Abstract
The development of efficient and reliable acidic oxygen evolution reaction (OER) electrocatalysts represents a crucial step in the process of water electrolysis. RuO2, a benchmark OER catalyst, suffers from limited large-scale applicability due to its tendency toward the less stable lattice oxygen mechanism (LOM). This work reports the synthesis of Co-doped RuO2 nanosheets with a unique porous morphology composed of interconnected grains via a facile molten salt method. Co doping modulates the grain size, effectively increasing the specific surface area and introducing oxygen vacancies. These oxygen vacancies, coupled with the Co dopants, form Co-O(V) motifs that tune the electronic configuration of Ru. This structural engineering promotes a shift in the OER mechanism from the detrimental LOM pathway to the more efficient adsorbate evolution mechanism (AEM), significantly enhancing the stability of the RuO2 matrix in acidic environments. The optimized Co0.108-RuO2 catalyst exhibits a low overpotential of 214 mV at 10 mA cm-2 and remarkable stability over commercial RuO2 and undoped counterparts, owing to the synergistic effect of the increased surface area, Co-O(V) motifs, and favored AEM pathway. This strategy of utilizing Co doping to engineer morphology, electronic structure, and reaction mechanism offers a promising avenue for developing high-performance OER electrocatalysts. © 2025 American Chemical Society.
| Original language | English |
|---|---|
| Pages (from-to) | 19734–19744 |
| Journal | ACS Applied Materials and Interfaces |
| Volume | 17 |
| Issue number | 13 |
| Online published | 19 Mar 2025 |
| DOIs | |
| Publication status | Published - 2 Apr 2025 |
Research Keywords
- acidic oxygen evolution reaction
- AEM pathway
- Co-doped RuO2 nanosheets
- electrocatalyst
- oxygen vacancy engineering
Publisher's Copyright Statement
- This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/
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