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One-step synthesis of Nickle Iron-layered double hydroxide/reduced graphene oxide/carbon nanofibres composite as electrode materials for asymmetric supercapacitor.

ABSTRACT: A novel NiFe-LDH/RGO/CNFs composite was produced by using a facile one-step hydrothermal method as electrode for supercapacitor. Compared with NiFe-LDH/CNFs, NiFe-LDH/CNTs and NiFe-LDH/RGO, NiFe-LDH/RGO/CNFs demonstrated a high specific capacitance of 1330.2 F g^-1 at 1 A g^-1 and a super rate capability of 64.2% from 1 to 20 A g^-1, indicating great potential for supercapacitor application. Additionally, an asymmetric supercapacitor using NiFe-LDH/RGO/CNFs composite as positive electrode material and activated carbon as negative electrode material was assembled. The asymmetric supercapacitor can work in the voltage range of 0-1.57 V. It displayed high energy density of 33.7 W h kg^-1 at power density of 785.8 W kg^-1 and excellent cycling stability with 97.1% of the initial capacitance after 2500 cycles at 8 A g^-1. Two flexible AC//LDH-RGO-CNFs ASC devices connected in series were able to light up a red LED indicator after being fully charged. The results demonstrate that the AC//LDH-RGO-CNFs ASC has a promising potential in commercial application.

SUBMITTER: Wang F

PROVIDER: S-EPMC5995954 | biostudies-literature |

REPOSITORIES: biostudies-literature

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High performance asymmetric supercapacitor based on Cobalt Nickle Iron-layered double hydroxide/carbon nanofibres and activated carbon.

Project description:A novel Cobalt Nickle Iron-layered double hydroxide/carbon nanofibres (CoNiFe-LDH/CNFs-0.5) composite was successfully fabricated through an easy in situ growth approach. The morphology and composition of the obtained materials were systematically investigated. When the two derived materials were used for supercapacitor electrodes, the CoNiFe-LDH/CNFs-0.5 composite displayed high specific surface area (114.2?m2?g-1), specific capacitance (1203?F?g-1 at 1?A?g-1) and rate capability (77.1% from 1?A?g-1 to 10?A?g-1), which were considerably higher than those of pure CoNiFe-LDH. Moreover, the specific capacitance of CoNiFe-LDH/CNFs-0.5 composite remained at 94.4% after 1000 cycles at 20?A?g-1, suggesting excellent long-time cycle life. The asymmetric supercapacitor based on CoNiFe-LDH/CNFs-0.5 as a positive electrode and activated carbon as a negative electrode was manufactured and it exhibited a specific capacitance of 84.9?F?g-1 at 1?A?g-1 and a high energy density of 30.2?W?h kg-1. More importantly, this device showed long-term cycling stability, with 82.7% capacity retention after 2000 cycles at 10?A?g-1. Thus, this composite with outstanding electrochemical performance could be a promising electrode material for supercapacitors.

| S-EPMC5498571 | biostudies-literature

Formation of a CoMn-Layered Double Hydroxide/Graphite Supercapacitor by a Single Electrochemical Step.

Project description:Hybrid electric storage systems that combine capacitive and faradaic materials need to be well designed to benefit from the advantages of batteries and supercapacitors. The ultimate capacitive material is graphite (GR), yet high capacitance is usually not achieved due to restacking of its sheets. Therefore, an appealing approach to achieve high power and energy systems is to embed a faradaic 2D material in between the graphite sheets. Here, a simple one-step approach was developed, whereby a faradaic material [layered double hydroxide (LDH)] was electrochemically formed inside electrochemically exfoliated graphite. Specifically, GR was exfoliated under negative potentials by CoII and, in the presence of MnII , formed GR-CoMn-LDH, which exhibited a high areal capacitance and energy density. The high areal capacitance was attributed to the exfoliation of the graphite at very negative potentials to form a 3D foam-like structure driven by hydrogen evolution as well as the deposition of CoMn-LDH due to hydroxide ion generation inside the GR sheets. The ratio between the CoII and MnII in the CoMn-LDH was optimized and analyzed, and the electrochemical performance was studied. Analysis of a cross-section of the GR-CoMn-LDH confirmed the deposition of LDH inside the GR layers. The areal capacitance of the electrode was 186 mF cm-2 at a scan rate of 2 mV s-1 . Finally, an asymmetric supercapacitor was assembled with GR-CoMn-LDH and exfoliated graphite as the positive and negative electrodes, respectively, yielding an energy density of 96.1 μWh cm-3 and a power density of 5 mW cm-3 .

| S-EPMC9826322 | biostudies-literature

Electrochemically Stable Cobalt⁻Zinc Mixed Oxide/Hydroxide Hierarchical Porous Film Electrode for High-Performance Asymmetric Supercapacitor.

