The design and synthesis of three-dimensional covalent organic frameworks (3D COFs) have still been considered as a big challenge. Here we report the design and synthesis of an AIEgen-based 3D COF (3D-TPE-COF), with a high surface area (1084 m² g⁻¹). According to powder X-ray diffraction and continuous rotation electron diffraction analyses, 3D-TPE-COF is identified to adopt a seven-fold interpenetrated pts topology. Interestingly, 3D-TPE-COF emits yellow fluorescence upon excitation, with a photoluminescence quantum yield of 20%. Moreover, by simply coating 3D-TPE-COF onto a commercial blue light-emitting diode (LED), a prototype white LED (WLED) under continuously driving without degradation for 1200 h was demonstrated. The present work suggests the possibility of using COF materials for stable WLEDs, which will greatly inspire us to design and synthesize fluorescent 3D COFs and facilitate the development of COF-based WLEDs in future.

Covalent organic frameworks (COFs) represent an emerging class of porous crystalline materials and have recently shown interesting applications in energy storage. Herein, we report the construction of a cycle-stable sulfur electrode by embedding sulfur into a 2D COF. The designed porphyrin-based COF (Por-COF), featuring a relatively large pore volume and narrow pore size distribution, has been employed as a host material for sulfur storage in Li–S batteries. With a 55% sulfur loading in the composite, the thus-prepared cathode delivers a capacity of 633 mA h g⁻¹ after 200 cycles at 0.5C charge/discharge rates. Therefore, embedding sulfur in the nanopores of the Por-COF significantly improves the performance of the sulfur cathode. Considering the flexible design of COFs, we believe that it is possible to synthesize a 2D COF host with a suitable pore environment to produce more stable Li–S batteries, which may help in exploration of the structure–property relationship between the host material and cell performance.

Magnesium oxysulfate (MOS) cement is a typical eco-friendly cementitious material, which presents excellent performances. In this work, a novel multiscale modeling strategy is proposed to simulate the hydration and pore structure of MOS cement system. This work collected and evaluated the Gibbs free energy of formation for main hydrates and equilibrium constant of main reactions in MOS cement system based on a first principle calculation using Material Studio. Followingly, the equilibrium phase compositions of MOS cement system were simulated through PHREEQC to investigate the molar ratio dependence of equilibrium phase compositions. Results showed that large M (MgO/MgSO₄) was beneficial for the formation of 5Mg(OH)₂·MgSO₄·7H₂O (Phase 517) and large H (H₂O/MgSO₄) tended to decompose MOS cement paste and cause leaching. The microstructure-based method visualized the hydration status of MOS cement systems at initial and ultimate stages via MATLAB and the results showed that large M was significant to reduce porosity, and similar results for the case of small H. Fractal analysis confirms that fractal dimension of pore structure (D_f) was significantly decreased after the hydration of MOS and was positively correlated to the porosity of the paste. In addition, it can be referred that large M and small H were beneficial for modifying the microstructure of MOS paste by decreasing the value of D_f.