Issue 44, 2024

Single and dual-atom catalysts towards electrosynthesis of ammonia and urea: a review

Abstract

Ammonia and urea represent two important chemicals that have contributed to the rapid development of humanity. However, their industrial production requires harsh conditions, consuming excessive energy and resulting in significant greenhouse gas emission. Therefore, there is growing interest in the electrocatalytic synthesis of ammonia and urea as it can be carried out under ambient conditions. Recently, atomic catalysts (ACs) have gained increased attention for their superior catalytic properties, being able to outperform their micro and nano counterparts. This review examines the advantages and disadvantages of ACs and summarises the advancement of ACs in the electrocatalytic synthesis of ammonia and urea. The focus is on two types of AC – single-atom catalysts (SACs) and diatom catalysts (DACs). SACs offer various advantages, including the 100% atom utilization that allows for low material mass loading, suppression of competitive reactions such as hydrogen evolution reaction (HER), and alternative reaction pathways allowing for efficient synthesis of ammonia and urea. DACs inherit these advantages, possessing further benefits of synergistic effects between the two catalytic centers at close proximity, particularly matching the N[triple bond, length as m-dash]N bond for N2 reduction and boosting C–N coupling for urea synthesis. DACs also possess the ability to break the linear scaling relation of adsorption energy of reactants and intermediates, allowing for tuning of intermediate adsorption energies. Finally, possible future research directions using ACs are proposed.

Graphical abstract: Single and dual-atom catalysts towards electrosynthesis of ammonia and urea: a review

Article information

Article type
Minireview
Submitted
10 Jun 2024
Accepted
08 Oct 2024
First published
22 Oct 2024

Nanoscale, 2024,16, 20463-20483

Single and dual-atom catalysts towards electrosynthesis of ammonia and urea: a review

W. Luo, J. Liu, Y. Hu and Q. Yan, Nanoscale, 2024, 16, 20463 DOI: 10.1039/D4NR02387K

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