Block copolymers (BCPs) are known to self-assemble into
various
structures. In particular, crystallization-driven self-assembly (CDSA)
strategies revealed a high potential for expanding the scope of obtainable
structures at the nanometer length scale. Herein, we report the characterization
of different self-assembled structures of a series of amorphous-crystalline
BCPs poly(dimethyl silacyclobutane)-block-poly(2-vinyl
pyridine) (PDMSB-b-P2VP). The polymers and their
structure formation in different solvents were analyzed, and their
response toward different solvent vapors and temperatures in the deposited
state was evaluated by transmission and scanning electron microscopy
(TEM, SEM) and atomic force microscopy (AFM). The influence of additional
solvents, temperature, and ultrasonication on colloidal dispersions
was investigated with additional dynamic light scattering (DLS) and
differential scanning calorimetry (DSC) experiments. Finally, the
polymer was introduced to a colloidal confinement by employing the
solvent evaporation method in the presence of cetyl-N,N,N-trimethylammoniumbromide (CTAB) or 16-hydroxycetyl-N,N,N-triethylammoniumbromide (CTEAB-OH) as surfactants, resulting in
a plethora of additional colloidal structures.