Mechanical and electrical properties of carbon nanotube buckypaper reinforced silicon carbide nanocomposites

The nanocomposite was produced via phenolic resin infiltrating into a carbon nanotube (CNT) buckypaper preform containing B₄C fillers and amorphous Si particles followed by an in-situ reaction between resin-derived carbon and Si to form SiC matrix. The buckypaper preform combined with the in-situ reaction avoided the phase segregation and increased significantly the volume fraction of CNTs. The nanocomposites prepared by this new process were dense with the open porosities less than 6%. A suitable CNT–SiC bonding was achieved by creating a B₄C modified interphase layer between CNTs and SiC. The hardness increased from 2.83 to 8.58 GPa, and the indentation fracture toughness was estimated to increase from 2.80 to 9.96 MPa m^1/2, respectively, by the reinforcing effect of B₄C. These nanocomposites became much more electrically conductive with high loading level of CNTs. The in-plane electrical resistivity decreased from 124 to 74.4 μΩ m by introducing B₄C fillers.     

Microstructure and physicomechanical properties of pressureless sintered multiwalled carbon nanotube/alumina nanocomposites

Multiwalled carbon nanotube (MWCNT)/alumina (Al₂O₃) nanocomposites containing CNT from 0.15 vol.% to 2.4 vol.% have been successfully fabricated by simple wet mixing of as-received commercial precursors followed by pressureless sintering. Extent of densification of nanocomposites sintered at low temperature (e.g. 1500 °C) was <90%, but increased up to ∼99% when sintered at 1700 °C and offered superior performance compared to pure Al₂O₃. Nanocomposites containing 0.3 vol.% MWCNT and sintered at 1700 °C for 2 h in Argon led to ∼23% and ∼34% improvement in hardness and fracture toughness, respectively, than monolithic Al₂O₃. In addition, the highest improvement (∼20%) in bending strength was obtained for 0.15 vol.% MWCNT/Al₂O₃ nanocomposite compared to pure Al₂O₃. Weibull analysis indicated reliability of nanocomposites increased up to 0.3 vol.% MWCNT, whereas, beyond that loading consistency was the same as obtained for pure Al₂O₃. Detailed microstructure and fractographic analysis were performed to assess structure-property relationship of present nanocomposites.     

Remarkable improvement in tribological behavior of plasma sprayed carbon nanotube and graphene nanoplatelates hybrid reinforced alumina nanocomposite coating

Addition of 0.5?wt% of graphene nanoplatelates (GNPs) and 1?wt% carbonnanotube (CNTs) in plasma sprayed Al₂O₃ coating showed the reduction of 93.25% in wear volume loss and 90.94% in wear rate. This could be attributed to the simultaneous effect of enhanced densification, presence of the transferred layer from the counterpart, strong interface between Al₂O₃, GNP and CNTs and toughening offered by the GNPs and CNTs. The lowest COF value of 0.27 was recorded on addition of 0.5?wt% of GNP in Al₂O₃ coating, which could be attributed to the graphitic lubrication on the worn track during the wear.     

Mechanical properties and electrical conductivity in a carbon nanotube reinforced silicon nitride composite

The influence of carbon nanotubes (CNTs) addition on basic mechanical, thermal and electrical properties of the multiwall carbon nanotube (MWCNT) reinforced silicon nitride composites has been investigated. Silicon nitride based composites with different amounts (1 or 3 wt%) of carbon nanotubes have been prepared by hot isostatic pressing. The fracture toughness was measured by indentation fracture and indentation strength methods and the thermal shock resistance by indentation method. The hardness values decreased from 16.2 to 10.1 GPa and the fracture toughness slightly decreased by CNTs addition from 6.3 to 5.9 MPa m^1/2. The addition of 1 wt% CNTs enhanced the thermal shock resistance of the composite, however by the increased CNTs addition to 3 wt% the thermal shock resistance decreased. The electrical conductivity was significantly improved by CNTs addition (2 S/m in 3% Si₃N₄/CNT nanocomposite).     

