Search Results (85)

Electrospinning has emerged as a powerful technique for fabricating customised nanofibrous materials with integrated functional nanostructures, offering significant advantages for electrochemical energy applications. This review highlights recent advances in using electrospun nanofibres directly as active components in devices such as batteries, supercapacitors, and fuel cells. The emphasis is on the role of composite design, fibre morphology and surface chemistry in enhancing charge transport, catalytic activity and structural stability. Integrating carbon-based frameworks, conductive polymers, and inorganic nanostructures into electrospun matrices enables multifunctional behaviour and improves device performance. The resulting nanofibrous composite materials, often after heat treatment, can be used directly as electrodes or self-supporting layers, eliminating the need for additional processing steps such as size reduction or preparation of slurries and inks for creating functional nanofibre-based deposits. The importance of composite nanofibres as an emerging strategy for overcoming challenges related to scalability, long-term durability, and interface optimisation is also discussed. This review summarises the key results obtained to date and highlights the potential of electrospun nanofibres as scalable, high-performance materials for next-generation energy technologies, outlining future directions for their rational design and integration. 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

In this study, we investigate the effect of varying the loading of molecularly imprinted polymer nanoparticles (MIP-NPs) on the morphology and sensing performance of electrospun nanofibres for the selective detection of linalool, a representative plant-emitted monoterpene. The proposed strategy combines two synergistic technologies: molecular imprinting, to introduce chemical selectivity, and electrospinning, to generate high-surface-area nanofibrous sensing layers with tuneable architecture. Linalool-imprinted MIP-NPs were synthesized via precipitation polymerization using methacrylic acid (MAA) and ethylene glycol dimethacrylate (EGDMA), yielding spherical particles with an average diameter of ~135 nm. These were embedded at increasing concentrations into a polyvinylpyrrolidone (PVP) matrix containing multi-walled carbon nanotubes (MWCNTs) and processed into nanofibrous mats by electrospinning. Atomic force microscopy (AFM) revealed that MIP content modulates fibre roughness and network morphology. Electrical sensing tests performed under different relative humidity (RH) conditions showed that elevated humidity (up to 60% RH) improves response stability by enhancing ion-mediated charge transport. The formulation with the highest MIP-NP loading exhibited the best performance, with a detection limit of 8 ppb (±1) and 84% selectivity toward linalool over structurally related terpenes (α-pinene and R-(+)-limonene). These results demonstrate a versatile sensing approach in which performance can be precisely tuned by adjusting MIP content, enabling the development of humidity-tolerant, selective VOC sensors for environmental and plant-related applications. Full article

Background/Objectives: A nanostructured membrane of polycaprolactone (a synthetic polymer) was synthesized using an electrospinning technique aiming to enhance its hydrophilicity and rate of degradation by surface modification via aminolysis. Since polycaprolactone nanofibrous films are naturally hydrophobic and with slow degradation, which restricts their use in biological systems, amino groups were added to the fiber surface using the aminolysis technique, greatly increasing the wettability of the membranes. Methods: Polycaprolactone nanofibrous membranes were synthesized via the electrospinning technique and surface modification by aminolysis. Trypsin, pepsin, and pancreatin were conjugated onto the aminolyzed PNF surface to further strengthen biocompatibility by enhancing the hydrophilicity, porosity, and biodegradation rate. SEM, FTIR, EDX, and liquid displacement method were performed to investigate proteolytic efficiency and morphological and physical characteristics such as hydrophilicity, porosity, and degradation rates. Results: Enzyme activity tests, which showed a zone of clearance, validated the successful enzyme conjugation and stability over a wide range of pH and temperatures. Scanning electron microscopy (SEM) confirms the smooth morphology of nanofibers with diameters ranging from 150 to 950 nm. Fourier transform infrared spectroscopy (FTIR) revealed the presence of O–H, C–O, C=O, C–N, C–H, and O–H functional groups. Energy-dispersive X-ray (EDX) elemental analysis indicates the presence of carbon, oxygen, and nitrogen atoms owing to the presence of peptide and amide bonds. The liquid displacement technique and contact angle proved that Pepsin-PNFs possess notably increased porosity (88.50% ± 0.31%) and hydrophilicity (57.6° ± 2.3 (L), 57.9° ± 2.5 (R)), respectively. Pancreatin-PNFs demonstrated enhanced enzyme activity and degradation rate on day 28 (34.61%). Conclusions: These enzyme-conjugated PNFs thus show improvements in physicochemical properties, making them ideal candidates for various biomedical applications. Future studies must aim for optimization of enzyme conjugation and in vitro and in vivo performance to investigate the versatility of these scaffolds. Full article

