Unveiling Surface Chemistry of Ultrafast-Sintered LLZO Solid-State Electrolytes for High-Performance Li-Garnet Solid-State Batteries

Abstract

Ultrafast (UF) sintering emerges as a game-changing sintering methodology for fabricating Li₇La₃Zr₂O₁₂ (LLZO) solid-state electrolytes, representing a pivotal stride toward the advancement and prospective commercialization of Li-garnet solid-state batteries. Despite its widespread use in the fabrication of LLZO ceramics, the chemical composition of the UF-sintered LLZO surface remains largely unexplored. This study presents an in-depth analysis of the surface chemistry of UF-sintered LLZO using comprehensive techniques, including depth-profiling X-ray photoelectron spectroscopy (XPS) and focused-ion-beam time-of-flight secondary ion mass spectroscopy (FIB-TOF-SIMS). Our investigation uncovers a striking difference between the surface of UF-sintered and conventionally sintered LLZO, revealing predominant surface contamination by Li₂O up to ca. 40 nm depth in the case of UF processing. Comparative synchrotron X-ray diffraction data during UF and conventional sintering elucidate the origin of surface contamination. We propose a viable solution to this issue through an additional heat treatment (HT) step at 900 °C after UF sintering, as corroborated by XPS and FIB-TOF-SIMS measurements. Furthermore, we present a comparative assessment of the electrochemical performance of Li/LLZO/Li symmetric cells based on UF-sintered LLZO pellets, both with and without the post-HT step, underscoring the pivotal role of an uncontaminated LLZO surface.