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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.
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页码:32262 / 32266
页数:5
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