Photoluminescence and Electroluminescence of Carbazole-based Conjugated Dendritic Molecules

  • Cho, Min-Ju (Department of Chemistry, College of Science, Korea University) ;
  • Kim, Young-Min (Display and Nanosystem Laboratory, College of Engineering, Korea University) ;
  • Ju, Byeong-Kwon (Display and Nanosystem Laboratory, College of Engineering, Korea University) ;
  • Choi, Dong-Hoon (Department of Chemistry, College of Science, Korea University)
  • 발행 : 2008.09.30

초록

A novel class of conjugated dendritic molecules bearing N-hexyl-substituted carbazoles as peripheral groups and various conjugative aromatic cores was synthesized through Heck coupling and the Horner-Emmons reaction. A multilayered structure of ITO/PEDOT:PSS (30 nm)/emitting material (50 nm)/BCP (10 nm)/$Alq_3$ (10 nm)/LiF (1 nm)/Al (100 nm) was employed to evaluate the synthesized dendritic materials. The electroluminescence spectrum of the multilayered device made of 3Cz predominantly exhibited blue emissions. Similar emissions were observed in the PL spectra of it's the device's thin film. The multilayered devices made of 3Cz, 3BCz, and 4BCz showed luminance values of 6,250 cd $m^{-2}$ at 24 V, 3,000 cd $m^{-2}$ at 25 V, and 1,970 cd $m^{-2}$ at 36 V, respectively. The smallest molecule, 3Cz, which bore three carbazole peripheral groups, exhibited a blue-like emission with CIE 1931 chromaticity coordinates of x = 0.17 and y = 0.21.

키워드

참고문헌

  1. R. H. Friend, R. W. Gymer, A. B. Holmes, J. H. Burroughes, R. N. Marks, C. Taliani, D. D. Bradley, D. A. Dos Santos, J. L. Brédas, M. Logdlund, and W. R. Salaneck. Nature, 397, 121 (1999) https://doi.org/10.1038/16393
  2. C. D. Dimitrakopoulos and P. R. L. Malenfant. Adv. Mater., 14, 99 (2002) https://doi.org/10.1002/1521-4095(20020116)14:2<99::AID-ADMA99>3.0.CO;2-9
  3. B. Crone, A. Dodabalapur, Y.-Y. Lin, R. W. Filas, Z. Bao, A. LaDuca, R. Sarpeshkar, H. E. Katz, and W. Li. Nature, 403, 521 (2000) https://doi.org/10.1038/35000530
  4. C. Adachi, M. A. Baldo, and S. R. Forrest. J. Appl. Phys., 87, 8049 (2000) https://doi.org/10.1063/1.373496
  5. Z. Hong, C. Liang, R. Li, W. Li, D. Zhao, D. Fan, D. Wang, B. Chu, F. Zang, L. S. Hong, and S. T. Lee. Adv. Mater., 13, 1241 (2001) https://doi.org/10.1002/1521-4095(200108)13:16<1241::AID-ADMA1241>3.0.CO;2-6
  6. P. P. Sun, J.-P. Duan, H. T. Shih, and C. H. Cheng. Appl. Phys. Lett., 81, 792 (2002) https://doi.org/10.1063/1.1497714
  7. F. Liang, Q. Zhou, Y. Cheng, L. Wang, D. Ma, X. Jing, and F. Wang. Chem. Mater., 15, 1935 (2003) https://doi.org/10.1021/cm0257724
  8. M. Sun, H. Xin, K. Z. Wang, Y. A. Zhang, L. P. Jin, and C. H. Huang. Chem. Commun., 6, 702 (2003)
  9. P. P. Sun, J.-P. Duan, J. J. Lih, and C. H. Cheng. Adv. Funct. Mater., 13, 683 (2003) https://doi.org/10.1002/adfm.200304378
  10. Y. Shirota. J. Mater. Chem., 15, 75 (2005) https://doi.org/10.1039/b413819h
  11. A. Kimoto, J.-S. Cho, K. Ito, D. Aoki, T. Miyake, and K. Yamamoto. Macromol. Rapid. Commun., 26, 597 (2005) https://doi.org/10.1002/marc.200400657
  12. T. W. Kwon, M. M. Alam, and S. A. Jenekhe. Chem. Mater., 16, 4657 (2004) https://doi.org/10.1021/cm0494711
  13. P. Furuta, J. Brooks, M. E. Thompson, and J. M. J. Frechet. J. Am. Chem. Soc., 125, 13165 (2003) https://doi.org/10.1021/ja0371348
  14. S.-C. Lo, T. D. Anthopoulos, E. B. Namdas, P. L. Burn, and I. D. W. Samuel. Adv. Mater., 17, 1945 (2005) https://doi.org/10.1002/adma.200500020
  15. Y. Kuwabara, H. Ogawa, H. Inada, N. Noma, and Y. Shirota. Adv. Mater., 6, 677 (1994) https://doi.org/10.1002/adma.19940060913
  16. P.-W. Wang, Y.-J. Liu, C. Devadoss, P. Bharathi, and J. S. Moore. Adv. Mater., 8, 237 (1996) https://doi.org/10.1002/adma.19960080311
  17. H. Yan, B. J. Scott, Q. Huang, and T. Marks. Adv. Mater., 16, 1948 (2004) https://doi.org/10.1002/adma.200400627
  18. Y. H. Niu, B. Chen, S. Liu, H. Yip, J. Bardecker, A. K. Y. Jen, J. Kavitha, Y. Chi, C. F. Shu, Y. H. Tseng, and C. H. Chien. Appl. Phys. Lett., 85, 1619 (2004) https://doi.org/10.1063/1.1786369
  19. X. H. Zhang, S. H. Choi, D. H. Choi, and K. H. Ahn. Tetrahedron Lett., 46, 5273 (2005) https://doi.org/10.1016/j.tetlet.2005.06.051
  20. J. Y. Li, D. Liu, C. Ma, O. Lengyel, C. S. Lee, C. H. Tung, and S. Lee. Adv. Mater., 16, 1538 (2004) https://doi.org/10.1002/adma.200305838
  21. J. Y. Li, D. Liu, Y. Li, C. S. Lee, H. L. Kwong, and S. Lee. Chem. Mater., 17, 1208 (2005) https://doi.org/10.1021/cm034731k
  22. M. J. Cho, T. W. Lee, H. S. Kim, J.-I. Jin, D. H. Choi, Y. M. Kim, and B. K. Ju. Macromol. Res., 15, 595 (2007) https://doi.org/10.1007/BF03218937