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    Molecular approach for engineering interfacial interactions in magnetic/topological insulator heterostructures

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    Identificadores
    URI: https://hdl.handle.net/10902/34975
    DOI: 10.1021/acsnano.0c02498
    ISSN: 1936-0851
    ISSN: 1936-086X
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    Autoría
    González Cuxart, Marc; Valbuena, Miguel Ángel; Robles, Roberto; Moreno Sierra, CésarAutoridad Unican; Bonell, Frédéric; Sauthier, Guillaume; Imaz, Inhar; Xu, Heng; Nistor, Corneliu; Barla, Alessandro; Gargiani, Pierluigi; Valvidares, Manuel; Maspoch Comamala, Daniel; Gambardella, Pietro; Valenzuela, Sergio O.; Mugarza, Aitor
    Fecha
    2020-05
    Derechos
    © ACS. This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Nano, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see: https://dx.doi.org/10.1021/acsnano.0c02498.
    Publicado en
    ACS Nano, 2020, 14(5), 6285-6294
    Editorial
    American Chemical Society
    Enlace a la publicación
    https://dx.doi.org/10.1021/acsnano.0c02498?ref=pdf
    Palabras clave
    Metal-organic molecules
    Topological insulators
    Interfacial interactions
    Scanning tunneling microscopy
    Angle-resolved photoelectron spectroscopy
    X-ray magnetic circular dichroism
    Density functional theory
    Resumen/Abstract
    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 Bi₂Se₃ 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 Bi₂Se₃ 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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    UNIVERSIDAD DE CANTABRIA

    Repositorio realizado por la Biblioteca Universitaria utilizando DSpace software
    Contacto | Sugerencias
    Metadatos sujetos a:licencia de Creative Commons Reconocimiento 4.0 España