ABSTRACT
The integration of diverse components into a single heterostructure represents an innovative approach that boosts the quantity and variety of active centers, thereby enhancing the catalytic activity for both hydrogen evolution reactions (HER) and oxygen evolution reactions (OER) in the water splitting process. In this study, a novel, hierarchically porous one-dimensional nanowire array comprising zinc cobalt sulfide and molybdenum disulfide (MoS2@Zn0.76Co0.24S) was successfully synthesized on a Ni foam substrate using an efficient and straightforward hydrothermal synthesis strategy. The incorporation of the metallic phase of molybdenum disulfide elevates the electronic conductivity of MoS2@Zn0.76Co0.24S, resulting in impressively low overpotentials. At 20, 50, and 100 mA cm-2, the overpotentials for oxygen evolution reaction (OER) are merely 90 mV, 170 mV, and 240 mV, respectively. Similarly, for hydrogen evolution reaction (HER), the overpotentials are 169 mV, 237 mV, and 301 mV at the same current densities in 1.0 M potassium hydroxide solution. The utilization of the MoS2@Zn0.76Co0.24S /NF electrolyzer demonstrates its exceptional performance as a catalyst in alkaline electrolyzers. Operating at a mere 1.45 V and 10 mA cm-2, it showcases outstanding efficiency. Achieving a current density of 405 mA cm-2, the system generates hydrogen at a rate of 3.1 mL/min with a purity of 99.997%, achieving an impressive cell efficiency of 68.28% and a voltage of 1.85 V. Furthermore, the MoS2@Zn0.76Co0.24S /NF hybrid exhibits seamless integration with solar cells, establishing a photovoltaic electrochemical system for comprehensive water splitting. This wireless assembly harnesses the excellent performance of the hybrid nanowire, offering a promising solution for efficient, durable, and cost-effective bifunctional electrocatalysts in the realm of renewable energy.
ABSTRACT
Heterointerface engineering enhances catalytic active centers and charge transfer capabilities to increase oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) kinetics. In this study, a novel heterostructure of manganese cobalt sulfide-molybdenum disulfide on nickel foam (MnCo2S4-MoS2/NF) was synthesized via a two-step hydrothermal process. The nanowire-shaped MnCo2S4-MoS2 on NF displayed accelerated charge transfer ability and multiple integrated active sites. When tested in one molar (1 M) potassium hydroxide (KOH) electrolyte, it furnished low overpotentials of 105 and 171 mV for the HER and 220 and 300 mV for the OER at the current densities of 20 and 50 mA cm-2, respectively. An electrolyzer based on MnCo2S4-MoS2/NF required low operating potentials of 1.41 and 1.49 V to yield the current densities of 10 and 20 mA cm-2, respectively, surpassing commercial and previously reported catalysts. Density functional theory (DFT) analysis revealed that the MnCo2S4-MoS2 heterostructure possesses the optimal adsorption free energies for the reactants, an extended electroactive surface area, good charge transfer ability, and reasonable density of electronic states close to the Fermi level, all of which contribute to the high activity of catalyst. Thus, heterointerface engineering is a promising strategy for creating efficient catalysts for overall water splitting.
