Thermal property improvement of polytetrafluoroethylene nanocomposites with graphene nanoplatelets

Thermal properties including the crystallization behavior, thermal stability and thermal conductivity for a series of graphene nanoplatelet (GNP)–polytetrafluoroethylene (PTFE) nanocomposites were studied. The GNP–PTFE nanocomposites were fabricated via solvent-assisted blending followed by cold-pressing and sintering. The results indicated that the GNP–PTFE nanocomposites retained the good thermal stability of the PTFE matrix, and possessed better crystallization and much higher thermal conductivity than pure PTFE. The thermal conductivity of PTFE nanocomposites with a GNP mass fraction of 20% could reach 4.02 W (m K)⁻¹, which was increased by 1300% compared with pure PTFE. Additionally, a theoretical model was proposed to analyze the thermal conductivity of GNP–PTFE nanocomposites. It is demonstrated that adding GNPs into PTFE homogeneously can effectively improve the thermal properties of the nanocomposites.

Adding GNPs into PTFE can significantly improve the thermal properties of nanocomposites.     

The chemical functionalization of graphene nanoplatelets through solvent-free reaction

Graphene nanoplatelets (GNPs) were functionalized through 1,3-dipolar cycloaddition of azomethine ylide using a solvent-free approach and under different reaction conditions. The yield and the functionality of the carboxyl-terminated pyrrolidine ring attached on the surface of GNPs could be affected by varying the reaction temperature as well as the reactant to GNP weight ratio. The functionalized GNPs were characterized extensively using a range of spectroscopic and microscopy techniques.

Carboxyl-terminated pyrrolidine functionalized graphene nanoplatelets through a solvent-free reaction.     

NiCo alloy nanoparticles electrodeposited on an electrochemically reduced nitrogen-doped graphene oxide/carbon-ceramic electrode: a low cost electrocatalyst towards methanol and ethanol oxidation

In this work, nickel–cobalt alloy nanoparticles were electrodeposited on/in an electrochemically reduced nitrogen-doped graphene oxide (ErN-GO)/carbon-ceramic electrode (CCE) and the resulting nanocomposite (NiCo/ErN-GO/CCE) was evaluated as a low cost electrocatalyst for methanol and ethanol electrooxidation. Field-emission scanning electron microscopy coupled with energy dispersive X-ray spectroscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy were used for the physical characterization of the electrocatalyst. To study the electrochemical behavior and electrocatalytic activity of the prepared electrocatalyst towards the oxidation of methanol and ethanol in alkaline media, cyclic voltammetry, chronoamperometry and electrochemical impedance spectroscopy were utilized. Electrochemical investigation of the introduced electrocatalysts (NiCo alloy and Ni nanoparticles alone electrodeposited on/in different substrates) indicated that NiCo/ErN-GO/CCE has highest activity and stability towards methanol (J_p = 88.04 mA cm⁻²) and ethanol (J_p = 64.23 mA cm⁻²) electrooxidation, which highlights its potential use as an anodic material in direct alcohol fuel cells.

NiCo alloy nanoparticles on the electrochemically reduced nitrogen-doped graphene oxide/carbon-ceramic electrode: a low cost electrocatalyst towards methanol and ethanol oxidation.     

Boron carbide composites with highly aligned graphene nanoplatelets: light-weight and efficient electromagnetic interference shielding materials at high temperatures

