Kinetics of Li Transport in Vanadium-Based Disordered Rocksalt Structures

Abstract

Disordered rocksalt Li-excess (DRX) compounds have emerged as promising new cathode materials for lithium-ion batteries, as they can consist solely of resource-abundant metals and eliminate the need for cobalt or nickel. A deeper understanding of the lithium-ion transport kinetics in DRX compounds is essential for enhancing their rate performance. This study employs first-principles calculations, cluster expansion techniques, and kinetic Monte Carlo simulations to investigate the Li + transport properties in DRX Li 2−x VO 3 , where 0 ≤ x ≤ 1. Our findings underscore (i) the necessity of accounting for both tetrahedral and octahedral Li occupancy when predicting the transport properties in DRX materials, (ii) the factors influencing the variation in the diffusion coefficients with Li content in Li 2−x VO 3 , and (iii) the impact of Li + correlated motion on the kinetics of Li + transport. We reveal that the relative stability of tetrahedral and octahedral Li determines the number of active sites within the percolation network, subsequently affecting the Li + transport properties. Furthermore, we demonstrate that the wide site energy distribution causes correlated motion in Li 2−x VO 3 , which hinders Li + transport.