arXiv subjects

V. A. Levashov

Publications and source records attributed to V. A. Levashov.

10 recordsLinked to original sources

arXiv2025

Collineations of particles in the Kob-Andersen system

Numerous indications suggest that subtle changes occurring in the structures of liquids on supercooling are connected to the phenomenon of the glass transition and that detailed understanding of these changes is crucial for the development of new glasses with desired properties. J.D. Bernal in his 1962 Bakerian lecture, in particular, reported about an observation of approximately linear chains of several particles, referred to as collineations. He found that in the studied hard sphere system, these collineations can contain up to eight particles. Since then, the collineations of three particles have been discussed in many papers in the context of the splitting of the second peak in pair density functions of supercooled liquids and glasses. However, it appears that longer collineations involving more that three particles have not been systematically studied. Here, we report on our study of such collineations for the Kob-Andersen system of particles on cooling for the parent and inherent structures. Contrary to intuition, our findings reveal that below the potential energy landscape crossover temperature, the number of collineations in the parent structures can exceed that of the corresponding inherent structures. We also introduce a model that connects long collineations with the pair density and angular density distribution functions and demonstrate that this model describes long collineations quite well. The second part of the paper explores potential connections between collineations and: 1) the disclination lines associated with the geometric frustration approach, 2) low-energy clusters from the topological cluster classification approach, 3) chain-like cooperative motion of particles in low-temperature supercooled liquids. For the studied system, according to the used methods, no clear connection was found between collineations and these phenomena.

cond-mat.soft↗

arXiv2021

Investigation of the degree of local structural similarity between the parent-liquid and children-crystal states for a model soft matter system

We investigate the degree of local structural similarity between the parent-liquid and children-crystal states for a model soft-matter system of particles interacting through the harmonic-repulsive pair potential. At different pressures, this simple system crystallizes into several significantly different crystal structures. Therefore, the model is well suited for addressing the question under consideration. In our studies, we carefully analyze the developments of the pair and triple correlation functions for the parent-liquid as the pressure increases. In particular, these considerations allow us to address the similarities in the orientational orderings of the corresponding liquid and solid phases. It is demonstrated that the similarities in the orientational ordering between the two states extend beyond the first and second neighbors. Currently, it is widely accepted that orientational ordering is important for understanding the behaviors of liquids, supercooled liquids, and the development of detailed theories of the crystalization process. Our results suggest that, up to a certain degree, it might be possible to predict the structures of the children-solids from studies of the parent-liquids. Our results raise anew a general question of how much insight into the properties of the liquid-state can be gained from drawing a parallel with the solid-state.

cond-mat.soft↗

arXiv2020

Structure of the simple harmonic-repulsive system in liquid and glassy states studied by the triple correlation function

An efficient description of the structures of liquids and, in particular, the structural changes that happen with liquids on supercooling remains to be a challenge. The systems composed of soft particles are especially interesting in this context because they often demonstrate non-trivial local orders that do not allow to introduce the concept of the nearest-neighbor shell. For this reason, the use of some methods, developed for the structure analysis of atomic liquids, is questionable for the soft-particle systems. Here we report about our investigations of the structure of the simple harmonic-repulsive liquid in 3D using the triple correlation function (TCF), i.e., the method that does not rely on the nearest neighbor concept. The liquid is considered at reduced pressure ($P=1.8$) at which it exhibits remarkable stability against crystallization on cooling. It is demonstrated that the TCF allows addressing the development of the orientational correlations in the structures that do not allow drawing definite conclusions from the studies of the bond-orientational order parameters. Our results demonstrate that the orientational correlations, if measured by the heights of the peaks in the TCF, significantly increase on cooling. This rise in the orientational ordering is not captured properly by the Kirkwood's superposition approximation. Detailed considerations of the peaks' shapes in the TCF suggest the existence of a link between the orientational ordering and the slowdown of the system's dynamics. Our findings support the view that the development of the orientational correlations in liquids may play a significant role in the liquids' dynamics and that the considerations of the pair distribution function may not be sufficient to understand intuitively all the structural changes that happen with liquids on supercooling.

cond-mat.soft↗

arXiv2019

Anomalous behavior and structure of a liquid of particles interacting through the harmonic-repulsive pair potential near the crystallization transition