B₄C-based ceramic composites containing 0–2 vol% highly aligned graphene nanoplatelets (GNPs) are fabricated. The electromagnetic interference (EMI) shielding properties of the obtained composites are investigated at X-band (8.2–12.4 GHz) frequency range from room-temperature up to 800 °C. All composites exhibit outstanding EMI shielding properties with satisfactory frequency- and thermal-stability. The shielding effectiveness (SE) of GNP/B₄C composites increases monotonically with increasing GNP loading. Superior room-temperature SE close to 40 dB is achieved with only 2 vol% GNPs and high SE around 35 dB still persists at 800 °C. Considering their relatively low density, GNP/B₄C composites possess a high specific shielding effectiveness (SSE) of 16 dB cm³ g⁻¹ which is among the highest values in reported ceramic-based shielding composites. Especially, the GNP/B₄C composite with 2 vol% GNPs exhibits the highest SSE/t (SSE divided by thickness) values at temperatures above 200 °C for all reported shielding composites, indicating that GNP/B₄C composites belong to the most promising high-temperature shielding composites. The excellent shielding properties of GNP/B₄C composites arise mainly from the high electrical conductivity, high dielectric loss and the multiple reflections by the highly aligned and large-sized GNP layers.

The incorporation of a small amount of highly aligned graphene nanoplatelets into boron carbide leads to light-weight and efficient high-temperature electromagnetic interference shielding composites.     

Synthesis of styrene maleic anhydride copolymer grafted graphene and its dispersion in aqueous solution

In this study, three simple methods were described to synthesize covalently functionalized graphene nanoplatelets (GNPs) with poly(styrene-co-maleic anhydride) (SMA) via ester linkages. Furthermore, the dispersibility of modified GNPs in aqueous solution was characterized by several techniques. Anchoring of SMA long-chains on GNPs via chemical bonds was confirmed by Fourier transform infrared spectroscopy. Furthermore, field emission scanning electron microscopy analysis indicated that the SMA unevenly covered the surface and edges of the GNPs. Solubility measurements showed that the modified GNPs prepared by the designed method had excellent dispersibility in aqueous solution, and the grafting rate of modified GNPs showed an obvious positive correlation with the concentration in aqueous solution as revealed by ultraviolet absorbency and thermogravimetric analysis results. Markedly, the modified GNPs during ultrasonic treatment exhibited better dispersibility and grafting rate compared to others. Moreover, the experimental results confirmed that GNP concentration reached up to 0.32 mg mL⁻¹ in aqueous solution and the grafting rate was 18.02%. The content of SMA had little effect on grafting rate; however, the ultrasonic duration significantly affected the process.

Three simple and cost-effective method were described to synthesize covalently functionalized graphene nanoplatelets (GNPs) with poly(styrene-co-maleic anhydride) (SMA), which offer the possibility of using graphene for low-value products such as cement-based materials.     

Nanofiller-conjugated percolating conductive network modified polymerization reaction characteristics of aromatic thermosetting copolyester resin

Deliberately controlled interfacial interactions between incorporated nanofiller particles and host polymer backbone chains constitute a critical element in the realm of polymer nanocomposites with tailorable multifunctional properties. We demonstrate the physicochemical effects induced by graphene nanoplatelets (GNP) of different sizes on the condensation polymerization reaction of aromatic thermosetting copolyester (ATSP) through the formation of electrically conductive percolating networks as enabled by interfacial interactions. Carboxylic acid and acetoxy-capped precursor oligomers of ATSP are solid-state mixed with chemically pristine GNP particles at various loading levels. Upon in situ endothermic condensation polymerization reaction, crosslinked backbone of the ATSP foam matrix is formed while the carbonaceous nanofillers are incorporated into the polymer network via covalent conjugation with functional end-groups of the oligomers. The controlled GNP size promotes different electrical percolation thresholds and ultimate electrical conductivities. Microstructural analysis demonstrates GNP distributions in the matrix as well as morphological modifications induced by the formation of conductive percolating GNP networks. Cure characteristics reveal the thermochemical changes prompted in the polymerization processes for GNP content above the requirement for percolation formation. Chemical spectroscopy of the ATSP nanocomposite morphology exhibits the formation of a robust interfacial coupling mechanism between the GNPs and ATSP backbone. The findings here may guide the developmental efforts of nanocomposites through better identifying roles of the morphology and content of nanofillers in polymerization processes.

Physicochemical effects induced by graphene nanoplatelets on the in situ polycondensation reaction of aromatic thermosetting copolyester through the formation of conductive percolating network assembled via interfacial interactions.     

