Fluid pumping by liquid metal droplet utilizing ac electric field.

We report a unique phenomenon in which liquid metal droplets (LMDs) under a pure ac electric field pump fluid. Unlike the directional pumping that occurs upon reversing the electric field polarity under a dc signal, this phenomenon allows the direction of fluid motion to be switched by simply shifting the position of the LMD within the cylindrical chamber. The physical mechanism behind this phenomenon has been termed Marangoni flow, caused by nonlinear electrocapillary stress. Under the influence of a localized, asymmetric ac electric field, the polarizable surface of the position-offset LMD produces a net time-averaged interfacial tension gradient that scales with twice the field strength, and thus pumps fluid unidirectionally. However, the traditional linear RC circuit polarization model of the LMD/electrolyte interface fails to capture the correct pump-flow direction when the thickness of the LMD oxide skin is non-negligible compared to the Debye length. Therefore, we developed a physical description by treating the oxide layer as a distributed capacitance with variable thickness and connected with the electric double layer. The flow profile is visualized via microparticle imaging velocimetry, and excellent consistency is found with simulation results obtained from the proposed nonlinear model. Furthermore, we investigate the effects of relevant parameters on fluid pumping and discuss a special phenomenon that does not exist in dc control systems. To our knowledge, no previous work addresses LMDs in this manner and uses a zero-mean ac electric field to achieve stable, adjustable directional pumping of a low-conductivity solution.

Single-Atom Zinc and Anionic Framework as Janus Separator Coatings for Efficient Inhibition of Lithium Dendrites and Shuttle Effect.

The two key problems for the industrialization of Li-S batteries are the dendrite growth of lithium anode and the shuttle effect of lithium polysulfides (LiPSs). Herein, we report the Janus separator prepared by coating anionic Bio-MOF-100 and its derived single-atom zinc catalyst on each side of the Celgard separator. The anionic metal-organic framework (MOF) coating induces the uniform and rapid deposition of lithium ions, while its derived single-atom zinc catalyzes the rapid transformation of LiPSs, thus inhibiting the lithium dendrite and shuttle effect simultaneously. Consequently, compared with other reported Li-S batteries assembled with single-atomic catalysts as separator coatings, our SAZ-AF Janus separator showed stable cyclic performance (0.05% capacity decay rate at 2 C with 1000 cycles), outstanding performance in protecting lithium anode (steady cycle 2800 h at 10 mAh cm-2), and equally excellent cycling performance in Li-SeS2 or Li-Se batteries. Our work provides an effective separator coating design to inhibit shuttle effect and lithium dendrite.

Community composition and functional genes explain different ecological roles of heterotrophic bacteria attached to two bloom-forming cyanobacterial genera.

Eutrophication leads to frequent outbreaks of cyanobacterial blooms, however, the effect of heterotrophic bacteria attached to cyanobacterial cells is unclear. Field investigations were carried out to gain a deeper understanding of the community composition and functional role of heterotrophic bacteria attached to Dolichospermum and Microcystins cells. The significantly positive relationships between Dolichospermum density and total nitrogen (TN) and between Microcystins density and particle nitrogen (PN) indicated the strong nitrogen (N) demand of these two species. The lack of functional genes that mediate the nitrification process in bacteria attached to both Microcystins and Dolichospermum cells indicated that these two genera preferred ammonium (NH4+-N). Dolichospermum cells obtained more available N through N2 fixation, which was expressed by high nitrogenase gene abundance. Bacteria attached to Microcystins cells showed a higher activity of leucine aminopeptidase and a significantly higher abundance of functional genes that mediate dissimilatory nitrate reduction to ammonium (DNRA) than those attached to Dolichospermum cells. The significantly higher abundance of carbon degradation genes and ß-glucosidase activity of bacteria attached to Microcystins cells compared with those of bacteria attached to Dolichospermum cells suggested that abundant organic carbon was bound to Microcystins cells, which is a prerequisite for DNRA. In addition, Microcystins cells exhibited a great advantage in soluble reactive phosphorus (SRP) production through high levels of organic phosphorus (P) hydrolysis associated with high levels of phosphatase genes of attached bacteria. In conclusion, bacteria attached to Microcystins cells performed more important functions on NH4+-N and SRP production through ammonification and DNRA, as well as phosphatase hydrolysis respectively, compared to those attached to Dolichospermum. Thus, algal growth is the result of different variables such as nutrient concentration, their ratio and the microbial ability.

