Assembly of high-performance hybrid supercapacitors using FeCo2O4 microflowers as battery-type cathode materials

In this work, FeCo₂O₄ microflowers (MFs) and microparticles (MPs) were respectively prepared at different temperatures via a wet chemical method, along with a post annealing treatment in air. These MFs and MPs exhibited huge specific surface area and a large number of mesopores. Several electrochemical tests were conducted in a three-electrode configuration. The FeCo₂O₄ MFs delivered a specific capacity of 301.3C g^?1, higher than 253.9C g^?1 for FeCo₂O₄ MPs. A hybrid supercapacitor (HSC) device was assembled with FeCo₂O₄ as cathode and activated carbon (AC) as anode to investigate the practical applications in electrochemical energy storage. The FeCo₂O₄ MFs//AC HSC delivered a capacity of 107.2C g^?1 at 1 A g^?1 and an energy density (E_d) of 25.7 W h kg^?1 at 862.6 W kg^?1, respectively, while the FeCo₂O₄ MPs//AC HSC showed an E_d of 23.8 W h kg^?1 at the power density (P_d) of 878.9 W kg^?1. The two HSCs showed little capacity decay after 3000 cycles at 6 A g^?1. The capacity of FeCo₂O₄ MFs and the obtained E_d of HSC were in a high status among those of transition metal oxides (TMOs)-based electrodes reported earlier. The current synthetic strategy can be used as a reference to the synthesis of other similar electrochemical materials for HSC electrodes.     

MOFs derived (Ni0.75Co0.25)Se2 nanoparticles embedded in N-doped nanocarbon for hybrid supercapacitors

Bimetallic selenides have aroused great interest as the electroactive materials for energy storage because of their high conductivity, robust electrochemical activity, and the synergistic effect. Herein, (Ni_0.75Co_0.25)Se₂ nanoparticles embedded in N-doped nanocarbon ((Ni_0.75Co_0.25)Se₂@NC) hybrids were derived from nickel and cobalt bimetal-organic frameworks (NiCo-MOFs), which were synthesized by ethylene glycol solvothermal method. Due to the synergistic contributions and unique architecture, (Ni_0.75Co_0.25)Se₂@NC hybrids electrode presents a considerable specific capacity of 536.6 C g^?1 at a discharge current density of 1 A g^?1. In addition, an as-assembled (Ni_0.75Co_0.25)Se₂@NC//activated carbon (AC) hybrid supercapacitor (HSC) ((Ni_0.75Co_0.25)Se₂@NC//AC HSC) shows large specific capacitance (73.6 F g^?1 at 0.5 A g^?1), outstanding energy density (26.2 Wh kg^?1 at 400 W kg^?1) with superior cyclic performance (88.7% of capacity retention after 5000 cycles). Furthermore, a (Ni_0.75Co_0.25)Se₂@NC//AC device could drive a mini-fan running for 67 s. Thus, (Ni_0.75Co_0.25)Se₂@NC is an outstanding active material for electrochemical energy storage.     

Facile fabrication of flower-like binary metal oxide as a potential electrode material for high-performance hybrid supercapacitors

Developing efficient electrode material with rational design and structure remains a crucial and great challenge for the significant improvement of high-performance hybrid supercapacitors (HSCs). Particularly, the performance of the HSCs can be largely enhanced by designing the battery-type Faradaic material with well-defined morphology and defective engineering. Here, a facile and effective strategy is utilized to develop oxygen-deficient flower-like three-dimensional NiMoO_4?δ (O_d-NMO) nanomaterial via hydrothermal process and following thermal-treatment under an inert-gas atmosphere. The presence of oxygen deficiency in the O_d-NMO is evaluated utilizing various spectroscopy techniques by comparing the pristine NiMoO₄ (P-NMO) heat treated under an ambient atmosphere. The electrochemical studies indicate that the oxygen defect sites in the O_d-NMO electrode have a considerable role in the betterment of supercapacitive performances. Hence, the O_d-NMO electrode provides a large specific capacity of 789 mA h g^?1 at 1 A g^?1 with an excellent rate capability than the P-NMO (579 mA h g^?1). Besides, the fabricated HSC based on O_d-NMO flower and activated carbon as the positive and negative electrodes, delivers a specific capacitance as high as 153 F g^?1 and accomplishes a large energy density (47.76 W h kg^?1) and power density (51.69 kW kg^?1) with improved long-term stability.     

