In the last decade, halide perovskites have attracted great interest due to many reasons, including their low cost, solution-processability, superior PL properties, broad range of color tunability, color purity, and defect tolerance, among others. They are in increasing demand for a wide range of applications, such as solar cells, light emitting diodes (LEDs), white LEDs (WLED), and lasers. Yellow phosphors have been heavily employed in solidstate lighting, since its illumination by blue yields white light with various optical features, such as high/low CRI, CCT, and luminous efficiency. However, phosphors as pigments are seldom found and are costly material. In this sense, halide perovskites may offer a promising alternative to phosphors for future solid-state lighting. In this study, the synthesis and optical properties of halide perovskites, as well as their application in WLED as a conversion layer are investigated.

Conversion of clean solar energy to chemical fuels is one of the promising and up-and-coming applications of metal–organic frameworks. However, fast recombination of photogenerated charge carriers in these frameworks remains the most significant limitation for their photocatalytic application. Although the construction of homojunctions is a promising solution, it remains very challenging to synthesize them. Herein, we report a well-defined hierarchical homojunction based on metal–organic frameworks via a facile one-pot synthesis route directed by hollow transition metal nanoparticles. The homojunction is enabled by two concentric stacked nanoplates with slightly different crystal phases. The enhanced charge separation in the homojunction was visualized by in-situ surface photovoltage microscopy. Moreover, the as-prepared nanostacks displayed a visible-light-driven carbon dioxide reduction with very high carbon monooxide selectivity, and excellent stability. Our work provides a powerful platform to synthesize capable metal–organic framework complexes and sheds light on the hierarchical structure-function relationships of metal–organic frameworks.

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The interest in all-inorganic halide perovskites has been increasing dramatically due to their high quantum yield, band gap tunability, and ease of fabrication in compositional and geometric diversity. In this study, we synthesized µm long and ~4 nm thick CsPbBr3 nanowires (NWs). They were, then, integrated into electrospun polyurethane (PU) fibers to examine polarization behavior of the composite fiber assembly. Aligned electrospun fibers containing CsPbBr3 nanowires show remarkable increase in degree of polarization from 0.17 to 0.30. This combination of NWs and PU fibers provides a promising composite material for various applications such as optoelectronic devices and solar cells.

Recent advances in colloidal synthesis methods have led to increased research focus on halide perovskites. Due to highly ionic crystal structure of perovskite materials, stability issue pops up especially against polar solvents such as water. In this study, we investigate water-driven structural evolution of CsPbBr 3 by performing experiments and state-of-the-art first-principles calculations.It is seen that while optical image shows the gradual degradation of yellowish-colored CsPbBr 3 structure under daylight, UV illumination reveals that the degradation of crystals takes place in two steps; transition from blue-emitting to green-emitting structure and and then transition from green-emitting phase to complete degradation. We found that as-synthesized CsPbBr 3 NWs emit blue light under 254 nm UV source and before the degradation, first CsPbBr 3 NWs undergoes a water-driven structural transition to form large bundles. It is also seen that formation of such bundles provide longer-term environmental stability. In addition theoretical calculations revealed how strong is the interaction of water molecules with ligands and surfaces of CsPbBr 3 and provide atomistic-level explanation to transition from ligand-covered nanowires to bundle formation. Further interaction of green-light-emitting bundles with water causes complete degradation of CsPbBr 3 and photoluminescence signal is entirely quenched. Moreover, Raman and XRD measurements revealed that completely degraded regions are decomposed to PbBr 2 and CsBr precursors. We believe that findings of this study may provide further insight into the degradation mechanism of CsPbBr 3 perovskite by water.