Article ID Journal Published Year Pages File Type
1329364 Journal of Solid State Chemistry 2009 5 Pages PDF
Abstract

The identity of the pyrochlore phase seen during the synthesis of ferroelectric Bi4−xLnxTi3O12 Aurivillius oxides is shown to be Bi2/3Ln4/3Ti2O7. This pyrochlore is only stable for Ln3+=Sm3+ or smaller. For larger lanthanides the layered Aurivillius oxide is favoured. The presence of six-fold disorder, associated with the Bi 6s2 lone pair electrons, is believed to stabilise the unexpected stoichiometry of this oxide. Precise structures, obtained by Rietveld refinement from synchrotron X-ray diffraction data, of three examples Ln3+=Eu, Ho and Yb are presented.

Graphical AbstractThe pyrochlore phase formed during the synthesis of the ferroelectric oxides Bi4−xLnxTi3O12 is shown to be Bi2/3Ln4/3Ti2O7. This is found to be stable only for Ln3+cations smaller than Sm3+. Displacive disorder of the Bi and Ln cations is observed.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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