4.8 Article

Carbon-Armored Co9S8 Nanoparticles as All-pH Efficient and Durable H2-Evolving Electrocatalysts

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 7, Issue 1, Pages 980-988

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/am507811a

Keywords

carbon; cobalt; hydrogen evolution; sulfide; water splitting

Funding

  1. NSFC [21371070, 21401066]
  2. National Basic Research Program of China [2013CB632403]
  3. Jilin province science and technology development projects [20150520003JH, 20140101041JC, 20130204001GX]
  4. Graduate Innovation Fund of Jilin University [2014083]

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Splitting water to produce hydrogen requires the development of non-noble-metal catalysts that are able to make this reaction feasible and energy efficient. Herein, we show that cobalt pentlandite (Co9S8) nanoparticles can serve as an electrochemically active, noble-metal-free material toward hydrogen evolution reaction, and they work stably in neutral solution (pH 7) but not in acidic (pH 0) and basic (pH 14) media. We, therefore, further present a carbon-armoring strategy to increase the durability and activity of Co9S8 over a wider pH range. In particular, carbon-armored Co9S8 nanoparticles (Co9S8@C) are prepared by direct thermal treatment of a mixture of cobalt nitrate and trithiocyanuric acid at 700 degrees C in N-2 atmosphere. Trithiocyanuric acid functions as both sulfur and carbon sources in the reaction system. The resulting Co9S8@C material operates well with high activity over a broad pH range, from pH 0 to 14, and gives nearly 100% Faradaic yield during hydrogen evolution reaction under acidic (pH 0), neutral (pH 7), and basic (pH 14) media. To the best of our knowledge, this is the first time that a transition-metal chalcogenide material is shown to have all-pH efficient and durable electrocatalytic activity. Identifying Co9S8 as the catalytically active phase and developing carbon-armoring as the improvement strategy are anticipated to give a fresh impetus to rational design of high-performance noble-metal-free water splitting catalysts.

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