Search Results (6)

The increased demand for alternative sustainable energy sources has boosted research in the field of fuel cells (FC). Among these, microbial fuel cells (MFC), based on microbial anodes and different types of cathodes, have been the subject of renewed interest due to their ability to simultaneously perform wastewater treatment and bioelectricity generation. Several different MFCs have been proposed in this work using different conditions and configurations, namely cathode materials, membranes, external resistances, and microbial composition, among other factors. This work reports the design and optimization of MFC performance and evaluates a hydrogel (Ion Jelly^®) modified air-breathing cathode, with and without an immobilized laccase enzyme. This MFC configuration was also compared with other MFC configuration performances, namely abiotic and biocathodes, concerning wastewater treatment and electricity generation. Similar efficiencies in COD reduction, voltage (375 mV), PD (48 mW/m²), CD (130 mA/m²), and OCP (534 mV) were obtained. The results point out the important role of Ion Jelly^® in improving the MFC air-breathing cathode performance as it has the advantage that its electroconductivity properties can be designed before modifying the cathode electrodes. The biofilm on MFC anodic electrodes presented a lower microbial diversity than the wastewater treatment effluent used as inocula, and inclusively Geobacteracea was also identified due to the high microbial selective niches constituted by MFC systems. Full article

Biofuel cells (BFCs) with enzymatic electrocatalysts have attracted significant attention, especially as power sources for wearable and implantable devices; however, the applications of BFCs are limited owing to the limited O₂ supply. This can be addressed by using air-diffusion-type bilirubin oxidase (BOD) cathodes, and thus the further development of the hierarchical structure of porous electrodes with highly effective specific surface areas is critical. In this study, a porous layer of gold is deposited over magnesium-oxide-templated carbon (MgOC) to form BOD-based biocathodes for the oxygen reduction reaction (ORR). Porous gold structures are constructed via electrochemical deposition of gold via dynamic hydrogen bubble templating (DHBT). Hydrogen bubbles used as a template and controlled by the Coulomb number yield a porous gold structure during the electrochemical deposition process. The current density of the ORR catalyzed by BOD without a redox mediator on the gold-modified MgOC electrode was 1.3 times higher than that of the ORR on the MgOC electrode. Furthermore, the gold-deposited electrodes were modified with aromatic thiols containing negatively charged functional groups to improve the orientation of BOD on the electrode surface to facilitate efficient electron transfer at the heterogeneous surface, thereby achieving an ORR current of 12 mA cm⁻² at pH 5 and 25 °C. These results suggest that DHBT is an efficient method for the fabrication of nanostructured electrodes that promote direct electron transfer with oxidoreductase enzymes. Full article

Green hydrogen from photocatalytic water-splitting and photocatalytic lignocellulosic reforming is a significant proposition for renewable energy storage in global net-zero policies and strategies. Although photocatalytic water-splitting and photocatalytic lignocellulosic reforming have been investigated, their integration is novel. Furthermore, biosynthesis can store the evolved hydrogen and fix the atmospheric carbon dioxide in a biocathode chamber. The biocathode chamber is coupled to the combined photocatalytic water-splitting and lignocellulose oxidation in an anode chamber. This integrated system of anode and biocathode mimics a (bio)electrosynthesis system. A visible solar radiation-driven novel hybrid system comprising photocatalytic water-splitting, lignocellulose oxidation, and atmospheric CO₂ fixation is, thus, investigated. It must be noted that there is no technology for reducing atmospheric CO₂ concentration. Thus, our novel intensified technology enables renewable and sustainable hydrogen economy and direct CO₂ capture from air to confront climate change impact. The photocatalytic anode considered is CdS nanocomposites that give a low absorption onset (200 nm), high absorbance range (200–800 nm), and narrow bandgap (1.58–2.4 V). The biocathode considered is Ralstonia eutropha H16 interfaced with photocatalytic lignocellulosic oxidation and a water-splitting anode. The biocathode undergoes autotrophic metabolism fixing atmospheric CO₂ and hydrogen to poly(3-hydroxybutyrate) biosynthesis. As the hydrogen evolved can be readily stored, the electron–hole pair can be separated, increasing the hydrogen evolution efficiency. Although there are many experimental studies, this study for the first time sets the maximum theoretical efficiency target from mechanistic deductions of practical insights. Compared to physical/physicochemical absorption with solvent recovery to capture CO₂, the photosynthetic CO₂ capture efficiency is 51%. The maximum solar-to-hydrogen generation efficiency is 33%. Lignocelluloses participate in hydrogen evolution by (1–4)-glycosidic bond decomposition, releasing accessible sugar monomers or monosaccharides forming a Cd–O–R bond with the CdS/CdO_x nanocomposite surface used as a photocatalyst/semiconductor, leading to $\mathrm{C}{\mathrm{O}}_3^{2-}$ in oxidised carboxylic acid products. Lignocellulose dosing as an oxidising agent can increase the extent of water-splitting. The mechanistic analyses affirm the criticality of lignocellulose oxidation in photocatalytic hydrogen evolution. The critical conditions for success are increasing the alcohol neutralising agent’s strength, increasing the selective (ligno)cellulose dosing, broadening the hybrid nanostructure of the photocatalyst/semiconductor, enhancing the visible-light range absorbance, and increasing the solar energy utilisation efficiency. Full article

