English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Fe3O4(111) surface structure determined by LEED crystallography

MPS-Authors
/persons/resource/persons22012

Ritter,  Michael
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons22230

Weiss,  Werner
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Ritter, M., & Weiss, W. (1999). Fe3O4(111) surface structure determined by LEED crystallography. Surface Science, 432(1-2), 81-94. doi:10.1016/S0039-6028(99)00518-X.


Cite as: https://hdl.handle.net/21.11116/0000-0006-0888-8
Abstract
The surface structure formed on epitaxial Fe3O4(111) magnetite films grown onto Pt(111) was re-examined by a full dynamical low energy electron diffraction (LEED) intensity analysis. Prior to the LEED measurements the films were investigated with scanning tunneling microscopy regarding their surface defect concentrations and the possible coexistence of different surface terminations. After a final oxidation at 1000 K in 10-6 mbar oxygen partial pressure one defined surface structure is formed, and for films with low surface defect concentrations the best fit structure reveals a Pendry R-factor of 0.20 based on a data set with a total energy range of 1300 eV. It corresponds to an unreconstructed bulk termination of Fe3O4(111), which exposes 1/4 monolayer of iron atoms over a hexagonal close-packed oxygen layer underneath. The outermost iron plane is relaxed inward towards the underlying oxygen plane by 41±7% of the corresponding bulk spacing, followed by strong relaxations of the next three interlayer spacings. The same surface termination with slightly different relaxations was obtained in an earlier analysis, which corresponded to a local R-factor minimum in parameter space [W. Weiss et al., Phys. Rev. Lett. 71 (1993) 1848]. The energetics of the Fe3O4(111) surface structure is discussed considering the mixed iono-covalent bond character in this oxide.