M. Brinkmann et al., Room-temperature synthesis of alpha-SiO2 thin films by UV-assisted ozonolysis of a polymer precursor, CHEM MATER, 13(3), 2001, pp. 967-972
A room-temperature synthesis route for thin films of amorphous silica (a-Si
O2) based on irradiation of a silicon-containing polymer by UV light in pur
e O-2 atmosphere has been developed. The chemical conversion of spin-coated
films of poly(pentamethyldisilylstyrene) (pPMDSS) to silicon oxycarbide an
d finally to amorphous silica is achieved by UV-assisted ozonolysis. The co
nversion process has been followed by Fourier transform infrared spectrosco
py (FTIR), ellipsometry, and X-ray photoelectron (XPS) and Auger electron s
pectroscopies (AES). The control of the irradiation time allows for control
of the chemical composition of the converted films ranging from that of a
silicon oxycarbide for short exposure times to that of a-SiO2 after 18 h of
exposure. The surface composition pf the fully converted films obtained by
XPS is characterized by an atomic ratio O/Si = 2.00 +/- 0.07. Auger electr
on depth profiles reveal a uniform chemical composition of the a-SiO2 films
with a residual carbon content in the bulk of the films below 1%. Converte
d a-SiO2 films of thicknesses up to 150 nm were achieved. Ellipsometry show
s that the conversion of the films in a-SiO2 is accompanied by a progressiv
e decrease of the film thickness and evolution of the refractive index to a
n asymptotic value of 1.44. The film surface of the converted films probed
by optical microscopy over large areas and by atomic force microscopy (AFM)
does not show any cracks and is atomically flat with a RMS roughness below
0.4 nm.