A new strategy for porous carbon synthesis: Starch hydrogel as a carbon source for Co3O4@C supercapacitor electrodes

A novel Co₃O₄@C composite with a three-dimensional (3D) interconnected network morphology was successfully fabricated by anchoring cobalt oxide nanocrystals onto porous carbon originating from starch hydrogels via freeze drying, precarbonization and thermal treatment in an aqueous system. Benefiting from unique structural features, the optimized electrode delivers an excellent capacitance of 1314.0 F g^?1 (1 A g^?1) and outstanding durability in terms of capacity preservation (93.5% over 10,000 cycles). In addition, an asymmetric supercapacitor consisting of DF-2 and active carbon exhibits an energy density of 149.1 Wh?kg^?1 at 800 W kg^?1 while maintaining great stability. The observed excellent performance is attributed to the unique 3D network, good conductivity and high surface-to-volumetric ratio of the carbon skeleton derived from the starch gel, which has wide scope for applications.     

MWCNTs-GONRs/Co3O4 electrode with needle-like arrays for outstanding supercapacitors

Multiwalled carbon nanotubes-graphene oxide nanoribbons (MWCNTs-GONRs) exhibit high specific surface area and good electroconductivity because of their unique three-dimensional cross-linking structure with the properties of both CNTs and GONRs. In this study, a hydrothermal method was employed to anchor MWCNTs–GONRs onto a Ni foam (NF) to obtain a precursor substrate. Subsequently, Co₃O₄ arrays were grown on the NF substrate to synthesize a MWCNTs–GONR/Co₃O₄ electrode. The electrode showed a capacitance of 846.2 F g⁻¹ at 1 A g⁻¹ and a capacitance retention of 90.1% after 3000 cycles. Furthermore, MWCNTs–GONRs/Co₃O₄ and active carbon (AC) were used as the positive and negative electrodes, respectively, to assemble a supercapacitor, which delivered a maximum energy density of 38.23 W h kg⁻¹ and a high power density of 6.80 kW kg⁻¹. In addition, the specific capacitance of the device reached a maximum of 91.5% after 9000 cycles. Thus, the MWCNTs–GONRs/Co₃O₄ electrode showed huge potential for supercapacitor applications.     

Nanoengineering of ZnCo2O4@CoMoO4 heterogeneous structures for supercapacitor and water splitting applications

A hybrid ZnCo₂O₄@CoMoO₄ heterogeneous structure deposited onto nickel foam was synthesized via a two-step hydrothermal process. The results demonstrate that the hybrid architecture exhibits excellent electrochemical performance, including the specific capacitance of 1040C g^?1 at 1 A g^?1 for hybrid structures, high energy density of 87.3 Wh kg^?1 at a power density of 2700 W kg^?1 for an as-assembled supercapacitor and excellent cycle stability with a capacity retention of 99% undergoing 8000 charge-discharge for the device. Moreover, it also shows favorable electrocatalytic activity with low overpotentials of 237 mV at 20 mA cm^?2 for oxygen evolution reaction and 114 mV at 10 mA cm^?2 for hydrogen evolution reaction, and low cell voltage of 1.54 V at 10 mA cm^?2 for overall water splitting. In addition, the stability maintains well for the long-term use of 13 h. We believe that this hybrid ZnCo₂O₄@CoMoO₄ heterogeneous structure could be a promising candidate for future energy storage and conversion.     

