journal article·2022-07-01Open access

3-(N,N-Diphenylamino)carbazole Donor Containing Bipolar Derivatives with Very High Glass Transition Temperatures as Potential TADF Emitters for OLEDs

Daiva Tavgeniene, Raminta Beresneviciute, Dovydas Blazevicius, Gintare Krucaite, Greta Jacunskaite, Sujith Sudheendran Swayamprabha, Jwo-Huei Jou, Saulius Grigalevicius

Coatings· Volume 12· Issue 7

Abstract

Well-defined electroactive bipolar derivatives of new structure have been synthesized from 3-(N,N-diphenylamino)-9H-carbazole and bis(4-fluorophenyl)sulfone, 4-fluorophenylsulfone or 4,4′-difluorobenzophenone, respectively. The full characterization of their structure is described. The amorphous materials with very high glass transition temperatures of 111–173 °C also possess high thermal stability, with onset decomposition temperatures of 351–398 °C. Some of the compounds having the best solubility were tested as the emitters dispersed in 4,4′-bis(N-carbazolyl)-1,1′-biphenyl (CBP) host for preparation of organic light emitting diodes (OLEDs). A device containing 15 wt% of the guest bis[4-{3-(N,N-diphenylamino)carbazol-9-yl}phenyl] sulfone demonstrated the best overall characteristics with maximum brightness exceeding 2630 cd/m2, current efficiency of 3.2 cd/A, power efficiency of 2.2 lm/W, and external quantum efficiency exceeding 1.7% at 100 cd/m2.
Source: crossref · Quality: baseline

Research context

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

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

Affiliations

Department of Polymer Chemistry and Technology, Kaunas University of Technology, Radvilenu Plentas 19, LT 50254 Kaunas, Lithuania

Department of Materials Science and Engineering, National Tsing-Hua University, No. 101, Kaungfu Rd., Hsin-Chu 30013, Taiwan

Funding

Research Council of Lithuania

References (41)

