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The mixed valent tellurate SrTe{sub 3}O{sub 8}: Electronic lone pair effect of Te{sup 4+}

Journal Article · · Journal of Solid State Chemistry
 [1];  [1];  [2];  [1];  [1]
  1. Laboratoire CRISMAT, UMR 6508 CNRS Ensicaen, 6 bd Marechal Juin, 14050 Caen Cedex 4 (France)
  2. UMR 6226 CNRS-Universite de Rennes 1 Sciences Chimiques de Rennes, Equipe Materiaux inorganiques: chimie douce et reactivite, Bat. 10B, campus de Beaulieu, 263, avenue du General Leclerc, F-35042 Rennes (France)
A novel mixed valent tellurium oxide, SrTe{sub 3}O{sub 8}, has been synthesized and its crystal structure was determined ab initio from powder X-ray diffraction data. This oxide, which crystallizes in a tetragonal unit-cell, P4{sub 2}/m space group, with very close a and c cell parameters (6.8257(1) and 6.7603(1) A, respectively), exhibits a very original structure built up of corner-sharing TeO{sub 6} (Te{sup 6+}) octahedra and Te{sub 2}O{sub 8} (Te{sup 4+}) twin-pyramidal units. The latter ones form [Te{sub 3}O{sub 8}]{sub {infinity}} chains running along the [001] and the [110] directions. Besides the four sided tunnels where the Sr{sup 2+} cations are located, there are very large four sided tunnels running along the c-axis which are obstructed by the electronic lone pairs of the Te{sup 4+} cations. -- Graphical abstract: Tunnel structure of the mixed valent tellurate SrTe{sub 3}O{sub 8} determined ab initio against powder X-ray diffraction; structure viewed along [001] direction with E the electronic lone pairs of the Te{sup 4+} cations.
OSTI ID:
20900889
Journal Information:
Journal of Solid State Chemistry, Journal Name: Journal of Solid State Chemistry Journal Issue: 11 Vol. 179; ISSN 0022-4596; ISSN JSSCBI
Country of Publication:
United States
Language:
English

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