Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6922
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dc.contributor.advisorAndronescu, Corinaen_US
dc.contributor.authorKUMBHAR, VAIBHAVen_US
dc.date.accessioned2022-05-13T08:59:43Z-
dc.date.available2022-05-13T08:59:43Z-
dc.date.issued2022-05-
dc.identifier.citation43en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6922-
dc.description.abstractIn today´s world, every human being faces problems like global warming, pollution and energy demand crises. The scientific community believes that the long term solution for these problems is reducing CO2 into energy-dense products. CO2 reduction reaction (CO2RR) requires active catalysts for efficient conversion. Developing catalysts based on earth-abundant elements for CO2RR is needed. Activity, selectivity and stability are the evaluation parameter for CO2RR catalysts. In this thesis, various manganese and nickel based nitrogen-doped carbon materials were synthesized and investigated as potential candidates for CO2RR aiming to achieve a minimum 50% faradic efficiency (FE) for carbon monoxide (CO) at -220 mA current, i.e. -194 mA/cm2 of current density. Optimised Ni-based catalysts show 58% FE for CO at -194 mA/cm2 with 112 mA/cm2 partial current density of CO, whereas Mn materials only favour hydrogen evolution reaction (HER), reaching a maximum 10 % FE for CO at -23 mA/cm2. A later part of this study includes various approaches to improve CO2RR activity, selectivity and stability, such as the addition of benzoxazine polymer, and changing precursors mass loadings.en_US
dc.language.isoenen_US
dc.subjectCO2RRen_US
dc.subjectelectroreductionen_US
dc.subjectselectivityen_US
dc.subjectelectrodesen_US
dc.subjectCOen_US
dc.subjectstabilityen_US
dc.subjectactivityen_US
dc.titleCO2 electroreduction on Mn-N-C and Ni-N-C electrocatalyst embedded in gas diffusion electrodesen_US
dc.typeThesisen_US
dc.typeDissertationen_US
dc.typeWorking Paperen_US
dc.type.degreeBS-MSen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.contributor.registration20161159en_US
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