Search Results (71)

This work presents a multifactorial strategy for reusing waste thermoplastics and generating multifunctional filaments for additive manufacturing. Acrylonitrile–butadiene–styrene (ABS) waste and commercial poly(methyl methacrylate) (PMMA) were compounded with carbon black (CB), graphene (G), or graphene foam (GF) at different loadings and extruded into composite filaments. The aim is to couple filler-induced bulk modifications with atmospheric pressure plasma jet (APPJ) surface coatings of TiO₂ and graphene oxide (GO) to obtain waste-derived filaments with tunable morphology, wettability, and thermal stability for advanced 3D-printed architectures. The filaments were subsequently coated with TiO₂ and/or GO using an APPJ process, which tailored surface wettability and enabled the formation of photocatalytically relevant interfaces. Digital optical microscopy and SEM revealed that CB, G, and GF were reasonably well dispersed in both polymer matrices but induced distinct surface and cross-sectional morphologies, including a carbon-rich outer crust in ABS and filler-dependent porosity in PMMA. For ABS composites, static contact-angle measurements show that APPJ coatings broaden the apparent wettability window from ~60–80° for uncoated filaments to ~40–50° (TiO₂/GO) up to >90° (GO), corresponding to a ≈150% increase in contact-angle span. For PMMA/CB composites, TiO₂/GO coatings expand the accessible contact-angle range to ~15–125° while maintaining surface energies around 50 mN m⁻¹. TGA/DSC analyses confirm that the composites and coatings remain thermally stable within typical extrusion and APPJ processing ranges, with graphene showing only ≈3% mass loss over the explored temperature range, compared with ≈65% for CB and ≈10% for GF. Fused deposition modeling trials verify the printability and dimensional fidelity of ABS-based composite filaments, whereas PMMA composites were too brittle for reliable FDM printing. Overall, combining waste polymer reuse, tailored carbonaceous fillers, and APPJ TiO₂/GO coatings provides a versatile route to design surface-engineered filaments for applications such as photocatalysis, microfluidics, and soft robotics within a circular polymer manufacturing framework. Full article

Nanomaterials play a beneficial role in regulating the function of cement-based materials. The effects and mechanism of graphene oxide (GO) on foam behavior in solutions and air-entraining behavior of cement mortar were studied, and its effect on the microstructure of cement mortar was also investigated. The results show that a synergy between GO’s hydrophobicity and the air-entraining agent’s hydrophobic chains drove more agent molecules to adsorb onto the GO surface, subsequently spreading and aggregating across the bubbles. GO effectively assisted the air entraining agent to refine the bubble size, improved the bubble stability of aqueous solutions, and had excellent air entraining performance in the fresh cement mortar, as well as the optimum air-void adjustment performance of hardened cement mortars. With the addition of 0.4‰ GO, the loss rate of gas content in the GO mixed mortar was 10.3%, which was 55.8% lower than that when only using AEA. The addition of 0.4‰ of GO effectively increased the volume fraction of the cement mortar system. GO reduced the pore volume in the mortar through the filling effect and nucleation effect to reduce the total porosity and refine the microstructure of the mortar. Full article

