2D Coordination Network of Trioxotriangulene with Multiple Redox Abilities and Its Rechargeable Battery Performance.

A three-fold symmetric trioxotriangulene derivative with three pyridyl groups as coordinating sites was designed and synthesized. In a cyclic voltammetry measurement, the trioxotriangulene skeleton exhibited a multi-stage redox ability from neutral radical to radical tetra-anion species. In the zinc complex of monoanion species, three pyridyl groups coordinated to the zinc ion to build up a two-dimensional coordination network with a cavity larger than 12 Å in diameter. This complex was utilized as a cathode active material of a lithium ion battery, and it exhibited a capacity of ca. 60 mAh g-1 per the weight of the active material with a stable cycling performance up to 1000 cycles. This work shows that the coordination network formed by the trioxotriangulene-based ligand was effective in the improvement of cycle performance of the organic rechargeable battery.

Characterisation of the biofouling community on a floating wave energy device.

Wave energy devices are novel structures in the marine environment and, as such, provide a unique habitat for biofouling organisms. In this study, destructive scrape samples and photoquadrats were used to characterise the temperate epibenthic community present on prototypes of the Pelamis wave energy converter. The biofouling observed was extensive and diverse with 115 taxa recorded including four non-native species. Vertical zonation was identified on the sides of the device, with an algae-dominated shallow subtidal area and a deeper area characterised by a high proportion of suspension-feeding invertebrates. Differences in species composition and biomass were also observed between devices, along the length of the device and between sampling dates. This research provides an insight into the variation of biofouling assemblages on a wave energy device as well as the potential technical and ecological implications associated with biofouling on marine renewable energy structures.

Biofouling community composition across a range of environmental conditions and geographical locations suitable for floating marine renewable energy generation.

Knowledge of biofouling typical of marine structures is essential for engineers to define appropriate loading criteria in addition to informing other stakeholders about the ecological implications of creating novel artificial environments. There is a lack of information regarding biofouling community composition (including weight and density characteristics) on floating structures associated with future marine renewable energy generation technologies. A network of navigation buoys were identified across a range of geographical areas, environmental conditions (tidal flow speed, temperature and salinity), and deployment durations suitable for future developments. Despite the perceived importance of environmental and temporal factors, geographical location explained the greatest proportion of the observed variation in community composition, emphasising the importance of considering geography when assessing the impact of biofouling on device functioning and associated ecology. The principal taxa associated with variation in biofouling community composition were mussels (Mytilus edulis), which were also important when determining loading criteria.

Bacterial nanometric amorphous Fe-based oxide: a potential lithium-ion battery anode material.

Amorphous Fe(3+)-based oxide nanoparticles produced by Leptothrix ochracea, aquatic bacteria living worldwide, show a potential as an Fe(3+)/Fe(0) conversion anode material for lithium-ion batteries. The presence of minor components, Si and P, in the original nanoparticles leads to a specific electrode architecture with Fe-based electrochemical centers embedded in a Si, P-based amorphous matrix.

Nanoparticle decorated anodes for enhanced current generation in microbial electrochemical cells.

The development of highly efficient anode materials is critical for enhancing the current output of microbial electrochemical cells. In this study, Au and Pd nanoparticle decorated graphite anodes were developed and evaluated in a newly designed multi-anode microbial electrolysis cell (MEC). The anodes decorated with Au nanoparticles produced current densities up to 20-fold higher than plain graphite anodes by Shewanella oneidensis MR-1, while those of Pd-decorated anodes with similar morphologies produced 50-150% higher than the control. Significant positive linear regression was obtained between the current density and the particle size (average Feret's diameter and average area), while the circularity of the particles showed negative correlation with current densities. On the contrary, no significant correlation was evident between the current density and the particle density based on area fraction and particle counts. These results demonstrated that nano-decoration can greatly enhance the performance of microbial anodes, while the chemical composition, size and shape of the nanoparticles determined the extent of the enhancement.

Fabrication of stainless steel mesh gas diffusion electrode for power generation in microbial fuel cell.

