Search Results (903)

The primary objective of this work is to provide new solutions to increase impact protection, using a three-dimensional textile imbibed with a shear-thinning fluid. An extensive analysis showed a scarcity of research papers related to the damping capacity of deformable porous materials imbibed with non-Newtonian fluid. No studies were found for shear-thinning fluid flow inside highly compressible foams or other soft, porous materials. The damping capacity of the imbibed material was evaluated using impact with a dropping weight. Polyvinyl alcohol solution mixed with water was used for imbibition of a three-dimensional textile. Hydrophilized carbon nanofibers were also added to the solution to augment the shear-thinning behavior. The measured impact force for imbibed samples showed an important reduction compared to the impact force for the dry material. This research does not focus on flow phenomena at the microstructural level but instead aims to highlight the macroscopic attenuation effect that occurs during the compression of the imbibed material. Full article

Electrospinning of poly(lactic acid) (PLA) commonly relies on toxic organic solvents, which limit its sustainability and biomedical applicability. In this work, a green electrospinning process was developed using dimethyl carbonate (DMC), a biodegradable and low-toxicity solvent, combined with acetone as a volatile co-solvent to promote efficient jet solidification. Three commercial PLA grades were evaluated for solubility and spinnability, and PLA 4043D was identified as the most suitable for DMC and acetone systems. The electrospinning parameters, including solvent ratio, flow rate, and applied voltage, were systematically optimized to achieve stable jet formation and uniform fiber morphology. Under optimized conditions, the process produced continuous, bead-free nanofibers with a mean diameter of ~1 µm and uniform nanoscale surface porosity resulting from differential solvent evaporation. The resulting fibers were characterized in terms of morphology, structure, thermal behavior, and mechanical performance, confirming increased amorphous content, high porosity (about 78%), and tensile strength of ~3 MPa for the selected electrospinning condition. This study demonstrates that DMC-based solvent systems enable a sustainable and potentially biocompatible route, considering the lower toxicity of the solvents employed, offering a green alternative to conventional toxic processes for the fabrication of medical scaffolds. Full article

At present, composite phase change materials are widely studied for battery thermal management. However, to ensure the battery’s thermal safety, it is necessary not only to control the temperature during regular operation, but also to prevent sudden thermal runaway. This basic function depends on the flame-retardant properties of the composite phase change materials. In this study, a hexagonal double-layer hollow nanocage S2 with defect orientation was prepared and combined with carbon nanotubes (PNT) derived from polypyrrole (PPy) tubes to form a high adsorption mixture. Multifunctional composite phase change material PNT/S2@PEG/TEP was prepared by adsorbing and coating polyethylene glycol 8000 (PEG-8000) and triethyl phosphate (TEP) with microfibrillated cellulose nanofibers (CNF) as the skeleton. The characterization shows that its thermal conductivity is 0.65 W/m·K and its phase transition enthalpy is 146.1 J/g, demonstrating its excellent thermal regulation. Microcalorimetric testing (MCC) confirmed its flame-retardant ability, attributed to the strong adsorption of PNT/S2 on PEG-8000 and TEP, the improvement in PNT’s thermal conductivity, and the contribution of CNF to flexibility. This composite phase change material, with excellent comprehensive properties, has broad application prospects in thermal safety for electronic equipment, significantly expanding its practical scope. Full article

The development of membranes and patches for controlled drug release to enhance therapeutic efficacy is a promising approach to addressing the challenge posed by poor adherence to pharmacological therapies for chronic diseases. In this study, we designed an electrospun polycaprolactone (PCL) nanofibrous membrane reinforced with different concentrations (0.04%, 0.05%, 0.075%, and 0.2%) of functionalized multi-walled carbon nanotubes (f-MWCNTs) intended for biomedical applications, such as transdermal devices. We characterized the resulting composites using scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), atomic force microscopy (AFM), and dynamic mechanical analysis (DMA) to evaluate their morphology, chemical composition, and mechanical properties. We also measured their cytotoxicity upon contact with peripheral blood mononuclear cells. The nanofibers had diameters below 100 nm and inclusions of microspheres, which were attributed to the electrospinning expansion phenomenon. Spectroscopic and mechanical analyses confirmed molecular interactions between the PCL matrix and the f-MWCNTs. Finally, biological tests demonstrated that both the dispersion of f-MWCNTs and the nanofiber sizing render the membranes biocompatible, supporting their potential use as drug-delivery systems. Full article

