Hyperuniformity classes of quasiperiodic tilings via diffusion spreadability.

Hyperuniform point patterns can be classified by the hyperuniformity scaling exponent α>0, that characterizes the power-law scaling behavior of the structure factor S(k) as a function of wave number k≡|k| in the vicinity of the origin, e.g., S(k)∼|k|^{α} in cases where S(k) varies continuously with k as k→0. In this paper, we show that the spreadability is an effective method for determining α for quasiperiodic systems where S(k) is discontinuous and consists of a dense set of Bragg peaks. It has been shown in [Phys. Rev. E 104, 054102 (2021)10.1103/PhysRevE.104.054102] that, for media with finite α, the long-time behavior of the excess spreadability S(∞)-S(t) can be fit to a power law of the form t^{-(d-α)/2}, where d is the space dimension, to accurately extract α for the continuous case. We first transform quasiperiodic and limit-periodic point patterns into two-phase media by mapping them onto packings of identical nonoverlapping disks, where space interior to the disks represents one phase and the space in exterior to them represents the second phase. We then compute the spectral density χ[over ̃]_{_{V}}(k) of the packings, and finally compute and fit the long-time behavior of their excess spreadabilities. Specifically, we show that the excess spreadability can be used to accurately extract α for the one-dimensional (1D) limit-periodic period-doubling chain (α=1) and the 1D quasicrystalline Fibonacci chain (α=3) to within 0.02% of the analytically known exact results. Moreover, we obtain a value of α=5.97±0.06 for the two-dimensional Penrose tiling and present plausible theoretical arguments strongly suggesting that α is exactly equal to six. We also show that, due to the self-similarity of the structures examined here, one can truncate the small-k region of the scattering information used to compute the spreadability and obtain an accurate value of α, with a small deviation from the untruncated case that decreases as the system size increases. This strongly suggests that one can obtain a good estimate of α for an infinite self-similar quasicrystal from a modestly sized finite sample. The methods described here offer a simple and general procedure to characterize accurately the large-scale translational order present in quasicrystalline and limit-periodic media in any space dimension that are self-similar. Moreover, the scattering information extracted from these two-phase media encoded in χ[over ̃]_{_{V}}(k), can be used to estimate their physical properties, such as their effective dynamic dielectric constants, effective dynamic elastic constants, and fluid permeabilities.

Local number fluctuations in ordered and disordered phases of water across temperatures: Higher-order moments and degrees of tetrahedrality.

The isothermal compressibility (i.e., related to the asymptotic number variance) of equilibrium liquid water as a function of temperature is minimal under near-ambient conditions. This anomalous non-monotonic temperature dependence is due to a balance between thermal fluctuations and the formation of tetrahedral hydrogen-bond networks. Since tetrahedrality is a many-body property, it will also influence the higher-order moments of density fluctuations, including the skewness and kurtosis. To gain a more complete picture, we examine these higher-order moments that encapsulate many-body correlations using a recently developed, advanced platform for local density fluctuations. We study an extensive set of simulated phases of water across a range of temperatures (80-1600 K) with various degrees of tetrahedrality, including ice phases, equilibrium liquid water, supercritical water, and disordered nonequilibrium quenches. We find clear signatures of tetrahedrality in the higher-order moments, including the skewness and excess kurtosis, which scale for all cases with the degree of tetrahedrality. More importantly, this scaling behavior leads to non-monotonic temperature dependencies in the higher-order moments for both equilibrium and non-equilibrium phases. Specifically, under near-ambient conditions, the higher-order moments vanish most rapidly for large length scales, and the distribution quickly converges to a Gaussian in our metric. However, under non-ambient conditions, higher-order moments vanish more slowly and hence become more relevant, especially for improving information-theoretic approximations of hydrophobic solubility. The temperature non-monotonicity that we observe in the full distribution across length scales could shed light on water's nested anomalies, i.e., reveal new links between structural, dynamic, and thermodynamic anomalies.

