A scalable Li-Al-Cl stratified structure for stable all-solid-state lithium metal batteries

被引:11
作者
Su, Han [1 ]
Li, Jingru [1 ]
Zhong, Yu [1 ]
Liu, Yu [1 ]
Gao, Xuhong [1 ]
Kuang, Juner [1 ]
Wang, Minkang [1 ]
Lin, Chunxi [1 ]
Wang, Xiuli [1 ]
Tu, Jiangping [1 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon & Adv Semicond Mat, Key Lab Adv Mat & Applicat Batteries Zhejiang Prov, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
INTERFACE;
D O I
10.1038/s41467-024-48585-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sulfides are promising electrolyte materials for all-solid-state Li metal batteries due to their high ionic conductivity and machinability. However, compatibility issues at the negative electrode/sulfide electrolyte interface hinder their practical implementation. Despite previous studies have proposed considerable strategies to improve the negative electrode/sulfide electrolyte interfacial stability, industrial-scale engineering solutions remain elusive. Here, we introduce a scalable Li-Al-Cl stratified structure, formed through the strain-activated separating behavior of thermodynamically unfavorable Li/Li9Al4 and Li/LiCl interfaces, to stabilize the negative electrode/sulfide electrolyte interface. In the Li-Al-Cl stratified structure, Li9Al4 and LiCl are enriched at the surface to serve as a robust solid electrolyte interphase and are diluted in bulk by Li metal to construct a skeleton. Enabled by its unique structural characteristic, the Li-Al-Cl stratified structure significantly enhances the stability of negative electrode/sulfide electrolyte interface. This work reports a strain-activated phase separation phenomenon and proposes a practical pathway for negative electrode/sulfide electrolyte interface engineering. Sulfide electrolytes' incompatibility with Li metal hinders their use in all-solid-state Li metal batteries. Here, the authors propose a scalable Li-Al-Cl stratified structure, formed via strain-activated phase separation, to effectively stabilize the negative electrode/electrolyte interface.
引用
收藏
页数:10
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