Graphene-Wrapped MgO/Poly(vinyl alcohol) Composite Sheets: Dielectric and Electromagnetic Interference Shielding Properties at Elevated Temperatures.

Different amounts of graphene-wrapped magnesium oxide (G@MgO) powders are uniformly dispersed in poly(vinyl alcohol) (PVA) solution in different experiments to obtain solutions which are coagulated to obtain solid materials, which are then hot pressed at 413 K and 3 t of pressure to finally obtain 1 mm thick freestanding G@MgO/PVA composite sheets in which the constituents, namely, graphene and MgO (in the form of G@MgO), are the nanofillers in PVA matrix. During synthesis of G@MgO powder, MgO nanoparticles are in situ wrapped by the graphene nanosheets as revealed by electron microscopy. Uniformity of G@MgO dispersion in PVA was confirmed by secondary electron micrographs and the consistency in X-ray diffraction and Raman scattering data collected from different locations of the samples. Temperature (303-393 K) dependent complex permittivity of G@MgO/PVA composite sheets (including those prepared by casting) in low frequency (20 Hz to 2 MHz) and high frequency (i.e., X-band, 8.2-12.4 GHz) ranges are measured. In both frequency ranges, G@MgO/PVA composite sheets prepared by coagulation exhibited dielectric properties superior to those of PVA and G@MgO/PVA composite sheets prepared by casting. A strong interfacial polarization is observed in coagulated and as-cast G@MgO/PVA composite sheets. It is noticed from the calculated activation energies that conduction is the dominating mechanism for energy transfer in both composite sheets' cases, while it is predominating in coagulated composite sheets due to the better network formation of the fillers in the coagulated samples than in the cast composite samples. The electromagnetic interference shielding effectiveness (EMI SE) values in the X-band frequency range (i.e., 8.2-12.4 GHz) of the G@MgO/PVA composite sheets prepared by coagulation are more than those prepared by casting for a particular weight fraction of G@MgO. At 393 K, for a particular G@MgO/PVA composite sheet prepared by coagulation, an excellent EMI SE of ∼27.5 dB is measured. It is also experimentally elucidated that the absorption is the dominating mechanism for EMI SE in the prepared composite sheets.

In vitro and in vivo evaluation of anti-cancer activity: Shape-dependent properties of TiO2 nanostructures.

Cancer is a complex and widespread disease, and it is going to be the first cause of death in the world. Chemotherapy has been used to treat cancer, but it is detrimental to immune cells and known to induce numerous side effects. Therefore it is imperative to develop new drugs for the treatment of cancer without any side effects and toxicity. TiO2 nanomaterials are human safe, cost effective, chemically stable and have numerous biomedical applications. Spherical TiO2 fine particles (TFP), TiO2 nanosquares (TNS) and TiO2 nanotubes (TNT) were developed and evaluated for anti-cancer activity in vitro and in vivo. Our data suggest that these nanostructured materials significantly inhibited proliferation of breast cancer MDAMB 231 cells in in vitro shape dependent manner. In addition, we found that TiO2 nanostructures inhibited the migration and colony formation of breast cancer MDAMB231 cells. More importantly, we found that TNS/TNT/TFP had anti-angiogenic effect in CAM assay and TNT had comparable anti-angiogenic effect with the positive control staurosporine. Additional qRT-PCR data suggest that TiO2 nanostructures induced the upregulation of tumor suppressor genes p53, MDA7, TRAIL and transcription factor STAT3, which suggests the probable mechanism for the anticancer activity of TiO2 nanostructures. Finally, analysis of TEM confirms the dispersion and interaction of nanostructures in the cells. Thus these materials could be potential therapeutic targets for the treatment of cancer.

Fascinating Magnetic Energy Storage Nanomaterials: A Brief Review.

OBJECTIVE: In this brief review, the importance of nanotechnology in developing novel magnetic energy storage materials is discussed. METHOD: The discussion covers recent patents on permanent magnetic materials and especially covers processing of permanent magnets (rare-earth and rare-earth free magnets), importance of rare-earth permanent magnets and necessity of rare-earth free permanent magnets. Magnetic energy storage materials are those magnetic materials which exhibit very high energy product (BH)max (where B is the magnetic induction in Gauss (G) whereas H is the applied magnetic field in Oersted (Oe)). (BH)max is the direct measure of the ability of a magnetic material to store energy. RESULT: In this context, processing of magnetic energy storage composite materials constituted by soft and hard magnetic materials played a predominant role in achieving high (BH)max values due to the exchange coupling phenomenon between the soft and hard magnetic phases within the composite. Magnetic energy storage composites are normally composed of rare-earth magnetic materials as well as rare-earth free magnetic materials. CONCLUSION: Nanotechnology's influence on the enhancement of energy product due to the exchange coupling phenomenon is of great prominence and therefore discussed in this review.

