Dynamic Transition between Monomer and Excimer Phosphorescence in Organic Near-Infrared Phosphorescent Crystals

被引:21
作者
Deng, Zihao [1 ,2 ]
Zhang, Jianyu [1 ,2 ]
Zhou, Jiaming [3 ]
Shen, Wei [4 ]
Zuo, Yunfei [1 ,2 ]
Wang, Jin [1 ,2 ]
Yang, Shengyi [1 ,2 ]
Liu, Junkai [1 ,2 ]
Chen, Yuyang [1 ]
Chen, Chun-Chao [2 ,4 ]
Jia, Guocheng [1 ,2 ]
Alam, Parvej [5 ]
Lam, Jacky W. Y. [1 ,2 ]
Tang, Ben Zhong [1 ,2 ,6 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Hong Kong Branch Chinese Natl Engn Res Ctr Tissue, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[3] Univ Hong Kong, Dept Mech Engn, Pokfulam Rd, Hong Kong, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, Shanghai 200240, Peoples R China
[5] Chinese Univ Hong Kong Shenzhen CUHK Shenzhen, Affiliated Hosp 2, Clin Translat Res Ctr Aggregat Induced Emiss, Sch Med,Sch Sci & Engn, Shenzhen 518172, Peoples R China
[6] Chinese Univ Hong Kong Shenzhen CUHK Shenzhen, Inst Aggregate Sci & Technol, Sch Sci & Engn, Shenzhen 518172, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
dynamic transition; excimer phosphorescence; near-infrared phosphors; noncovalent interactions; room-temperature phosphorescence; ROOM-TEMPERATURE PHOSPHORESCENCE; TRIPLET EXCITED-STATES; ENERGY-GAP LAW; EFFICIENCY; COLOR;
D O I
10.1002/adma.202311384
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Achieving efficient near-infrared room-temperature phosphorescence of purely organic phosphors remains scarce and challenging due to strong nonradiative decay. Additionally, the investigation of triplet excimer phosphorescence is rarely reported, despite the fact that excimer, a special emitter commonly formed in crystals with strong pi-pi interactions, can efficiently change the fluorescent properties of compounds. Herein, a series of dithienopyrrole derivatives with low triplet energy levels and stable triplet states, exhibiting persistent near-infrared room-temperature phosphorescence, is developed. Via the modification of halogen atoms, the crystals display tunable emissions of monomers from 645 to 702 nm, with a maximum lifetime of 3.68 ms under ambient conditions. Notably, excimer phosphorescence can be switched on at low temperatures, enabled by noncovalent interactions rigidifying the matrix and stabilizing triplet excimer. Unprecedentedly, the dynamic transition process is captured between the monomer and excimer phosphorescence with temperature variations, revealing that the unstable triplet excimers in crystals with a tendency to dissociate can result in the effective quench of room-temperature phosphorescence. Excited state transitions across varying environments are elucidated, interpreting the structural dynamics of the triplet excimer and demonstrating strategies for devising novel near-infrared phosphors. The novel phosphors are developed by the modification of dithienopyrrole, exhibiting efficient and persistent near-infrared room temperature phosphorescence. At low temperatures, excimer phosphorescence can be activated, enabled by the enhanced noncovalent interactions. With environmental variations, the dynamic transition process between the monomer and excimer phosphorescence is captured, establishing a framework to understand the photophysical mechanisms governing organic phosphorescence.image
引用
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页数:12
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