Inhibiting Formation and Reduction of Li2CO3 to LiCx at Grain Boundaries in Garnet Electrolytes to Prevent Li Penetration

Abstract

AbstractPoor ion and high electron transport at the grain boundaries (GBs) of ceramic electrolytes are the primary reasons for lithium filament infiltration and short‐circuiting of all‐solid‐state lithium metal batteries (ASLMBs). Herein, it is discovered that Li2CO3 at the GBs of Li7La3Zr2O12 (LLZO) sheets is reduced to highly electron‐conductive LiCx during cycling, resulting in lithium penetration of LLZO. The ionic and electronic conductivity of the GBs within LLZO can be simultaneously tuned using sintered Li3AlF6. The generated LiAlO2 (LAO) infusion and F‐doping at the GBs of LLZO (LAO‐LLZOF) significantly reduce the Li2CO3 content and broaden the energy bandgap of LLZO, which decreases the electronic conductivity of LAO‐LLZOF. LAO forms a 3D continuous ion transport network at the GB that significantly improves the total ionic conductivity. Lithium penetration within LLZO is suppressed and an all‐solid‐state LiFePO4/LAO‐LLZOF/Li battery stably cycled for 5500 cycles at 3 C. This work reveals the chemistry of Li2CO3 at the LLZO GBs during cycling, presents a novel lithium penetration mechanism within garnet electrolytes, and provides an innovative method to simultaneously regulate the ion and electron transport at the GBs in garnet electrodes for advanced ASLMBs.