Search Results (2,924)

The contamination of drinking water by per- and polyfluoroalkyl substances (PFASs) presents a global concern due to their extreme persistence, driven by strong C–F bonds. This study investigated the potential of graphene as a filtration material for PFAS removal, focusing on six key compounds regulated by the U.S. EPA: PFOA, PFNA, GenX, PFBS, PFOS, and PFHxS. Using molecular simulations, adsorption energy, diffusion coefficients, and PFAS-to-graphene distances were analyzed. The results showed that adsorption strength increased with molecular weight; PFOS (500 g/mol) exhibited the strongest adsorption (−171 kcal/mol). Compounds with sulfonic acid head groups (e.g., PFOS) had stronger interactions than those with carboxylate groups (e.g., PFNA), highlighting the importance of head group chemistry. Shorter graphene-to-PFAS distances also aligned with higher adsorption energies. PFOS, for example, had the shortest distance at 8.23 Å (head) and 6.15 Å (tail) from graphene. Diffusion coefficients decreased with increasing molecular weight and carbon chain length, with lower molecules like PFBS (four carbon atoms) diffusing more rapidly than heavier ones like PFOS and PFNA. Interestingly, graphene enhanced PFAS mobility in water, likely by disrupting the water structure and lowering intermolecular resistance. These results highlight graphene’s promise as a high-performance material for PFAS removal and future water purification technologies. Full article

The widespread adoption of sodium-ion batteries (SIBs) remains constrained by the inherent limitations of conventional anode materials, particularly their inadequate electronic conductivity, limited active sites, and pronounced structural degradation during cycling. To overcome these limitations, we propose a novel redox engineering approach to fabricate oxygen-vacancy-rich SnO₂ dots anchored on reduced graphene oxide (rGO), which are encapsulated within N-doped carbon nanofibers (denoted as ov-SnO₂/rGO@N-CNFs) through electrospinning and subsequent carbonization. The introduction of rich oxygen vacancies establishes additional sodium intercalation sites and enhances Na⁺ diffusion kinetics, while the conductive N-doped carbon network effectively facilitates charge transport and mitigates SnO₂ aggregation. Benefiting from the well-designed architecture, the hierarchical ov-SnO₂/rGO@N-CNFs electrode achieves remarkable reversible specific capacities of 351 mAh g⁻¹ after 100 cycles at 0.1 A g⁻¹ and 257.3 mAh g⁻¹ after 2000 cycles at 1.0 A g⁻¹ and maintains 177 mAh g⁻¹ even after 8000 cycles at 5.0 A g⁻¹, demonstrating exceptional long-term cycling stability and rate capability. This work offers a versatile design strategy for developing high-performance anode materials through synergistic interface engineering for SIBs. Full article

Films of a Ni/Al-layered double hydroxide intercalated with reduced graphene oxide were deposited, by means of a simple and rapid electrochemical synthesis, on Pt electrodes previously submitted to a special cleaning procedure. The aim of the research was to determine whether the better electrocatalytic properties of the Ni(III)/Ni(II) couple, due to the presence of the carbon nanomaterial, as compared to the Ni/Al-LDH alone, could allow glucose detection at physiological pHs, as normally LDHs work as redox mediators in basic solutions. Chronoamperometric experiments were carried out by applying a potential of 1.0 V vs. SCE to the electrode soaked in solutions buffered at pHs from 5.0 to 9.0 to which glucose was continuously added. The steady-state currents increased as the pH solution increased, but at pH = 7.0 the modified electrode exhibited a fast and rather sensitive response, which was linear up to 10.0 mM glucose, with a sensitivity of 0.56 A M⁻¹ cm⁻² and a limit of detection of 0.05 mM. Our results suggest the potential application of Ni/Al-LDH(ERGO) composite for the non-enzymatic detection of glucose or other oxidizable analytes under biological conditions. Full article

