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The NASICON-structured Na3MnZr(PO4)3 compound is a promising high-voltage cathode material for sodium-ion batteries (SIBs). In this study, an easy and scalable electrospinning approach was used to synthesize self-standing cathodes based on Na3MnZr(PO4)3 loaded into carbon nanofibers (CNFs). Different strategies were applied to load the active material. All the employed characterization techniques (X-ray powder diffraction (XRPD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), thermal gravimetric analysis (TGA), and Raman spectroscopy) confirmed the successful loading. Compared to an appositely prepared tape-cast electrode, Na3MnZr(PO4)3/CNF self-standing cathodes demonstrated an enhanced specific capacity, especially at high C-rates, thanks to the porous conducive carbon nanofiber matrix. Among the strategies applied to load Na3MnZr(PO4)3 into the CNFs, the electrospinning (vertical setting) of the polymeric solution containing pre-synthesized Na3MnZr(PO4)3 powders resulted effective in obtaining the quantitative loading of the active material and a homogeneous distribution through the sheet thickness. Notably, Na3MnZr(PO4)3 aggregates connected to the CNFs, covered their surface, and were also embedded, as demonstrated by TEM and EDS. Compared to the self-standing cathodes prepared with the horizontal setting or dip–drop coating methods, the vertical binder-free electrode exhibited the highest capacity values of 78.2, 55.7, 38.8, 22.2, 16.2, 12.8, 10.3, 9.0, and 8.5 mAh/g at C-rates of 0.05C, 0.1C, 0.2C, 0.5C, 1C, 2C, 5C, 10C, and 20C, respectively, with complete capacity retention at the end of the measurements. It also exhibited a good cycling life, compared to its tape-cast counterpart: it displayed higher capacity retention at 0.2C and 1C, and, after cycling 1000 cycles at 1C, it could be further cycled at 5C, 10C, and 20C. [ABSTRACT FROM AUTHOR]

Lightweight and low-cost one-dimensional carbon materials, especially biomass carbon fibers with multiple porous structures, have received wide attention in the field of electromagnetic wave absorption. In this paper, graphene-coated N-doped porous carbon nanofibers (PCNF) with excellent wave absorption properties were successfully synthesized via electrostatic spinning, electrostatic self-assembly, and high-temperature carbonization. The obtained results showed that the minimum reflection loss of the absorbing carbon fiber obtained under the carbonization condition of 800 °C is −51.047 dB, and the absorption bandwidth of reflection loss below −20 dB is 10.16 GHz. This work shows that carbonization temperature and filler content have a certain effect on the wave-absorbing properties of fiber, graphene with nanofiber, and the design and preparation of high-performance absorbing materials by combining the characteristics of graphene and nanofibers and multi-component coupling to provide new ideas for the research of absorbing materials. [ABSTRACT FROM AUTHOR]

Supercapacitors have attracted attention as efficient energy storage systems owing to their high power density and cycling stability. The use of appropriate electrode materials is important for high-performance supercapacitors, and various carbon materials have been studied as supercapacitor electrodes. In this study, carbon nanofibers with high specific surface areas were fabricated via a simple electrospinning process. Carbon nanofibers were fabricated by adjusting the ratio of polyacrylonitrile (PAN) to bisphenol A (BPA) and evaluated as electrode materials for supercapacitors. With the addition of BPA, improved specific surface area and oxygen functional groups were observed compared with nanofibers using only PAN. Therefore, BPA3, which had the highest specific surface area, exhibited a 28% improvement in capacitance (162 F/g) compared with BPA0 fabricated using only PAN. Carbon nanofibers fabricated by adjusting the ratio of BPA to PAN are promising electrodes for supercapacitors owing to their high capacitance and stability. [ABSTRACT FROM AUTHOR]

Carbon nanofiber (CNF) films or mats have great conductivity and thermal stability and are widely used in different technological processes. Among all the fabrication methods, electrospinning is a simple yet effective technique for preparing CNF mats, but the electrospun CNF mats are often brittle. Here, we report a feasible protocol by which to control the alignment of carbon black nanoparticles (CB NPs) within CNF to enhance the flexibility. The CB NPs (~45 nm) are treated with non-ionic surfactant Triton-X 100 (TX) prior to being blended with a solution containing poly(vinyl butyral) and polyacrylonitrile, followed by electrospinning and then carbonization. The optimized CB-TX@CNF mat has a boosted elongation from 2.25% of pure CNF to 2.49%. On the contrary, the untreated CB loaded in CNF displayed a lower elongation of 1.85% because of the aggregated CB spots created weak joints. The controlled and uniform dispersion of CB NPs helped to scatter the applied bending force in the softness test. This feasible protocol paves the way for using these facile surface-treated CB NPs as a commercial reinforcement for producing flexible CNF films. [ABSTRACT FROM AUTHOR]

This contribution describes the preparation, coupled with detailed characterization, of Nb2O5 nanofibers and their application in lithium–sulfur batteries for the improvement of electrochemical performance. The utilization of reactive needle-less electrospinning allowed us to obtain, in a single step, amorphous pre-ceramic composite PAN/Nb2O5 fibers, which were transformed into porous ceramic Nb2O5 nanofibers via calcination. Thermogravimetric studies defined that calcination at 600 °C results in crystalline ceramic fibers without carbon residues. The fibrous morphology and mean diameter (614 ± 100 nm) of the ceramic nanofibers were analyzed via scanning and transmission electron microscopy. A surface area of 7.472 m2/g was determined through nitrogen adsorption measurements, while a combination of X-ray diffraction and Raman spectroscopy was used to show the crystallinity and composition of the fibers after calcination—single T-phase Nb2O5. Its performance in the cathode of lithium–sulfur batteries was defined through electrochemical tests, and the obtained results were compared to a similar blank electrode. The initial discharge capacity of 0.5 C reached a value of 570 mAh∙g−1, while the reversible capacity of 406 mAh∙g−1 was retained after 200 cycles, representing a capacity retention of 71.3%. The presence of Nb2O5 nanofibers in the carbon cathode inhibits the shuttle effect through polysulphide confinement, which originates from porosity and chemical trapping. [ABSTRACT FROM AUTHOR]

Two-dimensional molybdenum disulfide (MoS2) is considered as a highly promising anode material for lithium-ion batteries (LIBs) due to its unique layer structure, large plane spacing, and high theoretical specific capacity; however, the overlap of MoS2 nanosheets and inherently low electrical conductivity lead to rapid capacity decay, resulting in poor cycling stability and low multiplicative performance. This severely limits its practical application in LIBs. To overcome the above problems, composite fibers with a core//sheath structure have been designed and fabricated. The sheath moiety of MoS2 nanosheets is uniformly anchored by the hydrothermal treatment of the axial of carbon nanofibers derived from an electrospinning method (CNFs//MoS2). The quantity of the MoS2 nanosheets on the CNFs substrates can be tuned by controlling the amount of utilized thiourea precursor. The influence of the MoS2 nanosheets on the electrochemical properties of the composite fibers has been investigated. The synergistic effect between MoS2 and carbon nanofibers can enhance their electrical conductivity and ionic reversibility as an anode for LIBs. The composite fibers deliver a high reversible capacity of 866.5 mA h g−1 after 200 cycles at a current density of 0.5 A g−1 and maintain a capacity of 703.3 mA h g−1 after a long cycle of 500 charge–discharge processes at 1 A g−1. [ABSTRACT FROM AUTHOR]

