Very thin liquid jets can be obtained using electric field, whereas an electrically-driven bending instability occurs that enormously increases the jet path and effectively leads to its thinning by very large ratios, enabling the production of nanometre size fibres. This mechanism, although it was discovered almost one century ago, is not yet fully understood. In the following study, experimental data are collected, with the dual goal of characterizing the electro-spinning of different liquids and evaluating the pertinence of a theoretical model.

Neodymium-Iron-Boron (Nd-Fe-B) magnets are considered to have the highest energy density, and their applications include electric motors, generators, hard disc drives, and MRI. It is well known that a fiber structure with a high aspect ratio and the large specific surface area has the potential to overcome the limitations, such as inhomogeneous structures and the difficulty in alignment of easy axis, associated with such magnets obtained by conventional methods. In this work, a suitable heat-treatment procedure based on single-step and multistep treatments to synthesize sound electrospun Nd-Fe-B-O nanofibers of Φ572 nm was investigated. The single-step heat-treated (directly heat-treated at 800°C for 2 h in air) samples disintegrated along with the residual organic compounds, whereas the multistep heat-treated (sequential three-step heat-treated including three steps;: dehydration (250°C for 30 min in an inert atmosphere), debinding (650°C for 30 min in air), and calcination (800°C for 1 h in air)) fibers maintained sound fibrous morphology without any organic impurities. They could maintain such fibrous morphologies during the dehydration and debinding steps because of the relatively low internal pressures of water vapor and polymer, respectively. In addition, the NdFeO3 alloying phase was dominant in the multistep heat-treated fibers due to the removal of barriers to mass transfer in the interparticles.

Polyvinylidene fluoride (PVDF) is one of the most important piezoelectric polymers. Piezoelectricity in PVDF appears in polar b and ɣ phases. Piezoelectric fibers obtained by means of electrospinning may be used in tissue engineering (TE) as a smart analogue of the natural extracellular matrix (ECM). We present results showing the effect of rotational speed of the collecting drum on morphology, phase content and in vitro biological properties of PVDF nonwovens. Morphology and phase composition were analyzed using scanning electron microscopy (SEM) and Fourier-transform infrared spectroscopy (FTIR), respectively. It was shown that increasing rotational speed of the collector leads to an increase in fiber orientation, reduction in fiber diameter and considerable increase of polar phase content, both b and g. In vitro cell culture experiments, carried out with the use of ultrasounds in order to generate electrical potential via piezoelectricity, indicate a positive effect of polar phases on fibroblasts. Our preliminary results demonstrate that piezoelectric PVDF scaffolds are promising materials for tissue engineering applications, particularly for neural tissue regeneration, where the electric potential is crucial.

The growing interest in one-dimensional tin oxide-based nanomaterials boosts research on both high-quality nanomaterials as well as production methods. This is due to the fact that they present unique electrical and optical properties that enable their application in various (opto)electronic devices. Thus, the aim of the paper was to produce ceramic SnO₂ nanowires using electrospinning with the calcination method, and to investigate the influence of the calcination temperature on the morphology, structure and optical properties of the obtained material. A scanning electron microscope (SEM) and Fourier-transform infrared spectroscopy (FTIR) were used to examine the morphology and chemical structure of obtained nanomaterials. The optical properties of manufactured one-dimensional nanostructures were investigated using UV-Vis spectroscopy. Moreover, based on the UV-Vis spectra, the energy band gap of the prepared nanowires was determined. The analysis of the morphology of the obtained nanowires showed that both the concentration of the precursor in the spinning solution and the calcination temperature have a significant impact on the diameter of the nanowires and, consequently, on their optical properties.

The aim of this work was to produce a thin SnO2 film by a technique combining the sol-gel method and electrospinning from a solution based on polyvinylpyrrolidone and a tin chloride pentahydrate as a precursor. The spinning solution was subjected to an electrospinning process, and then the obtained nanofiber mats were calcined for 10 h at 500°C. Then, the scanning electron microscopy morphology analysis and chemical composition analysis by X-ray microanalysis of the manufactured thin film was performed. It was shown that an amorphous-crystalline layer formed by the SnO2 nanofiber network was obtained. Based on the UV-Vis spectrum, the width of the energy gap of the obtained layer was determined.

