Despite the widespread use of polyaniline as a pseudocapacitor material, the cycling stability and rate capability of polyaniline- based electrodes are of concern because of the structural instability caused by repeated volumetric swelling and shrinking during the charge/discharge process. Herein, nanofiber-structured polyaniline was synthesized onto activated carbon textiles to ensure the long-term stability and high-rate capability of pseudocapacitors. The nanoporous structures of polyaniline nanofibers and activated textile substrate enhanced the ion and electron transfer during charge/discharge cycles. The resulting pseudocapacitor electrodes showed high gravimetric, areal, and volumetric capacitance of 769 F g− 1, 2638 mF cm− 2, and 845.9 F cm− 3, respectively; fast charge/discharge capability of 92.6% capacitance retention at 55 mA cm− 2; and good longterm stability of 97.6% capacitance retention over 2000 cycles. Moreover, a symmetric supercapacitor based on polyaniline nanofibers exhibited a high energy of 21.45 Wh cm− 3 at a power density of 341.2 mW cm− 3 in an aqueous electrolyte.

Gold nanoparticles (Au NPs) decorated carbon nanofibers (CNFs) have been prepared by an electrospinning approach and then carbonized. The prepared Au-CNFs were employed to modifying a screen printed electrode (SPE) for simultaneous determination of ascorbic acid (AA), dopamine (DA) and uric acid (UA). Au NPs are uniformly dispersed on carbon nanofibers were confirmed by the structure and morphological studies. The modified electrodes were tested in cyclic voltammetry (CV), differential pulse voltammetry (DPV) and chronoamperometry (CA) to characterize their electrochemical responses. Compared to bare SPE, the Au-CNFs/SPE had a better sensing response to AA, DA, and UA. The electrochemical oxidation signal of AA, DA and UA are well separated into three distinct peaks with peak potential separation of 280 mV, 159 mV and 439 mV between AA-DA, DA-UA and AA-UA respectively in CV studies and the corresponding peak potential separation in DPV studies are 290 mV, 166 mV and 456 mV. The Au-CNFs/SPE has a wide linear response of AA, DA and UA in DPV analysis over the range of 5–40 μM ( R2 = 0.9984), 2–16 μM ( R2 = 0.9962) and 2–16 μM ( R2 = 0.9983) with corresponding detection limits of 0.9 μM, 0.4 μM and 0.3 μM at S/N = 3, respectively. The developed modified SPE based sensor exhibits excellent reproducibility, stability, and repeatability. The excellent sensing response of Au-CNFs could reveal to a promising approach in electrochemical sensor.

This study examines the effects of the TiO2 content and TiO2 position in the core or shell within tubular carbon nanofibers on the photocatalytic activity under visible light. Core–shell tubular carbon nanofiber composites whose cores are filled with TiO2 nanoparticles (PMTi(10)P) are fabricated through coaxial electrospinning and subsequent heat treatment. The PMTi(10)P composites with well-preserved TiO2 nanoparticles in the core part induce more oxygen vacancies, Ti3+ species, chemisorbed oxygen species, and anatase phases, significantly improving the photocatalytic performance. They act as photoelectron traps, allowing more photoelectrons and holes to participate in the photocatalytic reaction and extending the absorbance of TiO2 to the visible light region. The resulting PMTi(10)P photocatalyst exhibits excellent performance of 100% removal of methylene blue within 30 min and maintains nearly 100% removal of 15 ppm methylene blue over 10 regeneration cycles, indicating consistent and stable photocatalytic performance.

