Pressure-energy correlations and thermodynamic scaling in viscous Lennard-Jones liquids

被引:63
作者
Coslovich, D. [1 ,2 ]
Roland, C. M. [3 ]
机构
[1] Vienna Univ Technol, Inst Theoret Phys, A-1040 Vienna, Austria
[2] Univ Trieste, Dipartimento Fis Teor, I-34100 Trieste, Italy
[3] USN, Res Lab, Washington, DC 20375 USA
基金
奥地利科学基金会;
关键词
fluctuations; liquid mixtures; liquid structure; molecular dynamics method; potential energy functions; thermodynamics; EQUATION-OF-STATE; MOLECULAR-DYNAMICS; SOFT SPHERES; FLUID; RELAXATION; DIFFUSION; LANDSCAPE; POLYMERS; MODEL;
D O I
10.1063/1.3054635
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
We use molecular dynamics simulation results on viscous binary Lennard-Jones mixtures to examine the correlation between the potential energy and the virial. In accord with a recent proposal [U. R. Pedersen , Phys. Rev. Lett. 100, 015701 (2008)], the fluctuations in the two quantities are found to be strongly correlated, exhibiting a proportionality constant, Gamma, numerically equal to one-third the slope of an inverse power law approximation to the intermolecular potential function. The correlation is stronger at higher densities, where interatomic separations are in the range where the inverse power law approximation is more accurate. These same liquids conform to thermodynamic scaling of their dynamics, with the scaling exponent equal to Gamma. Thus, the properties of strong correlation between energy and pressure and thermodynamic scaling both reflect the ability of an inverse power law representation of the potential to capture interesting features of the dynamics of dense, highly viscous liquids.
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页数:5
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