Search Results (5,250)

Borophene, a two-dimensional (2D) allotrope of boron, has emerged as a highly promising material owing to its exceptional mechanical strength, electronic conductivity, and diverse structural phases. Unlike graphene and other 2D materials, borophene exhibits inherent anisotropy, flexibility, and metallicity, offering unique opportunities for advanced nanotechnological applications. This review presents a comprehensive summary of recent progress in borophene synthesis methods, highlighting both bottom–up strategies such as chemical vapor deposition (CVD) and molecular beam epitaxy (MBE), and top–down approaches, including liquid-phase exfoliation and sonochemical techniques. A key challenge discussed is the stabilization of borophene’s polymorphs, as bulk boron’s non-layered structure complicates exfoliation. The influence of substrates and doping strategies on structural stability and phase control is also explored. Moreover, the intrinsic physicochemical properties of borophene, including its high flexibility, oxidation resistance, and anisotropic charge transport, were examined in relation to their implications for electronic, catalytic, and sensing devices. Particular attention was given to borophene’s performance in hydrogen storage and hydrogen evolution reactions (HERs), where functionalization with alkali and transition metals significantly enhances H₂ adsorption energy and storage capacity. Studies demonstrate that certain borophene–metal composites, such as Ti- or Li-decorated borophene, can achieve hydrogen storage capacities exceeding 10 wt.%, surpassing the U.S. Department of Energy targets for hydrogen storage materials. Despite these promising characteristics, large-scale synthesis, long-term stability, and integration into practical systems remain open challenges. This review identifies current research gaps and proposes future directions to facilitate the development of borophene-based energy solutions. The findings support borophene’s strong potential as a next-generation material for clean energy applications, particularly in hydrogen production and storage systems. Full article

This study explores a green synthesis approach for creating a nanocomposite material consisting of zinc oxide (ZnO) nanoparticles decorated with reduced graphene oxide (rGO), utilizing Clitoria ternatea flower extract as a biogenic reducing agent. The objective was to leverage the phytochemicals present in the flower extract to form ZnO nanoparticles, enhance their properties through rGO integration, and evaluate their structural and photocatalytic characteristics. The nanocomposite was characterized using a comprehensive suite of techniques, including XRD, FTIR, UV–Vis spectroscopy, DLS, zeta potential, SEM, and EDAX. To assess the in vitro biocompatibility, an MTT assay was performed on the normal fibroblast cell line 3T3L1. The nanocomposite exhibited minimal cytotoxicity with over 86% cell viability at concentrations up to 320 μg/mL. Additionally, hemolysis assays demonstrated that the nanocomposite induced less than 5% hemolysis, indicating excellent hemocompatibility. In an in vivo evaluation, zebrafish embryos exhibited no deformities, and the cumulative hatchability was also not affected up to a dose of 50 μg/mL. The exploration of environmental remediation was studied using bromophenol dye degradation, which showed a 65% dye degradation within 30 min of exposure to the composite and sunlight. The outcome of the study showed successful formation of ZnO and its composite with rGO (CT-rGO-ZnO), exhibiting excellent biocompatibility and improved photocatalytic properties. The material demonstrates promise for applications in environmental remediation and energy-related fields. The environmentally friendly nature of the synthesis approach also makes it a valuable contribution toward sustainable nanotechnology. Full article

Uric acid (UA) detection is critical for human health monitoring, necessitating the development of electrochemical sensing electrodes suitable for physiological environments. This study evaluated four 2D conductive metal–organic frameworks (2D c-MOFs), namely Cu-HHTP, Ni-HHTP, Cu-HAB, and Ni-HAB, which share identical graphene-like 2D sheet structures but differ in π-conjugation extent and catalytic active centers [MX₄] (M = Cu or Ni; X = O or NH) as electrosensing electrodes. Electrochemical sensing performance was compared by detecting UA in phosphate-buffered saline (PBS). Herein, the Ni-HHTP electrode demonstrated superior sensitivity (6.79 μA·μM⁻¹·cm⁻²), the lowest oxidation potential (0.272 V), and the lowest detection limit (0.44 μM). Langmuir adsorption isotherm analysis revealed that the Ni-HHTP electrode possesses the highest surface coverage (Γ_A) (5061.16 pmol cm⁻²) and the most favorable Gibbs adsorption free energy (ΔG°) (−18.775 kJ mol⁻¹), indicating its strongest UA adsorption capacity and molecular interaction. This enhanced performance is attributed to the optimal synergy between [NiO₄] catalytic centers and extended ligand π-conjugation, facilitating greater analyte adsorption and electron transfer efficiency. This work establishes clear structure–performance relationships for 2D c-MOF electrodes in UA detection, providing key insights for designing advanced electrosensing materials. Full article

