Keywords: nanoparticle, polymer, nanocomposite
Summary:There is considerable on-going interest in controlling the spatial dispersion of nanoparticles (NP) in a polymer matrix to create materials with significantly improved properties. We begin with the idea that NPs grafted with polymer chains behave akin to surfactants and assemble into a variety of structures when they are placed in amorphous polymer hosts. The consequences of these different dispersion states on mechanical properties, especially how these results are affected by the glassiness of the matrix are probed next. We then go beyond these equilibrium, surfactant-inspired paradigms and show that the isothermal crystallization rate of a polymer host can be used to dramatically vary NP spatial organization. Since the resulting nacre-like NP self-assembly significantly improves the polymer’s mechanical properties, we conclude that crystal growth kinetics represents an underappreciated handle to tailor the NP spatial dispersion and hence the properties of this class of commercially relevant polymer nanocomposites.