Electrode For Asymmetric Supercapacitors Research Articles

High-energy Mn2V2O7//C asymmetric supercapacitors in aqueous/organic hybrid electrolytes

The demand for advanced energy storage devices, such as high-energy density supercapacitors, has spurred efforts to develop new environmentally friendly and efficient electrode materials and electrolyte solutions for sustainable development. A prominent strategy is the fabrication of high-voltage and energy-density asymmetric supercapacitors (AS). In this study, dimanganese divanadate (Mn2V2O7, MVO) particles were synthesized via a hydrothermal process and used as pseudocapacitive electrodes for AS. The pseudocapacitive MVO electrode offered synergistic advantages of reversible surface or near-surface Faradaic reactions for charge storage. Another approach to address the challenges of limited energy density in supercapacitors was modifying the electrolyte solution to widen the operating voltage window and increase energy density. A hybrid electrolyte solution of 5 M sodium perchlorate (NaClO4) in a mixture of (2:1) volume ratio of acetonitrile (AN) and water (H2O) was introduced to expand the voltage window in the AS. The fabricated AS with MVO as a pseudocapacitive electrode and activated carbon as a double-layer capacitive electrode operated in a voltage window > 2.0 V with the hybrid electrolyte. The AS device exhibited a capacitance of 156.9 F g−1 at 0.1 A g−1 and a high energy density of 87.2 Wh kg−1, surpassing the carbon-based symmetric supercapacitor (58.9 Wh kg−1). Furthermore, the pseudocapacitive supercapacitor showed exceptional long-term stability over 50,000 cycles. Structural and surface characterization of the MVO electrode after CV testing validated that the charge storage mechanism in Mn2V2O7//C was a surface-controlled process. The performance of the AS pouch cell revealed the great promise of the pseudocapacitive electrode in practical applications.

Hydrothermal synthesis of rGO-decorated NiMn2O4 nanoneedles for high-performance positive electrode in asymmetric supercapacitors

Pseudocapacitive electrode materials inherently have low electron conductivity, which prevents an energetic material from being fully utilised. We were able to produce effective hierarchical NiMn2O4/rGO composites, which provide an appealing solution to this issue. The composites were synthesised using a one-step hydrothermal approach. Due to the high electrical conductivity of reduced graphene oxide (rGO), the needles on plate like morphology of NiMn2O4, and the strong hold of dynamic materials to the current collector, the resulting hybrid electrodes exhibit a specific capacitance of 1628 Fg−1 at a current density of 1 Ag−1. They also demonstrate excellent rate performance and remarkable cycling stability, with a capacitance retention of 97.4 % after 10,000 cycles. In addition, the NiMn2O4/rGO//AC asymmetric supercapacitor (ASC) exhibits a peak energy density of 45Whkg−1 when operated at a power density of 3240 Wkg−1. The ASC device has an impressive ultralong cycling life, with a capacitance retention rate of 89.1 % after undergoing 10,000 charge/discharge cycles. The NiMn2O4/rGO composites provide a scalable production method and demonstrate outstanding electrochemical performance. This presents an opportunity to create innovative hybrid electrodes for enhanced supercapacitors.

Solar-driven induced photoelectron remember effect involved in core–shell NiCo2S4@Ni3V2O8 composite electrode with superior electrochemical energy storage for asymmetric supercapacitor

Photo-assisted supercapacitor systems offer a compelling approach to effectively harnessing both solar and electrical energy. In this study, the core–shell heterostructure NiCo2S4@Ni3V2O8 (NCS@NVO) was successfully synthesized for the development of photosensitive supercapacitor electrodes. NCS@NVO demonstrated a pronounced photoelectron memory effect under illumination, attributed to the solar-driven contributions of both NCS and NVO, as photon absorption facilitated electron-hole pair separation and transport. Compared to the specific capacitance in the dark (2292F g−1 at 1 A g−1), the capacitance of the NCS@NVO composite electrode increased dramatically to 3025F g−1 when exposed to light. Moreover, the capacitance retention rate remained remarkably high at 99.83 % after 10,000 cycles at 20 A g−1. In addition, the NCS@NVO hybrid supercapacitor achieved an outstanding energy density of 63.56 W h kg−1 under illumination, alongside a power density of 789.84 W kg−1. This study thoroughly investigated the solar-induced photoelectron memory effect in the NCS@NVO composite electrode for asymmetric supercapacitors, paving the way for the design of high-performance photosensitive nano-electrodes in advanced electrochemical energy storage applications.

