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dc.contributor.authorChen Q.
dc.contributor.authorEl Gabaly F.
dc.contributor.authorAksoy Akgul F.
dc.contributor.authorLiu Z.
dc.contributor.authorMun B.S.
dc.contributor.authorYamaguchi S.
dc.contributor.authorBraun A.
dc.date.accessioned2019-08-01T13:38:39Z
dc.date.available2019-08-01T13:38:39Z
dc.date.issued2013
dc.identifier.issn0897-4756
dc.identifier.urihttps://dx.doi.org/10.1021/cm401977p
dc.identifier.urihttps://hdl.handle.net/11480/779
dc.description.abstractThe interaction of metal oxides with their ambient environment at elevated temperatures is of significant relevance for the functionality and operation of ceramic fuel cells, electrolyzers, and gas sensors. Proton conductivity in metal oxides is a subtle transport process which is based on formation of oxygen vacancies by cation doping and substitution and oxygen vacancy filling upon hydration in water vapor atmosphere. We have investigated the conductivity and electronic structure of the BaCeY-oxide proton conductor under realistic operation conditions from 373 to 593 K and water vapor pressures up to 200 mTorr in situ by combining ambient pressure X-ray photoelectron spectroscopy and electrochemical impedance spectroscopy. We provide element specific spectroscopic evidence that oxygen vacancies are filled by oxygen upon water exposure and partly oxidize Ce3+ and Y2+ toward Ce 4+ and Y3+. Moreover, the resonant valence band spectra of dry and hydrated samples show that oxygen ligand holes in the proximity of the Y dopant are by around 0.5 eV closer to the Fermi level than the corresponding hole states from Ce. Both hole states become substantially depleted upon hydration, while the proton conductivity sets on and increases systematically. Charge redistribution between lattice oxygen, Ce, and Y when BCY is exposed to water vapor at ambient and high temperature provides insight in the complex mechanism for proton incorporation in BCY. © 2013 American Chemical Society.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectambient pressure XPSen_US
dc.subjectAP-XPSen_US
dc.subjectimpedance spectroscopyen_US
dc.subjectin situ spectroscopyen_US
dc.subjectoxygen vacancyen_US
dc.subjectperovskiteen_US
dc.subjectproton conductoren_US
dc.subjectproton diffusivityen_US
dc.subjectresonant photoemissionen_US
dc.subjectvalence banden_US
dc.titleObservation of oxygen vacancy filling under water vapor in ceramic proton conductors in situ with ambient pressure XPSen_US
dc.typearticleen_US
dc.relation.journalChemistry of Materialsen_US
dc.departmentNiğde ÖHÜen_US
dc.identifier.volume25en_US
dc.identifier.issue23en_US
dc.identifier.startpage4690en_US
dc.identifier.endpage4696en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthor[0-Belirlenecek]
dc.identifier.doi10.1021/cm401977p


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