Abstract

The electrochemical insertion of divalent magnesium cations into orthorhombic molybdenum(VI) oxide was studied with regard to their use as electroactive species in ion-transfer battery systems and compared to the insertion of Li + and Na +. Specific charges of up to 300 and 240 Ah kg −1 were obtained in organic, propylene carbonate-based electrolytes for the lithium and sodium insertion, respectively, in the first reduction half-cycle. Reversible Mg 2+ insertion could be demonstrated in a room temperature molten salt electrolyte consisting of 3 wt.% MgCl 2, 41 wt.% 1-ethyl-3-methylimidazolium chloride, and 56 wt.% AlCl 3. Specific charges of up to 160 Ah kg −1 were obtained with MoO 3 in the first reduction half-cycle. The Mg 2+ insertion process can be enhanced using an organic electrolyte with traces of H 2O. In 1 M Mg(ClO 4) 2/acetonitrile with 3 mol% of H 2O, specific charges of up to 210 Ah kg −1 were measured in the first reduction.

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