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Register a new userLocal structure controls shear and bulk moduli in disordered solids
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Paradigmatic model systems, which are used to study the mechanical response of matter, are random networks of point-atoms, random sphere packings, or simple crystal lattices, all of these models assume central-force interactions between particles/atoms. Each of these models differs in the spatial arrangement and the correlations among particles. In turn, this is reflected in the widely different behaviours of the shear (G) and compression (K) elastic moduli. The relation between the macroscopic elasticity as encoded in G, K and their ratio, and the microscopic lattice structure/order, is not understood. We provide a quantitative analytical connection between the local orientational order and the elasticity in model amorphous solids with different internal microstructure, focusing on the two opposite limits of packings (strong excluded-volume) and networks (no excluded-volume). The theory predicts that, in packings, the local orientational order due to excluded-volume causes less nonaffinity (less softness or larger stiffness) under compression than under shear. This leads to lower values of G/K, a well-documented phenomenon which was lacking a microscopic explanation. The theory also provides an excellent one-parameter description of the elasticity of compressed emulsions in comparison with experimental data over a broad range of packing fractions.
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Shearing stresses can change the volume of a material via a nonlinear effect known as shear dilatancy. We calculate the elastic dilatancy coefficient of soft sphere packings and random spring networks, two canonical models of marginal solids close to their rigidity transition. We predict a dramatic enhancement of dilatancy near rigidity loss in both materials, with a surprising distinction: while packings expand under shear, networks contract. We show that contraction in networks is due to the destabilizing influence of increasing hydrostatic or uniaxial loads, which is counteracted in packings by the formation of new contacts.
The holographic principle has proven successful in linking seemingly unrelated problems in physics; a famous example is the gauge-gravity duality. Recently, intriguing correspondences between the physics of soft matter and gravity are emerging, including strong similarities between the rheology of amorphous solids, effective field theories for elasticity and the physics of black holes. However, direct comparisons between theoretical predictions and experimental/simulation observations remain limited. Here, we study the effects of non-linear elasticity on the mechanical and thermodynamic properties of amorphous materials responding to shear, using effective field and gravitational theories. The predicted correlations among the non-linear elastic exponent, the yielding strain/stress and the entropy change due to shear are supported qualitatively by simulations of granular matter models. Our approach opens a path towards understanding complex mechanical responses of amorphous solids, such as mixed effects of shear softening and shear hardening, and offers the possibility to study the rheology of solid states and black holes in a unified framework.
We measure experimentally the rearrangements due to a small localized cyclic displacement applied to a packing of rigid grains under gravity in a 2D geometry. We analyze the evolution of the response to this perturbation by considering the individual particle displacement and the coarse grained displacement field, as well as the mean packing fraction and coordination number. We find that the displacement response is rather long ranged, and evolves considerably with the number of cycles. We show that a small difference in the preparation method (induced by tapping the container) leads to a significant modification in the response though the packing fraction changes are minute. Not only the initial response but also its further evolution change with preparation, demonstrating that the system still retains a memory of the initial preparation after many cycles. Nevertheless, after a sufficient number of cycles, the displacement response for both preparation methods converges to a nearly radial field with a 1/r decay from the perturbation source. The observed differences between the preparation methods seem to be related to the changes in the coordination number (which is more sensitive to the evolution of the packing than the packing fraction). Specifically, it may be understood as an effect of the breaking of local arches, which affects the lateral transmission of forces.
We study two lattice models, the honeycomb lattice (HCL) and a special square lattice (SQL), both reducing to the Dirac equation in the continuum limit. In the presence of disorder (gaussian potential disorder and random vector potential), we investigate the behaviour of the density of states (DOS) numerically and analytically. While an upper bound can be derived for the DOS on the SQL at the Dirac point, which is also confirmed by numerical calculations, no such upper limit exists for the HCL in the presence of random vector potential. A careful investigation of the lowest eigenvalues indeed indicate, that the DOS can possibly be divergent at the Dirac point on the HCL. In spite of sharing a common continuum limit, these lattice models exhibit different behaviour.
Low-temperature properties of crystalline solids can be understood using harmonic perturbations around a perfect lattice, as in Debyes theory. Low-temperature properties of amorphous solids, however, strongly depart from such descriptions, displaying enhanced transport, activated slow dynamics across energy barriers, excess vibrational modes with respect to Debyes theory (i.e., a Boson Peak), and complex irreversible responses to small mechanical deformations. These experimental observations indirectly suggest that the dynamics of amorphous solids becomes anomalous at low temperatures. Here, we present direct numerical evidence that vibrations change nature at a well-defined location deep inside the glass phase of a simple glass former. We provide a real-space description of this transition and of the rapidly growing time and length scales that accompany it. Our results provide the seed for a universal understanding of low-temperature glass anomalies within the theoretical framework of the recently discovered Gardner phase transition.
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