請用此 Handle URI 來引用此文件：
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/46870完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 謝國煌(Kuo-Huang Hsieh) | |
| dc.contributor.author | Hsin-Jou Chuang | en |
| dc.contributor.author | 莊欣柔 | zh_TW |
| dc.date.accessioned | 2021-06-15T05:42:30Z | - |
| dc.date.available | 2010-08-20 | |
| dc.date.copyright | 2010-08-20 | |
| dc.date.issued | 2010 | |
| dc.date.submitted | 2010-08-20 | |
| dc.identifier.citation | 1. Grazulevicius, J.V.；Strohriegl, P.；Pielichowski, J.；Pielichowski, K. Prog. Polym. Sci. 2003, 28, 1297.
2. Ku, C. H. ; Kuo, C. H. ; Chen, C. Y. ; Leung, M. K. ; Hsieh, K. H. J. Mater. Chem., 2008, 18, 1296. 3. Peng, O.；Xu, J.；Li, M.；Zheng, W. Macromolecules 2009, 42, 5478. 4. Tsai, M. H.；Hong, Y. H.；Chang, C. H.；Su, H. C.；Wu. C. C. Adv. Mater. 2007, 19, 862. 5. Pickup, D. F.；Yi, H.；Kun, H.；Iraqi, A.；Stevenson, M.；Lidzey, D. G. Thin Solid Film. 2009, 517, 2840. 6. Tao, Y.；Wang, Q.；Yang, C.；Wang, Q.；Zhang, Z.；Zou, T.；Qin, J.；Ma, D. Angew. Chem. Int. Ed. 2008, 47, 8104. 7. Lin, Y.；Chen, Y.；Chen, Z.；Mac, D.；Zhang, B.；Ye, T.；Dai, Y. European Polymer Journal 2010, 46, 997. 8. Zeng, L.；Lee, T. Y. H.；Merkelb, Paul B.；Chen, S. H. J. Mater. Chem. 2009, 19, 8772. 9. Chien, C. H.；Kung, L. R.；Wu, C. H.；Shu, C. F.；Chang, S. Y.；Chi, Y. J. Mater. Chem. 2008, 18, 3461. 10. Tao, Y.；Wang, Q.；Shang, Y.；Yang, C.；Ao, L.；Qin, J.；Ma, D.；Shuai. Z. Chem. Commun. 2009, 77, 77. 11. Chen, C. H.；Huang, W. S.；Lai, M. Y.；Tsao, W. C.；Lin, J. T.；Wu, Y. H.；Ke, T. H.；Chen, L. Y.；Wu, C. C. Adv. Funct. Mater. 2009, 19, 2661. 12. Bernanose, E.; Comte, M.; Vouaux, P. J. Chem. Phys. 1953, 50, 64. 13. Bernanose, E.; Vouaux, P. J. Chem. Phys. 1953, 50, 261. 14. Bernanose, E. J. Chem. Phys. 1955, 52, 396. 15. Bernanose, E.; Vouaux, P.; J. Chem. Phys. 1955, 52, 509. 16. Pope, M.; Kallmann, H. P.; Magnante, P. J. Chem. Phys. 1963, 38,2042. 17. Helfrich, W.; Schneider, W. G. J. Chem. Phys. 1966, 44, 2902. 18. Roberts, G. G.; McGinnity, M. M.; Barlow, W. A.; Vincett, P. S. Solid State Commun. 1979, 32, 683. 19. Vincett, P. S.; Barlow, W. A.; Hann, R. A.; Roberts, G. G. Thin Solid Films 1982, 94, 171. 20. Tang, C. W.; VanSlyke, S. A. Appl. Phys. Lett. 1987, 51, 913. 21. Patridge, R. H. Polymer 1983, 24, 733. 22. Burrouhted, J. H.; Bradley, D. D. C.; Brown, A. R.; Mackay, R. N.; Friend, R. H.; Burns, P. L.; Homes, A. B. Nature 1990, 347, 539. 23. Braun, D.; Heeger, A. Appl. Phys. Lett. 1991, 58, 1982. 24. Ohmori, Y.; Uchida, M.; Muro, K.; Yoshino, K. Jpn. J. Appl. Phys. 1991, 30, 1928. 25. Ohmori, Y.; Morishita, C.; Uchida, M.; Yoshino, K. Jpn. J. Appl. Phys.1992, 31, 568. 