局域尺度Fe60A40薄膜中无序诱导铁磁现象的特性。

A. Smekhova, E. L. Torre, T. Szyjka, B. Eggert, B. Cöster, K. Ollefs, D. Walecki, S. Salamon, R. Bali, J. Lindner, F. Wilhelm, A. Rogalev, E. Weschke, D. Többens, R. Banerjee, B. Sanyal, C. Schmitz-Antoniak, H. Wende
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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 $( \\mathrm {B}2 \\rightarrow {A}2$) 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.","PeriodicalId":6571,"journal":{"name":"2018 IEEE International Magnetic Conference (INTERMAG)","volume":"39 1","pages":"1-1"},"PeriodicalIF":0.0000,"publicationDate":"2018-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Peculiarities of Disorder-Induced Ferromagnetism Phenomena in Fe60A40 films on a local scale.\",\"authors\":\"A. Smekhova, E. L. Torre, T. Szyjka, B. Eggert, B. Cöster, K. Ollefs, D. Walecki, S. Salamon, R. Bali, J. Lindner, F. Wilhelm, A. Rogalev, E. Weschke, D. Többens, R. Banerjee, B. Sanyal, C. Schmitz-Antoniak, H. 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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. 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引用次数: 0

摘要

富铁过渡金属铝化物Fe60Al40 (at)薄膜。%)在现代技术中非常有希望实现,因为有可能具有定制的磁性。Fe60Al40薄膜在室温下为化学有序的B2相弱铁磁性,通过离子辐照可在可控条件下可逆地转变为具有较高磁化强度的化学无序的A2相。先前的研究指出了化学无序对Fe60Al40薄膜静态和动态磁性能的重要影响,而磁性图化和磁化反转研究的成果也显示了其在自旋输运器件中的进一步应用前景[1-3]。在局部尺度上进行详细的研究可以通过了解局部环境和Fe-Al杂化特征对磁性能的影响,阐明Fe60Al40薄膜中无序诱导铁磁性现象的隐藏机制。在我们的工作中,应用元素特异性x射线吸收光谱(EXAFS, XANES和XMCD)在硬能谱和软能谱范围内以及基于同步加速器的XRD (SR-XRD),通过20keV Ne+离子辐照(低影响~1014离子cm-2)引发的有序-无序$(\ mathm {B}2 \右行{A}2$)相变,探测了40 nm厚度的Fe60Al40裸露薄膜中Fe和Al原子的局部重排和相关的磁性和电子性质。在室温(RT)和低温5K (LT)下,在Fe和Al K边缘记录的扩展x射线吸收精细结构(EXAFS)光谱和SR-XRD显示,辐照前后Fe和Al吸收剂的局部环境发生了显著变化。在转变过程中,有序B2相和完全无序A2相的Fe-Fe近邻数从3.47(7)增加到5.0(1),胞体体积膨胀约1%。在Fe L2、3和Fe K边的RT XMCD和Al K边的LT XANES分别证明了由于无序导致Fe和Al配位的明显变化,导致Fe三维自旋和4p轨道极化增加,Al原子的电子结构发生了特征变化[4,5]。通过在Fe - K边缘以上~60 eV记录XMCD信号,实现了用硬x射线探测三维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峰值振幅及其综合强度的分析显示,其随通量的变化趋势与利用XMCD谱分别在Fe L2、3边得到的三维有效自旋磁矩和三维轨道磁矩相似。此外,该分析指出,(0.75-6)× 1014离子cm-2的通量增加了A2相中Fe 3d态的局域化。XMCD记录的Fe - K或L3吸收边的元素特异性磁滞回线(ESHL)证实了辐照膜具有优先的面内磁各向异性;用ESHL法测定了Fe - L3边缘矫顽力场随温度和辐照强度的变化。在原位氢等离子体处理的帮助下,揭示了铁和铝之间杂化效应的特殊肩。结果表明,表面氧化层的还原导致表面Fe三维自旋磁矩随处理时间的增加或减少。这表明,使用封盖层既可以保护薄膜免受持续不受控制的氧化,也可以进一步提高薄膜的宏观磁化强度,这对技术应用更有利。应用VASP程序包对松弛模型系统进行自洽DFT计算,提供了理论支持。在B2和A2相中,局部构型发生了明显变化,随后Fe和Al磁矩发生了相当大的变化。这项工作部分由亥姆霍兹协会(青年研究小组“边缘性磁学”,VH-NG-1031)资助。作者感谢ESRF (ID12波束线)和HZB-BESSY II (UE46_PGM-1和KMC-2波束线)提供同步辐射设施和分配同步辐射;瑞典国家计算基础设施(SNIC)因提供高性能超级计算时间而得到认可。
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Peculiarities of Disorder-Induced Ferromagnetism Phenomena in Fe60A40 films on a local scale.
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 $( \mathrm {B}2 \rightarrow {A}2$) 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.
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