Аннотация:In the 1970s, the Ln2O3- Mo(WO3) (Ln = La-Tb) systems were intensively studied with the
aim of finding double molybdates and tungstates in them. It is known that in a number of
Ln2O3-MoO3 systems there are compounds with the composition 5:6 (Ln5Mo3O16) with the
fluorite-like structure [1].
Fluorite-like Ln5Mo3O16+δ (0 ≤ δ ≤ 0.5) compounds have mixed oxygen-electronic conductivity,
with a magnitude of the order of 10-2 S/cm at 800 °C [2, 3]. A study by Faurie [4]
showed that when one rare earth element is replaced by an alkaline element and one oxygen
by fluorine, MeLn4Mo3O15F compounds (Me = Li, K, Na) are formed with the safekeeping
of the fluorite structure. However, the properties of these compounds changed dramatically, a
phase transition occurred in the region of which the conductivity increased abruptly [5]. The
reason for this phenomenon has not yet been explained.
In this work, we synthesized the solid solutions in La5Mo3O16.5 - LiF join of the LiF - La2O3
- MoO3 ternary system in air. We study the conditions of solid state synthesis, polymorphism
and the properties of LixLa5–xMo3O16.5–yFx (x = 0–1.6) compounds using X-ray, DSC and
measuring the electrophysical properties, in particular, their piezoelectric response was investigated.
Wide region of LixLa5–xMo3O16.5–yFx solid solutions (x = 0–1.6) with a cubic fluorite-like
structure have been found in La5Mo3O16.5 - LiF join. It should be noted that successful synthesis
of these compounds significantly depends on the temperature and time of synthesis. The
upper limit of time and temperature is strongly limited by the volatility of fluorine, which,
according to thermogravimetry, evaporates from the compounds above 750–800 °C, and then
the LixLa5–xMo3O16.5–yFx compounds decompose. The optimum synthesis temperature was in
the region of 600–700 °C.
Polymorphism and properties of LixLa5–xMo3O16.5–yFx samples with high fluorine content
are of particular interest. At a temperature of about 580 °C, a reversible phase transition is
observed for these samples, which is accompanied by DSC anomalies, a peak of the dielectric
constant (Fig. 1) and an intense jump in conductivity by two orders of magnitude. These
samples also demonstrate significant piezoelectric response, which may indicate the ferroelectric
nature of the phase transition. XRD study did not reveal any difference between XRD
diffraction patterns of pure La5Mo3O16 and LixLa5–xMo3O16.5–yFx. However, it can be assumed,
taking into account the above mentioned changes in physical properties, that upon doping,
the cubic structure is distorted, although only slightly.