Journal
CHEMCATCHEM
Volume 13, Issue 7, Pages 1824-1833Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.202001838
Keywords
doping; nickel; foam; electrocatalysis; hydrogen evolution reaction; synergistic catalytic
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Funding
- National Science Foundation of China [21802126]
- Science Foundation of Shanxi Province [201801D221083]
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Cu-doped Ni3S2/NF catalyst was prepared and optimized for enhanced electrocatalytic activity in the hydrogen evolution reaction. Density functional theory calculations showed that the superior electrocatalytic activities were attributed to optimized water adsorption energy and enhanced electrical conductivity. The stability of the catalyst was tested in 1 M KOH for 12 hours, indicating no apparent attenuation in current density.
Ni3S2 has been widely reported as an effective electrochemical catalyst for hydrogen evolution reaction (HER). However, the electrochemical activity of the cathode reduction reaction needs to be further improved due to the drawback of strong S-H bond interaction on the surface of Ni3S2. Herein, a series of non-precious metal Cu element doped Ni3S2 materials were prepared on the Nickel foam support (Cu-Ni3S2/NF) though a two-step hydrothermal method. Moreover, we optimized the performance of the catalyst by adjusting the molar amount of doped copper ion in the first hydrothermal process. When the molar ratio of copper ion and nickel ion is 1 : 4, the Cu-Ni3S2/NF-1/4 material with independent and clustered rose-shaped cross-nanosheet arrays structure have been used as a highly efficient electrochemical hydrogen evolution reaction (HER) catalyst. In HER process, the Cu-Ni3S2/NF-1/4 material drives the current densities of 10 mA cm(-2) and 50 mA cm(-2) under low overpotentials of 92 mV and 256 mV respectively, while Ni3S2/NF needs 210 mV and 397 mV to reach the same current densities. Density functional theory (DFT) calculation shows that the superior electrocatalytic activities are attributed to optimized water adsorption energy and enhanced electrical conductivity. The stability of catalyst was tested in 1 M KOH for 12 hours by chronoamperometry, indicating the current density has no an apparent attenuation.
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