Electrical conductivity of chemically modified multiwalled carbon nanotube/epoxy composites

The electrical conductivity of oxidized multiwalled carbon nanotubes (MWNT)/epoxy composites is investigated with respect to the chemical treatment of the MWNT. The oxidation is carried out by refluxing the as-received MWNT in concentrated HNO₃ and H₂O₂/NH₄OH solutions, respectively, under several different treatment conditions. The oxidized MWNT are negatively charged and functionalized with carboxylic groups by both solutions. The MWNT oxidized under severe conditions are well purified, but their crystalline structures are partially damaged. It is recognized that the damage to the MWNT has considerable influence on the electrical properties of the MWNT composites, causing the electrical conductivity to be lowered at a low content of MWNT and the percolation threshold to be raised. The MWNT oxidized by the mixture of H₂O₂ and NH₄OH solution provides epoxy composites with a higher conductivity than those produced with the MWNT oxidized by nitric acid over the whole range of MWNT, independently of the oxidation conditions.     

The effect of nano-size additives on the electrical conductivity of matrix suspension and properties of self-flowing low-cement high alumina refractory castables

Influence of two nano-size additives on electrical properties of suspension matrix of self-flowing low-cement high alumina refractory castable is investigated. For this purpose, castament FS 10 and FS 20 on the basis of polycarboxylate ether were considered. The self-flow value, workability and mechanical strength of the castable are evaluated and their relations with electrical conductivity are determined. Using these relations, the type and optimum amount of proper additive for these refractory castables are determined. It was shown that if the electrical conductivity of matrix suspension is less than 0.71 mS/cm, high alumina low-cement self-flowing refractory castable can be obtained. The best self-flow, sufficient working time and adequate mechanical strength in the castables are obtained with 0.08 wt.% FS 20.     

Nitrogen-doped-CNTs/Si3N4 nanocomposites with high electrical conductivity

Novel highly electrically conducting nanocomposites consisting of a silicon nitride (Si₃N₄) ceramic matrix containing up to 13.6 vol.% of nitrogen-doped multi-walled carbon nanotubes (CNx) were fabricated. As-synthesized CNx were treated with hydrogen peroxide in order to efficiently detach/isolate the nanotubes from bundles, then they were mixed with the ceramic powders and fully densified using the spark plasma sintering (SPS) technique. Composites containing 13.6 vol.% CNx reached an electrical conductivity of 2174 S m⁻¹ that is the highest value reported hitherto for carbon nanotubes/Si₃N₄ nanocomposites. The nitrogen doping also favored a strong mechanical interlocking between the nanotubes and the Si₃N₄ matrix; when compared to the undoped carbon nanotubes. These novel nanocomposites could be used in devices associated to power generation or telecommunications.     

Microstructure and electrical conductivity of NiO–YSZ nano-powder synthesized by aerosol flame deposition

The aerosol flame deposition (AFD) process was capable of producing mixed metal oxide powders with 10–500 nm size from low-cost liquid precursors. The nickel oxide–yttria stabilized zirconia (NiO–YSZ) powders used as an anode of SOFC has been synthesised by using AFD process. It was demonstrated that this process is suitable for fabricating the nano-sized and spherical NiO–YSZ particles capable of enhancing three phase boundary areas. The synthesis process was studied by changing processing parameters such as the concentration and the composition ratio of the precursor solution and the flow rates of the flame gases. The sufficiently crystallized and spherically shaped NiO–YSZ particles were synthesized successfully and the size distribution was bimodal when observed by TEM. As changing contents of Ni and YSZ, the conductivities of NiO–YSZ pellet exhibited a typical mixed conductor behaviour of which the ionic conduction is in high temperature range and the electronic conduction is in lower temperature range.     

Strong and ultra-flexible polymer-derived silicon carbonitride nanocomposites by aligned carbon nanotubes

We report the synthesis of flexible ceramic composites with a high tensile strength (536.33±7.23 MPa) using carbon nanotube sheet aligned by mechanically stretching process. The process is based on the infiltration and pyrolysis of liquid ceramic precursor into aligned carbon nanotube sheet. Mechanical properties and microstructure of the resultant composites are investigated. The resultant nanocomposites maintain well-aligned carbon nanotube morphology with high volume fraction (60%) and long pullout (15 µm), contributing to a high degree of load-transfer efficiency and toughening. Flexibility test reveals that such ceramic nanocomposites retain the original mechanical properties and microstructures after one thousand repetitions of 75% bending deformation, showing excellent compliance and durability. Applications requiring materials with high flexibility and mechanical properties can benefit from this research.     