Mesenchymal stem cells (MSCs) represent a promising strategy in the field of regenerative medicine due to their multipotent differentiation capacity and immunomodulatory properties. The interaction of these cells with the extracellular matrix (ECM) and biomaterials, notably graphene oxide (GO), has proven decisive in modulating cell behavior, with the potential to optimize tissue regeneration processes. This review was conducted using the MEDLINE, Scopus, and Cochrane databases, covering studies published between 2018 and 2025, from which seven studies met the inclusion criteria, with an emphasis on in vitro and in vivo investigations regarding the association between GO and MSCs. The main findings demonstrate that GO, particularly when conjugated with polymers such as poly(L-lactic acid) (PLLA), enhances cell adhesion, stimulates proliferation, and promotes the osteogenic differentiation of MSCs, in addition to positively modulating intracellular signaling pathways. However, significant gaps remain in understanding the mechanisms and safety of GO’s therapeutic use in association with MSCs. Therefore, this review reinforces the need for further studies to deepen the characterization of the bioactive properties of GO-MSCs, aiming to enable safer and more effective clinical applications. Full article

The accumulation of blood toxins, including urea, uric acid, creatinine, bilirubin, p-cresyl sulfate, and indoxyl sulfate, poses severe health risks for patients with renal failure. Effective removal strategies are essential to mitigate complications associated with chronic kidney disease (CKD) and improve patient outcomes. Functional carbon-based materials, such as activated carbon (activated charcoal) and graphene oxide, have emerged as promising adsorbents due to their large surface area, adjustable porosity, and biocompatibility. This review comprehensively explores the latest advancements in carbon-based materials for blood purification across three key therapeutic modalities: (1) Hemoperfusion, where activated and modified carbonaceous materials enhance the adsorption of small-molecule and protein-bound toxins; (2) Hemodialysis, where functionalized carbon materials improve clearance rates and reduce treatment duration; and (3) Oral Therapeutics, where orally administered carbon adsorbents show potential in lowering systemic toxin levels in CKD patients. Furthermore, we present a comparative analysis of these approaches, highlighting their advantages, limitations, and future research directions for optimizing carbon-based detoxification strategies. The findings discussed in this review emphasize the significance of material engineering in advancing blood purification technologies. By enhancing the efficiency of toxin removal, carbon-based materials have the potential to revolutionize renal failure treatment, offering improved clinical outcomes and enhanced patient quality of life. Full article

The treatment of organic phosphate ester (OPE) pollutants in water is a challenging but highly necessary task. In this study, an advanced oxidation process through light activation of peroxymonosulfate (PMS) involving graphene oxide (GO) as a promoter was developed to degrade OPE in water, taking triphenyl phosphate (TPhP) as an example. The developed “Light+PMS+GO” system demonstrated good convenience, high TPhP degradation efficiency, tolerance in a near-neutral pH, satisfactory re-usability, and a low toxicity risk of degradation products. Under the investigated reaction conditions, viz., the full spectrum of a 300 W Xe lamp, PMS of 200 mg L⁻¹, GO of 4 mg L⁻¹, and TPhP of 10 μmol L⁻¹, the “Light+PMS+GO” system achieved nearly 100% TPhP degradation efficiency during a 15 min reaction duration with a 5.81-fold enhancement in the reaction rate constant, compared with the control group without GO. Through quenching experiments and electron paramagnetic resonance studies, singlet oxygen was identified as the main reactive species for TPhP degradation. Further studies implied that GO could accumulate both oxidants and pollutants on the surface, providing additional reaction sites for PMS activation and accelerating electron transfer, which all contributed to the enhancement of TPhP degradation. Finally, the TPhP degradation pathway was proposed and a preliminary toxicity evaluation of degradation intermediates was conducted. The convenience, high removal efficiency, and good re-usability indicates that the developed “Light+PMS+GO” reaction system has great potential for future applications. Full article

Graphene, a two-dimensional material with remarkable electrical, thermal, and mechanical properties, has revolutionized the fields of electronics, energy storage, and nanotechnology. This review presents a comprehensive analysis of graphene synthesis techniques, which can be classified into two primary approaches: top-down and bottom-up. Top-down methods, such as mechanical exfoliation, oxidation-reduction, unzipping carbon nanotubes, and liquid-phase exfoliation, are highlighted for their scalability and cost-effectiveness, albeit with challenges in controlling defects and uniformity. In contrast, bottom-up methods, including chemical vapor deposition (CVD), arc discharge, and epitaxial growth on silicon carbide, offer superior structural control and quality but are often constrained by high costs and limited scalability. The interplay between synthesis parameters, material properties, and application requirements is critically examined to provide insights into optimizing graphene production. This review also emphasizes the growing demand for sustainable and environmentally friendly approaches, aligning with the global push for green nanotechnology. By synthesizing current advancements and identifying critical research gaps, this work offers a roadmap for selecting the most suitable synthesis techniques and fostering innovations in scalable and high-quality graphene production. The findings serve as a valuable resource for researchers and industries aiming to harness graphene’s full potential in diverse technological applications. Full article

