Physical Review E 75, 051407 (2007)

Defect Fluctuations and Lifetimes in Disordered Yukawa Systems

C. Reichhardt and C.J. Olson Reichhardt

Theoretical Division and Center for Nonlinear Studies, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA

(Received 30 April 2006; published 23 May 2007)

We examine the time dependent defect fluctuations and lifetimes for a bidisperse disordered assembly of Yukawa particles. At high temperatures, the noise spectrum of fluctuations is white and the coordination number lifetimes have a stretched exponential distribution. At lower temperatures, the system dynamically freezes, the defect fluctuations exhibit a 1/f spectrum, and there is a power law distribution of the coordination number lifetimes. Our results indicate that topological defect fluctuations may be a useful way to characterize disordered systems.
I. INTRODUCTION
II. SIMULATION
III. DEFECT FLUCTUATIONS AND POWER SPECTRA
IV. DIFFUSION
V. DEFECT LIFETIMES
VI. YIELDING BEHAVIOR
VII. DISCUSSION
VIII. SUMMARY
References



I.  INTRODUCTION

In two dimensional systems of interacting repulsive particles such as dusty plasmas [1,2,3] and colloidal assemblies [4,5,6,7], heterogeneous particle motions have been observed in the dense liquid phase. The heterogeneity appears close to the disordering transition where the system changes from having predominantly hexagonal ordering to being heavily defected. Recently, it was demonstrated that in the disordered regime where dynamical heterogeneities are present, the time dependent density fluctuations of the topological defects exhibits a 1/f power spectrum [7]. The heterogeneous motion disappears at higher temperatures, and simultaneously the noise spectrum changes to a white form and the noise power is strongly reduced, indicating a lack of correlations in the fluctuations. It was argued that motion in the regime with dynamical heterogeneities occurs in a correlated manner and is spatially concentrated in areas containing a higher density of topological defects. As a result, the creation and annihilation of topological defects is strongly correlated, leading to the 1/f noise signature. Recent experiments on two-dimensional colloidal systems exhibiting heterogeneous motion have confirmed that the colloids with more rapidly changing coordination number are correlated with the regions of motion [5].
In the systems mentioned so far, the ground state at low temperatures is an ordered hexagonal lattice; however, it is known that intrinsically disordered or glassy systems also exhibit dynamical heterogeneities [8,9]. A natural question to ask is how do topological defect fluctuations behave in systems that are inherently disordered and that have no transition to an ordered state as the temperature is lowered. Although there is no ordering transition in an intrinsically disordered system, there can be a temperature at which a dynamical slowing down occurs, giving rise to glassy type behaviors. It would be interesting to study how or if the defect fluctuations change as dynamical freezing is approached. In the disordered system, the length scale of the dynamical heterogeneities increases as the temperature is lowered [8,9]. If the moving regions are associated with more highly defected regions, this may also be reflected in the defect fluctuations.
In this work we examine a two-dimensional system of a bidisperse mixture of Yukawa particles. Previously, this system has been shown to form a disordered state at all temperatures [10]. We analyze the time dependent defect fluctuations, noise spectra, noise power, and the coordination number lifetimes for varied temperatures. At high temperatures where there is no heterogeneous motion, the defect fluctuations have a white power spectrum, the coordination number lifetimes are very short, and there is an exponential decay in the distribution of lifetimes. As the temperature is lowered, the defect fluctuations show a 1/f power spectrum with increased noise power. We also find a peak in the noise power at a finite temperature we label Tn. Near this temperature, the motion is highly heterogeneous and the coordination lifetimes are power law distributed. For temperatures below Tn, the noise power is reduced and the coordination number lifetimes become extremely long. We also probe the system by examining the motion of a single particle driven by an external force. At T = 0 there is a well defined threshold force for motion [10]. At finite temperatures, creep occurs; however, there is a well defined kink in the velocity force curves at a threshold force which vanishes at Tn. These results suggest that measuring topological defect fluctuations may be a useful probe for understanding glassy and jamming behaviors in disordered systems.

