High efficiency and stable-yellow phosphorescence from OLEDs with a novel fluorinated heteroleptic iridium complex
Source abstract
Abstract
Abstract The performance of a heteroleptic bis-cyclometalated iridium complex based on 2-(2,3,4-trifluorophenyl)benzo[d]thiazole [(tfbt)2Ir(acac)] was investigated as a new phosphorescent emitter in OLEDs. The devices showed very high efficiency at various dopant concentrations and maximum efficiency was achieved at 6 wt% dopant concentration. A comparison of the performances of phosphorescent OLEDs with the new emitter versus those with prototype-based (bt)2Ir(acac) emitter revealed a remarkable improvement of efficiency at all dopant concentrations. These preliminary results obtained with the tfbt-based emitter indicate that this family of cyclometalated ligands with multi-fluorine functionalization is a promising compound for the development of highly emissive complexes.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Lanthanide and Transition Metal Complexes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (37)
Show source-provided references
1. Chi · Chem. Soc. Rev. · 2010 · 39 · 63810.1039/B916237B ↗
2. Fan · Chem. Soc. Rev. · 2014 · 43 · 643910.1039/C4CS00110A ↗
3. Ho · Coord. Chem. Rev. · 2013 · 257 · 161410.1016/j.ccr.2012.08.023 ↗
4. Panigati · Coord. Chem. Rev. · 2012 · 256 · 162110.1016/j.ccr.2012.03.006 ↗
5. You · Dalton Trans. · 2009 · 126710.1039/B812281D ↗
6. Ma · Synth. Met. · 1998 · 94 · 24510.1016/S0379-6779(97)04166-0 ↗
7. Baldo · Nature · 1998 · 395 · 15110.1038/25954 ↗
8. Lai · J. Mater. Chem. · 2011 · 21 · 498310.1039/c0jm04174b ↗
9. Peng · J. Mater. Chem. · 2011 · 21 · 355110.1039/c0jm03645e ↗
10. Shih · Appl. Phys. Lett. · 2006 · 88 · 25111010.1063/1.2214141 ↗
11. Chen · Appl. Phys. Lett. · 2007 · 91 · 02350510.1063/1.2757096 ↗
12. Li · Dalton Trans. · 2011 · 40 · 715310.1039/c1dt10305a ↗
13. Li · J. Mater. Chem. C · 2013 · 1 · 417110.1039/c3tc30586d ↗
14. Xiao · Synth. Met. · 2009 · 159 · 70510.1016/j.synthmet.2008.12.019 ↗
15. Xu · Synth. Met. · 2012 · 162 · 142110.1016/j.synthmet.2012.06.009 ↗
16. Liu · Dyes Pigm. · 2013 · 98 · 31710.1016/j.dyepig.2013.03.025 ↗
17. Li · Dyes Pigm. · 2014 · 106 · 5110.1016/j.dyepig.2014.02.025 ↗
18. Xiao · Synth. Met. · 2012 · 162 · 49710.1016/j.synthmet.2012.01.014 ↗
19. Li · Opt. Mater. · 2012 · 35 · 30010.1016/j.optmat.2012.09.002 ↗
20. Grushin · Chem. Commun. · 2001 · 21 · 149410.1039/b103490c ↗
21. Hu · Synth. Met. · 2008 · 158 · 91210.1016/j.synthmet.2008.06.012 ↗
22. Koech · Chem. Mater. · 2010 · 22 · 392610.1021/cm1002737 ↗
23. Wu · Dyes Pigm. · 2013 · 96 · 23710.1016/j.dyepig.2012.08.008 ↗
24. Xu · J. Mater. Chem. C · 2015 · 3 · 369410.1039/C5TC00073D ↗
25. Li · J. Phys. Chem. C · 2012 · 116 · 2050410.1021/jp3028929 ↗
26. Wang · Appl. Phys. Lett. · 2001 · 79 · 44910.1063/1.1384903 ↗
27. Chang · J. Organomet. Chem. · 2004 · 689 · 488210.1016/j.jorganchem.2004.07.003 ↗
28. Laskar · Chem. Mater. · 2004 · 16 · 11110.1021/cm030410x ↗
29. Wang · Adv. Mater. · 2011 · 23 · 282310.1002/adma.201100302 ↗
30. Yun · Opt. Mater. · 2012 · 34 · 116510.1016/j.optmat.2012.01.024 ↗
31. Fan · J. Phys. Chem. C · 2013 · 117 · 1913410.1021/jp406220c ↗
32. Lin · Proc. SPIE · 2014 · 9183
33. Zhang · New J. Chem. · 2015
34. Nonoyama · Bull. Chem. Soc. Jpn. · 1974 · 47 · 76710.1246/bcsj.47.767 ↗
35. Lamansky · J. Am. Chem. Soc. · 2001 · 123 · 430410.1021/ja003693s ↗
36. Baldo · Phys. Rev. B · 2000 · 62 · 1096710.1103/PhysRevB.62.10967 ↗
37. Reineke · Phys. Rev. B · 2007 · 75 · 12532810.1103/PhysRevB.75.125328 ↗