Abstract

Processes related to electronically excited states are central in many areas of science; however, accurately determining excited-state energies remains a major challenge in theoretical chemistry. Recently, higher energy stationary states of non-linear methods have themselves been proposed as approximations to excited states, although the general understanding of the nature of these solutions remains surprisingly limited. In this letter, we present an entirely novel approach for exploring and obtaining excited stationary states by exploiting the properties of non-Hermitian Hamiltonians. Our key idea centres on performing analytic continuations of conventional quantum chemistry methods. Considering Hartree-Fock theory as an example, we analytically continue the electron-electron interaction to expose a hidden connectivity of multiple solutions across the complex plane, revealing a close resemblance between Coulson-Fischer points and non-Hermitian degeneracies. Finally, we demonstrate how a ground-state wave function can be morphed naturally into an excited-state wave function by constructing a well-defined complex adiabatic connection.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.