Dynamic kinetic energy potential for orbital-free density functional theory

被引:30
|
作者
Neuhauser, Daniel [1 ]
Pistinner, Shlomo [1 ]
Coomar, Arunima [1 ]
Zhang, Xu [2 ]
Lu, Gang [2 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Calif State Univ Northridge, Dept Phys & Astron, Northridge, CA 91330 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2011年 / 134卷 / 14期
关键词
DEPENDENT THOMAS-FERMI; FREE MOLECULAR-DYNAMICS; LINEAR-RESPONSE; CLUSTERS;
D O I
10.1063/1.3574347
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A dynamic kinetic energy potential (DKEP) is developed for time-dependent orbital-free (TDOF) density function theory applications. This potential is constructed to affect only the dynamical (omega not equal 0) response of an orbital-free electronic system. It aims at making the orbital-free simulation respond in the same way as that of a noninteracting homogenous electron gas (HEG), as required by a correct kinetic energy, therefore enabling extension of the success of orbital-free density functional theory in the static case (e. g., for embedding and description of processes in bulk materials) to dynamic processes. The potential is constructed by expansions of terms, each of which necessitates only simple time evolution (concurrent with the TDOF evolution) and a spatial convolution at each time-step. With 14 such terms a good fit is obtained to the response of the HEG at a large range of frequencies, wavevectors, and densities. The method is demonstrated for simple jellium spheres, approximating Na(9)(+) and Na(65)(+) clusters. It is applicable both to small and large (even ultralarge) excitations and the results converge (i.e., do not blow up) as a function of time. An extension to iterative frequency-resolved extraction is briefly outlined, as well as possibly numerically simpler expansions. The approach could also be extended to fit, instead of the HEG susceptibility, either an experimental susceptibility or a theoretically derived one for a non-HEG system. The DKEP potential should be a powerful tool for embedding a dynamical system described by a more accurate method (such as time-dependent density functional theory, TDDFT) in a large background described by TDOF with a DKEP potential. The type of expansions used and envisioned should be useful for other approaches, such as memory functionals in TDDFT. Finally, an appendix details the formal connection between TDOF and TDDFT. (C) 2011 American Institute of Physics. [doi:10.1063/1.3574347]
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页数:10
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