Phenanthroimidazole-Based Diphenylborane Dimers as Blue Emitters for OLEDs

被引:0
|
作者
Nayak, Prakash [1 ]
Mukherjee, Susmita [2 ]
Patel, Dhairya [1 ]
Mahapatra, Adya Anwesa [1 ]
Murali, Anna Chandrasekar [1 ]
Perumal, Ajay [2 ]
Venkatasubbaiah, Krishnan [1 ]
机构
[1] Natl Inst Sci Educ & Res NISER, OCC Homi Bhabha Natl Inst, Bhubaneswar 752050, Odisha, India
[2] Indian Inst Sci Educ & Res IISER, Dept Phys Sci, Funct NANO & Optoelect Lab FNOL, Berhampur 760010, Odisha, India
来源
ACS APPLIED OPTICAL MATERIALS | 2024年 / 2卷 / 08期
关键词
phenanthroimidazole; B-N coordination; tetra-coordinated boron compounds; blue emitters; OLEDs; POLYCYCLIC AROMATIC-HYDROCARBONS; AGGREGATION-INDUCED EMISSION; LIGHT-EMITTING-DIODES; OPTOELECTRONIC PROPERTIES; OPTICAL-PROPERTIES; BORON; FLUORESCENCE; SUBSTITUENT; MOLECULES; DESIGN;
D O I
10.1021/acsaom.4c00176
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Herein, the design and synthesis of pi-conjugated diphenylboron-doped phenanthroimidazole dimers having intramolecular B-N coordination have been reported, along with their unique photophysical properties. The synthesized compounds exhibit bright blue fluorescence with high solution-state quantum yields reaching up to 99%, and they retain a 38% quantum yield in the solid-state thin films. Encouraged by excellent photophysical properties, we used diphenylboron-doped phenanthroimidazole dimers as blue emitters in the organic light-emitting diode (OLED) devices. The OLED devices with a host-guest emission layer having the diphenylboron-doped phenanthroimidazole dimer (blue emitter) as a guest emitter (20 wt %) in a 4,4 '-bis(N-carbazoyl)-1,1 '-biphenyl (CBP) host exhibited a high external quantum efficiency of 3.41% with current and power efficiencies of 4.53 cd/A and 1.75 lm/W and a maximum brightness of 2159 cd/m2. The deep blue electroluminescence (EL) emission corresponds to CIE (x, y) coordinates of (0.16, 0.16) and shows the potential of diphenylboron-doped phenanthroimidazole dimers as the efficient deep blue class of emitter molecules in blue OLEDs.
引用
收藏
页码:1523 / 1532
页数:10
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