A Co-Doped MnO2 catalyst for Li-CO2 batteries with low overpotential and ultrahigh cyclability.

Li-CO2 batteries can not only capture CO2 to solve the greenhouse effect but also serve as next-generation energy storage devices on the merits of economical, environmentally-friendly, and sustainable aspects. However, these batteries are suffering from two main drawbacks: high overpotential and poor cyclability, severely postponing the acceleration of their applications. Herein, a new Co-doped alpha-MnO2 nanowire catalyst is prepared for rechargeable Li-CO2 batteries, which exhibits a high capacity (8160 mA h g−1 at a current density of 100 mA g−1), a low overpotential (≈0.73 V), and an ultrahigh cyclability (over 500 cycles at a current density of 100 mA g−1), exceeding those of Li‐CO2 batteries reported so far. The reaction mechanisms are interpreted depending on in situ experimental observations in combination with density functional theory calculations. The outstanding electrochemical properties are mostly associated with a high conductivity, a large fraction of hierarchical channels, and a unique Co interstitial doping, which might be of benefit for the diffusion of CO2, the reversibility of Li2CO3 products, and the prohibition of side reactions between electrolyte and electrode. These results shed light on both CO2 fixation and new Li-CO2 batteries for energy storage

Heterojunction-composited architecture for Li–O2 batteries with low overpotential and long-term cyclability.

The crucial issue among lithium−oxygen batteries (LOBs) lies in the development of highly efficient catalysts to improve their large discharge−charge polarization, poor rate capability, and short cycle life. Herein, a composite of three-dimensional honeycomb graphene-supported a Mo/Mo2C heterojunction has been synthesized and can be utilized as a self-supported LOB cathode directly. The LOBs based on the Mo/Mo2C heterojunction composite cathode show a low overpotential of 0.52 V, a high discharge capacity of about 12016 mAh g−1 at 100 mA g−1, and a long-term cyclability (about 360 cycles) under a restricted capacity of 1000 mAh g−1 at 100 mA g−1, which exceeds the features of the majority of Mo-based catalysts for LOBs reported so far. Based on both experimental tests and density functional calculations, it is confirmed that the outstanding electrochemical performance is closely associated with a hierarchical porous structure for convenient oxygen/electrolyte diffusion, a large number of activity sites (interfaces/defects) for high capacity, and a high conductivity with metallic bonds for good rate capability. The method can be extended to prepare other metal based heterojunctions

An equatorial ultra iron-poor star identified in BOSS

We report the discovery of SDSS J131326.89-001941.4, an ultra iron-poor red giant star ([Fe/H] ~ -4.3) with a very high carbon abundance ([C/Fe]~ +2.5). This object is the fifth star in this rare class, and the combination of a fairly low effective temperature (Teff ~ 5300 K), which enhances line absorption, with its brightness (g=16.9), makes it possible to measure the abundances of calcium, carbon and iron using a low-resolution spectrum from the Sloan Digital Sky Survey. We examine the carbon and iron abundance ratios in this star and other similar objects in the light of predicted yields from metal-free massive stars, and conclude that they are consistent. By way of comparison, stars with similarly low iron abundances but lower carbon-to-iron ratios deviate from the theoretical predictions.Comment: 6 pages, 4 figures, accepted for publication in A&

5G multimedia massive MIMO communications systems

In the fifth generation (5G) wireless communication systems, a majority of the traffic demands are contributed by various multimedia applications. To support the future 5G multimedia communication systems, the massive multiple-input multiple-output (MIMO) technique is recognized as a key enabler because of its high spectral efficiency. The massive antennas and radio frequency chains not only improve the implementation cost of 5G wireless communication systems but also result in an intense mutual coupling effect among antennas because of the limited space for deploying antennas. To reduce the cost, an optimal equivalent precoding matrix with the minimum number of radio frequency chains is proposed for 5G multimedia massive MIMO communication systems considering the mutual coupling effect. Moreover, an upper bound of the effective capacity is derived for 5G multimedia massive MIMO communication systems. Two antennas that receive diversity gain models are built and analyzed. The impacts of the antenna spacing, the number of antennas, the quality-of-service (QoS) statistical exponent, and the number of independent incident directions on the effective capacity of 5G multimedia massive MIMO communication systems are analyzed. Comparing with the conventional zero-forcing precoding matrix, simulation results demonstrate that the proposed optimal equivalent precoding matrix can achieve a higher achievable rate for 5G multimedia massive MIMO communication systems

Achieving high strength and ductility in magnesium alloys via densely hierarchical double contraction nanotwins.

