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Recently, carbazole‐based self‐assembled monolayers (SAMs) have been utilized as hole transport layers (HTLs) in perovskite solar cells. However, their application in Sn or mixed Sn/Pb perovskite solar cells has been hindered by the poor wettability of the perovskite precursor solution on the carbazole surface. Here a self‐assembled bilayer (SAB) comprising a covalent monolayer (Br‐2PACz) and a noncovalent wetting layer (4CzNH3I) as the HTL in a Cs0.25FA0.75Sn0.5Pb0.5I3 perovskite solar cell is proposed. It is demonstrated that the wetting layer completely solves the problem due to the higher polarity of the surface and, furthermore, the ammonium groups help in the passivation of trap states at the buried SAB/perovskite interface. The introduction of the SAB enhances the device reproducibility with an average efficiency of 18.98 ± 0.28% (19.45% for the best device), compared to 11.54 ± 9.36% (19.34% for the best device) for the SAM‐only devices. Furthermore, the improved perovskite processability on the SAB helps to increase the reproducibility of larger size device, where, a 12.5% efficiency for a 0.8 cm2 active area device compared to 0.68% for the best SAM‐based solar cell is demonstrated. Finally, the device's operational stability is also improved to 358 hours (T80%), compared to 220 hours for the SAM‐based solar cell. [ABSTRACT FROM AUTHOR]

AgBiS2 nanocrystals have been shown to be a promising material for solar cell applications due to their high absorption coefficient, solution-processability and stability. However, detailed and systematic insight into how different surface passivation agents affect the overall material properties and corresponding device performance is still limited. Herein, a study about AgBiS2 nanocrystals treated with five different halide-based compounds – TBAI, TMAI, TBABr, TMABr and TMACl – is presented, with the nanocrystals themselves being synthesised via a newly adapted route under atmospheric conditions. For the differently passivated samples, variation in the ligand uptake, as well as shifts in the position of the valence and conduction bands could be observed. Incorporating these ligand-treated thin films into solar cell devices allowed for further investigation of their overall performance as well as into their respective charge carrier dynamics. Markedly longer charge carrier lifetimes were observed for the bromide- and chloride-passivated samples through transient photovoltage and photocurrent measurements as well as impedance spectroscopy. The effect of the surface modification on the charge carrier transport behaviour, on the other hand, was found to be less pronounced. Overall, this work demonstrates the importance of better understanding how different ligands affect nanocrystal properties, showcasing how it influences a wide variety of parameters controlling final device performance. [ABSTRACT FROM AUTHOR]