Influences of Simultaneous Substitution of Ce4+ and Cu2+ in LaFeO3 Perovskites on Surface Chemistry and Catalytic Activity for CO Oxidation
Influences of Simultaneous Substitution of Ce4+ and Cu2+ in LaFeO3 Perovskites on Surface Chemistry and Catalytic Activity for CO Oxidation
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摘要: Carbon monoxide (CO) in cigarette smoke is a product of tobacco pyrolysis and combustion. The purpose of this study was to investigate the effects of simultaneous substitutions of Ce4+ and Cu2+ in LaFeO3 perovskites on catalytic activity for CO oxidation. La1-xCexFe1-yCuyO3 perovskites were prepared from citrate,and the bulk structure and the surface properties were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and temperature-programmed reduction in H2 (H2-TPR). It was observed that, when La3+ (A-site) and Fe3+ (B-site) of LaFeO3 perovskites were partially substituted by Ce4+ and Cu2+, the catalytic activity was greatly improved. La0.7Ce0.3Fe0.9M0.1O3 showed the best catalytic activity for oxidation of CO in the presence of O2. When A-site (La3+ ) of LaFeO3 perovskites was partially substituted by Ce4+, the catalytic oxidation activity was directly correlated with its redox properties, which indicated that the catalytic oxidation reaction on the La1-xCexFeO3 perovskites followed the process of intrafacial reactions. When A-site (La3+ ) and B-site (Fe3+ ) of LaFeO3 perovskites was simultaneously substituted by Ce4+ and Cu2+, its catalytic oxidation activity was closely correlated with both the anion defect concentration and redox properties, which indicated that the catalytic oxidation reaction on the La1-xCexFe1-yCuyO3 perovskites followed both suprafacial process and intrafacial reactions.Abstract: Carbon monoxide (CO) in cigarette smoke is a product of tobacco pyrolysis and combustion. The purpose of this study was to investigate the effects of simultaneous substitutions of Ce4+ and Cu2+ in LaFeO3 perovskites on catalytic activity for CO oxidation. La1-xCexFe1-yCuyO3 perovskites were prepared from citrate,and the bulk structure and the surface properties were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and temperature-programmed reduction in H2 (H2-TPR). It was observed that, when La3+ (A-site) and Fe3+ (B-site) of LaFeO3 perovskites were partially substituted by Ce4+ and Cu2+, the catalytic activity was greatly improved. La0.7Ce0.3Fe0.9M0.1O3 showed the best catalytic activity for oxidation of CO in the presence of O2. When A-site (La3+ ) of LaFeO3 perovskites was partially substituted by Ce4+, the catalytic oxidation activity was directly correlated with its redox properties, which indicated that the catalytic oxidation reaction on the La1-xCexFeO3 perovskites followed the process of intrafacial reactions. When A-site (La3+ ) and B-site (Fe3+ ) of LaFeO3 perovskites was simultaneously substituted by Ce4+ and Cu2+, its catalytic oxidation activity was closely correlated with both the anion defect concentration and redox properties, which indicated that the catalytic oxidation reaction on the La1-xCexFe1-yCuyO3 perovskites followed both suprafacial process and intrafacial reactions.
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