Vapor-liquid nucleation of argon: Exploration of various intermolecular potentials

Matthew J. McGrath, Julius N. Ghogomu, Narcisse T. Tsona, J. Ilja Siepmann, Bin Chen, Ismo Napari, Hanna Vehkamäki

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Abstract

The homogeneous vapor-liquid nucleation of argon has been explored at T=70 and 90 K using classical nucleation theory, semiempirical density functional theory, and Monte Carlo simulations using the aggregation-volume-bias algorithm with umbrella sampling and histogram-reweighting. In contrast with previous simulation studies, which employed only the Lennard-Jones intermolecular potential, the current studies were carried out using various pair potentials including the Lennard-Jones potential, a modified Buckingham exponential-six potential, the Barker-Fisher-Watts pair potential, and a recent ab initio potential developed using the method of effective diameters. It was found that the differences in the free energy of formation of the critical nuclei between the potentials cannot be explained solely in terms of the difference in macroscopic properties of the potentials, which gives a possible reason for the failure of classical nucleation theory.

Original languageEnglish (US)
Article number084106
JournalJournal of Chemical Physics
Volume133
Issue number8
DOIs
StatePublished - Aug 28 2010

Bibliographical note

Funding Information:
M.J.M. gratefully acknowledges support from a National Science Foundation International Research grant (Grant No. OISE-0853294). J.I.S. would like to acknowledge support from NSF Grant No. CBET-0756641. B.C. gratefully acknowledges NSF Grant No. CHE/MCB-0448918. I.N. and H.V. gratefully acknowledge funding from the Academy of Finland (LASTU Research Programme). The authors also gratefully acknowledge the donation of computers to the Department of Chemistry, Faculty of Science, University of Dschang by the Peace Corps-Cameroon on behalf of Montgomery County, Maryland, USA. Part of the computing resources was provided by the Minnesota Supercomputing Institute and CSC, Helsinki.

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