材料科学
苝
二亚胺
发色团
光致发光
共价键
聚合物
纳米技术
超分子化学
多孔性
化学物理
发光
共价有机骨架
化学工程
组分(热力学)
分子
自组装
有机半导体
多孔介质
单晶
光化学
晶体工程
超短脉冲
光电子学
表征(材料科学)
作者
Ling Zhang,Zixuan Chen,Lukas Mühlnickel,Lukas Sporrer,Jakub D. Jasinski,Megha Koottungal,Kevin Synnatschke,Paul-Felix Jordan,Silvia Paasch,Eike Brunner,Zhehao Huang,Alexey Chernikov,Florian Auras
标识
DOI:10.1002/adma.202523646
摘要
ABSTRACT Two‐dimensional covalent organic frameworks (2D COFs) are crystalline porous polymers with highly tunable structural and electronic properties. Although single crystals of these materials are highly desirable for fundamental research and potential applications, their synthesis has so far been limited to only a few examples. We have developed a high‐temperature double‐modulator synthetic strategy that enables the growth of single crystals from fully dissolved precursors. We applied this approach to generate a series of perylene diimide (PDI)‐based 2D COFs. These materials crystallize as platelets with lateral dimensions reaching up to 50 µm for the biphenyl‐linked PDI(Me) 8 ‐2P COF, providing a suitable platform for studying electronic processes via micro‐spectroscopy. Photoluminescence (PL) measurements revealed ultrafast monomer‐like emission together with a slower excimer‐related component. The availability of COF single crystals further enabled polarization‐dependent measurements, which revealed that the fast PL component is linearly polarized due to the parallel orientation of the PDI chromophores in the frameworks. These findings highlight the importance of COF single crystals for elucidating structure—photophysical property relationships of these intriguing materials.
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