulfides and inspiring rational designs of high performance electrodes for sodium-ion batteries.
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