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High electrochemical reversibility is required for the application of high-energy- density lithium (Li) metal batteries; however, inactive Li formation and SEI (solid electrolyte interface)-instability- induced electrolyte consumption cause low Coulombic efficiency (CE). The prior interfacial chemical designs in terms of alloying kinetics have been used to enhance the CE of Li metal anode; however, the role of its redox chemistry at heterointerfaces remains a mystery. Herein, the relationship between heterointerfacial redox chemistry and electrochemical transformation reversibility is investigated. It is demonstrated that the lower redox potential at heterointerface contributes to higher CE, and this enhancement in CE is primarily due to the regulation of redox chemistry to Li deposition behavior rather than the formation of SEI films. Low oxidation potential facilitates the formation of the surface with the highly electrochemical binding feature after Li stripping, and low reduction potential can maintain binding ability well during subsequent Li plating, both of which homogenize Li deposition and thus optimize CE. In particular, Mg hetero-metal with ultra-low redox potential enables Li metal anode with significantly improved CE (99.6%) and stable cycle life for 700 cycles at 3.0 mA cm-2. This work provides insight into the heterointerfacial design principle of next-generation negative electrodes for highly reversible metal batteries. [ABSTRACT FROM AUTHOR]

Development of new power anode material with both high capacity and high-rate capability for lithium-ion batteries is highly desired. In this paper, a novel soft carbon anode for rechargeable lithium-ion batteries was developed using coal-based mesophase pitch. The structures of the materials were characterized by X-ray diffraction (XRD), Raman, N2 adsorption–desorption, Scanning Electron Microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The electrochemical characteristics of the new anode material were investigated. It was found that the soft carbon anode from coal-based mesophase pitch carbonized under vacuum conditions can deliver higher energy density and higher rate capability compared to soft carbon carbonized under a nitrogen atmosphere. The enhanced electrochemical properties are attributed to smaller nanocrystallites, more porosity, defects and carbon species of the resulting anode material. [ABSTRACT FROM AUTHOR]

In this paper, an efficient laser surface ablation strategy for producing binder‐free carbon‐coated nanocotton CoO‐Co integrated anode is reported. The fabrication process introduces in‐situ growing nanocotton‐like CoO on the surface of Co foil via ablating with a nanosecond laser. After that, coated with dopamine as carbon source, the CoO‐Co composite foil is heated in Argon atmosphere to form a CoO@C‐Co foil as an anode of LIB. The laser surface ablation exhibits high fabrication speed (~10 minutes) and significantly reduces the processing time. The obtained binder‐free CoO@C‐Co integrated anode shows a unique cotton‐like villous structure with large specific surface area and an active material/current collector integrated architecture, which provides a stabilized rapid electronic conduction path. When tested as an anode for LIBs, the CoO@C‐Co integrated anode possesses superior performance: First discharge capacity of 1301.5 mAh g−1 is achieved at a current density of 0.1 A g−1. Also at a high current density of 1.5 A g−1, the second discharge capacity of 791.7 mAh g−1 is achieved. After 800 cycles, reversible capacities of 799.8 mAh g−1 can still be achieved with an average coulombic efficiency of nearly 100%. In addition, this strategy is suitable for the production of other carbon coated transition metal oxides integrated anodes, such as NiO@C‐Ni, Fe2O3/Fe3O4@C‐Fe, and CuO/Cu2O@C‐Cu integrated anodes. [ABSTRACT FROM AUTHOR]

A novel anode was developed by coating reduced graphene oxide (rGO) and manganese oxide (MnO 2 ) composite on the carbon felt (CF) surface. With a large surface area and excellent electrical conductivity, this binder-free anode was found to effectively enhance the enrichment and growth of electrochemically active bacteria and facilitate the extracellular electron transfer from the bacteria to the anode. A microbial fuel cell (MFC) equipped with the rGO/MnO 2 /CF anode delivered a maximum power density of 2065 mW m −2 , 154% higher than that with a bare CF anode. The internal resistance of the MFC with this novel anode was 79 Ω, 66% lower than the regular one's (234 Ω). Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) analyses affirmed that the rGO/MnO 2 composite significantly increased the anodic reaction rates and facilitated the electron transfer from the bacteria to the anode. The findings from this study suggest that the rGO/MnO 2 /CF anode, fabricated via a simple dip-coating and electro-deposition process, could be a promising anode material for high-performance MFC applications. [ABSTRACT FROM AUTHOR]