26. Braun, D.; Gustaffson, G.; MacBranch, D.; Heeger, A. J. Appl. Phys. 1992, 72, 564. 27. Ohmori, Y.; Uchida, M.; Muro, K.; Yoshino, K. Jpn. J. Appl. Phys. 1991, 30, 1941. 28. Grem, G.; Leditzky, G.; Ulrich, B.; Leising, G. Adv. Mater. 1992, 4, 36. 29. Fukuda, M.; Sawada, K.; Morita, S.; Yoshino, K. Synth, Met. 1991, 41,855. 30. Adachi, C.; Baldo, M. A.; Thompson, M. E.; Forrest, S. R. J. Appl. Phys. 2001, 90, 5048. 31. Chen, C. H.; Shi, J.; Tang, C. W. Macromol. Symp. 1997, 125, 1. 32. Braun, D.; Heeger, A. Appl. Phys. Lett. 1991, 58, 1982. 33. O’Brien, D. F.; Baldo, M. A.; Thompson, M. E.; Forrest, S. R. Appl. Phys. Lett. 1999, 74, 442. 34. Baldo, M. A.; O’Brien, D. F.; You, Y.; Shoustikov, A.; Sibley, S.; Thompson, M. E.; Forrest, S. R. Nature. 1998, 395, 151. 35. Baldo, M. A.; O’Brien, D. F.; Thompson, M. E.; Forrest, S. R.; Phys. Rev. B. 1999, 60, 14422. 36. 陳金鑫,石建民,鄧青雲,化學, 1996, 54, 125. 37. Adachi, C.; Tsutsui, T.; Saito, S. Appl. Phys. Lett. 1989, 55, 1489. 38. (a) Pommerehne, J.; Vestwebber, H.; Guss, W.; Mahrt, R. F.; Bässler, H.; Porsch, M.; Daub, J. Adv. Mater. 1995, 7, 551. (b) Tak, Y. H.; Bässler, H.; Leuninger, J.; Müllen, K. J. Phys. Chem. 1998, 102, 4887. (c) Cao, Y.; Parker, I. D.; Yu, G.; Zhang, C.; Heeger, A. J. Nature 1999, 397, 414. 39. Weinfurner, K. H.; Weissötel, F.; Harmgarth, G.; Salbeck, J. Proc. SPIE Int. Soc. Opt. Eng. 1998, 40, 3476. 40. (a) Berleb, S.; Brütting, W.; Schwoerer, M.; Wehrmann, R.; Elschner, A. J. Appl. Phys. 1998, 83, 4403. (b) Bettenhausen, J.; Strohriegl, P.; Brütting, W.; Tokuhisa, H.; Tsutsui, T. J. Appl. Phys. 1997, 82, 4957. 41. Bettenhausen, J.; Greczmiel, M.; Jandke, M.; Strohriegl, P. Synth. Met.1997, 91, 223. 42. Kido, J.; Ontaki, C.; Hongawa, K.; Oknyama, K.; Nagai, K. Jpn. J. Appl. Phys. 1993, 32, 917. 43. Hamada, Y.; Sano, T.; Fujita, M.; Fujii, T.; Nishio, Y.; Shibata, K. Chem. Lett. 1993, 22, 905. 44. Hosokawa C.; Tokalin H.; Higashi H. ; Kusumoto T. Appl. Phys. Lett., 1992, 60, 1220. 45. An single crystal X-ray crystallography of AlQ3 was performed by Analytical Technology Division, Eastman Kodak Company. 46. Bryan P. S.; Lovecchio F. V.; VanSlyke S. A. US 5,141,672, 1992. 47. Hamada Y.; Sano T.; Fujita M.; Fujii T.; Nishio Y.; Shibata K. Chem. Lett., 1993, 905. 48. Hamada Y.; Sano T.; Shibata K.; Kuroki K.; Japan J. Appl. Phys., 1995, Part 2, 34,824-826. 49. Burroughes, J. H.; Bradley, D. D. C.; Brown, A. R.; Marks,R. N.; Mackay, K.; Friend, R. H.; Burn, D. L.; Holmes, A.B. Nature, 1990, 347, 539. 50. Tang, C. W.; VanSlyke, S. A. Appl. Phys. Lett. 1987, 51, 913. 51. Cao, G. Y.; Treacy G. M.; Klavetter, F.; Colaneri, N.; Heeger, A. J. Nature 1993, 357, 111. 