Coupling N 2 and CO 2 in H 2 O to synthesize urea under ambient conditions
The use of nitrogen fertilizers has been estimated to have supported 27% of the world's population over the past century. Urea (CO(NH ) ) is conventionally synthesized through two consecutive industrial processes, N + H → NH followed by NH + CO → urea. Both reactions operate under harsh con...
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Veröffentlicht in: | Nature chemistry 2020-08, Vol.12 (8), p.717 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The use of nitrogen fertilizers has been estimated to have supported 27% of the world's population over the past century. Urea (CO(NH
)
) is conventionally synthesized through two consecutive industrial processes, N
+ H
→ NH
followed by NH
+ CO
→ urea. Both reactions operate under harsh conditions and consume more than 2% of the world's energy. Urea synthesis consumes approximately 80% of the NH
produced globally. Here we directly coupled N
and CO
in H
O to produce urea under ambient conditions. The process was carried out using an electrocatalyst consisting of PdCu alloy nanoparticles on TiO
nanosheets. This coupling reaction occurs through the formation of C-N bonds via the thermodynamically spontaneous reaction between *N=N* and CO. Products were identified and quantified using isotope labelling and the mechanism investigated using isotope-labelled operando synchrotron-radiation Fourier transform infrared spectroscopy. A high rate of urea formation of 3.36 mmol g
h
and corresponding Faradic efficiency of 8.92% were measured at -0.4 V versus reversible hydrogen electrode. |
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ISSN: | 1755-4349 |
DOI: | 10.1038/s41557-020-0481-9 |