Search Results (131)

rGO/ZnO composites have been widely studied for use as toxic gas sensors due to the synergistic effect between the materials and the reduction in sensor operating temperature promoted by rGO. However, few studies have employed rGO/ZnO sensors for ozone detection, as graphene materials are oxidized and/or degraded when exposed to ozone. This paper reports on a study of ZnO/rGO/ZnO-based sensors with different ZnO NP morphologies for ozone sensing. ZnO nanoparticles with needle-like and donut-like morphologies were synthesized by the precipitation method, and bare ZnO and ZnO/rGO/ZnO composite sensors were fabricated by layer-deposition of ZnO and/or rGO via drop-casting, forming a “sandwiched” structure that protects the rGO sheets. Bare ZnO and ZnO/rGO/ZnO composites were analyzed by varying the temperature from 200 to 300 °C. The ZnO/rGO/ZnO sensor provided a high 13.3 response (R_gas/R_air) and recovery times of 442 s and 253 s, respectively, for 50 ppb of O₃, as well as high selectivity to ozone gas compared to CO, NH₃, and NO₂ gases. No oxidation or degradation of the sensor was observed during ozone detection measurements, indicating that the adopted manufacturing methodology was successful. Full article

In this work, we analyze how the coupling prism governs the performance of reduced-graphene-oxide (rGO)-assisted surface plasmon resonance (SPR) sensors for trace heavy-metal detection in water. A Kretschmann multilayer at 633 nm with a fixed Cu/Si₃N₄/rGO stack (45.0/5.00/1.41 nm) is modeled by transfer-matrix methods while varying the prism material among CaF₂, BK7, SiO₂, and SF₆. Performance optimization is carried out using angular sensitivity, full width at half maximum (FWHM), figure of merit (FoM), detection accuracy (DA), quality factor (QF), and a practical limit of detection (LoD). The analyte is represented by refractive-index typical of clean and contaminated water (n = 1.330 and 1.340). SF₆ yields the narrowest angular resonances but compresses analyte-induced angle spacing; CaF₂ provides larger analyte separations and consequently higher FoM and lower LoD under angle-encoded readout. The rGO interlayer enhances surface interaction across all prisms when co-tuned with the Cu and Si₃N₄ thicknesses. The sensitivity peaks around 310–320°·RIU⁻¹ for CaF₂. These results highlight the prism as a primary design variable in rGO-enhanced SPR sensing and position CaF₂-coupled architectures as promising for compact water-quality monitoring. Full article

The rapid advancement of next-generation energy storage technologies demands advanced manufacturing strategies that offer structural precision, scalability, and compositional tunability. Three-dimensional (3D) printing has emerged as a transformative approach to constructing energy storage architectures. In this work, we report a 3D-printed LiCoO₂//Li₄Ti₅O₁₂ full battery featuring a hierarchically porous and conductive reduced graphene oxide-carbon nanotubes (rGO-CNTs) framework that enables desirable ion-electron transport. The resulting full cells exhibit a high capacity of 151.4 mAh g⁻¹ at the rate of 0.1 C, superior rate performance, and outstanding cycling stability, maintaining 97.1% capacity after 3000 cycles. Furthermore, the fully printed cell successfully powers a digital stopwatch, demonstrating its practical applicability for devices. This study presents a structural and compositional study for constructing high-performance customizable 3D-printed batteries, advancing the digital manufacturing of next-generation energy systems. Full article

This work evaluates the CO₂-adsorption relevance and cycling stability of graphene oxide–silica (GO-SiO₂) and reduced graphene oxide–silica (rGO-SiO₂) gels after amine functionalization, demonstrating high-capacity retention under repeated adsorption–desorption cycles: rGO-SiO₂-APTMS retains ≈96.3% of its initial uptake after 50 cycles, while GO-SiO₂-APTMS retains ≈90.0%. The use of surfactants to control the organization of inorganic and organic molecules has enabled the development of ordered mesostructures, such as mesoporous silica and organic/inorganic nanocomposites. Owing to the outstanding properties of graphene and its derivatives, synthesizing mesostructures intercalated between graphene sheets offers nanocomposites with novel morphologies and enhanced functionalities. In this study, GO-SiO₂ and rGO-SiO₂ gels were synthesized and characterized by X-ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TG), mass spectrometry (MS), N₂ adsorption–desorption isotherms, and transmission electron microscopy (TEM). The resulting materials exhibit a laminar architecture, with mesoporous silica domains grown between graphene-based layers; the silica contents are 83.6% and 87.6%, and the specific surface areas reach 446 and 710 m²·g⁻¹, respectively. The laminar architecture is retained regardless of the surfactant-removal route; however, in GO-SiO₂ obtained by solvent extraction, a fraction of the surfactant remains partially trapped. Together with their high surface area, hierarchical porosity, and amenability to surface functionalization, these features establish amine-grafted graphene–silica gels, particularly rGO-SiO₂-APTMS, as promising CO₂-capture adsorbents. Full article