Algae-assisted microbial desalination cells represent a sustainable technology for low-energy fresh water production in which microalgae culture is integrated into the system to enhance oxygen reduction reaction in the cathode chamber. However, the water production (desalination rate) is low compared to conventional technologies (i.e., reverse osmosis and/or electrodialysis), as biocathodes provide low current generation to sustain the desalination process. In this sense, more research efforts on this topic are necessary to address this bottleneck. Thus, this study provides analysis, from the electrochemical point of view, on the cathode performance of an algae-assisted microbial desalination cell (MDC) using Chlorella vulgaris. Firstly, the system was run with a pure culture of Chlorella vulgaris suspension in the cathode under conditions of an abiotic anode to assess the cathodic behavior (i.e., cathode polarization curves in light-dark conditions and oxygen depletion). Secondly, Geobacter sulfurreducens was inoculated in the anode compartment of the MDC, and the desalination cycle was carried out. The results showed that microalgae could generate an average of 9–11.5 mg/L of dissolved oxygen during the light phase, providing enough dissolved oxygen to drive the migration of ions (i.e., desalination) in the MDC system. Moreover, during the dark phase, a residual concentration of oxygen (ca. 5.5–8 mg/L) was measured, indicating that oxygen was not wholly depleted under our experimental conditions. Interestingly, the oxygen concentration was restored (after complete depletion of dissolved oxygen by flushing with N₂) as soon as microalgae were exposed to the light phase again. After a 31 h desalination cycle, the cell generated a current density of 0.12 mA/cm² at an efficiency of 60.15%, 77.37% salt was removed at a nominal desalination rate of 0.63 L/m²/h, coulombic efficiency was 9%, and 0.11 kWh/m³ of electric power was generated. The microalgae-assisted biocathode has an advantage over the air diffusion and bubbling as it can self-sustain a steady and higher concentration of oxygen, cost-effectively regenerate or recover from loss and sustainably retain the system’s performance under naturally occurring conditions. Thus, our study provides insights into implementing the algae-assisted cathode for sustainable desalination using MDC technology and subsequent optimization. Full article

Bio-electrochemical systems (BES) are a flexible biotechnological platform that can be employed to treat several types of wastewaters and recover valuable products concomitantly. Sulfate-rich wastewaters usually lack an electron donor; for this reason, implementing BES to treat the sulfate and the possibility of recovering the elemental sulfur (S⁰) offers a solution to this kind of wastewater. This study proposes a novel BES configuration that combines bio-electrochemical sulfate reduction in a biocathode with a sulfide–air fuel cell (FC) to recover S⁰. The proposed system achieved high elemental sulfur production rates (up to 386 mg S⁰-S L⁻¹ d⁻¹) with 65% of the sulfate removed recovered as S⁰ and a 12% lower energy consumption per kg of S⁰ produced (16.50 ± 0.19 kWh kg⁻¹ S⁰-S) than a conventional electrochemical S⁰ recovery system. Full article

The electricity output from microbial fuel cell (MFC) with a microalgae assisted cathode is usually higher than that with an air cathode. The output of electricity from a photosynthetic microalgae MFC was positively correlated with the dissolved oxygen (DO) level in the microalgae assisted biocathode. However, DO is highly affected by the photosynthesis of microalgae, leading to the low stability in the electricity output that easily varies with the change in microalgae growth. In this study, to improve the electricity output stability of the MFC, a partially submerged carbon cloth cathode electrode was first investigated to use oxygen from both microalgae and air, with synthetic piggery wastewater used as the anolyte and anaerobically digested swine wastewater as the catholyte. When the DO levels dropped from 13.6–14.8 to 1.0–1.6 mg/L, the working voltages in the MFCs with partially submerged electrodes remained high (256–239 mV), whereas that for the conventional completely submerged electrodes dropped from 259 to 102 mV. The working voltages (average, 297 ± 26 mV) of the MFCs with the 50% submerged electrodes were significantly (p < 0.05) higher than with other partially or completely submerged electrodes. The associated maximum lipid production from wastewater was 250 ± 42 mg/L with lipid content of 41 ± 6% dry biomass. Although the partially submerged electrode had no significant effects on lipid production or nitrogen removal in wastewater, there was significant improvement in the stability of the electricity generated under variable conditions. Full article