博碩士論文 106223062 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator駱薇伃zh_TW
DC.creatorWei-Yu Loen_US
dc.date.accessioned2019-7-23T07:39:07Z
dc.date.available2019-7-23T07:39:07Z
dc.date.issued2019
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=106223062
dc.contributor.department化學學系zh_TW
DC.description國立中央大學zh_TW
DC.descriptionNational Central Universityen_US
dc.description.abstract本論文主要可以分為有機薄膜電晶體 (OTFTs)、有機光伏打電池 (OPVs) 、電洞傳輸層 (HTL) 和染料敏化太陽能電池 (DSSC) 的材料開發。 延續實驗室之前開發出n 型有機薄膜電晶體材料-醌型噻吩並吡咯酮二聚體 (DTPQ),DTPQ-b8 與 DTPQ-b16,其碳鏈分別為 b-C8H17 與 b-C16H33,兩者元件電性分別已到達 0.65 cm2V-1s-1 和 2.54 cm2V-1s-1。本研究繼續探討碳鏈之鏈長效應,開發出碳鏈為 C10H21 之 DTPQ-10 (1) 與 b-C17H35 之 DTPQ-b17 (2),並用不同之合成路徑開發出具有不對稱碳鏈 b-C16H33 和 C8H17 之 DTP’Q-8 (3),並獲得電性最高之 DTPQ-b16 的單晶結構,證明了所設計分子具有相當好的共平面性,且呈現磚塊型 face to face 的分子堆疊。 電洞傳輸層的部分,開發以噻吩並吡咯酮二聚體 (DTP) 為核心之兩個新型小分子材料,TPA-DTP-2 (4) 與 TPA-DTP-b8 (5),碳鏈分別為 C2H5 與 b-C8H17。因核心具 N 之原子亦同時具拉電子基團,此材料之 HOMO/ LUMO 電位與其它常見之電洞傳輸層材料有相當的不同,其 HOMO 可高達 -4.73 eV,藉由改變碳鏈長度來探討溶解度對製程的影響,應用於 Pb-based 的鈣鈦礦太陽能電池目前初步測試具有 9.6 % 之光電轉換效率。 有機光伏打電池電池的部分,以 CDT 為單元開發出雙聯 CDT 之 BCDT,並在末端分別接上拉電子基團羅丹寧 (Rh) 與 3-(二氰基亞甲基)茚-1-酮 (IN),開發出兩種可溶性有機光伏打太陽能電池材料: INBCDT (6)、RhBCDT (7)。多併環噻吩之核心有助於電荷轉移進而增加載子移動率,藉由引入長碳鏈確保分子之溶解度,同時可避免元件製膜時分子之嚴重堆疊,目前正進行其 OPV 元件之測試。 染料敏化太陽能電池的部分,以本實驗室已發表光電轉換效率可達 10.1% 的有機染料 TPA-TTAR-TA 之 D-π-A 設計為基礎,將具硫醚鏈聯噻吩 (SBT) 作為核心取代 TTAR,開發出新的有機染敏 TPA-SBT6-A (8)。以此新有機染料分子與 Ru-based 的染敏進行共染敏太陽能電池的測試,目前所得的元件效能可高達 ~9.8 % 之光電轉換效率。 zh_TW
dc.description.abstractA series of new organic optoelectronic materials were synthesized and characterized for organic thin film transistors (OTFTs), organic photovoltaic cells (OPVs), hole transporting layer (HTL) and dye sensitized solar cell (DSSC). For the OTFTs, n-type DTPQ-b8 (DTP with b-C8H17 chains) and DTPQ-b16 (DTP with b-C16H33 chains) exhibited mobility of 0.65 cm2V-1s-1 and 2.54 cm2V-1s-1. To further complete the side chains effect study, DTPQ-10 (1; R= C10H21), DTPQ-b17 (2; R= b-C17H35) and DTP’Q-8 (3; R= b-C16H33, C8H17) was synthesized and characterized. Single-crystal X-ray diffraction of DTPQ-b16 reveals the planarity of DTP core via the intramolecular S···O interaction. DTP showed brick-type face to face molecular stacking, with a short intermolecular stacking distance of 3.28 Å and short intermolecular N···H contacts of 2.52 Å. Furthermore, two new DTP-based hole transporting molecules were developed where the DTP core were end-capped with triphenylamino (TPA) unit. TPA-DTP-2 (4) exhibits the PCE up to 9.6% in Pb-based PSC. For the organic photovoltaics, one new core of a CDT-based, the dimerized CDT (BCDT), were developed. Via knoevenagel condensation, the new BCDT core were end-capped with electron withdrawing groups, such as rhodanine (Rh) or indane-1,3-dione (IN) to afford two new small molecules INBCDT (6) and RhBCDT (7). For DSSC, a new organic dye TPA-SBT6-A (8) were synthesized. Co-sensitization of TPA-SBT6-A (8) with Ru-based dyes exhibits the PCE up to 9.8% in dye sensitized solar cell. The optical and electrochemical properties (HOMO and LUMO) of these new materials were characterized by UV-vis and DPV. Thermal properties were investigated by DSC and TGA. Optoelectronic devices used these new developed small molecules are under optimization. en_US
DC.subject可溶性噻吩zh_TW
DC.title可溶性噻吩並吡咯酮二聚體衍生物 有機薄膜電晶體材料之開發zh_TW
dc.language.isozh-TWzh-TW
DC.titleDevelopment of Soluble Thienopyrroledione Dimer (DTP) Derivatives for Organic Optoelectronic Applicationsen_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

若有論文相關問題,請聯絡國立中央大學圖書館推廣服務組 TEL:(03)422-7151轉57407,或E-mail聯絡  - 隱私權政策聲明