The application of microbial fuel cell (MFC)-based toxicity sensors to real-world water monitoring is partly impeded by the limited sensitivity. To address this limitation, this study optimized the flow configurations and the control modes. Results revealed that the sensitivity increased by ∼15–41 times with the applying of a flow-through anode, compared to those with a flow-by anode. The sensors operated in the controlled anode potential (CP) mode delivered better sensitivity than those operated in the constant external resistance (ER) mode over a broad range of anode potentials from −0.41 V to +0.1 V. Electrodeposition of Cu(II) was found to bias the toxicity measurement at low anode potentials. The optimal anode potential was approximately −0.15 V, at which the sensor achieved an unbiased measurement of toxicity and the highest sensitivity. This value was greater than those required for electrodeposition while smaller than those for power overshoot. [ABSTRACT FROM AUTHOR]

In this study, a microbial fuel cell (MFC) with granular activated carbon packed anode (GAC-MFC) is developed and compared with a MFC with granular graphite packed anode (GG-MFC), to evaluate the adsorptive effect of the granular activated carbon anode on MFC’s performance. The current output of GAC-MFC (11.1 mA, 18.1 mA and 21.6 mA) is much higher than that of GG-MFC (4.87 mA, 12.5 mA and 17.9 mA) at low substrate COD concentrations (∼50, ∼100 and ∼200 mg/L) when a low external resistance (20 Ω) and high circulation flow rate (20 mL/min) are applied. The half-saturation constant ( K s ) of GAC-MFC is about half as much as that of GG-MFC, suggesting that GAC-MFC has more affinity for anode substrate and deliver better kinetic performance than GG-MFC. Internal resistance distribution shows that mass diffusion resistance of GAC-MFC is at least 50% lower than that of GG-MFC when the substrate COD is ∼50 mg/L, indicating that the adsorptive effect of granular activated carbon packed anode helps to effectively facilitate mass transfer at low COD concentrations. Otherwise, the substrates adsorbed on GAC surface also serve to buffer the impact of COD concentration plummeting in bulk solution. [ABSTRACT FROM AUTHOR]

Abstract: The performance and cost of electrodes are the most important aspects in the design of microbial fuel cell (MFC) reactors. A wide range of electrode materials and configurations have been tested and developed in recent years to improve MFC performance and lower material cost. As well, anodic electrode surface modifications have been widely used to improve bacterial adhesion and electron transfer from bacteria to the electrode surface. In this paper, a review of recent advances in electrode material and a configuration of both the anode and cathode in MFCs are provided. The advantages and drawbacks of these electrodes, in terms of their conductivity, surface properties, biocompatibility, and cost are analyzed, and the modification methods for the anodic electrode are summarized. Finally, to achieve improvements and the commercial use of MFCs, the challenges and prospects of future electrode development are briefly discussed. [Copyright &y& Elsevier]

Silicon and lithium metal are promising anode materials toward high energy densities Li (ion) batteries. However, silicon and lithium generally have dramatic volume change during lithiation/delithiation cycles. With the repeated expansion/shrinkage, the internal stress fluctuations and electrode pulverization can cause high interfacial resistance and the failure of electrodes. Herein, a novel strategy is proposed to engineer the current collector by using a polydopamine-assisted electroless metallization process to prepare an elastic deformable current collector covered with a high electrical conductivity Cu nano-network surface. The deformable current collectors can not only stabilize the interfacial stress as an artificial-spring, but also improve the electrical conductivity of anodes without any binders and conductive agents. Featured with outstanding deformable structure, the well-designed current collector achieves a low surface resistance of 0.06 Ω/sq and excellent electrochemical performance when applied in the commercial Si anode batteries, solid-state batteries, and ionic liquid electrolyte batteries at room-temperature. • A highly elastic and low resistance deformable current collector. • The deformable current collector achieves a low surface resistance of 0.06 Ω/sq. • Stabilized the interface stress of anodes as an artificial-spring. • Improve the electrical conductivity of anodes without binders and conductive agents. • Achieved >400 stable cycling performance when applied in a commercial Si anode. [ABSTRACT FROM AUTHOR]