This study reports the impact of a silver nanoparticles/reduced graphene oxide@titanium dioxide nanocomposite (Ag/rGO@TiO₂) on the mechanical and biocompatibility properties of poly(styrene-co-methylmethacrylate)/poly methyl methacrylate (PS-PMMA/PMMA)-based bone cement. The chemical, structural, mechanical, and thermal characteristics of Ag/rGO@TiO₂ nanocomposite-reinforced PS-PMMA bone cement ((Ag/rGO@TiO₂)/(PS-PMMA)/PMMA) were evaluated using Fourier Transform Infrared spectroscopy (FT-IR), X-ray diffraction (XRD), nano-indentation, and electron microscopy. FT-IR, XRD, and transmission electron microscopy results confirmed the successful synthesis of the nanocomposite and the nanocomposite-incorporated bone cement. The elastic modulus (E) and hardness (H) of the ((Ag/rGO@TiO₂)/(PS-PMMA)/PMMA) bone cement were measured to be 5.09 GPa and 0.202 GPa, respectively, compared to the commercial counterparts, which exhibited E and H values of 1.7 GPa to 3.7 GPa and 0.174 GPa, respectively. Incorporating Ag/rGO@TiO₂ nanocomposites significantly enhanced the thermal properties of the bone cement. Additionally, in vitro studies demonstrated that the bone cement was non-toxic to the MG63 cell line. Full article

Objectives: This study aims to investigate the impact of Gossypol on human cervical cancer cells and elucidate its mechanism of action to establish a foundation for further clinical investigations. Methods: Cell proliferation, migration, and invasion were evaluated through CCK−8, wound healing, and Transwell assays. Fe₃O₄-BP-Gossypol (Fe₃O₄@Gossypol) conjugates were synthesized by linking Fe₃O₄ with Gossypol using benzophenone crosslinking. Successful conjugation was confirmed through scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and ultraviolet–visible spectrophotometry (UV-Vis). Subsequent to co-incubation with HeLa cell lysates, Fe₃O₄@Gossypol complexes facilitated the magnetic enrichment and purification of target proteins, which were identified using high-resolution mass spectrometry (HR-MS). The identified targets underwent KEGG pathway and GO analyses, followed by molecular docking with Gossypol. HeLa cells were exposed to Gossypol at concentrations of 7.48, 14.96, and 29.92 μmol·L⁻¹ for 48 h, and protein expression levels were quantified via Western blotting. Results: Gossypol notably suppressed cervical cancer cell proliferation, migration, and invasion. The integration of target fishing, network pharmacology, and molecular docking highlighted PIK3R2, MAPK1, and GRB2 as potential therapeutic targets. Western blot analysis revealed a dose-dependent reduction in PIK3R2, GRB2, and MAPK1 expression in Gossypol-treated groups compared to controls (p < 0.05). Conclusions: Gossypol may exhibit anti-cervical cancer effects by modulating the PI3K/AKT signaling pathway. Full article

