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Zinc-mediated passivation improves hydrogen evolution activity in NiMo catalysts, indicating stability for renewable energy use.
Integrating water electrolyzers with intermittent renewable energy poses critical durability challenges from dynamic load fluctuations inducing catalyst degradation. We report a zinc‐mediated sacrificial protection strategy enhancing NiMo catalyst stability through in situ dendritic passivation. Zinc‐decorated NiMo on nickel felt (Zn‐NiMo/NF) exhibits considerable hydrogen evolution activity (94.6 mV overpotential at 50 mA cm −2 ) comparable to Pt/C. Under stringent load fluctuation cycling protocols (−500/50 mA cm −2 ), the zinc overlayer spontaneously reconstructs into laterally oriented, NiMo‐enriched dendrites providing dual protection: physical barriers suppressing dissolution (order‐of‐magnitude reductions in metal leaching) and sacrificial buffering wherein zinc preferentially oxidizes to zincate, shielding nickel from irreversible hydroxide formation. Zn‐NiMo/NF maintains stable performance while pristine NiMo/NF degrades substantially. Anion exchange membrane electrolyzer validation confirms minimal voltage escalation over 100 h cycling (1.645– 1.667 V), outperforming Pt/C (1.7028–1.857 V). This establishes sacrificial interface engineering as an effective paradigm for robust earth‐abundant electrocatalysts in renewable energy‐integrated hydrogen production.
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Jeong et al. (2026) studied this question.
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