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Temperature-Induced Metamagnetic Transition and Domain Structures of Single-Crystalline FeRh Thin Films on MgO(100)

机译:MgO(100)上单晶FeRh薄膜的温度诱导亚磁跃迁和畴结构

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摘要

Exchange systems of FeRh with a hard magnetic layer are a promising approach for heat-assisted magnetic recording that can largely increase the storage density of hard disk drives. The FeRh alloy is known to undergo a temperature-induced metamagnetic transition from antiferromagnetic (AFM) to ferromagnetic (FM) just above the room temperature. But the AFM and FM phases coexist across the transition in single-crystalline FeRh thin lms with thin capping layers (e.g. Au, Al, or MgO). In order to investigate the intrinsic surface magnetic properties, singlecrystalline FeRh lms without capping layer are prepared by two kinds of experimentalprocedures. For the ex-situ sample preparation procedure, two 40nm thick, single-crystalline FeRh lms are prepared on MgO(100) by separate layer deposition of Fe and Rh. X-ray photoemission spectroscopy (XPS) immediately after the deposition shows that one sample is Rh-rich and the other Fe-rich. The samples are exposed to air and transferred to a second ultra-high vacuum (UHV) system to perform themagnetic characterization. This transfer results in a contamination by C and O. After surface cleaning by high-temperature annealing the Rh-rich sample is still slightly contaminated with C, while the Fe-rich surface is oxidized. Magneto-optical Kerr eect (MOKE) measurements reveal that only the Rh-rich sample shows the metamagnetic transition below room temperature. The Fe-rich sample is FM at 193 and 293 K. Scanning electron microscopy with polarization analysis (SEMPA) reveals that the Rh-rich surface is FM at all temperatures between 160 and 450K although the bulk is AFM below room temperature.For the in-situ sample preparation procedure, a 10nm single-crystalline FeRh lm is prepared on MgO(100) again by separate layer deposition of Fe and Rh but now in the same UHV system as all characterizations. Thus, the intrinsic properties of the single-crystalline FeRh lm are investigated without exposure to air and additional cleaning steps. The in-situ prepared FeRh lm also exhibits the metamagnetic phase transition below room temperature as indicated by MOKE. The temperature dependent domain structure obtained by SEMPA reveals that FM domains exist at the surface while the bulk is AFM. In contrast to the ex-situ prepared samplethe domain size changes drastically at the transition temperature. This is related to a spin reorientation transition from out-of-plane to in-plane between 350 to 400 K.
机译:具有硬磁层的FeRh交换系统是一种有前途的热辅助磁记录方法,可以大大提高硬盘驱动器的存储密度。众所周知,FeRh合金会发生温度诱导的从正铁磁(AFM)到正好高于室温的铁磁(FM)的亚磁转变。但是AFM和FM相共存于具有薄覆盖层(例如Au,Al或MgO)的单晶FeRh薄膜中。为了研究固有的表面磁性能,通过两种实验方法制备了不具有覆盖层的单晶FeRh lms。对于异地样品制备程序,通过分别沉积铁和铑,在MgO(100)上制备了两个40nm厚的单晶FeRh lms。沉积后立即进行的X射线光电子能谱(XPS)显示,一个样品富含Rh,而另一个富含Fe。将样品暴露在空气中,然后转移到第二个超高真空(UHV)系统中,以进行磁表征。这种转移导致C和O的污染。在通过高温退火进行表面清洁后,富含Rh的样品仍被C轻微污染,而富含Fe的表面被氧化。磁光克尔效应(MOKE)测量表明只有富Rh的样品在室温以下才显示出亚磁性跃迁。富铁样品在193和293 K时为FM。带有极化分析(SEMPA)的扫描电子显微镜显示,在160至450K的所有温度下,富Rh的表面都是FM,尽管大部分在室温以下仍为AFM。在原位样品制备过程中,通过分别沉积Fe和Rh的层,再次在MgO(100)上制备了10nm单晶FeRh lm,但是现在所有特征都在同一UHV系统中。因此,在不暴露于空气和不进行额外清洁步骤的情况下,研究了单晶FeRh lm的固有性质。如MOKE所示,原位制备的FeRh lm在室温以下也表现出亚磁相变。 SEMPA获得的温度相关的畴结构表明,FM畴存在于表面,而大部分为AFM。与异地制备的样品相反,在转变温度下,畴尺寸急剧变化。这与在350至400 K之间从平面外到平面内的自旋重新定向过渡有关。

著录项

  • 作者

    Zhou Xianzhong;

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  • 年度 2013
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  • 原文格式 PDF
  • 正文语种 eng
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