Polymer matrix composites (PMCs) are crucial for their applications in aerospace, electronics, defense, and structural materials. PMCs reinforced with nanofillers offer substantial potential for enhanced thermal and mechanical performance. Although there have been significant developments in nanofiller-based high-performance composites involving graphene, carbon nanotubes, and metal oxides, the smallest of all the fillers, the graphene quantum dot (GQD), has not been explored thoroughly. The objective of this study is to investigate the effects of GQDs on the thermal properties of epoxy nanocomposites using all-atom molecular dynamics (MD) simulations. Specifically, the influence of GQDs on the glass transition temperature (T_g) and coefficient of linear thermal expansion (CTE) of the bisphenol F epoxy is evaluated. Further, the effects of surface functionalization and edge functionalization of GQDs are analyzed. Results demonstrate that the inclusion of functionalized GQDs leads to a 16% improvement in T_g, attributed to enhanced interfacial interactions and restricted molecular mobility in the epoxy network. MD simulations reveal that functional groups on GQDs form strong physical and chemical interactions with the polymer matrix, effectively altering its dynamics at the T_g. These results provide key molecular-level insights into the design of the next generation of thermally stable epoxy nanocomposites for high-performance applications in aerospace and defense. Full article

Geopolymer concrete uses a geopolymer binder instead of traditional Portland cement; thus, it reduces carbon emissions by a significant amount. In this study, Edge-Oxidized Graphene Oxide (EOGO), a carbon-based nanomaterial, was added into a metakaolin-based geopolymer, and its effect on the mechanical and rheological properties of the mixture was investigated. EOGO was added into the mixture at 0% (control), 0.1%, 0.5%, and 1% of the metakaolin mass. Several experiments were conducted to characterize the properties of the metakaolin–EOGO (MKGO) geopolymer, including its compressive strength, free–free resonance column (FFRC), void content, water absorption, setting time, flow, and rheology. It was found that the compressive strength and stiffness showed their maximum values and the void content was minimized at 0.1% EOGO. In addition, as the EOGO addition rate increased, the setting time tended to shorten, and the fluidity tended to decrease. This suggests that 0.1% EOGO is the most optimal content in metakaolin paste. This study confirms that EOGO is an additive material that can improve the performance of metakaolin-based geopolymers and presents opportunities for the development of sustainable construction materials through optimization of EOGO addition. Full article

This short review provides a focused overview of recent advances in catalytic systems for water purification, with particular attention to photocatalysis, Fenton-like processes, and biocatalysis. While not intended as a comprehensive survey, this review is grounded primarily in recent work from our research group, supported by comparisons with relevant studies from the broader literature. Emphasis is placed on the role of graphene-based materials, particularly aerogels, hydrogels, and xerogels, as functional platforms for catalytic nanoparticles inclusion and enzyme immobilization. This review aims to highlight key insights, practical limitations, and emerging strategies to improve catalyst reusability, stability, and scalability for real-world water treatment applications. Full article

Wastewater treatment plants generally lack a specialized design for the efficient removal of sulfamethoxazole (SMX), a toxic and bio-resistant compound. In this study, secondary effluent from a Beijing wastewater reclamation treatment plant was spiked with SMX and used to investigate the filtration performance and fouling mechanisms of thermo-responsive membranes. Thermo-responsive materials were prepared using polyvinylidene fluoride, N-isopropylacrylamide (NIPAM), and graphene oxide through Ce (IV)-induced redox radical polymerization. The results showed that the removal of SMX and COD reached 42% and 92%, respectively, with a NIPAM dosage of 1 g, and the removal of UV₂₅₄ reached its highest value at 57.9%. Additionally, the filtration flux was higher at a temperature of 35 °C with a NIPAM dosage of 1 g. The fluorescence intensity of the organic matter from the secondary effluent spiked with SMX and decreased after the thermo-responsive membranes were implemented, and filtration with the membrane containing 1 g of NIPAM achieved a lower intensity at a value of 3074.6, according to the analysis of three-dimensional fluorescence excitation–emission spectroscopy. According to the extended Derjaguin–Laudau–Verwey–Overbeek theory analysis, the interfacial free energies of the thermo-responsive membrane with a 1 g dose of NIPAM were higher than the others during filtration. Full article

