Diameter Of Nanofibers Research Articles

Impact of polycaprolactone, alginate, chitosan and zein nanofiber physical properties on immune cells for safe biomedical applications.

Nanofiber safety, especially immunogenicity, is important for their successful translation to clinical setting. This study provides a comprehensive evaluation of how nanofiber physical properties influence immune cells cultured on them, specifically peripheral blood mononuclear cells (PBMCs). We prepared nanofibers with a wide range of physical properties including various diameters, interfibrillar pore sizes and mat thicknesses, using four main polymers: polycaprolactone, alginate, chitosan, and zein. Our findings show that nanofiber diameters had only a marginal influence on the activity of immune cells, whereas interfibrillar nanofiber pore sizes had a significant effect, and mat thickness proved to have the greatest impact. Cells that penetrated deeper into the thick nanofiber mats ceased to proliferate but did not experience cytotoxicity. Moreover, we discovered that PBMCs penetrating the zein/PVP nanofiber mesh exhibited increased metabolic activity, indicating potential immunogenicity, whereas the other tested non-immunogenic nanofibers reduced it. To best of our knowledge, this study is the first to report on the impact of various nanofiber physical properties on in vitro immune cell behavior, thereby expanding the knowledge in the relatively unexplored field of nanofiber immunological safety. It underscores the need for rigorous preclinical nanofiber assessment and setting new standards for designing nanofiber-based biomedical products.

Morphological Modulation of Electrospun PVDF/PVP Nanofibers

ABSTRACTIn electrohydrodynamics, the regulation of the morphology and structures of electrospun nanofibers is crucial for tuning the properties of the final product. In the electrospinning process, the uniform and smooth morphology of polyvinylidene fluoride (PVDF) nanofibers can be obtained by controlling experimental parameters, environmental parameter, and system parameters. However, there is inadequate research on the effect of polymer addition on the morphology enhancement of PVDF nanofibers and the underlying mechanisms. In this study, the effects of the polyvinylpyrrolidone (PVP) molecular weight and content on various process parameters (i.e., Taylor cone length, straight fluid jet length, and spray angle) are evaluated. The obtained electrospun PVDF/PVP nanofibers were further characterized by SEM, EDS, FTIR, and XRD. The results indicate that the solution viscosity, which was controlled by varying the molecular weight and content of PVP, was linearly correlated with the process parameters. As the PVP molecular weight and content increased, the nanofiber diameter increased and the nanofiber morphology became smoother. The EDS results revealed that the nanofibers consisted of PVDF encapsulated by PVP. The FTIR and XRD results indicated that hydrogen bonding between PVP and PVDF weakened the crystallization of PVDF, leading to the formation of smooth PVDF/PVP nanofibers.

Fluorescent sensing copolymers: Synthesis, nanofiber fabrication and application in picric acid sensors

Increasing attention has been paid to the detection of explosives due to the occurrence of terrorist attacks around the world. Here, we used free radical polymerization to develop two different types of fluorescent copolymers for use in detecting picric acid. One exhibits aggregation-caused quenching (ACQ) and is called PNNS [poly (N-isopropyl acrylamide-co-N-hydroxymethyl acrylamide -co-styrene-pyrene), poly (NIPAAm-co-NMA-co-St-Py)]. The other possesses aggregation-induced emission (AIE) properties and is called PNNP [poly (N-isopropyl acrylamide-co-N-hydroxymethyl acrylamide-co-2-(1,2,3,4,5-pentaphenyl-1H-silol-1-yloxy) ethyl methacrylate), poly (NIPAAm-co-NMA-co-PPS-HEMA)]. Nanofibrous thin films of these copolymers were obtained by electrospinning. Upon interaction with picric acid, the fluorescence intensity of each copolymer was quenched due to photo-induced electron transfer (PET). The average diameters of PNNS and PNNP nanofibers were 179 ± 28 nm and 235 ± 143 nm, respectively. Sensing performance was evaluated by Stern-Volmer analysis. The Stern-Volmer constant (Ksv) values for PNNS and PNNP nanofibers were 0.012 μΜ−1 and 0.119 μΜ−1, respectively. Since the aggregated state of PNNP nanofibrous thin films can increase dramatically, the AIE property of this material provides a large dynamic range. Finally, the reusability of water- and methanol-washed nanofiber thin films was tested, revealing that the nanofiber sensors were reusable for detecting picric acid.

