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dc.contributor.authorOgugu, Edward B.
dc.contributor.authorGillanders, Ross N.
dc.contributor.authorTurnbull, Graham
dc.identifier.citationOgugu , E B , Gillanders , R N & Turnbull , G 2021 , ' Thermal desorption of explosives vapour from organic fluorescent sensors ' , Chemistry Proceedings , vol. 5 , no. 1 , 11 .
dc.identifier.otherPURE: 276920912
dc.identifier.otherPURE UUID: 576a8267-da3b-4be5-8da8-5df68d670ed3
dc.identifier.otherORCID: /0000-0002-8825-3234/work/104252453
dc.descriptionFunding: This research was funded by the Commonwealth Scholarships Commision, and the NATO Science for Peace & Security Programme under grant agreement MYP G5355.en
dc.description.abstractOrganic semiconductors can be used as highly sensitive fluorescent sensors for the detection of trace-level vapours of nitroaromatic explosives. This involves fluorescence quenching of the sensors and indicates the presence of explosives in the surrounding environment. However, for many organic fluorescent sensors, the quenching of fluorescence is irreversible and imposes a limitation in terms of the reusability of the sensors. Here, we present a study of thermal desorption of 2,4-DNT from thin-film explosives sensors made from the commercial fluorescent polymers Super Yellow and poly(9-vinyl carbazole). Thermal cycling of the sensor results in recovery of fluorescence, thereby making them reusable.
dc.relation.ispartofChemistry Proceedingsen
dc.rightsCopyright: © 2021 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 (CC BY) license (https://
dc.subjectOrganic semiconductorsen
dc.subjectNitroaromatic explosivesen
dc.subjectFluorescence quenchingen
dc.subjectThermal desorptionen
dc.subjectQC Physicsen
dc.subjectQD Chemistryen
dc.subjectU Military Scienceen
dc.titleThermal desorption of explosives vapour from organic fluorescent sensorsen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews.School of Physics and Astronomyen
dc.contributor.institutionUniversity of St Andrews.Sir James Mackenzie Institute for Early Diagnosisen
dc.contributor.institutionUniversity of St Andrews.Centre for Biophotonicsen
dc.description.statusPeer revieweden

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