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Electrocatalytic activity of tungsten carbide hybrids with two different MOFs for water splitting: a comparative
Umair Sohail1, Erum Pervaiz1, Rafiq Khosa1
1Heterogeneous Catalysis Lab, Department of Chemical Engineering, School of Chemical and Materials Engineering (SCME), National University of Sciences and Technology (NUST) Islamabad 44000 Pakistan erum.pervaiz@scme.nust.edu.pk +92 3324001027.
Abstract:
Conventional energy resources are diminishing, and environmental pollution is constantly increasing because of the excessive use of fossil fuels to sustain the ever-increasing population and industrialization. This has raised concerns regarding a sustainable future. In the pursuit of addressing sustainability in industrial processes and energy systems, the production of green hydrogen is considered a promising and crucial solution to meet the growing energy demands. Water-splitting is one of the most effective technologies for producing clean and carbon-neutral hydrogen. Water-splitting is a scientifically emerging application, but it is commercially limited due to its economic non-viability. The sluggish kinetics and the high overpotential needed for the water-splitting reactions (HER and OER) have encouraged the scientific community to design electrocatalysts that address the concerns of low activity, efficiency and stability. Designing a hybrid catalyst using metal-organic frameworks (MOFs) with transition metal carbides can be a suitable approach to address the deficiencies of conventional water-splitting catalysts. In this study, we have designed and fabricated an electrocatalyst of tungsten carbide (WC) with two different MOFs (Zr-based and Fe-based) and explored their electrocatalytic activity for hydrogen generation in an alkaline medium. It should be noted that hybrids of tungsten carbide with a zirconia MOF (UiO-66) showed better electrocatalytic activity with low overpotentials of 104 mV (HER) and 152 mV (OER) at a current density of 10 mA cm-2. This superior activity of WC with the Zr-MOF in comparison to the Fe-MOF is due to the synergistic effect of Zr present in UiO-66 grown on the WC matrix. Moreover, UiO-66 provides a larger electrocatalytic active surface area, so available active sites are more in UiO-66 as compared to the Fe-MOF. These findings set the stage for the systematic development and production of bi-functional hybrid catalysts with the potential to be utilized in water-splitting processes.
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