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.

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.

Hydrothermal synthesis of rGO and MnCoS composite for enhanced supercapacitor application

Nanostructured materials incorporating transition metal sulfides have demonstrated considerable potential across various applications, particularly in the realms of energy production and storage. Sulfide-based material preparation is a challenging and costly procedure that requires a high temperature and reducing atmosphere. This work reports that manganese cobalt sulfide (MCS) and reduced graphene oxide composite manganese cobalt sulfide (rMCS) were successfully prepared through a hydrothermal method. Various characterization techniques were employed to analyze the prepared materials, including X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Teller analysis, and X-ray photoelectron spectroscopy. In a three-electrode system, MCS and rMCS electrodes exhibit an excellent specific capacitance of 1695 and 1925 F g−1 at 1 A g−1 current density respectively. MCS delivers the capacitance retention of 99% and rMCS exhibits the capacitance retention of 100% capacitance retention over 5000 consecutive cycles. The constructed asymmetric supercapacitor electrode (rMCS//rGO) exhibits the energy and power density of 64 Wh kg−1 at 799 W kg−1, respectively with outstanding cyclic stability of 97.4% even after 10,000 cycles. The exceptional electrochemical properties of MCS with rGO composite electrode indicate that they would make an outstanding electrode material for cutting-edge energy storage devices.

Electrochemical synthesis of Mn–Ni–S on titania nanotubes as new dual-function electrodes for photo-assisted asymmetric supercapacitors

Photo-assisted energy storage systems, by which solar energy can be both converted and stored, have been of interest in the past few years. Novel energy conversion and storage technology is offered by photo-supercapacitors through the combination of an energy collecting unit and a supercapacitor. This dual-application system effectively generates and stores power in a single device, which makes it appropriate for various purposes. In this work, the electrochemical anodization-electrodeposition has been employed to fabricate manganese-nickel sulfide (Mn–Ni–S) nanostructures on titania nanotubes (TNs) and used them as photoelectrodes in photo-supercapacitors. The high surface area and improved properties make TNs considerably important for energy production and storage. Photoelectrochemical analysis was carried out in a three-electrode system under a xenon (Xe) lamp irradiation using the film prepared as the photoelectrode. The highest photocurrent and photovoltage were shown by MnNiS-3/TN electrode, indicating its superior photosensitivity. Upon illumination under a 0.7 mA/cm2 current density, the area-specific capacitance of MnNiS-3/TN electrode increased from 388.3 to 723.3 mF/cm2, which is 2.0, 3.6, and 12.8 times higher than the corresponding values for NiS/TN, MnS/TN, and bare TN electrodes under similar conditions, respectively. This indicates the considerable enhancement of the capacitance of this electrode induced by light. The desirable light-sensitive properties of MnNiS/TN make it capable of simultaneous solar energy harvesting and storage. Light sensitivity makes it possible to charge MnNiS/TN optically. More importantly, upon light irradiation, the capacity can be increased from 374.7 to 630.2 mF/cm2 (current density 0.5 mA/cm2) compared to the corresponding value in the dark. Using MnNiS-3/TN as the best photoelectrode and MnS/FTO, NiS/FTO, MnNiS-1/FTO, MnNiS-2/FTO, and MnNiS-3/FTO as the counter electrodes, photo-charged through light illumination on their surfaces, five asymmetric solid-state photo-supercapacitors (ASSPS) were prepared. MnNiS-3/TN//MnNiS-3/FTO device showed the largest CV curve area, which indicated its highest areal capacitance. High capacitance gain under irradiation (155.7% at 2.0 mA/cm2) and outstanding capacitance maintenance (97.9% over 10000 cycles) were shown by this ASSPS. Furthermore, a great energy density of 4855.4 mWh/cm2 was shown by the MnNiS-3/TN//MnNiS-3/FTO device under light irradiation. This research introduces a novel approach to the development of powerful solar energy conversion/storage devices.

