Search Results (606)

Titanium dioxide (TiO₂), owing to its excellent photocatalytic performance and environmental friendliness, holds great potential in the remediation of water pollution. In this study, we introduce a green and facile strategy to fabricate TiO₂-based hybrid aerogels, in which the peptide FQFQFIFK first self-assembles into peptide nanofibers (PNFs), followed by in situ biomineralization of TiO₂ on the PNFs. The TiO₂-loaded PNFs are then combined with graphene oxide (GO) via π–π interactions and integrated with microcrystalline cellulose (MCC) to construct a stable three-dimensional (3D) porous framework. The resulting GO/MCC/PNFs-TiO₂ aerogels exhibit high porosity, low density, and good mechanical stability. Photocatalytic experiments show that the aerogels efficiently degrade various organic dyes (methylene blue, rhodamine B, crystal violet, and Orange II) and antibiotics (e.g., tetracycline) under visible-light irradiation, achieving final degradation efficiencies higher than 90%. The excellent performance is attributed to the synergistic effect of the ordered interface provided by the PNF template, the stabilization and uniform dispersion facilitated by GO, and the mechanically robust 3D scaffold constructed by MCC. This work provides an efficient and sustainable strategy for designing functional hybrid aerogels and lays a foundation for their application in water treatment and environmental remediation. Full article

This research proposes an intelligent modeling and optimization strategy for abrasive waterjet machining (AWJM) of magnesium-based fiber metal laminates (FMLs) reinforced with reduced graphene oxide (r-GO). Experiments were designed using the Box–Behnken method, considering waterjet pressure, stand-off distance, traverse speed, and r-GO content as inputs, while kerf taper (Kt), surface roughness (Ra), and material removal rate (MRR) were evaluated as outputs. Adaptive Neuro-Fuzzy Inference System (ANFIS) models were developed for each response, with their critical optimized hyperparameters such as cluster radius, quash factor, and training data split through the dragonfly optimization (DFO) algorithm. The optimized ANFIS networks yielded a high predictive accuracy, with low RMSE and MAPE values and close agreement between predicted and measured results. Four metaheuristic algorithms including particle swarm optimization (PSO), salp swarm optimization (SSO), whale optimization algorithm (WOA), and the antlion optimizer (ALO) were applied for simultaneous optimization, using a TOPSIS-based single-objective formulation. ALO outperformed the others, identifying 325 MPa waterjet pressure, 2.5 mm stand-off, 800 mm/min traverse speed, and 0.00602 wt% r-GO addition in FMLs as optimal conditions. These settings produced a kerf taper of 2.595°, surface roughness of 8.9897 µm, and material removal rate of 138.13 g/min. The proposed ANFIS-ALO framework demonstrates strong potential for achieving precision and productivity in AWJM of hybrid laminates. Full article

Tryptophan (Trp) and tryptamine (Tryp), critical biomarkers in mood regulation, immune function, and metabolic homeostasis, are increasingly recognized for their roles in both oral and systemic pathologies, including neurodegenerative disorders, cancers, and inflammatory conditions. Their rapid, sensitive detection in biofluids such as saliva—a non-invasive, real-time diagnostic medium—offers transformative potential for early disease identification and personalized health monitoring. This review synthesizes advancements in electrochemical sensor technologies tailored for Trp and Tryp quantification, emphasizing their clinical relevance in diagnosing conditions like oral squamous cell carcinoma (OSCC), Alzheimer’s disease (AD), and breast cancer, where dysregulated Trp metabolism reflects immune dysfunction or tumor progression. Electrochemical platforms have overcome the limitations of conventional techniques (e.g., enzyme-linked immunosorbent assays (ELISA) and mass spectrometry) by integrating innovative nanomaterials and smart engineering strategies. Carbon-based architectures, such as graphene (Gr) and carbon nanotubes (CNTs) functionalized with metal nanoparticles (Ni and Co) or nitrogen dopants, amplify electron transfer kinetics and catalytic activity, achieving sub-nanomolar detection limits. Synergies between doping and advanced functionalization—via aptamers (Apt), molecularly imprinted polymers (MIPs), or metal-oxide hybrids—impart exceptional selectivity, enabling the precise discrimination of Trp and Tryp in complex matrices like saliva. Mechanistically, redox reactions at the indole ring are optimized through tailored electrode interfaces, which enhance reaction kinetics and stability over repeated cycles. Translational strides include 3D-printed microfluidics and wearable sensors for continuous intraoral health surveillance, demonstrating clinical utility in detecting elevated Trp levels in OSCC and breast cancer. These platforms align with point-of-care (POC) needs through rapid response times, minimal fouling, and compatibility with scalable fabrication. However, challenges persist in standardizing saliva collection, mitigating matrix interference, and validating biomarkers across diverse populations. Emerging solutions, such as AI-driven analytics and antifouling coatings, coupled with interdisciplinary efforts to refine device integration and manufacturing, are critical to bridging these gaps. By harmonizing material innovation with clinical insights, electrochemical sensors promise to revolutionize precision medicine, offering cost-effective, real-time diagnostics for both localized oral pathologies and systemic diseases. As the field advances, addressing stability and scalability barriers will unlock the full potential of these technologies, transforming them into indispensable tools for early intervention and tailored therapeutic monitoring in global healthcare. 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