Holey graphene interpenetrating networks for boosting high-capacitive Co3O4 electrodes via an electrophoretic deposition process

A composite of Co₃O₄/holey graphene (Co₃O₄/HG) was prepared via a facile hydrothermal route, and was then processed into an electrode by an electrophoretic deposition process. Holey graphene (HG) wrapped Co₃O₄ to form a 3D skeleton network, thereby providing high electrical conductivity, and the holes in HG could further shorten the electrolyte ion diffusion pathway. Therefore, by adjusting the mass ratio of Co₃O₄ to HG, the Co₃O₄/HG composite afforded an enhanced capacitance of 2714 F g⁻¹ (at a current density of 1 A g⁻¹), which is 20 times higher than that of pure Co₃O₄. To further explore the practical applications of Co₃O₄/HG, a symmetric supercapacitor employing Co₃O₄/HG was fabricated. The supercapacitor functioned stably at potentials up to 1.2 V, with an enhanced energy density of 165 Wh kg⁻¹ and a high power density of 0.6 kW kg⁻¹ at 1 A g⁻¹.     

Construction of pseudocapacitive Li2-xLaxZnTi3O8 anode for fast and super-stable lithium storage

Lithium-ion capacitors (LICs) composed of battery-type anodes with large energy densities and capacitor-type cathodes with high power densities are considered as appealing energy-storage devices. Here, a LIC with good performance is constructed using active carbon (AC) as the cathode and Li_1.95La_0.05ZnTi₃O₈ (LL5ZTO) as the anode. LL5ZTO doped with La is synthesized via a one-step solid-state route. The kinetics and structural stability of LZTO are enhanced by La-doping. Thus, LL5ZTO exhibits good Li-storage performance. The discharge specific capacity reaches 182.6 mAh g^?1 at 3 A g^?1 (120th cycle) for LL5ZTO. The LIC based on the LL5ZTO anode and the AC cathode delivers an energy density of 59.72 Wh kg^?1 at 846.4 W kg^?1, and a high power density of 8771 W kg^?1 at 19.49 Wh kg^?1. Furthermore, the capacity retention is over 90% after 3000 cycles for the LIC at 2 A g^?1. The good electrochemical performance indicates that the constructed LIC is expected to use in advanced energy storage devices.     

Interface bonding engineering for constructing a battery-type supercapacitor cathode with ultralong cycle life and high rate capability

The low rate and poor cycle greatly limit the large-scale applications of supercapacitors electrodes in energy storage field. In this work, the SnS₂/Ni₃S₂ nanosheets arrays are bonded on N/S co-doped graphene nanotubes though N–Sn/Ni and S–Sn/Ni interface bonds employing a simple hydrothermal method to form a self-supported battery-type supercapacitors cathode. A series of characterization and DFT calculations indicate that the interface bonding not only automatically generates the internal electric field and allows more redox reactions to carry out easily, but also effectively reduces the OH^? ions adsorption energy and maintains the integration of the electrode structure. This unique design greatly promotes the electronics/ions transfer and reaction kinetics of the cathode, and substantially enhances its rate capability and durability. Detailedly, a high specific capacity of 296.9 mAh g^?1 at 2 A g^?1 is obtained. More impressively, the cathode still holds 155.6 mAh g^?1 when the current density is enlarged to 100 A g^?1, as well as it can retain 84% initial capacity over 50,000 cycles. Besides, an assembled asymmetric supercapacitor utilizing the prepared N/S-GNTs@B–SnS₂/Ni₃S₂ nanosheets arrays cathode and activated carbon anode presents a large energy density of 51 W h kg^?1 at 850 W kg^?1 and outstanding cycling stability. This work provides an effective strategy for improving rate capability and cycle lifespan of battery-type supercapacitors electrodes, and pushes the metal compounds forward a significant step in the practical applications of energy storage devices.     

