• Energy Research

3D printing of a living bioanode holds the potential for the rapid and efficient production of bioelectrochemistry systems. However, the ink (such as sodium alginate, SA) that formed the matrix of the 3D-printed bioanode may hinder extracellular electron transfer (EET) between the microorganism and conductive materials. Here, we proposed a biomimetic design of a 3D-printed Shewanella bioanode, wherein riboflavin (RF) was modified on carbon black (CB) to serve as a redox substance for microbial EET. By introducing the medicated EET pathways, the 3D-printed bioanode obtained a maximum power density of 252 ± 12 mW/m2, which was 1.7 and 60.5 times higher than those of SA-CB (92 ± 10 mW/m2) and a bare carbon cloth anode (3.8 ± 0.4 mW/m2). Adding RF reduced the charge-transfer resistance of a 3D-printed bioanode by 75% (189.5 ± 18.7 vs 47.3 ± 7.8 Ω), indicating a significant acceleration in the EET efficiency within the bioanode. This work provided a fundamental and instrumental concept for constructing a 3D-printed bioanode.

Abstract Highly-efficient solar steam generator holds promise in seawater desalination and wastewater treatment with low energy consumption. The efficiency of generator highly depends on several factors including the kind of the absorber layer, the structure and the thickness of the generators. In this study, a model for calculating the optimal thickness was established based on the water transfer rate and thermal conduction loss. An optimal thickness of generator was determined by the calculation and experiment, taking carbonized wood based solar steam generator (CWSG) as an example. CWSG with optimal thickness about 22 mm performed a highest evaporation rate of 6.89 kg m−2 h−1, corresponding to efficiency of 87.7% under 5 sun. CWSG also served for seawater desalination and dye removal, which exhibited a stable performance even after 20 cycles. The results indicate that maximizing the efficiency of solar steam generator by thermal calculation could provide a new choice to design highly efficient solar steam generator for seawater desalination and dye removal.

Scaling up of microbial fuel cells (MFCs) without losing power density requires a thorough understanding of the effect of hydraulic pressure on MFC performance. In this work, the performance of an activated carbon air-cathode MFC was evaluated under different hydraulic pressures. The MFC under 100 mmH2O hydraulic pressure produced a maximum power density of 1260 ± 24 mW m(-2), while the power density decreased by 24.4% and 44.7% as the hydraulic pressure increased to 500 mmH2O and 2000 mmH2O, respectively. Notably, the performance of both the anode and the cathode had decreased under high hydraulic pressures. Electrochemical impedance spectroscopy tests of the cathode indicated that both charge transfer resistance and diffusion transfer resistance increased with the increase in hydraulic pressure. Denaturing gradient gel electrophoresis of PCR-amplified partial 16S rRNA genes demonstrated that the similarity among anodic biofilm communities under different hydraulic pressures was ≥ 90%, and the communities of all MFCs were dominated by Geobacter sp. These results suggested that the reduction in power output of the single chamber air-cathode MFC under high hydraulic pressures can be attributed to water flooding of the cathode and suppression the metabolism of anodic exoelectrogenic bacteria.

As the core component of microbial fuel cells, the conductivity and biocompatibility of anode are hard to achieve simultaneously but significantly influence the power generation performance and the overall cost of microbial fuel cells. Stainless steel felt has a low price and high conductivity, making it a potential anode for the large-scale application of microbial fuel cells. However, its poor biocompatibility limits its application. This study provides a one-step binder-free modification method of a stainless steel felt anode with reduced graphene oxide to retain the high conductivity while greatly improving biocompatibility. The maximum power density achieved by reduced graphene oxide modified stainless steel felt was 951.89 mW/m2, 5.49 and 1.91 times higher than the unmodified stainless steel felt anode and reduced graphene oxide coated stainless steel felt by Nafion, respectively. The robust reduced graphene oxide modification markedly improved the biocompatibility by forming a uniform biofilm and utilizing the high conductivity of reduced graphene oxide to enhance the charge transfer rate. It led to 92.7 and 37.9% decreases in charge transfer resistance of reduced graphene oxide modified stainless steel felt compared to the unmodified one and the anode modified with reduced graphene oxide by Nafion, respectively. The excellent performance and green synthesis method of the anode validated its potential as a high-performance anode material for scaled-up microbial fuel cell applications.

