Excellent Crystallinity and Stability Covalent-Organic Frameworks with High Emission and Anions Sensing.

Covalent-organic frameworks (COFs) are a new class of porous crystalline frameworks with high π-conjugation and periodical skeletons. The highly ordered π-conjugation structures in some COFs allow exciton migration and energy transfer over the frameworks, which leads to good fluorescence probing ability. In this work, two COFs (TFHPB-TAPB-COF and TFHPB-TTA-COF) are successfully condensed via the Schiff base condensation reaction. The intramolecular hydrogen bonds between imine bonds and hydroxyl groups form the excited-state intramolecular proton transfer (ESIPT) strategy. Owing to intramolecular hydrogen bonds in the skeleton, the two COFs show high crystallinity, remarkable stability, and excellent luminescence. The COFs represent a good sensitivity and selectivity to fluoride anions via fluorescence turn-off. Other halogen anions (chloride, bromide, and iodine) and acid anions (nitrate and hydrogen carbonate) remain inactive. These results imply that only fluoride anion is capable of opening the hydrogen bond interaction and hence break the ESIPT strategy. The detection limit toward fluoride anion is down to nanomoles level, ranking the best performances among fluoride anion sensors systems.

Effect of Polymer Encapsulation on the Mechanoluminescence of Mn2+-Doped CaZnOS.

Rare earth and transition metal ion-doped CaZnOS has garnered significant attention for its exceptional mechanoluminescence (ML) performance under mild mechanical stimuli and its capability for multicolor emissions. Since powdered phosphors are not directly usable, they require encapsulation within with polymers to create stable structures. This study investigates Mn2+-doped CaZnOS (CaZnOS:Mn2+) as the ML phosphor, optimizing its performance by varying the Mn2+ content, resulting in bright orange-red emissions from the d-d transitions of the Mn2+ activator. A quantum efficiency of 59.08% was achieved through the self-sensitization of the matrix lattice and energy transfer to the Mn2+ luminescent centers. The enhancement in ML due to Mn2+ doping is attributed to the reduced trap depth and increased trap concentration. Encapsulation with four polymers-PDMS, PU, SIL, and RTV-2-was explored to further optimize ML performance. Among these, PDMS provides the best ML output and sensitivity, owing to its slightly cross-linked structure and good triboelectric properties. The optimized CaZnOS:0.03Mn2+/PDMS composite, featuring excellent flexibility and recoverability, shows great potential for applications in anti-counterfeiting encryption, stress sensors, and wearable devices.

Vinylene-Linked Emissive Covalent Organic Frameworks for White-Light-Emitting Diodes.

Covalent organic frameworks (COFs) have gained considerable attention due to their highly conjugated π-skeletons, rendering them promising candidates for the design of light-emitting materials. In this study, we present two vinylene-linked COFs, namely, VL-COF-1 and VL-COF-2, which were synthesized through the Knoevenagel condensation of 2,4,6-trimethyl-1,3,5-triazine with terephthalaldehyde or 4,4'-biphenyldicarboxaldehyde. Both VL-COF-1 and VL-COF-2 exhibited excellent chemical and thermal stability. The presence of vinylene linkages between the constituent building blocks in these COFs resulted in broad excitation and emission properties. Remarkably, the designed VL-COFs demonstrated bright emission, fast fluorescence decay, and high stability, making them highly attractive for optoelectronic applications. To assess the potential of these VL-COFs in practical devices, we fabricated white-light-emitting diodes (WLEDs) coated with VL-COF-1 and VL-COF-2. Notably, the WLEDs coated with VL-COF-1 achieved high-quality white light emission, closely approximating standard white light. The promising performance of VL-COF-coated WLEDs suggests the feasibility of utilizing COF materials for stable and efficient lighting applications.

Combinatorial optimization of La, Ce-co-doped pyrosilicate phosphors as potential scintillator materials.

A combinatorial method was employed to rapidly screen the effects of La, Ce-co-doping on the luminescent properties of Gd2Si2O7 pyrosilicate using an 8 × 8 library. The candidate formulations (Gd1-x-yLax)2Si2O7:Ce2y were evaluated by luminescence pictures under ultraviolet excitation. The optimal composition was found to be (Gd0.89La0.1)2Si2O7:Ce0.02 after scaled-up preparation and detailed characterization of powder samples, which shows an excellent light output under both ultraviolet and X-ray excitation (about 5.43 times of commercial YAG:Ce powders). The XRD results indicate that the phase structure sequence is tetragonal-orthorhombic-triclinic for different calcination temperatures and doping ions. The (Gd0.89La0.1)2Si2O7:Ce0.02 powder sample also demonstrated excellent temperature stability of luminescence up to 200 °C and a short decay time of several tens of nanoseconds, suggesting that this may represent a new kind of scintillation material, such as single crystals, ceramics, glass, or phosphors.