Exploring anode materials with an excellent electrochemical performance is of great significance for supercapacitor applications. In this work, a N-doped-carbon-nanofiber (NCNF)-supported Fe3C/Fe2O3 nanoparticle (NCFCO) composite was synthesized via the facile carbonizing and subsequent annealing of electrospinning nanofibers containing an Fe source. In the hybrid structure, the porous carbon nanofibers used as a substrate could provide fast electron and ion transport for the Faradic reactions of Fe3C/Fe2O3 during charge–discharge cycling. The as-obtained NCFCO yields a high specific capacitance of 590.1 F g−1 at 2 A g−1, superior to that of NCNF-supported Fe3C nanoparticles (NCFC, 261.7 F g−1), and NCNFs/Fe2O3 (NCFO, 398.3 F g−1). The asymmetric supercapacitor, which was assembled using the NCFCO anode and activated carbon cathode, delivered a large energy density of 14.2 Wh kg−1 at 800 W kg−1. Additionally, it demonstrated an impressive capacitance retention of 96.7%, even after 10,000 cycles. The superior electrochemical performance can be ascribed to the synergistic contributions of NCNF and Fe3C/Fe2O3. [ABSTRACT FROM AUTHOR]

The present study involves the synthesis of photocatalytic composite nanofibers (NFs) comprising ilmenite nickel titanite-supported carbon nanofibers (NiTiO3/TiO2@CNFs) using an electrospinning process. The photocatalytic composite NFs obtained were utilized in hydrogen (H2) production from the photohydrolysis of ammonia borane (AB). The experimental findings show that the photocatalytic composite NFs with a loading of 25 mg had a good catalytic performance for H2 generation, producing the stoichiometric H2 in 11 min using 1 mmol AB under visible light at 25 °C and 1000 rpm. The increase in catalyst load to 50, 75, and 100 mg leads to a corresponding reduction in the reaction time to 7, 5, and 4 min. The findings from the kinetics investigations suggest that the rate of the photohydrolysis reaction is directly proportional to the amount of catalyst in the reaction system, adhering to a first-order reaction rate. Furthermore, it was observed that the reaction rate remains unaffected by the concentration of AB, thereby suggesting a reaction of zero order. Increasing the reaction temperature results in a decrease in the duration of the photohydrolysis reaction. Furthermore, an estimated activation energy value of 35.19 kJ mol−1 was obtained. The composite nanofibers demonstrated remarkable and consistent effectiveness throughout five consecutive cycles. The results suggest that composite NFs possess the capacity to function as a feasible substitute for costly catalysts in the process of H2 generation from AB. [ABSTRACT FROM AUTHOR]

The combination of multiple electrode materials and their reasonable structural design are conducive to the preparation of composite electrodes with excellent performance. In this study, based on carbon nanofibers grown with Ni(OH)2 and NiO (CHO) prepared by electrospinning, hydrothermal growth, and low-temperature carbonization, five transition metal sulfides (MnS, CoS, FeS, CuS, and NiS) were hydrothermally grown on their surfaces, exhibiting that CHO/NiS had the optimal electrochemical properties. Subsequently, the effect of hydrothermal growth time on CHO/NiS revealed that the electrochemical performance of CHO/NiS-3h was optimal, with a specific capacitance of up to 1717 F g−1 (1 A g−1), due to its multistage core–shell structure. Moreover, the diffusion-controlled process of CHO/NiS-3h dominated its charge energy storage mechanism. Finally, the asymmetric supercapacitor assembled with CHO/NiS-3h as the positive electrode demonstrated an energy density of 27.76 Wh kg−1 at a maximum power density of 4000 W kg−1, and it still maintained a power density of 800 W kg−1 at a maximum energy density of 37.97 Wh kg−1, exhibiting the potential application of multistage core–shell composite materials in high-performance supercapacitors. [ABSTRACT FROM AUTHOR]

Molybdenum carbide co-catalyst and carbon nanofiber matrix are suggested to improve the nickel activity toward methanol electrooxidation process. The proposed electrocatalyst has been synthesized by calcination electrospun nanofiber mats composed of molybdenum chloride, nickel acetate, and poly (vinyl alcohol) under vacuum at elevated temperatures. The fabricated catalyst has been characterized using XRD, SEM, and TEM analysis. The electrochemical measurements demonstrated that the fabricated composite acquired specific activity for methanol electrooxidation when molybdenum content and calcination temperature were tuned. In terms of the current density, the highest performance is attributed to the nanofibers obtained from electrospun solution having 5% molybdenum precursor compared to nickel acetate as a current density of 107 mA/cm2 was generated. The process operating parameters have been optimized and expressed mathematically using the Taguchi robust design method. Experimental design has been employed in investigating the key operating parameters of methanol electrooxidation reaction to obtain the highest oxidation current density peak. The main effective operating parameters of the methanol oxidation reaction are Mo content in the electrocatalyst, methanol concentration, and reaction temperature. Employing Taguchi's robust design helped to capture the optimum conditions yielding the maximum current density. The calculations revealed that the optimum parameters are as follows: Mo content, 5 wt.%; methanol concentration, 2.65 M; and reaction temperature, 50 °C. A mathematical model has been statistically derived to describe the experimental data adequately with an R2 value of 0. 979. The optimization process indicated that the maximum current density can be identified statistically at 5% Mo, 2.0 M methanol concentration, and 45 °C operating temperature. [ABSTRACT FROM AUTHOR]

A flexible CoNi@CNF electrochemical catalyst was developed using coaxial electrostatic spinning technology. The distribution and content of CoNi alloy nanoparticles on the surface of carbon fibers were adjusted by regulating the feed speed ratio of the outer and inner axes of coaxial electrostatic spinning. The results indicate that the content of the CoNi alloy distributed on the carbon fiber surface increased from 26.7 wt.% to 38.4 wt.% with an increase in the feed speed of the inner axis. However, the excessive precipitation of the CoNi alloy on the carbon fiber surface leads to the segregation of the internal CoNi alloy, which is unfavorable for the exposure of active sites during the electrolytic reaction. The best electrocatalytic performance of the composite was achieved when the rate of the outer axis feed speed was constant (3 mm/h) and the rate of the inner axis was 1.5 mm/h. The initial oxygen reduction potential and half-slope potential were 0.99 V and 0.92 V (VS RHE), respectively. The diffusion-limited current density was 6.31 mA/cm−2 and the current strength retention was 95.2% after the 20,000 s timed current test. [ABSTRACT FROM AUTHOR]

