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Tuning the strength of emergent correlations in a Brownian gas via batch resetting

Gabriele de Mauro, Satya N. Majumdar, Gregory Schehr

Abstract

We study a gas of $N$ diffusing particles on the line subject to batch resetting: at rate $r$, a uniformly random subset of $m$ particles is reset to the origin. Despite the absence of interactions, the dynamics generates a nonequilibrium stationary state (NESS) with long-range correlations. We obtain exact results, both for the NESS and for the time dependence of the correlations, which are valid for arbitrary $m$ and $N$. By varying $m$, the system interpolates between an uncorrelated regime ($m=1$) and the fully synchronous resetting case ($m=N$). For all $1<m<N$, correlations exhibit a non-monotonic time dependence due to the emergence of an intrinsic decorrelation mechanism. In the stationary state, the correlation strength can be tuned by varying $m$, and it displays a transition at a critical value $N_c=6$. Our predictions extend straightforwardly to any spatial dimension $d$ and the critical value $N_c=6$ remains the same in all dimensions. Our predictions are testable in existing experimental setups on optically trapped colloidal particles.

Tuning the strength of emergent correlations in a Brownian gas via batch resetting

Abstract

We study a gas of diffusing particles on the line subject to batch resetting: at rate , a uniformly random subset of particles is reset to the origin. Despite the absence of interactions, the dynamics generates a nonequilibrium stationary state (NESS) with long-range correlations. We obtain exact results, both for the NESS and for the time dependence of the correlations, which are valid for arbitrary and . By varying , the system interpolates between an uncorrelated regime () and the fully synchronous resetting case (). For all , correlations exhibit a non-monotonic time dependence due to the emergence of an intrinsic decorrelation mechanism. In the stationary state, the correlation strength can be tuned by varying , and it displays a transition at a critical value . Our predictions extend straightforwardly to any spatial dimension and the critical value remains the same in all dimensions. Our predictions are testable in existing experimental setups on optically trapped colloidal particles.
Paper Structure (4 sections, 20 equations, 3 figures)

This paper contains 4 sections, 20 equations, 3 figures.

Figures (3)

  • Figure 1: Schematic representation of batch resetting for $N=3$ and $m=2$. Four resetting events are shown (light-blue dots).
  • Figure 2: Plot of the function $V(m,N)$ (Eq. \ref{['eq:C2stat']}) compared with numerical simulations, shown as a function of $m$ for different values of $N$. For $N<N_c=6$, $V(m,N)$ increases monotonically with $m$, whereas for $N>N_c$ it becomes non–monotonic: the global maximum shifts from $m=N$ to $m=2$ and a shallow local minimum develops at $m=N-1$. This minimum is clearly visible in the central panel but it is also present for all $N\geq N_c$. At the critical value $N=N_c$, the points $m=2,3,N$ all give the same maximal value $V(m,N_c)=1$. The rightmost point corresponds to fully synchronous resetting Biroli2023 for all values of $N$.
  • Figure 3: Scaling function $A(z;\beta)$ defined in Eq. \ref{['eq:a_APP']} of the End Matter, shown for several values of $\beta=\frac{2N-m-1}{N-1}\in[1,2]$. For $1<m<N$ ($1<\beta<2$), $A(z;\beta)$ develops a maximum at a finite time $z$ (indicated by red dots), while for $m=N$ ($\beta=1$) it increases monotonically. For any $1<\beta<2$, $A(z;\beta)$ decays exponentially fast to its stationary value $(2/\beta-1)/5$.