Search Results (126)

This study employed the solid-state method to prepare perovskite-type high-entropy oxide materials La(Co_0.2Cr_0.2Fe_0.2Mn_0.2Ni_0.2)O₃ and La(Co_0.2Cr_0.2Ni_0.2Ga_0.2Ge_0.2)O₃ with equimolar ratios at the B-site and explored the effects of sintering temperature on the phase structure and electrochemical properties of high-entropy oxide ceramics. The results show that after sintering at 1300$°\mathrm{C}$, both samples exhibit orthorhombic perovskite structures. Both have a relative density of >97%, while La(Co_0.2Cr_0.2Ni_0.2Ga_0.2Ge_0.2)O₃ has a significantly larger grain size. Using these materials as electrodes, the cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) results indicate that the working electrode made of La(Co_0.2Cr_0.2Ni_0.2Ga_0.2Ge_0.2)O₃ shows higher oxidation reaction activity in CV measurements and achieved a specific capacitance of 74.3 F/g at a current density of 1 A/g in GCD measurements, which still maintained 73% of its initial specific capacitance (54.3 F/g) when the current density was increased to 10 A/g. Its capacitance retention rate is 10 percentage points higher than that of La(Co_0.2Cr_0.2Fe_0.2Mn_0.2Ni_0.2)O₃ at high current densities, demonstrating superior rate performance. Full article

Different composites of manganese oxides (Mn_xO_y) containing sodium (Na) and silver (Ag) were synthesized by the molten salt method with various MnSO₄·H₂O/NaNO₃ (M/N) molar ratios (between 0.3 and 1), and different AgNO₃ and NaOH amounts, obtaining two groups of materials: without the addition of AgNO₃ (labeled as M/N) and with AgNO₃ (labeled as M/N-A). As for the M/N group, the system with the lowest M/N ratio yielded the highest specific capacitance (160.5 F ${\mathrm{g}}^{-1}$), attributed to the formation of Mn₃O₄ and sodium birnessite. In the M/N-A group, the 1 M/N-0.5A system, produced with M/N ratio of 1 and addition of 0.5 g of AgNO₃, exhibited the highest specific capacitance (229.1 F ${\mathrm{g}}^{-1}$), associated with the presence of Mn₂O₃, silver hollandite, and metallic Ag. This enhancement is attributed to the synergistic effects of Na⁺ and Ag⁺ ions, which improve charge transfer kinetics and electrochemical performance. It was demonstrated that decreasing the MnSO₄·H₂O/NaNO₃ ratio in the M/N group and increasing AgNO₃ content in the M/N-A group enhances the electrochemically active surface area. Galvanostatic charge–discharge (GCD) and electrochemical impedance spectroscopy (EIS) techniques confirmed that the 1 M/N-0.5A system exhibited the best performance, characterized by high energy retention, stable cycling behavior, and low capacitance dispersion, indicating its strong potential as an active material for pseudocapacitor applications. Full article

Environmental sustainability and responsible resource utilization are critical global challenges. In this work, we present a sustainable and circular-economy-based approach for synthesizing CuFe₂O₄ nanoparticles by directly utilizing copper oxide minerals sourced from Chilean mining operations. Copper sulfate (CuSO₄) was extracted from these minerals through acid leaching and used as a precursor for nanoparticle synthesis via both chemical co-precipitation and microwave-assisted methods. The influence of different precipitating agents—NaOH, Na₂CO₃, and NaF—was systematically evaluated. XRD and FESEM analyses revealed that NaOH produced the most phase-pure and well-dispersed nanoparticles, while NaF resulted in secondary phase formation. The microwave-assisted method further improved particle uniformity and reduced agglomeration due to rapid and homogeneous heating. Electrochemical characterization was conducted to assess the suitability of the synthesized CuFe₂O₄ for supercapacitor applications. Cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) measurements confirmed pseudocapacitive behavior, with a specific capacitance of up to 1000 F/g at 2 A/g. These findings highlight the potential of CuFe₂O₄ as a low-cost, high-performance electrode material for energy storage. This study underscores the feasibility of converting primary mined minerals into functional nanomaterials while promoting sustainable mineral valorization. The approach can be extended to other critical metals and mineral residues, including tailings, supporting the broader goals of a circular economy and environmental remediation. Full article

