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dc.contributor.author
Garcés, D.  
dc.contributor.author
Wang, H.  
dc.contributor.author
Barnett, S.A.  
dc.contributor.author
Leyva, Adelma Graciela  
dc.contributor.author
Napolitano, Federico Ricardo  
dc.contributor.author
Fuentes, Rodolfo Oscar  
dc.contributor.author
Troiani, Horacio Esteban  
dc.contributor.author
Mogni, Liliana Verónica  
dc.date.available
2020-08-26T15:10:45Z  
dc.date.issued
2018-08  
dc.identifier.citation
Garcés, D.; Wang, H.; Barnett, S.A.; Leyva, Adelma Graciela; Napolitano, Federico Ricardo; et al.; An insight into the electrochemical performance of La0.5-XPrxBa0.5CoO3- δ as cathodes for solid oxide fuel cells: Study of the O2-reduction reaction; Royal Society of Chemistry; Journal of Materials Chemistry A; 6; 34; 8-2018; 16699-16709  
dc.identifier.issn
2050-7488  
dc.identifier.uri
http://hdl.handle.net/11336/112434  
dc.description.abstract
New LT-SOFC cathodes with La0.5-xPrxBa0.5CoO3-δ (0 ≤ x ≤ 0.5) compositions were studied. The La-rich compounds exhibit an inter-growing cubic and tetragonal structure whereas the Pr-rich show a tetragonal structure. Cathode polarization resistances, estimated from electrochemical impedance (EIS), take values around 0.15 and 0.04 Ω cm2 in air at 600 and 700 °C, respectively. The O2-reduction mechanism and its kinetic coefficients, O-ion diffusion (Dchem) and O-surface exchange (kchem), were studied by applying the ALS model for macro homogenous porous electrodes to the EIS data, in combination with microstructural parameters obtained from three-dimensional tomography using focused ion beam-scanning electron microscopy (3D FIB-SEM). The diffusion coefficients for samples with mixing of phases take values of Dchem ∼ 10-6 cm2 s-1, at 700 °C in air, whereas the pure tetragonal phases present lower values Dchem ∼ 10-8 cm2 s-1. On the contrary the kchem for all samples takes values ranging between 0.4 and 1 × 10-4 cm s-1 at 700 °C in air. In addition, the origin of time evolution of polarization at 700 °C in air was evaluated by combining the EIS spectra as a function of time and the ex situ sample characterization of fresh and tested samples by 3D FIB-SEM tomography and inductively coupled plasma-optical emission spectrometry (ICP-OES). Little changes of microstructures were detected, whereas an increasing of the amount of a water-soluble Ba surface species in comparison with total cation surface segregation was observed for all samples after the ageing. This may constitute the main reason causing the polarization resistance degradation. However, the analysis of time evolution shows, that contrary to the situations reported for SrO segregation in Sr-based perovskites, the Dchem is the coefficient mainly affected for compositions with inter-grown phases. At the same time, both Dchem and kchem decreases with time when only the tetragonal phase is present.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Royal Society of Chemistry  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
IT-SOFC  
dc.subject
cathode  
dc.subject
degradation  
dc.subject
FIB-SEM  
dc.subject.classification
Ingeniería de los Materiales  
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Ingeniería de los Materiales  
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INGENIERÍAS Y TECNOLOGÍAS  
dc.title
An insight into the electrochemical performance of La0.5-XPrxBa0.5CoO3- δ as cathodes for solid oxide fuel cells: Study of the O2-reduction reaction  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-10-15T17:54:26Z  
dc.identifier.eissn
2050-7496  
dc.journal.volume
6  
dc.journal.number
34  
dc.journal.pagination
16699-16709  
dc.journal.pais
Reino Unido  
dc.description.fil
Fil: Garcés, D.. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina  
dc.description.fil
Fil: Wang, H.. Northwestern University; Estados Unidos  
dc.description.fil
Fil: Barnett, S.A.. Northwestern University; Estados Unidos  
dc.description.fil
Fil: Leyva, Adelma Graciela. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Universidad Nacional de San Martín. Escuela de Ciencia y Tecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Napolitano, Federico Ricardo. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina  
dc.description.fil
Fil: Fuentes, Rodolfo Oscar. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Troiani, Horacio Esteban. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina  
dc.description.fil
Fil: Mogni, Liliana Verónica. Comisión Nacional de Energía Atómica. Centro Atómico Bariloche; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Patagonia Norte; Argentina  
dc.journal.title
Journal of Materials Chemistry A  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://xlink.rsc.org/?DOI=C8TA04338H  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/c8ta04338h