Adsorption mechanisms of Mo2CrC2 MXenes as potential anode materials for metal-ion batteries: A first-principles investigation

Abstract

Two dimensional MXene are attracting increasing interests as electrode materials for metal ion batteries (MIBs) because metal ions can diffuse in a 2D lattice surface. In this work, first-principles calculations were carried out to investigate the adsorption performance of monolayer Mo2CrC2 for Li, Na, and K. The results show strong storage ability for various metal cations. There are three layers of Li, two layers of Na, one layer of K, and four layers of Mg on both sides of the monolayer. The electrochemical and thermodynamics of the intercalation of metal ions on the Mo2CrC2 Mxene have been intensively investigated. There is no band gap at the Fermi level of any configuration indicating that it has excellent electronic conductivity leading to an asymmetric electron localization distribution. The binding energy of metal ions decreases as the ion concentration increases. The adsorption of metal ions on a mono-layer of Mo2CrC2 has been studied, and the results indicate that the metal ions obviously improved the diffusion of metal ions. The CI-NEB method was used to study the diffusion of a cation on a Mo2CrC2 surface and search for its lowest energy along the diffusion pathway. Their structural transformations were studied via ab initio molecular dynamic (AIMD) simulations at a series of temperatures. The metal ions gradually evolved via thermal motion with increasing temperature. These results suggest that Mo2CrC2 could be a promising electrode material for Li- and Na-ion batteries in terms of Mo2CrC2 specific capacity, diffusion dynamics, and structural stability.