Simultaneous Cr(VI) reduction and electricity generation in Plant-Sediment Microbial Fuel Cells (P-SMFCs): Synthesis of non-bonding Co3O4 nanowires onto cathodes.

Journal: Environmental Pollution (Barking, Essex : 1987)
Published:
Abstract

Development of low-cost cathode materials for Plant-Sediment Microbial Fuel Cells (P-SMFCs) has gained increasing interest, due to improved performance levels in terms of power and pollutant removal. A novel low cost three-dimensional cathode prepared by simple three-step strategy with growth of Co3O4 in-situ biofilm was successfully prepared. Different cathodes were applied to the six parallel P-SMFCs systems (reactor: R1-R6), such as graphite felt (GF), Pt/C, GF@Co3O4 (non-bonding Co3O4 nanowires on GF), GF@SG-Co3O4 (using argon as shielding gas (SG)). Its performances (R1, R2: control groups) were evaluated by electricity generation and Cr(VI) reduction at initial cadmium concentrations (4.97, 10.29 and 21.16 mg L-1). A significant Cr(VI) removal efficiency of 99.76%, maximum power density of 75.12 ± 2.90 mW m-2 and Cr(VI) adsorption capacity of 1.67 mg g-1 were obtained at initial Cr(VI) concentration of 21.16 mg L-1 with non-bonding GF@Co3O4 and bio-GF@SG-Co3O4 as cathodes. This indicated that these two materials were better than others (GF, Pt/C and GF@Co3O4) as cathodes. Characterization analysis including scanning electron microscope (SEM), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), Polarization curve, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) showed that high current generation Cr(VI) removal mainly attributed to transportation of plants, adsorption of bio-cathode, formation of a relatively high concentration region and abundant oxygen vacancies of GF@SG-Co3O4. The results show that P-SMFCs with GF@SG-Co3O4 cathode may be a potentially novel approach for remediating Cr(VI) contaminated waster or soil.

Authors
Ce Cheng, Yongyou Hu, Sicheng Shao, Jiayuan Yu, Weijia Zhou, Jianhua Cheng, Yuancai Chen, Shengnan Chen, Junfeng Chen, Lihua Zhang