Searcharxiv⌕ Search

arXiv subjects

D. Zeb Rocklin

Publications and source records attributed to D. Zeb Rocklin.

28 records · Page 2Linked to original sources

Directional mechanical response in the bulk of topological metamaterials

Mechanical metamaterials are those structures designed to convey force and motion in novel and desirable ways. Recently, Kane and Lubensky showed that lattices at the point of marginal mechanical stability (Maxwell lattices) possess a topological invariant that describes the distribution of floppy, zero-energy edge modes. Here, we show that applying force at a point in the bulk of these lattices generates a directional mechanical response, in which stress or strain is induced only on one side of the force. This provides both a bulk metric for mechanical polarization and a design principle to convey stresses and strains towards or away from parts of the structure. We also characterize the effects of removing bonds on the material's structure and floppy modes, establishing a relationship between edge modes and bulk response.

cond-mat.mtrl-sci↗

Fiber networks below the isostatic point: fracture without stress concentration

Crack nucleation is a ubiquitous phenomena during materials failure, because stress focuses on crack tips. It is known that exceptions to this general rule arise in the limit of strong disorder or vanishing mechanical stability, where stress distributes over a divergent length scale and the material displays diffusive damage. Here we show, using simulations, that a class of diluted lattices displays a new critical phase when they are below isostaticity, where stress never concentrates, damage always occurs over a divergent length scale, and catastrophic failure is avoided.

cond-mat.soft↗

Deformation of crystals: Connections with statistical physics

We give a bird's-eye view of the plastic deformation of crystals aimed at the statistical physics community, and a broad introduction into the statistical theories of forced rigid systems aimed at the plasticity community. Memory effects in magnets, spin glasses, charge density waves, and dilute colloidal suspensions are discussed in relation to the onset of plastic yielding in crystals. Dislocation avalanches and complex dislocation tangles are discussed via a brief introduction to the renormalization group and scaling. Analogies to emergent scale invariance in fracture, jamming, coarsening, and a variety of depinning transitions are explored. Dislocation dynamics in crystals challenges non equilibrium statistical physics. Statistical physics provides both cautionary tales of subtle memory effects in nonequilibrium systems, and systematic tools designed to address complex scale-invariant behavior on multiple length and time scales.

cond-mat.mtrl-sci↗

Transformable topological mechanical metamaterials

Mechanical metamaterials are engineered materials that gain their remarkable mechanical properties, such as negative Poisson's ratios, negative compressibility, phononic bandgaps, and topological phonon modes, from their structure rather than composition. Here we propose a new design principle, based on a uniform soft deformation of the whole structure, to allow metamaterials to be immediately and reversibly transformed between states with contrasting mechanical and acoustic properties. These properties are protected by the topological structure of the phonon band of the whole structure and are thus highly robust against disorder and noise. We discuss the general classification of all structures that exhibit such soft deformations, and provide specific examples to demonstrate how to utilize soft deformations to transform a system between different regimes such that remarkable changes in their properties, including edge stiffness and speed of sound, can be achieved.

cond-mat.soft↗

Mechanical Weyl Modes in Topological Maxwell Lattices

Topological mechanical structures exhibit robust properties protected by topological invariants. In this letter, we study a family of deformed square lattices that display topologically protected zero-energy bulk modes analogous to the massless fermion modes of Weyl semimetals. Our findings apply to sufficiently complex lattices satisfying the Maxwell criterion of equal numbers of constraints and degrees of freedom. We demonstrate that such systems exhibit pairs of oppositely charged Weyl points, corresponding to zero-frequency bulk modes, that can appear at the origin of the Brillouin zone and move away to the zone edge (or return to the origin) where they annihilate. We prove that the existence of these Weyl points leads to a wavenumber-dependent count of topological mechanical states at free surfaces and domain walls.

cond-mat.mes-hall↗

Rigidity percolation by next-nearest-neighbor braces on generic and regular isostatic lattices

We study rigidity percolation transitions in two-dimensional central-force isostatic lattices, including the square and the kagome lattices, as next-nearest-neighbor bonds ("braces") are randomly added to the system. In particular, we focus on the differences between regular lattices, which are perfectly periodic, and generic lattices with the same topology of bonds but whose sites are at random positions in space. We find that the regular square and kagome lattices exhibit a rigidity percolation transition when the number of braces is $\sim L\ln L$, where $L$ is the linear size of the lattice. This transition exhibits features of both first order and second order transitions: the whole lattice becomes rigid at the transition, whereas there exists a diverging length scale. In contrast, we find that the rigidity percolation transition in the generic lattices occur when the number of braces is very close to the number obtained from the Maxwell's law for floppy modes, which is $\sim L$. The transition in generic lattices is a very sharp first-order-like transition, at which the addition of one brace connects all small rigid regions in the bulk of the lattice, leaving only floppy modes on the edge. We characterize these transitions using numerical simulations and develop analytic theories capturing each transition. Our results relate to other interesting problems including jamming and bootstrap percolation.

