Search Results (217)

Carbon layer-coated μm-sized carbon fiber has the potential to be developed as an electrode, as it can be directly used as an electrode without any preparation process in the absence of an insulating binder. In our work, a carbon layer-coated carbon fiber (C@CF) coaxial structure is constructed by in situ conversion of the epoxy resin around the carbon fiber into a carbon layer, in which a sandwich scaffold of cover/CFRP/screen is designed and adopted. The activated SC@CF, i.e., A-SC@CF, can be directly served as the electrode, and has excellent supercapacitor performance: a high specific capacity of 227.1 F g⁻¹ at 0.5 A g⁻¹, with a capacitance retention of 98.9% after 20,000 cycles for the electrode, and an energy density of 16.68 Wh kg⁻¹ at the power density of 1400 W kg⁻¹ for its symmetrical supercapacitor (SSC). Full article

In this study, sugarcane bagasse (SCB), an abundant agricultural byproduct, was transformed into activated carbon via a controlled thermochemical pyrolysis route for high-performance energy storage applications. Herein, we utilized the activated carbon derived from pure sugarcane bagasse (SCB-AC) and further activated using KOH (SCB-KOH-AC) as an electrode material in aqueous symmetric supercapacitor configurations. The synthesized activated carbon was subjected to analysis using a range of characteristics including FT-Raman spectroscopy, which was employed to confirm the functional groups present in the carbon materials. The XPS analysis provided insights into the elemental composition and ionic states. The SEM analysis revealed that both activated carbon and KOH/activated carbon materials exhibited a layered or stacked, albeit slightly random, orientation. Electrochemical studies demonstrated that the synthesized carbon electrodes exhibited impressive specific capacitance values of (SCB) activated carbon (132.20 F/g) and KOH-activated, pure SCB AC (SCB-A) 253.41 F/g at 0.5 A/g. Furthermore, the SCB KOH-activated carbon (AC) electrode revealed a higher specific capacitance value and A//SCB-A symmetric devices delivered energy density reaching 17.91 Wh/kg and power density up to 2990 W/kg. The KOH-activated carbon electrode demonstrated remarkable cycling stability retaining 93.89%, even after 10,000 cycles. These results suggest that the sugarcane bagasse-derived activated carbon is a sustainable and low-cost candidate for next-generation supercapacitor electrodes. The results demonstrate enhanced capacitance, stability, and pore structure tailored for energy storage applications. The KOH-activated carbon SCB carbon symmetric device with symmetric electrodes exhibited a suitable bio-mass carbon for future energy storage applications. Full article

Electrochromic supercapacitors (ECSCs), which visually indicate their operating status through color changes, have attracted considerable attention in the field of wearable electronics. The conductive polymer polyaniline (PANI) shows great potential for integrated intelligent devices by combining bi-functional electrochromic spectral modulation and energy storage capabilities. In this work, a microsphere-like structured PANI-based composite film was fabricated on a porous Au/nylon 66 electrode via a one-step electrochemical copolymerization process, using 1,3,6,8-pyrenetetrasulfonic acid tetrasodium salt (PTSA) as both the dopant and cross-linking agent for the PANI backbone, serving as the ECSC electrode. Compared to the pristine PANI electrode, the PANI-PTSA composite film exhibits lower intrinsic resistance and higher electrical conductivity, delivering a higher specific capacitance of 310.0 F g⁻¹@1 A g⁻¹ and an areal capacitance of 340.0 mF cm⁻²@1 mA cm⁻², respectively. The dopant facilitates enhanced electrochemical performance by promoting charge transport within the PANI polymer network. Meanwhile, as a counter anion to the PANI backbone, PTSA regulates the growth of PANI chains and acts as a morphological controller. Furthermore, a symmetric ECSC based on the PANI-PTSA_8:1 electrode was assembled, and its electrochemical properties were thoroughly investigated. The device demonstrated a high specific capacitance of 169.2 mF cm⁻² at 1 mA cm⁻², a notable energy density of 23.5 μWh cm⁻² at a power density of 0.5 mW cm⁻², and excellent cycling stability with 79% capacitance retention after 3000 cycles at a current density of 5 mA cm⁻², alongside remarkable mechanical flexibility. Additionally, the working status of the ECSCs can be directly monitored through reversible color changes from yellow-green to deep blue during charge–discharge processes. Full article

