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DC Field | Value | Language |
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dc.contributor.advisor | Bocarsly, Andrew B. | - |
dc.contributor.author | Rock, Justin L. | - |
dc.date.accessioned | 2015-07-27T19:16:44Z | - |
dc.date.available | 2015-07-27T19:16:44Z | - |
dc.date.created | 2015-04-20 | - |
dc.date.issued | 2015-07-27 | - |
dc.identifier.uri | http://arks.princeton.edu/ark:/88435/dsp01k0698986h | - |
dc.description.abstract | Finding new catalysts for CO\(_{2}\) reduction is a growing field of interest. Previous research has shown that Group 6 metals might be a good source for producing these catalysts. One such potential catalyst that has previously gone uninvestigated is 2,2’- bipyridine tetracarbonyl chromium. In this study, this complex is investigated using cyclic voltammetry and bulk electrolysis to assess the possibility of acting as catalyst for the reduction of CO\(_{2}\). The complex exhibits two reduction peaks at negative potential,one reversible at approximately -1.7V vs. SCE and one irreversible at approximately -2.1V vs. SCE Despite showing current enhancements under CO\(_{2}\) in the CV data, electrolysis results showed poor production of CO\(_{2}\) reduction products, namely CO. An electrolysis run with labeled CO\(_{2}\) showed that in fact, the complex was not catalytically reducing CO\(_{2}\). Briefly, a few improvements to the system are considered, such as modifications to the bipyridine ligand and alternative ways of making up the solvent; however, these improvements are still a work in progress. | en_US |
dc.format.extent | 56 pages | en_US |
dc.language.iso | en_US | en_US |
dc.title | EXPLORING TETRACARBONYL CHROMIUM COMPLEXES WITH BIPYRIDINE DERIVATIVES AS POTENTIAL ELECTROCATALYSTS FOR CO2 REDUCTION | en_US |
dc.type | Princeton University Senior Theses | - |
pu.date.classyear | 2015 | en_US |
pu.department | Chemistry | en_US |
pu.pdf.coverpage | SeniorThesisCoverPage | - |
Appears in Collections: | Chemistry, 1926-2020 |
Files in This Item:
File | Size | Format | |
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PUTheses2015-Rock_Justin_L..pdf | 3.59 MB | Adobe PDF | Request a copy |
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