Issue 6, 2016

Unique reaction mechanism of preferential oxidation of CO over intermetallic Pt3Co catalysts: surface-OH-mediated formation of a bicarbonate intermediate

Abstract

A mechanistic study was performed regarding the preferential oxidation of CO in excess H2 (PROX) over a Pt3Co intermetallic compound supported on various metal oxides (Pt3Co/MOx: MOx = SiO2, Al2O3, MgO, CaO, and La2O3). The Pt3Co/MgO catalyst exhibited the highest catalytic activity (97% CO conversion at 100 °C). CO chemisorption analysis revealed that (1) the Pt dispersion differed depending on the nature of the support and preparation conditions, and (2) the catalytic activity strongly depended on the Pt dispersion but not on the acid–base properties of the support. The kinetic study suggested that CO and O2 adsorbed competitively on Co sites. In situ Fourier transform infrared analysis using D2 indicated that, at a low temperature (<60 °C), a bicarbonate species was formed as a reaction intermediate from CO, O2, and hydrogen that was supplied by the surface hydroxyl groups, not gas phase H2, followed by its decomposition to CO2 and H2O in a 1 : 1 ratio. At a high temperature (>80 °C), gas phase H2 is likely to participate in the formation of the bicarbonate-like intermediate. This study provides the first spectroscopic evidence of bicarbonate formation as an intermediate and the contribution of surface hydroxyl groups toward catalysis. The proposed reaction mechanism based on bicarbonate formation is unique compared with those reported for other PROX systems.

Graphical abstract: Unique reaction mechanism of preferential oxidation of CO over intermetallic Pt3Co catalysts: surface-OH-mediated formation of a bicarbonate intermediate

Supplementary files

Article information

Article type
Paper
Submitted
29 Sep 2015
Accepted
10 Dec 2015
First published
15 Dec 2015

Catal. Sci. Technol., 2016,6, 1642-1650

Author version available

Unique reaction mechanism of preferential oxidation of CO over intermetallic Pt3Co catalysts: surface-OH-mediated formation of a bicarbonate intermediate

S. Furukawa, K. Ehara and T. Komatsu, Catal. Sci. Technol., 2016, 6, 1642 DOI: 10.1039/C5CY01652E

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