60Al Peculiarities of Disorder-Induced Ferromagnetism Phenomena in Fe<inf>60</inf>A<inf>40</inf> films on a local scale.
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Peculiarities of Disorder-Induced Ferromagnetism Phenomena in Fe60A40 films on a local scale.

机译:Fe 60 A 40 薄膜在局部尺度上无序诱发的铁磁性现象的特殊性。

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Thin films of Fe-rich transition metal aluminide Fe60Al40 (at. %) are very promising for implementation in modern technology due to a possibility of having tailored magnetic properties. Being weakly ferromagnetic at room temperature in the chemically ordered B2 phase, Fe60Al40 films can be reversibly transformed into the ferromagnetic chemically disordered A2 phase with much higher magnetization in a well controlled way by means of ion irradiation. Prior studies point on important influence of created chemical disorder on static and dynamic magnetic properties of Fe60Al40 films while achievements in magnetic patterning and studies of magnetization reversal have shown their perspective for further use in spin-transport devices [1-3]. Detailed studies performed on a local scale can clarify hidden mechanisms of disorder induced ferromagnetism phenomena in Fe60Al40 films via understanding the influence of the local surrounding and features of Fe-Al hybridization on the magnetic properties. In our work, element-specific X-ray absorption spectroscopy (EXAFS, XANES, and XMCD) in hard-and soft energy ranges together with synchrotron-based XRD (SR-XRD) have been applied to probe the local rearrangements and related magnetic and electronic properties of Fe and Al atoms in bare Fe60Al40 thin films of 40 nm thickness through the order-disorder (B2 → A2) phase transition initiated by 20keV Ne+ ion irradiation with low fluences ~1014 ions cm-2). Extended X-ray absorption fine structure (EXAFS) spectra recorded at the Fe and Al K edges at room temperature (RT) and low temperature of 5K (LT) and SR-XRD have shown significant changes in the local environment of Fe and Al absorbers before and after the irradiation. In the course of the transition a number of Fe-Fe nearest-neighbors grew from 3.47(7) up to 5.0(1) for the ordered B2 and the fully disordered A2 phases, correspondingly, and ~1% of the unit cell volume expansion was found. Distinct changes of Fe and Al coordination due to disordering resulted in increased Fe 3d spin and 4p orbital polarizations and characteristic changes in electronic structure of Al atoms as was demonstrated by RT XMCD at the Fe L2,3 and Fe K edges as well as LT XANES at the Al K edge, respectively [4, 5]. A unique possibility to probe the magnetism of 3d states by hard X-rays has been realized by recording the XMCD signal at ~60 eV above the Fe K edge where so-called magnetic multi-electronic excitations (MEE, secondary processes) are present [6, 7]. The analysis of MEE peak amplitude and its integrated intensity has revealed similar tendencies in their changes with fluence as for 3d effective spin and 3d orbital magnetic moments obtained from XMCD spectra at the Fe L2,3 edges, respectively. Moreover, this analysis