Fabrication and characteristics of graphene‐reinforced silver nanowire/polybenzoxazine/epoxy copolymer composite thin films

In this study, composite thin films were fabricated by mixing one‐dimensional silver nanowires (AgNWs) with graphene, polybenzoxazine (PBZ) and epoxy. Their electrical and thermal properties under different environmental conditions were investigated. The AgNWs were prepared by a polyol reduction method using ethylene glycol as a reducing agent and polyvinylpyrrolidone as a soft template to reduce silver ions. High aspect ratio AgNWs were then mixed into polymer matrices to allow them to form electrical and thermal conductive paths. Next, a trace amount of graphene was added into the nanocomposites in order to enhance their electrical and thermal properties. The results showed that the addition of graphene and AgNWs improved the threshold leakage current, and a 33% increase in thermal diffusivity was observed. The water resistance and gas barrier properties of PBZ and graphene effectively improved the thermal oxidation stability, and a 200% increase in electrical conductivity was achieved after 120 h of thermal oxidation treatment. A considerable difference was observed between the moduli of epoxy and PBZ. Hardness and phase analyses using atomic force microscopy showed that material modulus mismatch occurred across the interface between the materials, triggering phonon scattering. However, the increase in thermal conductivity was not significant for either material. © 2018 Society of Chemical Industry     

Large-area reduced graphene oxide thin film with excellent thermal conductivity and electromagnetic interference shielding effectiveness

In this work, we fabricated reduced large-area graphene oxide (rLGO) with maximum surface area of 1592 μm² through a cost-effective chemical reduction process at low temperature. The product revealed large electrical conductivity of 243 ± 12 S cm⁻¹ and thermal conductivity of 1390 ± 65 W m⁻¹ K⁻¹, values much superior to those of a conventional reduced small-area graphene oxide (with electrical conductivity of 152 ± 7.5 S cm⁻¹ and thermal conductivity of 900 ± 45 W m⁻¹ K⁻¹). The rLGO thin film also exhibited not only excellent stiffness and flexibility with Young’s modulus of 6.3 GPa and tensile strength of 77.7 MPa, but also an efficient electromagnetic interference (EMI) shielding effectiveness of ∼20 dB at 1 GHz. The excellent performance of rLGO is attributed to the fact that the larger area LGO sheets include much fewer defects that are mostly caused by the damage of graphene sp² structure around edge boundaries, resulting in large electrical conductivity. The manufacturing process of rLGO is an economical and facile approach for the large scale production of highly thermally conducting graphene thin films with efficient EMI shielding properties, greatly desirable for future portable electronic devices.     

Enhancement of electrical and thermal conductivity of Su-8 photocrosslinked coatings containing graphene

Graphene platelets were dispersed into photocurable SU-8 resin. A strong increase of the T_g value as a function of the graphene content was observed and attributed to a mobility hindering effect on the polymeric chains caused by the graphene filler. A significant increase of electrical conductivity is achieved for composites containing functionalized graphene sheets (FGS) between 3 and 4 wt%. The thermal diffusivity of the polymer was observed to increase as a function of filler content in the nanocomposites confirming the conducting nature of the polymeric coating with incorporation of graphene.     

Highly electrically and thermally conductive silicon carbide-graphene composites with yttria and scandia additives

Dense silicon carbide/graphene nanoplatelets (GNPs) and silicon carbide/graphene oxide (GO) composites with 1 vol.% equimolar Y₂O₃–Sc₂O₃ sintering additives were sintered at 2000 °C in nitrogen atmosphere by rapid hot-pressing technique. The sintered composites were further annealed in gas pressure sintering (GPS) furnace at 1800 °C for 6 h in overpressure of nitrogen (3 MPa). The effects of types and amount of graphene, orientation of graphene sheets, as well as the influence of annealing on microstructure and functional properties of prepared composites were investigated. SiC-graphene composite materials exhibit anisotropic electrical as well as thermal conductivity due to the alignment of graphene platelets as a consequence of applied high uniaxial pressure (50 MPa) during sintering. The electrical conductivity of annealed sample with 10 wt.% of GNPs oriented parallel to the measuring direction increased significantly up to 118 S·cm⁻¹. Similarly, the thermal conductivity of composites was very sensitive to the orientation of GNPs. In direction perpendicular to the GNPs the thermal conductivity decreased with increasing amount of graphene from 180 W·m⁻¹ K⁻¹ to 70 W·m⁻¹ K⁻¹, mainly due to the scattering of phonons on the graphene – SiC interface. In parallel direction to GNPs the thermal conductivity varied from 130 W·m⁻¹ K⁻¹ up to 238 W·m⁻¹ K⁻¹ for composites with 1 wt.% of GO and 5 wt.% of GNPs after annealing. In this case both the microstructure and composition of SiC matrix and the good thermal conductivity of GNPs improved the thermal conductivity of composites.     

