Fully analytic implementation of density functional theory for efficient calculations on large molecules
Abstract
Fullerene like cages and naonotubes of carbon and other inorganic materials are currently under intense study due to their possible technological applications. First principle simulations of these materials are computationally challenging due to large number of atoms. We have recently developed a fast, variational and fully analytic density functional theory (ADFT) based model that allows study of systems larger than those that can be studied using existing density functional models. Using polarized Gaussian basis sets (6-311G**) and ADFT, we optimize geometries of large fullerenes, fullerene-like cages and nanotubes of carbon, boron nitride, and aluminum nitride containing more than two thousand atoms. The calculation of C2160 using nearly 39000 orbital basis functions is the largest calculation on any isolated molecule reported to-date at this level of theory, and it includes full geometry optimization. The electronic structure related properties of the inorganic cages and other carbon fulerenes have been studied.
Cite
@article{arxiv.cond-mat/0610060,
title = {Fully analytic implementation of density functional theory for efficient calculations on large molecules},
author = {Rajendra R. Zope and Brett I. Dunlap},
journal= {arXiv preprint arXiv:cond-mat/0610060},
year = {2007}
}
Comments
Manuscript for Proceedings of American Chemical Society, Washington DC (Large Scale Molecular Dynamics, Nanoscale, and Mesoscale Modeling and Simulation Symposium)