Exact molecular direct, cavity, and bridge functions in water system

Luc Belloni 1
1 LIONS - Laboratoire Interdisciplinaire sur l'Organisation Nanométrique et Supramoléculaire
NIMBE UMR 3685 - Nanosciences et Innovation pour les Matériaux, la Biomédecine et l'Energie (ex SIS2M)
Abstract : The exact molecular bridge function of the extended simple point charge model of liquid water at room temperature is extracted from Monte Carlo (MC) simulation data. The projections gmnlμν(r) onto rotational invariants of the highly directional pair distribution function g(r,Ω) are accumulated during simulation performed with N = 512 molecules (cubic box size L ≈ 25 Å). Making intensive use of anisotropic integral equation techniques, the molecular Ornstein-Zernike equation fed with the MC data available at short distances and completed beyond L/2 with the hypernetted chain closure valid at long distances is then inverted in order to derive on the whole r range the direct correlation function cmnlμν(r), the cavity function ymnlμν(r), the negative excess potential of mean force lnymnlμν(r), and, finally, the holy grail in such liquid state theory, the bridge function bmnlμν(r) projections. For completeness, the short distance domain inside the soft core can be reached, thanks to the use of a specially designed anisotropic finite potential which replaces the true one between a single pair of molecules in the simulation. The final bridge function b(r,Ω) of bulk water presents strong, non-universal directional features and can now serve as a reference for approximated bridge functions or functionals in liquid physics of aqueous solvents and solutions.
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Journal of Chemical Physics, American Institute of Physics, 2017, 147 (16), pp.164121. 〈http://aip.scitation.org/doi/abs/10.1063/1.5001684〉. 〈10.1063/1.5001684〉
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Soumis le : lundi 6 novembre 2017 - 08:56:04
Dernière modification le : mercredi 8 novembre 2017 - 01:12:45

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Luc Belloni. Exact molecular direct, cavity, and bridge functions in water system. Journal of Chemical Physics, American Institute of Physics, 2017, 147 (16), pp.164121. 〈http://aip.scitation.org/doi/abs/10.1063/1.5001684〉. 〈10.1063/1.5001684〉. 〈cea-01629086〉

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