Electrochemical Oxidation of Organic Pollutants Powered by a Silicon-Based Solar Cell
Author(s) -
Paula PerezRodriguez,
Carlos Maqueira Gonzalez,
Yasmina Bennani,
L.C. Rietveld,
Miro Zeman,
Arno H. M. Smets
Publication year - 2018
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.8b02502
Subject(s) - graphite , degradation (telecommunications) , electrochemistry , pollutant , materials science , decoupling (probability) , chemical engineering , methylene blue , silicon , electrochemical cell , solar cell , chemical oxygen demand , electrode , chemistry , photocatalysis , environmental engineering , environmental science , optoelectronics , electrical engineering , organic chemistry , catalysis , composite material , wastewater , control engineering , engineering
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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