通过改变应变和薄膜厚度精确控制Sr2IrO4外延薄膜的Jeff=12磁性能

S. Geprägs, B. Skovdal, M. Scheufele, M. Opel, D. Wermeille, P. Thompson, A. Bombardi, V. Simonet, S. Grenier, P. Lejay, G. Chahine, D. Quintero-Castro, R. Gross, D. Mannix
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引用次数: 1

摘要

本文采用先进的x射线散射技术,全面研究了应变和薄膜厚度对原型$J_\ mathm {eff}=1/2$化合物Sr$_2$IrO$_4$外延薄膜结构和磁性的影响。我们发现Sr$_2$IrO$_4$薄膜可以完全应变生长到108 nm的厚度。通过x射线共振散射,我们发现面外磁相关长度与薄膜厚度密切相关,而与薄膜的应变状态无关。这可以作为一个微调表盘来调节面外磁相关长度,并通过增加薄膜厚度将磁各向异性从二维(2D)转变为三维(3D)行为。这些结果为Sr$_2$IrO$_4$外延薄膜的磁性自由度的系统控制提供了更清晰的图像,并为探索$5d$过渡金属化合物的物理学提供了丰富的平台。
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Precise control of Jeff=12 magnetic properties in Sr2IrO4 epitaxial thin films by variation of strain and thin film thickness
We report on a comprehensive investigation of the effects of strain and film thickness on the structural and magnetic properties of epitaxial thin films of the prototypal $J_\mathrm{eff}=1/2$ compound Sr$_2$IrO$_4$ by advanced X-ray scattering. We find that the Sr$_2$IrO$_4$ thin films can be grown fully strained up to a thickness of 108 nm. By using X-ray resonant scattering, we show that the out-of-plane magnetic correlation length is strongly dependent on the thin film thickness, but independent of the strain state of the thin films. This can be used as a finely tuned dial to adjust the out-of-plane magnetic correlation length and transform the magnetic anisotropy from two-dimensional (2D) to three-dimensional (3D) behavior by incrementing film thickness. These results provide a clearer picture for the systematic control of the magnetic degrees of freedom in epitaxial thin films of Sr$_2$IrO$_4$ and bring to light the potential for a rich playground to explore the physics of $5d$-transition metal compounds.
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