Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/24784
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dc.contributor.authorHeras-Juaristi, G.pt_PT
dc.contributor.authorAmador, U.pt_PT
dc.contributor.authorFuentes, R. O.pt_PT
dc.contributor.authorChinelatto, A. L.pt_PT
dc.contributor.authorDe Paz, J.Romeropt_PT
dc.contributor.authorRitter, C.pt_PT
dc.contributor.authorFagg, D. P.pt_PT
dc.contributor.authorPérez-Coll, D.pt_PT
dc.contributor.authorMather, Glenn C.pt_PT
dc.date.accessioned2018-11-30T15:16:33Z-
dc.date.available2018-11-30T15:16:33Z-
dc.date.issued2018-
dc.identifier.issn2050-7488pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/24784-
dc.description.abstractA 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.pt_PT
dc.language.isoengpt_PT
dc.publisherRoyal Society of Chemistrypt_PT
dc.relationFCT-PTDC/CTM-ENE/6319/2014pt_PT
dc.rightsrestrictedAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.titleThermal evolution of structures and conductivity of Pr-substituted BaZr0.7Ce0.2Y0.1O3-:δ: Potential cathode components for protonic ceramic fuel cellspt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
ua.distributioninternationalpt
degois.publication.firstPage5324pt_PT
degois.publication.issue13pt_PT
degois.publication.lastPage5334pt_PT
degois.publication.titleJournal of Materials Chemistry Apt_PT
degois.publication.volume6pt_PT
dc.relation.publisherversionhttps://pubs.rsc.org/en/content/articlelanding/2018/ta/c7ta09570hpt_PT
dc.identifier.doi10.1039/c7ta09570hpt_PT
dc.identifier.essn2050-7496pt_PT
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DEM - Artigos



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