Thin Films and Solar Cells Based on Semiconducting Two-Dimensional Ruddlesden-Popper (CH3(CH2)3NH3)2(CH3NH3)n-1SnnI3n+1 i Perovskites

Low electrical resistivity (high dark carrier concentration) of CH3NH3SnI3 often leads to short-circuiting in solar cells, and appropriate thin-film modifications are required to ensure functional devices. The long-term durability of organicinorganic perovskite solar cells necessitates the protection of perovskite thin films from moisture to prevent material decomposition. Herein, we report that the electrical resistivity and the moisture stability of two-dimensional (2D) RuddlesdenPopper (CH3(CH2)(3)NH3)(2)(CH3NH3)(n-1)SnnI3n+1 perovskites are considerably improved compared to those of the three-dimensional (3D) CH3NH3SnI3 perovskite and subsequently show the solar cell fabrication using a simple one-step spin-coating method. These 2D perovskites are semiconductors with optical band gaps progressively decreasing from 1.83 eV (n = 1) to 1.20 eV (n = 8). The n = 3 and n = 4 members with optimal band gaps of 1.50 and 1.42 eV for solar cells, respectively, were thus chosen for in-depth studies. We demonstrate that thin films of 2D perovskites orient the {(CH3NH3)(n-1)SnnI(3n+1)}(2-) slabs parallel to the substrate when dimethyl sulfoxide solvent is used for deposition, and this orientation can be flipped to perpendicular when N,N-dimethylformamide solvent is used. We find that high-purity, single-phase films can be grown only by using precursor solutions of pre-synthesized single-phase bulk perovskite materials. We introduce for the first time the use of triethylphosphine as an effective antioxidant, which suppresses the doping level of the 2D films and improves film morphology. The resulting semiconducting 2D Sn-based iodide perovskite films were incorporated in solar cells yielding a power conversion efficiency of 2.5% from the Sn4I13 member. From the temporal stability standpoint, the 2D Sn perovskite solar cells outperform their 3D analogs.