Optimization of metal atomic ratio of PdxRuyNiz on carbon support for ethanol oxidation

The catalytic activity of palladium (Pd) on an alloy catalyst on carbon supports with regards to ethanol oxidation was enhanced by systematically varying the atomic ratio of Pd, ruthenium (Ru), and nickel (Ni) alloy catalyst. Each atomic ratio catalyst was investigated so as to find the highest current density per mass of palladium. Functionalized carbon black (C) and reduced graphene oxide (rGO) were used as carbon supports. The PdxRuyNiz/carbon catalysts were prepared by impregnation and reduction method with sodium borohydride (NaBH4) being used as the reducing agent. Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA) were used to characterize the functionalized carbon supports, and the synthesized PdxRuyNiz/carbon catalysts were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS), and inductively coupled plasma (ICP). The electrical properties of catalyst were performed by cyclic voltammetry (CV), chronoamperometry (CA), and CO-stripping to investigate the catalytic activity compared to 20%wt synthesized Pd/C. The results showed that Pd:Ru:Ni = 60:0:40 on rGO (Pd60Ni40/rGO) had the best metal atomic ratio and support for the electro-oxidation of ethanol. The maximum current density and the electrochemical surface area were 11,074 mA cm−2 mg−1Pd and 55.6 m2 g−1Pd, which were 1.7 and 2.67 times the corresponding values of synthesized Pd/C, respectively.