We
explored thiocyanate (SCN)-based two-dimensional (2D) organometal
lead halide perovskite families toward photovoltaic applications.
Using an SCN axial ligand and various cation species, we examined
AA′PbI<sub>2</sub>(SCN)<sub>2</sub>-type 2D perovskite by replacing
the cation species (AA′) between methylammonium (MA), formamidinium
(FA), and cesium. Among various cation compositions, only all-inorganic
cesium-based SCN perovskite, Cs<sub>2</sub>PbI<sub>2</sub>(SCN)<sub>2</sub>, film showed high thermal stability compared to known 2D
perovskites. Perovskite solar cells (PSCs) using the Cs<sub>2</sub>PbI<sub>2</sub>(SCN)<sub>2</sub> absorber yielded approximately 2%
conversion efficiency on the mesoscopic device. Relatively low efficiency
is attributed, in addition to optical properties (large band gap (2.05
eV) and exciton absorption), to the orientation of perovskite layer
parallel to the layered structure, preventing carrier extraction from
the light-absorber perovskite. In device stability, the Cs-based 2D
perovskite was stable against oxygen (oxidation), whereas it was found
to be unstable against humidity. X-ray diffraction and X-ray photoelectron
spectroscopy measurements showed that, unlike long alkylammonium-based
2D perovskite families such as BA<sub>2</sub>PbI<sub>4</sub> (BA =
butylammonium), the Cs-based 2D perovskite can undergo hydrolysis
due to the hydrophilic Cs cations.