Highly Luminescent Aluminum Complex with β-Diketone Ligands Exhibiting Near-Unity Photoluminescence Quantum Yield, Thermally Activated Delayed Fluorescence, and Rapid Radiative Decay Rate Properties in Solution-Processed Organic Light-Emitting Devices

被引:18
|
作者
Matsuya, Misaki [1 ]
Sasabe, Hisahiro [1 ,2 ,3 ]
Sumikoshi, Shunsuke [1 ]
Hoshi, Keigo [1 ]
Nakao, Kohei [1 ]
Kumada, Kengo [1 ]
Sugiyama, Ryo [1 ]
Sato, Ryoma [1 ]
Kido, Junji [1 ,2 ]
机构
[1] Yamagata Univ, Dept Organ Mat Sci, 4-3-16 Jonan, Yonezawa, Yamagata 9928510, Japan
[2] Yamagata Univ, Res Ctr Organ Elect ROEL, 4-3-16 Jonan, Yonezawa, Yamagata 9928510, Japan
[3] Yamagata Univ, Frontier Ctr Organ Mat FROM, 4-3-16 Jonan, Yonezawa, Yamagata 9928510, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
Organic light-emitting devices; Thermally activated delayed fluorescence (TADF); -diketone ligands; HIGH-EFFICIENCY; HOST MATERIALS; EMITTERS; DIODES; CONVERSION; OLEDS;
D O I
10.1246/bcsj.20220327
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A highly luminescent mononuclear Al complex with beta-diketone ligands exhibiting superior thermally activated de-layed fluorescence (TADF) properties was developed in this work. The complex showed yellow emission with promising photofunctions, including a near-unity photoluminescence quantum yield (PLQY), a rapid radiative decay rate, and a short delayed fluorescence lifetime in the solid state. When applied in a solution-processed organic light-emitting device, an external quantum efficiency (EQE) exceeding 18% and a low turn-on voltage of 2.9 V at 1 cd/m2 were obtained, sur-passing those of the corresponding beta-diketone ligand. Metal complexation with Al generated unique electronic structures that significantly strengthened the photofunctions of the origi-nal beta-diketone ligand in the solid state.
引用
收藏
页码:183 / 189
页数:7
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