Two-Dimensional Melting of Two- and Three-Component Mixtures.

We elucidate the interplay between diverse two-dimensional melting pathways and establish solid-hexatic and hexatic-liquid transition criteria via the numerical simulations of the melting transition of two- and three-component mixtures of hard polygons and disks. We show that a mixture's melting pathway may differ from its components and demonstrate eutectic mixtures that crystallize at a higher density than their pure components. Comparing the melting scenario of many two- and three-component mixtures, we establish universal melting criteria: the solid and hexatic phases become unstable as the density of topological defects, respectively, overcomes ρ_{d,s}≃0.046 and ρ_{d,h}≃0.123.

Entropy-Driven Thermo-gelling Vitrimer.

Thermo-gelling polymers have been envisioned as promising smart biomaterials but limited by their weak mechanical and thermodynamic stabilities. Here, we propose a new thermo-gelling vitrimer, which remains at a liquid state because of the addition of protector molecules preventing the crosslinking, and with increasing temperature, an entropy-driven crosslinking occurs to induce the sol-gel transition. Moreover, we find that the activation barrier in the metathesis reaction of vitrimers plays an important role, and experimentally, one can use catalysts to tune the activation barrier to drive the vitrimer to form an equilibrium gel at high temperature, which is not subject to any thermodynamic instability. We formulate a mean-field theory to describe the entropy-driven crosslinking of the vitrimer, which agrees quantitatively with computer simulations and paves the way for the design and fabrication of novel vitrimers for biomedical applications.

Interplay between jamming and motility-induced phase separation in persistent self-propelling particles.

In living and engineered systems of active particles, self-propulsion induces an unjamming transition from a solid to a fluid phase and phase separation between a gas and a liquidlike phase. We demonstrate an interplay between these two nonequilibrium transitions in systems of persistent active particles. The coexistence and jamming lines in the activity-density plane meet at the jamming transition point in the limit of hard particles or zero activity. This interplay induces an anomalous dynamic in the liquid phase and hysteresis at the active jamming transition.

Local Plastic Response and Slow Heterogeneous Dynamics of Supercooled Liquids.

We demonstrate, via numerical simulations, that the relaxation dynamics of supercooled liquids correlates well with a plastic length scale measuring a particle's response to impulsive localized perturbations and weakly to measures of local elasticity. We find that the particle averaged plastic length scale vanishes linearly in temperature and controls the super-Arrhenius temperature dependence of the relaxation time. Furthermore, we show that the plastic length scale of individual particles correlates with their typical displacement at the relaxation time. In contrast, the local elastic response only correlates with the dynamics on the vibrational timescale.

Unifying Description of the Vibrational Anomalies of Amorphous Materials.

The vibrational density of states D(ω) of solids controls their thermal and transport properties. In crystals, the low-frequency modes are extended phonons distributed in frequency according to Debye's law, D(ω)∝ω^{2}. In amorphous solids, phonons are damped, and at low frequency D(ω) comprises extended modes in excess over Debye's prediction, leading to the so-called boson peak in D(ω)/ω^{2} at ω_{bp}, and quasilocalized ones. Here we show that boson peak and phonon attenuation in the Rayleigh scattering regime are related, as suggested by correlated fluctuating elasticity theory, and that amorphous materials can be described as homogeneous isotropic elastic media punctuated by quasilocalized modes acting as elastic heterogeneities. Our numerical results resolve the conflict between theoretical approaches attributing amorphous solids' vibrational anomalies to elastic disorder and localized defects.

Unconventional rheological properties in systems of deformable particles.

We demonstrate the existence of unconventional rheological and memory properties in systems of soft-deformable particles whose energy depends on their shape, via numerical simulations. At large strains, these systems experience an unconventional shear weakening transition characterized by an increase in the mechanical energy and a drastic drop in shear stress, which stems from the emergence of short-ranged tetratic order. In these weakened states, the contact network evolves reversibly under strain reversal, keeping memory of its initial state, while the microscopic dynamics is irreversible.