Influence of carbon nanotubes on thermal and electrical conductivity of zirconia-based composite

Carbon nanotubes (CNTs) are widely used in ceramic-matrix composites (CMC) as a filler. An individual carbon nanotube exhibits extremely high thermal conductivity, however, the influence of CNTs on the thermal conductivity of CMCs is moderate. In contrast, even a small quantity of CNTs significantly increases the electrical conductivity of CMCs. The present paper studies this contradictory influence for ZrO₂-CNTs composites with 3, 5, 10 and 20 vol% multi-wall carbon nanotubes (MWCNTs). Their thermal and electrical conductivity was studied by the laser flash method and electrochemical impedance spectroscopy. The analysis reveals that the moderate influence of MWCNTs on the thermal conductivity of composites originates from the similar thermal conductivity of MWCNTs in a bundle and zirconia. On the other hand, the substantial difference in the electrical conductivity of MWCNTs and zirconia leads to an exponential increase in the electrical conductivity of the ZrO₂-CNTs composite even with small additions of nanotubes.     

Influence of oxygen ion enrichment on optical,mechanical, and electrical properties of LSCF perovskite nanocomposite

La_0.6Sr_0.4Co_0.2Fe_0.8O_3-δ (LSCF) is a mixed ionic electronic conductor with excellent surface catalytic activity for oxygen reduction. This work demonstrated that introduction of pure oxygen ion conductor to LSCF particles can significantly influence in-plane electronic conduction at the surface of LSCF-samarium-doped ceria (SDC) composite. The composite functional layer was prepared by mixing 50?wt% SDC particles with LSCF particles obtained from glycine–nitrate process. Homogeneous LSCF-SDC composite layer deposited by screen printing on an SDC substrate has been studied with and without LSCF current-collecting layer (CCL). The microstructural, optical, Raman, mechanical and electrical properties, and interfacial polarization resistance (R_p) of the prepared powders were evaluated. Results revealed that addition of oxygen ion conductor SDC exerted negligible effect on the phase structure and specific surface area but significantly influenced the band gap, oxygen vacancies, and electrical conductivity of LSCF. SDC addition significantly increased area specific resistance (ASR) of LSCF from 0.138?Ω?cm² to 0.481?Ω?cm² at 800?°C, thereby blocking the conduction path among LSCF particles. R_p value of LSCF-SDC composite can be improved by more than six times by enlarging the in-plane electronic conduction with thin CCL. Electrochemical measurement revealed that LSCF CCL reduced the R_p value, resulting in the lowest ASR of 0.087?Ω?cm² at 800?°C for the LSCF–SDC composite.     

Optical emission spectroscopy study of the influence of nitrogen on carbon nanotube growth

In-situ optical emission spectroscopy was used to systematically study the influence of nitrogen on the growth of carbon nanotubes (CNTs) by microwave-plasma enhanced chemical vapor deposition at different CH₄ concentrations in a CH₄/N₂ gas mixture. The results show that CN and C₂ co-exist in the plasma and emission intensities of the two species are correlated. The morphology and microstructure of the samples vary with the CH₄ concentration. Well aligned nanotubes are obtained at 20% CH₄. With the participation of N₂, the CNTs present a polymerized nanobell structure. More importantly, the length and thickness of each nanobell can be modulated by varying the CH₄ concentration. Without N₂, conventional cylindrical CNTs are obtained.     