The main objective of the work was to create a layer of carbon nanofibre on the surface of the NiTi shape memory alloy. The coating process was carried out in three stages. First, polyacrylonitrile was deposited by electrospinning. Then it was stabilized at temperatures up to 250°C. The last stage was the carbonization performed below 1000°C. The microstructure of the obtained coatings was observed using a scanning electron microscope. The X-ray diffraction techniques were applied to analyze the coating structure. After the polyacrylonitrile deposition, the fibers had an average diameter of about 280 nm, and the final fibers were almost twice as tiny. The applied steps also changed the phase and crystalline state of the fibers, finally leading to the formation of amorphous-nanocrystalline graphite.

In this study, we demonstrated a method of controllably synthesizing one-dimensional nanostructures having a dense or a hollow structure using fibrous sacrificial templates with tunable crystallinity. The fibrous Ga2O3 templates were prepared by calcining the polymer/gallium precursor nanofiber synthesized by an electrospinning process, and their crystallinity was varied by controlling the calcination temperature from 500oC to 900oC. GaN nanostructures were transformed by nitriding the Ga2O3 nanofibers using NH3 gas. All of the transformed GaN nanostructures maintained a one-dimensional structure well and exhibited a diameter of about 50 nm, but their morphology was clearly distinguished according to the crystallinity of the templates. When the templates having a relatively low crystallinity were used, the transformed GaN showed a hollow nanostructure, and as the crystallinity increased, GaN was converted into a denser nanostructure. This morphological difference can be explained as being caused by the difference in the diffusion rate of Ga depending on the crystallinity of Ga2O3 during the conversion from Ga2O3 to GaN. It is expected that this technique will make possible the tubular nanostructure synthesis of nitride functional nanomaterials.

Electrospun membranes exhibit very promising properties, such as high surface area, high surface area-to-pore volume ratio, high pore interconnectivity, and uniform pore distribution. Nanoparticles are a promising alternative for improving the properties of the electrospun membranes. Titania nanoparticles, which are stable, resistant, and non-toxic, have various applications including water treatment, sensors, food additive and cosmetics. Due to the high hydrophilicity of titania nanoparticles, membrane fouling is reduced in titania nanoparticles doped membranes. Titania nanoparticle doped polyacrylonitrile (PAN) nanocomposite electrospun membranes were prepared by electrospinning method in this work. Compared to bare PAN electrospun membranes 0.05% titania nanoparticles doped electrospun membranes have thinner nanofibers, higher hydrophilicity and almost 2 times lower bovine serum albumin adsorption, which shows lower fouling tendency.

The technique of electrospinning was employed to fabricate uniform one-dimensional inorganic-organic composite nanofibers at room temperature from a solution containing equal volumes of aluminum 2, 4-pentanedionate in acetone and polyvinylpyrrolidone in ethanol. Upon firing and sintering under carefully pre-selected time-temperature profiles (heating rate, temperature and soak time), high-purity and crystalline alumina nanofibers retaining the original morphological features present in the as-spun composite (cermer) fibers were obtained. Tools such as laser Raman spectroscopy, scanning and transmission electron microscopy together with energy dispersive spectroscopy and selected area electron diffraction were employed to follow

the systematic evolution of the ceramic phase and its morphological features in the as-spun and the fired fibers. X-ray diffraction was used to identify the crystalline fate of the final product.

Constantly developing nanotechnology provides the possibility of manufacturing nanostructured composites with a polymer matrix doped with ceramic nanoparticles, including ZnO. A specific feature of polymers, i.e. ceramic composite materials, is an amelioration in physical properties for polymer matrix and reinforcement. The aim of the paper was to produce thin fibrous composite mats, reinforced with ZnO nanoparticles and a polyvinylpyrrolidone (PVP) matrix obtained by means of the electrospinning process and then examining the influence of the strength of the reinforcement on the morphology and optical properties of the composite nanofibers. The morphology and structure of the fibrous mats was examined by a scanning electron microscope (SEM) with an energy dispersive spectrometer (EDS) and Fourier-transform infrared spectroscopy (FTIR). UV –Vis spectroscopy allowed to examine the impact of zinc oxide on the optical properties of PVP/ZnO nanofibers and to investigate the width of the energy gap.

