4.8 Article

An efficient and pH-universal ruthenium-based catalyst for the hydrogen evolution reaction

Journal

NATURE NANOTECHNOLOGY
Volume 12, Issue 5, Pages 441-446

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/NNANO.2016.304

Keywords

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Funding

  1. Creative Research Initiative (CRI) [2014R1A3A2069102]
  2. BK21 Plus [10Z20130011057]
  3. Science Research Center (SRC) [2016R1A5A1009405]
  4. Creative Materials Discovery Program through the National Research Foundation (NRF) of Korea [2016M3D1A1900035]
  5. National Research Foundation of Korea [2016M3D1A1900035, 2016R1A5A1009405] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The hydrogen evolution reaction (HER) is a crucial step in electro-chemical water splitting and demands an efficient, durable and cheap catalyst if it is to succeed in real applications(1-3). For an energy-efficient HER, a catalyst must be able to trigger proton reduction with minimal overpotential(4) and have fast kinetics(5-9). The most efficient catalysts in acidic media are platinum-based, as the strength of the Pt-H bond(10) is associated with the fastest reaction rate for the HER11,12. The use of platinum, however, raises issues linked to cost and stability in non-acidic media. Recently, non-precious-metal-based catalysts have been reported, but these are susceptible to acid corrosion and are typically much inferior to Pt-based catalysts, exhibiting higher overpotentials and lower stability(13-15). As a cheaper alternative to platinum, ruthenium possesses a similar bond strength with hydrogen (similar to 65 kcal mol(-1))(16), but has never been studied as a viable alternative for a HER catalyst. Here, we report a Ru-based catalyst for the HER that can operate both in acidic and alkaline media. Our catalyst is made of Ru nanoparticles dispersed within a nitrogenated holey two-dimensional carbon structure (Ru@C2N). The Ru@C2N electrocatalyst exhibits high turnover frequencies at 25 mV (0.67 H-2 s(-1) in 0.5 M H2SO4 solution; 0.75 H-2 s(-1) in 1.0 M KOH solution) and small overpotentials at 10 mA cm(-2) (13.5 mV in 0.5 M H2SO4 solution; 17.0 mV in 1.0 M KOH solution) as well as superior stability in both acidic and alkaline media. These performances are comparable to, or even better than, the Pt/C catalyst for the HER.

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