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All‐inorganic lead halide perovskite (IHP) nanocrystals (NC) have demonstrated to be a promising active material in a wide range of optoelectronic applications due to their chemical and thermal stability compared to organic‐inorganic perovskite NCs. However, the synthetic procedure of IHP NC generally requires a high‐temperature reaction of the precursors due to their limited solubility. Alternatively, the affinity of the precursor elements to the solvent was controlled to enhance their solubility in the liquid phase, and thus the enhanced kinetics in the crystallization process. Here, we show how the controlled solubility of Cs salts (i. e., Cs halide, acetate, carbonate) influences on their crystallization process and their optical properties. The formation of highly luminescent CsPbX3 (X=Cl, Br, and mixed Br/Cl and Br/I) NCs with a well‐controlled crystallinity and morphology provide fundamental insights into their crystallization process, broadening their applications in the optoelectronic devices. [ABSTRACT FROM AUTHOR]

A thermally stable 2D array of spheres and their morphology control become important for the fabrication of novel nanostructures. Here, a simple method is presented for fabrication of large-area and well-ordered arrays of carbonized polystyrene (PS) hollow spheres with a controlled (close-packed or non-close-packed hexagonal) morphology, prepared by combining the self-assembly of PS-grafted silica nanoparticles, etching, electron irradiation, and subsequent thermal annealing. Fine control in the 2D or 3D nanostructure of carbon materials can open up new opportunities for high-performance nanoscale applications that require an efficient fabrication method for preparation of the porous carbon array. [ABSTRACT FROM AUTHOR]