Show source-provided references
1. Anthracene-based fluorescent emitters toward superior-efficiency nondoped TTA-OLEDs with deep blue emission and low efficiency roll-off10.1016/j.cej.2020.127748 ↗
2. Deep-blue high-efficiency triplet-triplet annihilation organic light-emitting diodes using donor- and acceptor-modified anthracene fluorescent emitters10.1016/j.mtener.2021.100727 ↗
3. Bis(carbazol-9-yl)phenyl end-caped polyaromatics as solution-processed deep blue fluorescent emitters for simple structure solution-processed electroluminescent devices10.1016/j.dyepig.2020.109065 ↗
4. A deep blue fluorescent emitter functioning as host material in highly efficient phosphorescent and hybrid white organic light-emitting devices10.1016/j.orgel.2020.105848 ↗
5. High performance blue and white fluorescent organic electroluminescent devices with conventional electron transport material as blue emitter10.1016/j.dyepig.2020.108354 ↗
6. Towards high-power-efficiency solution-processed OLEDs: Material and device perspectives10.1016/j.mser.2020.100547 ↗
7. Semitransparent circularly polarized phosphorescent organic light-emitting diodes with external quantum efficiency over 30% and dissymmetry factor close to 10−210.1002/adfm.202102898 ↗
8. Purely organic phosphorescent organic light emitting diodes using alkyl modified phenoselenazine10.1039/D1TC01741A ↗
9. Recent progress in phosphorescent Ir(III) complexes for nondoped organic light-emitting diodes10.1016/j.ccr.2020.213283 ↗
10. Manipulation of exciton distribution for high-performance fluorescent/phosphorescent hybrid white organic light-emitting diodes10.1039/C7TC01477E ↗
11. Organic materials for deep blue phosphorescent organic light-emitting diodes10.1002/adma.201200627 ↗
12. Phenanthro[9,10-d]imidazole based new host materials for efficient red phosphorescent OLEDs10.1016/j.dyepig.2016.11.003 ↗
13. Xie, G., Wang, J., Cao, Y., Xue, X., Zhang, X., Liu, C., Li, H., Tao, Y., and Chen, R. (2021). Phosphine sulfide-based bipolar host materials for blue phosphorescent organic light-emitting diodes. Molecules, 26.10.3390/molecules26134079 ↗
14. Recent progress in the use of fluorescent and phosphorescent organic compounds for organic light-emitting diode lighting10.1117/1.JPE.5.057608 ↗
15. Degradation mechanism and lifetime improvement strategy for blue phosphorescent organic light-emitting diodes10.1002/adom.201600901 ↗
16. Structure–property relationship of 4-substituted-spirobifluorenes as hosts for phosphorescent organic light emitting diodes: An overview10.1039/C7TC00746A ↗
17. Phosphorescent and TADF polymers and dendrimers in solution-processed self-host organic light-emitting diodes: Structure analysis and design perspectives10.1039/C9QM00188C ↗
18. Identification of the key parameters for horizontal transition dipole orientation in fluorescent and TADF organic light-emitting diodes10.1002/adma.202100677 ↗
19. Recent progress of narrowband TADF emitters and their applications in OLEDs10.1039/D0TC02682D ↗
20. Thermally activated delayed fluorescence (TADF) path toward efficient electroluminescence in purely organic materials: Molecular level insight10.1021/acs.accounts.8b00174 ↗
21. Crystal organic light-emitting diodes with perfectly oriented non-doped pt-based emitting layer10.1002/adma.201705600 ↗
22. Recent advancements in and the future of organic emitters: TADF- and RTP-active multifunctional organic materials10.1002/asia.201801791 ↗
23. Cross-linkable aromatic amines as materials for insolublehole-transporting layers in light-emitting devices10.1016/j.synthmet.2008.01.004 ↗
24. Kotowicz, S., Korzec, M., Malarz, K., Krystkowska, A., Mrozek-Wilczkiewicz, A., Golba, S., Siwy, M., Mackowski, S., and Schab-Balcerzak, E. (2021). Luminescence and electrochemical activity of new unsymmetrical 3-imino-1,8-naphthalimide derivatives. Materials, 14.10.3390/ma14195504 ↗
25. Branched azomethines based on tris(2-aminoethyl)amine: Impact of imine core functionalization on thermal, electrochemical and luminescence properties10.1016/j.matchemphys.2019.122246 ↗
26. Photophysical and electrical properties of highly luminescent 2/6-triazolyl-substituted push–pull purines10.1021/acsomega.1c06359 ↗
27. Impact of the donor structure in new D–π–A systems based on indolo[3,2,1-jk]carbazoles on their thermal, electrochemical, optoelectronic and luminescence properties10.1039/D1TC01208H ↗
28. Organic Semiconductors for Solution-Processable Field-Effect Transistors (OFETs)10.1002/anie.200701920 ↗
29. Novel β-ketoenamines versus azomethines for organic electronics: Characterization of optical and electrochemical properties supported by theoretical studies10.1007/s10853-019-04210-3 ↗
30. Synthesis, photophysical and photoelectrical properties of glass-forming phenothiazinyl- and carbazolyl-substituted ethylenes
31. Photoconductive, photoluminescent and glass-forming 6,6-di(N-diphenylamino)-9,9-dialkyl-3,3-bicarbazoles10.1016/S1010-6030(03)00346-0 ↗
32. A review on low-molar-mass carbazole- based derivatives for organic light emitting diodes10.1016/j.synthmet.2018.11.017 ↗
33. Hole-transporting [3,3′]bicarbazolyl-based polymers and well-defined model compounds10.1016/j.eurpolymj.2006.06.023 ↗
34. Synthesis and properties of the polymers containing 3,3-dicarbazyl units in the main chain and their model compounds10.1016/S0032-3861(02)00466-4 ↗
35. Iodination in the carbazole series10.1039/JR9262900546 ↗
36. High-efficiency organic light-emitting diodes utilizing thermally activated delayed fluorescence from triazine-based donor–acceptor hybrid molecules10.1063/1.4749285 ↗
37. Organic electroluminescent diodes10.1063/1.98799 ↗
38. PEDT/PSS for efficient hole-injection in hybrid organic light-emitting diodes10.1016/S0379-6779(99)00328-8 ↗
39. Modulation of the physicochemical properties of donor–spiro–acceptor derivatives through donor unit planarisation: Phenylacridine versus indoloacridine—New hosts for green and blue phosphorescent organic light-emitting diodes (PhOLEDs)10.1002/chem.201600652 ↗
40. Electron-rich 4-substituted spirobifluorenes: Toward a new family of high triplet energy host materials for high-efficiency green and sky blue phosphorescent OLEDs10.1021/acsami.6b14285 ↗
41. Simple bipolar host materials for high-efficiency blue, green, and white phosphorescence OLEDs10.1021/acsami.6b05355 ↗