2025/04/09 by Stephen Fuller, Jingxu Zheng · 1 voice
Engineering · #Advancements in Battery Materials #Advanced Battery Materials and Technologies #Advanced battery technologies research
paper · doi:10.1073/pnas.2425752122
openalex publication_date 2025/04/09 · openalex created_date 2025/10/10 · openalex updated_date 2026/06/11
The solid-electrolyte interphase (SEI) formed on a battery electrode has been a central area of research for decades. This structurally complex layer profoundly impacts the electrochemical deposition morphology and stability of metal anodes. Departing from conventional approaches, we investigate metal dissolution-the reverse reaction of deposition-in battery environments using a state-of-the-art electroanalytical system combining a rotating-disk electrode and operando visualization. Our key finding is the presence of a transient SEI (T-SEI) that forms during fast discharging at high dissolution rates. We attribute T-SEI formation to local supersaturation and resultant electrolyte salt deposition. The T-SEI fundamentally alters the dissolution kinetics at the electrochemical interface, yielding a flat, clean surface. Unlike a classical SEI formed due to electrolyte decomposition, the T-SEI is "relaxable" upon removal of the enforced dissolution current; that is, the T-SEI dissolves back into the electrolyte when rested. The formation of T-SEI plays an unexpected critical role in the subsequent electrodeposition. When the metal is redeposited on a fully relaxed T-SEI surface, the morphology is remarkably different from that deposited on pristine or low-rate-discharged metal electrodes. Electron backscatter diffraction analysis suggests that the deposition occurs via growth of the original grains; this is in stark contrast to the isolated, new nuclei seen on standard metal electrodes without T-SEI formation. Using 3D profilometry, we observe a 42% reduction in surface roughness due to T-SEI formation. Our findings provide important insights into the kinetics at ion-producing electrochemical interfaces, and suggest a new dimension for engineering next generation batteries.