The potential, limitations, and challenges of divide and conquer quantum electronic structure calculations on energetic materials.

Tucker, Jon R. ; Magyar, Rudolph J.

关键词: APPROXIMATIONS;    ATOMS;    BONDING;    CALCULATION METHODS;    CHEMICAL EXPLOSIVES;    CHEMICAL REACTIONS;    COMPUTERIZED SIMULATION;    DENSITY MATRIX;    ELECTRONIC STRUCTURE;    EXPLOSIONS;    EXPLOSIVES;    HARMONICS;    QUANTUM ELECTRONICS;    QUANTUM MECHANICS;    WEAPONS;   

DOI  :  10.2172/1038199
RP-ID  :  SAND2012-1298
PID  :  OSTI ID: 1038199
Others  :  TRN: US201208%%574

美国|英语

来源: SciTech Connect

【 摘 要 】

High explosives are an important class of energetic materials used in many weapons applications. Even with modern computers, the simulation of the dynamic chemical reactions and energy release is exceedingly challenging. While the scale of the detonation process may be macroscopic, the dynamic bond breaking responsible for the explosive release of energy is fundamentally quantum mechanical. Thus, any method that does not adequately describe bonding is destined to lack predictive capability on some level. Performing quantum mechanics calculations on systems with more than dozens of atoms is a gargantuan task, and severe approximation schemes must be employed in practical calculations. We have developed and tested a divide and conquer (DnC) scheme to obtain total energies, forces, and harmonic frequencies within semi-empirical quantum mechanics. The method is intended as an approximate but faster solution to the full problem and is possible due to the sparsity of the density matrix in many applications. The resulting total energy calculation scales linearly as the number of subsystems, and the method provides a path-forward to quantum mechanical simulations of millions of atoms.