II.  SIMULATION

We consider a two-dimensional system with sides of length L and with periodic boundary conditions in the x and y directions. The system contains N particles interacting via a Yukawa or screened Coulomb potential. For any two particles i and j of charge qi and qj located at positions ri and rj, the pair interaction potential is V(rij) = qiqj exp(−κrij)/rij. Here rij=|rirj| and 1/κ is the screening length which is set equal to 2.0. We consider a 50:50 mixture of particles with charges q1 and q2 where q1/q2 = 1/2. We have previously shown that this system forms a disordered assembly at all temperatures [10]. The particles obey overdamped dynamics and the time dependent particle positions and velocities are obtained by integrating the overdamped Brownian dynamics [11] equations of motion, which for a single particle i is
η d ri

dt
= Fi + FT + Fd
(1)
Here η is the damping coefficient and Fi = −∑jiNi V(rij). The particle-particle interactions are cut off at lengths larger than 2/κ and are calculated using a neighbor index method for computational efficiency. Further cutoff lengths have negligible effects. The thermal force is modeled as random Langevin kicks with 〈FTi〉 = 0 and 〈FT(t)FT(t)〉 = 2ηkBTδ(tt). The initial conditions are obtained by simulated annealing. For our parameters, if all the charges are set equal to the larger charge q2, melting as defined by the onset of defects occurs at a temperature of T = 4.0. The driving force Fd is applied to a single particle only, such that Fd=fdx for the driven particle and Fd=0 for all other particles. For most of this work, we set fd=0. We anneal from a temperature of T = 8.0 down to a final temperature in steps of ∆T=0.25 and sit at each increment temperature for over 106 Brownian dynamics (BD) time steps. After annealing, we analyze the topological defect density and particle motions at a fixed temperature. Unless otherwise noted, we consider systems of size L=32 containing N=830 particles.
Fig1.png
Figure 1: (a) Voronoi construction for a snapshot of a bidisperse particle system at T = 1.5. White polygons have 6 neighbors, while black and gray polygons have 5 and 7 neighbors respectively. (b) The particle positions (black dots) and trajectories (black lines) for the same system during 105 simulation time steps.
In Fig. 1(a) we show the topological defects as obtained from a Voronoi construction for a system at T = 1.5. The Voronoi construction forms a polygon around each particle and is used to define the coordination number Cn of the particle. Particles with five, six, and seven neighbors corresponding to Cn=5, 6, and 7 are marked black, white, and gray, respectively. The system is also highly defected at other temperatures and there is little change in the average defect density with temperature; however, the time dependent fluctuation rate of the defects changes significantly with temperature as we show later. In Fig. 1(b) we illustrate the particle trajectories during 105 BD time steps at T=1.5. The motion is highly heterogeneous, and certain regions show motion during this time interval while other regions do not. At higher temperatures the motion becomes more homogeneous throughout the sample.
Fig2.png
Figure 2: (a) Power spectra S(ν,T) obtained from the time series of the topological defect density fluctuations P6(t) obtained at T = 1.5 (upper curve) with a fit (solid line) of α = 0.98 and T = 4.5 (lower curve) with a fit (solid line) of α = 0.1. The T = 4.5 curve has been shifted down for presentation purposes. Inset: the fitted values of α obtained from the power spectra vs T. (b) The noise power S0 vs T. Inset: S0 for T = 1.0 to T = 2.5 for varied system sizes L = 16 (squares), 32 (diamonds), 48 (triangles), and 54 (circles).

