Setiawan Dedy, Chae Munseok S, Hong Seung-Tae
Department of Energy Science and Engineering, DGIST (Daegu Gyeongbuk Institute of Science and Technology), Daegu, 42988, Republic of Korea.
Present address: Department of Nanotechnology Engineering, Pukyong National University, Busan, 48513, Republic of Korea.
ChemSusChem. 2023 Nov 8;16(21):e202300758. doi: 10.1002/cssc.202300758. Epub 2023 Aug 16.
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.
由于理论能量密度高且镁资源丰富,镁电池已成为锂离子电池的一种有前景的替代方案。二氧化钒VO(B)已被报道为镁电池的一种高容量正极材料。然而,由于对结构-性能关系的理解有限,其电化学嵌入机制需要进一步阐明。在本研究中,我们重新评估了该材料的储镁能力,特别关注非水电解质中水分含量的影响。仅在水分含量为650 ppm的湿电解质中实现了250 mAh g的较高放电容量。在水分含量为40 ppm的干电解质溶液中观察到的容量显著较低,为51 mAh g。通过X射线结构和元素分析,以及使用键价能景观计算的镁离子扩散途径分析,通过研究反应机制阐明了容量受限的原因。根据这项研究,除非适当调节电解质的水分含量,否则由于非镁离子插入的参与,镁离子电池正极令人印象深刻的容量可能被夸大。