Triple Electron Attachments with a New Intermediate-Hamiltonian Fock-Space Coupled-Cluster Method

The implementation of a new intermediate-Hamiltonian Fock-space coupled-cluster (IHFSCC) scheme for the (3,0) sector of the Fock space is reported. In this IHFSCC approach, the three-body contributions in the cluster operator <i>S</i>^(3,0) corresponding to the (3,0) sector of the Fock space are considered, while <i>S</i>^(1,0) and <i>S</i>^(2,0) at the (1,0) and (2,0) level only include one- and two-body operators. By introducing a suitable partition of the wave operator, the intermediate Hamiltonian, which only depends on the two-body operator of S^(1,0), is obtained. <i>S</i>^(2,0) and <i>S</i>^(3,0) are not required within this new IHFSCC scheme, and a large reference space can be possibly employed. The performance of this (3,0) IHFSCC method in calculating triple ionization potentials and excitation energies for atoms and cations with a ground p³ configuration as well as adiabatic excitation energies for some molecules is investigated. The effect of the number of active virtual orbitals and three different types of orbitals, i.e., reference orbitals, restricted open-shell Hartree-Fock orbitals (ROHF) of the target systems, and canonicalized ROHF orbitals, on IHFSCC results, is also studied. Our calculations indicate that reasonable results can be achieved with this (3,0) IHFSCC method when a minimal reference space is employed. Further increasing the number of active orbitals does not necessarily improve the results. In addition, the IHFSCC results using canonicalized ROHF orbitals generally agree well with reference values, and they are not very sensitive to the number of active orbitals compared with results using the reference orbitals. The new (3,0) IHFSCC method can be applied to open-shell systems with three unpaired electrons with reasonable accuracy at a relatively low computational cost.