The electronic structure of the triiodide ion from relativistic correlated calculations: a comparison of different methodologies.

Andre Severo Pereira Gomes (1) , Lucas Visscher (2) , Hélène Bolvin (3) , Trond Saue (4) , Stefan Knecht (5, 6) , Timo Fleig (4) , Ephraim Eliav (7)

1 PhLAM - Laboratoire de Physique des Lasers, Atomes et Molécules - UMR 8523
2 Amsterdam Center for Multiscale Modeling
3 SEM - Systèmes étendus et magnétisme (LCPQ)
4 GMO - Groupe THEO (LCPQ)
5 LCQMM - Laboratoire de chimie quantique et de modélisation moléculaire
6 Institute of Theoretical and Computational Chemistry
7 School of Chemistry

The triiodide ion I(3)(-) exhibits a complex photodissociation behavior, the dynamics of which are not yet fully understood. As a first step toward determining the full potential energy surfaces of this species for subsequent simulations of its dissociation processes, we investigate the performance of different electronic structure methods [time-dependent density functional theory, complete active space perturbation theory to second order (CASPT2), Fock-space coupled cluster and multireference configuration interaction] in describing the ground and excited states of the triiodide ion along the symmetrical dissociation path. All methods apart from CASPT2 include scalar relativity and spin-orbit coupling in the orbital optimization, providing useful benchmark data for the more common two-step approaches in which spin-orbit coupling is introduced in the configuration interaction. Time-dependent density functional theory with the statistical averaging of model orbital potential functional is off the mark for this system. Another choice of functional may improve performance with respect to vertical excitation energies and spectroscopic constants, but all functionals are likely to face instability problems away from the equilibrium region. The Fock-space coupled cluster method was shown to perform clearly best in regions not too far from equilibrium but is plagued by convergence problems toward the dissociation limit due to intruder states. CASPT2 shows good performance at significantly lower computational cost, but is quite sensitive to symmetry breaking. We furthermore observe spikes in the CASPT2 potential curves away from equilibrium, signaling intruder state problems that we were unable to curb through the use of level shifts. Multireference configuration interaction is, in principle, a viable option, but its computational cost in the present case prohibits use other than for benchmarking purposes.

Mots clés: spin-orbit interactions; photodissociation; perturbation theory; negative ions; molecule-photon collisions; molecular electronic states; iodine; ground states; excited states; density functional theory; coupled cluster calculations; configuration interactions; relativistic corrections; potential energy surfaces

Domaines: Chimie théorique et/ou physique

Andre Severo Pereira Gomes, Lucas Visscher, Hélène Bolvin, Trond Saue, Stefan Knecht, et al.. The electronic structure of the triiodide ion from relativistic correlated calculations: a comparison of different methodologies.. Journal of Chemical Physics, 2010, 133 (6), pp.064305. ⟨10.1063/1.3474571⟩. ⟨hal-00760969⟩