Adsorption of primary substituted hydrocarbons onto solid gallium substrates

dc.contributor.authorDe Silva, Chrishani Maheshwari
dc.date.accessioned2013-04-29T14:43:56Z
dc.date.available2013-04-29T14:43:56Z
dc.date.graduationmonthMay
dc.date.issued2013-04-29
dc.date.published2013
dc.description.abstractAdsorption of a series of primarily substituted hydrocarbons (RX; C[subscript]18H[subscript]37PO(OH)[subscript]2 (ODPA), C[subscript]17H[subscript]35COOH, C[subscript]18H[subscript]37OH, C[subscript]18H[subscript]37NH[subscript]2 and C[subscript]18H[subscript]37SH) onto solid gallium substrates with and without UV/ozone treatment was studied using contact angle goniometry, spectroscopic ellipsometry and cyclic voltammetry (CV). UV/ozone treatment offered a hydrophilic surface (water contact angle ([theta][superscript]water) less than 10°), reflecting the formation of a surface oxide layer with the maximum thickness of ca. 1 nm and possibly the removal of surface contaminants. Upon immersion in a toluene solution of a RX, [theta][superscript]water increased due to adsorption of the RX onto gallium substrates. In particular, UV/ozone-treated gallium substrates (UV-Ga) immersed in an ODPA solution exhibited [theta][superscript]water close to 105°. The ellipsometric thickness of the adsorbed ODPA layer was ca. 2.4 nm and CV data measured in an acetonitrile solution showed significant inhibition of redox reaction on the substrate surface. These results indicate the formation of a densely-packed ODPA monolayer on UV-Ga. The coverage of a C[subscript]17H[subscript]35COOH layer adsorbed onto UV-Ga was lower, as shown by smaller [theta][superscript]water (ca. 99°), smaller ellipsometric thickness (ca. 1.3 nm) and smaller electrode reaction inhibition. Adsorption of the other RX onto UV-Ga was weaker, as indicated by smaller [theta][superscript]water (82-92°). ODPA did not strongly adsorb onto UV-untreated gallium substrates, suggesting that the ODPA adsorption mainly originates from hydrogen bond interaction of a phosphonate group with surface oxide. These results will provide a means for controlling the surface properties of oxide-coated gallium that play an essential role in monolayer conductivity measurements and electroanalytical applications.
dc.description.advisorTakashi Ito
dc.description.degreeMaster of Science
dc.description.departmentDepartment of Chemistry
dc.description.levelMasters
dc.description.sponsorshipDivision of Chemical Sciences, Geosciences and Biosciences, Office of Basic Energy Sciences of the U.S
dc.identifier.urihttp://hdl.handle.net/2097/15673
dc.language.isoen_US
dc.publisherKansas State University
dc.rights© the author. This Item is protected by copyright and/or related rights. 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).
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectAdsorption
dc.subjectPrimary substituted
dc.subjectOctadecylphosphonic acid
dc.subjectGallium
dc.subject.umiChemistry (0485)
dc.titleAdsorption of primary substituted hydrocarbons onto solid gallium substrates
dc.typeThesis

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