Molecular Locking with All‐Organic Surface Modifiers Enables Stable and Efficient Slot‐Die‐Coated Methyl‐Ammonium‐Free Perovskite Solar Modules

The power conversion efficiency (PCE) of the state‐of‐the‐art large‐area slot‐die‐coated perovskite solar cells (PSCs) is now over 19%, but issues with their stability persist owing to significant intrinsic point defects and a mass of surface imperfections introduced during the fabrication process. Herein, the utilization of a hydrophobic all‐organic salt is reported to modify the top surface of large‐area slot‐die‐coated methylammonium (MA)‐free halide perovskite layers. Bearing two molecules, each of which is endowed with anchoring groups capable of exhibiting secondary interactions with the perovskite surfaces, the organic salt acts as a molecular lock by effectively binding to both anion and cation vacancies, substantially enhancing the materials’ intrinsic stability against different stimuli. It not only reduces the ingression of external species such as oxygen and moisture, but also suppresses the egress of volatile organic components during the thermal stability testing. The treated PSCs demonstrate efficiency of 19.28% (active area of 58.5 cm2) and 17.62% (aperture area of 64 cm2) for the corresponding mini‐module. More importantly, unencapsulated slot‐die‐coated mini‐modules incorporating the all‐organic surface modifier show ≈80% efficiency retention after 7500 h (313 days) of storage under 30% relative humidity (RH). They also remarkably retain more than 90% of the initial efficiency for over 850 h while being measured continuously. A hydrophobic all‐organic salt is reported to modify the top surface of large‐area slot‐die‐coated methylammonium (MA)‐free halide perovskite layers to achieve an active area efficiency of 19.28% (58.5 cm2) with the retention of ≈80% efficiency after 7500 h (313 days).