It is found that Mo doping can enhance the supercapacitor performance of VS₂ microflowers. The X-ray diffraction combined with energy dispersive X-ray, X-ray photoelectron spectroscopy, and Raman spectra results verify the successful doping of Mo atoms into the VS₂ matrix. As the electrode material of supercapacitors, the Mo-doped VS₂ performs better electrochemical performance than pristine VS₂, achieving the specific capacitance of 170 F g⁻¹ at 0.5 A g⁻¹ and 389.5 F g⁻¹ at 5 mV s⁻¹. Furthermore, the symmetric supercapacitor based on the Mo-doped VS₂ exhibits good stability and ideal rate capability. The enhanced capability is presumably ascribed to the more accessible active sites and faster electrons/ions diffusion kinetics, which are caused by the increased specific surface area, expanded interlayer spacing, and improved conductivity after Mo doping. This strategy can also be extended to strengthen the capacitive properties of other transition metal dichalcogenides for advanced energy storage devices. Full article

The demand for high-performance supercapacitors has driven extensive research into novel electrode materials with superior electrochemical properties. This study explores the supercapacitive behavior of quaternary CuNiCoZnO (CNCZO) films engineered into a three-dimensional (3D) flower-like morphology and developed on versatile substrates, including carbon cloth, stainless steel mesh, and nickel foam. The unique structural design, comprising interconnected nanosheets, enhances the electroactive surface area, facilitates ion diffusion, and improves charge storage capability. The synergistic effect of the multi-metallic composition contributes to remarkable electrochemical characteristics, including high specific capacitance, excellent rate capability, and outstanding cycling stability. Furthermore, the influence of different substrates on the electrochemical performance is systematically investigated to optimize material–substrate interactions. Electrochemical evaluations reveal outstanding specific capacitance values of 2318.5 F/g, 1993.7 F/g, and 2741.3 F/g at 2 mA/cm² for CNCZO electrodes on stainless steel mesh, carbon cloth, and nickel foam, respectively, with capacitance retention of 77.3%, 95.7%, and 86.1% over 5000 cycles. Furthermore, a symmetric device of CNCZO@Ni exhibits a peak specific capacitance of 67.7 F/g at a current density of 4 mA/cm², a power density of 717.4 W/kg, and an energy density of 25.6 Wh/kg, maintaining 84.5% stability over 5000 cycles. The straightforward synthesis of CNCZO on multiple substrates presents a promising route for the development of flexible, high-performance energy storage devices. Full article

Modulating the oxidation states of transition metal species is a practical approach to enhance redox activity and increase the number of active sites in electrode materials. Herein, we describe a simple one-step hydrothermal approach to prepare Co_xS_y with two different phases, cobalt pyrite (CoS₂) and cobalt pentlandite (Co₉S₈), to explain the influence of material microstructure and properties on electrochemical performance. The as-prepared CoS₂ and Co₉S₈ were investigated as symmetric supercapacitor (SC) devices for potential energy storage applications. Co₉S₈ exhibited the highest specific gravimetric capacitance of 14.12 Fg⁻¹ at 0.2 mAcm⁻² with capacitance retention of 91.3% after 10,000 cycles, indicating robust cycling stability. In addition, the Co₉S₈ SC device showed the highest energy (E) and power (P) density of 9.14 Whkg⁻¹ and 0.23 kWkg⁻¹. These results highlight a simple approach of tailoring different phase syntheses of Co_xS_y structure toward high-performance electrode material for energy storage and conversion. Full article

This study successfully demonstrates the synthesis of foxtail millet carbon-activated (FMCA) materials using a two-step carbonization process from foxtail millet husk (FMH). The pre-carbonized biomass-derived millet husk was chemically activated with KOH at 500 °C and subsequently carbonized in an inert argon atmosphere at 800 °C in a tubular furnace. XRD analysis revealed a diffraction peak at 2θ = 23.67°, corresponding to the (002) plane, indicating the presence of graphitic structures. The Raman analysis of FMCA materials showed an intensity ratio (I_G/I_D) of 1.13, signifying enhanced graphitic ordering and structural stability. The as-prepared FMC and FMCA electrode materials demonstrate efficient charge storage electrochemical symmetric devices. Electrochemical analysis revealed the charge–discharge curves and a specific capacitance of Csp (FMC//FMC) 55.47 F/g and (FMCA//FMCA) 82.94 F/g at 0.5 A/g. Additionally, the FMCA//FMCA symmetric device exhibits superior performance with a higher capacity retention of 94.89% over 5000 cycles. The results confirm the suitability of FMCA for energy storage applications, particularly in electrochemical double-layer capacitors (EDLCs), making it a promising material for next-generation supercapacitors. Full article

