Fabrication of CuO/T-ZnOw nanocomposites using photo-deposition and their photocatalytic property

CuO/tetrapod-like ZnO whisker (T-ZnOw) nanocomposites were successfully synthesized using a simple photo-deposition method. Some nanocomposites exhibit remarkably improved photocatalytic property, while the extents of the improvements vary with different Cu/Zn molar ratios and polyethylene glycol (PEG) concentrations. Moreover, it is found that excessively high Cu/Zn molar ratio or PEG concentration would reduce the photocatalytic property of the nanocomposites. A direct relationship between the morphology and the photocatalytic property of CuO/T-ZnOw was established and then analyzed by discussing the photocatalytic mechanism of the CuO/T-ZnOw nanocomposites.     

EMI shielding effectiveness of graphene decorated with graphene quantum dots and silver nanoparticles reinforced PVDF nanocomposites

Graphene decorated with graphene quantum dots (G-D-GQDs) have been successfully synthesized using solvothermal cutting of graphene oxide. The incorporation of G-D-GQDs in polyvinyledene fluoride (PVDF) matrix shows the total EMI shielding effectiveness (SE_T) of 31 dB at 8 GHz. The main mechanism of high EMI shielding effectiveness is reflection and absorption of EM radiation. The high absorption of EM radiation is due to tunneling of electrons from GQDs. Further, decoration of G-D-GQDs with conducting Ag nanoparticles (G-D-GQDsAg) enhances the SE_T value to 43 dB at 8 GHz of PVDF/G-D-GQDsAg nanocomposite, due to increase in electrical conductivity of PVDF/G-D-GQDsAg nanocomposite and enhanced dispersion of G-D-GQDsAg in PVDF matrix. The incorporation of G-D-GQDs and G-D-GQDsAg in PVDF matrix also increases the thermal stability and crystallinity of PVDF. The increase in thermal stability and crystallinity are more for PVDF/G-D-GQDsAg nanocomposite as compare to PVDF/G-D-GQDs nanocomposite, due to better dispersion of G-D-GQDsAg in PVDF matrix. Thus, PVDF/G-D-GQDsAg nanocomposite having high SE_T value can shield 99.9% of electromagnetic radiation in X-band range, which make it suitable for EMI shielding application for consumer electronic equipment’s.     

Influence of covalent and non-covalent modification of graphene on the mechanical,thermal and electrical properties of epoxy/graphene nanocomposites: a review

Abstract

Graphene is emerged as a highly sought after reinforcing filler for epoxy matrix in view of its superior electrical, mechanical and thermal properties. Dispersion of low concentration of graphene can significantly enhance the epoxy/graphene nanocomposites properties. Dispersion of graphene in epoxy matrix depends on processing protocols used, and interfacial interaction between epoxy matrix and graphene. Interfacial interaction between epoxy matrix and graphene can be achieved by covalent and non-covalent modification of graphene. This paper comprehensively review the influence of different processing protocols adopted for the processing of epoxy/graphene nanocomposites, and its effect on mechanical, thermal and electrical properties. In addition, covalent and non-covalent strategies adopted for modification of graphene, and its influence on mechanical, thermal and electrical properties of epoxy/graphene nanocomposites are extensively discussed. The future challenges associated with graphene reinforced epoxy nanocomposites processing have been discussed.     

Effect of Surface Structure of Nano-CaCO3 Particles on Mechanical and Rheological Properties of PVC Composites

To study the effect of different surface structures on resultant mechanical and rheological properties, nano-CaCO₃ particles were treated with isopropyl tri-stearyl titanate (H928), isopropyl tri-(dodecylbenz-enesulfonyl) titanate (JN198), and isopropyl tri-(dioctylpyrophosphato) titanate (JN114). Scanning electron microscopy (SEM) and dynamic mechanic analysis (DMA), carried out to characterize the effective interfacial interaction between the nano-CaCO₃ particles and a poly(vinyl chloride) (PVC) matrix, indicated that JN114 treated nano-CaCO₃ particles had the strongest interfacial interaction with a PVC matrix, while H928 treated nano-CaCO₃ had the weakest. The rheological and mechanical properties of PVC/nano-CaCO₃ composites were investigated as a function of surface structure and filler volume fraction. The tensile yield stress and elongation at break decreased with the increasing of calcium carbonate content while tensile modulus increased. PVC filled with JN114 treated nano-CaCO₃ had the highest tensile modulus and tensile yield stress, while those filled with H928 treated nano-CaCO₃ had the highest elongation at break at the same filler content. The impact strength of PVC/nano-CaCO₃ composites increased with the increasing of CaCO₃ content, and PVC composites filled with JN198 treated nano-CaCO₃ particle had a higher impact strength than those with JN114 or H928 treated, with the value reaching 23.9 ± 0.7 kJ/m² at 11 vol% CaCO₃, four times as high as that of pure PVC. Rheological properties indicated that a suitable interfacial interaction and a good dispersion of inorganic filler in a PVC matrix could reduce the viscosity of PVC/nano-CaCO₃ composites. The interfacial interaction was quantitatively characterized by semiempirical parameters calculated from the tensile strength of PVC/nano-CaCO₃ composites to confirm the results from the SEM and DMA experiments.     

Rheological Behaviors of Poly(Vinylidene Fluoride)/“Bud-Branched” Nanotubes Nanocomposites

Bud-branched nanotubes, fabricated by growing metal particles on the surfaces of multiwall carbon nanotubes (MWCNTs), were used to prepare poly(vinylidene fluoride) (PVDF)-based nanocomposites. The melt viscoelastic behaviors of PVDF and its nanocomposites were characterized. The results showed that the introduction of both the MWCNTs and bud-branched nanotubes (MWCNTs-B) increased the storage modulus, loss modulus, and complex viscosity of the nanocomposites. However, the bud-branched nanotubes were more efficient to increase the elasticity than the MWCNTs that have relatively smooth surfaces. In particular, it was observed that the bud-branched nanotubes caused an increase of normal force and crossover modulus, while for MWCNTs, no variation in the normal force and a decrease of the crossover modulus were observed.     