Strategic design of MXene/CoFe2O4/g-C3N4 electrode for high-energy asymmetric supercapacitors

MXenes are emerging as the next-generation materials for energy storage due to their substantial surface area, exceptional conductivity, and abundant surface-terminating groups. However, the tortuous path for ion transfer within the restacked layers significantly limits the electrochemical performance of multilayered MXenes. To overcome this, interlayer spacers have been introduced. These spacers help mitigate ion diffusion barriers and enhance the accessibility of active sites, thereby improving the overall efficiency and longevity of MXene-based supercapacitors and related devices. In this study, a rational material is designed by incorporating CoFe2O4 and g-C3N4 into the layers of MXene through ultrasonication for supercapacitor application. The physicochemical properties of the synthesized materials have been comprehensively characterized using diverse techniques, revealing that MXene/CoFe2O4/g-C3N4 has successfully evolved into a multilayered structure possessing enhanced surface area, low restacking tendency, high pore diameter, and excellent pore volume. Leveraging these properties, it performs as a viable material for fabricating the working electrode with a specific capacitance (Csp) of 1506.2 F g−1 at a current density of 5 A g−1 in 3 M KOH. It shows good stability with 89 % capacitance retention over 7000 cycles. An asymmetric supercapacitor (ASC) constructed with MXene/CoFe2O4/g-C3N4 as positive electrode and activated carbon as negative electrode exhibits an energy density of 79.8 Wh Kg−1 and power density of 1343.3 W Kg−1. Furthermore, it shows a capacitive retention of 91 % over 10,000 cycles. This MXene based composite, with excellent capacitance and outstanding stability, offers an appreciable performance in the field of sustainable energy storage.

Binder-free copper manganese sulfide nanoflake arrays electrodeposited on reduced graphene oxide-wrapped nickel foam as an efficient battery-type electrode for asymmetric supercapacitors

In the current study, 2D interconnected copper manganese sulfide (CMS) nanoflake arrays are successfully electrodeposited on nickel foam (NF) and reduced graphene oxide-coated NF (NF/rGO). A pulsed current electrodeposition method is used to prepare a uniform and homogeneous coverage of rGO on NF. By using rGO as a conductive carbon-based template, an ultrathin nanoflake structure of CMS with smaller dimensions and higher electrochemically active surface area (ECSA) is achieved. The results reveal the battery-type behavior of the as-synthesized CMS electroactive materials. At a current density of 5 A g−1 this electrode delivers a significant specific capacity of 667 C g-1 and maintained a considerable proportion of its initial capacity, with a retention value of 83.2 % even after undergoing 3000 charge/discharge cycles. In addition, an asymmetric supercapacitor is fabricated by setting up the synthesized NF/rGO/CMS sample as the positive electrode and activated carbon as the negative electrode. The constructed device not only delivers an impressive energy density of 63.3 Wh kg-1 accompanied by an outstanding power density of 11214.5 W kg−1, but also exhibits a considerable cycling durability, enduring only a 12 % decline in specific capacitance after 3000 charge/discharge cycles at a current density of 5 A g−1.

N‐Doped Carbon Coated Bimetallic CoFe2O4 Nanomembranes as An Enhanced Negative Electrode for Asymmetric Supercapacitors

AbstractIn‐suit nitrogen‐doped carbon layer coated on CoFe2O4 nanomembrane (NC−CoFe2O4) directly grown on carbon cloth was successfully fabricated. The electrochemical performance was conveniently manipulated by regulating the molar ration of Co2+ : Fe3+ (molar ration=1 : 2, CoFe2O4 nanomembrane, 2.9 F cm−2). Nitrogen‐doped (N‐doped) carbon coating strategy on CoFe2O4 nanomembrane (NC−CoFe2O4) via annealing of polypyrrole (PPy) was presented and NC−CoFe2O4 nanomembranes displayed a prominent capacitance of 12.1 F cm−2 (2563.8 F g−1) at 5 mA cm−2. More important, the composite demonstrated more stable microstructure and showed long‐term cycling stability (16.0 % decrease after 7000 cycles), which was significantly better than the unmodified CoFe2O4 (55.8 % decrease after 1000 cycles). To verify the practicability of the materials, an aqueous asymmetric supercapacitor has been fabricated using NC−CoFe2O4 composite anode and MnO2/CNTs cathode, and the device has a remarkable wide operating voltage range of 1.9 V. In addition, the assembled device has an exceptional specific capacity of 1.3 F cm−2 at 10 mA cm−2, high energy density (43.3 Wh kg−1 at a power density of 642.9 W kg−1), and also with a good capacity retention rate of 84.9 % after 1000 cycles.

