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非晶态钴钒氧化物作为一种高效析氧电催化剂

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

作者信息

Liardet Laurent, Hu Xile

机构信息

Laboratory of Inorganic Synthesis and Catalysis, Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.

出版信息

ACS Catal. 2018 Jan 5;8(1):644-650. doi: 10.1021/acscatal.7b03198. Epub 2017 Dec 6.

Abstract

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 (CoVO ) is X-ray amorphous and provides a 10 mA cm 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 CoVO catalyst is highly active, reaching 10 mA cm at 254 mV overpotential, with a Tafel slope of only 35 mV dec. This work demonstrates CoVO as a promising electrocatalyst for oxygen evolution and validates M-OH bond strength as a practical descriptor in OER catalysis.

摘要

水分解反应提供了一种很有前景的机制,可将可再生能源以氢燃料的形式储存起来。氧化半反应,即析氧反应(OER),是一个复杂的四电子过程,构成了水分解中的效率瓶颈。在此,我们报道了一种高活性的OER催化剂——钴钒氧化物。该催化剂是基于金属-OH键强度与活性的火山图设计的。该催化剂可通过简便的水热路线合成。最具活性的纯相材料(CoVO )是X射线非晶态的,当固定在平面基底上时,在1 M KOH电解液中,在347 mV的过电位下可提供10 mA cm 的电流密度。该合成方法也可用于涂覆高表面积基底,如泡沫镍。在这种三维基底上,CoVO 催化剂具有高活性,在254 mV过电位下达到10 mA cm ,塔菲尔斜率仅为35 mV dec 。这项工作证明CoVO 是一种很有前景的析氧电催化剂,并验证了M-OH键强度作为OER催化中一种实用描述符的作用。

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