Ha Nguyen Thi Ngoc, Paltiel Yossi, Baczewski Lech T, Tegenkamp Christoph
Solid Surface Analysis, Institute of Physics, Chemnitz University of Technology, Reichenhainer Strasse 70, Chemnitz 09126, Germany.
Department of Applied Physics, Hebrew University of Jerusalem, Jerusalem 91905, Israel.
ACS Appl Mater Interfaces. 2023 Apr 5;15(13):17406-17412. doi: 10.1021/acsami.3c01429. Epub 2023 Mar 23.
Propagation of electrons along helical molecules adsorbed on surfaces comes along with a robust spin polarization effect called chirality induced spin selectivity CISS. However, experiments on the molecular scale that allow a true correlation of spin effects with the molecular structure are quite rare. Here we have studied the structure of self-assembled chiral molecules and the electronic transmission and spin polarization of the current through the system by means of ambient scanning tunneling microscopy and spectroscopy in heterostructures of various α-helix polyalanine-based molecules (PA) adsorbed on AlO/Pt/Au/Co/Au substrates with perpendicular magnetic anisotropy. We have found a phase separation of the molecules into well-ordered enantiopure 2D hexagonal phases and quasi-1D heterochiral-dimer structures, which allows for the analysis of the spin polarization with almost atomic precision of PA in different phases. The spin polarization reaches up to 75% for chemisorbed molecules arranged in a hexagonal phase. On the contrary, for weakly coupled PA molecules without cysteine anchoring groups in a quasi-1D phase, a spin polarization of around 50% was found. Our results show that both the intermolecular interaction as well as the coupling to the substrate are important and point out that collective effects within the molecules and at the interfaces are required to achieve a high chiral induced spin selectivity.
电子沿着吸附在表面的螺旋分子传播时,会伴随一种强大的自旋极化效应,即手性诱导自旋选择性(CISS)。然而,在分子尺度上能够将自旋效应与分子结构真正关联起来的实验却相当罕见。在此,我们借助环境扫描隧道显微镜和光谱技术,研究了自组装手性分子的结构以及通过吸附在具有垂直磁各向异性的AlO/Pt/Au/Co/Au衬底上的各种基于α-螺旋聚丙氨酸的分子(PA)的异质结构系统的电流电子传输和自旋极化。我们发现分子相分离成有序的对映体纯二维六方相和准一维异手性二聚体结构,这使得能够以几乎原子级的精度分析不同相中PA的自旋极化。对于排列成六方相的化学吸附分子,自旋极化率高达75%。相反,对于在准一维相中没有半胱氨酸锚定基团的弱耦合PA分子,发现自旋极化率约为50%。我们的结果表明,分子间相互作用以及与衬底的耦合都很重要,并指出分子内部和界面处的集体效应对于实现高的手性诱导自旋选择性是必需的。