| dc.contributor.advisor | Yogesh Surendranath. | en_US |
| dc.contributor.author | Oh, Seokjoon. | en_US |
| dc.contributor.other | Massachusetts Institute of Technology. Department of Chemistry. | en_US |
| dc.date.accessioned | 2019-11-04T20:20:43Z | |
| dc.date.available | 2019-11-04T20:20:43Z | |
| dc.date.copyright | 2019 | en_US |
| dc.date.issued | 2019 | en_US |
| dc.identifier.uri | https://hdl.handle.net/1721.1/122714 | |
| dc.description | Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 2019 | en_US |
| dc.description | Cataloged from PDF version of thesis. Page 156 blank. | en_US |
| dc.description | Includes bibliographical references. | en_US |
| dc.description.abstract | This interconversion occurs via complex multistep, multielectron reactions, which can be carried out by either metallic heterogeneous or molecular homogeneous electrocatalysts. Metallic heterogeneous catalysts have a continuum of electronic states that distribute the redox burden of multielectron reactions, allowing for efficient catalysis. However, heterogeneous catalysts display a variety of active sites and local electronic structures, and are difficult to fine-tune at a molecular level. On the other hand, homogeneous catalysts allow a great degree of synthetic control over the catalytic active site. Moreover, the relative ease in spectroscopic characterization allows a mechanistic understanding of molecular catalysis at a level that is unattainable for heterogeneous catalysis. To bridge the advantages of both types of catalysts, we have developed a surface functionalization strategy for conjugating molecularly well-defined active sites to graphitic carbon surfaces. | en_US |
| dc.description.abstract | First, I will discuss the preparation and characterization of two new types of conjugating N-heterocyclic linkages to graphitic carbon surfaces. This work presents a general method for characterizing modified carbon surfaces with molecular-level structural detail. Then, I will present the electrocatalytic carbon dioxide reduction activity of a graphite-conjugated rhenium catalyst, and compare its catalytic behavior to that of a molecular analog. Electrochemical and spectroscopic data show that graphite-conjugated catalysts do not behave identically to their molecular analogs, but rather show properties similar to that of metallic heterogeneous catalysts, providing a unique bridge between the worlds of heterogeneous and homogeneous catalysis. | en_US |
| dc.description.abstract | Finally, in the appendix, I will present a chapter on the stability of graphite-conjugated linkages under electrochemical polarization, followed by a chapter on catalyzing the reduction of molecular pyridinium species using a graphite-conjugated rhodium catalyst. | en_US |
| dc.description.statementofresponsibility | by Seokjoon Oh. | en_US |
| dc.format.extent | 156 pages | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Massachusetts Institute of Technology | en_US |
| dc.rights | MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission. | en_US |
| dc.rights.uri | http://dspace.mit.edu/handle/1721.1/7582 | en_US |
| dc.subject | Chemistry. | en_US |
| dc.title | Graphite-conjugated catalysts : bridging heterogeneous and homogeneous catalysts | en_US |
| dc.type | Thesis | en_US |
| dc.description.degree | Ph. D. | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
| dc.identifier.oclc | 1124073519 | en_US |
| dc.description.collection | Ph.D. Massachusetts Institute of Technology, Department of Chemistry | en_US |
| dspace.imported | 2019-11-04T20:20:42Z | en_US |
| mit.thesis.degree | Doctoral | en_US |
| mit.thesis.department | Chem | en_US |