Transition metal oxides (TMOs) are considered to be highly promising materials for supercapacitor electrodes due to their low cost, multiple convertible valence states, and excellent electrochemical properties. However, inherent limitations, including restricted specific surface area and low electrical conductivity, have largely restricted their application in supercapacitors. In this paper, core–shell heterostructures of nickel–iron layered double hydroxide (NiFe-LDH) nanosheets uniformly grown on CuCo₂O₄ nanoneedles were synthesized by hydrothermal and calcination methods. It is found that the novel core–shell structure of CuCo₂O₄@NiFe-LDH improves the electrical conductivity of the electrode materials and optimizes the charge transport path. Under the synergistic effect of the two components and the core–shell heterostructure, the CuCo₂O₄@NiFe-LDH electrode achieves an ultra-high specific capacity of 323.4 mAh g⁻¹ at 1 A g⁻¹. And the capacity retention after 10,000 cycles at 10 A g⁻¹ is 90.66%. In addition, the assembled CuCo₂O₄@NiFe-LDH//RGO asymmetric supercapacitor device achieved a considerable energy density (68.7 Wh kg⁻¹ at 856.3 W kg⁻¹). It also has 89.36% capacity retention after 10,000 cycles at 10 A g⁻¹. These properties indicate the great potential application of CuCo₂O₄@NiFe-LDH in the field of high-performance supercapacitors. Full article

The widespread presence of pesticides—especially malathion—in aquatic environments presents a major obstacle to conventional remediation strategies, while the ongoing global energy crisis underscores the urgency of developing renewable energy sources such as hydrogen. In this context, photocatalytic water splitting emerges as a promising approach, though its practical application remains limited by poor charge carrier dynamics and insufficient visible-light utilization. Herein, we report the design and evaluation of a series of TiO₂-based ternary nanocomposites comprising commercial P25 TiO₂, reduced graphene oxide (rGO), and molybdenum disulfide (MoS₂), with MoS₂ loadings ranging from 1% to 10% by weight. The photocatalysts were fabricated via a two-step method: hydrothermal integration of rGO into P25 followed by solution-phase self-assembly of exfoliated MoS₂ nanosheets. The composites were systematically characterized using X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM), UV-Vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. Photocatalytic activity was assessed through two key applications: the degradation of malathion (20 mg/L) under simulated solar irradiation and hydrogen evolution from water in the presence of sacrificial agents. Quantification was performed using UV-Vis spectroscopy, gas chromatography–mass spectrometry (GC-MS), and thermal conductivity detection (GC-TCD). Results showed that the integration of rGO significantly enhanced surface area and charge mobility, while MoS₂ served as an effective co-catalyst, promoting interfacial charge separation and acting as an active site for hydrogen evolution. Nearly complete malathion degradation (~100%) was achieved within two hours, and hydrogen production reached up to 6000 µmol g⁻¹ h⁻¹ under optimal MoS₂ loading. Notably, photocatalytic performance declined with higher MoS₂ content due to recombination effects. Overall, this work demonstrates the synergistic enhancement provided by rGO and MoS₂ in a stable P25-based system and underscores the viability of such ternary nanocomposites for addressing both environmental remediation and sustainable energy conversion challenges. Full article

Gold nanoparticles–cuprous oxide/reduced graphene oxide/polypyrrole (AuNPs-Cu₂O/rGO/PPy) hybrid nanocomposites were synthesized for surface acoustic wave (SAW) sensors, achieving high sensitivity (2 Hz/ppb), selectivity, and fast response (~2 min) at room temperature. The films, deposited via spin-coating, were characterized by SEM, EDS, and XRD, revealing a rough, wrinkled morphology beneficial for gas adsorption. The sensor showed significant frequency shifts to NH₃, enhanced by AuNPs, Cu₂O, rGO, and PPy. It had a 6.4-fold stronger response to NH₃ compared to CO₂, H₂, and CO, confirming excellent selectivity. The linear detection range was 12–1000 ppb, with a limit of detection (LOD) of 8 ppb. Humidity affected performance, causing negative frequency shifts, and sensitivity declined after 30 days due to resistivity changes. Despite this, the sensor demonstrated excellent NH₃ selectivity and stability across multiple cycles. In simulated breath tests, it distinguished between healthy and patient-like samples, highlighting its potential as a reliable, non-invasive diagnostic tool. Full article

