4.8 Article

Partial-Single-Atom, Partial-Nanoparticle Composites Enhance Water Dissociation for Hydrogen Evolution

期刊

ADVANCED SCIENCE
卷 8, 期 2, 页码 -

出版社

WILEY
DOI: 10.1002/advs.202001881

关键词

electrocatalysis; multiple sites; single‐ atom catalysts; theoretical calculations; water dissociation

资金

  1. Science and Technology Commission of Shanghai Municipality [19ZR1465100, 19ZR1479500]
  2. Equipment Research Program [6140721050215]
  3. National Natural Science Foundation of China [21973107, 51702345]
  4. Science AMP
  5. Technology Innovation Major Program of Ningbo (Ningbo 2025 Program) [2018B10056]
  6. Program of Shanghai Academic Research Leader [20XD1424300]
  7. U.S. National Science Foundation (NSF) under the CAREER award [DMR-1945380]
  8. Oregon State University
  9. E. I. duPont de Nemours Co.
  10. Northwestern University
  11. Dow Chemical Company
  12. DOE [DE-AC02-06CH11357]

向作者/读者索取更多资源

This study reports an energy-efficient hydrogen evolution reaction (HER) electrocatalyst in alkaline medium, showing outstanding activity, surpassing commercial Pt/C and other reported electrocatalysts in alkaline conditions.
The development of an efficient electrocatalyst toward the hydrogen evolution reaction (HER) is of significant importance in transforming renewable electricity to pure and clean hydrogen by water splitting. However, the construction of an active electrocatalyst with multiple sites that can promote the dissociation of water molecules still remains a great challenge. Herein, a partial-single-atom, partial-nanoparticle composite consisting of nanosized ruthenium (Ru) nanoparticles (NPs) and individual Ru atoms as an energy-efficient HER catalyst in alkaline medium is reported. The formation of this unique composite mainly results from the dispersion of Ru NPs to small-size NPs and single atoms (SAs) on the Fe/N codoped carbon (Fe-N-C) substrate due to the thermodynamic stability. The optimal catalyst exhibits an outstanding HER activity with an ultralow overpotential (9 mV) at 10 mA cm(-2) (eta(10)), a high turnover frequency (8.9 H-2 s(-1) at 50 mV overpotential), and nearly 100% Faraday efficiency, outperforming the state-of-the-art commercial Pt/C and other reported HER electrocatalysts in alkaline condition. Both experimental and theoretical calculations reveal that the coexistence of Ru NPs and SAs can improve the hydride coupling and water dissociation kinetics, thus synergistically enhancing alkaline hydrogen evolution performance.

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