Explore the vast range of titles available.

Exploring lightweight microwave attenuation materials with strong and tunable wideband microwave absorption is highly desirable but remains a significant challenge. Herein, three-dimensional （3D） porous hybrid composites consisting of NiFe nanoparticles embedded within carbon nanocubes decorated on graphene oxide （GO） sheets （NiFe@C nanocubes@GO） as high-performance microwave attenuation materials have been rationally synthesized. The 3D porous hybrid composites are fabricated by a simple method, which involves one-step pyrolysis of NiFe Prussian blue analogue nanocubes in the presence of GO sheets. Benefiting from the unique structural features that exhibit good magnetic and dielectric losses as well as a proper impedance match, the resulting NiFe@C nanocubes@GO composites show excellent microwave attenuation ability. With a minimum reflection loss （RL） of -51 dB at 7.7 GHz at a thickness of 2.8 mm and maximum percentage bandwidth of 38.6% for RL 〈 -10 dB at a thickness of 2.2 mm, the NiFe@C nanocubes@GO composites are superior to the previously reported state-of-the-art carbon-based microwave attenuation materials.

We report the preparation of nanocomposites of reduced graphene oxide with embedded Fe3O4/Fe nanorings （FeNR@rGO） by chemical hydrothermal growth. We illustrate the use of these nanocomposites as novel electromagnetic wave absorbing materials. The electromagnetic wave absorption properties of the nanocomposites with different compositions were investigated. The preparation procedure and nanocomposite composition were optimized to achieve the best electromagnetic wave absorption properties. Nanocomposites with a GO：cx-Fe203 mass ratio of 1：1 prepared by annealing in HdAr for 3 h exhibited the best properties. This nanocomposite sample （thickness = 4.0 mm） showed a minimum reflectivity of -23.09 dB at 9.16 GHz. The band range was 7.4-11.3 GHz when the reflectivity was less than -10 dB and the spectrum width was up to 3.9 GHz. These figures of merit are typically of the same order of magnitude when compared to the values shown by traditional ferric oxide materials. However, FeNR@rGO can be readily applied as a microwave absorbing material because the production method we propose is highly compatible with mass production standards.

Graphene has attracted the interest of chemists, physicists, and materials scientists due to its extraordinary structural, mechanical, and electronic properties. While pristine graphene is desirable for applications that require a high electrical conductivity, many other applications require modified or functionalized forms of graphene, such as graphene oxide, reduced graphene, or other functionalized forms. Structurally modifying graphene through chemical functionalization reveals the numerous possibilities for tuning its structure; several chemical and physical functionalization methods have been explored to improve the stabilization and modification of graphene. In this review, we report recent progress towards the chemical modification of graphene, including both covalent and noncovalent methods, for use in various applications.

Scrupulous design and fabrication of advanced electrode materials are vital for developing high-performance sodium ion batteries. Herein, we report a facile one-step hydrothermal strategy for construction of a C-MoSe2/rGO composite with both high porosity and large surface area. Double modification of MoSe2 nanosheets is realized in this composite by introducing a reduced graphene oxide （rGO） skeleton and outer carbon protective layer. The MoSe2 nanosheets are well wrapped by a carbon layer and also strongly anchored on the interconnected rGO network. As an anode in sodium ion batteries, the designed C-MoSe2/rGO composite delivers noticeably enhanced sodium ion storage, with a high specific capacity of 445 mAh-g-1 at 200 mA.g-1 after 350 cycles, and 228 mAh-g 1 even at 4 A.g-1; these values are much better than those of C-MoSe2 nanosheets （258 mAh.g-a at 200 mA-g-1 and 75 mAh-g-1 at 4 A.g-~）. Additionally, the sodium ion storage mechanism is investigated well using ex situ X-ray diffraction and transmission electron microscopy methods. Our proposed electrode design protocol and sodium storage mechanism may pave the way for the fabrication of other high-performance metal diselenide anodes for electrochemical energy storage.

Nanostructured silicon has generated significant excitement for use as the anode material for lithium-ion batteries; however, more effort is needed to produce nanostructured silicon in a scalable fashion and with good performance. Here, we present a direct preparation of porous silicon nanoparticles as a new kind of nanostructured silicon using a novel two-step approach combining controlled boron doping and facile electroless etching. The porous silicon nanoparticles have been successfully used as high performance lithium-ion battery anodes, with capacities around 1,400 mA.h/g achieved at a current rate of 1 A/g, and 1,000 mA.h/g achieved at 2 A/g, and stable operation when combined with reduced graphene oxide and tested over up to 200 cycles. We attribute the overall good performance to the combination of porous silicon that can accommodate large volume change during cycling and provide large surface area accessible to electrolyte, and reduced graphene oxide that can serve as an elastic and electrically conductive matrix for the porous silicon nanoparticles.

