The Sc 2 (WO 4 ) 3 type structure has been used in order to create new trivalent cation conducting solid electrolytes by forming solid solutions of the type (Sc 2 (WO 4 ) 3 ) 1– x (M 2 (MoO 4 ) 3 ) x (M=Nd, Sm, Gd, Lu). In these compounds, the anionic part of the structure is partly replaced by molybdate (WO 4 →MoO 4 ) whereas the Sc 3+ cations are substituted by different larger lanthanide cations M (Sc→M). Increasing the size of M gradually leads to a restriction of the M 2 (WO 4 ) 3 solubility in the scandium tungstate phase (e.g., x=0-1 for M=Lu but x=0-0.1 for M=Nd). The electrical properties of the resulting materials have been characterized in detail. All solid solutions exhibit neither electronic nor anionic O 2– conduction but rather a mixed trivalent Sc 3+ /M 3+ cationic conduction with the Sc 3+ cations as the main charge carrying species for low M 2 (MoO 4 ) 3 concentrations (x<0.5) and the ionic transference number is >99%. For a given substitution rate of M for Sc, the electrical conductivity increases with increasing size of M. The highest conduction data were observed for the solid solution (Sc 2 (WO 4 ) 3 ) 0.75 (Sm 2 (MoO 4 ) 3 ) 0.25 exhibiting a conductivity of 2.4×10 –4 S cm –1 at 600 °C with an activation energy of 45.8 kJ mol –1 . Furthermore, in all different systems the maximum conductivity appears for the same average trivalent cationic radius indicating an optimized spatial spacing for the mobile cationic species.
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Köhler et al. (1999) studied this question.
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