Iridium- and ruthenium-based materials show high activity for oxygen evolution reaction (OER) in acidic media while Ru-based catalysts exhibit low stability, but Ir-based materials are limited by their high cost and low reserves. The rational design of the OER electrocatalysts to balance activity, stability, and cost is facing a challenge. Herein, we report a strategy to synthesize Ir-RuOx@WO3 catalyst using a low-temperature wet reflux method to deposit Ir-RuOx nanoparticles on ultrafine WO3 nanowires. Due to the metal–metal support interaction (MMSI) between Ir-RuOx and WO3, the abundant hydroxyl groups on the surface, and the protection of active sites by the mild catalyst synthesis method, Ir-RuOx@WO3 demonstrates the OER activity with a low overpotential of 148 mV at 10 mA/cm2 while the total precious metal usage is only 7.673 wt % (2.990 wt % Ir and 4.647 wt % Ru). Besides, with Ru activating the valence state of Ir to improve the activity and Ir stabilizing the Ru site to improve the stability, Ir-RuOx@WO3 achieved relative activity-stability balance as there was no noticeable degradation when operating at 10 mA/cm2 for 12 h. This study presents design concepts of acidic OER catalysts to balance activity, stability, and cost, promoting the widespread use of PEMWE technology in industrial settings.
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Li et al. (2024) studied this question.
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