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.

Hydroxypropyl cellulose (HPC) is a biocompatible cellulose derivative capable of self‐assembling into a lyotropic chiral nematic phase in aqueous solution. This liquid crystalline phase reflects right‐handed circular polarized light of a specific color as a function of the HPC weight fraction. Here, it is demonstrated that, by introducing a crosslinking agent, it is possible to drastically alter the visual appearance of the HPC mesophase in terms of the reflected color, the scattering distribution, and the polarization response, resulting in an exceptional matte appearance in solid‐state films. By exploiting the interplay between order and disorder, a robust and simple methodology toward the preparation of polarization and angular independent color is developed, which constitutes an important step toward the development of real‐world photonic colorants.

When a dispersion droplet dries, a rich variety of spatial and temporal heterogeneities emerge. Controlling these phenomena is essential for many applications yet requires a thorough understanding of the underlying mechanisms. Although the process of film formation from initially dispersed polymer particles is well documented and is known to involve three main stages - evaporation, particle deformation and coalescence - it is impossible to fully disentangle the effects of particle deformation and coalescence, as these stages are closely linked. We circumvent this problem by studying suspensions of colloidal rubber particles that are incapable of coalescing. Varying the crosslink density allows us to tune the particle deformability in a controlled manner. We develop a theoretical framework of the main regimes and stresses in drying droplets of these suspensions, and validate this framework experimentally. Specifically, we show that changing the particle modulus by less than an order of magnitude can completely alter the stress development and resulting instabilities. Scanning electron microscopy reveals that particle deformability is a key factor in stress mitigation. Our model is the suspension equivalent of the widely used Routh-Russel model for film formation in drying dispersions, with additional focus on lateral nonuniformities such as cracking and wrinkling inherent to the droplet geometry, thus adding a new dimension to the conventional view of particle deformation.

Additive manufacturing is becoming increasingly important as a flexible technique for a wide range of products, with applications in the transportation, health, and food sectors. However, to develop additional functionality it is important to simultaneously control structuring across multiple length scales. In 3D printing, this can be achieved by employing inks with intrinsic hierarchical order. Liquid crystalline systems represent such a class of self-organizing materials; however, to date they are only used to create filaments with nematic alignment along the extrusion direction. In this study, cholesteric hydroxypropyl cellulose (HPC) is combined with in situ photo-crosslinking to produce filaments with an internal helicoidal nanoarchitecture, enabling the direct ink writing of solid, volumetric objects with structural color. The iridescent color can be tuned across the visible spectrum by exploiting either the lyotropic or thermotropic behavior of HPC during the crosslinking step, allowing objects with different colors to be printed from the same feedstock. Furthermore, by examining the microstructure after extrusion, the role of shear within the nozzle is revealed and a mechanism proposed based on rheological measurements simulating the nozzle extrusion. Finally, by using only a sustainable biopolymer and water, a pathway toward environmentally friendly 3D printing is revealed.

The structural coloration of arthropods often arises from helicoidal structures made primarily of chitin. Although it is possible to achieve analogous helicoidal architectures by exploiting the self‐assembly of chitin nanocrystals (ChNCs), to date no evidence of structural coloration has been reported from such structures. Previous studies are identified to have been constrained by both the experimental inability to access sub‐micrometer helicoidal pitches and the intrinsically low birefringence of crystalline chitin. To expand the range of accessible pitches, here, ChNCs are isolated from two phylogenetically distinct sources of α‐chitin, namely fungi and shrimp, while to increase the birefringence, an in situ alkaline treatment is performed, increasing the intensity of the reflected color by nearly two orders of magnitude. By combining this treatment with precise control over ChNC suspension formulation, structurally colored chitin‐based films are demonstrated with reflection tunable from blue to near infrared.