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  1. NTU Theses and Dissertations Repository
  2. 工學院
  3. 高分子科學與工程學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/23010
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dc.contributor.advisor謝國煌
dc.contributor.authorWei-Lin Wuen
dc.contributor.author吳韋霖zh_TW
dc.date.accessioned2021-06-08T04:37:38Z-
dc.date.copyright2009-08-20
dc.date.issued2009
dc.date.submitted2009-08-17
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/23010-
dc.description.abstract本研究目的為合成出帶有苯並噻雙唑(Benzothiadiazole)側鏈的卡唑單體,再透過Yamamoto反應聚合均聚物(Homopolymer) P1,以及利用Stille反應與雙錫官能機的噻吩共聚成共聚物(Copolymer)P2。由凝膠滲透層析儀(Gel permeation chromatography, GPC)分析結果,P1之重量平均分子量(M¬¬w)為3775 g/mol而P2之Mw分佈在1000~2000 g/mol左右。熱重分析(Thermogravimetry analysis)結果則顯示P1和P2足以耐熱至200 oC以上,具有很好的熱穩定性。由光學性質的測試,P1和P2由於都帶有分子內的電子予體/電子施體(Donor/Acceptor)結構,所以在紫外-可見光(UV-visible)吸收光譜皆有兩個特性吸收峰,從光譜上可得出P1及P2之能隙(Band gap)分別為2.33 eV及2.38 eV。經循環伏安法(Cyclic voltammetry, CV)測試電化學性質,P2比P1擁有更高的氧化電位(1.3 eV),表示引入噻吩共聚可以有效提升分子的抗氧化性質,同時具有較低的最高電子填滿軌域(Highest occupied molecular orbital, HOMO)能階,較有機會作為高效率的高分子太陽能電池材料。zh_TW
dc.description.abstractIn this studies, carbaozle derivative monomers with benzothiadiazole side chain were synthesized and polymerized. Two novel polymer, Poly[9-(2,5-bis(hexyloxy)-4- (4-(5-methyl- thiophen-2-yl)benzo[c][1,2,5]thiadiazol-7-yl)phenyl)-9H-carbazole] (P1)
and poly[9-(2,5-bis(hexyloxy)-4-(4-(5-methyl-thiophen-2-yl)benzo[c][1,2,5]thiadiazol-
7-yl) phenyl)-9H-carbazole-alt-thiophene] (P2) were synthesized via Yamamoto coupling and Stille coupling reactions. According to thermogravimetry analysis, P1 and P2 possess great thermal stability. Due to the intramolecular electron donor-acceptor structure, the UV-visible absorption spectrum of polymers have two significant peak. From the absorption spectrum, P1 exhibits lower band gap (2.33 eV) than P2 (2.38 eV). In electrochemical analysis, copolymer P2 possesses lower highest occupied molecular orbital (HOMO) level (-5.57 eV) than homopolymer P1 (5.16 eV). Althogh P2 has higher band gap, P2 has lower HOMO which is essential parameter for high efficiency polymer solar cells. From the above analysis, carbazole derivatives with benzothiadiazoel side chain have potential for applications of polymer photovoltaics.
en
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en
dc.description.tableofcontents摘要 I
ABSTRACT II
目錄 III
表目錄 V
圖目錄 VI
第一章 緒論 1
1-1 前言 1
1-2 研究動機 1
第二章 文獻回顧 3
2-1 有機太陽能電池歷史簡介 3
2-2 有機太陽能電池運作原理 4
2-2.1 雙層(或多層)異質接面元件簡介 9
2-2.2 單層異質接面元件介紹 10
2-3 有機太陽能電池特性分析 11
2-3.1 開路電壓 11
2-3.2 短路電流 12
2-3.3 填充因子 12
2-3.4 能量轉換效率 13
2-3.5 影響元件效率之製程參數 14
2-3.6 提升元件效率之製程 14
2-4 高分子太陽能電池材料回顧 16
2-4.1 聚芴(Polyfluorene)系列 18
2-4.2 含矽原子聚合物系列 19
2-4.3 聚卡唑(Polycarbazole)系列 19
2-4.4 共軛側鏈聚合物 20
2-4.5 總結 21
第三章 實驗部分 33
3-1 實驗藥品與溶劑 33
3-3 實驗儀器 36
3-4 單體及聚合流程 39
3-5 合成步驟 43
第四章 結果與討論 50
4-1 合成結果分析 50
4-2 熱穩定性質探討 51
4-3 光學性質探討 53
4-4 電化學性質探討 56
第五章 結論 59
參考文獻 60
附錄 69
dc.language.isozh-TW
dc.subject共軛高分子zh_TW
dc.subject電子施體/受體zh_TW
dc.subject低能隙zh_TW
dc.subject太陽能電池zh_TW
dc.subject異質接面zh_TW
dc.subjectBulk heterojunctionen
dc.subjectElectron donor/acceptoren
dc.subjectSolar cellsen
dc.subjectConjugated polymersen
dc.subjectLow band gapen
dc.title含苯並噻雙唑側鏈之卡唑高分子衍生物之合成及其光電特性zh_TW
dc.titleSyntheses and Photovoltaic Characterizations of Polycarbazole Derivatives with Benzothiadiazole Side Chainen
dc.typeThesis
dc.date.schoolyear97-2
dc.description.degree碩士
dc.contributor.oralexamcommittee韓錦鈴,王怡仁
dc.subject.keyword低能隙,異質接面,電子施體/受體,太陽能電池,共軛高分子,zh_TW
dc.subject.keywordLow band gap,Bulk heterojunction,Electron donor/acceptor,Solar cells,Conjugated polymers,en
dc.relation.page82
dc.rights.note未授權
dc.date.accepted2009-08-17
dc.contributor.author-college工學院zh_TW
dc.contributor.author-dept高分子科學與工程學研究所zh_TW
顯示於系所單位:高分子科學與工程學研究所

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