Unique CNTs-chained Li4Ti5O12 nanoparticles as excellent high rate anode materials for Li-ion capacitors

Composite anode materials with a unique architecture of carbon nanotubes (CNTs)-chained spinel lithium titanate (Li₄Ti₅O₁₂, LTO) nanoparticles are prepared for lithium ion capacitors (LICs). The CNTs networks derived from commercial conductive slurry not only bring out a steric hindrance effect to restrict the growth of Li₄Ti₅O₁₂ particles but greatly enhance the electronic conductivity of the CNTs/LTO composites, both have contributed to the excellent rate capability and cycle stability. The capacity retention at 30 C (1 C = 175 mA g^?1) is as high as 89.7% of that at 0.2 C with a CNTs content of 11 wt%. Meanwhile, there is not any capacity degradation after 500 cycles at 5 C. The LIC assembled with activated carbon (AC) cathode and such a CNTs/LTO composite anode displays excellent energy storage properties, including a high energy density of 35 Wh kg^?1 at 7434 W kg^?1, and a high capacity retention of 87.8% after 2200 cycles at 1 A g^?1. These electrochemical performances outperform the reported data achieved on other LTO anode-based LICs. Considering the facile and scalable preparation process proposed herein, the CNTs/LTO composites can be very potential anode materials for hybrid capacitors towards high power-energy outputs.     

Electrochemical behavior of CuO/rGO nanopellets for flexible supercapacitor,non-enzymatic glucose,and H2O2 sensing application

In the present article, graphene oxide (GO) sheets and monoclinic copper oxide (CuO) nanocrystals are connected with each other and result in the formation of CuO/rGO nanopellets, and these nanopellets synthesized using coprecipitation method. The nanopellet structured CuO/rGO composite on carbon cloth, which act as current collector exhibits specific capacitance of 188 F g^?1 at a current density of 0.2 A g^?1 and up to 96.3% capacity retention after 2000 charge-discharge cycles. It shows a maximum energy density of 7.32 Wh kg^?1 and power density of 53 W kg^?1. The glucose sensing characteristics of CuO/rGO nanopellet is investigated on carbon cloth and ITO substrate. It shows glucose sensitivity of 0.805 mA mM^?1 cm^?2 and 0.2982 mA mM^?1 cm^?2 for a bundle like structured CuO/rGO composite on carbon cloth and ITO substrate, respectively. Further H₂O₂ sensing is studied on ITO substrate, which manifests H₂O₂ sensitivity of 84.39 μA mM^?1 cm^?2. The results indicate that nanopellet structured CuO/rGO composite could be a promising electrode material for supercapacitor, glucose, and H₂O₂ sensor.     

Oxygen vacancy-rich flower-like nickel cobalt layered double hydroxides for supercapacitors with ultrahigh capacity

One of the main difficulties for high-performance supercapacitors (SCs) is to design rational structures with excellent electrochemical properties. Herein, oxygen vacancy-rich nickel-cobalt layered double hydroxide, which has excellent supercapacitor performance, is prepared through an electrodeposition procedure and in situ oxidation process on nickel foam substrate. The conductivity and electrochemical properties are significantly improved by oxygen vacancies, which can be adjusted via hydrogen peroxide treatment. NiCo-LDH with oxygen vacancy (O_v-NiCo-LDH) attains a superior specific capacity of 1160 C g^?1 at the current density of 1 A g^?1 and shows a good capacity retention rate (61% of its original specific capacity is left at 20 A g^?1). Significantly, when the power density is 1.75 kW kg^?1, the energy density of the assembled symmetric supercapacitor (SSC) device is up to 216.19 Wh·kg^?1. This vacancy engineering strategy is helpful to the design of active materials for energy storage devices in the future.     

