Properties of Pt/C catalyst modified by chemical vapor deposition of Cr as a cathode of phosphoric acid fuel cell
- 1. School of Chemical and Biological Engineering and Institute of Chemical Process, Seoul National University, San 56-1, Shillim-dong, Kwanak-ku, Seoul 151-744 (Korea, Republic of)
Description
Cr-modified Pt/C catalysts were prepared by the chemical vapour deposition (CVD) of Cr on Pt/C, and their performance as a cathode of phosphoric acid fuel cell (PAFC) was compared with the case of catalysts containing Cr added by impregnation (IMP). The catalyst prepared by CVD showed a higher activity for oxygen reduction reaction (ORR) than one prepared by IMP. There was an optimum amount of Cr that yielded the maximum mass activity of the catalyst because the gain in the intrinsic activity due to the promotional effect of Cr was counterbalanced by the loss of exposed Pt surface area as a result of the Cr introduction. Nevertheless, the activity increase at the optimum amount of Cr was greater for the CVD catalyst than for the IMP catalyst. Also, the optimum amount of Cr to yield the maximum activity was smaller for the former catalyst [Cr/Pt]CVD = 0.6, than for the latter, [Cr/Pt]IMP = 1.0. The enhancement of the Pt catalyst activity by Cr addition is attributed to two factors: changes in the surface Pt-Pt spacing and the electronic modification of the Pt surface. The formation of a Pt-Cr alloy, as confirmed by X-ray diffraction, decreased the lattice parameter of Pt, which was beneficial to the catalyst activity for ORR. X-ray photoelectron spectroscopy results showed that the binding energies of Pt electrons were shifted to higher energies due to Cr modification. Accordingly, the electron density of Pt was lowered and the Pt-O bond became weak on the Cr-modified catalysts, which was also beneficial to the catalyst activity for ORR. The promotion of oxygen reduction on Cr-modified catalysts was confirmed by measuring the cyclic voltammograms of the catalysts. All the above changes were made more effectively for catalysts prepared by CVD than for those prepared by IMP because the former method allowed Cr to interact more closely with the Pt surface than the latter, which was demonstrated by the characterization of catalysts in this study
Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2006.03.104;
- PII
- S0013-4686(06)00416-6;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 52
- Journal Issue
- 4
- Journal Page Range
- p. 1676-1682
- ISSN
- 0013-4686
- CODEN
- ELCAAV
Conference
- Title
- 56. annual meeting of the International Society of Electrochemistry
- Dates
- 25-30 Sep 2005
- Place
- Busan (Korea, Republic of)
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 38028950
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ACID ELECTROLYTE FUEL CELLS; BINDING ENERGY; CATHODES; CHEMICAL VAPOR DEPOSITION; ELECTROCATALYSTS; ELECTRON DENSITY; LATTICE PARAMETERS; PERFORMANCE; PHOSPHORIC ACID; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- CATALYSTS; CHEMICAL COATING; COHERENT SCATTERING; DEPOSITION; DIFFRACTION; DIRECT ENERGY CONVERTERS; ELECTROCHEMICAL CELLS; ELECTRODES; ELECTRON SPECTROSCOPY; ENERGY; FUEL CELLS; HYDROGEN COMPOUNDS; INORGANIC ACIDS; INORGANIC COMPOUNDS; OXYGEN COMPOUNDS; PHOSPHORUS COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; SCATTERING; SPECTROSCOPY; SURFACE COATING
Optional Information
- Copyright
- Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.