Synthesis,structure and optical properties of x(CuO)/(1−x)Ni(OH)2 [x=0, 0.1 and 0.3] nanocomposites

The x(CuO)/(1−x)Ni(OH)₂ [x=0, 0.1 and 0.3] nanocomposites were prepared by the hydrothermal method in the presence of the surfactant polyethylenglycol-10000 (PEG-10000). X-ray diffraction (XRD), infrared (IR) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to characterize the as-prepared samples. The increase of the CuO content led to the increase of the crystallite size of both, the β-Ni(OH)₂ and the CuO. The increase in the crystallite size greatly affects the band gap energy of the as-prepared nanocomposites. The band gap energies of the x(CuO)/(1−x)Ni(OH)₂ nanocomposites were estimated by UV–vis spectroscopic method. UV–vis spectroscopic results showed an apparent decrease in the direct band gap energies. The x(CuO)/(1−x)Ni(OH)₂ [x=0, 0.1 and 0.3] nanocomposites show low band gap energies compared to the Ni(OH)₂ bulk materials. The enhanced optical properties lead to their possible use in photocatalytic and photovoltaic applications.     

Synergistic effect in structural and supercapacitor performance of well dispersed CoFe2O4/Co3O4 nano-hetrostructures

Herein, we report a facile homogeneous urea – assisted hydrothermal approach for the design of CoFe₂O₄/Co₃O₄ nano hetrostructure. A variation in Co concentration leads to smartly designed composite material namely CFC-11 and CFC-12 where CFC-12 appreciates the benefits of both CoFe₂O₄ and Co₃O₄ nanoparticles. The physico – chemical properties of as developed materials were investigated by X-ray diffraction (XRD), field emission electron microscopy (FE-SEM), high resolution transmission electron microscopy (HR-TEM), X-ray photoelectron microscopy (XPS) and Raman spectroscopy. The specific surface area and pore size distribution was determined by Brunauer-Emmett-Teller (BET) and Barrett-Joyner-Halendo (BJH) respectively. Magnetic measurements via. vibrating sample magnetometer (VSM) demonstrate that saturation magnetization decreases with the incorporation of Co₃O₄ antiferromagnetic nanoparticles. To explore the utility of as designed nano-hetrostructures as supercapacitor electrodes, we employed cyclic voltammetry (CV) and electrochemical impedence spectroscopy (EIS) measurements. A high specific capacitance of 761.1?F?g^?1 at 10?mV?s^?1, admirable cyclic durability of 92.2% and a low resistance value obtained from impedence measurements was observed for CFC-12. The favorable performance demonstrates the synergistic effect of CoFe₂O₄ and Co₃O₄ nanoparticles and thus promise an excellent material for energy storage devices.     

Dielectric relaxation and electrical conductivity in Ca5Nb4TiO17 ceramics

The temperature dependence of dielectric properties and electrical conduction of Ca₅Nb₄TiO₁₇ ceramics were characterized in a broad temperature range. A dielectric anomaly with strong frequency dispersion was detected in the temperature range 700–1010 °C. This dielectric relaxation could be almost removed completely by annealing in an oxidizing atmosphere. Complex impedance analysis confirmed the electrical inhomogeneity of the ceramics with different contributions from the bulk and grain boundaries. This suggests that the main mechanism for the observed relaxation is the Maxwell–Wagner polarization. ac conductivity results revealed the variation of conduction mechanism with increasing temperatures from localized hopping to long-range motion of the doubly ionized oxygen vacancies.     

Structural,optical, and electrical properties of cellulose/titanate nanosheets composite with enhanced protection against gamma irradiation

Two-dimensional (2D) materials have emerged as a promising functional filler in nanocomposites due to their unique anisotropy and resilience to harsh conditions. We report herein the use of Ti_0.91O₂ nanosheets as a protective component against γ-irradiation to cellulose paper. The titanate nanosheets were prepared via a sequence of solid-state synthesis of lepidocrocite-type Cs_0.7Ti_1.825O₄, proton exchange to H_0.7Ti_1.825O₄·H₂O, and exfoliation with tetrabutylammonium hydroxide. The nanosheets were incorporated into the commercial cellulose filter paper by a simple dip coating up to 0.6 mg cm⁻², equivalent to 10 wt% TiO₂. The nanosheets distribution was demonstrated by energy dispersive X-ray (EDX) mapping, synchrotron radiation X-ray tomographic microscopy (SRXTM), and atomic force microscopy (AFM). It is found that γ-irradiation (up to 50 kGy) destroyed the cellulose Iβ crystallinity of uncoated paper, but this is less pronounced in the cellulose/titanate nanosheets composite. This was also confirmed by the lack of a 235 nm-absorption characteristics of irradiation-induced decomposition product(s) in nanosheets-containing papers, which also exhibit UVA shielding property. The coated samples remained white while the uncoated ones were darkened with γ-irradiation. In addition, the nanosheets-coated papers showed dielectric permittivity, loss tangent, and AC conductivity which were invariant of the γ-dose, unlike those from the uncoated ones. Our work demonstrates the use of lead-free Ti_0.91O₂ nanosheets as a γ-shielding component to slow down/prevent structural, optical, and electrical properties damages in cellulose paper, which could extend to other nature-derived materials.     

