论文标题

磁性绝缘体异质结构中的工程界面相互作用的分子方法

A Molecular Approach for Engineering Interfacial Interactions in Magnetic-Topological Insulator Heterostructures

论文作者

Cuxart, Marc G., Valbuena, Miguel Angel, Robles, Roberto, Moreno, César, Bonell, Frédéric, Sauthier, Guillaume, Imaz, Inhar, Xu, Heng, Nistor, Corneliu, Barla, Alessandro, Gargiani, Pierluigi, Valvidares, Manuel, Maspoch, Daniel, Gambardella, Pietro, Valenzuela, Sergio O., Mugarza, Aitor

论文摘要

在磁性/拓扑绝缘子异质结构中控制界面相互作用是新型自旋依赖性电子现象出现的主要挑战。至于任何依赖接近效应的异质结构的合理设计,理想情况下应保留每个组件的整体属性,同时调整界面处的相互作用。但是,在大多数无机界面中,相互作用太强,因此在界面每一侧的磁矩和拓扑表面状态都扰动,甚至淬灭。在这里,我们表明可以通过使用配体化学来调整磁离子与表面状态的相互作用来保存这些特性。通过将基于CO的卟啉和邻苯烷氨酸单层沉积在Bi $ _2 $ _2 $ _3 $薄膜的表面上,形成了强大的界面,可以保留不依存的拓扑表面状态以及师团的原始磁矩。选定的配体使我们能够在这种弱相互作用方面调整界面杂交。这些结果与观察到的抑制表面状态在BI $ _2 $ _2 $ SE $ _3 $的第一个五五倍层的抑制形成鲜明对比,这是与与CO邻苯烷的相互作用引起的,证明了平面金属有机分子的能力,可以从强度到弱极限到弱极限。

Controlling interfacial interactions in magnetic/topological insulator heterostructures is a major challenge for the emergence of novel spin-dependent electronic phenomena. As for any rational design of heterostructures that rely on proximity effects, one should ideally retain the overall properties of each component while tuning interactions at the interface. However, in most inorganic interfaces interactions are too strong, consequently perturbing, and even quenching, both the magnetic moment and the topological surface states at each side of the interface. Here we show that these properties can be preserved by using ligand chemistry to tune the interaction of magnetic ions with the surface states. By depositing Co-based porphyrin and phthalocyanine monolayers on the surface of Bi$_2$Te$_3$ thin films, robust interfaces are formed that preserve undoped topological surface states as well as the pristine magnetic moment of the divalent Co ions. The selected ligands allow us to tune the interfacial hybridization within this weak interaction regime. These results, which are in stark contrast with the observed suppression of the surface state at the first quintuple layer of Bi$_2$Se$_3$ induced by the interaction with Co phthalocyanines, demonstrate the capability of planar metal-organic molecules to span interactions from the strong to the weak limit.

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