Use of Electrospun Cellulose Acetate/Silica Composites as Multifunctional Ingredients in Eco‐Friendly Semisolid Lubricant Formulations

ABSTRACTCellulose acetate/silica (CA/SIL) nanocomposites are prepared by electrospinning and investigated as multifunctional ingredients in eco‐friendly semisolid lubricant formulations. The structuring ability of these electrospun composites in castor oil and the antifriction and antiwear properties are examined through rheological and tribological experiments. The multifunctionality of CA/SIL composites arises from a balance between the silica content and the formation of nanofiber‐dominated structures. The linear viscoelasticity functions in the oleo‐dispersions increase by several orders of magnitude with both the spinning solution concentration and the CA:SIL ratio. However, the rheological response primarily depends on the morphology of the nanofiber mat obtained, specifically nanofiber diameter and the presence of beads. In contrast, the silica content significantly impacts the tribological performance of the oleo‐dispersions regardless of nanofiber morphology. For similar nanoarchitectures and rheological responses, the friction coefficient is reduced from 0.227 to 0.108 by incorporating silica in a 10:1 CA:SIL ratio, compared with the SIL‐free electrospun CA nanofibers, while wear is completely prevented. Increasing the composite concentration from 5 to 12.5 wt. % enhances wear protection and the gel strength of oleo‐dispersions, for example, the plateau modulus rises from 800 to 42,000 Pa using a composite with a 10:1 CA:SIL ratio.

Fabrication of composite RGD-tagged poly(lactic acid)-graphene oxide nanofiber containing bone-forming peptide-3 loaded-dendritic silica nanoparticles for bone regeneration in rabbit

In the current study, polylactic acid (PLA)/graphene oxide (GO) based composite scaffolds were fabricated by electrospinning method and then covalently modified with bone-forming peptide-3 (BFP-3)-loaded thiol-functionalized dendritic mesoporous silica nanoparticles (BFP-3@HS-DMSNs) and RGD. In this regard, PLA electrospinning nanofibers and composite of PLA/GO electrospinning nanofibers containing 0.02, 0.01, 0.04, 0.1, 0.2 % of GO were prepared and characterized in terms of mechanical strength, nanofibers diameter, thermal stability, crystallinity, specific surface area, total pore volume and cell adhesion properties. Among the prepared composites, PLA nanofibers containing 0.02 % GO demonstrated superior mechanical and morphological characteristics along with better cell adhesion for mesenchymal stem cell. Then, the PLA/0.02 %GO nanofiber was treated with plasma and consequently modified with N-(2-aminoethyl)maleimide linker which was applied for Cys-RGD and BFP-3@HS-DMSNs conjugation. The obtained results showed desirable adhesion of PLA/0.02 %GO nanofiber after incorporation of RGD (5 % of maleimide groups of the linker) and DMSNs which significantly increase cell adhesion potency (1.53 folds). By incorporation of BFP-3@HS-DMSNs (equivalent to 0.1 µg of BFP-3) to the RGD-tagged PLA/0.02 %GO nanofiber, the scaffold demonstrated better cytocompatibility and MSC differentiation to osteoblast based on biomineralization assay via alizarin red (4.2 folds) and alkaline phosphatase activity (1.7 folds) tests. In preclinical stage, after skull defect creation in rabbits, 5 treatments groups comprising PLA/0.02 %GO nanofiber, PLA/0.02 %GO/DMSNs, PLA/0.02 %GO/DMSNs/Cys-RGD, PLA/0.02 %GO/BFP-3@DMSNs and PLA/0.02%GO/BFP-3@DMSNs/Cys-RGD were used for bone regeneration in skull defects. After 3 months, the implantation of PLA/0.02GO/BFP-3@DMSNs/Cys-RGD showed higher bone regeneration based on CBCT imaging (18.875 mm2 bone formed area) in comparison with other treatment groups. This hybrid multimodal platform is purposely organized interactive processes which lead to potential bone regeneration.

