Catalyst nanoscale assembly from the vapor phase on corrosion resistant supports
Creators
- 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.2013.06.063Additional 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
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45053101
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- CATALYSTS; CATHODES; CORROSION RESISTANCE; DEPOSITION; NANOSTRUCTURES; OXYGEN; PERCHLORIC ACID; PLATINUM IONS; PROTON EXCHANGE MEMBRANE FUEL CELLS; SENSITIVITY; STABILITY; SURFACE AREA; SURFACES; SYNTHESIS; TRANSMISSION ELECTRON MICROSCOPY; X RADIATION; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- CHARGED PARTICLES; CHLORINE COMPOUNDS; COHERENT SCATTERING; DIFFRACTION; DIRECT ENERGY CONVERTERS; ELECTROCHEMICAL CELLS; ELECTRODES; ELECTROMAGNETIC RADIATION; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ELEMENTS; FUEL CELLS; HALOGEN COMPOUNDS; HYDROGEN COMPOUNDS; INORGANIC ACIDS; INORGANIC COMPOUNDS; IONIZING RADIATIONS; IONS; MICROSCOPY; NONMETALS; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; RADIATIONS; SCATTERING; SOLID ELECTROLYTE FUEL CELLS; SPECTROSCOPY; SURFACE PROPERTIES
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.