Analysis of the Dynamics of Heavy-Rydberg Ion Pair Formation Through Studies of Electron Capture Reactions
| dc.contributor.advisor | Dunning, F. Barry | |
| dc.creator | Kelley, Michael John | |
| dc.date.accessioned | 2019-05-16T20:43:18Z | |
| dc.date.available | 2019-05-16T20:43:18Z | |
| dc.date.created | 2017-12 | |
| dc.date.issued | 2017-09-06 | |
| dc.date.submitted | December 2017 | |
| dc.date.updated | 2019-05-16T20:43:18Z | |
| dc.description.abstract | Scattering of K(np) Rydberg atoms by electron-attaching molecules can result in the formation of positive-negative ion pairs through electron transfer reactions. These reactions can involve the dissociation of a transient intermediate negative ion into a smaller negative ion and a neutral fragment, or they can result in the parent molecule forming a metastable negative ion, with the excess energy being distributed among its internal modes. For Rydberg atoms of intermediate n, it is possible for these ion pairs to orbit each other at large separation, weakly bound by their mutual electrostatic attraction, forming what are known as heavy-Rydberg states. Measurements of the binding energy and velocity distributions of the ion pairs are used to probe the dynamics of electron transfer reactions. The data are analyzed using a semiclassical Monte Carlo collision code to explore the lifetime of the intermediate, the nature of its dissociation, the distribution of the excess energy of reaction, and the branching ratio of the various reaction channels. Results obtained using a variety of attaching targets including CF3I, CCl4, SF6, CH2Br2, 1,1,1-C2Cl3F3, CCl3Br, Fe(CO)5, and CH3NO2 have demonstrated both the wide variety of different behaviors that can accompany electron capture as well as the different behaviors of the product ion-pair states themselves. Remarkably, despite previous work showing that it was possible for CH3NO2 to form long-lived valence-bound negative ions through Rydberg electron transfer, the present work showed that such collisions do not result in the formation of long-lived bound ion-pair states. Rather, the data show that collisions lead to very strong Rydberg atom scattering through formation of transient ion-pair states. These results are consistent with theoretical work that predicts significant collisional quenching of Rydberg atoms by highly polar molecules and highlight a new mechanism for Rydberg atom scattering. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.citation | Kelley, Michael John. "Analysis of the Dynamics of Heavy-Rydberg Ion Pair Formation Through Studies of Electron Capture Reactions." (2017) Diss., Rice University. <a href="https://hdl.handle.net/1911/105537">https://hdl.handle.net/1911/105537</a>. | |
| dc.identifier.uri | https://hdl.handle.net/1911/105537 | |
| dc.language.iso | eng | |
| dc.rights | Copyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder. | |
| dc.subject | Rydberg atoms | |
| dc.subject | electron attachment | |
| dc.title | Analysis of the Dynamics of Heavy-Rydberg Ion Pair Formation Through Studies of Electron Capture Reactions | |
| dc.type | Thesis | |
| dc.type.material | Text | |
| thesis.degree.department | Physics and Astronomy | |
| thesis.degree.discipline | Natural Sciences | |
| thesis.degree.grantor | Rice University | |
| thesis.degree.level | Doctoral | |
| thesis.degree.name | Doctor of Philosophy |
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