This review article compiled previous reports in the fabrication of hydroquinone (HQ) electrochemical sensors using differently modified electrodes. The electrode materials, which are also called electrocatalysts, play a crucial role in electrochemical detection of biomolecules and toxic substances. Metal oxides, MXenes, carbon-based materials such as reduced graphene oxide (rGO), carbon nanotubes (CNTs), layered double hydroxides (LDH), metal sulfides, and hybrid composites were extensively utilized in the fabrication of HQ sensors. The electrochemical performance, including limit of detection, linearity, sensitivity, selectivity, stability, reproducibility, repeatability, and recovery for real-time sensing of the HQ sensors have been discussed. The limitations, challenges, and future directions are also discussed in the conclusion section. It is believed that the present review article may benefit researchers who are involved in the development of HQ sensors and catalyst preparation for electrochemical sensing of other toxic substances. Full article

Polymer-based electrothermal composites (PECs) have been increasingly attracting attention in recent years owing to their flexibility, low density, and high electrothermal efficiency. However, although a large number of reviews have focused on flexible and transparent film heaters as well as polymer-based conductive composites, comprehensive reviews of polymer-based electrothermal composites remain limited. Herein, we provide a comprehensive review of recent advancements in polymer-based electrothermal materials. This review begins with an introduction to the electrothermal theoretical basis and the research progress of PECs incorporating various conductive fillers, such as graphene, carbon nanotubes (CNTs), carbon black (CB), MXenes, and metal nanowires. Furthermore, a critical discussion is provided to emphasize the factors influencing the electrothermal conversion efficiency of these composites. Meanwhile, the development of multi-functional electrothermal materials has been also summarized. Finally, the application progress, future prospects, limitations, and potential directions for PEC are discussed. This review aims to serve as a practical guide for engineers and researchers engaged in the development of polymer-based electrothermal composites. Full article

The electrochemical conversion of CO₂ into high-purity Graphene NanoCarbon (GNC) materials provides a compelling path to address climate change while producing economically valuable nanomaterials. This work presents the progress and prospects of new large-scale syntheses of GNC allotropes via the C2CNT (CO₂ to Carbon Nano Technology) process. The C2CNT molten carbonate electrolysis technique enables the formation of Carbon NanoTubes (CNTs), Magnetic CNTs (MCNTs), Carbon Nano-Onions (CNOs), Carbon Nano-Scaffolds (CNSs), and Helical CNTs (HCNTs) directly from atmospheric or industrial CO₂. We discuss the morphology control enabled through variations in electrolyte composition, temperature, current density, and nucleation additives. We present results from scaled operations reaching up to 1000 tons/year CO₂ conversion and propose design approaches to reach megaton scales to support climate mitigation and GNC mass production. The products demonstrate high crystallinity, as evidenced by Raman, XRD, SEM, and TGA analyses, and offer promising applications in electronics, construction, catalysis, and medical sectors. Full article

Water scarcity poses a formidable challenge around the world, especially in arid regions where limited availability of freshwater resources threatens both human well-being and ecosystem sustainability. Membrane-based desalination technologies offer a viable solution to address this issue by providing access to clean water. This work ultimately aims to develop a novel permselective polymeric membrane material to be employed in an electrochemical desalination system. This part of the study addresses the optimization, preparation, and characterization of a polyvinylidene difluoride (PVDF) polymeric membrane using the electrospinning technique. The membranes produced in this work were fabricated under specific operational, environmental, and material parameters. Five different additives and nano-additives, i.e., graphene oxide (GO), carbon nanotubes (CNTs), zinc oxide (ZnO), activated carbon (AC), and a zeolitic imidazolate metal–organic framework (ZIF-8), were used to modify the functionality and selectivity of the prepared PVDF membranes. Each membrane was synthesized at two different levels of additive composition, i.e., 0.18 wt.% and 0.45 wt.% of the entire PVDF polymeric solution. The physiochemical properties of the prepared membranes were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), zeta potential, contact angle, conductivity, porosity, and pore size distribution. Based on findings of this study, PVDF/GO membrane exhibited superior results, with an electrical conductivity of 5.611 mS/cm, an average pore size of 2.086 µm, and a surface charge of −38.33 mV. Full article

