4.6 Article

Electrocatalytic Properties of Pulse-Reverse Electrodeposited Nickel Phosphide for Hydrogen Evolution Reaction

Journal

FRONTIERS IN CHEMISTRY
Volume 9, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fchem.2021.781838

Keywords

nickel phosphide; pulse-reverse electrodeposition; hydrogen evolution reaction; Ni precipitate; volmer-heyrovsky route

Funding

  1. National Research Foundation of Korea (NRF) - Ministry of Science and ICT [NRF-2020M3H4A3081760]

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Nickel phosphide films were fabricated as a catalytic cathode for the hydrogen evolution reaction using a pulse-reverse electrodeposition technique. The composition of the electrodeposited Ni-P alloys was controlled by adjusting duty cycles. The electrochemical properties of the Ni-P electrodeposits, including overpotentials, Tafel slopes, and electrochemical impedance spectrometry, were analyzed to study their HER electrocatalytic properties.
Nickel phosphide (Ni-P) films as a catalytic cathode for the hydrogen evolution reaction (HER) of a water splitting were fabricated by a pulse-reverse electrodeposition technique. The electrochemical behaviors for the electrodeposition of Ni-P were investigated by the characterization of peaks in a cyclic voltammogram. The composition of the electrodeposited Ni-P alloys was controlled by adjusting duty cycles of the pulse-reverse electrodeposition. The HER electrocatalytic properties of the Ni-P electrodeposits with an amorphous phase as a function of phosphorous contents existing in Ni-P were electrochemically characterized by the analysis of overpotentials, Tafel slopes, and electrochemical impedance spectrometry. Additionally, the elemental Ni-embedded crystalline Ni3P was prepared by an annealing process with the amorphous Ni69P31 electrodeposit with high contents of phosphorus. The crystalline structure with Ni inclusions in the matrix of Ni3P was formed by the precipitation of excess Ni. The electrocatalytic properties of crystalline Ni3P with elemental Ni inclusions were also investigated by electrochemical characterization.

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