Abstract
A Ce0.9Pr0.1O2 catalyst has been prepared using nitrates as metal precursors, which have been infiltrated into a polymethylmethacrylate colloidal crystal template and calcined at 500 °C. Its catalytic activity for CO oxidation (4.3 μmolCO s−1 gcatalyst −1 at 300 °C) is far superior compared to a reference catalyst prepared in the same way but without the template (1.4 μmolCO s−1 gcatalyst −1 at 300 °C), and even superior to a three dimensionally ordered macroporous (3DOM) catalyst prepared forming metal citrates to obtain the macroporous structure into the template (0.7 μmolCO s−1 gcatalyst −1 at 300 °C). It is demonstrated that infiltration of nitrates into the colloidal crystal template is more positive for catalytic oxidation of CO than formation of the 3DOM structure using citrates, despite the collapse of the macroporous structure. The 3DOM catalyst prepared with citrates has lower surface area (51 m2 g−1) than catalysts prepared using nitrates (118 and 87 m2 g−1 for the infiltrated and non infiltrated catalysts, respectively). The infiltrated catalyst prepared with nitrates reaches the highest surface area, and also develops more micro and mesoporosity and presents smaller crystallite size (8 vs. 16 nm) than the counterpart non infiltrated catalyst. In addition, the population of oxygen vacancies is also much higher in the infiltrated catalyst prepared with nitrates, and it is postulated that this improves oxygen mobility into the mixed oxide lattice and favors the catalyst reduction. On the contrary, it has been ruled out any effect of the infiltration step in the insertion of Pr cations into the ceria lattice.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.