To investigate the impermeability of foam concrete in various challenging environments, this study evaluates its water resistance by measuring the water contact angle and water absorption. Polyurethane (PU) was used to fabricate polyurethane foam concrete (PFC), enabling a monolithic hydrophobic modification to improve the permeation performance of foam concrete. The study also examines the effects of carbonation and freeze–thaw environments on the permeation resistance of PFC. Graphene oxide (GO), KH-550, and a composite hydrophobic coating (G/S) consisting of GO and KH-550 were employed to enhance the permeation resistance of PFC through surface hydrophobic modification. The functionality of the G/S composite hydrophobic coating was confirmed using energy dispersive X-ray spectrometry (EDS) and Fourier transform infrared spectroscopy (FTIR). The results showed the following: (1) The water contact angle of PFC increased by 20.2° compared to that of ordinary foam concrete, indicating that PU-based hydrophobic modification can significantly improve its impermeability. (2) After carbonation, a micro–nano composite structure resembling the surface of a lotus leaf developed on the surface of PFC, further enhancing its impermeability. However, freeze–thaw cycles led to the formation and widening of microcracks in the PFC, which compromised its hydrophobic properties. (3) Surface hydrophobic modifications using GO, KH-550, and the G/S composite coating improved the anti-permeability properties of PFC, with the G/S composite showing the most significant enhancement. (4) GO filled the tiny voids and pores on the surface of the PFC, thereby improving its anti-permeability properties. KH-550 replaced water on the surface of PFC and encapsulated surface particles, orienting its R-groups outward to enhance hydrophobicity. The G/S composite emulsion coating formed a hydrophobic silane layer inside the concrete, which enhanced water resistance by blocking water penetration, reducing microscopic pores in the hydrophobic layer, and improving impermeability characteristics. Full article

Early diagnosis of Alzheimer’s disease (AD) is essential for effective treatment; however current diagnostic methods are often complex, costly, and unsuitable for point-of-care testing. Graphene-based biosensors offer an alternative due to their affordability, versatility, and high conductivity. However, graphene’s conductivity can be compromised when its carbon lattice is oxidized to introduce functional groups for biomolecule immobilization. This study addresses this challenge by developing an electrochemical immunosensor using carboxyl-modified commercial graphene foam (COOH-GF) electrodes. The conductivity of graphene is preserved by enabling efficient COOH modification through π–π non-covalent interactions, while antibody immobilization is optimized via EDC-NHS carbodiimide chemistry. The immunosensor detects tau-441, an AD biomarker, using differential pulse voltammetry (DPV), achieving a detection range of 1 fM–1 nM, with a limit of detection (LOD) of 0.14 fM both in PBS and human serum. It demonstrates high selectivity against other AD-related proteins, including tau-217, tau-181, amyloid beta (Aβ_1-40 and Aβ_1-42), and 1% BSA. These findings underscore its potential as a highly sensitive, cost-effective tool for early AD diagnosis. Full article

Thin films of manganese–nickel–cobalt oxide with graphene (G@MNCO) were deposited on copper foam using electrochemical deposition. NiCo₂O₄ is the main phase in these films. As the proportion of graphene in the precursor solution increases, the oxygen vacancies in the samples also increase. The microstructure of these samples evolves into hierarchical vertical flake structures. Cyclic voltammetry measurements conducted within the potential range of 0–1.2 V reveal that the electrode with the highest graphene content achieves the highest specific capacitance, approximately 475 F/g. Furthermore, it exhibits excellent cycling durability, maintaining 95.0% of its initial capacitance after 10,000 cycles. The superior electrochemical performance of the graphene-enhanced, manganese-doped nickel–cobalt oxide electrode is attributed to the synergistic contributions of the hierarchical G@MNCO structure, the three-dimensional Cu foam current collector, and the binder-free fabrication process. These features promote quicker electrolyte ion diffusion into the electrode material and ensure robust adhesion of the active materials to the current collector. Full article

To address the protective demands of marine engineering equipment in complex corrosive environments, this study proposes an environmentally friendly composite coating based on carboxylated graphene oxide (CGO)-modified water-based epoxy organosilicon resin. By incorporating varying mass fractions (0.05–0.25%) of CGO into the resin matrix via mechanical blending, the microstructure, corrosion resistance, and long-term corrosion kinetics of the coatings were systematically investigated. The results demonstrate that the coating with 0.15 wt.% CGO (designated as KCG15) exhibited optimal comprehensive performance: its corrosion current density (I_corr = 4.37 × 10⁻⁸ A/cm²) was two orders of magnitude lower than that of the pure resin coating, while its low-frequency impedance modulus (∣Z∣_0.1Hz = 4.99 × 10⁶ Ω⋅cm²) is significantly enhanced, accompanied by improved surface compactness. The coating achieved a 97% inhibition rate against sulfate-reducing bacteria (SRB) through synergistic physical disruption and electrostatic repulsion mechanisms. Long-term corrosion kinetics analysis via 60-day seawater immersion identified three degradation phases—permeation (0–1 day), blockage (1–4 days), and failure (7–60 days)—with structural evolution from microcrack networks to foam-like blistering ultimately reducing by 97.8%. Furthermore, a 180-day atmospheric exposure test confirms the superior weatherability and adhesion of the KCG15 coating, with only minor discoloration observed due to its hydrophobic surface. This work provides theoretical and technical foundations for developing marine anti-corrosion coatings that synergize environmental sustainability with long-term protective performance. Full article