Extraordinary optical and transport properties of disordered stealthy hyperuniform two-phase media.

Disordered stealthy hyperuniform two-phase media are a special subset of hyperuniform structures with novel physical properties due to their hybrid crystal-liquid nature. We have previously shown that the rapidly converging strong-contrast expansion of a linear fractional form of the effective dynamic dielectric constantεek1,ω(Torquato and Kim 2021Phys. Rev.X11021002) leads to accurate approximations for both hyperuniform and nonhyperuniform two-phase composite media when truncated at the two-point level for distinctly different types of microstructural symmetries in three dimensions. In this paper, we further elucidate the extraordinary optical and transport properties of disordered stealthy hyperuniform media. Among other results, we provide detailed proofs that stealthy hyperuniform layered and transversely isotropic media are perfectly transparent (i.e. no Anderson localization, in principle) within finite wavenumber intervals through the third-order terms. Remarkably, these results imply that there can be no Anderson localization within the predicted perfect transparency interval in stealthy hyperuniform layered and transversely isotropic media in practice because the localization length (associated with only possibly negligibly small higher-order contributions) should be very large compared to any practically large sample size. We further contrast and compare the extraordinary physical properties of stealthy hyperuniform two-phase layered, transversely isotropic media, and fully three-dimensional isotropic media to other model nonstealthy microstructures, including their attenuation characteristics, as measured by the imaginary part ofεek1,ω, and transport properties, as measured by the time-dependent diffusion spreadabilityS(t). We demonstrate that there are cross-property relations between them, namely, we quantify how the imaginary parts ofεek1,ωand the spreadability at long times are positively correlated as the structures span from nonhyperuniform, nonstealthy hyperuniform, and stealthy hyperuniform media. It will also be useful to establish cross-property relations for stealthy hyperuniform media for other wave phenomena (e.g. elastodynamics) as well as other transport properties. Cross-property relations are generally useful because they enable one to estimate one property, given a measurement of another property.

Designer pair statistics of disordered many-particle systems with novel properties.

The knowledge of exact analytical functional forms for the pair correlation function g2(r) and its corresponding structure factor S(k) of disordered many-particle systems is limited. For fundamental and practical reasons, it is highly desirable to add to the existing database of analytical functional forms for such pair statistics. Here, we design a plethora of such pair functions in direct and Fourier spaces across the first three Euclidean space dimensions that are realizable by diverse many-particle systems with varying degrees of correlated disorder across length scales, spanning a wide spectrum of hyperuniform, typical nonhyperuniform, and antihyperuniform ones. This is accomplished by utilizing an efficient inverse algorithm that determines equilibrium states with up to pair interactions at positive temperatures that precisely match targeted forms for both g2(r) and S(k). Among other results, we realize an example with the strongest hyperuniform property among known positive-temperature equilibrium states, critical-point systems (implying unusual 1D systems with phase transitions) that are not in the Ising universality class, systems that attain self-similar pair statistics under Fourier transformation, and an experimentally feasible polymer model. We show that our pair functions enable one to achieve many-particle systems with a wide range of translational order and self-diffusion coefficients D, which are inversely related to one another. One can design other realizable pair statistics via linear combinations of our functions or by applying our inverse procedure to other desirable functional forms. Our approach facilitates the inverse design of materials with desirable physical and chemical properties by tuning their pair statistics.

Computational design of anisotropic stealthy hyperuniform composites with engineered directional scattering properties.

