Search Results (29)

As a sustainable alternative technology to the cost- and energy-intensive Haber–Bosch method, electrochemical nitrogen (N₂) reduction offers direct conversion of N₂ to NH₃ under ambient conditions. Direct use of noble metals or non-noble metals as electrocatalytic materials results in unsatisfactory electrocatalytic properties because of their low electrical conductivity and stability. Herein, three-dimensional flexible carbon nanofiber (CNF/TiO₂@CoS) nanostructures were prepared on the surface of CNF by using electrospinning, a hydrothermal method, and in situ growth. We investigated the behavior of CNFs/TiO₂@CoS as an electrocatalytic material in 0.1 M sodium sulfate. The highest ammonia yield of the material was 4.61 × 10⁻¹¹ mol s⁻¹ cm⁻² at −0.45 V vs. RHE, and the highest Faraday efficiency, as well as superior long-term durability, was 8.3% at −0.45 V vs. RHE. This study demonstrates the potential of firecracker-shaped nanofiber templates for loading varied noble metals or non-noble metals as a novel development of hybrid composites for electrocatalytic nitrogen reduction. Full article

As an important component of LIBs, the electrode material plays a crucial role in determining the lithium (Li) storage performance in LIBs. In this study, MoS₂ nano-flowers were synthesized using a one-pot hydrothermal method. The resulting MoS₂ nano-flower, along with PAN, were used as raw materials for electrospinning. After annealing treatment, MoS₂/(carbon nanofibers) CNFs nano-composites coated with carbon fibers were formed. The CNFs coating exhibited electrical conductivity and enhanced structural stability of the MoS₂ due to the stabilizing effect of the carbon fibers. Additionally, electrochemical tests, including CV and GCD, indicated that the optimal capacity and cycling stability were achieved when the MoS₂ content was 10%. The results indicated that the charge/discharge capacity of MoS₂/CNFs-10% at a current density of 100 mA/g was ~650 mAh/g. After the cycling current returned to 100 mA/g, the current recovery was ~600 mAh/g, thereby indicating outstanding cycling stability. Accordingly, our fabrication technique and new insight could both widen design strategy of multicomponent composite electrode materials and promote the practical applications of the latest emerging transition metal sulfides in next-generation high-performance lithium-ion 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

Lithium metal is regarded as ideal anode material due to its high theoretical specific capacity and low electrode potential. However, the uncontrollable growth of lithium dendrites seriously hinders the practical application of lithium-metal batteries (LMBs). Among various strategies, carbon nanofiber materials have shown great potential in stabilizing the lithium-metal anode (LMA) due to their unique functional and structural characteristics. Here, the latest research progress on carbon nanofibers (CNFs) for LMA is systematically reviewed. Firstly, several common preparation techniques for CNFs are summarized. Then, the development prospects, strategies and the latest research progress on CNFs for dendrite-free LMA are emphatically introduced from the perspectives of neat CNFs and CNF-based composites. Finally, the current challenges and prospects of CNFs for stabilizing LMA are summarized and discussed. These discussions and proposed strategies provide new ideas for the development of high-performance LMBs. Full article

Carbon nanomaterials are promising microwave catalytic materials due to their abundant inhomogeneous interfaces capable of producing ideal interfacial polarization and multiple relaxation, which are favorable for microwave attenuation and dissipation. However, the microwave absorption performance of carbon materials is not ideal in practical applications due to poor impedance matching and single dielectric loss. To solve this problem, a ternary system of “carbon-magnetic” Ni@SiC/CNFs (C/Ni, C/SiC) composites was synthesized by electrostatic spinning, and they efficiently degraded methylene blue under microwave radiation. The results imply that the catalyst Ni@SiC/CNFs with a double-shell structure gave a 99.99% removal rate in 90 s for the degradation of methylene blue under microwave irradiation, outperforming the C/Ni and C/SiC and most other reported catalysts in similar studies. On the one hand, the possible mechanism of the methylene blue degradation should be ascribed to the fact that the double-shell structure increases the polarization source of the material, resulting in excellent microwave absorption properties; and on the other, the in situ generation of ·OH and O₂⁻ active species under microwave radiation and the synergistic coupling effect of metal plasma greatly improved the degradation efficiency of methylene blue. The findings of this study could provide a valuable reference for the green degradation of industrial dye wastewater and its sustainable development process. Full article

