Tuning effect of vanadium substitution on the structural and electronic properties of potassium hollandite surfaces

Abstract

Metal oxide surfaces possess unique properties that are crucial for a wide variety of applications. Herein, density functional theory calculations are performed to study surfaces of potassium hollandite, KMn8O16, a promising cathode material for electrochemical energy storage, and the vanadium-substituted analog KMn7VO16. The results show that there is a clear increase in the stability of KMn8O16 with (001) < (110) < (100) or (010), apt to adopt an elongated rod-like morphology. The vanadium (V)-substitution lowers the crystal symmetry and prefers to occupy the surface sites, resulting in electron redistribution and selective tuning of surface energy depending on the surface structures. In particular, the higher stability of substituted V4+ compared with Mn4+ ions leads to stabilization of the (001) surface due to the direct interaction of reduced Mnδ+ ions on the surface, while such tuning effect decreases with the increase in surface stability, (110) > (100) and (010). As a result, the KMnO16 rod is shortened upon V-substitution as observed experimentally, effectively facilitating the ion transport during discharge. The V substituents also introduce stabilization to the defect surfaces resulting from Mn2+ dissolution during cycling, thereby hindering further structural decay. Our study demonstrates the potential tuning effect of V-substitution to promote the ion transport and mitigate the capacity degradation of α-MnO2-based materials.