The development of π‐conjugated molecular systems with high‐efficiency generation of UV and blue light plays an important role in the fields of light‐emitting diodes, fluorescent imaging, and information storage. Herein, supramolecular construction of solid‐state UV/blue luminescent materials are assembled using 2,5‐diphenyloxazole (DPO) with four typical co‐assembled building blocks (1,4‐diiodotetrafluorobenzene, 4‐bromotetrafluorobenzene carboxylic acid, pentafluorophenol, and octafluoronaphthalene). Compared with the pristine DPO sample, the as‐prepared two‐component molecular materials feature ease of crystallization, high crystallinity, enhanced thermal stability and tunable luminescence properties (such as emissive wavelength, color, fluorescence lifetime, and photoluminescence quantum yield) as well as multicolor polarized emission in the UV/blue region. Moreover, pump‐enhanced luminescence and reversible mechanochromic fluorescence (MCF) properties can also be obtained for these molecular solids, which are absent for the pristine DPO sample. Therefore, this work provides a procedure for the facile self‐assembly of ordered two‐component molecular materials with tunable UV/blue luminescence properties, which have potential application in the areas of light‐emitting displays, polarized emission, frequency doubling, and luminescent sensors.

Based on a supramolecular assembly strategy, Yan and co‐workers obtain two‐component molecular solid‐state materials of diphenyloxazole (DPO) through a solution‐growth process. On page 587, the DPO‐based high‐quality single crystals display tunable luminescence properties (such as emissive wavelength, color, and fluorescence lifetime) as well as multicolor polarized emission in the UV/blue/green region. This is similar to, in a macroscopic scenario, the variable light emitted from Canton tower (the highest tower in China, shown here) at the side of the Zhujiang river.

Although the fabrication of hierarchical architectures with highly ordered functional units is of great importance for both fundamental science and practical application, the development of one-dimensional (1D) organic hierarchical micro/nanostructures based on low-molecular-weight (LMW) building blocks remains at an early stage. Herein, we report two types of micro/nanoscaled multicomponent fluorescent fiber systems with tunable hierarchical morphologies through a one-step coassembly process. With the aid of hydrogen-bonding motifs, LMW precursors (1,4-bis(5-phenyloxazol-2-yl)benzene (A) and two coassembled building blocks: 4-bromotetrafluorobenzene carboxylic acid (B) and 2,3,4,5,6-pentafluorophenol (C)) have been self-organized into fibers and flexible free-standing films, which show hierarchical micro/nanostructures as well as tunable one-/two-photon luminescence. The disassembly of the multicomponent A.B and A.C fibers occurs at high temperature, which further alters the luminescence properties of the multicomponent materials. Therefore, this work provides a facile wet chemical route for fabricating multicomponent LMW self-assembled fibers and free-standing film systems with tunable hierarchical structures and photoemission behaviors, and such self-organized systems may have potential applications in fields of two-photon luminescence and thermal sensors.

Organic luminescent materials play an important role in the fields of light-emitting diodes and fluorescent imaging. Moreover, new synthetic approaches towardsπ-conjugated molecular systems with high fluorescence quantum efficiency are highly desired. Herein, different 2,5-diphenyloxazole-octafluoronaphthalene (DPO-OFN) films with tunable fluorescence have been prepared by Low Vacuum Physical Vapor Deposition (LVPVD) method. DPO-OFN films showed some changed properties, such as molecular vibration and fluorescence. All films exhibited blue/bluish violet fluorescence and showed blue shift, in comparison with pristine DPO. This work introduced a new method to fabricate two-component molecular materials with tunable blue/bluish violet luminescence properties and provided a new perspective to prepare organic luminescent film materials, layer film materials, cocrystal materials, and cocrystal film materials. Importantly, these materials have potential applications in the fields of next generation of photofunctional materials.

Electronic transport properties in an Al cluster are investigated theoretically in this paper. We propose a possible illustration of Coulomb blockade based on variable electrostatic potential (ESP). Density functional theory (DFT) was used to achieve the global minimum structure and wave function for analyzing the ESP and density of states (DOS) of Al 68 in different charged states. Al 68 is able to contain multiple electrons. According to the calculation of systematic energy and surface ESP, respectively, the surface of Al 68 presents a 0-6.33 eV ESP barrier after electron injection, which is 0 eV at first. The probability density of flow of electrons was calculated under onedimensional model with double barriers. Expected results were obtained, containing a nonlinear relationship between J and V and flow density steps. Moreover, an assumption is proposed associated with nonlinear conductance phenomenon of zero-dimensional nanomaterials. Significantly, Al films with different thicknesses were prepared by the low vacuum physical vapor deposition (LVPVD) method, exhibiting novel fluorescent behaviors. In addition, the I-V curve of a 25-nm Al film exhibited two steps at 7 and 27 V, respectively, which meant that the step effect was caused by Coulomb blockade, in accordance with the theoretical calculation.