Glinel, K.K.GlinelMoussa, A.A.MoussaJonas, A.M.A.M.JonasLaschewsky, A.A.Laschewsky2022-03-032022-03-032002https://publica.fraunhofer.de/handle/publica/20313610.1021/la0113670The influence of the charge density of polyelectrolytes on the growth of polyelectrolyte multilayers via layer-by-layer self-assembly from pure aqueous solutions was studied. Multilayers were built from strong polyanions, namely poly(styrenesulfonate) and an exfoliated synthetic hectorite, and cationic copolymers of diallyldimethylammonium chloride (DADMAC) with N-methyl-N-vinylformamide (NMVF) for which the composition and thus the charge density was varied systematically. The analysis of the system {cationic copolymer/poly(styrenesulfonate)} reveals that a critical linear charge density c of 0.036 elementary charge/Å of contour length is necessary to obtain Stable multilayer growth in pure water. Above c, the increment of thickness/deposition cycle varies with the linear charge density of the cationic copolymers, in good agreement with current theories of polyelectrolyte solutions. As linear charge density increases, the system passes successively through a charge-dep endent "Debye-Hückel" regime and then through a charge-independent "strong-screening" regime where counterion condensation dominates the behavior. Analogous results were obtained for the variation of the basal spacing of internally structured hybrid multilayers {cationic copolymer/hectorite}. However, by contrast with the first system, no critical linear charge density was found for the hybrid system. This is explained by additional, nonelectrostatic interactions between the clay platelets and the formamide fragment.en668541journal article