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一种基于咔唑的八元环分子骨架用于电致发光材料的开发。

An Eight-Membered Ring Molecular Framework Based on Carbazole for the Development of Electroluminescent Materials.

作者信息

Yan An, Xu Shipan, Du Xuyang, Zhu Chengyun, Li Shengli, Yang Xiaolong, Zhou Guijiang, Sun Yuanhui

机构信息

School of Chemistry, Xi'an Key Laboratory of Sustainable Energy Material Chemistry, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, Xi'an Jiaotong University, Xi'an 710049, China.

出版信息

Molecules. 2025 Feb 5;30(3):716. doi: 10.3390/molecules30030716.

DOI:10.3390/molecules30030716
PMID:39942822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11819814/
Abstract

The organic light-emitting diode (OLED) has been regarded as the most prominent product in the current market of organic electronics, which has attracted growing attention because of their applications in full-color displays and solid-state lighting. Organic materials that exhibit strong luminescence in the solid state constitute the core position of OLED. Extensive research efforts to probe the structure of organic luminescent materials have attracted considerable attention to the conjugated fusion ring architecture. This is because it can confer molecular rigidity and helps to inhibit intermolecular interactions and non-radiative transitions, thus enhancing the performance of luminescent materials. Here, we use an efficient and simple method to construct an eight-membered ring molecular framework based on carbazole. Moreover, we have introduced groups with different electron-withdrawing abilities to develop a series of luminescent molecules. The results show that the nonplanar structure based on the eight-membered ring suppresses fluorescence quenching caused by molecular aggregation. As the doping concentration increases, the electroluminescence spectrum remains basically unchanged, indicating that the eight-membered ring structure can effectively suppress the intermolecular interaction. Notably, DCBz-pm exhibits deep blue emission with a Commission Internationale de l'Eclairage (CIE) coordinate of (0.158, 0.046), which nearly meets the BT. 2020 standards. The DCBz-CN device reaches a maximum external quantum efficiency (EQE) of 4.36%. These results offer a new design strategy for improving the performance of OLEDs.

摘要

有机发光二极管(OLED)被认为是当前有机电子市场上最突出的产品,由于其在全彩显示器和固态照明中的应用而受到越来越多的关注。在固态中表现出强发光的有机材料构成了OLED的核心地位。对有机发光材料结构进行探测的广泛研究工作引起了人们对共轭稠合环结构的相当关注。这是因为它可以赋予分子刚性,并有助于抑制分子间相互作用和非辐射跃迁,从而提高发光材料的性能。在此,我们使用一种高效且简单的方法构建了基于咔唑的八元环分子框架。此外,我们引入了具有不同吸电子能力的基团来开发一系列发光分子。结果表明,基于八元环的非平面结构抑制了由分子聚集引起的荧光猝灭。随着掺杂浓度的增加,电致发光光谱基本保持不变,这表明八元环结构可以有效抑制分子间相互作用。值得注意的是,DCBz-pm呈现出深蓝色发射,其国际照明委员会(CIE)坐标为(0.158, 0.046),几乎符合BT. 2020标准。DCBz-CN器件的最大外量子效率(EQE)达到4.36%。这些结果为提高OLED性能提供了一种新的设计策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/4dd5fc5c86f1/molecules-30-00716-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/4e61b547ffdb/molecules-30-00716-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/0cbe08d41b91/molecules-30-00716-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/bc643620b896/molecules-30-00716-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/5fe0f2d13416/molecules-30-00716-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/b4fda12c1814/molecules-30-00716-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/7a309a767bc0/molecules-30-00716-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/b3e0ce347922/molecules-30-00716-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/4a89af1606e2/molecules-30-00716-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/e36888c82052/molecules-30-00716-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/2fb84723d8dd/molecules-30-00716-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/9ecd2bc1ad48/molecules-30-00716-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/4dd5fc5c86f1/molecules-30-00716-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/4e61b547ffdb/molecules-30-00716-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/0cbe08d41b91/molecules-30-00716-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/bc643620b896/molecules-30-00716-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/5fe0f2d13416/molecules-30-00716-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/b4fda12c1814/molecules-30-00716-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/7a309a767bc0/molecules-30-00716-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/b3e0ce347922/molecules-30-00716-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/4a89af1606e2/molecules-30-00716-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/e36888c82052/molecules-30-00716-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/2fb84723d8dd/molecules-30-00716-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/9ecd2bc1ad48/molecules-30-00716-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc5/11819814/4dd5fc5c86f1/molecules-30-00716-g010.jpg

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