Formic acid oxidation reaction on a PdxNiy bimetallic nanoparticle catalyst prepared by a thermal decomposition process using ionic liquids as the solvent

• PdxNiy nanoparticles were prepared by using RTILs as the solvent.
• The peak current on the Pd3Ni2 was about three times higher than that on the Pd.
• The lower electrode potential and easier hydrogen evolution were the main reasons.

The nano-catalysts of PdxNiy bimetallic nanoparticles (NPs, the nominal atomic ratios of Pd to Ni are 2:1, 3:2 and 1:1) supported on multi-walled carbon nanotubes (MWCNTs) (denoted as PdxNiy/MWCNTs) have been synthesized by a thermal decomposition process using room temperature ionic liquids (RTILs) of N-butylpyridinium tetrafluoroborate (BPyBF4) as the solvent. X-ray diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscopy (TEM) were employed to characterize the morphology of the samples, revealing that the prepared PdxNiy NPs were quite uniformly dispersed on the surface of MWCNTs with an average particle size of ∼8.0 nm. Formic acid oxidation reaction (FAOR) was investigated on the as-prepared catalysts by using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), demonstrating that the peak current on the Pd3Ni2/MWCNTs catalyst was about three times higher than that on the Pd/MWCNTs. The lower electrode potential and easier hydrogen evolution, based on the results obtained from chronopotentiometry and CV, respectively, were thought as the main reasons for the excellent electrocatalysis of the Pd3Ni2/MWCNTs toward formic acid oxidation reaction (FAOR) when compared to other samples.

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