镁
电解质
电化学
阴极
无机化学
钒
化学
价(化学)
储能
离子
化学工程
电极
物理化学
热力学
有机化学
功率(物理)
物理
工程类
作者
Dedy Setiawan,Munseok S. Chae,Seung‐Tae Hong
出处
期刊:Chemsuschem
[Wiley]
日期:2023-07-30
卷期号:16 (21): e202300758-e202300758
被引量:9
标识
DOI:10.1002/cssc.202300758
摘要
Abstract Magnesium batteries have emerged as a promising alternative to lithium‐ion batteries due to their theoretical high energy density and abundant magnesium resources. Vanadium dioxide, VO 2 (B), has been reported as a high‐capacity cathode material for magnesium batteries. However, the electrochemical intercalation mechanism requires further elucidation due to a limited understanding of the structure‐property relationship. In this study, we re‐evaluated the magnesium storage capability of the material, with a particular focus on the influence of water content in nonaqueous electrolytes. The higher discharge capacity of 250 mAh g −1 is achieved exclusively in the wet electrolyte with 650 ppm water content. A significantly lower capacity of 51 mAh g −1 was observed in the dry electrolyte solution containing 40 ppm water content. Through X‐ray structural and elemental analyses, as well as magnesium‐ion diffusion pathway analysis using bond‐valence‐energy‐landscape calculations, the restricted capacity was clarified by examining the reaction mechanism. According to this study, the impressive capacity of magnesium‐ion battery cathodes may be exaggerated due to the involvement of non‐magnesium‐ion insertion unless the electrolytes′ water content is appropriately regulated.
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