Chiral self-assembly of cellulose nanocrystals is driven by crystallite bundles

The transfer of chirality across length-scales is an intriguing and universal natural phenomenon. However, connecting the properties of individual building blocks to the emergent features of their resulting large-scale structure remains a challenge. In this work, we investigate the origins of mesoph...

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Veröffentlicht in:Nature communications 2022-05, Vol.13 (1), p.2657-9, Article 2657
Hauptverfasser: Parton, Thomas G., Parker, Richard M., van de Kerkhof, Gea T., Narkevicius, Aurimas, Haataja, Johannes S., Frka-Petesic, Bruno, Vignolini, Silvia
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Sprache:eng
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Zusammenfassung:The transfer of chirality across length-scales is an intriguing and universal natural phenomenon. However, connecting the properties of individual building blocks to the emergent features of their resulting large-scale structure remains a challenge. In this work, we investigate the origins of mesophase chirality in cellulose nanocrystal suspensions, whose self-assembly into chiral photonic films has attracted significant interest. By correlating the ensemble behaviour in suspensions and films with a quantitative morphological analysis of the individual nanoparticles, we reveal an inverse relationship between the cholesteric pitch and the abundance of laterally-bound composite particles. These ‘bundles’ thus act as colloidal chiral dopants, analogous to those used in molecular liquid crystals, providing the missing link in the hierarchical transfer of chirality from the molecular to the colloidal scale. Chirality transfer across length-scales is an intriguing phenomenon but connecting the properties of individual building blocks to the emergent features of their resulting large-scale structure remains challenging. Here, the authors investigate the origins of mesophase chirality in cellulose nanocrystal suspensions, whose self-assembly into chiral photonic films has attracted significant interest.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-022-30226-6