Wh. Thompson et al., ROOM-TEMPERATURE OXIDATION ENHANCEMENT OF POROUS SI(001) USING ULTRAVIOLET-OZONE EXPOSURE, Journal of applied physics, 80(9), 1996, pp. 5415-5421
The interaction of porous silicon (001) with ozone and ultraviolet (uv
) was investigated at room temperature and ambient pressure. The O/Si
atomic ratio in oxidized samples, as measured by Auger depth profiling
, was similar to those measured from thermally oxidized samples. For l
ong exposure times (>15 min), the O/Si ratio stayed constant throughou
t the porous layer, indicating full oxidation of the porous structure.
Additionally, the carbon concentration decreased significantly in the
uv-ozone oxidized layers as compared to the untreated porous layers.
Oxide layers up to 400 nm were measured. Fourier transform ir absorpti
on measurements show both an increase in the oxygen concentration and
a decrease in hydrogen concentration after oxidation. Photoluminescenc
e data show that this method of oxidation quenches light emission from
the porous layer. We believe that uv induced excitation of valence el
ectrons results in higher reactivity and diffusion of oxygen and ozone
as well as bond softening. The large volume of voids in the porous st
ructure assist penetration of ozone and atomic oxygen throughout the p
orous structure while the narrow lateral dimensions of the Si skeleton
requires a short diffusion length for full oxidation. (C) 1996 Americ
an Institute of Physics.