Fabrication of all-solid-state dye-sensitized solar cells and synthesis of triphenylamine-based organic dyes

碩士 === 國立高雄大學 === 化學工程及材料工程學系碩士班 === 100 === In this study, light-sensitive and all-organic of dye molecules have been synthesized by triphenylamine linked with N-Methylpyrrole structure. All-organic dye molecules, compared to the commercially-available ruthenium-based complexe type, hvae the advant...

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Main Authors: Yu-jyun Pan, 潘俞均
Other Authors: Chien-hsin Yang
Format: Others
Language:zh-TW
Published: 2012
Online Access:http://ndltd.ncl.edu.tw/handle/97784484415165753277
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spelling ndltd-TW-100NUK050630112016-07-15T04:17:16Z http://ndltd.ncl.edu.tw/handle/97784484415165753277 Fabrication of all-solid-state dye-sensitized solar cells and synthesis of triphenylamine-based organic dyes 全固態染料敏化太陽能電池製作與三苯胺系列染料合成 Yu-jyun Pan 潘俞均 碩士 國立高雄大學 化學工程及材料工程學系碩士班 100 In this study, light-sensitive and all-organic of dye molecules have been synthesized by triphenylamine linked with N-Methylpyrrole structure. All-organic dye molecules, compared to the commercially-available ruthenium-based complexe type, hvae the advantages of high absorption coefficient, the designable and metal-free. We made use of the Vilsmeier-Haack reaction, bromination, Kumada coupling reaction, Suzuki coupling reaction and Knoevenagel condensation reaction for the photosensitive organic dye molecules. We chelated titanium dioxide nanoparticles by the groups of cyanoacetic acid. And then Optical, electrical and photoelectric conversion efficiency were measured. The optimal efficiency of DSSCs reaches to 0.34% for MTPA1 dye. In addition, We fabricated all-solid-state dye-sensitized solar cells and used Poly(3-hexylthiophene) as the Hole Transfer Materials. We compared the photoelectric conversion efficiency of the market organic dye (N3, D131 and D149) with the inorganic dye (Sb2S3).The optimal efficiency of DSSCs reaches to 2.48% for N3 dye. Chien-hsin Yang 楊乾信 2012 學位論文 ; thesis 146 zh-TW
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language zh-TW
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description 碩士 === 國立高雄大學 === 化學工程及材料工程學系碩士班 === 100 === In this study, light-sensitive and all-organic of dye molecules have been synthesized by triphenylamine linked with N-Methylpyrrole structure. All-organic dye molecules, compared to the commercially-available ruthenium-based complexe type, hvae the advantages of high absorption coefficient, the designable and metal-free. We made use of the Vilsmeier-Haack reaction, bromination, Kumada coupling reaction, Suzuki coupling reaction and Knoevenagel condensation reaction for the photosensitive organic dye molecules. We chelated titanium dioxide nanoparticles by the groups of cyanoacetic acid. And then Optical, electrical and photoelectric conversion efficiency were measured. The optimal efficiency of DSSCs reaches to 0.34% for MTPA1 dye. In addition, We fabricated all-solid-state dye-sensitized solar cells and used Poly(3-hexylthiophene) as the Hole Transfer Materials. We compared the photoelectric conversion efficiency of the market organic dye (N3, D131 and D149) with the inorganic dye (Sb2S3).The optimal efficiency of DSSCs reaches to 2.48% for N3 dye.
author2 Chien-hsin Yang
author_facet Chien-hsin Yang
Yu-jyun Pan
潘俞均
author Yu-jyun Pan
潘俞均
spellingShingle Yu-jyun Pan
潘俞均
Fabrication of all-solid-state dye-sensitized solar cells and synthesis of triphenylamine-based organic dyes
author_sort Yu-jyun Pan
title Fabrication of all-solid-state dye-sensitized solar cells and synthesis of triphenylamine-based organic dyes
title_short Fabrication of all-solid-state dye-sensitized solar cells and synthesis of triphenylamine-based organic dyes
title_full Fabrication of all-solid-state dye-sensitized solar cells and synthesis of triphenylamine-based organic dyes
title_fullStr Fabrication of all-solid-state dye-sensitized solar cells and synthesis of triphenylamine-based organic dyes
title_full_unstemmed Fabrication of all-solid-state dye-sensitized solar cells and synthesis of triphenylamine-based organic dyes
title_sort fabrication of all-solid-state dye-sensitized solar cells and synthesis of triphenylamine-based organic dyes
publishDate 2012
url http://ndltd.ncl.edu.tw/handle/97784484415165753277
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