SearcharxivSearch

arXiv · 2103.12952

Hyperuniform Density Distributions of Brownian Particles via Designer External Potentials

Abstract

Disordered hyperuniformity (DHU) is a recently discovered novel state of many-body systems that is characterized by vanishing normalized infinite-wavelength density fluctuations similar to a perfect crystal, yet possesses an amorphous structure like a liquid or glass. Here we investigate equilibrium DHU states of Brownian particles induced by external potentials. In particular, we analytically derive sufficient conditions on the external potentials in order to achieve distinct classes of DHU density distributions of Brownian particles in thermal equilibrium, based on the stationary-state solutions of the corresponding Smoluchowski equation. We show for a wide spectrum of tight-binding potentials, the desirable DHU states of Brownian particles can be controlled and achieved by imposing proper hyperuniformity conditions on the potentials. Moreover, we find that thermal motions in these systems tend to enhance hyperuniformity. We also analyze the evolution dynamics of an initial density distribution (hyperuniform or non-hyperuniform) to the desirable equilibrium DHU state determined by the prescribed external potentials, which is shown to be coupled with the full spectra of the force fields associated with the imposed potentials. We find that although the transient density distribution can rapidly develop local patterns reminiscent of those in the equilibrium distribution, which is governed by the fast dynamics induced by the external potential, the overall distribution is still modulated by the initial density fluctuations which are relaxed through slow diffusive dynamics. Our study has implications for the fabrication of designer DHU materials.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Yang Jiao. 2021-03-24. Hyperuniform Density Distributions of Brownian Particles via Designer External Potentials. https://doi.org/10.1016/j.physa.2021.126435

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Slow Dynamics and the Geometry of Jammed Packings

Saddle points in the energy landscape of granular packings dominate the discrete steepest descent dynamics and ultimately determine the path that an out of mechanical equilibrium packing will follow and the resulting stable minimum that it will find. The saddle points that ultimately determine the resulting minima tend to be low-index saddle points. For models with an analytic energy landscape, such as the $p$-spin model, the steepest descent minimization path is affected by higher-index saddle points, which pull the system towards saddle points of decreasing index before arriving at the minima. Here, we examine the steepest descent minimization path of granular packings and compare them to the $p$-spin model. We show that the granular packing steepest descent minimization paths act like their smooth energy landscape counterparts and get attracted by saddle points. The index versus time curves for all models follow a shifted, stretched exponential. We further show that the shape parameter for the granular packings is unchanged when the energy landscape is modified to become analytic (Gaussian potential in a harmonic well) or non-local (Mari-Krzakala-Kurchan). The $p$-spin, on the other hand, has a significantly larger shape parameter. The reason is not due to the dimensionality, packing fraction, nonanalyticity, or the locality of the Hamiltonian of the models. The exact reason for the discrepancy in the shape parameter is \st{still} an unsolved mystery.

cond-mat.soft

A Phase-Field Study of Desiccation Crack Pattern Maturation under Drying-Wetting Cycles

The characteristic intersection angle of the desiccation crack relaxes from near \ang{90} toward \ang{120} under repeated drying--wetting cycles. However, the theoretical understanding of this relaxation is insufficient, especially the modeling of the drying--wetting cycles. Here we introduce a phase-field model of desiccation fracture, extending the model proposed in previous studies by adding crack healing and a scar effect left by past cracks. By repeating drying--wetting cycles in a finite element simulation, we find that the angle distribution develops a growing peak near \ang{120} as the cycle number increases, consistent with experiments. The standard deviation of the intersection angle from \ang{120} relaxes exponentially with a characteristic time of about 2.85 cycles. These results are consistent with experiments, except that the characteristic time is slightly smaller than the experimental value. Crack energy dominates the total energy and also relaxes exponentially with nearly the same characteristic cycle as the angle relaxation. This decay is driven mainly by a shortening of the effective crack length rather than a change in effective fracture toughness.

cond-mat.soft

Kinetics of ferritin crystal formation and melting in acoustically levitated droplets

Understanding protein crystallization pathways is essential for controlling crystallization in structural biology, materials science, and pharmaceutical applications. Classical nucleation theory does not fully capture crystallization processes for several proteins, including ferritin. Here, we combine acoustic levitation with small- and wide-angle X-ray scattering (SAXS and WAXS) to monitor ferritin crystallization in evaporating aqueous polyethylene glycol (PEG) solutions. Acoustic levitation rapidly drives the droplets through a broad range of protein and polymer concentrations, enabling time-resolved measurements of crystallization during evaporation. The scattering data show that ferritin crystals form during evaporation and subsequently lose their crystalline order upon further dehydration. Varying the PEG molecular weight switches between distinct crystallization pathways: one dominated by attractive protein-protein interactions and another dominated by repulsive interactions and excluded-volume effects. Furthermore, we find that lower molecular weight PEG (1000 g/mol) suppresses the dehydration-induced loss of crystalline order observed for higher molecular weight PEG (6000 g/mol), providing a simple strategy for improving protein crystal stability.

cond-mat.soft