2005 APS March Meeting
Monday–Friday, March 21–25, 2005;
Los Angeles, CA
Session J2: Heterostructures of Correlated Oxide Materials
11:15 AM–2:15 PM,
Tuesday, March 22, 2005
LACC
Room: 151
Sponsoring
Unit:
DCMP
Chair: Allen Goldman, University of Minnesota
Abstract ID: BAPS.2005.MAR.J2.5
Abstract: J2.00005 : Enhancing Ferroelectrics using Strain
1:39 PM–2:15 PM
Preview Abstract
Abstract
Author:
Darrell Schlom
(Penn State University)
We have used epitaxy and the misfit strain imposed by an underlying
substrate to shift the paraelectric-to-ferroelectric transition temperature
($T_{c})$ by \textit{hundreds} of degrees and to enhance the ferroelectric properties of
SrTiO$_{3}$ and BaTiO$_{3}$. Although SrTiO$_{3}$ is normally not
ferroelectric at any temperature, predictions based on thermodynamic
analysis imply that a biaxial strain of order 1{\%} will shift its $T_{c}$ to
the vicinity of room temperature. Such strains are also predicted to elevate
the $T_{c}$ of BaTiO$_{3}$ by comparable amounts. In practice, the synthesis
of uniformly strained ferroelectric films is challenging. Epitaxial
ferroelectric films are often grown to thicknesses greatly exceeding their
critical values, resulting in undesirable relaxation toward a zero-strain
state by the introduction of dislocations. Dislocation densities of $\sim
$10$^{11}$~cm$^{-2}$ are common in epitaxial ferroelectric films grown on
lattice-mismatched substrates, and the resulting inhomogeneous strain smears
out the ferroelectric phase transition. Our approach to controlling the
properties of ferroelectric SrTiO$_{3}$ and BaTiO$_{3}$ films centers on the
development of new substrates (DyScO$_{3}$ and GdScO$_{3})$ that enable the
growth of uniformly strained films below, or at least far closer to, the
critical thickness for relaxation. Our results$^{1,2}$ demonstrate not only
the largest strain-induced shift in $T_{c}$ ever achieved, but also manifest
a paradigm shift in how to manipulate the properties of ferroelectric thin
films. Strain is a viable alternative to the traditional method of chemical
substitutions for shifting $T_{c}$ by large amounts. These strained
SrTiO$_{3}$ and BaTiO$_{3}$ films have better structural perfection
(narrower rocking curve widths) than SrTiO$_{3}$ and BaTiO$_{3}$ single
crystals. An unexpected surprise is that the strained SrTiO$_{3}$ films
exhibit a frequency dependence of their dielectric constant consistent with
\textit{relaxor} ferroelectricity.
$^{1 }$J.H. Haeni, P. Irvin, W. Chang, R. Uecker, P. Reiche, Y.L. Li, S.
Choudhury, W. Tian, M.E. Hawley, B. Craigo, A.K. Tagantsev, X.Q. Pan, S.K.
Streiffer, L.Q. Chen, S.W. Kirchoefer, J. Levy, and D.G. Schlom, \textit{Nature}
\textbf{430} (2004) 758-761.
$^{2 }$K.J. Choi, M. Biegalski, Y.L. Li, A. Sharan, J. Schubert, R. Uecker,
P. Reiche, Y.B. Chen, X.Q. Pan, V. Gopalan, L.-Q. Chen, D.G. Schlom, and
C.B. Eom, \textit{Science} \textbf{306} (2004) 1005-1009.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2005.MAR.J2.5