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Improving Alkaline Hydrogen Oxidation through Dynamic Lattice Hydrogen Migration in Pd@Pt Core-Shell Electrocatalysts
Tonghui Zhao1, Mengting Li2, Dongdong Xiao3
1Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan, 430074, P. R. China.
A new dynamic lattice hydrogen migration mechanism significantly boosts alkaline hydrogen oxidation reaction (HOR) activity on Pd@Pt catalysts. This advance enhances catalyst design for efficient hydrogen electro-catalysis.
Area of Science:
- Electrochemistry
- Materials Science
- Catalysis
Background:
- Designing efficient catalysts for hydrogen electro-catalysis requires understanding hydrogen intermediate behavior.
- Synergetic multi-component catalysts offer improved performance through a division of chemical labor.
Purpose of the Study:
- To demonstrate a novel dynamic lattice hydrogen migration mechanism.
- To investigate its impact on alkaline hydrogen oxidation reaction (HOR) activity.
Main Methods:
- Utilizing Palladium-Platinum core-shell (Pd@Pt) nanoparticles.
- Employing electrochemical hydrogenation and dehydrogenation processes.
- In situ analysis to track lattice hydrogen (LH) dynamics.
Main Results:
- Pd@Pt catalysts exhibited a two orders of magnitude increase in alkaline HOR activity compared to pure Pd.
- Mass activity enhancement reached approximately 31.8 times that of commercial Pt.
- Demonstrated a dynamic LH migration mechanism involving PdHₓ formation and dehydrogenation, enhancing surface Pt sites and lowering the Volmer step energy barrier.
Conclusions:
- The dynamic lattice hydrogen migration mechanism significantly enhances HOR activity.
- PdHₓ acts as a hydrogen reservoir, facilitating continuous hydrogen supply to Pt surface sites.
- This mechanism offers a new avenue for designing advanced electro-catalysts for hydrogen-related energy applications.
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