This study explores a simple method of fabricating hybrid supercapacitor electrodes, which could potentially broaden the application of this technology. The method involves electrospinning a uniform solution of Matrimid/Metal−Organic Polyhedra 18 (MOP−18) followed by carbonization at a relatively low temperature of 700 °C in air, rather than in an inert atmosphere, to create free−standing, redox−active hybrid supercapacitor electrodes. Additionally, the synthesis procedure requires no stabilization or activation steps, which enhances the cost effectiveness of the synthesized electrode materials. The resulting C/CuO composite was used as the working electrode, with a polyacrylonitrile (PAN)/Poly(methyl methacrylate) (PMMA) carbon nanofiber (CNF) electrode as the counter and 6 M KOH as the electrolyte in a T−cell configuration. The cell performance and redox activity were evaluated using cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), electrochemical impedance spectroscopy (EIS) and cycling stability tests. Additionally, the physical and chemical structures of the electrode materials were assessed using X−ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron spectroscopy (TEM), X−ray diffractometry (PXRD), surface area analysis and other characterization techniques. The electrode material demonstrated a specific capacitance of up to 206 F/g. Supercapacitors utilizing this material display an energy density of 10.3 Wh/kg (active material) at a current density of 1 A/g in electrochemical testing. Full article

Metal–organic frame (MOF) materials may have the advantages of a regular pore structure, large porosity, and large specific surface area, which could provide better catalytic activity, but they have some disadvantages in electrocatalysis. In contrast, carbon nanofibers (CNFs) prepared by electrospinning methods have good conductivity and stability. Therefore, this research aimed to generate MOF/CNFs composite materials to improve the electrochemical properties of MOF materials and apply them to the field of electrochemical sensing. This experiment was based on the preparation of straight unidirectional CNFs by an electrospinning method at 2000 RPM. The original method of preparing zeolitic imidazolate frameworks (ZIF-8) was improved and ZIF-8 was uniformly dispersed on the surface of CNFs to form a ZIF-8/CNF composite with a fiber diameter of about 0.10 to 0.35 µm. The specific surface area of the CNFs was about 42.28 m²/g, while that of the ZIF-8/CNF composite was about 999.82 m²/g. The specific surface area of the ZIF-8/CNF composite was significantly larger than that of CNFs. The GCE/ZIF-8/CNF electrode had an excellent electrochemical reaction, with an oxidation peak at about 216 μA, which proved that the ZIF-8/CNF composite material would have good catalytic activity and excellent electrochemical properties for the detection of nitrofurazone compared to other modified electrodes. Full article

Supercapacitors (SCs) are widely used in energy storage devices due to their superior power density and long cycle lifetime. However, the limited energy densities of SCs hinder their industrial application to a great extent. In this study, we present a new combination of metallic phosphide–carbon composites, synthesized by directly carbonizing (Ni_1−xCo_x)₅TiO₇ nanowires via thermal chemical vapor deposition (TCVD) technology. The new method uses one-dimensional (1D) (Ni_1−xCo_x)TiO₇ nanowires as precursors and supporters for the in situ growth of intertwined porous CNF microspheres. These 1D nanowires undergo microstructure transformation, resulting in the formation of CoNiP nanoparticles, which act as excellent interconnected catalytic nanoparticles for the growth of porous 3D CNF microspheres. Benefiting from the synergistic effect of a unique 1D/3D structure, the agglomeration of nanoparticles can effectively be prevented. The resulting CNF microspheres exhibit an interconnected conductive matrix and provide a large specific surface area with abundant ion/charge transport channels. Consequently, at a scanning rate of 10 mV s⁻¹, its specific capacitance in 1.0 M Na₂SO₄ + 0.05 M Fe(CN)₆^3−/4− aqueous solution is as high as 311.7 mF cm⁻². Furthermore, the CoNiP@CNFs composite film-based symmetrical SCs show an ultrahigh energy density of 20.08 Wh kg⁻¹ at a power density of 7.20 kW kg⁻¹, along with outstanding cycling stability, with 87.2% capacity retention after 10,000 cycles in soluble redox electrolytes. This work provides a new strategy for designing and applying high-performance binary transition metal phosphide/carbon composites for next-generation energy storage devices. Full article

The extensive use of antibiotics has rapidly spread antibiotic resistance, which poses significant health risks to humans. Unfortunately, despite this pressing issue, there is still a lack of a reliable on-site detection method for the residues of antibiotics, such as nilutamide (Nlu). Consequently, there is an urgent need to develop and perfect such a detection method to effectively monitor and control antibiotic residues. In this study, the hydrothermal development of copper-metal-organic framework (Cu-MOF) polyhedrons on the functionalized carbon nanofiber (f-CNF) matrix allowed for the detection of Nlu in biological liquids via a sensitive amperometry technique. Further electrochemical detection of Nlu took place with the cyclic voltammetry (CV) technique Cu-MOF/f-CNF. Analytical and spectroscopic approaches were used to confirm the successful synthesis of Cu-MOF/f-CNF. The prepared material was decorated on the surface of GCE and performed as an electrochemical Nlu sensor, with a broad linear range of 0.01 to 141.4 μM and 2 nM as a lower limit of detection. In addition, the composites had a large surface area and many dedicated sites, which improved electrocatalysis. In practical applications, Cu-MOF/f-CNF/GCE provides a novel strategy for improving electrochemical activity by measuring Nlu concentrations in biological samples. Full article

