High rate performance activated carbons prepared from ginkgo shells for electrochemical supercapacitors

Partially graphitized ginkgo-based activated carbon (GGAC) is fabricated from ginkgo shells by pyrolysis, KOH activation and heat treatment using cobalt nitrate as graphitization catalyst. The graphitization temperature is 900 °C. The GGAC has a microporous structure and its specific surface area is 1775 m² g⁻¹. XRD patterns show that the carbon becomes more graphitic after heat treatment. The specific capacitance of the GGAC reaches to 178 F g⁻¹ at a potential scan rate of 500 mV s⁻¹, which is superior to that of commercial activated carbons and ordered mesoporous carbons. The high electrochemical performance of the GGAC is attributed to its good electronic conductivity and high surface area. Partially graphitized activated carbon is a promising electrode material for electrochemical supercapacitors with high rate performance.     

Hydrothermal synthesis and activation of graphene-incorporated nitrogen-rich carbon composite for high-performance supercapacitors

Graphene-incorporated nitrogen-rich carbon composite with nitrogen content of ca. 10 wt.% has been synthesized by an effective yet simple hydrothermal reaction of glucosamine in the presence of graphene oxide (GO). The nitrogen content of carbon composite is nearly twice as high as that of hydrothermal carbon without graphene. GO is favorable for the high nitrogen doping in the carbon composite by the reaction between the glucosamine-released ammonia and GO. The hydrothermal carbon composite is further activated by KOH, and graphene in the activated carbon composite demonstrates a positive effect of increasing specific surface area, pore volume and electrical conductivity, resulting in superior electrochemical performance. The activated carbon composite with higher specific surface area and micropore volume possesses higher specific capacitance with a value of 300 F g⁻¹ at 0.1 A g⁻¹ in 6 M KOH aqueous solution in the two electrode cell. Larger mesopore volume and higher conductivity of the activated carbon composite will provide fast ion and electron transfer, thus leading to higher rate capacity with a capacitance retention of 76% at 8 A g⁻¹ in comparison to the activated hydrothermal carbon without graphene.     

Thick vertically aligned carbon nanotube/carbon composite electrodes for electrical double-layer capacitors

We present a new method for synthesis of thick, self-standing porous carbon electrodes with improved physicochemical properties and unique porous structure. The synthesis is based on the use of vertically aligned carbon nanotubes (VACNT) as templates for polymer-based activated carbon materials. The VACNT template enables the production of 1 mm thick, binder-free electrodes with high capacity values even at high rates (>160 Fg⁻¹ at more than 1 Ag⁻¹ for 1 mm thick electrode), and very good stability upon cycling. The electrochemical performance after more than 50,000 cycles, the pore characterization by adsorption isotherms, and the structural analysis of the composite electrode are also reported.     

Electrochemical detection of catechol at integrated carbon nanotubes electrodes

The mechanical stability of the electrode plays a very important role in the long-term stability of electrochemical behavior. In this paper, multi-wall carbon nanotubes (MWCNTs) electrodes were prepared in the holes of glass directly by microwave plasma chemical vapor deposition and the electrochemical behavior of catechol at the integrated MWCNT electrodes was investigated. The oxygen plasma treated CNTs had excellent electrochemical behavior for the analysis of catechol. The catechol was detected in the linear concentration range of 1.0 × 10^− 6 mol L^− 1–1.0 × 10^− 3 mol L^− 1. And because CNTs were integrated directly on the substrate, the stable response to catechol solution showed that the carbon nanotubes electrodes had long-term stability.     

Amperometric study of hydrogen peroxide biosensor with butadiene rubber as immobilization matrix

A carbon paste electrode bound by butadiene rubber has been newly constructed and its electrochemical properties have been investigated to test the practicability of the enzyme electrode. The binder of carbon powder was butadiene rubber dissolved in toluene and ground cabbage tissue was embedded in the matrix as an enzyme source. The electrode, which showed a mechanical robustness after volatilization of solvent, displayed good catalytic power (detection limit = 2.5 × 10^?5 M, S/N = 2) and electrochemically irreversible characteristics. Its symmetry factor and the exchange current density of the electrode used were 0.23 and 1.71 × 10^?3 A cm^?2, respectively.     

