Search Results (3,527)

In the shift toward sustainable energy, there is a strong demand for efficient and durable energy storage solutions. Supercapacitors, in particular, are a promising technology, but they require high-performance materials that can be produced using simple, eco-friendly methods. This has led researchers to investigate new materials and composites that can deliver high energy and power densities, along with long-term stability. Herein, we report a green synthesis approach to create a composite material consisting of reduced graphene oxide and silver nanoparticles (rGO/Ag). The method uses ascorbic acid, a natural compound found in fruits and vegetables, as a non-toxic agent to simultaneously reduce graphene oxide and silver nitrate. To enhance electrochemical performance, the incorporation of silver nanoparticles into the rGO structures is optimized. In this study, different molar concentrations of silver nitrate (1.0, 0.10, and 0.01 M) are used to control silver nanoparticle loading during the synthesis and reduction process. A correlation between silver concentration, defect density in rGO, and the resulting capacitive behavior was assessed by systematically varying the silver molarity. The synthesized materials exhibited excellent performance as supercapacitor electrodes in a three-electrode configuration, with the rGO/Ag 1.0 M composite showing the best performance, reaching a maximum specific capacitance of 392 Fg⁻¹ at 5 mVs⁻¹. Furthermore, the performance of this optimized electrode material was investigated in a two-electrode configuration as a coin cell device, which demonstrates a maximum areal-specific capacitance of 22.63 mFcm⁻² and a gravimetric capacitance of 19.00 Fg⁻¹, which is within the range of commercially viable devices and a significant enhancement, outperforming low-level graphene-based devices. Full article

In this work, general purpose rubber composites were created based on a mixture of non-polar cis-1,4-isoprene rubber and cis-1,4-divinyl rubber as components. The main filler used was carbon black, while various graphite-like materials (graphite oxide, reduced graphite oxide, expanded graphite, and graphite nanoplatelets) served as additives. It was determined that the addition of these graphite-like materials resulted in a reduction in Mooney viscosity, with the introduction of graphene nanoplatelets having the most significant effect, contributing to a viscosity decrease of 8.5%. The relaxation rate increased, positively impacting elastic recovery and consequently reducing shrinkage. The introduction of graphite oxide, graphite nanoplatelets, and expanded graphite also increased the time to the onset of the vulcanization reaction; moreover, these additives lengthened the time needed to reach the optimum level of vulcanization. The addition of various graphite-like materials significantly affected the elongation at break, with the highest increase attributable to the addition of expanded graphite and reduced graphite oxide. It was found that the conditional tensile strength of these additives had little effect. Upon assessing the elastic-strength properties after aging, it was found that the inclusion of graphite-like materials reduced the elongation at break. Full article

The integration of nanoengineered materials into concrete systems has emerged as a promising strategy for enhancing structural performance and sustainability. This study presents a hybrid experimental-analytical investigation into the use of multilayer graphene as a smart admixture in high-performance concrete. The research combines mechanical testing, microstructural characterization, and a multi-objective optimization model to determine the optimal graphene dosage that maximizes strength gains while minimizing carbon emissions. Concrete specimens incorporating multilayer graphene (ranging from 0.01% to 0.10% by weight of cement) were tested over 7 to 90 days for compressive, tensile, and flexural strengths. Simultaneously, X-ray diffraction, scanning electron microscopy, and energy-dispersive X-ray analyses revealed crystallinity enhancement, pore densification, and favorable elemental redistribution due to graphene inclusion. A normalized composite objective function was formulated to balance three maximization targets—compressive, tensile, and flexural strength—and one minimization goal—carbon emission. The highest objective score (Z = 1.047) was achieved at 0.10% graphene dosage, indicating the optimal balance of strength performance and environmental efficiency. This dual-framework study not only confirms graphene’s reinforcing effects experimentally but also validates the 0.10% dosage through mathematical scoring. The outcomes position of multilayer graphene as a powerful additive for high-strength, low-carbon concrete, especially suited for infrastructure in hot and arid environments. The proposed optimization approach provides a scalable pathway for performance-based graphene dosing in future innovative concrete formulations. Full article

