“…Hybrid organic–inorganic perovskites have emerged as a promising alternative to existing solar cell technologies owing to their bandgap tunability, − facile processing methods, , and competitive performance. − The perovskite crystal structure consists of an A-site cation (e.g., formamidinium, FA + , CH(NH 2 ) 2 + ; methylammonium, MA + , CH 3 NH 3 + ) in a three-dimensional (3D) network of lead halide octahedra as shown in Figure a. As the photoactive phases of hybrid perovskite materials are not intrinsically stable under ambient conditions, methods to stabilize them are of intense current interest, with strategies based today either on elemental doping with inorganic cations (Cs + , K + , Rb + , Mn 2+ , Co 2+ , Sb 3+ , In 3+ ) − or on passivation by a surface treatment of organic molecules or salts. − When bulky molecular cations are used, two-dimensional (2D) layered perovskites can form where inorganic perovskite slabs are separated by layers of organic cations (Figure a). − Bulk layered perovskites are more stable than their 3D counterparts but typically have lower photoconversion efficiencies. , 2D/3D heterostructures, where the layered perovskite forms at the surface of the bulk perovskite, combine the higher stability provided by the 2D phase and the superior optoelectronic properties of the 3D perovskite, while further passivating interfacial vacancies to reduce nonradiative recombination. − The detailed manner in which organic moieties interact with the perovskite structure has been thought to modify the energy landscape of the material and thereby template the photoactive α-FAPbI 3 phase. ,, …”