Electrode Material For Supercapacitor Applications Research Articles

Cobalt ferrite (CoFe2O4)–activated carbon fabric (ACF) based composite electrode material for supercapacitor application

In the present article, rayon based activated carbon fiber/fabric (ACF) has been developed and explored as an active electrode material in combination with metal oxide for ultracapacitor application. Herein, the ACF is derived from rayon-based carbon fabric through activation and carbonization processes in a tubular furnace and prepared composite material of cobalt ferrite (CoFe2O4, Cof) and activated carbon fabric/fiber. The ACF, cobalt ferrite, and electrode material derived thereof are analyzed by FTIR, XPS, BET surface area analyzer, and XRD methods. The surface morphology and composition of prepared composite is examined by FESEM and EDX. The electrochemical properties of Cof-ACF composite are scrutinized by cyclic voltammetry. The composite material produces considerably high electrochemical supercapacitances in the order of 1287 F/g and 788 F/g at a potential sweep rate of 2 mV/s in 0.5 M phosphoric acid and 0.5 M sulphuric acid electrolytes, respectively. The electrochemical behavior of the cobalt ferrite decorated ACF electrode material exhibits a slightly higher energy density (176.98 Wh/kg) in H3PO4 than in H2SO4 (150.79 Wh/kg) electrolyte. The stability (~74 %) of electrode materials is retained even after 3500 cycles of charge/discharge in acid electrolytes. Thus, Cof-ACF composite material could be used as a cost-effective, compact, and light-weight electrode material with enhanced stability and improved performance for ultracapacitor and energy storage device applications in acid electrolytes.

Synthesis and characterization of nickel doped ternary oxide thin film as electrode materials for supercapacitor application

Synthesis and characterization of nickel doped ternary oxide thin film as electrode materials for supercapacitor application

Significant Electrochemical Performance of Zirconia Nanoparticles Decorated with Polyaniline for Next Generation Electrode Materials in Supercapacitor Applications

Significant Electrochemical Performance of Zirconia Nanoparticles Decorated with Polyaniline for Next Generation Electrode Materials in Supercapacitor Applications

Rare-earth (Eu3+) substitution impact on the structural, morphological, magneto-dielectric, and electrochemical properties of Cd0.45Co0.55Fe2−y Eu y O4 spinel nanoferrites

A series of Cd0.45Co0.55Fe2−yEuyO4 (y = 0.0, 0.1, 0.2, 0.3) spinel nanoferrites (SNFs) were synthesized using a self-igniting process and employed as electrode materials for supercapacitor applications. The results demonstrated the formation of a single SNFs phase, as shown by the XRD data. The crystallite size lies between the range of 29.30–51.12 nm. The porosity percentage is within the range of 31.37%–32.99%. Rietveld refinement of XRD and Raman analysis revealed the pure spinel phase and no secondary phase was observed. The saturation magnetization and magnetic anisotropy were also decreased with the addition of Eu3+ in Cd–Co SNFs. The high coercive field was enhanced for Eu3+ doping as compared to pure Cd–Co SNFs. The dielectric constant was improved with the substitution of Eu3+ in Cd–Co SNFs. The dielectric tangent loss was reduced with the doping of Eu3+. The electrochemical performance of the Eu3+ doped Cd–Co SNFs achieved an impressive maximum specific capacitance at a lower scan rate. Based on these findings, the outstanding electrochemical performance of the Eu3+ doped Cd–Co SNFs suggests their potential as promising materials for high-frequency, magnetic ferrofluid, and supercapacitor electrodes.

Polypyrrole doped zirconium dioxide composite as electrode material for super-capacitor applications

Polypyrrole doped zirconium dioxide composite as electrode material for super-capacitor applications