A novel gelatin/chitosan-based “sandwich” antibacterial nanofiber film loaded with perillaldehyde for the preservation of chilled chicken

Quality deterioration caused by microorganisms is a crucial problem in food industry. Herein, to enhance the antibacterial effect and extend the storage life of chilled chicken, a gelatin/chitosan (GC)-based “sandwich” nanofiber film was prepared by sandwiching GP2 (gelatin nanofibers loaded with 2 % (v/v) perillaldehyde) between two layers of GC nanofibers. The diameter of GP nanofibers was positively correlated with perillaldehyde concentration. However, the thermal stability of GP nanofibers was negatively correlated. The thermal degradation temperature (Tm) of GP2 was the lowest. Fortunately, GC nanofibers improved Tm of GP2 from 98.91 °C to 111.60 °C. Besides, FTIR absorption bands at 1636 and 1442 cm−1 indicated that perillaldehyde was successfully embedded. Moreover, poor water resistance of gelatin nanofibers was also improved. Specifically, benefiting from the synergy between perillaldehyde and chitosan, the shelf-life of chilled chicken was efficiently prolonged (over 10 days). Thus, this “sandwich” nanofiber film shows promise for food packaging.

Preparation and adsorption application of PLA/GO/PDA nanofiber membrane

Abstract In this study, PLA(polylactic acid)/GO(graphene oxide)/DA(Dopamine) porous nanofiber membrane was prepared by electrospinning. L16(43) orthogonal experiment was designed to investigate the effects of reaction temperature, reaction time, and DA concentration on the adsorption performance of DA oxidized and self-polymerized on the fiber. Based on the characterization of scanning electron microscopy and the determination of the adsorption performance of the fiber membrane to MB(methylene blue dye), data visualization analysis, variance analysis, and F-test were conducted to determine the optimal process parameters: reaction temperature of 45 ℃, reaction time of 30 h, and DA concentration of 2 mg/ml. PLA/GO/PDA(Polydopamine) nanofiber was prepared and characterized under the optimal process parameters. The results showed that the average diameter of the PDA-loaded nanofiber increased from 737 nm to 996 nm, and a layer of PDA with a thickness of about 129 nm was loaded on the outer surface of the fiber, making the contact angle of the fiber membrane with 0° and becoming a hydrophilic material. In adsorption performance testing of MB, the PLA/GO/PDA nanofiber membrane prepared based on the PLA/GO/DA fiber membrane with an adsorption rate of 98.81 % in 24 h was superior to the PLA/GO/PDA nanofiber membrane prepared based on the PLA/GO fiber membrane.

Fabrication of Anthocyanidin-Encapsulated Polyvinyl Alcohol Nanofibrous Membrane for Smart Packaging.

Smart colorimetric packaging has been an important method to protect human health from external hazardous agents. However, the currently available colorimetric detectors use synthetic dye probes, which are costly, toxic, difficult to prepare, and non-biodegradable. Herein, an environmentally friendly cellulose nanocrystal (CNC)-supported polyvinyl alcohol (PVA) nanofibrous membrane was developed for the colorimetric monitoring of food spoilage. Anthocyanidin (ACY) is a naturally occurring spectroscopic probe that was isolated from pomegranate (Punica granatum L.). By encapsulating the anthocyanin probe in electrospun polyvinyl alcohol fibers in the presence of a mordant (M), M/ACY nanoparticles were generated. After exposure to rotten shrimp, an investigation on the colorimetric changes from purple to green for the smart nanofibrous fabric was conducted using the coloration parameters and absorbance spectra. In response to increasing the length of exposure to rotten shrimp, the absorption spectra of the anthocyanin-encapsulated nanofibrous membrane showed a wavelength blueshift from 580 nm to 412 nm. CNC displayed a diameter of 12-17 nm. The nanoparticle diameter of M/ACY was monitored in the range of 8-13 nm, and the nanofiber diameter was shown in the range of 70-135 nm. Slight changes in comfort properties were monitored after encapsulating M/ACY in the nanofibrous fabric.

