Structural Heterogeneity Induced Li Dendrite Growth in Li0.33La0.56TiO3 Solid-State Electrolytes

被引:11
|
作者
Xu, Lei [1 ]
Feng, Tianshi [1 ]
Huang, Jinqiu [1 ]
Hu, Yubing [1 ]
Zhang, Lifeng [1 ]
Luo, Langli [1 ]
机构
[1] Tianjin Univ, Inst Mol Plus, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Li0.33La0.56TiO3; solid-state electrolyte; Li dendrite; short circuit; structural heterogeneity; CONDUCTIVITY; PROPAGATION;
D O I
10.1021/acsaem.2c00181
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
Solid-state electrolytes (SSEs) are driving next-generation Li-ion batteries (LIBs) with higher energy density and improved safety compared with organic liquid electrolytes. However, the gradual Li dendrite growth during cycling is still a critical issue limiting the long-term service of SSEs, the mechanism of which remains largely unclear. Her; we investigate the Li dendrite growth-induced short circuiting of Li0.33La0.56TiO3 (LLTO) ceramic pellets through detailed electron microscopy and spectroscopy analysis. Under both electrochemical cycling and thermal chemical reaction between Li and LLTO, we find that the Li dendrites prefer to nucleate at the voids in the LLTO pellet, followed by vertical growth along the grain boundaries, and finally result in the buildup of internal stress and the cracking of LLTO. In addition, Li dendrite growth accompanies the decomposition of Li0.33La0.56TiO3 because of the reduction of Ti4+ to Ti3+, which inevitably alters the bulk diffusion of Li ions.
引用
收藏
页码:3741 / 3747
页数:7
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