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 high-voltage 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 MgCl(2) additive of electrolyte impairs the Mgâ¦Oâ=âC interaction to reduce the Mg(2+) desolvation barrier for accelerated redox kinetics, while the Mg(2+)-conducting polymer coating on the Mg surface ensures the facile Mg(2+) migration and the effective 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 (>â2.0 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.
Reversible Magnesium Metal Anode Enabled by Cooperative Solvation/Surface Engineering in Carbonate Electrolytes.
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作者:Wang Caiyun, Huang Yao, Lu Yunhao, Pan Hongge, Xu Ben Bin, Sun Wenping, Yan Mi, Jiang Yinzhu
| 期刊: | Nano-Micro Letters | 影响因子: | 36.300 |
| 时间: | 2021 | 起止号: | 2021 Sep 14; 13(1):195 |
| doi: | 10.1007/s40820-021-00716-1 | ||
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