Cu2+/polyacrylonitrile composite fibers were prepared by electrospinning, and then Cu/carbon nanofibers (denoted as Cu/ CNF-X; X = Cu content, 0, 3, or 5 wt%) were formed by calcining them. The effects of Cu2+ content and carbonization temperature on the conductivity and electrothermal conversion of Cu/CNF-X were investigated. The results revealed that the conductivity and electrothermal properties of Cu/CNF-X improve with the increase in the Cu2+ content and carbonization temperature. When the carbonization temperature was 800, 900, or 1000 °C, the conductivity of Cu/CNF-5 (0.08, 0.68, or 2.48 S/cm, respectively) increased to 1.6, 1.5, or 1.6 times that of Cu/CNF-0, respectively. The highest instantaneous surface temperatures of Cu/CNF-5 calcined at 800, 900, and 1000 °C (36, 145, and 270.2 °C, respectively) increased by 4, 25.5, and 44.6 °C, respectively, compared with those of the corresponding Cu/CNF-0 samples (32, 120.3, and 225.6 °C, respectively). Thus, the addition of a small amount of Cu2+ effectively improved the conductivity and electrothermal conversion performance of Cu/CNF-X, which has potential application value in industrial products in the future.

The pursuit of sustainable and durable cementitious composites has led to a growing interest in alternative materials that can improve mechanical performance while reducing CO2 emissions. Nanomaterials, in particular, offer promising avenues due to their unique properties, including high surface area to volume ratio and increased reactivity. This study investigates the efficacy of Cellulose Nanofibers (CNF) in enhancing the durability of mortar exposed to sulfate attacks and alkali-silica reactions (ASR). Both MgSO4 and Na2SO4 solutions were employed to simulate sulfate attacks, while the role of CNF in mitigating ASR was also evaluated. Results indicate that CNF incorporation positively impacts the resistance of mortar against sulfate attacks and ASR, paving the way for eco-friendly and durable cement-based structures with extended service life.

Seawater evaporation and purification powered by solar energy are considered as a promising approach to alleviate the global freshwater crisis, and the development of photothermal materials with high efficiency is imminent. In this study, cellulose nanofiber (CNF)/MXene/Ni chain (CMN) aerogels were successfully synthesized by electrostatic force and hydrogen bond interaction force. CMN10 achieved a favorable evaporation rate as high as 1.85 kg m− 2 h− 1 in pure water, and the corresponding evaporation efficiency could be up to 96.04%. Even if it is applied to seawater with multiple interference factors, its evaporation rate can still be 1.81 kg m− 2 h− 1. The superior seawater evaporation activity origins from the promoted separation of photoexcited charges and photothermal conversion by the synergy of Ni chain and MXene, as well as the water transport channel supported by the 3D structure frame of CNF. Most importantly, CMN aerogel can maintain water vapor evaporation rates above 1.73 kg m− 2 h− 1 under extreme conditions such as acidic (pH 2) and alkaline (pH 12) conditions. In addition, various major ions, heavy metals and organic pollutants in seawater can be rejected by CMN10 during desalination, and the rejection rates can reach more than 99.69%, ensuring the purity of water resources after treatment. This work shows the great potential of CMN aerogel as a high-efficiency solar evaporator and low-cost photothermal conversion material. Cellulose nanofiber (CNF)/MXene/Ni chain (CMN) aerogels demonstrated high evaporation of water from sea water.

In order to increase the usability of PLA in tissue engineering, we tried to improve the hydrophobicity and low mechanical properties of PLA. The basic solutions were prepared by mixing 3, 5, and 7wt.% of PLA in a solution of chloroform and acetone in a volume ratio of 3:1. Several types of nanofiber mats were fabricated using a mixed solution in which 0.5, 1, and 3wt.% of PEO and PVAc, which are biodegradable polymers, were added to these solutions, respectively, through the SBS method. As a result, it was found that when the content of PEO increased, the diameter and surface state of nano fibers became uniform and the water contact angle significantly decreased, but it did not affect the tensile strength. In addition, the hydrophobicity of PLA was improved to hydrophilicity by mixing with PVAc, but the strain was greatly reduced.

