On the Hidden Transient Interphase in Metal Anodes: Dynamic Precipitation Controls Electrochemical Interfaces in Batteries

TL;DR

This study uncovers a transient interphase, T-SEI, that forms during rapid metal dissolution in batteries, significantly influencing electrode surface morphology and electrochemical kinetics, with implications for battery design and performance.

Contribution

It reveals the existence and role of a transient, relaxable interphase during fast metal dissolution, a phenomenon not previously characterized in battery interfaces.

Findings

T-SEI forms during high-rate metal dissolution and alters kinetics.

T-SEI leads to flatter, cleaner electrode surfaces after dissolution.

Electrodeposition on T-SEI differs markedly from standard deposition processes.

Abstract

The Solid-Electrolyte Interphase, SEI, formed on a battery electrode has been a central area of research for decades. This thin, complex layer profoundly impacts the electrochemical deposition morphology and stability of the metal in battery 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 in-operando visualization. Our key finding is the presence of a Transient Solid-Electrolyte Interphase, T-SEI, that forms during fast discharging at high dissolution rates. We attribute T-SEI formation to transient local supersaturation and resultant electrolyte salt deposition. The T-SEI fundamentally alters the dissolution kinetics at the electrochemical interface, leading to a self-limiting morphological evolution and eventually yielding a flat, clean surface. Unlike a classical SEI formed due to electrolyte decomposition, the T-SEI is fully relaxable upon removal of the enforced dissolution current. The formation of T-SEI, surprisingly, plays a 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 the deposition occurs via growth of the original grains. This is in stark contrast to the isolated, particulate nuclei seen on standard metal electrodes without T-SEI formation. Our findings provide important insights into the electrochemical kinetics at the metal-electrolyte interface, particularly in concentrated or water-in-salt electrolytes that are close to the salt saturation limit. The results suggest a new dimension for electrochemical engineering in batteries.