Polymer-stabilized graphene dispersions at high concentrations in organic solvents for composite production

We demonstrate a simple and effective technique for dispersing pristine (unfunctionalized) graphene at high concentrations in a wide range of organic solvents by use of a stabilizing polymer (polyvinylpyrrolidone, PVP). These polymer-stabilized graphene dispersions are shown to be highly stable and readily redispersible even after freeze-drying. This technique yields significantly higher graphene concentrations compared to prior studies. An excellent increase in the thermal conductivity of the fluid by the addition of pristine graphene is also demonstrated. These well-dispersed pristine graphene sheets were then used as a strong and conductive nano-filler for polymer composites. Graphene/PVP composites were produced by the bulk polymerization of N-vinylpyrrolidone loaded with dispersed graphene, resulting in excellent load transfer and improved mechanical and electrical properties.     

Thermal ageing of electrical conductivity in carbon nanotube/polyaniline composite films

The influence of carbon nanotubes on the thermal ageing effect of the electrical conductivity of composite thin films is presented. The composite thin films comprise carbon nanotube/polyaniline nanofibers. When subject to thermal treatment, the presence of nanotubes retards the loss of dopants from the polyaniline and enhances the thermal stability in electrical conductivity of the composite thin films. Specifically, an increase in temperature for the conductivity degradation and a significant reduction in the rate of the conductivity degradation of the composite thin films are observed. Upon prolonged heating, the composite thin films exhibit relative large conductivity at high nanotube content, while the polyaniline thin films become insulating.     

Electromagnetic interference shielding behavior of chemically and thermally reduced graphene based multifunctional polyurethane nanocomposites: A comparative study

This article presents the effect of exfoliation, dispersion, and electrical conductivity of graphene sheets onto the electrical, electromagnetic interference (EMI) shielding, and gas barrier properties of thermoplastic polyurethane (TPU) based nanocomposite films. The chemically reduced graphene (CRG) and thermally reduced/annealed graphene (TRG) having Brunauer–Emmett–Teller surface areas of 18.2 and 159.6 m²/g, respectively, when solution blended with TPU matrix using N,N-dimethylformamide as a solvent. Graphene sheets based TPU nanocomposites have been evaluated and compared for EMI shielding in Ku band, electrical conductivity, and gas barrier property. TRG/TPU nanocomposite films showed excellent gas barrier against N₂ gas as compared to CRG/TPU. The EMI shielding effectiveness for neat CRG and TRG graphene sheets is found to be −80, −45 dB, respectively, at 2 mm thickness. The EMI shielding data revealed that TRG/TPU nanocomposites showed better shielding at lower concentration (10 wt %), while CRG displayed better attenuation at higher concentrations. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47666.     

Mechanically robust,electrically and thermally conductive graphene-based epoxy adhesives

This study develops a facile approach to fabricate adhesives consists of epoxy and cost-effective graphene platelets (GnPs). Morphology, mechanical properties, electrical and thermal conductivity, and adhesive toughness of epoxy/GnP nanocomposite were investigated. Significant improvements in mechanical properties of epoxy/GnP nanocomposites were achieved at low GnP loading of merely 0.5?vol%; for example, Young’s modulus, fracture toughness (K_1C) and energy release rate (G_1C) increased by 71%, 133% and 190%, respectively compared to neat epoxy. Percolation threshold of electrical conductivity is recorded at 0.58?vol% and thermal conductivity of 2.13?W m^?1 K^?1 at 6?vol% showing 4 folds enhancements. The lap shear strength of epoxy/GnP nanocomposite adhesive improved from 10.7?MPa for neat epoxy to 13.57?MPa at 0.375?vol% GnPs. The concluded results are superior to other composites or adhesives at similar fractions of fillers such as single-walled carbon nanotubes, multi-walled carbon nanotubes or graphene oxide. The study promises that GnPs are ideal candidate to achieve multifunctional epoxy adhesives.     

