Modelling interfacial ionic transport in Li2VO2F cathodes during battery operation

Abstract

Transition metal oxyflourides have gained considerable interest as potential high-capacity cathode materials for Li-ion batteries. So far, commercialization has been hindered by the poor cyclability and fast degradation of this class of materials. The degradation process is believed to start at the surface and progresses toward the bulk. In this context, a suitable cathode-electrolyte interphase (CEI) appears to be a crucial factor where the formation of LiF has been identified as a key component promoting interfacial stability. In the current work, we make use of a combined density functional theory (DFT) and kinetic Monte Carlo (kMC) approach. Using DFT, we determine relevant interfaces between Li₂VO₂F and LiF. Rejection-free kMC simulations with parameters based on DFT are then used to probe the kinetics in the charging and discharging process of the Li₂VO₂F phase. We find that the interface formed by joining Li₂VO₂F and LiF via their most stable surface terminations has a modest but positive effect on the charging rate, where the LiF phase acts as a funnel that facilitates the Li extraction from the bulk of the Li₂VO₂F phase. However, the same interface has a severe impeding effect on the discharging of partially delithiated structures, which is orders of magnitudes slower than in the charging process. We find that the key property controlling the kinetics in the discharging process is the difference in stability of Li vacancies in the Li₂VO₂F and LiF phases.