4.7 Article

Intercalation synthesis of graphene-capped iron silicide atop Ni(111): Evolution of electronic structure and ferromagnetic ordering

Journal

APPLIED SURFACE SCIENCE
Volume 392, Issue -, Pages 715-722

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2016.09.103

Keywords

Graphene; Intercalation; Iron silicides; Photoelectron spectroscopy; Ferromagnetic materials; Thin films

Funding

  1. Russian German laboratory at BESSY II of HZB in Berlin, Germany
  2. Resource Center Physical methods of surface investigation of Research Park of Saint Petersburg State University, Russia [S-RC-5/4]
  3. Russian Foundation for Basic Research [16-02-00387]
  4. Saint Petersburg State University [15.61.202.2015]
  5. ITMO University

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A new method for synthesis of graphene-protected iron silicides has been tested, which consists in formation of graphene on Ni(111) followed by two-step intercalation of the system with Fe and Si. Characterization of the samples was performed in situ by low-energy electron diffraction, angular-resolved photoelectron spectroscopy, core-level photoelectron spectroscopy with synchrotron radiation and magnetic linear dichroism in photoemission of Fe 3p electrons. It is shown, that at 400 degrees C the intercalation of graphene/Ni(111) with iron occurs in a range up to 14 ML. The graphene layer strongly interacts with the topmost Fe atoms and stabilizes the fcc structure of the film. The in-plane ferromagnetic ordering of the film has a threshold nature and arises after the intercalation of 5 ML Fe due to the thickness-driven spin reorientation transition. Subsequent intercalation of graphene/Fe/Ni(111) with Si leads to the formation of the inhomogeneous system consisted of intercalated and nonintercalated areas. The intercalated islands coalesce at 2 ML Si when a Fe-Si solid solution covered with the Fe3Si surface silicide is formed. The Fe3Si silicide is ferromagnetic and has an ordered (root 3 x root 3)R30 degrees structure. The graphene layer is weakly electronically coupled to the silicide phase keeping its remarkable properties ready for use. (C) 2016 Elsevier B.V. All rights reserved.

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