journal article·2014-10-22

Constructive Effects of Long Alkyl Chains on the Electroluminescent Properties of Cationic Iridium Complex-Based Light-Emitting Electrochemical Cells

Chozhidakath Damodharan Sunesh, George Mathai, Youngson Choe

Publisher page

Abstract

A series of cationic iridium complexes (1-6) were synthesized using alkylated imidazole-based ancillary ligands, and the photophysical and electrochemical properties of these complexes were subsequently evaluated. Light-emitting electrochemical cells (LECs) were fabricated from these complexes, and the effects of the alkyl chain length on the electroluminescent properties of the devices were investigated. The LECs based on these complexes resulted in yellow emission (complexes 1, 3, and 5) and green emission (complexes 2, 4, and 6) with Commission Internationale de L'Eclairage (CIE) coordinates of (0.49, 0.50) and (0.33, 0.59), respectively. Our results indicate that the luminance and efficiency of the LECs can consistently be enhanced by increasing the alkyl chain length of the iridium complexes as a result of suppressed intermolecular interaction and self-quenching. Subsequently, a high luminance of 7309 cd m(-2) and current efficiency of 3.85 cd A(-1) were achieved for the LECs based on complex 5.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Conducting polymers and applications · Organic Electronics and Photovoltaics

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Polymer Science and Chemical Engineering, Pusan National University, Busan 609-735, South Korea

Department of Chemistry, Sacred Heart College, Thevara, Kochi 682-013, India

Funding

National Research Foundation of Korea

References (53)

