A Guideline to Mitigate Interfacial Degradation Processes in Solid-State Batteries Caused by Cross Diffusion

Abstract

Diffusion of transition metals across the cathode–electrolyte interface is identified as a key challenge for the practical realization of solid-state batteries. This is related to the formation of highly resistive interphases impeding the charge transport across the materials. Herein, the hypothesis that formation of interphases is associated with the incorporation of Co into the Li7La3Zr2O12 lattice representing the starting point of a cascade of degradation processes is investigated. It is shown that Co incorporates into the garnet structure preferably four-fold coordinated as Co2+ or Co3+ depending on oxygen fugacity. The solubility limit of Co is determined to be around 0.16 per formula unit, whereby concentrations beyond this limit causes a cubic-to-tetragonal phase transition. Moreover, the temperature-dependent Co diffusion coefficient is determined, for example, D700 °C = 9.46 × 10−14 cm2 s−1 and an activation energy Ea = 1.65 eV, suggesting that detrimental cross diffusion will take place at any relevant process condition. Additionally, the optimal protective Al2O3 coating thickness for relevant temperatures is studied, which allows to create a process diagram to mitigate any degradation with a minimum compromise on electrochemical performance. This study provides a tool to optimize processing conditions toward developing high energy density solid-state batteries.The incorporation of Co into Li7La3Zr2O12 is identified to play a key role in the degradation processes taking place at the interface formed with LiCoO2 during high temperature processing. It is found that the degradation is unavoidable but can be mitigated with a minimum compromise in performance by tailoring the interfacial coating layer thickness for any relevant processing conditions.