Dissipation in monotonic and non-monotonic relaxation to equilibrium

被引:5
|
作者
Petersen, Charlotte F. [1 ,3 ]
Evans, Denis J. [2 ]
Williams, Stephen R. [1 ]
机构
[1] Australian Natl Univ, Res Sch Chem, GPO Box 4, Canberra, ACT 2600, Australia
[2] Australian Natl Univ, Dept Appl Math, Res Sch Phys & Engn, GPO Box 4, Canberra, ACT 0200, Australia
[3] Aalto Univ, Aalto COMP Ctr Excellence, Dept Appl Phys, Espoo 00076, Finland
来源
JOURNAL OF CHEMICAL PHYSICS | 2016年 / 144卷 / 07期
基金
澳大利亚研究理事会;
关键词
STATE FLUCTUATION RELATION; STEADY-STATE; IRREVERSIBLE CYCLES; CHEMICAL-REACTIONS; THEOREM; INCREASE; ENTROPY;
D O I
10.1063/1.4941584
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Using molecular dynamics simulations, we study field free relaxation from a non-uniform initial density, monitored using both density distributions and the dissipation function. When this density gradient is applied to colour labelled particles, the density distribution decays to a sine curve of fundamental wavelength, which then decays conformally towards a uniform distribution. For conformal relaxation, the dissipation function is found to decay towards equilibrium monotonically, consistent with the predictions of the relaxation theorem. When the system is initiated with a more dramatic density gradient, applied to all particles, non-conformal relaxation is seen in both the dissipation function and the Fourier components of the density distribution. At times, the system appears to be moving away from a uniform density distribution. In both cases, the dissipation function satisfies the modified second law inequality, and the dissipation theorem is demonstrated. (C) 2016 AIP Publishing LLC.
引用
收藏
页数:8
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