Facial fabrication of few-layer functionalized graphene with sole functional group through Diels–Alder reaction by ball milling

The widespread use of graphene as a next-generation material in various applications requires developing an environmentally friendly and efficient method for fabricating functionalized graphene. Chemically, graphene can be used as an electron donor or attractor. Here, graphite was successfully exfoliated, and an in situ Diels–Alder reaction (D–A) was carried out to fabricate functionalized graphene with sole functional groups via mechanochemical ball milling. The reactivities of graphene acting as a diene or a dienophile were investigated. Few-layer (≤2 layers) graphene specimens were obtained by wet ball milling, heating in a nitrogen atmosphere, and solvent ultrasonic treatment. The ball-milling method was more effective than heating in a nitrogen atmosphere, and the [2 + 4] D–A of graphene was more dominant than the [4 + 2] D–A in the ball-milling process. The surface tension of functionalized graphene decreased, which provided a theoretical basis for the dispersion and exfoliation of graphite in a suitable solvent. Functionalized graphene still had a high electrical conductivity, which has far-reaching significance for functionalized graphene to be applied in electronic semiconductors and related applications. Meanwhile, functionalized graphene was applied to polymer composite fibers, the tensile strength and the Young''s modulus could reach 780 MPa and 19 GPa. The volume resistivity was two orders of magnitude lower than that of pure fiber. Thus, the use of ball milling to efficiently exfoliate and in situ functionalize graphite will help to develop a strategy that can be widely used to manufacture nanomaterials for various application fields.

The widespread use of graphene as a next-generation material in various applications requires developing an environmentally friendly and efficient method for fabricating functionalized graphene.     

In situ production of a two-dimensional molybdenum disulfide/graphene hybrid nanosheet anode for lithium-ion batteries

A solvent-free, low-cost, high-yield and scalable single-step ball milling process is developed to construct 2D MoS₂/graphene hybrid electrodes for lithium-ion batteries. Electron microscopy investigation reveals that the obtained hybrid electrodes consist of numerous nanosheets of MoS₂ and graphene which are randomly distributed. The MoS₂/graphene hybrid anodes exhibit excellent cycling stability with high reversible capacities (442 mA h g⁻¹ for MoS₂/graphene (40 h); 553 mA h g⁻¹ for MoS₂/graphene (20 h); 342 mA h g⁻¹ for MoS₂/graphene (10 h)) at a high current rate of 250 mA g⁻¹ after 100 cycles, whereas the pristine MoS₂ electrode shows huge capacity fading with a retention of 37 mA h g⁻¹ at 250 mA g⁻¹ current after 100 cycles. The incorporation of graphene into MoS₂ has an extraordinary effect on its electrochemical performance. This work emphasises the importance of the construction of the 2D MoS₂/graphene hybrid structure to prevent capacity fading issues with the MoS₂ anode in lithium-ion batteries.

A solvent-free, low-cost, high-yield and scalable single-step ball milling process is developed to construct 2D MoS₂/graphene hybrid electrodes for lithium-ion batteries.     

The design and fabrication of a multilayered graded GNP/Ni/PMMA nanocomposite for enhanced EMI shielding behavior

A multilayered graded structure can maximize the electromagnetic interference (EMI) shielding properties of a nanocomposite for a specific amount of a conductive filler in a polymer matrix. In this study, multilayered graded nanocomposites of graphene nanoplatelet (GNP)/Ni/polymethyl methacrylate (PMMA) were developed to achieve enhanced EMI shielding behavior. Both multilayered and monolayered nanocomposites were fabricated by controlling the compositions of GNP/Ni in the PMMA matrix. The contributions of the multilayered nanocomposite to EMI shielding were investigated and compared with the shielding effectiveness of the monolayered nanocomposite. The multilayered nanocomposite shows enhanced shielding effectiveness of around 61 dB in the X-band, which is more than three orders of magnitude higher than that of the monolayered nanocomposite. It has been confirmed that the measurements of reflection, absorption and total shielding effectiveness are in good accordance with the theoretically calculated results. The primary shielding mechanism was absorption due to conductive dissipation. The enhanced absorption of electromagnetic waves is attributed to an abrupt increase in the conductivity between layers in the direction of wave propagation in a multilayered nanocomposite due to impedance matching with the air and internal reflection between layers.

