博碩士論文 952203029 詳細資訊




以作者查詢圖書館館藏 以作者查詢臺灣博碩士 以作者查詢全國書目 勘誤回報 、線上人數:169 、訪客IP:3.128.78.41
姓名 陳柚全(Yu-Chuan Chen)  查詢紙本館藏   畢業系所 化學學系
論文名稱 單硫紫質衍生物的合成及光電轉換效率研究
(Synthesis of Thiophene Containing Thiaporphyrin Derivativesand their Application as Photo-sensitizing Dyes)
相關論文
★ 紫質衍生物研究:間位苯卟啉分子的鋅離子感測及大環紫質的構型★ N,N,O-蠍狀三牙基配位銅錯合物合成及C−H鍵活化反應研究
★ {Fe(NO)2}10 雙亞硝基鐵金屬錯合物的合成與鑑定及其產生過氧化亞硝酸根反應機制研究★ 氟苯取代氮碳異位紫質鐵錯合物之合成、鑑定與氧化反應
★ 氟取代與環氧化碳氮異位紫質錯合物研究★ 含噻吩基配位聚合物之合成,結構與螢光性質之探討
★ 具硝基和胺基取代之八乙基紫質金屬錯合物應 用於電催化二氧化碳還原研究★ 異位紫質釩氧錯合物之合成、光譜分析與 催化反應研究
檔案 [Endnote RIS 格式]    [Bibtex 格式]    [相關文章]   [文章引用]   [完整記錄]   [館藏目錄]   [檢視]  [下載]
  1. 本電子論文使用權限為同意立即開放。
  2. 已達開放權限電子全文僅授權使用者為學術研究之目的,進行個人非營利性質之檢索、閱讀、列印。
  3. 請遵守中華民國著作權法之相關規定,切勿任意重製、散佈、改作、轉貼、播送,以免觸法。

摘要(中) 本研究主要目的為研發新穎染料分子-單硫紫質化合物,將其應用於染料敏化太陽能電池並分析效能上的影響,我們將單硫紫質結合酸基利用相關非對稱合成文獻合成出10-(4-carboxyphenyl)-5,15,20-tris(p-tolyl)-21-monothiaporphyrin (8)、10,15-bis(4-carboxyphenyl)-5,20-bis(p-tolyl)-21-monothiaporphyrin (9)、
5,10,15,20-tetra(4-carboxyphenyl)-21-thiaporphyrin (13) 與推電子基3,4,5-trimethoxylbenzene 置入的單硫紫質化合物
10,15-bis(4-carboxyphenyl)-5,20-bis(3,4,5-trimethoxyphenyl)
-21-monothiaporphyrin (19),也將以上化合物的性質和光譜鑑定做初步探討。另外我們首度成功合出和鋅金屬化的Zinc(II) complex (20),也做了單晶X-ray 繞射分析。由偵測光電轉換效率實驗結果顯示,化合物8、9、13、19 的光電轉換率分別為0.11%、0.07%、0.06%、0.12%,化合物9 和19 的比照中發現經由推拉電子基設計的染料分子其光電轉換效率可提升約71%,因此推測取代基的推電子和立體結構特性,能降低染料分子在TiO2 上產生堆疊效應及電荷重組的可能,使電子能夠有效在染料和半導體導帶間進行傳遞。我們嘗試將附著酸基單硫紫質化合物的TiO2 film,利用第二次浸泡含有2,6-lutidine 的ZnCl2 溶液方式和鋅進行金屬化反應,經Uv-vis 光譜做初步分析和探討。
摘要(英) The purpose of this research is to synthesize novel molecular dyes that possess a potential of applying on the fabrication of dye-sensitized solar cells. Synthesis and
spectroscopic characterization of asymmetric free-base thisaporphyrins that are attached by various numbers of carboxylic acid and electron donating groups, 10-(4-carboxyphenyl)-5,15,20-tris(p-tolyl)-21-monothiaporphyrin (8),10,15-bis(4-carboxyphenyl)-5,20-bis(p-tolyl)-21-monothiaporphyrin (9), 5,10,15,20-tetra(4-carboxyphenyl)-21-thiaporphyrin (13), and 10,15-bis(4-carboxyphenyl)-5,20-bis(3,4,5-trimethoxyphenyl)-21-mono-thiaporphyrin (19), have been achieved. Moreover, the first zinc(II) thiaporphyrin complex (20) has also been successfully prepared, and the structural characterization was unambiguously corroborated with single-crystal X-ray diffraction analysis. From the measured result of solar energy to electricity conversion efficiency (η), the h values are 0.11, 0.07, 0.06, and 0.12% for compounds 8, 9, 13, and 19, respectively. With introduction of electron donating groups, 3,4,5-trimethoxylphenyl, into the skeleton of thiaporphyrin 9, the push-and-pull functional thiaporphyrin molecule (19) can be highly promoted ca. 71% on η value. By means of modification with push-and-pull
and steric crowded groups, the possibility of molecular aggregation as well as charge recombination could be decreased, i.e. the electronic communication between a
molecular dye and the conductive band of TiO2 could be improved. On the other hand, zinc metallation of thiaporphyrin molecules has been directly carried out on the surface of TiO2 film, which was attached by thiaporphyrin molecules, by monitoring the shift on the Uv-vis spectrum.