Crystallization,Flame Retardancy and Mechanical Properties of Poly(Butylene Terephthalate)/Brominated Epoxy/Nano-Sb2O3 Composites Dispersed By High Energy Ball Milling

Nano-Sb2O3 particles and brominated epoxy resin (BEO) powders were dispersed in poly (butylene terephthalate) (PBT) by high energy ball milling (HEBM). Then the nanocomposites were prepared by a twin screw extruder. The influence of the nano-Sb2O3 particles on the crystallization, thermal stability, flame retardancy and mechanical properties of the PBT/BEO/nano-Sb2O3 composites were investigated by X-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), limiting oxygen index (LOI), UL-94 tests and scanning electron microscopy (SEM). The results showed that the nano-Sb2O3 particles improved the crystallizability, thermal stability and flame retardancy properties of the PBT/BEO/nano-Sb2O3 composites. When the content of nano-Sb2O3 particles was 2.0?wt%, the LOI of nano-Sb2O3/BEO/PBT composites increased from 22.0 to 27.8 and the tensile strength reached its maximum value (62.44?MPa), which indicated that the optimum value of flame retardancy and mechanical properties of PBT/BEO/nano-Sb2O3 composites were obtained.     

Resistive switching behaviors of Cu/TaOx/TiN device with combined oxygen vacancy/copper conductive filaments

Forming-free and self-compliant bipolar resistive switching is observed in Cu/TaO_x/TiN conductive bridge random access memory. Generally, Pt has been investigated as an inert electrode. However, Pt is not desirable material in current semiconductor industry for mass production. In this study, all electrodes are adapted to complementary metal-oxide-semiconductor compatible materials. The self-compliant resistive switching is achieved via usage of TiN bottom electrode. Also, dissolved Cu ions in TaO_x lead to forming-free resistive switching behavior. The resistive switching mechanism is formation and rupture of combined oxygen vacancy/metallic copper conductive filament. We propose that Cu/TaO_x/TiN is a promising candidate for a conductive bridge random access memory structure.     

Electrical characterization of Schottky diodes based on boron doped homoepitaxial diamond films by conducting probe atomic force microscopy

A large planar tungsten carbide (WC) Schottky diode on p-type homoepitaxial diamond was mainly investigated on a microscopic level by atomic force microscopy (AFM) and conducting probe atomic force microscopy (CP-AFM), allowing simultaneous topographic and local electrical resistance imaging measurements. These techniques revealed the existence of a specific microstructure on the WC Schottky contact consisting of electrically insulating islands surrounded by conductive paths. The islands are found to be insulating in the whole range of explored bias [−5 V, +5 V], whereas the current flowing between the islands is 1000 times lower at a reverse bias of −5 V than at a forward bias of +5 V, in agreement with the rectifying ratio found from macroscopic current–voltage (I–V) measurements. CP-AFM provides a prospective imaging tool which is well suited for analyzing the local electrical properties and instabilities of Schottky junctions.     

Extrinsic Magnetoelectricity in Barium Titanate/Nickel Nanocomposites: Effect of Compaction Pressure on Interfacial Anisotropy

The dynamic control of the dielectric response in magnetoelectric (ME) nanocomposites (NCs) renders an entire additional degree of freedom to the functionality of miniaturized magnetoelectronics and spintronics devices. In composite materials, the ME effect is realized by using the concept of product properties. Through the investigation of the microwave properties of a series of BaTiO₃/Ni NCs fabricated by compaction of nanopowders, we present experimental evidence that the compaction (uniaxial) pressure in the range of 33–230 MPa significantly affects the ME features. We report here data for only one composition (17.1 vol.% of Ni in the BaTiO₃/Ni NC sample). Our findings revealed that the ME coupling coefficient exhibits a large enhancement for specific values of the Ni volume fraction and compaction pressure. Overall, these observations are considered to be evidence of stress-induced microstructural changes under pressure that strongly affect the elastic interaction between the magnetostrictive and piezoelectric phases in these NCs. These results have a potential technological impact for designing precise tunable ME NCs for microwave devices such as tunable phase shifters, resonators, and delay lines.     

Structure of trans-1,4-polybutadiene synthesized with a new catalyst system

Abstract

The structure, phase composition, and temperature behavior of two trans-1,4-polybutadienes (TPBs) were studied by means of x-ray scattering and differential scanning calorimetry (DSC) techniques. The two samples examined were (1) PB synthesized using an immobilized titanium-magnesium catalyst and (2) a random copolymer based on PB prepared with a homogeneous vanadium-containing catalyst used as a reference material. It was found that the nascent structure of the first PB involves three phases: crystalline, mesomorphic (low-temperature form), and amorphous. In the vicinity of 65°C, a first-order phase transition occurs. The system becomes biphasic and contains the high-temperature form of the mesophase, as well as the amorphous phase, component. Above 165°C, the polymer melts to form a single-phase isotropic melt with a structure typical of liquids. The lateral dimension of crystallites reversibly changes at the crystal-mesophase transition. It is suggested that during annealing of the mesophase formed by cooling of the isotropic melt, the chains acquire an extended conformation. Loss of regularity of the structure of macromolecules of TPB causes a reduction of phase transition temperatures, an increase of the imperfection of the crystalline phase, and a contraction of the temperature range of existence of the mesophase.