Supercapacitor Electrode Research Articles

In-situ growth of FeCo layered double hydroxide nanorods on MXene for high-performance supercapacitor electrodes

In the pursuit of clean energy solutions, supercapacitors have gained attention due to their exceptional energy storage capabilities. Layered double hydroxide (LDH), a notable material in this field, faces some challenges such as slow charge transfer speed and volumetric expansion. To tackle these issues, a novel FeCo-LDH/MXene composite was synthesized through in-situ hydrothermal growth of FeCo layered double hydroxide (FeCo-LDH) nanorods on MXene using ionic self-assembly, forming a three-dimensional (3D) composite with enhanced rate capability and cycling stability due to the synergetic coupling of MXene and LDH. The FeCo-LDH/MXene electrode significantly improves surface capacitance control performance and exhibits exceptional electrochemical performance, achieving a specific capacitance of 2058.2 F g−1 at 1 A g−1 and maintaining 1732.7 F g−1 at 10 A g−1, with 82.4 % capacity retention. Furthermore, the assembled supercapacitor delivers an energy density of 48.8 Wh kg−1 at 750 W kg−1 and 25.7 Wh kg−1 at 15000 W kg−1, demonstrating excellent rate performance, as well as 80.3 % capacitance after 5000 cycles at 2 A g−1, highlighting its durability. This advancement not only overcomes the specific capacitance challenge of MXene electrodes but also enhances the conductivity and cyclic stability of LDH, making FeCo-LDH/MXene a promising candidate for future high-performance energy storage applications.

Biopolymers as three-dimensional structural binders for nickel-cobalt sulfide supercapacitor electrodes

Ion diffusion and electron transfer are hindered by commonly used hydrophobic binders, which directly affect the electrochemical performance of the electrodes. Hydrophilic binders are selected to efficaciously solve the problem of relatively low actual specific capacitance and rate performance in the field of nickel cobalt sulfide electrode materials. In the paper, RuCoNiS electrodes were prepared using polytetrafluoroethylene (PTFE), carboxymethyl cellulose (CMC), xanthan gum (XG), and chitosan (CS) as binders. The surface wettability, morphological structure, specific surface area, and electrochemical performance of electrodes with different binders were analyzed by XRD, SEM, BET, CV, GCD, and EIS, etc. It's shown that the synthesis of CoNi2S is confirmed by XRD. The XPS results verify the existence of RuO2 and Ni2+/Ni3+ and Co2+/Co3+ redox couples. A cross-linked network structure is formed on the surface of the RuCoNiS by CS. The CS-RuCoNiS electrode has the largest specific surface area and microporosity. Ion migration in the electrolyte is facilitated by the excellent wettability of the CS-RuCoNiS electrode. The CS-RuCoNiS electrode reachs 1193.52 F g-1, which is 1.74 times higher than that of the PTFE-RuCoNiS electrode at 1 A g-1. The CS binder with its three-dimensional structure has the highest ionic conductivity of 2.29 × 10-4 S cm-1, a lower Rct, good cycling stability with a capacity retention of 84.3% after 5000 cycles at 200 mV s-1, and excellent rate performance of 85.6%. It can provide a practical application in supercapacitors.

Microwave-assisted vanadium interpolated cobalt-MOF cathode assembled 3 V high performing asymmetric supercapacitor with ionic liquid gel polymer electrolyte

To ameliorate energy storage and conversion, metal synergy, and structural stability, bimetal-assembled metal–organic frameworks (MOFs) are delved into. Augmented surface area, pseudo capacitance, and the ability to alter the MOF edifice of layered oxide have drawn interest in MOF-based oxide layered structures. Simple microwave and hydrothermal techniques use dimethyl formamide and water as solvents and annealing methods to generate the bimetallic organic framework’s Co3V2O8 and Co3VO4 cathode material. Those customized shapes boost redox sites and reduce ion electron distance. Due to cobalt’s faradaic process and vanadium’s highly layered attributes, supercapacitor electrode response is significant. Co3V2O8 has 1391F/g specific capacitance at 2 mV/s scan rate and 1309F/g at 4 mA/cm2 implemented current value. After 10,000 cycles, the cathode material depicts 89 % capacity retention and 98 % coulombic efficiency. Biowaste-derived activated carbon is combined with a Co3V2O8 cathode for asymmetric supercapacitor storage. That device works on 3 V windows with ionic liquid gel polymer electrolyte. With a maximum specific energy of 329.3 Wh/kg and specific power of 15250 W/kg, the achieved galvanometric capacitance is 263.5F/g and 220 mAh/g at the 9 mA/cm2 current and showed 88.5 % potential stability after 10,000 cycles. These findings corroborate its use as a supercapacitor cathode.

