Long-Lived Luminescence Emitted from Imide Compounds Dispersed in Polymer Matrices after Continuous Ultraviolet Irradiation and its Relation to Oxygen Quenching

被引:7
作者
Doi, Marina [1 ]
Ishige, Ryohei [1 ]
Ando, Shinji [1 ]
机构
[1] Tokyo Inst Technol, Dept Chem Sci & Engn, Ookayama,2 12 1 E4 5,Meguro ku, Tokyo 1528552, Japan
关键词
Host-guest systems; imide compounds; long-lived luminescence; polymers; room-temperature phosphorescence; singlet oxygen; ROOM-TEMPERATURE PHOSPHORESCENCE; SINGLET OXYGEN; DIFFUSION; FLUORESCENCE; PERMEABILITY; POLYIMIDES; EXCITATION; LIFETIME; HARD;
D O I
10.1002/cptc.202200310
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Long-lived room-temperature delayed phosphorescence, called prolonged irradiation-induced delayed luminescence (PIDL), was observed in air for three imide compounds (ICs) dispersed in polymethyl methacrylate under UV irradiation after an induction time of 1.60-6.78 min, whereas the ICs alone showed only fluorescence after a short period of UV irradiation. The PIDL emission continued as an afterglow for several seconds (0.36-1.30 s) after the irradiation was stopped. In the initial stage of irradiation, the ICs in the excited triplet state (T-1) generated via intersystem crossing were immediately quenched by ground state triplet molecular oxygen (O-3(2)), and the excited state energy of ICs was transferred by photosensitization to O-3(2), generating singlet oxygen (O-1(2)), causing a gradual depletion of the concentration of O-3(2) in the host matrix. When most of the O-3(2) adjacent to the ICs had been consumed, the ICs started to emit a PIDL. The induction time until the appearance of PIDL was linearly proportional to the O-3(2) concentration. Optical measurements and numerical simulations based on the Jablonski diagram support the PIDL generation mechanism and reveal the relationships between the rate constants and oxygen permeabilities of the host matrices.
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页数:15
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