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In Situ Reconstruction of Metal Oxide Cathodes for Ammonium Generation from High-Strength Nitrate Wastewater: Elucidating the Role of the Substrate in the Performance of CoO. | LitMetric

In Situ Reconstruction of Metal Oxide Cathodes for Ammonium Generation from High-Strength Nitrate Wastewater: Elucidating the Role of the Substrate in the Performance of CoO.

Environ Sci Technol

The Key Lab of Pollution Control and Ecosystem Restoration in Industry Clusters, Ministry of Education, School of Environment and Energy, South China University of Technology, Guangzhou 510006, P. R. China.

Published: March 2023

AI Article Synopsis

  • In situ electrochemical reconstruction significantly enhances the performance of transition metal oxide cathodes used for electrochemical nitrate reduction reactions (ENRRs), specifically on Co, Fe, Ni, Cu, Ti, and W oxides.
  • The freestanding ER-CoO/CF cathode demonstrated exceptional ammonium yield (0.46 mmol h cm), 100% selectivity, and 99.9% Faradaic efficiency at -1.3 V in a NO-N solution, outperforming its unreconstructed version and other cathodes.
  • The study revealed that the carbon cloth substrate mainly supports CoO without substantial electronic interaction, while the self-reconstruction of CoO favors the formation of metallic Co and oxygen vacancies, enhancing nitrate adsorption

Article Abstract

In situ electrochemical reconstruction is important for transition metal oxides explored as electrocatalysts for electrochemical nitrate reduction reactions (ENRRs). Herein, we report substantial performance enhancement of ammonium generation on Co, Fe, Ni, Cu, Ti, and W oxide-based cathodes upon reconstruction. Among them, the performance of a freestanding ER-CoO/CF (CoO grown on Co foil subjected to electrochemical reduction) cathode was superior to its unreconstructed counterpart and other cathodes; e.g., an ammonium yield of 0.46 mmol h cm, an ammonium selectivity of 100%, and a Faradaic efficiency of 99.9% were attained at -1.3 V in a 1400 mg L NO-N solution. The reconstruction behaviors were found to vary with the underlying substrate. The inert carbon cloth only acted as a supporting matrix for immobilizing CoO, without appreciable electronic interactions between them. A combination of physicochemical characterizations and theoretical modeling provided compelling evidence that the CF-promoted self-reconstruction of CoO induced the evolution of metallic Co and the creation of oxygen vacancies, which promoted and optimized interfacial nitrate adsorption and water dissociation, thus boosting the ENRR performance. The ER-CoO/CF cathode performed well over wide ranges of pH and applied current and at high nitrate loadings, ensuring its high efficacy in treating high-strength real wastewater.

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Source
http://dx.doi.org/10.1021/acs.est.2c09147DOI Listing

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