Heyang Yuan

Oxygen reduction reaction catalysts used in microbial fuel cells for energy-efficient wastewater treatment: a review

Microbial fuel cells (MFCs) as an energy-efficient wastewater treatment technology have attracted increasing interest in the past decade. Cathode catalysts for the oxygen reduction reaction (ORR) present a major challenge for the practical applications of MFCs. An ideal cathode catalyst should be scalable, durable, and cost-effective. A variety of non-precious metal catalysts have been developed for MFC applications, including carbon-based catalysts, metal-based catalysts, metal–carbon hybrids, metal–nitrogen–carbon complexes, and biocatalysts. This paper comprehensively reviews these materials with emphasis on their synthesis, performance, durability, and cost. It is anticipated that insights offered in this review could facilitate the development of ORR catalysts for MFC applications towards energy-efficient wastewater treatment.

Integrating membrane filtration into bioelectrochemical systems as next generation energy-efficient wastewater treatment technologies for water reclamation: A review.

Bioelectrochemical systems (BES) represent an energy-efficient approach for wastewater treatment, but the effluent still requires further treatment for direct discharge or reuse. Integrating membrane filtration in BES can achieve high-quality effluents with additional benefits. Three types of filtration membranes, dynamic membrane, ultrafiltration membrane and forward osmosis membrane that are grouped based on pore size, have been studied for integration in BES. The integration can be accomplished either in an internal or an external configuration. In an internal configuration, membranes can act as a separator between the electrodes, or be immersed in the anode/cathode chamber as a filtration component. The external configuration allows BES and membrane module to be operated independently. Given much progress and interest in the integration of membrane filtration into BES, this paper has reviewed the past studies, described various integration methods, discussed the advantages and limitations of each integration, and presented challenges for future development.

Porous Carbon Nanosheets Codoped with Nitrogen and Sulfur for Oxygen Reduction Reaction in Microbial Fuel Cells

In this work, a simple synthesis strategy has been developed for the preparation of nitrogen- and sulfur-codoped porous carbon nanosheets (N/S-CNS) as a cathode catalyst for microbial fuel cells (MFCs). The as-prepared N/S-CNS showed favorable features for electrochemical energy conversion such as high surface area (1004 m(2) g(-1)), defect structure, and abundant exposure of active sites that arose primarily from porous nanosheet morphology. Benefiting from the unique nanostructure, the resulting nanosheets exhibited effective electrocatalytic activity toward oxygen reduction reaction (ORR). The onset potential of the N/S-CNS in linear-sweep voltammetry was approximately -0.05 V vs Ag/AgCl in neutral phosphate buffer saline. Electrochemical impedance spectroscopy showed that the ohmic and charge-transfer resistance of the codoped catalyst were 1.5 and 14.8 Ω, respectively, both of which were lower than that of platinum/carbon (Pt/C). Furthermore, the electron-transfer number of the N/S-CNS was calculated to be ∼3.5, suggesting that ORR on the catalyst proceeds predominantly through the favorable four-electron pathway. The MFC with N/S-CNS as a cathode catalyst generated current density (6.6 A m(-2)) comparable to that with Pt/C (7.3 A m(-2)). The high durability and low price indicate that N/S-CNS can be a competitive catalyst for applications of MFCs.

Effect of acclimation and nutrient supply on 5-tolyltriazole biodegradation with activated sludge communities

The corrosion inhibitor 5-tolyltriazole (5-TTri) can have a detrimental impact on aquatic systems thus implying an acute need to reduce the effluent concentrations of 5-TTri. In this study, 5-TTri biodegradation was enhanced through acclimation and nutrient supply. Activated sludge communities (ASC) were setup in nine subsequent ASC generations. While generation two showed a lag phase of five days without biodegradation, generations four to nine utilized 5-TTri right after inoculation, with biodegradation rates from 3.3 to 5.2 mg L(-1)d(-1). Additionally, centrifuged AS supernatant was used to simulate the nutrient conditions in wastewater. This sludge supernatant (SS) significantly enhanced biodegradation, resulting in removal rates ranging from 3.2 to 5.0 mg L(-1)d(-1) without acclimation while the control groups without SS observed lower rates of ⩽ 2.2 mg L(-1)d(-1).

