Search Results (838)

Graphene has emerged as a promising material for transforming conventional textiles into smart, multi-functional platforms due to its exceptional electrical, thermal, and mechanical properties. This review aims to provide a comprehensive overview of the latest advances in graphene-enhanced fabrics over the past ten years, focusing on their functional properties and real-world applications. This article examines the main strategies used to incorporate graphene and its derivatives—such as graphene oxide and reduced graphene oxide—into textile substrates through coating, printing, or composite formation. The structural, electrical, thermal, mechanical, and electrochemical properties of these fabrics are discussed based on characterization techniques including microscopy, Raman spectroscopy, and cyclic voltammetry. Functional evaluations in wearable strain sensors, biosignal acquisition, electrothermal systems, and energy storage devices are highlighted to demonstrate the versatility of these materials. Although challenges remain in scalability, durability, and washability, recent developments in fabrication and encapsulation methods show significant potential to overcome these limitations. This review concludes by outlining the major opportunities and future directions for graphene-based textiles in areas such as personalized health monitoring, active thermal wear, and integrated wearable electronics. Full article

White-light-emitting diodes (wLEDs) are central to next-generation lighting technologies, yet their reliance on critical raw materials (CRMs), such as rare-earth elements, raises concerns regarding sustainability and supply security. In this work, we present a simple, low-cost method to produce photoluminescent carbon-based nanostructures—known as oxidative debris (OD)—via alkaline treatment of graphene oxide (GO) using KOH solutions ranging from 0.04 M to 1.78 M. The resulting OD, isolated from the supernatant after acid precipitation, exhibits strong and tunable photoluminescence (PL) across the visible spectrum. Emission peaks shift from blue (~440 nm) to green (~500 nm) and yellow (~565 nm) as a function of treatment conditions, with excitation wavelengths between 300 and 390 nm. Optical, morphological. and compositional analyses were performed using UV-Vis, AFM, FTIR, and Raman spectroscopy, confirming the presence of highly oxidized aromatic domains. The blue-emitting (S2) and green/yellow-emitting (R2) fractions were successfully separated and characterized, demonstrating potential color tuning by adjusting KOH concentration and treatment time. This study highlights the feasibility of reusing GO-derived byproducts as sustainable phosphor alternatives in wLEDs, reducing reliance on CRMs and aligning with green chemistry principles. Full article

Thylakoid-based photosynthetic biofuel cells (TBFCs) harness the inherent light-driven electron transfer pathways of photosynthesis to enable sustainable solar-to-electrical energy conversion. While TBFCs offer a unique route toward biohybrid energy systems, their practical deployment is hindered by sluggish electron transfer kinetics, unstable redox mediators, and inefficient interfacing between biological and electrode components. This review critically examines recent advances in TBFCs, with a focus on three key surface engineering strategies: (i) incorporation of nanostructured materials to enhance electrode conductivity and surface area; (ii) application of redox mediators to facilitate charge transfer between photosynthetic proteins and electrodes; and (iii) functional exploitation of individual thylakoid components, including Photosystem I (PSI) and Photosystem II (PSII), to augment photogenerated current output. By systematically evaluating current advancements, this review highlights the synergistic role of materials and biological components in advancing TBFC technology and offers insights into next generation biohybrid solar energy systems with enhanced efficiency and scalability. Full article

Nanozymes constitute a rapidly advancing frontier in scientific research, attracting widespread international interest, particularly for their role in facilitating cascade reactions. Despite their initial discovery a few years ago, significant hurdles persist in optimizing their catalytic performance and substrate specificity—challenges that are especially critical in the context of biomedical diagnostics. Within this domain, nitrogen-containing graphene oxide-based nanozymes exhibiting peroxidase-mimicking activity have emerged as particularly promising candidates, owing to the exceptional electrical conductivity, mechanical flexibility, and structural resilience of reduced graphene oxide-based materials. Intensive efforts have been devoted to engineering graphene oxide structures to enhance their peroxidase-like functionality. Nonetheless, the practical implementation of such nanozymes remains under active investigation and demands further refinement. This review synthesizes the current developments in nitrogen heteroatom-containing graphene oxide nanozymes and their derivative nanozymes, emphasizing recent breakthroughs and biomedical applications. It concludes by exploring prospective directions and the broader potential of these materials in the biomedical landscape. Full article

