Using precision coefficients on recurrence times and integrated currents to lower bound the average dissipation rate
Alberto Garilli, Diego Frezzato
TL;DR
This paper extends the Thermodynamic Uncertainty Relation (TUR) by incorporating the statistics of recurrence times for forward and backward transitions along an observable channel in a continuous-time Markov jump process. Using a transition-based framework, it introduces an effective affinity $\mathcal{A}$ and defines a refined bound on the stationary entropy production rate $\sigma^{\rm ss}$ in terms of the long-time precision $\mathcal{T}_\infty$ of the integrated current and the recurrence-time precisions, yielding $\sigma^{\rm ss} \geq 2J \coth^{-1}\left(J\mathcal{T}_\infty - \Delta \mathcal{P}^\tau\right)$. This augmented TUR saturates for unicyclic networks and remains tight far from equilibrium, outperforming the standard TUR in many regimes and enabling dissipation inference from observable currents and recurrence statistics, with potential applications to nanoscale molecular machines and biochemical sensing networks. Practically, the framework connects experimentally accessible fluctuations to a fundamental energetic cost, offering design principles for optimizing precision versus dissipation in nonequilibrium processes.
Abstract
For continuous-time Markov jump processes on irreducible networks and time-independent rate constants, we employ a transition-based formalism to express the long-time precision of a single integrated current over an observable channel in terms of precisions of the recurrence times of the forward and backward jumps, and of an effective affinity that captures the thermodynamic driving on that channel. This leads to a general lower bound for the stationary entropy production rate that extends the well-known Thermodynamic Uncertainty Relation (TUR). Such an augmented TUR, which incorporates the statistics of the recurrences, proves to be tighter than the standard one far from equilibrium, and potentially offers new opportunities for the optimization and design of biological and chemical out-of-equilibrium systems at the nanoscale.
