Assembly of single layers: Three-dimensional assembly of single-layered MoS2 is achieved on a large scale via a solution method. The as-prepared tubular architectures have tunable size and mesopores in the shell, which are desirable for applications. As a example, they exhibit excellent lithium storage properties and are highly active for hydrodesulfurization of thiophene resulting from their structural advantages.
In this article, hierarchical flower-like ZnO nanostructures with controlled morphology and dimensions have been synthesized by solution phase approach and functionalized by Au nanoparticles (AuNPs) with the combination of electrodeposition to explore novel applications. The photocatalytic activity and lithium storage capacity of these hybrid nanostructures have been investigated. It has been found that hybrid nanostructure combining the large specific surface area, stability and catalytic activity of small AuNPs, demonstrate the higher photocatalytic activity than that of pure ZnO. Furthermore, an initial discharge capacity of 1280 mA h g À1 and a reversible capacity over 392 mA h g À1 at the 50 cycles are achieved for the Au-ZnO hybrid nanostructure, which is found to be much better than that of any previously reported ZnO anodes. The improved lithium storage capacity and cycle life of the Au-ZnO electrode result from the Li activity of Au-ZnO phase. The photocatalytic and electrochemical activity of Au-ZnO hybrid nanostructures provide a new platform for energy storage, environmental remediation and photocatalysis applications.
Nitrogen-enriched porous carbon nanofiber networks (NPCNFs) were successfully prepared by using lowcost melamine and polyacrylonitrile as precursors via electrospinning followed by carbonization and NH 3 treatments. The NPCNFs exhibited inter-connected nanofibrous morphology with a large specific surface area, well-developed microporous structure, relatively high-level nitrogen doping and great amount of pyridinic nitrogen. As free-standing new anode materials in lithium-ion batteries (LIBs), the NPCNFs showed ultrahigh capacity, good cycle performance and superior rate capability with a reversible capacity of as high as 1323 mA h g À1 at a current density of 50 mA g À1 . These attractive characteristics make the NPCNFs materials very promising anode candidates for high-performance LIBs and, as free-standing electrode materials to be used in other energy conversion and storage devices.
Through a facile hydrothermal method with a special surfactant triethanolamine (TEA) followed by thermal treatment, monodispersed micro-/nanostructured Co3O4 powders with unique morphology (cube) have been synthesized successfully as anode material for Li-ion batteries (LIBs). The regular Co3O4 microcubes (∼2.37 μm in the average side length) consist of many irregular nanoparticles (20-200 nm in diameter, 30-40 nm in thickness) bonded to each other, which greatly inherit the morphology and size of the precursor CoCO3. The specific surface area of Co3O4 powders is about 5.10 m(2)·g(-1) by the Brunauer-Emmett-Teller (BET) method, and the average pore size is about 3.08 nm by the Barrett-Joyner-Halenda (BJH) method. In addition, the precursor is verified as a single-crystal, while the mesoporous cubic Co3O4 is a polycrystalline characteristic assembled by numerous single-crystal nanoparticles. More remarkable, the high performance of the micro-/nanostructured cubic Co3O4 powders has been obtained by the electrochemical measurements including high initial discharge capacities (1298 mAhg(-1) at 0.1 C and 1041 mAhg(-1) at 1 C), impressive rate capability, and excellent capacity retention (99.3%, 97.5%, 99.2%, and 89.9% of the first charge capacities after 60 cycles at 0.1 C, 0.2 C, 0.5 C, and 1 C, respectively).
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