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The ferroelectric and cubic phases in BaTiO_3 ferroelectrics are also antiferroelectric

Zhang, Qingsong and Çağin, Tahir and Goddard, William A., III (2006) The ferroelectric and cubic phases in BaTiO_3 ferroelectrics are also antiferroelectric. Proceedings of the National Academy of Sciences of the United States of America, 103 (40). pp. 14695-14700. ISSN 0027-8424. PMCID PMC1595414. http://resolver.caltech.edu/CaltechAUTHORS:ZHApnas06

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Abstract

Using quantum mechanics (QM, Density Functional Theory) we show that all four phases of barium titanate (BaTiO3) have local Ti distortions toward <111> (an octahedral face). The stable rhombohedral phase has all distortions in phase (ferroelectric, FE), whereas higher temperature phases have antiferroelectric coupling (AFE) in one, two, or three dimensions (orthorhombic, tetragonal, cubic). This FE–AFE model from QM explains such puzzling aspects of these systems as the allowed Raman excitation observed for the cubic phase, the distortions toward <111> observed in the cubic phase using x-ray fine structure, the small transition entropies, the heavily damped soft phonon modes, and the strong diffuse x-ray scattering in all but the rhombohedral phase. In addition, we expect to see additional weak Bragg peaks at the face centers of the reciprocal lattice for the cubic phase. Similar FE–AFE descriptions are expected to occur for other FE materials. Accounting for this FE–AFE nature of these phases is expected to be important in accurately simulating the domain wall structures, energetics, and dynamics, which in turn may lead to the design of improved materials.


Item Type:Article
Related URLs:
URLURL TypeDescription
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1595414/PubMed CentralArticle
ORCID:
AuthorORCID
Çağin, Tahir0000-0002-3665-0932
Goddard, William A., III0000-0003-0097-5716
Alternate Title:The ferroelectric and cubic phases in BaTiO3 ferroelectrics are also antiferroelectric
Additional Information:© 2006 by The National Academy of Sciences of the USA. Contributed by William A. Goddard III, August 1, 2006. Published online on September 25, 2006, 10.1073/pnas.0606612103. This work was initiated with funding by the Army Research Office (ARO, MURI-DAAD19-01-1-0517) and by the National Science Foundation (MRSEC-CSEM-DMR0080065) and completed with funding from Defense Advanced Research Planning Agency (Predicting Real Optimized Materials) through the Office of Naval Research (N00014-02-1-0839). The Molecular Simulation Center computational facilities used in these calculations were provided by grants from Defense University Research Instrumentation Program (DURIP)–ARO, DURIP–Office of Naval Research, and National Science Foundation Major Research Instrumentation. Author contributions: W.A.G. designed research; Q.Z. performed research; Q.Z. and T.C. analyzed data; and Q.Z. wrote the paper. The authors declare no conflict of interest.
Funders:
Funding AgencyGrant Number
Army Research Office (ARO)DAAD19-01-1-0517
NSFDMR-0080065
Defense Advanced Research Projects Agency (DARPA)UNSPECIFIED
Office of Naval Research (ONR)N00014-02-1-0839
Subject Keywords:barium titanate; phase transition
Issue or Number:40
PubMed Central ID:PMC1595414
Record Number:CaltechAUTHORS:ZHApnas06
Persistent URL:http://resolver.caltech.edu/CaltechAUTHORS:ZHApnas06
Alternative URL:http://dx.doi.org/10.1073/pnas.0606612103
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:9957
Collection:CaltechAUTHORS
Deposited By: Archive Administrator
Deposited On:28 Mar 2008
Last Modified:20 Apr 2017 17:44

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