Fragmentation of molecular ions in ultrafast laser pulses

dc.contributor.authorAblikim, Utuqen_US
dc.date.accessioned2015-04-21T20:23:50Z
dc.date.available2015-04-21T20:23:50Z
dc.date.graduationmonthMayen_US
dc.date.issued2015-04-21
dc.date.published2015en_US
dc.description.abstractImaging the interaction of molecular ion beams with ultrafast intense laser fields is a very powerful method to understand the fragmentation dynamics of molecules. Femtosecond laser pulses with different wavelengths and intensities are applied to dissociate and ionize molecular ions, and each resulting fragmentation channel can be studied separately by implementing a coincidence three-dimensional (3D) momentum imaging method. The work presented in this master’s report can be separated into two parts. First, the interaction between molecular ion beams and femtosecond laser pulses, in particular, the dissociation of CO[superscript]+ into C[superscript]++O, is studied. For that purpose, measurements are conducted at different laser intensities and wavelengths to investigate the possible pathways of dissociation into C[superscript]++O. The study reveals that CO[superscript]+ starts to dissociate from the quartet electronic state at low laser intensities. Higher laser intensity measurements, in which a larger number of photons can be absorbed by the molecule, show that the doublet electronic states with deeper potential wells, e.g. A [superscript]2Π, contribute to the dissociation of the molecule. In addition, the three-body fragmentation of CO[subscript]2[superscript]+ into C[superscript]++O[superscript]++O[superscript]+ is studied, and two breakup scenarios are separated using the angle between the sum and difference of the momentum vectors of two O[superscript]+ fragments. In the second part, improvements in experimental techniques are discussed. Development of a reflective telescope setup intended to increase the conversion efficiency of ultraviolet (UV) laser pulse generation is described, and the setup is used in the studies of CO[superscript]+ dissociation described in this report. The other technical study presented here is the measurement of the position dependence of timing signals picked off of a microchannel plate (MCP) surface. The experimental method is presented and significant time spread over the surface of the MCP detector is reported [1].en_US
dc.description.advisorItzik Ben-Itzhaken_US
dc.description.degreeMaster of Scienceen_US
dc.description.departmentDepartment of Physicsen_US
dc.description.levelMastersen_US
dc.description.sponsorshipthe Chemical Sciences, Geosciences, and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energyen_US
dc.identifier.urihttp://hdl.handle.net/2097/18962
dc.language.isoen_USen_US
dc.publisherKansas State Universityen
dc.subjectUltrafast lasersen_US
dc.subjectMolecular Physicsen_US
dc.subjectCO+ dissociationen_US
dc.subjectMicrochannel plate detectorsen_US
dc.subjectCO2+ fragmentationen_US
dc.subject.umiPhysics (0605)en_US
dc.titleFragmentation of molecular ions in ultrafast laser pulsesen_US
dc.typeReporten_US

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