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dc.contributor.advisorTimothy M. Swager.en_US
dc.contributor.authorJeon, Intaken_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Materials Science and Engineering.en_US
dc.date.accessioned2018-09-17T14:49:45Z
dc.date.available2018-09-17T14:49:45Z
dc.date.copyright2018en_US
dc.date.issued2018en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/117790
dc.descriptionThesis: Ph. D., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2018.en_US
dc.descriptionThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.en_US
dc.descriptionCataloged student-submitted from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (pages 137-146).en_US
dc.description.abstractStrong attractive interactions between extended π-systems of graphene in various graphites have been studied for several decades. However, to date, no effective scalable exfoliation mechanism has been reported to exclusively synthesize dispersible single layer graphene in liquid environments. The first feature of this thesis is to use the repulsive electrostatic effect to modify the geometry of [pi]-[pi] interaction of graphenes against attractive van der Waals interactions. We explored an electrochemical method, inducing the large offset from ideal tight stacked [pi]-[pi] geometry, to generate Hyperstage-1 graphite intercalation compounds. Subsequently, highly functionalized graphenes are spontaneously exfoliated from Hyperstage-1 graphite intercalation compounds by reaction with an aryl diazonium salt solution under electrochemical reducing conditions. The covalent functionalization of graphene successfully provided the appropriate chemical activity/reactivity for the desired applications. Through the reactivity of functional graphene, we developed the fluid-like graphene matrix to attain a superlubric state. In addition, Janus graphenes are simply synthesized by Meisenheimer complexes reactions of hydrocarbon, perfluorocarbon and water-soluble alkyl amines on the surface of graphene at room temperature. This approach opens the door to a rich variety of functional single layer graphenes for applications.en_US
dc.description.statementofresponsibilityby Intak Jeon.en_US
dc.format.extent146 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.subjectMaterials Science and Engineering.en_US
dc.titleGraphene at interfacesen_US
dc.typeThesisen_US
dc.description.degreePh. D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.identifier.oclc1051211579en_US


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