The development of effective catalysts for the pyrolysis of light hydrocarbons with the production of carbon nanomaterials represents a relevant direction. In the present work, the influence of copper addition on performance of a self-dispersed Ni-catalyst and structural features of the obtained carbon nanofibers (CNFs) was studied. The precursors of Ni and Ni-Cu catalysts were prepared by activation of metal powders in a planetary mill. During contact with the C₂H₄/H₂ reaction mixture, a rapid disintegration of the catalysts with the formation of active particles catalyzing the growth of CNFs has occurred. The kinetics of CNF accumulation during ethylene decomposition on Ni- and Ni-Cu catalysts was studied. The effect of temperature on catalytic performance was explored and it was shown that introduction of copper promotes 1.5–2-fold increase in CNFs yield in the range of 525–600 °C; the maximum CNFs yield (100 g/g_cat and above, for 30-min reaction) is reached on Ni-Cu-catalyst at 575–600 °C. A comparative analysis of the morphology and structure of CNF was carried out using electron microscopy methods. The growth mechanism of carbon filaments in the shape of “railway crossties” on large nickel crystals (d > 250 nm) was proposed. It was found that the addition of copper leads to a decrease in the bulk density of the carbon product from 40–60 to 25–30 g/L (at T = 550–600 °C). According to the low-temperature nitrogen adsorption data, specific surface area (SSA) of CNF samples (at T < 600 °C) lies in the range of 110–140 m²/g, regardless of the catalyst composition; at T = 600 °C the introduction of copper contributed to an increase in the specific surface of CNF by 100 m²/g. Full article

The unique physical and chemical properties of composite materials based on carbon nanofibers (CNFs) makes them attractive to scientists and manufacturers. One promising method to produce CNFs is catalytic chemical vapor deposition (CCVD). In the present work, a method based on carbon erosion (CE) of bulk microdispersed Ni-Cu alloys has been proposed to prepare efficient catalysts for the synthesis of CNF-based composites. The initial Ni-Cu alloys were obtained by mechanochemical alloying (MCA) of metallic powders in a planetary mill. The effect of MCA duration on the phase composition of Ni-Cu samples was studied by X-ray diffraction analysis and temperature-programmed reduction in hydrogen. It has been also revealed that, during such stages as heating, reduction, and short-term exposure to the reaction mixture (C₂H₄/H₂/Ar) at 550 °C, the formation of a Ni-based solid solution from the initial Ni-Cu alloys takes place. The early stages of the CE process were monitored by transmission electron microscopy combined with energy-dispersive X-Ray analysis. It was found that the composition of the catalytic particles is identical to that of the initial alloy. The morphological and structural features of the prepared Ni-Cu-CNF composites were studied by scanning and transmission electron microscopies. The textural characteristics of the composites were found to be dependent on the reaction time. Full article

Herein, unique three-dimensional (3D) hierarchically structured carbon nanofiber (CNF)/metal oxide/conducting polymer composite materials were successfully synthesized by combinations of various experimental methods. Firstly, base CNFs were synthesized by carbonization of electrospun PAN/PVP fibers to attain electric double-layer capacitor (EDLC) characteristics. To further enhance the capacitance, tin oxide (SnO₂) and iron oxide (Fe₂O₃) were coated onto the CNFs via facile hydrothermal treatment. Finally, polypyrrole (PPy) was introduced as the outermost layer by a dispersion polymerization method under static condition to obtain 3D-structured CNF/SnO₂/PPy and CNF/Fe₂O₃/PPy materials. With each synthesis step, the morphology and dimension of materials were transformed, which also added the benign characteristic for supercapacitor application. For the practical application, as-synthesized CNF/SnO₂/PPy and CNF/Fe₂O₃/PPy were applied as active materials for supercapacitor electrodes, and superb specific capacitances of 508.1 and 426.8 F g⁻¹ (at 1 A g⁻¹) were obtained (three-electrode system). Furthermore, an asymmetric supercapacitor (ASC) device was assembled using CNF/SnO₂/PPy as the positive electrode and CNF/Fe₂O₃/PPy as the negative electrode. The resulting CNF/SnO₂/PPy//CNF/Fe₂O₃/PPy device exhibited excellent specific capacitance of 101.2 F g⁻¹ (at 1 A g⁻¹). Notably, the ASC device displayed a long-term cyclability (at 2000 cycles) with a retention rate of 81.1%, compared to a CNF/SnO₂//CNF/Fe₂O₃ device of 70.3% without an outermost PPy layer. By introducing the outermost PPy layer, metal oxide detachment from CNFs were prevented to facilitate long-term cyclability of electrodes. Accordingly, this study provides an effective method for manufacturing a high-performance and stable supercapacitor by utilizing unique 3D hierarchical materials, comprised of CNF, metal oxide, and conducting polymer. Full article

