氧化还原
阳离子聚合
电化学
钾
化学
无机化学
电极
高分子化学
有机化学
物理化学
作者
Ajay Piriya Vijaya Kumar Saroja,Yupei Han,Charlie Nason,Gopinathan Sankar,Pan He,Yi Lu,Henry R. Tinker,Andrew Stewart,Verónica Celorrio,Min Zhou,Jiayan Luo,Yang Xu
标识
DOI:10.1021/acsmaterialslett.4c01455
摘要
MoS2 is regarded as one of the most promising potassium-ion battery (PIB) anodes. Despite the great progress to enhance its electrochemical performance, understanding of the electrochemical mechanism to store K-ions in MoS2 remains unclear. This work reports that the K storage process in MoS2 follows a complex reaction pathway involving the conversion reactions of Mo and S, showing both cationic redox activity of Mo and anionic redox activity of S. The presence of dual redox activity, characterized in-depth through synchrotron X-ray absorption, X-ray photoelectron, Raman, and UV-vis spectroscopies, reveals that the irreversible Mo oxidation during the depotassiation process directs the reaction pathway toward S oxidation, which leads to the occurrence of K-S electrochemistry in the (de)potassiation process. Moreover, the dual reaction pathway can be adjusted by controlling the discharge depth at different cycling stages of MoS2, realizing a long-term stable cycle life of MoS2 as a PIB anode.
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