Renewed interest in the reinforced carbon graphite composites has intrigued the community in the advanced materials fields. In this work, we present a simple carbon nanofibers reinforced carbon graphite composites synthetic method by incorporating mixture of coal tar pitch, synthetic graphite, pitch coke and the dispersion liquid of carbon nanofibers via liquid-phase mixing process. The impact of carbon nanofiber utilization on the microstructures and mechanical properties of carbon graphite composites are studied systematically. The covalent surface modification of carbon nanofibers effectively improves its microstructure and thereby promotes the carbon graphite composites’ dispersion behavior. We propose that a small amount of carbon nanofibers could promote the carbonization process of carbon graphite composites, facilitating the densification of carbon graphite composites and reducing the undesired open porosity. The amount of 0.7 wt % of carbon nanofiber concentration allows the enhancement of bend and compressive strength of carbon graphite composites up to 36.50 MPa and 60.46 MPa, increased by 167.9% and 146.9% compared with the pure carbon graphite composite, respectively. Our findings can be rationalized due to the improvement in the mechanical strength of carbon graphite composites could be attributed due to pull-out of carbon nanofibers from the matrix and bridging effect across the crack pores within the matrix.

Transition-metal phosphides (TMPs), a promising anode material for lithium-ion batteries (LIBs), are limited in application because of its serious volume effect in the cycle. In this work, a simple electrospinning strategy was proposed to restrict the grain size of CoP nanocrystals by nano-confined effect of carbon nanofibers with ligands. The addition of ligands not only could realize the uniform dispersion of CoP nanocrystals, but also strengthen the bond between the metals and carbon nanofibers. As a result, the CoP/CNF composite exhibits excellent lithium storage performance, and its reversible specific capacity could reach 1016.4 mAh g− 1 after 200 cycles at a current density of 200 mA g− 1. The research is anticipated to provide a new idea for the preparation of anode materials for lithium ion batteries.

In this work, a nanocomposite containing gold (Au) nanofibers decorated iron-metal–organic framework (Fe-MOF) was successfully synthesized for electrochemical detection of acetaminophen (AAP). The as-synthesized Au@Fe-MOF nanocomposite was confirmed by various characterization techniques. Morphological analysis showed that the Au nanofibers with an average size of less than 10 nm were dispersed on the Fe-MOF. Cyclic voltammetric analysis showed that the Au@Fe-MOF nanocomposite showed well-defined redox peaks with higher current than that of GCE and Fe-MOF. The Au@Fe-MOF/ GCE exhibited a linear range, sensitivity, and detection limit of 0.5–18 μM, 4.95 μM/μA/cm2, and 0.12 μM, respectively. The Au@Fe-MOF/GCE showed a very low response for the interference materials. The real sample analysis revealed that the Au@Fe-MOF/GCE showed good recovery towards the AAP in urine and paracetamol. Therefore, the developed sensor can be used for quality control of AAP.

In this article, nitrogen (N) doped porous carbon nanofibers (N-PCNF) were prepared by carbonization of polymer-silica nanocomposite precursor, and its application for heavy metal ion removal was demonstrated. Carbon–silica composite nanofibers were obtained by carbonization of electrospun polyacrylonitrile (PAN)-silica nanofiber composites. Subsequent selective etching of silica porogen produced porous carbon nanofibers (PCNF). It was revealed by surface characterization with X-ray photoelectron spectroscopy (XPS) that the surface of the PCNF was nitrogen-doped because N atom from cyanide group in PAN chains remained in the hexagonal carbon structure. The use of the obtained N-PCNF for heavy metal ion ( Hg2+) removal was demonstrated using a simple adsorption test apparatus and 5, 10, 15, 20-tetraphenylporphine tetrasulfonic acid (TPPS) as an indicator. The N-PCNF showed a removal efficiency of 96 and 99% in 10 and 120 min, respectively, indicating a maximum heavy metal ion adsorption capacity at pH 7.0. In addition, heavy metal ion adsorption behavior was also analyzed using common adsorption isotherms. This article provides important information for future research activities regarding control over hazardous substances.

