Abstract
Porous Ni, Ni-Ir, and Ni-Pt electrodes were prepared on Ni substrates by molten-salt Al co-deposition followed by dealloying. SEM/EDS and XRD confirmed a Raney-type porous network with Ir or Pt present across the layer. A urea oxidation reaction (UOR) was tested in 1 M NaOH + 0.33 M urea by cyclic voltammetry and chronoamperometry at +0.40 V vs. SCE (60 min). Smooth Ni showed near-zero current. Porous Ni resulted in ~11 mA cm(-2) initially and ~9 mA cm(-2) after 60 min. Porous Ni-Ir started at ~7 mA cm(-2) and fell to ~2 mA cm(-2) within 5 min, indicating fast deactivation, likely due to Ir-oxide formation that suppresses the Ni(2+)/Ni(3+) redox couple. Porous Ni-Pt remained at ~11 mA cm(-2) over 60 min, consistent with a stable Ni-Pt effect in which Pt aids urea adsorption/activation while Ni provides the redox path for oxidation. Overall, Pt improves UOR performance, whereas Ir lowers it under these conditions.