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 (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 is achieved exclusively in the wet electrolyte with 650 ppm water content. A significantly lower capacity of 51 mAh g 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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http://dx.doi.org/10.1002/cssc.202300758 | DOI Listing |
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