Chalcogen-substituted PCBM derivatives as ternary components in PM6:Y6 solar cells

Ternary organic solar cells (TOSCs) are a promising approach to enhance the power conversion efficiency in organic-based solar cells. The combination of fullerene and non-fullerene acceptors is employed to optimize the Eight absorption and phase separation for better charge dissociation and collection. Herein, we describe the synthesis and characterization of three chalcocogen substituted PCBM derivatives with a 5-membered aromatic ring [inked to the methyl ester position with the objective to study the relationship between interphase separation and power conversion efficiency. Therefore, the effects of furan, thiophene and selenophene in the PCBM derivatives (PCBFu, PCBTh and PCBSe, respectively) are investigated on the photovoltaic performance of ternary organic solar cells based on PM6:Y6. We observed that the addition of the PCBTh and PCBSe derivatives increases the short circuit current density and the fill factor pointing to the suppression of charge recombination. In addition, surface and thermal analysis confirms that the morphology is optimized in both cases, which implies that organized thin film nanomorphology is key for the suppression of carrier Losses. The TOSC with PCBTh exhibited the highest power conversion efficiency among all the devices reaching 14.6%.

Automated summary

Ternary organic solar cells hold promise in enhancing power conversion efficiency through the combination of fullerene and non-fullerene acceptors for better charge dissociation and collection. The study on chalcogen-substituted PCBM derivatives revealed that the addition of PCBTh and PCBSe derivatives improved short circuit current density and fill factor, suppressing charge recombination. Surface and thermal analysis confirmed the importance of organized thin film nanomorphology in optimizing morphology and reducing carrier losses, with TOSC containing PCBTh exhibiting the highest power conversion efficiency at 14.6%.