關鍵字(中) ★ 染料
★ 染料敏化太陽能電池
★ 光電轉換率
★ 單硫紫質
★ 紫質
關鍵字(英) ★ solar cells
★ dssc
★ thiaporphyrins
★ porphyrins
論文目次 章節 頁次
摘要
Abstract
謝誌
第一章 緒論 1
1-1. 紫質化合物簡介 1
1.2. 紫質衍生物 3
1-3. 紫質電子吸收光譜原理 3
1-4. 太陽能源的重要性 4
1-5. 太陽能電池的傳統發電原理 5
1-6. 染料敏化太陽能電池 6
1-7. 染料敏化太陽能電池工作原理 7
1-8. 染料敏化劑 8
1-9. 太陽能電池的重要參數 11
1-10. 研究動機與方向 12
第二章 單硫紫質的合成 15
單硫紫質染料及其衍生物的合成 15
第三章 實驗結果與討論 27
第四章 結論 88
第五章 未來展望 90
第六章 實驗步驟 91
參考文獻 110
參考文獻 (1) L. R., M. The Colours of Life:An Introduction to the Chemistry of Porphyrins and Related Compounds OUP, Oxford, 1997.
(2) Dolphin, ed. D. The Porphyrins Academic Press, New York, 1978.
(3) Campbell, W. M.; Burrell, A. K.; Officer, D. L.; Jolley, K. W. Coord. Chem. Rev. 2004, 248, 1363.
(4) Ghosh, A. Angew. Chem. Int. Ed. 2004, 43, 1918-1931.
(5) Narayanan, S. J.; Sridevi, B.; Chandrashekar, T. K.; Vij, A.; Roy, R. J. Am. Chem. Soc. 1999, 121, 9053-9068.
(6) Chmielewski, P. J.; Latos-Grazynski, L. Coordination Chemistry Reviews 2005, 249, 2510-2533.
(7) Furuta, H.; Ishizuka, T.; Osuka, A.; Ogawa, T. J. Am. Chem. Soc. 1999, 121, 2945-2946.
(8) Pushpan, S. K.; Srinivasan, A.; Anand, V. G.; Venkatraman, S.; Chandrashekar, T. K.; Joshi, B. S.; Roy, R.; Furuta, H. J. Am. Chem. Soc. 2001, 123,
5138-5139.
(9) Fowler, C. J.; Sessler, J. L.; Lynch, V. M.; Waluk, J.; Gebauer, A.; Lex, J.; Heger, A.; Zuniga-y-Rivero, F.; Vogel, E. Chem. Eur. J. 2002, 8, 3485-3496.
(10) Gouterman, M. J. Mol. Spectroscopy 1961, 6, 138.
(11) http://www.solar-i.com/know.html#12
(12) Frank Hurd and Robert Livingston. J. Phys. Chem. 1940, 44, 865.
(13) S. Chaberek, A. Shepp and R. J. Allen. J. Phys. Chem. 1965, 69, 641.
(14) S. Chaberek, A. Shepp and R. J. Allen. J. Phys. Chem. 1965, 69, 647.
(15) S. Chaberek, A. Shepp and R. J. Allen. J. Phys. Chem. 1965, 69, 2834.
(16) Kearns et al. J. Am. Chem. Soc. 1967, 89, 5456.
(17) H. Tsubomura.; M. Matsumura.; Y. Nomura and T. Amamiya. Nature. 1976, 261, 402.
(18) O’Regan, B. and M. Grätzel. Nature 1991, 353, 737.
(19) M. Grätzel. Inorg. Chem. 2005, 44, 6841.
