Surface pressure-area (pi-A) isotherm characteristics of 5.10,15-(4-hydroxy
phenyl)-20-(4-hexadecyloxy- phenyl) porphyrin monolayers on both the water
and TiO2 hydrosol subphases, the UV-vis absorption and fluorescence spectra
of the monolayers deposited onto CaF2 substrates are investigated. pi-A is
otherms find that the porphyrin ring extends to lie more flat on a TiO2 hyd
rosol surface than on a water surface. The UV-vis absorption spectra of the
deposited monolayers prove that the porphyrin TiO2 nanoparticle heterostru
cture assembly is formed, in which the J-aggregated affect of porphyrin is
weakened, comparing with that in the monolayer deposited from water subphas
e. The fluorescence spectra show that the fluorescent emission quenching by
the photoinduced electron transfer from the excited porphyrin molecule to
TiO2 nanoparticle, occurs under excitation in the Soret band region of porp
hyrin. (C) 1998 Elsevier Science Limited. All rights reserved.