Non-collinear ferromagnetic short range order in MgO decked multi-layered graphene.

A careful magnetic study of MgO decked multi-layered graphene (MDMLG), synthesized by a combustion process that does not involve the use of graphite (which can be a source of magnetic impurities) was conducted and an elaborate analysis of high-precision magnetization data permits us to completely rule out the presence of a long-range ferromagnetic (FM) ordering at temperatures T ≥ 2.5 K. Instead, a non-collinear FM short-range order persists up to temperatures as high as 300 K and a concomitant paramagnetic component is present at all the temperatures. The observed exponential temperature variations of the 'field-cooled' and 'zero-field-cooled' magnetizations, remanent magnetization, saturation magnetization, coercive field, exchange field and random anisotropy field are shown to basically reflect the exponential growth of the correlation length for the spins at the zigzag edges of graphene as the temperature falls below the temperature, Tx ≅ 10 K where a crossover from extremely weak to moderately weak magnetic anisotropy occurs. In sharp contrast, a paramagnetic response is induced by the defects in nanometer-sized MgO crystallites in MDMLG.

Phoenix dactylifera mediated green synthesis of Cu2O particles for arsenite uptake from water.

In this study, an environmentally friendly, cost-effective, and single-step procedure is used for the synthesis of polycrystalline Cu2O particles with controlled morphologies. Simple sugars are extracted from date fruit pulp (Phoenix dactylifera) and used as a reducing agent for the formation of Cu2O particles in aqueous medium. The feasibility of this solution is compared with the standard glucose solution. The Cu2O particles are characterized by electron microscopy, X-ray diffraction, optical absorption and Raman scattering techniques. It is concluded that the morphology of the particles is mainly influenced by the solvents. The obtained Cu2O particles are then used as an adsorbent to uptake As(III) ions from water. The maximum adsorption capacity (Qmax) is estimated by Langmuir and Freundlich isotherms and it is found that Qmax = 14.3 mg g-1. Adsorption kinetics study showed that the adsorption equilibrium could be achieved in 1 h and that the purified water meets the standards of World Health Organization (WHO) for acceptable amount of As(III) in drinking water. Adsorption kinetic models showed that the adsorption is chemisorption in nature.

Perspectives on State-of-the-Art Carbon Nanotube/Polyaniline and Graphene/Polyaniline Composites for Hybrid Supercapacitor Electrodes.

Supercapacitors are attractive alternative energy storage sources. They offer high energy/power density with other characteristics like fast discharge/charge time, long operation stability, safety etc. In a supercapacitor, working electrode material is the principal constituent. At present there are numerous electrode materials (with properties) suitable for their use in hybrid type supercapacitors. Carbon/polyaniline (PANi) composites are one class of such electrode materials. Here, perspectives on state-of-the-art carbon/PANi composites namely carbon nanotube/polyaniline and graphene/polyaniline composites expedient as hybrid type supercapacitor electrode materials will be presented.

Carbon- and Polyaniline Nanofibers Containing Composite Electrode Material for Supercapacitors.

Rapid mixing chemical oxidative polymerization method is used to synthesize carbon nanofibers (CNFs) and polyaniline nanofibers (PANI NF) containing composite. Morphological, structural and phase analyses reveal that the composite is constituted by PANI coated CNFs and PANI NF. The intrinsic defects on the CNFs' surfaces allowed the nucleation and growth of PANI on them. At the same time, the use of optimal aniline concentration facilitated the simultaneous nucleation and growth of PANI NF The composite exhibits an excellent electrochemical activity with a specific capacitance of -156.92 F/g. The synergic contribution of the constituents to the overall electrochemical activity of the composite are identified.

Electrochemically Active Polyaniline (PANi) Coated Carbon Nanopipes and PANi Nanofibers Containing Composite.

