Synthesis of Thiophene Derivatives as π-conjugated linker Photosensitized Dyes

碩士 === 國立臺北科技大學 === 有機高分子研究所 === 98 === In this thesis, several triphenylamine dyes, containing high hole mobility of thienothiophene , bithiophene and n-hexyl-substituted thienothiophene as π-conjugated linker, were synthesized . The organic dyes with the structure of donor-conjugated chain-acce...

Full description

Bibliographic Details
Main Authors: Chih-Hong Huang, 黃志弘
Other Authors: 張淑美
Format: Others
Language:zh-TW
Published: 2010
Online Access:http://ndltd.ncl.edu.tw/handle/233yrn
id ndltd-TW-098TIT05310004
record_format oai_dc
spelling ndltd-TW-098TIT053100042019-05-15T20:33:23Z http://ndltd.ncl.edu.tw/handle/233yrn Synthesis of Thiophene Derivatives as π-conjugated linker Photosensitized Dyes 含併二噻吩及二噻吩π共軛鏈之光敏染料合成 Chih-Hong Huang 黃志弘 碩士 國立臺北科技大學 有機高分子研究所 98 In this thesis, several triphenylamine dyes, containing high hole mobility of thienothiophene , bithiophene and n-hexyl-substituted thienothiophene as π-conjugated linker, were synthesized . The organic dyes with the structure of donor-conjugated chain-acceptor have been synthesized for dye sensitized solar cell (DSSC). The effects of both the length of the π-conjugated unit and of the alkyl chain up on the photophysical, electrochemical and photovoltaic properties of the dyes were studied. All of these compounds were characterized by UV/VIS spectrophotometer, fluorescence spectrophotometer and cyclic voltammetry. The photoconversion of these compounds were inspected using the AM 1.5 simulated solar light system. 張淑美 2010 學位論文 ; thesis 132 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 國立臺北科技大學 === 有機高分子研究所 === 98 === In this thesis, several triphenylamine dyes, containing high hole mobility of thienothiophene , bithiophene and n-hexyl-substituted thienothiophene as π-conjugated linker, were synthesized . The organic dyes with the structure of donor-conjugated chain-acceptor have been synthesized for dye sensitized solar cell (DSSC). The effects of both the length of the π-conjugated unit and of the alkyl chain up on the photophysical, electrochemical and photovoltaic properties of the dyes were studied. All of these compounds were characterized by UV/VIS spectrophotometer, fluorescence spectrophotometer and cyclic voltammetry. The photoconversion of these compounds were inspected using the AM 1.5 simulated solar light system.
author2 張淑美
author_facet 張淑美
Chih-Hong Huang
黃志弘
author Chih-Hong Huang
黃志弘
spellingShingle Chih-Hong Huang
黃志弘
Synthesis of Thiophene Derivatives as π-conjugated linker Photosensitized Dyes
author_sort Chih-Hong Huang
title Synthesis of Thiophene Derivatives as π-conjugated linker Photosensitized Dyes
title_short Synthesis of Thiophene Derivatives as π-conjugated linker Photosensitized Dyes
title_full Synthesis of Thiophene Derivatives as π-conjugated linker Photosensitized Dyes
title_fullStr Synthesis of Thiophene Derivatives as π-conjugated linker Photosensitized Dyes
title_full_unstemmed Synthesis of Thiophene Derivatives as π-conjugated linker Photosensitized Dyes
title_sort synthesis of thiophene derivatives as π-conjugated linker photosensitized dyes
publishDate 2010
url http://ndltd.ncl.edu.tw/handle/233yrn
work_keys_str_mv AT chihhonghuang synthesisofthiophenederivativesaspconjugatedlinkerphotosensitizeddyes
AT huángzhìhóng synthesisofthiophenederivativesaspconjugatedlinkerphotosensitizeddyes
AT chihhonghuang hánbìngèrsāifēnjíèrsāifēnpgòngèliànzhīguāngmǐnrǎnliàohéchéng
AT huángzhìhóng hánbìngèrsāifēnjíèrsāifēnpgòngèliànzhīguāngmǐnrǎnliàohéchéng
_version_ 1719100544404946944