Development of a ReaxFF reactive force field for tetrabutylphosphonium glycinate/CO2 mixtures

Bo Zhang, Adri Van Duin, J. Karl Johnson

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Carbon dioxide interacts with the ionic liquid tetrabutylphosphonium glycinate, [P(C4)4][Gly], through both physical and chemical absorption. We present a parametrization of the ReaxFF force field for this system that accounts for both chemical and physical interactions. The parametrization was developed from an extensive training set including periodic density functional theory (DFT) calculations of reaction pathways between CO2 and the anion [Gly]- in the condensed phase, condensed-phase molecular dynamics (MD) configurations, gas-phase CO2-anion and CO2-cation interactions, and gas-phase cluster calculations for intra-ion interactions. The optimized ReaxFF parameters capture the essential features of both physical and chemical interactions between CO2 and [P(C4)4][Gly] as compared with experiments, van der Waals-corrected DFT calculations, or, in the case of physical interactions, classical force field calculations. The probability distributions of the distance between C (from CO2) and N (from the anion) and the CO2 bend angles calculated from MD simulations with the optimized ReaxFF force field are in good general agreement with those from DFT-based MD simulations. We predict that the density of CO2/[P(C4)4][Gly] mixtures increases with increasing CO2 concentration up to at least 50 mol % CO2. We attribute the significant increase in density to the small effective volume occupied by chemically bound CO2 in the mixture. The predicted increase in density may be tested experimentally.

Original languageEnglish (US)
Pages (from-to)12008-12016
Number of pages9
JournalJournal of Physical Chemistry B
Volume118
Issue number41
DOIs
StatePublished - Oct 16 2014

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glycyl-glycyl-glycyl-glycine
field theory (physics)
Density functional theory
Anions
Molecular dynamics
Negative ions
molecular dynamics
density functional theory
anions
Gases
interactions
Ionic Liquids
vapor phases
Computer simulation
Ionic liquids
Carbon Dioxide
Probability distributions
Cations
Carbon dioxide
Positive ions

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films
  • Materials Chemistry

Cite this

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title = "Development of a ReaxFF reactive force field for tetrabutylphosphonium glycinate/CO2 mixtures",
abstract = "Carbon dioxide interacts with the ionic liquid tetrabutylphosphonium glycinate, [P(C4)4][Gly], through both physical and chemical absorption. We present a parametrization of the ReaxFF force field for this system that accounts for both chemical and physical interactions. The parametrization was developed from an extensive training set including periodic density functional theory (DFT) calculations of reaction pathways between CO2 and the anion [Gly]- in the condensed phase, condensed-phase molecular dynamics (MD) configurations, gas-phase CO2-anion and CO2-cation interactions, and gas-phase cluster calculations for intra-ion interactions. The optimized ReaxFF parameters capture the essential features of both physical and chemical interactions between CO2 and [P(C4)4][Gly] as compared with experiments, van der Waals-corrected DFT calculations, or, in the case of physical interactions, classical force field calculations. The probability distributions of the distance between C (from CO2) and N (from the anion) and the CO2 bend angles calculated from MD simulations with the optimized ReaxFF force field are in good general agreement with those from DFT-based MD simulations. We predict that the density of CO2/[P(C4)4][Gly] mixtures increases with increasing CO2 concentration up to at least 50 mol {\%} CO2. We attribute the significant increase in density to the small effective volume occupied by chemically bound CO2 in the mixture. The predicted increase in density may be tested experimentally.",
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Development of a ReaxFF reactive force field for tetrabutylphosphonium glycinate/CO2 mixtures. / Zhang, Bo; Van Duin, Adri; Johnson, J. Karl.

In: Journal of Physical Chemistry B, Vol. 118, No. 41, 16.10.2014, p. 12008-12016.

Research output: Contribution to journalArticle

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AU - Johnson, J. Karl

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N2 - Carbon dioxide interacts with the ionic liquid tetrabutylphosphonium glycinate, [P(C4)4][Gly], through both physical and chemical absorption. We present a parametrization of the ReaxFF force field for this system that accounts for both chemical and physical interactions. The parametrization was developed from an extensive training set including periodic density functional theory (DFT) calculations of reaction pathways between CO2 and the anion [Gly]- in the condensed phase, condensed-phase molecular dynamics (MD) configurations, gas-phase CO2-anion and CO2-cation interactions, and gas-phase cluster calculations for intra-ion interactions. The optimized ReaxFF parameters capture the essential features of both physical and chemical interactions between CO2 and [P(C4)4][Gly] as compared with experiments, van der Waals-corrected DFT calculations, or, in the case of physical interactions, classical force field calculations. The probability distributions of the distance between C (from CO2) and N (from the anion) and the CO2 bend angles calculated from MD simulations with the optimized ReaxFF force field are in good general agreement with those from DFT-based MD simulations. We predict that the density of CO2/[P(C4)4][Gly] mixtures increases with increasing CO2 concentration up to at least 50 mol % CO2. We attribute the significant increase in density to the small effective volume occupied by chemically bound CO2 in the mixture. The predicted increase in density may be tested experimentally.

AB - Carbon dioxide interacts with the ionic liquid tetrabutylphosphonium glycinate, [P(C4)4][Gly], through both physical and chemical absorption. We present a parametrization of the ReaxFF force field for this system that accounts for both chemical and physical interactions. The parametrization was developed from an extensive training set including periodic density functional theory (DFT) calculations of reaction pathways between CO2 and the anion [Gly]- in the condensed phase, condensed-phase molecular dynamics (MD) configurations, gas-phase CO2-anion and CO2-cation interactions, and gas-phase cluster calculations for intra-ion interactions. The optimized ReaxFF parameters capture the essential features of both physical and chemical interactions between CO2 and [P(C4)4][Gly] as compared with experiments, van der Waals-corrected DFT calculations, or, in the case of physical interactions, classical force field calculations. The probability distributions of the distance between C (from CO2) and N (from the anion) and the CO2 bend angles calculated from MD simulations with the optimized ReaxFF force field are in good general agreement with those from DFT-based MD simulations. We predict that the density of CO2/[P(C4)4][Gly] mixtures increases with increasing CO2 concentration up to at least 50 mol % CO2. We attribute the significant increase in density to the small effective volume occupied by chemically bound CO2 in the mixture. The predicted increase in density may be tested experimentally.

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