Seniority and Hierarchy Configuration Interaction for Radicals and Excited States

Hierarchy configuration interaction (hCI) has recently been introduced as an alternative configuration interaction (CI) route combining excitation degree and seniority number and has been shown to efficiently recover both dynamic and static correlations for closed-shell molecular systems [J. Phys. Chem. Lett. 2022, 13, 4342]. Here we generalize hCI for an arbitrary reference determinant, allowing calculations for radicals and excited states in a state-specific way. We gauge this route against excitation-based CI (eCI) and seniority-based CI (sCI) by evaluating how different ground-state properties of radicals converge to the full CI limit. We find that hCI outperforms or matches eCI, whereas sCI is far less accurate, in line with previous observations for closed-shell molecules. Employing second-order Epstein–Nesbet (EN2) perturbation theory as a correction significantly accelerates the convergence of hCI and eCI. We further explore various hCI and sCI models to calculate the excitation energies of closed- and open-shell systems. Our results underline that the choice of both the reference determinant and the set of orbitals drives the fine balance between correlation of ground and excited states. State-specific hCI2 and higher-order models perform similarly to their eCI counterparts, whereas lower orders of hCI deliver poor results unless supplemented by the EN2 correction, which substantially improves their accuracy. In turn, sCI1 produces decent excitation energies for radicals, encouraging the development of related seniority-based coupled-cluster methods.