52. Kraft, A.; Grimsdale, A. C.; Holmes, A. B. Angew. Chem. Int. Ed. 1998, 37, 402. 53. Hwang, D. H.; Kim, S. T.; Li, X. C.; Chuah, B. S.; DeMello, J. C.; Friend, R. H.; Moratti, S. C.; Holmes, A. B. Abstr. Pap. Am. Chem. S. 1997, 213, 319. 54. Koch, F.; Heitz, W. Macromol. Chem. Phys. 1997, 198, 1531. 55. Pfeiffer, S.; Horhold, H. H. Macromol. Chem. Phys. 1997, 200, 1870. 56. Sarnecki, G. J.; Brun, P. L.; Kraft, A.; Reiend, R. H.; Holmes, A. B. Synth. Met. 1993, 55, 91. 57. Hoger, F. W. S.; Zhang, C.; Pakbz, K.; Heeger, A. J. Polym. Prepr. 1993, 34, 197. 58. Gurge, R. M.; Sarker, A.; Lathti, P. M.; Hu, B.; Karasz, F. E. Macromolecules 1996, 29, 4287. 59. Gowri, R.; Mandal, D.; Shivkumar, B.; RamaKrishnan, S. Macromolecules 1998, 31, 1819. 60. Tang, C. W. ;Van Slyke, S. A. Appl, Phys. Lett 1987, 51, 913. 61. Tsutsui T.; Saito S., in “Polymers for Microelectronics”, eds. Tabata Y., Kodansha,Tokyo, 1990, 591-600. 62. Ishida T.; Kobayashi H.; Nakato Y. J. Appl. Phys., 1993, 73, 4344. 63. VanSlyke S. A.; Tang C. W.; Roberts L. C. US 4,720, 432, 1988. 64. Wakimoto T. ; Fukuda Y. ; Nagayama K. ; Yokoi A. ; Nakada H. ; Tsuchida M. IEEE Trans. Electron. Devices, 1997, 44, 1245. 65. Stoßel M. ; Staudigel J. ; Steuber F. ; Blassing J. ; Simmerer J. ; Winnacker A. Appl. Phys. Lett., 2000, 76, 115. 66. Ying, L.；Yu, C.；Zhikuan, C.；Dongge, M.；Bin, Z.；Tengling, Y.；Yanfeng, D. European Polymer Journal, 2010, 46, 997. 67. Kousuke, T.；Kota, S.；Hidemasa, K.；Akira, K.；Hideo, T.；Hiroshi, K.；Kenji ,O. Polymer, 2010, 51, 616. 68. Chen, Y. C. ; Huang, G. S. ; Hsiao, C. C. ; Chen, S. A. J. Am. Chem. Soc., 2006, 128, 8549. 69. Lichang, Z. ; Thomas, Y. H. ; Lee, Paul B. ; Merkel ; Chen, S. H. J. Mater. Chem., 2009, 19, 8772. 70. Yamamoto, T.; Maruyama, T.; Zhou, Z. H.; Ito, T.; Fukuda, T.; Yoneda, Y.; Begum, F.; Ikeda, T.; Sasaki, S.; Takezoe, H.; Fukuda, A.; Kubota, K. J. Am. Chem. Soc. 1994 ,116, 4832. 71. Chen, Y. C.; Huang, G. S.; Hsiao, C. C.; Chen, S. A. J. Am. Chem. Soc. 2006, 128, 8549. 72. Tucker, S. H. J. Chem. Soc. 1926, 1, 548. 73. Ku, C. H. ; Kuo, C. H. ; Chen, C. Y. ; Leung, M. K. ; Hsieh, K. H. J. Mater. Chem., 2008, 18, 1296. 74. Gilman, H.; Honeycutt, J. B. J. Org. Chem. 1957, 22, 226. 75. Tsuie, B.; Reddinger, J. L.; Sotzing, G. A.; Soloducho, J.; Katrizky, A. R. Reynolds, R. J. Mater. Chem., 1999, 9, 2189-2200. 76. Ashutosh, A. ; Kelkar ; Nandkumar, M. Tetrahedron Letters, 2002, 43, 7143. 77. Chen, S. H. ;Shim, S. C. ; Jung, B. J. ; Shim, H. K. Polymer, 2002, 43, 297. 78. Saulius, G. ; Liang, M. ; Gang, Q. ; Zhiyuan, X. ; Michael F. ; Ullrich, S. Macromol. Chem. Phys., 2007, 208, 349. 