Efficient Light-Emitting Devices Based on Platinum-Complexes-Anchored Polyhedral Oligomeric Silsesquioxane Materials
Source abstract
Abstract
The synthesis, photophysical, and electrochemical characterization of macromolecules, consisting of an emissive platinum complex and carbazole moieties covalently attached to a polyhedral oligomeric silsesquioxane (POSS) core, is reported. Organic light-emitting devices based on these POSS materials exhibit a peak external quantum efficiency of ca. 8%, which is significantly higher than that of the analogous devices with a physical blend of the platinum complexes and a polymer matrix, and they represent noticeable improvement in the device efficiency of solution-processable phosphorescent excimer devices. Furthermore, the ratio of monomer and excimer/aggregate electroluminescent emission intensity, as well as the device efficiency, increases as the platinum complex moiety presence on the POSS macromolecules decreases.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Silicone and Siloxane Chemistry · Organic Light-Emitting Diodes Research · Semiconductor materials and devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials, Advanced Photovoltaic Center, Arizona State University, Tempe, Arizona, 85287-6006
Nitto Denko Technical Corporation, 501 Via Del Monte, Oceanside, California 92058
References (35)
Show source-provided references
1. Tang C. W. · Appl. Phys. Lett. · 1987 · 51 · 91310.1063/1.98799 ↗
2. Burroughes J. H. · Nature · 1990 · 347 · 53910.1038/347539a0 ↗
3. Singh M. · Adv. Mater. · 2010 · 22 · 67310.1002/adma.200901141 ↗
4. Laine R. M. · J. Mater. Chem. · 2005 · 15 · 372510.1039/b506815k ↗
5. Chan K. L. · J. Mater. Chem. · 2009 · 19 · 910310.1039/b909234j ↗
6. Sellinger A. · Chem. Commun. · 2005 · 29 · 370010.1039/b505048k ↗
7. Chen K. B. · Thin Solid Films. · 2006 · 504 · 10310.1016/j.tsf.2006.02.059 ↗
8. Froehlich J. D. · Chem. Mater. · 2007 · 19 · 499110.1021/cm070726v ↗
9. Lo M. Y. · J. Am. Chem. Soc. · 2007 · 129 · 580810.1021/ja070471m ↗
10. Yang X. H. · Adv. Funct. Mater. · 2009 · 19 · 262310.1002/adfm.200900050 ↗
11. Singh M. · Soft. Mater. · 2009 · 5 · 300210.1039/b903531a ↗
12. Ma B. W. · Adv. Funct. Mater. · 2006 · 16 · 243810.1002/adfm.200600614 ↗
13. Williams E. L. · Adv. Mater. · 2007 · 19 · 19710.1002/adma.200602174 ↗
14. Cocchi M. · Appl. Phys. Lett. · 2007 · 90 · 16350810.1063/1.2722675 ↗
15. Yang X. H. · Adv. Mater. · 2008 · 20 · 240510.1002/adma.200702940 ↗
16. Yang X. H. · Appl. Phys. Lett. · 2008 · 93 · 19330510.1063/1.3013324 ↗
17. Furuta P. T. · J. Am. Chem. Soc. · 2004 · 126 · 1538810.1021/ja0446247 ↗
18. Cho J. Y. · Organometallics · 2007 · 26 · 481610.1021/om700373c ↗
19. You Y. M. · J. Am. Chem. Soc. · 2005 · 127 · 1243810.1021/ja052880t ↗
20. Lohse O. · Synlett. · 1999 · 1 · 4510.1055/s-1999-2533 ↗
21. Xu M. L. · Appl. Organomet. Chem. · 2005 · 19 · 122510.1002/aoc.985 ↗
22. Brooks J. · Inorg. Chem. · 2002 · 41 · 305510.1021/ic0255508 ↗
23. Cockburn B. N. · J. Chem. Soc. Dalton. Trans. · 1973 · 4 · 40410.1039/DT9730000404 ↗
24. Davis R. B. · J. Am. Chem. Soc. · 1955 · 77 · 328410.1021/ja01617a039 ↗
25. Vaeth K. M. · J. Appl. Phys. · 2002 · 92 · 344710.1063/1.1501748 ↗
26. Yang X. H. · Adv. Mater. · 2004 · 16 · 16110.1002/adma.200305621 ↗
27. Yang X. H. · Appl. Phys. Lett. · 2004 · 84 · 247610.1063/1.1691194 ↗
28. Wu F. I. · J. Mater. Chem. · 2005 · 15 · 103510.1039/b415754k ↗
29. Wu F. I. · J. Phys. Chem. B · 2005 · 109 · 1400010.1021/jp051747k ↗
30. Wu F. I. · Macromolecules · 2005 · 38 · 902810.1021/ma051842r ↗
31. Yang X. H. · Appl. Phys. Lett. · 2006 · 88 · 02110710.1063/1.2162693 ↗
32. Yang X. H. · Adv. Mater. · 2006 · 18 · 94810.1002/adma.200501867 ↗
33. Yang X. H. · Adv. Funct. Mater. · 2006 · 16 · 215610.1002/adfm.200500834 ↗
34. Zacharias P. · Angew. Chem., Int. Ed. · 2007 · 46 · 438810.1002/anie.200605055 ↗
35. Huang F. · Adv. Mater. · 2007 · 19 · 201010.1002/adma.200602967 ↗