The rapid advancement of modern infrastructure and construction industries demands cementitious materials with superior mechanical performance, durability, and sustainability, surpassing the limitations of conventional concrete. To address these challenges, carbon-based nanomaterials—including carbon nanofibers (CNFs), carbon nanotubes (CNTs), and graphene—have gained significant attention as next-generation reinforcement agents due to their exceptional strength, high aspect ratio, and unique interfacial properties. This review presents a critical analysis of the latest technological developments in carbon-enhanced cement and concrete composites, focusing on their role in achieving high-performance construction materials, as there is a shortage of reviews of cement concretes based on carbon nanoadditives. We systematically explore the underlying mechanisms, processing techniques, and structure–property relationships governing carbon-modified cementitious systems. First, we discuss advanced synthesis methods and dispersion strategies for carbon nanomaterials to ensure uniform reinforcement within the cement matrix. Subsequently, we analyze the mechanical enhancement mechanisms, including crack bridging, nucleation seeding, and interfacial bonding, supported by experimental and computational studies. Despite notable progress, challenges such as long-term durability, cost-effectiveness, and large-scale processing remain key barriers to practical implementation. Finally, we outline emerging trends, including multifunctional smart composites and sustainable hybrid systems, to guide future research toward scalable and eco-friendly solutions. By integrating fundamental insights with technological advancements, this review not only advances the understanding of carbon-reinforced cement composites but also provides strategic recommendations for their optimization and industrial adoption in next-generation construction. Full article

In order to study the durability of graphene oxide concrete composite in chloride and sulfate environments, graphene oxide concrete composite specimens were immersed in a mixed solution of 5% sodium sulfate and sodium chloride. After dry–wet cycle immersion and long-term natural immersion, the compressive strength, strength reduction rate, and mass loss rate of concrete specimens were tested. The microstructure was analyzed by scanning electron microscopy (SEM), and the durability of graphene oxide concrete composite in chloride and sulfate environments was analyzed. The results show that with the increase in corrosion age, under dry–wet cycle immersion and long-term natural immersion, the compressive strength reduction coefficient and mass loss rate of graphene oxide concrete composite specimens with 0.07% content are the smallest. The stress–strain curve of concrete after corrosion is flatter than that of uncorroded concrete, and the ductility of concrete specimens after corrosion increased. Through microstructure analysis, it can be seen that the internal structure of graphene oxide concrete composite test block is more compact, the hydration products are regulated, the corrosion of concrete is delayed, and the durability performance is better. Graphene oxide is used to improve the strength and durability of concrete, and the recommended dosage is 0.07%. Full article

Magnesium alloys, like AZ31, possess a desirable low weight and high specific strength, which make them favorable for aerospace and auto applications, yet their difficulty to machine limits their broader implementation for the industry. Electrical discharge machining (EDM) is an effective technology for machining difficult-to-machine materials, particularly when the materials are reinforced with ceramic and graphene-based fillers. This study examines the impact of reinforcement percentage (R) and different electrical discharge machining (EDM) parameters such as current (I), pulse on time (T_on) and pulse off time (T_off) on the material removal rate (MRR) and surface roughness (SR) of AZ31/B₄C/GNPs composites. The combined reinforcement range varies from 2 wt.% to 4 wt.%. The Taguchi design (L27) is utilized to conduct the experiments in this study. ANOVA of the experimental data indicated that current (I) significantly affects MRR and SR, exhibiting the greatest contribution of 44.93% and 51.39% on MRR and SR, respectively, among the variables analyzed. The surface integrity properties of EDMed surfaces are examined using SEM under both higher and lower material removal rate settings. Diverse machine learning techniques, including linear regression (LR), polynomial regression (PR), Random Forest (RF), and Gradient Boost Regression (GBR), are employed to construct an efficient predictive model for outcome estimation. The built models are trained and evaluated using 80% and 20% of the total data points, respectively. Statistical measures (MSE, RMSE, and R²) are utilized to evaluate the performance of the models. Among all the developed models, GBR exhibited superior performance in predicting MRR and SR, achieving high accuracy (exceeding 92%) and lower error rates compared to the other models evaluated in this work. This work demonstrated the synergy between techniques in optimizing EDM performance for hybrid composites using a statistical design and machine learning strategies that will facilitate greater use of hybrid composites in high-precision engineering applications and advanced manufacturing sectors. Full article

