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Updated: Jul 20, 2026

Excitonic Hamiltonians for Calculating Optical Absorption Spectra and Optoelectronic Properties of Molecular Aggregates and Solids
Published on: May 27, 2020
Extensions of r12 corrections to CC2-R12 for excited states
Christian Neiss1, Christof Hättig, Wim Klopper
1Institut für Nanotechnologie, Forschungszentrum Karlsruhe, P.O. Box 3640, D-76021 Karlsruhe, Germany. christian.neiss@int.fzk.de
Abstract:
As known since about two decades, R12 methods, which include terms linear in the interelectronic distance r(12) in the wave function, improve substantially the basis set convergence of the ground state correlation energy. In a previous study, however, it was found that the same approach does not give a similar systematic improvement if applied to excited states in the framework of coupled cluster response theory. In the present work, we examine the reason for this behavior and show that the inclusion of additional orbitals in the construction of the r(12) pair functions leads to an enhanced basis set convergence (and thus a balanced description) also for the excited states.
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