4.8 Article

Palladium-Tin Alloyed Catalysts for the Ethanol Oxidation Reaction in an Alkaline Medium

Journal

ACS CATALYSIS
Volume 2, Issue 2, Pages 287-297

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cs2005955

Keywords

Pd-Sn; ethanol oxidation reaction; alkaline fuel cell; rate law; DFT calculations

Funding

  1. University of New Hampshire
  2. U.S. Department of Energy, Office of Basic Energy Sciences [DE-AC02-98CH10886]

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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, Pd86Sn14/C catalysts showed much enhanced current densities in cyclic voltammetric and chronoamperometric measurements, compared to commercial Pd/C (Johns,:on Matthey). The overall rate law of ethanol oxidation reaction for both Pd86Sn14/C and commercial Pd/C were also determined, which clearly showed that Pd86Sn14/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.

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