Bifunctional catalysts for single-stage water-gas shift reaction in fuel cell applications. Part 1. Effect of the support on the reaction sequence.

K.G.H. Azzam, Igor V. Babych, Kulathuiyer Seshan, Leonardus Lefferts

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Abstract

Oxide support plays a significant role in the mechanistic reaction sequence for the water–gas shift (WGS) reaction over Pt-based catalysts. In situ FTIR spectroscopic and transient kinetic studies have been used to follow the reactions that occur. CeO2-, TiO2-, and ZrO2-supported Pt catalysts have been studied at 300 °C. In all cases, CO is adsorbed on Pt. The role of the support oxide is to activate water, completing the WGS reaction sequence. We have taken into consideration four different pathways that may be involved in the complex WGS reaction scheme: (A) red–ox route, (B) associative formate route, (C) associative formate route with red–ox regeneration of the oxide support, and (D) carbonate route. In the case of Pt/ZrO2, the WGS reaction follows the associative formate route with red–ox regeneration (route C). On Pt/TiO2, both the red–ox route (A) and the associative formate route with red–ox regeneration (C) contribute. The associative formate route (B) is the relevant reaction pathway on Pt/CeO2.
Original languageUndefined
Pages (from-to)153-162
Number of pages10
JournalJournal of catalysis
Volume251
Issue number1
DOIs
Publication statusPublished - 2007

Keywords

  • Carbonate
  • Platinum
  • METIS-244069
  • Associative formate mechanism
  • Zirconia
  • Reaction mechanism
  • Ceria
  • Water-gas shift
  • Titania
  • Red–ox
  • IR-78816

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