Insights into Nitrogenase Bioelectrocatalysis for Green Ammonia Production

There is a growing interest in using ammonia as a liquid carrier of hydrogen for energy applications. Currently, ammonia is produced industrially by the Haber‐Bosch process, which requires high temperature and high pressure. In contrast, bacteria have naturally evolved an enzyme known as nitrogenase...

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Veröffentlicht in:ChemSusChem 2020-09, Vol.13 (18), p.4856-4865
Hauptverfasser: Rapson, Trevor D., Gregg, Christina M., Allen, Robert S., Ju, HyungKuk, Doherty, Cara M., Mulet, Xavier, Giddey, Sarbjit, Wood, Craig C.
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Sprache:eng
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Zusammenfassung:There is a growing interest in using ammonia as a liquid carrier of hydrogen for energy applications. Currently, ammonia is produced industrially by the Haber‐Bosch process, which requires high temperature and high pressure. In contrast, bacteria have naturally evolved an enzyme known as nitrogenase, that is capable of producing ammonia and hydrogen at ambient temperature and pressure. Therefore, nitrogenases are attractive as a potentially more efficient means to produce ammonia via harnessing the unique properties of this enzyme. In recent years, exciting progress has been made in bioelectrocatalysis using nitrogenases to produce ammonia. Here, the prospects for developing biological ammonia production are outlined, key advances in bioelectrocatalysis by nitrogenases are highlighted, and possible solutions to the obstacles faced in realising this goal are discussed. Let the enzymes work for us! Nitrogenases are remarkable catalysts that have evolved to carry out arguably the most challenging of chemical reactions, cleaving the triple nitrogen bond. This enzyme has a huge potential to allow us to transition to the industrial production of ammonia at room temperature and atmospheric pressure. There are still hurdles to overcome, but there are multiple reasons to be optimistic that this is achievable. This Minireview outlines these advances and points towards future research that is required.
ISSN:1864-5631
1864-564X
DOI:10.1002/cssc.202001433