Ambient Room Temperature Phosphorescence and Thermally Activated Delayed Fluorescence from a Core-Substituted Pyromellitic Diimide Derivative

被引:0
|
作者
Kuila, Suman [1 ,2 ]
Garain, Swadhin [1 ,2 ]
Banappanavar, Gangadhar [3 ]
Garain, Bidhan Chandra [4 ]
Kabra, Dinesh [3 ]
Pati, Swapan K. [4 ]
George, Subi J. [1 ,2 ]
机构
[1] Jawaharlal Nehru Ctr Adv Sci Res JNCASR, New Chem Unit, Bangalore 560064, Karnataka, India
[2] Jawaharlal Nehru Ctr Adv Sci Res JNCASR, Sch Adv Mat SAMat, Bangalore 560064, Karnataka, India
[3] Indian Inst Technol, Dept Phys, Mumbai 400076, Maharashtra, India
[4] Jawaharlal Nehru Ctr Adv Sci Res JNCASR, Theoret Sci Unit, Bangalore 560064, Karnataka, India
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2021年 / 125卷 / 17期
关键词
STATE; MECHANISM; POLYMER;
D O I
10.1021/acs.jpcb.1c02253
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
Triplet harvesting under ambient conditions plays a crucial role in improving the luminescence efficiency of purely organic molecular systems. This requires elegant molecular designs that can harvest triplets either via room temperature phosphorescence (RTP) or by thermally activated delayed fluorescence (TADF). In this context, here we report a donor core-substituted pyromellitic diimide (acceptor) derivative as an efficient charge-transfer molecular design from the arylene diimide family as a triplet emitter. Solution-processed thin films of carbazole-substituted CzPhPmDI display both RTP- and TADF-mediated twin emission with a long lifetime and high efficiency under ambient conditions. The present study not only sheds light on the fundamental photophysical process involved in the triplet harvesting of donor-acceptor organic systems, but also opens new avenues in exploring an arylene diimide class of molecules as potential organic light-emitting materials.
引用
收藏
页码:4520 / 4526
页数:7
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