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Amorphous Cobalt Vanadium Oxide as a Highly ActiveElectrocatalyst for Oxygen Evolution

机译:非晶态高活性氧化钒钒析氧电催化剂

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摘要

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-CoVOx) 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-CoVOx 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-CoVOx as a promising electrocatalyst for oxygen evolution and validates M–OH bond strength as a practical descriptor in OER catalysis.
机译:水分解反应提供了以氢燃料形式存储可再生能源的有希望的机制。氧化半反应,即放氧反应(OER),是一个复杂的四电子过程,构成了水分解的效率瓶颈。在这里,我们报告了一种高活性的OER催化剂钴钒氧化物。该催化剂是根据金属-OH键强度和活性的火山图设计的。催化剂可以通过容易的水热途径合成。最具活性的纯相材料(a-CoVOx)是X射线无定形的,固定在平面上的1 M KOH电解质中,在347 mV的超电势下提供10 mA cm –2 的电流密度基质。合成方法也可以用于涂覆高表面积的基材,例如泡沫镍。在此三维衬底上,a-CoVOx催化剂具有很高的活性,在254 mV超电势下达到10 mA cm –2 ,Tafel斜率仅为35 mV dec -1 sup>。这项工作证明了a-CoVOx是一种有希望的氧气释放电催化剂,并证明了M-OH键强度是OER催化中的一种实用描述。

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