Search Results (57)

Microbial fuel cells (MFCs) are a sustainable approach to wastewater treatment and energy recovery. However, their practical utility is often limited by sluggish cathode kinetics. For this technology, developing cost-effective biocatalysts that do not compromise effectiveness is a primary challenge. In this study, we utilized anthocyanin molecularly functionalized Escherichia coli (Cya-WT) to promote the formation of electroactive biofilms and regulate the intrinsic catalytic activity of single cells, thereby enhancing extracellular electron transfer. MFCs incorporating Cya-WT-loaded carbon cloth (CC) biocathodes were configured to simultaneously evaluate power generation and glucose degradation activity. The results indicated that Cya-WT exhibited significantly improved oxygen reduction reaction (ORR) activity, achieving a reduction peak current of 3.61 mA cm⁻², compared to 2.02 mA cm⁻² for wild-type E. coli (WT). The assembled MFC offers a peak power density of 268 ± 13.4 μW cm⁻² and decomposes 17.1 ± 1.15 mM of glucose in 150 h, maintaining a consistent voltage output for 800 h. These results demonstrate that anthocyanin functionalization significantly enhances the electrocatalytic performance and metabolic capabilities of E. coli. This novel catalyst design method offers a new strategy for low-cost, renewable MFC cathode catalysts and shows good promise in MFC biopower generation through the assembly of carbon-based biocathodes. Full article

The increasing generation of industrial wastewater necessitates sustainable treatment strategies combined with resource recovery. Brewery wastewater, characterized by high organic content and low toxicity, represents a promising substrate for bio-electrochemical systems such as microbial fuel cells (MFCs). This study evaluates the feasibility of electricity generation from wastewater originating from a small-scale research brewery using a dual-chamber glass MFC equipped with a carbon felt anode and a foamed-glass separator. The system was operated in a repeated fed-batch mode over six consecutive 100 h cycles, with fresh wastewater supplied when the cell voltage decreased to 60% of its maximum value. Stable electrochemical performance was observed, with an average cell voltage of 304 mV and a maximum power density of 24 mW·m⁻². A consistent decrease in COD concentration of approximately 8.66% per 100 h operational cycle was recorded, along with a 4.93% reduction in NO₃⁻ concentration, while NH₄⁺ levels remained largely unchanged. The results indicate that brewery wastewater from small-scale facilities can support sustained bio-electrochemical activity under simplified, non-optimized conditions. Although power output and contaminant concentration changes were limited, the study provides a laboratory-scale study and highlights the need for further optimization of reactor configuration and operational parameters. Full article

Electroactive biofilms (EABs) are essential for the performance of bioelectrochemical systems (BESs), but their formation in Geobacter, critically on conductive pili and exopolysaccharides, limits application under conditions where these components are deficient. Herein, we investigated the restorative effects of exogenous flavin mononucleotide (FMN) on EAB formation and extracellular electron transfer (EET) in two defective mutants of Geobacter sulfurreducens: the pili-deficient PCAΔ1496 and exopolysaccharides-deficient PCAΔ1501. Results show that FMN significantly promoted biofilm thickness in PCAΔ1496 (250%) and PCAΔ1501 (33%), while boosting maximum current outputs by 175-fold and 317.7%, respectively. Spectroscopic and electrochemical analyses revealed that FMN incorporates into biofilms, binds to outer membrane c-type cytochromes (c-Cyts), and enhances electron exchange capacity. Differential pulse voltammetry further confirmed that FMN did not exist independently in the biofilm but bound to outer membrane c-Cyts as a cofactor. Collectively, exogenous FMN plays dual roles (electron shuttle and cytochrome-bound cofactor) in defective Geobacter EABs, effectively restoring biofilm formation and enhancing EET efficiency. This study expands the understanding of the formation mechanism of Geobacter EABs and provides a novel strategy for optimizing BES performance. Full article

