arXiv subjects

Tom C. Lubensky

Publications and source records attributed to Tom C. Lubensky.

18 recordsLinked to original sources

arXiv2026

Odd elasticity in disordered chiral active materials

Chiral active materials are abundant in nature, including the cytoskeleton with attached motor proteins, rotary clusters of bacterial flagella, and self-spinning starfish embryos. These materials break both time reversal and mirror-image (parity) symmetries due to injection of torques at the microscale. It was recently discovered that chiral active materials show a new type of elastic response termed `odd' elasticity. Currently, odd elasticity is understood microscopically only in ordered structures, e.g., lattice designs of metamaterials. It remains to explore how odd elasticity emerges in natural or biological systems, which are usually disordered. To address this, we propose a minimal generic model for disordered `odd solids', using micropolar (Cosserat) elasticity in the presence of local active torques. We find that odd elasticity naturally emerges as a nonlinear effect of internal particle rotations. Exploring the viscoelasticity of such a solid, when immersed in an odd fluid, we discover new dynamically unstable regions driven by the odd solid-fluid coupling, and, in the underdamped regime, also by inertia. Remarkably, in the overdamped limit, this odd solid-fluid coupling allows for bulk wave propagation near these unstable regions.

cond-mat.soft↗

arXiv2024

Chiral active fluids: what can we learn from the total momentum?

Chiral active materials are those that break both time-reversal symmetry and parity microscopically, which results in average rotation of the material's complex molecules around their center-of-mass (CM). These materials are far from equilibrium due to their local non-vanishing spin angular momentum. In this paper we show that, unlike passive fluids, the non vanishing spin angular momentum brings about a difference between the CM momentum and the total momentum, which accounts for the momentum of all atoms that compose the complex rotating molecules. This is in stark contrast to equilibrium fluids where the CM stress and the total momentum are essentially equivalent. In fact, we find that generally the CM dynamics are insufficient to describe the dynamics of a chiral active material. The total momentum, other than being experimentally accessible in simple rheological experiments, also imposes another constraint -- its stress must be allowed to be written in a symmetric way. We find that the latter imposes a relation between possible central-force interactions and spin-spin interactions, and constraints the ammount of {\it odd} viscosities in the system to the well-known odd (Hall) viscosity and the odd pressure.

cond-mat.soft↗

arXiv2024

Nonreciprocity and odd viscosity in chiral active fluids

Odd viscosity couples stress to strain rate in a dissipationless way. It has been studied in plasmas under magnetic fields, superfluid ${\rm He}^3$, quantum-Hall fluids, and recently in the context of chiral active matter. In most of these studies, odd terms in the viscosity obey Onsager reciprocal relations. Although this is expected in equilibrium systems, it is not obvious that Onsager relations hold in active materials. By directly coarse graining the kinetic energy and independently using both the Poisson-bracket formalism and a kinetic theory derivation, we find that the appearance of a non-vanishing angular momentum density, which is a hallmark of chiral active materials, necessarily breaks Onsager reciprocal relations. This leads to a non-Hermitian dynamical matrix for the total hydrodynamic momentum and to the appearance of odd viscosity and other non-dissipative contributions to the viscosity. Furthermore, by accounting for both the angular momentum density and interactions that lead to odd viscosity, we find regions in the parameter space in which 3D odd mechanical waves propagate and regions in which they are mechanically unstable. The lines separating these regions are continuous lines of exceptional points, suggesting a possible non-reciprocal phase transition.

cond-mat.soft↗

arXiv2021

Odd viscosity in active matter: microscopic origin and 3D effects

In common fluids, viscosity is associated with dissipation. However, when time-reversal-symmetry is broken a new type of non-dissipative `viscosity' may emerge. Recent theories and experiments on classical 2D systems with active spinning particles have heightened interest in odd viscosity, but a microscopic theory for it in active materials is still absent. Here we present such first-principles microscopic Hamiltonian theory, valid for both 2D and 3D, showing that odd viscosity is present in any system, equilibrium or not, with aligned spinning components. Our work substantially extends the applicability of odd viscosity into 3D fluids, and specifically to internally driven active materials, such as living matter (e.g., actomyosin gels). We find intriguing 3D effects of odd viscosity such as propagation of anisotropic bulk shear waves and breakdown of Bernoulli's principle.

cond-mat.soft↗

arXiv2021

Emergent Potts Order in a Coupled Hexatic-Nematic XY model

Addressing the nature of an unexpected smectic-A' phase in liquid crystal 54COOBC films, we perform large scale Monte Carlo simulations of a coupled hexatic-nematic XY model. The resulting finite-temperature phase diagram reveals a small region with composite Potts $\mathbb{Z}_3$ order above the vortex binding transition; this phase is characterized by relative hexatic-nematic ordering though both variables are disordered. The system develops algebraic hexatic and nematic order only at a lower temperature. This multi-step melting scenario agrees well with the experimental observations of a sharp specific heat anomaly that emerges above the onset of hexatic positional order. We therefore propose that the smectic-A' phase is characterized by composite Potts order and bound-states of fractional vortices.

