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A Knudsen cell for controlled deposition of L-cysteine and L-methionine on Au(111)

dc.contributor.advisorMitchell, Caroline E. J. (Katie)en_US
dc.contributor.committeeMemberPaige, Matthew F.en_US
dc.contributor.committeeMemberMoewes, Alexanderen_US
dc.contributor.committeeMemberMcWilliams, Kathryn A.en_US
dc.contributor.committeeMemberManson, Alanen_US
dc.contributor.committeeMemberBradley, Michael P.en_US
dc.creatorDubiel, Evan Alozieen_US
dc.date.accessioned2006-11-17T13:36:11Zen_US
dc.date.accessioned2013-01-04T05:08:35Z
dc.date.available2006-11-20T08:00:00Zen_US
dc.date.available2013-01-04T05:08:35Z
dc.date.created2006-11en_US
dc.date.issued2006-11-20en_US
dc.date.submittedNovember 2006en_US
dc.description.abstractThis thesis details the development of expertise and tools required for the study of amino acids deposited on Au(111), with a primary focus on the design and testing of a Knudsen cell for controlled deposition of L-cysteine and L-methionine. An ultra-high vacuum preparation chamber designed by Dr. Katie Mitchell and built by Torrovap Industries Inc. was installed. This chamber is connected to the existing scanning tunneling microscopy chamber via a gate valve, and both chambers can operate independently. Various instruments such as a mass spectrometer, quartz crystal microbalance, ion source, and sample manipulator were installed on the preparation chamber. Scanning tunneling microscopy was performed on both homemade and commercial Au(111) thin films. High resolution images of "herringbone" reconstruction and individual atoms were obtained on the commercial thin films, and optimal tunneling conditions were determined. A Knudsen cell was designed to be mounted on the preparation chamber. The Knudsen cell operates over the temperature range 300-400K, with temperatures reproducible to ±0.5K, and stable to ±0.1K over a five minute period. Reproducible deposition rates of less than 0.2Å/s were obtained for both L-cysteine and L-methionine. Electron impact mass spectrometry and heat of sublimation measurements were performed to characterize the effusion of L-cysteine and L-methionine from the Knudsen cell. The mass spectrometry results suggest that L-cysteine was decomposing at 403K while L-methionine was stable during effusion. Heats of sublimation of 168.3±33.2kJ/mol and 156.5±10.1kJ/mol were obtained for L-cysteine and L-methionine respectively.en_US
dc.identifier.urihttp://hdl.handle.net/10388/etd-11172006-133611en_US
dc.language.isoen_USen_US
dc.subjectknudsen cosine lawen_US
dc.subjectAmino Acidsen_US
dc.subjectMetal Surfacesen_US
dc.subjectScanning Tunneling Microscopyen_US
dc.subjectMass Spectrometryen_US
dc.subjectquartz crystal microbalanceen_US
dc.subjectself-assembled monolayersen_US
dc.subjectalkanethiolsen_US
dc.subjectadsorptionen_US
dc.subjecteffusionen_US
dc.subjectproteinsen_US
dc.titleA Knudsen cell for controlled deposition of L-cysteine and L-methionine on Au(111)en_US
dc.type.genreThesisen_US
dc.type.materialtexten_US
thesis.degree.departmentPhysics and Engineering Physicsen_US
thesis.degree.disciplinePhysics and Engineering Physicsen_US
thesis.degree.grantorUniversity of Saskatchewanen_US
thesis.degree.levelMastersen_US
thesis.degree.nameMaster of Science (M.Sc.)en_US

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