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| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 謝國煌 | |
| dc.contributor.author | Shao-Chieh Chen | en |
| dc.contributor.author | 陳紹傑 | zh_TW |
| dc.date.accessioned | 2021-06-15T00:21:29Z | - |
| dc.date.available | 2011-02-12 | |
| dc.date.copyright | 2009-02-12 | |
| dc.date.issued | 2009 | |
| dc.date.submitted | 2009-02-04 | |
| dc.identifier.citation | 1. Brabec, C. J.; Sariciftci, N. S.; Hummelen, J. C. Adv. Funct. Mater. 2001, 11, 15 – 26.
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| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/41518 | - |
| dc.description.abstract | 高分子太陽能電池由於其價格低廉，可利用溶液態時以捲式塗佈技術進行大面積加工，且於應用上具可撓性，使這項研究近幾年來受到極大重視。目前由P3HT/PCBM混成系統做成的太陽能電池元件效率為4%，為了製備效率超越P3HT/PCBM混成的太陽能電池元件，尋找一具備適當能階的低能隙高分子便成一重要課題。低能隙高分子對太陽光譜中可見光至近紅外光區段有較廣的吸收因而能有效提升太陽能元件之效率。在本篇碩士論文中，藉由Suzuki連結聚合法成功合成出施體與受體交替式之高分子PF-co-DMOTB及PC-co-DMOTB，合成之兩種高分子對一般溶劑具良好的溶解性，UV吸收光譜亦可發現其對可見光有良好的吸收。電化學及光學上測量判斷其能隙與能階，PF-co-DMOTB 其能隙為1.90eV ，PC-co-DMOTB則為1.82eV，其低能隙及施體受體交替之特性使其對光譜有較廣之吸收。由循環伏安法測量高分子HOMO之能階， PF-co-DMOTB為-5.19eV ，PC-co-DMOTB為-5.70eV，均低於P3HT之HOMO能階，此項優點使其製成元件時能形成較高之開路電壓。塊材異質接面型太陽能電池製做時將高分子與碳材PCBM混掺做主動層，導電玻璃 ITO為陽極，上層鋁金屬為陰極，實驗結果顯示，製備太陽能電池之最佳效率為由高分子PF-co-DMOTB與PCBM混掺比例為1：4時而得，各項參數如下：開路電壓Voc=0.69 eV，短路電流Jsc=1.06 mA cm-2 ，填充系數FF=0.25，及元件效率0.18%，此結果於太陽光模擬器A.M.1.5強度為100 mW cm-2下測得。 | zh_TW |
| dc.description.abstract | Polymer solar cells (PSCs) have attracted stong interest in recent years due to the prospect of low cost, solution-based processing and the capability to fabricate flexible devices. To further enhance the power conversion efficiency of 4% achieved from solar cells made of regioregular poly(3-hexylthiophene)/[6,6]-phenyl-C61-butyric acid methyl ester (P3HT/PCBM), a low band gap conjugated polymers with proper energy levels for charge transfer are required. Low optical bandgap conjugated polymers may improve the efficency of organic photovoltaic devices by increasing the absorption in the visible and near infrared region of the solar spectrum. In this master thesis work, I synthesized two new highly soluble and strongly visible-light absorbing alternating polymers using Suzuki coupling polymerization method that are based on 4,7-Bis-(3,4-dimethoxy-thiophen-2-yl)-benzo[1,2,5]thiadiazole monomers: poly[2,7-(9,9-dihexylfluoren)-alt-5,5-(4,7-Bis-(3,4-dimethoxy-thiophen-2-yl)-benzo[1,2,5]thiadiazole] (PF-co-DMOTB) and poly[9-eicosyl-3,6-carbazole-alt-5,5-(4,7-Bis-
(3,4-dimethoxy-thiophen-2-yl)-benzo[1,2,5]thiadiazole](PC-co-DMOTB). Electrochemical and photophysical studies reveal band gaps of 1.90eV for PF-co-DMOTB and 1.82eV for PC-co-DMOTB, which could effectively harvest broader solar spectrum. The cyclic voltammetry measurements show that the HOMO level of the polymers are -5.19eV for PF-co-DMOTB and -5.70eV for PC-co-DMOTB which are significantly lower than that of P3HT. Bulk heterojuncion photovoltaic devices were fabricated using blends of these copolymers with PCBM as the active layer, ITO-glass as the anode, and aluminum as the cathode. It is observed that the best performing solar cell device which made from polymer PF-co-DMOTB (80 wt% PCBM) delivers an open circuit voltage Voc=0.69 eV, Jsc=1.06 mA cm-2 , FF=0.25 and power conversion efficiency 0.18% under an illumination of A.M.1.5 with an intensity of 100 mW cm-2. | en |