Thermochemical energy storage (TCES) has gained significant attention as a high-capacity, long-duration solution for renewable energy integration, yet material-level challenges hinder its widespread adoption. This review for the first time systematically examines recent advancements in nano-engineered composite thermochemical materials (TCMs), focusing on their ability to overcome intrinsic limitations of conventional systems. Sorption-based TCMs, especially salt hydrates, benefit from nano-engineering through carbon-based additives like CNTs and graphene, which enhance thermal conductivity and reaction kinetics while achieving volumetric energy densities exceeding 200 kWh/m³. For reversible reaction-based systems operating at higher temperatures (250–1000 °C), the strategies include (1) nanoparticle doping (e.g., SiO₂, Al₂O₃, carbonaceous materials) for the mitigation of sintering and agglomeration; (2) flow-improving agents to enhance fluidization; and (3) nanosized structure engineering for an enlarged specific surface area. All these approaches show promising results to address the critical issues of sintering and agglomeration, slow kinetics, and poor cyclic stability for reversible reaction-based TCMs. While laboratory results are promising, challenges still persist in side reactions, scalability, cost reduction, and system integration. In general, while nano-engineered thermochemical materials (TCMs) demonstrate transformative potential for performance enhancement, significant research and development efforts remain imperative to bridge the gap between laboratory-scale achievements and industrial implementation. Full article

This paper provides an overview of various size-dependent theories based on modified/consistent couple stress and strain gradient theories (CSTs and SGTs), highlighting the development of two-dimensional (2D) refined and advanced shear deformation theories (SDTs) and three-dimensional (3D) pure analytical and semi-analytical numerical methods, including their applications, for analyzing the static and dynamic behaviors of microscale plates and shells made from advanced materials such as fiber-reinforced composites, functionally graded (FG) materials, and carbon nanotube/graphene platelet-reinforced composite materials. The strong and weak formulations of the 3D consistent CST, along with their corresponding boundary conditions for FG microplates, are derived and presented for illustration. A comparison study is provided to show the differences in the results of a simply supported FG microplate’s central deflection, stress, and lowest natural frequency obtained using various 2D size-dependent SDTs and 3D analytical and numerical methods based on the consistent CST. A parametric study is conducted to examine how primary factors, such as the effects of dilatational and deviatoric strain gradients and couple stress, impact the static bending and free vibration behaviors of a simply supported FG microplate using a size-dependent local Petrov–Galerkin meshless method based on the consistent SGT. Influences such as the inhomogeneity index and length-to-thickness ratio are considered. It is shown that the significance of the impact of various material length-scale parameters on the central deflection and its lowest natural frequency (in the flexural mode) of the FG microplate is ranked, from greatest to least, as follows: the couple stress effect, the deviatoric strain gradient effect, and finally the dilatational strain gradient effect. Additionally, when the microplate’s thickness is less than 10⁻⁷ m, the couple stress effect on its static and dynamic behaviors becomes saturated. Conversely, the impact of the dilatational and deviatoric strain gradients consistently influences the microplate’s static and dynamic behaviors. Full article

This study presents a green, single-step method for synthesizing nanocomposites based on reduced graphene oxide (RGO) and gold nanoparticles (AuNPs), using sodium citrate as a mild reducing and stabilizing agent. AuNPs were generated from chloroauric acid (HAuCl₄) directly on the surface of graphene oxide (GO), which was simultaneously reduced to RGO. Structural characterization via Transmission Electron Microscopy (TEM), High Resolution TEM (HRTEM) and Selected Area Electron Diffraction (SAED) confirms spherical AuNPs (10–60 nm) distributed on RGO sheets, with indications of nanoparticle aggregation. Dynamic Light Scattering (DLS) and zeta potential analysis support these findings, suggesting colloidal instability with higher RGO content. Biological evaluation demonstrates dose-dependent cytotoxicity in HaCaT keratinocytes, with IC₅₀ values (half maximal inhibitory concentration) decreasing as RGO content is increased. At moderate dilutions (1–25 µL/100 µL), the composites show acceptable cell viability (>70%). Antibacterial assays reveal strong synergistic effects against Escherichia coli, Staphylococcus aureus, and Bacillus subtilis, with sample RGO/Au 0.500/0.175 g/L showing complete E. coli inhibition at low Au content (0.175 g/L). The composite retained activity even in protein-rich media, suggesting potential for antimicrobial applications. These findings highlight the potential of RGO/AuNPs composites as multifunctional materials for biomedical uses, particularly in antimicrobial coatings and targeted therapeutic strategies. Full article

