Abstract

Molybdenum sulphide is an emerging precious-metal-free catalyst for cathodic water splitting. As its active sites catalyse the Volmer hydrogen adsorption step, it is particularly active in acidic media. This study focused on the electrochemical deposition of MoS2 on copper foam electrodes and the characterisation of their electrocatalytic properties. In addition, the electrodeposition was modified by adding a reducing agent—sodium hypophosphite—to the electrolyte. To reveal the role of hypophosphite, X-ray photoelectron spectroscopy (XPS) analysis was carried out in addition to scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX). MoS2 films, electrodeposited at various charges passed through the cell (catalyst loadings), were tested for their catalytic activity towards hydrogen evolution in 0.5 M H2SO4. Polarisation curves and Tafel slope analysis revealed that the electrodeposited MoS2 films are highly active. Namely, Tafel slopes fell within the 40–50 mV dec−1 range. The behaviour of as-deposited films was also evaluated by electrochemical impedance spectroscopy over a wide overpotential range (0 to −0.3 V), and two clear time constants were distinguished. Through equivalent electrical circuit analysis, the experimental data were fitted to the appropriate model, and the obtained values of the circuit components were examined as a function of overpotential. It was found that the addition of NaH2PO2 into the electrodeposition solution affects the intrinsic activity of the material. Finally, a method is proposed to approximate the number of active sites from impedance data.

Highlights

  • Within the field of renewable energy generation, storage and transportation, H2 is considered a feasible energy carrier due to its significant gravimetric energy density when compared to carbon-based fuels [1]

  • The mechanism of hydrogen evolution reaction (HER) in acidic solutions consists of three steps: electrochemical hydrogen adsorption (Volmer reaction), followed by electrochemical (Heyrovsky reaction) and/or chemical (Tafel reaction) hydrogen desorption [6]

  • Because the S 2p signal does not change in any major way, it is assumed that the material retains the same 2H-MoS2 structure, and that the effect of NaH2 PO2 on the electrochemical deposition of MoS2 is mainly targeting the suppression of Mo-O bond formation, or, the assistance of Mo-S bond formation

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Summary

Introduction

Within the field of renewable energy generation, storage and transportation, H2 is considered a feasible energy carrier due to its significant gravimetric energy density when compared to carbon-based fuels [1]. The most widely used industrial-scale hydrogen production method currently is the steam reforming process, where hydrocarbons react with steam, yielding H2 and CO2 [2]. With the application of sufficient overpotential on an electrode in an aqueous solution, the H2 O molecules spontaneously split into H2 and O2. The cathodic half-reaction is called the hydrogen evolution reaction (HER) [5]. The mechanism of HER in acidic solutions consists of three steps: electrochemical hydrogen adsorption (Volmer reaction), followed by electrochemical (Heyrovsky reaction) and/or chemical (Tafel reaction) hydrogen desorption [6]. The rate of HER depends on the adsorption

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