The outstanding performance of halide perovskites in optoelectronic applications can be partly attributed to their high absorption coefficient and long carrier lifetime, which are also desirable for photocatalysts. Herein, we report that cesium lead iodide perovskite quantum dots (CsPbI₃ QDs) can be used as catalysts to promote the polymerization of 2,2′,5′,2″-ter-3,4-ethylenedioxythiophene under visible light illumination while preserving the quantum dot in the desirable cubic crystal phase. Simultaneously, the generated conducting poly(3,4-ethylenedioxythiophene), PEDOT, encapsulates and stabilizes the morphology of the CsPbI₃ QDs. The photocatalytic polymerization clearly depends on the concentration of the CsPbI₃ QDs, and the CsPbI₃ QDs maintain the desirable perovskite phase when the concentration of the QD increases. Molecular oxygen and 1,4-benzoquinone can serve as electron acceptors during the photocatalytic polymerization reaction. When molecular oxygen is used, the structure of the CsPbI₃ QD transforms from cubic to orthorhombic, while usage of 1,4-benzoquinone preserves the cubic phase of CsPbI₃ QD. This novel approach enables the one-step formation of CsPbI₃/PEDOT composite, which could be promising for the preparation of novel optoelectronic materials and high performance devices.

This review gives a perspective on different synthetic methodologies for the preparation of halide perovskites and highlights the structural effects on their optoelectronic properties.

A novel nitroamine/energetic ionic salt cocrystal explosive composed of CL-20 and 1-AMTN in a 1 : 1 molar ratio was discovered and characterized. It shows an appropriate explosive power and good mechanical sensitivity relative to RDX currently in use.

The influence of twinned crystals on the performance of TKX-50 is investigated using normal TKX-50 and twinned TKX-50 supercells. ReaxFF-lg reactive molecular dynamics simulations are performed to study thermal decomposition and oxidation.