Emergence of linear isotropic elasticity in amorphous and polycrystalline materials.

We investigate the emergence of isotropic linear elasticity in amorphous and polycrystalline solids via extensive numerical simulations. We show that the elastic properties are correlated over a finite length scale ξ_{E}, so that the central limit theorem dictates the emergence of continuum linear isotropic elasticity on increasing the specimen size. The stiffness matrix of systems of finite size L>ξ_{E} is obtained, adding to that predicted by linear isotropic elasticity a random one of spectral norm (L/ξ_{E})^{-3/2} in three spatial dimensions. We further demonstrate that the elastic length scale corresponds to that of structural correlations, which in polycrystals reflect the typical size of the grain boundaries and length scales characterizing correlations in the stress field. We finally demonstrate that the elastic length scale affects the decay of the anisotropic long-range correlations of locally defined shear modulus and shear stress.

Mechanical disorder of sticky-sphere glasses. II. Thermomechanical inannealability.

Many structural glasses feature static and dynamic mechanical properties that can depend strongly on glass formation history. The degree of universality of this history dependence and what it is possibly affected by are largely unexplored. Here we show that the variability of elastic properties of simple computer glasses under thermal annealing depends strongly on the strength of attractive interactions between the glasses' constituent particles-referred to here as glass "stickiness." We find that in stickier glasses the stiffening of the shear modulus with thermal annealing is strongly suppressed, while the thermal-annealing-induced softening of the bulk modulus is enhanced. Our key finding is that the characteristic frequency and density per frequency of soft quasilocalized modes becomes effectively invariant to annealing in very sticky glasses; the latter are therefore deemed "thermomechanically inannealable." The implications of our findings and future research directions are discussed.

Softness, anomalous dynamics, and fractal-like energy landscape in model cell tissues.

Epithelial cell tissues have a slow relaxation dynamics resembling that of supercooled liquids. Yet, they also have distinguishing features. These include an extended short-time subdiffusive transient, as observed in some experiments and recent studies of model systems, and a sub-Arrhenius dependence of the relaxation time on temperature, as reported in numerical studies. Here we demonstrate that the anomalous glassy dynamics of epithelial tissues originates from the emergence of a fractal-like energy landscape, particles becoming virtually free to diffuse in specific phase space directions up to a small distance. Furthermore, we clarify that the stiffness of the cells tunes this anomalous behavior, tissues of stiff cells having conventional glassy relaxation dynamics.

Mechanical disorder of sticky-sphere glasses. I. Effect of attractive interactions.

Recent literature indicates that attractive interactions between particles of a dense liquid play a secondary role in determining its bulk mechanical properties. Here we show that, in contrast with their apparent unimportance to the bulk mechanics of dense liquids, attractive interactions can have a major effect on macro- and microscopic elastic properties of glassy solids. We study several broadly applicable dimensionless measures of stability and mechanical disorder in simple computer glasses, in which the relative strength of attractive interactions-referred to as "glass stickiness"-can be readily tuned. We show that increasing glass stickiness can result in the decrease of various quantifiers of mechanical disorder, on both macro- and microscopic scales, with a pair of intriguing exceptions to this rule. Interestingly, in some cases strong attractions can lead to a reduction of the number density of soft, quasilocalized modes, by up to an order of magnitude, and to a substantial decrease in their core size, similar to the effects of thermal annealing on elasticity observed in recent works. Contrary to the behavior of canonical glass models, we provide compelling evidence indicating that the stabilization mechanism in our sticky-sphere glasses stems predominantly from the self-organized depletion of interactions featuring large, negative stiffnesses. Finally, we establish a fundamental link between macroscopic and microscopic quantifiers of mechanical disorder, which we motivate via scaling arguments. Future research directions are discussed.

Frictional active Brownian particles.

