Spherical polyelectrolyte block copolymer micelles: structural change in presence of monovalent salt

Spherical polyelectrolyte block copolymer micelles were investigated as a function of added NaCl salt concentration using Small-Angle Neutron Scattering (SANS) and Light Scattering (LS). The micelles are formed by the self-association of charged-neutral copolymers made of a long deuterated polyelectrolyte moiety (NaPSS(d))251 and a short hydrophobic moiety (PEP)52. In presence of salt, the core shape and the aggregation number of the micelles are not affected. The hydrodynamic radius of the micelle is found to be identical to the radius of the whole micelle deduced from neutron scattering and thus the hydrodynamic radius is a valid measure of the corona thickness. At the lowest salt concentrations investigated the thickness of the corona, R(s), remains essentially constant and a contraction is observed above an added-salt concentration c(s) of 2 x 10(-2) M where this crossover concentration corresponds to the average ionic strength of the free counterions in the corona. The contraction takes place while maintaining a rod-like behavior of the chains at short scale and obeys to: R(s) approximately c(s)(-0.18). The exponent 0.18 suggests an electrostatic persistence length proportional to the Debye screening length.