Mechanosynthesis of pseudocapacitive MnCO3 and CoCO3 electroactive materials

Transition metals are known for their enormous potential as electrode materials for supercapacitor applications, however anhydrous carbonate minerals, namely Mn-carbonate, and Co-carbonate, are less explored and exhibit competitive energy storage performance compared to oxide and hydroxide forms. For the first time, MnCO3 (Rhodochrosite), CoCO3 (Spherocobaltite) and MnCo mixture (Mn1-xCoxCO3) were synthesized via mechanochemistry by a one-pot approach and used to prepare pseudocapacitive electrode materials for electrochemical energy storage. In this work, these materials were tested in alkaline electrolyte, and the morphological and structural features of the materials were examined using SEM (Scanning Electron Microscope), Transmission Electron Microscopy (TEM) and X-ray Diffraction (XRD). The surface composition was studied by X-ray photoelectron spectroscopy (XPS). After milling, the microstructures showed an increase in dislocations and microstrains in their crystal lattices which influenced the electrochemical performance. The crystallinity of the carbonate materials was also affected by grinding. In 1 M KOH electrolyte, milled MnCO3 evidenced the highest specific capacitance (354.3 F/g at 1.0 A/g), while milled CoCO3, revealed impressive capacitance retention of 94.8 % after 20000 continuous charge–discharge cycles at 10 A/g. Interestingly, the composite (Mn-Co)CO3 evidenced superior rate capability (58.8 %) and enhanced capacitance retention under cycling compared to the individual cobalt and manganese carbonates. The results evidence the excellent electrochemical behavior of Mn and Co carbonates prepared by a simple, low-cost, and green route and prove their potential as electroactive electrode materials for electrochemical energy storage applications, particularly pseudocapacitors.

Enhancing capacitive performance of MoS2 through Fe doping: Synthesis, characterization, and electrochemical evaluation for supercapacitor applications

The capacitive performance of bare MoS2 is limited due to its poor electronic conductivity. Therefore, we tried to dope different weight percentages (2 %, 4 %, 6 %, 8 %, and 10 %) of Iron (Fe) into the MoS2 to promote more active sites to improve its energy storage capacity. Given this, we have synthesized bare MoS2 and Fe-doped MoS2 using the hydrothermal method for electrochemical charge storage application. The effect of doping was well assessed using different physicochemical tests. The electrochemical properties of the bare MoS2 and Fe-doped MoS2 were evaluated using a three-electrode setup in a 3 M KOH aqueous electrolyte. As a result, the 8 % Fe-doped MoS2 electrode material demonstrates the maximum specific capacitance (CSP) of 545 F/g @ 1 A/g with 84.8 % capacitive retention over 2000 cycles at 5 A/g. Additionally, we fabricated an asymmetric solid-state supercapacitor device, which reveals a high CSP of 74.28 F/g at 4 A/g with an energy density of 72.79 Wh/kg and a power density of 10.07 kW/kg. The results asserted that the Fe-doped MoS2 is a potential electrode material for supercapacitor application.

Microwave assisted synthesis of NiMn<sub>2</sub>O<sub>4</sub> as electrode material for supercapacitor applications

In this work, spinel NiMn2O4 was successfully synthesized through microwave assisted co-precipitation method and followed by calcination at 500°C. The crystal structure and the presence of functional groups in NiMn2O4 were characterized through X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). The surface morphology was examined by field emission scanning electron microscopy (FE SEM). From the BET analysis surface area and average pore diameter of the mesoporous NMO nanoparticles are calculated to be 10.513 m2g-1and 8.55nm. The electrochemical performance of material as electrode material for supercapacitor applications was analysed by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The specific capacitance of the NMO electrode increased from 290.56 F/g to 751.57F/g with increase concentration from IM KOH to 6M KOH at scan rate of 5mV/s. These results indicate spinel NiMn2O4 as a promising candidate for high performance energy storage applications.

Hierarchical nanostructured Co0.5Mn0.5WO4 efficient electrode material for asymmetric supercapacitor application

BackgroundThis research focuses on the electrochemical characteristics of binary metal tungstates for asymmetric supercapacitor applications. Metal tungstates such as Cobalt tungstate (CoWO4) and Manganese tungstate (MnWO4) exhibit excellent electrical conductivity and redox characteristics. Different combinations of binary metal tungstates can serve as effective electrode materials for supercapacitor applications. MethodHerein, Co0.5Mn0.5WO4 nanoparticles was synthesized by the co-precipitation method followed by calcination. The prepared nanoparticles was used as an electrode material for the supercapacitor application. For study the two electrode system, Co0.5Mn0.5WO4 and activated carbon were worked as anode and cathode electrode, respectively. Significant findingsThe prepared electrode materials exhibit a battery type pusudocapacitance in cyclic voltammetry (CV). The charging and discharging properties of the material was analysed by galvanic charging and discharging (GCD) studies and it displays the specific capacitance value of 444 F/g at the current density of 1 A/g and it shows the specific capacitance retention of 91% after 1500 cycles. AC//Co0.5Mn0.5WO4 ASC device shows good energy density, power density and specific capacitance values of 30.5 Wh/Kg, 2800 W/Kg and 112 F/g at 1 A/g current density, respectively.

