The SIESTA method for ab initio order-N materials simulation
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We have developed and implemented a selfconsistent density functional method using standard norm-conserving pseudopotentials and a flexible, numerical linear combination of atomic orbitals basis set, which includes multiple-zeta and polarization orbitals. Exchange and correlation are treated with the local spin density or generalized gradient approximations. The basis functions and the electron density are projected on a real-space grid, in order to calculate the Hartree and exchange-correlation potentials and matrix elements, with a number of operations that scales linearly with the size of the system. We use a modified energy functional, whose minimization produces orthogonal wavefunctions and the same energy and density as the Kohn-Sham energy functional, without the need for an explicit orthogonalization. Additionally, using localized Wannier-like electron wavefunctions allows the computation time and memory required to minimize the energy to also scale linearly with the size of the system. Forces and stresses are also calculated efficiently and accurately, thus allowing structural relaxation and molecular dynamics simulations.
Gale, Julian and Soler, Joser and Artacho, Emilio and Garcia, Alberto and Junquera, Javiera and Ordejon, Pablo and Sanchez-Portal, Daniel (2002) The SIESTA method for ab initio order-N materials simulation, Journal of Physics: Condensed Matter 14:2745-2779.
Journal of Physics: Condensed Matter copyright (2002) IOP Publishing Ltd.
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