Rate-dependent deformation of amorphous sulfide glass electrolytes for solid-state batteries

Abstract

Sulfide glasses are emerging as potential electrolytes for solid-state batteries. The mechanical behavior of these materials can significantly impact cell performance, and it is thus imperative to understand their deformation and fracture mechanisms. Previous work mainly reports properties obtained under quasi-static loading conditions, but very little is known about deformation under dynamic conditions. The current investigation shows that the sulfide glass mechanical behavior is dominated by viscoplasticity, differing substantially from polycrystalline oxide and sulfide solid electrolytes. Finite element modeling indicates that the sulfide glass stiffness is high enough to maintain good contact with softer lithium metal electrodes under moderate stack pressures. The observed viscoplasticity also implies that battery operating conditions will play an important role in electro-chemo-mechanical processes that are associated with dendritic lithium penetration. In general, the rate-dependent mechanical behavior of the sulfide glass electrolytes documented here offers a new dimension for designing next-generation all-solid-state batteries.