Revealing the Perovskite Film Formation Using the Gas Quenching Method by In Situ GIWAXS: Morphology, Properties, and Device Performance

The optoelectronic properties, morphology, and consequently the performance of metal halide perovskite solar cells are directly related to the crystalline phases and intermediates formed during film preparation. The gas quenching method is compatible with large-area deposition, but an understanding of how this method influences these properties and performance is scarce in the literature. Here, in situ grazing incidence wide angle X-ray scattering is employed during spin coating deposition to gain insights on the formation of MAPbI(3)and Cs(x)FA(1-)(x)Pb(I0.83Br0.17)(3)perovskites, comparing the use of dimethyl sulfoxide (DMSO) and 2-methyl-n-pyrrolidone (NMP) as coordinative solvents. Intermediates formed using DMSO depend on the perovskite composition (e.g., Cs content), while for NMP the same intermediate [PbI2(NMP)] is formed independently on the composition. For MAPbI(3)and Cs(x)FA(1-)(x)Pb(I0.83Br0.17)(3)with a small amount of Cs (10% and 20%), the best efficiencies are achieved using NMP, while the use of DMSO is preferred for higher (30% and 40%) amount of Cs. The inhibition of the 2H/4H hexagonal phase when using NMP is crucial for the final performance. These findings provide a deep understanding about the formation mechanism in multication perovskites and assist the community to choose the best solvent for the desired perovskite composition aiming to perovskite-on-silicon tandem solar cells.

Automated summary

This study investigates the formation mechanism of MAPbI(3) and Cs(x)FA(1-)(x)Pb(I0.83Br0.17)(3) perovskites during deposition process using X-ray scattering, comparing the influence of DMSO and NMP solvents. The results show that the choice of optimal solvent varies for different Cs content, which is crucial for the final performance of the solar cells.