The mobilities of trivalent ions are generally considered to be low in solid oxides and thus trivalent ionic conductors are rare. Sc 2 (WO 4 ) 3 and related compounds have been described as Sc 3+ ionic conductors. However, there has not been conclusive experimental evidence whether Sc 3+ is the major or the only mobile species. Here, we report 45 Sc, 17 O, and 27 Al MAS NMR studies at ambient and high temperature of Sc 2 (WO 4 ) 3 -type compounds including Sc 2 (WO 4 ) 3, Sc 2 (MoO 4 ) 3 (scandium tungstate and scandium molybdate), and their solid solutions, as well as aluminum-doped Sc 2 (WO 4 ) 3 . 45 Sc MAS NMR spectra at ambient temperature of the Sc 2 (WO 4 ) 3 −Sc 2 (MoO 4 ) 3 binary are consistent with random mixing of W 6+ and Mo 6+ on tetrahedral sites. 17 O spectra show that the details of the end-member short-range structure are preserved throughout this solid solution, indicating that lattice distortion is minimized by the close similarity of the radii of the hexavalent cations. Al 3+ substitutes only into the octahedral sites. At high temperatures (600−700 °C), only the 17 O high spectra show noticeable line shape changes, whereas 45 Sc high-temperature spectra maintain a constant peak width and shift in position only, suggesting that the oxide anion may be a more mobile species but not excluding the possibility of a minor number of mobile scandium ions. 17 O high-temperature NMR data also suggest that oxide ions bonded to molybdenum ions may be more mobile than those in tungstate groups.
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Kim et al. (2008) studied this question.
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