Three layered graded compositions of GNP/Ni/PMMA nanocomposite shows higher shielding effectiveness compared to that of monolayer nanocomposite.     

Practical PBT/PC/GNP composites with anisotropic thermal conductivity

Most of the highly thermally conductive polymer-based composites currently face problems that must be solved before they can be directly used in industrial production. Herein, a practical polybutylene terephthalate (PBT)/polycarbonate (PC)/graphite nanoplatelet (GNP) thermally conductive composite with relative low filler content was prepared by a conventional melt-blending technique. GNPs selectively distributed and oriented in the PBT phase afford the composite a low percolation threshold and anisotropic thermal conductivity. Investigation of the influence of filler content on the final comprehensive performance showed that a prepared PBT/PC/GNP composite with 20 vol% GNPs exhibited superior performance in thermal conductivity, heat resistance, and mechanical properties. The in-plane and through-plane thermal conductivities of the composite were 5.82 W m⁻¹ K⁻¹ and 1.06 W m⁻¹ K⁻¹, respectively, which were increased by 2430% and 361% as compared to that of a neat PBT/PC blend. The Vicat softening temperature increased by 17.7 °C and reached 213.7 °C, while the mechanical properties also maintained a good application level.

The selective distribution of thermally conductive fillers in a co-continuous polymer blends provides an industrialized preparation method that takes into account both the properties and functions of thermally conductive composites.     

A dopamine electrochemical sensor based on a platinum–silver graphene nanocomposite modified electrode

A platinum–silver graphene (Pt–Ag/Gr) nanocomposite modified electrode was fabricated for the electrochemical detection of dopamine (DA). Electrochemical studies of the Pt–Ag/Gr nanocomposite towards DA detection were performed by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The CV analysis showed that Pt–Ag/Gr/GCE had enhanced electrocatalytic activity towards DA oxidation due to the synergistic effects between the platinum–silver nanoparticles and graphene. The DPV results showed that the modified sensor demonstrated a linear concentration range between 0.1 and 60 μM with a limit of detection of 0.012 μM. The Pt–Ag/Gr/GCE presented satisfactory results for reproducibility, stability and selectivity. The prepared sensor also showed acceptable recoveries for a real sample study.

A platinum–silver graphene nanocomposite was synthesized and characterized. A nanocomposite modified electrode was fabricated in order to investigate the electrochemical detection of dopamine.     

Segregated poly(arylene sulfide sulfone)/graphene nanoplatelet composites for electromagnetic interference shielding prepared by the partial dissolution method

Segregated conductive polymer composites have been proved to be outstanding electromagnetic interference shielding (EMI) materials at low filler loadings. However, due to the poor interfacial adhesion between the pure conductive filler layers and segregated polymer granules, the mechanical properties of the segregated composites are usually poor, which limit their application. Herein, a simple and effective approach, the partial dissolution method, has been proposed to fabricate segregated poly(arylene sulfide sulfone) (PASS)/graphene nanoplatelet (GNP) composites with superior EMI shielding effectiveness (SE) and high tensile strength. Morphology examinations revealed that the GNPs were restricted in the dissolved outer layer by the undissolved cores, and there was a strong interaction between the PASS/GNP layer and the pure PASS core. The resultant PASS/GNP composites showed excellent electrical conductivity (60.3 S m⁻¹) and high EMI SE (41 dB) with only 5 wt% GNPs. More notably, the tensile strength of the PASS/GNPs prepared by partial dissolution reached 36.4 MPa, presenting 136% improvement compared to that of the conventional segregated composites prepared by mechanical mixing. The composites also exhibited high resistance to elevated temperatures and chemicals owing to the use of the special engineering polymer PASS as a matrix.