Fabrication of gallic acid containing poly(vinyl alcohol)/chitosan electrospun nanofibers with antioxidant and drug delivery properties

Chitosan-based nanofibers with excellent properties are attractive materials for specific industrial applications of contemporary interest. This work aims to fabricate functional nanofibers based on poly(vinyl alcohol)/chitosan (CS) with an antioxidant and model drug molecule, gallic acid (GA), by electrospinning, followed by cross-linking through glutaraldehyde (PVA-CS-GAs). PVA-CS-GAs were electrospun at two different concentrations by the adjustment of the CS feeding ratio. The detailed characteristics of the as-prepared electrospun nanofibers were elucidated by Fourier Transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), water contact angle (WCA) measurements, thermogravimetric and differential scanning calorimetry (TGA and DSC) analyses. SEM images indicated that the average fiber diameter distribution was in the range of 90–110 nm. The results show that morphology, mean diameter, wettability, and thermal characteristics of the composite nanofibers were affected by the CS feeding ratio. Although the increase in the amount of polar -OH groups with the addition of GA caused an improvement in the hydrophilicity and thermal stability of the electrospun nanofibers, it also caused a decrease in the thermal transition temperatures. Furthermore, antioxidant tests based on DPPH radical scavenging ability and in vitro release studies demonstrated that the cross-linked PVA-CS-GA composite nanofibers have good antioxidant activity and a pH-dependent drug release rate, indicating their potential for implementation in wound healing and drug delivery applications.

Piezoelectric silk fibroin nanofibers: Structural optimization to enhance piezoelectricity and biostability for neural tissue engineering

Silk fibroin (SF) has garnered significant interest in tissue engineering due to its excellent biocompatibility and bioactivity. Notably, SF exhibits piezoelectric properties that can be harnessed to electrically stimulate cells, enhancing tissue morphogenesis. However, a systematic approach to control SF's piezoelectricity and biodegradation, and its application in neural morphogenesis, has not been fully explored. In this study, SF was electrospun into nanofibers of various sizes and subjected to a post-electrospinning chemical treatment to examine the effects of phase composition, especially the β-sheet formation, on the piezoelectricity and biostability of SF. The optimized SF scaffolds having a nanofiber diameter of 750 nm and a scaffold thickness of 250 µm allowed for the maintenance of nanofibrous structure for at least 6 weeks in aqueous environments while maintaining piezoelectric potential outputs of at least 200 mVp-p. This enabled cell membrane depolarization over an extended cell culture duration, facilitating the functional maturation of human neural stem cells (hNSCs). Specifically, acoustic piezo-activation of the SF scaffolds, resulting in mechano-electrical stimulation (MES) of the cells, accelerated their differentiation into neurons, astrocytes, and especially oligodendrocytes, leading to robust axon myelination within two weeks. Furthermore, MES enhanced neural connectivity and functional maturity, as evidenced by significant increases in excitatory and inhibitory synapse formation (46 % and 58 %, respectively), action potential amplitude (252 %), and velocity (210 %) compared to static control conditions. These findings demonstrate the potential of biodegradable electrospun SF nanofibers with balanced piezoelectricity and biostability for advancing neural tissue engineering.

Preparation and properties of bio-based PA56/SiO2–NH2 composite nanofiber membranes for high efficiency oil-water separation

With the continuous development of environmental protection and resource recycling demands, the development of bio-based separation membrane materials has increasingly attracted attention. Bio-based polyamide 56 (PA56), exhibiting excellent hydrophilicity, spinnability, and mechanical properties, is expected to complement and replace traditional separation membrane materials. In this study, the electrospinning preparation and structural control of PA56 nanofiber membranes were achieved through the optimization of PA56 content and mixed solvent ratios. The study found that when the PA56 content was 16 wt% and the formic acid to acetone ratio in the mixed solvent was 8:2, the nanofiber diameter distribution was the most uniform. Building on this, amino-functionalized modified silica (SiO2–NH2) nanoparticles were introduced to prepare PA56/SiO2–NH2 composite nanofiber membranes featuring a cobweb-like nanofiber network and micro-nodule structure. The effects of the addition of SiO2–NH2 nanoparticles on the morphology, structure, and properties of the fiber membranes were studied. The results indicate that the control of the mixed solvent ratio and the addition of SiO2–NH2 nanoparticles led to the formation of a cobweb-like nanofiber network and micro-nano nodular structure on the nanofiber surface, enhancing the hydrophilicity of PA56 nanofiber membranes. The M − 3 membrane with a nanoparticle addition amount of 0.8 wt% exhibited high hydrophilicity and underwater superoleophobic properties, achieving efficient separation of stable oil-in-water emulsions with a separation efficiency of 99.8 %. This work provides a new bio-based membrane material and its preparation method for treating oily wastewater using the membrane separation method.

