研究生: |
楊承翰 Yang-Cheng Han |
---|---|
論文名稱: |
合成具丙烯酸之錨基之染料敏化太陽能電池染料及其光物理性質研究 Synthesis and Photophysics of DSSC dyes with acrylic acidanchoring group |
指導教授: |
何郡軒
Jinn-Hsuan Ho |
口試委員: |
鄭志嘉
Chih-Chia Cheng 許智偉 Chih-Wei Hsu |
學位類別: |
碩士 Master |
系所名稱: |
工程學院 - 化學工程系 Department of Chemical Engineering |
論文出版年: | 2017 |
畢業學年度: | 105 |
語文別: | 中文 |
論文頁數: | 96 |
中文關鍵詞: | 分子內電荷轉移 、染料光敏化劑 |
外文關鍵詞: | (solvent effect), DMABN |
相關次數: | 點閱:178 下載:6 |
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本論文是合成具有噻吩及接有三苯胺為骨架之染料敏化電池之染料,增加推電子基強度及使用不同的拉電子基來探討結構的調整對吸收波長的影響,在三苯胺骨架中加上甲氧基,能增加共軛長度並且在實驗中發現能使吸收波長更加紅移在拉電子基方面,以改變不同官能基使染料之吸收波長更加紅移,並且使分子能吸收到更多可見光波長範圍。在本研究中是以鈴木偶聯反應(Suzuki coupling reaction)來合成,三苯胺作為骨架,噻吩作為共軛橋基及cyanoacrylic acid 及acetic acid 為拉電子基,並以核磁共振光譜圖(NMR)及質譜儀鑑定結構,利用紫外/光可見光光譜儀與循環電位儀來探討這四種染料性質。
Abstract
In this research, a series of DSSCs dyes with thien-2-yltriphenylamines (H and OMe substituent on triphenylamine part) skeleton and cyanoacrylic acid or acrylic acid anchoring groups have been synthesized by Suzuki coupling reaction and identified by nuclear magnetic resonance spectroscopy (NMR) and mass spectrometer. The photophysics of these dyes has been measured and were related to the substituents on triphenylamine group and anchoring groups. The most red-shift was showed in the case of the dye MOTTC containing methoxy substituents as electron-donating group and cyanoacrylic acid as electron-withdrawing group. MOTTC and its derivatives can absorb the visible light and is suitable for the application of solar cell
1.Tuning the HOMO and LUMO Energy Levels of Organic Chromophores for Dye Sensitized Solar Cells
2.F. Hurd, RLivingston, The quantum yields of some dye-sensitized photooxidations.
J. Phys. Chem, 1940, 44(7), 865-873.
3.M. K. Nazeeruddin, A. Kay, I. Rodicio, R. H. Baker, E.Miiller, P. Liska, N .
VlachopoulouM.Gratzel,Conversionoflighttoelectricitybycis-X2bis(2,2-bipyridyl-4,4-dicarboxylate)rutheniumcharge-transfer seensitizers(X=Cl-,Br-,I-,CN-and SCN-) on nanocrystalline titanium dioxide electrodes.J.Am.Chem.Soc.1993
4. M. Gratzel, Photoelectrochemical cells,” Nature, vol. 414, pp. 338-344, 2001a.
5. B. O’Regan and M. Grätzel, “A low-cost, high efficiency solar cell based on dye-sensitized colloidal TiO2 films,” Nature, vol. 353, pp. 737-740, 1991.
6. H. Tsubomura, M. Matsumura, Y, Nomura, T. Amamiya, Dye sensitised zinc
oxide: Aqueous electrolyte:platinum photocell.Nature, 1976, 261(5599)
7. Daniel P. Hagberg, Tannia Marinado, Karl Martin Karlsson, Kazuteru Nonomur
Peng Qin, Gerrit Boschloo, Tore Brinck,Anders Hagfeldt, and Licheng
8 . M.K. Nazeeruddin, F. De Angelis, S. Fantacci, A. Selloni, G. Viscardi, P.Liska,
S. Ito, B. Takeru, M. Grätzel, J.Am.Chem.Soc.127, 2005, 16835.
9. 許文碩國立台灣科技大學碩士論文 2015
10. S. Ito, S. M. Zakeeruddin, R. Humphry-Baker, P. Liska, R. Charvet,
P. Comte, M. K. Nazeeruddin, P. Péchy, M. Takata, H. Miura, S. UGchida, and M.
Grätzel, Adv. Mater. 2006, 18, 1202.
11. H. Choi, C. Baik, S. O. Kang, J. Ko, M.-S. Kang, Md. K. Nazeeruddin,
and M. Grätzel, Angew. Chem., Int. Ed. 2008,47, 327.
12. W. H. Liu, I. C. Wu, C. H. Lai, C. H. LaP.T.Chou, Y. T . Li, C. L.hen,Y.Y. Hsu, Y.Chi , Simple organic molecules bearing a 3,4-ethlenedioxythiophene linker for efficient dye-sensitized solar cells .Chem. Commun,2008
13. 陳志強, 有機發光二極體顯示器, 全華圖書,2007
14. T. Horiuchi, H. Miura, S. Uchida, Chem. Commun. 2003, 3036-3037
15.A. Yella, H. W. Lee, H. N. Tsao, C. Y. Yi, A. K. Chandiran, Md. haJaNazeeruddin,
W. G. Diau, C. Y, Yeh, S. M. Zakeeruddin, M. Gratzel, Science .334,629-634
16. N. Miyaura, K. Yamada, A. Suzuki, Tetrahedron Letters.1979, 36, 3437-3440
17.M. A. Green, K. emery, Y, Hishikawa, W. Warta, E .D. Dunlop,Solar cell efficiency
tables (Version45). Prog. Photovolt. Res. App. 2015, 23
18. W. E. Spear, P. G. Le Comber, Substitutional doping of amorphous silicon.
Solid State Commun , 1975, 17(9), 1193-1196. .
19. Ferrere, Suzanne, B. A. Gregg, New perylenes for dye sensitization of TiO2 solar cells. Chem. Mater.2004, 16(9), 1806-1812
20. GW Wheland, Resonance in organic chemistry, John Wiley&Sons, 1955.106.
21. G. L. Zhuo, X. Z. Jiang, B.Zhang, Z.H. Ge, Appl. Catal.A.2008,339,68-75.
22. M. Velusamy, K. R. J. Thomas, J. T. Lin, Y. C. Hsu, K. C. Ho, Org. Lett.2005, 1899-1902