Reversible Control of Magnetic Interactions by Electric Field in a Single Phase Material
arXiv:1206.5181 · doi:10.1038/ncomms2329
Abstract
Intrinsic magnetoelectric coupling describes the interaction between magnetic and electric polarization through an inherent microscopic mechanism in a single phase material. This phenomenon has the potential to control the magnetic state of a material with an electric field, an enticing prospect for device engineering. We demonstrate 'giant' magnetoelectric cross-field control in a single phase rare earth titanate film. In bulk form, EuTiO3 is antiferromagnetic. However, both anti and ferromagnetic interactions coexist between different nearest neighbor europium ions. In thin epitaxial films, strain can be used to alter the relative strength of the magnetic exchange constants. Here, we not only show that moderate biaxial compression precipitates local magnetic competition, but also demonstrate that the application of an electric field at this strain state, switches the magnetic ground state. Using first principles density functional theory, we resolve the underlying microscopic mechanism resulting in the EuTiO3 G-type magnetic structure and illustrate how it is responsible for the 'giant' cross-field magnetoelectric effect.
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- Emergence of a Dynamic Super-Structural Order Integrating Antiferroelectric and Antiferrodistortive Competing Instabilities in EuTiO3
- Room-temperature paramagnetoelectric effect in magnetoelectric multiferroics Pb(Fe1/2Nb1/2)O3 and its solid solution with PbTiO3
- Origin of giant spin-lattice coupling and the suppression of ferroelectricity in EuTiO3 from first principles
- Universal emergence of spatially-modulated structures induced by flexo-antiferrodistortive coupling in multiferroics
- Correlated materials design: prospects and challenges
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- Structural control of magnetic anisotropy in a strain driven multiferroic EuTiO3 thin film
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- Ultrafast transient increase of oxygen octahedral rotations in a perovskite
- Low-symmetry monoclinic phase stabilized by oxygen octahedra rotations in thin strained EuxSr1-xTiO3 films
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