A composite constituted by carbon nanopipes (CNPs) and polyaniline nanofibers (PANi NFs) is synthesized using in-situ chemical oxidative polymerization. Owing to its electrochemical activity the composite is found to be suitable as a working electrode material in hybrid type supercapacitors. Microstructural and phase analyses of the composite showed that (i) CNP surfaces are coated with PANi and (ii) PANi coated CNPs are distributed among PANi NFs. The composite shows an excellent electrochemical activity and a high specific capacitance of ~224.39 F/g. The electro-chemical activity of the composite is explicated in correlation with crystallinity, intrinsic oxidation state, and doping degree of PANi in the composite. The electro-chemical activity of the composite is also explicated in correlation with BET surface area and ordered meso-porosity pertaining to the composite. Charge/discharge curves indicate that the specific capacitance of the composite is a result of electric double-layer capacitance offered by CNPs and Faradaic pseudo capacitance offered by PANi NFs.

Strong interfacial polarization in ZnO decorated reduced-graphene oxide synthesized by molecular level mixing.

Globally, there is a great demand for energy storage materials and devices. In this context, charge storage capacitors are of great prominence. Metal oxide-graphene composites are excellent candidates for charge storage materials. This is because the dielectric properties of these composites can be controlled by the nature, dimensions and spatial distribution of the conductive components in these composites. ZnO decorated reduced-graphene oxide (r-GO) is synthesized and studied in this context. ZnO-r-GO composites are synthesized using molecular-level mixing. The composites are named as ZnO-0.1G, ZnO-0.2G and ZnO-0.3G in the order of increasing r-GO content. At 1 kHz, the dielectric permittivity (ε') values of ZnO-0.1G, ZnO-0.2G and ZnO-0.3G are nearly 11 (ε' = 114), 15 (ε' = 153) and 40 (ε' = 400) times greater than that of ZnO (ε' = 10). The strong interfacial polarization (Maxwell-Wagner polarization) in these composites is attributed to the presence of functional groups (which are polar in nature) on the r-GO sheets and also to the presence of lattice and/or topological defects in the r-GO. Temperature dependent electric modulus (M'') studies further confirm the observed interfacial polarization.

MgO-decorated few-layered graphene as an anode for li-ion batteries.

Combustion of magnesium in dry ice and a simple subsequent acid treatment step resulted in a MgO-decorated few-layered graphene (FLG) composite that has a specific surface area of 393 m(2)/g and an average pore volume of 0.9 cm(3)/g. As an anode material in Li-ion batteries, the composite exhibited high reversible capacity and excellent cyclic performance in spite of high first-cycle irreversible capacity loss. A reversible capacity as high as 1052 mAh/g was measured during the first cycle. Even at the end of the 60th cycle, more than 83% of the capacity could be retained. Cyclic voltammetry results indicated pseudocapacitance behavior due to electrochemical absorption and desorption of lithium ions onto graphene. An increase in the capacity has been observed during long-term cycling owing to electrochemical exfoliation of graphene sheets. Owing to its good thermal stability and superior cyclic performance with high reversible capacities, MgO-decked FLG can be an excellent alternative to graphite as an anode material in Li-ion batteries, after suitable modifications.

Possible gas-phase reactions of H2/CH4/tetramethylsilane in diamond/beta-SiC nanocomposite film deposition: an ab-initio study.

The Si-C bond breakings in tetramethylsilane (TMS) when interacting with H/H2 and the successive H abstractions from SiH4/CH4 in the gas mixture of H2/ CH4/TMS were studied at the CCSD(T)/6-311+G**//MP2/6-31+G** level of theory. Their rate constants between 1500 and 2500 K were estimated using a conventional transition state theory. The results indicate that (i) it is mainly the H radical that causes the Si-C bond breaking in TMS, and (ii) the successive H abstractions from SiH4 are much easier and faster than those from CH4. At low temperatures the differences of rate constants among the four types of the reactions are large, but generally reduced at high temperatures. The reaction rates show no selectivity over the pressure as verified at P = 0.00025, 0.025, 1, and 100 atm, respectively. Our results could provide the following microscopic level understanding of reactions in the synthesis of diamond/beta-SiC nanocomposite films. Although the Si content is smaller than that of C in the precursor gases, the gas mixture activated by microwave plasma technique could provide Si sources with a higher rate. The produced Si sources with excellent rigidity in sp3 hybridization competitively occupy the space on the substrate together with C sources, resulting in the deposition of diamond/beta-SiC nanocomposite films.