Investigation of the NO reduction by CO reaction over oxidized and reduced NiOx/CeO2 catalysts

Abstract

CeO2-supported NiOx catalysts have been widely studied in various catalytic reactions including NO reduction by CO. This work is mainly focused on investigation of the impact of catalyst synthesis conditions (e.g., oxidation and reduction) on the physicochemical properties of NiOx/CeO2 catalysts and the catalytic response for the NO reduction by CO reaction. The oxide NiOx/CeO2 sample was prepared by an incipient wetness impregnation (IWI) method and reduced under hydrogen reduction treatment at high temperatures (500 and 700 °C). The physicochemical properties of the synthesized samples were characterized by BET analysis, Raman spectroscopy, XRD, XPS, EELS and high-resolution transmission electron microscopy (HR-TEM). The results showed that higher reduction temperature led to the decrease in specific surface area (SSA), fewer oxygen vacancy/defect site, larger crystallite size of the CeO2 support, and formation of metallic Ni on the surface. The oxidized NiOx/CeO2 catalyst showed the highest catalytic activity, indicating that the presence of oxygen vacancy/defect sites, Ni2+ oxidation state, and smaller crystallite size are believed to enhance the catalytic activity. In situ DRIFTS confirmed the generation of several intermediate species, such as nitrate, carbonate, and N2O. On the basis of in situ DRIFTS and activity results, the possible reaction mechanism of NO reduction by CO over NiOx/CeO2 was proposed.

Graphical abstract: Investigation of the NO reduction by CO reaction over oxidized and reduced NiOx/CeO2 catalysts

Supplementary files

Article information

Article type
Paper
Submitted
07 Jul 2021
Accepted
08 Oct 2021
First published
11 Oct 2021

Catal. Sci. Technol., 2021, Advance Article

Investigation of the NO reduction by CO reaction over oxidized and reduced NiOx/CeO2 catalysts

K. Lee, G. Kwon, S. Hwang, J. A. Boscoboinik and T. Kim, Catal. Sci. Technol., 2021, Advance Article , DOI: 10.1039/D1CY01215K

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