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Dendritic copper oxide catalyst engineering weak-polarity Cu-O bond for high-efficiency nitrate electroreduction
Haiyan Ma1, Jing Yan1, Junjie Xu1
1The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081, China; Hubei Province Key Laboratory of Coal Conversion and New Carbon Materials, Wuhan University of Science and Technology, Wuhan 430081, China.
A novel dendritic copper oxide catalyst (Cu-B2) efficiently converts nitrate to ammonia, offering a promising pathway for sustainable ammonia synthesis and water purification with high selectivity and stability.
Area of Science:
- Electrochemistry
- Catalysis
- Materials Science
Background:
- Nitrate reduction reaction (NO3RR) is crucial for ammonia synthesis and water purification.
- Developing efficient, selective, and stable catalysts for NO3RR remains a significant challenge.
Purpose of the Study:
- To develop a dendritic copper oxide catalyst (Cu-B2) for efficient nitrate reduction reaction (NO3RR) to produce ammonia.
- To investigate the catalytic performance, selectivity, and stability of the Cu-B2 catalyst.
Main Methods:
- Electrochemical synthesis of dendritic copper oxide (Cu-B2).
- In situ characterization using attenuated total reflection surface enhanced infrared absorption spectroscopy (ATR-SEIRAS).
- Density functional theory (DFT) calculations to understand reaction mechanisms.
Main Results:
- Cu-B2 catalyst achieved 94% NH3 Faradaic efficiency and a yield of 16.9 mg h-1 cm-2 at -0.6 V.
- In situ reduction formed active Cu0/Cu+ sites while preserving dendritic morphology.
- Cu-B2 demonstrated potential-independent nitrate adsorption and efficient nitrite conversion to ammonia.
Conclusions:
- The dendritic Cu-B2 catalyst exhibits superior activity and durability for NO3RR to ammonia.
- Weaker Cu-O bond polarity in Cu-B2 leads to lower oxidation states of active Cu sites.
- Enhanced NO3- adsorption and conversion of intermediates contribute to improved catalytic performance.
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