Catalytic graphene formation in coal tar pitch- derived carbon structure in the presence of SiO2 nanoparticles

A simple and effective way to manufacture graphene from a coal tar pitch (CTP) is demonstrated. Silica (SiO₂) nanoparticles were used to modify the CTP as carbon precursor. A silica nanofiller introduced into the CTP matrix underwent carboreduction during heat treatment to 2000 °C, resulting in the formation of silicon carbide. Surfaces of SiC grains were sites for graphene formation. The influence of SiO₂ on the structure and microstructure of CTP- based carbon matrix, after annealing up to 2800 °C, was studied. Carbon samples were analyzed using X- ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and Raman Spectroscopy. Crystallite sizes (L_a, L_c) and interplanar distance (d₀₀₂) were determined. The presence of SiO₂ in CTP carbon precursor favored the crystallites’ growth in the ‘a′ crystallographic graphite direction, and inhibited their growth on the ‘c′ axis. The crystallites composing of graphene layers, were characterized by an elongated dimension in the ‘a′ axis direction. Above 2000 °C silicon carbide decomposed, followed by the sublimation of silicon from the carbon matrix.     

Low-temperature exfoliated graphene oxide incorporated with different types of natural rubber latex: Electrical and morphological properties and its capacitance performance

A simple with cost-effective method in the production and fabrication of graphene-based rubber nanocomposites as electrode materials is still remain a global challenge. In this work, we proposed one- and two-step approaches to fabricate an exfoliated graphene oxide (GO) as nanofiller in three different types of rubber latex polymer, namely, low ammonia natural rubber latex (NRL), radiation vulcanized NRL (RVNRL), and epoxy NRL 25 (ENRL 25). The electrical conductivity and capacitive behavior of nanocomposite samples were investigated under a four-point probe and cyclic voltammetry measurements, respectively. Meanwhile, the morphological properties were observed using field emission scanning electron microscopy, energy dispersive X-ray, optical polarization microscope, high-resolution transmission electron microscopy, Fourier-transform infrared spectroscopy, micro-Raman spectroscopy, and X-ray diffraction. The thermal stabilities of the nanocomposites were also investigated by thermogravimetric analysis. Among all, the GO/RVNRL polymer nanocomposite samples performed a better homogeneity with an improved electrical conductivity (~8.6 × 10⁻⁴ Scm⁻¹) as compared with the GO/ENRL 25 (~3.1 × 10⁻⁴ Scm⁻¹) and GO/NRL (~2.6 × 10⁻⁴ Scm⁻¹) polymer nanocomposite samples. In addition, the GO/RVNRL polymer nanocomposite electrodes showed acceptable specific capacitance (5 Fg^-1). The successfully fabricated conductive GO-based rubber nanocomposites are suitable for new supercapacitor electrodes.     

Effect of iodine incorporation on the electrical properties of amorphous conducting carbon films

In this work, the influence of iodine incorporation on the electrical properties of amorphous conducting carbon films, prepared by the vapor phase pyrolysis of maleic anhydride, is reported and discussed. X-ray diffraction (XRD) and scanning electron microscopy (SEM) studies reveal structural changes in the system. The anomalous behavior in the electrical properties of the intercalated system at low temperatures is investigated. The system shows a positive temperature coefficient of resistance (TCR) at low temperatures, which suggests reasons for the induced ordering of the system at low temperatures with the iodine incorporation. Also, a systematic increase in the conductivity of the sample is observed. The crossover temperature depends on the disorder in the system. The results indicate the possibility of metal-insulator (M-I) transition as a function of preparation temperature, iodine concentration and magnetic field.