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Neutral atoms and molecules are subject to two distinct forces in the limit of large distance, and short distance: an attractive van der Waals force, or dispersion force, at long ranges, and a repulsion force, the result of overlapping electron orbitals, referred to as Pauli repulsion (from Pauli exclusion principle). The Lennard-Jones potential (also referred to as the L-J potential, 6-12 potential or, less commonly, 12-6 potential)is a simple mathematical model that represents this behavior. It was proposed in 1931 by John Lennard-Jones of Bristol University. The L-J potential is of the form V(r) = 4varepsilon left left( rac{sigma}{r} ight)^{12} - left( rac{sigma}{r} ight)^{6} ight where is the depth of the potential well and is the hard sphere diameter. These parameters can be fitted to reproduce experimental data or deduced from results of accurate quantum chemistry calculations. The term describes repulsion and the term describes attraction. The force function is the negative of the gradient of the above potential: abla V(r) = - rac V(r) hat = 4 epsilon left( 12,-6, ight) hat The L-J potential is approximate. The form of the repulsion term has no theoretical justification; the repulsion force should depend exponentially on the distance, but the repulsion term of the L-J formula is more convenient due to the ease and efficiency of computing r12 as the square of r6. The attractive long-range potential, however, is derived from dispersion interactions. The L-J potential is a relatively good approximation and due to its simplicity often used to describe the properties of gases, and to model dispersion and overlap interactions in molecular models. It is particularly accurate for noble gas atoms and is a good approximation at long and short distances for neutral atoms and molecules. On the graph, Lennard-Jones potential for argon dimer is shown. Small deviation from the accurate empirical potential due to incorrect long range part of the repulsion term can be seen. Other more recent methods, such as the Stockmayer equation and the so-called multi equation, describe the interaction of molecules more accurately. Quantum chemistry methods, Møller-Plesset perturbation theory, coupled cluster method or full configuration interaction can give extremely accurate results, but require large computational cost.
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