Synthetic poly-dioxolane as universal solid electrolyte interphase for stable lithium metal anodes

被引:35
作者
Chen, Tao [1 ]
Wu, Haiping [2 ]
Wan, Jing [3 ]
Li, Mengxue [1 ]
Zhang, Yucheng [1 ]
Sun, Lin [1 ]
Liu, Yuncong [1 ]
Chen, Lili [1 ]
Wen, Rui [3 ]
Wang, Chao [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[2] BYD Shanghai Co Ltd, Dept Battery Technol, Shanghai 201611, Peoples R China
[3] Chinese Acad Sci, Ctr Excellence Mol Sci, CAS Res Educ, Key Lab Mol Nanostruct & Nanotechnol, Beijing 100190, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2021年 / 62卷
基金
中国国家自然科学基金;
关键词
Polymer; Lithium metal anodes; Solid electrolyte interphase; Lithium-ion batteries; PERFORMANCE; LI; SECONDARY; DESIGN; PROTECTION; STRATEGY; SOLVENT; SAFE; FILM;
D O I
10.1016/j.jechem.2021.03.018
中图分类号
O69 [应用化学];
学科分类号
081704 ;
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. (C) 2021 Published by ELSEVIER B.V. and Science Press on behalf of Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences.
引用
收藏
页码:172 / 178
页数:7
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