Light-weight magnesium alloys with high strength are especially desirable for the applications in transportation, aerospace, electronic components, and implants owing to their high stiffness, abundant raw materials, and environmental friendliness. Unfortunately, conventional strengthening methods mainly involve the formation of internal defects, in which particles and grain boundaries prohibit dislocation motion as well as compromise ductility invariably. Herein, we report a novel strategy for simultaneously achieving high specific yield strength (∼160 kN m kg-1) and good elongation (∼23.6%) in a duplex magnesium alloy containing 8 wt % lithium at room temperature, based on the introduction of densely hierarchical {1011}-{101 1} double contraction nanotwins (DCTWs) and full-coherent hexagonal close-packed (hcp) particles in twin boundaries by ultrahigh pressure technique. These hierarchical nanoscaled DCTWs with stable interface characteristics not only bestow a large fraction of twin interface but also form interlaced continuous grids, hindering possible dislocation motions. Meanwhile, orderly aggregated particles offer supplemental pinning effect for overcoming latent softening roles of twin interface movement and detwinning process. The processes lead to a concomitant but unusual situation where double contraction twinning strengthens rather than weakens magnesium alloys. Those cutting-edge results provide underlying insights toward designing alternative and more innovative hcp-type structural materials with superior mechanical properties

In-situ atomic-scale phase transformation of Mg under hydrogen conditions.

Magnesium hydrogenation issue poses a serious obstacle to designing strong and reliable structural materials, as well as offering a safe alternative for hydrogen applications. Understanding phase transformation of magnesium under hydrogen gas plays an essential role in developing high performance structural materials and hydrogen storage materials. Herein, we report in-situ atomic-scale observations of phase transformation of Mg and Mg-1wt.%Pd alloy under hydrogen conditions in an aberration-corrected environmental transmission electron microscopy. Compare with magnesium hydrogenation reaction, magnesium oxidation reaction predominately occurs at room temperature even under pure hydrogen gas (99.9%). In comparison, magnesium hydrogenation is readily detected in the interface between Mg and Mg6Pd, due to catalytic role of Mg6Pd. Note that the nanoscale MgH2 compound transfers into MgO spontaneously, and the interface strain remarkably varies during phase transformation. These atomic-level observations and calculations provide fundamental knowledge to elucidate the issue of magnesium hydrogenation

Thermal conductivity measurements of proton-heated warm dense aluminum.

Thermal conductivity is one of the most crucial physical properties of matter when it comes to understanding heat transport, hydrodynamic evolution, and energy balance in systems ranging from astrophysical objects to fusion plasmas. In the warm dense matter regime, experimental data are very scarce so that many theoretical models remain untested. Here we present the first thermal conductivity measurements of aluminum at 0.5-2.7 g/cc and 2-10 eV, using a recently developed platform of differential heating. A temperature gradient is induced in a Au/Al dual-layer target by proton heating, and subsequent heat flow from the hotter Au to the Al rear surface is detected by two simultaneous time-resolved diagnostics. A systematic data set allows for constraining both thermal conductivity and equation-of-state models. Simulations using Purgatorio model or Sesame S27314 for Al thermal conductivity and LEOS for Au/Al release equation-of-state show good agreement with data after 15 ps. Discrepancy still exists at early time 0-15 ps, likely due to non-equilibrium conditions

Electrochemical determination of chemical oxygen demand using Ti/TiO2 electrode.

