Polypyrrole (PPy) was prepared by electrochemical polymerization with the p
olyelectrolyte (PE) as a dopant. The PEs were copolymers of the water solub
le polymers and 2-acrylamido-2-methyl-1-propane sulfonic acid (AMPS). The w
ater soluble polymers were thermally sensitive poly(N-isopropyl acrylamide)
, P(NiPAAm) and thermally insensitive poly(acrylamide), P(AAm). The surface
of PPy/PE film observed by SEM was smoother than that of PPy film doped wi
th a monoelectrolyte. PPy/PE composites were fairly conductive, whose elect
rical conductivities measured by the four-probe method were in the range of
10(-1) to 10(-2) S/cm. The characteristics of cation and anion exchange du
ring redox processes were investigated by applying potential from -0.8 to 0
.5 V vs, an Ag/AgCl reference electrode to the PPy. The effect of temperatu
re on the doping-dedoping behavior and mass change of PPy composites was in
vestigated by potentiodynamic voltammetry and electrochemical quartz crysta
l microbalance (EQCM). The electrochemical activity of the PPy/PE gradually
decreased with increasing temperature. PPy/P(NiPAAm/AMPS) showed much grea
ter mass change with increasing temperature than PPy/P(AAm/AMPS), mainly be
cause of a decrease in the degree of swelling of thermally sensitive moiety
. This confirms that PPy/P(NiPAAm/AMPS) possesses temperature-dependent ele
ctrochemical activity, which indicates that it can be utilized for many att
ractive applications. The thermal volume transition temperature of PPy/P(Ni
PAAm/AMPS) was estimated from the slope change of mass decrease. The transi
tion temperature of the oxidized state of PPy/P(NiPAAm/AMPS) was higher tha
n that of the reduced state. (C) 1999 Elsevier Science S.A. All rights rese
rved.