Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/8742
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dc.contributorInstitute of Textiles and Clothingen_US
dc.creatorHu, Hen_US
dc.creatorXin, JHen_US
dc.creatorHu, Hen_US
dc.creatorWang, Xen_US
dc.creatorLu, Xen_US
dc.date.accessioned2014-12-19T07:07:28Z-
dc.date.available2014-12-19T07:07:28Z-
dc.identifier.issn1420-3049en_US
dc.identifier.urihttp://hdl.handle.net/10397/8742-
dc.language.isoenen_US
dc.publisherMDPI AGen_US
dc.rights© 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).en_US
dc.rightsThe following publication Hu, H., Xin, J. H., Hu, H., Wang, X., & Lu, X. (2014). Organic liquids-responsive β-cyclodextrin-functionalized graphene-based fluorescence probe : label-free selective detection of tetrahydrofuran. Molecules, 19(6), (Suppl. ), 7459-7479 is available at https://dx.doi.org/10.3390/molecules19067459en_US
dc.subjectChemical reduction and functionalizationen_US
dc.subjectFluorescence probeen_US
dc.subjectFluorescence quenchingen_US
dc.subjectFluorescence switch-onen_US
dc.subjectFunctionalized grapheneen_US
dc.subjectGraphene oxideen_US
dc.subjectRhodamine Ben_US
dc.subjectSensing platformen_US
dc.subjectSensoren_US
dc.subjectβ-cyclodextrinen_US
dc.titleOrganic liquids-responsive β-cyclodextrin-functionalized graphene-based fluorescence probe : label-free selective detection of tetrahydrofuranen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage7459en_US
dc.identifier.epage7479en_US
dc.identifier.volume19en_US
dc.identifier.issue6en_US
dc.identifier.doi10.3390/molecules19067459en_US
dcterms.abstractIn this study, a label-free graphene-based fluorescence probe used for detection of volatile organic liquids was fabricated by a simple, efficient and low-cost method. To fabricate the probe, a bio-based β-cyclodextrin (β-CD) was firstly grafted on reduced graphene surfaces effectively and uniformly, as evidenced by various characterization techniques such as Ultraviolet/Visible spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, thermogravimetric analysis, scanning electron microscopy and transmission electron microscopy. The subsequent inclusion of Rhodamine B (RhB) into the inner cavities of the β-CD grafted on the graphene surfaces was achieved easily by a solution mixing method, which yielded the graphene-based fluorescent switch-on probe. In addition, the gradual and controllable quenching of RhB by Fluorescence Resonance Energy Transfer from RhB to graphene during the process of stepwise accommodation of the RhB molecules into the β-CD-functionalized graphene was investigated in depth. A wide range of organic solvents was examined using the as-fabricated fluorescence probe, which revealed the highest sensitivity to tetrahydrofuran with the detection limit of about 1.7 μg/mL. Some insight into the mechanism of the different responsive behaviors of the fluorescence sensor to the examined targets was also described.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationMolecules, June 2014, v. 19, no. 6, p. 7459-7479en_US
dcterms.isPartOfMoleculesen_US
dcterms.issued2014-
dc.identifier.scopus2-s2.0-84903289195-
dc.identifier.rosgroupidr72685-
dc.description.ros2013-2014 > Academic research: refereed > Publication in refereed journalen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRA-
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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