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| S-EPMC6474017 | biostudies-literature

Facile Synthesis of CoSe/Co<sub>3</sub>O<sub>4</sub>-CNTs/NF Composite Electrode for High-Performance Asymmetric Supercapacitor.

Project description:Electrode materials are key factors for supercapacitors to endow them with excellent electrochemical properties. Here, a novel hybrid structure of a CoSe/Co3O4-CNTs binder free composite electrode on nickel foam was prepared via a facile flame method, followed by an electrodeposition process. Benefitting from the synergetic effects of the multicomponent (with low resistances of 1.542 Ω cm2 and a moderate mesoporous size of 3.12 nm) and the enlarged specific surface area of the composite material (77.4 m2 g-1), the CoSe/Co3O4-CNTs composite electrode delivers a high specific capacitance of 2906 F g-1 at 5 mV s-1 with an excellent rate stability. The fabricated CoSe/Co3O4-CNTs/NF//AC ASC exhibits a high energy density of 43.4 Wh kg-1 at 0.8 kW kg-1 and a long cycle life (92.7% capacitance retention after 10,000 cycles).

| S-EPMC9457315 | biostudies-literature

Modified Activation Process for Supercapacitor Electrode Materials from African Maize Cob.

Project description:In this work, African maize cobs (AMC) were used as a rich biomass precursor to synthesize carbon material through a chemical activation process for application in electrochemical energy storage devices. The carbonization and activation were carried out with concentrated Sulphuric acid at three different temperatures of 600, 700 and 800 °C, respectively. The activated carbon exhibited excellent microporous and mesoporous structure with a specific surface area that ranges between 30 and 254 m2·g-1 as measured by BET analysis. The morphology and structure of the produced materials are analyzed through Field Emission Scanning Electron Microscopy (FESEM), Fourier Transform Infrared Spectroscopy (FTIR), X-Ray Diffraction (XRD), Boehm titration, X-ray Photoelectron Spectroscopy (XPS) and Raman Spectroscopy. X-ray photoelectron spectroscopy indicates that a considerable amount of oxygen is present in the materials. The functional groups in the activated carbon enhanced the electrochemical performance and improved the material's double-layer capacitance. The carbonized composite activated at 700 °C exhibited excellent capacitance of 456 F g-1 at a specific current of 0.25 A g-1 in 6 M KOH electrolyte and showed excellent stability after 10,000 cycles. Besides being a low cost, the produced materials offer good stability and electrochemical properties, making them suitable for supercapacitor applications.

| S-EPMC7731031 | biostudies-literature

Animal- and Human-Inspired Nanostructures as Supercapacitor Electrode Materials: A Review.

Project description:Human civilization has been relentlessly inspired by the nurturing lessons; nature is teaching us. From birds to airplanes and bullet trains, nature gave us a lot of perspective in aiding the progress and development of countless industries, inventions, transportation, and many more. Not only that nature inspired us in such technological advances but also, nature stimulated the advancement of micro- and nanostructures. Nature-inspired nanoarchitectures have been considered a favorable structure in electrode materials for a wide range of applications. It offers various positive attributes, especially in energy storage applications, such as the formation of hierarchical two-dimensional and three-dimensional interconnected networked structures that benefit the electrodes in terms of high surface area, high porosity and rich surface textural features, and eventually, delivering high capacity and outstanding overall material stability. In this review, we comprehensively assessed and compiled the recent advances in various nature-inspired based on animal- and human-inspired nanostructures used for supercapacitors. This comprehensive review will help researchers to accommodate nature-inspired nanostructures in industrializing energy storage and many other applications.

| S-EPMC9537411 | biostudies-literature

Tailoring morphology of cobalt-nickel layered double hydroxide via different surfactants for high-performance supercapacitor.