Morphology and methanol permeability of sulfosuccinic acid cross‐linked polyvinyl alcohol and polyvinyl alcohol/Nafion nanofibrous membranes

AbstractCross‐linking of polyvinyl alcohol (PVA) and polyvinyl alcohol/Nafion (PVA/Nafion) electrospun nanofibers with sulfosuccinic acid (SSA) was investigated to assess their characterization and the effects of cross‐linking on the methanol permeability performance of the nanofibrous membranes. SSA was directly incorporated into the electrospinning polymer solution. The morphology, chemical functional groups, thermal stability, water stability and water swelling of the resulting nanofibers were examined. The effects of SSA concentration on ion exchange capacity (IEC) and methanol permeability of the nanofibrous membranes were discussed. Bead‐free and smooth nanofibers were produced for all SSA concentrations with a mean nanofiber diameter of 240–270 nm. It was shown that 15% SSA concentration was suitable for preserving the morphology of PVA nanofibers against water, while the morphology of PVA/Nafion nanofibers was preserved even without cross‐linking. The increase in SSA concentration led to increase in swelling in water. SSA cross‐linking was also shown to increase the thermal stability of the produced nanofibers. IEC increased by the increase in SSA concentration, while increase in SSA concentration led to a decrease in methanol permeability.

Advances in Electrospun Poly(ε-caprolactone)-Based Nanofibrous Scaffolds for Tissue Engineering.

Tissue engineering has great potential for the restoration of damaged tissue due to injury or disease. During tissue development, scaffolds provide structural support for cell growth. To grow healthy tissue, the principal components of such scaffolds must be biocompatible and nontoxic. Poly(ε-caprolactone) (PCL) is a biopolymer that has been used as a key component of composite scaffolds for tissue engineering applications due to its mechanical strength and biodegradability. However, PCL alone can have low cell adherence and wettability. Blends of biomaterials can be incorporated to achieve synergistic scaffold properties for tissue engineering. Electrospun PCL-based scaffolds consist of single or blended-composition nanofibers and nanofibers with multi-layered internal architectures (i.e., core-shell nanofibers or multi-layered nanofibers). Nanofiber diameter, composition, and mechanical properties, biocompatibility, and drug-loading capacity are among the tunable properties of electrospun PCL-based scaffolds. Scaffold properties including wettability, mechanical strength, and biocompatibility have been further enhanced with scaffold layering, surface modification, and coating techniques. In this article, we review nanofibrous electrospun PCL-based scaffold fabrication and the applications of PCL-based scaffolds in tissue engineering as reported in the recent literature.

Fabrication and characterization of electrospun core-shell nanofibers of bilayer zein/pullulan emulsions crosslinked by genipin

In this study, the electrospun core-shell nanofibers of zein/pullulan stabilized bilayer emulsions before and after genipin crosslinking were fabricated. The experimental results indicated that the addition of pullulan increased the apparent viscosity and elastic modulus of the bilayer emulsions, which was further increased after the chemical crosslinking of genipin. The nanofiber diameter increased from 102.9 nm to 169.9 nm with the increasing ratio of pullulan, but increased significantly to a range of 405.6–708.0 nm after genipin crosslinking. The electrospun nanofiber films of crosslinked emulsions had higher thermal stability and stronger water stability. The FTIR result proved the existence of hydrogen bond interaction between the zein, pullulan, and genipin molecules. In addition, before and after crosslinking, the encapsulation efficiency of electrospun fiber films for camellia oil was >77.68 %, and the maximum encapsulation efficiency could reach 87.94 %, and there was no significant change during the 7-day storage period, showing good stability. These research results can provide a theoretical basis for the encapsulation of hydrophobic active substances in zein-based emulsion electrospun core-shell nanofibers.

Optimization of Polyvinylidene Fluoride/Polyvinyl Alcohol Electrospun using Taguchi Method for Tissue Engineering Application

Composite nanofibers for tissue engineering applications were prepared with polyvinylidene fluoride and polyvinyl alcohol via a horizontal electrospinning process. The effect of the processing parameters (polymer concentration, voltage, feed rate and tip-to-collector distance) on the fibre diameter was studied using L9 orthogonal arrays of the Taguchi Method, S/N ratio, and ANOVA to produce uniform and finest fibre. The optimum parameters were at 90 wt% PVDF ratios for polymer concentration, applied voltage at 10 kV, feed rate at 0.5 mL/h and tip-to-collector distance at 15 cm. The PVDF/PVA electrospun compromises 171.60 nm nanofiber diameter with homogenous morphology and no bead formed. MTT and live/dead kit assay analysis toward human (HSF) cells confirmed the potential of the PVDF/PVA electrospun to be used as an alternative tissue template to allow new cell or tissue formation in the future.

