Manipulating Ligand Density at the Surface of Polyoxovanadate-Alkoxide Clusters.

We present the post-synthetic modification of a polyoxovanadate-alkoxide (POV-alkoxide) cluster via the reactivity of its cationic form, [V6O7(OCH3)12]1+, with water. This result indicates that cluster oxidation increases the lability of bridging methoxide ligands, affording a ligand exchange reaction that serves to compensate for the increased charge of the cluster core. This synthetic advance affords the isolation of a series of POV-alkoxide clusters with varying degrees of µ2-O2- ligands incorporated at the surface, namely, [V6O8(OCH3)11], [V6O9(OCH3)10], and [V6O10(OCH3)9]. Characterization of the POV-alkoxide clusters is described; changes in the infrared and electronic absorption spectra are consistent with the oxidation of the cluster core. We also examine the consequences of ligand substitution on the redox properties of the series of POV-alkoxide clusters via cyclic voltammetry; decreased alkoxide ligand density translates to a cathodic shift of analogous redox events. Ligand substitution also increases comproportionation constants of the Lindqvist core, indicating electron exchange between vanadium centers is promoted in structures with greater numbers of µ2-O2- ligands.

Molecular Engineering of Polyoxovanadate-Alkoxide Clusters and Microporous Polymer Membranes to Prevent Crossover in Redox-Flow Batteries.

The ongoing development of redox-active charge carriers for nonaqueous redox-flow batteries has led to energy-dense storage concepts and chemistries with high cell voltages. However, rarely are these candidates for flowable energy storage evaluated in tandem with cell separators compatible with organic solvent, limiting progress in the identification of suitable charge carrier-separator pairings. This is important, as the efficiency of a redox-flow battery is dictated by extent of active species crossover through a separator, dividing the two cells, and the contribution of the separator to cell resistance. Here, we report the size-dependent crossover behavior of a series of redox-active vanadium(III) acetoacetonate, and two polyoxovanadate-alkoxide clusters, [V6O7(OR)12] (R = CH3, C5H11) through separators derived from polymers of intrinsic microporosity (PIMs). We find that highly efficacious active-material blocking requires both increasing the size of the vanadium species and restricting pore swelling of the PIMs in nonaqueous electrolyte. Notably, increasing the size of the vanadium species does not significantly affect its redox reversibility, and reducing swelling decreases the conductivity of the separator by only 50%. By pairing polyoxometalate clusters with PIM membranes in nonaqueous redox-flow batteries, more efficient systems may well be within reach.