Covalency competition induced selective bond breakage and surface reconstruction in manganese cobaltite towards enhanced electrochemical charge storage

Abstract

Manganese cobaltite (MnCo2O4) is a promising electrode material because of its attractive redox chemistry and excellent charge storage capability. Our previous work demonstrated that the octahedrally-coordinated Mn are prone to react with the hydroxyl ions in alkaline electrolyte upon electrochemical cycling and separates on the surface of spinel to reconstruct into δ-MnO2 nanosheets irreversibly, thus results in a change of the reaction mechanism with K+ ion intercalation. However, the low capacity has greatly limited its practical application. Herein, we found that the tetrahedrally-coordinated Co2+ ions were leached when MnCo2O4 was equilibrated in 1 mol L−1 HCl solution, leading to the formation of layered CoOOH on MnCo2O4 surface which is originated from the covalency competition induced selective breakage of the CoT–O bond in CoT–O–CoO and subsequent rearrangement of free CoO6 octahedra. The as-formed CoOOH is stable upon cycling in alkaline electrolyte, exhibits conversion reaction mechanism with facile proton diffusion and is free of massive structural evolution, thus enables utilization of the bulk electrode material and realizes enhanced specific capacity as well as facilitated charge transfer and ion diffusion. In general, our work not only offers a feasible approach to deliberate modification of MnCo2O4's surface structure, but also provides an in-depth understanding of its charge storage mechanism, which enables rational design of the spinel oxides with promising charge storage properties.

Keywords

• Manganese cobaltite
• Tetrahedrally-coordinated Co2+ leaching
• Selective bond breakage
• Surface reconstruction
• Charge storage mechanisms