Bone tissue engineering integrates biomaterials, cells, and bioactive agents to propose sophisticated treatment options over conventional choices. Scaffolds have central roles in this scenario, and precisely designed and fabricated structures with the highest similarity to bone tissue have shown promising outcomes. On the other hand, using nanotechnology and nanomaterials as the enabling options confers fascinating properties to the scaffolds, such as precisely tailoring the physicochemical features and better interactions with cells and surrounding tissues. Among different nanomaterials, polymeric nanofibers and carbon nanofibers have attracted significant attention due to their similarity to bone extracellular matrix (ECM) and high surface-to-volume ratio. Moreover, bone ECM is a biocomposite of collagen fibers and hydroxyapatite crystals; accordingly, researchers have tried to mimic this biocomposite using the mineralization of various polymeric and carbon nanofibers and have shown that the mineralized nanofibers are promising structures to augment the bone healing process in the tissue engineering scenario. In this paper, we reviewed the bone structure, bone defects/fracture healing process, and various structures/cells/growth factors applicable to bone tissue engineering applications. Then, we highlighted the mineralized polymeric and carbon nanofibers and their fabrication methods. [ABSTRACT FROM AUTHOR]

ZnS–graphene composites (ZnSGO) were synthesized by a hydrothermal process and loaded onto carbon nanofibers (CNFs) by electrospinning (ZnS–GO/CNF), to obtain self-standing anodes for SIBs. The characterization techniques (XRPD, SEM, TEM, EDS, TGA, and Raman spectroscopy) confirm that the ZnS nanocrystals (10 nm) with sphalerite structure covered by the graphene sheets were successfully synthesized. In the ZnS–GO/CNF anodes, the active material is homogeneously dispersed in the CNFs' matrix and the ordered carbon source mainly resides in the graphene component. Two self-standing ZnS–GO/CNF anodes (active material amount: 11.3 and 24.9 wt%) were electrochemically tested and compared to a tape-casted ZnS–GO example prepared by conventional methods (active material amount: 70 wt%). The results demonstrate improved specific capacity at high C-rate for the free-standing anodes compared to the tape-casted example (69.93 and 92.59 mAh g−1 at 5 C for 11.3 and 24.9 wt% free-standing anodes, respectively, vs. 50 mAh g−1 for tape-casted). The 24.9 wt% ZnS–GO/CNF anode gives the best cycling performances: we obtained capacities of 255–400 mAh g−1 for 200 cycles and coulombic efficiencies ≥ 99% at 0.5 C, and of 80–90 mAh g−1 for additional 50 cycles at 5 C. The results suggest that self-standing electrodes with improved electrochemical performances at high C-rates can be prepared by a feasible and simple strategy: ex situ synthesis of the active material and addition to the carbon precursor for electrospinning. [ABSTRACT FROM AUTHOR]

The sluggish electron transfer at the interface of microorganisms and an electrode is a bottleneck of increasing the output power density of microbial fuel cells (MFCs). Mo-doped carbon nanofibers (Mo-CNFs) prepared with electrostatic spinning and high-temperature carbonization are used as an anode in MFCs here. Results clearly indicate that Mo2C nanoparticles uniformly anchored on carbon nanowire, and Mo-doped anodes could accelerate the electron transfer rate. The Mo-CNF ΙΙ anode delivered a maximal power density of 1287.38 mW m−2, which was twice that of the unmodified CNFs anode. This fantastic improvement mechanism is attributed to the fact that Mo doped on a unique nanofiber surface could enhance microbial colonization, electrocatalytic activity, and large reaction surface areas, which not only enable direct electron transfer, but also promote flavin-like mediated indirect electron transfer. This work provides new insights into the application of electrospinning technology in MFCs and the preparation of anode materials on a large scale. [ABSTRACT FROM AUTHOR]

Thermoplastic polyurethane (TPU) has been widely used as the elastic polymer substrate to be combined with conductive nanomaterials to develop stretchable strain sensors for a variety of applications such as health monitoring, smart robotics, and e-skins. However, little research has been reported on the effects of deposition methods and the form of TPU on their sensing performance. This study intends to design and fabricate a durable, stretchable sensor based on composites of thermoplastic polyurethane and carbon nanofibers (CNFs) by systematically investigating the influences of TPU substrates (i.e., either electrospun nanofibers or solid thin film) and spray coating methods (i.e., either air-spray or electro-spray). It is found that the sensors with electro-sprayed CNFs conductive sensing layers generally show a higher sensitivity, while the influence of the substrate is not significant and there is no clear and consistent trend. The sensor composed of a TPU solid thin film with electro-sprayed CNFs exhibits an optimal performance with a high sensitivity (gauge factor ~28.2) in a strain range of 0–80%, a high stretchability of up to 184%, and excellent durability. The potential application of these sensors in detecting body motions has been demonstrated, including finger and wrist-joint movements, by using a wooden hand. [ABSTRACT FROM AUTHOR]

Sol-gel electrospinning process was used to prepare electrospun carbon nanofibers (ECNFs) from polyacrylonitrile and graphite nanoplatelets. The nanofibers of as-electrospun carbon were calcinated in argon from room temperature to 500 °C for 1h. Scanning and transmission electron microscopy with energy-dispersive X-ray spectroscopy and X-ray diffractometry (XRD) were used to characterize the synthesized ECNFs. The smooth ECNFs with a diameter of 129 ± 43 nm comprised conical platelets of 30–200 µm length. The plane-layered nanofibers contained crystallites along the long fiber axis and were mainly parallel. [ABSTRACT FROM AUTHOR]

The booming demand for energy storage has driven the rapid development of energy storage devices such as supercapacitors, and the research on high-performance electrode materials, a key component of supercapacitors, has gained tremendous attention. In this research, phenolic resin-based multi-porous carbon nanofibers have been prepared by electrospinning, curing, carbonization and activation and then employed as advanced electrode materials in supercapacitors. We demonstrate that the material is nano-scale continuous fiber, and its surface has pore distribution of different sizes. It delivers a high specific capacitance of 242 F g−1 at a current density of 0.2 A g−1 and maintains 148 F g−1 even at a high current density of 20 A g−1. Moreover, it shows almost no capacitance decay at a current density of 2 A g−1 over 1000 cycles, demonstrating its great potential as high-performance electrodes in supercapacitors. [ABSTRACT FROM AUTHOR]

