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

被引:122
作者
Parton, Thomas G. [1 ]
Parker, Richard M. [1 ]
van de Kerkhof, Gea T. [1 ]
Narkevicius, Aurimas [1 ]
Haataja, Johannes S. [1 ]
Frka-Petesic, Bruno [1 ]
Vignolini, Silvia [1 ]
机构
[1] Univ Cambridge, Yusuf Hamied Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England
基金
英国生物技术与生命科学研究理事会; 欧盟地平线“2020”; 英国工程与自然科学研究理事会;
关键词
LIQUID-CRYSTALS; SUSPENSIONS; FILMS; MICROFIBRILS; TWIST; SHAPE;
D O I
10.1038/s41467-022-30226-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:9
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