
doi: 10.1021/am501995e
pmid: 25007291
pmc: PMC4251880
handle: 21.11116/0000-000B-FAD2-E , 10044/1/53166
doi: 10.1021/am501995e
pmid: 25007291
pmc: PMC4251880
handle: 21.11116/0000-000B-FAD2-E , 10044/1/53166
Cellulose nanocrystals (CNCs) form chiral nematic phases in aqueous suspensions that can be preserved upon evaporation of water. The resulting films show an intense directional coloration determined by their microstructure. Here, microreflection experiments correlated with analysis of the helicoidal nanostructure of the films reveal that the iridescent colors and the ordering of the individual nematic layers are strongly dependent on the polydispersity of the size distribution of the CNCs. We show how this affects the self-assembly process, and hence multidomain color formation in such bioinspired structural films.
0306 Physical Chemistry (Incl. Structural), 0904 Chemical Engineering, iridescence, Color, self-assembly, structural color, Microscopy, Electron, Scanning, Nanoparticles, Polystyrenes, chiral-nematic films, Nanoscience & Nanotechnology, Cellulose, cellulose nanocrystals, 0303 Macromolecular And Materials Chemistry
0306 Physical Chemistry (Incl. Structural), 0904 Chemical Engineering, iridescence, Color, self-assembly, structural color, Microscopy, Electron, Scanning, Nanoparticles, Polystyrenes, chiral-nematic films, Nanoscience & Nanotechnology, Cellulose, cellulose nanocrystals, 0303 Macromolecular And Materials Chemistry
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