The growing demand for fire-safe, sustainable materials has driven extensive research into advanced flame retardants particularly polystyrene (PS), a widely utilized yet inherently flammable polymer. Graphene-derived materials are considered effective flame retardants owing to their higher thermal stability, char-formation, and gas barrier properties. However, despite these advantages, challenges such as agglomeration, high thermal conductivity, poor interfacial compatibility, and processing limitations hinder their full-scale adoption in building insulation and other applications. This review presents an in-depth analysis of recent progress in graphene-enhanced flame-retardant systems for polystyrene applications, focusing on synthesis methods, flame-retardant mechanisms, and material performance. It also discusses strategies to address these challenges, such as surface functionalization, hybrid flame-retardant formulations, optimized graphene loading, and improved dispersion techniques. Furthermore, future research directions are proposed to enhance the effectiveness and commercial viability of graphene-based flame-retardant polystyrene composites. Overcoming these challenges is essential for high-performance, eco-friendly, flame-retardant materials on a larger scale. Full article

Carbon nanotubes (CNTs) are cylindrical nanostructures formed by rolling a graphene sheet—a hexagonal lattice of carbon atoms—into a tube. Based on the rolling direction, CNTs are categorized as armchair, zigzag, or chiral. The chiral vector, derived from the graphene lattice, defines the CNT’s structure, with chiral CNTs denoted by indices (n, m), where m > 0 and m ≠ n. The mechanical properties and structural stability of CNTs are highly sensitive to defects and impurities within their atomic framework. Among these, point defects such as single-atom vacancies are the most prevalent and can significantly degrade mechanical performance. These defects alter stress distribution, reduce stiffness, and impair strength, thereby limiting the functional reliability of CNTs in advanced applications such as nanocomposites, sensors, and electronic devices. This study examines the influence of vacancy defects on CNT mechanical behavior through a multiscale modeling framework. Molecular dynamics (MD) simulations are conducted using LAMMPS, with structural visualization via Visual Molecular Dynamics (VMD). Concurrently, a finite element (FE) model is developed in ANSYS, where the CNT is idealized as a space frame of elastic beam elements representing carbon–carbon bonds. The integration of atomistic and continuum approaches offers a comprehensive understanding of defect-induced mechanical degradation. The MD and FEM results are in strong agreement with findings in existing literature, validating the adopted methodology. These findings contribute valuable insights into the design and optimization of CNT-based materials for high-performance engineering applications. Full article

In this study, graphene production via liquid-phase exfoliation assisted by sonication was evaluated using deionized water as a solvent and two graphite sources: one recovered from spent lithium-ion batteries (LIBs) and a commercial counterpart. A 750 W, 20 kHz ultrasonic processor was used, with sonication amplitudes ranging from 50% to 80% for two hours while maintaining a constant temperature of 45 °C. The resulting dispersions were left undisturbed for 24 h at ambient temperature to allow natural phase separation between decanted and dispersed fractions. These fractions were subsequently dried and weighed to determine exfoliation yield. High-quality graphene was successfully obtained via direct liquid-phase exfoliation of graphite recovered from LIBs, assisted by sonication in deionized water. Graphene formation was confirmed in both suspended and decanted fractions after two hours of sonication at 80% amplitude through complementary characterization techniques, including UV-Vis, Raman spectroscopy, HRTEM, and XRD. Comparative experiments using thermally pretreated battery graphite and commercial graphite revealed that graphene dispersions derived from untreated LIB-derived graphite exhibited greater long-term stability than those obtained from commercial or thermally pretreated battery graphite before sonication. Full article

Past studies have offered insights into how graphite-derived graphene oxide (GDGO) can improve the mechanical properties and alter microstructural characteristics of concrete. These advantages can significantly impact the construction industry regarding cost, sustainability, and efficiency. However, the high cost of GDGO can make commercial implementation unattainable. This paper comprehensively investigates coal-derived GO as a cost-saving alternative to commercial GDGO while achieving comparable concrete performance. Different GO proportions were incorporated into concrete mixes through laboratory experiments to determine the effect on mechanical properties and microstructures. In this research, concrete mixes were formulated by replacing a portion of cement with coal-derived GO and adding this GO as an additive to concrete at varying percentages (0.05%, 0.10%, 0.25%, 0.50%, 1%, and 1.5% by weight of cement). The study revealed flexural, split tensile, and compressive strength improvements of 3.3%, 2.3%, and 21.2%, respectively, at a minimal 0.05 wt.% GO replacement. Optimal inclusions of GO as an additive ranging from 0.05 to 0.25 wt.% were identified to exhibit a maximum increase in mechanical properties. More precisely, adding 0.10 weight percent of GO as an additive to concrete showed increases in flexural, split tensile, and compressive strengths of 14.05%, 9.7%, and 34.2%, respectively. Furthermore, detailed analyses, including modulus of elasticity, Poisson’s ratio, heat of hydration, and microstructural analysis provided comprehensive insights into the enhanced mechanical performance of GO-incorporated concrete. Additionally, the study revealed a lower Ca/Si ratio in GO concrete, further validating the reinforcing properties of the GO. Full article

