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van Meer R, Gritsenko OV, Baerends EJ. Excitation energies with linear response density matrix functional theory along the dissociation coordinate of an electron-pair bond in N-electron systems. J Chem Phys. 2014;140(2):024101doi: 10.1063/1.4852195.
van Meer, R., Gritsenko, O. V., & Baerends, E. J. (2014). Excitation energies with linear response density matrix functional theory along the dissociation coordinate of an electron-pair bond in N-electron systems. The Journal of chemical physics, 140(2), 024101. https://doi.org/10.1063/1.4852195
van Meer, R, et al. "Excitation energies with linear response density matrix functional theory along the dissociation coordinate of an electron-pair bond in N-electron systems." The Journal of chemical physics vol. 140,2 (2014): 024101. doi: https://doi.org/10.1063/1.4852195
van Meer R, Gritsenko OV, Baerends EJ. Excitation energies with linear response density matrix functional theory along the dissociation coordinate of an electron-pair bond in N-electron systems. J Chem Phys. 2014 Jan 14;140(2):024101. doi: 10.1063/1.4852195. PMID: 24437859.
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J Chem Phys. 2014 Jan 14;140(2):024101. doi: 10.1063/1.4852195.

Excitation energies with linear response density matrix functional theory along the dissociation coordinate of an electron-pair bond in N-electron systems.

The Journal of chemical physics

R van Meer, O V Gritsenko, E J Baerends

Affiliations

  1. Faculty of Exact Sciences, Theoretical Chemistry, VU University, Amsterdam, The Netherlands.

PMID: 24437859 DOI: 10.1063/1.4852195

Abstract

Time dependent density matrix functional theory in its adiabatic linear response formulation delivers exact excitation energies ωα and oscillator strengths fα for two-electron systems if extended to the so-called phase including natural orbital (PINO) theory. The Löwdin-Shull expression for the energy of two-electron systems in terms of the natural orbitals and their phases affords in this case an exact phase-including natural orbital functional (PILS), which is non-primitive (contains other than just J and K integrals). In this paper, the extension of the PILS functional to N-electron systems is investigated. With the example of an elementary primitive NO functional (BBC1) it is shown that current density matrix functional theory ground state functionals, which were designed to produce decent approximations to the total energy, fail to deliver a qualitatively correct structure of the (inverse) response function, due to essential deficiencies in the reconstruction of the two-body reduced density matrix (2RDM). We now deduce essential features of an N-electron functional from a wavefunction Ansatz: The extension of the two-electron Löwdin-Shull wavefunction to the N-electron case informs about the phase information. In this paper, applications of this extended Löwdin-Shull (ELS) functional are considered for the simplest case, ELS(1): one (dissociating) two-electron bond in the field of occupied (including core) orbitals. ELS(1) produces high quality ωα(R) curves along the bond dissociation coordinate R for the molecules LiH, Li2, and BH with the two outer valence electrons correlated. All of these results indicate that response properties are much more sensitive to deficiencies in the reconstruction of the 2RDM than the ground state energy, since derivatives of the functional with respect to both the NOs and the occupation numbers need to be accurate.

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