N-doped hierarchically porous carbon from lignite-derived residue for high-performance supercapacitor

Lignite-derived residue with cross-linked aromatic structure and heteroatom groups is an alternative and low-cost precursor for porous carbon. Herein, N-doped hierarchically porous carbon (NDHPC) was prepared by KOH activation from lignite-derived residue using ZnO as the template and dicyandiamide as the nitrogen source. The optimal NDHPC presents hierarchically porous stacked layered structure with high specific surface area (2648.18 m2/g) and contains abundant O/N functional groups, making it promising candidate as the electrode material. Introducing nitrogen can provide more pseudocapacitors and meanwhile improve the wettability of the NDHPC, thus enhancing electrochemical performance. The optimal NDHPC exhibits a high specific capacitance of 336 F g−1 at the current density of 0.5 A g−1 with good rate performance. Additionally, the assembled NDHPC symmetrical supercapacitor presents outstanding cycle stability with 96.2 % capacitance retention and possesses energy density of 7.85 Wh kg−1 at power density of 250 W kg−1. This study offers an effective and low-cost approach to fully utilize the organic matter in coal-derived residue for preparing supercapacitor electrode materials.

Facile Synthesis of Highly Supercapacitive Mo‐doped Titanium Nanotube Arrays and Effect of Anodization Voltage

AbstractDesigning potential architectures by the modification of conventional electrode materials is an effective approach in the development of high performance supercapacitor electrodes. The present study investigated the effect of varying anodization voltages (50, 75, and 100 V) on the morphology and electrochemical properties of titanium nanotubes (TNT). Molybdenum was doped onto TNT using a simple hydrothermal procedure, followed by thermal treatment at 450 °C. The study effectively demonstrated control over the dimensions of the nanotube structure by adjusting the anodization voltage. Additionally, it was found that the tube diameters were increased due to etching during the hydrothermal treatment with the Mo precursor, which potentially enhanced the supercapacitive performance of Mo‐doped TNT. Further, structural analysis revealed that Mo doping improved both crystallinity and electrode stability. With an optimal anodization voltage of 100 V, TNT and Molybdenum‐doped TNT could exhibit capacitance value of 13.34 and 326.54 mF cm−2 respectively, at a current density of 1 mA cm−2. Furthermore, the electrode demonstrated good cyclic stability with 88% capacitance retention and 97% coulombic efficiency after 5000 cycles. An impressive energy density of 87.03 µWh cm−2 and a power density of 799.99 µW cm−2 could be achieved with this sample in an asymmetrical device.

Synthesis and surface engineering of carbon-modified cobalt ferrite for advanced supercapacitor electrode materials

The precise design and surface modification of electrode materials are crucial challenges for advancing the supercapacitor technology. In this study, we report a straightforward two-step process for the synthesis of a cobalt ferrite (CoFe2O4)/carbon hetero nanostructure. The CoFe2O4 nanoparticles were first synthesized using a simple chemical oxidation method, followed by carbon modification using glucose. The modified samples were calcined at 400 and 600 °C for 4 h in N2 atmosphere to optimize the structural and electrochemical properties.. The increase in the grain size of carbon modified cobalt ferrite magnetic nanoparticles (MNPs) was observed from 22 to 28 nm with post annealing temperature. The presence of carbon was confirmed by the FTIR spectroscopy, FESEM and TEM analyses. The carbon decoration on the cobalt ferrite partially showed a core–shell like morphology. The saturation magnetization of bare cobalt ferrite was observed to be 76 emu/g and the same was decreased by the surface modification with carbon. A high specific capacitance of 323 F/g was observed for the carbon-modified cobalt ferrite MNPs annealed at 600 °C. The electrochemical impedance spectroscopy (EIS) analysis demonstrated that the charge-transfer resistance (Rct) decreased significantly in the carbon-modified CoFe2O4 MNPs, particularly for the sample annealed at 600 °C, with an Rct value of 17 Ω. The carbon layer effectively enhanced conductivity and reduced the electrode/electrolyte interface, led to the improved electrochemical performance, as reflected in the enhanced specific capacitance. An improved capacitance retention of 84 % was achieved in the case of carbon-modified cobalt ferrite MNPs based electrode even after 4000 cycles. The study suggested that the prepared carbon-modified cobalt ferrite MNPs stand in the limelight as a better candidate electrode material for the electrochemical applications.

