Cerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cells
Highly homogeneous (Ce,Tb) oxides are prepared by a microemulsion technique, and their structural and electronic state after high temperature calcination is examined with X-ray diffraction, high resolution transmission electron microscopy, X-ray photoelectron and absorption (XANES) spectroscopies an...
| Autores: | , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2005 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/173090 |
| Acceso en línea: | http://hdl.handle.net/10261/173090 |
| Access Level: | acceso abierto |
| Palabra clave: | Cerium oxide Terbium oxide Solid oxide fuel cell Anode Structure Surface area |
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Cerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cellsMartínez Arias, ArturoHungría, Ana B.Iglesias Juez, AnaConesa Cegarra, José CarlosMather, Glenn C.Munuera, GuillermoFernández, M.Cerium oxideTerbium oxideSolid oxide fuel cellAnodeStructureSurface areaHighly homogeneous (Ce,Tb) oxides are prepared by a microemulsion technique, and their structural and electronic state after high temperature calcination is examined with X-ray diffraction, high resolution transmission electron microscopy, X-ray photoelectron and absorption (XANES) spectroscopies and impedance spectroscopy measurements. Addition of Tb stabilizes significantly (in comparison to pure ceria) specific surface area and small particles sizes during high temperature calcination (up to 1100 °C); phase decomposition at these high temperatures, similar to that occurring when stabilization of ceria is carried out with Zr, does not occur, and the mixed oxide remains homogeneous throughout. Tb addition to ceria may thus be beneficial when used as a component of SOFC anodes. TEM data indicate reshaping of oxide particles and provide evidence of crystal superstructures after high temperature treatments, while XPS and XANES reveal an increase in the Tb4+/Tb3+ ratio (for a given pretreatment) with the Tb/Ce ratio; Ce seems to be less reducible to Ce3+ in the presence of Tb. Total electrical conductivity of CT samples under H2 is mediated by electron transport (involving probably only Ce) and is lower than in gadolinia-doped ceria (GCO); in air conductivity is higher than for GCO, particularly at low temperatures, and it is probable that a p-type transport mechanism predominates in this case.Thanks are given to CICYT (Project MAT2003-03925) for financial support of this research, to the Universities of Madrid (Complutense) and Cádiz for the facilities given for the obtention of TEM data, to ICP-Unidad de Apoyo staff for chemical analysis results and XRD recording, to technical staff at Daresbury Laboratory Station 9.3 (Drs. I. Harvey and A.R. Lennie) for the help given during recording of the XAFS spectra, and to Mr. A. Macías for assistance in recording the XPS data.Peer reviewedElsevierComisión Interministerial de Ciencia y Tecnología, CICYT (España)Universidad Complutense de MadridUniversidad de CádizConsejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72]201820182005info:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501Postprintinfo:eu-repo/semantics/acceptedVersionhttp://hdl.handle.net/10261/173090reponame:DIGITAL.CSIC. Repositorio Institucional del CSICinstname:Consejo Superior de Investigaciones Científicas (CSIC)Ingléshttps://doi.org/10.1016/j.jpowsour.2005.02.079Síinfo:eu-repo/semantics/openAccessoai:digital.csic.es:10261/1730902026-05-22T06:33:51Z |
| dc.title.none.fl_str_mv |
Cerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cells |
| title |
Cerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cells |
| spellingShingle |
Cerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cells Martínez Arias, Arturo Cerium oxide Terbium oxide Solid oxide fuel cell Anode Structure Surface area |
| title_short |
Cerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cells |
| title_full |
Cerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cells |
| title_fullStr |
Cerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cells |
| title_full_unstemmed |
Cerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cells |
| title_sort |
Cerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cells |
| dc.creator.none.fl_str_mv |
Martínez Arias, Arturo Hungría, Ana B. Iglesias Juez, Ana Conesa Cegarra, José Carlos Mather, Glenn C. Munuera, Guillermo Fernández, M. |
| author |
Martínez Arias, Arturo |
| author_facet |
Martínez Arias, Arturo Hungría, Ana B. Iglesias Juez, Ana Conesa Cegarra, José Carlos Mather, Glenn C. Munuera, Guillermo Fernández, M. |
| author_role |
author |
| author2 |
Hungría, Ana B. Iglesias Juez, Ana Conesa Cegarra, José Carlos Mather, Glenn C. Munuera, Guillermo Fernández, M. |
| author2_role |
author author author author author author |
| dc.contributor.none.fl_str_mv |
Comisión Interministerial de Ciencia y Tecnología, CICYT (España) Universidad Complutense de Madrid Universidad de Cádiz Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72] |
| dc.subject.none.fl_str_mv |
Cerium oxide Terbium oxide Solid oxide fuel cell Anode Structure Surface area |
| topic |
Cerium oxide Terbium oxide Solid oxide fuel cell Anode Structure Surface area |
| description |
Highly homogeneous (Ce,Tb) oxides are prepared by a microemulsion technique, and their structural and electronic state after high temperature calcination is examined with X-ray diffraction, high resolution transmission electron microscopy, X-ray photoelectron and absorption (XANES) spectroscopies and impedance spectroscopy measurements. Addition of Tb stabilizes significantly (in comparison to pure ceria) specific surface area and small particles sizes during high temperature calcination (up to 1100 °C); phase decomposition at these high temperatures, similar to that occurring when stabilization of ceria is carried out with Zr, does not occur, and the mixed oxide remains homogeneous throughout. Tb addition to ceria may thus be beneficial when used as a component of SOFC anodes. TEM data indicate reshaping of oxide particles and provide evidence of crystal superstructures after high temperature treatments, while XPS and XANES reveal an increase in the Tb4+/Tb3+ ratio (for a given pretreatment) with the Tb/Ce ratio; Ce seems to be less reducible to Ce3+ in the presence of Tb. Total electrical conductivity of CT samples under H2 is mediated by electron transport (involving probably only Ce) and is lower than in gadolinia-doped ceria (GCO); in air conductivity is higher than for GCO, particularly at low temperatures, and it is probable that a p-type transport mechanism predominates in this case. |
| publishDate |
2005 |
| dc.date.none.fl_str_mv |
2005 2018 2018 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article http://purl.org/coar/resource_type/c_6501 Postprint info:eu-repo/semantics/acceptedVersion |
| format |
article |
| status_str |
acceptedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10261/173090 |
| url |
http://hdl.handle.net/10261/173090 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
https://doi.org/10.1016/j.jpowsour.2005.02.079 Sí |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
| eu_rights_str_mv |
openAccess |
| dc.publisher.none.fl_str_mv |
Elsevier |
| publisher.none.fl_str_mv |
Elsevier |
| dc.source.none.fl_str_mv |
reponame:DIGITAL.CSIC. Repositorio Institucional del CSIC instname:Consejo Superior de Investigaciones Científicas (CSIC) |
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Consejo Superior de Investigaciones Científicas (CSIC) |
| reponame_str |
DIGITAL.CSIC. Repositorio Institucional del CSIC |
| collection |
DIGITAL.CSIC. Repositorio Institucional del CSIC |
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1869413778031902720 |
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15,81155 |