The complete restoration of a perfect carbon lattice has been a central issue in the research on graphene derived from graphite oxide since this preparation route was first proposed several years ago, but such a goal has so far remained elusive. Here, we demonstrate that the highly defective structure of reduced graphene oxide sheets assembled into free-standing, paper-like films can be fully repaired by means of high temperature annealing （graphitization）. Characterization of the films by X-ray photoelectron and Raman spectroscopy, X-ray diffraction and scanning tunneling microscopy indicated that the main stages in the transformation of the films were （i） complete removal of oxygen functional groups and generation of atomic vacancies （up to 1,500 ~C）, and （ii） vacancy annihilation and coalescence of adjacent overlapping sheets to yield continuous polycrystalline layers （1,800-2,700 ~C） similar to those of highly oriented graphites. The prevailing type of defect in the polycrystalline layers were the grain boundaries separating neighboring domains, which were typically a few hundred nanometers in lateral size, exhibited long-range graphitic order and were virtually free of even atomic-sized defects. The electrical conductivity of the annealed films was as high as 577,000 S-m-1, which is by far the largest value reported to date for any material derived from graphene oxide, and strategies for further improvement without the need to resort to higher annealing temperatures are suggested. Overall, this work opens the prospect of truly achieving a complete restoration of the carbon lattice in graphene oxide materials.

The synthesis of a composite of cobalt phosphide nanowires and reduced graphene oxide （denoted CoP/RGO） via a facile hydrothermal method combined with a subsequent annealing step is reported. The resulting composite presents large specific surface area and enhanced conductivity, which can effectively facilitate charge transport and accommodates variations in volume during the lithiation/de-lithiation processes. As a result, the CoP/RGO nanocomposite manifests a high reversible specific capacity of 960 mA·h-g-1 over 200 cycles at a current density of 0.2 A·g-1 （297 mA·h·g-1 over 10,000 cycles at a current density of 20 A.g-1） and excellent rate capability （424 mA·h·g-1 at a current density of 10 A·g-1）.

We report a three-dimensional hierarchical ternary hybrid composite of molybdenum disulfide （MoS2）, reduced graphene oxide （GO）, and carbon nano- tubes （CNTs） prepared by a two-step process. Firstly, reduced GO-CNT composites with three-dimensional microstructuresare synthesized by hydrothermal treatment of an aqueous dispersion of GO and CNTs to form a composite structure via π-π interactions. Then, MoS2 nanoparticles are hydrothermally grown on the surfaces of the GO-CNT composite. This ternary composite shows superior electrocatalytic activity and stability in the hydrogen evolution reaction, with a low onset potential of only 35 mV, a Tafel slope of -38 mV.decade-1 and an apparent exchange current density of 74.25 mA.cm-2. The superior hydrogen evolution activity stemmed from the synergistic effect of MoS2 with its electrocatalytically active edge-sites and excellent electrical coupling to the underlying graphene and CNT network.

With the combination of surfactant and freeze-drying, we have developed two kinds of graphene spongy structures. On the one hand, using foams of soap bubbles as templates, three-dimensional porous graphene sponges with rich hierarchical pores have been synthesized. Pores of the material contain three levels of length scales, including millimeter, micrometer and nanometer. The structure can be tuned by changing the freezing media, adjusting the stirring rate or adding functional additives. On the other hand, by direct freeze-drying of a graphene oxide/surfactant suspension, a porous framework with directionally aligned pores is prepared. The surfactant gives a better dispersion of graphene oxide sheets, resulting in a high specific surface area. Both of the obtained materials exhibit excellent absorption capacity and good compression performance, providing a broad range of possible applications, such as absorbents, storage media, and carriers.

In this study, macroscopic graphene-wrapped melamine foams （MF-G） were fabricated by an MF-templated layer-by-layer （LBL） assembly using graphene oxide as building blocks, followed by solution-processed reduction. By concisely duplicating sponge-like, highly ordered three-dimensional architectures from MF, the resulting MF-G with an interconnected graphene-based scaffold and tunable nanostructure was explored as compressible, robust electrodes for efficient energy storage. A thin layer of pseudocapacitive polypyrrole （PPy） was then attached and uniformly coated on MF-G, resulting in a well-defined core- double-shell configuration of the MF-G-PPy ternary composite sponges. The as-assembled devices exhibited enhancement of supercapacitor performance, with a high specific capacitance of 427 F·g-1 under a compressive strain of 75% and an excellent cycling stability with only 18% degradation after 5,000 charge- discharge cycles. Besides, the MF-G-PPy electrode maintained stable capacitance up to 100 compression-release cycles, with a compressive strain of 75%. These encouraging results thus provide a new route towards the low-cost, easily scalable fabrication of lightweight and deformation-tolerant electrodes.