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Stable room-temperature ferromagnetic phase at the FeRh(100) surface

机译:FeRh(100)表面的稳定室温铁磁相

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摘要

Interfaces and low dimensionality are sources of strong modifications ofelectronic, structural, and magnetic properties of materials. FeRh alloys arean excellent example because of the first-order phase transition taking placeat $\sim$400 K from an antiferromagnetic phase at room temperature to a hightemperature ferromagnetic one. It is accompanied by a resistance change andvolume expansion of about 1\%. We have investigated the electronic and magneticproperties of FeRh(100) epitaxially grown on MgO by combining spectroscopiescharacterized by different probing depths, namely X-ray magnetic circulardichroism and photoelectron spectroscopy. We thus reveal that the symmetrybreaking induced at the Rh-terminated surface stabilizes a surfaceferromagnetic layer involving five planes of Fe and Rh atoms in the nominallyantiferromagnetic phase at room temperature. First-principles calculationsprovide a microscopic description of the structural relaxation and the electronspin-density distribution that fully support the experimental findings.
机译:界面和低尺寸是材料的电子,结构和磁性性质发生强烈改变的原因。 FeRh合金是一个很好的例子,因为从室温下的反铁磁相到高温铁磁相的一阶相变发生在$ \ sim $ 400K。伴随着电阻变化和体积膨胀约1%。我们通过结合不同探测深度(X射线磁性圆二色性和光电子能谱)表征的光谱学,研究了在MgO上外延生长的FeRh(100)的电子和磁性。因此,我们揭示了在Rh终止的表面上引起的对称性破坏稳定了表面铁磁层,该铁磁层在室温下在名义反铁磁相中包含五个Fe和Rh原子平面。第一性原理计算提供了结构弛豫和电子自旋密度分布的微观描述,完全支持了实验结果。

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