Enumerating low-frequency nonphononic vibrations in computer glasses.

In addition to Goldstone phonons that generically emerge in the low-frequency vibrational spectrum of any solid, crystalline or glassy, structural glasses also feature other low-frequency vibrational modes. The nature and statistical properties of these modes-often termed "excess modes"-have been the subject of decades-long investigation. Studying them, even using well-controlled computer glasses, has proven challenging due to strong spatial hybridization effects between phononic and nonphononic excitations, which hinder quantitative analyses of the nonphononic contribution DG(ω) to the total spectrum D(ω), per frequency ω.

Elasticity of self-organized frustrated disordered spring networks.

There have been some interesting recent advances in understanding the notion of mechanical disorder in structural glasses and the statistical mechanics of these systems' low-energy excitations. Here we contribute to these advances by studying a minimal model for structural glasses' elasticity in which the degree of mechanical disorder-as characterized by recently introduced dimensionless quantifiers-is readily tunable over a very large range. We comprehensively investigate a number of scaling laws observed for various macro, meso and microscopic elastic properties, and rationalize them using scaling arguments.

Effects of coordination and stiffness scale separation in disordered elastic networks.

Many fibrous materials are modeled as elastic networks featuring a substantial separation between the stiffness scales that characterize different microscopic deformation modes of the network's constituents. This scale separation has been shown to give rise to emergent complexity in these systems' linear and nonlinear mechanical response. Here we study numerically a simple model featuring said stiffness scale separation in two-dimensions and show that its mechanical response is governed by the competition between the characteristic stiffness of collective nonphononic soft modes of the stiff subsystem, and the characteristic stiffness of the soft interactions.

Elasticity and rheology of auxetic granular metamaterials.

The flowing, jamming, and avalanche behavior of granular materials is satisfyingly universal and vexingly hard to tune: A granular flow is typically intermittent and will irremediably jam if too confined. Here, we show that granular metamaterials made from particles with a negative Poisson's ratio yield more easily and flow more smoothly than ordinary granular materials. We first create a collection of auxetic grains based on a re-entrant mechanism and show that each grain exhibits a negative Poisson's ratio regardless of the direction of compression.

Scaling regimes and fluctuations of observables in computer glasses approaching the unjamming transition.

Under decompression, disordered solids undergo an unjamming transition where they become under-coordinated and lose their structural rigidity. The mechanical and vibrational properties of these materials have been an object of theoretical, numerical, and experimental research for decades. In the study of low-coordination solids, understanding the behavior and physical interpretation of observables that diverge near the transition is of particular importance.

Detecting low-energy quasilocalized excitations in computer glasses.

Soft, quasilocalized excitations (QLEs) are known to generically emerge in a broad class of disordered solids and to govern many facets of the physics of glasses, from wave attenuation to plastic instabilities. In view of this key role of QLEs, shedding light upon several open questions in glass physics depends on the availability of computational tools that allow one to study QLEs' statistical mechanics. The latter is a formidable task since harmonic analyses are typically contaminated by hybridizations of QLEs with phononic excitations at low frequencies, obscuring a clear picture of QLEs' abundance, typical frequencies, and other important micromechanical properties.

Boson-peak vibrational modes in glasses feature hybridized phononic and quasilocalized excitations.

A hallmark of structural glasses and other disordered solids is the emergence of excess low-frequency vibrations on top of the Debye spectrum DDebye(ω) of phonons (ω denotes the vibrational frequency), which exist in any solid whose Hamiltonian is translationally invariant. These excess vibrations-a signature of which is a THz peak in the reduced density of states D(ω)/DDebye(ω), known as the boson peak-have resisted a complete theoretical understanding for decades. Here, we provide direct numerical evidence that vibrations near the boson peak consist of hybridizations of phonons with many quasilocalized excitations; the latter have recently been shown to generically populate the low-frequency tail of the vibrational spectra of structural glasses quenched from a melt and of disordered crystals.

Low-energy quasilocalized excitations in structural glasses.

Glassy solids exhibit a wide variety of generic thermomechanical properties, ranging from universal anomalous specific heat at cryogenic temperatures to nonlinear plastic yielding and failure under external driving forces, which qualitatively differ from their crystalline counterparts. For a long time, it has been believed that many of these properties are intimately related to nonphononic, low-energy quasilocalized excitations (QLEs) in glasses. Indeed, recent computer simulations have conclusively revealed that the self-organization of glasses during vitrification upon cooling from a melt leads to the emergence of such QLEs.

Bond-space operator disentangles quasilocalized and phononic modes in structural glasses.

The origin of several emergent mechanical and dynamical properties of structural glasses is often attributed to populations of localized structural instabilities, coined quasilocalized modes (QLMs). Under a restricted set of circumstances, glassy QLMs can be revealed by analyzing computer glasses' vibrational spectra in the harmonic approximation. However, this analysis has limitations due to system-size effects and hybridization processes with low-energy phononic excitations (plane waves) that are omnipresent in elastic solids.

