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Proton conductivity of hexagonal and cubic BaTi1-XScxO3-delta (0.1 <= x <= 0.8)
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK). STFC Rutherford Appleton Laboratory, England.
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2014 (English)In: Dalton Transactions, ISSN 1477-9226, E-ISSN 1477-9234, Vol. 43, no 40, 15055-15064 p.Article in journal (Refereed) Published
Abstract [en]

BaTi1-xScxO3-delta (X = 0.1-0.8) was prepared via solid state reaction. High resolution X-ray powder diffraction was used to characterise the synthesised materials. It was found that low substitution (x = 0.1 and 0.2) of Ti4+ for Sc3+ gives a hexagonal perovskite structure, whereas high substitution (x = 0.5-0.7) results in a cubic perovskite structure. Thermogravimetric analysis revealed significant levels of protons in both as-prepared and hydrated samples. Electrical conductivity was measured by AC impedance methods under oxygen, argon and under dry and humid, both H(2)0 and D2O, conditions for BaTi1-xScXO3-delta,(x = 0.2, 0.6 and 0.7). In the temperature range of 150-600 C-circle, under humid conditions, the conductivity is significantly higher than that under the dry conditions. The increase in conductivity is especially prominent for the cubic phases, indicating that protons are the dominant charge carriers. The proton conductivity of hexagonal BaTi0.8,Sc0.2O3-delta is approx. two orders of magnitude lower than that of the more heavily substituted cubic phases. Conductivity is also found to be higher in dry O-2 than in Ar in the whole temperature range of 150-1000 C-circle, characteristic of a significant contribution from p-type charge carriers under oxidising atmospheres. Greater Sc3+ substitution leads to a higher proton concentration and the highest proton conductivity (sigma similar to 2 x 10(-3) S cm(-1) at 600 degrees C) is found for the BaTi(0.3)Sc(07)cO(3-delta) composition.

Place, publisher, year, edition, pages
2014. Vol. 43, no 40, 15055-15064 p.
National Category
Chemical Sciences
URN: urn:nbn:se:su:diva-109263DOI: 10.1039/c4dt01280aISI: 000343023200018OAI: diva2:765559


Available from: 2014-11-24 Created: 2014-11-17 Last updated: 2014-11-24Bibliographically approved

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