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Characterizing the fluorescence intermittency of individual cadmium selenide/zinc sulfide quantum dot clusters with spatially correlated single molecule fluorescence spectroscopy and atomic force microscopy

dc.contributor.authorYu, Ming, author
dc.contributor.authorVan Orden, Alan K., advisor
dc.date.accessioned2024-03-13T20:28:06Z
dc.date.available2024-03-13T20:28:06Z
dc.date.issued2008
dc.description.abstractIn this thesis, I describe work done to study the optical behaviors of CdSe/ZnS quantum dots, especially the fluorescence blinking behavior of small quantum dot clusters. QDs have unique optical properties that impart several key advantages over molecular dyes. However, when examined at the single-molecule level, QDs emission exhibit novel fluorescence intermittency, or "blinking," behavior. This blinking is believed to be caused by trapping and de-trapping of the photoexcited carriers, causing the QDs to fluctuate between emissive and non-emissive states. A spatially correlated single molecule fluorescence spectroscopy and atomic force microscopy (AFM) apparatus was used to carry out these studies. Single molecule spectroscopy examines the blinking behavior of individual, isolated QDs and QD clusters, while the AFM images the nanometer scale topography of the particles. When multiple isolated QDs were probed simultaneously, the fluorescence behavior was consistent with independent blinking of the individual QDs. However, when close-packed QD clusters were probed, the fluorescence intermittency became much more rapid and intense than could be explained by the summation of multiple particles blinking independently. This suggests when the small QDs aggregate together, they become electronically coupled in some way that enhances the fluorescence blinking. Subsequently, we studied variations of the emission wavelengths of isolated small QD clusters possessing the enhanced blinking behavior. The emission wavelength of the coupled enhanced blinking is red shifted relative to that of normal blinking. We propose that red-shifting in emission is one of the characteristics of electronic coupling in the QD clusters and resulted from the quantum confinement Stark effect. In the following chapters, environment and substrate dependence were also studied. Compared with ambient air, dry nitrogen decreases the population, intensity and/or durations of "on" times. Both CTAB- and Mg 2+-mica substrates quench the fluorescence of single QDs and QD clusters, which is due to the dissociation of electron hole pairs of excited QDs by the electron attractive sites in CTAB molecules and Mg2+ ions.
dc.format.mediumborn digital
dc.format.mediumdoctoral dissertations
dc.identifierETDF_Yu_2008_3332719.pdf
dc.identifier.urihttps://hdl.handle.net/10217/238035
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relation.ispartof2000-2019
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.rights.licensePer the terms of a contractual agreement, all use of this item is limited to the non-commercial use of Colorado State University and its authorized users.
dc.subjectcadmium selenide
dc.subjectfluorescence
dc.subjectquantum dot clusters
dc.subjectzinc sulfide
dc.subjectanalytical chemistry
dc.titleCharacterizing the fluorescence intermittency of individual cadmium selenide/zinc sulfide quantum dot clusters with spatially correlated single molecule fluorescence spectroscopy and atomic force microscopy
dc.typeText
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineChemistry
thesis.degree.grantorColorado State University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy (Ph.D.)

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