Ambient electrosynthesis of urea with nitrate and carbon dioxide over iron-based dual sites

Study realizes ambient electrosynthesis of urea with nitrate and carbon dioxide over iron-based dual-sites

(a). Schematic illustration of the synthetic process of Fe(a)@C-Fe3O4/CNTs; (b). Low- and (c) high-magnification TEM images of Fe(a)@C-Fe3O4/CNTs. HRTEM images of Fe(a)@C (d) (from the red dashed box in c) and Fe3O4 NPs (e) (from the yellow dashed box in c); (f), (g) HAADF-STEM images and corresponding elemental mapping images of Fe3O4 and Fe(a)@C. Credit: Geng Jing

Urea (CO(NH2)2) has been applied both in agricultural and pharmaceutical fields. The widely used Bosch-Meiser process has high energy consumption and CO2 emission. Therefore, it is imperative to explore energy-saving and economic routes for urea synthesis under mild conditions.

The electrosynthesis of urea with CO2 and NO3– under ambient conditions is an efficient way, but it is far from application. This is because the key step requires an efficient electrocatalyst enabling adsorption and activation of NO3– and CO2 to accomplish the CN coupling.

Researchers from the Hefei Institutes of Physical Science of the Chinese Academy of Sciences have now developed a liquid-phase laser irradiation route to fabricate symbiotic carbon encapsulated amorphous iron (Fe(a)@C) and iron oxide nanoparticles (Fe3O4 NPs) on carbon nanotubes (denoted as Fe(a)@C-Fe3O4/CNTs).

The as-fabricated Fe(a)@C-Fe3O4/CNTs contained two Fe-based active componentsnamely, [email protected] NPs with the particle sizes of 10~20 nm and Fe3O4 NPs with particle sizes of 1~5 nm.

The presence of two different structural units in Fe(a)@C-Fe3O4/CNTs made it possible to synergistically electrocatalytic activate CO2 and NO3– to realize the CN coupling for urea synthesis.

As expected, Fe(a)@C-Fe3O4/CNTs exhibited superior activity toward the electrocatalytic coupling of CO2 and NO3– for urea synthesis, affording a urea yield of 1341.3±112.6 μg h-1 mgcat-1 and a faradic efficiency of 16.5±6.1% at -0.65 V (vs. RHE) in 0.1 M KNO3 electrolyte.

Both experimental and theoretical results revealed that Fe(a)@C was mainly responsible for the electrocatalytic reduction of NO3– to form *NH2 intermediates, while Fe3O4 was more beneficial for the electrocatalytic reduction of CO2 to form *CO intermediates.

The synergistically catalytic effect contributes to the excellent electrocatalytic performance of urea synthesis at ambient conditions.

The research was published in Angewandte Chemie International Edition.

More information:
Jing Geng et al, Ambient Electrosynthesis of Urea with Nitrate and Carbon Dioxide over Iron-Based Dual-Sites, Angewandte Chemie International Edition (2022). DOI: 10.1002/anie.202210958

Citation: Ambient electrosynthesis of urea with nitrate and carbon dioxide over iron-based dual-sites (2022, November 25) retrieved 25 November 2022 from https://phys.org/news/2022-11-ambient-electrosynthesis-urea-nitrate- carbon.html

This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Leave a Comment