In this paper, we present a study of a series of carbon-supported Pd–Sn binary alloyed catalysts prepared through a modified Polyol method as anode electrocatalysts for direct ethanol fuel cell reactions in an alkaline medium. Transmission electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and aberration-corrected scanning transmission electron microscopy equipped with electron energy loss spectroscopy were used to characterize the Pd–Sn/C catalysts, where homogeneous Pd–Sn alloys were determined to be present with the surface Sn being partially oxidized. Among various Pd–Sn catalysts, Pd 86 Sn 14 /C catalysts showed much enhanced current densities in cyclic voltammetric and chronoamperometric measurements, compared to commercial Pd/C (Johnson Matthey). The overall rate law of ethanol oxidation reaction for both Pd 86 Sn 14 /C and commercial Pd/C were also determined, which clearly showed that Pd 86 Sn 14 /C was more favorable in high ethanol concentration and/or high pH environment. Density functional theory calculations also confirmed Pd–Sn alloy structures would result in lower reaction energies for the dehydrogenation of ethanol, compared to the pure Pd crystal.
No takes yet. Share an insight, caveat, or question.
Du et al. (2012) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: