Exact separation of radial and angular correlation energies in two-electron atoms

被引:1
|
作者
Kammath, Anjana R. [1 ,2 ]
Ramakrishnan, Raghunathan [2 ]
机构
[1] Indian Inst Sci Educ & Res, Mohali 140306, Punjab, India
[2] Tata Inst Fundamental Res, Ctr Interdisciplinary Sci, Hyderabad 500107, India
关键词
Schroedinger equation; Hylleraas; Correlation energy; Variational principle; HELIUM; STATE;
D O I
10.1016/j.cplett.2019.02.004
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
Partitioning of helium atom's correlation energy into radial and angular contributions, although of fundamental interest, has eluded critical scrutiny. Conventionally, radial and angular correlation energies of helium atom are defined for its ground state as deviations, from Hartree-Fock and exact values, of the energy obtained using a purely radial wavefunction devoid of any explicit dependence on the interelectronic distance. Here, we show this rationale to associate the contribution from radial-angular coupling entirely to the angular part underestimating the radial one, thereby also incorrectly predict non-vanishing residual radial probability densities. We derive analytic matrix elements for the high-precision Hylleraas basis set framework to seamlessly uncouple the angular correlation energy from its radial counterpart. The resulting formula agrees with numerical cubature yielding precise purely angular correlation energies for the ground as well as excited states. Our calculations indicate 60.2% of helium's correlation energy to arise from strictly radial interactions; when excluding the contribution from the radial-angular coupling, this value drops to 41.3%.
引用
收藏
页码:93 / 96
页数:4
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