Abstract

In this work, we investigated the effects of different acceptors (IT−4F and PC71BM) on the charge dynamics in PM6-based solar cells. The correlation between different acceptors and the performance of organic solar cells was studied by atomic force microscope, steady-state absorption spectrum, transient absorption spectrum, and electrical measurements. Optical absorption exhibited that IT−4F has strong absorption in the near-infrared region for the active layer. Transient absorption measurements showed that different acceptors (IT−4F and PC71BM) had a significant influence on the behaviors of PM6 excitons and charge dynamics. That is, the exciton dissociation rate and delocalized polaron transport in the PM6:IT−4F active layer were significantly faster than that in the PM6:PC71BM active layer. The lifetime of localized polaron in the PM6:PC71BM active layer was longer than that in the PM6:IT−4F active layer. Conversely, the lifetime of delocalized polaron in the PM6:IT−4F active layer was longer than that in the PM6:PC71BM active layer. Electrical measurement analysis indicated that lower bimolecular recombination, higher charge transport, and charge collection ability were shown in the PM6:IT−4F device compared with the PM6:PC71BM device. Therefore, PM6:IT−4F solar cells achieved a higher power conversion efficiency (12.82%) than PM6:PC71BM solar cells (8.78%).

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