Functionalized carbon onions,detonation nanodiamond and mesoporous carbon as cathodes in Li-ion electrochemical energy storage devices

Functionalization of carbon surface leads to the enhancement of ion storage capacity of carbon cathodes due to the additional pseudocapacitive reactions. In order to gain additional insights on the effects of the carbon specific surface area, porosity and oxygeni-containing functional groups on their electrochemical performance, we have investigated thick (>150 μm) electrodes based on carbon onion nanopowder with and without functional groups present on carbon surface as well as nanodiamond soot and mesoporous activated carbon. Oxidation of carbon onion surface was found to result in a 2.4–2.8-fold increase in their specific capacitance. The larger average pore size and the absence of micropores in carbon nanoparticles based electrodes resulted in a better rate performance compared to that of mesoporous activated carbon. However, significant self-discharge was observed in all the oxidized samples. The low electrode density combined with limited overall charge storage capacity of carbon samples resulted in a volumetric capacity of less than 23 mAh cm⁻³, compared to 450–700 mAh cm⁻³ offered by state of the art high-density cathodes used in commercial Li-ion batteries. Even with further improvements, our estimations suggest that porous carbon cathodes will unlikely be able to offer more than 15% of the energy density of traditional cathodes.     

Improved cyclability of lithium–sulfur battery cathode using encapsulated sulfur in hollow carbon nanofiber@nitrogen-doped porous carbon core–shell composite

Hollow carbon nanofiber@nitrogen-doped porous carbon (HCNF@NPC) core–shell composite, which was carbonized from HCNF@polyaniline, was prepared as an improved high conductive carbon matrix for encapsulating sulfur as a cathode composite material for lithium–sulfur batteries. The prepared HCNF@NPC-S composite with high sulfur content of 77.5 wt.% showed an obvious core–shell structure with an NPC layer coating on the surface of the HCNFs and sulfur homogeneously distributed in the coating layer. This material exhibited much better electrochemical performance than the HCNF-S composite, delivered initial discharge capacity of 1170 mAh g⁻¹, and maintains 590 mAh g⁻¹ after 200 cycles at the current density of 837.5 mA g⁻¹ (0.5 C). The significantly improved electrochemical performance of the HCNF@NPC-S composite was attributed to the synergetic effect between HCNF cores, which provided electronic conduction pathways and worked as mechanical support, and the NPC shells with relatively high surface area and pore volume, which could trap sulfur/polysulfides and provide Li⁺ conductive pathways.     

High energy density Li-ion capacitor assembled with all graphene-based electrodes

To meet the higher requirement of energy storage units, novel devices combining high power performance of supercapacitor and high energy density of Li-ion battery are in urgent demand. Herein we designed and fabricated a Li-ion capacitor device, which is composed of an electrochemical double layer capacitance electrode as the positive electrode and a Li-ion battery type electrode as the negative electrode. Both electrodes consist of graphene-based active materials: a three-dimensional graphene-based porous carbon material with ultrahigh specific surface area, appropriate pore size distribution and excellent conductivity for the positive electrode, and a flash-reduced graphene oxide with open-pore structure and superior rate capability for the negative electrode. With the benefit of the Li-ion capacitor structure, the device exhibits a comprehensive and excellent electrochemical performance in terms of high operating voltage (4.2 V), ultrahigh energy density of 148.3 Wh kg⁻¹ (with power density of 141 W kg⁻¹), maximum power density of 7800 W kg⁻¹ (with energy density kept at 71.5 Wh kg⁻¹) and long cycle life. Such a superior performance indicates that the Li-ion capacitor could be a promising novel energy storage device for wide applications in fast, high efficient and long life energy storage systems.     