Show source-provided references
1. Pei Q. · Science · 1995 · 269 · 108610.1126/science.269.5227.1086 ↗
2. Sun Q. J. · J. Disp. Technol. · 2007 · 3 · 21110.1109/JDT.2007.896737 ↗
3. Lee J. K. · Appl. Phys. Lett. · 1996 · 69 · 168610.1063/1.117028 ↗
4. Slinker J. · Chem. Commun. · 2003 · 19 · 239210.1039/B304265K ↗
5. Slinker J. D. · J. Mater. Chem. · 2007 · 17 · 297610.1039/B704017B ↗
6. deMello J. C. · Phys. Rev. B · 1998 · 57 · 1295110.1103/PhysRevB.57.12951 ↗
7. Rudmann H. · J. Appl. Phys. · 2001 · 90 · 433810.1063/1.1409577 ↗
8. Gao F. G. · J. Am. Chem. Soc. · 2000 · 122 · 742610.1021/ja000666t ↗
9. Bolink H. J. · Inorg. Chem. · 2005 · 44 · 596610.1021/ic0507058 ↗
10. Kalyuzhny G. · J. Am. Chem. Soc. · 2003 · 125 · 627210.1021/ja029550i ↗
11. Soltzberg L. J. · J. Am. Chem. Soc. · 2006 · 128 · 776110.1021/ja055782g ↗
12. Lyons C. H. · J. Am. Chem. Soc. · 1998 · 120 · 1210010.1021/ja981057c ↗
13. Gao F. G. · Chem. Mater. · 2002 · 14 · 346510.1021/cm020117h ↗
14. Hosseini A. R. · Chem. Mater. · 2005 · 17 · 611410.1021/cm050986h ↗
15. Armaroli N. · Adv. Mater. · 2006 · 18 · 131310.1002/adma.200502365 ↗
16. Kalsani V. · Inorg. Chem. · 2006 · 45 · 206110.1021/ic051828v ↗
17. Zhang Q. S. · Adv. Funct. Mater. · 2006 · 16 · 120310.1002/adfm.200500691 ↗
18. Felici M. · Molecules · 2010 · 15 · 203910.3390/molecules15032039 ↗
19. Slinker J. D. · J. Am. Chem. Soc. · 2004 · 126 · 276310.1021/ja0345221 ↗
20. Costa R. D. · Adv. Energy Mater. · 2011 · 1 · 28210.1002/aenm.201000069 ↗
21. He L. · Chem. Commun. · 2011 · 47 · 646710.1039/c1cc11263e ↗
22. Chen B. · Org. Electron. · 2011 · 12 · 76610.1016/j.orgel.2011.02.006 ↗
23. Sun L. · J. Mater. Chem. · 2011 · 21 · 1808310.1039/c1jm12984h ↗
24. Zhang J. · Adv. Funct. Mater. · 2013 · 23 · 466710.1002/adfm.201300344 ↗
25. Kessler F. · Dalton Trans. · 2012 · 41 · 18010.1039/C1DT10698H ↗
26. Sunesh C. D. · Mater. Chem. Phys. · 2012 · 136 · 17310.1016/j.matchemphys.2012.06.048 ↗
27. Tordera D. · J. Mater. Chem. · 2012 · 22 · 1926410.1039/c2jm33969b ↗
28. Sunesh C. D. · Polyhedron · 2013 · 57 · 7710.1016/j.poly.2013.04.029 ↗
29. Costa R. D. · Chem. Commun. · 2011 · 47 · 320710.1039/c0cc05084a ↗
30. Sunesh C. D. · Opt. Mater. · 2013 · 35 · 40710.1016/j.optmat.2012.09.023 ↗
31. Meier S. B. · J. Mater. Chem. C · 2013 · 1 · 5810.1039/C2TC00251E ↗
32. Chen B. · Org. Electron. · 2013 · 14 · 74410.1016/j.orgel.2012.12.026 ↗
33. Sunesh C. D. · Org. Electron. · 2014 · 15 · 66710.1016/j.orgel.2013.12.026 ↗
34. Su H. · Adv. Funct. Mater. · 2007 · 17 · 101910.1002/adfm.200600372 ↗
35. He L. · Adv. Funct. Mater. · 2009 · 19 · 295010.1002/adfm.200900723 ↗
36. Costa R. D. · Adv. Funct. Mater. · 2009 · 19 · 345610.1002/adfm.200900911 ↗
37. Liao C. T. · Phys. Chem. Chem. Phys. · 2012 · 14 · 126210.1039/C1CP23336J ↗
38. Costa R. D. · Chem. Commun. · 2009 · 388610.1039/b905367k ↗
39. Costa R. D. · Chem.—Eur. J. · 2010 · 16 · 985510.1002/chem.201000600 ↗
40. Liao C. T. · Phys. Chem. Chem. Phys. · 2012 · 14 · 977410.1039/c2cp40739f ↗
41. Su H. C. · J. Mater. Chem. · 2010 · 20 · 552110.1039/c0jm00429d ↗
42. Tamayo A. B. · Inorg. Chem. · 2005 · 44 · 872310.1021/ic050970t ↗
43. Costa R. D. · Angew. Chem., Int. Ed. · 2012 · 51 · 817810.1002/anie.201201471 ↗
44. Hu T. · J. Mater. Chem. · 2012 · 22 · 420610.1039/c2jm16185k ↗
46. Hwang S. W. · Macromolecules · 2001 · 34 · 298110.1021/ma001855z ↗
47. Nonoyama M. · Bull. Chem. Soc. Jpn. · 1974 · 47 · 76710.1246/bcsj.47.767 ↗
48. Sprouse S. · J. Am. Chem. Soc. · 1984 · 106 · 664710.1021/ja00334a031 ↗
49. He L. · Adv. Funct. Mater. · 2008 · 18 · 212310.1002/adfm.200701505 ↗
50. Colombo M. G. · Inorg. Chem. · 1993 · 32 · 308110.1021/ic00066a019 ↗
51. Lowry M. S. · J. Am. Chem. Soc. · 2004 · 126 · 1412910.1021/ja047156+ ↗
52. Adachi C. · Appl. Phys. Lett. · 2001 · 79 · 208210.1063/1.1400076 ↗
53. Lowry M. S. · Chem. Mater. · 2005 · 17 · 571210.1021/cm051312+ ↗