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dc.contributor.author
Vega Castillo, Jesús Eduardo  
dc.contributor.author
Ravella, Uday K.  
dc.contributor.author
Corbel, Gwenaël  
dc.contributor.author
Lacorre, Philippe  
dc.contributor.author
Caneiro, Alberto  
dc.date.available
2016-01-13T15:12:10Z  
dc.date.issued
2013-11  
dc.identifier.citation
Vega Castillo, Jesús Eduardo; Ravella, Uday K.; Corbel, Gwenaël; Lacorre, Philippe; Caneiro, Alberto; Thermodynamic stability of La2Mo2−yWyO9, La2Mo2−yWyO8.96+0.02y and La7Mo7(2−y)/2W7y/2O30 (y = 0, 0.5 and 1.0); Royal Society of Chemistry; Dalton Transactions; 43; 6; 11-2013; 2661-2669  
dc.identifier.issn
1477-9226  
dc.identifier.uri
http://hdl.handle.net/11336/3576  
dc.description.abstract
The role of W content on the limit oxygen partial pressure (pO2) for stability of fast oxygen-ion conductors La2Mo2−yWyO9 with y = 0, 0.5 and 1.0 has been studied by means of thermogravimetric analysis (TGA) under controlled atmospheres. At 718 °C, below the pO2 stability limit of La2Mo2−yWyO9, the perovskite related compounds La7Mo7(2−y)/2W7y/2O30 were stabilized even for y = 1.0. At 608 °C, the first stage of reduction of β-La2Mo2−yWyO9 leads to the formation of the crystallized oxygen deficient La2Mo2−yWyO8.6+0.02y phase. X-ray powder diffraction shows that the stabilization of the high temperature β-form through tungsten substitution observed in fully oxidized La2Mo2−yWyO9 samples is preserved upon slight reduction. The n-type conductivity arising from the mixed valence state of molybdenum becomes less and less predominant as the W content increases. Further reduction causes amorphization. At both temperatures, W substitution does not enhance the thermodynamic stability of the La2Mo2−yWyO9 ion conductor under a reducing atmosphere but only slows down the kinetics of reduction.  
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
Lamox  
dc.subject
Thermodynamic  
dc.subject
Stability  
dc.subject.classification
Química Inorgánica y Nuclear  
dc.subject.classification
Ciencias Químicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Thermodynamic stability of La2Mo2−yWyO9, La2Mo2−yWyO8.96+0.02y and La7Mo7(2−y)/2W7y/2O30 (y = 0, 0.5 and 1.0)  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2016-03-30 10:35:44.97925-03  
dc.journal.volume
43  
dc.journal.number
6  
dc.journal.pagination
2661-2669  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Cambridge  
dc.description.fil
Fil: Vega Castillo, Jesús Eduardo. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Patagonia Norte; Argentina  
dc.description.fil
Fil: Ravella, Uday K.. Université du Maine. Institut des Molécules et Matériaux du Mans; Francia  
dc.description.fil
Fil: Corbel, Gwenaël. Université du Maine. Institut des Molécules et Matériaux du Mans; Francia  
dc.description.fil
Fil: Lacorre, Philippe. Université du Maine. Institut des Molécules et Matériaux du Mans; Argentina  
dc.description.fil
Fil: Caneiro, Alberto. Comisión Nacional de Energía Atómica; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Area de Energía Nuclear. Instituto Balseiro; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Patagonia Norte; Argentina  
dc.journal.title
Dalton Transactions  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2014/DT/C3DT52174E#!divAbstract  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://dx.doi.org/DOI:10.1039/C3DT52174E