Three‐dimensional (3 D) perovskite has attracted a lot of attention owing to its success in photovoltaic (PV) solar cells. However, one of its major crucial issues lies in its stability, which has limited its commercialization. An important property of organic–inorganic perovskite is the possibility of forming a layered material by using long organic cations that do not fit into the octahedral cage. These long organic cations act as a “barrier” that “caps” 3 D perovskite to form the layered material. Controlling the number of perovskite layers could provide a confined structure with chemical and physical properties that are different from those of 3 D perovskite. This opens up a whole new batch of interesting materials with huge potential for optoelectronic applications. This Minireview presents the synthesis, properties, and structural orientation of low‐dimensional perovskite. It also discusses the progress of low‐dimensional perovskite in PV solar cells, which, to date, have performance comparable to that of 3 D perovskite but with enhanced stability. Finally, the use of low‐dimensional perovskite in light‐emitting diodes (LEDs) and photodetectors is discussed. The low‐dimensional perovskites are promising candidates for LED devices, mainly because of their high radiative recombination as a result of the confined low‐dimensional quantum well.
One of the attractive features of hybrid perovskite is the possibility to reduce its dimensionality, which enhances the perovskite's resistivity to moisture. In this work, we used 2D/3D perovskites to study different organic molecular spacers (aromatic ring vs cyclic ring); Cs was introduced as an additional small cation to methylammonium. It was found that Cs improves the photovoltaic performance; however, it reduces the cells' stability because two cations having a different ionic radius are mixed, which creates strains in the perovskite structure. The aromatic ring spacers display better stability in complete cells than does the cyclo spacer. Importantly, Cs has a greater effect on the stability than does the nature of the spacer molecule. The difference in the size of the organic cations as well as the inorganic cations plays a major role in the perovskite's stability in a film and in a complete solar cell.
Hybrid organic-inorganic perovskite has proved to be a superior material for photovoltaic solar cells. In this work we investigate the parameters influencing the growth of ZnO nanowires (NWs) for use as an efficient low temperature photoanode in perovskite-based solar cells. The structure of the solar cell is FTO (SnO2:F)-glass (or PET-ITO (In2O3·(SnO2) (ITO)) on, polyethylene terephthalate (PET)/ZnAc seed layer/ZnO NWs/CH3NH3PbI3/Spiro-OMeTAD/Au. The influence of the growth rate and the diameter of the ZnO NWs on the photovoltaic performance were carefully studied. The ZnO NWs perovskite-based solar cell demonstrates impressive power conversion efficiency of 9.06% on a rigid substrate with current density over 21 mA/cm2. In addition, we successfully fabricated flexible perovskite solar cells while maintaining all fabrication processes at low temperature, achieving power conversion efficiency of 6.4% with excellent stability for over 75 bending cycles.
A new approach for fine tuning of the metal work function (WF) in the range of 1 eV is described. WF control is achieved by 3D molecular doping of the metal rather than the classical 2D adsorption. Both small molecules (Congo red, thionine) and polymers (Nafion, poly(vinylbenzyltrimethylammonium)chloride) were shown to affect the work function of gold and silver. The in situ reaction of the dopants within the metallic matrix is a further tool for altering the WF, confirming that this effect is dopant-dependent. We attribute this effect to the charge transfer interactions between the dopant molecule and the surrounding 3D metallic cage.
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