Tracking of high-temperature thermal expansion and transport properties vs. oxidation state of cobalt between +2 and +3 in the La 2Co 1+z(Ti 1-xMg x) 1-zO 6-system
Artikel i vetenskaplig tidskrift, 2012

The high-temperature thermal expansion and electronic transport properties of the B-site substituted LaCoO 3 with both variable oxidation state of cobalt between +2 and +3 (La 2Co(Ti 1-xMg x)O 6, 0 ≤ x ≤ 0.5) and variable Co 3+-content relative to the other B-cations (La 2Co 1+z(Ti 0.5Mg 0.5) 1-zO 6, 0.2 ≤ z ≤ 0.6) have been investigated. Based on the temperature dependence of the thermal expansion, electronic transport properties and Seebeck coefficient, three different groups of compositions according to their symmetries can be allocated. It was found that the thermal expansion coefficients (TECs) of the studied compounds are mainly dependent on the proportion of Co 2+/Co 3+. For La 2Co(Ti 1-xMg x)O 6, the TEC increases from ∼9 (x = 0) to ∼19 ppm K -1 (x = 0.5) with an increase of the oxidation state of cobalt from +2 to +3, respectively. The TECs of La 2Co 1+z(Ti 0.5Mg 0.5) 1-zO 6, z = 0.2-0.6 with Co 3+-only, remain constant at ∼21 ppm K -1 independent of the cobalt content. Thermoelectric measurements of the system indicate that all samples in the system, except La 2Co 1.6(Ti 0.5Mg 0.5) 0.4O 6, are p-type conductors over the whole temperature range, 300 < T < 1175 K. The conductivities were found to increase with an increase of both Co 3+ and total cobalt content and are described with a small polaron hopping model. Due to an insignificant number of oxygen vacancies of La 2Co 1+z(Ti 1-xMg x) 1-zO 6 samples prepared in air at elevated temperatures, the investigated system is proposed as an excellent model system for the investigation of the influence of the Co oxidation state and stoichiometry on different properties in perovskite cobalt oxides. © The Royal Society of Chemistry 2012.


Samrand Shafeie

Stockholms universitet

J. Grins

Stockholms universitet

S. Y. Istomin

Moscow State University

A.A. Gippius

Moscow State University

L. Karvonen

Eidgenössische Materialprüfungs- und Forschungsanstalt (Empa)

S. Populoh

Eidgenössische Materialprüfungs- und Forschungsanstalt (Empa)

A. Weidenkaff

Eidgenössische Materialprüfungs- und Forschungsanstalt (Empa)

J. Köhler

Max-Planck Institute für Festkörperforschung

G. Svensson

Max-Planck Institute für Festkörperforschung

Journal of Materials Chemistry

0959-9428 (ISSN) 1364-5501 (eISSN)

Vol. 22 32 16269-16276


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