Disordered hyperuniform materials are an emerging class of exotic amorphous states of matter that endow them with singular physical properties, including large isotropic photonic band gaps, superior resistance to fracture, and nearly optimal electrical and thermal transport properties, to name but a few. Here we generalize the Fourier-space-based numerical construction procedure for designing and generating digital realizations of isotropic disordered hyperuniform two-phase heterogeneous materials (i.e., composites) developed by Chen and Torquato [Acta Mater. 142, 152 (2018)1359-645410.1016/j.actamat.2017.09.053] to anisotropic microstructures with targeted spectral densities. Our generalized construction procedure explicitly incorporates the vector-dependent spectral density function χ[over ̃]_{_{V}}(k) of arbitrary form that is realizable. We demonstrate the utility of the procedure by generating a wide spectrum of anisotropic stealthy hyperuniform microstructures with χ[over ̃]_{_{V}}(k)=0 for k∈Ω, i.e., complete suppression of scattering in an "exclusion" region Ω around the origin in Fourier space. We show how different exclusion-region shapes with various discrete symmetries, including circular-disk, elliptical-disk, square, rectangular, butterfly-shaped, and lemniscate-shaped regions of varying size, affect the resulting statistically anisotropic microstructures as a function of the phase volume fraction. The latter two cases of Ω lead to directionally hyperuniform composites, which are stealthy hyperuniform only along certain directions and are nonhyperuniform along others. We find that while the circular-disk exclusion regions give rise to isotropic hyperuniform composite microstructures, the directional hyperuniform behaviors imposed by the shape asymmetry (or anisotropy) of certain exclusion regions give rise to distinct anisotropic structures and degree of uniformity in the distribution of the phases on intermediate and large length scales along different directions. Moreover, while the anisotropic exclusion regions impose strong constraints on the global symmetry of the resulting media, they can still possess structures at a local level that are nearly isotropic. Both the isotropic and anisotropic hyperuniform microstructures associated with the elliptical-disk, square, and rectangular Ω possess phase-inversion symmetry over certain range of volume fractions and a percolation threshold ϕ_{c}≈0.5. On the other hand, the directionally hyperuniform microstructures associated with the butterfly-shaped and lemniscate-shaped Ω do not possess phase-inversion symmetry and percolate along certain directions at much lower volume fractions. We also apply our general procedure to construct stealthy nonhyperuniform systems. Our construction algorithm enables one to control the statistical anisotropy of composite microstructures via the shape, size, and symmetries of Ω, which is crucial to engineering directional optical, transport, and mechanical properties of two-phase composite media.

Molecular Rotations, Multiscale Order, Hyperuniformity, and Signatures of Metastability during the Compression/Decompression Cycles of Amorphous Ices.

We model, via large-scale molecular dynamics simulations, the isothermal compression of low-density amorphous ice (LDA) to generate high-density amorphous ice (HDA) and the corresponding decompression extending to negative pressures to recover the low-density amorphous phase (LDAHDA). Both LDA and HDA are nearly hyperuniform and are characterized by a dynamical HBN, showing that amorphous ices are nonstatic materials and implying that nearly hyperuniformity can be accommodated in dynamical networks. In correspondence with both the LDA-to-HDA and the HDA-to-LDAHDA phase transitions, the (partial) activation of rotational degrees of freedom activates a cascade effect that induces a drastic change in the connectivity and a pervasive reorganization of the HBN topology which, ultimately, break the samples' hyperuniform character. Key to this effect is the rapid rate at which changes occur, and not their magnitude. The inspection of structural properties from the short- to the long-range shows that signatures of metastability are present at all length-scales, hence providing further solid evidence in support of the liquid-liquid critical point scenario. LDA and LDAHDA differ in terms of HBN and structural properties, implying that they are distinct low-density glasses. Our work unveils the role of molecular rotations in the phase transitions between amorphous ices and shows how the unfreezing of rotational degrees of freedom generates a cascade effect that propagates over multiple length-scales. Our findings greatly improve our basic understanding of water and amorphous ices and can potentially impact the field of molecular network-forming materials at large.

Equilibrium states corresponding to targeted hyperuniform nonequilibrium pair statistics.

