Li mobility in the orthorhombic Li0.18La0.61TiO3 perovskite studied by NMRand impedance spectroscopies

Citation
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
Citations number
27
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
CHEMISTRY OF MATERIALS
ISSN journal
08974756 → ACNP
Volume
12
Issue
6
Year of publication
2000
Pages
1694 - 1701
Database
ISI
SICI code
0897-4756(200006)12:6<1694:LMITOL>2.0.ZU;2-O
Abstract
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.