The escalating demand for high-performance energy storage devices has driven extensive research into flexible electrode materials for supercapacitors. Integrating structured carbon nanomaterials with flexible substrates to construct binder-free electrode architectures represents a promising strategy for improving supercapacitor capacitance and rate capability. However, achieving stable, binder-free integration of structure-controlled nanostructured carbon materials with flexible substrates remains a critical challenge. In this study, we report a direct synthesis approach for one-dimensional (1D) carbon nanofibers (CNFs) on commercial flexible carbon fabric (CF) via chemical vapor deposition (CVD). The resulting CNFs exhibit two typical average diameters—approximately 25 nm and 50 nm—depending on the growth temperature, with both displaying highly graphitized structures. Electrochemical characterization of the CNFs/CF composites in 1 M H₂SO₄ electrolyte revealed typical electric double-layer capacitor (EDLC) behavior. Notably, the 25 nm-CNFs/CF electrode achieves a high specific capacitance of 87.5 F/g, significantly outperforming the 50 nm-CNFs/CF electrode, which reaches 50.2 F/g. Compared with previously reported carbon nanotube CNTs/CF electrodes, the 25 nm-CNFs/CF electrode exhibits superior capacitance and lower resistance. Full article

Silicon is considered one of the most promising anode materials for lithium-ion batteries because of its high theoretical capacity and low lithiation potential. However, its practical application is limited by significant volume expansion, unstable solid–electrolyte interphase formation, and poor intrinsic conductivity. This review summarizes recent advances in hybrid strategies using multi-walled carbon nanotubes (MWCNTs), single-walled carbon nanotubes (SWCNTs), graphene, carbon nanofibers (CNFs), and pitch-derived carbons. We compare their respective benefits and drawbacks regarding conductivity, structural resilience, and scalability, while also addressing critical challenges such as dispersion, defect control, and processing costs. The discussion emphasizes the importance of hierarchical, multifunctional architectures that combine different forms of carbon to achieve synergistic performance. Finally, we outline future directions in interfacial engineering, defect and doping optimization, and electrode design under high-loading conditions. We believe that this review can offer perspectives on developing durable, energy-dense, and commercially viable silicon anodes for next-generation lithium-ion batteries. Full article

This study investigates the synergistic influence of multi-walled carbon nanotubes (MWC-NTs), nanosilica powder (NSP), and polypropylene fiber waste (PFW) on the mechanical performance of mortar incorporating demolished concrete waste aggregates (DCWA). The replacement of natural aggregates with DCWA typically results in strength reductions and weak interfacial transition zones; therefore, the combined use of nanomaterials and microfibers is proposed as a mitigation strategy. A Taguchi Design of Experiments (DOE) approach was employed to optimize mix parameters, including MWCNT dosage, NSP content, PFW volume fraction, and DCWA replacement level. Mortar mixtures were prepared with MWCNTs (0–0.1% by binder weight), NSP (0–2% by binder weight), PFW (0–0.3% by volume), and DCWA (0–20% replacement of fine sand). Mechanical performance was assessed through compressive and flexural strength tests. A combined statistical approach using the Pareto chart and ANOVA identified the most influential parameters and their respective contributions to the response variable. The innovative aspect of this research lies in the synergistic integration of MWCNTs, NSP, demolished concrete waste, and polypropylene fiber waste within the mortar matrix, with the incorporation of nanomaterials specifically intended to compensate for the strength reduction typically induced by the use of demolition concrete waste aggregates. Although a potential nano-scale synergy between MWCNTs and NSP was initially considered, the experimental results indicated that the most relevant synergistic effects occurred among broader mix parameters rather than specifically between the two nanomaterials. Even so, when assessed individually, both nanomaterials contributed to improving the mechanical characteristics of the mortar—particularly nanosilica, which demonstrated a more pronounced effect—yet these individual enhancements did not translate into a distinct synergistic interaction between MWCNTs and NSP. The Taguchi DOE proved to be an efficient tool for multiple factor analysis, enabling reliable identification of the most influential parameters with a minimum number of tests. Its application facilitated the development of mortar mixtures that effectively integrate demolition waste while achieving enhanced mechanical performance through nano- and micro-scale reinforcement. Full article

Chitin-derived biomass carbon materials are promising supercapacitor electrode materials due to their wide availability, low cost, high specific surface area, and nitrogen doping capability. However, their practical application is limited by insufficient conductivity and cyclic stability, often requiring functional modification or integration with complementary materials. In this study, we present a novel strategy by incorporating copper sulfide (Cu₂S) into a chitin-based carbon matrix. Cu₂S, known for its high intrinsic conductivity, excellent electroactivity, and theoretical specific capacity (~335 mAh·g⁻¹), was uniformly doped into the three-dimensional carbon aerogel framework derived from chitin nanofibers (ChNF) through sol–gel, freeze-drying, and high-temperature carbonization processes. The resulting chitin-based carbon/Cu₂S composite aerogel (CChNF/Cu₂S) exhibited a hierarchical porous structure with Cu₂S nanoparticles (20–30 nm) uniformly distributed on the carbon fiber surface. Electrochemical tests demonstrated its excellent performance, achieving a specific capacitance of 852 F·g⁻¹ at 1 A·g⁻¹, highlighting the synergistic effects of the conductive Cu₂S and nitrogen-doped carbon framework for high-performance supercapacitor applications. Full article