Decoration of carbon cloth by manganese oxides for flexible asymmetric supercapacitors

Here we describe the production of carbon cloth coated with MnO₂ nanosheets or MnOOH nanorods through a normal temperature reaction or a hydrothermal approach, respectively. Of note, the electrochemical performance of MnO₂-coated carbon cloth was better (429.2 F g⁻¹) than that of MnOOH-coated carbon cloth. When the MnO₂-coated carbon cloth is introduced as the positive electrode and the Fe₂O₃-coated carbon cloth as the negative electrode, a flexible asymmetric supercapacitor was obtained with an energy density of 22.8 Wh kg⁻¹ and a power density of 159.4 W kg⁻¹. Therefore, such a hierarchical MnO₂-coated carbon cloth nanocomposite is a promising high-performance electrode for flexible supercapacitors.     

Unique cyclic performance of post-treated carbide-derived carbon as an anode electrode

Carbide-derived carbon (CDC) is an attractive anode material for Li-ion battery applications because diverse pore textures and structures from amorphous to highly ordered graphite can be controlled by changing the synthesis conditions and precursor, respectively. To elucidate the unique cycling behavior of the post air-treated CDC anode, electrochemical performance was studied under variation of C-rates with structural changes before and after cycling. By tailoring the pore texture of CDCs as removal of amorphous phase by post air-activation, the anode electrode showed a high increase of capacity under prolonged cycling and under high C-rate conditions such as 0.3–1.0 C-rates. The discharge capacities of the treated CDC increased from 400 mAh g⁻¹ to 913 mAh g⁻¹ with increasing cycle number and were close to high initial irreversible value, 1250 mAh g⁻¹, at the 220th cycle under a 0.1C-rate condition, which are unique and unusual cyclic properties in carbon anode applications. Under high C-rate conditions, the discharge capacities started to increase from around 160 mAh g⁻¹ and values of 415 mAh g⁻¹, 372 mAh g⁻¹, and 336 mAh g⁻¹, were observed at 0.3, 0.5, and 1.0 C-rates, respectively, at 600 cycles, demonstrating stable capacity performance.     

Highly porous carbon spheres for electrochemical capacitors and capacitive flowable suspension electrodes

In flowable and conventional electrochemical capacitors, the energy capacity is largely determined by the electrode material. Spherical active material, with high specific surface area (SSA) represents a promising material candidate for film and flow capacitors. In this study, we synthesized highly porous carbon spheres (CSs) of submicrometer size to investigate their performance in film and suspension electrodes. In particular, we studied the effects of carbonization and activation temperatures on the electrochemical performance of the CSs. The CSs activated at optimum conditions demonstrated narrow pore size distribution (<3 nm) with high SSA (2900 m²/g) and high pore volume (1.3 cc/g), which represent significant improvement as compared to similar materials reported in literature. Electrochemical tests of CSs in 1 M H₂SO₄ solution showed a specific capacitance of 154 F/g for suspension electrode and 168 F/g for film electrode with excellent rate performance (capacitive behaviors up to 100 mV/s) and cycling performance (95% of initial capacitance after 5000 cycles). Moreover, in the film electrode configuration, CSs exhibited high rate performance (78 F/g at 1000 mV/s) and volumetric power density (9000 W/L) in organic electrolytes, along with high energy density (21.4 Wh/L) in ionic liquids.     

Facile synthesis of activated carbon/carbon nanotubes compound for supercapacitor application

A large number of carbon nanotubes (CNTs) have been produced commingled in activated mesocarbon microbeads (AMCMBs) activated by potassium hydroxide in a stainless steel container at 900 °C, in which an especial buried-protection method with petroleum coke powders was used to protecting the product during activation. The CNTs were found to be about 50 nm in diameter and characteristic length more than 10 μm. In addition, the AMCMBs/CNTs compound when used for electrode material of electrochemical double-layer capacitors exhibited a specific capacitance of 243 F g^?1 in 6 M KOH aqueous solution.     

