Affiliation:
1. Material Chemistry Group for Thin Film Catalysis – CatLab Helmholtz-Zentrum Berlin für Materialien und Energie Albert-Einstein-Str. 15 12489 Berlin Germany
2. Department of Chemistry IIT (BHU) Varanasi UP-221005 India
3. Strategy Department of Energy and Information Helmholtz-Zentrum Berlin für Materialien und Energie Hahn-Meitner-Platz 1 14109 Berlin Germany
4. Department of Chemistry Technical University of Berlin Straße des 17 Juni 135. Sekr. C2 10623 Berlin Germany
Abstract
AbstractElectrochemical 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.