Materials
crystallizing in highly symmetric structures are of particular
interest as they display superior physical properties in many relevant
technological areas such as solid oxide fuels cells (SOFCs), catalysis,
or photoluminescent materials. While the rare earth molybdenum oxides
RE<sub>6</sub>MoO<sub>12</sub> with the large rare earth cations RE
= La to Dy crystallize in a cubic defect fluorite structure type (<i>Fm</i>3̅<i>m</i>, no. 225), the compounds with
the smaller cations RE = Tm–Lu could hitherto only be synthesized
in the rhombohedral defect fluorite structure type (<i>R</i>3̅, no. 148). In the following, new low temperature access
to the rare earth molybdenum oxides RE<sub>6</sub>MoO<sub>12−δ</sub> (RE = Tm–Lu) crystallizing in the highly symmetric cubic
bixbyite structure type (<i>Ia</i>3̅, no. 206) will
be discussed. The three-step method comprises preparation of the rhombohedral
phases by solution combustion (SC) reactions, their reduction including
simultaneous structural transitions from the rhombohedral to the cubic
phases, and subsequent reoxidations while preserving their cubic structures.
Detailed studies on this process were performed on the compound Yb<sub>6</sub>MoO<sub>12−δ</sub> using TG-DTA, XPS, EDX, and
X-ray powder diffraction (XRPD) measurements. In contrast to the rhombohedral
phase Yb<sub>6</sub>MoO<sub>12</sub>, which does not show any ionic
conductivity, the cubic bixbyite structured compound can be classified
as a promising ionic conductor. Electrochemical impedance spectroscopy
(EIS) revealed that bulk and grain boundary activation energy determined
to be 144.6 kJ mol<sup>–1</sup> and 150.4 kJ mol<sup>–1</sup>, respectively, range in the same regime as the conventional ionic
conductor 8-YSZ. Furthermore, the new cubic phase Yb<sub>6</sub>MoO<sub>12−δ</sub> displays improved coloristic properties (UV–Vis
spectroscopy) with a yellow hue value (CIE-Lab) being enhanced from <i>b</i>* = 26.0 of the rhombohedral to <i>b</i>* = 46.1
for the cubic phase, which is relevant for the field of inorganic
pigments