Reaction Kinetics of Carbonation at the Surface of Garnet-Type Li7La3Zr2O12 as Solid Electrolytes for All-Solid-State Li Ion Batteries

被引:10
作者
Nakayama, Masanobu [1 ]
Horie, Takuya [1 ]
Natsume, Ryosuke [1 ]
Hashimura, Shogo [1 ]
Tanibata, Naoto [1 ]
Takeda, Hayami [1 ]
Maeda, Hirotaka [1 ]
Kotobuki, Masashi [2 ]
机构
[1] Nagoya Inst Technol, Dept Adv Ceram, Nagoya, Aichi 4668555, Japan
[2] Ming Chi Univ Technol, Battery Res Ctr Green Energy, New Taipei 24301, Taiwan
基金
日本科学技术振兴机构;
关键词
LI+/H+ EXCHANGE; CONDUCTION; STABILITY; AIR;
D O I
10.1021/acs.jpcc.2c08588
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
Garnet-type Li7La3Zr2O12 has attracted attention as a promising candidate for solid electrolytes in all-solid-state lithium ion metal batteries because it exhibits high Li ion conductivity and is inert in the presence of metallic Li. However, this material is known to react with water and carbon dioxide gas, even under ambient conditions, which can cause degradation, such as a decrease in ionic conductivity. In this study, the reaction rate of the carbonation processes under both humid and dry conditions was evaluated using thermal analysis. We confirmed that carbonation did not occur at <700 K under dry conditions. The reaction kinetics were found to initially be phase-boundary controlled and then diffusion controlled, and the corresponding activation energies were estimated to be 0.5 and 0.8 eV, respectively.
引用
收藏
页码:7595 / 7601
页数:7
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