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MagneticContrast at Spin-Flip Excitations: An AdvancedX-Ray Spectroscopy Tool to Study Magnetic-Ordering

机译:磁性自旋翻转激发的对比:高级X射线光谱学工具研究磁序

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摘要

The determination of the local orientation and magnitude of the magnetization in spin textures plays a pivotal role in understanding and harnessing magnetic properties for technological applications. Here, we show that by employing the polarization dependence of resonant inelastic X-ray scattering (RIXS), we can directly probe the spin ordering with chemical and site selectivity. Applied on the prototypical ferrimagnetic mixed-valence system, magnetite ([Fe3+]A[Fe3+,Fe2+]BO4), we can distinguish spin-flip excitations at the A and B antiferromagnetically coupled Fe3+ sublattices and quantify the exchange field. Furthermore, it is possible to determine the orbital contribution to the magnetic moment from detailed angular dependence measurements. RIXS dichroism measurements performed at spin-flip excitations with nanometer spatial resolution will offer a powerful mapping contrast suitable for the characterization of magnetic ordering at interfaces and engineered spin textures.
机译:自旋织构中磁化的局部取向和大小的确定在理解和利用磁性能用于技术应用中起着关键作用。在这里,我们表明通过利用共振非弹性X射线散射(RIXS)的偏振依赖性,我们可以直接探测具有化学和位点选择性的自旋有序。应用于典型的亚铁磁混合价体系磁铁矿([Fe 3 + ] A [Fe 3 + ,Fe 2 + ] BO4) ,我们可以区分A和B反铁磁耦合的Fe 3 + 子晶格上的自旋翻转激发,并量化交换场。此外,可以通过详细的角度依赖性测量确定轨道对磁矩的贡献。在具有纳米空间分辨率的自旋翻转激励下执行的RIXS二向色性测量将提供强大的映射对比度,适用于表征界面处的磁序和工程自旋纹理。

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