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dc.contributor.author
Grunbaum, Nicolas
dc.contributor.author
Dessemond, L.
dc.contributor.author
Fouletier, J.
dc.contributor.author
Prado, Fernando Daniel
dc.contributor.author
Caneiro, Alberto
dc.date.available
2019-03-26T15:49:07Z
dc.date.issued
2006-03
dc.identifier.citation
Grunbaum, Nicolas; Dessemond, L.; Fouletier, J.; Prado, Fernando Daniel; Caneiro, Alberto; Electrode reaction of Sr1-xLaxCo0.8Fe0.2 O3-δ with x = 0.1 and 0.6 on Ce0.9Gd0.1O1.95 at 600 ≤ T ≤ 800 °C; Elsevier Science; Solid State Ionics; 177; 9-10; 3-2006; 907-913
dc.identifier.issn
0167-2738
dc.identifier.uri
http://hdl.handle.net/11336/72539
dc.description.abstract
The electrode reaction of the perovskite phases Sr1-xLaxCo0.8Fe0.2O 3-δ (x = 0.1 and 0.6) on Ce0.9Gd0.1O1.95 has been investigated by impedance spectroscopy in the temperature range 600 ≤ T ≤ 800 °C. Thick porous electrodes (t ∼ 20 μm) were sprayed on Ce0.9Gd0.1O1.95 and ac impedance spectra were recorded on symmetrical cells at the equilibrium. The analysis of the complex impedance diagrams clearly indicates the presence of two contributions. The low frequency one was assigned to the gas phase oxygen diffusion through the porous electrode and a finite length diffusion (Warburg) impedance was used to describe the high frequency (HF) data. The polarization resistance of the HF impedance contribution (Rw) is higher for x = 0.1 while the activation energy of Rw is higher for x = 0.6. The variations of Rw versus the La content, temperature and thickness indicate that the Warburg-type impedance contains information of both bulk oxygen diffusion and surface processes. © 2006 Elsevier B.V. All rights reserved.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Elsevier Science
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Cobaltites
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Electrode Reaction
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Impedance Spectroscopy
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Mixed Conductors
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Sofc
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Otras Ciencias Químicas
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Electrode reaction of Sr1-xLaxCo0.8Fe0.2 O3-δ with x = 0.1 and 0.6 on Ce0.9Gd0.1O1.95 at 600 ≤ T ≤ 800 °C
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2019-03-15T19:22:38Z
dc.journal.volume
177
dc.journal.number
9-10
dc.journal.pagination
907-913
dc.journal.pais
Países Bajos
dc.journal.ciudad
Amsterdam
dc.description.fil
Fil: Grunbaum, Nicolas. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina
dc.description.fil
Fil: Dessemond, L.. Laboratoire d'Electrochimie et de Physicochimie des Matériaux et des Interfaces; Francia
dc.description.fil
Fil: Fouletier, J.. Laboratoire d'Electrochimie et de Physicochimie des Matériaux et des Interfaces; Francia
dc.description.fil
Fil: Prado, Fernando Daniel. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina
dc.description.fil
Fil: Caneiro, Alberto. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina
dc.journal.title
Solid State Ionics
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1016/j.ssi.2006.02.009
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S0167273806000920
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