Wider adoption of membrane technology is hindered by fouling and flux/rejection challenges. Recent practice in mitigating these is to incorporate hydrophilic and porous fillers. Herein the addition of hydrophilic graphene oxide (GO) in conjunction with porous mixed ZIFs (ZIF-67/ZIF-8) crystallites were used as inorganic fillers in the preparation of polyphenylenesulfone (PPSU) ultrafiltration (UF) membranes. The morphology of the resultant composite membranes was assessed using atomic force microscopy (AFM) and scanning electron microscopy (SEM) whilst surface hydrophilicity through water contact angle. The pure water flux (PWF) and membrane permeability were found to increase with increasing filler content. This was attributed to the combined hydrophilicity of GO and porous structure of the ZIF materials because of increasing alternative water pathways in the membrane matrix with increasing filler content. Furthermore, the increase in the ZIF component led to increasing bovine serum albumin (BSA) fouling resistance as demonstrated by increasing fouling recovery ratio (FRR). The dye rejection was due to a combination of electrostatic interaction between the fillers and the dyes as well as size exclusion. The chemical interactions between the ZIFs and the dyes resulted in slightly different rejection profiles for the smaller dyes, the cationic methylene blue being rejected less efficiently than the anionic methyl orange, potentially leading to their separation. The larger anionic dye, Congo red was rejected predominately through size exclusion. Full article

Composite anion exchange membranes (AEMs) based on poly(terphenylene piperidinium) (PTPiQA) and impregnated with varying loadings of quaternized graphene oxide (QGO) as filler were developed, and their properties as anion exchange membranes for use in water electrolysis (AEMWEs) and fuel cells (AEMFCs) were explored. This study investigates the trade-off between mechanical robustness, ionic conductivity, and alkaline stability in QGO-reinforced twisted polymer backbones. QGO synthesized by functionalization with ethylenediamine (EDA), followed by quaternization with glycidyl trimethylammonium chloride (GTMAC), was used as a filler for PTPiQA, and the properties of the resulting composites PTPiQA-QGO-X investigated as a function of QGO loading for X between 0.1 and 0.7 wt%. Among all compositions, PTPiQA-QGO-0.3% exhibited the highest OH⁻ conductivity of 71.56 mS cm⁻¹ at room temperature, attributed to enhanced ionic connectivity and water uptake. However, this increase in conductivity was accompanied by a slight decrease in ion exchange capacity (IEC) retention (91.8%) during an alkaline stability test in 1 M KOH at 60 °C for 336 h due to localized cation degradation. Mechanical testing revealed that PTPiQA-QGO-0.3% offered optimal dry and wet tensile strength (dry TS of 42.77 MPa and wet TS of 30.20 MPa), whereas higher QGO loadings yielded low mechanical strength. These findings highlight that 0.3 wt% QGO balances ion transport efficiency and mechanical strength, while higher loadings improve alkaline durability, compromising mechanical durability and guiding the rational design of AEMs for AEMWEs and AEMFCs. Full article

This study presents a comprehensive evaluation of the behavior of fluoroelastomer (FKM) compounds reinforced with graphene nanoplatelets of various sizes such as 15 μm (GN15) and 5 μm (GN5). The study evaluates the mechanical, dynamic mechanical, thermal, wetting, and photothermal properties of the compounds when irradiated with an 808 nm laser. The results demonstrate that the size of the graphene nanoplatelets significantly impacts the mechanical properties, with smaller sizes exhibiting a stronger reinforcing effect compared to larger nanoplatelets. Additionally, clear evidence of an influence on dynamic mechanical properties was observed, particularly through the broadening of the damping factor (tan δ) peak. This suggests modifications to the material’s viscoelastic behavior. Regarding the photothermal response, it was found that smaller nanoplatelets (GN5) dispersed in the rubber matrix allow higher temperatures to be reached and thermal equilibrium to be achieved more efficiently under irradiation. Overall, the results suggest that FKM compounds containing graphene nanoplatelets can attain high temperatures with low-energy infrared irradiation. This makes them promising materials for technological applications in extreme environments, such as the Arctic, high mountains, or space, where materials with controlled thermal responses and high mechanical performance are required. Full article

