Boosting urea electrooxidation on oxyanion-engineered nickel sites via inhibited water oxidation

Xintong Gao, Xiaowan Bai, Pengtang Wang, Yan Jiao, Kenneth Davey, Yao Zheng () and Shi-Zhang Qiao ()
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Xintong Gao: The University of Adelaide
Xiaowan Bai: The University of Adelaide
Pengtang Wang: The University of Adelaide
Yan Jiao: The University of Adelaide
Kenneth Davey: The University of Adelaide
Yao Zheng: The University of Adelaide
Shi-Zhang Qiao: The University of Adelaide

Nature Communications, 2023, vol. 14, issue 1, 1-10

Abstract: Abstract Renewable energy-based electrocatalytic oxidation of organic nucleophiles (e.g.methanol, urea, and amine) are more thermodynamically favourable and, economically attractive to replace conventional pure water electrooxidation in electrolyser to produce hydrogen. However, it is challenging due to the competitive oxygen evolution reaction under a high current density (e.g., >300 mA cm−2), which reduces the anode electrocatalyst’s activity and stability. Herein, taking lower energy cost urea electrooxidation reaction as the model reaction, we developed oxyanion-engineered Nickel catalysts to inhibit competing oxygen evolution reaction during urea oxidation reaction, achieving an ultrahigh 323.4 mA cm−2 current density at 1.65 V with 99.3 ± 0.4% selectivity of N-products. In situ spectra studies reveal that such in situ generated oxyanions not only inhibit OH− adsorption and guarantee high coverage of urea reactant on active sites to avoid oxygen evolution reaction, but also accelerate urea’s C − N bond cleavage to form CNO − intermediates for facilitating urea oxidation reaction. Accordingly, a comprehensive mechanism for competitive adsorption behaviour between OH− and urea to boost urea electrooxidation and dynamic change of Ni active sites during urea oxidation reaction was proposed. This work presents a feasible route for high-efficiency urea electrooxidation reaction and even various electrooxidation reactions in practical applications.

Date: 2023
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DOI: 10.1038/s41467-023-41588-w

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