The growing scarcity of natural renewable resources has accelerated interest in producing nanomaterials from waste streams. Nanomaterials offer exceptional reinforcement capabilities for advanced composites, driving the need for sustainable and scalable production routes. While prior reviews have broadly examined nanomaterial synthesis from biomass or industrial residues, they often overlook textile waste as a strategic feedstock. This review uniquely focuses on the upcycling of textile waste—one of the most abundant yet underutilized waste streams—into high-value nanomaterials, thereby advancing circular economy principles. Unlike earlier studies that primarily discuss energy recovery or generic recycling, this work systematically explores mechanical, chemical, and thermal conversion routes tailored for textiles, leading to the production of cellulose nanofibers, cellulose nanocrystals, and carbon nanoparticles, which represent a significant class of biodegradable nanomaterials. Furthermore, a comprehensive analysis of the physicochemical properties of the nanomaterials and their emerging applications in water purification and environmental remediation is provided. An alternative pathway for nanomaterial synthesis from waste rather than renewable sources, providing information on the effective extraction of nanomaterials from mixed fiber compositions and dye residues present in textile waste, is also highlighted. By addressing current challenges and outlining future research directions, this review establishes a roadmap for sustainable textile waste valorization, marking a critical step toward eco-friendly nanomaterial production. Full article

This study is devoted to the determination of the role of aerosol spraying in the formation of NO₂ sensor properties of carbon nanofiber (CNF)-based films. This is the first paper to systematically apply the aerosol spraying technique to CNF-based films and link the spraying parameters directly to sensor performance metrics (response, signal-to-noise ratio, response times, etc.). Chemiresistive gas sensors were created based on CNFs and tested at room temperature (25 ± 1 °C). It has been shown that the increase in the concentration of the CNF/ethanol mixture used for spraying from 3 to 30 mg/mL led to a growth in sensor response from 1.2% to 12.0% at 2 ppm NO₂. The increase in the thickness of the CNF film of the sensor induced a growth in ΔR/R₀ to NO₂ that is attributed to the formation of a porous film. With increased film thickness, the response improves (from 7.0% to 10.6% at 2 ppm NO₂) as does the signal-to-noise ratio (from 735:1 to 1892:1). The creation of hybrid all-carbon composites based on CNFs and multi-walled carbon nanotubes (MWCNTs) resulted in a decrease in both sensor response and signal-to-noise ratio; however, the response time and recovery degree improved. Two types of hybrid materials based on CNFs and MWCNTs were created using aerosol spraying to enhance the sensor behavior of CNFs. The obtained data confirm the dominant role of the thickness of CNF-based films and their density (in terms of distance between nearest carbon inclusions within the film) in sensor characteristics. The machine learning data used to describe the sensing behavior of two gases with opposite resistance changes when in contact with CNFs, namely NO₂ and NH₃, showed final accuracies of 92.13% on training data and 91.98% on validation data. Full article

In this study, the tribological compatibility of ZrO₂-nanofiber-strengthened Al-matrix composites with graphene nanoplatelets (GNPs)-derived surface film acting as a solid lubricant was investigated. The substrate materials prepared by Spark Plasma Sintering (SPS) included the pure aluminum monolith (reference material) and two Al–ZrO₂ nanocomposites with either 1 or 3 wt.% of ZrO₂ nanofibers. The GNPs-derived solid lubricant films were dry mechanically burnished into the metallographically polished surfaces. The durability of these burnished films was evaluated by performing tribological friction experiments using a ball-on-disk method. Thus, a friction load capacity of GNP-derived tribofilms on the substrate materials and its effect on the coefficient of friction (COF) were evaluated. The results showed that the films burnished on the surfaces of Al–ZrO₂ nanofiber composites were more resistant to much higher loads than films burnished on monolithic aluminum. The obtained findings indicated that ZrO₂ nanofiber protrusions likely stabilize a GNP-derived carbon tribolayer on the polished composite surfaces. As a result, the reinforcement of aluminum with ceramic nanofibers led also to a significant reduction in COF. The highest improvement of tribological performance was observed for the Al–ZrO₂ nanofiber composite with 1 wt.% ZrO₂ nanofibers. The increase of ZrO₂ nanofibers up to 3 wt.% was no more efficient due to nanofiber clustering leading to lower stability of the carbon friction film. Our objective was to isolate the role of the aluminum substrate, specifically, ZrO₂ nanofiber protrusions in the formation and retention of a GNP-derived carbon tribofilm under room-temperature, ambient-air dry sliding. Full article