cond-mat.stat-mech↗

arXiv2016

Topological colloids

Abundant in nature, colloids also find increasingly important applications in science and technology, ranging from direct probing of kinetics in crystals and glasses to fabrication of third-generation quantum-dot solar cells. Because naturally occurring colloids have a shape that is typically determined by minimization of interfacial tension (for example, during phase separation) or faceted crystal growth, their surfaces tend to have minimum-area spherical or topologically equivalent shapes such as prisms and irregular grains (all continuously deformable - homeomorphic - to spheres). Although toroidal DNA condensates and vesicles with different numbers of handles can exist and soft matter defects can be shaped as rings and knots, the role of particle topology in colloidal systems remains unexplored. Here we fabricate and study colloidal particles with different numbers of handles and genus g ranging from 1 to 5. When introduced into a nematic liquid crystal - a fluid made of rod-like molecules that spontaneously align along the so-called "director" - these particles induce three-dimensional director fields and topological defects dictated by colloidal topology. Whereas electric fields, photothermal melting and laser tweezing cause transformations between configurations of particle-induced structures, three-dimensional nonlinear optical imaging reveals that topological charge is conserved and that the total charge of particle-induced defects always obeys predictions of the Gauss-Bonnet and Poincare-Hopf index theorems. This allows us to establish and experimentally test the procedure for assignment and summation of topological charges in three-dimensional director fields. Our findings lay the groundwork for new applications of colloids and liquid crystals that range from topological memory devices, through new types of self-assembly, to the experimental study of low-dimensional topology.

cond-mat.soft↗

arXiv2016

Mechanical Graphene

We present a model of a mechanical system with a vibrational mode spectrum identical to the spectrum of electronic excitations in a tight-binding model of graphene. The model consists of point masses connected by elastic couplings, called "tri-bonds," that implement certain three-body interactions, which can be tuned by varying parameters that correspond to the relative hopping amplitudes on the different bond directions in graphene. In the mechanical model, this is accomplished by varying the location of a pivot point that determines the allowed rigid rotations of a single tri-bond. The infinite system constitutes a Maxwell lattice, with the number of degrees of freedom equal to the number of constraints imposed by the tri-bonds. We construct the equilibrium and compatibility matrices and analyze the model's phase diagram, which includes spectra with Weyl points for some placements of the pivot and topologically polarized phases for others. We then discuss the edge modes and associated states of self stress for strips cut from the periodic lattice. Finally, we suggest a physical realization of the tri-bond, which allows access to parameter regimes not available to experiments on (strained) graphene and may be used to create other two-dimensional mechanical metamaterials with different spectral features.

cond-mat.soft↗

arXiv2015

Chiral structures and defects of lyotropic chromonic liquid crystals induced by saddle-splay elasticity

An experimental and theoretical study of lyotropic chromonic liquid crystals (LCLCs) confined in cylinders with degenerate planar boundary conditions elucidates LCLC director configurations. When the Frank saddle-splay modulus is more than twice the twist modulus, the ground state adopts an inhomogeneous escaped-twisted configuration. Analysis of the configuration yields a large saddle-splay modulus, which violates Ericksen inequalities but not thermodynamic stability. Lastly, we observe point defects between opposite-handed domains and explain a preference for point defects over domain walls.

cond-mat.soft↗

arXiv2013

The syncytial Drosophila embryo as a mechanically excitable medium

Mitosis in the early syncytial Drosophila embryo is highly correlated in space and time, as manifested in mitotic wavefronts that propagate across the embryo. In this paper we investigate the idea that the embryo can be considered a mechanically-excitable medium, and that mitotic wavefronts can be understood as nonlinear wavefronts that propagate through this medium. We study the wavefronts via both image analysis of confocal microscopy videos and theoretical models. We find that the mitotic waves travel across the embryo at a well-defined speed that decreases with replication cycle. We find two markers of the wavefront in each cycle, corresponding to the onsets of metaphase and anaphase. Each of these onsets is followed by displacements of the nuclei that obey the same wavefront pattern. To understand the mitotic wavefronts theoretically we analyze wavefront propagation in excitable media. We study two classes of models, one with biochemical signaling and one with mechanical signaling. We find that the dependence of wavefront speed on cycle number is most naturally explained by mechanical signaling, and that the entire process suggests a scenario in which biochemical and mechanical signaling are coupled.

physics.bio-ph↗

arXiv2011

Order-by-disorder in the antiferromagnetic Ising model on an elastic triangular lattice

Geometrically frustrated materials have a ground-state degeneracy that may be lifted by subtle effects, such as higher order interactions causing small energetic preferences for ordered structures. Alternatively, ordering may result from entropic differences between configurations in an effect termed order-by-disorder. Motivated by recent experiments in a frustrated colloidal system in which ordering is suspected to result from entropy, we consider in this paper, the antiferromagnetic Ising model on a deformable triangular lattice. We calculate the displacements exactly at the microscopic level, and contrary to previous studies, find a partially disordered ground state of randomly zigzagging stripes. Each such configuration is deformed differently and thus has a unique phonon spectrum with distinct entropy, thus lifting the degeneracy at finite temperature. Nonetheless, due to the free-energy barriers between the ground-state configurations, the system falls into a disordered glassy state.