Carbon nanofibrous materials from electrospinning are good candidate electrode materials for supercapacitor applications due to their straightforward processability, chemical stability, high porosity, and large surface area. In this research, a straightforward and effective way was revealed to significantly enhance the electrochemical performance of carbon nanofibrous electrode material from electrospinning of polyacrylonitrile (PAN). Fluorination of the electrospun carbon nanofibers (ECNF) was studied by comparing two types of hydrofluoric acid (HF) treatment, i.e., direct HF acid treatment on ECNF (Type I) vs. HF acid treatment on the stabilized PAN (Type II) followed by carbonization. The latter was found to be an advantageous way to introduce C-F bonds in the resultant carbon nanofibrous electrode material that contributed to pseudocapacitance. Furthermore, the Type II HF acid treatment demonstrated exciting synergistic effects with ECNF aerogel formation on carbon structure and porosity development and generated a superior fluorinated electrospun carbon nanofibrous aerogel (ECNA-F) electrode material for supercapacitor uses. The resultant ECNA-F electrode material demonstrated excellent electrochemical performance with great cyclic stability due to the large improvements in both pseudocapacitance and electrical double-layer capacitance. ECNA-F achieved a specific capacitance of 372 F/g at a current density of 0.5 A/g with 1 M H₂SO₄ electrolyte, and the device with ECNA-F and 1 M Na₂SO₄ electrolyte possessed an energy density of 29.1 Wh/kg at a power density of 275 W/kg. This study provided insight into developing high-performance and stable carbon nanofibrous electrode materials for supercapacitors. Full article

A 6-carbon short-chain per- and polyfluoroalkyl substance (PFAS), GenX, also known as hexafluoropropylene oxide dimer acid (HFPO-DA) and its ammonium salt, has been manufactured in recent years as a replacement for perfluorooctanoic acid (PFOA), a traditional long-chain PFAS, due to the increasing environmental regulation of PFAS compounds in recent years. GenX has received significant attention because of the fact that it is more toxic than people originally thought, and it is now one of the six PFAS compounds that are placed under legally enforceable restrictions in drinking water, i.e., 10 ppt, by the United States Environmental Protection Agency (US EPA). In this research, we extended the use of polyacrylonitrile (PAN) nanofibers from electrospinning for GenX removal from water by coating them with polyaniline (PANI) through in situ polymerization. The obtained PANI-coated electrospun PAN nanofibrous adsorbent (PANI-ESPAN) demonstrated excellent GenX adsorption capability and could remove nearly all GenX (>98%) from a 100 ppb aqueous solution. This research provided valuable insights into short-chain PFAS remediation from water by designing and developing high-performance adsorbent materials. Full article

To reduce solid waste production and enable the synergistic conversion of solid waste into high-value-added products, we introduce a novel, sustainable, and ecofriendly method. We fabricate nanofiber and nanosheet silicon carbides (SiC) through a carbothermal reduction process. Here, the calcined coal gangue, converted from coal gangue, serves as the silicon source. The carbon sources are the carbonized waste tire residue from waste tires and the pre-treated kerosene co-refining residue. The difference in carbon source results in the alteration of the morphology of the SiC obtained. By optimizing the reaction temperature, time, and mass ratio, the purity of the as-made SiC products with nanofiber-like and nanosheet-like shapes can reach 98%. Based on the influence of synthetic conditions and the results calculated from the change in the Gibbs free energy of the reactions, two mechanisms for SiC formation are proposed, namely the reaction of intermediate SiO with CO to form SiC-nuclei-driven nanofibrous SiC and the SiO-deposited carbon surface to fabricate nuclei-induced polymorphic SiC (dominant nanosheets). This work provides a constructive strategy for preparing nanostructured SiC, thereby achieving “turning trash into treasure” and broadening the sustainable utilization and development of solid wastes. Full article

