Quantifying Heterogeneous Degradation Pathways and Deformation Fields in Solid‐State Batteries

Mechanical, (electro)chemical degradation pathways in all solid-state batteries and associated deformation fields around them are quantified using an in situ, multimodal strategy. The effects of electrolyte processing, cell assembly, and cycling are isolated. At the electrode interface and the terminal crack, stress is an order of magnitude higher than yield strength of Li; allowing plastic flow of Li into defects.

Abstract

Solid-state batteries are compelling candidates for next-generation energy storage devices, promising both high energy density and improved safety, by utilizing metallic Li as the negative electrode. However, they suffer from poor cyclability and rate capability, which limits their wide application. Degradation in these devices occurs through complex mechanical, chemical and electrochemical pathways, all of which produce heterogeneous deformation fields. Therefore, isolating solid-state degradation mechanisms, and explicitly linking them to the associated deformation fields requires a multimodal characterization strategy. Here, a novel 3-D, in situ methodology for linking degradation to deformation in solid-state cells is presented. X-ray imaging is used to measure the morphological degradation, and combined with X-ray diffraction to quantify (electro)chemical aspects. Finally, the heterogeneous stress fields from these various pathways are mapped in situ. This heterogeneity is shown globally, from the interface to the bulk electrolyte, as well as locally, around features such as cracks and voids. Through these analyses, it is possible to delineate the effects of solid electrolyte processing, cell assembly, and cycling on the end-of-life state of the cell. Moreover, the importance of stress mitigation in these cells is highlighted, with mean stresses around the interface and some cracks comfortably exceeding the elastic limit of Li.