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Electrochemical Oxidation of Organic Pollutants Powered by a Silicon-Based Solar Cell
[Image: see text] Currently available (photo-)electrochemical technologies for water treatment establish a trade-off between low-pollutant concentration and costs. This paper aims at decoupling these two variables by designing a photo-oxidation device using earth abundant materials and an electronic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369653/ https://www.ncbi.nlm.nih.gov/pubmed/30775640 http://dx.doi.org/10.1021/acsomega.8b02502 |
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author | Perez-Rodriguez, Paula Maqueira Gonzalez, Carlos Bennani, Yasmina Rietveld, Luuk C. Zeman, Miro Smets, Arno H. M. |
author_facet | Perez-Rodriguez, Paula Maqueira Gonzalez, Carlos Bennani, Yasmina Rietveld, Luuk C. Zeman, Miro Smets, Arno H. M. |
author_sort | Perez-Rodriguez, Paula |
collection | PubMed |
description | [Image: see text] Currently available (photo-)electrochemical technologies for water treatment establish a trade-off between low-pollutant concentration and costs. This paper aims at decoupling these two variables by designing a photo-oxidation device using earth abundant materials and an electronic-free approach. The proposed device combines a graphite/graphite electrochemical system with a silicon-based solar cell that provides the necessary electrical power. First, the optimum operational voltage for the graphite/graphite electrochemical system was found to be around 1.6 V. That corresponded closely to the voltage produced by an a-Si:H/a-Si:H tandem solar cell of approximately 1.35 V. This configuration was shown to provide the best pollutant degradation in relation to the device area, removing 70% of the initial concentration of phenol and 90% of the methylene blue after 4 h of treatment. The chemical oxygen demand (COD) removal of these two contaminants after 4 h of treatment was also promising, 55 and 30%, respectively. Moreover, connecting several solar cells in series led to higher pollutant degradation but lower COD removal, suggesting that the degradation of the intermediate components is a limiting factor. This is expected to be due to the higher currents achieved by the series-connected configuration, which would favor other reactions such as polymerization over the degradation of intermediate species. |
format | Online Article Text |
id | pubmed-6369653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-63696532019-02-14 Electrochemical Oxidation of Organic Pollutants Powered by a Silicon-Based Solar Cell Perez-Rodriguez, Paula Maqueira Gonzalez, Carlos Bennani, Yasmina Rietveld, Luuk C. Zeman, Miro Smets, Arno H. M. ACS Omega [Image: see text] Currently available (photo-)electrochemical technologies for water treatment establish a trade-off between low-pollutant concentration and costs. This paper aims at decoupling these two variables by designing a photo-oxidation device using earth abundant materials and an electronic-free approach. The proposed device combines a graphite/graphite electrochemical system with a silicon-based solar cell that provides the necessary electrical power. First, the optimum operational voltage for the graphite/graphite electrochemical system was found to be around 1.6 V. That corresponded closely to the voltage produced by an a-Si:H/a-Si:H tandem solar cell of approximately 1.35 V. This configuration was shown to provide the best pollutant degradation in relation to the device area, removing 70% of the initial concentration of phenol and 90% of the methylene blue after 4 h of treatment. The chemical oxygen demand (COD) removal of these two contaminants after 4 h of treatment was also promising, 55 and 30%, respectively. Moreover, connecting several solar cells in series led to higher pollutant degradation but lower COD removal, suggesting that the degradation of the intermediate components is a limiting factor. This is expected to be due to the higher currents achieved by the series-connected configuration, which would favor other reactions such as polymerization over the degradation of intermediate species. American Chemical Society 2018-10-30 /pmc/articles/PMC6369653/ /pubmed/30775640 http://dx.doi.org/10.1021/acsomega.8b02502 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Perez-Rodriguez, Paula Maqueira Gonzalez, Carlos Bennani, Yasmina Rietveld, Luuk C. Zeman, Miro Smets, Arno H. M. Electrochemical Oxidation of Organic Pollutants Powered by a Silicon-Based Solar Cell |
title | Electrochemical Oxidation of Organic Pollutants Powered
by a Silicon-Based Solar Cell |
title_full | Electrochemical Oxidation of Organic Pollutants Powered
by a Silicon-Based Solar Cell |
title_fullStr | Electrochemical Oxidation of Organic Pollutants Powered
by a Silicon-Based Solar Cell |
title_full_unstemmed | Electrochemical Oxidation of Organic Pollutants Powered
by a Silicon-Based Solar Cell |
title_short | Electrochemical Oxidation of Organic Pollutants Powered
by a Silicon-Based Solar Cell |
title_sort | electrochemical oxidation of organic pollutants powered
by a silicon-based solar cell |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369653/ https://www.ncbi.nlm.nih.gov/pubmed/30775640 http://dx.doi.org/10.1021/acsomega.8b02502 |
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