Cost-effective and sustainable high-performance supercapacitor material was successfully prepared from cellulosic waste (Sapindus trifoliatus nut shells) biomass-derived activated carbon (CBAC) by physical activation method. The CBAC displays nanofiber morphology, high specific surface area (786 m2/ g), large pore volume (0.212 cm3 g− 1) which are evaluated using FESEM, BET and possessed excellent electrochemical behavior analyzed through various electrochemical methods. Moreover, the assembled symmetric CBAC//CBAC device exhibits high specific capacitance of 240.8 F g− 1 with current density of 0.2 A g− 1 and it is maintained to 65.6 F g− 1 at high current density of 2.0 A g− 1. In addition, the symmetric device delivers an excellent specific energy maximum of over 30 Wh kg− 1 at 400 W kg− 1 of specific power and excellent cycling stability in long term over 5000 cycles. The operation of the device was tested by light-emitting diode. Hence, CBAC-based materials pave way for developing large-scale, low-cost materials for energy storage device applications.

A carbon nanofiber was produced from the Areca catechu husk as a supercapacitor electrode, utilizing a chemical activation of potassium hydroxide (KOH) at different concentrations. One-stage integrated pyrolysis both carbonization and physical activation were employed for directly converting biomass to activated carbon nanofiber. The morphology structure, specific surface area, pore structure characteristic, crystallinity, and surface compound were characterized to evaluate the influence on electrochemical performance. The electrochemical performance of the supercapacitor was measured using cyclic voltammetry (CV) through a symmetrical system in 1 M H2SO4. The results show that the KOH-assisted or absence activation converts activated carbon from aggregate into a unique structure of nanofiber. The optimized carbon nanofiber showed the large specific surface area of 838.64 m2 g−1 with the total pore volume of 0.448 cm3 g−1, for enhancing electrochemical performance. Beneficial form its unique structural advantages, the optimized carbon nanofiber exhibits high electrochemical performance, including a specific capacitance of 181.96 F g−1 and maximum energy density of 25.27 Wh kg−1 for the power density of 91.07 W kg−1. This study examines a facile conventional route for producing carbon nanofiber from biomass Areca catechu husk in economical and efficient for electrode supercapacitor.

Tungsten disulfide (WS2), a typical 2D layerd structure, has received much attention as a pseudocapacitive material because of its high theoretical specific capacity and excellent ion diffusion kinetics. However, WS2 has critical limits such as poor long-term cycling stability owing to its large volume expansion during cycling and low electrical conductivity. Therefore, to increase the high-rate performance and cycling stability for pseudocapacitors, well-dispersed WS2 nanoparticles embedded in carbon nanofibers (WS2-CNFs), including mesopores and S-doping, are prepared by hydrothermal synthesis and sulfurizaiton. These unique nanocomposite electrodes exhibit a high specific capacity (159.6 F g−1 at 10 mV s−1), excellent high-rate performance (81.3 F g−1 at 300 mV s−1), and long-term cycling stability (55.9% after 1,000 cycles at 100 mV s−1). The increased specific capacity is attributed to well-dispersed WS2 nanoparticles embedded in CNFs that the enlarge active area; the increased high-rate performance is contributed by reduced ion diffusion pathway due to mesoporous CNFs and improved electrical conductivity due to S-doped CNFs; the long-term cycling stability is attributed to the CNFs matrix including WS2 nanoparticles, which effectively prevent large volume expansion.

The (Ga1-xZnx)(N1-xOx) solid solution is attracting extensive attention for photocatalytic water splitting and wastewater treatment owing to its narrow and controllable band gap. To optimize the photocatalytic performance of the solid solution, the key points are to decrease its band gap and recombination rate. In this study, (Ga1-xZnx)(N1-xOx) nanofibers with various Zn fractions are prepared by electrospinning followed by calcination and nitridation. The effect of the composition and crystallinity of electrospun oxide nanofibers on the morphology and optical properties of the obtained solid-solution nanofibers are systematically investigated. The results show that the final shape of the (Ga1-xZnx) (N1-xOx) material is greatly affected by the crystallinity of the oxide nanofibers before nitridation. The photocatalytic properties of (Ga1-xZnx)(N1-xOx) with different Ga:Zn atomic ratios are investigated by studying the degradation of rhodamine B under visible light irradiation.