Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1523057 | Materials Chemistry and Physics | 2012 | 8 Pages |
In the present study we report the synthesis, crystal structure and vibrational spectroscopy studies of Bi1−xTa1−xTe2xO4 orthorhombic solid solutions (0 ≤ x ≤ 0.2). Rietveld refinements showed that this solid solution is continuous adopting Pnna (no.52) space group. The structure is formed by (Bi/Te(1))O6 and (Ta/Te(2))O6 octahedra, The (Ta/Te(2))O6 octahedra linked over four comers and thus the structure can be viewed as consisting of sheets of [(Ta/Te(2))O6]3− units separated by Bi3+ cations. The infrared spectra of Bi1−xTa1−xTe2xO4 oxides at room temperature showed some characteristic vibration bands assigned to Bi–O and Ta–O vibrations. Raman spectra of this crystalline solid solution series are interpreted by means of “internal mode” approach. Assignments of the Ta–O and Bi–O vibrational stretching modes, as well as some of other modes, have been made.
► Synthesis and crystal structures are described for the Bi1−xTa1−xTe2xO4 solid solution with (0 ≤ x ≤ 0.2). ► The structure is formed by a three-dimensional network of octahedral (Ta/Te(2))O6 linked by the octahedral (Bi/Te(1))O6. ► The infrared spectra at room temperature showed some characteristic vibration bands assigned to Bi–O and Ta–O vibrations.