Flexible polymer-based piezoelectric nanogenerators (PENGs) have gained significant interest due to their ability to deliver clean and sustainable energy for self-powered electronics and wearable devices. Recently, the incorporation of fillers into the ferroelectric polymer matrix has been used to improve the relatively low piezoelectric properties of polymer-based PENGs. In this study, we investigated the effect of various nanofillers such as titania (TiO₂), zinc oxide (ZnO), reduced graphene oxide (rGO), and lead zirconate titanate (PZT) on the PENG performance of the nanocomposite thin films containing the nanofillers in poly(vinylidene fluoride-co-trifluoro ethylene) (P(VDF-TrFE)) matrix. The nanocomposite films were prepared by depositing molecularly thin films of P(VDF-TrFE) and nanofiller nanoparticles (NPs) spread at the air/water interface onto the indium tin oxide-coated polyethylene terephthalate (ITO-PET) substrate, and they were characterized by measuring their microstructures, crystallinity, β-phase contents, and piezoelectric coefficients (d₃₃) using SEM, FT-IR, XRD, and quasi-static meter, respectively. Multiple PENGs incorporating various nanofillers within the polymer matrix were developed by assembling thin film-coated substrates into a sandwich-like structure. Their piezoelectric properties, such as open-circuit output voltage (V_OC) and short-circuit current (I_SC), were analyzed. As a result, the PENG containing 4 wt% PZT, which was named P-PZT-4, showed the best performance of V_OC of 68.5 V with the d₃₃ value of 78.2 pC/N and β-phase content of 97%. The order of the maximum V_OC values for the PENGs of nanocomposite thin films containing various nanofillers was PZT (68.5 V) > rGO (64.0 V) > ZnO (50.9 V) > TiO₂ (48.1 V). When the best optimum PENG was integrated into a simple circuit comprising rectifiers and a capacitor, it demonstrated an excellent two-dimensional power density of 20.6 μW/cm² and an energy storage capacity of 531.4 μJ within 3 min. This piezoelectric performance of PENG with the optimized nanofiller type and content was found to be superior when it was compared with those in the literature. This PENG comprising nanocomposite thin film with optimized nanofiller type and content shows a potential application for a power source for low-powered electronics such as wearable devices. Full article

The performance development of rGO-FET biosensors by analyzing the influence of GO flake size on biosensing efficacy. GO flakes of varying sizes, from 1 µm to 20 µm, were prepared under controlled conditions, followed by characterization through SEM and XPS to evaluate their size, surface area, and C/O ratio. The biosensing performance was systematically assessed by rGO-FET biosensors, examining the effects of GO flake size, C/O ratio, and film thickness. PACAP38 was employed as a biomarker for receptor-mediated detection, while chlorine ions served as model analytes for receptor-free small molecule detection. The results indicate that decreasing the GO flake size enhanced the performance for both target biomolecules. These findings highlight the crucial importance of selecting GO flake sizes specific to target analytes and detection strategies, thereby optimizing biosensor efficiency. Full article

Green chemistry seeks to find alternative synthesis routes that are less harsh to living organisms and the environment. In this communication, a microwave-assisted hydrothermal technique and a thermal annealing method were used in the reduction of graphene oxide (GO) to make reduced GO (rGO). Graphite powder was oxidised using the Improved Hummers’ method, exfoliated, and freeze-dried. Thereafter, an aqueous suspension of GO was reduced under microwave (MW) irradiation for 10 min at 600 W with and without the help of a reducing agent (hydrazine hydrate). Thermal annealing reduction was also conducted under a nitrogen atmosphere at 300 °C for 1 h. Prepared samples were analysed using Raman laser spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), the Brunauer–Emmett–Teller (BET) method, and X-ray photoelectron spectroscopy (XPS). A successful reduction in the GO functional groups between the sheets was established using XRD. In the Raman analysis, the ratio of the intensity of the D and G band (I_D/I_G) in graphene sheets assisted in assessing the quality of the graphene films. An estimation of the number of structural defects was calculated using the I_D/I_G ratio. The Raman analysis showed an increase in the I_D/I_G ratio after both oxidation and reduction processes. The defect densities of both MW-treated samples were comparable while an increased defect density was evident in the thermally annealed sample. TEM micrographs confirmed the sheet-like morphology of the samples. The rGO sheets obtained from the MW-treated method appeared to be smaller when compared to the rGO ones obtained by thermal treatment. It was also evident from XRD analysis that thermal treatment promoted the coalition of graphitic layers, such that the estimated number of layers was larger than that of GO. The elemental analysis showed that the C/O ratio of GO increased from 2 to 7.8 after MW hydrazine reduction. Full article

