Modeling the Fluorescence Quantum Yields of Aromatic Compounds: Benchmarking the Machinery to Compute Intersystem Crossing Rates.

Abstract

The from-first-principles calculation of fluorescence quantum yields (FQYs) and lifetimes of organic dyes remains very challenging. In this article, we extensively test the machinery to calculate FQYs. Specifically, we perform an extensive analysis on the parameters influencing the intersystem crossing (ISC), internal conversion (IC), and fluorescence rate constants calculations. The impact of (i) the electronic structure (chosen exchange-correlation functional and spin-orbit Hamiltonian), (ii) the vibronic parameters (coordinate system, broadening function, and dipole expansion), and (iii) the excited-state kinetic models are systematically assessed for a series of seven rigid aromatic molecules. Our studies provide more insights into the choice of parameters and the expected accuracy for the computational protocols aiming to deliver FQY values. Some challenges are highlighted, such as, on the one hand, the difficulty to benchmark against the experimental nonradiative rate constants, for which the separation between the IC and ISC contributions is often not provided in the literature and, on the other hand, the need to go beyond the harmonic approximation for the calculation of the IC rates.