Tunability of the dielectric response of epitaxially strained SrTiO3 from first principles

Armin Antons, J. B. Neaton, Karin M. Rabe, and David Vanderbilt
Phys. Rev. B 71, 024102 – Published 13 January 2005

Abstract

The effect of in-plane strain on the nonlinear dielectric properties of SrTiO3 epitaxial thin films is calculated using density-functional theory within the local-density approximation. Motivated by recent experiments, the structure, zone-center phonons, and dielectric properties with and without an external electric field are evaluated for several misfit strains within ±3% of the calculated cubic lattice parameter. In these calculations, the in-plane lattice parameters are fixed, and all remaining structural parameters are permitted to relax. The presence of an external bias is treated approximately by applying a force to each ion proportional to the electric field. After obtaining zero-field ground state structures for various strains, the zone-center phonon frequencies and Born effective charges are computed, yielding the zero-field dielectric response. The dielectric response at finite electric field bias is obtained by computing the field dependence of the structure and polarization using an approximate technique. The results are compared with recent experiments and a previous phenomenological theory. The tunability is found to be strongly dependent on the in-plane lattice parameter, showing markedly different behavior for tensile and compressive strains. Our results are expected to be of use for isolating the role of strain in the tunability of real ultrathin epitaxial films.

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  • Received 23 June 2004

DOI:https://doi.org/10.1103/PhysRevB.71.024102

©2005 American Physical Society

Authors & Affiliations

Armin Antons*, J. B. Neaton, Karin M. Rabe, and David Vanderbilt

  • Department of Physics and Astronomy, Rutgers University, Piscataway, New Jersey 08854-8019, USA

  • *Electronic address: a.antons@fz-juelich.de; Present address: Institut of Solid State Research (IFF), Research Centre Jülich, 52425 Jülich, Germany.
  • Present address: The Molecular Foundry, Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.

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Issue

Vol. 71, Iss. 2 — 1 January 2005

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