Abstract

AbstractConverting PbI2 residues into low‐dimensional perovskites through post‐treatment with ammonium‐based large cations can passivate 3D perovskites, thus has emerged as an effective strategy to improve the performance of perovskite solar cells (PSCs). Herein, a dramatically improved efficiency is demonstrated for PSCs based on a two‐step‐processed FAPbI3 perovskite via post‐treatment with formamidinium (FA)‐based benzamidine hydrochloride (PFACl), outperforming the commonly used methylamine (MA)‐based benzylamine hydrochloride (PMACl). With an in‐depth exploration of the crystal structures and morphology changes of the FAPbI3 perovskite upon the PFACl post‐treatment, the preferential formation of 1D rather than 2D structures on the 3D perovskite film is identified. In contrast to the 2D counterpart, the more energetically favorable 1D structure enables a more effective elimination of PbI2 residues. As a consequence, the PFACl‐induced 1D/3D perovskite film is endowed with smoother morphology, more uniform surface potential distribution, lower trap density, faster charge transfer, and better film stability than the PMACl‐induced 2D/3D perovskite and control films, demonstrating champion efficiencies of 24.9% for a small‐size PSC, 23.6% for a 1 cm2 large‐size PSC, and 21.2% for a 5 × 5 cm2 mini‐module, which is the highest among the perovskite solar mini‐modules using the two‐step deposition method.

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