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铟酞菁在Pb(100)上的自旋态切换

Spin-state switching of indium-phthalocyanine on Pb(100).

作者信息

Ide Niklas, Banerjee Arnab, Weismann Alexander, Berndt Richard

机构信息

Institut für Experimentelle und Angewandte Physik, Christian-Albrechts-Universität zu Kiel D-24098 Kiel Germany

出版信息

RSC Adv. 2024 Dec 5;14(52):38506-38513. doi: 10.1039/d4ra07270g. eCollection 2024 Dec 3.

Abstract

Indium(iii) phthalocyanine chloride deposited on Pb(100) is studied by scanning tunnelling spectroscopy at cryogenic temperatures. The Cl ions are dissociated and the remaining indium phthalocyanine (InPc) is observed in two states with the metal ion pointing to (↓) or away (↑) from the substrate. Isolated molecules and islands with a superstructure and a unit cell of four inequivalent molecules, namely one InPc↑ and three InPc↓ in different sites, are observed. Using atomic resolution images of the substrate the adsorption sites and azimuthal orientation of InPc are determined and a structure model is proposed. Conductance spectra of the lowest unoccupied molecular orbital reveal differences that depend on the adsorption sites and azimuthal orientations of the complexes. Only InPc↑ molecules exhibit Shiba states, indicating the presence of a localized spin. By electron extraction isolated complexes as well as molecules in islands are converted from InPc↑ to InPc↓. At the same time, their spin state changes, as indicated by the disappearance of the Shiba states.

摘要

在低温下通过扫描隧道光谱对沉积在Pb(100)上的氯化铟(III)酞菁进行了研究。Cl离子发生解离,观察到剩余的铟酞菁(InPc)处于两种状态,金属离子指向(↓)或远离(↑)衬底。观察到了孤立分子以及具有超结构和由四个不等价分子组成的晶胞的岛,即在不同位置的一个InPc↑和三个InPc↓。利用衬底的原子分辨率图像确定了InPc的吸附位点和方位取向,并提出了一个结构模型。最低未占据分子轨道的电导光谱揭示了取决于配合物吸附位点和方位取向的差异。只有InPc↑分子表现出志波态,表明存在局域自旋。通过电子提取,孤立的配合物以及岛中的分子从InPc↑转变为InPc↓。与此同时,它们的自旋状态发生变化,如志波态的消失所示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e06f/11618534/6c1de47a6a08/d4ra07270g-f1.jpg

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