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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/66760


    Title: 新型固著基團於光敏劑在染料敏化太陽能電池元件之應用
    Authors: 李庭育;Li,Ting-Yu
    Contributors: 化學學系
    Keywords: 染料敏化太陽能電池;DSSC
    Date: 2015-01-06
    Issue Date: 2015-03-16 15:10:48 (UTC+8)
    Publisher: 國立中央大學
    Abstract: 有機染料部分,我們合成出由pyridinium ylide骨架作為受端(acceptor)與固著基團(anchoring group)組成之新型有機染料NO109-NO111應用於染料敏化太陽能電池(DSSC)中。這些新型受端染料比起pyridine-N-oxide (NO107)與N-(carboxymethyl)-pyridinium (NO108)染料,在優化與開發高效率染料開啟一扇窗。在染料敏化太陽能電池中,NO111染料雙芽螯合(bidentate chelation)於TiO2上,其效率表現是所合成的染料中最高的。
    有機金屬染料部分,我們設計了拉電子基官能化之N-heterocyclic carbene (NHC)-pyridine配位基,合成出NHC-pyridine Ru錯合物,即CB102、CB103、DC101與CC321染料。在CB102與CB103染料中,我們由一個線性路徑,合成出NHC-pyridine Ancillary配位基,並且以廉價且快速的合成途徑,來合成Bipyridine Anchoring配位基。在DC101染料中,我們以溶劑效應來控制中間物構型(Conformation),成功達到反應專一性結果。在CC321染料中,我們對於NHC與碳陰離子之Ru錯合物的合成,提供了一個可行的路徑。
    ;A set of new organic dyes (NO109-NO111) consisting of pyridinium ylide skeleton as an acceptor and anchoring group were synthesized and characterized for applications in DSSCs. The comparative study of these new acceptor dyes with the pyridine-N-oxide and N-(carboxymethyl)-pyridinium analogous dyes can open up a window to optimize and develop an efficient dyes. A DSSC of dye NO111 with its bidentate chelation on TiO2 showed the highest efficiency among the synthesized dyes.
    We designed new N-heterocyclic carbene (NHC)-pyridine ligands with an electron-withdrawing substituents to construct various Ru complexs, (CB102, CB103, DC101, and CC321.) The NHC-pyridine ancillary ligand utilized in CB102 and CB103 dyes were synthesize through an linear synthetic routes. Also, a simple and cheap synthetic strategy was developed to synthesize the bipyridine anchoring ligand. In case of DC101 dye, we achieved the stereospecificity by utilizing the solvent effect which controls the conformation of the intermediate. In case of CC321 dye, we provid the first synthetic strategy to develope Ru-complex bearing both NHC and carbanion ligands.
    Appears in Collections:[Graduate Institute of Chemistry] Electronic Thesis & Dissertation

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