Search Results (39)

Severe polysulfide shuttling and sluggish redox kinetics critically hinder lithium–sulfur (Li-S) battery commercialization. In this study, a multifunctional diatomite (DE)/TiO₂/MoS₂/N-doped carbon nanofiber (NCNF) composite separator was fabricated via hydrothermal synthesis, electrospinning, and carbonization. DE provides dual polysulfide suppression, encompassing microporous confinement and electrostatic repulsion. By integrating synergistic catalytic effects from TiO₂ and MoS₂ nanoparticles, which accelerate polysulfide conversion, and conductive NCNF networks, which facilitate rapid charge transfer, this hierarchical design achieves exceptional electrochemical performance: a 1245.6 mAh g⁻¹ initial capacity at 0.5 C and 65.94% retention after 200 cycles. This work presents a rational multi-component engineering strategy to suppress shuttle effects in high-energy-density Li-S batteries. Full article

The widespread adoption of sodium-ion batteries (SIBs) remains constrained by the inherent limitations of conventional anode materials, particularly their inadequate electronic conductivity, limited active sites, and pronounced structural degradation during cycling. To overcome these limitations, we propose a novel redox engineering approach to fabricate oxygen-vacancy-rich SnO₂ dots anchored on reduced graphene oxide (rGO), which are encapsulated within N-doped carbon nanofibers (denoted as ov-SnO₂/rGO@N-CNFs) through electrospinning and subsequent carbonization. The introduction of rich oxygen vacancies establishes additional sodium intercalation sites and enhances Na⁺ diffusion kinetics, while the conductive N-doped carbon network effectively facilitates charge transport and mitigates SnO₂ aggregation. Benefiting from the well-designed architecture, the hierarchical ov-SnO₂/rGO@N-CNFs electrode achieves remarkable reversible specific capacities of 351 mAh g⁻¹ after 100 cycles at 0.1 A g⁻¹ and 257.3 mAh g⁻¹ after 2000 cycles at 1.0 A g⁻¹ and maintains 177 mAh g⁻¹ even after 8000 cycles at 5.0 A g⁻¹, demonstrating exceptional long-term cycling stability and rate capability. This work offers a versatile design strategy for developing high-performance anode materials through synergistic interface engineering for SIBs. Full article

Lithium–sulfur batteries (LSBs) exhibit high theoretical specific capacities, abundant resource reserves, and low costs, making them promising candidates for next-generation lithium-ion batteries (LIBs). However, significant challenges, such as the shuttle effect and volume expansion, hinder their practical applications. To address these issues, this study introduces a unique intermediate layer comprising N-doped carbon nanofiber/TiO₂/diatomite (NCNF/TiO₂/DE) from the perspective of membrane modification. The intermediate layer comprises nitrogen-doped titanium dioxide/carbon nanofiber (NCNF/TiO₂) materials, with diatomite filling the fiber gaps. This forms a three-dimensional (3D) conductive network that provides ample space for sulfur volume expansion and numerous adsorption active sites, thereby accelerating electrolyte penetration and lithium-ion diffusion. These features collectively contribute to the outstanding electrochemical performance of the battery. At 0.1 C, the NCNF/TiO₂/DE-800-coated separator battery achieved a first-cycle discharge specific capacity of 1311.1 mAh g⁻¹, significantly higher than the uncoated lithium–sulfur battery (919.6 mAh g⁻¹). Under varying current densities, the NCNF/TiO₂/DE-800 material demonstrates good electrochemical reversibility and exhibits high lithium-ion diffusion rates and low charge-transfer resistance. Therefore, this study provides an advanced intermediate layer material that enhances the electrochemical performance of lithium–sulfur batteries. Full article

