Show simple item record

dc.contributor.advisorWalker, Robert Aen_US
dc.contributor.authorBrindza, Michael Rossen_US
dc.date.accessioned2010-11-23T06:30:15Z
dc.date.available2010-11-23T06:30:15Z
dc.date.issued2009en_US
dc.identifier.urihttp://hdl.handle.net/1903/10993
dc.description.abstractThis dissertation presents the results of nonlinear spectroscopic studies whose goal is to understand how the asymmetric nature of interfaces and intermolecular interactions give rise to interfacial solvation properties and solvent structure. The first part of this thesis uses resonance enhanced second harmonic generation to examine the polarity and hydrogen bonding opportunities at interfaces formed between hydrophilic silica and both weakly and strongly associating organic liquids. Measuring interfacial electronic spectra of probe molecules that exhibit solvatochromic sensitivity to polarity and hydrogen bonding, we saw that small changes in solvent structure affect interfacial polarity, and strongly associating alcohols solvents create a region of heterogeneous polarity at the interface. Silica appears to donate hydrogen bonds to adsorbates no matter what solvent (protic or aprotic) was chosen. The second part of this dissertation uses another nonlinear spectroscopic technique, vibrational sum frequency generation, to determine the structure and orientation of solvent molecules adsorbed to silica/vapor, silica/liquid, and neat liquid/vapor interfaces. By comparing spectral features appearing under different experimental polarization conditions, we have determined average solvent orientations and degree of organization. Our initial studies of alkanes adsorbed to the silica/vapor interface show that despite strong substrate-adsorbate interactions, molecules at the interface show some degree of long range order and organization. In order to examine how the strength of intermolecular forces between adsorbates and either the substrate or neighboring molecules affect interfacial organization, we measured vibrational spectra of octanol isomers as well as different functional group containing n-alkyl molecules at silica/vapor and silica/liquid interfaces. The octanol studies show that strongly associating molecules form ordered monolayers at the silica/vapor interface, but that strength of lateral interactions is important for preserving that order when the liquid is brought into contact. Branched isomers appeared very disordered at solid/liquid interfaces. Further examining this change in order between solvents at silica/vapor and silica/liquid interfaces using equal length but different functional group containing solvents, we see that the energetics of adsorption and solvation are likely to be responsible for the degree of order both at the solid/vapor surface (adsorption) and solid/liquid interface (both adsorption and solvation).en_US
dc.titleSolvation, Structure and Organization at Liquid Surfacesen_US
dc.typeDissertationen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.contributor.departmentChemistryen_US
dc.subject.pqcontrolledPhysical Chemistryen_US
dc.subject.pquncontrolledInterfaceen_US
dc.subject.pquncontrolledNonlinear Spectroscopyen_US
dc.subject.pquncontrolledSilicaen_US
dc.subject.pquncontrolledSolvationen_US
dc.subject.pquncontrolledSolvent Structureen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record