Wearable, non-invasive sweat sensors capable of continuously monitoring the pH of sweat, which is a key indicator related to metabolism and homeostasis level, are highly desirable for personal health management. However, ensuring the stability and accuracy of these sensors can be challenging when the body is in motion. In this work, we prepared a stretchable nanofibrous membrane-based electrochemical pH-sensing electrode by embedding carbon nanotubes (MWCNT) and silver nanowires (AgNWs) into an elastic electrospun nanofibrous membrane, followed by polyaniline electrodeposition. The as-prepared pH-sensing electrode showed a high sensitivity of 82.53 mV/pH and high accuracy in ionic solutions with pH ranging from 3 to 7. Notably, the electrode maintained stable sensing performance under deformations, including torsion, bending, and tensile strains up to 30%. Even after 1000 cycles of stretching at a 30% tensile strain, the detection sensitivity remained above 70 mV/pH, indicating its potential application as a wearable electrochemical sensor for monitoring sweat pH in personal health management. Full article

In this paper, we explore a straightforward two-step method to produce high-purity, vertically aligned multi-walled carbon nanofibres (MWCNFs) via chemical vapor deposition (CVD). Two distinct solutions are utilized for this CVD method: a catalytic solution consisting of ferrocene and acetonitrile (ACN) and a carbon source solution with camphor and ACN. The vapors of the catalytic solution inserted in the reaction chamber through external boiling result in a floating catalyst CVD approach that produces vertically aligned CNFs in a consistent manner. CNFs are grown in a conventional CVD horizontal reactor at 850 °C under atmospheric pressure and characterized by Raman spectroscopy, scanning and transmission electron microscopy (SEM and TEM), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Coating the MWCNTs with polymethyl methacrylate (PMMA) while still on the Si substrate retains the structure and results in a flexible, conductive thin film suitable for flexible electrodes. The film is 62 μm thick and stable in aqueous solutions, capable of withstanding further processing, such as electropolymerization with polyaniline, to be used for energy storage applications. Full article

Nanofiber mats with a high surface-to-volume ratio can be prepared by electrospinning. The Porosity is sometimes reported to be tunable by blending different materials, e.g., water-soluble poly(ethylene oxide) (PEO) with not water-soluble poly(acrylonitrile) (PAN). Here, nanofiber mats were electrospun from different PAN:PEO ratios, using a wire-based electrospinning machine “Nanospider Lab”. Investigations of the as-spun nanofiber mats as well as of membranes after washing off the water-soluble PEO by scanning electron microscopy (SEM) revealed severe differences in the nanofiber mat morphologies, such as varying fiber diameters and especially non-fibrous areas in the carbonized nanofiber mats, depending on the amount of PEO in the nanofiber mat as well as the molecular weight of the PEO. Similarly, the ratio and molecular weight of PEO influenced the results of stabilization and carbonization. This paper discusses the possibility of tailoring nanofiber porosity for the potential use of PAN nanofiber mats in tissue engineering, filtration, and other applications. Full article

In this work, non-precious electrocatalysts were synthesized using the electrospinning technique. Ni₁₂M₈/CNF (M = Cd, Co, and Cu) catalysts were successfully prepared in a fixed ratio to withstand the optimum transition metal co-catalyst in addition to the role of CNFs as support in ion-charge movement through the catalyst surface. The prepared catalysts were physically studied by XRD, SEM, and TEM. The electrochemical activity was verified using different fuel concentrations, different sweeping scan rates, and electrochemical impedance. Ni₁₂Cu₈/CNFs showed the highest electrochemical activity reaching 152 mA/cm² through different methanol concentrations. The outstanding performance is attributed to the large active surface area provided by carbon nanofibrous that eases the charge carrier transfer through the untrapped surface of the catalyst. The electrochemical tests suggest that Ni₁₂Cu₈/CNFs have the lowest ohmic impedance resistance ensuring the highest efficiency of the designed catalyst. The obtained results serve as an efficient catalyst for direct methanol electrooxidation reactions and suggest a possible application of a low-cost, easily accessible, and large surface area established via the preparing method. Full article

