Surface Functionalization of Graphene-based Materials

dc.contributor.advisorAjayan, Pulickel M.en_US
dc.contributor.committeeMemberBarrera, Enrique V.en_US
dc.contributor.committeeMemberMarti, Angel A.en_US
dc.creatorMathkar, Akshayen_US
dc.date.accessioned2013-09-16T15:56:13Zen_US
dc.date.accessioned2013-09-16T15:56:17Zen_US
dc.date.available2013-09-16T15:56:13Zen_US
dc.date.available2013-09-16T15:56:17Zen_US
dc.date.created2013-05en_US
dc.date.issued2013-09-16en_US
dc.date.submittedMay 2013en_US
dc.date.updated2013-09-16T15:56:18Zen_US
dc.description.abstractGraphene-based materials have generated tremendous interest in the past decade. Manipulating their characteristics using wet-chemistry methods holds distinctive value, as it provides a means towards scaling up, while not being limited by yield. The majority of this thesis focuses on the surface functionalization of graphene oxide (GO), which has drawn tremendous attention as a tunable precursor due to its readily chemically manipulable surface and richly functionalized basal plane. Firstly, a room-temperature based method is presented to reduce GO stepwise, with each organic moiety being removed sequentially. Characterization confirms the carbonyl group to be reduced first, while the tertiary alcohol is reduced last, as the optical gap decrease from 3.5 eV down to 1 eV. This provides greater control over GO, which is an inhomogeneous system, and is the first study to elucidate the order of removal of each functional group. In addition to organically manipulating GO, this thesis also reports a chemical methodology to inorganically functionalize GO and tune its wetting characteristics. A chemical method to covalently attach fluorine atoms in the form of tertiary alkyl fluorides is reported, and confirmed by MAS 13C NMR, as two forms of fluorinated graphene oxide (FGO) with varying C/F and C/O ratios are synthesized. Introducing C-F bonds decreases the overall surface free energy, which drastically reduces GO’s wetting behavior, especially in its highly fluorinated form. Ease of solution processing leads to development of sprayable inks that are deposited on a range of porous and non-porous surfaces to impart amphiphobicity. This is the first report that tunes the wetting characteristics of GO. Lastly as a part of a collaboration with ConocoPhillips, another class of carbon nanomaterials - carbon nanotubes (CNTs), have been inorganically functionalized to repel 30 wt% MEA, a critical solvent in CO2 recovery. In addition to improving the solution processability of CNTs, composite, homogeneous solutions are created with polysulfones and polyimides to fabricate CNT-polymer nanocomposites that display contact angles greater than 150o with 30 wt% MEA. This yields materials that are inherently supersolvophobic, instead of simply surface treating polymeric films, while the low density of fluorinated CNTs makes them a better alternative to superhydrophobic polymer materials.en_US
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationMathkar, Akshay. "Surface Functionalization of Graphene-based Materials." (2013) Diss., Rice University. <a href="https://hdl.handle.net/1911/72000">https://hdl.handle.net/1911/72000</a>.en_US
dc.identifier.slug123456789/ETD-2013-05-464en_US
dc.identifier.urihttps://hdl.handle.net/1911/72000en_US
dc.language.isoengen_US
dc.rightsCopyright 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.en_US
dc.subjectGraphene oxideen_US
dc.subjectWettingen_US
dc.subjectCarbon nanotubesen_US
dc.subjectFunctionalizationen_US
dc.titleSurface Functionalization of Graphene-based Materialsen_US
dc.typeThesisen_US
dc.type.materialTexten_US
thesis.degree.departmentMechanical Engineering and Materials Scienceen_US
thesis.degree.disciplineEngineeringen_US
thesis.degree.grantorRice Universityen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophyen_US
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