The synthesis of CoZn-MOF was accomplished via a simple hydrothermal method. The characterization of the synthesized materials was performed using X-ray diffraction (XRD), providing a thorough understanding of their structure and content. Subsequently, carbon nanotubes (CNTs) underwent three different pretreatment procedures prior to their application as an anode in a supercapacitor (SC) arrangement, with CoZn-MOF functioning as the cathode. The use of CNTs as electrode material led to an inherent improvement in conductivity and an intrinsic increase in the specific capacitance of the supercapacitor. Galvanostatic charge–discharge measurements of the three cells with different electrodes proved that the supercapacitor based on the CNT (acetic acid)//CoZn-MOF exhibited a capacity of 0.2285 F/g, a moderate energy density of 0.1944 Whkg⁻¹ at a power density of 26.48 Wkg⁻¹ as compared to the other two supercapacitors (CNT (nitric acid)//CoZn-MOF and CNT (unprocessed)//CoZn-MOF). This study utilized the advantages of carbon nanotubes in supercapacitor electrodes and examined the impact of CNT pretreatment. Full article

Boron nitride nanostructures (BNNs), including nanotubes, nanosheets, and nanoribbons, are renowned for their exceptional thermal stability, chemical inertness, mechanical strength, and high surface area, making them suitable for advanced material applications. Metal–organic frameworks (MOFs), characterized by their porous crystalline structures, high surface area, and tunable porosity, have emerged as excellent candidates for gas adsorption and storage applications, particularly in the context of hydrogen. This paper explores the synthesis and properties of BNNs and MOFs, alongside the innovative approach of integrating BNNs within MOFs to create composite materials with synergistic properties. The integration of BNNs into MOFs enhances the overall thermal and chemical stability of the composite while improving hydrogen sensing and storage performance. Various synthesis methods for both BNNs and MOFs are discussed, including chemical vapor deposition, solvothermal synthesis, and in situ growth, with a focus on their scalability and reproducibility. Furthermore, the mechanisms underlying hydrogen sensing and storage are examined, including physisorption, chemisorption, charge transfer, and work function modulation. Electrochemical characterization techniques, such as cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic charge–discharge, are used to analyze the performance of BNN-MOF systems in hydrogen storage and sensing applications. These methods offer insights into the material’s electrochemical behavior and its potential to store hydrogen efficiently. Potential industrial applications of BNN-MOF composites are highlighted, particularly in fuel cells, hydrogen-powered vehicles, safety monitoring in hydrogen production and distribution networks, and energy storage devices. The integration of these materials can contribute significantly to the development of more efficient hydrogen energy systems. Finally, this study outlines key recommendations for future research, which include optimizing synthesis techniques, improving the hydrogen interaction mechanisms, enhancing the stability and durability of BNN-MOF composites, and performing comprehensive economic and environmental assessments. BNN-MOF composites represent a promising direction in the advancement of hydrogen sensing and storage technologies, offering significant potential to support the transition toward sustainable energy systems and hydrogen-based economies. Full article

This study presents a novel approach to the development of high-performance supercapacitors through 3D printing technology. We synthesized a composite material consisting of silver-doped reduced graphene oxide (rGO) and dodecylbenzenesulfonic acid (DBSA)-doped polyaniline (PANI), which was further blended with polylactic acid (PLA) for additive manufacturing. The composite was extruded into filaments and printed into circular disc electrodes using fused deposition modeling (FDM). These electrodes were assembled into symmetric supercapacitor devices with a solid-state electrolyte. Electrochemical characterization, including cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) tests, demonstrated considerable mass-specific capacitance values of 136.2 F/g and 133 F/g at 20 mV/s and 1 A/g, respectively. The devices showed excellent stability, retaining 91% of their initial capacitance after 5000 cycles. The incorporation of silver nanoparticles enhanced the conductivity of rGO, while PANI-DBSA improved electrochemical stability and performance. This study highlights the potential of combining advanced materials with 3D printing to optimize energy storage devices, offering a significant advancement over traditional manufacturing methods. Full article

