CACO

Processes related to electronically excited states are central in chemistry, physics, and biology, playing a key role in ubiquitous processes such as photochemistry, catalysis, and solar cell technology. However, defining an effective method that reliably provides accurate excited-state energies remains a major challenge in theoretical chemistry. In CACO, we aim at developing a totally novel approach to obtain excited-state energies and wave functions in molecular systems thanks to the properties of non-Hermitian Hamiltonians. Our key idea is to perform an analytic continuation of conventional computational chemistry methods. Indeed, through the complex plane, ground and excited states can be naturally connected. In a non-Hermitian complex picture, the energy levels are sheets of a more complicated topological manifold called Riemann surface and they are smooth and continuous analytic continuation of one another. CACO's main goal is to develop a new theoretical approach allowing to connect, through the complex plane, electronic states. Instead of Hermitian Hamiltonians, we propose to use a more general class of Hamiltonians which have the property of being PT-symmetric, i.e., invariant with respect to combined parity reflection P and time reversal T. This weaker condition ensures a real energy spectrum in unbroken PT-symmetric regions. PT-symmetric Hamiltonians can be seen as analytic continuation of conventional Hermitian Hamiltonians. Using PT-symmetric quantum theory, an Hermitian Hamiltonian can be analytically continued into the complex plane, becoming non-Hermitian in the process and exposing the fundamental topology of eigenstates. Our gateway between ground and excited states are provided by exceptional points, the non-Hermitian analogs of conical intersections, which lie at the boundary between broken and unbroken PT-symmetric regions.