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Switchable Acidic Oxygen Evolution Mechanisms on Atomic Skin of Ruthenium Metallene Oxides
Tianyi Gao1, Dongxu Jiao1, Lina Wang2
1School of Materials Science and Engineering, Key Laboratory of Automobile Materials of MOE, Electron Microscopy Center, Jilin University, Changchun 130012, China.
Ruthenium dioxide (RuO2) catalysts for acidic oxygen evolution reaction (OER) show improved stability and activity. A novel metallene core-skin structure shifts the OER pathway, enhancing performance and durability.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Ruthenium dioxide (RuO2) is a promising catalyst for acidic oxygen evolution reaction (OER) due to its efficiency and low cost.
- However, RuO2 stability is limited by the lattice oxygen mechanism (LOM).
Purpose of the Study:
- To develop a stable and highly active RuO2-based catalyst for acidic OER.
- To investigate a novel metallene-based core-skin structure for tuning OER pathways.
Main Methods:
- Fabrication of metallene-based core-skin structures with varying core species (metallene oxides vs. metallenes).
- Electrochemical characterization of oxygen evolution reaction (OER) activity and stability.
- Spectroscopic analyses and theoretical calculations to elucidate reaction mechanisms.
Main Results:
- The Pd@RuO2 metallene catalyst exhibited a low overpotential of 189 mV at 10 mA cm-2 for acidic OER, outperforming PdO@RuO2 metallenes.
- The core-skin structure enabled a switch from LOM to an adsorbate evolution mechanism.
- The catalyst demonstrated robust stability with negligible decay over 100 hours at 50 mA cm-2.
Conclusions:
- The metallene-based core-skin structure effectively regulates the OER pathway and enhances catalyst performance.
- The Pd-metallene core acts as an electron donor, optimizing active site energetics and stability.
- This approach offers a new strategy for designing advanced electrocatalysts.
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