The current economic growth and increasing needs of society have led to developing processes that harm our environment and have severe long-term consequences. For this reason, different attempts have been made to mitigate these effects by substituting conventional toxic materials with environmentally friendly ones. Industry sectors related to energy storage, printed electronics, and wearable technology are moving towards applying sustainable strategies. Renewable biopolymers such as cellulose and its derivatives, as well as carbon-based alternatives, which include carbon nanotubes (CNTs), single-wall carbon nanotubes (SWCNTs), graphite, graphene, and carbon black (CB), are leading the advances in this field. The present research aimed to develop conductive cellulose paper using environmentally friendly components compatible with the paper recycling process. Coating formulations based on carbon black were proposed using three different types of binders: polytetrafluoroethylene (PTFE), latex (styrene butadiene), and sodium carboxymethyl cellulose (CMC). The formulation, composition, and preparation were studied, and they were related to the coating’s electrical resistance and integrity. This last parameter was determined through a new method described in this research, implementing a mechanical/optical technique to measure the coating’s durability. The formulation with the best performance in terms of electrical resistance (0.29 kΩ), integrity, and non-toxicity was obtained using sodium carboxymethyl cellulose (CMC) as a binder and dispersant. Full article

Promethazine hydrochloride (PMH) is a first-generation antipsychotic drug created from phenothiazine derivatives that is widely employed to treat psychiatric disorders in human healthcare systems. However, an overdose or long-term intake of PMH can lead to severe health issues in humans. Hence, establishing a sensitive, accurate, and efficient detection approach to detect PMH in human samples is imperative. In this study, we designed orthorhombic copper molybdate microspheres decorated on reduced graphene oxide (Cu₃Mo₂O₉/RGO) composite via the effective one-pot hydrothermal method. The structural and morphological features of the designed hybrid were studied using various spectroscopic methods. Subsequently, the electrochemical activity of the composite-modified screen-printed carbon electrode (Cu₃Mo₂O₉/RGO/SPCE) was assessed by employing voltammetric methods for PMH sensing. Owing to the uniform composition and structural benefits, the combination of Cu₃Mo₂O₉ and RGO has not only improved electrochemical properties but also enhanced the electron transport between PMH and Cu₃Mo₂O₉/RGO. As a result, the Cu₃Mo₂O₉/RGO/SPCE exhibited a broad linear range of 0.4–420.8 µM with a low limit of detection (LoD) of 0.015 µM, highlighting excellent electrocatalytic performance to PMH. It also demonstrated good cyclic stability, reproducibility, and selectivity in the presence of chlorpromazine and biological and metal compounds. Furthermore, the Cu₃Mo₂O₉/RGO/SPCE sensor displayed satisfactory recoveries for real-time monitoring of PMH in human urine and serum samples. This study delivers a promising electrochemical sensor for the efficient analysis of antipsychotic drug molecules. Full article

CO₂ capture by adsorption on proper solid materials appears to be a promising approach, due to its low energy requirements and ease of implementation. This study aimed to prepare efficient materials for CO₂ capture based on composites of nanocarbon and reduced graphene oxide, using graphite, L-ascorbic acid, and glycine as precursors. The materials were characterized by XRD, low-temperature N₂ adsorption, FTIR, Raman, and XPS spectroscopies, along with SEM and TEM. The CO₂ adsorption capacities, heats of adsorption, and selectivity were determined. A hierarchical porous structure was found for NC-LAA, NC/RGO-LAA, and NC/RGO-Gly. At 273 K and 100 kPa, the adsorption capacities for NC-LAA and NC-Gly reached 2.6 mmol/g and 2.5 mmol/g, respectively, while for the composites, the capacities were 1.7 mmol/g for NC/RGO-Gly and 3.5 mmol/g for NC/RGO-LAA. The adsorption ability of the glycine-derived materials is related to the presence of nitrogen-containing functional groups. The heats of adsorption for NC-LAA, NC-Gly, and NC/RGO-Gly reveal chemisorption with CO₂. Except for chemisorption, the NC/RGO-LAA material shows a sustained physical adsorption up to higher CO₂ coverage. The best adsorption of CO₂, observed for NC/RGO-LAA, is connected with the synergy between carbon dots and RGO. This composition ensures both sufficient oxygen surface functionalization and a proper hierarchical porous structure. Full article

