Realization of Mg2+ intercalation in a thermodynamically stable layer-structured oxide

被引:0
|
作者
Zhang, Junhao [1 ,2 ]
Guan, Haotian [1 ,2 ]
Yue, Jili [1 ,2 ]
Lu, Yangfan [1 ,2 ]
Li, Qian [1 ,2 ]
Huang, Guangsheng [1 ,2 ]
Wang, Jingfeng [1 ,2 ]
Qu, Baihua [1 ,2 ]
Pan, Fusheng [1 ,2 ]
机构
[1] Chongqing Univ, Coll Mat Sci & Engn, Natl Engn Res Ctr Magnesium Alloys, Natl Innovat Ctr Ind Educ Integrat Energy Storage, Chongqing 400044, Peoples R China
[2] Chongqing Inst New Energy Storage Mat & Equipment, Chongqing 401135, Peoples R China
基金
中国国家自然科学基金;
关键词
MAGNESIUM VANADIUM-OXIDE; ELECTROCHEMICAL INSERTION; BATTERY; PERFORMANCE; CATHODES; SODIUM; WATER;
D O I
10.1039/d4ra03923h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Magnesium batteries have emerged as one of the considerable choices for next-generation batteries. Oxide compounds have attracted great attention as cathodes for magnesium batteries because of their high output voltages and ease of synthesis. However, a majority of the reported results are based on metastable nanoscale oxide materials. This study puts forward a thermodynamically stable layer-structured oxide K0.5MnO2 with an enlarged lattice spacing as a model cathode material employing optimized electrolytes, enabling Mg2+ intercalation into the K0.5MnO2 framework in a real magnesium battery directly using Mg foil as the anode. First-principles calculations implied that the enlarged layer spacing could decrease the migration energy barrier of Mg2+ in the layered oxide. This work can pave the way to understanding the fundamental intercalation behavior of Mg2+ in magnesium batteries.
引用
收藏
页码:32262 / 32266
页数:5
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