The Zhang-Torquato conjecture [G. Zhang and S. Torquato, Phys. Rev. E, 2020, 101, 032124.] states that any realizable pair correlation function g2(r) or structure factor S(k) of a translationally invariant nonequilibrium system can be attained by an equilibrium ensemble involving only (up to) effective two-body interactions. To further test and study this conjecture, we consider two singular nonequilibrium models of recent interest that also have the exotic hyperuniformity property: a 2D "perfect glass" and a 3D critical absorbing-state model. We find that each nonequilibrium target can be achieved accurately by equilibrium states with effective one- and two-body potentials, lending further support to the conjecture. To characterize the structural degeneracy of such a nonequilibrium-equilibrium correspondence, we compute higher-order statistics for both models, as well as those for a hyperuniform 3D uniformly randomized lattice (URL), whose higher-order statistics can be very precisely ascertained. Interestingly, we find that the differences in the higher-order statistics between nonequilibrium and equilibrium systems with matching pair statistics, as measured by the "hole" probability distribution, provide measures of the degree to which a system is out of equilibrium. We show that all three systems studied possess the bounded-hole property and that holes near the maximum hole size in the URL are much rarer than those in the underlying simple cubic lattice. Remarkably, upon quenching, the effective potentials for all three systems possess local energy minima (i.e., inherent structures) with stronger forms of hyperuniformity compared to their target counterparts. Our methods are expected to facilitate the self-assembly of tunable hyperuniform soft-matter systems.

Hyperuniformity of maximally random jammed packings of hyperspheres across spatial dimensions.

The maximally random jammed (MRJ) state is the most random (i.e., disordered) configuration of strictly jammed (mechanically rigid) nonoverlapping objects. MRJ packings are hyperuniform, meaning their long-wavelength density fluctuations are anomalously suppressed compared to typical disordered systems, i.e., their structure factors S(k) tend to zero as the wave number |k| tends to zero. Here we show that generating high-quality strictly jammed states for Euclidean space dimensions d=3,4, and 5 is of paramount importance in ensuring hyperuniformity and extracting precise values of the hyperuniformity exponent α>0 for MRJ states, defined by the power-law behavior of S(k)∼|k|^{α} in the limit |k|→0. Moreover, we show that for fixed d it is more difficult to ensure jamming as the particle number N increases, which results in packings that are nonhyperuniform. Free-volume theory arguments suggest that the ideal MRJ state does not contain rattlers, which act as defects in numerically generated packings. As d increases, we find that the fraction of rattlers decreases substantially. Our analysis of the largest truly jammed packings suggests that the ideal MRJ packings for all dimensions d≥3 are hyperuniform with α=d-2, implying the packings become more hyperuniform as d increases. The differences in α between MRJ packings and the recently proposed Manna-class random close packed (RCP) states, which were reported to have α=0.25 in d=3 and be nonhyperuniform (α=0) for d=4 and d=5, demonstrate the vivid distinctions between the large-scale structure of RCP and MRJ states in these dimensions. Our paper clarifies the importance of the link between true jamming and hyperuniformity and motivates the development of an algorithm to produce rattler-free three-dimensional MRJ packings.

Wave propagation and band tails of two-dimensional disordered systems in the thermodynamic limit.

Understanding the nature and formation of band gaps associated with the propagation of electromagnetic, electronic, or elastic waves in disordered materials as a function of system size presents fundamental and technological challenges. In particular, a basic question is whether band gaps in disordered systems exist in the thermodynamic limit. To explore this issue, we use a two-stage ensemble approach to study the formation of complete photonic band gaps (PBGs) for a sequence of increasingly large systems spanning a broad range of two-dimensional photonic network solids with varying degrees of local and global order, including hyperuniform and nonhyperuniform types. We discover that the gap in the density of states exhibits exponential tails and the apparent PBGs rapidly close as the system size increases for nearly all disordered networks considered. The only exceptions are sufficiently stealthy hyperuniform cases for which the band gaps remain open and the band tails exhibit a desirable power-law scaling reminiscent of the PBG behavior of photonic crystals in the thermodynamic limit.

