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Variation of graphene/titanium dioxide concentration as electrocatalyst for an oxygen reduction reaction in constructed wetland-microbial fuel cells.
- Source :
-
Electrochemistry Communications . Dec2023, Vol. 157, pN.PAG-N.PAG. 1p. - Publication Year :
- 2023
-
Abstract
- [Display omitted] • ORR reaction mechanism in CW-MFCs occurred through the 4-electrons pathway. • Maximum power density was produced with 1 mg/cm2 of G/TiO 2 in CW-MFCs. • Photosynthetic compounds were used as substrate for the anodic biofilm in CW-MFCs. Constructed wetlands-microbial fuel cells (CW-MFC) are an innovative technology used for simultaneous bioelectricity generation and wastewater treatment. This is possible due to the installation of macrophytes in an electrode configuration, in which electroactive microorganisms use organic substrates as biofuel. One way to improve the electrochemical performance of CW-MFCs is through the impregnation of cathodic electrocatalysts. Therefore, in this study the bioelectricity production capacity of CW-MFCs was evaluated from the oxygen reduction reaction (ORR). For this study, the concentrations 0 (CW-MFC1), 0.5 (CW-MFC2), and 1 mg/cm2 (CW-MFC3) of graphene/titanium dioxide (G/TiO 2) as electrocatalyst on the cathodes were evaluated. Using the Koutecky-Levich analysis, it was determined that the ORR transfer mechanism arises via a 4-electron pathway. The electrokinetic parameters of Tafel slope, charge transfer coefficient, and exchange current density determined the efficiency of the ORR, registering 92 mV/dec, 0.93 (α), and 2.30 x10-3 mA/cm2, respectively for CW-MFC3. The highest electrochemical performance was obtained at a concentration of 1 mg/cm2 (CW-MFC3) of G/TiO 2 , generating 144 mW/m2 of power density, 157 Ω of internal resistance, −150 mV of anodic potential, and 383 mV of cathodic potential. The surface modification carried out on the cathodes resulted in a catalytic increase in the ORR. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 13882481
- Volume :
- 157
- Database :
- Academic Search Index
- Journal :
- Electrochemistry Communications
- Publication Type :
- Academic Journal
- Accession number :
- 174036816
- Full Text :
- https://doi.org/10.1016/j.elecom.2023.107618