Electrical stimulation is increasingly explored as a strategy to accelerate the development of electroactive biofilms in microbial fuel cells (MFCs), yet its integration with photosynthetic MFCs (pMFCs) remains insufficiently understood. This study evaluated how short-term anodic stimulation (0.5–5 V, 4 days) affects biofilm formation and COD removal, and how subsequent operation with photosynthetic cathodes—Chlorella sp., Arthrospira platensis and Tetraselmis subcordiformis—modulates anodic microbial communities and functional potential. Stimulation at 1 V yielded the best activation effect, resulting in the highest voltage output, power density and fastest COD removal kinetics, whereas 5 V inhibited biofilm development. During pMFC operation, Chlorella produced the highest voltage (0.393 ± 0.064 V), current density (0.14 ± 0.02 mA·cm⁻²) and Coulombic efficiency (~19%). Arthrospira showed moderate performance, while Tetraselmis generated no current despite efficient COD removal. 16S rRNA sequencing revealed distinct cathode-driven community shifts: Chlorella enriched facultative electroactive taxa, Arthrospira promoted sulfur-cycling bacteria and Actinobacteria, and Tetraselmis induced strong methanogenic dominance. Functional prediction and qPCR confirmed these trends, with Chlorella showing increased pilA abundance and Tetraselmis displaying enriched methanogenic pathways. Overall, the combined use of optimal anodic stimulation and photosynthetic cathodes demonstrates that cathodic microalgae strongly influence anodic redox ecology and energy recovery, with Chlorella-based pMFCs offering the highest electrochemical performance. Full article

Microbial electrolysis cells (MECs) are bioreactors that utilize electroactive microorganisms to catalyze the oxidation of organic substrates in wastewater, generating electron flow for hydrogen production. Despite the concept, a persistent performance gap exists where metabolically active anodic biofilms frequently fail to achieve expected current densities by the flow of electrons to produce hydrogen. This review examines the multiple causes that lead to the disconnect between robust biofilm development, electron transfer, and hydrogen production. Factors affecting biofilm generation (formation, substrate selection, thickness, conductivity, and heterogeneity) are discussed. Moreover, factors affecting electron transfer (electrode configuration, mass transfer constraints, key electroactive species, and metabolic pathways) are discussed. Also, substrate diffusion limitations, proton accumulation causing inhibitory pH gradients in stratified biofilms, elevated internal resistance, electron diversion to competing processes like hydrogenotrophic methanogenesis consuming H₂, and detrimental biofilm aging, impacting hydrogen production, are studied. The critical roles of electrode materials, reactor configuration, and biofilm electroactivity are analyzed, emphasizing advanced electrochemical (CV, EIS, LSV), imaging (CLSM, SEM, AFM), and omics (metagenomics, transcriptomics, proteomics) techniques essential for diagnosing bottlenecks. Strategies to enhance extracellular electron transfer (EET) (advanced nanomaterials, redox mediators, conductive polymers, bioaugmentation, and pulsed electrical operation) are evaluated for bridging this performance gap and improving energy recovery. The review presents an integrated framework connecting biofilm electroactivity, EET kinetics, and hydrogen evolution efficiency. It highlights that conventional biofilm metrics may not reflect actual electron flow. Combining electrochemical, microelectrode, and omics insights allows precise evaluation of EET efficiency and supports sustainable MEC optimization for enhanced hydrogen generation. Full article

Microbial fuel cell (MFC) is a novel and environmentally friendly technology for wastewater treatment and pollutant resource utilization. Although advances have been made in various aspects including electrode materials and synthetic biology approaches, the overall performance of MFC still requires improvement, with mass transfer efficiency and structural stability of biofilms emerging as key bottlenecks constraining their practical applications. This study investigated the regulation of substrate type and electrode potential during bioanode culture to optimize biofilm structure and enhance MFC performance. Results demonstrated that bioanodes cultured with glucose at −0.3 V formed vertically ordered biofilms that exhibited significant advantages in mass transfer characteristics, electrocatalytic activity, and structural stability. Under these culture conditions, enriched fermentative microorganisms facilitated the construction of porous biofilm scaffolds, while the electric field generated by the −0.3 V potential further induced vertical orientation and ordered arrangement of the biofilm. The superior mass transfer characteristics enabled the inner, middle, and outer layers of the biofilm to maintain high microbial activity (>50%), thereby maximizing the catalytic activity of electroactive microorganisms in each layer and enhancing biofilm structural stability. This study proposes a bioanode culture strategy centered on biofilm structural optimization, providing new theoretical foundations and technical pathways for achieving long-term stable and efficient MFC operation. Full article

