Amorphous Cobalt Vanadium Oxide as a Highly Active Electrocatalyst for Oxygen Evolution

[Image: see text] The water-splitting reaction provides a promising mechanism to store renewable energies in the form of hydrogen fuel. The oxidation half-reaction, the oxygen evolution reaction (OER), is a complex four-electron process that constitutes an efficiency bottleneck in water splitting. Here we report a highly active OER catalyst, cobalt vanadium oxide. The catalyst is designed on the basis of a volcano plot of metal–OH bond strength and activity. The catalyst can be synthesized by a facile hydrothermal route. The most active pure-phase material (a-CoVO(x)) is X-ray amorphous and provides a 10 mA cm(–2) current density at an overpotential of 347 mV in 1 M KOH electrolyte when immobilized on a flat substrate. The synthetic method can also be applied to coat a high-surface-area substrate such as nickel foam. On this three-dimensional substrate, the a-CoVO(x) catalyst is highly active, reaching 10 mA cm(–2) at 254 mV overpotential, with a Tafel slope of only 35 mV dec(–1). This work demonstrates a-CoVO(x) as a promising electrocatalyst for oxygen evolution and validates M–OH bond strength as a practical descriptor in OER catalysis.