Reduced-dimensional (2D or quasi-2D) perovskites have recently attracted considerable interest due to their superior long-term stability. The nature of the intercalating cations plays a key role in determining the physicochemical properties and stability of the quasi-2D perovskites. Here, the thermal stability of a series of 2D Ruddlesden−Popper (RP) perovskites is studied using seven types of intercalating cations with increasing linear carbon-chain length from ethylammonium (EA) to n-dodecylammonium (DA) through a high-throughput platform. The results show that long-chain cations in quasi-2D perovskite films lead to strong steric hindrance between adjacent perovskite domains, thus suppressing Ostwald ripening during the thermal-aging process. For short-chain cations, increased-dimensional phase redistribution during the aging period is observed, which can benefit a concomitant regeneration of the 3D/3D-like perovskite phases. The impact of steric hindrance on structural reconfiguration and the subsequent phase redistribution in quasi-2D perovskites are systematically characterized by UV-vis absorption spectra, photoluminescence spectra, and X-ray diffraction patterns. Due to the steric hindrance effect, an optimal chain length is found to maximize film stability by balancing the water/oxygen resistance and increased-dimensional phase redistribution. This study provides new insight into the thermal stability of quasi-2D perovskites.

Self-healing of defects imposed by external stimuli such as high energy radiation is a possibility to sustain the operational lifetime of electronic devices such as radiation detectors. Cs 3 Bi 2 Br 3 I 6 polycrystalline wafers are introduced here as novel X-ray detector material, which not only guarantees a high X-ray stopping power due to its composition with elements with high atomic numbers, but also outperforms other Bi-based semiconductors in respect to detector parameters such as detection limit, transient behavior, or dark current. The polycrystalline wafers represent a size scalable technology suitable for future integration in imager devices for medical applications. Most astonishingly, aging of these wafer-based devices results in an overall improvement of the detector performance-dark currents are reduced, photocurrents are increased, and one of the most problematic properties of X-ray detectors, the base line drift is reduced by orders of magnitude. These aging induced improvements indicate self-healing effects which are shown to result from recrystallization. Optimized synthetic conditions also improve the as prepared X-ray detectors; however, the aged device outperforms all others. Thus, self-healing acts in Cs 3 Bi 2 Br 3 I 6 as an optimization tool, which is certainly not restricted to this single compound, it is expected to be beneficial also for many further polycrystalline ionic semiconductors.

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Epitaxial growth methods usually need dedicated equipment, high energy consumption to maintain pure vacuum conditions and evaporation of source materials, and elevated substrate temperatures. Solution epitaxial growth requires nothing of that but is rarely used because the achieved microstructures are of low quality, not homogeneous, and finally exhibit worse performances in devices. Here, an antisolvent‐vapor‐assisted‐crystallization of metal‐halide‐perovskites as a method overcoming these disadvantages is demonstrated. The methylammonium lead tribromide exhibits van‐der‐Waals type of epitaxial growth on mica substrates, resulting in micro‐crystallites whose shape can be controlled to be either triangular micro‐prism or micro‐cuboid. These micro‐crystallites act as optical resonators supporting various optical modes and lasing is achieved under optical excitation with low thresholds and record high environmental stability. Selecting suitable resonators from a large variety of sizes allows control of mode spacing and finally mono‐mode operation, considered to be an important feature of semiconductor laser devices. The achieved results are essentially competitive to those obtained by vapor phase epitaxial microstructures, highlighting that epitaxy of high‐quality optoelectronic device structures is feasible by minimum technological efforts and energy consumption, which are of increasing importance considering issues such as global warming and the current energy crisis.

success of epitaxial growth of conventional inorganic semiconductors for (opto) electronics, there are various attempts to obtain single-crystalline structures by the epitaxial growth of metal halide perovskites (MHPs), as promising materials for optoelectronic applications. While most attempts have been pursued by some ways of chemical vapor deposition (CVD) on various substrates and also by molecular beam epitaxy, [1][2][3][4][5][6][7][8] albeit with elaborate equipment, the advantages of the MHPs are enrolled by solution processing them. Solution epitaxy is an inexpensive and facile approach to obtain high-quality films and microstructures. Simple techniques such as spin coating delivered already epitaxial crystalline films operating as highly sensitive photodetectors. [9] Thereafter, spin coating was introduced by Kelso et al., as a general technique for the epitaxial growth of inorganic High-quality epitaxial growth of oriented microcrystallites on a semiconductor substrate is demonstrated here for formamidinium lead bromide perovskite, by drop casting of precursor solutions in air. The microcrystallites exhibit green photoluminescence at room temperature, as well as lasing with low thresholds. Lasing is observed even though the substrate is fully opaque at the lasing wavelengths, and even though it has a higher refractive index as the perovskite active material. Moreover, the lasing is stable for more than 10 9 excitation pulses, which is more than what is previously achieved for devices kept in the air. Such highly stable lasing under pulsed excitation represents an important step towards continuous mode operation or even electrical excitation in future perovskite-based devices.

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