First-principles method for calculating the rate constants of internal-conversion and intersystem-crossing transitions

Abstract

A method for calculating the rate constants for internal-conversion (k_IC) and intersystem-crossing (k_ISC) processes within the adiabatic and Franck–Condon (FC) approximations is proposed. The applicability of the method is demonstrated by calculation of k_IC and k_ISC for a set of organic and organometallic compounds with experimentally known spectroscopic properties. The studied molecules were pyrromethene-567 dye, psoralene, hetero[8]circulenes, free-base porphyrin, naphthalene, and larger polyacenes. We also studied fac-Alq₃ and fac-Ir(ppy)₃, which are important molecules in organic light emitting diodes (OLEDs). The excitation energies were calculated at the multi-configuration quasi-degenerate second-order perturbation theory (XMC-QDPT2) level, which is found to yield excitation energies in good agreement with experimental data. Spin–orbit coupling matrix elements, non-adiabatic coupling matrix elements, Huang–Rhys factors, and vibrational energies were calculated at the time-dependent density functional theory (TDDFT) and complete active space self-consistent field (CASSCF) levels. The computed fluorescence quantum yields for the pyrromethene-567 dye, psoralene, hetero[8]circulenes, fac-Alq₃ and fac-Ir(ppy)₃ agree well with experimental data, whereas for the free-base porphyrin, naphthalene, and the polyacenes, the obtained quantum yields significantly differ from the experimental values, because the FC and adiabatic approximations are not accurate for these molecules.