Hierarchical structural design of cobalt sulphide nanoparticles/nickel sulphide for high-performance supercapacitors

Metal-organic framework (MOF) materials have become increasingly attractive in supercapacitor electrode research because of their regular crystal topology and tunable pore distribution. The strategy for the synthesis of the Ni3S4/Co3S4 electrode material with a layered structure was successfully devised using the layered Ni-MOF as a template and precursor. The characterisation techniques of XRD, FTIR, XPS, SEM, TEM and BET have provided confirmation of the assertion that the Ni3S4/Co3S4 composites exhibit an advanced hierarchical pore structure and considerable specific surface area. The specific capacity of the Ni3S4/Co3S4 composite is as high as 122.8 mAh g−1, and it can still maintain 72.6 % of the specific capacity after 3,000 cycles. Furthermore, the SEM morphology remains largely unchanged after cycling, which demonstrates excellent stability. Moreover, honeycomb-shape porous carbon (N-HAPC) with ultra-high specific surface area was selected as negative electrode material to fabricate a novel hybrid supercapacitor (Ni3S4/Co3S4//N-HAPC), which exhibits a broad operational voltage range of 1.6 V and superior energy density of 28.6 Wh kg−1. Simultaneously, HSCs exhibited remarkable charge-discharge stability, exhibiting a mere 17.2 % decline in capacitance stability following 7,000 GCD cycles. The combination of two Ni3S4/Co3S4//N-HAPC HSCs in series has been demonstrated to be capable of illuminating a small LED lamp, indicating the potential for their use in practical applications. Furthermore, this approach offers a novel strategy for the structural design of MOF-like materials.

Activated biomass-derived 3-dimensional porous graphene-like carbon for high-performance energy storage electrode materials

This article reports studies on the fabrication of active material for supercapacitor electrodes, from 3D porous graphene-like carbon (GLC), synthesized by carbonization from coffee waste (CW) and tea waste (TW) at 550 °C, followed by thermochemical activation in KOH at 850 °C in a quartz tubular furnace. The microstructure of coffee and tea waste shows the form of micro- and mesopores during carbonization and further chemical activation forms hierarchically highly porous 3D graphene-like carbon. GLC-CW exhibited a higher specific surface area (SSA) of 3486 m2/g according to the Brunauer-Emmett-Teller (BET) method, compared to GLC-TW, which had an SSA of 2407 m2/g. These results highlight the effectiveness of graphene-like carbon derived from coffee and tea waste, demonstrating its potential as a promising material for high-capacity supercapacitors. The electrochemical characteristics of the assembled supercapacitors using GLC-CW and GLC-TW revealed significantly higher specific capacitance values of 214 F/g and 182 F/g respectively, along with cycling stability of 98 % and 95 % during 5000 cycles of charge and discharge at 2 A/g current density. This approach can produce high-performance electrode materials for supercapacitors at a reasonable cost and with easy scalability.

A facile one-pot synthesis of hierarchical porous carbon for supercapacitor electrodes

This study presents a facile, environmentally friendly approach to fabricate hierarchical porous carbon for supercapacitor electrodes. The one-pot synthesis of PFO/silica/PTFE via co-pyrolysis generates ideal hierarchical porous carbon. Compared with traditional methods, this method eliminates toxic solvents and complex cleaning steps. PPC-2 obtained under the optimized activation time has the highest specific surface area (2657 m2 g−1) and a remarkable total pore volume (2.96 cm3 g−1). These properties result in a remarkable specific capacitance of 335.9–210.8 F g−1 at current densities of 0.5–10 A g−1 in KOH electrolyte. The electrochemical performance of the PPC-2 electrode in a symmetric supercapacitor device was measured in aqueous (6 M KOH) and ionic liquid (EMIM-TFSI) electrolytes. In EMIM-TFSI, PPC-2//PPC-2 provides an energy density of 48.5 Wh/kg even at a power density of 750 W kg−1. This facile one-pot synthesis method offers a sustainable and scalable approach to produce high-performance hierarchical porous carbon for supercapacitor applications.