Macroporous silica fibers having spherical cavities were fabricated by electrospinning using the spinning solution prepared from the mixed dispersion of tetraethylorthosilicate (TEOS) and polystyrene nanospheres as precursor and sacrificial templates, respectively, by injection through metallic nozzle. By applying electric field, the electro-spun fibers obtained by evaporation-driven self-assembly were collected on flat substrate or rotating drum, followed by the removal of the templates by calcination. The sound absorption coefficient of the porous fibers was measured by impedance tube, and the measured value was larger than 0.9 at high frequency region of incident waves. The surface of the resulting fibers was modified using fluorine-containing silane coupling agent to produce superhydrophobic fibrous materials to prevent the infiltration of humidity.

Stable dispersion of antimony-doped tin oxide nano-powder was prepared by wet attrition process by comminuting aggregated ATO nano-powder using the titanate coupling agent as a dispersant to form the chemisorbed layer on the particle surface. The feed solution of the ATO dispersion and PVP was prepared for electro-spun fibers on the glass substrate. The surface resistance of the fibrous ATO film after electrospinning for 30 minutes was in the order of 105 Ω/□, which is sufficient for anti-static coating. The optical transmittance of ATO fibers was confirmed by measuring the visible light transmittance.

Black TiO ₂nanofibers have recently emerged as a promising material that has both advantages of black metal oxide and one-dimensional nanostructure. However, current reduction-based synthesis approaches are not compatible with practical applications because these processes require high process costs, complicated processes, and sophisticated control. Therefore, it is still necessary to develop a simple and facile method that can easily introduce atomic defects during the synthesis process. This work suggests an electrospinning process with an antioxidant and subsequent calcination process for the facile synthesis of black TiO ₂ nanofibers. The synthesized black TiO ₂ nanofiber has an average diameter of 50.3 nm and a rutile structure. Moreover, this nanofiber represented a noticeable black color and a bandgap of 2.67 eV, clearly demonstrating the bandgap narrowing by the introduced atomic defects.

Textile industry emits daily huge amounts of sewage rich in non-biodegradable organic compounds, especially in textile dyes. Such contaminants are highly soluble in water, which makes their removal difficult. Other studies suggest their carcinogenicity, toxicity and mutagenicity. A promising chemical treatment of textile wastewater is the photodegradation of dye molecules in the process of photocatalysis in the presence of a photocatalyst. One-dimensional nanostructures exhibit a high surface-to-volume ratio and a quantum confinement effect, making them ideal candidates for nanophotocatalyst material. Nb2O5 is, among other metal oxides with a wide band gap, gaining popularity in optical applications, and electrospun niobium oxide nanostructures, despite their ease and low cost, can increase the chemical removal of textile dyes from wastewater. Facile synthesis of electrospun one-dimensional niobium oxide nanofibers is presented. The nanophotocatalysts morphology, structure, chemical bonds and optical properties were examined. Based on photodegradation of aqueous solutions (ph=6) of methylene blue and rhodamine B, the photocatalytic activity was established. The photocatalytic efficiency after 180 minutes of ultraviolet irradiation in the presence of Nb2O5 nanofibers was as follows: 84.9% and 31.8% for methylene blue and rhodamine B decolorization, respectively.

In this study, we demonstrate a facile and cost-effective way to synthesize Nd-Fe-B of various shapes such as powders, rods and fibers using electrospinning, heat-treatment and washing procedures. Initially Nd-Fe-B fibers were fabricated using electrospinning. The as-spun Nd-Fe-B fibers had diameters ranging 489 to 630 nm depending on the PVP concentration in reaction solutions. The different morphologies of the Nd2Fe14B magnetic materials were related to the difference in thickness of the as-spun fibers. The relationships between the as-spun fiber thickness, the final morphology, and magnetic properties were briefly elucidated. The intrinsic coercivity of Nd2Fe14B changed with the change in morphology from powder (3908 Oe) to fiber (4622 Oe). This work demonstrates the effect of the Nd-Fe-B magnetic properties with morphology and can be extended to the experimental design of other magnetic materials.