Facile synthesis of Ce2(WO4)3-decorated polyaniline composites as promising electrode material for supercapacitor applications

Facile synthesis of Ce2(WO4)3-decorated polyaniline composites as promising electrode material for supercapacitor applications

Waste PET bottles derived carbon black as electrode material for supercapacitor application

This study explores the conversion of polyethylene terephthalate (PET) waste into carbon black for its use in supercapacitors, offering a sustainable solution to waste management and energy storage needs. PET bottles were pyrolysed in an inert environment to produce carbon black. This plastic waste derived carbon was then characterised and used for electrode fabrication to explore its potential in supercapacitor applications. The supercapacitive properties of these electrodes were evaluated using cyclic voltammetry and charge–discharge techniques in various “Water-in-salt” electrolytes (WIS). WIS are the electrolytes in which the concentration of water is less than the concentration of salts by weight and volume. electrolytes. Sodium acetate (CH3COONa) exhibited the highest potential window and specific capacitance among the tested electrolytes. The derived carbon black demonstrated promising electrochemical performance, with a specific capacitance of 233 F/g and an energy density of 186.6 Wh/kg. These findings underscore the potential of carbon black derived from waste PET bottles as an effective material for supercapacitors, contributing to sustainable energy storage solutions and waste reduction.

Fabrication of rGO-modified ternary metal chalcogenide hybrid nanocomposite(rGO/Cu2MnSnS4) for high-performance supercapacitors

Efficient supercapacitor electrodes play a crucial role in addressing energy-related challenges and contributing to solutions for the global energy crisis. Recently, Metal chalcogenide/reduced graphene oxide (rGO) composites have garnered considerable attention due to their potential as electrode materials for supercapacitor applications. This study investigates the synergistic catalytic performance achieved by integrating ternary metal-based chalcogenides (Cu2MnSnS4) with 2D carbonaceous materials, highlighting their enhanced conductivity and catalytic activity for applications in energy conversion and environmental remediation. The current study involves the synthesis of a nanocomposite comprising rGO and copper manganese tin sulphide (Cu2MnSnS4), intended for use as an electrode material in energy storage devices. The structural characterization of the rGO/Cu2MnSnS4 nanocomposite was verified through X-ray diffraction, and the morphological analysis was conducted using scanning electron microscopy (SEM). The hybrid Cu2MnSnS4/rGO electrodes have demonstrated remarkable electrochemical characteristics, notably surpassing the performance of pure Cu2MnSnS4 in an alkaline electrolyte. Specifically, the maximum specific capacitance of Cu2MnSnS4/rGO reaches 1539 F g−1 at a scan rate of 10 mV s−1, whereas pure Cu2MnSnS4/rGO achieves a maximum specific capacitance of 948 F g−1 at the same scan rate. The findings from the electrochemical performance evaluation of the electrode material suggest that incorporating into rGO into Cu2MnSnS4 can significantly boost the supercapacitor performance of the Cu2MnSnS4 electrodes. This innovative combination has notably enhanced the overall electrochemical properties of the electrode materials, establishing it as a promising candidate for use in supercapacitor devices.

Enhanced electrochemical performance of CoMoO4/r-GO composites as electrode material for supercapacitor application

In the present work, a CoMoO4/r-GO hybrid was synthesized via a simple hydrothermal process. The phase purity and chemical binding energy were studied by powder XRD and XPS analytical techniques. The surface topography and internal morphology of the CoMoO4/r-GO hybrid were tested by FE-SEM and TEM analysis. The EDX elemental mapping was confirmed by the presence of Co, Mo, O, and C in the CoMoO4/r-GO hybrid. The CoMoO4/r-GO hybrid electrode material delivered a high specific capacitance of 556 F/g compared to 396 F/g (CoMoO4) at a current density of 0.5 A/g. The life cycle stability of the CoMoO4/r-GO hybrid exhibited 97 % and 95 % of columbic efficiency and capacitance retained over 1000 charge-discharge (GCD) cycles at a current density of 10 A/g.