A nanocomposite comprised of nickel titanate/titania nanoparticles decorated with carbon nanofibers (NiTiO3/TiO2-decorated CNFs) is successfully synthesized via electrospinning and further utilized for methylene blue (MB) photodegradation. The morphology, phase, structural and chemical composition of the nanocomposite is investigated via scanning electron microscope, X-ray diffraction and transmission electron microscope equipped with energy dispersive X-ray. A mathematical model is developed to predict the photocatalytic activity of the produced nanocomposite by considering parameters such as initial dye concentration, light intensity, reaction temperature, and catalyst dosage. The reaction rate constant K1 decreased from 0.0153 to 0.0044 min−1 with an increase in the MB concentration from 5 to 15 mg L−1, while K2, K3, and K4 were found to increase with the increase in reaction temperature (0.0153 to 0.0222 min−1), light intensity (0.0153 to 0.0228 min−1) and catalyst dose concentration (0.0153 to 0.0324 min−1), respectively. The results obtained are found to be in good agreement with the modeling results and showed effective photodegradation activity. The performance of our catalyst is found to be better compared to other catalysts previously reported in the literature. The recyclability data of the synthesized NiTiO3/TiO2-decorated CNFs catalyst for four runs show that the catalyst is quite stable and recyclable. This nanocomposite photocatalyst offers a low-cost solution for wastewater pollution problems and opens new avenues to further explore the electrospinning method for the synthesis of nanocomposites. [ABSTRACT FROM AUTHOR]

Semiconductor materials as photocatalysts hold great prospects for renewable energy substitutes and environmental protection. Nanostructured BiOX (X=Cl, Br, I) with favorable features of a unique layered crystal structure and suitable band gaps has been demonstrated to be a promising photocatalytic material. In this paper, a two-step synthesis route combining an electrospinning technique and SILAR reaction has been accepted as a straightforward protocol for the exploitation of BiOI/carbon nanofibers' (CNFs) hierarchical heterostructures. As expected, the BiOI/CNFs presented a much higher degradation rate of methyl orange than that of the pure BiOI under visible light. The degradation rate of methyl orange reaches 85% within 210 min. The enhanced photocatalytic activity could be attributed to the fact that conductive CNFs as substrate could effectively improve the separation and transformation of photogenerated charges. Moreover, the fabricated BiOI/CNFs after five cycles could be easily recycled without a decrease in photocatalytic activity due to their ultra-long one-dimensional nano-structural property. [ABSTRACT FROM AUTHOR]

Transition−metal−based materials show great promise for energy conversion and storage due to their excellent chemical properties, low cost, and excellent natural properties. In this paper, through simple strategies such as classical electrospinning, air calcination, and the one−step hydrothermal method, a large area of Ni(OH)2 nanosheets were grown on NiMoO4 nanofibers, forming NiMoO4@Ni(OH)2 nanofibers. The one−dimensional nanostructure was distributed with loose nanosheets, and this beneficial morphology made charge−transfer and diffusion more rapid, so the newly developed material showed good capacitance and conductivity. Under the most suitable experimental conditions, the optimal electrode exhibited the highest specific capacitance (1293 F/g at 1 A/g) and considerable rate capability (56.8% at 10 A/g) under typical test conditions. Most interestingly, the corresponding asymmetrical capacitors exhibited excellent electrochemical cycle stability, maintaining 77% of the original capacitance. NiMoO4@Ni(OH)2 nanofibers were verified to be simple to prepare and to have good performances as energy−storage devices within this experiment. [ABSTRACT FROM AUTHOR]

Carbon nanofiber-decorated graphite rods are introduced as effective and low-cost anodes for industrial wastewater-driven microbial fuel cells. Carbon nanofiber deposition on the surface of the graphite rods could be performed by the electrospinning of polyacrylonitrile/N,N-Dimethylformamide solution using the rod as nanofiber collector, which was calcined under inert atmosphere. The experimental results indicated that at 10 min electrospinning time, the proposed graphite anode demonstrates very good performance compared to the commercial anodes. Typically, the generated power density from sugarcane industry wastewater-driven air cathode microbial fuel cells were 13 ± 0.3, 23 ± 0.7, 43 ± 1.3, and 185 ± 7.4 mW/m2 using carbon paper, carbon felt, carbon cloth, and graphite rod coated by 10-min electrospinning time carbon nanofibers anodes, respectively. The distinct performance of the proposed anode came from creating 3D carbon nanofiber layer filled with the biocatalyst. Moreover, to annihilate the internal cell resistance, a membrane-less cell was assembled by utilizing a poly(vinylidene fluoride) electrospun nanofiber layer-coated cathode. This novel strategy inspired a highly hydrophobic layer on the cathode surface, preventing water leakage to avoid utilizing the membrane. However, in both anode and cathode modifications, the electrospinning time should be optimized. The best results were obtained at 5 and 10 min for the cathode and anode, respectively. [ABSTRACT FROM AUTHOR]

Nanocarriers are gaining significant importance in the modern era of drug delivery. Nanofiber technology is one of the prime paradigms in nanotechnology for various biomedical and theranostic applications. Nanofibers obtained after successful electrospinning subjected to surface functionalized for drug delivery, biomedical, tissue engineering, biosensing, cell imaging and wound dressing application. Surface functionalization entirely changes physicochemical and biological properties of nanofibers. In physicochemical properties, wettability, melting point, glass transition temperature, and initial decomposition temperature significantly change offer several advantageous for nanofibers. Similarly, biological properties include cell adhesion, biocompatibility, and proliferation, also changes by functionalization of nanofibers. Various natural and synthetic materials polymers, metals, carbon materials, functional groups, proteins, and peptides, are currently used for surface modification of nanofibers. Various research studies across the globe demonstrated the usefulness of surface functionalized nanofibers in tissue engineering, wound healing, skin cancers, melanoma, and disease diagnosis. The delivery of drug through surface functionalized nanofibers results in improved permeation and bioavailability of drug which is important for better targeting of disease and therapeutic efficacy. This review provides a comprehensive insight about various techniques of surface functionalization of nanofibers along with its biomedical applications, toxicity assessment and global patent scenario. [ABSTRACT FROM AUTHOR]

Biomass-based carbon nanofibers (CNF) were synthesized using lignin extracted from sawdust and polyacrylonitrile (PAN) (30:70) with the help of the electrospinning method and subsequent stabilization at 220 °C and carbonization at 800, 900, and 1000 °C. The synthesized CNFs were studied by scanning electron microscopy, energy-dispersive X-ray analysis, Raman spectroscopy, and the Brunauer–Emmett–Teller method. The temperature effect shows that CNF carbonized at 800 °C has excellent stability at different current densities and high capacitance. CNF 800 in the first test cycle at a current density of 100 mA/g shows an initial capacity of 798 mAh/g and an initial coulomb efficiency of 69.5%. The CNF 900 and 1000 show an initial capacity of 668 mAh/g and 594 mAh/g, and an initial Coulomb efficiency of 52% and 51%. With a long cycle (for 500 cycles), all three samples at a current density of 500 mA/g show stable cycling in different capacities (CNF 800 in the region of 300–400 mAh/g, CNF 900 and 1000 in the region of 100–200 mAh/g). [ABSTRACT FROM AUTHOR]