III.  DEFECT FLUCTUATIONS AND POWER SPECTRA

In order to characterize the defect fluctuations, we perform a series of simulations at different T and examine the time dependent density of six-fold coordinated particles, P6(t), defined as P6(t)=N−1i=1Nδ(Cni(t)−6), where Cni is the coordination number of particle i. The power spectrum of the resulting time series is defined as
S(ν,T) =

P6(t) e−2πiνtdt
2
 
(2)
The noise power S0 is defined as the average value of the noise spectrum at a particular value of the frequency ν. After annealing we wait 104 time steps before acquiring the time series P6(t) to avoid any transient behaviors. In Fig. 2(a) we show the power spectra of P6(t) for T = 1.5 and T = 4.5. At T = 1.5 the power spectrum has a 1/fα form with α ≈ 0.98, as indicated by the upper solid line. For T = 4.5 the noise spectrum is approximately white and α ≈ 0.1. We plot the evolution of α with T in the inset of Fig. 2(a). For T ≤ 2.0, we find 1/f noise with α ≈ 1, while at high T, the noise spectrum becomes white with α ≈ 0. The particle trajectories also indicate that the motion is no longer heterogeneous for T > 2.0. In monodisperse systems near the disorder transition, a similar 1/f noise signal was observed when the particle motions were highly heterogeneous [7]. We note that for T < 1.5 there is very little particle motion and the defect fluctuations are strongly suppressed. This can be more clearly seen by examining the noise power S0 at fixed ν = 5 as shown in Fig. 2(b). At high temperatures, S0 is low, but it increases rapidly to a peak value as the temperature is reduced to T = Tn = 1.5, and then decreases quickly for T < 1.5. We associate the peak in S0 at Tn with the temperature at which the system begins to undergo a dynamical freezing.
In the inset of Fig. 2(b), we plot the variation in S0 for systems of different sizes ranging from L=16 to 54. As L increases, the peak in the noise power becomes more pronounced. Additionally, although the height of the peak in S0 increases with L, at higher or lower T the noise power at the non-peak temperatures is reduced with increasing L. For temperatures away from T = 1.5, the individual power spectrum curves have a rollover to a white spectrum at the lowest frequencies. At T = 1.5, the α = 1.0 behavior persists down to the lowest frequencies, as shown in Fig. 2(a). The suppression of the noise power away from T=1.5 in the larger systems can be understood as arising from the fact that there is a length scale l associated with the correlated creation or annihilation of defects. The fluctuations with the largest l correspond to the lowest frequencies. If l is constant, then when the system size is small or comparable to l, the fluctuations will have a 1/f character down to the lowest observable frequencies and the noise power will be increased away from the peak in S0, as seen for L = 16 in the inset of Fig. 2(b). As the system is made larger, the fluctuations begin to average out, a low frequency cutoff appears in the 1/f spectrum, and the noise power is reduced. Near the dynamical freezing temperature Tn, the fluctuations grow with the system size and 1/f noise is present for all arbitrarily large L and low ν. For T < Tn, the fluctuations are again cut off and the noise power is reduced. We have compared our results against simulations of collections of non-interacting particles, where the motion is homogeneous and diffusive at all temperatures. In this case, there is no peak in S0 and the spectra are white for all temperatures.
Fig3.png
Figure 3: (a) The measure of the particle displacements d(t) vs t for (top curve to bottom curve) T = 3, 2.5, 1.5, 1.0, and 0.5. The dashed line is a linear fit showing the behavior expected for a system undergoing normal diffusion. (b) The value of d(t) at t = 107 time steps measured for the same system as a function of T.

IV.  DIFFUSION

To quantify the amount of motion present in the system as a function of temperature, we measure the diffusion of the particles by computing the square displacements of the particles from an initial position as a function of time,
d(t) = N

