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Supramolecular chirality typically originates from either chiral molecular building blocks or external chiral stimuli. Generating chirality in achiral systems in the absence of a chiral input, however, is non-trivial and necessitates spontaneous mirror symmetry breaking. Achiral nematic lyotropic chromonic liquid crystals have been reported to break mirror symmetry under strong surface or geometric constraints. Here we describe a previously unrecognised mechanism for creating chiral structures by subjecting the material to a pressure-driven flow in a microfluidic cell. The chirality arises from a periodic double-twist configuration of the liquid crystal and manifests as a striking stripe pattern. We show that the mirror symmetry breaking is triggered at regions of flow-induced biaxial-splay configurations of the director field, which are unstable to small perturbations and evolve into lower energy structures. The simplicity of this unique pathway to mirror symmetry breaking can shed light on the requirements for forming macroscopic chiral structures.

 

Supramolecular chirality typically originates from either chiral molecular building blocks or external chiral stimuli. Generating chirality in achiral systems in the absence of a chiral input, however, is non-trivial and necessitates spontaneous mirror symmetry breaking. Achiral nematic lyotropic chromonic liquid crystals have been reported to break mirror symmetry under strong surface or geometric constraints. Here we describe a previously unrecognised mechanism for creating chiral structures by subjecting the material to a pressure-driven flow in a microfluidic cell. The chirality arises from a periodic double-twist configuration of the liquid crystal and manifests as a striking stripe pattern. We show that the mirror symmetry breaking is triggered at regions of flow-induced biaxial-splay configurations of the director field, which are unstable to small perturbations and evolve into lower energy structures. The simplicity of this unique pathway to mirror symmetry breaking can shed light on the requirements for forming macroscopic chiral structures. 

When a hyperelastic hydrogel confined between two parallel glass plates begins to dry from a lateral boundary, the volume lost by evaporation is accommodated by an inward displacement of the air-hydrogel interface that induces an elastic deformation of the hydrogel. Once a critical front displacement is reached, we observe intermittent fracture events initiated by a geometric instability resulting in localized bursts at the interface. These bursts relax the stresses and irreversibly form air cavities that lead to cellular networks. We show that the spatial extent of the strain field prior to a burst, influenced by the air-hydrogel interfacial tension and the confinement of the gel, determines the characteristic size of the cavities. 

The interplay between viscoelasticity and inertia in dilute polymer solutions at high deformation rates can result in inertioelastic instabilities. The nonlinear evolution of these instabilities generates a state of turbulence with significantly different spatiotemporal features compared to Newtonian turbulence, termed elastoinertial turbulence (EIT). We ex- plore EIT by studying the dynamics of a submerged planar jet of a dilute aqueous polymer solution injected into a quiescent tank of water using a combination of schlieren imaging and laser Doppler velocimetry (LDV). We show how fluid elasticity has a nonmonotonic effect on the jet stability depending on its magnitude, creating two distinct regimes in which elastic effects can either destabilize or stabilize the jet. In agreement with linear stability analyses of viscoelastic jets, an inertioelastic shear-layer instability emerges near the edge of the jet for small levels of elasticity, independent of bulk undulations in the fluid column. The growth of this disturbance mode destabilizes the flow, resulting in a turbulence transition at lower Reynolds numbers and closer to the nozzle compared to the conditions required for the transition to turbulence in a Newtonian jet. Increasing the fluid elasticity merges the shear-layer instability into a bulk instability of the jet column. In this regime, elastic tensile stresses generated in the shear layer act as an “elastic membrane” that partially stabilizes the flow, retarding the transition to turbulence to higher levels of inertia and greater distances from the nozzle. In the fully turbulent state far from the nozzle, planar viscoelastic jets exhibit unique spatiotemporal features associated with EIT. The time-averaged angle of jet spreading, an Eulerian measure of the degree of entrainment, and the centerline velocity of the jets both evolve self-similarly with distance from the nozzle. The autocovariance of the schlieren images in the fully turbulent region of the jets shows coherent structures that are elongated in the streamwise direction, consistent with the suppression of streamwise vortices by elastic stresses. These coherent structures give a higher spectral energy to small frequency modes in EIT characterized by LDV measurements of the velocity fluctuations at the jet centerline. Finally, our LDV measurements reveal a frequency spectrum characterized by a −3 power-law exponent, different from the well-known −5/3 power-law exponent characteristic of Newtonian turbulence.