Heterovalent substitutions in Na2M2TeO6 family: Crystal structure, fast sodium ion conduction and phase transition of Na2LiFeTeO6

• Published in: Solid state ionics 2013-02, Vol.233, p.7-11
• Main Authors: Nalbandyan, V.B., Petrenko, А.А., Evstigneeva, M.A.
• Format: Article
• Language: English
• Subjects: Aluminum; Bottleneck; Diffraction; Gallium; Heating; High temperature; Ion conduction; Iron; Layered structure; Nickel; Order disorder; Phase transition; Rietveld; Sodium; Tellurate
• ISSN: 0167-2738; 1872-7689
• DOI: 10.1016/j.ssi.2012.12.002

A new solid electrolyte Na2LiFeTeO6 has been prepared by solid-state reactions in air at 700°C and characterized by powder X-ray diffraction, redox titration and impedance measurements on ceramic samples. It is a new superstructure type of the well-known hexagonal layered P2 type with complete ordering of Li, Fe and Te in octahedral brucite-like layers: orthorhombic, P212121, a=5.2109(1), b=8.9791(2), c=11.2389(2)Å, Z=4. At room temperature, sodium ions in the interlayer gap are concentrated in two of the six non-equivalent trigonal prisms; at elevated temperatures, they exhibit high ionic conductivity, e.g., 4S/m at 300°C. Orthorhombic distortion decreases on heating, presumably due to sodium movement, and vanishes at ca. 400°C giving rise to the hexagonal Na2Co2TeO6-type structure. Analogous Na2LiRTeO6 (R=Al or Ga), Na2LiFeWO6, Na2Mn2TeO6, Na2M2WO6 (M=Ni or Cu), Na2NiMSbO6 (M=Al or Fe) and Na2NiAlTO6 (T=Nb or Ta) could not be prepared. ► Na2LiFeTeO6 is a new orthorhombic superlattice of the known hexagonal layered P2 type. ► The distortion seems to be only due to Na+ ion ordering in the interlayer prisms. ► On heating, high Na+ ion conductivity is observed, e.g., 4S/m at 300°C. ► With Na+ ion movement, distortion decreases and vanishes at ca. 400°C. ► 10 other variants of M and/or Te substitutions in Na2M2TeO6 family were unsuccessful.