Efficient production of activated carbons from PET for organic supercapacitor applications: A single-step approach

This study introduces a novel approach for synthesizing supercapacitor electrode materials using polyethylene terephthalate (PET), a plastic facing recycling challenges. Unlike conventional methods that involve separate carbonization and activation steps, we employ a single-step method. In this process, activated carbons are synthesized using potassium hydroxide (KOH) as an activating agent. Remarkably, the yield via the single-step method (S_PACXs) exceeds that of the two-step method (T_PACYs) by at least 1.7 times. During the single-step process, KOH forms a layer on the PET surface before activation, which leads to increased yields, higher specific surface areas, and more developed mesopores. Furthermore, S_PACXs exhibit superior specific surface areas compared to commercial activated carbon. These enhanced properties significantly improve electrochemical performance, with S_PACXs demonstrating superior performance compared to T_PACYs. Ultimately, this study validates the efficiency of the single-step method in producing high-quality activated carbon from PET, saving time and energy, and outperforming the two-step method.

A Flexible Asymmetric Supercapacitor with High-Performance and Long-Lifetime: Fabrication of Nanoworm-Like-Structured Electrodes Based on Polypyrrole-Thiosemicarbazone Complex.

A thiosemicarbazone-based iron(III) complex is prepared and used in the preparation of a supercapacitor electrode material. This electrode is produced by a solvothermal reaction of polypyrrole and the complex on carbon felt. The characterization of the complex and material is carried out using UV-vis, elemental analysis, FT-IR, XRD, BET, and TGA methods, and the surface morphology is examined using SEM technique. Because the interaction of electrode and electrolyte is of great importance in energy storage systems, as the surface area and pore volume increase, electrode ions at the electrode/electrolyte interface leak to the inner surfaces and interact with the larger surface area, which increases the charge storage performance. The electrode material, nano-worm structure, reached the highest specific capacitance value of 764.6 F g-1 at 5 mV s-1. Compared to the capacitance value of polypyrrole in its pure form, it is observed to exhibit an 187.2% increase. The highest specific capacitance value of the asymmetric supercapacitor (ASC) formed with a graphite electrode is 318.1 F g-1 at the current density of 1 Ag-1. Moreover, ASC reached a wide working potential of 1.8 V in an aqueous electrolyte and exhibited ultra-long cycle life (112%), maintaining its stability after 10000 cycles.

High-performance supercapacitor of ZnO-incorporated structurally modified g-C3N4 with circular mesoporous channels attained via a template-free approach

Abstract Here, the superior structural features of graphitic carbon nitride (g-C3N4) in combination with integrated mesoporous channels have been explored for its use as a supercapacitor electrode material. A facile template-free strategy is adopted for the preparation of ZnO-incorporated modified g-C3N4 nanocomposite, where material characterization via x-ray difraction, Fourier transfrom infrared spectroscopy, field-emission scanning electron microscopy, transmission electron microscopy and x-ray photoelectron spectroscopy analysis revealed the presence of structurally modified g-C3N4 having uniform circular mesoporous channels with well-dispersed ZnO with strong Zn–C and Zn–N interactions. The electrical double-layer capacitance together with the pseudocapacitance of the ZnO/g-C3N4 electrode material resulted in improved performance, leading to a specific capacitance of 146.3 F g−1 at a current density of 0.5 A g−1; an increased capacitance is observed in 5000 repeated charge–discharge cycles. A symmetric coin cell supercapacitor fabricated from the material displayed an energy density of 38.8 mWh kg−1 at a power density of 4259 mW kg−1. Additionally, the long life of 6000 cycles (retaining 100% specific capacitance) exhibited by the coin cell supercapacitor further indicates the promising energy storage nature of the ZnO-incorporated modified g-C3N4 mesoporous nanoarchitecture. Real life application of the ZnO/g-C3N4-derived supercapacitor is illustrated by lighting up a green LED with a series connection of four coin cells.

Initial Study of Reduced Graphene Oxide Foams Modified by Mn and Bi as Capacitive Electrode Materials

In a view of application of porous materials in wearable electronics and self-powered systems, reduced graphene oxide (rGO) foams modified by Mn or/and Bi were produced in this study to be used as electrodes for supercapacitors. The hydrothermal method and the freeze-drying processes were used for the preparation of the materials further morphologically, elementally and structurally analyzed. Based on the electrochemical characterization, Bi-modified rGO foam was found to be more a promising material for capacitive electrodes in comparison to the other prepared materials.

