Issue 35, 2015

Pt/porous nanorods of ceria as efficient high temperature catalysts with remarkable catalytic stability for carbon dioxide reforming of methane

Abstract

Porous nanorods of ceria (PN-ceria) with a large oxygen storage capacity and a high concentration of oxygen vacancies exhibited better thermal stability compared to other nanocerias. No obvious structural deconstruction of PN-ceria was observed when the material was annealed at 800 °C. As the support of metal nanocatalysts, Pt exhibited a high dispersion on PN-ceria and presented a high activity and catalytic stability for the carbon dioxide reforming of methane (CRM) reaction at a high temperature of 800 °C. The catalytic activity of Pt/PN-ceria catalysts in terms of methane conversion only slightly decreased from 77.3% to 74.2% with a slow carbon deposition rate of 0.1 mg coke gcat−1 h−1 after 72 hours of the CRM reaction at 800 °C. In contrast, a large decay in methane conversion (16.2%) was observed for Pt/nonporous nanorods of ceria under the same reaction conditions. The high and robust catalytic activity of Pt/PN-ceria catalysts can be ascribed to the unique physicochemical properties of PN-ceria, by preventing the sintering of Pt nanocatalysts into big particles and the formation of coke under rigid reaction conditions. Hence, more accessible active sites of Pt/PN-ceria catalysts are provided for the CRM. Besides, the high concentration of oxygen vacancies and fast mobility of the lattice oxygen of PN-ceria also benefited the catalytic activity, stability and anti-coke deposition.

Graphical abstract: Pt/porous nanorods of ceria as efficient high temperature catalysts with remarkable catalytic stability for carbon dioxide reforming of methane

Supplementary files

Article information

Article type
Paper
Submitted
11 May 2015
Accepted
24 Jul 2015
First published
27 Jul 2015

J. Mater. Chem. A, 2015,3, 18074-18082

Author version available

Pt/porous nanorods of ceria as efficient high temperature catalysts with remarkable catalytic stability for carbon dioxide reforming of methane

Z. Zhang, J. Li, W. Gao, Y. Ma and Y. Qu, J. Mater. Chem. A, 2015, 3, 18074 DOI: 10.1039/C5TA03448E

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