Electrochemical Stability Window and Electrolyte Breakdown Mechanisms of Lithium Lanthanum Titanate

Perovskite-type La0.57Li0.29TiO3 (LLTO) is a promising solid electrolyte material with high Li-ion conductivity. However, its experimental electrochemical stability window is not precisely known, and thus the compatibility with potential electrode materials is partly unclear. In this contribution, we present results from electrochemical and analytical experiments to elucidate the stability of LLTO when being polarized with Li-ion-blocking Pt electrodes. Above 2.5 V, a darkened color front starts moving from the cathode to the anode, leading to electrolyte degradation. While first-principles calculations predict the appearance of new phases as decomposition products, we find zones with modified defect chemical properties originating from the anode and cathode. The darkened zone forming at the cathode contains Ti3+ polarons with high mobility, which leads to a mixed ion-electron conductivity, already for a very small Li excess concentration. Next to the anode a spatially very confined, weakly conductive Li depletion zone forms. The spatially confined but substantial Li depletion near the anode could be quantified by analytical laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). In contrast to first-principles calculations, no new phases were found near the anode, according to synchrotron-based grazing incidence XRD measurements.

Automated summary

In this study, the electrochemical and analytical experiments were conducted to investigate the stability of LLTO with Li-ion-blocking Pt electrodes. It was found that at voltages above 2.5 V, the electrolyte degradation occurred due to the movement of a darkened color front from cathode to anode. The cathode region showed the presence of Ti3+ polarons with high mobility, leading to mixed ion-electron conductivity, while the anode region exhibited a spatially confined, weakly conductive Li depletion zone.