Dr. Carsten Walter, Ajit Kumar Singh, Dr. Tobias Sontheimer, Dr. Arindam Indra, Dr. Prashanth W. Menezes
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引用次数: 0
摘要
使用单原子催化剂(SACs)进行电化学水氧化反应因其原子利用率高、活性非凡以及反应机理清晰而备受关注。在单原子催化剂中,原子位点是底物结合和反应中间产物的活性中心,而原子位点与固体载体的相互作用则是稳定和提高催化活性的关键。原子位点周围的配位元素会形成类似配体的环境,从而影响电化学特性。因此,调整 SAC 的配位环境可以调节其氧进化反应(OER)活性。有鉴于此,问题出现了:在水氧化过程中,支持物在稳定单原子(SA)和控制其电化学活性方面的作用是什么?本综述通过最新实例来探讨这一问题。光谱特性分析和密度泛函理论(DFT)计算提供了直接答案:在 SAC 中,原子中心通过邻近原子与支撑物产生强烈的相互作用,从而影响 OER 活性。
Insights into the Single Atom and Support Interaction in Electrocatalytic Oxygen Evolution Reaction
Electrochemical water oxidation with single atom catalysts (SACs) has garnered immense interest because of their high atom utilization, extraordinary activity, and elucidation of the reaction mechanism. In SACs, while the atomic sites offer active centers for substrate binding and reaction intermediates, their interaction with the solid support is crucial for the stabilization and enhancement of catalytic activity. Coordinated elements surrounding the atomic site create a ligand-like environment that influences electrochemical properties. As a result, tuning the coordination environment of SACs allows for modulation of their oxygen evolution reaction (OER) activity. In light of this, the question arises: What is the role of the support in stabilizing single atoms (SAs) and controlling their electrochemical activity during water oxidation? This review addresses this question using recent examples. Spectroscopic characterizations and density functional theory (DFT) calculations provide a direct answer: In SACs, the atomic centers exhibit strong interactions with the support via neighboring atoms, influencing OER activity.
期刊介绍:
ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.