Surface chemistry of alkylsilanes on Si(100)2x1

被引:25
作者
Foster, M [1 ]
Darlington, B [1 ]
Scharff, J [1 ]
Campion, A [1 ]
机构
[1] UNIV TEXAS,SCI & TECHNOL CTR SYNTH GROWTH & ANAL ELECT MAT,AUSTIN,TX 78712
基金
美国国家科学基金会;
关键词
alkylsilanes; chemical vapor deposition; electron energy loss spectroscopy; silicon; single crystal epitaxy; surface chemical reaction; thermal desorption spectroscopy; vibrations of adsorbed molecules;
D O I
10.1016/S0039-6028(96)01260-5
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
The adsorption and thermal decomposition of ethylsilane, diethylsilane, triethylsilane, tetraethylsilane, dimethylsilane and di-isobutylsilane were studied on the Si(100)2 x 1 reconstructed surface using temperature-programmed desorption mass spectrometry and high-resolution electron energy-loss spectroscopy. Ethylsilane, diethylsilane and di-isobutylsilane each adsorbs dissociatively onto the surface up to a saturation coverage of approximately 0.25 ML. Thermal decomposition proceeds via beta-hydride elimination. Ethylene and hydrogen desorption occurs at 700 and 800 K, respectively, for ethylsilane and diethylsilane. Isobutylene desorption is observed at 635 K, followed by hydrogen desorption at 800 K for di-isobutylsilane. Dimethylsilane adsorbs dissociatively up to a saturation coverage of 0.25 ML. Thermal decomposition proceeds via dehydrogenation of the methyl groups. Hydrogen desorption is observed at 800 K for low coverages with a 5-10 K peak shift to higher temperatures for higher coverages. Triethylsilane adsorbs dissociatively, but saturation coverage could not be established in these experiments. Thermal decomposition proceeds via P-hydride elimination, resulting in the desorption of ethylene at 700 K and hydrogen at 800 K. Adsorption of tetraethylsilane is not observed. For every precursor, except tetraethylsilane, hydrogen adsorbs exclusively as the (2 x 1) monohydride. No adsorption of any of these precursors on the native SiO2 surface is observed at 100 K. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:35 / 44
页数:10
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