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ABSTRACT The hydrogen (H) spillover effect on metal‐support electrocatalysts plays a significant role in improving the catalytic efficiency of the hydrogen evolution reaction (HER). However, the long reaction path and undesirable interfacial resistance cause considerable barriers in the H migration process. Herein, a small platinum atom‐island (Pt ai ) featuring multifunctional active centers embedded in Mo 2 C is designed, which exhibits an interface‐free atomic‐scale H spillover effect typically observed in single‐component catalysts. Experiments and calculations co‐reveal that a built‐in ultra‐short H spillover channel is established within the Pt ai , which strikingly mitigates H migration barriers. When applied in alkaline HER, exceptionally low overpotentials ( η 10 = 11.8 mV, η 100 = 52.9 mV) are obtained for the catalyst. More importantly, corresponding alkaline anion‐exchange membrane water electrolyzers exhibit an ultralow cell voltage (1.77 V cell ) and high stability (200 h) at an industrial current density of 1.0 A·cm −2 . This study proposes a novel strategy to accelerate hydrogen spillover in multicomponent catalysts through the design of interface‐free multifunctional active centers.
Li et al. (Wed,) studied this question.
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