Abstract
Magnetic nanoparticle chains are found in biosystems, such as in the brain of migratory birds. Inspired by natural assemblies, in a novel approach, the facile assembly of magnetically aligned polymer grafted cobalt nanoparticle (MPGNP) chains in thin polymer films was accomplished by using low strength permanent magnets directly during the flow-casting process. Unlike previous studies of MPGNP chain alignment in the high viscosity melt phase, the high mobility of such dispersed MPGNPs during casting by magnetic flow coating of polystyrene (PS) nanocomposite thin films from a dispersion allowed for formation of well-aligned MPGNP chains at the PS film/air interface. Both spherical (symmetric) and cylindrical (asymmetric) MPGNP aligned chains were obtained with distinct properties. The average chain length and width, number of particles per chain, spacing between parallel chains, and chain alignment were quantified using surface probe and electron microscopy, and grazing incidence X-ray. The aligned chains did not randomize when annealed above the film glass temperature, apparently due to the high translational entropic barrier for macroscopic (GISAXS) chain realignment. The Young’s bending modulus of the aligned MPGNP nanocomposite films as revealed by a thin film wrinkling metrology showed that the elastic modulus along the chain axis direction was higher for the film with the cylindrical but not the spherical MPGNP chains. This suggests that PGNP chain flexural properties depend on asymmetry of the local MPGNP unit, much like the persistence length “stiffness” effect of polymer chains. The ferromagnetic nature of the aligned PGMNP chains resulted in film rotation, as well as repulsive and attractive translation under an applied external magnetic field. Such magnetically responsive films can be useful for sensors and other applications.