Ghosh Supriya, Mishra Suryakant, Avigad Eytan, Bloom Brian P, Baczewski L T, Yochelis Shira, Paltiel Yossi, Naaman Ron, Waldeck David H
Chemistry Department , University of Pittsburgh , Pittsburgh , Pennsylvania 15260 , United States.
Department of Chemical and Biological Physics , Weizmann Institute , Rehovot 76100 , Israel.
J Phys Chem Lett. 2020 Feb 20;11(4):1550-1557. doi: 10.1021/acs.jpclett.9b03487. Epub 2020 Feb 11.
Kelvin-probe measurements on ferromagnetic thin film electrodes coated with self-assembled monolayers of chiral molecules reveal that the electron penetration from the metal electrode into the chiral molecules depends on the ferromagnet's magnetization direction and the molecules' chirality. Electrostatic potential differences as large as 100 mV are observed. These changes arise from the applied oscillating electric field, which drives spin-dependent charge penetration from the ferromagnetic substrate to the chiral molecules. The enantiospecificity of the response is studied as a function of the magnetization strength, the magnetization direction, and the handedness and length of the chiral molecules. These new phenomena are rationalized in terms of the chiral-induced spin selectivity (CISS) effect, in which one spin orientation of electrons from the ferromagnet penetrates more easily into a chiral molecule than does the other orientation. The large potential changes (>kT at room temperature) manifested here imply that this phenomenon is important for spin transport in chiral spintronic devices and for magneto-electrochemistry of chiral molecules.
对手性分子自组装单分子层包覆的铁磁薄膜电极进行开尔文探针测量发现,电子从金属电极渗透到 chiral 分子中取决于铁磁体的磁化方向和分子的手性。观察到高达 100 mV 的静电势差。这些变化源于施加的振荡电场,该电场驱动自旋相关的电荷从铁磁基底渗透到手性分子中。研究了响应的对映体特异性与磁化强度、磁化方向以及手性分子的手性和长度的函数关系。这些新现象根据手性诱导自旋选择性(CISS)效应得到合理解释,在该效应中,来自铁磁体的电子的一种自旋取向比另一种取向更容易渗透到手性分子中。此处表现出的大的电势变化(室温下 >kT)意味着这种现象对手性自旋电子器件中的自旋输运以及手性分子的磁电化学很重要。