Effects of electron acceptors on removal of antibiotic resistant Escherichia coli, resistance genes and class 1 integrons under anaerobic conditions.

Anaerobic biotechnologies can effectively remove antibiotic resistant bacteria (ARB) and antibiotic resistance genes (ARGs), but there is a need to better understand the mechanisms. Here we employ bioelectrochemical systems (BES) as a platform to investigate the fate of a native tetracycline and sulfonamide-resistant Escherichia coli strain and its ARGs. The E. coli strain carrying intI1, sulI and tet(E) was isolated from domestic wastewater and dosed into a tubular BES. The BES was first operated as a microbial fuel cell (MFC), with aeration in the cathode, which resulted in enhanced removal of E. coli and ARGs by ~2 log (i.e., order of magnitude) when switched from high current to open circuit operation mode. The BES was then operated as a microbial electrolysis cell (MEC) to exclude the effects of oxygen diffusion, and the removal of E. coli and ARGs during the open circuit configuration was again 1-2 log higher than that at high current mode. Significant correlations of E. coli vs. current (R(2)=0.73) and ARGs vs. E. coli (R(2) ranged from 0.54 to 0.87), and the fact that the BES substrate contained no electron acceptors, implied that the persistence of the E. coli and its ARGs was determined by the availability of indigenous electron acceptors in the BES, i.e., the anode electrode or the electron shuttles generated by the exoelectrogens. Subsequent experiments with pure-culture tetracycline and sulfonamide-resistant E. coli being incubated in a two-chamber MEC and serum bottles demonstrated that the E. coli could survive by respiring anode electrode and/or electron shuttles released by exoelectrogens, and ARGs persisted with their host E. coli.

Unravelling and Reconstructing the Nexus of Salinity, Electricity and Microbial Ecology for Bioelectrochemical Desalination

Microbial desalination cells (MDCs) are an emerging concept for simultaneous water/wastewater treatment and energy recovery. The key to developing MDCs is to understand fundamental problems, such as the effects of salinity on system performance and the role of microbial community and functional dynamics. Herein, a tubular MDC was operated under a wide range of salt concentrations (0.05-4 M), and the salinity effects were comprehensively examined. The MDC generated higher current with higher salt concentrations in the desalination chamber. When fed with 4 M NaCl, the MDC achieve a current density of 300 A m-3 (anode volume), which was one of the highest among bioelectrochemical system studies. Community analysis and electrochemical measurements suggested that electrochemically active bacteria Pseudomonas and Acinetobacter transferred electrons extracellularly via electron shuttles, and the consequent ion migration led to high anode salinities and conductivity that favored their dominance. Predictive functional dynamics and Bayesian networks implied that the taxa putatively not capable of extracellular electron transfer (e.g., Bacteroidales and Clostridiales) might indirectly contribute to bioelectrochemical desalination. By integrating the Bayesian network with logistic regression, current production was successfully predicted from taxonomic data. This study has demonstrated uncompromised system performance under high salinity and thus has highlighted the potential of MDCs as an energy-efficient technology to address water-energy challenges. The statistical modeling approach developed in this study represents a significant step toward understating microbial communities and predicting system performance in engineered biological systems.

Platinum Group Metal-free Catalysts for Hydrogen Evolution Reaction in Microbial Electrolysis Cells

Hydrogen gas is a green energy carrier with great environmental benefits. Microbial electrolysis cells (MECs) can convert low-grade organic matter to hydrogen gas with low energy consumption and have gained a growing interest in the past decade. Cathode catalysts for the hydrogen evolution reaction (HER) present a major challenge for the development and future applications of MECs. An ideal cathode catalyst should be catalytically active, simple to synthesize, durable in a complex environment, and cost-effective. A variety of noble-metal free catalysts have been developed and investigated for HER in MECs, including Nickel and its alloys, MoS2 , carbon-based catalysts and biocatalysts. MECs in turn can serve as a research platform to study the durability of the HER catalysts. This personal account has reviewed, analyzed, and discussed those catalysts with an emphasis on synthesis and modification, system performance and potential for practical applications. It is expected to provide insights into the development of HER catalysts towards MEC applications.