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Bonding Structure of Ultrathin Oxides on Si(110) Surface

Published online by Cambridge University Press:  01 February 2011

Yoshihisa Yamamoto
Affiliation:
yamamoto@cir.tohoku.ac.jp, Tohoku University, Tohoku University, 6-3 Aza-Aoba, Aramaki, Aobaku, Sendai, 980-8578, Japan
Hideaki Togashi
Affiliation:
togashi@suemitsu.riec.tohoku.ac.jp, Tohoku University, 6-3 Aza-Aoba, Aramaki, Aoba-ku,, Sendai, 980-8578, Japan
Atsushi Kato
Affiliation:
kato@suemitsu.riec.tohoku.ac.jp, Tohoku University, 6-3 Aza-Aoba, Aramaki, Aoba-ku,, Sendai, 980-8578, Japan
Maki Suemitsu
Affiliation:
suemitsu@cir.tohoku.ac.jp, Tohoku University, 6-3 Aza-Aoba, Aramaki, Aoba-ku,, Sendai, 980-8578, Japan
Yuzuru Narita
Affiliation:
narita@ele.kyutech.ac.jp, Kyusyu Institute of Technology, 1-1, Sensui-mach, Tobata-ku, Kitakyushu, 804-8550, Japan
Yuden Teraoka
Affiliation:
yteraoka@spring8.or.jp, Japan Atomic Energy Agency, 1-1-1, Kouto, Sayo-cho, 679-5148, Japan
Akitaka Yoshigoe
Affiliation:
yoshigoe@spring8.or.jp, Japan Atomic Energy Agency, 1-1-1, Kouto, Sayo-cho, 679-5148, Japan
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Abstract

The thermal oxidation kinetics of Si(110) surface up to oxide layer thickness of 1 ML has been investigated by real-time monitoring of chemical shifted in the Si 2p core-level photoemission using synchrotron radiation. The uptake profiles of every Si oxidation states (Sin+: n = 1 − 4) indicate that the top surface Si(110) oxidation proceeds through a two-step oxidation pathway via Si2+ state, just like the Si(001) surface. In contrast to the Si(001) oxidation, however, Si3+ state is always more abundant than Si4+ state during oxidation. This is related to occurrence of imperfect oxidation of this surface, most probably due to accumulation of compressive strain during oxidation.

Type
Research Article
Copyright
Copyright © Materials Research Society 2008

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References

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