电解质
二甲醚
二甲氧基乙烷
阳极
碳酸二甲酯
金属
分解
碳酸丙烯酯
无机化学
化学
有机化学
甲醇
物理化学
电极
作者
Tao Li,Yan Li,Yiling Sun,Zhengfang Qian,Renheng Wang
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2021-05-20
卷期号:3 (6): 838-844
被引量:67
标识
DOI:10.1021/acsmaterialslett.1c00276
摘要
Localized high-concentration electrolytes (LHCEs) have captured considerable attention, since they retain the merits of high-concentration electrolytes while circumventing the disadvantages of high viscosity and high costs. Herein, a systematic comparison between two representative LHCEs (i.e., dimethyl carbonate (DMC)-based LHCE and 1,2-dimethoxyethane (DME)-based LHCE) in high-voltage Li metal batteries was performed. The results showed that DME-based LHCE possesses better compatibilty with Li metal anodes than DMC-based LHCE, and the underlying mechanism is clarified from the point of solid electrolyte interphase (SEI) formation. The two representative LHCEs showed comparable reductive stability, while Li+–DME showed better reductive stability than Li+–DMC. This means the more prominent decomposition of anions in DME-based LHCE, since SEI is derived from the competitive decomposition products of solvents and anions, which is further verified by the more-complete anion decomposition products found in SEI formed in DME-based LHCE. The inorganic-rich SEI with superior passivating ability is reponsible for the good compatibility of DME-based LHCE with Li metal anodes. The findings in this study provides fresh understandings on the stable nature of ether-based LHCE with Li metal anodes, which can serve as guidelines for advanced electrolytes engineering.
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