High-efficiency turquoise-blue electrophosphorescence from a Pt(II)-pyridyltriazolate complex in a phosphine oxide host

被引:36
作者
Bhansali, Unnat S. [1 ]
Polikarpov, Evgueni [2 ]
Swensen, James S. [2 ]
Chen, Wei-Hsuan [3 ]
Jia, Huiping [1 ]
Gaspar, Daniel J. [2 ]
Gnade, Bruce E. [1 ]
Padmaperuma, Asanga B. [2 ]
Omary, Mohammad A. [3 ]
机构
[1] Univ Texas Dallas, Dept Mat Sci & Engn, Richardson, TX 75083 USA
[2] Pacific NW Natl Lab, Energy & Environm Directorate, Richland, WA 99352 USA
[3] Univ N Texas, Dept Chem, Denton, TX 76203 USA
基金
美国国家科学基金会;
关键词
LIGHT-EMITTING DEVICES; ORGANIC ELECTROPHOSPHORESCENCE; ENERGY-TRANSFER; PHOSPHORESCENT EMISSION; TRIPLET ENERGY; CONFINEMENT; DIODES;
D O I
10.1063/1.3268434
中图分类号
O59 [应用物理学];
学科分类号
摘要
We demonstrate high-efficiency turquoise-blue electrophosphorescence from bis[3,5-bis(2-pyridyl)-1,2,4-triazolato]platinum(II) [Pt(ptp)(2)] doped in 4-(diphenyl-phosphoryl)-N, N-diphenylaniline (HM-Al). Organic light-emitting diodes (OLEDs) with 5% Pt(ptp)(2):HM-A1 attain peak power efficiency of 61.2 lm/W, versus 40.8 lm/W for analogous devices employing the standard turquoise-blue phosphor bis[4,6-difluorophenyl)-pyridinato-N,C-2'](picolinato)iridium(III) (FIrpic). Devices with x% Pt (ptp)(2): HM-A1 exhibit blue emission maxima (lambda(max) similar to 480 nm) with monotonic increase in excimer/monomer intensity ratio at higher doping levels within 1%-10%, causing color shift toward green and less charge balance. This work represents a significant step toward optimizing future white OLEDs from the same phosphor via combination of low-doped and higher-doped or neat films. (C) 2009 American Institute of Physics. [doi: 10.1063/1.3268434]
引用
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页数:3
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