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Optimization of Redox and Catalytic Performance of LaFeO3 Perovskites: Synthesis and Physicochemical Properties
La 1− x Ce x FeO 3 perovskites were synthesized through a citric-acid assisted co-precipitation process. X-ray diffraction, transmission electron microscopy, energy dispersive x-ray analysis, thermogravimetric analysis, UV/Vis absorption spectroscopy, Fourier transform infrared spectroscopy, x-ray p...
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Published in: | Journal of electronic materials 2019-07, Vol.48 (7), p.4351-4361 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | La
1−
x
Ce
x
FeO
3
perovskites were synthesized through a citric-acid assisted co-precipitation process. X-ray diffraction, transmission electron microscopy, energy dispersive x-ray analysis, thermogravimetric analysis, UV/Vis absorption spectroscopy, Fourier transform infrared spectroscopy, x-ray photoelectron spectroscopy, and an N
2
-adsorption–desorption technique were applied for characterization of the perovskites. The x-ray analysis exhibited highly purified single-phase orthorhombic nanocrystals. The loading of Ce improved the specific surface area and affects the thermal stability along with the O
2
desorption characteristics. The BET analysis and textural characterization of a high concentration of the Ce-ion-doped LaFeO
3
perovskite revealed a relatively high specific surface area with respect to a low concentration of the doped perovskites, indicating the homogeneous dispersion of Ce ions within the crystal matrix. The oxidation states of trivalent La, Fe, O, and C in all perovskites were identified through an XPS study. The redox behavior was examined using temperature program reduction/oxidation techniques. The La
0.95
Ce
0.05
FeO
3
perovskites exhibited a high specific surface area and the best redox, catalytic, and reusability performances among the prepared catalysts, as revealed by the TPR/TPO, BET, and catalytic activity analyses. |
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ISSN: | 0361-5235 1543-186X |
DOI: | 10.1007/s11664-019-07216-4 |