Realizability of iso-g2 processes via effective pair interactions.

An outstanding problem in statistical mechanics is the determination of whether prescribed functional forms of the pair correlation function g2(r) [or equivalently, structure factor S(k)] at some number density ρ can be achieved by many-body systems in d-dimensional Euclidean space. The Zhang-Torquato conjecture states that any realizable set of pair statistics, whether from a nonequilibrium or equilibrium system, can be achieved by equilibrium systems involving up to two-body interactions. To further test this conjecture, we study the realizability problem of the nonequilibrium iso-g2 process, i.e., the determination of density-dependent effective potentials that yield equilibrium states in which g2 remains invariant for a positive range of densities. Using a precise inverse algorithm that determines effective potentials that match hypothesized functional forms of g2(r) for all r and S(k) for all k, we show that the unit-step function g2, which is the zero-density limit of the hard-sphere potential, is remarkably realizable up to the packing fraction ϕ = 0.49 for d = 1. For d = 2 and 3, it is realizable up to the maximum "terminal" packing fraction ϕc = 1/2d, at which the systems are hyperuniform, implying that the explicitly known necessary conditions for realizability are sufficient up through ϕc. For ϕ near but below ϕc, the large-r behaviors of the effective potentials are given exactly by the functional forms exp[ - κ(ϕ)r] for d = 1, r-1/2 exp[ - κ(ϕ)r] for d = 2, and r-1 exp[ - κ(ϕ)r] (Yukawa form) for d = 3, where κ-1(ϕ) is a screening length, and for ϕ = ϕc, the potentials at large r are given by the pure Coulomb forms in the respective dimensions as predicted by Torquato and Stillinger [Phys. Rev. E 68, 041113 (2003)]. We also find that the effective potential for the pair statistics of the 3D "ghost" random sequential addition at the maximum packing fraction ϕc = 1/8 is much shorter ranged than that for the 3D unit-step function g2 at ϕc; thus, it does not constrain the realizability of the unit-step function g2. Our inverse methodology yields effective potentials for realizable targets, and, as expected, it does not reach convergence for a target that is known to be non-realizable, despite the fact that it satisfies all known explicit necessary conditions. Our findings demonstrate that exploring the iso-g2 process via our inverse methodology is an effective and robust means to tackle the realizability problem and is expected to facilitate the design of novel nanoparticle systems with density-dependent effective potentials, including exotic hyperuniform states of matter.

Precise determination of pair interactions from pair statistics of many-body systems in and out of equilibrium.

The determination of the pair potential v(r) that accurately yields an equilibrium state at positive temperature T with a prescribed pair correlation function g_{2}(r) or corresponding structure factor S(k) in d-dimensional Euclidean space R^{d} is an outstanding inverse statistical mechanics problem with far-reaching implications. Recently, Zhang and Torquato [Phys. Rev. E 101, 032124 (2020)2470-004510.1103/PhysRevE.101.032124] conjectured that any realizable g_{2}(r) or S(k) corresponding to a translationally invariant nonequilibrium system can be attained by a classical equilibrium ensemble involving only (up to) effective pair interactions. Testing this conjecture for nonequilibrium systems as well as for nontrivial equilibrium states requires improved inverse methodologies. We have devised an optimization algorithm to precisely determine effective pair potentials that correspond to pair statistics of general translationally invariant disordered many-body equilibrium or nonequilibrium systems at positive temperatures. This methodology utilizes a parameterized family of pointwise basis functions for the potential function whose initial form is informed by small-, intermediate- and large-distance behaviors dictated by statistical-mechanical theory. Subsequently, a nonlinear optimization technique is utilized to minimize an objective function that incorporates both the target pair correlation function g_{2}(r) and structure factor S(k) so that the small intermediate- and large-distance correlations are very accurately captured. To illustrate the versatility and power of our methodology, we accurately determine the effective pair interactions of the following four diverse target systems: (1) Lennard-Jones system in the vicinity of its critical point, (2) liquid under the Dzugutov potential, (3) nonequilibrium random sequential addition packing, and (4) a nonequilibrium hyperuniform "cloaked" uniformly randomized lattice. We found that the optimized pair potentials generate corresponding pair statistics that accurately match their corresponding targets with total L_{2}-norm errors that are an order of magnitude smaller than that of previous methods. The results of our investigation lend further support to the Zhang-Torquato conjecture. Furthermore, our algorithm will enable one to probe systems with identical pair statistics but different higher-body statistics, which will shed light on the well-known degeneracy problem of statistical mechanics.

