铁磁性
材料科学
钙钛矿(结构)
价(化学)
自旋电子学
外延
离子
凝聚态物理
晶格常数
顺磁性
化学计量学
铁磁性
结晶学
纳米技术
化学
磁化
衍射
磁场
物理化学
物理
光学
有机化学
量子力学
图层(电子)
作者
Zhaoting Zhang,Hong Yan,Zhen Huang,Xiao Chi,Changjian Li,Zhi Shiuh Lim,Shengwei Zeng,Kun Han,Ganesh Ji Omar,Kexin Jin,Ariando Ariando
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-12-16
卷期号:22 (24): 9900-9906
被引量:3
标识
DOI:10.1021/acs.nanolett.2c03206
摘要
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 (PO2) and lattice mismatch (ε), on tuning magnetic properties in epitaxial double-perovskite Sr2FeReO6 films. In a nearly lattice matched Sr2FeReO6/SrTiO3 film, the ferrimagnetic-to-paramagnetic phase transition occurs when PO2 is reduced to 30 mTorr, probably due to the formation of Re4+ ions that replace the stoichiometric Re5+ to cause disorders of B-site ions. On the other hand, a large compressive strain or tensile strain shifts this critical PO2 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.
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