Eu-viologen based bimetal–organic frameworks nanosheets with Mn atoms anchored on Eu-µ-O skeletons as high-performance negative electrode for flexible asymmetric supercapacitors

Exploring advanced negative electrode materials is imperative to develop high-performance asymmetric supercapacitors for breaking through current energy density limits of supercapacitors, but remains challenging. Herein, a strategy is proposed to create a novel negative electrode by anchoring Mn single-atoms on Eu-viologen metal–organic frameworks (EV-Mn MOFs) nanosheets flowery architectures that self-supported on oxidized carbon cloths (OCC). Such EV-Mn/OCC achieves a negative broadened voltage window (−1 ∼ 0 V) and boosted areal capacitance (840.82 mF cm−2), which is four folds of the isostructural EV/OCC without Mn atoms and surpasses most of currently reported negative electrodes. Also, the EV-Mn/OCC manifests good cycling stability (∼80 % retention for 10,000 cycles). As deduced by the thorough studies of X-ray absorption fine spectra and X-ray photoelectron spectroscopies, the enhanced pseudocapacitance of EV-Mn/OCC definitely correlates to the valence modulation of Mn and Eu through internal electron transfer via Eu-O-Mn bonds on Eu-µ-O skeleton in EV-Mn MOFs. Subsequently, the constructed flexible all-solid-state symmetric supercapacitors employing EV-Mn/OCC as negative electrode can deliver a high energy density (86.89 μWh cm−2) at 1600 μW cm−2, outperforming many asymmetric devices based on traditional negative electrode materials. This work can spur the development of single-atom metallic electronic-modulation strategy for MOFs negative electrode material (MOFs-NEM), and accelerate their applications in flexible energy conversion and storage devices.

MXene and polyaniline coated 3D-printed carbon electrode for asymmetric supercapacitor

ABSTRACT 3D printing has emerged as an attractive manufacturing technique in supercapacitor electrodes owing to the precise and customisable fabrication of complex electrode designs, enhancing the performance and efficiency of the device. Despite the advantages, 3D-printed electrodes are limited by their low conductivity and electrochemical properties, predominantly due to the lack of availability of suitable conductive materials. To address this limitation, we modified the 3D-printed nanocarbon (3D-PnC) electrode by activation and surface deposition of Ti3C2Tx MXene. A solid-state asymmetric supercapacitor was fabricated by using 3D-PnC/Ti3C2Tx as the negative electrode and polyaniline (PANI) electrodeposited 3D-printed nanocarbon electrode (3D-PnC@PANI) as the positive electrode. The fabricated symmetric supercapacitor exhibits enhancement in overall voltage window, areal capacitance and energy density. The successful operation of the supercapacitor was demonstrated by the illumination of the red light-emitting diodes. Furthermore, this research opens the possibility of utilising MXene-modified 3D-printed electrodes for various electrochemical applications and devices.

The rational design of Fe2O3@MnO2 derived from Fe[Fe(CN)6]∙4H2O as negative electrode for asymmetric supercapacitor

Metal–organic frameworks (MOF)-derived nanomaterial have shown great promise as a supercapacitor anode materials. In this work, we successfully synthesized a novel Fe2O3@MnO2 composite with core–shell by hydrothermal techniques. MnO2 nanorods decorated on the Fe2O3 nanoparticles which was direct pyrolysis of Fe-PBA can combine of advantages of Fe2O3 and evenly dispersed MnO2 to obtain an ultra-wide voltage window of −1.1 V - 0.4 V and an excellent specific capacitance of 449 F g−1. The further constructed NiCo-LDH/rGO//Fe2O3@MnO2 asymmetric supercapacitor achieves a high energy density of 33.4 Wh kg−1 at a high power density of 800 W kg−1 and a capacity retention of more than 75 % after 10,000 cycle tests. This study not only corroborates the considerable potential of Fe2O3@MnO2 as anode material for supercapacitors, but also offers a novel approach to the design of asymmetric supercapacitors, which will facilitate the advancement of supercapacitor technology towards higher energy density and longer lifetime.

Complex polycation redox material interfaced with renewable porous carbon for asymmetric supercapacitors

Mixed polycation transition metal ferrites are known to exhibit unique and superior characteristics for structural, electrical, magnetic, and optical applications. Although a few binary transition metal ferrites are found to be suitable for electrochemical energy storage application, ternary transition metal ferrites are not investigated for asymmetric supercapacitors (ASCs). Mixed polycation oxides are expected to have increased active sites that can facilitate proton and electron transfer impacting the redox reactions. Specific crystal structure and associated lattice parameters as well as surface and morphological characteristics can also influence the energy storage properties. This study for the first time reports a novel complex polycation redox material, (CupMnqZnr)xFeyOz and renewable pinewood (PW) derived porous carbon (POC) as electrodes for ASC. Both (CupMnqZnr)xFeyOz and PW-POC are subjected to electrochemical characterization and used in ASC configuration with aqueous KOH electrolyte. It is anticipated that the Faradaic characteristics of (CupMnqZnr)xFeyOz will make it to serve as a cathode while PW-POC with capacitive behavior will act as anode in ASCs. Relatively higher specific capacitance of > 200 F/g is observed for the (CupMnqZnr)xFeyOz reference electrode and fabricated ASCs. Capacitance retention rate is tested in 10,000 cycles for the working electrodes whereas for ASC, the stability tests are performed over 100 charging-discharging cycles exhibiting relatively higher capacitance retention. (CupMnqZnr)xFeyOz appears to be a promising material for a supercapacitor.

Effects of ultrasonic power on the electrochemical characteristics of high-performance nanosized zinc–cobalt oxide electrodes for asymmetric supercapacitors

This study reports the preparation of ZnCo2O4 oxide (ZCO) electrode materials with favorable microstructure and porosity arrangement via ultrasonic electrodeposition-calcination. The application of ultrasonic waves at a power of 200 W (using ZCO-2) led to the development of a smooth and flat microstructure, characterized by the presence of numerous micropores. The lattice constant of ZnCo2O4 in the ZCO-2 oxide electrode material was determined to be 0.428 nm via TEM analysis. Furthermore, the XRD analysis of ZCOs demonstrated the effective synthesis of ZnCo2O4 electrode materials. The main lattice diffraction planes of ZCOs were observed at (111), (220), (311), (400), (511), and (440), with corresponding diffraction angles of 29.8°, 36.4°, 42.9°, 45.2°, 62.3°, and 66.5°, respectively. The application of 200 W ultrasonic power during electrochemical experiments significantly improved the electrochemical performance of ZCO-2. The ZCO-2 oxide electrode demonstrated remarkable area capacitance and negligible electrical impedance. At a current density of 3 mA/cm2, the area capacitance was measured to be 1.803 F/cm2. The ZCO-2 oxide electrode showed remarkable capacitance retention of 67.3 % even under high current density conditions. Furthermore, the asymmetric supercapacitor composed of ZCO-2 and AC (ZCO-2/AC ASC) showed outstanding electrochemical performance. The ZCO-2/AC ASC showed a capacitance of 5.721 F/cm3 at a current density of 0.5 mA/cm2. Furthermore, it demonstrated an energy density of 68.2 Wh/kg at a power density of 250 W/kg. The capacitor showed consistent performance and retained 63.8 % of its initial capacitance even after undergoing 24,000 cycles. Furthermore, the findings of this research provide substantial implications for the combination of ultrasonic electrodeposition with capacitors, while also presenting an innovative concept for electrode materials in high-performance supercapacitors.

