Urea electrooxidation reaction (UOR) plays an important
role in
environmental protection and energy regeneration. The extensively
studied nickel-based catalysts exhibit good activity for UOR, but
urea is more prone to be overelectrooxidized to another pollutant
NO
x
– (x = 2, 3). Herein, the Cu/Ni-B interface catalyst is presented. The
introduction of Cu significantly enhances the Faradaic efficiency
of N2 (nearly 70% at 1.70 V versus RHE). Electrochemical
tests and in situ Raman spectroscopy results show that the introduction
of Cu significantly affects the density of OH* species on the catalyst
in the UOR process. It is proposed that with a moderate decrease in
OH* density, the catalyst can provide enough sites for urea molecules
to allow simultaneous adsorption of the two N atoms, facilitating
the process of N-N coupling to form N2. This work is also
instructive for the design of electrocatalysts for other nucleophile
electrooxidation reactions.