335818 A Reactive Interatomic Potential for the Molecular Dynamics Simulations of Saturated Hydrocarbons Using the Modified Embedded-Atom Method

Friday, November 8, 2013: 8:30 AM
Union Square 16 (Hilton)
Sasan Nouranian, Center for Advanced Vehicular Systems (CAVS), Mississippi State University, Starkville, MS, Michael I. Baskes, Mechanical and Aerospace Engineering, University of California, San Diego, La Jolla, CA, Mark A. Tschopp, Materials & Manufacturing Science Division, Lightweight and Specialty Metals Branch (RDRL-WMM-F), Army Research Laboratory, Adelphi, MD, Steven R. Gwaltney, Department of Chemistry, Mississippi State University, Mississippi State, MS and M.F. Horstemeyer, Center for Advanced Vehicular Systems, Mississippi State University, Mississippi State, MS

In this work, an interatomic potential for saturated hydrocarbons was developed using the modified embedded-atom method (MEAM), a semi-empirical N-body potential based on density functional theory and pair potentials.  The potential was parameterized by fitting to a large experimental and first-principles (FP) database consisting of 1) bond distances, bond angles, and atomization energies at 0 K of a homologous series of alkanes and their select isomers from methane to n-octane, 2) the potential energy curves of H2, CH, and C2 diatomics, 3) the potential energy curves of hydrogen, methane, ethane, and propane dimers, i.e., (H2)2, (CH4)2, (C2H6)2, and (C3H8)2, respectively, and 5) pressure-volume-temperature (PVT) data of a dense high-pressure methane system with the density of 0.5534 g/cc.  The atomization energies and geometries of a range of linear alkanes, cycloalkanes, and free radicals calculated from the MEAM potential were compared to those calculated by other commonly used potentials for hydrocarbons, i.e., second-generation reactive empirical bond order (REBO) and reactive force field (ReaxFF).  MEAM reproduced the experimental and/or FP data with great accuracy, comparable to or better than REBO or ReaxFF.  The experimental PVT data for a relatively large series of methane, ethane, propane, and butane systems with different densities were predicted reasonably well by MEAM.

Although the MEAM formalism has been applied to atomic systems with predominantly metallic bonding in the past, the current work demonstrates the promising extension of the MEAM potential to covalently bonded molecular systems, specifically saturated hydrocarbons and saturated hydrocarbon-based polymers.  The MEAM potential has already been parameterized for a large number of metallic unary, binary, ternary, carbide, nitride, and hydride systems, and extending it to saturated hydrocarbons provides a reliable and transferable potential for atomistic/molecular studies of complex material phenomena involving hydrocarbon-metal or polymer-metal interfaces, polymer-metal nanocomposites, fracture and failure in hydrocarbon-based polymers, etc.  The latter is especially true since MEAM is a reactive potential that allows for dynamic bond formation and bond breaking during simulation.  However, it is important to note that the current parameterization does not accurately reproduce the energetics and structures of unsaturated hydrocarbons and, therefore, should not be applied to such systems.

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