The synthesis of BaSn(OH)(6) acicular crystals by precipitation at 100 degreesC from aqueous solutions and their transformation in the perovskitelike compound BaSnO3 was investigated. Single acicular crystals 100-200 mum in length were obtained from a 0.05 M solution, whereas bundlelike aggregates of 20-40 mum 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 Angstrom, b = 6.340 +/- 0.001 Angstrom, c = 10.563 +/- 0.001 Angstrom, beta = 128.51 +/- 0.01degrees, alpha = gamma = 90degrees. The BaSn(OH)(6) particles decomposed to BaSnO3 and water at approximately 270 degreesC and the original morphology was retained. The resulting product had specific surface area up to 30-40 m(2)/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 degreesC 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 degreesC.

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

M T Buscaglia;M Viviani;V Buscaglia;A Martinelli;
2003

Abstract

The synthesis of BaSn(OH)(6) acicular crystals by precipitation at 100 degreesC from aqueous solutions and their transformation in the perovskitelike compound BaSnO3 was investigated. Single acicular crystals 100-200 mum in length were obtained from a 0.05 M solution, whereas bundlelike aggregates of 20-40 mum 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 Angstrom, b = 6.340 +/- 0.001 Angstrom, c = 10.563 +/- 0.001 Angstrom, beta = 128.51 +/- 0.01degrees, alpha = gamma = 90degrees. The BaSn(OH)(6) particles decomposed to BaSnO3 and water at approximately 270 degreesC and the original morphology was retained. The resulting product had specific surface area up to 30-40 m(2)/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 degreesC 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 degreesC.
2003
Istituto di Chimica della Materia Condensata e di Tecnologie per l'Energia - ICMATE
POWDER DIFFRACTION PATTERNS
BARIUM STANNATE
MICROSTRUCTURAL DEVELOPMENT
HALL MEASUREMENTS
TEMPERATURE
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/52292
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