Li self-diffusion in lithium niobate single crystals at low temperatures
Author(s) -
Johanna Rahn,
Erwin Hüger,
Lars Dörrer,
Benjamin Ruprecht,
Paul Heitjans,
Harald Schmidt
Publication year - 2012
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/c2cp23548j
Subject(s) - diffusion , chemistry , arrhenius equation , vacancy defect , analytical chemistry (journal) , self diffusion , ion , atmospheric temperature range , activation energy , enthalpy , lithium (medication) , isotope , thermodynamics , crystallography , medicine , physics , self service , organic chemistry , chromatography , marketing , quantum mechanics , business , endocrinology
Li self-diffusion in Li(2)O-deficient LiNbO(3) single crystals is investigated in the temperature range between 423 and 773 K (150-500 °C) by secondary ion mass spectrometry. A thin layer of ion-beam sputtered isotope enriched (6)LiNbO(3) was used as a tracer source, which allows one to study pure isotope interdiffusion. The diffusivities can be described by the Arrhenius law with an activation enthalpy of (1.33 ± 0.03) eV, which is in acceptable agreement with the migration energy of a single Li vacancy as determined by ab initio calculations given in the literature. Charge diffusivities as derived from impedance spectroscopy measurements on the same type of samples are identical to the tracer diffusivities within error limits. No indication of the formation of defect-complexes at low temperatures could be found in the diffusion behaviour.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom