Organiczne diody elektroluminescencyjne na bazie pochodnych pirazolochinoksalin

• Autorzy: Pokladko-Kowar Monika , Wojtasik Katarzyna

Identyfikatory

DOI

10.15199/48.2022.09.51

Warianty tytułu

EN

Organic light-emitting diodes based on pyrazoloquinoxaline derivatives

• Języki publikacji: PL

Abstrakty

PL

Pochodne pirazolochinoksalin (A-PQX) badano pod kątem zastosowań w organicznych diodach elektroluminescencyjnych (OLED). Wykonane zostały pomiary widm absorpcyjnych, fotoluminescencyjnych oraz elektroluminescencyjnych. Zbudowane zostały jednowarstwowe komórki o strukturze ITO/PEDOT:PSS/PVK+A-PQX/Ca/Al. Wyznaczone zostały parametry charakterystyczne dla OLED. Maksymalna luminescencja otrzymana dla tych struktur wynosiła 884 cd/m2 dla diody na bazie 7-N,N-dietylo-1-fenylo-3-metylo-1H-pirazolo[3,4-b]chinoksaliny (7- PQX).

EN

Pyrazoloquinoxaline derivatives (A-PQX) have been studied for applications in organic light emitting diodes (OLEDs). Single-layer OLEDs with the structure: ITO/PEDOT:PSS/PVK+A-PQX/Ca/Al were built. Parameters characteristic for OLED were determined. The absorption, photoluminescent and electroluminescent spectra were measured. The maximum luminescence obtained for these structures was 884 cd/m2 for a diode based on 7-N,N-diethyl-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]quinoxaline (7A-PQX).

Słowa kluczowe

PL

organiczne diody elektroluminescencyjne; OLED; absorpcja; elektroluminescencja; fotoluminescencja

EN

organic light emitting diode; OLED; absorption; electroluminescence; photoluminescence

• Wydawca: Wydawnictwo SIGMA-NOT
• Czasopismo: Przegląd Elektrotechniczny
• Rocznik: 2022
• Tom: R. 98, nr 9
• Strony: 220--223
• Opis fizyczny: Bibliogr. 23 poz., rys., tab.