In the present paper, the interaction between metal oxide nanoparticles and carbon materials was studied, and the results showed a synergetic effect, leading to an improvement in the properties of the obtained hybrid composites. The In₂O₃ NPs were prepared by the precipitation method and thermal treatment at 550 °C. The composites were obtained using an ex situ method, by mixing the In₂O₃ NPs with reduced oxide graphene (rGO) in a ratio of 10:1. The structural, morphological, and chemical composition studies of the In₂O₃ NPs and In₂O₃-rGO composites were investigates by FTIR and EDX spectroscopy, SEM microscopy, and XRD analysis. These techniques have highlighted the obtaining of In₂O₃ of high purity, and crystallinity, with the mean particle size in the range of 8–25 nm, but also, the dispersion of In₂O₃ NPs onto rGO sheets. We examined the influence of the In₂O₃ nanostructure morphology and In₂O₃-rGO composites on the electrochemical properties using cyclic voltammetry. The surface properties of the In₂O₃ and composite films were studied by contact angles, which indicate the maintenance of the hydrophilic nature. The obtained results establish the synergy between the main components to form In₂O₃-rGO, which can be used for the development of biosensors to enhance the device performance. Full article

The observed increase in the diversity and level of pollutant content in the water environment forces the development of more effective technologies for their removal. Using nanomaterials in water and wastewater treatment offers numerous opportunities to remove organic and inorganic contaminants that are hardly removable in conventional processes. In this group, carbon-based nanomaterials, mainly carbon nanotubes (CNTs), graphene (Gr), and graphene oxide (GO), are very popular. This review aims to present the directions and diversity of applications of carbon-based nanomaterials (CNMs) in water and wastewater technology, as well as the challenges and environmental dangers that new solutions entail. Authors also present the results of the research on the changes in properties of GO produced in the laboratory as water suspension and a freeze-dried product over time. The results confirm the significant influence of the form of graphene oxide and its storage time on the structural properties, hydrophilicity, and stability of GO. Therefore, they should be considered when selecting an adsorbent or reaction catalyst in environmental applications for developing new greener and sustainable methods of treatment and purification, which use fewer reagents and release safer products. Full article

Periodontal disease in dogs leads to progressive bone loss and adversely impacts overall health. However, cost-effective regenerative strategies are still limited in veterinary practice. This study aimed to develop and evaluate a novel tannic acid (TA)–gelatin-based hydrogel (Gel), incorporating graphene oxide (GO) and hydroxyapatite nanoparticles (HA), as a potential barrier material for guided tissue regeneration (GTR) applications. The hydrogels—Gel, Gel-GO, Gel-HA, and Gel-GO-HA—were characterized for chemical structure, molecular interactions, surface morphology, nanoparticle dispersion, and tensile strength. Cytotoxicity was assessed using L929 fibroblasts (ISO 10993-5), while cell viability/proliferation, morphology, and alkaline phosphatase (ALP) production were evaluated using canine periodontal ligament-derived cells. Results show that crosslinking with tannic acid enhanced the incorporation of graphene oxide and hydroxyapatite nanoparticles via hydrogen bonding into TA–gelatin-based hydrogels. This combination increased surface roughness, reduced degradation rate, and enabled shape memory behavior, critical for guided tissue regeneration (GTR) membranes. The extracts from Gel-HA-GO showed that cytotoxicity was both time- and concentration-dependent in L929 fibroblasts, whereas enhanced cell proliferation and increased ALP production were observed in cultures derived from canine periodontal ligament cells. These findings suggest that TA–gelatin-based hydrogels incorporating GO and HA demonstrated favorable mechanical and physicochemical properties, biocompatibility, and osteogenic potential. These attributes suggest their viability as a promising composite for the development of innovative GTR strategies to address periodontal tissue loss in veterinary medicine. Full article

Integrating two-dimensional transition-metal dichalcogenides with graphene is attractive for low-power memory and neuromorphic hardware, yet sequential wet transfer leaves polymer residues and high contact resistance. We demonstrate a complementary metal–oxide–semiconductor (CMOS)-compatible, transfer-free route in which an atomically thin amorphous MoS₂ precursor is RF-sputtered directly onto chemical vapor-deposited few-layer graphene and crystallized by confined-space sulfurization at 800 °C. Grazing-incidence X-ray reflectivity, Raman spectroscopy, and X-ray photoelectron spectroscopy confirm the formation of residue-free, three-to-four-layer 2H-MoS₂ (roughness: 0.8–0.9 nm) over 1.5 cm × 2 cm coupons. Lateral MoS₂/graphene devices exhibit reproducible non-volatile resistive switching with a set transition (SET) near +6 V and an analogue ON/OFF ≈2.1, attributable to vacancy-induced Schottky-barrier modulation. The single-furnace magnetron sputtering + sulfurization sequence avoids toxic H₂S, polymer transfer steps, and high-resistance contacts, offering a cost-effective pathway toward wafer-scale 2D memristors compatible with back-end CMOS temperatures. Full article