4.7 Article

Ni-WC nanoparticles/carbon aerogel electrocatalytic electrode for methanol and urea electrooxidation

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 48, Issue 3, Pages 991-1000

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.09.311

Keywords

Catalytic electrooxidation; Methanol oxidation; Urea oxidation; Ni-WC

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Efficient bacterial cellulose (BC)-derived carbon aerogel loaded with Ni-based catalyst and WC nanoparticles co-catalyst was developed for the electrooxidation of methanol and urea. The catalytic electrode exhibits high electrocatalytic activity for methanol and urea electrooxidation due to the synergistic effect between Ni and WC. The electrode shows good durability with significant retention of peak current density after cycling.
Direct methanol fuel cells and direct urea fuel cells are significant for mitigating the energy crisis and protecting the environment. However, as the common critical anodes for the electrooxidation of methanol and urea, most Ni-based catalysts are severely poisoned by the CO group, resulting in a decrease in current densities and stability of fuel cells. Herein, efficient bacterial cellulose (BC)-derived carbon aerogel loaded with Ni-based catalyst and WC nanoparticles co-catalyst was developed for the electrooxidation of methanol and urea. As a result, the catalytic electrode exhibits high electrocatalytic activity for methanol electrooxidation (105.7 mA cm-2 at 0.8 V) and urea electrooxidation (90.4 mA cm-2 at 0.8 V). The synergistic effect between Ni and WC can significantly weaken the surface adsorption of CO on the electrode to obtain excellent and durable electrochemical performance. For methanol oxidation reaction and urea oxidation reaction, the retentions of the peak cur-rent density after 2000 cycles in the original electrolytes are 48.94% and 74.79%, respectively. Moreover, applying the new electrolyte, the peak current density can return to 88.42% and 84.4% of the original value. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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