Published September 30, 2013 | Version v1
Journal article

Catalyst nanoscale assembly from the vapor phase on corrosion resistant supports

  • 1. Center for Clean Energy Engineering, University of Connecticut, 44 Weaver Road, Storrs, CT 06269 (United States)
  • 2. Department of Materials Science and Engineering, University of Connecticut, 191 Auditorium Road, Storrs, CT 06269 (United States)
  • 3. Departamento de Materiales Metálicos y Cerámicos, Instituto de Investigaciones en Materiales, Universidad Nacional Autónoma de México, Mexico D.F. 04510 (Mexico)
  • 4. Department of Chemical and Biomolecular Engineering, University of Connecticut, Storrs, CT 06269 (United States)
  • 5. Department of Chemical, Materials and Biomolecular Engineering, University of Connecticut, Storrs, CT 06269 (United States)

Description

The synthesis process, reactive spray deposition technology (RSDT), utilized a jet-flame to produce Pt nanoparticles. The RSDT process bypasses traditional wet chemical routes by simultaneously nucleating the catalyst on a support and sequential deposition of catalyst layer via the gas phase. Pt nanoparticles were attached, in the process gas during the time-of-flight, to the surface of several supports. The supports show promising corrosion resistance under the cathode conditions of a proton exchange membrane fuel cell (PEMFC). The supported Pt catalysts were then studied in regards to structure, stability and electrochemical behavior toward the oxygen reduction reaction (ORR) in perchloric acid. Transmission electron microscopy studies showed that the average Pt particle diameter is ∼2.5 nm. The average diameter and distribution of the Pt particles are independent of the support type and a high degree of catalyst dispersion has been achieved on all supports. The greatest surface area and electrochemical mass activity were obtained using Vulcan XC-72R, while a graphitized carbon support produced the highest specific activity. Based on X-ray photoelectric spectroscopy (XPS) measurements, approximately 30% of the surface of the Pt particles is comprised of Pt2+. This oxide coverage does not extend into the bulk and is below the detection limits of X-ray diffraction (XRD). The electrochemical reduction of oxygen exhibits a typical Tafel slope of −65 to −71 mV/dec

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2013.06.063

Additional details

Identifiers

DOI
10.1016/j.electacta.2013.06.063;
PII
S0013-4686(13)01169-9;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
107
Journal Page Range
p. 632-655
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.