Search Results (391)

This study investigates CaCu_3−xSr_xTi₄O₁₂ (CCSTO) systems synthesized using the solid-state method, with x compositions of 0.00, 0.15, and 3.00. The samples were modified using 6 wt% graphene oxide (GO) and reduced GO (rGO) prepared via Hummer’s method to evaluate their performance as electrodes in supercapacitors. The results indicate that the addition of 6wt% rGO to CCTO (CCTO-6rGO) led to an improvement in specific capacitance, reaching 237.76 mF·g⁻¹ at a scan rate of 10 mV/s, compared to 29.86 mF·g⁻¹ for pure CCTO and only 7.83 mF·g⁻¹ for CCTO-6GO, suggesting that rGO enhances charge storage. For the CCTO15Sr samples, CCTO15Sr-6rGO exhibited the highest specific capacitance, with 321.63 mF·g⁻¹ at 10 mV/s, surpassing both pure CCTO15Sr (80.19 mF·g⁻¹) and CCTO15Sr-6GO (25.73 mF·g⁻¹). These results stem from oxygen and metal vacancies, which aid charge accumulation and ion diffusion. In contrast, adding GO generally reduced specific capacitance in all samples. The findings highlight CCSTO’s potential—especially with rGO modification—as a supercapacitor electrode while also indicating areas for further optimization. Full article

Due to their excellent physicochemical properties, the nanoparticles (NPs) have been utilized in various potential applications, including environmental remediation, energy storage, and nanomedicine. In this work, the ultrasonic and manual stirring approaches were used to integrate yttrium oxide (Y₂O₃) nanoparticles (NPs) into reduced graphene oxide (RGO) and carbon nanotubes (CNTs) to enhance their photocatalytic and anticancer properties. Pure Y₂O₃NPs, Y₂O₃/RGO NCs, and Y₂O₃/CNTs NCs were characterized using different analytical techniques, such as XRD, SEM, EDX with Elemental Mapping, FTIR, UV-Vis, PL, and DLS to investigate their improved structural, surface morphological, chemical bonding, optical, and surface charge properties. XRD data confirmed the successful integration of Y₂O₃into RGO and CNTs, with minor changes in crystallite sizes. SEM images with EDX analysis revealed that Y₂O₃NPs were uniformly distributed on RGO and CNTs, reducing aggregation. Chemical bonding and interactions between Y₂O₃and carbon materials were investigated using Fourier Transform Infrared (FTIR) analysis. UV and PL results suggest that the optical studies showed a shift in absorption peaks upon integration with RGO and CNTs. This indicates enhanced light absorption and modifications to the band gap between (3.79–4.40 eV) for the obtained samples. In the photocatalytic experiment, the degradation efficiency of bromophenol blue (BPB) dye for Y₂O₃RGO NCs was up to 87.3%, outperforming pure Y₂O₃NPs (45.83%) and Y₂O₃/CNTs NCs (66.78%) after 120 min of UV irradiation. Additionally, the MTT assay demonstrated that Y₂O₃/RGO NCs exhibited the highest anticancer activity against MG-63 bone cancer cells with an IC50 value of 45.7 µg/mL compared to Y₂O₃CNTs NCs and pure Y₂O₃NPs. This work highlights that Y₂O₃/RGO NCs could be used in significant applications, including environmental remediation and in vivo cancer therapy studies. 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

Calcareous sand, characterized by numerous pore spaces, easy fragmentation, and low strength, is commonly used as fill material in island construction projects. Due to these limitations, it often fails to meet the requirements of actual engineering applications. This paper uses oxidized graphene in combination with fly ash cement to modify calcareous sand. The effects of oxidized graphene, fly ash cement, and curing time on the modification effect were investigated through triaxial tests and numerical simulations. The experimental results show the following: (1) Both the extension of curing age and the increase in the dosage of fly ash cement can improve the shear performance of calcareous sand, with the increase in the dosage of fly ash cement able to ensure thorough bonding between calcareous sand particles. (2) Graphene oxide can significantly improve the shear performance of calcareous sand cement mortar, with the optimal dosage being 0.06%. Excess amounts result in a reduced performance improvement, which is related to the degree of the catalysis of oxidized graphene on hydration reactions. (3) The numerical simulation shows that when the maximum shear stress reached 3437 kPa, cracks began appearing on the specimen, consistent with the experimental results. Meanwhile, the numerical simulation results reveal the crack propagation pattern in the specimens, showing that the stress at crack initiation is lower than the peak stress. Full article

