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Synthesis and structural characterization of perovskite type proton conducting BaZr1-xInxO3-delta (0.0 <= x <= 0.75)
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2006 (English)In: Solid State Ionics, ISSN 0167-2738, E-ISSN 1872-7689, Vol. 177, no 17-18, 1395-1403 p.Article in journal (Refereed) Published
Abstract [en]

Solid state sintering has been used to prepare the cubic perovskite structured compounds BaZr1-xInxO3-delta (0.0 <= x <= 0.75). Analysis of X-ray powder diffraction (XRPD) data reveals that the unit cell parameter, a, increases linearly with an increased Indium concentration. XRPD data was also used to demonstrate the completion of sample hydration, which was reached when the materials showed a set of single-phase Bragg-peaks. Dynamic thermogravimetric analysis (TGA) data showed that approx. 89% of the total number of available oxygen vacancies can be filled in BaZr1-xInxO3-delta for x=0.50, and that the maximum water uptake occurs below 300 degrees C. Rietveld analysis of the room temperature neutron powder diffraction (NPD) data confirmed the average cubic symmetry (space group Pm-3m), and an expansion of the unit cell parameter after the hydration reaction. The strong O-H stretch band, 2500-3500 cm(-1), in the infrared absorbance spectrum clearly manifests the presence of protons in the hydrated material. Proton conductivity of hydrated BaZr1-xInxO3-delta, x=0.75 was investigated during heating and cooling cycles under dry argon atmosphere. The total conductivity during the heating cycle was nearly two orders of magnitude greater than that of cooling cycle at 300 degrees C, whilst these values were similar at higher temperatures i.e. T > 600 degrees C.

Place, publisher, year, edition, pages
2006. Vol. 177, no 17-18, 1395-1403 p.
Keyword [en]
X-ray diffraction, neutron diffraction, proton conductors, rietveld refinement, perovskite
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:uu:diva-153659DOI: 10.1016/j.ssi.2006.07.009ISI: 000241714000001OAI: oai:DiVA.org:uu-153659DiVA: diva2:417446
Available from: 2011-05-17 Created: 2011-05-17 Last updated: 2017-12-11Bibliographically approved

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