ELECTRICITY GENERATION CHARACTERISTICS OF AN ANAEROBIC FLUIDIZED BED MICROBIAL FUEL CELL

Anaerobic fluidized bed microbial fuel cell (AFBMFC) was developed to investigate the effect of fluidization behaviors on the electrogenesis capacity. Waste water and active carbon were used as liquid and solid phase, respectively. The fuel cell was started up successfully using anaerobic activated sludge as inoculums. The power density is increased with increasing circular liquid velocity up to 450 mW·m-2. High COD remove rate reached 93% after five days operation. Meanwhile, the effects of cathode area on the electrogenesis capacity of AFB MFC were also investigated

Supporting nickel on vanadium nitride for comparable hydrogen evolution performance to platinum in alkaline solution

The hydrogen evolution reaction (HER) is an effective means to producing hydrogen from electrolytic water splitting. However the best-performing catalysts use expensive Pt-group metals. Cheaper non-precious metal alternatives have shown low activity as their mechanism of H-2 formation (Volmer-Heyrovsky) leads to high overpotentials. Here, we report an outstanding HER catalyst (Ni/VN) highly dispersed nickel supported on vanadium nitride that matches the turnover frequency of the platinum on carbon (Pt/C) benchmark material. It is more durable than Pt/C in alkaline solution. Ni/VN follows the low-overpotential (Volmer-Tafel) mechanism of H-2 formation, with a 43 mV overpotential at a current density of 10 mA cm(-2). This value is even below that of Pt/C (57 mV). The support of VN enhances the dispersion of nickel, weakens the surface oxidation, decreases the hydrogen binding energy, and therefore significantly improves the HER catalysis. This result removes one of the major barriers for scalability of electrolytic water-splitting by demonstrating that nitride-based materials can match and even surpass the efficiency and durability of precious metal catalysts

Surface Functionalized Sensors for Humidity-Independent Gas Detection

Semiconducting metal oxides (SMOXs) are used widely for gas sensors. However, the effect of ambient humidity on the baseline and sensitivity of the chemiresistors is still a largely unsolved problem, reducing sensor accuracy and causing complications for sensor calibrations. Presented here is a general strategy to overcome water-sensitivity issues by coating SMOXs with a hydrophobic polymer separated by a metal-organic framework (MOF) layer that preserves the SMOX surface and serves a gas-selective function. Sensor devices using these nanoparticles display near-constant responses even when humidity is varied across a wide range [0-90 % relative humidity (RH)]. Furthermore, the sensor delivers notable performance below 20 % RH whereas other water-resistance strategies typically fail. Selectivity enhancement and humidity-independent sensitivity are concomitantly achieved using this approach. The reported tandem coating strategy is expected to be relevant for a wide range of SMOXs, leading to a new generation of gas sensors with excellent humidity-resistant performance

In Situ TEM Study of the Degradation of PbSe Nanocrystals in Air

PbSe nanocrystals have attracted widespread attention due to a variety of potential applications. However, the practical utility of these nanocrystals has been hindered by their poor air stability, which induces undesired changes in the optical and electronic properties. An understanding of the degradation of PbSe nanocrystals when they are exposed to air is critical for improving the stability and enhancing their applications. Here, we use in situ transmission electron microscopy (TEM) with an environmental cell connected to air to study PbSe nanocrystal degradation triggered by air exposure. We have also conducted a series of complementary studies, including in situ environmental TEM study of PbSe nanocrystals exposed to pure oxygen and PbSe nanocrystals in H2O using a liquid cell, and ex situ experiments, such as O2 plasma treatment and thermal heating of PbSe nanocrystals under different air exposure. Our in situ observations reveal that when PbSe nanocrystals are exposed to air (or oxygen) under electron beam irradiation, they experience a series of changes, including shape evolution of individual nanocrystals with the cuboid intermediates, coalescence between nanocrystals, and formation of PbSe thin films through drastic solid-state fusion. Further studies show that the PbSe thin films transform into an amorphous Pb rich phase or eventually pure Pb, which suggest that Se reacts with oxygen and can be evaporated under electron beam illumination. These various in situ and ex situ experimental results indicate that PbSe nanocrystal degradation in air is initiated by the dissociation and removal of ligands from the PbSe nanocrystal surface

Selective and Continuous Electrosynthesis of Hydrogen Peroxide on Nitrogen-doped Carbon Supported Nickel

Hydrogen peroxide is a widely used industrial oxidant, the large-scale production of which continues to be done by an indirect process. Direct electrosynthesis of hydrogen peroxide from aerial oxygen and water is a sustainable alternative, but this remains challenging because hydrogen peroxide is highly reactive and robust catalysts are vital. Here, we report direct and continuous electrosynthesis of hydrogen peroxide under alkaline conditions using a nitrogen-doped-carbon-supported nickel catalyst. Both experiment and theoretical calculations confirm that the existence of nickel particles suppresses the further reduction of hydrogen peroxide on Ni-N-C matrix. In air-saturated 0.1 M potassium hydroxide, the energy-efficient non-precious metal electrocatalyst exhibits a consistent Faraday efficiency over 95% at a steady rate of hydrogen peroxide production (15.1 mmol min−1 gcat−1) for 100 h. This sustainable, efficient, and safe process is an important step toward continuous production of hydrogen peroxide

