Two-dimensional
(2D) MXenes and their composites are increasingly
performing as efficient catalysts for the production of hydrogen (H2) and oxygen (O2). Herein, we report a strategy
for the surface modification of V2CT
x
MXene as an efficient bifunctional hybrid electrocatalyst
for water splitting application by optimized loading of spherical
silver nanoparticles (Ag-NPs) on V2CT
x
nanosheets (NSs). In 1.0 M KOH solution, the V2CT
x
/Ag-NPs nanohybrid (labeled as HII)
attained an overpotential of 310 mV (vs RHE) and a Tafel slope of
62 mV/dec for the oxygen evolution reaction (OER), and an overpotential
of 32 mV (vs RHE) and a Tafel slope of 114 mV/dec for the hydrogen
evolution reaction (HER). The hybrid showed significantly improved
values than those of their constituents (MXene nanosheets and Ag-NPs)
and was even comparable to the industrial RuO2 and Pt electrocatalysts.
The uniform loading of silver nanoparticles (Ag-NPs) on 2D MXene sheets
acted as a conductive agent and their large surface area facilitated
ion transport by ensuring short conductive pathways at the electrode–electrolyte
interface. Moreover, the strong contact and electrical coupling with
charge transfer between Ag-NPs and V2CT
x
MXene provided much higher water-splitting performance and
structural stability as well as low charge transfer resistance, which
eventually enhanced the intrinsic activity of the catalyst. This HER
reaction followed the Volmer–Heyrovsky mechanism for H2 production at the cathode. The dispersion of Ag-NPs increases
the Raman signals of V2CT
x
for
the hybrid, demonstrating the surface-enhanced activity of Raman scattering.
The three-dimensional frame structure of nickel foam helped in easing
the release of oxygen and hydrogen gas bubbles from the reaction sites.