Waste catkins-derived graphitic carbon/Co3O4 composites as long-life and high-rate anodes for lithium-ion battery

Upgrading waste re-utilization has been regarded as an important concept to promote the sustainable development of social economy. Herein, waste catkins were used as carbon source and template to prepare graphitic carbon/Co₃O₄ composites through cobalt salt immersion, in-situ carbonization and calcination. The obtained Co₃O₄/C composites inherit the microtubular structure of catkins with ultra-thin tube wall and large tube cavity. Particularly, the sample (Co₃O₄/C-280) calcined at 280 °C in air shows a morphology of the hollow Co₃O₄ spheres (av. 50 nm) evenly embedded on the biocarbon tube. As an anode for lithium-ion battery, such unique structure is more conductive to alleviate volume expansion. As expected, Co₃O₄/C-280 electrode has excellent rate capability at 5 A g⁻¹ and stable long-cycle performance (647.3 mA h g⁻¹, 1800 cycles, 1 A g⁻¹). The presence of pseudo-capacitance behavior plays an important role in improving the capacity of material. The good electrochemical properties of Co₃O₄/C-280 can be ascribed to the synergistic effect of hollow tubular structure and graphitic carbon. Therefore, the strategy of making waste profitable is in line with the theme of green and sustainable development, and provides a reference for improving lithium storage performance of Co₃O₄-based anode materials.     

Anchoring mesoporous Fe3O4 nanospheres onto N-doped carbon nanotubes toward high-performance composite electrodes for supercapacitors

Fe-based oxide electrodes for practical applications in supercapacitors (SCs) suffer from low conductivity and poor structural stability. To settle these issues, we report on the design and synthesis of Fe₃O₄/carbon nanocomposites via firmly anchoring mesoporous Fe₃O₄ nanospheres onto N-doped carbon nanotubes (N-CNTs) via C–O–Fe bonds. Mesoporous Fe₃O₄ nanospheres are featured by rich electroactive sites and short ion diffusion pathways. The N-CNTs, on the other hand, serve as the scaffolds, which not only provide conductive networks but also suppress the accumulation between mesoporous Fe₃O₄ nanospheres as well as alleviate volume changes during charge/discharge cycles. Accordingly, the constructed Fe₃O₄/N-CNTs nanocomposite electrode demonstrates improved specific capacity values of up to 314 C g⁻¹ at 1 A g⁻¹, with 92% retention of the initial capacity after 5000 cycles at 10 A g⁻¹. In addition, the assembled Fe₃O₄/N-CNTs//active carbon (AC) asymmetric supercapacitor (ASC) device possesses an energy density of 25.3 Wh kg⁻¹, suggesting that the prepared Fe₃O₄/N-CNTs nanocomposites are promising electrode materials for use in SCs.     

Highly porous metal organic framework derived NiO hollow spheres and flowers for oxygen evolution reaction and supercapacitors

In this study, metal-organic-framework (MOF) derived porous NiO hollow spheres and flowers were obtained using facile solvothermal synthesis and heat treatment. After pyrolyzing, the flower like and hollow spherical like morphology of NiO nanoparticles was successfully inherited from the initial MOF-based templates. The electrochemical studies demonstrated that the porous NiO hallow spheres unveiled a better supercapacitive performance (specific capacitance (C_s) = 1058 F g^?1 at current density (j) = 2 A g^?1) and oxygen evolution reaction (OER) catalytic activity (overpotential (?) = 323 mV) compared to porous NiO flowers (C_s = 857 F g^?1 at j = 2 A g^?1 and ? = 346 mV). Moreover, excellent capacity retention of over 93% was obtained in porous NiO-hs nanoparticles even after 5000 cycles. The fabricated NiO//Fe₂O₃ asymmetric supercapacitor delivered an energy density (E) of 35.75 W h Kg^?1 under power density (P) of 780 W kg^?1 and showed promising stability over 3000 cycles. Considering the ease of preparation and high catalytic activity and supercapacitive performance, these prous NiO hallow structures can be considered as a potential electrode material for next generation energy storage devices and OER catalysts.     