Saclike-silicon nanoparticles anchored in ZIF-8 derived spongy matrix as high-performance anode for lithium-ion batteries.

The carbon layer with good electrical conductivity and outstanding mechanical stability are essential in designing high-performance silicon/carbon (Si/C) anodes to replace the commercial graphite in lithium-ion batteries (LIBs). In terms of solving the two inherent defects of poor conductivity and big volume change of silicon, we fabricate a spongy carbon matrix derived from ZIF-8 to anchor saclike silicon synthesized by molten salt magnesiothermic reduction method. This spongy matrix can anchor saclike silicon to provide a stable reaction interface and support fast electronic transmission. At the same time, buffer space in saclike Si nanoparticles and spongy matrix can synergistically accommodate the volume change of Si to maintain the integrity of the electrode. The resulting composite with a high Si content of 77.58% exhibits good capacities of 1448 mAh g-1 at 2 A g-1 and 848 mAh g-1 at 4 A g-1 after 500 cycles. High initial coulombic efficiency of 84% at 0.2 A g-1 is also exhibited in the first three activation cycles. Therefore, this novel multifunctional N-doped spongy matrix can supply multifaceted benefits in accommodation of volumetric variation, enhancement of conductivity, and integrity of structure during cycling.

Cerium Based Metal-Organic Frameworks as an Efficient Separator Coating Catalyzing the Conversion of Polysulfides for High Performance Lithium-Sulfur Batteries.

In this work, we demonstrate cerium (Ce) based metal-organic frameworks (MOFs) combined with carbon nanotubes (CNTs) to form Ce-MOF/CNT composites as separator coating material in the Li-S battery system, which showed excellent electrochemical performance even under high sulfur loading and much better capacity retention. At the sulfur loading of 2.5 mg/cm2, initial specific capacity of 1021.8 mAh/g at 1C was achieved in the Li-S cell with the Ce-MOF-2/CNT coated separator, which was slowly reduced to 838.8 mAh/g after 800 cycles with a decay rate of only 0.022% and the Coulombic efficiency of nearly 100%. Even at a higher sulfur loading of 6 mg/cm2, the cell based on Ce-MOF-2/CNT separator coating still exhibited excellent performance with initial specific capacity of 993.5 mAh/g at 0.1 C. After 200 cycles, the specific capacity of 886.4 mAh/g was still retained. The excellent performance is ascribed to the efficient adsorption of the Ce-MOF-2 to Li2S6 species and its catalytic effect toward conversion of polysulfides, resulting in suppressed shuttle effect of polysulfides in the Li-S batteries.

An enzymatic mechanism for balancing the stoichiometry of nitrogen and phosphorus in a shallow Chinese eutrophic lake.

The over-enrichment of lake waters with nitrogen (N) and phosphorus (P) has become a serious environmental problem, but modes of change in stoichiometry and enzymatic regeneration along trophic gradients are largely unknown. Seasonal variations in the kinetics of extracellular aminopeptidase (LAP) and alkaline phosphatase (AP), together with the composition of phytoplankton and concentrations of N and P, were examined from Jun 2013 to September 2014 in a Chinese shallow lake in which two basins had contrasting trophic states. The turbid basin had a significantly higher concentration of chlorophyll a and lower ratios of N to P. In parallel, the turnover time of organic N mediated by LAP (LAPT) was significantly shorter, and its maximum velocity (Vmax) was significantly higher compared to those in the clear basin. Considering data from both basins, there were linear decreases in N/P and the ratios between dissolved inorganic N and total N with an increasing trophic state index, coupled with a significantly positive relationship between N/P and LAPT. Additionally, with decreasing TN/TP, the Michaelis constant (Km) of the AP increased linearly, reducing the efficiency of P regeneration. In contrast, the Km value of LAP decreased, and Vmax increased, which enhanced N mineralization by simultaneously increasing the reaction velocity and improving the affinity for substrate. Additionally, the Km value of LAP was significantly related to that of AP and the ammonium concentration. Thus, substrate affinity acted as a key factor modifying the pathways of enzymatic degradation of organic N and P according to their stoichiometry in the water column. Phytoplankton composition was directly linked to LAPT. Overall, this study seemed to be the first to connect a stoichiometric shift of N and P with kinetics of extracellular enzymes responsible for their regeneration along trophic gradients, presenting an additional pathway to overcome nitrogen deficiency in eutrophic lakes.

Efficient Encapsulation of Small S2-4 Molecules in MOF-Derived Flowerlike Nitrogen-Doped Microporous Carbon Nanosheets for High-Performance Li-S Batteries.