Water-resistant perovskite nanodots enable robust two-photon lasing in aqueous environment

Abstract: Owing to their large absorption cross-sections and high photoluminescence quantum yields, lead halide perovskite quantum dots (PQDs) are regarded as a promising candidate for various optoelectronics applications. However, easy degradation of PQDs in water and in a humid environment is a critical hindrance for applications. Here we develop a Pb-S bonding approach to synthesize water-resistant perovskite@silica nanodots keeping their emission in water for over six weeks. A two-photon whispering-gallery mode laser device made of these ultra-stable nanodots retain 80% of its initial emission quantum yield when immersed in water for 13 h, and a two-photon random laser based on the perovskite@silica nanodots powder could still operate after the nanodots were dispersed in water for up to 15 days. Our synthetic approach opens up an entirely new avenue for utilizing PQDs in aqueous environment, which will significantly broaden their applications not only in optoelectronics but also in bioimaging and biosensing

Water-resistant perovskite nanodots enable robust two-photon lasing in aqueous environment

Abstract: Owing to their large absorption cross-sections and high photoluminescence quantum yields, lead halide perovskite quantum dots (PQDs) are regarded as a promising candidate for various optoelectronics applications. However, easy degradation of PQDs in water and in a humid environment is a critical hindrance for applications. Here we develop a Pb-S bonding approach to synthesize water-resistant perovskite@silica nanodots keeping their emission in water for over six weeks. A two-photon whispering-gallery mode laser device made of these ultra-stable nanodots retain 80% of its initial emission quantum yield when immersed in water for 13 h, and a two-photon random laser based on the perovskite@silica nanodots powder could still operate after the nanodots were dispersed in water for up to 15 days. Our synthetic approach opens up an entirely new avenue for utilizing PQDs in aqueous environment, which will significantly broaden their applications not only in optoelectronics but also in bioimaging and biosensing

Concave Ni(OH)₂ Nanocube Synthesis and Its Application in High-Performance Hybrid Capacitors

The controlled synthesis of hollow structure transition metal compounds has long been a very interesting and significant research topic in the energy storage and conversion fields. Herein, an ultrasound-assisted chemical etching strategy is proposed for fabricating concave Ni(OH)2 nanocubes. The morphology and composition evolution of the concave Ni(OH)2 nanocubes suggest a possible formation mechanism. The as-synthesized Ni(OH)2 nanostructures used as supercapacitor electrode materials exhibit high specific capacitance (1624 F g−1 at 2 A g−1) and excellent cycling stability (77% retention after 4000 cycles) due to their large specific surface area and open pathway. In addition, the corresponding hybrid capacitor (Ni(OH)2//graphene) demonstrates high energy density (42.9 Wh kg−1 at a power density of 800 W kg−1) and long cycle life (78% retention after 4000 cycles at 5 A g−1). This work offers a simple and economic approach for obtaining concave Ni(OH)2 nanocubes for energy storage and conversion

An alginic acid assisted rheological phase synthesis of carbon coated Li3V2(PO4)(3) with high-rate performance

A nanoscaled Li3V2(PO4)(3)/C(LVP/C) composite is successfully synthesized via a modified rheological phase method. Alginic acid is applied as a new carbon source and ethylene glycol is used as the dispersant, and both of which play multifaceted roles during the synthetic route. A series of intensive investigations shows that the LVP/C composite possesses a three-dimensional carbon network and a loose structure, which provide discontinuous electronic and ionic pathways. The electrochemical performance of the LVP/C cathode is revealed to be impressive in terms of capacity, high-rate capability and long-life cycleability. Between 3.0 and 4.3 V, it delivers a discharge capacity of 132.3 mAh g(-1) at 0.5 degrees C rate, approaching the theoretical value, and can cycle at a rate as high as 40 C without obvious capacity fading. Most distinctively, when discharged at 90 C ultrahigh rate (charged at 5 C rate), the largest capacity of 61.4 mAh g(-1), can still be available, after 600 cycles the capacity retention can still maintain 76%. When operated within 3.0-4.8 V, it cannot only discharge the initial capacity of 184.1 mAh g(-1) at 0.1 degrees C, but also exhibit a stable cycling performance at 20 C for 400 cycles. These excellent performances can be fundamentally attributed to the high electronic/ionic conductivities which are related closely to the modified rheological phase preparation route and the promising new carbon source. (C) 2014 Elsevier B.V. All rights reserved