Control of wettability by anion exchange on Si/SiO2 surfaces

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dc.contributor.authorChi, YSko
dc.contributor.authorLee, JKko
dc.contributor.authorLee, Sko
dc.contributor.authorChoi, Insungko
dc.date.accessioned2009-11-19T06:42:30Z-
dc.date.available2009-11-19T06:42:30Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2004-04-
dc.identifier.citationLANGMUIR, v.20, no.8, pp.3024 - 3027-
dc.identifier.issn0743-7463-
dc.identifier.urihttp://hdl.handle.net/10203/12921-
dc.description.abstractWater wettability Of Si/SiO2 surfaces was controlled by the formation of SAMs terminating in 1-alkyl-3-(3-silylpropyl)imidazolium ions and the anion exchange on the surfaces ("direct anion exchange"). The exchange was confirmed by X-ray photoelectron spectroscopy, and the water wettability was measured as a water contact angle by contact angle goniometry. We found that anions played a great role in determining water wettability Of Si/SiO2 surfaces. For example, water contact angles Of Si/SiO2 surfaces presenting 1-methyl-3-(3-silylpropyl)imidazolium ions changed from 28 to 42degrees when the counteranion Cl- was exchanged with PF6- In addition to the anions, the N-alkyl groups of imidazolium cations were also found to be important in determining water wettability: we did not observe any significant changes in the contact angles of Si/SiO2 surfaces presenting 1-butyl-3-(3-silylpropyl)imidazolium ions by the anion exchange. We also demonstrated that the reaction rate of the direct anion exchange was affected by a choice of solvents: the anion exchange from Cl- to PF6- was the fastest in an aqueous solution.-
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherAMER CHEMICAL SOC-
dc.subjectSELF-ASSEMBLED MONOLAYERS-
dc.subjectIONIC LIQUIDS-
dc.subjectORGANIC-SURFACES-
dc.subjectCATALYSIS-
dc.subjectPOLYMERS-
dc.subjectFILMS-
dc.subjectGOLD-
dc.subjectHEXAFLUOROPHOSPHATE-
dc.subjectCHEMISTRY-
dc.subjectCRYSTALS-
dc.titleControl of wettability by anion exchange on Si/SiO2 surfaces-
dc.typeArticle-
dc.identifier.wosid000220750300007-
dc.identifier.scopusid2-s2.0-2342418879-
dc.type.rimsART-
dc.citation.volume20-
dc.citation.issue8-
dc.citation.beginningpage3024-
dc.citation.endingpage3027-
dc.citation.publicationnameLANGMUIR-
dc.identifier.doi10.1021/la036340q-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorChoi, Insung-
dc.contributor.nonIdAuthorChi, YS-
dc.contributor.nonIdAuthorLee, JK-
dc.contributor.nonIdAuthorLee, S-
dc.type.journalArticleArticle-
dc.subject.keywordPlusSELF-ASSEMBLED MONOLAYERS-
dc.subject.keywordPlusIONIC LIQUIDS-
dc.subject.keywordPlusORGANIC-SURFACES-
dc.subject.keywordPlusCATALYSIS-
dc.subject.keywordPlusPOLYMERS-
dc.subject.keywordPlusFILMS-
dc.subject.keywordPlusGOLD-
dc.subject.keywordPlusHEXAFLUOROPHOSPHATE-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusCRYSTALS-
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