论文标题

具有单向过渡的系统的热力学不确定性关系

Thermodynamic uncertainty relation for systems with unidirectional transitions

论文作者

Pal, Arnab, Reuveni, Shlomi, Rahav, Saar

论文摘要

我们为具有单向转变的系统提供了热力学不确定性关系(TUR)。不确定性关系涉及热力学和动态术语的混合物。也就是说,来自双向转变的熵产生以及单向跃迁的净通量。该派生不假定稳态,结果同样适用于任意初始条件的瞬态过程。由于每个双向过渡也可以看作是一对单独的单向转变,因此我们的方法具有固有的自由度。因此,对于任何给定的系统,都可以得出有效的TUR的集合。但是,我们发现选择一种在观察时间中最能匹配系统动力学的表示形式将产生与波动有关的更紧密结合的TAR。更确切地说,当与两个状态之间的过渡相关的熵产生大于它们之间的净通量之和时,我们表明的双向表示应被单向替换。因此,除了为以前无法​​使用此类关系的系统提供TUR外,本文提供的结果还提供了一种系统的方法,可以通过以实际动机的方式替换双向过渡,从而改善TUR界限。我们的方法及其实施的力量在随机重置的随机行走模型和酶促催化模型上展示。

We derive a thermodynamic uncertainty relation (TUR) for systems with unidirectional transitions. The uncertainty relation involves a mixture of thermodynamic and dynamic terms. Namely, the entropy production from bidirectional transitions, and the net flux of unidirectional transitions. The derivation does not assume a steady-state, and the results apply equally well to transient processes with arbitrary initial conditions. As every bidirectional transition can also be seen as a pair of separate unidirectional ones, our approach is equipped with an inherent degree of freedom. Thus, for any given system, an ensemble of valid TURs can be derived. However, we find that choosing a representation that best matches the systems dynamics over the observation time will yield a TUR with a tighter bound on fluctuations. More precisely, we show a bidirectional representation should be replaced by a unidirectional one when the entropy production associated with the transitions between two states is larger than the sum of the net fluxes between them. Thus, in addition to offering TURs for systems where such relations were previously unavailable, the results presented herein also provide a systematic method to improve TUR bounds via physically motivated replacement of bidirectional transitions with pairs of unidirectional transitions. The power of our approach and its implementation are demonstrated on a model for random walk with stochastic resetting and on the Michaelis-Menten model of enzymatic catalysis.

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