Carbon fiber is known for being lightweight and adaptable, making it useful for various current and future applications. However, to broaden the use of carbon fibers beyond niche applications, production costs must be lowered. A potential approach to achieving this is by using more affordable raw materials, such as lignin, which is renewable, cost-effective, and widely available compared with the materials commonly used in industry today. This study explores the impact of metal ions on the quality of carbon fiber derived from lignin, focusing on its mechanical and electrochemical properties and morphology. The effect of a specific metal ion (Ni(NO₃)₂·6H₂O) was examined by incorporating it into the spinning solution. The carbonization stage of the fiber was conducted at temperatures of 800, 900, and 1000 °C in an inert atmosphere. Scanning electron microscopy (SEM) analysis showed no defects or damage in any of the fibers. Therefore, it was concluded that moderate concentrations of Ni²⁺ ions in the fibers do not influence the stabilization or carbonization processes, thus leaving the mechanical properties of the final carbon fiber unchanged. These carbon nanofibers were also tested as a sustainable alternative to the non-renewable materials used in electrodes for energy storage and conversion devices, such as supercapacitors. Electrochemical performance was assessed in a 6 M KOH solution using a two-electrode cell configuration. Galvanostatic charge–discharge tests were performed at different current densities (0.1, 0.25, 0.5, 1.0, and 2.0 A g⁻¹). The specific capacitance of the carbon nanofibers was determined from CVA data at various scan rates: 5, 10, 20, 40, 80, and 160 mV s⁻¹. The results indicated that at 0.1 A g⁻¹, the capacitance reached 108 F g⁻¹, and at a scan rate of 5 mV s⁻¹, it was 91 F g⁻¹. The innovation of this work lies in its use of lignin, a renewable and widely available material, to produce carbon fibers, reducing costs compared with traditional methods. Additionally, the incorporation of nickel ions enhances the electrochemical properties of the fibers for supercapacitor applications without compromising their mechanical performance. Full article

This study investigates nitrogen-doped carbon synthesis and electrochemical properties as electrode material for energy storage devices, an additional focus of the work is on the electrochemical exfoliation synthesis of nitrogen-doped carbon using various precursors and doping methods. The physical properties of the synthesized sample are characterized using X-ray photoelectron spectroscopy, scanning electron microscopy, and Raman spectroscopy. The electrochemical properties of the N-doped carbons are studied using cyclic voltammetry and galvanostatic charge-discharge cycling. Finally, the work explores the potential application of the N-doped carbons as electrode material for energy storage devices, such as supercapacitors. The results show that N-doped carbons exhibit electrochemical performance superior to that of graphene oxide, with higher electrical capacitance. The results demonstrate the potential of N-doped carbons as high-performance electrode materials for electrochemical energy storage applications. This paper aims to explain the advantages of N-doping in carbon materials more precisely in graphene and the use of these materials in creating electrodes for application in supercapacitors and batteries. Full article

