论文标题

电子在磁性薄膜的杂化纳米结构中旋转极化的合作效应,该薄膜具有吸附的手性分子,并用非自旋偏振扫描隧道显微镜研究

Cooperative effect of electrons spin polarization in a hybrid nanostructure of a magnetic thin film with adsorbed chiral molecules studied with non-spin-polarized scanning tunneling microscopy

论文作者

Ha, Nguyen T. N., Rasabathina, L., Hellwig, O., Sharma, A., Salvan, G., Yochelis, S., Paltiel, Y., Baczewski, L. T., Tegenkamp, C.

论文摘要

带有α-螺旋构象的多酰胺分子(PA)最近引起了很多兴趣,因为电子通过手性骨架结构的传播随着传输电子的自旋极化而伴随着。通过在环境条件下扫描隧道显微镜和光谱,研究了PA分子吸附在具有垂直方向异性的外部磁Al2O3/pt/au/au/co/au纳米结构上的表面上。因此,在表面上排序的PA分子与跨该混合系统的电子隧穿之间的相关性是底物磁化方向的函数以及观察到覆盖率和螺旋的效果。发现最高的自旋极值P,用于有序的自组装单层,并具有将分子与磁性底物表面定义的化学耦合,这表明当前诱导的自旋选择性是一种合作效应。因此,与从占用的分子轨道得出的值相比,从螺旋分子的未占用分子轨道沿电子传输推导的P更大。显然,较大的轨道重叠会导致较高的电子迁移率产生较高的P值。通过切换共层的磁化方向,可以证明非自旋偏振的STM可用于研究具有亚分子分辨率的手性分子,以检测埋入磁性层的特性,并检测分子的自旋偏振,从这种氢结构的磁磁性变化中旋转。

Polyalanine molecules (PA) with an α-helix conformation gathered recently a lot of interest as the propagation of electrons through the chiral backbone structure comes along with spin polarization of the transmitted electrons. By means of scanning tunneling microscopy and spectroscopy at ambient conditions, PA molecules adsorbed on surfaces of epitaxial magnetic Al2O3/Pt/Au/Co/Au nanostructures with perpendicular anisotropy were studied. Thereby, a correlation between the PA molecules ordering at the surface with the electron tunneling across this hybrid system as a function of the substrate magnetization orientation as well as the coverage density and helicity of the was observed. The highest spin polarization values, P, were found for well-ordered self-assembled monolayers and with a defined chemical coupling of the molecules to the magnetic substrate surface, showing that the current induced spin selectivity is a cooperative effect. Thereby, P deduced from the electron transmission along unoccupied molecular orbitals of the helical molecules is larger as compared to values derived from the occupied molecular orbitals. Apparently, the larger orbital overlap is resulting in a higher electron mobility yielding a higher P value. By switching the magnetization direction of the Co-layer, it was demonstrated that the non-spin-polarized STM can be used to study chiral molecules with a sub-molecular resolution, to detect properties of buried magnetic layers and to detect the spin polarization of the molecules from the change of the magnetoresistance of such hybrid structures.

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