High-Speed Electrospinning of Ethyl Cellulose Nanofibers via Taylor Cone Optimization.

Ethyl cellulose (EC) is one of the most widely used cellulose derivatives. Nevertheless, challenges such as the formation of beaded fibers, low yield, and nonporous internal structure persist in electrospinning, limiting functional improvements and industrial applications. This study invented a groundbreaking high-speed electrospinning technique through sheath liquid assistance to optimize the Taylor cone, dramatically enhancing the yield, morphology, and formation of porous structures of EC nanofibers beyond what has been seen in the literature to date. Our study emphasizes the crucial role of the sheath liquid's physical and chemical properties in controlling the morphology and diameter of EC nanofibers. It was discovered that highly polar and viscous sheath liquids led to the formation of beaded structures. Most importantly, the sheath liquid-assisted method substantially increased the ejection rate of the EC solution tens and hundreds of times compared to the current low-speed electrospinning method (0.1-1 mL/h) by refining the shape of the Taylor cone and resolving low productivity challenges in conventional nanofiber production. Meanwhile, increasing the flow rate of the EC or the sheath liquid accelerated the phase separation of EC solutions, thereby promoting the formation of porous structures in EC nanofibers. A pronounced porous structure was observed when the core EC flow rate reached 25 mL/h or the sheath chloroform flow rate reached 20 mL/h. Furthermore, our sheath liquid-assisted high-speed electrospinning technique demonstrated universal applicability to ECs with varying molecular weights. This study comprehensively addressed challenges in controlling the yield, morphology, and internal structure of EC nanofibers through sheath-solution-assisted high-speed electrospinning technology. These findings provide an innovative approach to developing next-generation electrospinning technologies to enhance the yield and properties of natural polymers for sustainability.

Nanofiber power: Reinforcing in-situ hydrogel for enhanced rivastigmine delivery

Rivastigmine, used in the treatment of Alzheimer's disease (AD), faces challenges of poor stability and low permeability when delivered through conventional methods. To address these issues, rivastigmine-loaded nanofibers were systematically prepared via an electrospinning process utilizing the Design of Experiments (DoE) methodology and subsequently transformed into an in-situ hydrogel using the cold process method. Preliminary experiments determined optimal polymer concentration, ratio, and electrospinning parameters. A 32 factorial design optimized nanofibers, with polyvinyl alcohol (PVA) concentration (X1) and PVA: chitosan ratio (X2) as independent variables, and % cumulative drug release (Y1) and % entrapment efficiency (Y2) as dependent variables. Using the desirability model, the final batch achieved % cumulative drug release and % entrapment efficiency of 90.17 ± 2.64 and 91.46 ± 4.83 respectively. Fourier Transform Infrared Spectroscopy (FTIR) and X-ray diffraction (XRD) studies showed no significant excipient interactions. Field emission scanning electron microscopy (FE-SEM) analysis revealed nanofiber diameters of 160–230 nm. Findings demonstrated that the nanofiber-reinforced in-situ hydrogel exhibited significantly improved gelling capacity at 34.2 °C and increased spreadability (19.51 ± 1.75 cm2) compared to the hydrogel formulations without nanofibers. In-vitro and ex-vivo studies showed controlled rivastigmine release over 8 h. Additionally, enhanced mucoadhesion (236.7 ± 8.83 gm/cm2), pH compatibility (5.9 ± 0.12) with nasal fluid, and moisture resistance uptake highlight suitability for nasal drug delivery. Therefore, this approach offers an efficient delivery platform for rivastigmine with enhanced delivery characteristics and promising therapeutic potential.

MOF Nanosheet-Functionalized Poly(lactic acid) Meta-membranes for Long-Term Air Purification and Intelligent Monitoring.

