DOI

The paper is focused on the Fe for Co substitution effect on the redox and catalytic properties in the perovskite structure of GdFeO3. The solid oxides with the composition GdFe1−xCoxO3 (x = 0; 0.2; 0.5; 0.8; 1) were obtained by the sol-gel method and characterized by var-ious methods: X-Ray diffraction (XRD), temperature-programmed reduction (H2-TPR), N2 sorp-tion, temperature-programmed desorption of oxygen (TPD-O2), simultaneous thermal analysis (STA), and X-ray photoelectron spectroscopy (XPS). The H2-TPR results showed that an increase in the cobalt content in the GdFe1−xCoxO3 (x = 0; 0.2; 0.5; 0.8; 1) leads to a decrease in the reduction temperature. Using the TPD-O2 and STA methods, the lattice oxygen mobility is increasing in the course of the substitution of Fe for Co. Thus, the Fe substitution in the perovskite leads to an im-provement in the oxygen reaction ability. Experiments on the soot oxidation reveal that catalytic oxidation ability increases in the series: GdFe0.5Co0.5O3 ˂ GdFe0.2Co0.8O3 ˂ GdCoO3, which is in good correlation with the increasing oxygen mobility according to H2-TPR, TPD-O2, and STA results. The soot oxidation over GdFeO3 and GdFe0.8Co0.2O3 is not in this range due to the impurities of iron oxides and higher specific surface area.

Original languageEnglish
Article number1256
Number of pages10
JournalCatalysts
Volume11
Issue number10
DOIs
StatePublished - 19 Oct 2021

    Scopus subject areas

  • Catalysis
  • Physical and Theoretical Chemistry

    Research areas

  • Perovskites, Soot oxidation, Temperature-programmed reaction, Transition metal oxides, perovskites, NO, MN, COMBUSTION, transition metal oxides, temperature-programmed reaction, CO, soot oxidation, CALCINATION TEMPERATURE, METHANE PARTIAL OXIDATION, REMOVAL, RARE-EARTH, XPS, LATTICE OXYGEN

ID: 87764313