This work investigated the use of microbial fuel cells (MFCs) for the degradation of polyethylene terephthalate (PET) and the simultaneous generation of electricity. The study implemented two separate single-chamber MFCs, one with a co-culture of Ideonella sakaiensis and Geobacter sulfurreducens (I.S-G.S) and the other with Ideonella sakaiensis and activated sludge (I.S-AS). The effectiveness of microplastic (MP) degradation was assessed based on the electroactivity of the anodic biofilm, the reduction in particle size, and the decrease in PET mass. Both systems achieved a significant reduction in MP size and mass, with the I.S-AS system notably surpassing the I.S-G.S in terms of efficiency and electricity generation. The I.S-AS system achieved a 30% mass reduction and 80% size reduction, along with a peak voltage of 222 mV. The study concludes that MFCs, particularly with the activated sludge co-culture, offer a viable and more environmentally friendly alternative for MP degradation and energy recovery. These findings suggest a promising direction for improving waste management practices and advancing the capabilities of bio-electrochemical systems in addressing plastic pollution. Further research is recommended to optimize the operational conditions and to test a broader range of MP sizes for enhanced degradation efficacy. Full article

This study discussed the influence of acetate and sodium chloride concentration on monitoring 2,4-dichlorophenol(2,4-DCP) by electroactive bacteria. The performance of the reactor was represented by power density, and the electrochemical activity was represented by redox capacity. At the same time, micro-electrodes were used to detect the redox potential between biofilms, and the changes in extracellular polymers and microbial community structure under different conditions were also explored. With acetate concentration of 1 g/L and sodium chloride concentration of 0.0125 g/L, the electroactive microorganisms were more sensitive to toxic substances and responded fast. The biofilm also evenly covered on the surface of the carrier, which aided in the diffusion of substances. Although the maximum power density monotonically increased with acetate concentration, high concentration of substrate may mask the inhibitory effect and affect the judgment of inhibitory results. The content of protein and polysaccharide increased monotonically with sodium chloride concentration. However, more polysaccharides would lead to high resistance to electron transfer. Compared to sodium chloride, the microbial content was more affected by acetate. The electroactive microorganisms had strong adaptability to salinity. In practical application, it is conducive to increase the sensitivity of MFCs to reasonably reduce the concentration of acetic acid and sodium chloride. Full article

Microbial Fuel Cell (MFC) is a novel bioelectrochemical system that catalyzes the oxidation of chemical energy in organic waste and converts it directly into electrical energy through the attachment and growth of electroactive microorganisms on the electrode surface. This technology realizes the synergistic effect of waste treatment and renewable energy production. A CF-NiO-PANI capacitor composite anode was prepared by loading polyaniline on a CF-NiO electrode to improve the capacitance of a CF electrode. The electrochemical characteristics of the composite anode were evaluated using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), and the electrode materials were analyzed comprehensively by scanning electron microscopy (SEM), energy diffusion spectrometer (EDS), and Fourier transform infrared spectroscopy (FTIR). MFC system based on CF-NiO-PANI composite anode showed excellent energy conversion efficiency in potato starch wastewater treatment, and its maximum power density increased to 0.4 W/m³, which was 300% higher than that of the traditional CF anode. In the standard charge–discharge test (C1000/D1000), the charge storage capacity of the composite anode reached 2607.06 C/m², which was higher than that of the CF anode (348.77 C/m²). Microbial community analysis revealed that the CF-NiO-PANI anode surface formed a highly efficient electroactive biofilm dominated by electrogenic bacteria (accounting for 47.01%), confirming its excellent electron transfer ability. The development of this innovative capacitance-catalytic dual-function anode material provides a new technical path for the synergistic optimization of wastewater treatment and energy recovery in MFC systems. Full article