This study aimed to develop a novel biomaterial for neural tissue regeneration by combining chitosan (CS), a natural polymer, with graphene oxide (GO) at concentrations of 3%, 6%, and 9%. The homogeneity, conductivity, three-dimensional characteristics, and ability to support cell viability of the composite materials were systematically evaluated. Fourier-Transform Infrared (FTIR) spectroscopy confirmed the successful incorporation of GO into the CS matrix, while UV-Vis and photoluminescence (PL) spectrometry revealed modifications in the optical properties with increasing GO content. Thermogravimetric analysis (TG-DSC) demonstrated improved thermal stability of the composites, and swelling tests indicated enhanced water absorption capacity. Although some agglomerates were observed, the homogeneity was reasonable at both macroscopic and microscopic level (optical visualization–FTIR and electron microscopy). The composite films exhibited promising physical and electrochemical properties, highlighting their potential for neural tissue engineering applications. Their biological activity was assessed by culturing neuronal cells on the CS-GO scaffolds. Results from MTT, LDH, and LIVE/DEAD assays demonstrated excellent cell viability, moderate-to-good cell attachment, and the promotion of intercellular network formation. Among the tested formulations, the CS-GO 6% scaffold showed the most favorable biological response, with a significant increase in SH-SY5Y cell viability after 7 days (p < 0.05) compared to the CS control. LIVE/DEAD imaging confirmed enhanced cell attachment and elongated morphology, while the LDH assay indicated minimal cytotoxicity. Notably, a critical threshold was identified between 6% and 9% GO, where conductivity increased by approximately 52-fold. Future studies should focus on optimizing the composite parameters, loading them with specific biologically active agents and thus targeting specific neuronal applications. Full article

The presence of secondary electromagnetic waves (EMWs) results in EMW pollution and a large need for EMW-shielding materials. Therefore, new, lightweight, flexible, chemically resistant, and durable EMW shielding materials are demanded, while graphene and its derivatives meet the above-mentioned requirements. Among graphene derivatives, N-doped graphene exhibits promising electrical properties for shielding applications, although achieving sufficient N-incorporation in the graphene sheets remains a challenge. Herein, we produced graphene oxide using the modified Hummers’ method (GO) and the electrochemical exfoliation of highly ordered pyrolytic graphite. These two GO samples were thermally treated at 500 °C and 800 °C under a pure NH₃ gas for 1 h. UV-Vis, infrared, and Raman spectroscopies and X-ray diffraction, elemental, and thermogravimetric analyses were used to investigate the structural properties of modified GO. One of the highest levels of N-doping of GO was measured (11.25 ± 0.08 at%). The modification under a NH₃ atmosphere leads to simultaneous N-doping and reduction of graphene, resulting in the formation of electrically conductive and EMW shielding materials. Density functional theory (DFT) revealed the effect of heteroatoms on the energy band gap of GO. The cluster corresponding to N-doped rGO had a reduced bandgap of 0.77 eV. Full article

We have demonstrated the fabrication of laminate composites with functional features to demonstrate energy storage capabilities. The present study investigates the surface modification of carbon fibers by coating dual materials of reduced graphene oxide (rGO) and cellulose-based activated carbon to enhance their energy storage capacitance for the development of structural supercapacitors. The dual coating on carbon fibers enabled a near 210-fold improvement in surface area, surpassing that of pristine carbon fibers. This formed a highly porous graphene network with activated carbon, resulting in a well-connected fiber–graphene-activated carbon network on carbon fibers. The electrochemical supercapacitor, fabricated from surface-functionalized carbon fibers, provides the best performance, with a specific capacitance of 172 F g⁻¹ in an aqueous electrolyte. Furthermore, the symmetrical structural supercapacitor (SSSC) device delivered a specific capacitance of 227 mF g⁻¹ across a wide potential window of 6 V. The electrochemical stability of the SSSC device was validated by a high capacitance retention of 97.3% over 10,000 cycles. Additionally, the study showcased the practical application of this technology by successfully illuminating an LED using the proof-of-concept SSSC device with G-aC/CF electrodes. Overall, the findings of this study highlight the potential of carbon fiber composites as a promising hybrid material, offering both structural integrity and a functional performance suitable for aerospace and automobile applications. Full article