i=1 
|
~
r
 

i 
(t) −
~
r
 

i 
(t0)|2 ,
(3)
where ~ri(t) is the position of particle i at time t with the effect of crossing the periodic boundary conditions removed. For particles undergoing normal diffusion, d(t) ∝ t. In Fig. 3(a) we plot d(t) at T = 3.0, 2.5, 1.5, 1.0, and 0.5 from top to bottom. The data was taken over a period of 107 time steps which started after the system had entered a stationary state. In general, we find a transient time period which lasts for 103 time steps after annealing. This transient behavior was excluded from the analysis so that t0 > 103 time steps. For T > 1.5, the long time behavior of the system is consistent with normal diffusion, as indicated by the dashed line showing a linear slope in Fig. 3(a). For T < 1.5, within our time frame d(t) saturates to a constant value, while at T = 1.5 the long time behavior is more consistent with subdiffusion, d(t) ∝ tα where α < 1.0. We note that this agrees with the measures of the noise fluctuations which indicate that the 1/f noise which appears at T = Tn = 1.5 is associated with the presence of system-wide slow dynamics. For T < 1.5 the fluctuations are instead associated with the rattling motions of single particles rather than long time system wide motions. In Fig. 3(b) we plot the value of d obtained at the end of 107 steps. For T < 1.5, d saturates to a constant value since within our time frame the particles are no longer diffusing significantly, while d increases with T for higher T.
We note that since we are restricted to performing simulations over finite periods of time, we cannot be certain that the subdiffusive motion at T=1.5 does not cross over to regular diffusion at extremely long times. If this were the case, the power spectrum of the corresponding very long time series would show a low frequency cutoff in the 1/f signature at the time scale where the regular diffusion begins to dominate. What we can conclude from our data is that over the time regimes which we are able to access, the appearance of the 1/f defect fluctuations is correlated with the subdiffusive behavior.
Fig4.png
Figure 4: (a) The coordination number Cn vs time for a single particle at T = 1.5 showing occasional changes. (b) Cn vs time for a single particle at T = 3.5 showing much more rapid changes. (c) The histogram of the coordination number lifetimes P(tl) for T = 3.5 (lower curve) and T = 1.5 (upper curve). The solid line is a power law fit with β = 1.6. Inset: P(tl) at T = 5.0, 3.5, 2.5, and 1.5, from left to right.

V.  DEFECT LIFETIMES

We next consider the lifetimes of the coordination numbers. In Fig. 4(a) we show the coordination number Cn as a function of time for one particle in a system at T = 1.5. During this time frame, the particle is predominantly sixfold coordinated with Cn=6, while there are occasional jumps to a configuration with Cn=5 or 7. In some cases, such as for t > 7000, the particle maintains Cn ≠ 6 for a longer period of time. We obtain a similar plot regardless of which particle in the system is selected. In Fig. 4(b) we plot Cn vs time for the same particle at T = 3.5, showing that the particle coordination number is changing much more rapidly. The coordination lifetimes tl are obtained by measuring the length of time that elapses between changes in Cn for a given particle. We histogram this quantity over all the particles, and plot the resulting P(tl) in Fig. 4(c) for two systems at T = 3.5 (lower curve) and T = 1.5 (upper curve). The straight solid line is a power law fit to P(tl) ∝ tl−β with β = 1.6, while the curve at T = 3.5 is fit well to a stretched exponential. In the inset of Fig. 4(c) we plot P(tl) for T = 5.0, 3.5, 2.5, and 1.5, which shows that for the higher temperatures the average lifetime 〈tl〉 is shorter. For T = 5.0, P(tl) can be fit reasonably well to an exponential distribution. For the intermediate temperatures, we can fit the data with a stretched exponential form, and at T = 1.5 we obtain a power law fit. For T < 1.5, the lifetimes become extremely long and we observe close to a bimodal distribution where there are a few particles jumping back and forth giving rise to short values of tl, while Cn of the other particles does not change for the duration of the simulations over times of 2.5×107 BD steps.
Fig5.png
Figure 5: The velocity Vx vs fd for a single driven probe particle for T = 3.5, 2.0, 1.25, 1.0, and 0 from left to right. The peak in the noise power of the defect fluctuation power spectra occurs at T = Tn = 1.5, which also corresponds to the onset of the subdiffusive motion. Inset: the threshold force fc extracted from the velocity-force curves vs T.

