TY - JOUR
T1 - Diarylboron-Based Asymmetric Red-Emitting Ir(III) Complex for Solution-Processed Phosphorescent Organic Light-Emitting Diode with External Quantum Efficiency above 28%
AU - Yang, Xiaolong
AU - Guo, Haoran
AU - Liu, Boao
AU - Zhao, Jiang
AU - Zhou, Guijiang
AU - Wu, Zhaoxin
AU - Wong, Wai Yeung
N1 - Funding Information:
The authors gratefully acknowledge the financial support from the National Natural Science Foundation of China (Grant Nos. 21602170 and 21572176), the Natural Science Foundation of Shaanxi Province (Grant No. 2016JQ2011), the China Postdoctoral Science Foundation (Grant Nos. 2015M580831 and 20130201110034), the Fundamental Research Funds for the Central Universities (Grant Nos. xjj2016061 and cxtd2015003), and the Creative Scientific Research Team in Yulin City.
PY - 2018/5
Y1 - 2018/5
N2 - Organic light-emitting diodes (OLEDs) are one of the most promising technologies for future displays and lighting. Compared with the blue and green OLEDs that have achieved very high efficiencies by using phosphorescent Ir(III) complexes, the red OLEDs still show relatively low efficiencies because of the lack of high-performance red-emitting Ir(III) complexes. Here, three highly efficient asymmetric red-emitting Ir(III) complexes with two different cyclometalating ligands made by incorporating only one electron-deficient triarylboron group into the nitrogen heterocyclic ring are reported. These complexes show enhanced photoluminescence quantum yields up to 0.96 and improved electron transporting capacity. In addition, the asymmetric structure can help to improve the solubility of Ir(III) complexes, which is crucial for fabricating OLEDs using the solution method. The photoluminescent and oxidation–reduction properties of these Ir(III) complexes are investigated both experimentally and theoretically. Most importantly, a solution-processed red OLED achieves extremely high external quantum efficiency, current efficiency, and power efficiency with values of 28.5%, 54.4 cd A−1, and 50.1 lm W−1, respectively, with very low efficiency roll-off. Additionally, the related device has a significantly extended operating lifetime compared with the reference device. These results demonstrate that the asymmetric diarylboron-based Ir(III) complexes have great potential for fabricating high-performance red OLEDs.
AB - Organic light-emitting diodes (OLEDs) are one of the most promising technologies for future displays and lighting. Compared with the blue and green OLEDs that have achieved very high efficiencies by using phosphorescent Ir(III) complexes, the red OLEDs still show relatively low efficiencies because of the lack of high-performance red-emitting Ir(III) complexes. Here, three highly efficient asymmetric red-emitting Ir(III) complexes with two different cyclometalating ligands made by incorporating only one electron-deficient triarylboron group into the nitrogen heterocyclic ring are reported. These complexes show enhanced photoluminescence quantum yields up to 0.96 and improved electron transporting capacity. In addition, the asymmetric structure can help to improve the solubility of Ir(III) complexes, which is crucial for fabricating OLEDs using the solution method. The photoluminescent and oxidation–reduction properties of these Ir(III) complexes are investigated both experimentally and theoretically. Most importantly, a solution-processed red OLED achieves extremely high external quantum efficiency, current efficiency, and power efficiency with values of 28.5%, 54.4 cd A−1, and 50.1 lm W−1, respectively, with very low efficiency roll-off. Additionally, the related device has a significantly extended operating lifetime compared with the reference device. These results demonstrate that the asymmetric diarylboron-based Ir(III) complexes have great potential for fabricating high-performance red OLEDs.
KW - asymmetric Ir(III) complexes
KW - diarylboron
KW - high efficiency diodes
KW - red phosphor
KW - solution-processed organic light-emitting diodes
UR - http://www.scopus.com/inward/record.url?scp=85043233361&partnerID=8YFLogxK
U2 - 10.1002/advs.201701067
DO - 10.1002/advs.201701067
M3 - Journal article
AN - SCOPUS:85043233361
SN - 2198-3844
VL - 5
JO - Advanced Science
JF - Advanced Science
IS - 5
M1 - 1701067
ER -