The effect of nanoparticle location and shape on thermal transitions observed in hydrated layer-by-layer assemblies

Nanoparticles can have a profound effect on thermal transitions observed in polymer nanocomposites. Many layer-by-layer (LbL) assemblies contain nanoparticles for added functionality, but the resulting effects of nanoparticles on an LbL film's thermal properties are not known. Previously, we have shown that a nanoparticle-free LbL film containing strong polyelectrolytes, poly(diallyldimethylammonium chloride)/poly(styrene sulfonate) (PDAC/PSS), exhibited a single reversible thermal transition much like a glass-melt transition. In the work presented here, nanoparticles of either spherical (SiO₂) or platelet (Laponite clay) shape are inserted at varying vertical locations throughout PDAC/PSS LbL films. Temperature-controlled quartz crystal microbalance (QCM-D) and modulated differential scanning calorimetry (MDSC) are applied, for which QCM-D proved to be more sensitive to the transition. All Laponite-containing films possess two thermal transitions. During growth, Laponite-containing films exhibit steady increases in dissipation, which is proposed to arise from mechanically decoupled regions separated by the Laponite nanoparticles. For SiO₂-containing films, three transitions are detectable only when the SiO₂ nanoparticles are placed in the middle of the film; no transitions are observed for SiO₂ placed at the bottom or top, perhaps because of a weakening of the transition. The lowest transition is close in value to that of neat PDAC/PSS LbL films, and was assigned to a “bulk” response. The higher transition(s) is attributed to polymer chains in an interfacial region near the nanoparticle. We propose that nanoparticles restrict segmental mobility, thus elevating the transition temperature in the interfacial region.