Flexible conductive graphene/poly(vinyl chloride) composite thin films with high mechanical strength and thermal stability

The fabrication and characterization of ultrathin composite films of surfactant-wrapped graphene nanoflakes and poly(vinyl chloride) is described. Free-standing composite thin films were prepared by a simple solution blending, drop casting and annealing route. A significant enhancement in the mechanical properties of pure poly(vinyl chloride) films was obtained with a 2 wt.% loading of graphene, such as a 58% increase in Young’s modulus and an almost 130% improvement of tensile strength. Thermal analysis of the composite films showed an increase in the glass transition temperature of the polymer, which confirms their enhanced thermal stability. The composite films had very low percolation threshold of 0.6 vol.% and showed a maximum electrical conductivity of 0.058 S/cm at 6.47 vol.% of the graphene loading.     

Flexible cellulose composite film incorporated by carbon nitride@graphene oxide prepared by a “compressed-aerogel” approach for efficient thermal management

Heat dissipation films originating from polymer composite with improved thermal conductivity are becoming potential candidates for effective thermal management of next-generation electronic products, profiting from their soft nature and good electrical insulation. In this work, a novel hybrid filler composed of carbon nitride (C₃N₄) and graphene oxide (GO) is synthesized and further introduced into the cellulose matrix. The electrical insulation of the composite is maintained, attributed to the low electrical conductivity of C₃N₄. Meanwhile, the bridged chemical bond between C₃N₄ and GO reduces the interfacial thermal resistance and promotes heat transfer. By hot-pressing the aerogel intermediate, the directional arrangement of fillers is achieved, leading to favorable flexibility and mechanical behavior, and superior in-plane thermal conductivity (5.74 W/mK) of the composite. Thermal characterizations reveal that lower thermal contact resistance (TCR), improved thermal stability, and the relatively lower coefficient of thermal expansion (CTE) together facilitate its practical application in thermal management. The practical performance test is also performed which fully demonstrates its favorable temperature regulation ability, reflected by a 2.7 °C temperature decrement observed in the cell phone battery heat dissipation test.     

Electrical ac and dc behavior of epoxy nanocomposites containing graphene oxide

This article deals with the investigation of electrical properties of epoxy‐based nanocomposites containing graphene oxide nanofillers dispersed in the polymer matrix through two‐phase extraction. Broadband dielectric spectroscopy and dc electrical conductivity as a function of electric field have been evaluated in specimens containing up to 0.5 wt % of nanofiller. Nanocomposites containing pristine graphene oxide do not show significant changes of electrical properties. On the contrary, the same materials after a proper thermal treatment at 135°C, able to provoke the in situ reduction of graphene oxide, exhibit higher permittivity and electrical conductivity, without showing large decrease of breakdown voltage. Moreover, a nonlinear behavior of the electrical conductivity is observed in the range of electric fields investigated, i.e. 2–30 kV mm^?1. A new relaxation phenomenon with a very low temperature dependence is also evidenced at high frequency in reduced graphene oxide composites, likely associated to induced polarization of electrically conductive nanoparticles. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41923.     

Improving electrical conductivity and wear resistance of hafnium nitride films via tantalum incorporation

Transition metal nitrides are being widely applied, as durable sensors, semiconductor and superconductor devices, their electrical conductivity and wear resistance having a significant influence on these applications. However, there are few reports about how to improve above properties. In this paper, tantalum was incorporated into hafnium nitride films through Hf_1-xTa_xN_y [x=Ta/(Hf+Ta), y=N/(Hf+Ta)] solid solution. The electrical conductivity and wear resistance of the films were significantly improved, due to the increase of the electron concentration (tantalum has one more valence electron than hafnium) and the increase in H/E and H³/E² ratios caused by the effect of solid solution hardening, respectively. The highest electrical conductivity of Hf_1-xTa_xN_y films is 8.3×10⁵ S m⁻¹, which is 1.7 times and 5.2 times of that of hafnium nitride and tantalum nitride films, respectively. In addition, the lowest wear rate of films is 1.2×10⁻⁶ mm³/N m, which is only 10% and 48% of that of hafnium nitride and tantalum nitride films, respectively. These results indicate that alloying with another transition metal is an effective method to improve electrical conductivity and wear resistance of transition metal nitrides.     

