Covalency competition induced selective bond breakage and surface reconstruction in manganese cobaltite towards enhanced electrochemical charge storage
Peng Gao, Pei Tang, Ying Mo, Peitao Xiao, Zhou Wang, Shi Chen, Hongliang Dong, Ziwei Li, Chaohe Xu, Jilei Liu
Abstract
Manganese cobaltite (MnCo 2 O 4 ) 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-MnO 2 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 Co 2+ ions were leached when MnCo 2 O 4 was equilibrated in 1 mol L −1 HCl solution, leading to the formation of layered CoOOH on MnCo 2 O 4 surface which is originated from the covalency competition induced selective breakage of the Co T –O bond in Co T –O–Co O and subsequent rearrangement of free CoO 6 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 MnCo 2 O 4 '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.