Enhanced catalytic performance of cobalt and iron co-doped ceria catalysts for soot combustion
A series of promising Ce–Co–Fe catalysts were successfully synthesized using a cetyl-trimethylammonium-bromide-assisted co-precipitation method and investigated for diesel soot combustion. The surface morphological and structural properties were systematically examined using various techniques: X-ra...
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Veröffentlicht in: | Journal of materials science 2020, Vol.55 (1), p.283-297 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A series of promising Ce–Co–Fe catalysts were successfully synthesized using a cetyl-trimethylammonium-bromide-assisted co-precipitation method and investigated for diesel soot combustion. The surface morphological and structural properties were systematically examined using various techniques: X-ray diffraction, scanning electron microscope, N
2
adsorption–desorption, Raman spectroscopy, temperature-programmed reduction and in situ diffuse reflection infrared Fourier transform spectroscopy. The catalyst–soot combustion activities were tested in O
2
and NO + O
2
using a temperature-programmed technique. Nanometer crystalline solid solutions were formed with high surface areas when the Fe and Co cations were co-doped in the ceria lattice. Transition metals doping played a key role in increasing oxygen vacancies and promoting the redox performance of Ce–Co–Fe catalysts. Co–Fe co-doping accelerated the oxidation of soot under both “tight” and “loose” contact conditions. Among all the ceria-based catalysts, Ce
80
Co
15
Fe
5
showed superior activity with
T
10
= 256 °C and high selectivity with
S
CO
2
=
100
%
under tight a contact mode. The observed high catalytic activity following co-doping was proved to have occurred because of various reasons such as improved redox properties, increased oxygen vacancies and high surface area. The presence of NO in O
2
also promoted soot oxidation, which follows the NO
2
-assisted mechanism. Moreover, the in situ DRIFTS performed under an isothermal condition in NO + O
2
confirmed the strong adsorption capacity for NO
x
species on the doped ceria catalyst. |
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ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-019-03973-z |