The efficient use of renewable energy sources requires development of new electrocatalytic materials for electrochemical energy storage systems, particularly fuel cells. To increase durability of high temperature polymer electrolyte fuel cell (HT-PEMFC), Pt/carbon black based catalysts should be replaced by more durable ones, for example Pt/carbon nanofibers (CNF). Here, we report for the first time the quantitative ascorbic acid assisted deposition of Pt onto electrospun polyacrylonitrile-based CNF composite materials. The effect of their subsequent post-treatment at various temperatures (250 and 500 °C) and media (vacuum or argon-hydrogen mixture) on the Pt/C catalyst morphology is investigated. All obtained samples are thoroughly studied by high resolution electron microscopy, and Pt electrochemically active specific surface area was evaluated by cyclic voltammetry. [ABSTRACT FROM AUTHOR]

In recent years, spinel-type structural cobalt salts (NiCo2O4, CuCo2O4, etc.) have been widely used electrocatalysis because of their superior properties such as large crustal reserves, low cost, environmental friendliness, high electrochemical activity, abundant oxidation valence, and stable chemical properties. In this paper, hollow carbon nanofibers loaded CuCo2O4 nanowires (CuCo2O4@CNFs) were prepared by electrospinning technique and solvothermal method. The CuCo2O4@CNFs exhibit enhances electrocatalytic activity for oxygen evolution reaction (OER), requiring an overpotential of 273 mV in a 1.0 M KOH solution to achieve a current density of 10 mA cm−2. In addition, the overpotential remained almost constant after 3000 cycles of voltammetry measurements. The enhanced electrocatalytic activity may be attributed to the unique one-dimensional hollow nanostructure of CNFs and high dispersion of CuCo2O4 nanowires, which enhanced the charge transfer and improved the diffusion of the electrolyte ions at the surface. [ABSTRACT FROM AUTHOR]

Titanium oxynitride carbon composite nanofibers (TiON/C-CNFs) were synthesised with electrospinning and subsequent heat treatment in ammonia gas. In situ four-probe electrical conductivity measurements of individual TiON/C-CNFs were performed. Additionally, the TiON/C-CNFs were thoroughly analysed with various techniques, such as X-ray and electron diffractions, electron microscopies and spectroscopies, thermogravimetric analysis and chemical analysis to determine the crystal structure, morphology, chemical composition, and N/O at. ratio. It was found that nanofibers were composed of 2–5 nm sized titanium oxynitride (TiON) nanoparticles embedded in an amorphous carbon matrix with a small degree of porosity. The average electrical conductivity of a single TiON/C-CNF was 1.2 kS/m and the bulk electrical conductivity of the TiON/C-CNF fabric was 0.053 kS/m. From the available data, the mesh density of the TiON/C-CNF fabric was estimated to have a characteristic length of 1.0 µm and electrical conductivity of a single TiON/C-CNF was estimated to be from 0.45 kS/m to 19 kS/m. The electrical conductivity of the measured TiON/C-CNFs is better than that of amorphous carbon nanofibers and has ohmic behaviour, which indicates that it can effectively serve as a new type of support material for electrocatalysts, batteries, sensors or supercapacitors. [ABSTRACT FROM AUTHOR]

In this study, polyacrylonitrile (PAN)-based activated nanofiber composites, which were embedded inside zeolitic imidazolate framework-8 (ZIF-8) crystals or ZIF-8-derived carbons (ZDC-850), were fabricated using an electrospinning process, to serve as CO2 adsorbents. The adsorbents were characterized using various techniques. The degree of crystallinity of ZDC-850 totally changed compared to that of ZIF-8. For nanofiber composites, the timing of the ligand decomposition of ZIF-8 significantly affected the material properties. The Zn metals in the ZIF-8/PAN or ZDC-850/PAN could be embedded and protected by the PAN fibers from excess volatilization in the following treatments: ZIF-8 had significant pore volumes in the range of 0.9–1.3 nm, but ZDC-850 and ZIF-8/PAN exhibited a distinct peak at approximately 0.5 nm. The CO2 adsorption capacities at 25 °C and 1 atm followed the order: ZIF-8/PAN (4.20 mmol/g) > ZDC-850 (3.50 mmol/g) > ZDC-850/PAN (3.38 mmol/g) > PAN (2.91 mmol/g) > ZIF-8 (0.88 mmol/g). The slope in the log–linear plot of isosteric heat of adsorption was highly associated with CO2 adsorption performance. Under 1 atm at 25 °C, for Zn metal active sites inside the pores, the pores at approximately 0.5 nm and in C-N (amines) groups could promote CO2 adsorption. At low CO2 pressures, for a good CO2 adsorbent, the carbon content in the adsorbent should be higher than a threshold value. Under this condition, the percentage of ultra-micropore and micropore volumes, as well as the functional groups, such as the quaternary or protonated N (amines), N=C (imines or pyridine-type N), C-OH, and -COOH groups, should be considered as significant factors for CO2 adsorption. [ABSTRACT FROM AUTHOR]

Recently, electrocatalysts for oxygen reduction reaction (ORR) as well as oxygen evolution reaction (OER) hinged on electrospun nanofiber composites have attracted wide research attention. Transition metal elements and heteroatomic doping are important methods used to enhance their catalytic performances. Lately, the construction of electrocatalysts based on metal-organic framework (MOF) electrospun nanofibers has become a research hotspot. In this work, nickel-cobalt zeolitic imidazolate frameworks with different molar ratios (NixCoy-ZIFs) were synthesized in an aqueous solution, followed by NixCoy-ZIFs/polyacrylonitrile (PAN) electrospun nanofiber precursors, which were prepared by a simple electrospinning method. Bimetal (Ni-Co) porous carbon nanofiber catalysts doped with nitrogen, oxygen, and sulfur elements were obtained at high-temperature carbonization treatment in different atmospheres (argon (Ar), Air, and hydrogen sulfide (H2S)), respectively. The morphological properties, structures, and composition were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Moreover, the specific surface area of materials and their pore size distribution was characterized by Brunauer-Emmett-Teller (BET). Linear sweep voltammetry curves investigated catalyst performances towards oxygen reduction and evolution reactions. Importantly, Ni1Co2-ZIFs/PAN-Ar yielded the best ORR activity, whereas Ni1Co1-ZIFs/PAN-Air exhibited the best OER performance. This work provides significant guidance for the preparation and characterization of multi-doped porous carbon nanofibers carbonized in different atmospheres. [ABSTRACT FROM AUTHOR]

