Visualisation and orbital-free parametrisation of the large-Z scaling of the kinetic energy density of atoms

被引:22
|
作者
Cancio, Antonio C. [1 ]
Redd, Jeremy J. [2 ]
机构
[1] Ball State Univ, Dept Phys & Astron, Muncie, IN 47306 USA
[2] Utah Valley Univ, Dept Phys, Orem, UT USA
关键词
Density functional theory; kinetic energy density; orbital-free DFT; meta-GGA; Thomas-Fermi theory; THOMAS-FERMI THEORY; ELECTRON LOCALIZATION; QUANTUM CORRECTIONS; GRADIENT EXPANSION; APPROXIMATION; FUNCTIONALS; PARAMETER; SYSTEMS;
D O I
10.1080/00268976.2016.1246757
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
The scaling of neutral atoms to large Z, combining periodicity with a gradual trend to homogeneity, is a fundamental probe of density functional theory, one that has driven recent advances in understanding both the kinetic and exchange-correlation energies. Although research focus is normally upon the scaling of integrated energies, insights can also be gained from energy densities. We visualise the scaling of the positive-definite kinetic energy density (KED) in closed-shell atoms, in comparison to invariant quantities based upon the gradient and Laplacian of the density. We notice a striking fit of the KED within the core of any atom to a gradient expansion using both the gradient and the Laplacian, appearing as an asymptotic limit around which the KED oscillates. The gradient expansion is qualitatively different from that derived from first principles for a slowly varying electron gas and is correlated with a nonzero Pauli contribution to the KED near the nucleus. We propose and explore orbital-free meta-GGA models for the kinetic energy to describe these features, with some success, but the effects of quantum oscillations in the inner shells of atoms make a complete parametrisation difficult. We discuss implications for improved orbital-free description of molecular properties.
引用
收藏
页码:618 / 635
页数:18
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