New nanosized Si/O/C composites have been synthesized by laser-aerosol
interaction. The Si-29 spectra revealed a deep rearrangement of Si bo
nding in the samples with respect to the original aerosol. From the si
loxane (CH3)(3)SiOSi(CH3)(3) (MDSO) and the silane C2H5OSi(CH3)(3) (ET
MS) aerosols with M environments, solids with a wide variety of SiOxC4
-x environments were produced. These environments were shown to be ran
domly distributed. On the other hand, the same Q environment from the
Si(OC2H5)(4) (TEOS) aerosol remained in the powders. This can be ratio
nalized in terms of Si-O and Si-C bond exchanges. After pyrolysis and
before crystallization, there was a clear deviation from the random mo
del indicating that the material started to organize. C-13 and H-1 NMR
distinguished Si-C and aromatic free C. Both spectroscopies indicated
that there was less C in the Si/O/C phase of the ex-MDSO powder than
in the ex-ETMS one. The ex-MDSO Si/O/C was therefore less oxygenated,
contained less carbon,and consequently the most condensed of the two.
This study illustrates the great versatility of the method. The local
environment of the Si in the precursor is modified through a limited b
ond redistribution and condensation during the synthesis and before py
rolysis. The choice of a Q organosilane, not allowing bond redistribut
ion, leads to a highly porous, nanosized silica, because excess aromat
ic carbon is burned off by thermal oxidation. On the other hand, a cho
ice of a precursor with a mixed SiOxC4-x environment leads after pyrol
ysis under an inert atmosphere to a mixture of Sii O/C and free aromat
ic carbon.