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dc.contributor.advisorRobert W. Field.en_US
dc.contributor.authorBarnum, Timothy J.(Timothy James)en_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Chemistry.en_US
dc.date.accessioned2020-10-18T21:33:08Z
dc.date.available2020-10-18T21:33:08Z
dc.date.copyright2020en_US
dc.date.issued2020en_US
dc.identifier.urihttps://hdl.handle.net/1721.1/128066
dc.descriptionThesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 2020en_US
dc.descriptionCataloged from the PDF of thesis.en_US
dc.descriptionIncludes bibliographical references (pages 313-326).en_US
dc.description.abstractRydberg states of molecules with high orbital angular momentum (l >/~ 3) are a unique class of electronic states. These high-l Rydberg states escape the rapid non-radiative decay by predissociation, which is typical of the intensively studied low-4 Rydberg states. Access to high-4 Rydberg states is challenging due to the [delta]l = ±1 transition propensity rule in combination with the short lifetimes of the optically accessible, low- Rydberg states. To address these dual challenges, we implement optical-millimeter-wave stimulated Raman adiabatic passage (optical-mmW STIRAP), which enables efficient population transfer from a low-lying electronic state to a high-l Rydberg state without directly populating a lossy, low-e Rydberg state. Our demonstration of optical-mmW STIRAP on an atomic system includes examination of the experimental and theoretical details of every step of this coherent process and demonstrates its promise for molecular applications.en_US
dc.description.abstractWe explore the physics of the Rydberg electron <->ion-core system through investigation of the spectroscopy and dynamics of high-l Rydberg states of NO. We populate ng Rydberg states of NO by a three-color triple-resonance excitation scheme and probe Rydberg-Rydberg transitions by chirped-pulse millimeter-wave (CPmmW) spectroscopy. The precision of the experimental data obtained and the breadth of the state space examined by CPmmW spectroscopy provides challenges to the existing theory of the structure of high-l Rydberg states. We apply a long-range electrostatic model to disentangle and describe the physical mechanisms that contribute to the autoionization dynamics of NO Rydberg states. Our model accounts for the decay rates of vibrationally excited ng Rydberg states.en_US
dc.description.abstractWe explain the previously measured NO⁺ ion rotational state population distributions produced by autoionization of NO nf states and propose methods to generate single quantum state-selected NO⁺ ions by selective population of specific ng Rydberg states.en_US
dc.description.statementofresponsibilityby Timothy J. Barnum.en_US
dc.format.extent326 agesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectChemistry.en_US
dc.titleSpectroscopy and dynamics of high orbital angular momentum Rydberg statesen_US
dc.typeThesisen_US
dc.description.degreePh. D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.identifier.oclc1199082884en_US
dc.description.collectionPh.D. Massachusetts Institute of Technology, Department of Chemistryen_US
dspace.imported2020-10-18T21:33:04Zen_US
mit.thesis.degreeDoctoralen_US
mit.thesis.departmentChemen_US


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