Enhancing High Humidity Stability of Quasi‐2D Perovskite Thin Films through Mixed Cation Doping and Solvent Engineering

Abstract Perovskite materials show excellent photovoltaic performance along with simple processing and low‐energy requirements. Despite their high power conversion efficiency (PCE), instability in the presence of moisture is still a major challenge. An effective method to enhance perovskite stability is by reducing dimensionality through incorporation of long organic cations into the perovskite crystal, which improves charge‐carrier extraction efficiency of the perovskites compared to conventional 3D perovskites. Quasi‐2D perovskites or 2D/3D perovskites strike a good balance between PCE and stability, having much improved stability compared to 3D structures while retaining excellent optoelectronic properties. Yielding better thermal stability and broader absorption into the near‐infrared, formamidinium iodide (FAI) doping has positive influences yet tends to cause poor surface morphology. Here, we introduce highly stable MA/FA‐based quasi‐2D perovskite fabricated by mixed cation doping (MCD), which is repeated deposition of MA and FA cations onto a quasi‐2D perovskite layer. MCD enables better morphology and surface passivation, leading to fewer defects. MA/FA‐based quasi‐2D perovskite with quasi‐cubic structure has high humidity resistivity, remaining intact after 90 days under 60% relative humidity without encapsulation. The underlying mechanism is further explained by binding and formation energies of cation mixture in solution and perovskite structure through computational analysis.