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Experimental Evidence for a State-Point-Dependent Density-Scaling Exponent of Liquid Dynamics
A large class of liquids obey density scaling characterized by an exponent, which quantifies the relative roles of temperature and density for the dynamics. We present experimental evidence that the density-scaling exponent γ is state-point dependent for the glass formers tetramethyl-tetraphenyl-tri...
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Published in: | Physical review letters 2019-02, Vol.122 (5), p.055501-055501, Article 055501 |
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container_title | Physical review letters |
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creator | Sanz, Alejandro Hecksher, Tina Hansen, Henriette Wase Dyre, Jeppe C Niss, Kristine Pedersen, Ulf R |
description | A large class of liquids obey density scaling characterized by an exponent, which quantifies the relative roles of temperature and density for the dynamics. We present experimental evidence that the density-scaling exponent γ is state-point dependent for the glass formers tetramethyl-tetraphenyl-trisiloxane (DC704) and 5-polyphenyl ether (5PPE). A method is proposed that from dynamic and thermodynamic properties at equilibrium estimates the value of γ. The method applies at any state point of the pressure-temperature plane, both in the supercooled and the normal liquid regimes. We find that γ is generally state-point dependent, which is confirmed by reanalyzing data for 20 metallic liquids and two model liquids. |
doi_str_mv | 10.1103/PhysRevLett.122.055501 |
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subjects | Density Liquids Polyphenyl ether Scaling Thermodynamic equilibrium Thermodynamic properties |
title | Experimental Evidence for a State-Point-Dependent Density-Scaling Exponent of Liquid Dynamics |
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