Repository logo
  • English
  • 中文
Log In
Have you forgotten your password?
  1. Home
  2. College of Science / 理學院
  3. Chemistry / 化學系
  4. Synthesis of Oligo-biphenylene-(E)-vinyl with Hole-transport Group Side Chains, and Electron-transport Main Chain, and the Applications on OLED
 
  • Details

Synthesis of Oligo-biphenylene-(E)-vinyl with Hole-transport Group Side Chains, and Electron-transport Main Chain, and the Applications on OLED

Date Issued
2007
Date
2007
Author(s)
Yang, Chin-Fu
DOI
zh-TW
URI
http://ntur.lib.ntu.edu.tw//handle/246246/51976
Abstract
Abstract We used 2,2’-diiodobiphenyl as starting material to couple with hole transporting compounds such as triphenylamines and phenylcarbazoles on 2,2’position by Suzuki reaction. After that, the derivates of 4,4’-bis(diethyl methylphosphonate) were synthesized, and oligomerized with π electron dialdehydes by Wadsworth-Emmons reaction to generate the oligomers, which have electrotransport main chain and holetransport side chain. The aforementioned oligomers were used as light emitters or electro-polymerization precursors in Light Emitting Devices. And the respectively electrical and optical properties were studied. All the oligomers, P1~27, have high Td,5% which ranged from 320 to 580 oC. And the Tg of these oligomers are between 75 and 242 oC. From the results of experiments, the best device of oligomers mixed with PBD as emitting layer : we got electroluminescence of P9 as green-blue; low turn on voltage was 4V; the best brightness was1240 cd/m2, and the best efficiency was 1.69 cd/A . In the device of oligomer as HIT(ITO/CV(P1∼P27)/41+PVK+PBD/Ca/Mg) : we got P8 as 3 cycles(85nm) with 15~16V turn on voltage , 15300 cd/m2 on best brighness, and 11 cd/A on best efficiency.
Subjects
發光二極體:寡聚物
螢光
電洞注入層
電子傳輸層
發光層
PLED
OLED
HTL
HIL
emitter
triphenyl amine
Type
thesis
File(s)
Loading...
Thumbnail Image
Name

ntu-96-D89223017-1.pdf

Size

23.31 KB

Format

Adobe PDF

Checksum

(MD5):01142042cea2edd6c6d4b5afca498e57

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

總館學科館員 (Main Library)
醫學圖書館學科館員 (Medical Library)
社會科學院辜振甫紀念圖書館學科館員 (Social Sciences Library)

開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

  • 請確認所上傳的全文是原創的內容,若該文件包含部分內容的版權非匯入者所有,或由第三方贊助與合作完成,請確認該版權所有者及第三方同意提供此授權。
    Please represent that the submission is your original work, and that you have the right to grant the rights to upload.
  • 若欲上傳已出版的全文電子檔,可使用Open policy finder網站查詢,以確認出版單位之版權政策。
    Please use Open policy finder to find a summary of permissions that are normally given as part of each publisher's copyright transfer agreement.
  • 網站簡介 (Quickstart Guide)
  • 使用手冊 (Instruction Manual)
  • 線上預約服務 (Booking Service)
  • 方案一:臺灣大學計算機中心帳號登入
    (With C&INC Email Account)
  • 方案二:ORCID帳號登入 (With ORCID)
  • 方案一:定期更新ORCID者,以ID匯入 (Search for identifier (ORCID))
  • 方案二:自行建檔 (Default mode Submission)
  • 方案三:學科館員協助匯入 (Email worklist to subject librarians)

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science