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A Survey of Catalytic Materials for Ammonia Electrooxidation to Nitrite and Nitrate

Studies of the ammonia oxidation reaction (AOR) for the synthesis of nitrite and nitrate (NO(2/3) (−)) have been limited to a small number of catalytic materials, majorly Pt based. As the demand for nitrate‐based products such as fertilisers continues to grow, exploration of alternative catalysts is...

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Autores principales: Johnston, Sam, Cohen, Sam, Nguyen, Cuong K., Dinh, Khang N., Nguyen, Tam D., Giddey, Sarbjit, Munnings, Christopher, Simonov, Alexandr N., MacFarlane, Douglas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827930/
https://www.ncbi.nlm.nih.gov/pubmed/35879863
http://dx.doi.org/10.1002/cssc.202200614
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author Johnston, Sam
Cohen, Sam
Nguyen, Cuong K.
Dinh, Khang N.
Nguyen, Tam D.
Giddey, Sarbjit
Munnings, Christopher
Simonov, Alexandr N.
MacFarlane, Douglas R.
author_facet Johnston, Sam
Cohen, Sam
Nguyen, Cuong K.
Dinh, Khang N.
Nguyen, Tam D.
Giddey, Sarbjit
Munnings, Christopher
Simonov, Alexandr N.
MacFarlane, Douglas R.
author_sort Johnston, Sam
collection PubMed
description Studies of the ammonia oxidation reaction (AOR) for the synthesis of nitrite and nitrate (NO(2/3) (−)) have been limited to a small number of catalytic materials, majorly Pt based. As the demand for nitrate‐based products such as fertilisers continues to grow, exploration of alternative catalysts is needed. Herein, 19 metals immobilised as particles on carbon fibre electrodes were tested for their catalytic activity for the ammonia electrooxidation to NO(2/3) (−) under alkaline conditions (0.1 m KOH). Nickel‐based electrodes showed the highest overall NO(2/3) (−) yield with a rate of 5.0±1.0 nmol s(−1) cm(−2), to which nitrate contributed 62±8 %. Cu was the only catalyst that enabled formation of nitrate, at a rate of 1.0±0.4 nmol s(−1) cm(−2), with undetectable amounts of nitrite produced. Previously unexplored in this context, Fe and Ag also showed promise and provided new insights into the mechanisms of the process. Ag‐based electrodes showed strong indications of activity towards NH(3) oxidation in electrochemical measurements but produced relatively low NO(2/3) (−) yields, suggesting the formation of alternate oxidation products. NO(2/3) (−) production over Fe‐based electrodes required the presence of dissolved O(2) and was more efficient than with Ni on longer timescales. These results highlight the complexity of the AOR mechanism and provide a broad set of catalytic activity and nitrate versus nitrite yield data, which might guide future development of a practical process for the distributed sustainable production of nitrates and nitrites at low and medium scales.
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spelling pubmed-98279302023-01-10 A Survey of Catalytic Materials for Ammonia Electrooxidation to Nitrite and Nitrate Johnston, Sam Cohen, Sam Nguyen, Cuong K. Dinh, Khang N. Nguyen, Tam D. Giddey, Sarbjit Munnings, Christopher Simonov, Alexandr N. MacFarlane, Douglas R. ChemSusChem Research Articles Studies of the ammonia oxidation reaction (AOR) for the synthesis of nitrite and nitrate (NO(2/3) (−)) have been limited to a small number of catalytic materials, majorly Pt based. As the demand for nitrate‐based products such as fertilisers continues to grow, exploration of alternative catalysts is needed. Herein, 19 metals immobilised as particles on carbon fibre electrodes were tested for their catalytic activity for the ammonia electrooxidation to NO(2/3) (−) under alkaline conditions (0.1 m KOH). Nickel‐based electrodes showed the highest overall NO(2/3) (−) yield with a rate of 5.0±1.0 nmol s(−1) cm(−2), to which nitrate contributed 62±8 %. Cu was the only catalyst that enabled formation of nitrate, at a rate of 1.0±0.4 nmol s(−1) cm(−2), with undetectable amounts of nitrite produced. Previously unexplored in this context, Fe and Ag also showed promise and provided new insights into the mechanisms of the process. Ag‐based electrodes showed strong indications of activity towards NH(3) oxidation in electrochemical measurements but produced relatively low NO(2/3) (−) yields, suggesting the formation of alternate oxidation products. NO(2/3) (−) production over Fe‐based electrodes required the presence of dissolved O(2) and was more efficient than with Ni on longer timescales. These results highlight the complexity of the AOR mechanism and provide a broad set of catalytic activity and nitrate versus nitrite yield data, which might guide future development of a practical process for the distributed sustainable production of nitrates and nitrites at low and medium scales. John Wiley and Sons Inc. 2022-09-29 2022-10-21 /pmc/articles/PMC9827930/ /pubmed/35879863 http://dx.doi.org/10.1002/cssc.202200614 Text en © 2022 The Authors. ChemSusChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Johnston, Sam
Cohen, Sam
Nguyen, Cuong K.
Dinh, Khang N.
Nguyen, Tam D.
Giddey, Sarbjit
Munnings, Christopher
Simonov, Alexandr N.
MacFarlane, Douglas R.
A Survey of Catalytic Materials for Ammonia Electrooxidation to Nitrite and Nitrate
title A Survey of Catalytic Materials for Ammonia Electrooxidation to Nitrite and Nitrate
title_full A Survey of Catalytic Materials for Ammonia Electrooxidation to Nitrite and Nitrate
title_fullStr A Survey of Catalytic Materials for Ammonia Electrooxidation to Nitrite and Nitrate
title_full_unstemmed A Survey of Catalytic Materials for Ammonia Electrooxidation to Nitrite and Nitrate
title_short A Survey of Catalytic Materials for Ammonia Electrooxidation to Nitrite and Nitrate
title_sort survey of catalytic materials for ammonia electrooxidation to nitrite and nitrate
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827930/
https://www.ncbi.nlm.nih.gov/pubmed/35879863
http://dx.doi.org/10.1002/cssc.202200614
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