Collective motion of self-propelled organisms or synthetic particles, often termed "active fluid," has attracted enormous attention in the broad scientific community because of its fundamentally nonequilibrium nature. Energy input and interactions among the moving units and the medium lead to complex dynamics. Here, we introduce a class of active matter--living liquid crystals (LLCs)--that combines living swimming bacteria with a lyotropic liquid crystal. The physical properties of LLCs can be controlled by the amount of oxygen available to bacteria, by concentration of ingredients, or by temperature. Our studies reveal a wealth of intriguing dynamic phenomena, caused by the coupling between the activity-triggered flow and long-range orientational order of the medium. Among these are (i) nonlinear trajectories of bacterial motion guided by nonuniform director, (ii) local melting of the liquid crystal caused by the bacteria-produced shear flows, (iii) activity-triggered transition from a nonflowing uniform state into a flowing one-dimensional periodic pattern and its evolution into a turbulent array of topological defects, and (iv) birefringenceenabled visualization of microflow generated by the nanometersthick bacterial flagella. Unlike their isotropic counterpart, the LLCs show collective dynamic effects at very low volume fraction of bacteria, on the order of 0.2%. Our work suggests an unorthodox design concept to control and manipulate the dynamic behavior of soft active matter and opens the door for potential biosensing and biomedical applications.motile bacteria | self-organization | cromonic liquid crystals A ctive matter has recently emerged as an important physical model of living systems that can be described by the methods of nonequilibrium statistical mechanics and hydrodynamics (1-3). Active matter is driven by the internal sources of energy, associated with the self-propelled particles such as bacteria or synthetic swimmers. The interaction of these active particles among themselves and with the medium produces a rich variety of dynamic effects and patterns. Most of the studies deal with active particles embedded into a Newtonian isotropic fluid. In this case the interactions among particles are caused by longrange hydrodynamic and short-range excluded volume effects (4-13). In this work, we conceive a general class of active fluids, termed living liquid crystals (LLCs). The suspending medium is a nontoxic liquid crystal (LC) that supports the activity of selfpropelled particles, namely bacteria. At the very same time, the medium imposes long-range anisotropic interactions onto bacteria, thanks to the intrinsic orientational order that persists even when the bacteria are not active. The importance of this system is twofold. Firstly, the bacterial activity modifies the orientational order of the system, by producing well-defined and reproducible patterns with or without topological defects. Secondly, the orientational order of the suspending medium reveals facets of bacterial behavior, allowing one t...
Using a magnetic Frederiks transition technique, we measure the temperature and concentration dependences of splay K1, twist K2, and bend K3 elastic constants for the lyotropic chromonic liquid crystal sunset yellow formed through noncovalent reversible aggregation of organic molecules in water. K1 and K3 are comparable to each other and are an order of magnitude higher than K2. At higher concentrations and lower temperatures, K1 and the ratios K1/K3 and K1/K2 increase, which is attributed to elongation of self-assembled lyotropic chromonic liquid crystal aggregates, a feature not found in conventional thermotropic and lyotropic liquid crystals formed by covalently bound units of a fixed length.
Using dynamic light scattering, we study orientational fluctuation modes in the nematic phase of a self-assembled lyotropic chromonic liquid crystal (LCLC) disodium cromoglycate and measure the Frank elastic moduli and viscosity coefficients. The elastic moduli of splay (K1) and bend (K3) are in the order of 10 pN while the twist modulus (K2) is an order of magnitude smaller. The splay constant K1 and the ratio K1/K3 both increase substantially as the temperature T decreases, which we attribute to the elongation of the chromonic aggregates at lower temperatures. The bend viscosity is comparable to that of thermotropic liquid crystals, while the splay and twist viscosities are several orders of magnitude larger. The temperature dependence of bend viscosity is weak. The splay and twist viscosities change exponentially with the temperature. In addition to the director modes, the fluctuation spectrum reveals an additional mode that is attributed to diffusion of structural defects in the column-like aggregates.
We have experimentally and theoretically investigated the dependence of the intrinsic Gilbert damping parameter α0 on the spin-orbital coupling strength ξ by using L10 ordered FePd1−xPtx ternary alloy films with perpendicular magnetic anisotropy. With the time-resolved magneto-optical Kerr effect, α0 is found to increase by more than a factor of ten when x varies from 0 to 1.0. Since changes of other leading parameters are found to be neglected, the α0 has for the first time been proven to be proportional to ξ 2 .
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