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http://arks.princeton.edu/ark:/88435/dsp01cf95jf08b
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DC Field | Value | Language |
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dc.contributor.advisor | Loo, Lynn | - |
dc.contributor.author | Burd, Joshua | - |
dc.date.accessioned | 2017-07-20T18:10:30Z | - |
dc.date.available | 2017-07-20T18:10:30Z | - |
dc.date.created | 2017-05-01 | - |
dc.date.issued | 2017-5-1 | - |
dc.identifier.uri | http://arks.princeton.edu/ark:/88435/dsp01cf95jf08b | - |
dc.description.abstract | The electrochromic polymer made by template polymerization of aniline on poly(2-acryl-amido-2-methyl-1propanesulfonic acid (PAAMPSA) has shown potential in independent visible and near-infrared modulating smart window applications. PANI-PAAMPSA can be switched reversibly by an applied voltage through three oxidation states that change the polymer from clear to green/IR absorbing to dark blue. A suitable counter electrode is an electrochromic polymer which is colored in its oxidized state and clear in its reduced state, which is opposite the behavior of PANI-PAAMPSA. This thesis examines the potential to use ECP-magenta, an ethylhexyl substituted version of the homopolymer ProDOT (3,4 propylenedioxythiophene), as the counter electrode. The charge required to fully switch states for PANI-PAAMPSA is double that required for ECP-magenta for the same thickness, meaning the required thickness for PANI-PAAMPSA can be significantly less and still provide a balanced charge capacity for the cell. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Improvement of Electrochromic Windows through Materials Optimization | en_US |
dc.type | Princeton University Senior Theses | - |
pu.date.classyear | 2017 | en_US |
pu.department | Chemical and Biological Engineering | en_US |
pu.pdf.coverpage | SeniorThesisCoverPage | - |
pu.contributor.authorid | 960862108 | - |
pu.contributor.advisorid | 310070790 | - |
pu.certificate | Materials Science and Engineering Program | en_US |
Appears in Collections: | Chemical and Biological Engineering, 1931-2019 |
Files in This Item:
File | Size | Format | |
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jburd_thesis_final.pdf | 1.17 MB | Adobe PDF | Request a copy |
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