Tuning cholesteric cellulose nanocrystal self-assembly in spherical confinement via salt and sonication

Fuente: arXiv
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Autori principali: Saraiva, Diogo Vieira, Hogeweg, Anne Meike, Tran, Lisa
Natura: Preprint
Pubblicazione: 2026
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author Saraiva, Diogo Vieira
Hogeweg, Anne Meike
Tran, Lisa
author_facet Saraiva, Diogo Vieira
Hogeweg, Anne Meike
Tran, Lisa
contents Cellulose nanocrystals (CNCs) self-assemble into cholesteric liquid crystals that produce structural color upon solvent removal. Although most studies examine this process in planar films, confinement within micron-sized water-in-oil droplets provides a powerful platform for resolving self-assembly dynamics in real time. Here, we investigate how two common pitch-tuning strategies, sodium chloride addition and tip sonication, govern the kinetics and structure of CNC self-assembly under spherical confinement. Polarized optical microscopy timelapses capture the evolution from isotropic suspension through tactoid nucleation and annealing to kinetic arrest and final buckling. Consistent with prior work, pitch-concentration analysis reveals a universal post-arrest regime governed by droplet shrinkage. Beyond this established behavior, we identify a pre-arrest regime in which pitch decreases rapidly and whose kinetics accelerate with increasing salt concentration and sonication dose. These parameters shift the onset of cholesteric order and gelation, thereby tuning the concentration window for tactoid coalescence. Together, these results establish droplet confinement as a quantitative platform for probing out-of-equilibrium CNC self-assembly and for kinetically programming structurally colored soft materials.
format Preprint
id arxiv_https___arxiv_org_abs_2601_07429
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Tuning cholesteric cellulose nanocrystal self-assembly in spherical confinement via salt and sonication
Saraiva, Diogo Vieira
Hogeweg, Anne Meike
Tran, Lisa
Soft Condensed Matter
Cellulose nanocrystals (CNCs) self-assemble into cholesteric liquid crystals that produce structural color upon solvent removal. Although most studies examine this process in planar films, confinement within micron-sized water-in-oil droplets provides a powerful platform for resolving self-assembly dynamics in real time. Here, we investigate how two common pitch-tuning strategies, sodium chloride addition and tip sonication, govern the kinetics and structure of CNC self-assembly under spherical confinement. Polarized optical microscopy timelapses capture the evolution from isotropic suspension through tactoid nucleation and annealing to kinetic arrest and final buckling. Consistent with prior work, pitch-concentration analysis reveals a universal post-arrest regime governed by droplet shrinkage. Beyond this established behavior, we identify a pre-arrest regime in which pitch decreases rapidly and whose kinetics accelerate with increasing salt concentration and sonication dose. These parameters shift the onset of cholesteric order and gelation, thereby tuning the concentration window for tactoid coalescence. Together, these results establish droplet confinement as a quantitative platform for probing out-of-equilibrium CNC self-assembly and for kinetically programming structurally colored soft materials.
title Tuning cholesteric cellulose nanocrystal self-assembly in spherical confinement via salt and sonication
topic Soft Condensed Matter
url https://arxiv.org/abs/2601.07429