析氧
钴
氧气
钥匙(锁)
氧还原反应
化学
机制(生物学)
催化作用
材料科学
纳米技术
化学工程
组合化学
无机化学
计算机科学
物理化学
电化学
电极
生物化学
有机化学
物理
工程类
量子力学
计算机安全
作者
Kenneth Crossley,Thomas J. Schmidt,Emiliana Fabbri
摘要
Focusing on five key concepts, we review the roles of cation and oxygen vacancies in determining the surface reconstruction pathway, reaction mechanism, and ultimate activity of cobalt-based oxygen evolution reaction (OER) electrocatalysts. Cation and oxygen vacancies can initiate reactant adsorption, facilitating active surface reconstruction, and can switch the dominant mechanism from the adsorbate evolution mechanism (AEM) to the lattice oxygen evolution mechanism (LOEM). However, these effects are facet-dependent. Rigorous oxygen vacancy quantification promises to identify the OER mechanism steering thresholds and unlock the full potential of vacancy engineering. Finally, oxygen vacancy quantification strategies are critically examined to facilitate this goal.
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