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MOx/Rh Metallene with Energetic Interfaces as Efficient Bifunctional Electrocatalyst for Durable Water Splitting
Ruilong Wei1, Yuner Lin1, Shanshan Ye1
1Key Lab of Porous Functional Materials of Jiangxi Province, College of Chemistry and Materials, Jiangxi Normal University, Nanchang, China.
This study developed novel ultrathin metal oxide/rhodium (MOx/Rh) heterostructures for alkaline water splitting. The FeOx/Rh catalyst shows excellent bifunctional activity and stability, enabling efficient solar-driven hydrogen production.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Developing efficient and stable bifunctional electrocatalysts for alkaline water splitting is crucial for clean energy technologies.
- Current catalysts often face challenges in activity, stability, and cost-effectiveness.
Purpose of the Study:
- To design and synthesize ultrathin metal oxide/rhodium (MOx/Rh) metallene heterostructures for enhanced alkaline water splitting.
- To investigate the interfacial effects and catalytic mechanisms of these novel heterostructures.
Main Methods:
- Atmosphere-controlled solvothermal synthesis was employed to create uniform MOx nanoclusters on Rh metallene.
- Electrochemical characterization was performed to evaluate bifunctional activity and durability for overall water splitting.
- Mechanistic studies, including DFT calculations, were used to understand the role of the interface and electronic coupling.
Main Results:
- The FeOx/Rh catalyst exhibited superior bifunctional activity, achieving 1.53 V for overall water splitting at 10 mA cm-2 with robust durability.
- Optimized interfaces between FeOx and Rh significantly accelerated the kinetics of the oxygen evolution reaction.
- FeOx promoted water dissociation, while electronically modulated Rh optimized hydrogen adsorption.
Conclusions:
- Interfacial engineering of MOx/Rh heterostructures is a viable strategy for developing high-performance electrocatalysts.
- This approach enables efficient solar-driven hydrogen production, offering a new paradigm for catalyst design.
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