This review article investigates the rising global energy demand, which is primarily driven by population growth and industrialization, raising significant environmental concerns due to the extensive reliance on fossil fuels. In response, hydrogen is being explored as a potential eco-friendly energy solution to meet the urgent need for sustainable energy. This review covers various hydrogen storage methods, including compressed gas, cryogenic liquids, solid materials, and electrochemical techniques. Among these, electrochemical technology is highly regarded as a leading experimental approach for hydrogen storage, and it is noted for its outstanding performance under normal conditions. The characteristics of a material’s surface play a crucial role in determining its electrochemical hydrogen storage capacity. Innovative materials, such as graphene oxide and 3D graphene oxide, are particularly significant in this regard, as they can significantly enhance hydrogen storage capacity; electrochemical hydrogen storage functions by incorporating atomic hydrogen into carbon materials following the reduction of water. This article underscores the significance of green energy and the need to ensure safety and precision at room temperature and ambient pressure using electrochemical hydrogen storage techniques and mechanisms. Furthermore, it offers a comprehensive review of developments in electrochemical hydrogen storage and its mechanisms, focusing on carbon, graphene oxide, and the contributions of 3D graphene foam. Full article

Achieving high energy density while maintaining high power density and long cycle life in supercapacitors, particularly in supercapatteries (SCs), through a thermally stable, greener ionic liquid approach remains a significant challenge for an advanced energy storage application. In this work, we prepared high conductive and high charge storage capability bimetallic transition metal molybdate [Ag₂Mo₂O₇ (AgM)], synergistic with reduced graphene oxide (rGO) coated on nickel foam (AgM/rGO/NF). The physio-chemical characterization revealed a ball-like cluster morphology wrapped in rGO nanosheets and a spinel-type cubic structure using scanning electron microscopy (FE-SEM) displays and X-ray diffraction (XRD) analyses. Further, the electrochemical performance of AgM/rGO/NF electrode achieved a remarkable specific C_sp value of 573.63 F/g at a current density of 1.0 A/g in 3 M KOH electrolyte. An asymmetric SCs (ASCs) device was fabricated using AgM/rGO/NF as the positive and rGO as the negative electrodes, achieving a wide potential window of 1.3 V. The ASC demonstrated an energy density of 16.71 Wh/kg at a power density of 642.98 W/kg, highlighting AgM/rGO/NF’s potential as an advanced electrode material for energy storage applications. Full article

In a view of application of porous materials in wearable electronics and self-powered systems, reduced graphene oxide (rGO) foams modified by Mn or/and Bi were produced in this study to be used as electrodes for supercapacitors. The hydrothermal method and the freeze-drying processes were used for the preparation of the materials further morphologically, elementally and structurally analyzed. Based on the electrochemical characterization, Bi-modified rGO foam was found to be more a promising material for capacitive electrodes in comparison to the other prepared materials. Full article