Poly(3,4-ethylenedioxythiophene) (PEDOT) and PEDOT-functionalized carbon nanoparticles (f-CNPs) were synthesized by in situ chemical oxidative polymerization and pyrolysis methods. f-CNP-PEDOT nanocomposites were prepared by varying the concentration of PEDOT from 1 to 20% by weight (i.e., 1, 2.5, 5, 10, and 20 wt%). Several characterization techniques, such as field-emission scanning electron microscopy (FESEM), attenuated total reflectance-Fourier transform infrared (ATR-FTIR), X-ray diffraction (XRD), N₂ Brunauer–Emmett–Teller (BET) and Barrett–Joyner–Halenda (BJH) analyses, as well as cyclic voltammetry (CV), galvanostatic charge discharge (GCD), and electrochemical impedance spectroscopy (EIS), were applied to investigate the morphology, the crystalline structure, the N₂ adsorption/desorption capability, as well as the electrochemical properties of these new synthesized nanocomposite materials. FESEM analysis showed that these nanocomposites have defined porous structures, and BET surface area analysis showed that the standalone f-CNP exhibited the largest surface area of 801.6 m²/g, whereas the f-CNP-PEDOT with 20 wt% exhibited the smallest surface area of 116 m²/g. The BJH method showed that the nanocomposites were predominantly mesoporous. CV, GCD, and EIS measurements showed that f-CNP functionalized with 5 wt% PEDOT had a higher capacitive performance compared to the individual f-CNPs and PEDOT constituents, exhibiting an extraordinary specific capacitance of 258.7 F/g, at a current density of 0.25 A/g, due to the combined advantage of enhanced electrochemical activity induced by PEDOT doping, and highly developed porosity of f-CNPs. Symmetric aqueous supercapacitor devices were fabricated using the optimized f-CNP-PEDOT doped with 5 wt% of PEDOT as active material, exhibiting a high capacitance of 96.7 F/g at 1.4 V, holding practically their full charge, after 10,000 charge–discharge cycles at 2 A/g, thus providing the highest electrical electrodes performance. Hereafter, this work paves the way for the potential use of f-CNP-PEDOT nanocomposites in the development of high-energy-density supercapacitors. Full article

Solid-state supercapacitors with gel electrolytes have emerged as a promising field for various energy storage applications, including electronic devices, electric vehicles, and mobile phones. In this study, nanocomposite gel membranes were fabricated using the solution casting method with perfluorosulfonic acid (PFSA) ionomer dispersion, both with and without the incorporation of 10 wt.% montmorillonite (MMT). MMT, a natural clay known for its high surface area and layered structure, is expected to enhance the properties of supercapacitor systems. Manganese oxide, selected for its pseudocapacitive behavior in a neutral electrolyte, was synthesized via direct co-precipitation. The materials underwent structural and morphological characterization. For electrochemical evaluation, a two-electrode Swagelok cell was employed, featuring a carbon xerogel negative electrode, a manganese dioxide positive electrode, and a PFSA polymer membrane serving as both the electrolyte and separator. The membrane was immersed in a 1 M Na₂SO₄ solution before testing. A comprehensive electrochemical analysis of the hybrid cells was conducted and compared with a symmetric carbon/carbon supercapacitor. Cyclic voltammetric curves were recorded, and galvanostatic charge–discharge tests were conducted at various temperatures (20, 40, 60 °C). The hybrid cell with the PFSA/MMT 10 wt.% exhibited the highest specific capacitance and maintained its hybrid profile after prolonged cycling at elevated temperatures, highlighting the potential of the newly developed membrane. Full article

