Statistical mechanics of Roskilde liquids: Configurational adiabats, specific heat contours and density dependence of the scaling exponent

Abstract

We derive exact results for the rate of change of thermodynamic quantities, in particular the configurational specific heat at constant volume, $C_V$, along configurational adiabats (curves of constant excess entropy $S_{\textrm{ex}}$). Such curves are designated isomorphs for so-called Roskilde liquids, in view of the invariance of various structural and dynamical quantities along them. Their slope in a double logarithmic representation of the density-temperature phase diagram, $γ$ can be interpreted as one third of an effective inverse power-law potential exponent. We show that in liquids where $γ$ increases (decreases) with density, the contours of $C_V$ have smaller (larger) slope than configurational adiabats. We clarify also the connection between $γ$ and the pair potential. A fluctuation formula for the slope of the $C_V$-contours is derived. The theoretical results are supported with data from computer simulations of two systems, the Lennard-Jones fluid and the Girifalco fluid. The sign of $dγ/dρ$ is thus a third key parameter in characterizing Roskilde liquids, after $γ$ and the virial-potential energy correlation coefficient $R$. To go beyond isomorph theory we compare invariance of a dynamical quantity, the self-diffusion coefficient along adiabats and $C_V$-contours, finding it more invariant along adiabats.