The segregated structure prepared by controlling the dissolution process endows the composites with both excellent EMI SE and high mechanical strength.     

Anisotropic tough poly(vinyl alcohol)/graphene oxide nanocomposite hydrogels for potential biomedical applications

Hydrogels, one of the most important bioinspired materials, are receiving increasing attention because of their potential applications as scaffolds for artificial tissue engineering and vehicles for drug delivery, etc. However, these applications are always severely limited by their microstructure and mechanical behavior. Here we report the fabrication of a tough polyvinyl alcohol/graphene oxide (PVA/GO) nanocomposite hydrogel through a simple and effective directional freezing–thawing (DFT) technique. The resulting hydrogels show well-developed anisotropic microstructure and excellent mechanical properties with the assistance of DFT method and lamellar graphene. The hydrogels with anisotropic porous structures that consisted of micro-sized fibers and lamellas exhibit high tensile strengths, up to 1.85 MPa with a water content of 90%. More interestingly, the PVA/GO composite hydrogels exhibit the better thermostability, which can maintain the original shape when swollen in hot water (65 °C). In addition, the hydrogels with biocompatibility show good drug release efficiency due to the unique hierarchical structure. The successful synthesis of such hydrogel materials might pave the way to explore applications in biomedical and soft robotics fields.

Tough PVA/GO nanocomposite hydrogel with well-developed anisotropic microstructure and excellent mechanical properties.     

Effect of surfactant concentration in electrolyte on the fabrication and properties of nickel-graphene nanocomposite coating synthesized by electrochemical co-deposition

Long-time environmental protection of metallic materials is still required in the manufacturing and engineering applications. Nickel-graphene nanocomposite coatings have been prepared on carbon steel using sodium dodecyl sulfate (SDS) as a dispersant in the electrolyte by an electrochemical co-deposition technique. In this study, the effects of surfactants on graphene dispersion, carbon content in the coatings, surface morphology, microstructures, microhardness and corrosion resistance properties of the nanocomposite coatings are explored. The results indicate that the reasonably good graphene dispersion, coarser surface morphology and reduction in grain sizes are achieved upon increasing the surfactant concentration in the electrolyte. The surfactant also influences the preferred orientation of grains during electrodeposition; the (200) plane is the preferred orientation for the nanocomposite produced with SDS in the bath electrolyte. The microhardness, adhesive strength and corrosion performance of the nickel-graphene nanocomposite coatings are found to increase with the increasing concentration of sodium dodecyl sulfate in the deposition bath. Moreover, the influencing mechanism of surfactant concentration on the properties of nanocomposite coatings has been discussed.

Long-time environmental protection of metallic materials is still required in the manufacturing and engineering applications.     

A stable TiO2–graphene nanocomposite anode with high rate capability for lithium-ion batteries

A rapid microwave hydrothermal process is adopted for the synthesis of titanium dioxide and reduced graphene oxide nanocomposites as high-performance anode materials for Li-ion batteries. With the assistance of hydrazine hydrate as a reducing agent, graphene oxide was reduced while TiO₂ nanoparticles were grown in situ on the nanosheets to obtain the nanocomposite material. The morphology of the nanocomposite obtained consisted of TiO₂ particles with a size of ∼100 nm, uniformly distributed on the reduced graphene oxide nanosheets. The as-prepared TiO₂–graphene nanocomposite was able to deliver a capacity of 250 mA h g⁻¹ ± 5% at 0.2C for more than 200 cycles with remarkably stable cycle life during the Li⁺ insertion/extraction process. In terms of high rate capability performance, the nanocomposite delivered discharge capacity of ca. 100 mA h g⁻¹ with >99% coulombic efficiency at C-rates of up to 20C. The enhanced electrochemical performance of the material in terms of high rate capability and cycling stability indicates that the as-developed TiO₂–rGO nanocomposites are promising electrode materials for future Li-ion batteries.