This study focuses on the growth of Cu₂O/CuO nanowires by one-step thermal oxidation using a flexible copper mesh at oxidation temperatures in the range of 300 to 600 °C in a controlled atmosphere of mixed-flow Ar and O₂ gases. Thermal oxidation is one of the simplest used methods to obtain nanowires on a metal surface, offering advantages such as low production costs and the ability to produce metal oxides on a large scale without the use of hazardous chemical compounds. The growth of metal oxides on a conductive substrate, forming metal/oxide structures, has proven to be an effective method for enhancing charge-transfer efficiency. The as-synthesized Cu/Cu₂O/CuO (Nw) electrodes were structurally and morphologically characterized using techniques such as XRD and SEM/EDX analysis to investigate the structure modification and morphologies of the materials. The supercapacitor properties of the as-developed Cu/Cu₂O/CuO (Nw) electrodes were then examined using cyclic voltammetry (CV), galvanostatic charge–discharge (GCD) measurements, and electrochemical impedance spectroscopy (EIS). The CV curves show that the Cu/Cu₂O/CuO (Nw) structure acts as a positive electrode, and, at a scan rate of 5 mV s ⁻¹, the highest capacitance values reached 26.158 mF cm⁻² for the electrode oxidized at a temperature of 300 °C. The assessment of the flexibility of the electrodes was performed at various bending angles, including 0°, 45°, 90°, 135°, and 180°. The GCD analysis revealed a maximum specific capacitance of 21.198 mF cm⁻² at a low power density of 0.5 mA cm⁻² for the oxidation temperature of 300 °C. The cycle life assessment of the all of the as-obtained Cu/Cu₂O/CuO (Nw) electrodes over 500 cycles was performed by GCD analysis, which confirmed their electrochemical stability. Full article

Graphite is a versatile material used in various fields, particularly in the power source manufacturing industry. Nowadays, graphite holds a unique position in materials for anode electrodes in lithium-ion batteries. With a carbon content of over 99% being a requirement for graphite to serve as an electrode material, the graphite refinement process plays a pivotal role in the research and development of anode materials for lithium-ion batteries. This study used three different processes to purify spherical graphite through wet chemical methods. The spherical graphite after the purification processes was analysed for carbon content by using energy-dispersive X-ray (EDX) spectroscopy and was evaluated for structural and morphological characteristics through X-ray diffraction (XRD), scanning electron microscopy (SEM), and Brunauer–Emmett–Teller (BET) analyses. The analyses results indicate that the three-step process via H₂SO₄–NaOH–HCl cleaning can elevate the carbon content from 90% to above 99.9% while still maintaining the graphite structure and spherical morphology, thus enhancing the surface area of the material for anode application. Furthermore, the spherical graphite was studied for electrochemical properties when used as an anode for Li-ion batteries using cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) measurements. The results demonstrated that the purification process significantly improves the material’s capacity with a specific capacity of 350 mAh/g compared to the 280 mAh/g capacity of the anode made of spherical graphite without purification. Full article

Sodium-ion batteries (SIBs) have emerged as a promising alternative to lithium-ion batteries (LIBs) due to the abundance and low cost of sodium resources. Cathode material plays a crucial role in the performance of sodium ion batteries determining the capacity, cycling stability, and rate capability. Na₃V₂(PO₄)₃ (NVP) is a promising cathode material due to its stable three-dimensional NASICON structure, but its discharge capacity is low and its decay is serious with the increase of cycle period. We focused on modifying NVP cathode material by coating carbon and doping Nb⁵⁺ ions for synergistic electrochemical properties of carbon-coated NVP@C as a cathode material. X-ray diffraction analysis was performed to confirm the phase purity and crystal structure of the Nb⁵⁺ doped NVP material, which exhibited characteristic diffraction peaks that matched well with the NASICON structure. Nb⁵⁺-doped NVP@C@Nb_x materials were prepared using the sol–gel method and characterized by X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Raman and Brunauer -Emmett-Teller (BET) analysis. First-principles calculations were performed based on density functional theory. VASP and PAW methods were chosen for these calculations. GGA in the PBE framework served as the exchange-correlation functional. The results showed the NVP unit cell consisted of six NVP structural motifs, each containing octahedral VO₆ and tetrahedral PO₄ groups to form a polyanionomer [V₂(PO₄)₃] along with the c-axis direction by PO₄ groups, which had Na1(6b) and Na2(18e) sites. And PDOS revealed that after Nb doping, the d orbitals of the Nb atoms also contributed electrons that were concentrated near the Fermi surface. Additionally, the decrease in the effective mass after Nb doping indicated that the electrons could move more freely through the material, implying an enhancement of the electron mobility. The electrochemical properties of the Nb⁵⁺ doped NVP@C@Nb cathode material were evaluated through cyclic voltammetry (CV), galvanostatic charge-discharge tests, electrochemical impedance spectroscopy (EIS), and X-ray photoelectric spectroscopy (XPS). The results showed that NVP@C@Nb_0.15 achieved an initial discharge capacity as high as 114.27 mAhg⁻¹, with a discharge capacity of 106.38 mAhg⁻¹ maintained after 500 cycles at 0.5C, and the retention rate of the NVP@C@Nb_0.15 composite reached an impressive 90.22%. NVP@C@Nb_0.15 exhibited low resistance and high capacity, enabling it to create more vacancies and modulate crystal structure, ultimately enhancing the electrochemical properties of NVP. The outstanding performance can be attributed to the Nb⁵⁺-doped carbon layer, which not only improves electronic conductivity but also shortens the diffusion length of Na⁺ ions and electrons, as well as reduces volume changes in electrode materials. These preliminary results suggested that the as-obtained NVP@C@Nb_0.15 composite was a promising novel cathode electrode material for efficient sodium energy storage. Full article

