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Cation interdiffusion in polycrystalline calcium and strontium titanate

Journal Article · · Journal of the American Ceramic Society; (United States)
; ;  [1]
  1. Dept. of Materials Science and Engineering, Whitaker Lab., No. 5, Lehigh Univ., Bethlehem, PA (US)
This paper discusses a method that has been developed to study bulk lattice interdiffusion between calcium and strontium titanate by fabrication of a diffusion couple using cosintering. The measured interdiffusion coefficients, D(C), indicate that strontium impurity diffusion in calcium titanate occurs at a faster rate than calcium impurity diffusion in strontium titanate. These interdiffusion coefficients are composition independent when the concentration of the calcium cation exceeds that of the strontium cation; otherwise D(C) is strongly composition dependent. Investigations into the effect of cation nonstoichiometry give results that are consistent with a defect incorporation reaction in which excess TiO{sub 2}, within the solid solubility limit, produces A-site cation vacancies as compensating defects. The interdiffusion coefficients increase with increasing concentrations of TiO{sub 2}, so it is concluded that interdiffusion of these alkaline-earth cations in their titanates occurs via a vacancy mechanism.
OSTI ID:
5159799
Journal Information:
Journal of the American Ceramic Society; (United States), Journal Name: Journal of the American Ceramic Society; (United States) Vol. 74:4; ISSN 0002-7820; ISSN JACTA
Country of Publication:
United States
Language:
English