Order-disorder phase transition of the subsurface cation vacancy reconstruction on Fe3O4(001)

B. Arndt, B. A. J. Lechner, A. Bourgund, E. Grånäs, M. Creutzburg, K. Krausert, J. Hulva, G. S. Parkinson, M. Schmid, V. Vonk, F. Esch, A. Stierle

Deutsches Elektronen-Synchrotron (DESY), D-22607 Hamburg, Germany.
University of Hamburg, Physics Department, D-20355 Hamburg, Germany
Department of Chemistry & Catalysis Research Center, Technical University of Munich, D-85748 Garching, Germany.
Institut für Angewandte Physik, TU Wien, 1040 Wien, Austria

Phys. Chem. Chem. Phys. 22 (2020) 8336-8343

We present surface X-ray diffraction and fast scanning tunneling microscopy results to elucidate the nature of the surface phase transition on magnetite (001) from a reconstructed to a non-reconstructed surface around 720 K. In situ surface X-ray diffraction at a temperature above the phase transition, at which long-range order is lost, gives evidence that the subsurface cation vacancy reconstruction still exists as a local structural motif, in line with the characteristics of a 2D second-order phase transition. Fast scanning tunneling microscopy results across the phase transition underpin the hypothesis that the reconstruction lifting is initiated by surplus Fe ions occupying subsurface octahedral vacancies. The reversible near-surface iron enrichment and reduction of the surface to stoichiometric composition is further confirmed by in situ low-energy ion scattering, as well as ultraviolet and X-ray photoemission results.

Corresponding authors: Barbara Lechner and Andreas Stierle. Reprints also available from Gareth Parkinson (parkinson at iap_tuwien_ac_at).

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