In this paper, we design a self-powered photoelectrochemical (PEC)-type photodetector based on a hybridization of two-dimensional (2D) few-layer antimony (Sb) nanosheets (NSs) and reduced graphene oxide (rGO). The few-layer Sb NSs obtained by liquid-phase exfoliation can be anchored on the surface of rGO through hydrothermal treatment. Specifically, during photoexcitation, the electron–hole pairs photogenerated on the surface of Sb NSs can be well stimulated and transferred by rGO, reducing the photogenerated carriers recombine on Sb NSs. The excellent electrochemical performance is confirmed by PEC tests. The photobehavior performance of the Sb NSs-rGO composite is significantly improved; its photocurrent density reaches 48.830 nA/cm² at zero potential, approximately twice that of pure Sb NSs. The hybrid exhibits a faster photoresponse speed, with the response time and recovery time being 0.140 s and 0.163 s, respectively. This enhancement arises from the conductive role of rGO as a conductive channel, and as a result, the efficient separation of photoinduced electron–hole pairs is facilitated. This study is a further exploration of hybrid engineering of 2D materials in photochemical photodetectors and demonstrates significant progress in this field. Full article

The growing challenge of biofilm-associated infections in dentistry necessitates advanced solutions. This review highlights the potential of smart bioactive and antibacterial materials—bioactive glass ceramics (BGCs), silver nanoparticle (AgNP)-doped polymers, and pH-responsive chitosan coatings—in transforming restorative dentistry. BGCs reduce biofilms by >90% while promoting bone integration. AgNP-polymers effectively combat S. mutans and C. albicans but require controlled dosing (<0.3 wt% in PMMA) to avoid cytotoxicity. Chitosan coatings enable pH-triggered drug release, disrupting acidic biofilms. Emerging innovations like quaternary ammonium compounds, graphene oxide hybrids, and 4D-printed hydrogels offer on-demand antimicrobial and regenerative functions. However, clinical translation depends on addressing cytotoxicity, standardizing antibiofilm testing (≥3-log CFU/mL reduction), and ensuring long-term efficacy. These smart materials pave the way for self-defending restorations, merging infection control with tissue regeneration. Future advancements may integrate AI-driven design for multifunctional, immunomodulatory dental solutions. 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

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

Alginate-based materials are widely studied for biomedical use, but their limited mechanical properties and variable biocompatibility pose challenges. In this work, hybrid composites composed of alginate, calcium, and graphene oxide were fabricated using a freeze-drying method and cross-linked with calcium ions via calcium chloride at different concentrations. Structural and morphological features were assessed using SEM, EDS, ICP-MS, and BET analysis. The resulting composites exhibited a porous architecture, with calcium incorporation confirmed by elemental analysis. Surface characteristics and pore parameters were influenced by the presence of graphene oxide and the cross-linking process. The effects of the materials on haemostasis were evaluated through activated partial thromboplastin time (aPTT) and prothrombin time (PT) assays, revealing modulation of the intrinsic coagulation pathway without significant changes in the extrinsic pathway. In this study, we analysed the effect of alginate–graphene oxide composites on the viability of peripheral blood mononuclear (PBM) cells and human foreskin fibroblasts from the Hs68 cell line. We also assessed the genotoxic potential of alginate–graphene oxide composites on these cells. Our results showed no cyto- or genotoxic effects of the material on either cell type. These findings suggest the biocompatibility and safe character of alginate–graphene oxide composites for use with blood and skin cells. Full article

