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The quality and the performance of hybrid perovskite (HP)'s films strongly depend on the complete conversion into MAPbI3 of a spin-coated solution of methylammonium iodide (MAI) and PbI2. Highly crystalline PbI2 on a substrate limits such a conversion and, consequently, the HP's solar cell performances. We investigate for the first time the use of short-chain organic acids as additives in a non-complexing solvent like γ-butyrolactone (GBL), that can retard retard the crystallization of PbI2. Based on XRD analyses of the spin coated films, the acetic acid is the most effective additive in retarding the PbI2 crystallization, making Pb2+ available for a subsequent reaction with MAI. These results open a new experimental path for fabricating perovskite films by single or sequential step methods involving acid additives. [ABSTRACT FROM AUTHOR]

In this study, the structure and morphology, as well as time, ultraviolet radiation, and humidity stability of thin films based on newly developed 1D (PRSH)PbX3 (X = Br, I) pseudo-perovskite materials, containing 1D chains of face-sharing haloplumbate octahedra, are investigated. All films are strongly crystalline already at room temperature, and annealing does not promote further crystallization or film reorganization. The film microstructure is found to be strongly influenced by the anion type and, to a lesser extent, by the DMF/DMSO solvent volume ratio used during film deposition by spin-coating. Comparison of specular X-ray diffraction and complementary grazing incidence X-ray diffraction analysis indicates that the use of DMF/DMSO mixed solvents promotes the strengthening of a dominant 100 or 210 texturing, as compared the case of pure DMF, and that the haloplumbate chains always lie in a plane parallel to the substrate. Under specific DMF/DMSO solvent volume ratios, the prepared films are found to be highly stable in time (up to seven months under fluxing N2 and in the dark) and to highly moist conditions (up to 25 days at 78% relative humidity). Furthermore, for representative (PRSH)PbX3 films, resistance against ultraviolet exposure (λ = 380 nm) is investigated, showing complete stability after irradiation for up to 15 h at a power density of 600 mW/cm2. These results make such thin films interesting for highly stable perovskite-based (opto)electronic devices. [ABSTRACT FROM AUTHOR]