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
Hauptverfasser: Gao, Yibo, Teng, Shichang, Wang, Zhongpeng, Wang, Baoqin, Liu, Wei, Liu, Wenxu, Wang, Liguo
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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.
ISSN:0022-2461
1573-4803
DOI:10.1007/s10853-019-03973-z