The organic–inorganic Sn–Pb mixed perovskite has achieved great progress during the last 10 years and is considered as one of the most promising low‐bandgap photovoltaic materials. It has lower toxicity, outstanding optoelectrical properties, and achieved remarkable performance. However, there are still plenty of challenges in controlling the morphology, crystallinity, and defects of the Sn–Pb mixed perovskite film because of the inferior chemical stability of Sn compared with Pb. Herein, it is found that the synergistic effect of potassium thiocyanate (KSCN) in the Sn–Pb mixed perovskites can enlarge the grain size, enhance the crystallization, improve the film morphology, and obtain high‐quality perovskite films which effectively eliminate the bulk defects and smooth carrier transportation of Sn–Pb mixed perovskite solar cells. Through optimizing the concentration of KSCN, a high‐performance MA0.5FA0.5Pb0.5Sn0.5I3 solar cell with an efficiency of 15.14% and improved stability is obtained. This work lays a key foundation for the fabrication of efficient and stable Sn‐based or Sn–Pb mixed perovskite solar devices.
Two-dimensional
(2D) perovskites show better resistance and optoelectronic
characteristics than three-dimensional compounds. However, the high
exciton energy and insufficient interfacial charge flow significantly
reduce perovskite device performance. In this regard, a strategy to
obtain high-performance 2D perovskite solar cells employing synergistic
impact of coadditives (NH4SCN and HCl) to enable the proper
alignment of perovskite films through the substrate, which eventually
increases crystallinity and charge transport of 2D perovskites and
reduces defect states, is presented. This coadditive method successfully
generates homogeneous 2D perovskite films with consistent crystal
structures and higher film quality. The champion 2D perovskite device
exhibited a photovoltaic performance of 16.45% with an improved J
sc. These results suggest that developing additive
engineering might result in remarkably stable and efficient 2D perovskite
materials.
Perovskite solar cells have been intensively studied recently due to their superb optoelectronic properties and rapidly increasing power conversion efficiency. However, perovskite solar cells with the AMX3 structure as the light‐absorbing layer have a big stability problem. Multiple alternatives have been developed to ensure their stability, such as dimensional engineering (2D and 2D/3D), which consists of the incorporation of large organic cations into the perovskite structure. Research in dimensional engineering has been prevalent in the Ruddlesden–Popper phases. The presence of this large cation slows the decomposition and improves the stability of perovskites. Thus, new 2D perovskites are being studied based on Dion–Jacobson (DJ) phases, consisting of the addition of diammonium cations and leading to the formation of 2D and 2D/3D perovskites with better stability due to their hydrogen bonding on both sides. Moreover, 2D DJ perovskites offer the advantage of decreasing the gap between layers with higher contacts, which improves not only their optoelectronic properties, but also their charge transport properties. This article begins with an overview of the crystal structure and optoelectronic characteristics of 2D perovskites. Then, the progress achieved currently in using DJ‐phase perovskites in photovoltaic is assessed. Finally, the possible research routes for producing low‐dimensional perovskites are highlighted.
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