79. Tao, Y.；Wang, Q.；Shang, Y.；Yang, C.；Ao, L.；Qin, J.；Ma, D.；Shuai. Z. Chem. Commun., 2009, 77, 77. 80. Lee, R. H. ; Hsu, H. F. Journal of Applied Polymer Science, 2007, 106, 2863. 81. Dijken, A. V.; Bastiaansen, J. J. A. M.; Kiggen, N. M. M.; Langeveld, B.M. W.; Rothe, C.; Monkman, A. P.; Bach, I.; Stössel, P.; Brunner, . J. Am. Chem. Soc. 2004, 126, 7718. 82. Zhang, F.; Xu, Z.; Zhao, S.; Liu, L.; Sun, B.; Pei, J. Physica B. 2006, 381,256. 83. Pu, Y. J. ; Kurata, T. ; Minoru, S. ; Junji, K. ; Hiroyuki, N. Synthetic Metals, 2004, 143, 207. 84. Kousuke, T. ; Kota, S. ; Hidemasa, K. ; Kenji, O. Polymer , 2010, 51 , 616. 85. Yang, Y.；Pei, Q. J. Appl. Phys., 1995, 77, 4807. 86. Tsuchiya, K. ; Sakaguchi, K.; Kasuga, H. ; Kawakami, A.; Taka, H. ; Kita, H.; Ogino K. Polymer, 2010, 51, 616. 87. Zhang, K. ; Tao, Y.; Yang, C. ; You, H. ; Zou, Y. ; Qin, J. ; Ma, D. Chem. Mater., 2008, 20, 7324. | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/46870 | - |
| dc.description.abstract | 在本研究中，主要合成以咔唑(carbazole)為主體，於咔唑的9-號氮上做改質，以YAMAMOTO聚合法，合成一系列以咔唑為主鏈的均聚物(homopolymer)與共聚物(copolymer)，均聚物的的部分，首先引入具有良好的傳導電洞效果及高三重態能階的卡唑，將其應用於高分子發光二極體的主體發光材料；共聚物(copolymer)的部分引入具有發光與傳導電洞特性的三苯胺(triphenylamine)與傳導電子特性的噁唑(oxadiazole)，因分子內具有Donor-Acceptor的結構而呈現雙極性(bipolar)特性，進而提高電荷轉移的效率，將其應用於藍光螢光材料；接著對合成出的一系列高分子利用凝膠滲透層析儀、熱重分析儀、微差掃描卡計、螢光光譜儀及電激發光實驗做光電性質分析與探討，進而應用於高分子發光二極體元件的製作與討論。在元件應用的部分，藍色螢光元件中，元件結構：ITO/PEDOT:PSS/P2/TPBi /Mg/Ag在亮度上有最好的表現，啟動電壓為7.5V，電壓於17V時達最大亮度為104 cd/m2，電壓於13.5V時達最大效率為0.12cd/A。綠色磷光元件中，元件結構：ITO /PEDOT:PSS / P6 + Ir(ppy)3(8 %) + PBD(20%) /Mg /Ag在亮度上有最好的表現，啟動電壓為7V，電壓於13V時達最大亮度為1080cd/m2，電壓於13V時達最大效率為0.42cd/A，其中磷光元件ITO /PEDOT:PSS / P6 + Ir(ppy)3(1%) + PBD(20%) /Mg /Ag，在效率的表現上為最佳，電壓於8V時達最大效率為2cd/A。 | zh_TW |
| dc.description.abstract | In this study, polycarbaozle derivatives were synthesized and polymerized via Yamamoto coupling reaction. Firstly, we synthesized the conjugated polycarbazole P6 which combined the structure characteristics of carbazole in the side chain as host material. Moreover, we synthesized the conjugated polycarbazole P1-P5 which combined the structure characteristics of triphenylamine and oxadiazole in the side chain as blue fluorescent materials. Polymers P1-P5 contained both of electron- and hole-transporting properties to achieve high efficiency. All the polymers were fully characterized by gel permeation chromatography (GPC), thermal gravimetric analyzer (TGA), differential scanning calorimeter (DSC), photoluminescence spectrophotometer (PL), and electroluminescent (EL) spectroscopy. Lastly, all the polymers were application on the device of polymer light emitting diode, and