Promising electrode material of Fe3O4 nanoparticles decorated on V2O5 nanobelts for high-performance symmetric supercapacitors

Bundled V₂O₅ nanobelts decorated with Fe₃O₄ nanoparticles (F3V nanostructures) were successfully synthesized to develop a low-cost electrode material for energy storage applications. The synthesized samples were subjected to structural, morphological and electrochemical studies. The Fe₃O₄ nanoparticles decorated over bundled V₂O₅ nanobelts exhibited better electrochemical properties than the pristine Fe₃O₄ nanoparticles and V₂O₅ nanobelts. The electrochemical behavior of the fabricated electrodes was investigated in an electrolyte of 3 M KOH, demonstrated an exceptional specific capacity values of 750.1, 660.3, and 1519 F g^–1 for V₂O₅, Fe₃O₄, and F3V respectively at a current density of 15 A g^–1. The assembled F3V symmetric supercapacitor (SSC) device exhibited an excellent specific capacitance of 93 F g^–1 at a current density of 0.5 A g^–1, delivering energy and power densities of 13 Wh.kg^–1 and 1530 W kg^–1, respectively, and superior long-term cycling stability of ～84% capacity retention over 5000 galvanostatic charge–discharge cycles. These findings demonstrate the extraordinary electrochemical characteristics of the F3V nanostructures, indicating their potential use in energy storage applications.     

Three-dimensional carbon-based endogenous-exogenous MoO2 composites as high-performance negative electrode in asymmetric supercapacitors and efficient electrocatalyst for oxygen evolution reaction

It is not an easy way to design composite electrodes with a high concentration of the constituent. This study cleverly exploited the phase transformation of molybdenum oxide to synthesize three-dimensional carbon-based endogenous-exogenous MoO₂ composites (EEC) by a two-step process. MC-15 exhibited the most outstanding electrochemical performance among EEC, with a specific capacitance up to 411.1 F g^?1 in Na₂SO₄, due to the design of MoO₂, which could be highly loaded with three-dimensional carbon. In addition, the electrode capacitance remains up to 94.1% after 5000 cycles, attributed to the synergy effect of three-dimensional carbon and molybdenum dioxide by providing an abundance of active sites for MoO₂ and overcoming its stacking. In this way, the electrochemical properties of the EEC electrode are not compromised by the volume expansion during the electrochemical process. The energy density of the asymmetric supercapacitor using this material as the negative electrode and MnO₂@CC is 14 W h kg^?1 at a power density of 802 W kg^?1, showing a significant increase in energy density over the asymmetric supercapacitor with a conventional negative electrode (activated carbon, energy density of 3.36 W h kg^?1 and power density of 700 W kg^?1). Its specific capacitance remained 84.9% after 2500 cycles. In addition, an overpotential of only 348 mV was required to drive oxygen evolution in alkaline electrolytes with a Tafel slope as low as 88.7 mV dec^?1; the 20 h stability test retains almost 100%. The results show that the design optimization of the negative electrode material provides a simple and effective strategy to increase the energy density of supercapacitors, and EEC electrode materials are a great candidate to be utilized in supercapacitors with excellent performance as well as electrolytic water.     

Polypyrrole-wrapped NiCo2S4 nanoneedles as an electrode material for supercapacitor applications

In this study, dicobalt tetrasulfide (NiCo₂S₄) nanoneedles were successfully synthesized by a two-step hydrothermal method on nickel foam. A layer of polypyrrole (PPy) was further wrapped on the surface of the NiCo₂S₄ nanoneedles by in-situ polymerization. The obtained NiCo₂S₄@PPy composite was investigated for supercapacitor applications, which exhibited a capacitance of 1842.8 F g^?1 at 1 A g^?1. An asymmetric supercapacitor device fabricated with an activated carbon negative electrode and NiCo₂S₄@PPy positive electrodes exhibited an energy density of 41.2 Wh kg^?1 at 402.2 W kg^?1 with a high charge–discharge cycling stability (92.8% after 5000 cycles). These results demonstrate that NiCo₂S₄@PPy electrodes have broad application prospects as energy storage electrode materials.     

