过电位
塔菲尔方程
催化作用
材料科学
吸附
化学工程
电解
无机化学
交换电流密度
解吸
电解水
碱金属
氢
电化学
分解水
双功能
离子交换
双功能催化剂
析氧
碱性水电解
纳米线
电流密度
密度泛函理论
金属
氢燃料
合金
制氢
过渡金属
作者
Dunyuan Jin,Yirong Zhai,Yun Huang,Longxiang Wang,Yifan Ye,J. Ge,Guiqiang Li
出处
期刊:Small
[Wiley]
日期:2026-01-09
卷期号:22 (7): e12365-e12365
被引量:3
标识
DOI:10.1002/smll.202512365
摘要
Abstract Hydrogen, with its high energy density and positive environmental impact, offers an ideal solution for energy storage via water electrolysis. Anion exchange membrane water electrolysis (AEMWE) has gained significant attention due to its high current density and low‐cost advantages, but the slow kinetics of the hydrogen evolution reaction (HER) remain a bottleneck. Here, a multiscale‐engineered catalyst is developed by growing CuRu single‐atom alloy nanosheets on Ni‐wrapped Cu nanowires (CuRu 1 ‐1/Ni). Electronic structure optimization alleviates the strong hydrogen adsorption on Ru sites, while the tip effect of nanosheets promotes alkali metal cation accumulation and rapid adsorbed hydroxyl (OH ad ) desorption. The CuRu 1 ‐1/Ni catalyst achieves optimized hydrogen adsorption through synergistic electronic interactions between CuRu single‐atom alloys and the Ni substrate. In situ Raman spectroscopy, CO stripping, alkali metal ion probe experiments, and finite element simulations confirm that the tip effect accelerates OH ad desorption and OH − transport. The CuRu 1 ‐1/Ni catalyst demonstrates excellent alkaline HER performance with the overpotential at 10 mA cm −2 of 30 mV, a Tafel slope of 30.2 mV dec −1 , and a mass activity of 0.347 A mg Ru −1 at 50 mV overpotential, surpassing Pt/C by 12‐fold. The catalyst also exhibits favorable stability, achieving a high current density of 1 A cm −2 in AEMWE.
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