Aqueous zinc-ion batteries (AZIBs) have attracted considerable attention due to their intrinsic safety, low cost, and environmental friendliness. However, drastic volume expansion, sluggish reaction kinetics, and the insufficient structural stability of electrode materials still remain key challenges. In this work, a cascade structure-guided electron transport strategy was used to construct a vanadium nitride@carbon nanosheet/carbon nanofiber (VN@CNS/CNF) composite as a high-performance cathode for AZIBs. In this rationally engineered architecture, carbon-coated VN nanoparticles are uniformly anchored on a conductive carbon nanofiber network, forming a multidimensional interconnected structure that enables fast electron/ion transport and robust mechanical stability. The carbon shell effectively alleviates volume expansion and prevents VN nanoparticle agglomeration, while the continuous carbon fiber backbone reduces charge transfer resistance and enhances reaction kinetics. Benefiting from this synergistic structural design, the VN@CNS/CNF electrode delivers a high specific capacity of 564 mAh g⁻¹ at 0.1 A g⁻¹, maintains 99% capacity retention after 50 cycles, and retains 280 mAh g⁻¹ even at 8 A g⁻¹ after prolonged cycling. This study provides a new structural engineering strategy for vanadium nitride-based electrodes and provides strategic guidance for the development of fast-charging, durable aqueous zinc-ion batteries. Full article

This study explores the development of new room-temperature NO₂ sensors utilizing carbon nanofibers (CNFs), single-walled carbon nanotubes (SWCNTs), and their hybrids with reduced graphite oxide (rGO), fabricated via a facile drop casting method with varying concentrations of carbon/ethanol mixtures. The concentration-dependent relation of sensor response to NO₂ has been found. Comprehensive characterization techniques, including electron microscopy, Raman spectroscopy, optical microscopy, and X-ray diffraction were employed to analyze the sensing materials. Our results reveal that CNFs exhibit superior sensitivity, reaching −1.32%/ppm at an optimal suspension concentration of 1.5 mg/mL, outperforming SWCNTs. The creation of hybrid composites, specifically CNFs/rGO and SWCNTs/rGO, further enhances sensing performance due to synergistic effects. Molecular dynamics simulations revealed increased adsorption behavior of the CNFs/rGO hybrid sensing material. The fabricated devices, based on all-carbon composites, are effective and energy-efficient platforms for NO₂ detection, offering promising solutions for environmental monitoring, the chemical industry, and industrial safety applications. Full article

Fiber-based and fabric batteries signify a groundbreaking development in energy storage, allowing for the straightforward incorporation of power sources into wearable fabrics, intelligent apparel, and adaptable electronics. In this study, we introduce a novel strategy for one-step fabrication of a flexible lithium titanate oxide (Li₄Ti₅O₁₂, LTO) anode directly on a copper current collector via electrospinning, eliminating the need for high-temperature post-processing. Based on our previous work with electrospun nanofiber cathodes and carbon-based current collector, we prepared the LTO electrode using polyethylene oxide (PEO) as a binder and carbon additives to enhance mechanical integrity and conductivity. LTO fiber mats detached from the current collector were found to endure multiple instances of bending, twisting, and folding without any structural damage. LTO/Li cells incorporating electrospun fiber LTO electrodes with 72 wt% active material loading deliver a high capacity of 170 mAh g⁻¹ at 0.05 C. In addition, they demonstrate excellent cycling stability with a capacity loss of only 0.01% per cycle over 200 cycles and maintain a capacity of 160 mAh g⁻¹ at 0.1 C. The scalability of the heat-treatment-free method for fabricating flexible LTO anodes, together with the improved mechanical durability and electrochemical performance, offers a promising route toward the development of next-generation flexible and wearable energy storage devices. Full article

Silicon (Si) is a promising high-capacity anode material for lithium–ion batteries but faces challenges such as severe volume fluctuations during cycles and the formation of unstable solid-electrolyte interphase films on the electrode surface. To address these limitations, we developed a bioinspired Si@C composite anode through polydopamine-mediated self-assembly of aromatic polyamide nanofibers and nano–Si, followed by controlled pyrolysis at 1000 °C under N₂. The resulting hierarchical architecture mimics the symbiotic root-nodule structure of legumes, featuring vascular bundle-like carbon frameworks and chemically bonded Si/C interfaces. The optimized composite delivers an initial capacity of 1107.0 mAh g⁻¹ at 0.1 A g⁻¹ and retains 580.0 mAh g⁻¹ after 100 cycles with 52.4% retention. The exceptional electrochemical properties arise from the optimized architecture and surface interactions. The nature-inspired carbon network minimizes ionic transport resistance via vertically aligned porous pathways while simultaneously boosting lithium–ion adsorption capacity. Furthermore, radially aligned graphitic ribbons are generated through controlled polyamide thermal transformation that effectively mitigates electrode swelling and maintains stable interfacial layers during cycling. Full article