High-frequency noise exceeding 1 kHz has emerged as a pressing public health issue in industrial and occupational settings. In response to this challenge, the present study explores the development of a graphene oxide–polyethyleneimine (GO-PEI) foam (GPF) featuring a hierarchically porous structure. The synthesis and optimization of GPF were carried out using a range of analytical techniques, including Raman spectroscopy, scanning electron microscopy (SEM), Braunauer–Emmett–Teller (BET) analysis, X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FT-IR). To evaluate its acoustic properties, GPF was subjected to sound absorption tests over the 1000–6400 Hz frequency range, where it was benchmarked against conventional melamine foam. The findings demonstrated that GPF with a GO-to-PEI composition ratio of 1:3 exhibited enhanced sound absorption performance, with improvements ranging from 15.0% to 118%, and achieved a peak absorption coefficient of 0.97. Additionally, we applied the Johnson–Champoux–Allard (JCA) model to further characterize the foam’s acoustic behavior, capturing key parameters such as porosity, flow resistivity, and viscous/thermal losses. The JCA model exhibited a superior fit to the experimental data compared to traditional models, providing a more accurate prediction of the foam’s complex microstructure and sound absorption properties. These findings underscore GPF’s promise as an efficient solution for mitigating high-frequency noise in industrial and environmental applications. Full article

The aggregation of graphene oxide (GO) during the hydration process limits its wide application. Polymer superplasticizers have been used to improve the dispersion state of GO due to their adsorption and site-blocking effects, though the formation of a large amount of foam during the mixing process weakens the mechanical properties of cement. A highly dispersed amphoteric polycarboxylate superplasticizer-stabilized graphene oxide (APC/GO) toughening agent was prepared by electrostatic self-assembly. Results demonstrate that the APC/GO composite dispersed well in a cement pore solution due to the steric effect offered by the APC. Additionally, the well-dispersed GO acted as an antifoaming agent in the cement since GO nanosheets can be absorbed at the air–liquid interface of APC foam via electrostatic interactions and eliminate the air-entraining effect. The well-dispersed APC/GO sheets promoted cement hydration and further refined its pore structure owing to the nucleation effect. The flexural and compressive strength of the cement containing the APC/GO composite were enhanced by 21.51% and 18.58%, respectively, after a 7-day hydration process compared with a blank sample. The improved hydration degree, highly polymerized C-S-H gel, and refined pore structure provided enhanced mechanical properties. Full article

A significant weakness of many organic and inorganic aerogels is their poor mechanical behaviour, representing a great impediment to their application. For example, polymer aerogels generally have higher ductility than silica aerogels, but their elastic modulus is considered too low. Herein, we developed extremely low loading (<1 wt%) 2D graphene oxide (GO) nanosheets modified poly (vinyl alcohol) (PVA) aerogels via a facile and environmentally friendly method. The aerogel shows a 9-fold increase in compressional modulus compared to a pure polymer aerogel. With a low density of 0.04 mg/mm³ and a thermal conductivity of only 0.035 W/m·K, it outperforms many commercial insulators and foams. As compared to a pure PVA polymer aerogel, a 170% increase in storage modulus is obtained by adding only 0.6 wt% GO nanosheets. The nanocomposite aerogel demonstrates strong fire resistance, with a 50% increase in burning time and little smoke discharge. After surface modification with 1H,1H,2H,2H-Perfluorodecyltriethoxysilane, the aerogel demonstrates water resistance, which is suitable for outdoor applications in which it would be exposed to precipitation. Our research demonstrates a new pathway for considerable improvement in the performance and application of polymer aerogels. Full article

NiFe-layered double hydroxides (NiFe-LDH) have been reported to possess exceptional oxygen evolution reaction (OER) activity. However, maintaining the stability of high activity over a long time remains a critical challenge that needs to be addressed for their practical application. Here, we report a custom-sized deep recombination of 2D graphene oxide with NiFe-LDH (NiFe-LDH/GO/NF) through a simple electrodeposition method that improves OER activity and achieves excellent stability. The excellent performance of the catalyst mainly comes from the three-phase interface and electron transport channel dredged by the three-dimensional structure constructed by the deep composite, which can not only significantly reduce its charge and electron transfer resistance, improving the material conductivity, but it also effectively increases the specific surface area, inhibits aggregation, and exposes rich active sites. In addition, GO with good conductivity not only supports NiFe-LDH well but also increases the heterogeneous interface, putting the NiFe-LDH/GO composites in close contact with Ni foam and increasing the electrocatalytic stability of the NiFe-LDH/GO/NF. The experimental results show that the overpotential of NiFe-LDH/20,000GO/NF is only 295 mV at a current density of 100 mA cm⁻²; the Tafel slope is 52 mV dec⁻¹, and the charge transfer resistance (Rct) is only 0.601 Ω in 1 M KOH. This indicates that GO has excellent potential to assist in constructing geometric and electronic structures of NiFe-LDH in long-term applications. Full article

