In situ p-block protective layer plating in carbonate-based electrolytes enables stable cell cycling in anode-free lithium batteries

被引:0
|
作者
Shi, Jie [1 ]
Koketsu, Toshinari [1 ,2 ]
Zhu, Zhenglu [1 ]
Yang, Menghao [1 ]
Sui, Lijun [1 ]
Liu, Jie [3 ]
Tang, Mingxue [3 ]
Deng, Zhe [4 ]
Liao, Mengyi [4 ]
Xiang, Jingwei [4 ]
Shen, Yue [4 ]
Qie, Long [4 ]
Huang, Yunhui [4 ]
Strasser, Peter [2 ]
Ma, Jiwei [1 ]
机构
[1] Tongji Univ, Inst New Energy Vehicles, Sch Mat Sci & Engn, Shanghai Key Lab R&D & Applicat Met Funct Mat, Shanghai, Peoples R China
[2] Tech Univ Berlin, Dept Chem, Berlin, Germany
[3] Ctr High Pressure Sci & Technol Adv Res, Beijing, Peoples R China
[4] Huazhong Univ Sci & Technol, Sch Mat Sci & Engn, State Key Lab Mat Proc & Die & Mold Technol, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL ANODE; LI-METAL; INTERPHASE; LIQUID; SALT; NMR; ELECTRODEPOSITION; CHALLENGES; ENERGY;
D O I
10.1038/s41563-024-01997-8
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
Anode-free' Li metal batteries offer the highest possible energy density but face low Li coulombic efficiency when operated in carbonate electrolytes. Here we report a performance improvement of anode-free Li metal batteries using p-block tin octoate additive in the carbonate electrolyte. We show that the preferential adsorption of the octoate moiety on the Cu substrate induces the construction of a carbonate-less protective layer, which inhibits the side reactions and contributes to the uniform Li plating. In the mean time, the reduction of Sn2+ at the initial charging process builds a stable lithophilic layer of Cu6Sn5 alloy and Sn, improving the affinity between the Li and the Cu substrate. Notably, anode-free Li metal pouch cells with tin octoate additive demonstrate good cycling stability with a high coulombic efficiency of similar to 99.1%. Furthermore, this in situ p-block layer plating strategy is also demonstrated with other types of p-block metal octoate, as well as a Na metal battery system, demonstrating the high level of universality.
引用
收藏
页码:1686 / 1694
页数:12
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