4.8 Article

The emergence of magnetic ordering at complex oxide interfaces tuned by defects

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NATURE COMMUNICATIONS
卷 11, 期 1, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-020-17377-0

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  1. Deutsche Forschungsgemeinschaft through the Collaborative Research Centre [Sonderforschungsbereich 762]
  2. European Commission [80127]
  3. Swedish Research Council (Vetenskapsradet)
  4. Swedish infrastructure for micro- and nanofabrication (MyFab)

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Complex oxides show extreme sensitivity to structural distortions and defects, and the intricate balance of competing interactions which emerge at atomically defined interfaces may give rise to unexpected physics. In the interfaces of non-magnetic complex oxides, one of the most intriguing properties is the emergence of magnetism which is sensitive to chemical defects. Particularly, it is unclear which defects are responsible for the emergent magnetic interfaces. Here, we show direct and clear experimental evidence, supported by theoretical explanation, that the B-site cation stoichiometry is crucial for the creation and control of magnetism at the interface between non-magnetic ABO(3)-perovskite oxides, LaAlO3 and SrTiO3. We find that consecutive defect formation, driven by atomic charge compensation, establishes the formation of robust perpendicular magnetic moments at the interface. Our observations propose a route to tune these emerging magnetoelectric structures, which are strongly coupled at the polar-nonpolar complex oxide interfaces. In the interfaces of non-magnetic complex oxides, it is unclear which defects are responsible for the magnetic interfaces. Here, the authors find the B-site cation stoichiometry is crucial for the creation and control of magnetism at the interface between non-magnetic ABO(3)-perovskite oxides.

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