Derivative discontinuities in density functional theory

被引:13
|
作者
Mosquera, Martin A. [1 ]
Wasserman, Adam [1 ,2 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Phys & Astron, W Lafayette, IN 47907 USA
基金
美国国家科学基金会;
关键词
molecular dissociation; exchange-correlation energy; fractional number of electrons; derivative discontinuity; density functional theory; GENERALIZED GRADIENT APPROXIMATION; CORRELATION POTENTIALS; EXCHANGE-ENERGY; BAND-GAPS; ACCURATE; MODEL; LIMITATIONS; EIGENVALUE; ORBITALS; FAILURE;
D O I
10.1080/00268976.2014.968650
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
Fifty years after the original formulation of density functional theory (DFT), subtle consequences of the mathematical mappings underlying its formalism continue to merit new views. In this article, we discuss the origin, the importance, and the challenges associated with finding the derivative discontinuity of the exchange-correlation (XC) energy of DFT at integer-electron numbers. We show how even the energy of a quantum electron gas with finite volume and number of electrons displays such derivative discontinuities, but continuous density functional approximations to the XC functional miss them entirely. We discuss some of the practical problems that arise due to this lack of derivative discontinuities in standard functionals, and explain new ways to recover them.
引用
收藏
页码:2997 / 3013
页数:17
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