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dc.contributor.advisorYogesh Surendranath.en_US
dc.contributor.authorOh, Seokjoon.en_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Chemistry.en_US
dc.date.accessioned2019-11-04T20:20:43Z
dc.date.available2019-11-04T20:20:43Z
dc.date.copyright2019en_US
dc.date.issued2019en_US
dc.identifier.urihttps://hdl.handle.net/1721.1/122714
dc.descriptionThesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 2019en_US
dc.descriptionCataloged from PDF version of thesis. Page 156 blank.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractThis 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.abstractFirst, 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.abstractFinally, 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.statementofresponsibilityby Seokjoon Oh.en_US
dc.format.extent156 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT 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.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectChemistry.en_US
dc.titleGraphite-conjugated catalysts : bridging heterogeneous and homogeneous catalystsen_US
dc.typeThesisen_US
dc.description.degreePh. D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.identifier.oclc1124073519en_US
dc.description.collectionPh.D. Massachusetts Institute of Technology, Department of Chemistryen_US
dspace.imported2019-11-04T20:20:42Zen_US
mit.thesis.degreeDoctoralen_US
mit.thesis.departmentChemen_US


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