化学计量学
化学气相沉积
粘着系数
氢
基质(水族馆)
反应机理
化学
反应速率常数
反应速率
沉积(地质)
增长率
粘着概率
化学反应
化学工程
分析化学(期刊)
动力学
物理化学
催化作用
有机化学
吸附
几何学
古生物学
地质学
沉积物
物理
海洋学
解吸
数学
量子力学
生物
工程类
作者
H.-W. Liu,Guan-Hong Chou,B.W. Lee,Yu-Hsun Cheng,Jhong-Ren Huang,Lu‐Sheng Hong
标识
DOI:10.1021/acs.iecr.4c02017
摘要
The film growth mechanism of stoichiometric SiC in a chemical vapor deposition reaction system using methyltrichlorosilane (MTS) and hydrogen (H2) as the reactants was investigated. Kinetic analysis of the film growth rate profiles was performed in two distinct reactors, a hot-wall tubular reactor and a macrocavity reactor. Macrocavity experiments at 1273 K revealed that MTS reacts at the substrate surface with a low sticking probability of 2.1 × 10–6, while the film growth is primarily contributed by the gas-phase reaction of the reactants. Moreover, the tubular reactor exhibited a unique film growth rate profile, featured by an initial increase followed by a decrease along the gas flow direction. This observation strongly suggested a stepwise reaction in which MTS/H2 reacts in the gas phase to form an intermediate species, which then contributes to film growth by reacting at the substrate surface. The apparent sticking probability of the gaseous intermediate species, derived from the best-fit surface reaction rate constant to the proposed stepwise reaction mechanism, was found to be approximately 1 × 10–3. The obtained sticking probability, being 3 orders of magnitude higher than that of MTS, indicated that the gaseous intermediate species may consist of a MTS/H2-derived active species that maintains the original Si–C bond structure, thereby leading to the stoichiometric SiC film growth.
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