Material degradation of liquid organic semiconductors analyzed by nuclear magnetic resonance spectroscopy
Source abstract
Abstract
Liquid organic light-emitting diodes (liquid OLEDs) are unique devices consisting only of liquid organic semiconductors in the active layer, and the device performances have been investigated recently. However, the device degradation, especially, the origin has been unknown. In this study, we show that material degradation occurs in liquid OLEDs, whose active layer is composed of carbazole with an ethylene glycol chain. Nuclear magnetic resonance (NMR) experiments clearly exhibit that the dimerization reaction of carbazole moiety occurs in the liquid OLEDs during driving the devices. In contrast, cleavages of the ethylene glycol chain are not detected within experimental error. The dimerization reaction is considered to be related to the device degradation.
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Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Conducting polymers and applications · Advanced MRI Techniques and Applications
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Affiliations
Kyoto University 1 Institute for Chemical Research, , Uji, Kyoto 611-0011, Japan
Kyusyu University 2 Center for Organic Photonics and Electronics Research (OPERA), , 744 Motooka, Nishi, Fukuoka 819-0395, Japan
Nissan Chemical Industries, LTD 3 , 722-1 Tsuboi, Funabashi 274-8507, Japan
References (21)
Show source-provided references
1. Appl. Phys. Lett. · 2009 · 95 · 05330410.1063/1.3200947 ↗
2. Adv. Mater. · 2011 · 23 · 88910.1002/adma.201003505 ↗
3. Jpn. J. Appl. Phys. · 2012 · 51 · 4160410.1143/JJAP.51.041604 ↗
4. Chem. Lett. · 2012 · 41 · 93410.1246/cl.2012.934 ↗
5. Sens. Actuators, B · 2015 · 207 · 48110.1016/j.snb.2014.09.101 ↗
6. Appl. Phys. Lett. · 1987 · 51 · 91310.1063/1.98799 ↗
7. Chem. Mater. · 1996 · 8 · 136310.1021/cm960152m ↗
8. Synth. Met. · 1997 · 89 · 17110.1016/S0379-6779(97)81214-3 ↗
9. Science · 1999 · 283 · 190010.1126/science.283.5409.1900 ↗
10. J. Appl. Phys. · 2007 · 101 · 02451210.1063/1.2430922 ↗
11. J. Fluorine Chem. · 2009 · 130 · 64010.1016/j.jfluchem.2009.04.009 ↗
12. Adv. Mater. · 2010 · 22 · 376210.1002/adma.200902624 ↗
13. Org. Electron. · 2011 · 12 · 34110.1016/j.orgel.2010.11.004 ↗
14. Electrochim. Acta · 2002 · 47 · 292710.1016/S0013-4686(02)00171-8 ↗
15. See supplementary material at http://dx.doi.org/10.1063/1.4928515 for full 1H NMR and 1H-1H COSY spectra of TEGCz and (TEGCz)2.
16. J. Am. Chem. Soc. · 1993 · 115 · 429110.1021/ja00063a053 ↗
17. Macromolecules · 1998 · 31 · 657310.1021/ma9801772 ↗
18. Prog. Nucl. Magn. Reson. Spectrosc. · 1999 · 34 · 20310.1016/S0079-6565(99)00003-5 ↗
19. J. Photochem. Photobiol. A · 2008 · 194 · 32710.1016/j.jphotochem.2007.08.031 ↗
20. Dyes Pigm. · 2008 · 78 · 20710.1016/j.dyepig.2007.12.003 ↗
21. Tetrahedron Lett. · 2011 · 52 · 474910.1016/j.tetlet.2011.07.002 ↗