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Cited 21 time in webofscience Cited 11 time in scopus
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dc.contributor.authorJung, KH-
dc.contributor.authorKim, KH-
dc.contributor.authorLee, DH-
dc.contributor.authorJung, DS-
dc.contributor.authorPark, CE-
dc.contributor.authorChoi, DH-
dc.date.accessioned2016-04-01T02:45:49Z-
dc.date.available2016-04-01T02:45:49Z-
dc.date.created2010-10-26-
dc.date.issued2010-09-
dc.identifier.issn1566-1199-
dc.identifier.other2010-OAK-0000021757-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/25720-
dc.description.abstractNew benzothieno[3,2-b]benzothiophene (BTBT)-based soluble semiconducting molecules have been synthesized through Horner-Emmons coupling reactions using 5-alkylthiophene- 2-carbaldehyde and BTBT-diethylphosphonate. The only difference between the two molecules is the length of alkyl chains as a substituent. The molecules are intrinsically thermotropic liquid crystalline (LC) and exhibit good solubility in common organic solvents. The semiconducting properties of the two LC molecules were evaluated in organic thin film transistors (OTFTs). After annealing the samples at the temperature at which liquid crystallinity appears, the TFT device performance improved significantly. The two conjugated molecules 4 and 5 exhibited fairly high charge carrier mobilities of 0.020 cm(2)/(Vs) (V(th) = -14.5 V, I(ON/OFF) = 1.42 x 10(5)) and 0.023 cm(2)/(Vs) (V(th) = -2.0 V, I(ON/OFF) = 1.20 x 10(6)), respectively. (C) 2010 Elsevier B.V. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.relation.isPartOfORGANIC ELECTRONICS-
dc.subjectConjugated molecule-
dc.subjectOrganic semiconductor-
dc.subjectLiquid crystallinity-
dc.subjectThin film transistor-
dc.subjectMobility-
dc.subjectFIELD-EFFECT TRANSISTORS-
dc.subjectHIGH-PERFORMANCE-
dc.subjectSEMICONDUCTORS-
dc.subjectMOBILITY-
dc.subjectMOLECULES-
dc.subjectTRANSPORT-
dc.subjectACENES-
dc.titleLiquid crystalline dialkyl-substituted thienylethenyl [1] benzothieno[3,2-b] benzothiophene derivatives for organic thin film transistors-
dc.typeArticle-
dc.contributor.college화학공학과-
dc.identifier.doi10.1016/J.ORGEL.2010.07.008-
dc.author.googleJung, KH-
dc.author.googleKim, KH-
dc.author.googleLee, DH-
dc.author.googleJung, DS-
dc.author.googlePark, CE-
dc.author.googleChoi, DH-
dc.relation.volume11-
dc.relation.issue9-
dc.relation.startpage1584-
dc.relation.lastpage1593-
dc.contributor.id10104044-
dc.relation.journalORGANIC ELECTRONICS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationORGANIC ELECTRONICS, v.11, no.9, pp.1584 - 1593-
dc.identifier.wosid000281519700016-
dc.date.tcdate2019-02-01-
dc.citation.endPage1593-
dc.citation.number9-
dc.citation.startPage1584-
dc.citation.titleORGANIC ELECTRONICS-
dc.citation.volume11-
dc.contributor.affiliatedAuthorPark, CE-
dc.identifier.scopusid2-s2.0-77954989362-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc15-
dc.description.scptc14*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusFIELD-EFFECT TRANSISTORS-
dc.subject.keywordPlusHIGH-PERFORMANCE-
dc.subject.keywordPlusSEMICONDUCTORS-
dc.subject.keywordPlusMOBILITY-
dc.subject.keywordPlusMOLECULES-
dc.subject.keywordPlusTRANSPORT-
dc.subject.keywordPlusACENES-
dc.subject.keywordAuthorConjugated molecule-
dc.subject.keywordAuthorOrganic semiconductor-
dc.subject.keywordAuthorLiquid crystallinity-
dc.subject.keywordAuthorThin film transistor-
dc.subject.keywordAuthorMobility-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-

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박찬언PARK, CHAN EON
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