This study reports the fabrication of a new membrane electrode assembly by using stainless steel mesh (SSM) as raw material and its effectiveness as gas diffusion electrode (GDE) for electrochemical oxygen reduction in microbial fuel cell (MFC). Based on feeding glucose (0.5 g L(-1)) substrate to a single-chambered MFC, power generation using SSM-based GDE was increased with the decrease of polytetrafluoroethylene (PTFE) content applied during fabrication, reaching the optimum power density of 951.6 mW m(-2) at 20% PTFE. Repeatable cell voltage of 0.51 V (external resistance of 400 Ω) and maximum power density of 951.6 mW m(-2) produced for the MFC with SSM-based GDE are comparable to that of 0.52 V and 972.6 mW m(-2), respectively obtained for the MFC containing typical carbon cloth (CC)-made GDE. Besides, Coulombic efficiency (CE) is found higher for GDE (SSM or CC) with membrane assembly than without, which results preliminarily from the mitigation of Coulombic loss being associated with oxygen diffusion and substrate crossover. This study demonstrates that with its good electrical conductivity and much lower cost, the SSM-made GDE suggests a promising alternative as efficient and more economically viable material to conventional typical carbon for power production from biomass in MFC.

Electricity generation of single-chamber microbial fuel cells at low temperatures.

Practical applications of microbial fuel cells (MFCs) for wastewater treatment will require operation of these systems over a wide range of wastewater temperatures. MFCs at room or higher temperatures (20-35°C) are relatively well studied compared those at lower temperatures. MFC performance was examined here over a temperature range of 4-30°C in terms of startup time needed for reproducible power cycles, and performance. MFCs initially operated at 15°C or higher all attained a reproducible cycles of power generation, but the startup time to reach stable operation increased from 50 h at 30°C to 210 h at 15°C. At temperatures below 15°C, MFCs did not produce appreciable power even after one month of operation. If an MFC was first started up at temperature of 30°C, however, reproducible cycles of power generation could then be achieved at even the two lowest temperatures of 4°C and 10°C. Power production increased linearly with temperature at a rate of 33±4 mW °C(-1), from 425±2 mW m(-2) at 4°C to 1260±10 mW m(-2) at 30°C. Coulombic efficiency decreased by 45% over this same temperature range, or from CE=31% at 4°C to CE=17% at 30°C. These results demonstrate that MFCs can effectively be operated over a wide range of temperatures, but our findings have important implications for the startup of larger scale reactors where low wastewater temperatures could delay or prevent adequate startup of the system.

Solar-driven microbial photoelectrochemical cells with a nanowire photocathode.

We report a self-biased, solar-driven microbial photoelectrochemical cell (solar MPC) that can produce sustainable energy through coupling the microbial catalysis of biodegradable organic matter with solar energy conversion. The solar MPC consists of a p-type cuprous oxide nanowire-arrayed photocathode and an electricigen (Shewanella oneidensis MR-1)-colonizing anode, which can harvest solar energy and bioenergy, respectively. The photocathode and bioanode are interfaced by matching the redox potentials of bacterial cells and the electronic bands of semiconductor nanowires. We successfully demonstrated substantial current generation of 200 µA from the MPC device based on the synergistic effect of the bioanode (projected area of 20 cm2) and photocathode (projected area of 4 cm2) at zero bias under white light illumination of 20 mW/cm2. We identified the transition of rate-limiting step from the photocathode to the bioanode with increasing light intensities. The solar MPC showed self-sustained operation for more than 50 h in batch-fed mode under continuous light illumination. The ability to tune the synergistic effect between microbial cells and semiconductor nanowire systems could open up new opportunities for microbial/nanoelectronic hybrid devices with unique applications in energy conversion, environmental protection, and biomedical research.

Factors affecting the performance of microbial fuel cells for sulfur pollutants removal.

A microbial fuel cell (MFC) has been developed for removal of sulfur-based pollutants and can be used for simultaneous wastewater treatment and electricity generation. This fuel cell uses an activated carbon cloth+carbon fibre veil composite anode, air-breathing dual cathodes and the sulfate-reducing species Desulfovibrio desulfuricans. 1.16gdm(-3) sulfite and 0.97gdm(-3) thiosulfate were removed from the wastewater at 22 degrees C, representing sulfite and thiosulfate removal conversions of 91% and 86%, respectively. The anode potential was controlled by the concentration of sulfide in the compartment. The performance of the cathode assembly was affected by the concentration of protons in the cation-exchanging ionomer with which the electrocatalyst is co-bound at the three-phase (air, catalyst and support) boundary.