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Synthesis and characterization of BaSn(OH)6 and BaSnO3 acicular particles

Published online by Cambridge University Press:  31 January 2011

M. T. Buscaglia
Affiliation:
Institute for Energetics and Interphases, National Research Council, via De Marini 6, I-16149 Genoa, Italy
M. Leoni
Affiliation:
Institute for Energetics and Interphases, National Research Council, via De Marini 6, I-16149 Genoa, Italy
M. Viviani
Affiliation:
Institute for Energetics and Interphases, National Research Council, via De Marini 6, I-16149 Genoa, Italy
V. Buscaglia*
Affiliation:
Institute for Energetics and Interphases, National Research Council, via De Marini 6, I-16149 Genoa, Italy
A. Martinelli
Affiliation:
Department of Chemistry and Industrial Chemistry, via Dodecaneso 31, I-16146 Genoa, Italy
A. Testino
Affiliation:
Department of Process and Chemical Engineering, University of Genoa, Fiera del Mare, Pad. D., I-16146 Genoa, Italy
P. Nanni
Affiliation:
Department of Process and Chemical Engineering, University of Genoa, Fiera del Mare, Pad. D., I-16146 Genoa, Italy
*
a)Address all correspondence to this author. e-mail: buscaglia@icfam.ge.cnr.it
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Abstract

The synthesis of BaSn(OH)6 acicular crystals by precipitation at 100 °C from aqueous solutions and their transformation in the perovskitelike compound BaSnO3 was investigated. Single acicular crystals 100–200 μm in length were obtained from a 0.05M solution, whereas bundlelike aggregates of 20–40 μm were precipitated from 0.2–0.6 M solutions. The x-ray diffraction pattern of barium hexahydroxostannate was indexed according to monoclinic symmetry with cell parameters a = 11.029 ± 0.002 Å, b = 6.340 ± 0.001 Å, c = 10.563 ± 0.001 Å = 128.51 ± 0.01°, α = γ = 90°. The BaSn(OH)6 particles decomposed to BaSnO3 and water at approximately 270 °C and the original morphology was retained. The resulting product had specific surface area up to 30–40 m2/g and consisted of 10–20 nm crystallites. The larger unit cell edge in comparison to the reference value and the continuous weight loss up to 1200 °C indicate that water is not completely released during decomposition and a substantial amount of proton defects (up to 0.4 mol per mole of BaSnO3) is incorporated in the perovskite lattice as OH groups. Normal crystallographic properties of BaSnO3 are restored only after calcination at 1300 °C.

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Articles
Copyright
Copyright © Materials Research Society 2003

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