As electronic devices advance toward higher power density, heat dissipation has emerged as a critical bottleneck limiting their reliability. Graphene oxide (GO)/epoxy resin (EP) composites, combining high-thermal-conductivity potential with polymer-matrix advantages, have become a key focus for overcoming the limitations of traditional metal heat-dissipation materials. This review systematically examines these composites, analyzing their thermal conductivity enhancement mechanisms, structural regulation strategies, and application challenges. We first elaborate on how GO’s intrinsic properties influence its enhancement capability, then explore the roles of physical dispersion strategies and interfacial modification techniques in optimizing filler dispersion and reducing interfacial thermal resistance, revealing the effects of preparation processes on thermal conduction network construction. Their remarkable potential is demonstrated in applications such as electronic packaging and electromagnetic shielding. However, challenges including cross-scale structural design and multi-physics collaborative regulation remain. This review aims to provide theoretical foundations and technical guidance for transitioning these composites from lab research to industrial application and advancing thermal management in high-performance electronics. Full article

Saxitoxin (STX) is a toxin with paralyzing and lethal properties, necessitating the development of a simple analytical method. This study developed a nucleic acid aptamer biosensor using graphene oxide (GO) as a fluorescence quencher for STX detection. GO was combined with M30-f, an STX nucleic acid aptamer modification with 5-carboxyfluorescein, which can produce fluorescence absorption under the conditions of an excitation wavelength of 408 nm and emission wavelength of 515 nm. Based on the principle of fluorescence resonance energy transfer, the fluorescence of M30-f was quenched. In the presence of STX, M30-f specifically binds to STX and dissociates from the GO surface, thereby restoring fluorescence. The STX content can be quantitatively detected through differences in fluorescence absorption. The influence of ultrasonic time on the fluorescence quenching ability of GO was investigated. The aqueous solution of graphene oxide, 30GO, optimized by ultrasound treatment for a duration of 30 min, demonstrated excellent fluorescence quenching capability. 30GO was analyzed utilizing various characterization techniques, including SEM, FT-IR, UV, XPS, XRD, AFM, and contact angle measurements. The methodological validation showed that the established STX sensor exhibits excellent linearity within a concentration range of 10–100,000 ng/L, with a limit of detection (LOD) as low as 0.098 μg/L. In addition, the results further demonstrated the sensor’s high specificity for detecting neurotoxic shellfish toxin STX. The recovery rate for clam samples ranged from 89.12% to 104.71%, while that for oyster samples ranged from 91.20% to 109.65%, with relative standard deviations (RSDs) all below 3%. This aptamer sensor is characterized by its simplicity, high sensitivity, and broad detection range, providing significant technical support for advancing marine biotoxin research. Full article

The replacement of natural aggregates with recycled aggregates in concrete production has gained attention as a sustainable approach for valorizing construction and demolition waste (CDW). Although regulatory frameworks in this area remain underdeveloped, extensive research has demonstrated that acceptable mechanical and durability properties can be achieved. However, the elevated water absorption associated with recycled materials—mainly due to residual attached mortar and increased porosity—continues to pose a challenge. When used without prior treatment, these particles absorb part of the mixing water intended for cement hydration, potentially compromising both fresh and hardened concrete performance. This study explores the use of graphene oxide (GO) nanocoating as a surface modification strategy to mitigate water absorption. Absorption test were performed to evaluate the effectiveness of the treatment, followed by the preparation of multiple concrete mixes incorporating varying substitution rates of natural aggregate with untreated and GO-treated recycled material. The mixtures were assessed for workability and compressive strength. Results indicate that GO nanocoating substantially reduces water (up to 30%) uptake and improves the overall performance of concrete containing recycled constituents, increasing its compressive strength by up to 32%, highlighting its potential as a viable pretreatment for sustainable concrete production. Full article