Frictional forces affect the rheology of hard-sphere colloids, at high shear rate. Here we demonstrate, via numerical simulations, that they also affect the dynamics of active Brownian particles and their motility-induced phase separation. Frictional forces increase the angular diffusivity of the particles, in the dilute phase, and prevent colliding particles from resolving their collision by sliding one past to the other. This leads to qualitatively changes of motility-induced phase diagram in the volume-fraction motility plane. While frictionless systems become unstable towards phase separation as the motility increases only if their volume fraction overcomes a threshold, frictional systems become unstable regardless of their volume fraction. These results suggest the possibility of controlling the motility-induced phase diagram by tuning the roughness of the particles.

Linker-mediated self-assembly of mobile DNA-coated colloids.

Developing construction methods of materials tailored for given applications with absolute control over building block placement poses an immense challenge. DNA-coated colloids offer the possibility of realising programmable self-assembly, which, in principle, can assemble almost any structure in equilibrium, but remains challenging experimentally. Here, we propose an innovative system of linker-mediated mobile DNA-coated colloids (mDNACCs), in which mDNACCs are bridged by the free DNA linkers in solution, whose two single-stranded DNA tails can bind with specific single-stranded DNA receptors of complementary sequence coated on colloids. We formulate a mean-field theory efficiently calculating the effective interaction between mDNACCs, where the entropy of DNA linkers plays a nontrivial role. Particularly, when the binding between free DNA linkers in solution and the corresponding receptors on mDNACCs is strong, the linker-mediated colloidal interaction is determined by the linker entropy depending on the linker concentration.

Hyperuniformity and density fluctuations at a rigidity transition in a model of biological tissues.

The suppression of density fluctuations at different length scales is the hallmark of hyperuniformity. Here, we explore the presence of this hidden order in a manybody interacting model of biological tissue, known to exhibit a transition, or sharp crossover, from a solid to a fluid like phase. We show that the density fluctuations in the rigid phase are only suppressed up to a finite lengthscale. This length scale monotonically increases and grows rapidly as we approach the fluid phase reminiscent to divergent behavior at a critical point, such that the system is effectively hyperuniform in the fluid phase. Furthermore, complementary behavior of the structure factor across the critical point also indicates that hyperuniformity found in the fluid phase is stealthy.

Attraction Tames Two-Dimensional Melting: From Continuous to Discontinuous Transitions.

Two-dimensional systems may admit a hexatic phase and hexatic-liquid transitions of different natures. The determination of their phase diagrams proved challenging, and indeed, those of hard disks, hard regular polygons, and inverse power-law potentials have only recently been clarified. In this context, the role of attractive forces is currently speculative, despite their prevalence at both the molecular and colloidal scale. Here, we demonstrate, via numerical simulations, that attraction promotes a discontinuous melting scenario with no hexatic phase. At high-temperature, Lennard-Jones particles and attractive polygons follow the shape-dominated melting scenario observed in hard disks and hard polygons, respectively. Conversely, all systems melt via a first-order transition with no hexatic phase at low temperature, where attractive forces dominate. The intermediate temperature melting scenario is shape dependent. Our results suggest that, in colloidal experiments, the tunability of the strength of the attractive forces allows for the observation of different melting scenarios in the same system.

Role of Attractive Forces in the Relaxation Dynamics of Supercooled Liquids.

The attractive tail of the intermolecular interaction affects very weakly the structural properties of liquids, while it affects dramatically their dynamical ones. Via the numerical simulations of model systems not prone to crystallization, both in three and in two spatial dimensions, here we demonstrate that the nonperturbative dynamical effects of the attractive forces are tantamount to a rescaling of the activation energy by the glass transition temperature T_{g}: systems only differing in their attractive interaction have the same structural and dynamical properties if compared at the same value of T/T_{g}.

Transition from Static to Dynamic Friction in an Array of Frictional Disks.

The nature of an instability that controls the transition from static to dynamical friction is studied in the context of an array of frictional disks that are pressed from above on a substrate. In this case the forces are all explicit and Newtonian dynamics can be employed without any phenomenological assumptions. We show that an oscillatory instability that had been discovered recently is responsible for the transition, allowing individual disks to spontaneously reach the Coulomb limit and slide with dynamic friction. The transparency of the model allows a full understanding of the phenomenon, including the speeds of the waves that travel from the trailing to the leading edge and vice versa.