The advancement of cost-effective, high-performance catalysts for both electrochemical oxygen reduction reactions (ORRs) and oxygen evolution reactions (OERs) is crucial for the widespread implementation of metal–air batteries. In this research, we fabricated leaf-like N-doped carbon frames embedded with Co nanoparticles by pyrolyzing a ZIF-L/carbon nanofiber (ZIF-L/CNF) composite. Consequently, the optimized ZIF-L/CNF-700 catalyst exhibit exceptional catalytic activities in both ORRs and OERs, comparable to the benchmark 20 wt% Pt/C and RuO₂. Addressing the issue of diminished cycle performance in the Zn–air battery cycle process, further detailed investigations into the post-electrolytic composition reveal that both the carbon framework and Co nanoparticles undergo partial oxidation during both OERs and ORRs. Owing to the varying local pH on the catalyst surface due to the consumption and generation of OH⁻ by OERs and ORRs, after OERs, the product is reduced-size Co particles, while after ORRs, the product is outer-layer Co(OH)₂-enveloping Co particles. Full article

The development of conducting polymer incorporated with carbon materials-based electrochemical biosensors has been intensively studied due to their excellent electrical, optical, thermal, physical and chemical properties. In this work, a label-free electrochemical dopamine (DA) biosensor based on polyaniline (PANI) and its aminated derivative, i.e., poly(3-aminobenzylamine) (PABA), composited with functionalized multi-walled carbon nanotubes (f-CNTs), was developed to utilize a conducting polymer as a transducing material. The electrospun nanofibers of the composites were fabricated on the surface of fluorine-doped tin oxide (FTO)-coated glass substrate under the optimized condition. The PANI/f-CNTs and PABA/f-CNTs electrospun nanofibers were characterized by attenuated total reflectance–Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), which confirmed the existence of f-CNTs in the composites. The electroactivity of the electrospun nanofibers was investigated in phosphate buffer saline solution using cyclic voltammetry (CV) before being employed for label-free electrochemical detection of DA using differential pulse voltammetry (DPV). The sensing performances including sensitivity, selectivity, stability, repeatability and reproducibility of the fabricated electrospun nanofiber films were also electrochemically evaluated. The electrochemical DA biosensor based on PANI/f-CNTs and PABA/f-CNTs electrospun nanofibers exhibited a sensitivity of 6.88 µA·cm⁻²·µM⁻¹ and 7.27 µA·cm⁻²·µM⁻¹ in the linear range of 50–500 nM (R² = 0.98) with a limit of detection (LOD) of 0.0974 µM and 0.1554 µM, respectively. The obtained DA biosensor showed great stability, repeatability and reproducibility with precious selectivity under the common interferences, i.e., glucose, ascorbic acid and uric acid. Moreover, the developed electrochemical DA biosensor also showed the good reliability under detection of DA in artificial urine. Full article

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. Full article

The advantages of low cost, high theoretical capacity, and dependable safety of aqueous zinc ion hybrid supercapacitors (ZHSCs) enable their promising use in flexible and wearable energy storage devices. However, achieving extended cycling stability in ZHSCs is still challenged by the limited availability of carbon cathode materials that can effectively pair with zinc anode materials. Here, we report a method for synthesising heteroatom-doped carbon nanofibers using electrostatic spinning and metal-organic frameworks (specifically ZIF-8). Assembled Zn//ZPCNF-1.5 ZHSCs exhibited 193 mA h g⁻¹ specific capacity at 1 A g⁻¹ and 162.6 Wh kg⁻¹ energy density at 841.2 kW kg⁻¹. Additionally, the device showed an ultra-long cycle life, maintaining 98% capacity after 20,000 cycles. Experimental analysis revealed an increase in the number of pores and active sites after adding ZIF-8 to the precursor. Furthermore, N doping effectively enhanced Zn²⁺ ions chemical adsorption and improved Zn-ion storage performance. This work provides a feasible design strategy to enhance ZHSC energy storage capability for practical applications. Full article

