Hj. Mick et al., HIGH-TEMPERATURE KINETICS OF SI ATOM OXIDATION BY NO BASED ON SI, N, AND O ATOM MEASUREMENTS, Journal of physical chemistry, 97(26), 1993, pp. 6839-6842
In the present investigation the well-known high-temperature thermal d
ecomposition of silane was used as Si atom source. Its oxidation by NO
was studied behind reflected shock waves in SiH4/NO/Ar systems by app
lying the atomic resonance absorption spectroscopy (ARAS) technique fo
r detecting Si, N, and O atoms. Initial mixtures of 0.5-10 ppm SiH4 an
d 75-300 ppm NO in Ar were used to perform experiments in the temperat
ure range 1660 K less-than-or-equal-to T less-than-or-equal-to 3360 K
at pressures 0.4 bar less-than-or-equal-to p less-than-or-equal-to 1.5
bar. From the measured Si atom absorption profiles the rate coefficie
nt for the reaction Si + NO half arrow right over half arrow left SiO
+ N (R3), k3, was determined by applying the first-order method, which
is known to be independent of calibration. The results were summarize
d by the Arrhenius expression k3 = 3.2 X 10(13) exp(-1775 K/T) cm3 mol
-1 S-1(+/- 40%). To confirm the correctness of reaction R3, N atoms we
re also measured in the SiH4/NO/Ar system. In that case the formation
of N atoms via reaction R3 and the consumption by reaction with NO, N
+ NO half arrow right over half arrow left N2 + O (R4), was observed.
By computer simulations all measured N atom concentrations were fitted
to the calculated ones by varying the rate coefficient k4. A temperat
ure-independent value of k4 = 2.0 x 10(13) cm3 mol-1 s-1 (+/- 50%) was
obtained. Finally, O atoms were measured in the SiH4/NO/Ar system. Al
l O atom profiles observed were well fit by computer simulations based
on a reaction scheme containing the dissociation of silane, reactions
of Si and N with NO, and the well-known O + H-2 half arrow right over
half arrow left OH + H reaction.