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Author:

Zhou, Kai Ling (Zhou, Kai Ling.) | Wang, Zelin (Wang, Zelin.) | Han, Chang Bao (Han, Chang Bao.) | Ke, Xiaoxing (Ke, Xiaoxing.) | Wang, Changhao (Wang, Changhao.) | Jin, Yuhong (Jin, Yuhong.) | Zhang, Qianqian (Zhang, Qianqian.) | Liu, Jingbing (Liu, Jingbing.) | Wang, Hao (Wang, Hao.) (Scholars:汪浩) | Yan, Hui (Yan, Hui.)

Indexed by:

Scopus SCIE

Abstract:

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 (Pt-SA-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 Pt-SA-NiO/Ni nanosheets on Ag nanowires to form a hierarchical three-dimensional morphology. Consequently, the fabricated Pt-SA-NiO/Ni catalyst displays high alkaline hydrogen evolution performances with a quite high mass activity of 20.6Amg(-1) for Pt at the overpotential of 100mV, significantly outperforming the reported catalysts. While H-2 evolution from water may represent a renewable energy source, there is a strong need to improve catalytic efficiencies while maximizing materials utilization. Here, authors examine single-atom Pt on nickel-based heterostructures as highly active electrocatalysts for alkaline H-2 evolution.

Keyword:

Author Community:

  • [ 1 ] [Zhou, Kai Ling]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China
  • [ 2 ] [Wang, Zelin]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China
  • [ 3 ] [Han, Chang Bao]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China
  • [ 4 ] [Ke, Xiaoxing]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China
  • [ 5 ] [Wang, Changhao]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China
  • [ 6 ] [Jin, Yuhong]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China
  • [ 7 ] [Zhang, Qianqian]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China
  • [ 8 ] [Liu, Jingbing]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China
  • [ 9 ] [Wang, Hao]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China
  • [ 10 ] [Yan, Hui]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China

Reprint Author's Address:

  • 汪浩

    [Han, Chang Bao]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China;;[Ke, Xiaoxing]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China;;[Wang, Hao]Beijing Univ Technol, Fac Mat & Mfg, Beijing, Peoples R China

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Source :

NATURE COMMUNICATIONS

ISSN: 2041-1723

Year: 2021

Issue: 1

Volume: 12

1 6 . 6 0 0

JCR@2022

ESI Discipline: Multidisciplinary;

ESI HC Threshold:169

JCR Journal Grade:1

Cited Count:

WoS CC Cited Count: 528

SCOPUS Cited Count: 523

ESI Highly Cited Papers on the List: 17 Unfold All

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WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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