4.7 Article

Transition metal doped MoS2 nanosheets for electrocatalytic hydrogen evolution reaction

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 47, Issue 88, Pages 37256-37263

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.01.109

Keywords

Molybdenum disulfide; 2D materials; Doping; Transition metal; Electrocatalytic water; Splitting

Funding

  1. Tamil Nadu State Council for Science and Technology
  2. DST-FIST
  3. RUSA R I
  4. PURSE
  5. [Chennai-600 025]

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This study explores the effect of transition metal doping on 2D MoS2 nanosheets for the electrocatalytic hydrogen evolution reaction (HER). High-quality MoS2 nanosheets with randomly doped metal ions were synthesized using a hydrothermal method. It was found that Ni-MoS2 exhibited superior HER performance compared to Co-MoS2 and Fe-MoS2.
In the present work, the effect of transition metals (Ni, Fe, Co) doping on 2-dimensional (2D) molybdenum disulfide (MoS2) nanosheets for electrocatalytic hydrogen evolution reaction (HER) was explored. A simple and cost-effective hydrothermal method was adopted to synthesis transition metals doped MoS2 nanosheets. The morphological and spectroscopic studies evidence the formation of high-quality MoS2 nanosheets with the randomly doped metal ions. Notably, the Ni-MoS2 displayed superior HER performance with an overpotential of-0.302 V vs. reversible hydrogen electrode (RHE) (to attain the current density of 10 mA cm-2) as compared to the other transition metals doped MoS2 (Co-MoS2, Fe-MoS2). From the Nyquist plot, superior charge transport from the electro-catalyst to the electrolyte in Ni-MoS2 was realized and confirmed that Ni doping provides the necessary catalytic active sites for rapid hydrogen production. The stable performance was confirmed with the cyclic test and chronoamperometry measurement and envisaged that hydrothermally synthesized Ni-MoS2 is a highly desirable cost-effective approach for electrocatalytic hydrogen generation.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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