晶界
电负性
锂(药物)
电解质
材料科学
烧结
快离子导体
离子
离子电导率
电导率
热稳定性
矿物学
化学工程
冶金
化学
微观结构
物理化学
电极
内分泌学
工程类
有机化学
医学
作者
Shiwei Deng,Huilin Zhu,Zhiyuan Zheng,Zi-Xiang Kong,Zixing Wang,Wang Zhou,Rui Tang,Jian‐Fang Wu,Jilei Liu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-08-01
卷期号:24 (32): 9801-9807
被引量:8
标识
DOI:10.1021/acs.nanolett.4c01266
摘要
Cation-doped cubic Li7La3Zr2O12 is regarded as a promising solid electrolyte for safe and energy-dense solid-state lithium batteries. However, it suffers from the formation of Li2CO3 and high electronic conductivity, which give rise to an unconformable Li/Li7La3Zr2O12 interface and lithium dendrites. Herein, composite AlF3-Li6.4La3Zr1.4Ta0.6O12 solid electrolytes were created based on thermal AlF3 decomposition and F/O displacement reactions under a high-temperature sintering process. When the AlF3 is thermally decomposed, it leaves Al2O3/AlF3 meliorating the grain boundaries and F– ions partially displacing O2– ions in the grains. Due to the higher electronegativity of F– in the grains and the grain-boundary modification, these AlF3-Li6.4La3Zr1.4Ta0.6O12 deliver optimized electronic conduction and chemical stability against the formation of Li2CO3. The Li/AlF3-Li6.4La3Zr1.4Ta0.6O12/Li cell exhibits a low interfacial resistance of ∼16 Ω cm2 and an ultrastable long-term cycling behavior for 800 h under a current density of 200 μA/cm2, leading to Li//LiCoO2 solid-state batteries with good rate performance and cycling stability.
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