Publication date: 17th February 2025
Mesoporous carbon-based (mC) hole-transporting-layer-free architectures offer a cost-effective solution for the commercialization of perovskite solar cells (PSCs). Adding 5-aminovaleric acid (AVA) to MAPbI3 reduces defect concentration and enhances pore filling, while Eu enrichment in CsPbI3 reduces cation migration and enables device reusability [1].
In this study, AVA-MAPbI3 mC-PSCs were encapsulated at room temperature (RT) with a solvent- and water-free polyurethane (PU) resin [2]. Under continuous ambient light, RT, and 40% relative humidity (RH), PU encapsulant acts as a barrier to extend device durability and enable reusability. The formation of a bump in the J-V curve after ~250 h, already reported at low scan-rate but here observed at 50 mV/s, strongly reduces the photovoltaic performances. We demonstrate that the bump is not linked to the formation of PbI2 but is explained by a water-vacancy interaction that increases cation mobility and enhances screening effects near the electron-transport layer. The photovoltaic performances are fully restored by drying the devices under N2 flow for ~48 hours.
A further addition of a hydrophobic Kapton tape interlayer between the PU and the device mitigates bump formation, boosts t90 to ~6000 h and projects t80 to ~10,800 h. Differently from the Kapton tape used alone, PU provides an effective sealing all around the devices, ensuring stability in 100% RH at 90 °C and even underwater.
For indoor applications, Eu:CsPbI3 mC-PSCs typically degrade from γ- to δ-phase within ~1 h in air, whereas PU-encapsulated devices achieve t80 ~250 h, extendable to 1250 h with an additional closure glass slide[3].