The Relationship between the Crystal Structure and Electrical Properties of Oxide Ion Conducting Ba3W1.2Nb0.8O8.6

Kirstie S McCombie, Eve J Wildman, Clemens Ritter, Ronald I Smith, Janet M S Skakle, Abbie C Mclaughlin* (Corresponding Author)

*Corresponding author for this work

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18 Citations (Scopus)
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The oxide ionic conductor Ba3W1.2Nb0.8O8.6 has been synthesised as part of an investigation into the new class of Ba3M’M’’O8.5 (M’ = W, Mo; M’’ = Nb) oxide-ion conducting hexagonal perovskite derivatives. The substitution of W6+ for Nb5+ in Ba3W1+xNb1-xO8.5+x/2 leads to an increase in the oxygen content, which enhances the low temperature ionic conductivity. However at 400 °C, the ionic conductivity of Ba3W1.2Nb0.8O8.6 is still significantly lower than the molybdenum compound Ba3MoNbO8.5. Remarkably, at 600 °C the bulk oxide ionic conductivities of Ba3MoNbO8.5, Ba3WNbO8.5 and Ba3W1.2Nb0.8O8.6 are very similar (σb = 0.0016 S cm-1, 0.0017 S cm-1 and 0.0022 S cm-1 respectively). The variable temperature neutron diffraction results reported here demonstrate that Ba3W1.2Nb0.8O8.6 undergoes a similar structural rearrangement to Ba3MoNbO8.5 above 300 °C but the ratio of (W/Nb)O4 tetrahedra to (W/Nb)O6 octahedra rises at a faster rate upon heating between 300 and 600 °C. There is a clear relationship between the ionic conductivity of Ba3M’1+xM’’1-xO8.5+x/2 (M’ = W, Mo; M’’= Nb) phases and the number of tetrahedrally coordinated M' and M" cations present within the crystal structure.
Original languageEnglish
Pages (from-to)11942-11947
Number of pages6
JournalInorganic Chemistry
Issue number19
Early online date12 Sept 2018
Publication statusPublished - 1 Oct 2018

Bibliographical note

This research was supported by the University of Aberdeen and EPSRC (research grant EP/L002493/1). We also acknowledge the UK Science and Technology Facilities Council (STFC) for provision of beamtime at ISIS and the ILL.


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