Wang Yixuan, Yin Yanfeng, Yang Binhao, Tian Wenming, Yang Xinyi, Zou Bo
Synergetic Extreme Condition High-Pressure Science Center, State Key Laboratory of Superhard Materials, College of Physics, Jilin University, Changchun 130012, China.
State Key Laboratory of Molecular Reaction Dynamics and the Dynamic Research Center for Energy and Environmental Materials, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Nano Lett. 2025 Feb 12;25(6):2141-2149. doi: 10.1021/acs.nanolett.4c04949. Epub 2025 Jan 23.
Covalent-organic frameworks (COFs) are dynamic covalent porous organic materials constructed from emissive molecular organic building blocks. However, most two-dimensional (2D) COFs are nonemissive or weakly emissive in the solid state owing to the intramolecular rotation and vibration together with strong π-π interactions. Herein, we report a pressure strategy to achieve the bright multicolor emission from yellow to red in the 2D triazine triphenyl imine COF (TTI-COF). Intriguingly, the TTI-COF experiences a 24-fold enhancement under a mild pressure of 2.7 GPa compared with the initial state. Joint experimental and theoretical results reveal that the restricted intramolecular chemical bond vibrations and the reduced π-π interactions originating from the offset stacking mode account for the significant pressure-induced emission enhancement. Furthermore, such piezochromic behavior may be ascribed to the decreased energy gap and enhanced intermolecular interaction. Our investigation offers constructive guidelines for designing 2D COF materials with high photoluminescence performance.
共价有机框架(COFs)是由发光分子有机结构单元构建而成的动态共价多孔有机材料。然而,由于分子内旋转和振动以及强π-π相互作用,大多数二维(2D)COFs在固态下是非发光的或弱发光的。在此,我们报道了一种压力策略,以实现二维三嗪三苯基亚胺COF(TTI-COF)从黄色到红色的明亮多色发射。有趣的是,与初始状态相比,TTI-COF在2.7 GPa的温和压力下发射增强了24倍。联合实验和理论结果表明,受限的分子内化学键振动以及源自错位堆积模式的π-π相互作用的减少是压力诱导发射显著增强的原因。此外,这种压致变色行为可能归因于能隙减小和分子间相互作用增强。我们的研究为设计具有高光致发光性能的二维COF材料提供了建设性的指导方针。