Design of Optimal Laser Pulses for Controlling Molecular Processes

dc.contributor.guideHarjinder Singh
dc.coverage.spatial
dc.creator.researcherSitansh Sharma
dc.date.accessioned2017-08-08T07:16:03Z
dc.date.available2017-08-08T07:16:03Z
dc.date.awarded31/07/2011
dc.date.completed30/07/2011
dc.date.registered30-12-2006
dc.description.abstractControl of molecular dynamics using external laser has achieved significant progress in recent years. Optimal control theory (OCT) has emerged as a powerful tool for laser desiging. In this work, we have used time dependent quantum mechanics along with OCT to design pulses for controlling processes, such as state-selective population transfer and dissociation in molecular systems in their ground electronic state. The generation of the highly excited vibrational states in a specified bond is an interesting problem in relation to intramolecular vibrational relaxation, bond dissociation and molecular quantum computing. We have treated the interaction of the molecule with the laser within the dipole approximation. The time dependent quantum mechanical propagation is achieved using the split-operator form of evolution operator together with Fast Fourier Transforms (FFT) and grid methods. The detailed analysis of laser pulses are carried out in terms of time dependent variation of electric field and its corresponding frequency spectrum. We have obtained fields for vibrational and rovibrational control in diatomic system (HF) using conjugate gradient method. Pulses are also designed to control nuclear dynamics in the fragments located in biomolecules, using simplified but realistic models. Optimized laser give nearly complete population transfer to the preselected molecular state at the end of pulse duration. The possibility of using Genetic Algorithm has also been investigated. This procedure allows us to select limited laser parameters to vary that correspond to those actually available to the experimentalist. Thus, it provides good control over pulse parameters, allowing optimized pulses with simple time and frequency structures. We have applied this method for selective state-to-state transitions in HF molecule and selective dissociation in HF molecule and the Fe CO bond in the CO-heme complex. It is shown that pulses designed in this way have simple time and frequency structures, and are experimentally feasible.
dc.description.note
dc.format.accompanyingmaterialNone
dc.format.dimensions
dc.format.extentxxii,185
dc.identifier.urihttp://hdl.handle.net/10603/165985
dc.languageEnglish
dc.publisher.institutionComputational Natural Sciences
dc.publisher.placeHyderabad
dc.publisher.universityInternational Institute of Information Technology, Hyderabad
dc.relation
dc.rightsself
dc.source.universityUniversity
dc.subject.keywordCO-heme complex
dc.subject.keywordconjugate gradient algorithm
dc.subject.keywordcontrol
dc.subject.keywordgenetic algorithm
dc.subject.keywordHF
dc.subject.keywordlaser lulse
dc.subject.keywordOptimization
dc.titleDesign of Optimal Laser Pulses for Controlling Molecular Processes
dc.title.alternative
dc.type.degreePh.D.

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