Conventional wastewater purification technologies consume large amounts of energy, while the abundant chemical energy and nutrient resources contained in sewage are wasted in such treatment processes. A microbial nutrient recovery cell (MNRC) has been developed to take advantage of the energy contained in wastewater, in order to simultaneously purify wastewater and recover nutrient ions. When wastewater was circulated between the anode and cathode chambers of the MNRC, the organics (COD) were removed by bacteria while ammonium and phosphate (NH4+-N and PO43−-P) were recovered by the electrical field that was produced using in situ energy in the wastewater without additional energy input. The removal efficiencies from wastewater were >82% for COD, >96% for NH4+-N, and >64% for PO43−-P in all the operational cycles. Simultaneously, the concentrations of NH4+ and PO43− in the recovery chamber increased to more than 1.5 and 2.2 times, respectively, compared with the initial concentrations in wastewater. The MNRC provides proof-of-concept as a sustainable, self-driven approach to efficient wastewater purification and nutrient recovery in a comprehensive bioelectrochemical system. [ABSTRACT FROM AUTHOR]

Although transition metal oxides anodes have attracted lots of attention, there are still many problems to be resolved. Complicated fabrication process, high cost and poor electrochemical performances are the most important ones, together hindering transition metal oxides anodes for practical use. Herein, we provide a new approach to fabricate a binder-free and conductive-additive-free TiO 2 /WO 3 -W integrative anode material through the nanosecond laser ablation and dip-coating technology, which simplifies the entire anode preparation process with no need for a conventional tape-casting procedure. Using this method, great time cost, machine cost and labor cost related to mixing and tape-casting process can be saved on the basis of good electrochemical performances. The prepared TiO 2 /WO 3 -W integrative anode realizes a first Coulombic efficiency of 75.6% and attains to a stable capacity within the first five cycles. It can still maintain a capacity of 600 mAh g −1 in the range of 0.01–3 V vs. Li + /Li at a current rate of 0.2 C after 500 cycles. This work offers a new way to achieve a fast fabrication of the integrative anode for lithium ion battery, which is universal for other transition metals (such as Fe, Cu, Ni, Co, Mo, W etc.). [ABSTRACT FROM AUTHOR]

Abstract: Four materials, carbon felt cube (CFC), granular graphite (GG), granular activated carbon (GAC) and granular semicoke (GS) were tested as packed anodic materials to seek a potentially practical material for microbial fuel cells (MFCs). The microbial community and its correlation with the electricity generation performance of MFCs were explored. The maximum power density was found in GAC, followed by CFC, GG and GS. In GAC and CFC packed MFCs, Geobacter was the dominating genus, while Azospira was the most populous group in GG. Results further indicated that GAC was the most favorable for Geobacter adherence and growth, and the maximum power densities had positive correlation with the total biomass and the relative abundance of Geobacter, but without apparent correlation with the microbial diversity. Due to the low content of Geobacter in GS, power generated in this system may be attributed to other microorganisms such as Synergistes, Bacteroidetes and Castellaniella. [Copyright &y& Elsevier]

Abstract: The combined use of brush anodes and glass fiber (GF1) separators, and plastic mesh supporters were used here for the first time to create a scalable microbial fuel cell architecture. Separators prevented short circuiting of closely-spaced electrodes, and cathode supporters were used to avoid water gaps between the separator and cathode that can reduce power production. The maximum power density with a separator and supporter and a single cathode was 75±1W/m3. Removing the separator decreased power by 8%. Adding a second cathode increased power to 154±1W/m3. Current was increased by connecting two MFCs connected in parallel. These results show that brush anodes, combined with a glass fiber separator and a plastic mesh supporter, produce a useful MFC architecture that is inherently scalable due to good insulation between the electrodes and a compact architecture. [ABSTRACT FROM AUTHOR]

