The re-equilibration kinetics of single crystal and thin films of SrTiO 3 were monitored by measuring electrical conductivity as a function of temperature, T, and oxygen partial pressure, p O 2 , over the ranges: 823 K Ο½ T Ο½ 1173 K and 10 Pa Ο½ p O 2 Ο½ 0.1 MPa. Application of the solution of Fick's s
Tracer diffusion and chemical diffusion of oxygen in acceptor doped SrTiO3
β Scribed by J. Claus; M. Leonhardt; J. Maier
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 263 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0022-3697
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β¦ Synopsis
Oxygen tracer and oxygen chemical diffusion coefficients have been determined for single crystalline SrTiO 3 under defined temperature (f ), oxygen partial pressure (p(O 2 )), and acceptor (Fe) dopant concentration (m Fe ) conditions. Oxygen tracer diffusion results were obtained 873 K Υ T Υ 1173 K; pO 2 10 5 Pa by means of 18 O isotope exchange with subsequent analysis of the 18 O in-diffusion profiles by secondary ion mass spectrometry (SIMS). In the case of chemical diffusion an in situ and spatially resolved, optical relaxation technique was applied 673 K Υ T Υ 973 K; 10 Pa Υ pO 2 Υ 10 5 Pa: The dopant concentration in both experiments was varied between 4:3 Γ 10 18 cm Οͺ3 Υ m Fe Υ 4:9 Γ 10 19 cm Οͺ3 : The evaluation of (ex situ) tracer and (in situ) concentration profiles are shown to be in excellent agreement with defect chemical calculations. In contrast to the tracer diffusion coefficients (D β«Ψ‘β¬ ) the chemical diffusion coefficients (D d ) are sensitive to ionic-electronic (short-range) defect interactions (internal buffer effects influence the thermodynamic factor) caused by valence changes of the redox-active Fe-doping.
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