Twórcy

autor

Pokladko-Kowar Monika

• Politechnika Krakowska, Katedra Fizyki ul. Podchorążych 1, 30-084 Kraków

• https://orcid.org/0000-0002-8413-5185

autor

Wojtasik Katarzyna

• Politechnika Krakowska, Katedra Fizyki ul. Podchorążych 1, 30-084 Kraków

Bibliografia

• [1] Sneha Kagatikar and Dhanya Sunil, A systematic review on 1,8-naphthalimide derivatives as emissive materials in organic light-emitting diodes, J. Mater. Sci., 57 (2022), 105–139.
• [2] Yeh P., Yeh N., Lee CH., Ding T.J., Applications of LEDs in optical sensors and chemical sensing devices to detect biochemicals, heavy metals, and environmental nutrients. Renew Sustain Energy Rev 75, (2017), 461–468.
• [3] Wang Y., Liu P., Wang H. et. al., Flexible organic light emitting devices with copper nanowire composite transparent conductive electrode, J Mater Sci, 54, (2019), 2343–2350.
• [4] Burroughes J., Bradley D., Brown A.R., Marks R.N., Mackay K., Friend R.H., Burn P.L., Holmes A., Light-emitting diodes based on conjugated polymers, Nature, 347, (1990), 539–541.
• [5] S. Reineke , F. Lindner , G. Schwartz , N. Seidler , K. Walzer , B. Luessem , K. Leo , White organic light-emitting diodes with fluorescent tube efficiency, Nature 459 (2009) 234–238 .
• [6] Nan-Chieh Chiu, Kyle Smith T., Stylianou Kyriakos C, Metalorganic frameworks for white light emission: From synthesis to device fabrication, Coordination Chemistry Reviews, 459, (2022), 214441.
• [7] Qian-Chong Zhang, Hui Xiao, Xu Zhang, Liang-Jin Xu, Zhong-Ning Chen, Luminescent oligonuclear metal complexes and the use in organic light-emitting diodes, Coordination Chemistry Reviews, 378, (2019), 121–133.
• [8] Yuan Q., Wang T., Panlong Y., Zhang H., Han Zhang, Ji W., Areview on the electroluminescence properties of quantum-dot light-emitting diodes”, Organic Electronics, 90, (2021) 106086
• [9] Luo X.F., Qu Z.Z., Han H.B., Su J., Yan Z., Zhang X.M., Tong J.J., Zheng Y.X., Zuo J.L., Carbazole-based Iridium(III) complexes for electrophosphorescence with EQE of 32.2% and low efficiency roll-off, Adv. Opt. Mater. 9, (2020), 2001390.
• [10] Wan S.P., Lu H. Y., Li M., Chen C.Feng., Advances in circularly polarized luminescent materials based on axially chiral compounds, Journal of Photochemistry & Photobiology, C: Photochemistry Reviews, 50, (2022) 100500.
• [11] Z. Chen , C.-L. Ho , L. Wang , W.-Y. Wong , Single-molecular white-light emitters and their potential WOLED applications, Adv. Mater., 32, (2020),1903269.
• [12] Chen D., Wei Li, Lin Gan, Mengke Z. W., Li, Shi-Jian Su Non-noble- metal-based organic emitters for OLED applications,Materials Science & Engineering R, 142, (2020), 100581.
• [13] Tang C.W., VanSlyke S.A., Organic electroluminescent diodes Appl. Phys. Lett. 51 (1987) 913.
• [14] Bernanose A., Vouaux P., Chim J., Électroluminescence organique : étude du mode d'émission, Phys., 50, (1953), 261.
• [15] Bernanose A., Comte M., Vouaux P., Chim J., Sur un nouveau mode d'émission lumineuse chez certains composés organiques, Phys. 50 (1953) 64.
• [16] Helfrich W., Schneider W.G., Recombination Radiation in Anthracene Crystals, Phys. Rev. Lett., 14, (1965) 229.
• [17] Jayanta Bauri, Ram Bilash Choudhary and Gobind Mandal, Recent advances in efficient emissive materials-based OLED applications: a review, J. Mater. Sci., 56, (2021), 18837–18866.
• [18] Danel, A.; Wojtasik, K.; Szlachcic, P.; Gryl, M.; Stadnicka, K., A new regiospecific synthesis method of 1H-pyrazolo[3,4-b]quinoxalines – Potential materials for organic optoelectronic devices, and a revision of an old scheme. Tetrahedron, 73, nr 34, (2017), 5072–5081, DOI: 10.1016/j.tet.2017.06.061.
• [19] Wojtasik, K.; Danel, A., The Synthesis of 1H-Pyrazolo[3,4-b]quinoxaline Derivatives Oriented towards Modification of Carbocyclic Ring in the Parent Skeleton. ChemistrySelect, 5, (2020), 5521–5525, DOI: 10.1002/slct.202000418 Table.
• [20] J.P. Wolfe, H. Tomori, J.P. Sadighi, J. Yin, S.L. Buchwald, Simple, Efficient Catalyst System for the Palladium-Catalyzed Amination of Aryl Chlorides, Bromides, and Triflates, The Journal of Organic Chemistry, 65, nr. 4, (2000), 1158-1174.
• [21] Yang, C., Zhang, J., Peng, WT. et al. Impact of Stokes Shift on the Performance of Near-Infrared Harvesting Transparent Luminescent Solar Concentrators. Sci Rep 8, (2018), 16359.
• [22] M. Brouwer Albert, Standards for photoluminescence quantum yield measurements in solution (IUPAC Technical Report),Pure and Applied Chemistry, (2011), p. 2213.
• [23] Kotowicz S., Kula S., Filapek M., et al. 2,2-Dicyanovinyl derivatives - Thermal, photophysical, electrochemical and electroluminescence investigations, Mater. Chem. Phys. 209, (2018), 249.

Uwagi

Opracowanie rekordu ze środków MEiN, umowa nr SONP/SP/546092/2022 w ramach programu "Społeczna odpowiedzialność nauki" - moduł: Popularyzacja nauki i promocja sportu (2022-2023).