摘要
Acidic oxygen evolution reaction (OER) is crucial for developing proton exchange membrane water electrolyzers, which has been hindered by the high overpotential of iridium oxide (IrO x )-based catalysts and the scarcity of iridium. Herein, we introduce a novel strategy to synthesize ultra-thin amorphous IrO x nanosheets with flexible mono/multi-element doping. Benefiting from synergistic W/Mo/Co co-doping effect, WMoCo-IrO x nanosheets (WMC-IrO x NS) sample optimally modulates the Ir electronic structure, maintains the neutral oxygen vacancy concentration and stabilizes Ir sites. Additionally, the nanosheets expose abundant Ir active centers. WMC-IrO x NS exhibits superior OER electrocatalysis performance with a low overpotential of 241 mV, excellent stability of 275 h at 10 mA cm −2 , and a high mass activity of 545.4 A/g Ir. The catalyst follows the lattice oxygen mechanism (LOM) pathway. As observed in in situ attenuated total reflectance Fourier transform infrared spectroscopy, compared to the un-doped sample, WMC-IrO x NS accumulates negligible Ir–O–O* intermediates. Therefore, through the multi-element synergistic co-doping effect, the catalyst weakens the adsorption energy of O–O* intermediates and promotes O 2 release, thereby lowering OER energy barriers in acidic conditions. This work opens an inspiring avenue for designing IrO x -based catalysts with high activity and low Ir usage.
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