Polyelectrolyte brushes consisting of polystyrene-poly(acrylic acid) (PS-PA
A) diblock copolymers were investigated experimentally using surface pressu
re isotherms and ellipsometry. The surface pressure pi of the block copolym
ers at the air/water interface was measured as a function of the grafting d
ensity sigma at various salt concentrations and pH. It is concluded that th
e scaling behavior of pi>(*) over bar *(sigma) of long PAA chains at high i
onic strengths and low pH agrees with predictions of analytical mean-field
models. The theoretical predicted scaling behavior of pi>(*) over bar *(sig
ma) for annealed brushes at low ionic strength and low pH is not observed b
ecause of adsorption of the polyacid chains to the air/water interface. The
thickness of PAA brushes on hydrophobically modified Si wafers was measure
d with ellipsometry as a function of pH, total ionic strength I, and sigma.
It is observed that at a given pH the brush thickness behaves nonmonotonic
ally as a function of I (i.e., it initially increases and subsequently decr
eases with increasing I). This nonmonotonic behavior agrees with theoretica
l predictions for annealed brushes. The experimentally observed scaling exp
onent alpha in the power law H similar to I-alpha is similar to0.1, which i
s less than that predicted theoretically (1/3).