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| dc.description.tableofcontents | 目錄
摘要………………….………………………..………………………...………………..I Abstract…..………………………………………………………………..……..……..II 目錄…………………………………………………………………………………….IV 圖索引………………………………...…………………………..……………………VI 表索引…………………………………………………………………................…..VIII 第一章 緒論 ………………………………………….…......…………….……...……1 第二章 文獻回顧 2-1 共軛高分子與碳材混掺之有機太陽能電池基本操作原理………….……...2 2-2 有機太陽能電池之元件結構………………………………………….……...5 2-2-1雙層結構……………………………………………………….……….5 2-2-2 塊材異質接面(Bulk heterojunction)結構………….……………...….5 2-3 應用於有機太陽能電池之高分子材料............................................................7 2-3-1有機太陽能電池材料簡介......................................................................7 2-3-2 PPV:PCBM系統之太陽能電池………………………………9 2-3-3 Poly(3-alkylthiophene) : PCBM系統之太陽能電池............................11 2-4交替式施體-受體共軛高分子..........................................................................12 2-4-1交替式施體-受體共軛高分子介紹………………….………………..12 2-4-2交替式施體-受體共軛高分子應用於太陽能電池………………..….13 2-5近年來應用於太陽能電池之高分子新材料介紹...........................................14 第三章 實驗方法…………………………………………….……………………..…22 3-1 實驗藥品..........................................................................................................22 3-2 使用儀器..........................................................................................................24 3-3 實驗流程…………………………………………………………….……….25 3-3-1 單體合成...............................................................................................25 3-4 實驗步驟................................……………...…………………………..…….27 3-4-1 單體合成方法………………..……….………………..……………..27 3-4-2 聚合反應……………………..……….................................................37 3-4-2-1 PF-co-DMOTB聚合反應……………….……………......….37 3-4-2-2 PC-co-DMOTB聚合反應………………………………...….38 3-5性質測試………….………………………………………..…….……..…….39 第四章 結果與討論……………………………………………………….………..…40 4-1單體及高分子合成方法與鑑定.......................................................................40 4-2 光學及電化學性質..........................................................................................41 4-3 太陽能元件製作及效率測試..........................................................................46 第五章 結論………………………………….………………………………………..57 參考文獻……………………………………….………………………………………58 附錄………………………………………..………………………………...…………64 GPC Data………………………………………………………………………….65 NMR Spectra..…………………………………….………..….………………….66 圖索引 圖2.1 光子轉換成自由載子機制示意圖………………………..……………………3 圖2.2 Bulk heterojunction結構與影響元件效率之各參數示意圖…………………..4 圖2.3 有機太陽能電池雙層結構示意圖………………………………..……..………5 圖2.4 Bulk heterojunction結構之示意圖……………………………………………..6 圖2.5 常用於有機太陽能電池材料之結構圖..............................................................7 圖2.6 施體(D)與受體(A)軌域混成D-A monomer低能隙示意圖................................12 圖3.1 單體4,7-Bis-(5-bromo-3,4-dimethoxy-thiophen-2-yl)-benzo[1,2,5]thiadiazole 之合成...............................................................................................................25 圖3.2 單體9-Eicosyl-3,6-bis-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)- 9H-carbazole之合成........................................................................................... 