Volume 42, Issue 10-11 p. 1581-1584
Research Article

Growth of thin epitaxial alumina films onto Ni(111): an electron spectroscopy and diffraction study

Slavomir Nemsak

Corresponding Author

Slavomir Nemsak

National Institute for Materials Science, Advanced Electronic Materials Center, Sakura 3-13, 305-0003 Tsukuba, Japan

National Institute for Materials Science, Advanced Electronic Materials Center, Sakura 3-13, 305-0003 Tsukuba, Japan.Search for more papers by this author
Tomas Skala

Tomas Skala

Sincrotrone Trieste, SCpA, Strada Statale 14, km 163.5, 34149 Basovizza-Trieste, Italy

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Michiko Yoshitake

Michiko Yoshitake

National Institute for Materials Science, Advanced Electronic Materials Center, Sakura 3-13, 305-0003 Tsukuba, Japan

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Nataliya Tsud

Nataliya Tsud

Charles University, Faculty of Mathematics and Physics, V Holesovickach 2, 180 00 Prague, Czech Republic

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Taeyoung Kim

Taeyoung Kim

National Institute for Materials Science, Advanced Electronic Materials Center, Sakura 3-13, 305-0003 Tsukuba, Japan

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Shinjiro Yagyu

Shinjiro Yagyu

National Institute for Materials Science, Advanced Electronic Materials Center, Sakura 3-13, 305-0003 Tsukuba, Japan

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Vladimir Matolin

Vladimir Matolin

Charles University, Faculty of Mathematics and Physics, V Holesovickach 2, 180 00 Prague, Czech Republic

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First published: 09 September 2010
Citations: 8

Abstract

An epitaxial ultra-thin alumina layer was prepared on Ni(111) by simultaneous Al deposition and oxidation at elevated temperatures. Different deposition procedures lead to creation of oxide layers of various thicknesses and quality. Low-energy electron diffraction revealed epitaxial parameters of the films and the relationship between the nickel substrate and the oxide overlayer. Core-level photoelectron spectroscopy using Al-Kα and synchrotron-generated photons show that the oxide-metal interface is formed by oxygen atoms, which is contrary to the case of epitaxial alumina layers prepared by the oxidation of NiAl(110) and Ni3Al(111) surfaces. The results of a photoelectric work function measurement are also discussed. Copyright © 2010 John Wiley & Sons, Ltd.