This work demonstrates the feasibility of using biochars derived from a variety of waste feedstocks, such as food organics and garden organics (FOGOs), garden organics (GOs), and biosolids (BSs), provided by Barwon Water (BW) and South East Water (SEW), as active electrode material for supercapacitor application. Four different biochars were produced by the co-pyrolysis of pre-treated mixed waste feedstocks, which were fabricated into a two-electrode symmetric supercapacitor set-up to evaluate their energy storage potential. Two different approaches, (i) carbon nanoparticle coating/modification and (ii) thermochemical activation, were employed to improve the electrochemical properties of the biochars. Potassium hydroxide-activated biochar derived from BW’s triple waste feedstock mixture (comprising 70% GOs, 20% FOGOs, and 10% BSs) demonstrated the highest specific capacitance (30.33 F/g at 0.1 A/g), energy density (4.21 Wh/kg), and power density (2.15 kW/kg) among the tested samples. Such waste-derived biochar offers several benefits for energy storage, including cost-efficiency and sustainable alternatives to traditional electrode materials. The biochar’s electrochemical performance can be further improved by improving the feedstock quality by different pre-treatments. Full article

Preparing carbon aerogel in an eco-friendly and inexpensive manner remains a significant challenge. The carbon aerogels derived from food waste (FWCAs) with a three-dimensional connected network structure are successfully synthesized using microwave radiation. The as-prepared FWCA-4 (The KOH/C ratio is 4) has a large specific surface area (1470 m²/g), pore volume (0.634 m³/g), and a high degree of graphitization. Band-like lattice stripes with a spacing of 0.34 nm, corresponding to the graphite plane, are observed. A high specific capacitance of 314 F/g at 1.0 A/g and an excellent capacitance retention (>90% after 10,000 cycles) make the FWCA-4 suitable for high-performance supercapacitor electrode materials. Furthermore, the specific surface area and pore volume of FWCA-4 are larger and the degree of graphitization is higher than in ordinary porous carbon derived from food waste (FWPC). The assembled symmetrical solid capacitor from FWCA-4 exhibits a maximum energy density of approximately 179.9 W/kg in neutral ion electrolytes. Thus, food waste is successfully used to prepare carbon aerogels through a gelation process using microwave radiation. The recycling of waste biomass is achieved, and the results provide insights for the preparation of carbon aerogels using biomass. Full article

Microplastic pollution represents a significant global environmental issue, with cigarette filters being a major contributor due to their slow biodegradation. To address this issue while creating valuable materials, we developed a novel approach to synthesize nitrogen-doped carbon nanotubes on carbonized cigarette filter powder (NCNT@cCFP) using a microwave irradiation and nickel-catalyzed process. The successful incorporation of nitrogen (~6.6 at.%) and the enhanced graphitic structure create a hierarchical conductive network with abundant active sites for electrochemical reactions. The resulting NCNT@cCFP electrode exhibits a specific capacitance of 452 F/g at 1 A/g in a three-electrode configuration. The integrated hierarchical structure facilitates efficient electron transport and ion diffusion, leading to excellent rate capability (91.6% at 10 A/g) and cycling stability (96.5% retention after 5000 cycles). Furthermore, a symmetric supercapacitor device demonstrates promising energy storage capability with a maximum energy density of 14.0 Wh/kg at 483.1 W/kg, while maintaining 10.4 Wh/kg at a high power density of 4419.1 W/kg. This synergistic waste recycling strategy combined with microwave-driven synthesis offers a sustainable pathway for developing high-performance energy storage materials. Full article

Solid polymer electrolytes (SPEs) for symmetrical supercapacitors are proposed herein with activated carbon as electrodes and optimized solid polymer electrolyte membranes, which serve as the separators and electrolytes. We propose the design of a low-cost solid polymer electrolyte consisting of guanidinium nitrate (GuN) and poly(ethylene oxide) (PEO) with poly(vinylpyrrolidone) (PVP). Using the solution casting approach, blended polymer electrolytes with varying GuN weight percentage ratios of PVP and PEO are prepared. On the blended polymer electrolytes, structural, morphological, vibrational, and ionic conductivity are investigated. The solid polymer electrolytes’ morphology and level of roughness are examined using an FESEM. The interlinking bond formation between the blended polymers and the GuN salt is verified by FTIR measurements, indicating that the ligands are chemically complex. We found that, up to 20 wt.% GuN, the conductivity value increased (1.84 × 10⁻⁶ S/cm) with an increase in mobile charge carriers. Notably, the optimized PVP/PEO/20 wt.% solid polymer electrolyte was fabricated into a solid-state symmetrical supercapacitor device, which delivered a potential window of 0 to 2 V, a superior energy density of 3.88 Wh kg⁻¹, and a power density of 1132 W kg⁻¹. Full article