Recently, it has been found that electrochemical sensing technology is one of the significant approaches for the monitoring of toxic and hazardous substances in food and the environment. Nitrofurazone (NFZ) and nitrofurantoin (NFT) possess a hazardous influence on the environment, aquatic life, and human health. Thus, various advanced materials such as graphene, carbon nanotubes, metal oxides, MXenes, layered double hydroxides (LDHs), polymers, metal–organic frameworks (MOFs), metal-based composites, etc. are widely used for the development of nitrofurazone and nitrofurantoin sensors. This review article summarizes the progress in the fabrication of electrode materials for nitrofurazone and nitrofurantoin sensing applications. The performance of the various electrode materials for nitrofurazone and nitrofurantoin monitoring are discussed. Various electrochemical sensing techniques such as square wave voltammetry (SWV), differential pulse voltammetry (DPV), linear sweep voltammetry (LSV), amperometry (AMP), cyclic voltammetry (CV), and chronoamperometry (CA) are discussed for the determination of NFZ and NFT. It is observed that DPV, SWV, and AMP/CA are more sensitive techniques compared to LSV and CV. The challenges, future perspectives, and limitations of NFZ and NFT sensors are also discussed. It is believed that present article may be useful for electrochemists as well materials scientists who are working to design electrode materials for electrochemical sensing applications. Full article

Hydrogen is widely recognized as a key enabler of the clean energy transition, but the lack of safe, efficient, and scalable storage technologies continues to hinder its broad deployment. Conventional hydrogen storage approaches, such as compressed hydrogen storage, cryo-compressed hydrogen storage, and liquid hydrogen storage, face limitations, including high energy consumption, elevated cost, weight, and safety concerns. In contrast, solid-state hydrogen storage using carbon-based adsorbents has gained growing attention due to their chemical tunability, low cost, and potential for modular integration into energy systems. This review provides a comprehensive evaluation of hydrogen storage using carbon-based materials, covering fundamental adsorption mechanisms, classical materials, emerging architectures, and recent advances in computationally AI-guided material design. We first discuss the physicochemical principles driving hydrogen physisorption, chemisorption, Kubas interaction, and spillover effects on carbon surfaces. Classical adsorbents, such as activated carbon, carbon nanotubes, graphene, carbon dots, and biochar, are evaluated in terms of pore structure, dopant effects, and uptake capacity. The review then highlights recent progress in advanced carbon architectures, such as MXenes, three-dimensional architectures, and 3D-printed carbon platforms, with emphasis on their gravimetric and volumetric performance under practical conditions. Importantly, this review introduces a forward-looking perspective on the application of artificial intelligence and machine learning tools for data-driven sorbent design. These methods enable high-throughput screening of materials, prediction of performance metrics, and identification of structure–property relationships. By combining experimental insights with computational advances, carbon-based hydrogen storage platforms are expected to play a pivotal role in the next generation of energy storage systems. The paper concludes with a discussion on remaining challenges, utilization scenarios, and the need for interdisciplinary efforts to realize practical applications. Full article

The development of lightweight composites with superior mechanical properties and electromagnetic interference (EMI) shielding performance is essential for various structural and functional applications. This study investigates the effect of hybrid nanocarbon (graphene nanosheet (GNS) and carbon nanotube (CNT)) reinforcements on the properties of magnesium (Mg) matrix composites. Specifically, the GNS-CNT hybrid, which forms a three-dimensional interconnected network structure, was analyzed and compared to composites reinforced with only GNSs or CNTs. The objective was to determine the benefits of hybrid reinforcements on the mechanical strength and EMI shielding capability of the composites. The results indicated that the GNS-CNT/Mg composite, at a nanocarbon content of 0.5 wt.% and a GNS-CNT ratio of 1:2, achieved optimal performance, with a 55% increase in tensile strength and an EMI shielding effectiveness of 70 dB. The observed enhancements can be attributed to several key mechanisms: effective load transfer, which promotes tensile twinning, along with improved impedance matching and multiple internal reflections within the GNS-CNT network, which enhance absorption loss. These significant improvements position the composite as a promising candidate for advanced applications requiring high strength, toughness, and efficient electromagnetic shielding, providing valuable insights into the design of high-performance lightweight materials. Full article