Conductive multi-walled carbon nanotubes (MWCNTs) as well as piezoelectric zinc oxide (ZnO) nanoparticles are frequently used as a single additive and dispersed in polyvinylidene fluoride (PVDF) solutions for the fabrication of piezoelectric composite films. In this study, MWCNT/ZnO binary dispersions are used as spinning liquids to fabricate composite nanofibrous films by electrospinning. Binary additives are conducive to increasing the crystallinity, piezoelectric voltage coefficient, and consequent piezoelectricity of as-spun films owing to the stretch-enhanced polarization of the electrospinning process under an applied electric field. PCZ–1.5 film (10 wt. % PVDF/0.1 wt. % MWCNTs/1.5 wt. % ZnO nanoparticles) contains the maximum β-phase content of 79.0% and the highest crystallinity of 87.9% in nanofibers. A sensor using a PCZ–1.5 film as a functional layer generates an open-circuit voltage of 10 V as it is subjected to impact loads with an amplitude of 6 mm at 10 Hz. The piezoelectric sensor reaches a power density of 0.33 μW/cm² and a force sensitivity of 582 mV/N. In addition, the sensor is successfully applied to test irregular motions of a bending finger and stepping foot. The result indicates that electrospun PVDF/MWCNT/ZnO nanofibrous films are suitable for wearable devices. Full article

A facile interconnected nanofibre electrode material derived from polybenzimidazol (PBI) was fabricated for a supercapacitor using a centrifugal spinning technique. The PBI solution in a mixture of dimethyl acetamide (DMA) and N, N-dimethylformamide (DMF) was electrospun to an interconnection of fine nanofibres. The as-prepared material was characterised by using various techniques, which include scanning electron microscopy (SEM), X-ray diffractometry (XRD), Raman, X-ray photoelectron spectroscopy (XPS), and Brunauer–Emmett–Teller (BET) among others. The specific surface area of the interconnected NCF material was noticed to be around 49 m² g⁻¹. Electrochemical properties of the material prepared as a single-electrode are methodically studied by adopting cyclic voltammetry, electrochemical impedance spectroscopy, and constant-current charge–discharge techniques. A maximum specific capacitance of 78.4 F g⁻¹ was observed for the electrode at a specific current of 0.5 A g⁻¹ in a 2.5 M KNO₃ solution. The electrode could also retain 96.7% of its initial capacitance after a 5000 charge–discharge cycles at 5 A g⁻¹. The observed capacitance and good cycling stability of the electrode are supported by its specific surface area, pore volume, and conductivity. The results obtained for this material indicate its potential as suitable candidate electrode for supercapacitor application. Full article

This study explored the design of an innovative stereoselective S-(-)-limonene sensor according to the molecular imprinting polymer (MIP) strategy using UV light to generate in situ polymer cross-linking. A conductive composite nanofibrous fabric of polyvinylpyrrolidone (PVP), polyacrylic acid (PAA) and carbon nanotubes (MWCNTs) was deposited on purpose in a single step by electrospinning onto interdigital microelectrodes. The nanostructured layer was investigated by microscopy (SEM, TEM, AFM) and infrared transmission measurements (FTIR). The resulting sensing features (carried out in environmental air) seemed to be mainly dependent on the peculiarity of the nanostructure and the phenomena occurring at the interfaces between the cross-linked PVP–PAA/cavity shape and MWCNTs. Furthermore, the specificity of the host–guest interaction was proven by the sensitivity, selectivity and stereoselectivity of the sensor when exposed to similar monoterpenes ((±)-α-pinene and (±)-linalool) and the enantiomer of limonene (R(+)), respectively. Full article

Desirable characteristics of electrospun chitosan membranes (ESCM) for guided bone regeneration are their nanofiber structure that mimics the extracellular fiber matrix and porosity for the exchange of signals between bone and soft tissue compartments. However, ESCM are susceptible to swelling and loss of nanofiber and porous structure in physiological environments. A novel post-electrospinning method using di-tert-butyl dicarbonate (tBOC) prevents swelling and loss of nanofibrous structure better than sodium carbonate treatments. This study aimed to evaluate the hypothesis that retention of nanofiber morphology and high porosity of tBOC-modified ESCM (tBOC-ESCM) would support more bone mineralization in osteoblast-fibroblast co-cultures compared to Na₂CO₃ treated membranes (Na₂CO₃-ESCM) and solution-cast chitosan solid films (CM-film). The results showed that only the tBOC-ESCM retained the nanofibrous structure and had approximately 14 times more pore volume than Na₂CO₃-ESCM and thousands of times more pore volume than CM-films, respectively. In co-cultures, the tBOC-ESCM resulted in a significantly greater calcium-phosphate deposition by osteoblasts than either the Na₂CO₃-ESCM or CM-film (p < 0.05). This work supports the study hypothesis that tBOC-ESCM with nanofiber structure and high porosity promotes the exchange of signals between osteoblasts and fibroblasts, leading to improved mineralization in vitro and thus potentially improved bone healing and regeneration in guided bone regeneration applications Full article