cond-mat.stat-mech↗

arXiv2008

Stripes, Zigzags, and Slow Dynamics in Buckled Hard Spheres

We study the analogy between buckled colloidal monolayers and the triangular-lattice Ising antiferromagnet. We calculate free volume-induced Ising interactions, show how lattice deformations favor zigzag stripes that partially remove the Ising model ground-state degeneracy, and identify the Martensitic mechanism prohibiting perfect stripes. Slowly inflating the spheres yields jamming as well as logarithmically slow relaxation reminiscent of the glassy dynamics observed experimentally.

cond-mat.soft↗

arXiv2008

Geometric Frustration in Buckled Colloidal Monolayers

Geometric frustration arises when lattice structure prevents simultaneous minimization of local interactions. It leads to highly degenerate ground states and, subsequently, complex phases of matter such as water ice, spin ice and frustrated magnetic materials. Here we report a simple geometrically frustrated system composed of closely packed colloidal spheres confined between parallel walls. Diameter-tunable microgel spheres are self-assembled into a buckled triangular lattice with either up or down displacements analogous to an antiferromagnetic Ising model on a triangular lattice. Experiment and theory reveal single-particle dynamics governed by in-plane lattice distortions that partially relieve frustration and produce ground-states with zigzagging stripes and subextensive entropy, rather than the more random configurations and extensive entropy of the antiferromagnetic Ising model. This tunable soft matter system provides an uncharted arena in which the dynamics of frustration, thermal excitations and defects can be directly visualized.

cond-mat.soft↗

arXiv2004

Nonlinear Elasticity in Biological Gels

Unlike most synthetic materials, biological materials often stiffen as they are deformed. This nonlinear elastic response, critical for the physiological function of some tissues, has been documented since at least the 19th century, but the molecular structure and the design principles responsible for it are unknown. Current models for this response require geometrically complex ordered structures unique to each material. In this Article we show that a much simpler molecular theory accounts for strain stiffening in a wide range of molecularly distinct biopolymer gels formed from purified cytoskeletal and extracellular proteins. This theory shows that systems of semi-flexible chains such as filamentous proteins arranged in an open crosslinked meshwork invariably stiffen at low strains without the need for a specific architecture or multiple elements with different intrinsic stiffnesses.

cond-mat.soft↗

arXiv2000

Quantum Theory of the Smectic Metal State in Stripe Phases

We present a theory of the electron smectic fixed point of the stripe phases of doped layered Mott insulators. We show that in the presence of a spin gap three phases generally arise: (a) a smectic superconductor, (b) an insulating stripe crystal and (c) a smectic metal. The latter phase is a stable two-dimensional anisotropic non-Fermi liquid. In the abscence of a spin gap there is also a more conventional Fermi-liquid-like phase. The smectic superconductor and smectic metal phases may have already been seen in Nd-doped LSCO.

cond-mat.str-el↗

arXiv1996

Multiple light scattering in anisotropic random media

In the last decade Diffusing Wave Spectroscopy (DWS) has emerged as a powerful tool to study turbid media. In this article we develop the formalism to describe light diffusion in general anisotropic turbid media. We give explicit formulas to calculate the diffusion tensor and the dynamic absorption coefficient, measured in DWS experiments. We apply our theory to uniaxial systems, namely nematic liquid crystals, where light is scattered from thermal fluctuations of the local optical axis, called director. We perform a detailed analysis of the two essential diffusion constants, parallel and perpendicular to the director, in terms of Frank elastic constants, dielectric anisotropy, and applied magnetic field. We also point out the relevance of our results to different liquid crystalline systems, such as discotic nematics, smectic-A phases, and polymer liquid crystals. Finally, we show that the dynamic absorption coefficient is the angular average over the inverse viscosity, which governs the dynamics of director fluctuations.

cond-mat.soft↗

arXiv1996

Direct Determination of DNA Twist-Stretch Coupling

The symmetries of the DNA double helix require a new term in its linear response to stress: the coupling between twist and stretch. Recent experiments with torsionally-constrained single molecules give the first direct measurement of this important material parameter. We extract its value from a recent experiment of Strick et al. [Science 271 (1996) 1835] and find rough agreement with an independent experimental estimate recently given by Marko. We also present a very simple microscopic theory predicting a value comparable to the one observed.

cond-mat.soft↗

arXiv1996

Multiple light scattering in nematic liquid crystals

We present a rigorous treatment of the diffusion approximation for multiple light scattering in anisotropic random media, and apply it to director fluctuations in a nematic liquid crystal. For a typical nematic material, 5CB, we give numerical values of the diffusion constants $D_{\|}$ and $D_{\perp}$. We also calculate the temporal autocorrelation function measured in Diffusing Wave Spectroscopy.

cond-mat↗

arXiv1995

Temporal Fluctuations in Nematic Liquid Crystals

We use a set of simplified non-linear Langevin equations to study the hydrodynamic excitations in a nematic liquid crystal. We calculate the one-loop self-energy corrections in the long wavelength limit.

cond-mat↗