The
development of diblock copolymer (DBC) nanocomposite films containing
magnetic nanoparticles (NPs) with diameters (D) over
20 nm is a challenging task. To host large iron oxide NPs (Fe3O4, D = 27 ± 0.6 nm), an
ultrahigh molecular weight (UHMW) linear DBC polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) is used as
a template in the present work. Due to hydrogen bonding between the
carboxylic acid ligands of the NPs and the ester groups in PMMA, the
NPs show an affinity to the PMMA block. The localization of the NPs
inside the DBC is investigated as a function of the NP concentration.
At low NP concentrations, NPs are located preferentially at the interface
between PS and PMMA domains to minimize the interfacial tension caused
by the strong segregation strength of the UHMW DBC. At high NP concentrations
(≥10 wt %), chain-like NP aggregates (a head-to-tail orientation)
are observed in the PMMA domains, resulting in a change of the morphology
from sphere to ellipsoid for part of the PMMA domains. Magnetic properties
of the hybrid films are probed via superconducting quantum interference
device magnetometry. All hybrid films show ferrimagnetism and are
promising for potential applications in magnetic data storage.