Abstract
The correct determination of the exciton diffusion length (L-D) in novel organic photovoltaics (OPV) materials is an important, albeit challenging, task required to understand these systems. Herein, a high-throughput approach to probe L-D in nonfullerene acceptors (NFAs) is reported, that builds upon the conventional photoluminescence (PL) surface quenching method using NFA layers with a graded thickness variation in combination with spectroscopic PL mapping. The method is explored for two archetypal NFAs, namely, ITIC and IT-4F, using PEDOT:PSS and the donor polymer PM6 as two distinct and practically relevant quencher materials. Interestingly, conventional analysis of quenching efficiency as a function of acceptor layer thickness results in a threefold difference in L-D values depending on the specific quencher. This discrepancy can be reconciled by accounting for the differences in light in- and outcoupling efficiency for different multilayer architectures. In particular, it is shown that the analysis of glass/acceptor/PM6 structures results in a major overestimation of L-D, whereas glass/acceptor/PEDOT:PSS structures give no significant contribution to outcoupling, yielding L-D values of 6-12 and 8-18 nm for ITIC and IT-4F, respectively. Hence, practical guidelines for quencher choice, sample geometries, and analysis approach for the accurate assessment of L-D are provided.