The increasing use of pharmaceutically active compounds (PhACs), endocrine-disrupting compounds (EDCs), and personal care products (PCPs) has led to the widespread presence of organic micropollutants (OMPs) in aquatic environments, posing a significant global challenge for environmental conservation. In recent years, advanced materials-based nanofiltration (NF) technologies have emerged as a promising solution for water and wastewater treatment. This review begins by examining the sources of OMPs, as well as the risk of OMPs. Subsequently, the key criteria of NF membranes for OMPs are discussed, with a focus on the roles of pore size, charge property, molecular interaction, and hydrophilicity in the separation performance. Against that background, this review summarizes and analyzes recent advancements in materials such as metal organic frameworks (MOFs), covalent organic frameworks (COFs), graphene oxide (GO), MXenes, hybrid materials, and environmentally friendly materials. It highlights the porous nature and structural diversity of organic framework materials, the advantage of inorganic layered materials in forming controllable nanochannels through stacking, the synergistic effects of hybrid materials, and the importance of green materials. Finally, the challenges related to the performance optimization, scalable fabrication, environmental sustainability, and complex separation of advanced materials-based membranes for OMP removal are discussed, along with future research directions and potential breakthroughs. Full article

In order to improve the durability performance of sticky rice–lime paste in ancient masonry restoration materials, the effect of graphene oxide–nanosilica hybrids (GO–NS) on its basic physical properties and durability performance was investigated. The surface morphology, physical phase characteristics and infrared spectra of GO–NS and its sticky rice–lime paste were analysed by SEM, FE-TEM, XRD and FTIR. It was shown that NS successfully attached to the GO surface and improved the interlayer structure of GO. GO–NS reduces the fluidity and shrinkage of sticky rice–lime paste, prolongs the initial setting, shortens the final setting and significantly improves the compressive strength, water resistance and freeze resistance. As NS improves the interlayer structure of GO, it provides nucleation sites for the hardening of the sticky rice–lime paste, improves the quantity and structural distribution of the hardening products and reduces the pores. The NS undergoes a hydration reaction with Ca(OH)₂ in the lime to produce calcium silicate hydrate (C–S–H), which further refines the internal pore structure of the sticky rice–lime paste. As a result, the GO–NS-modified sticky rice–lime paste has a denser interior and better macroscopic properties. 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

Lost circulation is a major challenge in oil and gas drilling operations, severely restricting drilling efficiency and compromising operational safety. Conventional bridging and plugging materials rely on precise particle-to-fracture size matching, resulting in low success rates. Self-healing gels penetrate loss zones as discrete particles that progressively swell, accumulate, and self-repair in integrated gel masses to effectively seal fracture networks. Self-healing gels effectively overcome the shortcomings of traditional bridging agents including poor adaptability to fractures, uncontrollable gel formation of conventional downhole crosslinking gels, and the low strength of conventional pre-crosslinked gels. This work employs stearyl methacrylate (SMA) as a hydrophobic monomer, acrylamide (AM) and acrylic acid (AA) as hydrophilic monomers, and graphene oxide (GO) as an inorganic dopant to develop a GO-based self-healing organic–inorganic hybrid plugging material (SG gel). The results demonstrate that the incorporation of GO significantly enhances the material’s mechanical and rheological properties, with the SG-1.5 gel exhibiting a rheological strength of 3750 Pa and a tensile fracture stress of 27.1 kPa. GO enhances the crosslinking density of the gel network through physical crosslinking interactions, thereby improving thermal stability and reducing the swelling ratio of the gel. Under conditions of 120 °C and 6 MPa, SG-1.5 gel demonstrated a fluid loss volume of only 34.6 mL in 60–80-mesh sand bed tests. This gel achieves self-healing within fractures through dynamic hydrophobic associations and GO-enabled physical crosslinking interactions, forming a compact plugging layer. It provides an efficient solution for lost circulation control in drilling fluids. Full article

This study reported covalent organic frameworks (COFs) and their hybrid composites with two-dimensional materials, graphene oxide (GO), graphitic carbon nitride (g-C₃N₄), and boron nitride (BN), to examine their structural, textural, and gas adsorption properties. Material characterization confirmed the crystallinity of COF-1 and the preservation of framework integrity after integrating the 2D nanomaterials. FT-IR spectra exhibited pronounced vibrational fingerprints of imine linkages and validated the functional groups from the COF and the integrated nanomaterials. TEM images revealed the integration of the two components, porous, layered structures with indications of interfacial interactions between COF and 2D nanosheets. Nitrogen adsorption–desorption isotherms revealed the microporous characteristics of the COFs, with hysteresis loops evident, indicating the development of supplementary mesopores at the interface between COF-1 and the 2D materials. The BET surface area of pristine COF-1 was maximal at 437 m²/g, accompanied by significant micropore and Langmuir surface areas of 348 and 1290 m²/g, respectively, offering enhanced average pore widths and hierarchical porous strcuture. CO₂ adsorption tests were investigated showing maximum adsorption capacitiy of 1.47 mmol/g, for COF-1, closely followed by COF@BN at 1.40 mmol/g, underscoring the preserved sorption capabilities of these materials. These findings demonstrate the promise of designed COF-based hybrids for gas capture, separation, and environmental remediation applications. Full article