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Ultrathin Carbon Shell Protecting Copper Sites to Boost Anodic Hydrogen Production via Low-Potential Formaldehyde
Xiafei Gao1, Heng Yang1, Jianghui Qiu1
1College of Chemistry and Chemical Engineering, State Key Laboratory of High-Efficiency Utilization of Coal and Green Chemical Engineering, Ningxia University, Yinchuan 750021, P. R. China.
This study developed a stable carbon-coated copper catalyst for efficient formaldehyde oxidation reaction (FOR), enabling simultaneous hydrogen production at both anode and cathode with high efficiency and durability.
Area of Science:
- Electrochemistry
- Materials Science
- Catalysis
Background:
- Copper-based electrocatalysts offer potential for bipolar hydrogen production via aldehyde oxidation.
- Current Cu-based catalysts suffer from insufficient activity and stability for practical applications.
- Formaldehyde oxidation reaction (FOR) coupled with hydrogen evolution reaction (HER) can generate H2 at both electrodes.
Purpose of the Study:
- To enhance the activity and stability of copper electrocatalysts for formaldehyde oxidation.
- To develop a bipolar hydrogen production system utilizing an improved catalyst.
- To investigate the mechanism behind the enhanced catalytic performance.
Main Methods:
- Coating copper spheres with an ultrathin carbon shell.
- Electrochemical characterization of the catalyst's performance in formaldehyde oxidation.
- Experimental and theoretical calculations to elucidate the reaction mechanism.
Main Results:
- The carbon-coated copper catalyst achieved high current density (100 mA cm-2) at a low potential (0.13 V vs RHE) for FOR.
- A bipolar system coupling FOR and HER demonstrated near 100% Faraday efficiency for H2 production.
- The catalyst exhibited stable operation for over 30 hours in a flow cell at a low voltage (0.1 V).
Conclusions:
- The ultrathin carbon shell protects Cu(0) sites, preventing oxidation and ensuring long-term catalyst stability.
- Electron transfer at the Cu/carbon interface lowers the reaction energy barrier, facilitating C-H bond cleavage and H2 generation.
- This work provides a design principle for durable and active copper-based electrocatalysts for hydrogen production.
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