Anion exchange strategy to synthesis of porous NiS hexagonal nanoplates for supercapacitors.

A facile anion exchange strategy was applied to the synthesis of porous NiS hexagonal nanoplates (NiS HNPs) as an electrode material for supercapacitors. It was found that Na2S concentration is a key factor to achieve porous NiS hexagonal nanoplates with well-defined architecture. Porous NiS hexagonal nanoplates exhibited a specific capacitance of 1897 F g-1 at a current density of 1 A g-1. NiS HNPs//activated carbon (AC) asymmetric supercapacitor (ASC) shows a long cycle lifespan (about 100% capacity retention after 4000 cycles at a current density of 3 A g-1) with a maximum energy density of 11.6 Wh kg-1 at a large loading mass of about 30 mg. Impressively, two NiS HNPs//AC ASCs in series could light up a red LED for about 30 min. The remarkable electrochemical performance of NiS HNPs is ascribed to their unique hierarchical porous architectures. The anion exchange method is a facile and versatile strategy for the synthesis of metal sulfides with high performance for energy storage.

Large-scale synthesis of monodisperse magnesium ferrite via an environmentally friendly molten salt route.

Sub-micrometer-sized magnesium ferrite spheres consisting of uniform small particles have been prepared using a facile, large-scale solid-state reaction employing a molten salt technique. Extensive structural characterization of the as-prepared samples has been performed using scanning electron microscope, transmission electron microscopy, high-resolution transmission electron microscopy, selected area electron diffraction, and X-ray diffraction. The yield of the magnesium ferrite sub-micrometer spheres is up to 90%, and these sub-micrometer spheres are made up of square and rectangular nanosheets. The magnetic properties of magnesium ferrite sub-micrometer spheres are investigated, and the magnetization saturation value is about 24.96 emu/g. Moreover, the possible growth mechanism is proposed based on the experimental results.

Synthesis of silicon carbide nanocrystals from waste polytetrafluoroethylene.

Resource utilization of waste plastic could solve the problem of environmental pollution and simultaneously relieve energy shortages, achieving sustainable development. In this study, the conversion of waste polytetrafluoroethylene (PTFE) to cubic silicon carbide (SiC) nanoparticles has been described. The structures and morphologies of the obtained SiC were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Furthermore, the FTIR spectrum of the obtained SiC sample suggests that the waste PTFE was completely converted into SiC in our approach.

Chemical synthesis of germanium nanoparticles with uniform size as anode materials for lithium ion batteries.

A simple Mg-thermal reduction reaction is reported to synthesize germanium (Ge) nanoparticles with a uniform size at a low temperature of 400 °C in an autoclave. The as-prepared Ge nanoparticles exhibit promising anode applications in lithium ion batteries with high capacity and excellent cycling stability.

Growth of conical carbon nanotubes by chemical reduction of MgCO3.

Carbon nanotubes were synthesized by chemical reduction of magnesium carbonate with metallic lithium at 600 degrees C. The nanotubes with an average length of 13 microm and diameter of 60 nm are made of short coaxial conical cylinder tubular graphite sheets with their cone axis parallel to the tube axis, different from the ordinary carbon nanotubes, composed of concentric cylindrical graphite layers with their normal perpendicular to the tube axis. It is suggested that nanoscale rough surface of lithium formed at the interface between supercritical carbon dioxide and liquid lithium takes the roles of both the reductant for reduction of carbon dioxide to carbon and the template for growth of carbon nanotubes.

Controlled Synthesis of Carbon Nanoparticles in a Supercritical Carbon Disulfide System.

Carbon nanoparticles with large surface areas were produced by the reduction of carbon disulfide with metallic lithium at 500 °C. The carbon nanoparticles account for about 80% of the carbon product. The carbon nanoparticles were characterized by X-ray powder diffraction, field emission scanning electron microscopy, transmission electron microscopy, high resolution transmission electron microscopy and N2 physisorption. The results showed that carbon nanoparticles predominate in the product. The influence of experimental conditions was investigated, which indicated that temperature plays a crucial role in the formation of carbon nanoparticles. The possible formation mechanism of the carbon nanoparticles was discussed. This method provides a simple and efficient route to the synthesis of carbon nanoparticles.

Diamond formation by reduction of carbon dioxide at low temperatures.

This Communication reports a low-temperature diamond synthesis technique, in which diamonds (10-250 mum) can form at a temperature as low as 440 degrees C by reduction of dense CO2 with metallic Na. The X-ray diffraction pattern of a powder sample shows three reflection peaks, indexed with 111, 220, and 311, corresponding unambiguously to cubic diamond. The Raman spectrum of the product exhibits an intense first-order peak at 1332 cm-1, which is the characteristic signature of the cubic diamond, indicating the formation of well-crystallized diamond. Carbon dioxide is a nontoxic low-energy molecule, abundant on earth. This novel reduction method could allow studies of large-size diamond growth using CO2 as the carbon source.