A Noble-Metal-Free Ce0.90Co0.10O2 – δ Catalyst with Enhanced
Three-Way Catalytic Performance1
Bhaskar Devu Mukri*
Independent Researcher, Uttara Kannada, Karnataka, 581327 India
Correspondence to: *e-mail: bhaskardm@gmail.com
1Abbreviations and notation: OSC, oxygen storage capacity; TWC, three-way catalytic reaction; HCM, honeycomb structured cordierite monolith; PXRD, powder X-ray diffraction; XPS, X-ray photoelectron spectroscopy; TEM, transmission electron microscopy; H2-TPR, H2-temperature programmed reduction; HC, hydrocarbon.
Received 16 January, 2021
Abstract—Co ion doped ceria, Ce0.90Co0.10O2 – δ, and Pd ion doped ceria, Ce0.98Pd0.02O2 – δ, were coated on honeycomb structured cordierite monolith by solution combustion method. The dip–dry–heat procedure was followed for the catalyst coating on the monolith. The color of the monolith confirmed the highly crystalline fluorite structure of the catalytic coating. X-ray diffraction and transmission electron microscopy studies confirmed the single phase of Co ion doped CeO2, and the particle size of about 9 nm was determined by the particle-size distribution curve. Ce0.90Co0.10O2 – δ showed little higher catalytic activities than Ce0.98Pd0.02O2 – δ in CO oxidation, hydrocarbons oxidation, and NO reduction by CO. Three-way catalytic reactions over Ce0.90Co0.10O2 – δ were competitively better than those over Ce0.98Pd0.02O2 – δ. The X-ray photoelectron spectroscopy study confirmed that some of Co3+ ions are reduced to Co2+ ions after three-way catalytic reactions on Ce0.90Co0.10O2 – δ catalyst due to the utilization of excess lattice oxygen for the oxidation reaction. Economically, Ce0.90Co0.10O2 – δ catalyst is far preferable than Ce0.98Pd0.02O2 – δ catalyst due to the high expense of noble metals compared to other transition metals.
Keywords: Ce0.90Co0.10O2 – δ catalyst, characterization, CO oxidation, HC oxidation, CO + NO reaction
DOI: 10.1134/S0023158421060136