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dc.contributor.advisorChen, De
dc.contributor.authorHjorth, Ida
dc.date.accessioned2015-10-06T07:37:51Z
dc.date.available2015-10-06T07:37:51Z
dc.date.created2012-06-19
dc.date.issued2012
dc.identifierntnudaim:8154
dc.identifier.urihttp://hdl.handle.net/11250/2351884
dc.description.abstractIn this thesis a thermoelectric cell is developed. Aligned Carbon Nanotubes and aligned Nitrogen-doped Carbon Nanotubes are used as electrode materials. Ferri/Ferrocyanide and Tetrabutylammonium Nitrate (TBAN) electrolytes have been tested for thermoelectric performance, with the two different electrode materials. It was found that Nitrogen doping of CNT's enhances reaction kinetics of the Ferro/Ferricyanide redox reaction. It is suggested that there will be an ideal level of doping, where the electron transfer rate is maximized. TBAN showed the highest open circuit voltage, but it was discovered that TBAN in dodecanol was unsuitable as an electrolyte for thermocells due to low conductivity and unstable current. The current decreased to less than 1 A in some seconds. The highest thermoelectric eciency obtained was for a symmetric NCNT elec- trode conguration, with the Ferrocyanide redox couple. The eciency was 0.007 % of the Carnot efficiency, which is less than state-of-the art electrolyte thermo- cells. The lower eciecy was due to non-optimized electrodes and current leakages in the test cell. Dense, uniform and aligned CNT's were grown on Aluminum foil but using a pre-deposited 2 nm layer of iron catalyst. Ammonia annealing was required before CVD. The treatment with ammonia lead to longer catalyst lifetimes and better alignment. Lengths up to 110 m was obtained, 15 nm in diameter. Growth of aligned N-doped CNT's on Aluminum was done using a floating catalyst method. Up to 1.5 % incorporation of Nitrogen was achieved.
dc.languageeng
dc.publisherNTNU
dc.subjectNanoteknologi, Nanoteknologi for materialer, energi og miljø
dc.titleOrganic Electrolytes for Thermoelectric Devices and CNT Electrode functionalization by Nitrogen-doping
dc.typeMaster thesis
dc.source.pagenumber87


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