Diffusion spreadability as a probe of the microstructure of complex media across length scales.

Understanding time-dependent diffusion processes in multiphase media is of great importance in physics, chemistry, materials science, petroleum engineering, and biology. Consider the time-dependent problem of mass transfer of a solute between two phases and assume that the solute is initially distributed in one phase (phase 2) and absent from the other (phase 1). We desire the fraction of total solute present in phase 1 as a function of time, S(t), which we call the spreadability, since it is a measure of the spreadability of diffusion information as a function of time. We derive exact direct-space formulas for S(t) in any Euclidean space dimension d in terms of the autocovariance function as well as corresponding Fourier representations of S(t) in terms of the spectral density, which are especially useful when scattering information is available experimentally or theoretically. These are singular results because they are rare examples of mass transport problems where exact solutions are possible. We derive closed-form general formulas for the short- and long-time behaviors of the spreadability in terms of crucial small- and large-scale microstructural information, respectively. The long-time behavior of S(t) enables one to distinguish the entire spectrum of microstructures that span from hyperuniform to nonhyperuniform media. For hyperuniform media, disordered or not, we show that the "excess" spreadability, S(∞)-S(t), decays to its long-time behavior exponentially faster than that of any nonhyperuniform two-phase medium, the "slowest" being antihyperuniform media. The stealthy hyperuniform class is characterized by an excess spreadability with the fastest decay rate among all translationally invariant microstructures. We obtain exact results for S(t) for a variety of specific ordered and disordered model microstructures across dimensions that span from hyperuniform to antihyperuniform media. Moreover, we establish a remarkable connection between the spreadability and an outstanding problem in discrete geometry, namely, microstructures with "fast" spreadabilities are also those that can be derived from efficient "coverings" of space. We also identify heretofore unnoticed, to our best knowledge, remarkable links between the spreadability S(t) and NMR pulsed field gradient spin-echo amplitude as well as diffusion MRI measurements. This investigation reveals that the time-dependent spreadability is a powerful, dynamic-based figure of merit to probe and classify the spectrum of possible microstructures of two-phase media across length scales.

Understanding degeneracy of two-point correlation functions via Debye random media.

It is well known that the degeneracy of two-phase microstructures with the same volume fraction and two-point correlation function S_{2}(r) is generally infinite. To elucidate the degeneracy problem explicitly, we examine Debye random media, which are entirely defined by a purely exponentially decaying two-point correlation function S_{2}(r). In this work, we consider three different classes of Debye random media. First, we generate the "most probable" class using the Yeong-Torquato construction algorithm [Yeong and Torquato, Phys. Rev. E 57, 495 (1998)1063-651X10.1103/PhysRevE.57.495]. A second class of Debye random media is obtained by demonstrating that the corresponding two-point correlation functions are effectively realized in the first three space dimensions by certain models of overlapping, polydisperse spheres. A third class is obtained by using the Yeong-Torquato algorithm to construct Debye random media that are constrained to have an unusual prescribed pore-size probability density function. We structurally discriminate these three classes of Debye random media from one another by ascertaining their other statistical descriptors, including the pore-size, surface correlation, chord-length probability density, and lineal-path functions. We also compare and contrast the percolation thresholds as well as the diffusion and fluid transport properties of these degenerate Debye random media. We find that these three classes of Debye random media are generally distinguished by the aforementioned descriptors, and their microstructures are also visually distinct from one another. Our work further confirms the well-known fact that scattering information is insufficient to determine the effective physical properties of two-phase media. Additionally, our findings demonstrate the importance of the other two-point descriptors considered here in the design of materials with a spectrum of physical properties.

