硅氢化物在多孔硅表面吸附二硅烷后的分解

A.C. Dillon, M.B. Robinson, S.M. George
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引用次数: 8

摘要

二硅烷(Si2H6)用于硅化学气相沉积(CVD),是硅表面原子层外延(ALE)的潜在前驱体。本研究采用傅里叶变换红外(FTIR)透射光谱研究了二硅烷在高比表面积多孔硅表面的吸附和分解。FTIR光谱显示,在200 K温度下,二硅烷在多孔硅表面发生离解吸附,形成大量SiH3表面物质和部分SiH2、SiH表面物质。采用2125 ~ 2156 cm−1的SiHx拉伸模式、862 cm−1的SiH3简并变形模式和907 cm−1的SiH2剪剪模式监测表面杂化物在退火过程中的分解情况。在200 ~ 600 K之间,硅表面的SiH3物质减少,并逐渐消失。同时,SiH2表面组分在200 ~ 440 K间增加,随后在440 ~ 620 K间减少。在620k时,多孔硅表面只剩下一氢化物。在640 K以上,随着H2的脱附,SiH表面种类减少。吸附研究也在不同的等温温度下进行。这些二硅烷吸附和分解实验为硅CVD和ALE加工过程中的表面化学提供了重要的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decomposition of silicon hydrides following disilane adsorption on porous silicon surfaces

Disilane (Si2H6) is used for silicon chemical vapor deposition (CVD) and is a potential precursor for atomic layer epitaxy (ALE) on silicon surfaces. In this study, Fourier transform infrared (FTIR) transmission spectroscopy was employed to examine the adsorption and decomposition of disilane on high surface area porous silicon surfaces. The FTIR spectra revealed that disilane dissociatively adsorbs on porous silicon surfaces at 200 K to form a large fraction of SiH3 surface species and some SiH2 and SiH surface species. The SiHx stretching modes between 2125–2156 cm−1, the SiH3 degenerate deformation mode at 862 cm−1 and the SiH2 scissor mode at 907 cm−1 were then employed to monitor the decomposition of the surface hybride species during thermal annealing. Between 200–600 K, the SiH3 species decreased and were depleted from the silicon surface. Concurrently, the SiH2 surface species were observed to increase between 200–440 K and subsequently to decrease between 440–620 K. Only monohydride species remained on the porous silicon surface at 620 K. Above 640 K, the SiH surface species decreased concurrently with H2 desorption. Adsorption studies were also conducted at various isothermal temperatures. These disilane adsorption and decomposition experiments provide important insights to the surface chemistry during silicon CVD and ALE processing.

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