Co-doped carbon nanofiber mats can be prepared by the addition of cobalt acetate to the polyacrylonitrile/DMF electrospun solution. Wastewater obtained from food industries was utilized as the anolyte as well as microorganisms as the source in single-chamber batch mode microbial fuel cells. The results indicated that the single Co-free carbon nanofiber mat was not a good anode in the used microbial fuel cells. However, the generated power can be distinctly enhanced by using double active layers of pristine carbon nanofiber mats or a single layer Co-doped carbon nanofiber mat as anodes. Typically, after 24 h batching time, the estimated generated power densities were 10, 92, and 121 mW/m2 for single, double active layers, and Co-doped carbon nanofiber anodes, respectively. For comparison, the performance of the cell was investigated using carbon cloth and carbon paper as anodes, the observed power densities were smaller than the introduced modified anodes at 58 and 62 mW/m2, respectively. Moreover, the COD removal and Columbic efficiency were calculated for the proposed anodes as well as the used commercial ones. The results further confirm the priority of using double active layer or metal-doped carbon nanofiber anodes over the commercial ones. Numerically, the calculated COD removals were 29.16 and 38.95% for carbon paper and carbon cloth while 40.53 and 45.79% COD removals were obtained with double active layer and Co-doped carbon nanofiber anodes, respectively. With a similar trend, the calculated Columbic efficiencies were 26, 42, 52, and 71% for the same sequence. [ABSTRACT FROM AUTHOR]

Recently, electrocatalysts for oxygen reduction reaction (ORR) as well as oxygen evolution reaction (OER) hinged on electrospun nanofiber composites have attracted wide research attention. Transition metal elements and heteroatomic doping are important methods used to enhance their catalytic performances. Lately, the construction of electrocatalysts based on metal-organic framework (MOF) electrospun nanofibers has become a research hotspot. In this work, nickel-cobalt zeolitic imidazolate frameworks with different molar ratios (NixCoy-ZIFs) were synthesized in an aqueous solution, followed by NixCoy-ZIFs/polyacrylonitrile (PAN) electrospun nanofiber precursors, which were prepared by a simple electrospinning method. Bimetal (Ni-Co) porous carbon nanofiber catalysts doped with nitrogen, oxygen, and sulfur elements were obtained at high-temperature carbonization treatment in different atmospheres (argon (Ar), Air, and hydrogen sulfide (H2S)), respectively. The morphological properties, structures, and composition were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Moreover, the specific surface area of materials and their pore size distribution was characterized by Brunauer-Emmett-Teller (BET). Linear sweep voltammetry curves investigated catalyst performances towards oxygen reduction and evolution reactions. Importantly, Ni1Co2-ZIFs/PAN-Ar yielded the best ORR activity, whereas Ni1Co1-ZIFs/PAN-Air exhibited the best OER performance. This work provides significant guidance for the preparation and characterization of multi-doped porous carbon nanofibers carbonized in different atmospheres. [ABSTRACT FROM AUTHOR]

Carbon nanofibers are used for a broad range of applications, from nano-composites to energy storage devices. They are typically produced from electrospun poly(acrylonitrile) nanofibers by thermal stabilization and carbonization. The nanofiber mats are usually placed freely movable in an oven, which leads to relaxation of internal stress within the nanofibers, making them thicker and shorter. To preserve their pristine morphology they can be mechanically fixated, which may cause the nanofibers to break. In a previous study, we demonstrated that sandwiching the nanofiber mats between metal sheets retained their morphology during stabilization and incipient carbonization at 500 °C. Here, we present a comparative study of stainless steel, titanium, copper and silicon substrate sandwiches at carbonization temperatures of 500 °C, 800 °C and 1200 °C. Helium ion microscopy revealed that all metals mostly eliminated nanofiber deformation, whereas silicone achieved the best results in this regard. The highest temperatures for which the metals were shown to be applicable were 500 °C for silicon, 800 °C for stainless steel and copper, and 1200 °C for titanium. Fourier transform infrared and Raman spectroscopy revealed a higher degree of carbonization and increased crystallinity for higher temperatures, which was shown to depend on the substrate material. [ABSTRACT FROM AUTHOR]

High temperature is required in carbon fiber synthesis in the carbonization step. However, direct high-temperature heating without the presence of additive materials would affect the yield and structure of carbon fibers produced. Thus, this study aims to synthesize carbon fibers from poly-vinyl alcohol (PVA), as the precursor and reducing agent, using silver nanoparticles (SNP) from silver nitrate (AgNO3) as additives. The pre-treatment of PVA was performed in three steps, i.e., mixing PVA/AgNO3, electrospinning, and iodination. The interaction of PVA and AgNO3 was assessed by FTIR, and SEM was used to characterize the electro-spun fibers prior and after iodination; Raman spectrophotometer was carried out to confirm the yield of carbon fibers. There was reduction in oxygen groups (3000–3800 cm−1) and emergence of –C=O (1100 cm−1) and –C=C– (1627 cm−1) functional groups, indicating formation of carbon layers. Based on the DT/GA results, the silver nanoparticles reduce the need of high temperature with optimum carbonization at 350 °C and lead to the formation of more regular graphene layers. Graphene layers with a size distribution of 0.438 nm and well-organized structures were successfully formed, and the Raman shifting showed higher intensities of G and G' bands in the presence of Ag. Based on DT/GA results, the yield of carbon fibers with iodinated PVA fibers and SNP as additive had higher rates around 800 µg/min, reaching 33% at 500 °C. Thus, it is demonstrated that iodinated PVA/AgNO3 samples can significantly improve carbon fiber yield at low temperatures. [ABSTRACT FROM AUTHOR]

Low-cost and simple methods are constantly chased in order to produce less expensive lithium-ion batteries (LIBs) while possibly increasing the energy and power density as well as the volumetric capacity in order to boost a rapid decarbonization of the transport sector. Li alloys and tin-carbon composites are promising candidates as anode materials for LIBs both in terms of capacity and cycle life. In the present paper, electrospinning was employed in the preparation of Sn/SnOx@C composites, where tin and tin oxides were homogeneously dispersed in a carbonaceous matrix of carbon nanofibers. The resulting self-standing and light electrode showed a greatly enhanced performance compared to a conventional electrode based on the same starting materials that are simply mixed to obtain a slurry then deposited on a Cu foil. Fast kinetics were achieved with more than 90% of the reaction that resulted being surface-controlled, and stable capacities of about 300 mAh/g over 500 cycles were obtained at a current density of 0.5 A/g. [ABSTRACT FROM AUTHOR]

To improve the performance of PtRu/nitrogen-doped graphene composite carbon nanofibers, the composite carbon nanofibers were thermally compensated by deep cryogenic treatment (DCT), which realized the morphology reconstruction of composite carbon nanofibers. The effects of different DCT times were compared: 12 h, 18 h, and 24 h. The morphology reconstruction mechanism was explored by combining the change of inner chain structure and material group. The results showed that the fibers treated for 12 h had better physical and chemical properties, where the diameter is evenly distributed between 500 and 800 nm. Combined with Fourier infrared analysis, the longer the cryogenic time, the more easily the water vapor and nitrogen enter polymerization reaction, causing changes of chain structure and degradation performance. With great performance of carbonization and group transformation, the PtRu/nitrogen-doped graphene composite carbon nanofibers can be used as an efficient direct alcohol fuel cell catalyst and promote its commercialization. [ABSTRACT FROM AUTHOR]

