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Letters to Nature
Nature 433, 395-399 (27 January 2005) | doi:10.1038/nature03261; Received 17 September 2004; Accepted 3 December 2004
There is an Addendum (7 April 2005) associated with this document.
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Strong polarization enhancement in asymmetric three-component ferroelectric superlattices
Ho Nyung Lee1, Hans M. Christen1, Matthew F. Chisholm1, Christopher M. Rouleau1 & Douglas H. Lowndes1
- Condensed Matter Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA
Correspondence to: Ho Nyung Lee1 Correspondence and requests for materials should be addressed to H.N.L. (Email: hnlee@ornl.gov).
Abstract
Theoretical predictions—motivated by recent advances in epitaxial engineering—indicate a wealth of complex behaviour arising in superlattices of perovskite-type metal oxides. These include the enhancement of polarization by strain1, 2 and the possibility of asymmetric properties in three-component superlattices3. Here we fabricate superlattices consisting of barium titanate (BaTiO3), strontium titanate (SrTiO3) and calcium titanate (CaTiO3) with atomic-scale control by high-pressure pulsed laser deposition on conducting, atomically flat strontium ruthenate (SrRuO3) layers. The strain in BaTiO3 layers is fully maintained as long as the BaTiO3 thickness does not exceed the combined thicknesses of the CaTiO3 and SrTiO3 layers. By preserving full strain and combining heterointerfacial couplings, we find an overall 50% enhancement of the superlattice global polarization with respect to similarly grown pure BaTiO3, despite the fact that half the layers in the superlattice are nominally non-ferroelectric. We further show that even superlattices containing only single-unit-cell layers of BaTiO3 in a paraelectric matrix remain ferroelectric. Our data reveal that the specific interface structure and local asymmetries play an unexpected role in the polarization enhancement.
- Condensed Matter Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA
Correspondence to: Ho Nyung Lee1 Correspondence and requests for materials should be addressed to H.N.L. (Email: hnlee@ornl.gov).
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