Unified quantifier of mechanical disorder in solids.

Mechanical disorder in solids, which is generated by a broad range of physical processes and controls various material properties, appears in a wide variety of forms. Defining unified and measurable dimensionless quantifiers, allowing quantitative comparison of mechanical disorder across widely different physical systems, is therefore an important goal. Two such coarse-grained dimensionless quantifiers (among others) appear in the literature: one is related to the spectral broadening of discrete phononic bands in finite-size systems (accessible through computer simulations) and the other is related to the spatial fluctuations of the shear modulus in macroscopically large systems.

Does mesoscopic elasticity control viscous slowing down in glassforming liquids?

The dramatic slowing down of relaxation dynamics of liquids approaching the glass transition remains a highly debated problem, where the crux of the puzzle resides in the elusive increase in the activation barrier ΔE(T) with decreasing temperature T. A class of theoretical frameworks-known as elastic models-attribute this temperature dependence to the variations of the liquid's macroscopic elasticity, quantified by the high-frequency shear modulus G(T). While elastic models find some support in a number of experimental studies, these models do not take into account the spatial structures, length scales, and heterogeneity associated with structural relaxation in supercooled liquids.

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.

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.

Statistical mechanics of local force dipole responses in computer glasses.

Soft quasilocalized modes (QLMs) are universally featured by structural glasses quenched from a melt, and are involved in several glassy anomalies such as the low-temperature scaling of their thermal conductivity and specific heat, and sound attenuation at intermediate frequencies. In computer glasses, QLMs may assume the form of harmonic vibrational modes under a narrow set of circumstances; however, direct access to their full distribution over frequency is hindered by hybridizations of QLMs with other low-frequency modes (e.g.

Elastic moduli fluctuations predict wave attenuation rates in glasses.

The disorder-induced attenuation of elastic waves is central to the universal low-temperature properties of glasses. Recent literature offers conflicting views on both the scaling of the wave attenuation rate Γ(ω) in the low-frequency limit (ω → 0) and its dependence on glass history and properties. A theoretical framework-termed Fluctuating Elasticity Theory (FET)-predicts low-frequency Rayleigh scattering scaling in -d spatial dimensions, Γ(ω) ∼ γ ω, where γ = γ(V) quantifies the coarse-grained spatial fluctuations of elastic moduli, involving a correlation volume V that remains debated.

Simple and Broadly Applicable Definition of Shear Transformation Zones.

Plastic deformation in amorphous solids is known to be carried by stress-induced localized rearrangements of a few tens of particles, accompanied by the conversion of elastic energy to heat. Despite their central role in determining how glasses yield and break, the search for a simple and generally applicable definition of the precursors of those plastic rearrangements-the so-called shear transformation zones (STZs)-is still ongoing. Here we present a simple definition of STZs-based solely on the harmonic approximation of a glass's energy.

An energy-landscape-based crossover temperature in glass-forming liquids.

The systematic identification of temperature scales in supercooled liquids that are key to understanding those liquids' underlying glass properties, and their formation-history dependence, is a challenging task. Here, we study the statistics of particles' squared displacements δr between equilibrium liquid configurations at temperature T and their underlying inherent states, using computer simulations of 11 different computer glass formers. We show that the relative fluctuations of δr are nonmonotonic in T, exhibiting a maximum whose location defines the crossover temperature T.

Extracting the properties of quasilocalized modes in computer glasses: Long-range continuum fields, contour integrals, and boundary effects.

Low-frequency nonphononic modes and plastic rearrangements in glasses are spatially quasilocalized, i.e., they feature a disorder-induced short-range core and known long-range decaying elastic fields.

Universality of the Nonphononic Vibrational Spectrum across Different Classes of Computer Glasses.

It has been recently established that the low-frequency spectrum of simple computer glass models is populated by soft, quasilocalized nonphononic vibrational modes whose frequencies ω follow a gapless, universal distribution D(ω)∼ω^{4}. While this universal nonphononic spectrum has been shown to be robust to varying the glass history and spatial dimension, it has so far only been observed in simple computer glasses featuring radially symmetric, pairwise interaction potentials. Consequently, the relevance of the universality of nonphononic spectra seen in simple computer glasses to realistic laboratory glasses remains unclear.

Finite-size effects in the nonphononic density of states in computer glasses.

The universal form of the density of nonphononic, quasilocalized vibrational modes of frequency ω in structural glasses, D(ω), was predicted theoretically decades ago, but only recently revealed in numerical simulations. In particular, it has been recently established that, in generic computer glasses, D(ω) increases from zero frequency as ω^{4}, independent of spatial dimension and of microscopic details. However, it has been shown [Lerner and Bouchbinder, Phys.