Local structure of Ba(Ti,Zr)O3 perovskite-like solid solutions and its relation to the band-gap behavior

Igor Levin, Eric Cockayne, Victor Krayzman, Joseph C. Woicik, Soonil Lee, Clive A. Randall

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

Local structures in BaTi1-xZrxO3 solid solutions were analyzed using x-ray absorption fine structure (XAFS) measurements and density-functional theory (DFT) calculations. We demonstrate that for low concentrations of Ti, isolated Ti atoms in the relatively large octahedral sites of the BaZrO3 lattice acquire centrosymmetric coordination with average Ti-O distances shorter than those in BaTiO 3. In contrast for higher concentrations of Ti, Ti atoms having one or more Ti as their B-site nearest neighbors undergo polar off-center displacements. Our DFT calculations confirm both effects. These results combined with the previously published data suggest that isolated polarizable ions on the B sites of a relatively expanded host perovskite lattice remain nonpolar by symmetric relaxation of the nearest-neighbor oxygen atoms to yield nearly ideal bond lengths around the dopant species. For neighboring Ti atoms, such symmetric relaxation is impossible, and these atoms are displaced off center. Our XAFS measurements did not detect any significant deviations from a random distribution of Ti and Zr in the present samples except for compositions close to BaTiO3. The DFT calculations suggest that the dominant effect of the local displacements on band-gap values for this system is determined by the shortest Ti-O bonds due to strong Ti 3d-O 2p hybridization; however, local displacements have only a secondary effect on the band-gap behavior.

Original languageEnglish (US)
Article number094122
JournalPhysical Review B - Condensed Matter and Materials Physics
Volume83
Issue number9
DOIs
StatePublished - Mar 30 2011

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Perovskite
Solid solutions
Energy gap
solid solutions
Atoms
Density functional theory
density functional theory
x ray absorption
atoms
fine structure
X rays
statistical distributions
Bond length
low concentrations
oxygen atoms
deviation
Doping (additives)
perovskite
Ions
Oxygen

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Condensed Matter Physics

Cite this

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title = "Local structure of Ba(Ti,Zr)O3 perovskite-like solid solutions and its relation to the band-gap behavior",
abstract = "Local structures in BaTi1-xZrxO3 solid solutions were analyzed using x-ray absorption fine structure (XAFS) measurements and density-functional theory (DFT) calculations. We demonstrate that for low concentrations of Ti, isolated Ti atoms in the relatively large octahedral sites of the BaZrO3 lattice acquire centrosymmetric coordination with average Ti-O distances shorter than those in BaTiO 3. In contrast for higher concentrations of Ti, Ti atoms having one or more Ti as their B-site nearest neighbors undergo polar off-center displacements. Our DFT calculations confirm both effects. These results combined with the previously published data suggest that isolated polarizable ions on the B sites of a relatively expanded host perovskite lattice remain nonpolar by symmetric relaxation of the nearest-neighbor oxygen atoms to yield nearly ideal bond lengths around the dopant species. For neighboring Ti atoms, such symmetric relaxation is impossible, and these atoms are displaced off center. Our XAFS measurements did not detect any significant deviations from a random distribution of Ti and Zr in the present samples except for compositions close to BaTiO3. The DFT calculations suggest that the dominant effect of the local displacements on band-gap values for this system is determined by the shortest Ti-O bonds due to strong Ti 3d-O 2p hybridization; however, local displacements have only a secondary effect on the band-gap behavior.",
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Local structure of Ba(Ti,Zr)O3 perovskite-like solid solutions and its relation to the band-gap behavior. / Levin, Igor; Cockayne, Eric; Krayzman, Victor; Woicik, Joseph C.; Lee, Soonil; Randall, Clive A.

In: Physical Review B - Condensed Matter and Materials Physics, Vol. 83, No. 9, 094122, 30.03.2011.

Research output: Contribution to journalArticle

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AU - Lee, Soonil

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