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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 周大新(Tashin J. Chow) | |
dc.contributor.author | Po-Ting Chou | en |
dc.contributor.author | 周柏廷 | zh_TW |
dc.date.accessioned | 2021-05-19T18:03:03Z | - |
dc.date.available | 2024-12-31 | |
dc.date.available | 2021-05-19T18:03:03Z | - |
dc.date.copyright | 2014-07-15 | |
dc.date.issued | 2014 | |
dc.date.submitted | 2014-07-15 | |
dc.identifier.citation | 第一章
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dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/8020 | - |
dc.description.abstract | 利用電子予體-共軛架橋-電子受體(Donor-π-Bridge-Acceptor)架構設計並合成染敏太陽能電池染料。使用奈米級二氧化鈦所做的工作電極、I-/I3-電解質與Pt對電極,製作出太陽能電池元件。
第二章使用不同第三丁基芳香環胺作為電子予體,以Stille coupling方式建構出具有末端醛基的phenylene-thiophene-phenylene (PSP)共軛架橋分子,再以Knoevenagel condensation,使用cyanoacetic acid與末端醛基去建構出含有末端酸基的電子受體,並製作成太陽能電池元件探討,電子予體的改變對於染料效率的影響。元件效率測得最好的為化合物CB-PSP,其轉換效率最高可達到6.70 %。為了證明第三丁基可幫助減少分子堆疊,使用CDCA作為共吸附劑,發現其元件效率呈現下降的趨勢,表示有可能減少二氧化鈦上的染料吸附量,造成元件Jsc減少。由此證明CB-PSP在具有第三丁基時,可能會減少分子堆疊的情況。 第三章為使用phenothiazine做為染料主體,由於其構型上為非平面,其構型亦可減少分子本身的堆疊。因此將phenothiazine作為一個單位,在氮上建構出兩種不同鏈長的官能基,再以NBS溴化、低溫下以正丁基鋰和N,N-二甲基甲醯胺或是三異丙基硼酸,製作具有溴基、醛基及硼酸官能基的phenothiazine結構,以Suzuki coupling建構出具有醛基的單體、雙聚體和三聚體的phenothiazine,再以Knoevenagel condensation,使用cyanoacetic acid與末端醛基去建構出含有末端酸基的電子受體。在元件效率測得以雙聚體系統有較好的效率,並且以具4-(hexyloxy)-phenyl group的PT2b其轉換效率可達到7.38 %,並且在加入共吸附劑DCA後,由於幫助調整染料在二氧化鈦上的排列和減少I3-和二氧化鈦接觸,轉換效率可達7.78 %。 第四章使用1,3-indandione-5,6-dicarboxylic acid做為電子受體,由於1,3-indandione具有相當強的拉電子性,相當容易將吸收範圍往紅光區移動,故使用其衍生物期望較短共軛系統下就可以得到較廣的吸收範圍。在酸性條件下使用1,3-indandione-5,6-dicarboxylic acid與具有醛基的芳香環胺作縮和反應,並且製作成太陽能電池元件探討。與cyanoacetic acid所作之染料相比,吸收光譜有約100 nm的紅位移,表示1,3-indandione-5,6-dicarboxylic acid具有相當強的拉電子基性質。將其作成元件後,其光電轉換效率並不高,以具有n-hexyloxy group的化合物2而言,其效率只有1.10 %,當加入莫爾比333倍的DCA後,其效率可達到2.51 %。 | zh_TW |
dc.description.abstract | In chapter 2, we have described the synthesis of a series of metal-free organic dyes containing phenylene-thiophene-phenylene (PSP) as conjugated spacer attached with various tert-butyl substituted arylamines as donor and cyanoacetic acid as acceptor for DSSCs studies. Presence of tert-butyl group in the donor unit not only suppressed intermolecular aggregation but also helped in reducing charge recombination rate. Compared to other dyes discussed in this chapter, the dye CB-PSP exhibited maximum overall conversion efficiency (6.70 %) with short-circuit photocurrent density (Jsc) of 14.63 mA•cm-2 and open-circuit photovoltage (Voc) of 0.685 V. For dye CB-PSP, the observed maximum photon-to-current conversion efficiency (IPCE) was more than 80% in the region of 420~480 nm. We have used CDCA (chenodeoxycholic acid) as co-adsorbent in order to demonstrate the effect of tert-butyl group for inhibition of dye-aggregation. By using CDCA, the overall performance was decreased as CDCA reduced the dye loading amount on TiO2. This observed result indicated that tert-butyl group effectively inhibited the dye-aggregation on TiO2 surface.
