In this letter we report {it in situ} small--angle neutron scattering results on the high--density (HDA) and low-density amorphous (LDA) ice structures and on intermediate structures as found during the temperature induced transformation of HDA into LDA. We show that the small--angle signal is characterised by two $Q$ regimes featuring different properties ($Q$ is the modulus of the scattering vector defined as $Q = 4pisin{(Theta)}/lambda_{rm i}$ with $Theta$ being half the scattering angle and $lambda_{rm i}$ the incident neutron wavelength). The very low--$Q$ regime ($< 5times 10^{-2}$ AA $^{-1}$) is dominated by a Porod--limit scattering. Its intensity reduces in the course of the HDA to LDA transformation following a kinetics reminiscent of that observed in wide--angle diffraction experiments. The small--angle neutron scattering formfactor in the intermediate regime of $5 times 10^{-2} < Q < 0.5$ AA$^{-1}$ HDA and LDA features a rather flat plateau. However, the HDA signal shows an ascending intensity towards smaller $Q$ marking this amorphous structure as heterogeneous. When following the HDA to LDA transition the formfactor shows a pronounced transient excess in intensity marking all intermediate structures as strongly heterogeneous on a length scale of some nano--meters.
We review a new theory of viscoelasticity of a glass-forming viscous liquid near and below the glass transition. In our model we assume that each point in the material has a specific viscosity, which varies randomly in space according to a fluctuating activation free energy. We include a Maxwellian elastic term and assume that the corresponding shear modulus fluctuates as well with the same distribution as that of the activation barriers. The model is solved in coherent-potential approximation (CPA), for which a derivation is given. The theory predicts an Arrhenius-type temperature dependence of the viscosity in the vanishing-frequency limit, independent of the distribution of the activation barriers. The theory implies that this activation energy is generally different from that of a diffusing particle with the same barrier-height distribution. If the distribution of activation barriers is assumed to have Gaussian form, the finite-frequency version of the theory describes well the typical low-temperature alpha relaxation peak of glasses. Beta relaxation can be included by adding another Gaussian with center at much lower energies than that responsible for the alpha relaxation. At high frequencies our theory reduces to the description of an elastic medium with spatially fluctuating elastic moduli (heterogeneous elasticity theory), which explains the occurrence of the boson-peak-related vibrational anomalies of glasses.
The mechanical response of naturally abundant amorphous solids such as gels, jammed grains, and biological tissues are not described by the conventional paradigm of broken symmetry that defines crystalline elasticity. In contrast, the response of such athermal solids are governed by local conditions of mechanical equilibrium, i.e., force and torque balance of its constituents. Here we show that these constraints have the mathematical structure of a generalized electromagnetism, where the electrostatic limit successfully captures the anisotropic elasticity of amorphous solids. The emergence of elasticity from local mechanical constraints offers a new paradigm for systems with no broken symmetry, analogous to emergent gauge theories of quantum spin liquids. Specifically, our $U(1)$ rank-2 symmetric tensor gauge theory of elasticity translates to the electromagnetism of fractonic phases of matter with the stress mapped to electric displacement and forces to vector charges. We corroborate our theoretical results with numerical simulations of soft frictionless disks in both two and three dimensions, and experiments on frictional disks in two dimensions. We also present experimental evidence indicating that force chains in granular media are sub-dimensional excitations of amorphous elasticity similar to fractons.
We show that the distribution of elements $H$ in the Hessian matrices associated with amorphous materials exhibit singularities $P(H) sim {lvert H rvert}^{gamma}$ with an exponent $gamma < 0$, as $lvert H rvert to 0$. We exploit the rotational invariance of the underlying disorder in amorphous structures to derive these exponents exactly for systems interacting via radially symmetric potentials. We show that $gamma$ depends only on the degree of smoothness $n$ of the potential of interaction between the constituent particles at the cut-off distance, independent of the details of interaction in both two and three dimensions. We verify our predictions with numerical simulations of models of structural glass formers. Finally, we show that such singularities affect the stability of amorphous solids, through the distributions of the minimum eigenvalue of the Hessian matrix.
Mechanical deformation of amorphous solids can be described as consisting of an elastic part in which the stress increases linearly with strain, up to a yield point at which the solid either fractures or starts deforming plastically. It is well established, however, that the apparent linearity of stress with strain is actually a proxy for a much more complex behavior, with a microscopic plasticity that is reflected in diverging nonlinear elastic coefficients. Very generally, the complex structure of the energy landscape is expected to induce a singular response to small perturbations. In the athermal quasistatic regime, this response manifests itself in the form of a scale free plastic activity. The distribution of the corresponding avalanches should reflect, according to theoretical mean field calculations (Franz and Spigler, Phys. Rev. E., 2017, 95, 022139), the geometry of phase space in the vicinity of a typical local minimum. In this work, we characterize this distribution for simple models of glass forming systems, and we find that its scaling is compatible with the mean field predictions for systems above the jamming transition. These systems exhibit marginal stability, and scaling relations that hold in the stationary state are examined and confirmed in the elastic regime. By studying the respective influence of system size and age, we suggest that marginal stability is systematic in the thermodynamic limit.
The present work deals with the behavior of fiber bundle model under heterogeneous loading condition. The model is explored both in the mean-field limit as well as with local stress concentration. In the mean field limit, the failure abruptness decreases with increasing order k of heterogeneous loading. In this limit, a brittle to quasi-brittle transition is observed at a particular strength of disorder which changes with k. On the other hand, the model is hardly affected by such heterogeneity in the limit where local stress concentration plays a crucial role. The continuous limit of the heterogeneous loading is also studied and discussed in this paper. Some of the important results related to fiber bundle model are reviewed and their responses to our new scheme of heterogeneous loading are studied in details. Our findings are universal with respect to the nature of the threshold distribution adopted to assign strength to an individual fiber.