Efficient and stable inverted perovskite solar cells enabled by inhibition of self-aggregation of fullerene electron-transporting compounds.

Fullerene-based electron-transporting layers (ETLs) significantly influence the defect passivation and device performance of inverted perovskite solar cells (PSCs). However, the π-cage structures of fullerenes lead to a strong tendency to self-aggregate, which affects the long-term stability of the corresponding PSCs. Experimental results revealed that [6,6]-phenyl-C-butyric acid methyl ester (PCBM)-based ETLs exhibit a certain degree of self-aggregation that affects the stability of the device, particularly under continuous irradiation stress. To modulate the aggregation behavior, we replaced a methyl hydrogen of PCBM with a phenyl group to yield [6,6]-phenyl-C-butyric acid benzyl ester (PCBB). As verified through X-ray crystallography, this minor structural modification results in more non-covalent intermolecular interactions, which effectively enhanced the electron-transporting ability of the PCBB-based ETL and led to an efficiency approaching 20%. Notably, the enhanced intermolecular forces of PCBB suppressed its self-aggregation, and the corresponding device showed significantly improved stability, retaining approximately 90% of its initial efficiency after 600 h under one-sun irradiation with maximum power point tracking. These findings provide a viable approach for the design of new fullerene derivatives to tune their intermolecular interactions to suppress self-aggregation within the ETL for high-performance PSCs.