材料科学
阳极
电解质
锂(药物)
电化学
电池(电)
磷酸钒锂电池
复合数
枝晶(数学)
化学工程
阴极
容量损失
二甲氧基乙烷
三元运算
离子电导率
锂电池
电极
复合材料
金属
离子键合
冶金
化学
离子
有机化学
程序设计语言
工程类
功率(物理)
物理化学
内分泌学
物理
医学
量子力学
计算机科学
数学
几何学
作者
Yingzhen Zhang,Chunwen Sun
标识
DOI:10.1021/acsami.1c00745
摘要
Lithium metal is considered as the ideal anode for next-generation rechargeable batteries due to its highest theoretical specific capacity and lowest electrochemical potential. However, lithium dendrite growth during lithium deposition could lead to a short circuit and even cause severe safety issues. Here, we use solid-state electrolyte Li3InCl6 as an additive in nonaqueous electrolytes because of its high ionic conductivity (10–3 to 10–4 S cm–1) and good electrochemical stability. It is found that Li3InCl6 can in situ react with metallic lithium to form a ternary composite solid electrolyte interphase (SEI) consisting of a Li–In alloy, LiCl, and codeposited Li3InCl6. The composite SEI can effectively suppress Li dendrite growth and thereby maintain stable long-term cycling performance in lithium metal batteries. The protected lithium electrode exhibits stable cycling performance in a symmetric Li|Li battery for nearly 1000 h at a current density of 1 mA cm–2. Besides, the full battery with a LiFePO4 cathode and a metallic lithium anode delivers a stable capacity of 140.6 mA h g–1 for 500 cycles with a capacity retention of 95%. The Li|S battery with Li3InCl6-added LiTFSI in 1,3-dioxolane/1,2-dimethoxyethane electrolyte also shows significant improvement in capacity retention at 0.5 C. This work demonstrates an effective approach to design dendrite-free metal anodes.
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