Self-Adaptation of Pseudomonas fluorescens Biofilms to Hydrodynamic Stress.

In some conditions, bacteria self-organize into biofilms, supracellular structures made of a self-produced embedding matrix, mainly composed of polysaccharides, DNA, proteins, and lipids. It is known that bacteria change their colony/matrix ratio in the presence of external stimuli such as hydrodynamic stress. However, little is still known about the molecular mechanisms driving this self-adaptation. In this work, we monitor structural features of Pseudomonas fluorescens biofilms grown with and without hydrodynamic stress. Our measurements show that the hydrodynamic stress concomitantly increases the cell density population and the matrix production. At short growth timescales, the matrix mediates a weak cell-cell attractive interaction due to the depletion forces originated by the polymer constituents. Using a population dynamics model, we conclude that hydrodynamic stress causes a faster diffusion of nutrients and a higher incorporation of planktonic bacteria to the already formed microcolonies. This results in the formation of more mechanically stable biofilms due to an increase of the number of crosslinks, as shown by computer simulations. The mechanical stability also relies on a change in the chemical compositions of the matrix, which becomes enriched in carbohydrates, known to display adhering properties. Overall, we demonstrate that bacteria are capable of self-adapting to hostile hydrodynamic stress by tailoring the biofilm chemical composition, thus affecting both the mesoscale structure of the matrix and its viscoelastic properties that ultimately regulate the bacteria-polymer interactions.

Phase behavior of Lennard-Jones particles in two dimensions.

The phase diagram of the prototypical two-dimensional Lennard-Jones (LJ) system, while extensively investigated, is still debated. In particular, there are controversial results in the literature with regard to the existence of the hexatic phase and the melting scenario. Here we study the phase behavior of two-dimensional range-limited LJ particles via large-scale numerical simulations. We demonstrate that at a high temperature, when the attraction in the potential plays a minor role, melting occurs via a continuous solid-hexatic transition followed by a first-order hexatic-fluid transition. The hexatic phase occurs in a density range that vanishes as the temperature decreases so that at low-temperature melting occurs via a first-order liquid-solid transition. The temperature where the hexatic phase disappears is well above the liquid-gas critical temperature. The evolution of the density of topological defects confirms this scenario.

Noise amplification in frictional systems: Oscillatory instabilities.

It was discovered recently that frictional granular materials can exhibit an important mechanism for instabilities, i.e., the appearance of pairs of complex eigenvalues in their stability matrix. The consequence is an oscillatory exponential growth of small perturbations which are tamed by dynamical nonlinearities. The amplification can be giant, many orders of magnitude, and it ends with a catastrophic system-spanning plastic event. Here we follow up on this discovery, explore the scaling laws characterizing the onset of the instability, the scenarios of the development of the instability with and without damping, and the nature of the eventual system-spanning events. The possible relevance to earthquake physics and to the transition from static to dynamic friction is discussed.

Nonequilibrium strongly hyperuniform fluids of circle active particles with large local density fluctuations.

Disordered hyperuniform structures are an exotic state of matter having vanishing long-wavelength density fluctuations similar to perfect crystals but without long-range order. Although its importance in materials science has been brought to the fore in past decades, the rational design of experimentally realizable disordered strongly hyperuniform microstructures remains challenging. Here we find a new type of nonequilibrium fluid with strong hyperuniformity in two-dimensional systems of chiral active particles, where particles perform independent circular motions of the radius R with the same handedness. This new hyperuniform fluid features a special length scale, i.e., the diameter of the circular trajectory of particles, below which large density fluctuations are observed. By developing a dynamic mean-field theory, we show that the large local density fluctuations can be explained as a motility-induced microphase separation, while the Fickian diffusion at large length scales and local center-of-mass-conserved noises are responsible for the global hyperuniformity.