Nanocomposites based on Fe₃O₄ and carbonaceous nanoparticles (CNPs), including carbon nanotubes (CNTs) and graphene derivatives (graphene oxide (GO) and reduced graphene oxide (RGO)), such as Fe₃O₄@GO, Fe₃O₄@RGO, and Fe₃O₄@CNT, have demonstrated considerable potential in a number of health applications, including tissue regeneration and innovative cancer treatments such as hyperthermia (HT). This is due to their ability to transport drugs and generate localized heat under the influence of an alternating magnetic field on Fe₃O₄. Despite the promising potential of CNTs and graphene derivatives as drug delivery systems, their use in biological applications is hindered by challenges related to dispersion in physiological media and particle agglomeration. Hence, a solid foundation has been established for the integration of various synthesis techniques for these nanocomposites, with the wet co-precipitation method being the most prevalent. Moreover, the dimensions and morphology of the composite nanoparticles are directly correlated with the value of magnetic saturation, thus influencing the efficiency of the composite in drug delivery and other significant biomedical applications. The current demand for this type of material is related to the loading of a larger quantity of drugs within the hybrid structure of the carrier, with the objective of releasing this amount into the tumor cells. A second demand refers to the biocompatibility of the drug carrier and its capacity to permeate cell membranes, as well as the processes occurring within the drug carriers. The main objective of this paper is to review the synthesis methods used to prepare hybrids based on Fe₃O₄ and CNPs, such as GO, RGO, and CNTs, and to examinate their role in the formation of hybrid nanoparticles and the correlation between their morphology, the dimensions, and optical/magnetic properties. Full article

Manganese dioxide (MnO₂) has drawn attention as a sensitiser to be incorporated in graphene-based chemoresistive sensors thanks to its promising properties. In this regard, a rGO@MnO₂ sensing material was prepared and deposited on two different substrates (silicon and Kapton). The effect of the substrate nature on the morphology and sensing behaviour of the rGO@MnO₂ material was thoroughly analysed and reported. These sensors were exposed to different dilutions of NO₂ ranging from 200 ppb to 1000 ppb under dry and humid conditions (25% RH and 70% RH) at room temperature. rGO@MnO₂ deposited on Kapton showed the highest response of 6.6% towards 1 ppm of NO₂ under dry conditions at RT. Other gases or vapours such as NH₃, CO, ethanol, H₂ and benzene were also tested. FESEM, HRTEM, Raman, XRD and ATR-IR were used to characterise the prepared sensors. The experimental results showed that the incorporation of nanosized MnO₂ in the rGO material enhanced its response towards NO₂. Moreover, this material also showed very good responses toward NH₃ both under dry and humid conditions, with the rGO@MnO₂ sensor on silicon showing the highest response of 18.5% towards 50 ppm of NH₃ under 50% RH at RT. Finally, the synthetised layers showed no cross-responsiveness towards other toxic gases. Full article

Lithium–sulfur batteries (Li-S batteries) have attracted wide attention due to their high theoretical energy density and the low cost of sulfur cathode material. However, the poor conductivity of the sulfur cathode, the polysulfide shuttle effect, and the slow redox kinetics severely affect their cycling performance and Coulombic efficiencies, especially under low-temperature conditions, where these effects are more exacerbated. To address these issues, this study designs and synthesizes a microspherical cobalt molybdate@reduced graphene oxide (CoMoO₄@rGO) composite material as the cathode material for Li-S batteries. By growing CoMoO₄ nanoparticles on the rGO surface, the composite material not only provides a good conductive network but also significantly enhances the adsorption capacity to polysulfides, effectively suppressing the shuttle effect. After 100 cycles at room temperature with a current density of 1 C, the reversible specific capacity of the battery stabilizes at 805 mAh g⁻¹. Notably, at −20 °C, the S/CoMoO₄@rGO composite achieves a reversible specific capacity of 840 mAh g⁻¹. This study demonstrates that the CoMoO₄@rGO composite has significant advantages in suppressing polysulfide diffusion and expanding the working temperature range of Li-S batteries, showing great potential for applications in next-generation high-performance Li-S batteries. Full article