Ma. Paris et al., Li mobility in the orthorhombic Li0.18La0.61TiO3 perovskite studied by NMRand impedance spectroscopies, CHEM MATER, 12(6), 2000, pp. 1694-1701
Electrical conductivity and NMR relaxation times (T-1 and T-2) have been de
termined in the Li0.18La0.61TiO3 perovskite. At room temperature, the unit
cell constants are a = 3.865(1), b = 3.876(1), and c = 7.788(2) Angstrom an
d the space group Pmmm (orthorhombic). In this doubled perovskite, the Riet
veld analysis of the X-ray powder pattern showed that La ions occupy prefer
entially one type of sites (z/c = 0), and Li and vacancies accommodate with
the remaining La at the second site (z/c = 0.5). From this fact, Li motion
should be favored in the plane ab; however, exchanges of Li between contig
uous layers are detected above 200 K by NMR spectroscopy. From T-1 and T-2
NMR data, two main relaxation mechanisms have been detected, which have bee
n ascribed to localized exchanges (200-273 K) and extended motions of Li (a
bove 273 K). The de conductivity shows a non-Arrhenius temperature dependen
ce, and local activation energies of 0.41 and 0.26 eV were obtained in the
low- and high-temperature ranges, respectively. Both NMR and electrical con
ductivity relaxations are described by "stretched exponential" functions, c
haracteristic of correlated ion motions.