Tracer diffusion and chemical diffusion of oxygen in acceptor doped SrTiO3

Citation
J. Claus et al., Tracer diffusion and chemical diffusion of oxygen in acceptor doped SrTiO3, J PHYS CH S, 61(8), 2000, pp. 1199-1207
Citations number
51
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS
ISSN journal
00223697 → ACNP
Volume
61
Issue
8
Year of publication
2000
Pages
1199 - 1207
Database
ISI
SICI code
0022-3697(200008)61:8<1199:TDACDO>2.0.ZU;2-E
Abstract
Oxygen tracer and oxygen chemical diffusion coefficients have been determin ed for single crystalline SrTiO3 under defined temperature (f), oxygen part ial pressure (p(O-2)), and acceptor (m(Fe)) dopant concentration (m(Fe)) co nditions. Oxygen tracer diffusion results were obtained (873 K less than or equal to T less than or equal to 1173 K, p(O-2)= 10(5) Pa) by means of O-1 8 isotope exchange with subsequent analysis of the O-18 in-diffusion profil es by secondary ion mass spectrometry (SIMS). In the case of chemical diffu sion an in situ and spatially resolved, optical relaxation technique was ap plied (673 K less than or equal to T less than or equal to 973 K, 10 Pa les s than or equal to P(O-2) less than or equal to 10(5) Pa). The dopant conce ntration in both experiments was varied between 4.3 X 10(18) cm(-3) less th an or equal to m(Fe) less than or equal to 4.9 X 10(19) cm(-3). The evaluat ion of (ex situ) tracer and (in situ) concentration profiles are shown to b e in excellent agreement with defect chemical calculations. In contrast to the tracer diffusion coefficients (D*) the chemical diffusion coefficients (D-delta) are sensitive to ionic-electronic (short-range) defect interactio ns (internal buffer effects influence the thermodynamic factor) caused by v alence changes of the redox-active Fe-doping. (C) 2000 Elsevier Science Ltd . All rights reserved.