Long-lived Triplet Excitons Allowed by Intermolecular Hydrogen Bonding in Amorphous Matrix

被引:5
|
作者
Tsubomoto, Yuichiro [1 ]
Hirata, Shuzo [2 ]
Totani, Kenro [1 ]
Vacha, Martin [2 ]
Watanabe, Toshiyuki [1 ]
机构
[1] Tokyo Univ Agr & Technol, Grad Sch Engn, Dept Appl Chem, Koganei, Tokyo 1848588, Japan
[2] Tokyo Inst Technol, Grad Sch Sci & Engn, Dept Organ & Polymer Mat, Meguro Ku, Tokyo 1528552, Japan
关键词
room-temperature phosphorescence; triplet exciton; long lifetime; hydrogen bonding; triplet excited state; ROOM-TEMPERATURE PHOSPHORESCENCE; ORGANIC MATERIALS; DELAYED FLUORESCENCE; EFFICIENT; LIGHT;
D O I
10.2494/photopolymer.28.573
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A purely organic guest material with a long triplet excited state lifetime (tau > 1 s) was doped into two different pi-conjugated amorphous hosts with similar glass transition temperatures (T-g). The phosphorescence quenching behavior of the guest material was investigated under vacuum conditions. When doped into a host that did not exhibit intermolecular hydrogen bonding, the tau of the guest decreased significantly at temperatures below the T-g of the host. Conversely, when doped into a host that did exhibit intermolecular hydrogen bonding, the tau remained almost unaffected at temperatures below the T-g of the host. The diffusion coefficient of oxygen, which was largely removed from the host materials under vacuum, was similar for both host materials. These results indicated that weak thermal diffusional motion of a host material intrinsically quenches long-lived triplet excitons of purely organic guest materials.
引用
收藏
页码:573 / 577
页数:5
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