Development of bifunctional Mo doped ZnAl2O4 spinel nanorods array directly grown on carbon fiber for supercapacitor and OER application

Electrochemical energy storage and water splitting strategies may be greatly improved with proper structural design and doping techniques. In the present study, molybdenum-doped ZnAl₂O₄ loaded on carbon fiber (Mo–ZnAl₂O₄/CF) was fabricated via a simple hydrothermal synthetic approach. Due to its unique hierarchical nanostructures and enhanced electrical, structural topologies, Mo-doped ZnAl₂O₄ demonstrates exceptional supercapacitor performance and electrocatalytic oxygen evolution reaction activity. The Mo-doped ZnAl₂O₄ electrode material exhibited 1477.63 F g^?1 specific capacitance, 46.57 Wh Kg^?1 specific energy and specific power of 476.4 W kg^?1 at 1 A g^?1. After 5000 cycles, the pseudo supercapacitor retains 97.46% of its capacitance and displays stable behavior over 50 h. During the OER reaction, the Mo–ZnAl₂O₄/CF as an electrocatalyst rapidly self-reconstructs, resulting in many oxygen vacancies, and causes a lower 38 mV dec^?1 Tafel slope and overpotential potential of 255 mV to achieved 10 mA cm^?2 current flow and responsible for the excellent stability of the electrocatalyst. These findings suggest that multifunctional materials based electrode for electrical energy conversion and storage become more efficient and stable by using Mo for doping to generate porous hierarchical structures and local amorphous phases.     

Facile synthesis and characterization of conducting polymer-metal oxide based core-shell PANI-Pr2O–NiO–Co3O4 nanocomposite: As electrode material for supercapacitor

Metal oxide nanoparticles and their composites with conducting polymers, specifically Polyaniline (PANI) were utilized for fabricating nanoscale supercapacitor (SC) electrode materials. In the present study, we have synthesized pristine Pr₂O₃, NiO, Co₃O₄ nanoparticles, binary PANI-Pr₂O₃, PANI-NiO, PANI-Co₃O₄, ternary Pr₂O₃–NiO–Co₃O₄, and quaternary PANI-Pr₂O₃–NiO–Co₃O₄ spherical core-shell nanocomposite using co-precipitation and ultra-sonication methods. The grown samples were characterized with different analytical techniques. The XRD pattern revealed that the as-synthesized products were crystalline with Pr₂O₃ hexagonal phase, NiO cubic phase, and Co₃O₄ cubic phase in pure and nanocomposites. The Williamson-Hall, Scherrer, and size-strain plot methods were employed to study the crystalline development and contribution of micro-strain. FTIR pattern exhibited the metal-oxygen and PANI bond vibrations. FE-SEM images shown the spherical core-shell shape morphology of quaternary nanocomposite. EDX evident the presence of praseodymium, cobalt, and nickel in synthesized samples. UV–vis spectroscopy confirmed the absorption in the visible region. The IV graphs showed a higher conductivity of quaternary nanocomposite. The cyclic voltammetry results revealed that the quaternary nanocomposite has a higher specific capacitance 500 Fg^-1 as compared to binary nanocomposites 134 F g^?1 (PANI-Pr₂O₃), 143 F g^?1 (PANI-Co₃O₄), 256 F g^?1 (PANI-NiO), and PANI (90.8 F g^?1) at a scan rate of 5 m Vs^?1. The GCD results also showed that the quaternary nanocomposite has a higher specific capacitance of 905 F g^?1 at current density 1 A g^?1 with maximum energy density and power density of 87.99 kWhkg^-1 and 2.6 k W kg^?1_, respectively. The EIS curve also confirmed that the quaternary nanocomposite has a lower polarization resistance (R_p) and solution resistance (R_s). The higher capacitance of quaternary nanocomposite can facilitate ion transfer, and the formation of its core-shell structure flourish to enhance surface-dependent electrochemical properties. Furthermore, this study gives a novel research idea to manufacture electrode materials for supercapacitors.