Amorphous Phase Induced Lithium Dendrite Suppression in Glass-Ceramic Garnet-Type Solid Electrolytes

Lithium metal-based solid-state batteries (SSBs) have attracted much attention due to their potentially higher energy densities and improved safety compared with lithium-ion batteries. One of the most promising solid electrolytes, garnet-type Li7La3Zr2O12 (LLZO), has been investigated intensively in recent years. It enables the use of a lithium metal anode, but its application is still challenging because of lithium dendrites that grow at voids, cracks, and grain boundaries of sintered bodies during cycling of the battery cell. In this work, glass-ceramic Ta-doped LLZO produced in a unique melting process was investigated. Upon cooling, an amorphous phase is generated intrinsically, whose composition and fraction are adjusted during the process. Herein, it was set to about 4 wt % containing Li2O and a Li2O–SiO2 phase. During sintering, it was shown to segregate into the grain boundaries and decrease porosity via liquid phase sintering. Sintering temperature and sintering time were found to be reduced compared with the LLZO fabricated by a solid-state reaction while maintaining high density and ionic conductivity. The glass-ceramic sintered at 1130 °C for 0.5 h showed a room-temperature ionic conductivity of 0.64 mS cm–1. Most importantly, the evenly distributed amorphous phase along the grain boundaries effectively hinders lithium dendrite growth. Besides mechanically blocking pores and voids, it helps to prevent inhomogeneous distribution of current density. The critical current density (CCD) of the Li|LLZTO|Li symmetric cell was determined as 1.15 mA cm–2, and in situ lithium plating experiments in a scanning electron microscope revealed superior dendrite stability properties. Therefore, this work provides a promising strategy to prepare a dense and dendrite-suppressing solid electrolyte for future implementation in SSBs.