Graphene oxide (GO), a derivative of graphene, has attracted significant attention in tribological applications due to its unique structural, mechanical, and chemical properties. This review highlights the influence of GO and its composites on friction and wear performance across various engineering systems. The paper explores GO’s key properties, such as its high surface area, layered morphology, and abundant functional groups. These features contribute to reduced shear resistance, tribofilm formation, and improved load-bearing capacity. A detailed analysis of GO-based composites, including polymer, metal, and ceramic matrices, reveals those small additions of GO (typically 0.1–2 wt%) result in substantial reductions in coefficient of friction and wear rate, with improvements ranging between 30–70%, depending on the application. The tribological mechanisms, including self-lubrication, dispersion, thermal stability, and interface interactions, are discussed to provide insights into performance enhancement. Furthermore, the effects of electrochemical environment, functional group modifications, and external loading conditions on GO’s tribological behavior are examined. Despite these advantages, challenges such as scalability, agglomeration, and material compatibility persist. Overall, the paper demonstrates that GO is a promising additive for advanced tribological systems, while also identifying key limitations and future research directions. Full article

Background: Graphene oxide (GO) is widely explored as a functional additive in polymer composites; however, its simple physical dispersion in dental resins often leads to poor interfacial stability and limited long-term performance. Covalent functionalization may overcome these limitations by enabling chemical integration into the polymer matrix. This study presents the synthesis and FT-IR/Raman characterization of GRAPHYMERE^®, a novel graphene oxide-based monomer obtained through exfoliation, amine functionalization with 1,6-hexanediamine, and transamidation with methyl methacrylate. Methods: A novel GO-based monomer, GRAPHYMERE^®, was synthesized through a three-step process involving GO exfoliation, amine functionalization with 1,6-hexanediamine, and transamidation with methyl methacrylate to introduce polymerizable acrylic groups. The resulting product was characterized using FT-IR and Raman spectroscopy. Results: Spectroscopic analyses confirmed the presence of aliphatic chains and amine functionalities on the GO surface. Although some expected signals were overlapped, the data suggest successful surface modification and partial insertion of methacrylamide groups. The process is straightforward, uses low-toxicity reagents, and avoids complex reaction steps. Conclusions: GRAPHYMERE^® represents a chemically modified GO monomer potentially suitable for copolymerization within dental resin matrices. While its structural features support compatibility with radical polymerization systems, further studies are required to assess its mechanical performance and functional properties in dental resin applications. 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

Due to its persistence and potential negative effects on ecosystems and human health, microplastic pollution in aquatic environments has become a major worldwide concern. Photocatalytic degradation is a sustainable manner to degrade microplastics to non-toxic by-products. In this review, comprehensive discussion focuses on the synergistic effects of various photocatalytic materials including TiO₂, ZnO, WO₃, graphene oxide, and metal–organic frameworks for producing heterojunctions and involving multidimensional nanostructures. Such mechanisms can include the generation of reactive oxygen species and polymer chain scission, which can lead to microplastic breakdown and mineralization. The advancements of material modifications in the (nano)structure of photocatalysts, doping, and heterojunction formation methods to promote UV and visible light-driven photocatalytic activity is discussed in this paper. Reactor designs, operational parameters, and scalability for practical applications are also reviewed. Photocatalytic systems have shown a lot of development but are hampered by shortcomings which include a lack of complete mineralization and production of intermediary secondary products; variability in performance due to the fluctuation in the intensity of solar light, limited UV light, and environmental conditions such as weather and the diurnal cycle. Future research involving multifunctional, environmentally benign photocatalytic techniques—e.g., doped composites or composite-based catalysts that involve adsorption, photocatalysis, and magnetic retrieval—are proposed to focus on the mechanism of utilizing light effectively and the environmental safety, which are necessary for successful operational and industrial-scale remediation. Full article