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Local electrical control of magnetic order and orientation by ferroelastic domain arrangements just above room temperature

机译:通过刚好高于室温的铁弹性域布置对磁序和取向进行局部电控制

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摘要

Ferroic materials (ferromagnetic, ferroelectric, ferroelastic) usually divide into domains with different orientations of their order parameter. Coupling between different ferroic systems creates new functionalities, for instance the electrical control of macroscopic magnetic properties including magnetization and coercive field. Here we show that ferroelastic domains can be used to control both magnetic order and magnetization direction at the nanoscale with a voltage. We use element-specific X-ray imaging to map the magnetic domains as a function of temperature and voltage in epitaxial FeRh on ferroelastic BaTiO3. Exploiting the nanoscale phase-separation of FeRh, we locally interconvert between ferromagnetic and antiferromagnetic states with a small electric field just above room temperature. Imaging and ab initio calculations show the antiferromagnetic phase of FeRh is favoured by compressive strain on c-oriented BaTiO3 domains, and the resultant magnetoelectric coupling is larger and more reversible than previously reported from macroscopic measurements. Our results emphasize the importance of nanoscale ferroic domain structure and the promise of first-order transition materials to achieve enhanced coupling in artificial multiferroics.
机译:铁性材料(铁磁,铁电,铁弹性)通常分为顺序参数不同取向的区域。不同铁磁系统之间的耦合产生了新的功能,例如对包括磁化和矫顽场在内的宏观磁性能进行电控制。在这里,我们表明,铁弹性域可用于控制纳米级电压的磁序和磁化方向。我们使用特定于元素的X射线成像将铁磁BaTiO3上外延FeRh中的磁畴映射为温度和电压的函数。利用FeRh的纳米级相分离,我们在室温以上的小电场下,在铁磁和反铁磁状态之间进行局部互变。成像和从头算计算表明,FeRh的反铁磁相受到c取向BaTiO3域上的压缩应变的促进,并且所产生的磁电耦合比以前从宏观测量中报道的更大,更可逆。我们的结果强调了纳米级铁磁畴结构的重要性以及一阶过渡材料在人工多铁磁学中实现增强耦合的希望。

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