Surface Modification in CsPb0.5Sn0.5I2Br Inorganic Perovskite Solar Cells: Effects of Bifunctional Dipolar Molecules on Photovoltaic Performance.

Inorganic tin-lead binary perovskites have piqued the interest of researchers as effective absorbers for thermally stable solar cells. However, the nonradiative recombination originating from the surface undercoordinated Sn2+ cations and the energetic offsets between different layers cause an excessive energy loss and deteriorate the perovskite device's performance. In this study, we investigated two thioamide derivatives that differ only in the polar part connected to their common benzene ring, namely, benzenecarbothioamide and 4-fluorophenylcarbothioamide (F-TBA). These two molecules were implemented as modifiers onto the inorganic tin-lead perovskite (CsPb0.5Sn0.5I2Br) surface in the perovskite solar cells. Modifiers that carry C═S and NH2 functional groups, equipped with lone electron pairs, can autonomously associate with surface Sn2+ through coordination and electrostatic attraction mechanisms. This interaction serves effectively to passivate the surface. In addition, due to the permanent dipole moment of the intermediate layer, an interfacial dipole field appears at the PCBM/CsPb0.5Sn0.5I2Br interface, reducing the electron extraction potential barrier. Consequently, the planar solar cell with an ITO/PEDOT:PSS/CsPb0.5Sn0.5I2Br/PCBM/BCP/Ag layered structure featuring an F-TBA surface post-treatment demonstrated a noteworthy power conversion efficiency of 14.01%. Simultaneously, after being stored for 1000 h in an inert atmosphere glovebox, the non-encapsulated CsPb0.5Sn0.5I2Br solar cells managed to preserve 94% of their original efficiency.

Fabrication of High-Quality CsPbI3 Perovskite Films with Phosphorus Pentachloride Additive for Highly Stable Solar Cells.

Fully inorganic perovskite cesium lead triiodide (CsPbI3 ) has garnered much attention from researcher for photovoltaic application because of its excellent thermal stability compared with the inorganic-organic hybrid counterparts, along with the potential to serve as the top cell in tandem devices with silicon solar cell. However, the active α-phase cubic CsPbI3 spontaneously tends to transform into the non-perovskite δ-CsPbI3 when subjected to ambient condition. This work proposes an effective method to fabricate high-quality and stable α-phase cubic CsPbI3 films by introducing phosphorus pentachloride (PCl5 ) as an additive. PCl5 acts as colloidal binder for modulating crystallization dynamics of perovskites, resulting in high-quality film and a significantly suppressed phase transition. Finally, highly stable CsPbI3 perovskite solar cells can be achieved with a power conversion efficiency up to 17.85 %, and a long-term stability in N2 filled glove box.