The kinetics of adsorption of poly(o-methoxyaniline) (POMA) via self-a
ssembly has been investigated using UV-vis spectroscopy. Though experi
mental conditions, including type of substrate, affect the amount of p
olymer adsorbed, adsorption of the first POMA layer on glass substrate
s was shown to occur in two stages, reaching saturation within a few m
inutes. The first stage is represented by a first-order kinetics with
characteristic times of 5-10 s. The second stage also has an exponenti
al behavior with t(1.5) and characteristic times of hundreds of second
s, which was valid for all substrates when the shift in the polaronic
band in the beginning of adsorption was taken into account. The t(1.5)
within the exponential is believed to indicate a diffusion-controlled
growth of small domains formed during the first stage of adsorption.
The appearance of small domains and their subsequent growth are consis
tent with scanning electron micrographs obtained at distinct time peri
ods of adsorption. When a POMA layer was made to adsorb on an already
formed POMA/poly(ethenesulfonic acid) self-assembly multilayer, the ad
sorption process became faster as the number of bilayers already depos
ited increased.