期刊
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 9, 期 16, 页码 4732-4737出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.8b02209
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资金
- Advanced Low Carbon Technology Research and Development Program (ALGA) of the Japan Science and Technology Agency (JST)
- Japan Society for the Promotion of Science (JSPS) [17J08120]
Mg(TFSA)(2)/triglyme(G3)-based electrolytes (TFSA: bis (trifluoromethanesulfonyl) amide) are one of candidates for magnesium rechargeable batteries, but the passivation of Mg-metal anode due to the TFSA anion is fatal in practical use. In this work we show that at elevated temperatures around 150 degrees C a comparable amount of MgCl2 salt can be dissolved in concentrated Mg(TFSA)(2)/G3 solutions, and the passivation of Mg metal is markedly suppressed in such highly concentrated solutions (1 <= G3/Mg-salts <= 2) in comparison with in the dilute solutions (G3/Mg-salts >> 2). By decreasing the amount of G3 solvent, the solvation structure of Mg2+ ions is modified in that free TFSA anions are drastically lowered, which would consequently decrease the reactivity of TFSA anions. We also demonstrate that a full-cell using MgCo2O4 cathode with the electrolyte of Mg(TFSA)(2)/MgCl2/G3 1:1:2 at 150 degrees C delivers a cell voltage of similar to 2 V versus Mg-metal anode.
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