Plasma advanced oxidation process (PAOP) has great ability to break recalcitrant pollutants into small molecular compounds but suffers from poor performance and low energy efficiency for mineralizing dyeing pollutants. Combining advanced oxidation process with biodegradation process is an effective strategy to improve mineralization performance and reduce cost. In this study, a combined process using PAOP as pre-treatment followed by microbial fuel cell (MFC) treatment was investigated to mineralize methylene blue (MB). The PAOP could degrade MB by 97.7%, but only mineralize MB by 23.2% under the discharge power of 35 W for 10 min. Besides, BOD5/COD ratio of MB solution raised from 0.04 to 0.38 while inhibition on E. coli growth decreased from 85.5% to 28.3%. The following MFC process increased MB mineralization percentage to 63.0% with a maximum output power density of 519 mW m-2. The combined process achieved a mineralization energy consumption of 0.143 KWh gTOC-1 which was only 41.8% of that of PAOP. FT-IR, UV-vis and pH variation demonstrated that PAOP could break the aromatic and heterocyclic structures in MB molecule to form organic acids. Possible degradation pathways of MB were accordingly proposed based on LC-MS, GC-MS, and density functional theory calculation.

Single-chamber microbial fuel cells (MFCs) can efficiently treat wastewater containing nitrate, probably because the interaction between exoelectrogens and denitrifying bacteria may enhance the denitrification activity of MFCs. In this study, the denitrification of nitrate with a wide range of concentrations was investigated by using single-chamber air cathode MFCs. The maximum average denitrification rate of the MFCs inoculated and operated under closed-circuit conditions (Group N-CC) was up to 12.2 ± 0.6 kg NO3--N m-3 d-1 at a high nitrate concentration of 2000 mg NO3-N L-1, which was 74.3% higher than that of the MFCs inoculated and operated under open-circuit conditions and which was significantly higher than those of other MFC systems and many traditional bioreactors. The high denitrification activity of the MFCs of Group N-CC was attributed to the significant reduction of nitrite accumulation through the possible bioelectrochemical nitrite reduction by exoelectrogens that were only enriched at the anodes of the MFCs of Group N-CC. In addition, the MFCs of Group N-CC showed good stability (over 3.5 years) and low apparent activation energy (34.0 kJ mol-1) of the denitrification, indicating the good coexistence of exoelectrogens (Geobacter) and denitrifying bacteria (Thauera) with high performance on denitrification during the long-term operation.

Poor anode performance is one of the main bottlenecks in the development of microbial fuel cells (MFCs) for practical applications. Multilayered Ti3C2 MXene (m-MXene) is an alternative anode modification material because of its high specific surface area and electrical conductivity. However, the multilayered structure, negatively charged surface, and electropositivity of m-MXene could limit its modification effects. In this work, we used a solution-phase flocculation method (ammonium ion method) to restack and aggregate MXene nanosheets as an anode modification material (n-MXene). The n-MXene-modified anode had a higher specific surface area, surface hydrophilicity and surface electropositivity than the m-MXene-modified anode. The n-MXene-modified anode obtained a maximum current density of 2.1 A m-2, which was 31.2% and 61.5% higher than that of the m-MXene-modified anode (1.6 A m-2) and bare carbon fiber cloth anode (1.3 A m-2). This improved anode performance was attributed to both the decrease in the charge transfer resistance and diffusion resistance, which were related to the increased quantity of biomass and microbial nanowire (or pili)-shaped filaments on the electrode surface. This work provides a simple and cost-effective approach to prepare MXene nanosheets for the modification of MFC anodes.

Microbial fuel cells (MFCs) provide a cost-effective method for treating swine wastewater treatment and simultaneously producing electricity, yet they need to be combined with other wastewater treatment processes to improve the effluent water quality. In this paper, we constructed single-chamber air-cathode MFCs with a compact configuration for nitrogen and COD removal and high electricity production and combined them with a low-cost flocculation process to discharge higher quality wastewater. We show that MFCs could remove ammonia at a rate of 269.2 ± 0.5 g m-3 d-1 (99.1± 0.1% ammonia removal efficiency) with a maximum power density of 37.5 W m-3 and 21.6% of coulombic efficiency at a 40:60 ratio of raw swine wastewater to denitrification effluent of swine wastewater. Up to 82.5 ± 0.5% COD could be removed with MFCs, from 2735 ± 15 mg L-1 to 480 ± 15 mg L-1, and flocculation further reduced levels to 90 ± 1 mg L-1 for a 96.6 ± 0.2% overall COD removal efficiency of the combination technology. Cost analysis of the combined MFC and flocculation process showed a net economic benefit of $ 0.026 m-3. In summary, this novel combination wastewater treatment method provides an effective way to treat swine wastewater to low pollutant levels in the effluent at low cost (a net gain).