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磁性表面上的对映选择性吸附

Enantioselective Adsorption on Magnetic Surfaces.

作者信息

Safari Mohammad Reza, Matthes Frank, Caciuc Vasile, Atodiresei Nicolae, Schneider Claus M, Ernst Karl-Heinz, Bürgler Daniel E

机构信息

Peter Grünberg Institute, Electronic Properties (PGI-6), Forschungszentrum Jülich, 52425, Jülich, Germany.

Jülich Aachen Research Alliance (JARA-FIT), Fundamentals of Future Information Technology, Forschungszentrum Jülich, 52425, Jülich, Germany.

出版信息

Adv Mater. 2024 Apr;36(14):e2308666. doi: 10.1002/adma.202308666. Epub 2024 Jan 6.

DOI:10.1002/adma.202308666
PMID:38153192
Abstract

From the beginning of molecular theory, the interplay of chirality and magnetism has intrigued scientists. There is still the question if enantiospecific adsorption of chiral molecules occurs on magnetic surfaces. Enantiomer discrimination was conjectured to arise from chirality-induced spin separation within the molecules and exchange interaction with the substrate's magnetization. Here, it is shown that single helical aromatic hydrocarbons undergo enantioselective adsorption on ferromagnetic cobalt surfaces. Spin and chirality sensitive scanning tunneling microscopy reveals that molecules of opposite handedness prefer adsorption onto cobalt islands with opposite out-of-plane magnetization. As mobility ceases in the final chemisorbed state, it is concluded that enantioselection must occur in a physisorbed transient precursor state. State-of-the-art spin-resolved ab initio simulations support this scenario by refuting enantio-dependent chemisorption energies. These findings demonstrate that van der Waals interaction should also include spin-fluctuations which are crucial for molecular magnetochiral processes.

摘要

从分子理论诞生之初起,手性与磁性之间的相互作用就一直吸引着科学家们。磁性表面是否会发生手性分子的对映体特异性吸附这一问题仍然存在。有人推测,对映体识别源于分子内手性诱导的自旋分离以及与底物磁化强度的交换相互作用。在此,研究表明单螺旋芳烃在铁磁钴表面发生对映选择性吸附。自旋和手性敏感扫描隧道显微镜显示,相反手性的分子更倾向于吸附在具有相反面外磁化强度的钴岛上。由于在最终化学吸附状态下迁移率停止,因此可以得出结论,对映体选择必定发生在物理吸附的瞬态前驱体状态。最新的自旋分辨从头算模拟通过反驳对映体依赖性化学吸附能来支持这一情形。这些发现表明,范德华相互作用也应包括对分子磁手性过程至关重要的自旋涨落。

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