Electrochemical Oxidation of Organic Pollutants Powered by a Silicon-Based Solar Cell

Journal Article (2018)
Author(s)

P. Perez Rodriguez (TU Delft - Photovoltaic Materials and Devices)

Carlos Maqueira Gonzalez (Student TU Delft)

Yasmina Bennani (TU Delft - Sanitary Engineering)

Luuk C. Rietveld (TU Delft - Sanitary Engineering)

M. Zeman (TU Delft - Electrical Sustainable Energy)

Arno Hendrikus Marie Smets (TU Delft - Photovoltaic Materials and Devices)

Research Group
Photovoltaic Materials and Devices
Copyright
© 2018 P. Perez Rodriguez, Carlos Maqueira Gonzalez, Y. Doekhi-Bennani, L.C. Rietveld, M. Zeman, A.H.M. Smets
DOI related publication
https://doi.org/10.1021/acsomega.8b02502
More Info
expand_more
Publication Year
2018
Language
English
Copyright
© 2018 P. Perez Rodriguez, Carlos Maqueira Gonzalez, Y. Doekhi-Bennani, L.C. Rietveld, M. Zeman, A.H.M. Smets
Research Group
Photovoltaic Materials and Devices
Issue number
10
Volume number
3
Pages (from-to)
14392-14398
Reuse Rights

Other than for strictly personal use, it is not permitted to download, forward or distribute the text or part of it, without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license such as Creative Commons.

Abstract

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.