| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1330481 | Journal of Solid State Chemistry | 2012 | 7 Pages |
The crystal structure of cerium brannerite, Ce0.975Ti2O5.95, was determined from Rietveld analysis of high resolution neutron powder diffraction data (space group C2/m, a=9.8320(1) Å, b=3.75287(6) Å, c=6.8852(1) Å, β=119.230(1)°). The presence of both cerium and oxygen vacancies was confirmed from Rietveld analysis and defect energy calculations, combined with careful investigation of the phase diagram. Formation of oxygen vacancies at the O1 site, charge compensated by Ce vacancies, relieves considerable Coulombic repulsion and hence structural strain associated with short O1–O1 contacts forming the shared edge of neighbouring TiO6 polyhedra. Consideration of the bond valence sum of Ce4+ in Ce0.975Ti2O5.95 afforded a revised value of the r0=2.098±0.039 Å for the reference bond length, based on analysis of 21 crystal structures mined from the ICSD.
Graphical abstractNeutron diffraction and atomistic defect energy calculations reveal the mechanism of nonstochiometry in cerium brannerite, Ce0.975Ti2O5.95.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► The defect brannerite Ce0.975Ti2O5.95 was prepared by solid state synthesis. ► Neutron diffraction confirmed the presence of Ce vacancies charge compensated by O vacancies. ► Defect energy calculations show oxygen vacancies relieve structural strain associated with short O–O contact distances.
