Electrical properties of the fast-ion conductor lanthanum fluoride
| Autor: | J R Igel, John J. Fontanella, C. G. Andeen, Alan V. Chadwick, Mary C. Wintersgill, V E Bean |
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| Rok vydání: | 1982 |
| Předmět: |
Materials science
Condensed matter physics Enthalpy General Engineering General Physics and Astronomy Dielectric Conductivity Atmospheric temperature range Condensed Matter Physics Thermal expansion Condensed Matter::Materials Science chemistry.chemical_compound Nuclear magnetic resonance chemistry Lanthanum trifluoride Relaxation (physics) Anisotropy |
| Zdroj: | Journal of Physics C: Solid State Physics. 15:7215-7228 |
| ISSN: | 0022-3719 |
| DOI: | 10.1088/0022-3719/15/35/019 |
| Popis: | Audio-frequency complex-impedance measurements have been performed on pure and alkaline-earth-doped lanthanum trifluoride at zero pressure over the temperature range 5.5-310K and at pressures up to 0.3 GPa in the vicinity of room temperature. Studies have been made both parallel and perpendicular to the optical axis. The real part of the dielectric constant is found to be given by epsilon '/sub /// approximately=12.6 and epsilon 'perpendicular to approximately=14.4 and both components increase slightly with temperature. Also, for the calcium-doped material, four relaxations have been observed. The activation enthalpy for the principal relaxation is close to that for the motion of free vacancies and thus is attributable to the reorientation of a bound vacancy. In addition, the anisotropy ratio for the relaxation is found to be Aperpendicular to /A/sub /// approximately=1.8, which is opposite to the anisotropy observed for DC conductivity. An explanation of the anisotropy ratio is discussed. Finally, the pressure-dependent conductivity has been measured in the association region, yielding an activation volume of about 2.4 cm3 mol-1. The thermal expansion coefficient of the activation volume is found to be negative. The value of 2.4 cm3 mol-1 is interpreted to be the activation volume for the motion of vacancies. |
| Databáze: | OpenAIRE |
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