The manufacturing and properties of a nano-laminate derived from graphene powder

The work presents a method of consolidation of graphene flakes (platelets) into a bulk material showing high anisotropy of thermal, electrical and mechanical properties. Such materials can be used as directional high-temperature thermal insulators similar to graphite foils, but due to much finer microstructure they may exhibit different, possibly enhanced properties. The graphene flakes were consolidated by a filter pressing of propanol suspension followed by a hot-pressing of produced green bodies at 2200 °C under 25 MPa in a protective atmosphere.The hot-pressing step was necessary to force orientation of the flakes and to densify the material. Microstructural observations, mechanical strength and elastic properties assessment, as well as thermal and electrical properties analysis were performed. Scanning electron microscopy revealed that microstructure of the material consisted of highly-oriented layers of the graphene flakes. It resulted in a distinct anisotropy of thermal conductivity (360 vs. 3 W/mK), coefficient of thermal expansion (25·10⁻⁶ vs. −1·10⁻⁶ 1/K) and electrical resistivity (60·10⁻⁶ vs. 850·10⁻⁶ Ω m) of the material in the in-plane and through plane direction, respectively. The material showed brittle behavior, but it could be machined.     

Development of Ethylene‐Vinyl Acetate Composites Reinforced with Graphene Platelets

Composites of ethylene‐vinyl acetate (EVA) reinforced with graphene platelets are fabricated. Morphological, thermal, mechanical, electrical properties as well as moisture absorption of the composites are characterized. Transmission electron microscopy shows a good dispersion of graphene platelets in the matrix. The unidirectional orientation of graphene platelets parallel to the surface of the composites is revealed by field emission scanning electron microscopy and is validated using the Halpin–Tsai model. Tensile strength and elongation of the composites are respectively improved by 109 and 83%, after the addition of 3 wt% graphene platelets. The incorporation of 5 wt% graphene platelets enhances the char residue of the composites from 0.544% for pure EVA to 6.63% for the composites. The electrical conductivity of the composite with 3 wt% graphene platelets is two orders of magnitude higher than that of pure EVA with 10⁻¹³ S cm^–1 electrical conductivity.

     

Thermal,mechanical and electrical properties of hard B4C,BCN, ZrBC and ZrBCN ceramics

We study the thermal, mechanical and electrical properties of B₄C, BCN, ZrBC and ZrBCN ceramics prepared in the form of thin films by magnetron sputtering. We focus on the effect of Zr_x(B₄C)_1−x sputter target composition, the N₂+Ar discharge gas mixture composition, the deposition temperature and the annealing temperature after the deposition. The thermal properties of interest include thermal conductivity (observed in the range 1.3–7.3 W m⁻¹ K⁻¹), heat capacity (0.37–1.6×10³ J kg⁻¹ K⁻¹ or 1.9–4.1×10⁶ Jm⁻³ K⁻¹), thermal effusivity (1.6–4.5×10³ J m⁻² s^−1/2 K⁻¹) and thermal diffusivity (0.38–2.6×10⁻⁶ m² s⁻¹). We discuss the relationships between materials composition, preparation conditions, structure, thermal properties, temperature dependence of the thermal properties and other (mechanical and electrical) properties. We find that the materials structure (amorphous×crystalline hexagonal ZrB₂-like×nanocrystalline cubic ZrN-like), more than the composition, is the crucial factor determining the thermal conductivity and other properties. The results are particularly important for the design of future ceramic materials combining tailored thermal properties, mechanical properties, electrical conductivity and oxidation resistance.     

Assembly and benign step-by-step post-treatment of oppositely charged reduced graphene oxides for transparent conductive thin films with multiple applications

We report a new approach for the fabrication of flexible and transparent conducting thin films via the layer-by-layer (LbL) assembly of oppositely charged reduced graphene oxide (RGO) and the benign step-by-step post-treatment on substrates with a low glass-transition temperature, such as glass and poly(ethylene terephthalate) (PET). The RGO dispersions and films were characterized by means of atomic force microscopy, UV-visible absorption spectrophotometery, Raman spectroscopy, transmission electron microscopy, contact angle/interface systems and a four-point probe. It was found that the graphene thin films exhibited a significant increase in electrical conductivity after the step-by-step post-treatments. The graphene thin film on the PET substrate had a good conductivity retainability after multiple cycles (30 cycles) of excessively bending (bending angle: 180°), while tin-doped indium oxide (ITO) thin films on PET showed a significant decrease in electrical conductivity. In addition, the graphene thin film had a smooth surface with tunable wettability.     

