Outstanding
optical and mechanical properties can be obtained from
hierarchical assemblies of nanoparticles. Herein, the formation of
helically ordered, chiral nematic films obtained from aqueous suspensions
of cellulose nanocrystals (CNCs) were studied as a function of the
initial suspension state. Specifically, nanoparticle organization
and the structural colors displayed by the resultant dry films were
investigated as a function of the anisotropic volume fraction (AVF),
which depended on the initial CNC concentration and equilibration
time. The development of structural color and the extent of macroscopic
stratification were studied by optical and scanning electron microscopy
as well as UV–vis spectroscopy. Overall, suspensions above
the critical threshold required for formation of liquid crystals resulted
in CNC films assembled with longer ranged order, more homogeneous
pitches along the cross sections, and narrower specific absorption
bands. This effect was more pronounced for the suspensions that were
closer to equilibrium prior to drying. Thus, we show that high AVF
and more extensive phase separation in CNC suspensions resulted in
large, long-range ordered chiral nematic domains in dried films. Additionally,
the average CNC aspect ratio and size distribution in the two separated
phases were measured and correlated to the formation of structured
domains in the dried assemblies