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Theoretical study of CeO(2) doped with tetravalent ions
KTH, Skolan för industriell teknik och management (ITM), Materialvetenskap.
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2007 (Engelska)Ingår i: Physical Review B Condensed Matter, ISSN 0163-1829, E-ISSN 1095-3795, Vol. 76, nr 7, s. 174119-Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

We have used density functional theory calculations within the LDA+U formulation to investigate how small amounts of dissolved SiO2, GeO2, SnO2, or PbO2 affect the redox thermodynamics of ceria (CeO2). Compared to pure ceria, reduction is facilitated and the reducibility increases in the sequence of CeO2-SnO2, CeO2-GeO2, and CeO2-SiO2, which correlates with the decrease of the ionic radii of the solutes. For low solute concentrations, there is an inverse relation between high reducibility and the solution energy of tetravalent solutes. CeO2-PbO2 is unique in the sense that the initial reduction occurs by Pb(IV)double right arrow Pb(II) instead of the usual Ce(IV)double right arrow Ce(III) reaction. Among the investigated ceria compounds, CeO2-PbO2 has the lowest reduction energy and rather low solution energy. We have studied how the solution and reduction energies depend on the concentration of Si, Ge, Sn, Pb, Ti, Zr, Hf, and Th solute ions. While the solution energy increases monotonously with concentration, the reduction energy first decreases, as compared to pure ceria (except for Th, which exhibits a small increase), and with further increase of solute concentration, it either remains almost constant (Zr, Hf, and Th) or slightly increases (Ti, Si, Ge, and Sn).

Ort, förlag, år, upplaga, sidor
2007. Vol. 76, nr 7, s. 174119-
Nationell ämneskategori
Övrig annan teknik
Identifikatorer
URN: urn:nbn:se:kth:diva-6890DOI: 10.1103/PhysRevB.76.174119ISI: 000251326600043Scopus ID: 2-s2.0-36648998537OAI: oai:DiVA.org:kth-6890DiVA, id: diva2:11730
Anmärkning
QC 20100622Tillgänglig från: 2007-03-14 Skapad: 2007-03-14 Senast uppdaterad: 2017-12-14Bibliografiskt granskad
Ingår i avhandling
1. From the Electronic Structure of Point Defects to Functional Properties of Metals and Ceramics
Öppna denna publikation i ny flik eller fönster >>From the Electronic Structure of Point Defects to Functional Properties of Metals and Ceramics
2007 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Point defects are an inherent part of crystalline materials and they influence important physical and chemical properties, such as diffusion, hardness, catalytic activity and phase stability. Increased understanding of point defects enables us to tailor the defect-related properties to the application at hand. Modeling and simulation have a prominent role in acquiring this knowledge. In this thesis thermodynamic and kinetic properties of point defects in metals and ceramics are studied using first-principles calculations based on density functional theory. Phenomenological models are used to translate the atomic level properties, obtained from the first-principles calculations, into functional materials properties. The next paragraph presents the particular problems under study.

The formation and migration of vacancies and simple vacancy clusters in copper are investigated by calculating the energies associated with these processes. The structure, stability and electronic properties of the low-oxygen oxides of titanium, TiOx with 1/3 < x < 3/2, are studied and the importance of structural vacancies is demonstrated. We develop an integrated first-principles and Calphad approach to calculate phase diagrams in the titanium-carbon-nitrogen system, with particular focus on vacancy-induced ordering of the substoichiometric

carbonitride phase, TiCxNy (x+y < 1). The possibility of forming higher oxides of plutonium than plutonium dioxide is explored by calculating the enthalpies for nonstoichiometric defect-containing compounds and the analysis shows that such oxidation is only produced by strong oxidants. For ceria (CeO2) doped with trivalent ions from the lanthanide series we probe the connection between the choice of a dopant and the improvement of ionic conductivity by studying the oxygen-vacancy formation and migration properties. The significance of minimizing the dopant-vacancy interactions is highlighted. We investigate the redox thermodynamics of CeO2-MO2 solid solutions with M being Ti, Zr, Hf, Th, Si, Ge, Sn or Pb and show that reduction is facilitated by small solutes.

The results in this thesis are relevant for the performance of solid electrolytes, which are an integral part of solid oxide fuel cells, oxygen storage materials in automotive three-way catalysts, nuclear waste materials and cutting tool materials.

Ort, förlag, år, upplaga, sidor
Stockholm: Materialvetenskap, 2007
Nyckelord
first principles, ab initio, density functional theory, Calphad, point defects, diffusion, solid electrolytes, oxygen storage materials
Nationell ämneskategori
Övrig annan teknik
Identifikatorer
urn:nbn:se:kth:diva-4309 (URN)978-91-7178-590-9 (ISBN)
Disputation
2007-03-30, F2, Lindstedtsvägen 26, Stockholm, 10:00
Opponent
Handledare
Anmärkning
QC 20100622Tillgänglig från: 2007-03-14 Skapad: 2007-03-14 Senast uppdaterad: 2012-03-22Bibliografiskt granskad

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Andersson, David A.Johansson, Börje
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