The temperature dependence of the dichlorosilane (SiH2Cl2) dissociativ
e adsorption kinetics on a Si(100)2 x 1 surface was investigated using
ultraviolet photoelectron spectroscopy (UPS). By observing in situ th
e UPS intensity of the surface state originated from the dimer danglin
g bonds, the time evolutions. of the surface chlorine and hydrogen cov
erage during SiH2Cl2 exposure onto a Si(100) clean surface were obtain
ed. They were successfully fitted with a rate equation assuming a comp
etition between the SiH2Cl2 adsorption and the desorption of H-2, HCl,
and SiCl. The reaction order and the reaction coefficient for the SiH
2Cl2 adsorption at RT were determined from the fitting to be 1.75 and
3.0 x 10(-2) ML/s, respectively, while they were changed to 1.80 and 9
.0 x 10(-3) ML/s at 400 degrees C or to 3.20 and 6.0 x 10(-3) ML/s at
600 degrees C as the adsorption temperature was raised. Based on this
strong temperature dependence of the parameters, we proposed a surface
reaction model of the SiH2Cl2 adsorption kinetics, which includes tem
perature dependent partial decomposition of the adsorption precursors.