An infrared study of H8Si8O12 cluster adsorption on Si(100) surfaces

被引:24
作者
Eng, J
Raghavachari, K [1 ]
Struck, LM
Chabal, YJ
Bent, BE
Banaszak-Holl, MM
McFeely, FR
Michaels, AM
Flynn, GW
Christman, SB
Chaban, EE
Williams, GP
Radermacher, K
Mantl, S
机构
[1] Lucent Technol, Bell Labs, Murray Hill, NJ 07974 USA
[2] Columbia Univ, Dept Chem, New York, NY 10027 USA
[3] Columbia Univ, Columbia Radiat Lab, New York, NY 10027 USA
[4] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[5] IBM Corp, TJ Watson Res Labs, Yorktown Hts, NY 10598 USA
[6] Brookhaven Natl Lab, Natl Synchrotron Light Source, Upton, NY 11973 USA
[7] Forschungszentrum Julich, Inst Schicht & Ionentech, W-5170 Julich, Germany
关键词
D O I
10.1063/1.476411
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Motivated by a controversy about the proper interpretation of x-ray photoelectron spectra of Si/SiO2 interfaces derived from the adsorption of H8Si8O12 spherosiloxane clusters on Si(100) surfaces, we have studied the adsorption geometry of the H8Si8O12 clusters on deuterium-passivated and clean Si(100) surfaces by using external reflection infrared spectroscopy. Access to frequencies below 1450 cm(-1) was made possible through the use of specially prepared Si(100) samples which have a buried metallic CoSi2 layer that acts as an internal mirror. A comparison of the infrared spectrum of the clusters on a deuterium-passivated Si(100) surface at 130 K with an infrared spectrum of the clusters in a carbon tetrachloride solution reveals that the clusters are only weakly physisorbed on the D/Si(100) surface and also provides evidence for the purity of the cluster source. We also present infrared spectra of clusters directly chemisorbed on a clean Si(100) surface and show evidence that the clusters are adsorbed on the Si(100) via attachment by one vertex. A complete assignment of the observed vibrational features, for both physisorbed and chemisorbed clusters, has been made based upon comparisons with the results obtained in ab initio calculations using gradient-corrected density functional methods. (C) 1998 American Institute of Physics. [S0021-9606(98)02820-7].
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收藏
页码:8680 / 8688
页数:9
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