A characteristic property of many soft matter systems is an ultrasoft effective interaction between their structural units. This softness often leads to complex behavior. In particular, ultrasoft systems under pressure demonstrate polymorphism of complex crystal and quasicrystal structures. Therefore, it is of interest to investigate how different can be the structure of the fluid state in such systems at different pressures. Here we address this issue for the model liquid composed of particles interacting through the harmonic-repulsive pair potential. This system can form different crystal structures as the liquid is cooled. We find that, at certain pressures, the liquid exhibits unusual properties, such as the negative thermal expansion coefficient. Besides, the volume and the potential energy of the system can increase during crystallization. At certain pressures, the system demonstrates high stability against crystallization and it is hardly possible to crystallize it on the timescales of the simulations. To address the liquid's structure at high pressures, we consider the scaled pair distribution function (PDF) and the bond-orientational order (BOO) parameters. The marked change happening with the PDF, as pressure increases, is the splitting of the first peak which is caused by the appearance of non-negligible interaction with the second neighbors and the following rearrangement of the structure. Our findings suggest that non-trivial effects, usually explained by different interactions at different spatial scales, can be observed also in one-component systems with simple one-length-scale ultrasoft repulsive interactions.

cond-mat.soft↗

arXiv2018

Green-Kubo stress correlation function at the atomic scale and a long-range bond-orientational ordering in a model liquid

Recently there have been several considerations by different authors of viscosity and the Green-Kubo stress correlation function from the microscopic perspective. In most of these and earlier works the atomic level stress is the minimal element of stress. It is also possible to consider, for pairwise interaction potentials, as the minimal elements of stress, the stress tensors associated with the pairs of interacting particles. From this perspective, the atomic level stress is not the minimal stress element, but a sum of all pair stress elements in which involved a selected particle. In this paper, we consider the Green-Kubo stress correlation function from a microscopic perspective using the stress tensors of interacting pairs as the basic stress elements. The obtained results show the presence of a long-range bond-orientational order in the studied model liquid and naturally elucidate the connection of the bond-orientational order with viscosity. It turns out that the long-range bond-orientational order is more clearly expressed in the pairs' stress correlation function than in the atomic stress correlation function. On the other hand, previously observed stress waves are much better expressed in the atomic stress correlation functions. We also address the close connection of our approach with the previous bond-orientational order considerations. Finally, we consider the probability distributions for the bond-stress and atomic stress correlation products at selected distances. The character of the obtained probability distributions raises questions about the meaning of the average correlation functions at large distances.

cond-mat.soft↗

arXiv2017

Contribution to Viscosity from the Structural Relaxation via the Atomic Scale Green-Kubo Stress Correlation Function

We studied the connection between the structural relaxation and viscosity for a binary model of repulsive particles in the supercooled liquid regime. The used approach is based on the decomposition of the macroscopic Green-Kubo stress correlation function into the correlation functions between the atomic level stresses. Previously we used the approach to study an iron-like single component system of particles. The role of vibrational motion has been addressed through the demonstration of the relationship between viscosity and the shear waves propagating over large distances. In our previous considerations, however, we did not discuss the role of the structural relaxation. Here we suggest that the contribution to viscosity from the structural relaxation can be taken into account through the consideration of the contribution from the atomic stress auto-correlation term only. This conclusion, however, does not mean that only the auto-correlation term represents the contribution to viscosity from the structural relaxation. Previously the role of the structural relaxation for viscosity has been addressed through the considerations of the transitions between inherent structures and within the mode-coupling theory by other authors. In the present work, we study the structural relaxation through the considerations of the parent liquid and the atomic level stress correlations in it. The comparison with the results obtained on the inherent structures also is made. Our results suggest that in the supercooled liquid regime the vibrational contribution to viscosity extends over the times which are much larger than the Einstein's vibrational period and much larger than the times which it takes for the shear waves to propagate over the model systems. Besides addressing the atomic level shear stress correlations, we also studied correlations between the atomic level pressure elements.

cond-mat.mtrl-sci↗

arXiv2017

Crystalline structures of particles interacting through the harmonic-repulsive pair potential

The behavior of identical particles interacting through the harmonic-repulsive pair potential has been studied in 3D using molecular dynamics simulations at a number of different densities. We found that at many densities, as the temperature of the systems decreases, the particles crystallize into complex structures whose formation have not been anticipated in previous studies on the harmonic-repulsive pair potential. In particular, at certain densities crystallization into the structure $Ia\bar{3}d$ (space group $\#230$) with 16 particles in the unit cell occupying Wyckoff special positions (16b) was observed. This crystal structure has not been observed previously in experiments or in computer simulations of single component atomic or soft matter systems. At another density we observed a liquid which is rather stable against crystallization. Yet, we observed crystallization of this liquid into the monoclinic $C2/c$ (space group $\#15$) structure with 32 particles in the unit cell occupying four different non-special Wyckoff (8f) sites. In this structure particles located at different Wyckoff sites have different energies. From the perspective of the local atomic environment, the organization of particles in this structure resembles the structure of some columnar quasicrystals. At a different value of the density we did not observe crystallization at all despite rather long molecular dynamics runs. At two other densities we observed the formation of the $βSn$ distorted diamond structures instead of the expected diamond structure. Possibly, we also observed the formation of the $R\bar{3}c$ hexagonal lattice with 24 particles per unit cell occupying non-equivalent positions.