Recently, graphene oxide (GO) has been largely investigated as a potential adsorbent towards dyes. However, the major obstacle to its full employment is linked to its natural powder consistence, which greatly complexifies the operations of recovery and reuse. With the aim to overcome this issue, the present work reports on the design of GO-modified carbon nanotubes buckypapers (BPs), in which the main component, GO, is entirely entrapped in the BP grid generated by CNTs for the double purpose of (a) increasing adsorption performance of GO-BPs and (b) ensure a fast process of regeneration and reuse. Adsorption experiments were performed towards several dyes: Acid Blue 29 (AB29), Crystal Violet (CV), Eosyn Y (EY), Malachite Green (MG), and Rhodamine B (RB) (C_i = 50 ppm, pH = 6). Results demonstrated that adsorption is strictly dependent on the charge occurring both on GO-BP and dye surfaces, observing great adsorption capacities towards MG (493.44 mg g⁻¹), RB (467.35 mg g⁻¹), and CV (374.53 mg g⁻¹), due to the best coupling of dye cationic form with negative GO-BP surface. Adsorption isotherms revealed that dyes capture onto GO-BPs is thermodynamically favored (ΔG < 0), becoming more negative at 313 K. Kinetic studies evidenced that the process can be described through a pseudo-first-order model, with MG, RB, and CV exhibiting the highest values of k₁. In view of these results, the following trend in GO-BP adsorption performance has been derived: MG ≈ RB > CV > AB29 > EY. Full article

Tribology is the branch of science and engineering that focuses on understanding friction, wear, and lubrication, which is essential for saving energy, improving performance, reducing vibration, and creating eco-friendly lubricants and wear resistance. Over the past decade, nanomaterials have captured the immense interest of tribology science. This review aimed to analyze how graphene and its derivatives can be incorporated into lubricants to enhance their properties, particularly in mitigating friction and wear. This is due to graphene’s excellent specific properties, such as a low friction coefficient, mechanical strength, high thermal and electrical conductivity, biocompatibility, high load-carrying capacity, wear resistance, and chemical stability. This study briefly introduces graphite, graphene, and graphene oxide, as well as presents graphene as a material for tribological applications. Among other things, the environmentally friendly possibilities of chemical reduction of reduced graphene oxide are analyzed here, as well as the macro-, micro-, and nano-tribological examination of graphene and its derivatives. Despite what is already known about graphene in tribology, further research is needed to gain a deeper understanding of development regarding integration with different materials, long-term performance, eco-friendly synthesis using green reducing agents, and comprehending how these approaches may affect systems at various scales. Full article

Oxygen reduction reaction (ORR) is one of the most important reactions in electrochemical energy storage and conversion devices. To overcome the slow kinetics, minimize the overpotential, and make this reaction feasible, efficient, and stable, electrocatalysts are needed. Metal-free graphene-based systems are considered promising and cost-effective ORR catalysts with adjustable structures. This review is meant to give a rational overview of the graphene-based metal-free ORR electrocatalysts, illustrating the huge amount of related research developed particularly in the field of fuel cells and metal–air batteries, with particular attention to the synthesis procedures. The novelty of this review is that, beyond general aspects regarding the synthesis and characterization of graphene, above 90% of the various graphene (doped and undoped species, composites)-based ORR electrocatalysts have been reported, which represents an unprecedented thorough collection of both experimental and theoretical studies. Hundreds of references are included in the review; therefore, it can be considered as a vademecum in the field. Full article

The efficient mass transport and enhanced accessibility of active sites are crucial for high-performance electrocatalysts in water splitting. Inspired by the hierarchical structure of natural wood, we engineered a monolithic electrocatalyst, cobalt nanoparticles encapsulated in nitrogen-doped carbon layers on carbonized wood (Co@NC/CW), by carbonizing wood to create a three-dimensional framework with vertically aligned macropores. The unique architecture encapsulates cobalt nanoparticles within in situ-grown nitrogen-doped graphene layers on wood-derived microchannels, facilitating ultrafast electrolyte infusion and anisotropic electron transport. As a result, the optimized freestanding Co@NC/CW electrode exhibits remarkable bifunctional activity, achieving overpotentials of 403 mV and 227 mV for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), respectively, at a current density of 50 mA cm⁻². Furthermore, the integrated hybrid electrolyzer combining the HER and the OER delivers an impressive 50 A cm⁻² at a cell voltage of 1.72 V while maintaining a Faradaic efficiency near 99.5% and sustaining long-term stability over 120 h of continuous operation. Co@NC/CW also demonstrates performance in the complete decomposition of alkaline seawater, underscoring its potential for scalable applications. This wood-derived catalyst design not only leverages the natural hierarchical porosity of wood but also offers a sustainable platform for advanced electrochemical systems. Full article