The rapid growth in plastic consumption, particularly polyethylene terephthalate (PET), has led to a significant increase in plastic waste, posing a major environmental challenge. Developing an integrated circular economy framework for nanomaterial-enhanced recycled PET (nrPET) can be a promising approach to address this issue and advance sustainable and resilient road construction practices. This comprehensive review examines the current use of rPET in road construction, its existing limitations, and the role of nanomaterials in enhancing the performance of these materials. The review explores the mechanisms by which nanomaterials, such as carbon nanotubes, graphene, nanosilica, and clay nanoplatelets, can improve the properties of rPET, leading to more durable, weather-resistant, and cost-effective road materials. Furthermore, the review analyzes the environmental and sustainability benefits of using nrPET in road construction, focusing on carbon footprint reduction, conservation of natural resources, and alignment with circular economy principles. The potential for job creation, social benefits, and support for circular economy initiatives are also discussed. The review then delves into the challenges associated with the implementation of this framework, including technical barriers, economic and market barriers, regulatory and policy challenges, and environmental and safety considerations. Strategies to address these challenges, such as advancements in nanotechnology, scaling up circular economy models, and fostering collaborative research, are presented. Finally, the article proposes a framework and outlines future directions and research opportunities, emphasizing the exploration of emerging nanomaterials, scaling up circular economy models, and encouraging collaborations between researchers, industry stakeholders, policymakers, and communities. 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

The aim was to investigate the impact of laser parameters on the surface morphology of ablated graphene and elucidate the interaction mechanism between carbon materials and femtosecond lasers. A pulsed laser with a wavelength of 1030 nm is employed to infer the ablation threshold of the surface and interface of graphene coatings formed through ultrasonic spraying. The ablation threshold of the coating–substrate interface is verified by numerical simulation. Incorporating the data of groove width and depth obtained from a three-dimensional profilometer and finite element simulation, an in-depth analysis of the threshold conditions of laser ablation in coating materials is accomplished. The results indicate that when the femtosecond laser frequency is 10 kHz, the pulse width is 290 fs, and the energy density reaches 0.057 J/cm², the graphene material can be effectively removed. When the energy density is elevated to 2.167 J/cm², a complete ablation of a graphite coating with a thickness of 1.5 μm can be achieved. The findings of this study validate the evolution law and linear relationship of ablation crater morphology, offering new references for microstructure design and the selection of controllable laser processing parameters. Full article

Efficient and rapid detection of bacterial pathogens is crucial for food safety and effective disease control. While conventional methods such as PCR and ELISA are accurate, they are time-consuming, costly, and often require specialized infrastructure. Recently, electrochemical biosensors integrating graphene nanomaterials with bacteriophages—termed graphages—have emerged as promising platforms for pathogen detection, offering fast, specific, and highly responsive detection. This review critically examines all electrochemical biosensors reported to date that utilize graphene–phage hybrids. Key aspects addressed include the types of graphene nanomaterials and bacteriophages used, immobilization strategies, electrochemical transduction mechanisms, and sensor metrics—such as detection limits, linear ranges, and ability to perform in real matrices. Particular attention is given to the role of phage orientation, surface functionalization, and the use of receptor binding proteins. Finally, current limitations and opportunities for future research are outlined, including prospects for genetic engineering and sensor miniaturization. This review serves as a comprehensive reference for researchers developing phage-based biosensors, especially those interested in integrating carbon nanomaterials for improved electroanalytical performance. 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