points towards increased localization of Fe 3d states in A2 phases created by fluencies of (0.75-6) × 1014 ions cm-2. Element-specific hysteresis loops (ESHL) recorded by XMCD either at the Fe K or L3 absorption edges have confirmed the preferential in-plane magnetic anisotropy of irradiated films; the variations in coercive fields depending on temperature and irradiation fluence have been checked by ESHL at the Fe L3 edge. The specific shoulder related to hybridization effects between Fe and Al has been uncovered with the help of in-situ hydrogen plasma treatment. It has been also illustrated that the reduction of the top oxide layer leads to increase or decrease of Fe 3d spin magnetic moments in the surface region depending on the time of treatment. This suggests that the use of a capping layer could either protect the films from continuous uncontrolled oxidation or further increase the macroscopic magnetization of films that is much more favorable for technological applications. A theory support was provided by self-consistent DFT calculations using the VASP program package applied to relaxed model systems. A clear variation of local configurations in B2 and A2 phases followed by sizable changes in Fe and Al magnetic moments has been found. The work was partially funded by Helmholtz Association (Young Investigator's Group “Borderline Magnetism”, VH-NG-1031). The authors thank the ESRF (ID12 beamline) and HZB-BESSY II (UE46_PGM-1 and KMC-2 beamlines) for provision of synchrotron radiation facilities and allocation of synchrotron radiation; Swedish National Infrastructure for Computing (SNIC) is acknowledged for providing high performance supercomputing time.
机译:富铁过渡金属铝化物Fe的薄膜 60 40 (at。%)由于具有定制的磁性能的可能性对于在现代技术中实现是非常有前途的。在室温下以化学有序的B2相Fe呈弱铁磁性 60 40 通过离子辐照,可以很好地控制薄膜以可控的方式将其可逆地转变为具有更高磁化强度的铁磁化学无序A2相。先前的研究指出了化学紊乱对铁的静态和动态磁性能的重要影响。 60 40 在磁性图案化和磁化反转研究方面取得的成就显示了它们在自旋传输设备中的进一步应用的前景[1-3]。在局部范围内进行的详细研究可以阐明铁中无序诱发铁磁性现象的隐藏机制 60 40 通过了解局部环境和Fe-Al杂化特征对磁性能的影响来形成薄膜。在我们的工作中,硬和软能范围内的元素特定X射线吸收光谱法(EXAFS,XANES和XMCD)以及基于同步加速器的XRD(SR-XRD)已用于探测局部重排以及相关的磁场和裸铁中铁和铝原子的电子性质 60 40 通过20keV Ne引发的有序(B2→A2)相变的40 nm厚度的薄膜 + 低通量的离子辐照〜10 14 离子厘米 -2 )。在室温(RT)和低温5K(LT)和SR-XRD下在Fe和Al K边缘记录的扩展X射线吸收精细结构(EXAFS)光谱显示,Fe和Al吸收剂的局部环境发生了重大变化辐照前后。在过渡过程中,有序的B2相和完全无序的A2相的Fe-Fe最近邻的数量从3.47(7)增长到5.0(1),并相应地增加了约1%的晶胞体积被找到。如通过RT XMCD在Fe L处证实的,由于无序引起的Fe和Al配位的明显变化导致Fe 3d自旋和4p轨道极化增加,并且Al原子的电子结构发生了特征性变化 2,3 Fe和Fe K边缘,以及Al K边缘的LT XANES [4,5]。通过在Fe K边缘上方〜60 eV处记录XMCD信号,从而实现了用硬X射线探测3d态磁性的独特可能性,其中存在所谓的磁性多电子激发(MEE,二次过程)[ 6、7]。对MEE峰振幅及其积分强度的分析表明,与在Fe L处的XMCD光谱获得的3d有效自旋和3d轨道磁矩有关,它们的通量变化趋势相似。 2,3 边缘。而且,该分析指出,由(0.75-6)×10的通量产生的Fe 3d态在A2相中的定位增加 14 离子厘米 -2 。 XMCD在Fe K或L处记录的元素特定磁滞回线(ESHL) 3 吸收边缘证实了辐照膜的优先面内磁各向异性。 ESHL在Fe L处检查了取决于温度和辐照通量的矫顽场的变化 3 边缘。在原位氢等离子体处理的帮助下,已经发现了与铁和铝之间的杂交效应有关的特定肩峰。还已经表明,取决于处理时间,顶部氧化物层的还原导致表面区域中Fe 3d自旋磁矩的增加或减少。这表明使用覆盖层可以保护膜免受连续的不受控制的氧化,或者可以进一步增加膜的宏观磁化强度,这对于技术应用而言更为有利。使用适用于松弛模型系统的VASP程序包,通过自洽DFT计算提供了理论支持。已发现B2和A2相的局部构型有明显变化,然后铁和铝磁矩发生了较大变化。这项工作部分由亥姆霍兹协会(青年研究者小组“边界磁力”,VH-NG-1031)资助。作者感谢ESRF(ID12光束线)和HZB-BESSY II(UE46_PGM-1和KMC-2光束线)提供同步辐射装置和分配同步辐射;瑞典国家计算机基础设施(SNIC)以提供高性能的超级计算时间而闻名。

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