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dc.identifier.urihttp://hdl.handle.net/11401/78202
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degreeen_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.typeThesis
dcterms.abstractAccording to the United States Environmental Protection Agency, as of 2015, transportation accounted for 32% of the carbon dioxide emissions in the United States (and all carbon dioxide emissions in the U.S. accounted for 82.2% of all greenhouse gases from human activity). A hydrogen fuel cell is a device that efficiently produces electrical energy directly from a chemical reaction, with zero carbon emissions, and therefore holds great promise in alleviating our dependence on harmful use of energy sources. Due to their clean emissions and high efficiencies, there has been focus on the hydrogen fuel cell for vehicle applications using proton exchange membrane and alkaline fuel cells. Although the proton exchange membrane fuel cell is currently being used in vehicles, their high cost limits their feasibility in the market. This has inspired the development of the alkaline fuel cell whose efficiency and simplicity suggest the possibility of manufacturing high power fuel cell vehicles at a low cost, since the electrocatalysts in the alkaline fuel cell can be made from non-noble metals. Although the hydrogen oxidation reaction is one of the fastest electrochemical reactions in acidic media, it is two orders of magnitude slower in alkaline media, which hinders the overall efficiency of the alkaline fuel cell. Pure platinum is currently the best catalyst for the hydrogen oxidation reaction, but platinum’s high cost and rarity yields economic issues, rendering the technology futile if it cannot be commercialized. Furthermore, platinum’s hydrogen binding energy is slightly stronger than the optimal hydrogen binding energy. As the hydrogen oxidation reaction happens only on the surface of the catalyst, there is no need for platinum content beyond the exterior. Since tungsten and nickel are cheap, as well as abundant, they are ideal elements to replace the core of the catalyst with, while leaving a platinum shell surrounding this core. The activity of the hydrogen oxidation reaction when using a platinum monolayer shell on a nickel tungsten core electrocatalyst is explored, and it was found that the novel catalyst created here exhibits kinetics that rival pure platinum, but at less than half the platinum content, suggesting that nickel and tungsten modify the electronic properties of platinum in a way that enhances its activity for the hydrogen oxidation reaction. Furthermore, the hydrogen binding energy of this novel electrocatalyst was found to be weaker than the optimal binding energy (rather than stronger, as seen in pure platinum), indicating the possibility of modifying the electronic properties of platinum for a more optimal hydrogen binding energy.
dcterms.available2018-03-22T22:39:18Z
dcterms.contributorAdzic, Radoslav R.en_US
dcterms.contributorSears, Trevor J.en_US
dcterms.contributorWhite, Michael G.en_US
dcterms.creatorTeeluck, Krishani
dcterms.dateAccepted2018-03-22T22:39:18Z
dcterms.dateSubmitted2018-03-22T22:39:18Z
dcterms.descriptionDepartment of Chemistry.en_US
dcterms.extent90 pg.en_US
dcterms.formatMonograph
dcterms.formatApplication/PDFen_US
dcterms.identifierhttp://hdl.handle.net/11401/78202
dcterms.issued2017-08-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2018-03-22T22:39:18Z (GMT). No. of bitstreams: 1 Teeluck_grad.sunysb_0771M_13428.pdf: 5208948 bytes, checksum: f4e6a85bcee2e855aa1321ed65959686 (MD5) Previous issue date: 2017-08-01en
dcterms.subjectChemistry -- Chemical engineering.
dcterms.subjectEnvironment
dcterms.subjectFuel cell
dcterms.subjectHydrogen oxidation reaction
dcterms.subjectNon-noble metal
dcterms.subjectPlatinum monolayer
dcterms.titlePlatinum Monolayer Shell on Non-Noble Metal Core Electrocatalysts for the Hydrogen Oxidation Reaction
dcterms.typeThesis


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