VI.  YIELDING BEHAVIOR

The results from Figs. 2, 3 and 4 suggest that near T = 1.5, some type of dynamical crossover or freezing occurs. We can also probe the system by slowly driving a single particle through it. If the system acts rigidly at low drives, then there is a threshold force fc above which the driven particle moves with respect to the background. Previous work on this system at T = 0 has characterized this threshold force [10]. Experiments have also shown evidence for a threshold force to motion for disordered colloidal systems [12]. In general, we find that creep can occur at low but finite temperatures; however, a threshold force can still be identified by a sudden increase or kink in the particle velocity vs applied force. In Fig. 5 we plot the velocity Vx vs applied drive fd for a single probe particle which has a charge q/q1 = 5.0 moving through a disordered assembly of particles at temperatures ranging from T=0 to T=3.5. If the surrounding particles are absent, the probe particle moves linearly with VFd. The velocity-force curves are obtained by slowly increasing the applied drive fd. For T < 1.5, Vx shows a sharp downward concavity at finite fd. We define the threshold force fc as the value at which Vx=5×10−5. For T > 1.5, the curves show a slight positive concavity and if we linearly extrapolate the curves to Vx = 0, the threshold force is indistinguishable from zero. In the inset of Fig. 5 we plot the threshold force fc extracted from the velocity-force curves. We have considered various rates of increasing fd and find no differences in the extracted values of fc. The threshold decreases with increasing temperature up to T = 1.5, and above this temperature there is no threshold for motion. These results add further evidence that there is a dynamical freezing or jamming that occurs near T = 1.5, as also reflected in the defect fluctuations. We note that it is beyond the scope of this paper to determine the true nature of the finite temperature dynamical freezing, such as whether it resembles a glass transition.

VII.  DISCUSSION

The main goal of this paper is to introduce a new measure, the fluctuations in the defect density, for characterizing disordered systems near freezing. The question of whether there is really a finite temperature freezing transition in the equilibrium system near T = 1.5 is beyond the scope of our paper. Although we have found several signatures for some form of dynamical slowing down at T = 1.5, it is possible that for very long times beyond our simulation time scales, the system would show linear diffusion and the fluctuations would lose the 1/f characteristic at very low frequencies. We note that there is other evidence that topological fluctuations and defects appear to be correlated with jamming. Recently, the shape features of topological defects have been utilized to study the jamming transition in two-dimensional granular materials [13]. In this case the fluctuations are nonthermal; however, a jamming transition can still occur. Measurements of fluctuations of P6(t) for the granular system, in the manner we suggest in the present work, reveal the same trends that we have found here. The defect fluctuations have a white noise characteristic away from the jamming transition which crosses over to a 1/f signature near jamming with a peak in the finite frequency noise power [14]. This indicates that the topological fluctuations near jamming or freezing may universally exhibit 1/f noise features.
There has also been recent work on two-dimensional binary glass forming systems showing correlations between the onset of glassy properties and the disappearance of certain types of topological defects at finite temperature. This adds further evidence that there may indeed be a finite temperature freezing or jamming transition in two-dimensional disordered systems that is connected with the motion of defects [15].

VIII.  SUMMARY

To summarize, we have shown that the topological defect fluctuations is a useful quantity that can be employed to understand dynamical freezing and heterogeneities in disordered systems. We specifically find that in regimes where there are dynamical heterogeneities, the time dependent defect density fluctuations show a 1/f characteristic noise spectrum, and that at higher temperatures where the motion is uniform, a white noise spectrum appears. The defect noise power also shows a peak just before the dynamics of the system freezes, and this effect is robust for increasing system sizes. The coordination number lifetimes show a power law distribution in the heterogeneous regions which crosses over to an exponential form at higher temperatures where the heterogeneities are lost. We correlate the peak in the noise power with the onset of subdiffusive behavior as well as with the temperature where a threshold force for the motion of a driven probe particle disappears. Our results should be testable for disordered charge-stabilized colloidal assemblies, dusty plasmas, and other disordered charged systems. We note that recent experiments on granular system near jamming have found the same type of behavior in the time series analysis of the defect fluctuations as the jamming transition is approached.
We thank M.B. Hastings for useful discussions. We also thank A. Abate for sharing his unpublished data with us. This work was supported by the U.S. DoE under Contract No. W-7405-ENG-36.

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