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Electrocatalytic Nitrate and Nitrite Reduction toward Ammonia using Cu2O Nanocubes: Active Species and Reaction Mechanisms

MPS-Authors
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Bai,  Lichen       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Franco,  Federico
Interface Science, Fritz Haber Institute, Max Planck Society;

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Timoshenko,  Janis       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Rettenmaier,  Clara       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Scholten,  Fabian
Interface Science, Fritz Haber Institute, Max Planck Society;

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Jeon,  Hyosang
Interface Science, Fritz Haber Institute, Max Planck Society;

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Yoon,  Aram       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Rüscher,  Martina
Interface Science, Fritz Haber Institute, Max Planck Society;

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Herzog,  Antonia       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Haase,  Felix       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Kühl,  Stefanie
Interface Science, Fritz Haber Institute, Max Planck Society;

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Chee,  See Wee       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Bergmann,  Arno       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Roldan Cuenya,  Beatriz       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Citation

Bai, L., Franco, F., Timoshenko, J., Rettenmaier, C., Scholten, F., Jeon, H., et al. (2024). Electrocatalytic Nitrate and Nitrite Reduction toward Ammonia using Cu2O Nanocubes: Active Species and Reaction Mechanisms. Journal of the American Chemical Society, 146(14), 9665-9678. doi:10.1021/jacs.3c13288.


Cite as: https://hdl.handle.net/21.11116/0000-000E-B34A-5
Abstract
The electrochemical reduction of nitrate (NO3–) and nitrite (NO2–) enables sustainable, carbon-neutral, and decentralized routes to produce ammonia (NH3). Copper-based materials are promising electrocatalysts for NOx– conversion to NH3. However, the underlying reaction mechanisms and the role of different Cu species during the catalytic process are still poorly understood. Herein, by combining quasi in situ X-ray photoelectron spectroscopy (XPS) and operando X-ray absorption spectroscopy (XAS), we unveiled that Cu is mostly in metallic form during the highly selective reduction of NO3–/NO2– to NH3. On the contrary, Cu(I) species are predominant in a potential region where the two-electron reduction of NO3– to NO2– is the major reaction. Electrokinetic analysis and in situ Raman spectroscopy was also used to propose possible steps and intermediates leading to NO2– and NH3, respectively. This work establishes a correlation between the catalytic performance and the dynamic changes of the chemical state of Cu, and provides crucial mechanistic insights into the pathways for NO3–/NO2– electrocatalytic reduction.