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Title: Synthesis, structure and characterisation of the n=4 Aurivillius phase Bi{sub 5}Ti{sub 3}CrO{sub 15}

Journal Article · · Journal of Solid State Chemistry
; ;  [1];  [1];  [2]
  1. Department of Materials Science and Engineering, The University of Sheffield, Mappin Street, Sheffield S1 3JD (United Kingdom)
  2. School of Chemistry, The University of Birmingham, Edgbaston, Birmingham B15 2 TT (United Kingdom)

The n=4 Aurivillius phase, Bi{sub 5}Ti{sub 3}CrO{sub 15}, was synthesised by solid state reaction. Rietveld analysis of high resolution neutron diffraction data demonstrated this material to adopt the polar space group A2{sub 1}am at room temperature, transforming to the aristotype I4/mmm structure above 650 {sup o}C. This phase transition is coincident with an anomaly in DSC signal and relative permittivity, which are characteristic of a ferroelectric-paraelectric phase transition. Bi{sub 5}Ti{sub 3}CrO{sub 15} exhibits paramagnetic behaviour at low temperature, with short range antiferromagnetic interactions, but no evidence for long range magnetic ordering. This is considered a consequence of significant disorder of Ti and Cr over the available octahedral sites, as demonstrated by analysis of neutron diffraction data. -- Graphical abstract: We report here the synthesis, structure and characterisation of the n=4 Aurivillius phase Bi{sub 5}Ti{sub 3}CrO{sub 15}. Analysis of neutron powder diffraction and XANES data, supported by Madelung energy calculations, demonstrate partial ordering of Ti and Cr cations in the component perovskite layer. Bi{sub 5}Ti{sub 3}CrO{sub 15} is paramagnetic in the temperature range studied but exhibits a dielectric and DSC anomaly at 660 {sup o}C, characteristic of a ferroelectric-paraelectric phase transition. Analysis of high temperature neutron diffraction data confirm a direct phase transition between space groups A2{sub 1}am and I4/mmm at {approx}660 {sup o}C. Display Omitted

OSTI ID:
21494209
Journal Information:
Journal of Solid State Chemistry, Vol. 184, Issue 2; Other Information: DOI: 10.1016/j.jssc.2010.09.031; PII: S0022-4596(10)00430-5; Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; ISSN 0022-4596
Country of Publication:
United States
Language:
English

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