Synergistic Enhancement of Supercapacitor Performance: Vanadium‐Substituted Phosphotungstic and Molybdic Acid Combined with Polypyrrole Using Pyridinium and Ammonium Ionic Containing Organic Cation Linkers with Improved Conductivity

High‐performance energy‐storage devices have emerged as a favored choice owing to their remarkable efficiency, sustainability, and environmental friendliness. Nowadays, polyoxometalate (POM)‐based supercapacitor (SC) electrode materials have gained much attention. Herein, a few new POMs and ionic liquid (IL) composites incorporated into conducting polymer as electrode materials for SC applications are reported. The H6[PV3Mo9O40]⋅34H2O (PV3Mo9) and H6[PV3W9O40].34H2O (PV3W9) POMs are treated with tetrabutylammonium chloride and 1‐butyl‐4‐methyl pyridinium chloride (BMP) and finally combined with polypyrrole (PPy) for the SC studies. An extensive array of analytical techniques is employed to delve into the interplay between the constituents within the composite materials, such as Fourier transform infrared spectroscopy, powder X‐ray diffraction, thermogravimetric analysis, nuclear magnetic resonance (1H and 13C), Field‐emission scanning electron microscopy, energy‐dispersive X‐ray stpectroscopy, X‐ray photoelectron spectroscopy, and Brunauer‐Emmett‐Teller surface area. The combined application of these techniques enables us to understand the interaction dynamics within composite materials comprehensively. POM–ILs combination improves the solubility issues of POMs, and doping of PPy enhances the electrochemical performances of the materials. The PV3W9–BMP–PPy symmetric SC cell shows a specific capacitance of 294.79 F g−1 and an energy density of 28.89 Wh kg−1 at 1 A g−1 current density in 0.25 M H2SO4 medium followed by an excellent cycle life of 78.6% after 10,000 galvanostatic charge–discharge cycles. The fabricated SC device is performed to light up the bulbs of red, yellow, and green light emitting diodes for 50, 30, and 28 s, respectively.

Facile synthesis of ternary potato-like Bi2O2CO3/β-Co(OH)2 wires/carbon aerogel heterostructures for supercapacitor applications

Advanced carbon-based materials supported by metal oxides are considered as potential candidates to achieve sustainable, green, and low-cost electrode materials for energy storage devices. Herein this work Bi2O2CO3/β-Co(OH)2/carbon aerogel composite has been successfully prepared via a simple solvothermal approach. The structural characterizations indicate a uniform and numerous potato-structured Bi2O2CO3 and β-Co(OH)2 nanowires anchored on carbon aerogel. In addition, the presence of carbon aerogel between Bi2O2CO3 and β-Co(OH)2 can effectively improve the ion transportation mechanism and also provide the regular framework for material stabilization. By combining these advantages, the synthesized materials modified with nickel foam as a working electrode delivers a higher specific capacitance value of 621.52 Fg−1 at 2 Ag−1 with a good capacitance retention of 97 % after the incessant 5000 cycles test. Such remarkable electrochemical results suggest the promising applications of Bi2O2CO3 and β-Co(OH)2 on stabilized carbon aerogel as alternate electrode material for supercapacitor applications.

Salvia officinalis leaf extract-stabilized NiO NPs, ZnO NPs, and NiO@ZnO nanocomposite: Green hydrothermal synthesis, characterization and supercapacitor application

AbstractIn this study, NiO nanoparticles (NiO NPs) and NiO@ZnO nanocomposite were synthesized for the first time using a Salvia officinalis (S. officinalis) extract-assisted hydrothermal process. The S. officinalis leaf extract served as a natural reducing and capping agent. The synthesized NiO NPs, ZnO NPs, and NiO@ZnO nanocomposite were thoroughly characterized using various techniques, including Fourier-transform infrared spectroscopy (FT-IR), ultraviolet–visible spectroscopy (UV–Vis), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), energy-dispersive spectrometry (EDS) mapping, vibrating sample magnetometer (VSM), and cyclic voltammetry (CV) analysis. The direct and indirect band gap energies of NiO NPs, ZnO NPs, and NiO@ZnO were found to be 3.00, 2.28, and 2.71 eV, and 2.63, 1.91, and 2.23 eV, respectively. The crystallite sizes were analyzed using PXRD spectra through Scherrer and Williamson–Hall (W–H) methods. TEM analysis revealed that the average particle sizes of NiO NPs, ZnO NPs, and NiO@ZnO were 16.0, 207.5, and 31.0 nm, respectively. The magnetic properties of all nanomaterials were assessed via the VSM technique. Specific capacitance (Cs) values, determined from CV voltammograms, were 196.8, 632.4, and 785 Fg-1 at a scan rate of 25 mVs-1 for NiO NPs, ZnO NPs, and NiO@ZnO, respectively. These findings suggest that the green-synthesized NiO@ZnO nanocomposite holds significant potential as a high-performance electrode material for supercapacitor applications.

