博碩士論文 100223049 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator黃啟銘zh_TW
DC.creatorChi-ming Huangen_US
dc.date.accessioned2013-7-22T07:39:07Z
dc.date.available2013-7-22T07:39:07Z
dc.date.issued2013
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=100223049
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本篇以文獻中的有機小分子2,6二苯基二噻吩併[3,2-b:2’,3’-d]噻吩(2,6-diphenyldithieno[3,2-b:2’,3’-d] thiophene ; DP-DTT;化合物 1)出發,設計並開發出以三併環噻吩(DTT)與雙三併環噻吩(BDT)作為中心結構的2-五氟苯基-6-苯基二噻吩併[3,2-b:2’,3’-d]噻吩(2-pentafluorophenyl-6-phenyldithieno[3,2-b:2’,3’-d]thiophene;FPP-DTT;化合物2)、2,6-二苯基雙二噻吩併[3,2-b:2’,3’-d]噻吩[2,6-diphenylbis(dithieno [3,2-b:2’,3’-d]thiophene) ; DP-BDT;化合物 3]、2-五氟苯基-6-苯基二噻吩併[3,2-b:2’,3’-d]噻吩(2-pentafluoro phenyl-6-phenylbis(dithieno [3,2-b:2’,3’-d]thiophene);FPP-BDT; 化合物4),將此四種材料經由物理氣相沈積法(physical vapor transport, PVT)分別養成單晶,經由單晶繞射實驗解得其立體結構後,製備成單晶及薄膜場效電晶體元件。利用單晶場效電晶體元件討論晶體結構與分子內在(intrinsic)電荷傳輸性質的關係,同時探討與薄膜表面形貌對於電荷傳輸的影響。 化合物1與 化合物3的單晶結構為魚骨狀排列方式,結晶成片狀,化合物2與化合物4則為面對面排列,結晶成針狀,其中化合物2 存在著最短的分子間距離3.756Å,其單晶場效電晶體元件電洞遷移率(hole mobility, µ)高達0.741cm2/V-s,開關電流比約為105,化合物 4電洞遷移率達0.725 cm2/V-s。化合物1與化合物3測得的最高載子遷移率分別為0.359 cm2/V-s、 0.405 cm2/V-s。 將以上四個有機小分子材料分別製成有機薄膜元件,在基板為25oC的條件下觀察薄膜表面形貌可發現化合物1在薄膜表面結晶性良好,為片狀結晶,載子遷移率可達0.202 cm2/V-s,化合物2製成元件表面形貌為長條狀結晶,載子遷移率可達0.134 cm2/V-s。另外也將蒸鍍基板升溫,觀察基板溫度對於薄膜表面晶粒大小提升與載子遷移率的影響。zh_TW
dc.description.abstractBased on the reported core structure of dithieno[3,2-b:2’,3’-d] thiophene (DTT), a series of organic semiconductor molecules was designed and synthesized, which are 2,6-diphenyldithieno[3,2-b:2’,3’-d] thiophene (DP-DTT,compound1), 2-pentafluorophenyl-6-phenyl- dithieno[3,2-b:2’,3’-d]thiophene(FPP-DTT, compound 2) 2,6-diphenyl- bis(dithieno [3,2-b:2’,3’-d]thiophene (DP-BDT, compound 3), and 2-pentafluorophenyl-6-phenylbis(dithieno[3,2-b:2’,3’-d]thiophene (FPP- BDT, compound 4). Single crystals for each compound were prepared by physical vapor transport (PVT) method in a home-made reactor, and were used for single crystal field-effect transistor (SCFET) devices fabrication in order to study their intrinsic charge transport behavior. Single crystals of compound 1 and compound 3 exhibit herring-bone structure, while compound 2 and compound 4 exhibit face-to-face π-π stacking. Among these, compound 2 exhibits the shortest intermolecular distance of 3.756Å, and a highest hole mobility of 0.741 cm2/V-s for SCFET, as well as a high current on-off ratio of 105. The hole mobilities for SCFET of compound 4, compound 1, and compound 3 were 0.725 cm2/V-s, 0.359 cm2/V-s, and 0.405 cm2/V-s, respectively. Meanwhile, organic thin-film transistor (OTFT) devices for each compound were also prepared in order to explore the correlation between the thin-film morphology and charge carrier mobility. With vacuum thermal evaporation at ambient substrate temperature of 25oC, compound 1 showed good crystallinity with 2-dimentional film morphology, as well as a high mobility of 0.202 cm2/V-s. Compound 2 exhibited 1-dimentional crystal structure, and hole mobility of 0.134 cm2/V-s for the film transistor. Substrate temperature was also raised during the evaporation process in order to study the effect of temperature on film morphology.en_US
DC.subject有機半導體材料zh_TW
DC.subject場效電晶體zh_TW
DC.subject三併環噻吩zh_TW
DC.subjectOFETen_US
DC.subjectthiopheneen_US
DC.subjectDTTen_US
DC.title有機半導體材料三併環噻吩衍生物之開發與其薄膜、單晶場效電晶體元件製備與分析zh_TW
dc.language.isozh-TWzh-TW
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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