4.8 Article

Ruthenium anchored on carbon nanotube electrocatalyst for hydrogen production with enhanced Faradaic efficiency

Journal

NATURE COMMUNICATIONS
Volume 11, Issue 1, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-020-15069-3

Keywords

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Funding

  1. Creative Research Initiative (CRI) Program through the National Research Foundation (NRF) of Korea - Ministry of Science, ICT, and Future Planning [2014R1A2069102]
  2. BK21 Plus Program through the National Research Foundation (NRF) of Korea - Ministry of Science, ICT, and Future Planning [10Z20130011057]
  3. Science Research Center (SRC) Program through the National Research Foundation (NRF) of Korea - Ministry of Science, ICT, and Future Planning [2016R1A5A1009405]
  4. Young Researcher Program through the National Research Foundation (NRF) of Korea - Ministry of Science, ICT, and Future Planning [2019R1C1C1006650]
  5. NRF [2019R1A2C2089332]
  6. National Research Foundation of Korea [2019R1A2C2089332] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Developing efficient and stable electrocatalysts is crucial for the electrochemical production of pure and clean hydrogen. For practical applications, an economical and facile method of producing catalysts for the hydrogen evolution reaction (HER) is essential. Here, we report ruthenium (Ru) nanoparticles uniformly deposited on multi-walled carbon nanotubes (MWCNTs) as an efficient HER catalyst. The catalyst exhibits the small overpotentials of 13 and 17 mV at a current density of 10 mA cm(-2) in 0.5M aq. H2SO4 and 1.0M aq. KOH, respectively, surpassing the commercial Pt/C (16 mV and 33 mV). Moreover, the catalyst has excellent stability in both media, showing almost zeroloss during cycling. In a real device, the catalyst produces 15.4% more hydrogen per power consumed, and shows a higher Faradaic efficiency (92.28%) than the benchmark Pt/C (85.97%). Density functional theory calculations suggest that Ru-C bonding is the most plausible active site for the HER.

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