Predicting vapor liquid equilibria using density functional theory: a case study of argon

Predicting vapor liquid equilibria (VLE) of molecules governed by weak van der Waals (vdW) interactions using the first principles approach is a significant challenge. Due to the poor scaling of the post Hartree-Fock wave function theory with system size/basis functions, the Kohn-Sham density functi...

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Main Authors: Goel, Himanshu, Ling, Sanliang, Ellis, Breanna Nicole, Taconi, Anna, Slater, Ben, Rai, Neeraj
Format: Article
Published: American Institute of Physics 2018
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Online Access:https://eprints.nottingham.ac.uk/52407/
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author Goel, Himanshu
Ling, Sanliang
Ellis, Breanna Nicole
Taconi, Anna
Slater, Ben
Rai, Neeraj
author_facet Goel, Himanshu
Ling, Sanliang
Ellis, Breanna Nicole
Taconi, Anna
Slater, Ben
Rai, Neeraj
author_sort Goel, Himanshu
building Nottingham Research Data Repository
collection Online Access
description Predicting vapor liquid equilibria (VLE) of molecules governed by weak van der Waals (vdW) interactions using the first principles approach is a significant challenge. Due to the poor scaling of the post Hartree-Fock wave function theory with system size/basis functions, the Kohn-Sham density functional theory (DFT) is preferred for systems with a large number of molecules. However, traditional DFT cannot adequately account for medium to long range correlations which are necessary for modeling vdW interactions. Recent developments in DFT such as dispersion corrected models and nonlocal van der Waals functionals have attempted to address this weakness with a varying degree of success. In this work, we predict the VLE of argon and assess the performance of several density functionals and the second order Møller-Plesset perturbation theory (MP2) by determining critical and structural properties via first principles Monte Carlo simulations. PBE-D3, BLYP-D3, and rVV10 functionals were used to compute vapor liquid coexistence curves, while PBE0-D3, M06-2X-D3, and MP2 were used for computing liquid density at a single state point. The performance of the PBE-D3 functional for VLE is superior to other functionals (BLYP-D3 and rVV10). At T = 85 K and P = 1 bar, MP2 performs well for the density and structural features of the first solvation shell in the liquid phase.
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spelling nottingham-524072020-05-04T19:40:32Z https://eprints.nottingham.ac.uk/52407/ Predicting vapor liquid equilibria using density functional theory: a case study of argon Goel, Himanshu Ling, Sanliang Ellis, Breanna Nicole Taconi, Anna Slater, Ben Rai, Neeraj Predicting vapor liquid equilibria (VLE) of molecules governed by weak van der Waals (vdW) interactions using the first principles approach is a significant challenge. Due to the poor scaling of the post Hartree-Fock wave function theory with system size/basis functions, the Kohn-Sham density functional theory (DFT) is preferred for systems with a large number of molecules. However, traditional DFT cannot adequately account for medium to long range correlations which are necessary for modeling vdW interactions. Recent developments in DFT such as dispersion corrected models and nonlocal van der Waals functionals have attempted to address this weakness with a varying degree of success. In this work, we predict the VLE of argon and assess the performance of several density functionals and the second order Møller-Plesset perturbation theory (MP2) by determining critical and structural properties via first principles Monte Carlo simulations. PBE-D3, BLYP-D3, and rVV10 functionals were used to compute vapor liquid coexistence curves, while PBE0-D3, M06-2X-D3, and MP2 were used for computing liquid density at a single state point. The performance of the PBE-D3 functional for VLE is superior to other functionals (BLYP-D3 and rVV10). At T = 85 K and P = 1 bar, MP2 performs well for the density and structural features of the first solvation shell in the liquid phase. American Institute of Physics 2018-06-12 Article PeerReviewed Goel, Himanshu, Ling, Sanliang, Ellis, Breanna Nicole, Taconi, Anna, Slater, Ben and Rai, Neeraj (2018) Predicting vapor liquid equilibria using density functional theory: a case study of argon. Journal of Chemical Physics, 148 (22). 224501/1-224501/10. ISSN 1089-7690 Density functional theory; Vapor liquid equilibria; Dispersion interactions; First principles Monte Carlo; Liquid structure http://dx.doi.org/10.1063/1.5025726 doi10.1063/1.5025726 doi10.1063/1.5025726
spellingShingle Density functional theory; Vapor liquid equilibria; Dispersion interactions; First principles Monte Carlo; Liquid structure
Goel, Himanshu
Ling, Sanliang
Ellis, Breanna Nicole
Taconi, Anna
Slater, Ben
Rai, Neeraj
Predicting vapor liquid equilibria using density functional theory: a case study of argon
title Predicting vapor liquid equilibria using density functional theory: a case study of argon
title_full Predicting vapor liquid equilibria using density functional theory: a case study of argon
title_fullStr Predicting vapor liquid equilibria using density functional theory: a case study of argon
title_full_unstemmed Predicting vapor liquid equilibria using density functional theory: a case study of argon
title_short Predicting vapor liquid equilibria using density functional theory: a case study of argon
title_sort predicting vapor liquid equilibria using density functional theory: a case study of argon
topic Density functional theory; Vapor liquid equilibria; Dispersion interactions; First principles Monte Carlo; Liquid structure
url https://eprints.nottingham.ac.uk/52407/
https://eprints.nottingham.ac.uk/52407/
https://eprints.nottingham.ac.uk/52407/