Shi Zhaoping, Wang Xian, Ge Junjie, Liu Changpeng, Xing Wei
State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin 130022, PR China.
Nanoscale. 2020 Jul 2;12(25):13249-13275. doi: 10.1039/d0nr02410d.
The oxygen evolution reaction (OER), as the anodic reaction of water electrolysis (WE), suffers greatly from low reaction kinetics and thereby hampers the large-scale application of WE. Seeking active, stable, and cost-effective OER catalysts in acidic media is therefore of great significance. In this perspective, studying the reaction mechanism and exploiting advanced anode catalysts are of equal importance, where the former provides guidance for material structural engineering towards a better catalytic activity. In this review, we first summarize the currently proposed OER catalytic mechanisms, i.e., the adsorbate evolution mechanism (AEM) and lattice oxygen evolution reaction (LOER). Subsequently, we critically review several acidic OER electrocatalysts reported recently, with focus on structure-performance correlation. Finally, a few suggestions on exploring future OER catalysts are proposed.
析氧反应(OER)作为水电解(WE)的阳极反应,因反应动力学较低而受到严重影响,从而阻碍了水电解的大规模应用。因此,寻找在酸性介质中具有活性、稳定性和成本效益的析氧反应催化剂具有重要意义。从这个角度来看,研究反应机理和开发先进的阳极催化剂同样重要,前者为材料结构工程提供指导以实现更好的催化活性。在这篇综述中,我们首先总结了目前提出的析氧反应催化机理,即吸附质析出机理(AEM)和晶格氧析出反应(LOER)。随后,我们批判性地综述了最近报道的几种酸性析氧反应电催化剂,重点关注结构与性能的相关性。最后,对探索未来的析氧反应催化剂提出了一些建议。