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In this work, we demonstrate that an external pressure of 15–30 kPa can significantly improve metal halide perovskite (MHP) film thermal stability. We demonstrate this through the application of weight on top of an MHP film during thermal aging in preserving the perovskite phase and the mobile ion concentration, an effect which we hypothesize reduces the extent to which volatile species can escape from the MHP lattice. This method is shown to be effective for a more scalable approach by only applying the weight to a cover glass during the lamination of an epoxy-based resin, after which the weight is removed. The amount of pressure applied during lamination is shown to correlate with stability in both 1 sun illumination and damp heat testing. Lastly, the performance of MHP photovoltaic devices is improved using pressure during lamination, an effect which is attributed to improved interfacial contact between the MHP and the adjacent charge transport layers and healing of any voids or defects that may exist at the buried interface after processing. As such, there are implications for tuning the amount of pressure that is applied during lamination to enable the durability of MHP solar modules toward manufacturing-scale deployment. 

Although C₆₀is usually the electron transport layer (ETL) in inverted perovskite solar cells, its molecular nature of C₆₀leads to weak interfaces that lead to non-ideal interfacial electronic and mechanical degradation. Here, we synthesized an ionic salt from C₆₀, 4-(1',5′-dihydro-1'-methyl-2'H-[5,6] fullereno-C₆₀-I_h-[1,9-c]pyrrol-2'-yl) phenylmethanaminium chloride (CPMAC), and used it as the electron shuttle in inverted PSCs. The CH₂-NH₃⁺head group in the CPMA cation improved the ETL interface and the ionic nature enhanced the packing, leading to ~3-fold increase in the interfacial toughness compared to C₆₀. Using CPMAC, we obtained ~26% power conversion efficiencies (PCEs) with ~2% degradation after 2,100 hours of 1-sun operation at 65°C. For minimodules (four subcells, 6 centimeters square), we achieved the PCE of ~23% with <9% degradation after 2,200 hours of operation at 55°C.