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dc.contributor.author
Kilo, Martin  
dc.contributor.author
Taylor, Marcela Andrea  
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Argirusis, Christos  
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Borchardt, Günter  
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Lerch, Martin  
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Kaïtasov, Odile  
dc.contributor.author
Lesage, Bernard  
dc.date.available
2019-04-15T14:27:36Z  
dc.date.issued
2004-11  
dc.identifier.citation
Kilo, Martin; Taylor, Marcela Andrea; Argirusis, Christos; Borchardt, Günter; Lerch, Martin; et al.; Nitrogen diffusion in nitrogen-doped yttria stabilised zirconia; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 6; 13; 11-2004; 3645-3649  
dc.identifier.issn
1463-9076  
dc.identifier.uri
http://hdl.handle.net/11336/74366  
dc.description.abstract
Nitrogen self-diffusion was measured in single crystalline nitrogen-doped yttria-stabilised zirconia (YZrON) containing 10 mol% yttrium oxide. Samples containing two different nitrogen contents (5 and 6 mol% N on the anion sublattice) were investigated as a function of temperature (650-1000 K) using implanted N as a stable tracer. For a given temperature, the nitrogen diffusivity was nearly independent of the nitrogen content in the nitrogen-doped yttria-stabilised zirconia, which can be only partially understood using defect chemistry. The activation enthalpy of nitrogen diffusion was between 2 and 2.5 eV with a preexponential factor of the order of 100 cm2 s-1, which corresponds to a migration entropy of 5 kB. The surface exchange reaction between nitrogen and the oxonitride surface was investigated at 1073 K using 200 mbar gaseous 15N2 and was found to be slow but considerable. Decreasing the oxygen content in the gas phase can enhance the nitrogen incorporation into the oxonitrides.  
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
Nitrogen Diffusion  
dc.subject
Sims  
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Astronomía  
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Ciencias Físicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Nitrogen diffusion in nitrogen-doped yttria stabilised zirconia  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-03-18T14:28:38Z  
dc.journal.volume
6  
dc.journal.number
13  
dc.journal.pagination
3645-3649  
dc.journal.pais
Reino Unido  
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CAMBRIDGE  
dc.description.fil
Fil: Kilo, Martin. Technische Universität Clausthal; Alemania  
dc.description.fil
Fil: Taylor, Marcela Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Física La Plata. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Física La Plata; Argentina. Technische Universität Clausthal; Alemania  
dc.description.fil
Fil: Argirusis, Christos. Technische Universität Clausthal; Alemania  
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Fil: Borchardt, Günter. Technische Universität Clausthal; Alemania  
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Fil: Lerch, Martin. Technishe Universitat Berlin; Alemania  
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Fil: Kaïtasov, Odile. Universite Paris-sud Xi; Francia  
dc.description.fil
Fil: Lesage, Bernard. Centre de Sciences Nucléaires Et de Sciences de la Matière; Francia  
dc.journal.title
Physical Chemistry Chemical Physics  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/b315123a  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/Content/ArticleLanding/2004/CP/B315123A#!divAbstract