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Phys. Rev. B 77, 085313 (2008) [10 pages]

Interfacial properties between CoO (100) and Fe3O4 (100)

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Hui-Qiong Wang1,3, Eric I. Altman2,3, and Victor E. Henrich1,3
1Department of Applied Physics, Yale University, P.O. Box 208284, New Haven, Connecticut 06520, USA
2Department of Chemical Engineering, Yale University, P.O. Box 208284, New Haven, Connecticut 06520, USA
3Center for Research on Interface Structures and Phenomena (CRISP), Yale University, P.O. Box 208284, New Haven, Connecticut 06520, USA

Received 21 October 2007; revised 19 January 2008; published 19 February 2008

Using molecular beam epitaxy 1–20 ML thick CoO (100) films were grown monolayer by monolayer on Fe3O4 (100) substrates. The stoichiometry of the films was verified by low-energy-electron diffraction and reflection-high-energy-electron diffraction patterns, as well as x-ray photoelectron spectroscopy. Auger measurements as a function of CoO film thickness indicated a layer-by-layer growth mode. Ultraviolet photoelectron spectroscopy (UPS) was used to monitor the thin film electronic properties. The evolution of the density of states in the O 2p∕Fe 3d and O 2p∕Co 3d bands exhibits a shift in the position of the CoO valence band for ultrathin films relative to bulklike thick films. The measured spectra (when aligned to cancel the band shift) are compared to models of the spectra that would be expected based on the bulk compounds, with and without additional interfacial electronic states. Electronic states at the Fe3O4-CoO interface have been identified, and their UPS spectrum has been determined.

© 2008 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevB.77.085313
DOI:
10.1103/PhysRevB.77.085313
PACS:
73.20.−r, 79.60.Jv, 79.60.Dp