cond-mat.soft↗

Self-assembly of three-dimensional open structures using patchy colloidal particles

Open structures can display a number of unusual properties, including a negative Poisson's ratio, negative thermal expansion, and holographic elasticity, and have many interesting applications in engineering. However, it is a grand challenge to self-assemble open structures at the colloidal scale, where short-range interactions and low coordination number can leave them mechanically unstable. In this paper we discuss the self-assembly of open structures using triblock Janus particles, which have two large attractive patches that can form multiple bonds, separated by a band with purely hard-sphere repulsion. Such surface patterning leads to open structures that are stabilized by orientational entropy (in an order-by-disorder effect) and selected over close-packed structures by vibrational entropy. For different patch sizes the particles can form into either tetrahedral or octahedral structural motifs which then compose open lattices, including the pyrochlore, the hexagonal tetrastack and the perovskite lattices. Using an analytic theory, we examine the phase diagrams of these possible open and close-packed structures for triblock Janus particles and characterize the mechanical properties of these structures. Our theory leads to rational designs of particles for the self-assembly of three-dimensional colloidal structures that are possible using current experimental techniques.

cond-mat.soft↗

Organization of strongly interacting directed polymer liquids in the presence of stringent constraints

The impact of impenetrable obstacles on the energetics and equilibrium structure of strongly repulsive directed polymers is investigated. As a result of the strong interactions, regions of severe polymer depletion and excess are found in the vicinity of the obstacle, and the associated free-energy cost is found to scale quadratically with the average polymer density. The polymer-polymer interactions are accounted for via a sequence of transformations: from the 3D line liquid to a 2D fluid of Bose particles to a 2D composite fermion fluid and, finally, to a 2D one-component plasma. The results presented here are applicable to a range of systems consisting of noncrossing directed lines.

cond-mat.soft↗

Directed-polymer systems explored via their quantum analogs: General polymer interactions and their consequences

The impact of polymer-polymer interactions of various types on the thermodynamics, structure, and accommodation of topological constraints is addressed for systems comprising many directed polymers in two spatial dimensions. The approach is predicated on the well-known equivalence between the classical equilibrium statistical mechanics of directed polymers in two spatial dimensions and the imaginary-time quantum dynamics of particles in one spatial dimension, originally exploited by P.-G. de Gennes [J.\ Chem.\ Phys.\ {\bf 48}, 2257 (1968)]. Known results concerning two exactly solvable microscopic models of quantum particles moving in one spatial dimension---the Lieb-Liniger model of contact interactions and the Calogero-Sutherland model of long-range interactions---are used to shed light on the behavior of the corresponding polymeric systems. In addition, the technique of bosonization is used to reveal how generic polymer interactions give rise to an emergent polymer fluid that has universal collective excitations. Comparison of the response to topological constraints of a fluid of simply noncrossing (i.e., noncrossing but otherwise noninteracting) directed polymers, explored in a companion Paper, to the response of a generically interacting directed polymer fluid reveals that the structure is quantitatively unchanged by the generic interactions on the line transverse to the pin, and is qualitatively unchanged by the generic interactions throughout the two dimensions of the system's extent. Furthermore, the free-energy cost associated with a pin that partitions a system having generic interactions is found to be proportional to the pin-partitioning cost for a system of simply noncrossing polymers.

cond-mat.soft↗

Directed-polymer systems explored via their quantum analogs: Topological constraints and their consequences

The equilibrium statistical mechanics of classical directed polymers in 2 dimensions is well known to be equivalent to the imaginary-time quantum dynamics of a 1+1-dimensional many-particle system, with polymer configurations corresponding to particle world-lines. This equivalence motivates the application of techniques originally designed for one-dimensional many-particle quantum systems to the exploration of many-polymer systems, as first recognized and exploited by P.-G. de Gennes [J.\ Chem.\ Phys.\ {\bf 48}, 2257 (1968)]. In this low-dimensional setting interactions give rise to an emergent polymer fluid, and we examine how topological constraints on this polymer fluid (e.g., due to uncrossable pins or barriers) and their geometry give rise to strong, entropy-driven forces. In the limit of large polymer densities, in which a type of mean-field theory is accurate, we find that a point-like pin causes a divergent pile-up of polymer density on the high-density side of the pin and a zero-density region (or gap) of finite area on the low-density. In addition, we find that the force acting on a pin that is only mildly displaced from its equilibrium position is sub-Hookean, growing less than linearly with the displacement, and that the gap created by the pin also grows sublinearly with the displacement. By contrast, the forces acting between multiple pins separated along the direction preferred by the polymers are super-Hookean. These nonlinear responses result from effective long-ranged interactions between polymer segments, which emerge via short-ranged interactions between distant segments of long polymer strands. In the present paper, we focus on the case of an infinitely strong, repulsive contact interaction, which ensures that the polymers completely avoid one another. In a companion paper, we consider the effects of a wider set of inter-polymer interactions.

cond-mat.soft↗