▎ 摘　　要

A new Molecular Dynamics Finite Element Method (MDFEM) with a coupled mechanical-charge/dipole formulation is proposed. The equilibrium equations of Molecular Dynamics (MD) are embedded exactly within the computationally more favourable Finite Element Method (FEM). This MDFEM can readily implement any force field because the constitutive relations are explicitly uncoupled from the corresponding geometric element topologies. This formal uncoupling allows to differentiate between chemical-constitutive, geometric and mixed-mode instabilities. Different force fields, including bond-order reactive and polarisable fluctuating charge-dipole potentials, are implemented exactly in both explicit and implicit dynamic commercial finite element code. The implicit formulation allows for larger length and time scales and more varied eigenvalue-based solution strategies.The proposed multi-physics and multi-scale compatible MDFEM is shown to be equivalent to MD, as demonstrated by examples of fracture in carbon nanotubes (CNT), and electric charge distribution in graphene, but at a considerably reduced computational cost. The proposed MDFEM is shown to scale linearly, with concurrent continuum FEM multi-scale couplings allowing for further computational savings. Moreover, novel conformational analyses of pillared graphene structures (PGS) are produced. The proposed model finds potential applications in the parametric topology and numerical design studies of nano-structures for desired electro-mechanical properties(e.g.stiffness, toughness and electric field induced vibrational/electron-emission properties). Copyright (c) 2014 John Wiley & Sons, Ltd.