Issue 2, 2013

An ultra-stable nanosized Ce0.9Fe0.1O2 solid solution with an excellent catalytic performance towards CH4 oxidation

Abstract

Activation of the C–H bonds in CH4 is relatively difficult, since CH4 is a quite a stable hydrocarbon with an extremely high ignition temperature (>1600 °C), which usually causes sintering and deactivation of catalysts. It remains a challenge to find catalysts that can show both good catalytic activity and thermal stability. In this work, Fe3+ doped CeO2 nanoparticles were initially prepared and tested for catalytic activity towards CH4 combustion. Systematic sample characterizations indicate that our nanoparticles were exposed by highly energetic facets (200), which yielded an excellent catalytic performance and thermal stability. The total conversion of CH4 at a specific velocity of 60 000 ml g−1 h−1 appeared at T100 = 520 °C, about 100 °C lower than that under similar test conditions previously reported for the best Ce–Fe–O solid solution catalysts. Strikingly, the present nanoparticles were also merited by an ultra-high thermal stability, since no particle growth or agglomeration is detected after high-temperature treatment, and since both the structure and oxygen species of the catalysts did not change at all before and after catalytic tests. The catalysts did not show any sign of deactivation, even when the test time was beyond 100 h. The surface oxygen species on the exposed (200) plane of the nanoparticles could be beneficial for the excellent catalytic performance towards CH4 combustion.

Graphical abstract: An ultra-stable nanosized Ce0.9Fe0.1O2 solid solution with an excellent catalytic performance towards CH4 oxidation

Supplementary files

Article information

Article type
Paper
Submitted
03 Sep 2012
Accepted
04 Oct 2012
First published
05 Oct 2012

J. Mater. Chem. A, 2013,1, 374-380

An ultra-stable nanosized Ce0.9Fe0.1O2 solid solution with an excellent catalytic performance towards CH4 oxidation

Y. Zuo, X. Huang, L. Li and G. Li, J. Mater. Chem. A, 2013, 1, 374 DOI: 10.1039/C2TA00167E

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