During the last two decades, electrospinning has become a very popular technique for the fabrication of nanofibers due to its low cost and simple handling. Nanofiber materials have found utilization in many areas such as medicine, sensors, batteries, etc. In catalysis, these materials also present important advantages, since they present a low resistance to internal diffusion and a high surface area to volume ratio. These advantages are mainly due to the diameter–length proportion. A bibliographic analysis on the applications of electrospun nanofibers in catalysis shows that there are two important groups of catalysts that are being investigated, based on TiO2 and in carbon materials. The main applications found are in photo- and in electro-catalysis. The present study contributes by reviewing these catalytic applications of electrospun nanofibers and demonstrating that they are promising materials as catalysts, underlining some works to prove the advantages and possibilities that these materials have as catalysts. On one hand, the possibilities of synthesis are almost infinite, since with coaxial electrospinning quite complex nanofibers with different layers can be prepared. On the other hand, the diameter and other properties can be controlled by monitoring the applied voltage and other parameters during the synthesis, being quite reproducible procedures. The main advantages of these materials can be grouped in two: one related to their morphology, as has been commented, relative to their low resistance and internal diffusion, that is, their fluidynamic behavior in the reactor; the second group involves advantages related to the fact that the active phases can be nanoscaled and dispersed, improving the activity and selectivity in comparison with conventional catalytic materials with the same chemical composition. [ABSTRACT FROM AUTHOR]

Carbon capture is amongst the key emerging technologies for the mitigation of greenhouse gases (GHG) pollution. Several materials as adsorbents for CO2 and other gases are being developed, which often involve using complex and expensive fabrication techniques. In this work, we suggest a sound, easy and cheap route for the production of nitrogen-doped carbon materials for CO2 capture by pyrolysis of electrospun poly(acrylonitrile) (PAN) fibers. PAN fibers are generally processed following specific heat treatments involving up to three steps (to get complete graphitization), one of these being stabilization, during which PAN fibers are oxidized and stretched in the 200–300 °C temperature range. The effect of stabilization temperature on the chemical structure of the carbon nanofibers is investigated herein to ascertain the possible implication of incomplete conversion/condensation of nitrile groups to form pyridine moieties on the CO2 adsorption capacity. The materials were tested in the pure CO2 atmosphere at 20 °C achieving 18.3% of maximum weight increase (equivalent to an uptake of 4.16 mmol g−1), proving the effectiveness of a high stabilization temperature as route for the improvement of CO2 uptake. [ABSTRACT FROM AUTHOR]

Silicon (Si) is expected to be a high-energy anode for the next generation of lithium-ion batteries (LIBs). However, the large volume change along with the severe capacity degradation during the cycling process is still a barrier for its practical application. Herein, we successfully construct flexible silicon/carbon nanofibers with a core–shell structure via a facile coaxial electrospinning technique. The resultant Si@C nanofibers (Si@C NFs) are composed of a hard carbon shell and the Si-embedded amorphous carbon core framework demonstrates an initial reversible capacity of 1162.8 mAh g−1 at 0.1 A g−1 with a retained capacity of 762.0 mAh g−1 after 100 cycles. In addition, flexible LIBs assembled with Si@C NFs were hardly impacted under an extreme bending state, illustrating excellent electrochemical performance. The impressive performances are attributed to the high electric conductivity and structural stability of the porous carbon fibers with a hierarchical porous structure, indicating that the novel Si@C NFs fabricated using this electrospinning technique have great potential for advanced flexible energy storage. [ABSTRACT FROM AUTHOR]

In this study, polyacrylonitrile (PAN) was mixed with a renewable polymer, lignin, to produce electrospun nanofibers by using an electrospinning technique. Lignin was utilized as a soft template that was removed from the nanofibers by using a selective dissolution technique to create porous PAN nanofibers. These nanofibers were characterized with Fourier transform infrared (FTIR), field emission scanning electron microscopy (FESEM), thermogravimetry analysis (TGA), X-ray diffraction (XRD), and Brunauer-Emmett-Teller (BET) to study their properties and morphology. The results showed that lignin can be homogeneously mixed into the PAN solution and successfully electrospun into nanofibers. FESEM results showed a strong relationship between the PAN: lignin ratio and the diameter of the electrospun fibers. Lignin was successfully removed from electrospun nanofibers by a selective chemical dissolution technique, which resulted in roughness and porousness on the surface of the nanofibers. Based on the BET result, the specific surface area of the PAN/lignin nanofibers was more than doubled following the removal of lignin compared to PAN nanofibers. The highest specific surface area of nanofibers after selective chemical dissolution was found at an 8:2 ratio of PAN/lignin, which was 32.42 m2g−1 with an average pore diameter of 5.02 nm. The diameter of electrospun nanofibers was also slightly reduced after selective chemical dissolution. Porous PAN nanofibers can be seen as the precursors to the production of highly porous carbon nanofibers. [ABSTRACT FROM AUTHOR]

The issue of heavy metal contamination has caused a great deal of concern among water quality experts today, as it contributes to water pollution. Activated carbon nanofibers (ACNFs) showed a significant ability in removing heavy metals from the wastewater. In this study, polyacrylonitrile (PAN) was blended and electrospun with an abundant and inexpensive biopolymer, lignin and a water soluble polymer, poly(ethylene glycol) (PEG), by using an electrospinning technique to form nanofibers. The electrospun nanofibers were then investigated as a precursor for the production of porous ACNFs to study the removal of nickel(II) ions by adsorption technique. PEG was added to act as a porogen and to create the porous structure of carbon nanofibers (CNFs). CNFs were prepared by thermal treatment of the electrospun nanofibers and followed by activation of CNFs by thermal and acid treatment on CNFs. Attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) spectral analysis of the ACNFs showed a strong absorption peak of the C-O functional group, indicating the increase in the oxygenated compound. Field emission scanning electron microscopy (FESEM) images concluded that the ACNFs have more porous and compact fibers with a smaller fiber diameter of 263 ± 11 nm, while the CNFs are less compact and have slightly larger fiber diameter of 323 ± 6 nm. The adsorption study showed that the ACNFs possessed a much higher adsorption capacity of 18.09 mg/g compared with the CNFs, which the amount adsorbed was achieved only at 2.7 mg/g. The optimum adsorption conditions that gave the highest percentage of 60% for nickel(II) ions removal were 50 mg of adsorbent dosage, 100 ppm of nickel(II) solution, pH 3, and a contact time of 60 min. The study demonstrated that the fabrication of ACNFs from PAN/lignin/PEG electrospun nanofibers have potential as adsorbents for the removal of heavy metal contaminants. [ABSTRACT FROM AUTHOR]