A simple activation method has been used to obtain porous carbon material from walnut shells. The effect of the activation duration at 400 °C in an atmosphere with limited air access on the structural, morphological, and electrochemical properties of the porous carbon material obtained from walnut shells has been studied. Moreover, the structure and morphology of the original and activated carbon samples have been characterized by SAXS, low-temperature adsorption porosimetry, SEM, and Raman spectroscopy. Therefore, the results indicate that increasing the duration of activation at a constant temperature results in a reduction in the thickness values of interplanar spacing (d₀₀₂) in a range of 0.38–0.36 nm and lateral dimensions of the graphite crystallite from 3.79 to 2.52 nm. It has been demonstrated that thermal activation allows for an approximate doubling of the specific S_BET surface area of the original carbon material and contributes to the development of its mesoporous structure, with a relative mesopore content of approximately 75–78% and an average pore diameter of about 5 nm. The fractal dimension of the obtained carbon materials was calculated using the Frenkel–Halsey–Hill method; it shows that its values for thermally activated samples (2.52, 2.69) are significantly higher than for the original sample (2.17). Thus, the porous carbon materials obtained were used to fabricate electrodes for electrochemical capacitors. Electrochemical investigations of these cells in a 6 M KOH aqueous electrolyte were conducted by cyclic voltammetry, galvanostatic charge/discharge, and impedance spectroscopy. Consequently, it was established that the carbon material activated at 400 °C for 2 h exhibits a specific capacity of approximately 110–130 F/g at a discharge current density ranging from 4 to 100 mA/g. Full article

Flexible electronic products, with their characteristics of flexibility and wearability, have attracted significant attention and have become an important direction in the research and development of the electronics industry. Planar micro-supercapacitors (MSCs) with flexible composite electrodes can provide reliable energy support for these products, propelling their further development. The research employed a quick, effective, and environmentally friendly method of laser scribing to create shape-controllable flexible composite electrodes on composite films of Poly(3,4-ethylenedioxythiophene) and graphene oxide (PEDOT/GO), which were subsequently assembled into MSCs. An analysis of the composite electrode morphology, structure, and elemental distribution was conducted through the utilization of SEM, TEM, and XPS techniques. Following this, a comprehensive evaluation of the electrochemical performance of the flexible MSCs was carried out, which included cyclic voltammetry (CV), galvanostatic charge/discharge (GCD), and assessment of cyclic stability. The analysis of the CV results indicated that the MSCs achieved the areal capacitance of 5.78 mF/cm² at 5 mV/s. After 5000 cycles at a current density of 0.05 mA/cm², the capacitance retention rate was 85.4%. The high areal capacitance and strong cycle stability of MSCs highlight the potential of PEDOT/reduced graphene oxide (PEDOT/rGO) electrodes in electrode applications. Full article