The wide use of conventional polymeric air filters is causing a dramatically increasing accumulation of plastic and microplastic pollution. The development of poly(lactic acid) (PLA) fibrous membranes for efficient air purification is of important significance but frequently challenged by the rapid decay of filtration performance due to the intrinsically poor electret properties of PLA. Here, we propose an electroactivity promotion methodology, involving the one-step synthesis and homogeneous incorporation of high-dielectric ZIF-8 nanosheets (ZIFNSs), to facilitate interfacial polarization and fiber refinement during electrospinning of PLA nanofibers. The preparative electrospun PLA/ZIFNS meta-membranes exhibited an unusual combination of significantly reduced nanofiber diameter (∼462 nm), enhanced surface potential (approaching 10 kV), and increased surface activity and facilitated the formation of electroactive phases. With well-controlled morphological features, the highly electroactive PLA/ZIFNS meta-membranes exhibited exceptional filtration efficiencies for PM2.5 and PM0.3 (99.2 and 96.0%, respectively) even at the highest airflow rate of 85 L/min, in clear contrast to that of its pure PLA counterpart (only 79.3 and 74.6%). Arising from the increased electroactivity and active contact sites, remarkable triboelectric performance and self-charging mechanisms were demonstrated for the PLA/ZIFNS meta-membranes, contributing to long-term efficient PM0.3 filtration (97.5% for over 360 min). Moreover, as triggered by physiological activities like respiration and speaking, the electroactive PLA/ZIFNS meta-membranes enabled real-time monitoring with high sensitivity and specificity. The proposed strategy affords significant promotion of electroactivity and triboelectric performance for PLA nanofibers, which may motivate the development of ecofriendly protective membranes for respiratory healthcare and real-time monitoring.

Piezoelectric Energy Harvesting in Poly(vinylidene Fluoride‐co‐hexafluoropropylene)/Barium Titanate Nanofibers and Ultrasonic Assisted Piezocatalytic Degradation of Ciprofloxacin

AbstractAn innovative approach has been adopted through the synthesis of a cost‐effective ferroelectric host polymer, which was integrated with Barium Titanate (BaTiO3) to develop an efficient electrospun Polyvinylidene Fluoride‐Hexafluoropropylene/BaTiO3 (PVdF‐HFP/BaTiO3) nanocomposite (PBT), designated for energy harvesting and piezocatalytic applications. FT‐IR affirmed the existence of the crystalline β‐phase within the nanofibers. SEM images showed that nanofiber diameter decreases as applied voltage is increased in electrospinning. The BaTiO3 nanoparticles were scattered evenly in PBT, but at lower voltages, they aggregate. PBT showed enhanced piezoelectric performance under higher voltage conditions, registering a maximum piezoelectric output of ~7.7 V and an output current of 0.77 μA. Moreover, the composite exhibited a power density of 14.15 mW/m2 at a load resistance of 20 MΩ. Fabricated piezoelectric nanogenerator (PENG) demonstrated practical utility in flexible electronics, notably in charging capacitors of 0.47 μF and 1 μF. Additionally, the piezocatalytic degradation of the antibiotic ciprofloxacin (CIP) was effectively achieved using the electrospun nanofibers, with an impressive degradation rate of up to 99.6 % within 30 minutes under acidic conditions, and the material displayed notable reusability, maintaining up to 95.5 % efficiency after five cycles. DFT calculations and COMSOL simulations alongside a comparative examination of the electronic properties of PBT.

Stimulated Brillouin scattering in silica optical nanofibers

Stimulated Brillouin scattering offers a broad range of applications, including lasers, sensors, and microwave photonics, most of which require strong Brillouin gain within a narrow bandwidth. Here, we experimentally report the first measurement of stimulated Brillouin scattering in silica optical nanofibers from both hybrid and surface acoustic waves. Using a pump–probe technique in the radio frequency domain, we measured a Brillouin gain as high as 15 m−1 W−1 and linewidth to 16 MHz for the L03 hybrid acoustic mode near 9 GHz using a 990-nm diameter nanofiber. This gain is 65 times larger than the highest gain obtained in standard single-mode fibers. In addition, we report a Brillouin gain of up to 5 m−1 W−1 from surface acoustic waves around 5 GHz. We further demonstrate a nanofiber-based Brillouin laser with a threshold of 350 mW. Our results create opportunities for advanced Brillouin-based applications utilizing optical nanofibers.