journal article·2020-12Open access

White Dendrimer Organic Light Emitting Diodes: Exciton Formation and Transfer

Lorenz Graf von Reventlow, Wei Jiang, Dani M. Stoltzfus, Steven M. Russell, Paul L. Burn, Alexander Colsmann

Advanced Optical Materials· Volume 8· Issue 24

Abstract

Abstract In this work solution‐processed organic white‐light emitting diodes comprising a blend of red and blue phosphorescent dendrimers are presented. In contrast to common small molecule blended‐dye organic light emitting diodes (OLEDs), the bulky dendrons between the light emitting moieties increase the spacing and hamper the transfer of excitons between the dyes. The reduced transfer of the excitons from the blue dye to the red dye enables greater control over OLED color avoiding the issue in which small variations in the concentration of the red dye can dramatically change the emission color. Thus, the approach leads to enhanced manufacturing reproducibility. Transient electroluminescence measurements provide detailed insights into the charge carrier and exciton formation and transfer dynamics within the device.
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Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials

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Affiliations

Karlsruhe Institute of Technology (KIT) Light Technology Institute Engesserstrasse 13 Karlsruhe 76131 Germany

Karlsruhe Institute of Technology (KIT) Material Research Center for Energy Systems Strasse am Forum 7 Karlsruhe 76131 Germany

Centre for Organic Photonics & Electronics The School of Chemistry and Molecular Biosciences The University of Queensland Queensland 4072 Australia

Funding

Australian Research Council · Bundesministerium für Bildung und Forschung

References (28)

Show source-provided references
1. Guo F. · Appl. Phys. Lett. · 2005 · 87 · 1
2. 10.1002/adma.20140033210.1002/adma.201400332 ↗
3. 10.1038/nature0800310.1038/nature08003 ↗
4. 10.1039/C1JM13846D10.1039/C1JM13846D ↗
5. Wu S. F. · Adv. Funct. Mater. · 2017 · 27 · 1
6. 10.1002/adma.20110475810.1002/adma.201104758 ↗
7. Zhang D. · Light: Sci. Appl. · 2015 · 4 · 1
8. 10.1039/C9QM00042A10.1039/C9QM00042A ↗
9. 10.1016/j.mser.2016.06.00110.1016/j.mser.2016.06.001 ↗
10. 10.1039/C7TC03134C10.1039/C7TC03134C ↗
11. Ding D. · Adv. Mater. · 2020 · 1906950 · 1
12. 10.1002/1521-4095(20020705)14:13/14<975::AID-ADMA975>3.0.CO;2-D10.1002/1521-4095(20020705)14:13/14<975::AID-ADMA975>3.0.CO;2-D ↗
13. 10.1002/adma.20050002010.1002/adma.200500020 ↗
14. 10.1039/C8TC05703F10.1039/C8TC05703F ↗
15. 10.1021/acs.jpcc.5b0708410.1021/acs.jpcc.5b07084 ↗
16. 10.1021/ol703087210.1021/ol7030872 ↗
17. 10.1016/j.orgel.2010.05.01510.1016/j.orgel.2010.05.015 ↗
18. 10.1002/adma.20030667010.1002/adma.200306670 ↗
19. 10.3390/molecules2110136510.3390/molecules21101365 ↗
20. 10.1021/acsami.8b0959510.1021/acsami.8b09595 ↗
21. Liu R. · Phys. Rev. B · 2011 · 83 · 1
22. 10.1063/1.354912810.1063/1.3549128 ↗
23. 10.1103/PhysRevB.86.07520410.1103/PhysRevB.86.075204 ↗
24. 10.1002/adfm.20080091810.1002/adfm.200800918 ↗
25. 10.1002/adma.20070167310.1002/adma.200701673 ↗
26. 10.1002/adfm.20110269910.1002/adfm.201102699 ↗
27. 10.1002/adfm.20130345310.1002/adfm.201303453 ↗
28. 10.1039/C8TC03491E10.1039/C8TC03491E ↗