A high-performance asymmetric supercapacitor based on carbon and carbon–MnO2 nanofiber electrodes

An asymmetric supercapacitor with high energy and power densities has been fabricated using MnO₂/carbon nanofiber composites as positive electrode and activated carbon nanofibers as negative electrode in Na₂SO₄ aqueous electrolyte. Both electrode materials are freestanding in nature without any conductive additives or binders and exhibit outstanding electrochemical performances. The as-assembled asymmetric supercapacitor with optimal mass ratio can be operated reversibly over a wide voltage range of 0–2.0 V, and presents a maximum energy density of 30.6 Wh kg⁻¹, which is much higher than those of symmetric supercapacitors. Moreover, the supercapacitor exhibits excellent rate capability (high power density of 20.8 kW kg⁻¹ at 8.7 Wh kg⁻¹) and long-term cycling stability with only 6% loss of its initial capacitance after 5000 cycles. These attractive results make these freestanding materials promising for applications in aqueous electrolyte-based asymmetric supercapacitors with high energy and power densities delivery.     

The composite material based on Dawson-type polyoxometalate and activated carbon as the supercapacitor electrode

A supercapacitor electrode assembled from activated carbon (AC) and (NH₄)₆[P₂Mo₁₈O₆₂]·14.2H₂O (P₂Mo₁₈) was fabricated for the first time, and showed remarkable electrochemical performance ascribed to the synergy of the double layer capacitance of AC and the pseudocapacitance of P₂Mo₁₈. The investigations indicate that the AC/P₂Mo₁₈ electrode exhibits a specific capacitance of 275 F g^− 1 at a high current density of 6 A g^− 1, which is substantially larger than the 182 F g^− 1 of the AC electrode. In addition, the AC/P₂Mo₁₈ electrode possesses a remarkable rate capability (89%) when the current density is increased from 2 to 6 A g^− 1.     

Synthesis of a graphene–carbon nanotube composite and its electrochemical sensing of hydrogen peroxide

Graphene, whose structure consists of a single layer of sp²-hybridized carbon atoms, provides an excellent platform for designing composite nanomaterials. In this study, we have demonstrated a facile process to synthesize graphene–multiwalled carbon nanotube (MWCNT) composite. The graphene–MWCNT composite material is endowed with a large electrochemical surface area and fast electron transfer properties in Fe(CN)₆^3?/4? redox species. A graphene–MWCNT composite modified electrode exhibits good performance in terms of the electrocatalytic reduction of H₂O₂; a sensor constructed from such an electrode shows a good linear dependence on H₂O₂ concentration in the range of 2 × 10^?5 to 2.1 × 10^?3 mol L^?1. The detection limit is estimated to be 9.4 × 10^?6 mol L^?1. This study provides a new kind of composite modified electrode for electrochemical sensors.     

High performance wire-shaped supercapacitive electrodes based onactivated carbon fibers core/manganese dioxide shell structures

Micro/nano hierarchical structures with uniformly patterned nanostructures shell and activated internal core are promising for boosting electrochemical performance. Here we report the fabrication of wire-shaped supercapacitive electrodes with manganese dioxide (MnO₂) nanostructures shell integrated onto activated carbon fiber (ACF) core. The ACF core is doped with nitrogen heteroatom and shows good conductivity and hydrophilicity, which endow fast ion and electron transport and high accessibility of electrolyte. The MnO₂ nanostructures shell integrated on the ACF core by electrodeposition method together provide significant pseudocapacitive contribution associated with fast faradaic reactions. The electrochemical performance of the fabricated electrodes was evaluated by cyclic voltammetry, galvanostatic charging/discharging and electrochemical impedance spectroscopy techniques. The integrated wire-shaped electrodes, which boost the synergetic effect of MnO₂ nanostructures and ACF, have excellent current collecting capabilities thus resulting high electrochemical performance (with the specific capacitance of 26.64 mF cm⁻¹ at the current density of 0.1 mA cm⁻¹ and 96% capacitance retention after 8000 charging/discharging cycles at the current density of 1 mA cm⁻¹).     