Investigating the Exfoliated Hexagonal Boron Nitride Nanosheets Embedded on Bi2S3 Nanorods Designed as a Positive Electrode for Hybrid Supercapacitors

Investigating the Exfoliated Hexagonal Boron Nitride Nanosheets Embedded on Bi₂S₃ Nanorods Designed as a Positive Electrode for Hybrid Supercapacitors

Polyoxometalate/α-Fe2O3/polyaniline composite: Tailored approaches for high-performance supercapacitors

The need for portable, high-performance electronics that have high power or energy density has increased significantly in recent years. In this work, a composite material was coated on stainless steel that consists of polyoxometalate (POM)/α-Fe2O3/polyaniline (PANI) as an electrode material for a symmetric supercapacitor. α-Fe2O3 was prepared using starch as a template while PANI was electrodeposited. The physical and chemical characteristics of the modified electrodes were investigated via Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy and electrochemical techniques such as cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic chargedischarge (GCD) experiments. In 1 M H2SO4, the composite had a specific capacitance of 528 F/g at a current density of 0.2 A/g. In addition, the composite exhibited a high energy density of 73.4 Wh kg−1 at a high-power density of 7.14 kW kg−1 and 91.62 % capacity retention after 10 cycles. The results show that POM/α-Fe2O3/PANI is a promising composite electrode for use as a supercapacitor electrode material.

Binder-Free Approach of Mixed-Valent Oxovanadates Anchored on MWCNTs as Supercapacitive Electrodes to Symmetric Supercapacitor Devices: Enriched Performance through the Incorporation of Guest Molecules in Capsular-Shaped Polyanions

Binder-Free Approach of Mixed-Valent Oxovanadates Anchored on MWCNTs as Supercapacitive Electrodes to Symmetric Supercapacitor Devices: Enriched Performance through the Incorporation of Guest Molecules in Capsular-Shaped Polyanions

Synthesis of Porous Carbons from Candlenut Shells Using Various Types of Activators for Environmentally Friendly Supercapacitors

Porous carbon is one of the promising electrode materials for supercapacitors due to its unique and engineerable microstructural properties. The study of the synthesis of porous carbon from waste biomass is very important due to the abundance of natural resources, low cost production and contribute to solving environmental problems. In this study, porous carbons derived from candlnut shell with various type of activator was studied the chemical structural, morphological and electrochemical properties then evaluated as electrodes for supercapacitor. We have been successfully synthesized of porous carbon from candlenut shells using three steps of the process, i.e.: carboni-zation, activation and calcination. Carbonization was carried out at 700°C in a furnace using a closed crucible to minimize the oxygen. The chemical activation conducted using three types of activators, i.e. ZnCl2, H3PO4 and KOH then calcination process by heated at 800°C for 1 h under Ar flow. The results of the Fourier-transform infrared (FTIR) analysis show that the carbonization process increases the content of aromatic C=C functional groups and reduce the OH, C-H, C-O and C=O functional groups. The carbonization process has also increased the electrical conductivity of the sample around 0.8525 S/m. The results of Scanning Electron Microscope (SEM) images can be observed that the activation process of carbon has formed which was indicated by the appearance of many pores on the surface area of carbon. N2 adsorption/desorption isotherms (Brunauer–Emmett–Teller (BET)) characterization was indicated that the porous carbon is dominated by mesoporous with a pore size around 2-50 nm. BET characterization also can be determined the surface area of porous carbon around 477 m2/g for ZnCl2, 636 m2/g for H3PO4, and 681 m2/g for KOH. This synthesized materials are further employed in a symmetric supercapacitor using simple glass cell. The best performance of supercapacitor achieved by KOH porous carbons with 16.30 F/g of specific capacitance, 2.26 Wh/kg of energy density and 1038 W/kg of power density.

Zinc cobalt sulfide with carbon (graphene oxide and CNT) based nanocomposite as positive electrode for asymmetric coin cell supercapacitors