Coaxial electrospinning has been considered a straightforward and convenient method for producing hollow nanofibers. Therefore, the objective of this study was to develop hollow activated carbon nanofibers (HACNFs) for CO2 capture in order to reduce emissions of CO2 to the atmosphere and mitigate global warming. Results showed that the sacrificing core could be decomposed at carbonization temperatures above 900 °C, allowing the formation of hollow nanofibers. The average outer diameters of HACNFs ranged from 550 to 750 nm, with a shell thickness of 75 nm. During the carbonization stage, the denitrogenation reactions were significant, while in the CO2 activation process, the release of carbon oxides became prominent. Therefore, the CO2 activation could increase the percentages of N=C and quaternary N groups. The major nitrogen functionalities on most samples were O=C–NH and quaternary N. However, =C and quaternary N groups were found to be crucial in determining the CO2 adsorption performance. CO2 adsorption on HACNFs occurred due to physical adsorption and was an exothermic reaction. The optimal CO2 adsorption performance was observed for HACNFs carbonized at 900 °C, where 3.03 mmol/g (1 atm) and 0.99 mmol/g (0.15 atm) were measured at 25 °C. The degradation of CO2 uptakes after 10 adsorption−desorption cyclic runs could be maintained within 8.9%. [ABSTRACT FROM AUTHOR]

We developed free-standing nitrogen-doped carbon nanofiber (CNF) electrodes incorporating Co/CoOx nanoparticles (NPs) as a new cathode material for removing Acid Orange 7 (AO7; a dye for wool) from wastewater by the heterogeneous electro-Fenton reaction. We produced the free-standing N-doped CNF electrodes by electrospinning a polyacrylonitrile (PAN) and cobalt acetate solution followed by thermal carbonation of the cobalt acetate/PAN nanofibers under a nitrogen atmosphere. We then investigated electro-Fenton-based removal of AO7 from wastewater with the free-standing N-doped-CNFs-Co/CoOx electrodes, in the presence or not of Fe2+ ions as a co-catalyst. The electrochemical analysis showed the high stability of the prepared N-doped-CNF-Co/CoOx electrodes in electrochemical oxidation experiments with excellent degradation of AO7 (20 mM) at acidic to near neutral pH values (3 and 6). Electro-Fenton oxidation at 10 mA/cm2 direct current for 40 min using the N-doped-CNF-Co/CoOx electrodes loaded with 25 wt% of Co/CoOx NPs led to complete AO7 solution decolorization with total organic carbon (TOC) removal values of 92.4% at pH 3 and 93.3% at pH 6. The newly developed N-doped-CNF-Co/CoOx electrodes are an effective alternative technique for wastewater pre-treatment before the biological treatment. [ABSTRACT FROM AUTHOR]

Supercapacitors have been considered as one of the main energy storage devices. Recently, electrospun nanofibers have served as promising supercapacitor electrodes because of their high surface area, high porosity, flexibility, and resistance to aggregation. Here, we investigate the effects of electrospinning parameters and nickel precursors on the nanostructure of electrospun nickel oxide (NiO), as well as on their electrochemical performance as supercapacitor electrodes. In contrast to the case of using nickel nitrate, increasing the nickel acetate molar concentration maintains the flexible fibrous sheet morphology of the as-spun sample during the polycondensation and calcination of NiO. As a result, our flexible electrode of NiO nanofibers derived from nickel acetate (NiO-A) exhibits much better electrochemical performance values than that of nickel nitrate-derived NiO. To further improve the electrochemical storage performance, we combined NiO-A nanofibers with single-walled carbon nanotubes (CNTs) as a hybrid electrode. In both half-cell and full-cell configurations, the hybrid electrode displayed a higher and steadier areal capacitance than the NiO-A nanofibers because of the synergetic effect between the NiO-A nanofibers and CNTs. Altogether, this work demonstrates the potency of the hybrid electrodes combined with the electrospun NiO-A nanofibers and CNTs for supercapacitor applications. [ABSTRACT FROM AUTHOR]

In this work, we prepared network-structured carbon nanofibers using polyacrylonitrile blends (PAN150 and PAN85) with different molecular weights (150,000 and 85,000 g mol−1) as precursors through electrospinning/hot-pressing methods and stabilization/carbonization processes. The obtained PAN150/PAN85 polymer nanofibers (PNFs; PNF-73, PNF-64 and PNF-55) with different weight ratios of 70/30, 60/40 and 50/50 (w/w) provided good mechanical and electrochemical properties due to the formation of physically bonded network structures between the blended PAN nanofibers during the hot-processing/stabilization processes. The resulting carbonized PNFs (cPNFs; cPNF-73, cPNF-64, and cPNF-55) were utilized as anode materials for supercapacitor applications. cPNF-73 exhibited a good specific capacitance of 689 F g−1 at 1 A g−1 in a three-electrode set-up compared to cPNF-64 (588 F g−1 at 1 A g−1) and cPNF-55 (343 F g−1 at 1 A g−1). In addition, an asymmetric hybrid cPNF-73//NiCo2O4 supercapacitor device also showed a good specific capacitance of 428 F g−1 at 1 A g−1 compared to cPNF-64 (400 F g−1 at 1 A g−1) and cPNF-55 (315 F g−1 at 1 A g−1). The cPNF-73-based device showed a good energy density of 1.74 W h kg−1 (0.38 W kg−1) as well as an excellent cyclic stability (83%) even after 2000 continuous charge–discharge cycles at a current density of 2 A g−1. [ABSTRACT FROM AUTHOR]

Electrospun poly(acrylonitrile) (PAN) nanofibers are typical precursors of carbon nanofibers. During stabilization and carbonization, however, the morphology of pristine PAN nanofibers is not retained if the as-spun nanofiber mats are treated without an external mechanical force, since internal stress tends to relax, causing the whole mats to shrink significantly, while the individual fibers thicken and curl. Stretching the nanofiber mats during thermal treatment, in contrast, can result in fractures due to inhomogeneous stress. Previous studies have shown that stabilization and carbonization of PAN nanofibers electrospun on an aluminum substrate are efficient methods to retain the fiber mat dimensions without macroscopic cracks during heat treatment. In this work, we studied different procedures of mechanical fixation via metallic substrates during thermal treatment. The influence of the metallic substrate material as well as different methods of double-sided covering of the fibers, i.e., sandwiching, were investigated. The results revealed that sandwich configurations with double-sided metallic supports not only facilitate optimal preservation of the original fiber morphology but also significantly accelerate the carbonization process. It was found that unlike regularly carbonized nanofibers, the metal supports allow complete deoxygenation at low treatment temperature and that the obtained carbon nanofibers exhibit increased crystallinity. [ABSTRACT FROM AUTHOR]