luminescent properties is discussed. At the results of blue fluorescence devices, device ITO/PEDOT:PSS/P2/TPBi /Mg/Ag has the best performance, turn on voltage is 7.5V, maximum brightness is 104 cd/m2 on 17V, and maximum efficiency is 0.12cd/A on 13.5V. At the results of green phosphorescence devices, device ITO /PEDOT:PSS / P6 + Ir(ppy)3(8 %) + PBD(20%) /Mg /Ag has the best performance, turn on voltage is 7 V, maximum brightness is 1080 cd/m2 on 13V, and maximum efficiency is 0.42cd/A on 13V. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-15T05:42:30Z (GMT). No. of bitstreams: 1 ntu-99-R97549010-1.pdf: 4970957 bytes, checksum: 4f95acdfa703d5674eb38a849d19e035 (MD5) Previous issue date: 2010 | en |
| dc.description.tableofcontents | 摘要 I
ABSTRACT II 目錄 III 圖目錄 V 表目錄 IX 第一章 緒論 1 1-1 前言 1 1-2 研究動機 1 第二章 文獻回顧 3 2-1 有機發光二極體之研究發展史 3 2-2 高分子發光二極體之發光原理 6 2-2.1 電激發光原理 6 2-2.2 螢光與磷光理論 7 2-2.3 主客能量轉移理論 10 2-3 有機電激發光材料 12 2-3.1 電洞傳輸材料 12 2-3.2 電子傳輸材料 13 2-3.3 小分子發光材料 16 2-3.4 高分子材料 17 2-4 高分子發光二極體之元件結構 18 2-4.1 陰陽電極 20 2-4.2 電子及洞子的再結合 21 2-4.3 電洞注入層材料 22 2-4.4 電子注入層材料 22 2-5 研究方向 23 第三章 實驗部分 24 3-1 實驗藥品與溶劑 24 3-2 實驗儀器 28 3-3合成步驟與數據 30 第四章 結果與討論 56 4-1 合成結果分析 56 4-1.1 單體小分子的合成 56 4-1.2 高分子的合成 63 4-1.3 高分子的分子量探討 64 4-2 熱穩定性質探討 67 4-3 光學性質探討 69 4-3.1 高分子P1-P5的光學性質探討 69 4-3.2 高分子P6的光學性質探討 74 4-4 電化學性質探討 79 4-5 PLED 元件結構及性質探討 87 4-5.1 PLED元件製備標準流程 87 4-5.2 螢光發光材料P1-P5之元件探討 90 4-5.3 主體發光材料P6之元件探討 101 第五章 結論 104 第六章 參考文獻 105 附錄 111 | |
| dc.language.iso | zh-TW | |
| dc.subject | 高分子發光二極體 | zh_TW |
| dc.subject | 雙極性 | zh_TW |
| dc.subject | 咔 | zh_TW |
| dc.subject | 唑 | zh_TW |
| dc.subject | carbazole | en |
| dc.subject | bipolar | en |
| dc.subject | Polymer light emitting diode | en |
| dc.title | 三苯胺、噁唑及咔唑之側鏈取代含咔唑共軛高分子衍生物的合成及其應用於高分子發光二極體之研究 | zh_TW |
| dc.title | Synthesis and Application on Polymer Light Emitting Diode of Polycarbazole-Based Conjugated Polymers Derivatives Containing Triphenylamine, Oxadiazole, and Carbazole | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 98-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.coadvisor | 梁文傑(Man-Kit Leung) | |
| dc.contributor.oralexamcommittee | 韓錦鈴,黃誌楷,郭昭輝 | |
| dc.subject.keyword | 高分子發光二極體,咔,唑,雙極性, | zh_TW |
| dc.subject.keyword | Polymer light emitting diode,carbazole,bipolar, | en |
| dc.relation.page | 161 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2010-08-20 | |
| dc.contributor.author-college | 工學院 | zh_TW |
| dc.contributor.author-dept | 高分子科學與工程學研究所 | zh_TW |
| 顯示於系所單位： | 高分子科學與工程學研究所 | |
文件中的檔案：
| 檔案 | 大小 | 格式 | |
|---|---|---|---|
| ntu-99-1.pdf 未授權公開取用 | 4.85 MB | Adobe PDF |
系統中的文件，除了特別指名其著作權條款之外，均受到著作權保護，並且保留所有的權利。