Abstract The world dependence on portable electronic devices has increased the demand for high-performance energy storage devices. The use of transition metal sulfides as faradaic electrode materials for electrochemical energy storage is rapidly increasing due to their high energy density. Herein Zinc Cobalt Sulfide (ZCS) with graphene oxide (GO) and carbon nanotubes (CNT) were used to create an interconnected ZCS composite network using a solvothermal technique. The materials were characterized by utilizing XRD, FT-Raman, TGA, FESEM/EDX, XPS, and BET. The electrochemical performance of the materials was examined using cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS). The prepared electrodes exhibited both pseudocapacitor behavior and double-layer capacitor behavior, indicating the hybrid nature. Furthermore, All the electrode ZCS, ZCS/GO, ZCS/CNT, and ZCS/GO/CNT electrodes demonstrated higher capacitance behavior, with values of 420, 551, 585 and 811 F g−1 at 1 A/g. Among these ZCS/GO/CNT electrode exhibits outstanding electrochemical properties, with a notable retention of 81.08% at 10 Ag−1 because Combining ZCS nanoparticles with interconnected GO and CNT provides excellent electronic conductivity and stability. The assembled ZCS/GO/CNT//graphene oxide asymmetric coin cell (ACC) supercapacitor showed a high energy density of 33.3 Wh kg–1 at a power density of 624 W kg–1. The 3D nanostructure of ZCS/GO/CNT/Graphene oxide has great potential for developing foldable energy storage devices.

Probing structural and electrochemical properties of a 2D CoMoO4@hBN nanocomposite as pseudocapacitive electrode for high-performance supercapacitors

The effectiveness of energy storage is largely determined by the electrode material's performance in critical areas. Enhancements in ion transport, cyclic stability, rate capability, and specific capacitance directly boost the supercapacitors' overall performance and broaden their application potential. This study aims to enhance these properties by incorporating hexagonal boron nitride (hBN) into cobalt molybdate (CoMoO4) material in a 1:1 stoichiometric ratio. The CoMoO₄@hBN nanocomposite was synthesized using a hydrothermal method followed by ball milling. The X-ray diffraction (XRD) analysis confirmed the formation of a single-phase CoMoO4@hBN composite, with a significant increase in crystallite size from 18.21 nm in pure CoMoO₄ to 25.6 nm, along with a slight shift in diffraction peaks, indicating enhanced crystallinity and structural defects due to the substitution of oxygen with boron atoms. Raman spectroscopy revealed that the composite retains the characteristic peaks of both CoMoO₄ and hBN, with stable sharp peaks at 936 cm−1 (Mo=O bond) and 1367 cm−1 (E2g peak of hBN) even after 20 depth measurements, confirming successful conjugation and consistent vibrational properties. The X-ray photoelectron spectroscopy (XPS) showed a slight shift in Co 2p and Mo 3d binding energies to higher values, suggesting improved electronic interactions between CoMoO4 and hBN, which could enhance the composite's conductivity. The electrochemical analysis demonstrated that incorporating h-BN significantly boosts the electrode's performance compared to pristine CoMoO4, with about 37 % increase in specific capacitance at 1 A g−1, reduced charge transfer resistance (0.11 Ω), and superior cyclic stability with 96 % capacitance retention after 5000 cycles. These findings indicate that hBN enhances both the electrical conductivity and structural integrity of CoMoO4, positioning the CoMoO4@hBN composite as a promising material for high-performance supercapacitors.

Synthesis and Electrochemical Performances of Fluffy Carbonized Hexagonal KCoPO4 as Pseudocapacitive Electrode for High performing Hybrid Supercapacitor Applications

AbstractElectrochemical energy storage is one of the effective ways that can address the mentioned issues as alternative energy/power produced through solar or windmills can effectively be stored for continuous usage. Hybrid/Asymmetric supercapacitors can deliver a significant amount of power density as well as increased energy density with better rate capability and longer lifespan. The fluffy carbonized hexagonal KCoPO4 synthesized via a simple sol‐gel method accompanied by calcination has delivered high capacitance and longer cyclibility as a positive electrode in aqueous asymmetric supercapacitors. The fluffy carbonized hexagonal KCoPO4 exhibited a specific capacitance equal to 725 F/g at 0.5 A/g current density with excellent cyclic stability. The predominant intercalative pseudocapacitive charge storage behavior seems to be the reason behind the high capacitance of the electrode due to the active involvement of Co2+/3+ redox couple mediate charge storage as intercalative (inner) and capacitive, (outer) surface charges storage on the electrode were close to 37 % and 63 % respectively. Aqueous Asymmetric supercapacitor mode with KCoPO4 being a positive electrode and activated carbon being a negative electrode (KCoPO4//AC) was designed to address its performance in 2 M KOH aqueous electrolyte. The fabricated device in AASc mode (AC//KCoPO4) achieved the highest energy density close to 121.1 Wh/kg with a high power density of 6945 W/kg in the potential window of 1.5 V in 2 M KOH electrolyte.