Mitigating Interfacial Capacity Fading in Vanadium Pentoxide by Sacrificial Vanadium Sulfide Encapsulation for Rechargeable Mg-Ion Batteries

Abstract

Rechargeable Mg-ion Batteries (RMB) containing a Mg metal anode offer the promise of higher specific volumetric capacity, energy density, safety, and economic viability than lithium-ion battery technology, but their realization is challenging. The limited availability of suitable inorganic cathodes compatible with electrolytes relevant to Mg metal anode restricts the development of RMBs. Despite the promising capability of some oxides to reversibly intercalate Mg+2 ions at high potential, its lack of stability in chloride-containing ethereal electrolytes, relevant to Mg metal anode hinders the realization of a full practical RMB. Here the successful in situ encapsulation of monodispersed spherical V2O5 (approximate to 200 nm) is demonstrated by a thin layer of VS2 (approximate to 12 nm) through a facile surface reduction route. The VS2 layer protects the surface of V2O5 particles in RMB electrolyte solution (MgCl2 + MgTFSI in DME). Both V2O5 and V2O5@VS2 particles demonstrate high initial discharge capacity. However, only the V2O5@VS2 material demonstrates superior rate performance, Coulombic efficiency (100%), and stability (138 mA h g-1 discharge capacity after 100 cycles), signifying the ability of the thin VS2 layer to protect the V2O5 cathode and facilitate the Mg+2 ion intercalation/deintercalation into V2O5. Rationally designed spherical V2O5 encapsulated with 2D VS2 endows with high discharge capacity and pronounced stability. The thin VS2 layer shields the surface of V2O5 and facilitates the dissociation of complex ions of the electrolyte solution toward the development of advanced cathode material for next-generation rechargeable Mg-ion battery.image