Lithium-sulfur (Li-S) battery is regarded as one of the most promising next-generation efficient energy storage systems because of its ultrahigh theoretical capacity of 1675 mAh/g and energy density of 2600 Wh/kg accompanied by the environmental benignity and abundance from natural sulfur. However, the insulating nature of sulfur and the dissolution of the polysulfides Li2S n (4 ≤ n ≤ 8) seriously restrict its practical application. The metastable small sulfur molecules (S2-4) stored in microporous carbon (pore size of <0.6 nm) as the active materials can avoid the production of the soluble polysulfide and solve the shuttle effect thoroughly. In addition, the conductivity of sulfur can be also improved. However, the preparation of microporous carbon materials with reasonable pore size and unique morphology for efficiently encapsulating S2-4 is still challenging. Herein, three flowerlike microporous nitrogen-doped carbon nanosheets with the pore size of <0.6 nm (namely, FMNCN-800, -900, and -1000) as the cathode materials in Li-S batteries were obtained from temperature-dependent carbonization of the metal-organic framework (MOF), Zn-TDPAT, which was from the simply reflux reaction of N-rich ligand H6TDPAT with Zn(II) salt. Our study showed that the FMNCN-900 from carbonization of Zn-TDPAT at 900 °C has suitable pore volume and nitrogen content, accommodating small S2-4 molecules in its micropores with the mass uptake of about 45%. Meanwhile, the appropriate amount of the nitrogen doping and the unique nanostructure of the flowerlike carbon nanosheet in the FMNCN-900 can effectively support its fast electronic transmission and lithium-ion conduction. The resulting S@FMNCN-900 composite cathode material presents the excellent electrochemical property in the Li-S battery (here the carbonate as electrolytes) with a reversible capacity of about 1220 mAh/g at 0.1C after 200 cycles and even 727 mAh/g at 2C after the long-term cycle of 1000 with only around 0.02% capacity loss per cycle. Obviously, the results indicate that the delicate construction of MOF-derived nitrogen-doped microporous carbon nanosheet is a promising strategy to develop novel electrode material for high-performing Li-S batteries.

The phosphorus release pathways and their mechanisms driven by organic carbon and nitrogen in sediments of eutrophic shallow lakes.

To reveal phosphorus (P) release pathways from sediment and their mechanisms induced by organic matter enrichment, 116 sampling sites (including surface water and sediment) in 29 shallow lakes with different eutrophic degrees in Wuhan city, China, were investigated from July 2011 to November 2011. Empirical relationship and structural equation model indicated that the decomposition of total organic matter (TOM), including proteins (PRT), carbo-hydrates (CHO) and lipids (especially PRT) mediated by extracellular enzymes, accelerated the formation of anaerobic status. On the other hand, coupled nitrification-denitrification caused by ammonium (NH4+-N) accumulation due to PRT decomposition further aggravated anaerobic status and nitrate removal in terms of the increase of dehydrogenase activity (DHA). As a consequence, ferric iron was reduced to ferrous iron and soluble reactive phosphorus (SRP) was released from iron-bound phosphorus (Fe(OOH)~P) in sediments. In addition, extracellular alkaline phosphatase can be induced by organic carbon and nitrogen on condition that the input of nitrogen (N) and carbon (C) exceeded by far that of P. Taken together, enrichment of N and C can result in P release through the formation of anaerobic status and alkaline phosphatase production. Hence, we indicated that a close coupling existed among C, N and P cycles.

A flexible and superhydrophobic upconversion-luminescence membrane as an ultrasensitive fluorescence sensor for single droplet detection.

A Ln3+-doped (Yb3+, Tm3+ or Yb3+, Er3+ co-doped) NaYF4 nanoparticle/polystyrene hybrid fibrous membrane (HFM) was fabricated using an electrospinning technique. The HFM shows upconversion luminescence (UCL), flexibility, superhydrophobicity and processability. The UCL membrane can be used as a fluorescence sensor to detect bioinformation from a single water droplet (~10 µl). Based on the fluorescence resonance energy transfer, the detection limits of this sensor can reach 1 and 10 ppb for the biomolecule, avidin, and the dye molecule, Rhodamine B, respectively, which are superior to most of the fluorescence sensors reported in previous works. After the fluorescence detection, the target droplet was easily removed without residues on the UCL membrane surface due to its superhydrophobic property, which exhibits an excellent recyclability that cannot be achieved by traditional liquid-based detection systems.