Nguyen Thi Ngoc Ha, Rasabathina Lokesh, Hellwig Olav, Sharma Apoorva, Salvan Georgeta, Yochelis Shira, Paltiel Yossi, Baczewski Lech T, Tegenkamp Christoph
Solid Surface Analysis, Institute of Physics, Chemnitz University of Technology, Reichenhainer Str. 70, 09126 Chemnitz, Germany.
Functional Magnetic Materials, Institute of Physics, Chemnitz University of Technology, Reichenhainer Str. 70, 09126 Chemnitz, Germany.
ACS Appl Mater Interfaces. 2022 Aug 24;14(33):38013-38020. doi: 10.1021/acsami.2c08668. Epub 2022 Aug 12.
Polyalanine molecules (PA) with an α-helix conformation have recently attracted a great deal 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 under ambient conditions, PA molecules adsorbed on surfaces of epitaxial magnetic AlO/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 PA molecules was observed. The highest spin polarization values, , 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, deduced from the electron transmission along unoccupied molecular orbitals of the chiral molecules is larger as compared to values derived from the occupied molecular orbitals. Apparently, the larger orbital overlap results in a higher electron mobility, yielding a higher 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 submolecular resolution, to detect properties of buried magnetic layers and to detect the spin polarization of the molecules from the change in the magnetoresistance of such hybrid structures.
具有α-螺旋构象的聚丙氨酸分子(PA)最近引起了广泛关注,因为电子通过手性主链结构的传播伴随着传输电子的自旋极化。通过在环境条件下的扫描隧道显微镜和光谱学,研究了吸附在外延磁性AlO/Pt/Au/Co/Au纳米结构表面的PA分子,该纳米结构具有垂直各向异性。由此,观察到表面PA分子的有序排列与作为底物磁化方向以及PA分子的覆盖密度和螺旋度函数的跨该混合系统的电子隧穿之间的相关性。对于有序的自组装单分子层以及分子与磁性底物表面具有确定的化学耦合,发现了最高的自旋极化值,表明电流诱导的自旋选择性是一种协同效应。由此,与从占据分子轨道得出的值相比,从沿着手性分子未占据分子轨道的电子传输推导得出的 更大。显然,更大的轨道重叠导致更高的电子迁移率,产生更高的 值。通过切换Co层的磁化方向,证明了非自旋极化STM可用于以亚分子分辨率研究手性分子、检测埋藏磁性层的性质以及从这种混合结构的磁阻变化检测分子的自旋极化。