A rapid microwave hydrothermal process is adopted for the synthesis of titanium dioxide and reduced graphene oxide nanocomposites as high-performance anode materials for Li-ion batteries.     

Ternary 3D reduced graphene oxide/Ni0.5Zn0.5Fe2O4/polyindole nanocomposite for supercapacitor electrode application

A facile two-step strategy has been reported for the preparation of a ternary 3D reduced graphene oxide/Ni_0.5Zn_0.5Fe₂O₄/polyindole nanocomposite (GNP) and this composite is applied as an electrode material for supercapacitor applications. Remarkably, Ni_0.5Zn_0.5Fe₂O₄ nanoparticles (NZF) decorated on reduced graphene oxide (GN2) are achieved by a facile hydrothermal method followed by coating with polyindole (PIN) through an in situ emulsion polymerization process. The structure, porosity, morphology, and thermal stability of the resulting ternary GNP hybrid material were characterized via X-ray diffraction (XRD), Raman spectroscopy, Brunauer–Emmett–Teller (BET) surface area measurements, transmission electron microscopy (TEM), and thermogravimetric analysis (TGA). This combination of hybrid material has a favorable mesoporous structure that enables high exposure of active sites for fast electron transport for supercapacitor applications. We demonstrate here that the ternary GNP hybrid electrode material is capable of delivering a favorable specific capacitance of ∼320 F g⁻¹ at 0.3 A g⁻¹ within the potential range from −0.1 to 1 V, with desirable rate stability and excellent cycling stability in the three-electrode system. Furthermore, an asymmetric supercapacitor (ASC) of a two-electrode configuration was fabricated using 3D RGO and GNP as the negative and positive electrodes, respectively. Such a device manifests a favourable C_sp of 48.9 F g⁻¹ at 0.5 A g⁻¹ and retains stability of 84% even after 2000 cycles. This ASC device exhibits a significant energy density of 16.38 W h kg⁻¹ at a power density of 1784 W kg⁻¹. The synergistic effects of pseudo and double layer capacitive contributions from PIN and GN2 make this ternary GNP hybrid electrode material of great promise in supercapacitor applications.

A facile two-step strategy has been reported for the preparation of a ternary 3D reduced graphene oxide/Ni_0.5Zn_0.5Fe₂O₄/polyindole nanocomposite (GNP) and this composite is applied as an electrode material for supercapacitor applications.     

Synthesis of graphene via electrochemical exfoliation in different electrolytes for direct electrodeposition of a Cu/graphene composite coating

Directly dispersing graphene into an electrolyte still remains a crucial difficulty in electrodepositing a graphene enhanced composite coating onto electrical contact materials. Herein, graphene was synthesized via electrochemical exfoliation in an N,N-dimethylformamide (DMF)/H₂O solution containing (NH₄)₂SO₄. The electrochemically exfoliated graphene nanosheets (GNs) were directly dispersed by sonication. In comparison with graphene synthesized from aqueous solution, the GNs electrochemically exfoliated in the DMF/H₂O–(NH₄)₂SO₄ solution exhibit a lower degree of oxidation. Cu/graphene composite coatings were subsequently electrodeposited onto Cu foils by adding Cu²⁺ into the as-fabricated graphene solution. The surface nanostructure of the Cu/graphene composite coatings was transformed from loose pine needles to a uniform and compact structure with an increase in the concentration of Cu²⁺, which indicated that the controllable synthesis of Cu/graphene composite coatings with different performances could be achieved in graphene dispersions after adding Cu²⁺. In order to synthesize graphene via electrochemical exfoliation and directly electrodeposit a Cu/graphene composite coating without adding CuSO₄ or any other additive, an attempt was made to directly electrodeposit a Cu/graphene composite coating in CuSO₄/DMF/H₂O solution after electrochemical exfoliation.

Electrochemically exfoliated graphene was directly dispersed in the DMF/H₂O solution for electrodeposition of a Cu/graphene composite coating.     

