4.6 Article

Heteroatom-doped MoSe2 Nanosheets with Enhanced Hydrogen Evolution Kinetics for Alkaline Water Splitting

Journal

CHEMISTRY-AN ASIAN JOURNAL
Volume 14, Issue 2, Pages 301-306

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.201801645

Keywords

heteroatom doping; hydrogen evolution reaction; molybdenum selenide nanosheets; water adsorption; water splitting

Funding

  1. Australian Research Council (ARC) DECRA Grant [DE160100596]
  2. AIIM FOR GOLD Grant
  3. UOWs Vice-Chancellor's Postdoctoral Research Fellowship Funding

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Electrochemical water splitting for hydrogen generation is a vital part for the prospect of future energy systems, however, the practical utilization relies on the development of highly active and earth-abundant catalysts to boost the energy conversion efficiency as well as reduce the cost. Molybdenum diselenide (MoSe2) is a promising nonprecious metal-based electrocatalyst for hydrogen evolution reaction (HER) in acidic media, but it exhibits inferior alkaline HER kinetics in great part due to the sluggish water adsorption/dissociation process. Herein, the alkaline HER kinetics of MoSe2 is substantially accelerated by heteroatom doping with transition metal ions. Specifically, the Ni-doped MoSe2 nanosheets exhibit the most impressive catalytic activity in terms of lower overpotential and larger exchange current density. The density functional theory (DFT) calculation results reveal that Ni/Co doping plays a key role in facilitating water adsorption as well as optimizing hydrogen adsorption. The present work paves a new way to the development of low-cost and efficient electrocatalysts towards alkaline HER.

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