4.8 Article

Study of LiCoO2/Li7La3Zr2O12:Ta Interface Degradation in All-Solid-State Lithium Batteries

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 9, 页码 11288-11299

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c22246

关键词

ASSLB; LCO/LLZO:Ta interface; interface degradation; Al diffusion; Co diffusion; electrochemical impedance spectroscopy

资金

  1. Federal Ministry of Education and Research (Bundesministerium fur Bildung und Forschung), Germany [13XP0134A, 13XP0305A, 13XP0223A]
  2. Ministry of Science and Technology, Taiwan [109-2636-E-006-012, 110-2636-E-006-016]

向作者/读者索取更多资源

The garnet-type Li7La3Zr2O12 (LLZO) ceramic solid electrolyte has high Li-ion conductivity and chemical stability at room temperature. However, capacity fading during cycling is a common issue. Investigation of the LiCoO2/LLZO interface revealed electrochemically driven cation diffusion, leading to the formation of an amorphous secondary phase interlayer with high impedance and causing capacity fading. Thermodynamic analysis also suggests the formation of low- or non-conducting secondary phases during cycling, further contributing to capacity fading. Understanding this degradation process is crucial for improving the cycling stability of garnet-based all-solid-state Li batteries.
The garnet-type Li7La3Zr2O12 (LLZO) ceramic solid electrolyte combines high Li-ion conductivity at room temperature with high chemical stability. Several all-solid-state Li batteries featuring the LLZO electrolyte and the LiCoO2 (LCO) or LiCoO2-LLZO composite cathode were demonstrated. However, all batteries exhibit rapid capacity fading during cycling, which is often attributed to the formation of cracks due to volume expansion and the contraction of LCO. Excluding the possibility of mechanical failure due to crack formation between the LiCoO2/LLZO interface, a detailed investigation of the LiCoO2/LLZO interface before and after cycling clearly demonstrated cation diffusion between LiCoO2 and the LLZO. This electrochemically driven cation diffusion during cycling causes the formation of an amorphous secondary phase interlayer with high impedance, leading to the observed capacity fading. Furthermore, thermodynamic analysis using density functional theory confirms the possibility of low- or non-conducting secondary phases forming during cycling and offers an additional explanation for the observed capacity fading. Understanding the presented degradation paves the way to increase the cycling stability of garnet-based all-solid-state Li batteries.

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