Energy-consistent relativistic pseudopotentials and correlation consistent basis sets for the 4d elements Y–Pd

<jats:p>Scalar-relativistic pseudopotentials and corresponding spin-orbit potentials of the energy-consistent variety have been adjusted for the simulation of the [Ar]3d10 cores of the 4d transition metal elements Y–Pd. These potentials have been determined in a one-step procedure using numerical two-component calculations so as to reproduce atomic valence spectra from four-component all-electron calculations. The latter have been performed at the multi-configuration Dirac-Hartree-Fock level, using the Dirac-Coulomb Hamiltonian and perturbatively including the Breit interaction. The derived pseudopotentials reproduce the all-electron reference data with an average accuracy of 0.03eV for configurational averages over nonrelativistic orbital configurations and 0.1eV for individual relativistic states. Basis sets following a correlation consistent prescription have also been developed to accompany the new pseudopotentials. These range in size from cc-pVDZ-PP to cc-pV5Z-PP and also include sets for 4s4p correlation (cc-pwCVDZ-PP through cc-pwCV5Z-PP), as well as those with extra diffuse functions (aug-cc-pVDZ-PP, etc.). In order to accurately assess the impact of the pseudopotential approximation, all-electron basis sets of triple-zeta quality have also been developed using the Douglas-Kroll-Hess Hamiltonian (cc-pVTZ-DK, cc-pwCVTZ-DK, and aug-cc-pVTZ-DK). Benchmark calculations of atomic ionization potentials and 4dm−25s2→4dm−15s1 electronic excitation energies are reported at the coupled cluster level of theory with extrapolations to the complete basis set limit.</jats:p>