In chapter 3, we have described the synthesis and studies of a series of organic oligo-dyes for DSSCs applications based on non-conjugated phenothiazine both as donor and spacer. As the geometry of phednothiazine is not planer, the dyes containing phenothiazine unit are expected to reduce the rate of charge recombination and dye-aggregation. All dyes discussed in this chapter exhibited an open-circuit photovoltage (Voc) more than 0.78 V under the AM 1.5 solar condition (100 mW∙cm-2). The overall conversion efficiencies of dyes followed the order dimer > monomer > trimer. The dye PT2b showed maximum efficiency (7.78 %) by using DCA as co-adsorbent with short-circuit photocurrent density (Jsc) of 14.3 mA•cm-2, open-circuit photovoltage (Voc) of 0.83 V and fill factor (FF) of 0.65. In chapter 4, we have demonstrated the synthesis and studies of dyes containing 1,3-indandione-5,6-dicarboxylic acid as an electron acceptor in place of commonly used conventional cyanoacetic acid. For these dyes, substituted triphenylamines have been used as donor units. The strong electron withdrawing nature of 1,3-indandione shifted the absorption maxima towards higher wavelength of these simple D-π-A systems. The dyes 1 and 2, showed about 100 nm red shift in their absorption maxima as compared to analogous 2-cyano-3-(4-(diphenylamino)phenyl)acrylic acid (TPA) which we have used as reference dye for comparison. The dye 2 exhibited maximum efficiency of 2.51 % in presence of DCA (100 mM) with short-circuit photocurrent density (Jsc) of 6.86 mA•cm-2, open-circuit photovoltage (Voc) of 0.58 V and fill factor (FF) of 0.63. | en |
dc.description.provenance | Made available in DSpace on 2021-05-19T18:03:03Z (GMT). No. of bitstreams: 1 ntu-103-D97223108-1.pdf: 13161133 bytes, checksum: 6917403c977bc98c5e2300b32639a2b5 (MD5) Previous issue date: 2014 | en |
dc.description.tableofcontents | 目錄
口試委員會審定書 I 謝誌 II 中文摘要 III 英文摘要 V 目錄 VII 圖目錄 X 表目錄 XIII 第一章 緒論 1 1-1 前言 2 1-2 太陽能簡介 3 1-3 太陽能電池簡介 3 1-3-1 矽太陽能電池 5 (1) 單晶矽太陽能電池 5 (2) 多晶矽太陽能電池 6 (3) 非晶矽太陽能電池 6 1-3-2 薄膜太陽能電池 7 (1) 矽薄膜太陽能電池 7 (2) 化合物半導體薄膜太陽能電池 8 1-3-3有機太陽能電池 8 (1) 單層及雙層太陽能電池 9 (2) 混合異質接面型太陽能電池 10 (3) 染敏化太陽能電池 11 1-4 理論說明 12 1-4-1 染敏化太陽能電池基本結構 12 1-4-2 染敏化太陽能電池工作原理 13 1-4-3 二氧化鈦薄膜 15 1-4-4 染料 17 (1) Coumarin 19 (2) Indoline 19 (3) Triarylamine 20 (4) Phenothiazine 21 1-4-5 電解質 22 1-4-6 對電極 24 1-5 太陽能電池測試條件與參數介紹 25 1-6 研究動機與目的 27 1-6實驗儀器 27 1-7 參考資料 30 第二章 具有第三丁基的不同電子予體染料在染敏化太陽能電池的應用 34 2-1 介紹 35 2-2 染料合成 36 2-3 光物理和電化學性質 39 2-4 理論計算 42 2-5 元件效率 44 2-6 結論 48 2-7 實驗步驟 50 2-8 參考資料 68 第三章 寡聚吩噻嗪在染敏化太陽能電池的應用 73 3-1 介紹 74 3-2 染料合成 75 3-3 光物理和電化學性質 77 3-4 理論計算 79 3-5 元件效率 81 3-6 結論 87 3-7 實驗步驟 88 3-8 參考資料 98 第四章 使用1,3-茚二酮衍生物在染敏化太陽能電池的應用 100 4-1 介紹 101 