4.6 Article

Coral-like S-doped CoSe2 with enriched 1T-phase as efficient electrocatalyst for hydrogen evolution reaction

Journal

ELECTROCHIMICA ACTA
Volume 322, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2019.134739

Keywords

Hydrogen evolution; Cobalt chalcogenides; Sulfur doping; Coral-like structure

Funding

  1. Danish National Research Foundation
  2. AUFF-NOVA project from Aarhus Universitets Forskningsfond
  3. EU
  4. National Program for Support of Top-notch Young Professionals
  5. National Natural Science Foundation of China [51773049]
  6. China Aerospace Science and Technology Corporation-Harbin Institute of Technology Joint Center for Technology Innovation Fund [HIT151A01]
  7. Shanghai Academy of Spaceflight Technology Fund [SAST2017-126]
  8. Harbin City Science and Technology Projects [2013DB4BP031, RC2014QN017035]
  9. China Postdoctoral Science Special Foundation [201003420, 20090460067]
  10. HIT Research Institute of New Materials and Intelligent Equipment Technology Co., Ltd. Scientific and Technological Cooperation and Development Fund [2017KJHZ002]
  11. Fundamental Research Funds for the Central Universities, China [YJ201893]
  12. State Key Lab of Advanced Metals and Materials, China [2019-Z03]

Ask authors/readers for more resources

Developing high-efficiency electrocatalysts for water splitting is considered as a promising strategy to generate hydrogen addressing the current energy issues. CoSe2 is a promising electrocatalyst for water splitting due to its intrinsic metallicity, but its application is limited by the chemically inert basal plane and thus lack of active sites. Herein, we investigate the effect of growth condition on hydrogen evolution by changing the doped sulfur amount. The optimized coral-like CoS0.1Se1.9 with enriched 1T-phase exhibits robust hydrogen evolution reaction(HER) activity, which is evidenced from mere -157 mV (vs. RHE) is needed to afford a current density of 10 mA cm(-2), a small Tafel slope of 28.2 mV dec(-1) and remarkable long-term stability. This enhancement may be attributed to the increase of active sites and improved conductivity, resulting from the tuned morphology and electronic structure of CoS0.1Se1.9. This work paves a novel route in the rational design and facile synthesis of superior nonprecious electro-catalysts with striking HER performance for practical utilization. (C) 2019 Elsevier Ltd. All rights reserved.

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