The selective laser sintering of a polyamide 11/BaTiO3/graphene ternary piezoelectric nanocomposite

Piezoelectric materials featuring the capability of converting mechanical energy to electricity are very important for harvesting discrete mechanical energy to meet the rapidly increasing demand for cleaner energy. However, the intrinsic poor flexibility and processability make it difficult for current piezoelectric materials to fulfill their potential. This study reports a novel polyamide 11 (PA11)/BaTiO₃ (BT)/graphene (Gr) ternary nanocomposite 3D printed part with significantly enhanced dielectric and piezoelectric properties due to its special discontinuous graphene network and microspores. The piezoelectric BT nanoparticles with excellent piezoelectric properties were uniformly dispersed into PA11 via a solid-state shear milling (S³M) technology. Moreover, via ultrasonic coating and selective laser sintering (SLS) technology, the discontinuous graphene network and microporous structures were both fabricated in the prepared 3D printed parts. The graphene interfaces acted as electrodes, and thus significantly increased the poling efficiency, while the porous structure further magnified the stress concentration. As a result, a piezoelectric coefficient (d₃₃) of 3.8 pC N⁻¹ and open-circuit voltage of 16.2 ± 0.4 V were obtained, exhibiting better comprehensive performances than those of most reported piezoelectric materials.

Polyamide 11/BaTiO₃/graphene nanocomposite SLS part with enhanced dielectric and piezoelectric properties due to its special discontinuous graphene network and microspores.     

Electrodeposited Pd/graphene/ZnO/nickel foam electrode for the hydrogen evolution reaction

Efficient electrocatalysts are crucial to water splitting for renewable energy generation. In this work, electrocatalytic hydrogen evolution from Pd nanoparticle-modified graphene nanosheets loaded on ZnO nanowires on nickel foam was studied in an alkaline electrolyte. The high electron mobility stems from the cylindrical ZnO nanowires and the rough surface on the graphene/ZnO nanowires increases the specific surface area and electrical conductivity. The catalytic activity arising from adsorption and desorption of intermediate hydrogen atoms by Pd nanoparticles improves the hydrogen evolution reaction efficiency. As a hydrogen evolution reaction (HER) catalyst, the Pd/graphene/ZnO/Ni foam (Pd/G/ZnO/NF) nanocomposite exhibits good stability and superior electrocatalytic activity. Linear sweep voltammetry (LSV) revealed an overpotential of −31 mV and Tafel slope of 46.5 mV dec⁻¹ in 1 M KOH. The economical, high-performance, and environmentally friendly materials have excellent prospects in hydrogen storage and hydrogen production.

Efficient electrocatalysts are crucial to water splitting for renewable energy generation.     

Electrochemical hydrodechlorination of perchloroethylene in groundwater on a Ni-doped graphene composite cathode driven by a microbial fuel cell

Enhancing the activity of the cathode and reducing the voltage for electrochemical hydrodechlorination of chlorohydrocarbon were always the challenges in the area of electrochemical remediation. In this study, a novel cathode material of Ni-doped graphene generated by Ni nanoparticles dispersed evenly on graphene was prepared to electrochemically dechlorinate PCE in groundwater. The reduction potential of Ni-doped graphene for PCE electrochemical hydrodechlorination was −0.24 V (vs. Ag/AgCl) determined by cyclic voltammetry. A single MFC with a voltage of 0.389–0.460 V and a current of 0.221–0.257 mA could drive electrochemical hydrodechlorination of PCE effectively with Ni-doped graphene as the cathode catalyst, and the removal rate of PCE was significantly higher than that with single Ni or graphene as the cathode catalyst. Moreover, neutral conditions were more suitable for Ni-doped graphene to electrochemically hydrodechlorinate PCE in groundwater and no byproduct was accumulated.

Ni-doped graphene was prepared to electrochemically dechlorinate PCE driven by a microbial fuel cell. Dechlorination efficiency and reduction potential were significantly higher than for bare Ni or graphene.