Supercapacitors have the characteristics of high power density, long cycle life, and fast charge and discharge rates, making them promising alternatives to traditional capacitors and batteries. The use of transition-metal compounds as electrode materials for supercapacitors has been a compelling research topic in recent years because their use can effectively enhance the electrical performance of supercapacitors. The current research on capacitor electrode materials can mainly be divided into the following three categories: carbon-based materials, metal oxides, and conductive polymers. Nickel hydroxide (Ni(OH)₂) is a potential electrode material for use in supercapacitors. Depending on the preparation conditions, two crystal phases of nickel hydroxide, α and β, can be produced. When compared to α-NiOH, the structure of β-Ni(OH)₂ does not experience ion intercalation. As a result, the carrier transmission rate of α-Ni(OH)₂ is slower, and its specific capacitance value is smaller. Its carrier transport rate can be improved by adding conductive materials, such as graphene. β-Ni(OH)₂ was chosen as an electrode material for a supercapacitor in this study. Homemade low-pressure chemical vapor deposition graphene (LPCVD-Graphene) conductive material was introduced to modify β-Ni(OH)₂ in order to increase its carrier transport rate. The LPCVD method was used to grow high-quality graphene films on three-dimensional (3D) nickel foam substrates. Then, a hydrothermal synthesis method was used to grow β-Ni(OH)₂ nanostructures on the 3D graphene/nickel foam substrate. In order to improve the electrical properties of the composite structure, a high-quality graphene layer was incorporated between the nickel hydroxide and the 3D nickel foam substrate. The effect of the conductive graphene layer on the growth of β-Ni(OH)₂, as well as its electrical properties and electrochemical performance, was studied. When this β-Ni(OH)₂/CVD-Graphene/3D-NF (nickel foam) material was used as the working electrodes of the supercapacitor under a current density of 1 A/g and 3 A/g, they exhibited a specific capacitance of 2015 F/g and 1218.9 F/g, respectively. This capacitance value is 2.62 times higher than that of the structure without modification with a graphene layer. The capacitance value remains at 99.2% even after 1000 consecutive charge and discharge cycles at a current density of 20 A/g. This value also improved compared to the structure without graphene layer modification (94.7%). Full article

Using thermal storage materials with excellent thermal properties in the energy utilization system enables efficient use of renewable energy sources. Organic phase change materials (PCMs) have the advantages of high heat storage density, no corrosion, and low cost, but low thermal conductivity and insufficient heat transfer capacity have always been the bottlenecks in their application. In this paper, melamine foam@ reduction graphene oxide (MF@rGO) and carbon foam@ reduction graphene oxide (CF@rGO) composite foams with double carbon networks were prepared by self-assembly method and further employed in 1-octadecinal (OD) PCMs. The microstructure, chemical composition, phase change behavior, thermal conductivity, and photothermal conversion performance of MF@rGO/OD and CF@rGO/OD were studied in detail using SEM, FTIR, Raman DSC, and LFA. The melting and solidification enthalpies of CF@rGO/OD composite PCMs were 208.3 J/g and 191.4 J/g, respectively, its thermal conductivity increased to 1.54 W/m·K, which is 6.42 times that of pure OD. The porous structure and high thermal conductivity of the double carbon network substantially enhance the efficiency of energy storage and release in composite PCMs. CF@rGO/OD composite PCMs have excellent heat storage performance and heat transfer capacity, and a wide range of application prospects in the fields of low-temperature solar heat storage, precision instrument temperature control, and intelligent buildings. Full article