The study demonstrates enhanced hydrogen evolution reaction performance in anion-exchange membranes using a novel catalyst.
Hydrogen spillover offers a promising approach to develop highly active and affordable electrocatalysts for the hydrogen evolution reaction by regulating hydrogen migration and kinetics. Herein, a catalyst composed of osmium nanoparticles supported on zirconium dioxide (Os/ZrO₂) is designed and synthesized. The Lewis-acid-rich ZrO₂ support not only promotes water dissociation but also triggers hydrogen spillover, thereby optimizing the desorption energetics of hydrogen intermediates. Then, Os/ZrO₂ delivers outstanding HER activity in both alkaline and acidic electrolytes, requiring overpotentials of only 16 and 14 mV to reach 10 mA cm⁻², surpassing commercial Pt/C and Os/C. Mechanistic studies have confirmed the occurrence of hydrogen spillover, whereby hydrogen intermediates migrate from the Os nanoparticles to the ZrO₂ surface, effectively tuning the adsorption/desorption kinetics and leading to significantly enhanced HER performance. Furthermore, in an anion-exchange membrane electrolyzer, Os/ZrO₂||RuO₂ achieves a low voltage of 1.82 V at 1 A cm⁻² and maintains stable operation, translating to a hydrogen production cost of $0.97 per gasoline gallon equivalent. This work presents an effective strategy for designing high-performance HER catalysts through hydrogen spillover engineering, providing a feasible route for enhanced electrocatalytic systems.
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Wang et al. (2026) studied this question.
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