Nanoparticle assemblies
with long-range packing order and preferred
crystallographic orientation of building blocks, i.e., mesocrystals, are of high interest not only because of their unique physical
properties but also due to their complex structure and morphogenesis.
In this study, faceted mesocrystals have been assembled from the dispersion
of truncated cubic-shaped iron oxide nanoparticles stabilized by oleic
acid (OA) molecules using the nonsolvent “gas phase diffusion
technique” into an organic solvent. The effects of synthesis
conditions as well as of the nanoparticle size and shape on the structure
and morphogenesis of mesocrystals were examined. The interactions
of OA-capped iron oxide nanoparticles with solvent molecules were
probed by analytical ultracentrifugation and double difference pair
distribution function analysis. It was shown that the structure of
the organic shell significantly depends on the nature and polarity
of solvent molecules. For the nonpolar solvents, the interaction of
the aliphatic chains of OA molecules with the solvent molecules is
favorable and the chains extend into the solvent. The solvation shell
around the nanoparticles is more extended in nonpolar and more compact
in polar solvents. There is a clear trend for more spherical particles
to be assembled into the fcc superlattice, whereas
less truncated cubes form rhombohedral and tetragonal structures.
The observed changes in packing symmetry are reminiscent of structural
polymorphism known for “classical” (atomic and molecular)
crystals.