材料科学
氧化还原
阴极
镁
钛
纳米技术
离子
化学
冶金
有机化学
物理化学
作者
Jianbiao Wang,Xian Yi Tan,Man‐Fai Ng,Gang Wu,Gaoliang Yang,Tanmay Ghosh,Carina Yi Jing Lim,Wutthikrai Busayaporn,Wanwisa Limphirat,Dechmongkhon Kaewsuwan,Deviprasath Chinnadurai,Zhenxiang Xing,Hongfei Liu,Yi Ren,Qingyu Yan,Zhi Wei Seh
标识
DOI:10.1002/adfm.202512519
摘要
Abstract Parasitic reactions have hampered transition metal chalcogenide cathodes in magnesium−ion batteries (MIBs), especially for conversion−type cathodes. To fully harness its high theoretical capacity and restrict undesirable side reactions, a defective titanium polyanion cathode ( V s −TiS 3 ) with exposed (001) facets is prepared via a fast−quenching treatment. The performance of the cathode material is investigated in MIBs for the first time, demonstrating a new hybrid energy storage mechanism involving both insertion and conversion reactions. Moreover, the defective TiS 2 formed during cycling is found to have a strong adsorption effect on the side products of magnesium polysulfides (MgS x ), boosting magnesium storage performance. Consequently, the electrodes delivered a substantial capacity of 717.3 mAh g −1 at 25 mA g −1 , and a high capacity of 291.5 mAh g −1 at 500 mA g −1 after 100 cycles, surpassing the performance of previously reported MIBs at the same current density. When employed in pouch cells, a high energy density of 220 Wh kg −1 is achieved. Lastly, this cathode material is also adapted for other mono/multivalent metal−ion batteries (e.g., Li + , Na + , Al 3+ ), demonstrating its versatility.
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