LiAlCl4•3SO2: a promising inorganic electrolyte for stable Li metal anode at room and low temperature

被引:9
作者
Gao, Tiantian [1 ]
Wang, Bo [1 ,2 ]
Wang, Fei [1 ]
Li, Ruopeng [1 ]
Wang, Lei [1 ]
Wang, Dianlong [1 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, Harbin 150001, Heilongjiang, Peoples R China
[2] Harbin Inst Technol, Sch Mat Sci & Engn, 92 West Dazhi St, Harbin 150001, Heilongjiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
LiAlCl4 center dot 3SO(2) electrolyte; Non-combustible; Li metal anode; Stable SEI film; Low temperature; FREE LITHIUM DEPOSITION; DENDRITIC GROWTH; ION; PERFORMANCE; BATTERIES; LIALCL4; CHEMISTRY; CELLS; SO2; BA;
D O I
10.1007/s11581-019-02994-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
LiAlCl4 center dot 3SO(2) is a promising electrolyte used for Li metal batteries. At room and low temperature, a stable solid electrolyte interface film can be formed in LiAlCl4 center dot 3SO(2) to achieve favorable protection for Li metal anodes. Here, Li|Cu cells with SO2-based inorganic electrolyte (LiAlCl4 center dot 3SO(2)) display higher average coulombic efficiency and more excellent cycling stability compared with a conventional organic electrolyte. Moreover, at 0.5 mA cm(-2), the coulombic efficiency of Li|Cu cells with LiAlCl4 center dot 3SO(2) electrolyte can reach 95% at - 20 degrees C, while the coulombic efficiency of the conventional organic electrolyte at - 20 degrees C is only about 79%. Furthermore, LiAlCl4 center dot 3SO(2) electrolyte is non-combustible. Based on all the experimental results, LiAlCl4 center dot 3SO(2) is a promising electrolyte candidate for safe Li metal batteries. Graphic abstract Lithium metal anode, protected by the stable and dense SEI films formed in non-flammable and inorganic non-aqueous liquid electrolyte-LiAlCl4 center dot 3SO(2) (IE), exhibits small and stable over-potential during Li stripping/plating compared with conventional organic electrolyte (OE) even at - 20 degrees C.
引用
收藏
页码:4137 / 4147
页数:11
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