Geometrically isomeric [Ir(C^N)(C’^N’)(N’’^O)-tris-heteroleptic [Ir(dFppy)(CN-ppz)(pic)] Ir(III)-complexes with blue-light: Forwards to efficient blue organic light-emitting diodes
Siyu Hou , Baowen Wang , Yan Zhang , Hui Chang , Xingqiang Lü , Guorui Fu , Hongyang Zhang
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引用次数: 0
Abstract
Despite the great success of Ir(III)-complex-based green/red-light OLEDs (OLED = organic light-emitting diode), the realization of their efficient blue-OLEDs is far behind and challenging. Herein, using HdFppy (2-(2,4-difluorophenyl)pyridine) and CN-ppzH (4-(1H-pyrazol-1-yl)benzonitrile) as the HC^N/HC’^N’ ligands and Hpic (2-picolinic acid) as the N’’^O-ancillary ligand, the [Ir(C^N)(C’^N’)(N’’^O)]-tris-heteroleptic molecular design strategy was adopted, obtaining the two [Ir(dFppy)(CN-ppz)(pic)]-configured blue-emitting (λPL (photoluminescence emission peak) = 466, 496(sh) nm; ΦPL (photoluminescence quantum efficiency) = 0.41–0.46) geometrical isomers 1a and 1b. Further through the doped and vacuum-deposited fabrication, their blue-OLEDs-1A/1B with the LMax (maximum luminance) values up to 18090–22528 cd/m2 and the ηEQEMax (maximum external quantum efficiency) sizes of 7.99–8.42 %, were realized, respectively. This study result shows that [Ir(dFppy)(CN-ppz)(pic)]-included [Ir(C^N)(C’^N’)(N’’^O)]-tris-heteroleptic Ir(III)-complexes can be used as the attractive blue-phosphor candidates forwards to efficient blue-OLEDs.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.