V. Bekiari et al., Time-resolved fluorescence quenching studies in nanocomposite materials made of silica and cetyltrimethylammonium bromide, J PHYS CH B, 103(43), 1999, pp. 9085-9089
Fluorescence quenching studies have been performed in silica/cetyltrimethyl
ammonium bromide nanocomposite materials made by the sol-gel method and by
mixing prehydrolyzed tetramethoxysilane with aqueous surfactant micelles. H
ydrophobic probes incorporated in these materials are solubilized in the:su
rfactant subphase where they can diffuse. Pyrene forms diffusion-controlled
excimers there. The subphase is organized, providing a polar hydrocarbon i
nterface and a hydrophobic interior, and it most probably consists of perco
lating surfactant clusters, each formed by fusion of several micelles. Hydr
ophilic molecules are incorporated in the embedding silica phase, and they
are immobilized. Quenching is much more restricted in films than in bulk ma
trices, even though films support a large number of molecular layers. This
result is consistent with the existence of alternating surfactant bilayer/s
ilica layer structure, previously proposed.