Project description:Tailoring the morphology of cobalt-nickel layered double hydroxide (LDH) electrode material was successfully achieved via the process of cathodic electrodeposition by adding different surfactants (hexamethylenetetramine, dodecyltrimethylammonium bromide (DTAB) or cetyltrimethylammonium bromide). The as-prepared Co0.75Ni0.25(OH)2 samples with surfactants exhibited wrinkle-like, cauliflower-like or net-like structures that corresponded to better electrochemical performances than the untreated one. In particular, a specific capacitance of 1209.1 F g-1 was found for the cauliflower-like Co0.75Ni0.25(OH)2 electrode material using DTAB as the surfactant at a current density of 1 A g-1, whose structure boosted ion diffusion to present a good rate ability of 64% with a 50-fold increase in current density from 1 A g-1 to 50 A g-1. Accordingly, the asymmetric supercapacitor assembled by current LDH electrode and activated carbon electrode showed an energy density as high as 21.3 Wh kg-1 at a power density of 3625 W kg-1. The relationship between surfactant and electrochemical performance of the LDH electrode materials has been discussed.

| S-EPMC6170540 | biostudies-literature

Facile synthesis approach of bifunctional Co-Ni-Fe oxyhydroxide and spinel oxide composite electrocatalysts from hydroxide and layered double hydroxide composite precursors.

Project description:Zinc-air batteries (ZABs) are promising candidates for the next-generation energy storage systems, however, their further development is severely hindered by kinetically sluggish oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). Facile synthesis approaches of highly active bifunctional electrocatalysts for OER and ORR are required for their practical applications. Herein, we develop a facile synthesis procedure for composite electrocatalysts composed of OER-active metal oxyhydroxide and ORR-active spinel oxide containing Co, Ni and Fe from composite precursors consisting of metal hydroxide and layered double hydroxide (LDH). Both hydroxide and LDH are simultaneously produced by a precipitation method with a controlled molar ratio of Co2+, Ni2+ and Fe3+ in the reaction solution, and calcination of the precursor at a moderate temperature provides composite catalysts of metal oxyhydroxides and spinel oxides. The composite catalyst shows superb bifunctional performances with a small potential difference of 0.64 V between a potential of 1.51 V vs. RHE at 10 mA cm-2 for OER and a half-wave potential of 0.87 V vs. RHE for ORR. The rechargeable ZAB assembled with the composite catalyst as an air-electrode exhibits a power density of 195 mA cm-2 and excellent durability of 430 hours (1270 cycles) of a charge-discharge cycle test.

| S-EPMC10071814 | biostudies-literature

Pseudocapacitance electrode and asymmetric supercapacitor based on biomass juglone/activated carbon composites.

Project description:A novel electrode material incorporating renewable biomass-derived juglone biomolecules with commercial activated carbon (AC) granules has been through simple ultrasonic dispersion and dissolution-recrystallization and was found to exhibit good electrochemical performance. The juglone biomolecules are prepared by an ultrasound-assisted extraction method from abandoned walnut peel, which decreases pollution and increases economic efficiency. Through the dissolution-recrystallization process with AC, a hierarchical structure with nanosized juglone particles was obtained, and the AC particles worked as scaffolding to strengthen the slight biomolecules, thus expanding the active sites and effectively reducing the dissolution of the active materials. The pseudocapacitance fading mechanism was investigated by ex situ FTIR measurement and the porous structure ensures that the composite electrode has an enhanced specific capacitance of 248 F g-1 compared to 172.8 and 62.5 F g-1 for the respective AC and juglone samples. Besides, the excellent cyclic stability (retained 75% after 3000 charge-discharge cycles) was demonstrated. The highest area-specific capacitance of the composites was 1300 mF cm-2. An asymmetric supercapacitor based on this composite electrode was assembled with an AC electrode as the counter electrode and exhibited good cyclic performance at a voltage of 1.2 V (retained 77% after 3000 charge-discharge cycles), which provides a high energy density of 12 W h kg-1 at a power density of 0.18 kW kg-1 and a high power density of 2 kW kg-1 at an energy density of 9 W h kg-1. This work explores the application of biomolecule-based composites in energy storage devices and provides a potential strategy for constructing environmentally friendly electrodes.

| S-EPMC9072198 | biostudies-literature

Nitrogen Doped Macroporous Carbon as Electrode Materials for High Capacity of Supercapacitor.

Project description:Nitrogen doped carbon materials as electrodes of supercapacitors have attracted abundant attention. Herein, we demonstrated a method to synthesize N-doped macroporous carbon materials (NMC) with continuous channels and large size pores carbonized from polyaniline using multiporous silica beads as sacrificial templates to act as electrode materials in supercapacitors. By the nice carbonized process, i.e., pre-carbonization at 400 °C and then pyrolysis at 700/800/900/1000 °C, NMC replicas with high BET specific surface areas exhibit excellent stability and recyclability as well as superb capacitance behavior (~413 F ⋅ g-1) in alkaline electrolyte. This research may provide a method to synthesize macroporous materials with continuous channels and hierarchical pores to enhance the infiltration and mass transfer not only used as electrode, but also as catalyst somewhere micro- or mesopores do not work well.

| S-EPMC6432412 | biostudies-literature

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