As serious water ecological pollution caused by toxicant leakage occurs frequently, early-warning for toxicity presented in water environment attracts increasing attentions as it saves time to retain water safety and human health. Electrochemically active biofilm (EAB) sensor is a promising device for in situ real-time water toxicity early-warning. To improve the sensitivity of EAB sensor particularly for low-concentration toxicity warning, this study employed titanium mesh (TiM) as the anode to construct an EAB sensor. Compared to traditional EAB sensor with carbon felt (CF) anode, the sensitivity of the TiM sensor was increased up to 37.4 times. The effects of mesh size (TiM50, TiM100, TiM150) and operation mode (flow-by and flow-through) on the sensitivity of TiM sensors were further investigated. Results showed the sensor with TiM100 anode had the highest inhibition rate (IR) in flow-by mode, attributed to low charge transfer resistance (R ct) and fast mass transfer. Flow-through operation could further enhance TiM100 sensor's sensitivity from flow-by operation and succeeded to signal as low as 0.0025% formaldehyde, the lowest so far tested in EAB sensor with sensing anode. Multiple toxicity shocks on flow-through TiM100 sensor revealed its good recoverability towards all tested formaldehyde concentration from 0.01% to 0.0025%, during which electrochemical activity degradation and biomass accumulation partially impaired the repeatability. This work highlights the great improvement of EAB sensors by utilizing titanium mesh as EAB carrier and provides a reference for the practical application of metallic materials for EAB sensors. [ABSTRACT FROM AUTHOR]

As a viable wastewater treatment and energy recovery technology, microbial fuel cell (MFC) requires more research with regard to the simultaneous achievement of high-quality effluent and high power generation. In this study, a novel flow-through carbon-based composite anode configuration is proposed, which combines the carbon cloth of two-dimensional anode with wooden granular activated carbon of three-dimensional anode. The proposed configuration enhances the performance of power production and chemical oxygen demand degradation by promoting the mass transfer, reducing internal resistance and increasing bioburden. Microbial fuel cell with the composite anode exhibited the highest maximum power density (1300 ± 50 mW m−2) and the highest chemical oxygen demand removal rate constant (0.155 ± 0.007 h−1) compared with the microbial fuel cell using the carbon cloth anode (1136 ± 46 mW m−2 and 0.072 ± 0.008 h−1) or the wooden granular activated carbon anode (1045 ± 32 mW m−2 and 0.129 ± 0.009 h−1). Meanwhile, at a lower chemical oxygen demand concentration (about 48 mg L−1), the microbial fuel cell with the composite anode maintained a current density of 2.4 A m−2, which is 18% higher than the wooden granular activated carbon anode (2.04 A m−2) and 400% higher than the carbon cloth anode (0.48 A m−2). The cyclic voltammetry and electrochemical impedance spectroscopy tests confirmed that the composite anodes displayed better electrochemical performance. Improving the flow rate and reducing the external resistance could effectively enhance the power production and chemical oxygen demand removal performance of microbial fuel cells, while the computational fluid dynamics simulation intuitively demonstrated the positive effect of the composite anode on chemical oxygen demand degradation. These results suggest that the flow-through composite anode provides a feasible strategy to simultaneously enhance the power generation and improve the effluent quality. Image 1 • A composite anode was constructed by optimizing 2D and 3D carbon anode materials.. • Flow-through composite anode MFC had higher power generation and COD removal rate. • Flow-through composite anode MFC maintained high power generation at low COD. • Reducing external resistance and improving flow rate enhanced the MFC performance. • Flow-through composite anode MFC was proved better COD removal in CFD simulation. [ABSTRACT FROM AUTHOR]