Oxygen Diffusion Studies in Mixed Ionic Electronic Conducting Compounds

dc.contributor.advisorJacobson, Allan J.
dc.contributor.committeeMemberGuloy, Arnold M.
dc.contributor.committeeMemberBaldelli, Steven
dc.contributor.committeeMemberArdebili, Haleh
dc.contributor.committeeMemberMeen, James K.
dc.creatorRupasov, Dmitry 1983-
dc.date.accessioned2017-07-17T20:47:28Z
dc.date.available2017-07-17T20:47:28Z
dc.date.createdAugust 2014
dc.date.issued2014-08
dc.date.submittedAugust 2014
dc.date.updated2017-07-17T20:47:28Z
dc.description.abstractCobalt-based oxides with perovskite-related structures are important candidate cathode materials for the next generation solid oxide fuel cells (SOFCs) because of their good catalytic properties and high values of electronic and ionic conductivity. The aim of the work described in the thesis is to investigate oxygen transport in Sr3YCo4O10.5 (SYC, the so-called 314 phase) and double perovskites LnBaCoFeO5+δ (Ln = La, Pr, Sm and Gd) with combination of theoretical and experimental methods. The oxygen transport properties of Sr3YCo4O10.5 were studied by three different techniques. Molecular dynamics simulations (MD) predicted an isotropic character of oxygen diffusion with an activation energy of 1.56 eV in the temperature range of 1000 – 1400 K. Values of tracer oxygen diffusion, D*, and the surface exchange coefficient, k*, were measured as a function of temperature (500 – 900 °C) with isotope exchange depth profiling combined with secondary ion mass spectrometry (IEDP/SIMS). Chemical oxygen diffusion coefficients, Dchem, and chemical surface exchange rates, kchem, were obtained from electrical conductivity relaxation experiments (ECR). Good agreement of the results obtained by different techniques was confirmed after application of thermodynamic factors to the ECR data. Electrochemical performance of symmetrical cells with Ce0.9Gd0.1O1.95 (GDC) as electrolyte (SYC/GDC/SYC) in the temperature range 620 – 770 °C was evaluated. Double perovskites LnBaCoFeO5+δ (Ln = La, Pr, Sm and Gd) were studied by combination of ECR, thermogravimetric analysis (TGA) and dilatometry. It was found that size of rare earth element (REE) has strong influence on electrochemical and mechanical properties of the samples. In case of La and Pr-containing compounds, fast degradation of the surface kinetics during ECR experiments at high oxygen partial pressure was associated with surface segregation. ECR measurements at low pO2 switches were performed for La, Pr and Gd-containing samples to avoid large deviation from chemical equilibrium during experiments. For SmBaCoFeO5+δ it was found that a linear model for the exchange kinetics works in a larger pO2(1)/pO2(2) interval. The effect of A-cation ordering in LaBaCoFeO5+δ on oxygen transport properties was investigated. Oxygen diffusion was found to be slower in ordered structure, due to the influence of ordering in A-cation sublattice on anion ordering.
dc.description.departmentChemistry, Department of
dc.format.digitalOriginborn digital
dc.format.mimetypeapplication/pdf
dc.identifier.citationPortions of this document appear in: D. Rupasov, A. Chroneos, D. Parfitt, J.A. Kilner, R.W. Grimes, S.Y. Istomin, E.V Antipov. "Oxygen diffusion in Sr3YCo4O10.5: A molecular dynamics study." Phys. Rev. B 79 (2009): 172102/1-172102/4. And in: D.P. Rupasov, A.V. Berenov, J.A. Kilner, S.Y. Istomin, E.V. Antipov. "Oxygen diffusion in Sr3YCo4O10.5." Solid State Ionics 197 (2011): 18-24. And in: D. Rupasov, T. Makarenko, A.J. Jacobson. "Oxygen diffusion in Sr3YCo4O10.5: An electrical conductivity relaxation and thermogravimetric analysis approach." Solid State Ionics 265 (2014): 68-72.
dc.identifier.urihttp://hdl.handle.net/10657/1901
dc.language.isoeng
dc.rightsThe author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
dc.subjectDouble perovskites
dc.subjectElectrical conductivity relaxation
dc.subjectIsotope exchange depth profiling
dc.subjectMolecular dynamics
dc.subjectSolid oxide fuel cells
dc.subjectOxygen diffusion
dc.subjectThermal Expansion
dc.titleOxygen Diffusion Studies in Mixed Ionic Electronic Conducting Compounds
dc.type.dcmitext
dc.type.genreThesis
thesis.degree.collegeCollege of Natural Sciences and Mathematics
thesis.degree.departmentChemistry, Department of
thesis.degree.disciplineChemistry
thesis.degree.grantorUniversity of Houston
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy

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