博碩士論文 972203015 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator張修絜zh_TW
DC.creatorHsiu-chieh Changen_US
dc.date.accessioned2010-7-22T07:39:07Z
dc.date.available2010-7-22T07:39:07Z
dc.date.issued2010
dc.identifier.urihttp://ir.lib.ncu.edu.tw:444/thesis/view_etd.asp?URN=972203015
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利用 “one-pot” reaction 開發出不對稱主體併環噻吩 (1) 與併環噻吩 (6),並且將併環噻吩 (1) 產率提升。其併環噻吩衍生物分子 (2) ~ (5) 也已開發成功,當中分子 (2)、分子 (3) 與分子 (5) 皆為 P 型半導體材料,載子移動率分別達 0.11 cm2 / Vs、0.088 cm2 / Vs 及 0.08 cm2 / Vs,而可溶性 P 型半導體材料分子 (4) 也表現高載子移動率為 0.606 cm2 / Vs。這些不對稱併環有機半導體材料皆表現相當良好的光、空氣與熱穩定性。 zh_TW
dc.description.abstractAsymmetric molecules (1) and (6) were synthesized by “one-pot” reaction, and the yield of molecule (1) was improved. Four asymmetric molecules (2), (3), (4) and (5) based on molecule (1) had been developed. All of the molecules are P-type semiconductor materials. Molecule (2) exhibits good field-effect performance with a high mobility of 0.11 cm2 / Vs. In addition, the mobilities of molecule (3) and (4) are 0.088 and 0.08 cm2 / Vs. Soluble molecule (4) had been developed by attaching a long n-octyl chain to the end position and exhibits excellent field-effect performance with a mobility as high as 0.606 cm2 / Vs via solution process. These organic semiconductor materials all show good stability under photo, air and thermal conditions. en_US
DC.subject五環素zh_TW
DC.subject併環噻吩zh_TW
DC.subject載子移動率zh_TW
DC.subject有機薄膜電晶體zh_TW
DC.subjectPentaceneen_US
DC.subjectfused-thiophenesen_US
DC.subjectmobilityen_US
DC.subjectOrganic thin-film transistoren_US
DC.title有機薄膜電晶體材料苯三併環噻吩及苯四併環噻吩衍生物之開發zh_TW
dc.language.isozh-TWzh-TW
DC.titleSynthesis of Functionalized Benzo[d,d′]thieno[3,2-b;4,5-b′]dithiophenes (BTDTs) and Benzothieno[3,2-b]thieno[2’,3’:4,5]thieno[2,3-d] thiophene (B4T) for Organic Thin-Film Transistorsen_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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