The development of new heterogeneous Pt-containing catalysts has retained its relevance over the past decades. The present paper describes the method to produce metal–carbon composites, Pt_1−xNi_x/CNF, with an adjustable Pt/Ni ratio. The composites represent Pt_1−xNi_x (x = 0.0–1.0) nanoparticles embedded within a structure of carbon nanofibers (CNF). The synthesis of the composites is based on a spontaneous disintegration of Pt_1−xNi_x alloys in an ethylene-containing atmosphere with the formation of CNF. The initial Pt_1−xNi_x alloys were prepared by thermolysis of multicomponent precursors. They possess a porous structure formed by fragments of 100–200 nm. As was shown by X-ray diffraction analysis, the crystal structure of the alloys containing 0–30 and 60–100 at.% Ni corresponds to a fcc lattice based on platinum (Fm-3m), while the Pt_0.50Ni_0.50 sample is an intermetallic compound with the tetragonal structure (P4/mmm). The impact of the Ni content in the Pt_1−xNi_x samples on their activity in ethylene decomposition was studied as well. As was revealed, the efficiency of Pt_1−xNi_x alloys in this process increases with the rise of Ni concentration. The composite samples were examined in an electrochemical hydrogen evolution reaction. The synthesized Pt_1-xNi_x/CNF composites demonstrated superior activity if compared with the Pt/Vulcan commercial catalyst. Full article

Lithium-Sulfur batteries (LSBs) are one of the most promising next-generation batteries to replace Li-ion batteries that power everything from small portable devices to large electric vehicles. LSBs boast a nearly five times higher theoretical capacity than Li-ion batteries due to sulfur’s high theoretical capacity, and LSBs use abundant sulfur instead of rare metals as their cathodes. In order to make LSBs commercially viable, an LSB’s separator must permit fast Li-ion diffusion while suppressing the migration of soluble lithium polysulfides (LiPSs). Polyolefin separators (commonly used in Li-ion batteries) fail to block LiPSs, have low thermal stability, poor mechanical strength, and weak electrolyte affinity. Novel nanofiber (NF) separators address the aforementioned shortcomings of polyolefin separators with intrinsically superior properties. Moreover, NF separators can easily be produced in large volumes, fine-tuned via facile electrospinning techniques, and modified with various additives. This review discusses the design principles and performance of LSBs with exemplary NF separators. The benefits of using various polymers and the effects of different polymer modifications are analyzed. We also discuss the conversion of polymer NFs into carbon NFs (CNFs) and their effects on rate capability and thermal stability. Finally, common and promising modifiers for NF separators, including carbon, metal oxide, and metal-organic framework (MOF), are examined. We highlight the underlying properties of the composite NF separators that enhance the capacity, cyclability, and resilience of LSBs. Full article

The application of transition metal oxides/hydroxides in energy storage has long been studied by researchers. In this paper, the core-shell CNFs@Ni(OH)₂/NiO composite electrodes were prepared by calcining carbon nanofibers (CNFs) coated with Ni(OH)₂ under an N₂ atmosphere, in which NiO was generated by the thermal decomposition of Ni(OH)₂. After low-temperature carbonization at 200 °C, 250 °C and 300 °C for 1 h, Ni(OH)₂ or/and NiO existed on the surface of CNFs to form the core-shell composite CNFs@Ni(OH)₂/NiO-X (X = 200, 250, 300), in which CNFs@Ni(OH)₂/NiO-250 had the optimal electrochemical properties due to the coexistence of Ni(OH)₂ and NiO. Its specific capacitance could reach 695 F g⁻¹ at 1 A g⁻¹, and it still had 74% capacitance retention and 88% coulomb efficiency after 2000 cycles at 5 A g⁻¹. Additionally, the asymmetric supercapacitor (ASC) assembled from CNFs@Ni(OH)₂/NiO-250 had excellent energy storage performance with a maximum power density of 4000 W kg⁻¹ and a maximum functional capacity density of 16.56 Wh kg⁻¹. Full article