Nanostructured silver for applications in surface enhanced Raman spectroscopy and photoelectrochemical reactions

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dc.contributorSzulczewski, Gregory J.
dc.contributorBakker, Martin G.
dc.contributorFrantom, Patrick A.
dc.contributorChopra, Nitin
dc.contributor.advisorPan, Shanlin
dc.contributor.authorClayton, Daniel Adam
dc.contributor.otherUniversity of Alabama Tuscaloosa
dc.date.accessioned2017-03-01T17:10:06Z
dc.date.available2017-03-01T17:10:06Z
dc.date.issued2014
dc.descriptionElectronic Thesis or Dissertationen_US
dc.description.abstractInitial work focused on characterizing silver and its surface enhanced Raman spectroscopy (SERS) capabilities. Silver nanowires were chosen as an ideal material and scanning confocal microscopy studies were performed to identify hot spots. The silver nanowires were found to exhibit fluorescence blinking that was attributed to small silver clusters undergoing rapid interchange from Ag<super>0</super> to Ag<sub>2</sub>O. Control of this blinking was accomplished through the removal of oxygen and through electrochemical control of the system. SERS was also recorded from these nanowires. Deconvolution of the SERS signal from the fluorescence was accomplished either by increasing the SERS analyte concentration or increasing the total number of "hot spots" in the focus volume. Silver applications were studied by performing a SERS study of Rhodamine 6G (R6G) and Poly(3-hexylthiophene-2,5-diyl) (P3HT). A Tollens' silver substrate was utilized as the SERS substrate and similar blinking effects were found to arise. P3HT was cast from 4 different solvents:dichloromethane, chlorobenzene, THF, and toluene. The solvent effects were studied, with kinking of the polymer noted in the non-chlorinated solvents. Single molecule studies in conjunction with polarization control indicated that the P3HT formed in an overlapping manner with only partial charge transfer within the molecule. Finally silvers interactions with TiO<sub>2</sub> were studied. Micron scale single crystal anatase TiO<sub>2</sub> was synthesized by using HF in a hydrothermal process forming a truncated bipyramidal structure consisting of [101] and [001] faces. Fluorine was present in small amounts on the surface of the TiO<sub>2</sub> as confirmed by x-ray photoelectron spectroscopy (XPS). An annealing process was used to remove the fluorine. Nitrogen doping was attempted, but was not found to occur in significant amounts. Visible light sensitivity was noted in annealed samples but did not occur in the bulk as demonstrated through photoelectrochemical measurements. Silver photoreduction directly on the surface of the TiO<sub>2</sub> crystals revealed visible light sensitivity at surface defects. No facial preference was noted for the silver growth through energy-dispersive X-ray spectroscopy (EDX) images. A secondary method of silver attachment through a linker molecule showed that on-resonance silver structures provided greater SERS enhancement dependent upon the direction of the linker molecule.en_US
dc.format.extent141 p.
dc.format.mediumelectronic
dc.format.mimetypeapplication/pdf
dc.identifier.otheru0015_0000001_0001665
dc.identifier.otherClayton_alatus_0004D_12044
dc.identifier.urihttps://ir.ua.edu/handle/123456789/2115
dc.languageEnglish
dc.language.isoen_US
dc.publisherUniversity of Alabama Libraries
dc.relation.hasversionborn digital
dc.relation.ispartofThe University of Alabama Electronic Theses and Dissertations
dc.relation.ispartofThe University of Alabama Libraries Digital Collections
dc.rightsAll rights reserved by the author unless otherwise indicated.en_US
dc.subjectAnalytical chemistry
dc.subjectMaterials science
dc.subjectPhysical chemistry
dc.titleNanostructured silver for applications in surface enhanced Raman spectroscopy and photoelectrochemical reactionsen_US
dc.typethesis
dc.typetext
etdms.degree.departmentUniversity of Alabama. Department of Chemistry
etdms.degree.disciplineChemistry
etdms.degree.grantorThe University of Alabama
etdms.degree.leveldoctoral
etdms.degree.namePh.D.

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