Synthesis of nano-crystalline La1-xSrxCoO3-delta perovskite oxides by EDTA-citrate complexing process and its catalytic activity for soot oxidation

Authors
Prasad, D. HariPark, S. Y.Oh, E-OJi, H.Kim, H-R.Yoon, K-J.Son, J-W.Lee, J-H.
Issue Date
2012-12-07
Publisher
ELSEVIER
Citation
APPLIED CATALYSIS A-GENERAL, v.447, pp.100 - 106
Abstract
In the present study, La1-xSrxCoO3-delta(x = 0.2, 03, 0.4, 0.5) perovskite nano-particles have been successfully prepared by EDTA-citrate complexing process and the catalytic performance was examined for the soot oxidation activity. The physio-chemical properties of these materials were characterized by means of X-ray diffraction (XRD), thermogravimetry-differential thermal (TG-DTA) analysis, BET surface area and X-ray photoelectron spectroscopy (XPS) analysis, scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS) analysis. TG-DTA analysis suggested that, in the temperature range of 350-500 degrees C, the pyrolysis of metal/nitrate/citrate/EDTA complexes takes place and the single phase La1-xSrxCoO3-delta perovskite oxides can be formed at 900 degrees C and the phase formation has been confirmed by XRD analysis. The surface composition of the samples derived from XPS analysis indicated an impoverishment of lanthanum content at the surface with the increase of strontium content. For La0.6Sr0.4CoO3-delta sample, Sr-enriched perovskite surface has been observed along with the more number of surface oxides (M(Sr, La, Co)-O) resulting in higher catalytic activity for soot oxidation than the others. (C) 2012 Elsevier B.V. All rights reserved.
Keywords
SURFACE CHARACTERIZATION; SOLID-SOLUTIONS; CEO2 CATALYSTS; FUEL-CELLS; TEMPERATURE; OXYGEN; BEHAVIOR; CATHODE; LACOO3; COPRECIPITATION; SURFACE CHARACTERIZATION; SOLID-SOLUTIONS; CEO2 CATALYSTS; FUEL-CELLS; TEMPERATURE; OXYGEN; BEHAVIOR; CATHODE; LACOO3; COPRECIPITATION; La1-xSrxCoO3-delta perovskite oxides; EDTA-citrate complexing process; Soot oxidation
ISSN
0926-860X
URI
https://pubs.kist.re.kr/handle/201004/128555
DOI
10.1016/j.apcata.2012.09.008
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KIST Article > 2012
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