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. Full article

Carbon materials with elusive 0D, 1D, 2D, and 3D nanostructures and high surface area provide certain emerging applications in electrocatalytic and photocatalytic CO₂ utilization. Since carbon possesses high electrical conductivity, it expels the photogenerated electrons from the catalytic surface and can tune the photocatalytic activity in the visible-light region. However, the photocatalytic efficiency of pristine carbon is comparatively low due to the high recombination of photogenerated carriers. Thus, supporting carbon materials, such as graphene, CNTs (Carbon nanotubes), g-C₃N₄, MWCNs (Multiwall carbon nanotubes), conducting polymers, and its other simpler forms like activated carbon, nanofibers, nanosheets, and nanoparticles, are usually combined with other metal and non-metal nanocomposites to increase the CO₂ absorption and conversion. In addition, carbon-based materials with transition metals and organometallic complexes are also commonly used as photocatalysts for CO₂ reduction. This review focuses on developing efficient carbon-based nanomaterials for the photoconversion of CO₂ into solar fuels. It is concluded that MWCNs are one of the most used materials as supporting materials for CO₂ reduction. Due to the multi-layered morphology, multiple reflections will occur within the layers, thus enhancing light harvesting. In particular, stacked nanostructured hollow sphere morphologies can also help the metal doping from corroding. Full article

The electrical conductivity (σ) and Seebeck coefficient (S) at temperatures from 40 °C to 100 °C of melt-processed polypropylene (PP) composites filled with 5 wt.% of industrial-grade carbon nanofibers (CNFs) is investigated. Transmission Electron Microscopy (TEM) of the two Pyrograf^® III CNFs (PR 19 LHT XT and PR 24 LHT XT), used in the fabrication of the PP/CNF composites (PP/CNF 19 and PP/CNF 24), reveals that CNFs PR 24 LHT XT show smaller diameters than CNFs PR 19 LHT XT. In addition, this grade (PR 24 LHT XT) presents higher levels of graphitization as deduced by Raman spectroscopy. Despite these structural differences, both Pyrograf^® III grades present similar σ (T) and S (T) dependencies, whereby the S shows negative values (n-type character). However, the σ (T) and S (T) of their derivative PP/CNF19 and PP/CNF24 composites are not analogous. In particular, the PP/CNF24 composite shows higher σ at the same content of CNFs. Thus, with an additionally slightly more negative S value, the PP/CNF24 composites present a higher power factor (PF) and figure of merit (zT) than PP/CNF19 composites at 40 °C. Moreover, while the σ (T) and S (T) of CNFs PR 19 LHT XT clearly drive the σ (T) and S (T) of its corresponding PP/CNF19 composite, the S (T) of CNFs PR 24 LHT XT does not drive the S (T) observed in their corresponding PP/CNF24 composite. Thus, it is inferred in PP/CNF24 composites an unexpected electron donation (n-type doping) from the PP to the CNFs PR 24 LHT XT, which could be activated when PP/CNF24 composites are subjected to that increase in temperature from 40 °C to 100 °C. All these findings are supported by theoretical modeling of σ (T) and S (T) with the ultimate aim of understanding the role of this particular type of commercial CNFs on the thermoelectrical properties of their PP/CNF composites. Full article

The sodium battery is one of the best energy storage technologies due to its abundant resource reserves and excellent energy storage ability. As a two-dimensional layered transition metal, molybdenum selenide (MoSe₂) has large interlayer spacing and a high theoretical capacity (470 mAh∙g⁻¹). Its structure is suitable for the negative electrode of sodium-ion batteries, with a large ionic radius and slow ion diffusion kinetics. However, it is difficult for the rate capability and cycling performance of MoSe₂ to meet practical needs due to a weak intrinsic electron transport ability and volume expansion during sodium absorption. The hydrothermal synthesis method was used to synthesize the MoSe₂ complex based on boron and nitrogen dual-doped 3D carbon fibers obtained from bacterial cellulose membranes (MoSe₂/N&B-BCM) for sodium batteries. Additionally, electrochemical analysis and experimental characterization were performed. In summary, the experimental analysis shows that MoSe₂/N&B-BCM has excellent conductivity, structural integrity, cyclability (328 mAh∙g⁻¹ after 100 cycles at a 0.5 c constant rate), and rate stability. Full article