(20) Zhong-Sheng Wang.; Masatoshi Yanagida.; Kazuhiro Sayama and Hideki Sugihara. Chem. Mater. 2006, 18, 2912-2916.
(21) O’Regan, B. and M Grätzel. Nature 1991, 353, 737-740.
(22) M. Grätzel. Nature 2001, 414, 338-344.
(23) M. Grätzel. J. Photochem. and Photobio. A:Chem. 2004, 164, 3-14.
(24) Robertson, N. Angew. Chem. Int. Ed. 2006, 45, 2338.
(25) M. Grätzel. J. Photochem. and Photobio.C- Photochem. Rev. 2003, 4, 145.
(26) C. Klein.; Md. K. Nazeeruddin.; D. Di. Censo.; P. Liska and M. Grätzel. Inorg. Chem. 2004﹐43﹐4216-4226.
(27) Nazeeruddin, M. K.; Penchy, P.; Grätzel, M. Chem. Commum. 1997, 1705.
(28) Nazeeruddin, M. K.; Zakeeruddin, S. M.; Humphrey-Baker, R.; Jirousek, M.; Liska, P.; Vlachopoulos, N.; Shklover, V.; Fischer, C.-H.; Grätzel, M. Inorg. Chem. 1999, 38, 6298.
(29) M. Grätzel. Prog. Photovolt. Res. Appl. 2000, 8, 171-185.
(30) A. Hagfeldt, M. Grätzel. Acc. Chem. Res. 2000, 33, 269-277.
(31) Kim. S. Finnie.; John R. Bartlett and James L. Woolfrey, Langmuir. 1998, 14, 2744-2749.
(32) Nazeeruddin, M. K.; Penchy, P.; Renouard, T. et al. J. Am. Chem. Soc. 2001, 123, 1613-1624.
(33) C. Bauer.; G. Boschloo.; E. Mukhtar.; A. Hagfeldt. J. Phys.Chem. B .2002, 106, 12693-12704.
(34) P. D. Cozzoli.; R. Comparelli.; E. Fanizza.; M. L. Curri.; A. Agostiano.; D. Laub. J. Am. Chem. Soc. 2004, 126, 3868-3879.
(35) S. Punidha.; Neeraj Agarwal.; Iti Gupta.; M. Ravikanth. Eur. J. Org. Chem. 2007, 1168-1175.
(36) Jerzy Lisowski.; Lechoslaw Latos-Grazynski.; Ludmila Szterenberg. Inorg. Chem. 1992, 31, 1933-1940.
(37) Piotr J. Chmielewski and Lechoslaw Latos-Grazynski. Inorg. Chem. 1992, 31, 5231-5235.
(38) J.-Y. Tung et al. Inorganic Chemistry Communications. 2002, 5, 150-155.
(39) Iti Gupta.; M. Ravikanth. J. Photochem. and Photobio. A:Chem. 2006, 177, 156-163.
(40) Andreas Gebauer.; Joseph A. R. Schmidt.; John Arnold. Inorg. Chem. 2000, 39, 3424-3427.
(41) Iti Gupta.; M. Ravikanth. J. Org. Chem. 2004, 69, 6796-6811.
(42) Won-Seob Cho.; Han-Je Kim.; Benjamin J. Littler.; Mark A. Miller.; Chang-Hee Lee.; Jonathan S. Lindsey. J. Org. Chem. 1999, 64, 7890-7901.
(43) Silvio Stute.; Kerstin Gloe.; Karsten Gloe. Tetrahedron, 2005, 61, 2907-2912.
(44) http://zh.wikipedia.org/w/index.php? title=Image:SolarCell_StructuralDrawing.JPG&variant=zh-tw
(45) M. Grätzel. Nature 2001, 414, 338-344.
(46) 林明獻編著,太陽電池技術入門.
(47) Suman Cherian and Carl C. Wamser. J. Phys. Chem. B, 2000, 104 (15), 3624 -3629.
指導教授 洪政雄(Chen-hsiung Hung) 審核日期 2008-11-11
推文 facebook   plurk   twitter   funp   google   live   udn   HD   myshare   reddit   netvibes   friend   youpush   delicious   baidu   
網路書籤 Google bookmarks   del.icio.us   hemidemi   myshare   

若有論文相關問題,請聯絡國立中央大學圖書館推廣服務組 TEL:(03)422-7151轉57407,或E-mail聯絡  - 隱私權政策聲明