Linda Susan Hirst

The ferroelectric nematic phase (N _F ) exhibits high spontaneous polarization with fluidity, enabling electric field-driven topological defect lattice formation. While molecular structure is known to govern the molecular shape, charge distribution, and subsequent phase behavior of ferroelectric nematics, its effect on electric field-driven lattice behavior remains poorly understood. In this work, we investigate the influence of molecular substituents on field-driven square defect lattices across five molecular series exhibiting low-temperature ferroelectric nematic phases. Focusing on the roles of lateral fluorination and the methoxy group, we find that a lateral methoxy group on the left-hand ring reduces the lattice period by 100–300 μ m. Fluorinated molecules exhibit more complex behavior: without a lateral methoxy group, fluorination decreases lattice size, whereas with a lateral methoxy group, it increases lattice size. The materials with the largest and smallest lattice sizes are selected to compare pattern formation dynamics through response time and memory effect measurements. These differences are attributed to variations in steric hindrance, charge density distribution, and material viscosity, highlighting the role of subtle molecular modifications in controlling topological defect lattices.

Non-equilibrium particle transport in liquid crystals (LCs) can be exploited to create a variety of complex composite morphologies such as capsules, foams and gels by cooling the system through a phase transition.

We report the design and use of calamitic ligands for quantum dot surface modification and nanoparticle assembly. Ligands incorporating a rigid aromatic rod-like core have previously been shown to facilitate the formation of porous nanoparticle-based structures, such as solid-walled capsules and multi-compartment quantum dot foams and networks via liquid crystal phase transition templating—a process in which the host phase is quenched through the isotropic-nematic phase transition. The effect of the calamitic ligand structure on particle dispersion, transport, and subsequent assembly, however, requires further investigation, particularly in the case of anisotropic liquid crystal solvents. In this report, we vary the structure of six new calamitic ligands and characterize quantum dot size and packing into superstructures when modified with each ligand. Dynamic light scattering is used to measure the effective nanoparticle size for each ligand in dilute toluene solution. Transmission electron microscopy reveals nanoparticle distribution in dense drop-cast films for each ligand, and small-angle x-ray scattering is used to measure interparticle separations in the assembled porous structures. Together, these methods provide a full picture of particle packing for each ligand. Notably, our findings demonstrate that while longer, more rigid aromatic cores promote a closer packing structure in drop-cast films (a slow quasi-equilibrium process)—such effects are not evident using a rapid quenching method. This study highlights the fact that when nanoparticles are formed into macroscopic assemblies, both ligand design and the particular method of assembly can contribute significantly to the final packing structure.

Platinum-coated Janus colloids exhibit self-propelled motion in aqueous solution via the catalytic decomposition of hydrogen peroxide. Here, we report their motion in a uniformly aligned nematic phase of lyotropic chromonic liquid crystal, disodium cromoglycate (DSCG). When active Janus colloids are placed in DSCG, we find that the anisotropy of the liquid crystal imposes a strong sense of direction to their motion; the Janus colloids tend to move parallel to the nematic director. Motion analysis over a range of timescales reveals a crossover from ballistic to anomalous diffusive behavior on timescales below the relaxation time for liquid crystal elastic distortions. Surprisingly we observe that smaller particles roll during ballistic motion, whereas larger particles do not. This result highlights the complexity of phoretically-driven particle motion, especially in an anisotropic fluid environment.

This work examines self-mixing in active nematics, a class of fluids in which mobile topological defects drive chaotic flows in a system comprised of biological filaments and molecular motors. We present experiments that demonstrate how geometrical confinement can influence the braiding dynamics of the defects. Notably, we show that confinement in cardioid-shaped wells leads to realization of the golden braid, a maximally efficient mixing state of exactly three defects with no defect creation or annihilation. We characterize the golden braid state using different measures of topological entropy and the Lyapunov exponent. In particular, topological entropy measured from the stretching rate of material lines agrees well with an analytical computation from braid theory. Increasing the size of the confining cardioid produces a transition from the golden braid, to the fully chaotic active turbulent state.

This work examines self-mixing in active nematics, a class of fluids in which mobile topological defects drive chaotic flows in a system comprised of biological filaments and molecular motors. We present experiments that demonstrate how geometrical confinement can influence the braiding dynamics of the defects. Notably, we show that confinement in cardioid-shaped wells leads to realization of the golden braid, a maximally efficient mixing state of exactly three defects with no defect creation or annihilation. We characterize the golden braid state using different measures of topological entropy and the Lyapunov exponent. In particular, topological entropy measured from the stretching rate of material lines agrees well with an analytical computation from braid theory. Increasing the size of the confining cardioid produces a transition from the golden braid, to the fully chaotic active turbulent state.

Forming Confining And Observing Microtubule Based Active Nematics. JoVE publishes peer-reviewed scientific video protocols to accelerate biological, medical, chemical and physical research. Watch our scientific video articles. JoVE is the world-leading producer and provider of science videos with the mission to improve scientific research, scientific journals, and education. Millions of scientists, educators and students at thousands of universities, colleges, hospitals and biopharmaceutical companies worldwide use JoVE for their research, teaching and learning.

Actively driven, bundled microtubule networks, powered by molecular motors have become a useful framework in which to study the dynamics of energy-driven defects, but achieving control of defect motions is still a challenging problem. In this paper, we present a method to confine active nematic fluid using wetting to curve a layer of oil over circular pillars. This geometry, in which submersed pillars impinge on an oil-water interface, creates a two-tier continuous active layer in which the material is confined above, and surrounds the pillars. Active flows above the pillars are influenced by the circular geometry and exhibit dynamics similar to those observed for active material confined by hard boundaries, e.g., inside circular wells. The thin oil layer beneath the active material is even thinner in the region above the pillars than outside their boundary, consequently producing an area of higher effective friction. Within the pillar region, active length scales and velocities are decreased, while defect densities increase relative to outside the pillar boundary. This new way to confine active flows opens further opportunities to control and organize topological defects and study their behavior in active systems.

Significance: Active nematics are ordered liquid crystalline fluids that exhibit spontaneous persistent flows and collective dynamics. The development of motile biopolymer systems inspired by nature has recently attracted considerable attention to out-of-equilibrium soft materials. We report the formation of an active nematic in which microtubules are propelled by kinesin motors coupled to a lipid membrane substrate. The system exhibits apolar order in a globally aligned nematic phase and locally ordered dynamic lanes. Use of a fluid substrate represents a significant advance for active matter as it allows for spatial re-organization of motors, which generate force, in response to the dynamics of the aligning microtubules. This self-organized feedback mechanism may have implications in vivo and for engineering efficient dynamic and reconfigurable materials.