Preferential
attraction of polymer chains to the substrate [i.e.,
poly(methyl methacrylate) (PMMA) on the hydroxyl-terminated Si substrate]
typically results in the initial phase separation of spin-cast immiscible
linear polymer blends [i.e., polystyrene (PS)/PMMA] with a characteristic
interfacial microstructure depending on their molecular weight. A
formation of the undesired microstructure in those blends is inevitable
because of the thermodynamic force driving their phase separation
combined with relatively rapid dynamics in solution. In contrast,
the polymer ligands, which are grafted from nanoparticles, are capable
of limited segmental interactions in the presence of segmental contacts
of chemically distinct chains as well as hindered mobility by interpenetration
(or entanglement) and thus exhibit a homogeneous but non-equilibrium
phase behavior. Here, the microstructure of the blends consisting
of immiscible polymer-grafted nanoparticles (PGNPs) was identified
by their neutron reflectivity, in which the scattering length density
was controlled by tethering deuterated PS on silica NPs. We demonstrate
that the single-phase homogeneous microstructure is attributed to
a significantly reduced particle dynamics arising from the cooperative
motion (or interpenetration) of polymer ligands during vitrification
of PGNP films despite a relatively high degree of segregation NχS/MMA. Furthermore, the slower segmental
interactions of polymer ligands promote the thermal stability of the
PGNP blends in the kinetically quenched non-equilibrium state. This
suggests a crucial role of polymer ligands to determine the relevant
properties relying on their microstructures in a wide range of blending
approaches utilizing nanoparticles and polymers.