Reversible Magnesium Metal Anode Enabled by Cooperative Solvation/Surface Engineering in Carbonate Electrolytes

被引:2
|
作者
Caiyun Wang [1 ,2 ]
Yao Huang [1 ,2 ]
Yunhao Lu [1 ]
Hongge Pan [1 ,3 ]
Ben Bin Xu [4 ]
Wenping Sun [1 ]
Mi Yan [1 ]
Yinzhu Jiang [1 ,2 ]
机构
[1] School of Materials Science and Engineering, State Key Laboratory of Clean Energy Utilization, Zhejiang University
[2] ZJU-Hangzhou Global Scientific and Technological Innovation Centre, Zhejiang University
[3] Institute of Science and Technology for New Energy, Xi'an Technological University
[4] Mechanical and Construction Engineering, Faculty of Engineering and Environment, Northumbria University
基金
中国国家自然科学基金; 中央高校基本科研业务费专项资金资助;
关键词
D O I
暂无
中图分类号
TM912 [蓄电池]; TG146.22 [];
学科分类号
080502 ; 0808 ;
摘要
Magnesium metal anode holds great potentials toward future high energy and safe rechargeable magnesium battery technology due to its divalent redox and dendrite-free nature. Electrolytes based on Lewis acid chemistry enable the reversible Mg plating/stripping, while they fail to match most cathode materials toward highvoltage magnesium batteries. Herein, reversible Mg plating/stripping is achieved in conventional carbonate electrolytes enabled by the cooperative solvation/surface engineering. Strongly electronegative Cl from the MgCl2additive of electrolyte impairs the Mg…O = C interaction to reduce the Mg2+desolvation barrier for accelerated redox kinetics,while the Mg2+-conducting polymer coating on the Mg surface ensures the facile Mg2+migration and the e ective isolation of electrolytes. As a result, reversible plating and stripping of Mg is demonstrated with a low overpotential of 0.7 V up to 2000 cycles. Moreover, benefitting from the wide electrochemical window of carbonate electrolytes, high-voltage(> 2.0 V) rechargeable magnesium batteries are achieved through assembling the electrode couple of Mg metal anode and Prussian blue-based cathodes. The present work provides a cooperative engineering strategy to promote the application of magnesium anode in carbonate electrolytes toward high energy rechargeable batteries.
引用
收藏
页码:117 / 127
页数:11
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