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双稳催化表面反应的非平衡热力学与随机动力学

Non-Equilibrium Thermodynamics and Stochastic Dynamics of a Bistable Catalytic Surface Reaction.

作者信息

Pineda Miguel, Stamatakis Michail

机构信息

Department of Chemical Engineering, University College London, Roberts Building, Torrington Place, London WC1E 7JE, UK.

出版信息

Entropy (Basel). 2018 Oct 23;20(11):811. doi: 10.3390/e20110811.

Abstract

Catalytic surface reaction networks exhibit nonlinear dissipative phenomena, such as bistability. Macroscopic rate law descriptions predict that the reaction system resides on one of the two steady-state branches of the bistable region for an indefinite period of time. However, the smaller the catalytic surface, the greater the influence of coverage fluctuations, given that their amplitude normally scales as the square root of the system size. Thus, one can observe fluctuation-induced transitions between the steady-states. In this work, a model for the bistable catalytic CO oxidation on small surfaces is studied. After a brief introduction of the average stochastic modelling framework and its corresponding deterministic limit, we discuss the non-equilibrium conditions necessary for bistability. The entropy production rate, an important thermodynamic quantity measuring dissipation in a system, is compared across the two approaches. We conclude that, in our catalytic model, the most favorable non-equilibrium steady state is not necessary the state with the maximum or minimum entropy production rate.

摘要

催化表面反应网络呈现出非线性耗散现象,如双稳性。宏观速率定律描述预测,反应系统会在双稳区域的两个稳态分支之一上无限期停留。然而,催化表面越小,覆盖度涨落的影响就越大,因为其幅度通常与系统大小的平方根成正比。因此,可以观察到稳态之间的涨落诱导转变。在这项工作中,研究了小表面上双稳催化CO氧化的模型。在简要介绍平均随机建模框架及其相应的确定性极限之后,我们讨论了双稳性所需的非平衡条件。比较了两种方法中作为测量系统耗散的重要热力学量的熵产生率。我们得出结论,在我们的催化模型中,最有利的非平衡稳态不一定是熵产生率最大或最小的状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7f6/7512375/6ef4b0f6cf3d/entropy-20-00811-g001.jpg

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