过电位
非阻塞I/O
催化作用
离解(化学)
材料科学
铂金
过渡金属
氢
异质结
制氢
金属
无机化学
氧化物
化学工程
化学
物理化学
电化学
冶金
有机化学
工程类
光电子学
电极
作者
Kai Zhou,Zelin Wang,Chang Bao Han,Xiaoxing Ke,Changhao Wang,Yuhong Jin,Qianqian Zhang,Jingbing Liu,Hao Wang,Hui Yan
标识
DOI:10.1038/s41467-021-24079-8
摘要
Single-atom catalysts provide an effective approach to reduce the amount of precious metals meanwhile maintain their catalytic activity. However, the sluggish activity of the catalysts for alkaline water dissociation has hampered advances in highly efficient hydrogen production. Herein, we develop a single-atom platinum immobilized NiO/Ni heterostructure (PtSA-NiO/Ni) as an alkaline hydrogen evolution catalyst. It is found that Pt single atom coupled with NiO/Ni heterostructure enables the tunable binding abilities of hydroxyl ions (OH*) and hydrogen (H*), which efficiently tailors the water dissociation energy and promotes the H* conversion for accelerating alkaline hydrogen evolution reaction. A further enhancement is achieved by constructing PtSA-NiO/Ni nanosheets on Ag nanowires to form a hierarchical three-dimensional morphology. Consequently, the fabricated PtSA-NiO/Ni catalyst displays high alkaline hydrogen evolution performances with a quite high mass activity of 20.6 A mg-1 for Pt at the overpotential of 100 mV, significantly outperforming the reported catalysts.
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