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可调谐的 SrFeReO 双钙钛矿的磁性。

Tunable Magnetic Properties in SrFeReO Double-Perovskite.

机构信息

Department of Physics, National University of Singapore, Singapore 117575, Singapore.

Shaanxi Key Laboratory of Condensed Matter Structures and Properties and MOE Key Laboratory of Materials Physics and Chemistry under Extraordinary Conditions, Northwestern Polytechnical University, Xi'an 710072, People's Republic of China.

出版信息

Nano Lett. 2022 Dec 28;22(24):9900-9906. doi: 10.1021/acs.nanolett.2c03206. Epub 2022 Dec 16.

Abstract

Double-perovskite oxides have attracted recent attention due to their attractive functionalities and application potential. In this paper, we demonstrate the effect of dual controls, i.e., the deposition pressure of oxygen () and lattice mismatch (ε), on tuning magnetic properties in epitaxial double-perovskite SrFeReO films. In a nearly lattice matched SrFeReO/SrTiO film, the ferrimagnetic-to-paramagnetic phase transition occurs when is reduced to 30 mTorr, probably due to the formation of Re ions that replace the stoichiometric Re to cause disorders of B-site ions. On the other hand, a large compressive strain or tensile strain shifts this critical to below 1 mTorr or above 40 mTorr, respectively. The observations can be attributed to the modulation of B-site ordering by epitaxial strain through affecting elemental valence. Our results provide a feasible way to expand the functional tunability of magnetic double-perovskite oxides that hold great promise for spintronic devices.

摘要

双钙钛矿氧化物由于其诱人的功能和应用潜力而受到了近期的关注。在本文中,我们展示了双控制(即氧沉积压力 () 和晶格失配 (ε))对双钙钛矿 SrFeReO 外延薄膜磁性能的调控作用。在近乎晶格匹配的 SrFeReO/SrTiO 薄膜中,当 降低至 30 毫托时,发生亚铁磁-顺磁相变,可能是由于形成取代了化学计量比 Re 的 Re 离子,导致 B 位离子无序。另一方面,较大的压应变或张应变分别将此临界 值移动至低于 1 毫托或高于 40 毫托。这些观察结果可以归因于外延应变通过影响元素价态来调制 B 位有序性。我们的结果为扩展具有自旋电子学器件应用前景的磁性双钙钛矿氧化物的功能可调性提供了一种可行的方法。

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