cond-mat.soft↗

arXiv2015

Analysis of spatial correlations in a model 2D liquid through eigenvalues and eigenvectors of atomic level stress matrices

Considerations of local atomic level stresses associated with each atom represent a particular approach to address structures of disordered materials at the atomic level. We studied structural correlations in a two-dimensional model liquid using molecular dynamics simulations in the following way. We diagonalized the atomic level stress tensors of every atom and investigated correlations between the eigenvalues and orientations of the eigenvectors of different atoms as a function of distance between them. It is demonstrated that the suggested approach can be used to characterize structural correlations in disordered materials. In particular, we found that changes in the stress correlation functions on decrease of temperature are the most pronounced for the pairs of atoms with separation distance that corresponds to the first minimum in the pair density function. We also show that the angular dependencies of the stress correlation functions previously reported in [Phys. Rev. E v.91, 032301 (2015)] related not to the alleged anisotropies of the Eshelby's stress fields, but to the rotational properties of the stress tensors.

cond-mat.soft↗

arXiv2014

Dependence of the Atomic Level Green-Kubo Stress Correlation Function on Wavevector and Frequency. Molecular Dynamics Results from a Model Liquid

We report on a further investigation of a new method that can be used to address vibrational dynamics and propagation of stress waves in liquids. The method is based on the decomposition of the macroscopic Green-Kubo stress correlation function into the atomic level stress correlation functions. This decomposition, as was demonstrated previously for a model liquid studied in molecular dynamics simulations, reveals the presence of stress waves propagating over large distances and a structure that resembles the pair density function. In this paper, by performing the Fourier transforms of the atomic level stress correlation functions, we elucidate how the lifetimes of the stress waves and the ranges of their propagation depend on their frequency, wavevector, and temperature. These results relate frequency and wavevector dependence of the generalized viscosity to the character of propagation of the shear stress waves. In particular, the results suggest that an increase in the value of the frequency dependent viscosity at low frequencies with decrease of temperature is related to the increase in the ranges of propagation of the stress waves of the corresponding low frequencies. We found that the ranges of propagation of the shear stress waves of frequencies less than half of the Einstein frequency, extend well beyond the nearest neighbor shell even above the melting temperature. The results also show that the crossover from quasilocalized to propagating behavior occurs at frequencies usually associated with the Boson peak.

cond-mat.mtrl-sci↗

arXiv2014

Atomic Level Green-Kubo Stress Correlation Function for a Model Crystal: An Insight into Molecular Dynamics Results on a Model Liquid

In order to get insight into the connection between the vibrational dynamics and the atomic level Green-Kubo stress correlation function in liquids we consider this connection in a model crystal instead. Of course, vibrational dynamics in liquids and crystals are quite different and it is not expected that the results obtained on a model crystal should be valid for liquids. However, these considerations provide a benchmark to which the results of the previous molecular dynamics simulations can be compared. Thus, assuming that vibrations are plane waves, we derive analytical expressions for the atomic level stress correlation functions in the classical limit and analyze them. These results provide, in particular, a recipe for analysis of the atomic level stress correlation functions in Fourier space and extraction of the wavevector and frequency dependent information. We also evaluate the energies of the atomic level stresses. Obtained energies are significantly smaller than the energies that were obtained in MD simulations of liquids previously. This result suggests that the average energies of the atomic level stresses in liquids and glasses are largely determined by the structural disorder. We discuss this result in the context of equipartition of the atomic level stress energies. Analysis of the previously published data suggests that it is possible to speak about configurational and vibrational contributions to the average energies of the atomic level stresses in a glass state. However, this separation in a liquid state is problematic. We also consider peak broadening in the pair distribution function with increase of distance. We find that peak broadening (by ~40%) occurs due to the transverse vibrational modes, while contribution from the longitudinal modes does not change with distance. Finally, we introduce and consider atomic level transverse current correlation function.

cond-mat.soft↗