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CoO纳米阵列的阴极电化学活化:一种显著提高析氢活性的巧妙策略。

Cathodic electrochemical activation of CoO nanoarrays: a smart strategy to significantly boost the hydrogen evolution activity.

作者信息

Yang Li, Zhou Huang, Qin Xin, Guo Xiaodong, Cui Guanwei, Asiri Abdullah M, Sun Xuping

机构信息

College of Chemistry, Sichuan University, Chengdu 610064, China.

出版信息

Chem Commun (Camb). 2018 Feb 22;54(17):2150-2153. doi: 10.1039/c7cc09416g.

Abstract

Co(hydro)oxides show unsatisfactory catalytic activity for the hydrogen evolution reaction (HER) in alkaline media, and it is thus highly desirable but still remains a challenge to design and develop Co(hydro)oxide derived materials as superb hydrogen-evolving catalysts using a facile, rapid and less energy-intensive method. Here, we propose a cathodic electrochemical activation strategy toward greatly boosted HER activity of a CoO nanoarray via room-temperature cathodic polarization in sodium hypophosphite solution. After activation, the overpotential significantly decreases from 260 to 73 mV to drive a geometrical catalytic current density of 10 mA cm in 1.0 M KOH. Notably, this activated electrode also shows strong long-term electrochemical durability with the retention of its catalytic activity at 100 mA cm for at least 40 h.

摘要

羟基氧化钴在碱性介质中对析氢反应(HER)表现出不尽人意的催化活性,因此,采用简便、快速且能耗较低的方法设计和开发衍生自羟基氧化钴的材料作为优异的析氢催化剂,是非常可取的,但仍然是一项挑战。在此,我们提出一种阴极电化学活化策略,通过在次磷酸钠溶液中进行室温阴极极化,极大地提高CoO纳米阵列的析氢活性。活化后,过电位从260 mV显著降至73 mV,以驱动在1.0 M KOH中10 mA cm²的几何催化电流密度。值得注意的是,这种活化电极还表现出很强的长期电化学耐久性,在100 mA cm²的电流密度下至少保持40小时的催化活性。

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