法拉第效率
阳极
电解质
金属锂
材料科学
溶解
化学工程
锂(药物)
枝晶(数学)
阴极
金属
化学
冶金
电极
物理化学
内分泌学
工程类
医学
数学
几何学
作者
Tao Chen,Haiping Wu,Jing Wan,Mengxue Li,Yucheng Zhang,Lin Sun,Yuncong Liu,Lili Chen,Rui Wen,Chao Wang
标识
DOI:10.1016/j.jechem.2021.03.018
摘要
Lithium (Li) metal is a promising anode for the next generation high-energy–density batteries. However, the growth of Li dendrites, low coulombic efficiency and dramatic volume change limit its development. Here, we report a new synthetic poly-dioxolane (PDOL) approach to constructing an artificial 'elastic' SEI to stabilize the Li/electrolyte interface and the Li deposition/dissolution behavior in a variety of electrolytes. By coating PDOL with optimized molecular weights and synthetic routes on Li metal anode, the 'elastic' SEI layer could be maintained on top of the Li metal anode to accommodate the Li deposition/dissolution. No dendrite formation was observed during the cycling process, and the interfacial side reactions were reduced significantly. Consequently, we successfully achieved 330 cycles with a CE of 98.4% in ether electrolytes and 90 cycles with a CE of 94.3% in carbonate electrolytes. Simultaneously, the Li-metal batteries with LiFePO4 as cathodes also exhibited improved cycling performance. This strategy could promote the development of dendrite-free metal anodes toward high-performance Li-metal batteries.
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