Rechargeable aqueous Zn-MnO₂ batteries are positioned as a highly promising candidate for next-generation energy storage, owing to their compelling combination of economic viability, inherent safety, exceptional capacity (with a theoretical value of ≈308 mAh·g⁻¹), and eco-sustainability. However, this system still faces multiple critical challenges that hinder its practical application, primarily including the ambiguous energy storage reaction mechanism (e.g., unresolved debates on core issues such as ion transport pathways and phase transition kinetics), dendrite growth and side reactions (e.g., the hydrogen evolution reaction and corrosion reaction) on the metallic Zn anode, inadequate intrinsic electrical conductivity of MnO₂ cathodes (≈10⁻⁵ S·cm⁻¹), active material dissolution, and structural collapse. This review begins by systematically summarizing the prevailing theoretical models that describe the energy storage reactions in Zn-Mn batteries, categorizing them into the Zn²⁺ insertion/extraction model, the conversion reaction involving MnO_x dissolution–deposition, and the hybrid mechanism of H⁺/Zn²⁺ co-intercalation. Subsequently, we present a comprehensive discussion on Zn anode protection strategies, such as surface protective layer construction, 3D structure design, and electrolyte additive regulation. Furthermore, we focus on analyzing the performance optimization strategies for MnO₂ cathodes, covering key pathways including metal ion doping (e.g., introduction of heteroions such as Al³⁺ and Ni²⁺), defect engineering (oxygen vacancy/cation vacancy regulation), structural topology optimization (layered/tunnel-type structure design), and composite modification with high-conductivity substrates (e.g., carbon nanotubes and graphene). Therefore, this review aims to establish a theoretical foundation and offer practical guidance for advancing both fundamental research and practical engineering of Zn-manganese oxide secondary batteries. Full article

The combination of polypyrrole (PPy) with graphene has attracted extensive attention as a nonlinear optical material with various optoelectronic applications. Here, we describe the development of PPy nanoplates prepared using a simple spin-coating method. The appropriate volume of the dropped PPy solution was determined to be 50 drops by comparing the surface morphologies, chain structures, elementary compositions, and optical properties of PPy saturable absorbers (SAs). The hybrid PPy/graphene heterostructure SA was obtained using the wet transfer process of a graphene layer. This approach led to significant improvements in optical properties, including a ~7.2% increase in linear optical absorption, a 2.5-fold increase in modulation depth, and a third decrease in saturable intensity at 1550 nm due to the additional optical absorption and the π-π interaction between PPy nanoplates and the graphene layer. By inserting the PPy/graphene heterostructure SA into the passively mode-locked fiber laser cavity, 1559 nm ultrashort laser pulses were generated, with an average output power of 1.24 mW, a 815 fs pulse width, and a repetition frequency of 3.26 MHz. Our experimental results demonstrate that the prepared PPy SA has excellent nonlinear optical characteristics, providing a new opportunity for the generation of ultrashort laser pulses. Full article

Waste lithium-ion batteries (LIBs), which usually contain dangerous organic electrolytes and transition metals, including nickel, cobalt, iron, and manganese, can hurt the environment and human health. Substantial advancements have been achieved in employing high-efficiency, economical, and environmentally sustainable techniques for the recycling of spent LIBs. Converting exhausted LIBs into efficient energy conversion catalysts straightforwardly is a good strategy for addressing metal resource constraints and clean energy concerns. This transforms waste cathodes, anodes, binders, and separators from depleted LIBs into electrocatalysts free of platinum group metals for the oxygen evolution reaction (OER) and the oxygen reduction reaction (ORR). The composite, including transition metal oxide, graphene oxide, and carbon mass, will be synthesized from spent LIBs, demonstrating enhanced electrocatalytic activity. Utilizing “waste-to-energy” methods for used LIBs as catalysts would provide substantial benefits in environmental preservation and the effective production of functional materials in metal–air batteries. Full article