硅烷和锗反应中Si1-xGex薄膜的低温外延生长机理

J. Murota, Y. Takasawa, H. Fujimoto, K. Goto, T. Matsuura, Y. Sawada
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摘要

采用超净热壁低压化学气相沉积(LPCVD)系统,在最干净的sih4, geh4和h2与ph3或b2h6的反应环境下,在550°C的Si(100)表面研究了未掺杂和掺杂Si 1-x Ge x薄膜的低温外延生长。根据Langmuir吸附等温线,假设一个sih4或geh4分子被吸附在一个单一的吸附位点上,并在那里分解,sih4和geh4的反应速率用Langmuir型速率方程表示。结果表明,sih4和geh4在Si-Ge对的键位上的吸附速率常数比其他基团的吸附速率常数大,而sih4在Ge-Ge对的键位上的表面反应速率常数最大。随着PH 3和b2h5的加入,P和B的掺入率成比例增加,且随着膜中Ge分数x的增加,P和B的掺入率也相应增加。根据Langmuir-type速率方程,这可以通过自由位点密度的增加和自由位点材料的差异来解释。在P掺杂的情况下,发现电非活性P与高Ge组分形成。
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Low-Temperature Epitaxial Growth Mechanism of Si1-xGex Films in the Silane and Germane Reactions
Low-temperature epitaxial growth of undoped and doped Si 1-x Ge x films on the Si(100) surface at 550°C was investigated under the cleanest possible reaction environment of SiH 4 , GeH 4 and H 2 with the PH 3 or B 2 H 6 addition using an ultraclean hot-wall low-pressure chemical vapour deposition (LPCVD) system. The SiH 4 and GeH 4 reaction rates are expressed by the Langmuir-type rate equation, assuming that one SiH 4 or GeH 4 molecule is adsorbed at a single adsorption site, according to the Langmuir's adsorption isotherm, and decomposes there. It is found that the SiH 4 and GeH 4 adsorption rate constants become larger at the bond site of the Si-Ge pair than those at the others, while the SiH 4 surface reaction rate constant becomes the largest at the bond site of the Ge-Ge pair. With the PH 3 and B 2 H 5 addition, the incorporation rate of P and B increased proportionally and was higher with a higher Ge fraction x in the film. This was explained by the increase of the free site density and the difference of free site materials according to the Langmuir-type rate equation. In the case of P doping, it is found that electrically inactive P is formed with high Ge fractions.
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