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dc.contributor.author
Heras Juaristi, Gemma
dc.contributor.author
Amador, Ulises
dc.contributor.author
Fuentes, Rodolfo Oscar
dc.contributor.author
Chinelatto, Adilson L.
dc.contributor.author
Romero De Paz, Julio
dc.contributor.author
Ritter, Clemens
dc.contributor.author
Fagg, Duncan P.
dc.contributor.author
Pérez Coll, Domingo
dc.contributor.author
Mather, Glenn C.
dc.date.available
2020-03-18T17:38:54Z
dc.date.issued
2018-03
dc.identifier.citation
Heras Juaristi, Gemma; Amador, Ulises; Fuentes, Rodolfo Oscar; Chinelatto, Adilson L.; Romero De Paz, Julio; et al.; Thermal evolution of structures and conductivity of Pr-substituted BaZr0.7Ce0.2Y0.1O3-:δ: Potential cathode components for protonic ceramic fuel cells; Royal Society of Chemistry; Journal of Materials Chemistry A; 6; 13; 3-2018; 5324-5334
dc.identifier.issn
2050-7488
dc.identifier.uri
http://hdl.handle.net/11336/100069
dc.description.abstract
A complete solid solution forms between the perovskite proton conductor BaZr0.7Ce0.2Y0.1O3-δ (BZCY72) and BaPr0.9Y0.1O3-δ (BPY) on synthesis by the Pechini method and high-temperature annealing. Phase fields of selected members of the Ba(Zr0.7Ce0.2)1-(x/0.9)PrxY0.1O3-δ series were studied as a function of composition and temperature by high-resolution neutron powder diffraction revealing symmetry changes in the sequence Pnma → Imma → → Pm3m. Higher symmetry is favoured for low Pr contents and high temperatures, as consideration of tolerance factor suggests. A volume contraction, ascribed to dehydration, is observed by synchrotron X-ray diffraction on heating in air for lower x. Magnetic measurements and structural data support the presence of Pr in the IV valence state on the perovskite B site. Thermogravimetric analysis in CO2 to ∼1253 K indicates better chemical stability for x ≤ 0.445, whereas decomposition occurred for higher x. Electrical conductivity increases by over two orders of magnitude in dry air at lower temperature from x = 0.225 to 0.675; total conductivity reaches a value of 0.4 S cm-1 at 1173 K for x = 0.675. The series exhibits electron-hole transport with a positive pO2 dependence which increases with temperature, consistent with participation of oxygen vacancies in charge compensation of the Y3+ acceptor dopant. The activation energy for thermally activated hole hopping in air in the range 523-773 K decreases from ∼1 eV for BZCY72 to ∼0.4 eV for x = 0.675. Conductivity is generally lower in humidified N2 and air (pH2O ≈ 0.023 atm) than the corresponding dry atmospheres, consistent with consumption of holes by less mobile protonic species; however for x ≤ 0.225 the lower concentration of electron holes concomitant with higher oxygen-vacancy content in N2 results in slightly higher conductivity in wet conditions due to hydration of vacancies.
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
Proton Conductors
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Neutron Diffraction
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XRD
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EIS
dc.subject.classification
Físico-Química, Ciencia de los Polímeros, Electroquímica
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Thermal evolution of structures and conductivity of Pr-substituted BaZr0.7Ce0.2Y0.1O3-:δ: Potential cathode components for protonic ceramic fuel cells
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2020-03-13T13:42:20Z
dc.journal.volume
6
dc.journal.number
13
dc.journal.pagination
5324-5334
dc.journal.pais
Reino Unido
dc.description.fil
Fil: Heras Juaristi, Gemma. Instituto de Cerámica y Vidrio de Madrid; España
dc.description.fil
Fil: Amador, Ulises. Universidad San Pablo Ceu; España
dc.description.fil
Fil: Fuentes, Rodolfo Oscar. Comisión Nacional de Energía Atómica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
dc.description.fil
Fil: Chinelatto, Adilson L.. Universidade Estadual de Ponta Grossa; Brasil
dc.description.fil
Fil: Romero De Paz, Julio. Universidad Complutense de Madrid; España
dc.description.fil
Fil: Ritter, Clemens. Institut Laue Langevin; Francia
dc.description.fil
Fil: Fagg, Duncan P.. Universidade de Aveiro; Portugal
dc.description.fil
Fil: Pérez Coll, Domingo. Instituto de Cerámica y Vidrio de Madrid; España
dc.description.fil
Fil: Mather, Glenn C.. Instituto de Cerámica y Vidrio de Madrid; España
dc.journal.title
Journal of Materials Chemistry A
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/C7TA09570H
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2018/TA/C7TA09570H
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