26 圖3.3 合成高分子PF-co-DMOTB…………………………………………………….37 圖3.4 合成高分子PC-co-DMOTB……………………………………………………38 圖4.3 PF-co-DMOTB UV吸收光譜............................................................................41 圖4.4 PC-co-DMOTB UV吸收光譜............................................................................42 圖4.5 (a)高分子PF-co-DMOTB CV量測之氧化電位圖 (b)高分子PC-co-DMOTB CV量測之氧化電位圖............................................44 圖4.6 (a)PF-co-DMOTB, PCBM, PEDOT:PSS, ITO與Al電極相對能階圖 (b)PC-co-DMOTB, PCBM, PEDOT:PSS, ITO與Al電極相對能階圖..............45 圖4.7 太陽能元件結構圖..............................................................................................46 圖4.8 PF-co-DMOTB與PCBM 混掺比例1：1製備太陽能元件之電流-電壓特性圖.........................................................................................................................48 圖4.9 PF-co-DMOTB與PCBM混掺於不同轉速成膜後之UV-vis吸收....................48 圖4.10 PF-co-DMOTB與PCBM混掺比例1：4製備太陽能元件電流-電壓特性圖.....50 圖4.11 PF-co-DMOTB與PCBM混掺於不同轉速成膜後之UV-vis吸收.....................50 圖4.12 PF-co-DMOTB與PCBM混掺 1：4時之AFM圖(a)高度圖(b)相圖(c)平均粗糙度.....................................................................................................................51 圖4.13 PC-co-DMOTB與PCBM混掺不同轉速下製備太陽能元件之電流-電壓特性圖.........................................................................................................................52 圖4.14 PC-co-DMOTB與PCBM混掺不同轉速及混掺比例下製備太陽能元件之電流-電壓特性圖....................................................................................................53 圖4.15 PC-co-DMOTB與PCBM混掺成膜之UV-vis吸收..........................................54 圖4.16 PC-co-DMOTB與PCBM混掺於Chloroform與DCB混合溶劑下製備太陽能元件之電流-電壓特性圖................................................................................55 表索引 表2.1 應用於太陽能電池之有機材料化學結構及其光電轉換效率........................15 表4.1 PF-co-DMOTB於不同轉速製備太陽能元件之效率與各項參數..................48 表4.2 PF-co-DMOTB於不同轉速製備太陽能元件之效率與各項參數..................50 表4.3 PC-co-DMOTB於不同轉速製備太陽能元件之效率與各項參數.................52 表4.3 PC-co-DMOTB以Chloroform為溶劑於不同混掺比例及轉速製備太陽能元 件之效率與各項參數.......................................................................................54 表4.4 PC-co-DMOTB以Chloroform與DCB混合溶劑於不同混掺比例及轉速製備太陽能元件之效率與各項參數...................................................................56 表4.5 PC-co-DMOTB以Chloroform溶劑固定混掺比例不同轉速下製備太陽能元件之效率與各項參數.......................................................................................56 | |
| dc.language.iso | zh-TW | |
| dc.subject | 電子施體/受體 | zh_TW |
| dc.subject | 高分子太陽能電池 | zh_TW |
| dc.subject | Suzuki 連結聚合法 | zh_TW |
| dc.subject | 低能隙 | zh_TW |
| dc.subject | Polymer solar sell | en |
| dc.subject | Low band gap | en |
| dc.subject | Donor-acceptor | en |
| dc.subject | Suzuki coupling | en |
| dc.title | 新穎施體-受體聚噻吩系共軛高分子衍生物之合成及有機太陽能電池應用 | zh_TW |
| dc.title | Novel Donor-Acceptor Conjugated Benzothiadiazole-based Copolymers Synthesis and Applications for Organic Solar Cell | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 97-1 | |
| dc.description.degree | 碩士 | |
| dc.contributor.coadvisor | 顏溪成 | |
| dc.contributor.oralexamcommittee | 韓錦鈴 | |
| dc.subject.keyword | 低能隙,Suzuki 連結聚合法,電子施體/受體,高分子太陽能電池, | zh_TW |
| dc.subject.keyword | Low band gap,Suzuki coupling,Donor-acceptor,Polymer solar sell, | en |
| dc.relation.page | 71 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2009-02-04 | |
| 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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|---|---|---|---|
| ntu-98-1.pdf 未授權公開取用 | 2.63 MB | Adobe PDF |
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