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反铁弹性自旋交叉金属超分子链中的集体自旋操纵

Collective Spin Manipulation in Antiferroelastic Spin-Crossover Metallo-Supramolecular Chains.

作者信息

Liu Jing, Gao Yifan, Wang Tong, Xue Qiang, Hua Muqing, Wang Yongfeng, Huang Li, Lin Nian

机构信息

Department of Physics, The Hong Kong University of Science and Technology, Hong Kong, China.

Division of Quantum State of Matter, Beijing Academy of Quantum Information Sciences, 100193 Beijing, China.

出版信息

ACS Nano. 2020 Sep 22;14(9):11283-11293. doi: 10.1021/acsnano.0c03163. Epub 2020 Aug 20.

Abstract

Coupled spin-crossover complexes in supramolecular systems feature rich spin phases that can exhibit collective behaviors. Here, we report on a molecular-level exploration of the spin phase and collective spin-crossover dynamics in metallo-supramolecular chains. Using scanning tunneling microscopy, spectroscopy, and density functional theory calculations, we identify an antiferroelastic phase in the metal-organic chains, where the Ni atoms coordinated by deprotonated tetrahydroxybenzene linkers on Au(111) are at a low-spin ( = 0) or a high-spin ( = 1) state alternately along the chains. We demonstrate that the spin phase is stabilized by the combined effects of intrachain interactions and substrate commensurability. The stability of the antiferroelastic structure drives the collective spin-state switching of multiple Ni atoms in the same chain in response to electron/hole tunneling to a Ni atom a domino-like magnetostructural relaxation process. These results provide insights into the magnetostructural dynamics of the supramolecular structures, offering a route toward their spintronic manipulations.

摘要

超分子体系中的耦合自旋交叉配合物具有丰富的自旋相,可表现出集体行为。在此,我们报告了对金属超分子链中自旋相和集体自旋交叉动力学的分子水平探索。利用扫描隧道显微镜、光谱学和密度泛函理论计算,我们在金属有机链中识别出一种反铁弹性相,其中在Au(111)上由去质子化的四羟基苯连接体配位的Ni原子沿着链交替处于低自旋((S = 0))或高自旋((S = 1))状态。我们证明,自旋相通过链内相互作用和衬底适配性的综合作用得以稳定。反铁弹性结构的稳定性驱动同一链中多个Ni原子响应电子/空穴隧穿到一个Ni原子而发生集体自旋态切换——这是一个多米诺骨牌式的磁结构弛豫过程。这些结果为超分子结构的磁结构动力学提供了见解,为其自旋电子学操纵提供了一条途径。

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