Critical pore radius and transport properties of disordered hard- and overlapping-sphere models.

Transport properties of porous media are intimately linked to their pore-space microstructures. We quantify geometrical and topological descriptors of the pore space of certain disordered and ordered distributions of spheres, including pore-size functions and the critical pore radius δ_{c}. We focus on models of porous media derived from maximally random jammed sphere packings, overlapping spheres, equilibrium hard spheres, quantizer sphere packings, and crystalline sphere packings. For precise estimates of the percolation thresholds, we use a strict relation of the void percolation around sphere configurations to weighted bond percolation on the corresponding Voronoi networks. We use the Newman-Ziff algorithm to determine the percolation threshold using universal properties of the cluster size distribution. The critical pore radius δ_{c} is often used as the key characteristic length scale that determines the fluid permeability k. A recent study [Torquato, Adv. Wat. Resour. 140, 103565 (2020)10.1016/j.advwatres.2020.103565] suggested for porous media with a well-connected pore space an alternative estimate of k based on the second moment of the pore size 〈δ^{2}〉, which is easier to determine than δ_{c}. Here, we compare δ_{c} to the second moment of the pore size 〈δ^{2}〉, and indeed confirm that, for all porosities and all models considered, δ_{c}^{2} is to a good approximation proportional to 〈δ^{2}〉. However, unlike 〈δ^{2}〉, the permeability estimate based on δ_{c}^{2} does not predict the correct ranking of k for our models. Thus, we confirm 〈δ^{2}〉 to be a promising candidate for convenient and reliable estimates of the fluid permeability for porous media with a well-connected pore space. Moreover, we compare the fluid permeability of our models with varying degrees of order, as measured by the τ order metric. We find that (effectively) hyperuniform models tend to have lower values of k than their nonhyperuniform counterparts. Our findings could facilitate the design of porous media with desirable transport properties via targeted pore statistics.

Gap Sensitivity Reveals Universal Behaviors in Optimized Photonic Crystal and Disordered Networks.

Through an extensive series of high-precision numerical computations of the optimal complete photonic band gap (PBG) as a function of dielectric contrast α for a variety of crystal and disordered heterostructures, we reveal striking universal behaviors of the gap sensitivity S(α)≡dΔ(α)/dα, the first derivative of the optimal gap-to-midgap ratio Δ(α). In particular, for all our crystal networks, S(α) takes a universal form that is well approximated by the analytic formula for a 1D quarter-wave stack, S_{QWS}(α). Even more surprisingly, the values of S(α) for our disordered networks converge to S_{QWS}(α) for sufficiently large α. A deeper understanding of the simplicity of this universal behavior may provide fundamental insights about PBG formation and guidance in the design of novel photonic heterostructures.

Manifestations of metastable criticality in the long-range structure of model water glasses.

Much attention has been devoted to water's metastable phase behavior, including polyamorphism (multiple amorphous solid phases), and the hypothesized liquid-liquid transition and associated critical point. However, the possible relationship between these phenomena remains incompletely understood. Using molecular dynamics simulations of the realistic TIP4P/2005 model, we found a striking signature of the liquid-liquid critical point in the structure of water glasses, manifested as a pronounced increase in long-range density fluctuations at pressures proximate to the critical pressure. By contrast, these signatures were absent in glasses of two model systems that lack a critical point. We also characterized the departure from equilibrium upon vitrification via the non-equilibrium index; water-like systems exhibited a strong pressure dependence in this metric, whereas simple liquids did not. These results reflect a surprising relationship between the metastable equilibrium phenomenon of liquid-liquid criticality and the non-equilibrium structure of glassy water, with implications for our understanding of water phase behavior and glass physics. Our calculations suggest a possible experimental route to probing the existence of the liquid-liquid transition in water and other fluids.