Bio-nanocomposite films were prepared using chitosan, gelatin, and varying concentrations (0, 0.5, 1.0, 2.0, and 5.0 wt%) of titanium dioxide (TiO₂) nanoparticles in acetic acid via a casting method. The incorporation of TiO₂ nanoparticles into the bio-chitosan matrix enhanced ultraviolet (UV) absorption and improved the films’ physical, mechanical, and electrical properties. Additionally, the TiO₂-loaded films exhibited antimicrobial activity, contributing to the extended preservation of packaged products by inhibiting microbial growth. Notably, the bio-nanocomposite films containing 1.0 wt% TiO₂ exhibited an electroactive response, bending under relatively low electric field strength (250 V/mm), whereas the control film without TiO₂ required higher field strength (550 V/mm) to achieve bending. This indicates potential applications in electroactive actuators requiring precise movement control. Among the tested concentrations, films containing 0.5 wt% and 1.0 wt% TiO₂ (Formulas 7 and 8) demonstrated optimal performance. These films presented a visually appealing appearance with no tear marks, low bulk density (0.91 ± 0.04 and 0.85 ± 0.18 g/cm³), a satisfactory electromechanical response at 250 V/m (17.85 ± 2.58 and 61.48 ± 6.97), low shrinkage percentages (59.95 ± 3.59 and 54.17 ± 9.28), high dielectric constant (1.80 ± 0.07 and 8.10 ± 0.73), and superior UV absorption compared with pure bio-chitosan films, without and with gelatin (Formulas 1 and 6). Full article

Microbial fuel cells (MFCs) generate electricity through the microbial oxidation of organic waste. However, the inherent electrochemical performance of carbon felt (CF) electrodes is relatively poor and requires enhancement. In this study, nickel oxide (NiO) was successfully loaded onto CF to improve its electrode performance, thereby enhancing the electricity generation capacity of MFCs during the degradation of treated wastewater. Scanning electron microscopy (SEM), X-ray diffraction (XRD), and energy diffusion spectrometer (EDS) analyses confirmed the successful deposition of NiO on the CF surface. The modification enhanced both the conductivity and capacitance of the electrode and increased the number of microbial attachment sites on the carbon fiber filaments. The prepared CF–NiO electrode was employed as the anode in an MFC, and its electrochemical and energy storage performance were evaluated. The maximum power density of the MFC with the CF–NiO anode reached 0.22 W/m², compared to 0.08 W/m² for the unmodified CF anode. Under the C1000-D1000 condition, the charge storage capacity and total charge output of the CF–NiO anode were 1290.03 C/m² and 14,150.03 C/m², respectively, which are significantly higher than the 452.9 C/m² and 6742.67 C/m² observed for the CF anode. These results indicate notable improvements in both power generation and energy storage performance. High-throughput gene sequencing of the anodic biofilm following MFC acclimation revealed that the CF–NiO anode surface hosted a higher proportion of electroactive bacteria. This suggests that the NiO modification enhances the biodegradation of organic matter and improves electricity generation efficiency. Full article

This study explores the feasibility of producing biohydrogen from winery wastewater using a dual-chamber microbial electrolysis cell (MEC). A mixed microbial consortium pre-adapted to heavy-metal environments and enriched with Geobacter sulfurreducens was anaerobically cultivated from diverse waste streams. Over 5000 h of development, the MEC system was progressively adapted to winery wastewater, enabling long-term electrochemical stability and high organic matter degradation. Upon winery wastewater addition (5% v/v), the system achieved a sustained hydrogen production rate of (0.7 ± 0.3) L H₂ L⁻¹ d⁻¹, with an average current density of (60 ± 4) A m⁻³, and COD removal efficiency exceeding 55%, highlighting the system’s resilience despite the presence of inhibitory compounds. Coulombic efficiency and cathodic hydrogen recovery reached (75 ± 4)% and (87 ± 5)%, respectively. Electrochemical impedance spectroscopy provided mechanistic insight into charge transfer and biofilm development, correlating resistive parameters with biological adaptation. These findings demonstrate the potential of MECs to simultaneously treat agro-industrial wastewaters and recover energy in the form of hydrogen, supporting circular resource management strategies. Full article

