Redox-inactive ions control the redox-activity of molecular vanadium oxides
Simon Greiner1,2, Benjamin Schwarz1, Mark Ringenberg3
1Institute of Inorganic Chemistry I, Ulm University Albert-Einstein-Allee 11 89081 Ulm Germany carsten.streb@uni-ulm.de.
Abstract:
Polyoxometalates are key materials for energy conversion and storage due to their unique chemical tunability and electrochemical reactivity. Herein, we report that functionalization of molecular vanadium oxides, polyoxovanadates, with redox-inert Ca2+ cations leads to a significant increase in their electron storage capabilities. The electrochemical performance of the Ca2+-functionalized dodecavanadate [Ca2V12O32Cl(DMF)3]2- (={Ca V }) was thus compared with that of the precursor compound (H2NMe2)2[V12O32Cl]3- (={V }). {Ca V } can store up to five electrons per cluster, while {V } only shows one reversible redox transition. In initial studies, we demonstrated that {Ca V } can be used as an active material in lithium-ion cathodes. Our results show how redox-inert cations can be used as structural and electrostatic stabilizers, leading to major changes in the redox-chemistry of polyoxovanadates.
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