To overcome the shortcomings of the conventional potassium dichromate method (PDM) for monitoring chemical oxygen demand (COD) of waters, many efforts have been made on developing quick and environment-friendly techniques. Among all alternatives, electrochemical (EC) techniques are very competitive due to their relatively simple devices and quickness. A number of electrodes have been fabricated to investigate electrochemical determination of COD. However, little work has been reported on Ti/TiO2 based electrode for this purpose. In the present work, Ti/Ti/TiO2 electrode was simply prepared by anodic oxidation of pure titanium. Aqueous solutions of potassium hydrogen phthalate and phenol were electrolyzed by chronocoulometry in a three-electrode system with Ti/Ti/TiO2 as working electrode (anode). Organic compounds were electrochemically oxidized on Ti/Ti/TiO2 electrode by hydroxyl radicals and the released electrons were recorded and transferred to currents. The electric currents were proportional to the COD values of the water samples being investigated. Based on data of COD values and corresponding currents, a linear regression equation was obtained for a certain kind of waste water. With the regression equation, current of an unknown water sample was transferred to its COD value. Conditions for the presented EC method were set up as cell voltage 2.0V v.s. SCE and pH 7.0. The linear range of COD was of about 25~530 mg/L. COD values of real waste water samples were measured by Ti/Ti/TiO2 electrode and the relative errors were all in the range of ±8% compared with data determined by conventional PDM. The electrochemicalmethodology was successfully applied to evaluate COD in waste water

Self-reductive synthesis of MXene/Na0.55Mn1.4Ti0.6O4 hybrids for high-performance symmetric lithium ion batteries.

Increasing environmental problems and energy challenges have created an urgent demand for the development of green and efficient energy-storage systems. The search for new materials that could improve the performance of Li-ion batteries (LIBs) is one of today's most challenging tasks. Herein, a stable symmetric LIB based on the bipolar material-MXene/Na0.55Mn1.4Ti0.6O4 was developed. This bipolar hybrid material showed a typical MXene-type layered structure with high conductivity, containing two electrochemically active redox couples, namely, Mn4+/Mn3+ (3.06 V) and Mn2+/Mn (0.25 V). This MXene/Na0.55Mn2O4-based symmetric full cell exhibited the highest energy density of 393.4 W h kg−1 among all symmetric full cells reported so far, wherein it is bestowed with a high average voltage of 2.81 V and a reversible capacity of 140 mA h g−1 at a current density of 100 mA g−1. In addition, it offers a capacity retention of 79.4% after 200 cycles at a current density of 500 mA g−1. This symmetric lithium ion full battery will stimulate further research on new LIBs using the same active materials with improved safety, lower costs and a long life-span

On the retrofitting and repowering of coal power plants with post-combustion carbon capture: An advanced integration option with a gas turbine windbox

Retrofitting a significant fraction of existing coal-fired power plants is likely to be an important part of a global rollout of carbon capture and storage. For plants suited for a retrofit, the energy penalty for post-combustion carbon capture can be minimised by effective integration of the capture system with the power cycle. Previous work on effective integration options has typically been focused on either steam extraction from the power cycle with a reduction of the site power output, or the supply of heat and electricity to the capture system via the combustion of natural gas, with little consideration for the associated carbon emissions. This article proposes an advanced integration concept between the gas turbine, the existing coal plant and post-combustion capture processes with capture of carbon emissions from both fuels. The exhaust gas of the gas turbine enters the existing coal boiler via the windbox for sequential combustion to allow capture in a single dedicated capture plant, with a lower flow rate and a higher CO2 concentration of the resulting flue gas. With effective integration of the heat recovery steam generator with the boiler, the existing steam cycle and the carbon capture process, the reference subcritical unit used in this study can be repowered with an electricity output penalty of 295 kWh/tCO2 – 5% lower than a conventional steam extraction retrofit of the same unit – and marginal thermal efficiency of natural gas combustion of 50% LHV – 5% point higher than in a configuration where the gas turbine has a dedicated capture unit