Structural characterization of many-particle systems on approach to hyperuniform states.

The study of hyperuniform states of matter is an emerging multidisciplinary field, impinging on topics in the physical sciences, mathematics, and biology. The focus of this work is the exploration of quantitative descriptors that herald when a many-particle system in d-dimensional Euclidean space R^{d} approaches a hyperuniform state as a function of the relevant control parameter. We establish quantitative criteria to ascertain the extent of hyperuniform and nonhyperuniform distance-scaling regimes as well as the crossover point between them in terms of the "volume" coefficient A and "surface-area" coefficient B associated with the local number variance σ^{2}(R) for a spherical window of radius R. The larger the ratio B/A, the larger the hyperuniform scaling regime, which becomes of infinite extent in the limit B/A→∞. To complement the known direct-space representation of the coefficient B in terms of the total correlation function h(r), we derive its corresponding Fourier representation in terms of the structure factor S(k), which is especially useful when scattering information is available experimentally or theoretically. We also demonstrate that the free-volume theory of the pressure of equilibrium packings of identical hard spheres that approach a strictly jammed state either along the stable crystal or metastable disordered branch dictates that such end states be exactly hyperuniform. Using the ratio B/A, as well as other diagnostic measures of hyperuniformity, including the hyperuniformity index H and the direct-correlation function length scale ξ_{c}, we study three different exactly solvable models as a function of the relevant control parameter, either density or temperature, with end states that are perfectly hyperuniform. Specifically, we analyze equilibrium systems of hard rods and "sticky" hard-sphere systems in arbitrary space dimension d as a function of density. We also examine low-temperature excited states of many-particle systems interacting with "stealthy" long-ranged pair interactions as the temperature tends to zero, where the ground states are disordered, hyperuniform, and infinitely degenerate. We demonstrate that our various diagnostic hyperuniformity measures are positively correlated with one another. The same diagnostic measures can be used to detect the degree to which imperfections in nearly hyperuniform systems cause deviations from perfect hyperuniformity. Moreover, the capacity to identify hyperuniform scaling regimes should be particularly useful in analyzing experimentally or computationally generated samples that are necessarily of finite size.

Kinetic Frustration Effects on Dense Two-Dimensional Packings of Convex Particles and Their Structural Characteristics.

The study of hard-particle packings is of fundamental importance in physics, chemistry, cell biology, and discrete geometry. Much of the previous work on hard-particle packings concerns their densest possible arrangements. By contrast, we examine kinetic effects inevitably present in both numerical and experimental packing protocols. Specifically, we determine how changing the compression/shear rate of a two-dimensional packing of noncircular particles causes it to deviate from its densest possible configuration, which is always periodic. The adaptive shrinking cell (ASC) optimization scheme maximizes the packing fraction of a hard-particle packing by first applying random translations and rotations to the particles and then isotropically compressing and shearing the simulation box repeatedly until a possibly jammed state is reached. We use a stochastic implementation of the ASC optimization scheme to mimic different effective time scales by varying the number of particle moves between compressions/shears. We generate dense, effectively jammed, monodisperse, two-dimensional packings of obtuse scalene triangle, rhombus, curved triangle, lens, and "ice cream cone" (a semicircle grafted onto an isosceles triangle) shaped particles, with a wide range of packing fractions and degrees of order. To quantify these kinetic effects, we introduce the kinetic frustration index K, which measures the deviation of a packing from its maximum possible packing fraction. To investigate how kinetics affect short- and long-range ordering in these packings, we compute their spectral densities χ̃V(k) and characterize their contact networks. We find that kinetic effects are most significant when the particles have greater asphericity, less curvature, and less rotational symmetry. This work may be relevant to the design of laboratory packing protocols.