Fluorescence concentration quenching occurs when increasing
molecular
concentration of fluorophores results in a decreasing fluorescence
quantum yield. Even though this phenomenon has been studied for decades,
its mechanisms and signatures are not yet fully understood. The complexity
of the problem arises due to energy migration and trapping in huge
networks of molecules. Most of the available theoretical work focuses
on integral quantities like fluorescence quantum yield and mean excitation
lifetime. In this work, we present a numerical study of the fluorescence
decay kinetics of three-dimensional and two-dimensional molecular
systems. We investigate the differences arising from the variations
in models of trap formations. We also analyze the influence of the
molecular orientations to the fluorescence decay kinetics. We compare
our results to the well-known analytical models and discuss their
ranges of validity. Our findings suggest that the analytical models
can provide inspiration for different ways of approximating the fluorescence
kinetics, yet more detailed analysis of the experimental data should
be done by comparison with numerical simulations.