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,Zixiang 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:1
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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