A novel three-dimensional porous biocarbon electrode with exceptional biocompatibility was synthesized via a facile approach using pumpkin as the precursor. The obtained pumpkin-derived biocarbon features a highly porous architecture and serves as an efficient biocarbon electrode (denoted as PBE) in a microbial fuel cell (MFC). This PBE could form robust biofilms to facilitate the adhesion of electroactive bacteria. When used in the treatment of real wastewater, the assembled PBE-MFC achieves a remarkable power density of 231 mW/m², much higher than the control (carbon brush—MFC, 164 mW/m²) under the identical conditions. This result may be attributed to the upregulation of flagellar assembly pathways and bacterial secretion systems in the electroactive bacteria (e.g., Hydrogenophaga, Desulfovibrio, Thiobacillus, Rhodanobacter) at the anode of the PBE-MFC. The increased abundance of nitrifying bacteria (e.g., Hyphomicrobium, Sulfurimonas, Aequorivita) and organic matter-degrading bacteria (e.g., Lysobacter) in the PBE-MFC also contributed to its exceptional wastewater treatment efficiency. With its outstanding biocompatibility, cost-effectiveness, environmental sustainability, and ease of fabrication, the PBE-MFC displays great potential for application in the field of high-performance and economic wastewater treatment. Full article

To address the limitations of conventional antibacterial therapies, we developed an injectable, conductive polyurethane-based composite gel system for sustained root canal disinfection. This gel incorporates piezoelectric nanoparticles (n-BaTiO₃) and conductive segments (aniline trimer, AT) within a polyurethane matrix, which synergistically interact with a static antimicrobial agent (n-ZnO) to achieve dynamic, mechano-responsive antibacterial activity. Under cyclic compression (simulating mastication), the piezoelectric gels exhibited enhanced electroactivity via the mechano-electric coupling effect, generating 2-fold higher voltage and a 1.8–1.9× increase in current compared to non-piezoelectric controls. The dynamic electroactivity of the gels enabled superior long-term performance, achieving 92–97% biofilm eradication, significantly higher than the static n-ZnO-only gel (88%). XPS and UV-vis spectroscopy analyses confirmed mechano-electrochemically amplified reactive oxygen species (ROS) generation, which contributed to improved biofilm disruption. The ISO-compliant gel provides durable, load-responsive disinfection while maintaining good biocompatibility, offering a promising solution to prevent post-treatment reinfection. Full article

Microbial biosensors are bioanalytical devices that can measure the toxicity of pollutants or detect specific substances. This is the greatest advantage of microbial biosensors which use whole cells of microorganisms as powerful tools for measuring integral parameters of environmental pollution. This review explores the core principles of microbial biosensors including biofuel devices, emphasizing their capacity to evaluate biochemical oxygen demand (BOD), toxicity, heavy metals, surfactants, phenols, pesticides, inorganic pollutants, and microbiological contamination. However, practical challenges, such as sensitivity to environmental factors like pH, salinity, and the presence of competing substances, continue to hinder their broader application and long-term stability. The performance of these biosensors is closely tied to both technological advancement and the scientific understanding of biological systems, which influence data interpretation and device optimization. The review further examines cutting-edge developments, including the integration of electroactive biofilms with nanomaterials, molecular biology techniques, and artificial intelligence, all of which significantly enhance biosensor functionality and analytical accuracy. Commercial implementations and improvement strategies are also discussed, providing a comprehensive overview of the state-of-the-art in this field. Overall, this work consolidates recent progress and identifies both the potential and limitations of microbial biosensors, offering valuable insights into their future development for environmental monitoring. Full article