A novel adsorbent of N-doped carbonized microspheres were developed from chitin (N-doped CM-chitin) for adsorption of Congo red (CR). The N-doped CM-chitin showed spherical shape and consisted of carbon nanofibers with 3D hierarchical architecture. There were many micro/nano-pores existing in N-doped CM-chitin with high surface area (455.703 m² g⁻¹). The N element was uniformly distributed on the carbon nanofibers and formed with oxidize-N graphitic-N, pyrrolic-N, and pyridinic-N. The N-doped CM-chitin showed excellent adsorption capability for CR and the maximum adsorption amount was approximate 954.47 mg g⁻¹. The π-π/n-π interaction, hydrogen-bond interactions, and pore filling adsorption might be the adsorption mechanisms. The adsorption of N-doped CM-chitin was considered as a spontaneous endothermic adsorption process, and which well conformed to the pseudo-second-order kinetic and Langmuir isotherm model. The N-doped CM-chitin exhibited an effective adsorption performance for dynamic CR water with good reusability. Therefore, this work provides new insights into the fabrication of a novel N-doped adsorbent from low-cost and waste biomasses. Full article

Owing to their high electrical conductivity, high surface area, low density, high thermal stability, and chemical stability, carbon nanofibers have been used in many fields, including energy storage, electromagnetic shielding, filtering, composites, sensors, and tissue engineering. Considering the environmental impact of petroleum-based polymers, it is vital to fabricate carbon nanofibers from environmentally-friendly materials using fast and safe techniques. PVA/PVP nanofibers were fabricated via centrifugal spinning and the effects of variations in the PVP content on the morphology and thermal properties of PVA/PVP-blend nanofibers were studied using SEM and DSC analyses. Moreover, the effects of carbonization conditions, including stabilization time, stabilization temperature, carbonization time, and carbonization temperature on the morphology and carbon yield, were investigated. Centrifugally spun PVA/PVP-based carbon nanofiber electrodes with an average fiber diameter around 300 nm are reported here for the first time. Furthermore, centrifugally spun PVA/PVP-based B, N, F-doped carbon nanofibers were fabricated by combining centrifugal spinning and heat treatment. Through B, N, F doping, CNFs demonstrated a high reversible capacity of more than 150 mAh/g in 200 cycles with stable cycling performance. Full article

A flexible N-doped carbon nanofiber membrane loaded with Nb and Ni nanoparticles (Nb/Ni@NC) was prepared using electrospinning technology and a subsequent thermal annealing method and used as a self-supporting anode material for lithium-ion batteries. The Nb/Ni@NC nanofiber membrane had excellent flexibility and could be folded and bent at will without fragmentation and wrinkling; the nanofibers also had a uniform and controllable morphology with a diameter of 300–400 nm. The electrochemical results showed that the flexible Nb/Ni@NC electrode could deliver a high discharge capacity of 378.7 mAh g⁻¹ after 200 cycles at 0.2 A g⁻¹ and an initial coulombic efficiency of 67.7%, which was higher than that of the pure flexible NC anode in contrast. Moreover, a reversible discharge capacity of 203.6 mAh g⁻¹ after 480 cycles at 1.0 A g⁻¹ was achieved by the flexible Nb/Ni@NC electrode with a capacity decay for each cycle of only 0.075%, which showed an excellent rate capability and cycling stability. Full article

The design of catalytic materials for NO_X removal by the selective catalytic reduction with NH₃ (NH₃-SCR) has been a focus of research in the field of waste gas treatment. In this work, pitch-based activated carbon fibers (ACFs) were impregnated with copper nitrate and cerium nitrate, and then the ACFs that were loaded with bimetallic nanoparticles (ACF@Cu/Ce) were obtained after the pyrolyzation and reduction were performed. Moreover, the ACF@Cu/Ce were furtherly treated through the chemical vapor deposition and NH₃ activation, through which the N-doped carbon nanofibers (N-CNFs) were grown on the surface of the ACFs. Thus, the catalytic material with a multi-dimensional metal nanoparticle distribution and nitrogen-rich network structure, namely the N-CNF/ACF@Cu/Ce, was constructed. In the NH₃-SCR reaction, the NO conversion of the N-CNF/ACF@Cu/Ce could be maintained at about 72~81% in a wide temperature window of 295~495 °C, which enabled the N-CNF/ACF@Cu/Ce to meet the requirements of the practical applications. Full article