High-performance supercapacitor based on V2O5/carbon nanotubes-super activated carbon ternary composite

A ternary composite of V₂O₅/carbon nanotubes/super activated carbon (V₂O₅/CNTs–SAC) was prepared by a simple hydrothermal method and used as a supercapacitor electrode material. The electrochemical performance of the electrode was analyzed using cyclic voltammetry, galvanostatic charge/discharge measurements, and electrochemical impedance spectroscopy, which were performed in 2 M NaNO₃ as the electrolyte. The V₂O₅/CNTs–SAC nanocomposite exhibited a specific capacitance as high as 357.5 F g⁻¹ at a current density of 10 A g⁻¹, which is much higher than that of either bare V₂O₅ nanosheets or a V₂O₅/CNTs composite. Furthermore, the capacitance increased to 128.7% of the initial value after 200 cycles, with 99.5% of the maximum value being retained after 1000 cycles. These results demonstrated that the V₂O₅/CNTs–SAC ternary composite is suitable for use as an electrode material for supercapacitors.     

Functionalized N-doped interconnected carbon nanofibers as an anode material for sodium-ion storage with excellent performance

The electrochemical performance of sodium-ion battery was improved by using functionalized interconnected N-doped carbon nanofibers (FN-CNFs) as the anode. The material was synthesized with polypyrrole as precursor by a simple method. The FN-CNF electrode exhibits excellent rate capability and cycling stability, delivering a capacity of 134.2 mAh g⁻¹ at a high current density of 200 mA g⁻¹ after 200 cycles and retains a capacity of 73 mAh g⁻¹ even at an extremely high current density of 20 A g⁻¹. The superior performance can be attributed to N-doped sites and functionalized groups, which are capable of capturing sodium ions rapidly and reversibly through surface adsorption and surface redox reactions.     

Carbonization temperature dependence of pore structure of silicon carbide spheres and their electrochemical capacitive properties as supercapacitors

Three-dimensional silicon carbide-based frameworks with hierarchical micro- and mesoporous structures (2MSiC) are prepared by employing the template method and carbonization reaction using aerosol-spray drying. The mesopores are generated by the self-assembly of a structure-directing agent, whereas the micropores originate from the partial evaporation of Si atoms during the carbonization process. During the carbonization process, the proportion of micro- and mesopores in 2MSiC can be controlled by the carbonization temperature by controlling the amount of partial evaporation of Si atoms. The 2MSiC electrode prepared using a Brij56 structure-directing agent as the mesopore template and carbonized at 1250 °C exhibits a high charge storage capacity with a specific capacitance of 259.9 F g⁻¹ at a scan rate of 5 mV s⁻¹ with 88.1% rate performance from 5 to 500 mV s⁻¹ in 1 M KCl aqueous electrolyte. This outstanding electrochemical performance can be attributed to the synergistic effect of both the enhanced electric double layer properties caused by micropores and reduced resistant pathways for ion diffusion in the pores as well as a large accessible surface area for ion transport/charge storage caused by mesopores. These encouraging results demonstrate that the 2MSiC electrode prepared with Brij56 and carbonized at 1250 °C is a promising candidate for high-performance electrode materials for supercapacitors.     

Three-dimensional MnO/reduced graphite oxide composite films as anode materials for high performance lithium-ion batteries

MnO/reduced graphite oxide (MnO/RGO) composite films with three dimensionally porous structures have been synthesized by an improved electrostatic spray deposition setup and their microstructure and electrochemical properties have been characterized by X-ray diffraction, scanning electron microscopy, thermal gravimetric, Raman spectrometry and galvanostatic cell cycling. The results show that the structure and electrochemical performance of the electrode film are influenced significantly by the RGO content. The three dimensionally porous structure collapse does not occur in the MnO/RGO thin films for a RGO content lower than 16.58 wt%, the 16.58 wt% reduced graphite oxide content being optimal. Such an improvement in the cycling performance (772 mAh g⁻¹ after 100 cycles at 1 C) and rate capability (425 mAh g⁻¹ at 6 C) might be attributed to the excellent microstructure and electrical conductivity of MnO/reduced graphite oxide composite film electrodes.