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Universalities among natural orbitals and occupation numbers pertaining to ground states of two electrons in central potentials.

Jerzy CioslowskiFilip Prątnicki
Published in: The Journal of chemical physics (2019)
Although both the natural orbitals (NOs) {ψnlm(r→)} and their occupation numbers {νnl} pertaining to the ground state of two electrons confined by a central potential are completely determined by the spatial component Ψ(r→1,r→2) of the underlying wavefunction through a homogeneous Fredholm equation of the second kind in which Ψ(r→1,r→2) plays the role of the kernel, for the species with a single positive-valued natural amplitude that corresponds to the strongly occupied NO ("the normal sign pattern"), these quantities turn out to depend almost entirely on the "on-top" wavefunction Ψ(r→,r→). For such species, for which the occupation numbers are found to have the large-n asymptotics of n-8, a universal expression involving only Ψ(r→,r→) that reproduces the weakly occupied NOs with remarkable accuracy is inferred from the electron-electron coalescence cusp in Ψ(r→1,r→2). These theoretical predictions are fully confirmed by comparisons among the benchmark-quality NOs computed for the helium atom, the isoelectronic cations with the nuclear charges ranging from 3 to 5, and the two-electron harmonium atom at the limit of an infinitely strong confinement.
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