Grain boundary engineered,multilayer graphene incorporated LaCoO3 composites with enhanced thermoelectric properties

Enhancement of thermoelectric properties by virtue of decreased electrical resistance through grain boundary engineering is realised in this study. A robust strategy of optimisation of the transport properties by tuning the energy filtering effects at the interfaces by decreasing the interfacial electrical resistance is achieved in LaCoO₃ (LCO). This is accomplished by the incorporation of multilayer graphene within the parent LCO matrix containing multi-scale nano/micro grains. The present work has attained a substantial increment in electrical conductivity from a value of 96 Scm^-1 for bare LCO to ～5300 Scm^-1 at 750 K by incorporating 0.08 wt% multilayer graphene in LCO. No significant change in thermal conductivity is observed due to the presence of multilayer graphene in LCO. A zT of 0.33 at 550 K for 0.08 wt% multi-layer graphene incorporated LCO composite is achieved which is the highest thermoelectric figure of merit value for undoped LCO reported until now.     

Enhancement of electrical and thermal conductivity of polypropylene by graphene nanoplatelets

One of disadvantages of polymer composites is poor electrical and thermal conductivity. As a first step in this direction, graphene‐modified polypropylene polymer is being developed to improve its electrical and thermal conductivity. Two techniques were investigated: surface coating and extrusion. In the case of coating technique, the percolation threshold was found to be 0.5 wt % of graphene and electrical conductivity of polypropylene increased around 13 log cycles. Coating technique breaks the agglomerations due to magnetic stirring followed by sonication and gives homogeneous graphene‐coated polypropylene pellets. When polymer melts under compression molding, the graphene platelets network formed on the surface of polypropylene pellets as well as through‐the‐thickness of the molded disk, which provide continuous network of graphene. However, in extrusion technique, graphene segregated and did not disperse properly in polypropylene. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45833.     

Pressureless sintering of multilayer graphene reinforced silicon carbide ceramics for mechanical seals

ABSTRACT

The silicon carbide (SiC) ceramics containing multilayer graphene derived from graphite exfoliation were successfully prepared by pressureless sintering, and the effect of graphene content on the sintering behaviours, microstructure, mechanical, tribological, electrical and thermal properties was investigated in detail. The bulk density, bending strength and hardness of the composite ceramics gradually decrease with the increase of graphene content, but the friction, conductance and thermal conductance properties are improved obviously. When the graphene content reaches 5?wt-%, the dry friction coefficient of 0.22, electrical conductivity of 2724.14 S?1?m?1 and thermal conductivity of 8.5?W?(m?1?K?1) can be obtained, indicating good comprehensive mechanical, tribological, electrical and thermal properties. This multilayer graphene reinforced silicon carbide ceramic is a promising seal material instead of SiC seal materials containing graphite to be applied in next-generation mechanical seals.     

Characterization of optical,thermal and electrical properties of SWCNTs/PMMA nanocomposite films

The optical, thermal and electrical behavior of single-wall carbon nanotubes (SWCNTs)/poly(methyl methacrylate) (PMMA) composite are studied as a function of SWCNTs concentration. The nanocomposites were prepared in the form of films by solution casting technique. The concentrations of SWCNTs in SWCNTs/PMMA films were 0, 0.5, 1, 1.5, 2, 3.5, 5, 7.5, and 10 wt%. High-resolution transmission electron microscopy showed that SWCNTs doped in PMMA is less fragmented as compared to the powder SWCNTs. This is due to the interactions with polymers as well as the fabrication method. X-ray diffraction patterns of SWCNTs/PMMA composite films indicated that there is no covalent interaction between SWCNTs and PMMA. In addition, it demonstrates a homogeneous dispersion of SWCNTs in PMMA matrix. The optical properties of SWCNTs/PMMA films of SWCNTs concentration from 0 to 2.0 wt% have shown that the absorption intensity of the composite was enhanced ≈8.5 times as compared to the plain PMMA. Photoacoustic spectroscopy technique was used as a powerful and non-destructive tool to determine the thermal diffusivity (α), thermal effusivity (e) and thermal conductivity (k). The composites exhibited ≈160 % improvement in k at 2.0 wt%. Furthermore, the DC electrical conductivity measurements of SWCNTs/PMMA showed that the percolation threshold value was about 2.0 wt% of SWCNTs loading.