Single‐Step One‐Pot Synthesis of NiCo2O4/Molybdate Nanocomposites for Flexible Supercapacitor Electrodes

Energy storage technology plays a critical role in integrating variable energy sources into the grid and ensuring energy consistency. Electrochemical supercapacitors are one of the most promising energy storage devices, as they present multiple advantages of high power density, rapid charge/discharge characteristics, and long‐term cycle stability. Herein, the NiCo2O4/molybdate nanocomposites are developed as electrode materials for supercapacitor applications. The NiCo2O4/molybdate nanocomposites are synthesized by a facile single‐pot hydrothermal method and are coated on a carbon cloth substrate to form flexible supercapacitor electrodes. The structures, chemical compositions, morphologies, and textural properties of these materials are carefully studied by X‐Ray diffraction, X‐Ray absorption spectroscopy, scanning electron microscopy/energy‐dispersive X‐Ray spectroscopy mapping, and N2 adsorption–desorption isotherms. The formation of spinel NiCo2O4 nanorods decorated with molybdate (AMoO4, A = Co, Ni) particles is confirmed for all samples. The NiCo2O4/CoMoO4 electrode exhibits pseudocapacitive behavior and provides the highest specific capacitance (287.28 F g−1 at current density 6 A g−1), about 5.5 times as high as that of NiCo2O4, with excellent cycle stability (107% specific capacitance retention after 1000 charge/discharge cycles at 1 A g−1). Therefore, the NiCo2O4/CoMoO4 composites can be considered as a promising pseudocapacitor electrode material.

Electrochemical performance of V2O5/TiO2 nanocomposite: As an emerging electrode material for supercapacitor application

This scrutiny encounters the hydrothermal approach of binary nanocomposites V2O5/TiO2 (VT). The XRD pattern substantiated the formation of the binary composites with 18 nm of the crystallite size without any extraneous impurities. Whereas, HR-SEM implies the efficient bonding and homogeneous distribution between V2O5 and TiO2 nanoparticles, which provokes high electrochemical performances. Additionally, the BET analysis exposes the specific surface area to be 251 m2 g−1 with an average pore size of 3.14 nm for the VT nanocomposite. The electrochemical performances of the binary VT nanocomposite exhibit high specific capacitance of 443.7 Fg−1 at a current density of 1 Ag−1 with an excellent cyclic retention of 90 % even after successive 5000 cycles at 5 Ag−1. Therefore, the results obtained in this study clearly demonstrates that the binary nanocomposite VT would be a favorable electrode material for the commercial energy storage applications.

Nickel sulfide and potato‐peel‐derived carbon spheres composite for high‐performance asymmetric supercapacitor electrodes

AbstractIn the present work, a novel composite of nickel sulfide (NiS) and potato peel‐derived carbon spheres (NiS/PPCS) with higher specific capacitance and cyclic performance was synthesized as electrode material for supercapacitor applications. The composite was deposited on a graphite rod to be use as an electrode. The electrochemical performance studies using CV, GCD, and EIS revealed that the prepared electrode showed an improved current response and higher specific capacitance than the pristine NiS electrode. The maximum specific capacitance for the NiS/PPCS electrode was found to be 2185 F/g at 0.2 A/g current density. More precisely, it was observed that the NiS/PPCS composite exhibited an excellent retention capacity of 95.04% after 20 000 continuous charge‐discharge cycles, showing its exceptional cyclic performance. The impedance studies revealed that the reaction between the NiS/PPCS electrode and electrolyte was rapid and highly reversible. Based on the findings of the electrochemical performances, NiS/PPCS electrode appears to be a potential candidate for highly efficient and economical asymmetric supercapacitors.

Influence of Biomass-derived Porous Activated Carbon on Polyaniline as Electrode Material for Supercapacitor Applications

Influence of Biomass-derived Porous Activated Carbon on Polyaniline as Electrode Material for Supercapacitor Applications