Transition metal polysulfides with high S content, such as VS4, TiS4, and MoS3, have high specific Li+ capacities, but their reaction mechanisms for lithium-ion batteries remain unclear due to unknown intermediate products. In this work, first-principles calculations based on the density functional theory were performed to reveal the electrochemical properties of VS4 for lithium-ion batteries. The results demonstrated multiple phase transformations during Li+ insertion, starting with nucleation transformation from VS4 to Li3VS4 and followed by gradual decomposition reactions. Enthalpy-driven long-range migration of Li2S molecules resulted in crystalline to amorphous transformation during decomposition. S and V successively behaved as redox centers for Li xVS4 before and after x = 3. Moreover, low activation energy and high Li+ diffusivity were observed at room temperature, revealing superior rate capability of the material.
Keywords: conversion reaction; structure prediction; structure transformation; transition metal polysulfide; vanadium tetra-sulfide.