中大學術數位典藏-NCU Institutional Repository-提供博碩士論文、考古題、期刊論文、研究計畫等下載:Item 987654321/97371
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 83956/83956 (100%)
造访人次 : 62490112      在线人数 : 719
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.lib.ncu.edu.tw/handle/987654321/97371


    题名: 雙噻吩(BT)及咪唑(Im)衍生物之電洞傳輸層及界面修飾層材料開發
    作者: 李昱錡;Li, Yu-Qi
    贡献者: 化學學系
    关键词: 封面;論文授權書;指導教授推薦書;中文摘要;英文摘要;謝誌;目錄;正文;附錄;參考文獻
    日期: 2025-06-25
    上传时间: 2025-10-17 11:12:34 (UTC+8)
    出版者: 國立中央大學
    摘要: 本研究以雙噻吩(Bithiophene, BT)及咪唑(Imidazole, Im)為核心,開發出5種電洞傳輸層材料以及5種界面層材料,應用於鈣鈦礦太陽能電池中,並依用途不同分為兩個系列。
    第一系列開發出五種自組裝單分子膜材料(Self-Assembled Monolayer, SAM)分為兩個部分,首先以酯基、羧基化雙噻吩為核心,於單、雙側接上三苯胺,合成出三種小分子電洞傳輸層材料DEBT-2D (1)、DABT-2D (2)、DABT-1D (3); 第二部分則以酯基、羧基化雙噻吩(DEBT、DABT)為單體,分別與硫烷基化雙噻吩(SBT)單元進行聚合製備出DEBT-SBT (4)、DABT-SBT (5)等高分子材料,其中目前DEBT-2D (1)、DABT-2D (2) 、DEBT-SBT (4)、DABT-SBT (5) 與本實驗室材料DTP-HP作為Co-SAM應用在錫鈣鈦礦太陽能電池中光電轉換效率(PCE)分別有7.36%、7.36%、7.3%、7.3%,而DABT-1D (3)則是與TPAT-PA作為Co-SAM具 7.93% PCE。
    第二系列則是用咪唑(Im)為核心,以噻吩及苯環延伸共軛,並以不同數量之FP當作外掛基團,分別合成出五種界面層材料,TFP-Im (6)、TFP-ImP (7)、TFP-ImT (8)、DFPIm-BT (9)、DFPIm-BP (10)。其中TFP-Im (6)和TFP-ImP (7)作為電洞傳輸界面層材料(HTIM)應用在鉛鈣鈦礦太陽能電池中PCE分別為21.05%、21%,而TFP-Im (8)當作電子傳輸界面層材料(ETIM) PCE 為21%,上述材料元件效能優化中。
    ;In this study, five hole transporting materials (HTM) and five interfacial materials (IM) were developed based on bithiophene (BT) and imidazole (Im) cores, respectively, and applied in perovskite solar cells. The materials are categorized into two series according to their intended functions.
    The first series involves the development of five self-assembled monolayer (SAM) materials, which can be further divided into two categories. The first category features three small-molecular HTMs, i.e. DEBT-2D (1), DABT-2D (2), and DABT-1D (3) which using ester- and carboxylated functionalized bithiophene cores (DEBT or DABT) and end capping with mono- or di-substituted triphenylamine groups. The second series of HTM include two polymeric materials DEBT-SBT (4) and DABT-SBT (5) synthesized by polymerizing DEBT or DABT with thioalkylated bithiophene (SBT) unit. Among these, DEBT-2D (1), DABT-2D (2), DEBT-SBT (4), and DABT-SBT (5), when co-dyed with our DTP-HP in tin-based perovskite solar cells, demonstrated preliminary power conversion efficiencies (PCE) of 7.36%, 7.36%, 7.30%, and 7.30%, respectively. In contrast, DABT-1D (3) co-dyed with TPAT-PA achieved a preliminary PCE of 7.93%.
    Five imidazole based interfacial materials (IM), i.e. TFP-Im (6), TFP-ImP (7), TFP-ImT (8), DFPIm-BT (9), and DFPIm-BP (10) were synthesized which were functionalized with varying numbers of fluorinated phenyl (FP) groups. TFP-Im (6) and TFP-ImP (7) was applied as hole transporting interfacial materials (HTIM) in lead-based perovskite solar cells and reached PCE of 21.05% and 21.0%, respectively. Meanwhile, TFP-Im (8), utilized as an electron transporting interfacial material (ETIM), exhibited PCE of 21.0%. Device optimization of these new materials is currently in progress
    显示于类别:[化學研究所] 博碩士論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML24检视/开启


    在NCUIR中所有的数据项都受到原著作权保护.

    社群 sharing

    ::: Copyright National Central University. | 國立中央大學圖書館版權所有 | 收藏本站 | 設為首頁 | 最佳瀏覽畫面: 1024*768 | 建站日期:8-24-2009 :::
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 隱私權政策聲明