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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...

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Autores principales: Perez-Rodriguez, Paula, Maqueira Gonzalez, Carlos, Bennani, Yasmina, Rietveld, Luuk C., Zeman, Miro, Smets, Arno H. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
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.
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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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