Improving Contact Impedance via Electrochemical Pulses Applied to Lithium–Solid Electrolyte Interface in Solid-State Batteries

Stabilizing interfaces in solid-state batteries (SSBs) is crucial for development of high energy density batteries. In this work, we report a facile electrochemical protocol to improve the interfacial impedance and contact at the interface of Li | Li6.25Al0.25La3Zr2O12 (LALZO). Application of short duration, high-voltage pulses to poorly formed interfaces leads to lower contact impedance. It is found that the local high current density that results from these pulses at the vicinity of the interfacial pores can lead to a better contact between Li and LALZO because of local Joule heating, as supported by theoretical simulations. The pulse technique, which has also been applied to a Li | Li6.4La3Zr1.4Ta0.6O12 (LLZTO) | LiNi0.6Mn0.2Co0.2O2 (NMC622) cell, results in remarkable reduction of the charge-transfer resistance. Ex situ characterizations, which include X-ray photoelectron spectroscopy and scanning electron microscopy techniques, reveal that there is no detrimental effects of the pulse on cathode and solid electrolyte bulks and interfaces. This electrochemical pulse technique sheds light on a facile, nondestructive method that has the potential to significantly improve the interfacial contacts in a solid-state battery configuration

Differences in the Interfacial Mechanical Properties of Thiophosphate and Argyrodite Solid Electrolytes and Their Composites

Interfacial mechanics are a significant contributor to the performance and degradation of solid-state batteries. Spatially resolved measurements of interfacial properties are extremely important to effectively model and understand the electrochemical behavior. Herein, we report the interfacial properties of thiophosphate (Li3PS4)- and argyrodite (Li6PS5Cl)-type solid electrolytes. Using atomic force microscopy, we showcase the differences in the surface morphology as well as adhesion of these materials. We also investigate solvent-less processing of hybrid electrolytes using UV-assisted curing. Physical, chemical, and structural characterizations of the materials highlight the differences in the surface morphology, chemical makeup, and distribution of the inorganic phases between the argyrodite and thiophosphate solid electrolytes