4-2 染料合成 102 4-3 光物理和電化學性質 102 4-4 理論計算 107 4-5 元件效率 109 4-6 結論 115 4-7 實驗步驟 116 4-8 參考資料 118 附圖 120 圖目錄 圖1-1: 太陽能幅射光譜分佈 3 圖1-2: 太陽能電池發電原理 4 圖1-3: 1954年貝爾實驗室測試太陽能電池 5 圖1-4: 非晶矽太陽能電池結構 7 圖1-5: 單層和雙層有機太陽能電池簡圖 10 圖1-6: 1991年所提出染敏化太陽能電池工作圖 11 圖1-7: 染敏化太陽能電池結構 13 圖1-8: 染敏化太陽能電池工作圖 14 圖1-9: 二氧化鈦Anatase和Rutile之結晶結構 16 圖1-10: 現在常用的Ru系列染料 18 圖1-11: Coumarin系列太陽能電池染料 19 圖1-12: Indoline系列太陽能電池染料 20 圖1-13: Triarylamine系列太陽能電池染料 21 圖1-14: Phenothiazine系列太陽能電池染料 22 圖1-15: 半固態的PGE電解質與全固態電解質和其作用機制 24 圖1-16: AM1.5光譜的光子流量在光強度為1000W/m2 25 圖1-17: 染敏化太陽能電池之電流-電壓圖 27 圖2-1: PSP系列分子結構 36 圖2-2: PSP系列分子合成路徑 38 圖2-3: PSP系列的吸收光譜 39 圖2-4: PSP系列吸附在二氧化鈦上的吸收光譜 40 圖2-5: PSP系列之HOMO-LUMO能階 41 圖2-6: PSP系列理論計算之分子結構 43 圖2-7: PSP系列理論計算之電子雲分布 43 圖2-8: PSP系列太陽能電池I-V圖和IPCE圖 44 圖2-9: PSP系列電化學阻抗光譜圖(上)與波特相位圖(下) 47 圖2-10: CB-PSP加入CDCA之太陽能電池I-V圖和電化學阻抗光譜圖 48 圖3-1: PT系列分子結構 75 圖3-2: PT系列分子合成路徑 76 圖3-3: PT系列的吸收光譜 77 圖3-4: PT系列吸附在二氧化鈦上的吸收光譜 78 圖3-6: PT系列理論計算之分子結構 80 圖3-7: PT系列理論計算之電子雲分布 80 圖3-8: PT系列Milliken charge在基態與激發態的差異 81 圖3-9: PT系列太陽能電池I-V圖和IPCE圖 83 圖3-10: PT系列染料吸附量 84 圖3-11: PT系列電化學阻抗光譜圖(上E1;下E2) 85 圖3-12: PTb系列加入DCA之太陽能電池I-V 圖 86 圖4-1: 化合物1和2之分子合成路徑 102 圖4-2: 化合物1和2的吸收光譜 103 圖4-3: 化合物1和2吸附在二氧化鈦上的吸收光譜 103 圖4-4: 不同溶劑下的螢光光譜化合物1(上);化合物2(下) 105 圖4-5: 化合物1和2的CV圖和HOMO-LUMO能階圖 106 圖4-6: 化合物1和2理論計算之分子結構 107 圖4-7: 化合物1和2理論計算之電子雲分布 108 圖4-8: 化合物1和2太陽能電池I-V圖和IPCE圖 110 圖4-9: 化合物1、2和N719電化學阻抗光譜圖(Light) 111 圖4-10: 化合物1和2之電子密度與電壓關係圖 112 圖4-11: 化合物1、2和N719之電子壽命與電壓關係圖 113 圖4-12: 化合物1和2加入DCA之太陽能電池I-V圖 114 表目錄 表1-1: 二氧化鈦Anatase和Rutile的物理性質 16 表2-1: PSP系列之光物理和電化學性質 42 表2-2: PSP系列太陽能電池元件性質 45 表2-3: CB-PSP加入CDCA之太陽能電池元件性質 48 表3-1: PT系列之光物理和電化學性質 79 表3-2: PTa系列在不同溶劑下之太陽能電池元件性質 82 表3-3: PT系列之太陽能電池元件性質 84 表3-4: PTb系列加入DCA之太陽能電池元件性質 86 表4-1: 化合物1和2之光物理和電化學性質 104 表4-2: 化合物1和2的基態和激發態偶級距 105 表4-3: 理論計算Transition energy level與實驗值的差異 109 表4-4: 化合物1和2之太陽能電池元件性質 111 表4-5: 化合物1和2加入DCA之太陽能電池元件性質 115 | |
dc.language.iso | zh-TW | |
dc.title | 新型芳香環有機材料之合成與其應用於染敏化太陽能電池 | zh_TW |
dc.title | Synthesis of New Type Aromatic Organic Material and Applications on Dye-Sensitized Solar Cells | en |
dc.type | Thesis | |
dc.date.schoolyear | 102-2 | |
dc.description.degree | 博士 | |
dc.contributor.oralexamcommittee | 孫世勝(Shih-Sheng Sun),劉陵崗(Ling-Kang Liu),劉清揚(Ching-Yang Liu),張源杰(Yuan Jay Chang) | |
dc.subject.keyword | 染敏化太陽能電池,二氧化鈦,第三丁基,吩??,1,3-?二酮-5,6-雙羧酸, | zh_TW |
dc.subject.keyword | DSSCs,TiO2,tert-butyl,phednothiazine,1,3-indandione-5,6-dicarboxylic acid, | en |
dc.relation.page | 166 | |
dc.rights.note | 同意授權(全球公開) | |
dc.date.accepted | 2014-07-15 | |
dc.contributor.author-college | 理學院 | zh_TW |
dc.contributor.author-dept | 化學研究所 | zh_TW |
dc.date.embargo-lift | 2024-12-31 | - |
顯示於系所單位: | 化學系 |
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