4.4 Article

Co doped MoS2 as Bifunctional Electrocatalyst for Hydrogen Evolution and Oxygen Reduction Reactions

Journal

INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE
Volume 14, Issue 10, Pages 9805-9814

Publisher

ESG
DOI: 10.20964/2019.10.29

Keywords

Co-MoS2; electrocatalysts; hydrogen evolution reaction; oxygen evolution reaction

Funding

  1. National Natural Science Foundation of China [51701001, 61804039]
  2. Academic funding projects for Top Talents in Subjects (Majors) of Universities [gxbjZD31]
  3. Natural Science Foundation of Anhui Higher Education Institution of China [KJ2019A0734, KJ2019A0736, KJ2017A924, KJ2017A002]
  4. Natural Science Foundation of Anhui Province [1808085QE126]
  5. Doctor Scientific Research Fund of Anhui University [J01001927]
  6. Youth Core Teacher Fund of Anhui University [J01005111]
  7. Foundation of Cooperative Innovation Research Center for Weak Signal-Detecting Materials and Devices Integration Anhui University [Y01008411, WRXH201703]

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Pure MoS2 and MoS2 compounds were doped with Co using a hydrothermal method. XRD results indicate that two of the five diffraction peak results at 9.2 degrees and 18.2 degrees may be attributed to low crystallinity of MoS2. The (002) diffraction peaks for the Co-doped MoS2 shifted to smaller angle, which may be due to the Mo4+ ions (r = 0.65 angstrom) having been replaced by larger Co2+ ions (r = 0.74 angstrom). Raman results show that the intensity of the A(1g) mode was greater than that of the E-2g(1) mode for our samples; this indicates that the samples have edge-terminated structures and possess more electrocatalytic active sites. The results of XPS also confirm that the cobalt ions substituted molybdenum atoms into the lattice of MoS2. Results from the electrocatalytic test confirms that cobalt doping reduces the charge transfer resistance and increases the electrocatalytic active sites, which are conducive to improving its electrocatalytic performance.

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