In this study, a novel multiscale carbon architecture was developed by integrating mesocarbon microbeads (MCMBs), graphitic nanofibers (GNFs), and mesoporous carbon, aimed at enhancing the performance of symmetric supercapacitors. The unique combination of spherical MCMB particles, conductive GNF nanofibers, and mesoporous carbon sheets resulted in a highly effective electrode material, offering improved conductivity, increased active sites for charge storage, and enhanced structural stability. The fabricated MCMB/GNF/MC architecture demonstrated a remarkable specific capacitance of 393 F g⁻¹ at 1 A g⁻¹ in a three-electrode system, significantly surpassing the performance of individual MCMBs and MCMB/GNF electrodes. Furthermore, the architecture was incorporated into a symmetric supercapacitor (SSC) device, where it achieved a capacitance of 86 F g⁻¹ at 1 A g⁻¹. The device exhibited excellent cycling stability, retaining 92% of its initial capacitance after 10,000 charge–discharge cycles, with an outstanding coulombic efficiency of 99%. At optimal operating conditions, the SSC device delivered an energy density of 11 Wh kg⁻¹ at a power density of 500 W kg⁻¹, making it a promising candidate for high-performance energy-storage applications. This multiscale carbon architecture represents a significant advancement in the design of electrode materials for symmetric supercapacitors, offering a balance of high energy and power density, long-term stability, and excellent scalability for practical applications. This work not only contributes to the development of high-performance electrode materials but also paves the way for scalable, long-lasting supercapacitors for future energy-storage technologies. Full article

Supercapacitors are advanced energy storage devices renowned for their rapid energy delivery and long operational lifespan, making them indispensable across various industries. Their relevance has grown in recent years due to the adoption of environmentally friendly materials. One such material is bacterial nanocellulose (BNC), produced entirely from microbial sources, offering sustainability and a bioprocess-driven synthesis. In this study, BNC was synthesized using a symbiotic microbial community. After production and purification, pristine BNC membranes, with an average thickness of 80 microns, were impregnated with an alkali-alcohol meta-polybenzimidazole (PBI) solution. This process yielded hybrid BNC/PBI membranes with improved ion-transport properties. The BNC membranes were then doped with a 6 M KOH solution, to enhance OH⁻ conductivity, and characterized using optical microscopy, ATR FT-IR, XRD, CVT, BET analysis, and impedance spectroscopy. Both BNC and BNC/PBI membranes were tested as separators in laboratory-scale symmetric supercapacitor cells, with performance compared to a commercial Viledon^® separator. The supercapacitors employing BNC membranes exhibited high specific capacitance and excellent cycling stability, retaining performance over 10,000 charge/discharge cycles. These findings underscore the potential of BNC/KOH membranes for next-generation supercapacitor applications. Full article

Utilizing lignin-derived activated carbon in supercapacitors has emerged as a promising approach to alleviating environmental pollution and promoting the high-value utilization of byproducts in the papermaking industry. In this study, activated carbons (LACs) were prepared using a simple one-step KOH activation approach and by employing enzymatic hydrolysis lignin (EHL). The impact of the KOH activation parameters on the microstructure and capacitive performance of the LACs was investigated by varying the KOH/EHL ratio and activation temperature. The optimized sample LAC_800-4 showed an interconnected porous structure with a high surface area of 2285 m²/g, abundant micropores, and a small number of mesopores, which makes it a suitable electrode material for supercapacitors. The sample LAC_800-4 demonstrated a high specific capacitance of 291.3 F/g in a three-electrode system. Under a symmetrical supercapacitor electrode system, the specific capacitance of the LAC_800-4 electrode reached 186.8 F/g at 0.5 A/g. After 10,000 cycles at 20 A/g, the capacitance retention rate remained at 96.1%. The symmetrical supercapacitor also demonstrated a superior energy density of 6.5 Wh/kg. This work provides valuable insights into the transformation of low-value natural biomass derivatives into environmentally friendly, high-performing supercapacitor electrode materials. Full article

Due to its low cost, natural abundance, non-toxicity, and high theoretical capacitance, cobalt oxide (CoO) stands as a promising candidate electrode material for supercapacitors. In this study, binder-less molybdenum doped CoO (Mo@CoO) integrated electrodes were one-step fabricated using a simple electric discharge corrosion (EDC) method. This EDC method enables the direct synthesis of Mo@CoO active materials with oxygen vacancy on cobalt substrates, without any pre-made templates, conductive additives, or chemicals. Most importantly, the EDC method enables precise control over the discharge processing parameter of pulse width, which facilitates tailoring the surface morphologies of the as-prepared Mo@CoO active materials. It was found that the fabricated Mo@CoO based symmetric supercapacitor prepared by a pulse width of 24 μs (Mo@CoO-SCs24) achieved a maximum areal capacitance 36.0 mF cm⁻² (0.15 mA cm⁻²), which is 1.83 and 1.97 times higher than that of Mo@CoO-SCs12 and Mo@CoO-SCs36. Moreover, the Mo@CoO-SCs24 devices could be worked at 10 V s⁻¹, which demonstrates their fast charge/discharge characteristic. These results demonstrated the significant potential of the EDC strategy for efficiency fabricating various metal oxide binder-less integrated electrodes for various applications, like supercapacitors, batteries and sensors. Full article