Copper Phosphosulfide Nanosheets on Cu-Coated Graphene Fibers as Asymmetric Supercapacitor Electrodes

Copper Phosphosulfide Nanosheets on Cu-Coated Graphene Fibers as Asymmetric Supercapacitor Electrodes

Chemical vapor deposition-grown single-layer graphene-supported nanostructured Co3O4 composite as binder-free electrode for asymmetric supercapacitor and electrochemical detection of caffeic acid

In this study, we developed a monolayer graphene/nanostructured cobalt oxide (MLG/Co3O4) composite for asymmetric supercapacitor and electrochemical sensor applications. The MLG was grown by chemical vapor deposition process and the Co3O4 nanostructures were electrodeposited on the MLG surface. Scanning electron microscopy proved that there were flower-like nanostructured Co3O4 densely electrodeposited on the MLG surface. At a current density of 3 mA cm−2, the MLG/Co3O4 composite produced an areal capacitance of 3.73 F cm−2. After 10,000 cycles, the composite electrode still had 93.6 % of its initial capacitance at 5 mA cm−2. The asymmetric system displayed an areal capacitance of 929 mF cm−2 at 4 mA cm−2 with good cycle stability. The asymmetric electrode produced a specific energy of 51 μWh cm−2 and a specific power of 11.1 mW cm−2. Cyclic voltammetric measurements demonstrated that the composite showed redox peaks at 0.48 eV and 0.09 eV toward the determination of CA. With a sensitivity of 0.13 µA/µM/cm2 and a limit of detection of 0.009 µM, the composite showed CA concentrations, ranging from 0.5 to 480 M. The composite displayed excellent selectivity and the current produced for the interfering compounds was exceedingly low. Using the composite electrode, the spiked CA in red wine and green tea samples recovered remarkably effectively.

Influence of Deposition Potential on Electrodeposited Bismuth–Copper Oxide Electrodes for Asymmetric Supercapacitor

AbstractThe modern research reported the simplest low–cost synthesis of Bismuth–Copper oxide (Bi2CuO4) with spruce–leaf–like morphology and its applications in supercapacitor devices. Bi (NO3)3 . 5H2O was used as a precursor during an electrodeposition (ED) method to create the spruce–leaf–like Bi2CuO4 electrode. XRD, XPS, FE−SEM, EDX, and TEM were used to characterize the structures and morphologies of the synthesized materials, while CV, CP, and EIS were used to determine their electrochemical characteristics. The Bi2CuO4 phase was confirmed by XRD patterns, and electrochemical testing demonstrated that the material had better rate capability and an SC of 431.2 F/g at a scan rate of 2 mV/s. After 5,000 cycles, it retained 81.4 % of its energy. Additionally, the maximum SC that was attained by the created asymmetric solid–state device ASSD (Bi0.6 Vǀǀ1 M PVA−KOHǀǀAC) was 73.7 F/g. The energy density was 55.3 Wh/Kg at a power density of 4570 W/Kg. The exceptional electrochemical performance of Bi2CuO4 thin film electrodes recommends it has a promising material.

Hierarchical flower bud-like P, W co-doped NiCo2S4@MoS2 composites as high-performance electrodes for asymmetric supercapacitor

Engineering binary transitional metal sulfides (BTMSs)-based electrode materials with a rationally designed constituent architecture is a viable strategy for improving their rate capability and electrochemical durability, which provides a possibility for their application in supercapacitors (SCs). Herein, a novel three-dimensional (3D) flower bud-like phosphorus and tungsten co-doped NiCo2S4 and MoS2 composites (P, W-NCS@MS) is prepared on conductive carbon cloth using the hydrothermal method. The effects of P, W-doping, or MoS2-combination on the morphology, structure and electrochemical properties of NiCo2S4-based electrode materials are systematically studied. The designed P, W-NCS@MS achieves a high specific capacity of 1250C g−1 at 1 A g−1 and a satisfactory capacity retention of 80 % after 10,000 cycles. In addition, the asymmetric supercapacitor (ASC) constructed through P, W-NCS@MS and activated carbon electrodes delivers a high energy density of 65.0 Wh kg−1 at the power density of 400 W kg−1 and shows satisfactory cycling stability of 85 % capacitance retention after 20,000 cycles. Notably, the assembled ASC device successfully powered electronic devices in a serial circuit, highlighting its prospective applications in energy storage. This work offers a viable design approach for heteroatom doping and hierarchical interface structures in composite electrode materials toward high-performance SCs.

V2O5-assembled NiAl-layered double hydroxide as high-performance electrode for asymmetric supercapacitor

V2O5-assembled NiAl-layered double hydroxide as high-performance electrode for asymmetric supercapacitor