Investigation of the water-stimulated Mg insertion mechanism in an electrodeposited MnO cathode using X-ray photoelectron spectroscopy.

Batteries based on magnesium chemistry are being widely investigated as an alternative energy storage system to replace lithium-ion batteries. Mg batteries have multiple challenges, especially on the cathode side. The divalent Mg ion has slow insertion kinetics in many metal oxide cathodes conventionally used in Li-ion batteries. One solution that has been explored is adding water molecules into an organic electrolyte, which has been shown to aid in Mg insertion and improve performance of manganese oxide (MnO) cathodes. While there have been studies on Mg insertion mechanisms into MnO in solely aqueous or organic electrolytes for some crystalline MnO polymorphs, our work is focused on water-containing organic electrolyte, where an HO to Mg ratio of 6 : 1 is present. In this study, we report results based on ex situ XPS experiments, including both angle resolved and depth profiling studies to assess the surface reactions and determine the mechanism of Mg insertion into an amorphous, electrodeposited MnO cathode. We propose that in this mixed electrolyte system, there is a combined insertion/conversion reaction mechanism whereby Mg and HO molecules co-insert into the MnO structure and a reaction between HO and Mg creates an observable Mg(OH) layer at the surface of the MnO. A more full understanding of the role of the water molecules is important to aid in the future design of cathode materials, especially when determining potential ways to integrate metal oxides in Mg batteries.