摘要
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 (Ptai) featuring multifunctional active centers embedded in Mo2C 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 Ptai, which strikingly mitigates H migration barriers. When applied in alkaline HER, exceptionally low overpotentials (η10 = 11.8 mV, η100 = 52.9 mV) are obtained for the catalyst. More importantly, corresponding alkaline anion-exchange membrane water electrolyzers exhibit an ultralow cell voltage (1.77 Vcell) 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.
| 源语言 | 英语 |
|---|---|
| 期刊 | Advanced Functional Materials |
| DOI | |
| 出版状态 | 已接受/待刊 - 2026 |
| 已对外发布 | 是 |
学术指纹
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