Electrodes For High-performance Asymmetric Supercapacitors Research Articles

Hierarchical multi-shelled nanoporous mixed copper cobalt phosphide hollow microspheres as a novel advanced electrode for high-performance asymmetric supercapacitors

Hierarchical multi-shelled nanoporous mixed copper cobalt phosphide microspheres have been for the first time developed as a novel advanced electrode with superior electrochemical properties.

Facile synthesis of carbon nanofibers/MnO2 nanosheets as high-performance electrodes for asymmetric supercapacitors

We reported the facile synthesis of hollow carbon nanofibers/MnO2 (CNFs/MnO2) composites for high performance supercapacitor electrodes. The nanocomposites were prepared via electrospinning of carbon nanofibers/MnOx and subsequent hydrothermal coating of MnO2 nanosheets on the surface. The unique hollow structure and numerous MnO2 nanosheets increased the contact area between the electrodes and electrolyte so that the CNFs/MnO2 electrode exhibited higher electrochemical performance than the CNFs/MnOx composites. The CNFs/MnO2 composites displayed a specific capacitance of 151.1F/g at 1A/g, and 90% of the initial specific capacitance was maintained after 8000 cycles. An asymmetric supercapacitor was assembled with the CNFs/MnO2 composites and the active carbon. The asymmetric supercapacitor exhibited a high performance in 1M Na2SO4 aqueous solution with a working potential window ranging from 0 to 1.8V. Furthermore, the asymmetric supercapacitor possessed a cycling stability with 93.5% capacitance retained after 1500 cycles at 1A/g.

Supercapacitors: Biomass-Derived Nitrogen-Doped Carbon Nanofiber Network: A Facile Template for Decoration of Ultrathin Nickel-Cobalt Layered Double Hydroxide Nanosheets as High-Performance Asymmetric Supercapacitor Electrode (Small 24/2016)

Supercapacitors: Biomass-Derived Nitrogen-Doped Carbon Nanofiber Network: A Facile Template for Decoration of Ultrathin Nickel-Cobalt Layered Double Hydroxide Nanosheets as High-Performance Asymmetric Supercapacitor Electrode (Small 24/2016)

Biomass-Derived Nitrogen-Doped Carbon Nanofiber Network: A Facile Template for Decoration of Ultrathin Nickel-Cobalt Layered Double Hydroxide Nanosheets as High-Performance Asymmetric Supercapacitor Electrode.

The development of biomass-based energy storage devices is an emerging trend to reduce the ever-increasing consumption of non-renewable resources. Here, nitrogen-doped carbonized bacterial cellulose (CBC-N) nanofibers are obtained by one-step carbonization of polyaniline coated bacterial cellulose (BC) nanofibers, which not only display excellent capacitive performance as the supercapacitor electrode, but also act as 3D bio-template for further deposition of ultrathin nickel-cobalt layered double hydroxide (Ni-Co LDH) nanosheets. The as-obtained CBC-N@LDH composite electrodes exhibit significantly enhanced specific capacitance (1949.5 F g(-1) at a discharge current density of 1 A g(-1) , based on active materials), high capacitance retention of 54.7% even at a high discharge current density of 10 A g(-1) and excellent cycling stability of 74.4% retention after 5000 cycles. Furthermore, asymmetric supercapacitors (ASCs) are constructed using CBC-N@LDH composites as positive electrode materials and CBC-N nanofibers as negative electrode materials. By virtue of the intrinsic pseudocapacitive characteristics of CBC-N@LDH composites and 3D nitrogen-doped carbon nanofiber networks, the developed ASC exhibits high energy density of 36.3 Wh kg(-1) at the power density of 800.2 W kg(-1) . Therefore, this work presents a novel protocol for the large-scale production of biomass-derived high-performance electrode materials in practical supercapacitor applications.

Hierarchical CuCo2S4 hollow nanoneedle arrays as novel binder-free electrodes for high-performance asymmetric supercapacitors.

Hierarchical CuCo2S4 hollow nanoneedle arrays have been firstly synthesized on a Ni foam using a facile template-free hydrothermal method and applied as novel binder-free electrodes for high-performance asymmetric supercapacitors with ultrahigh specific capacitance, high energy density, excellent rate capability and outstanding long-term cycling stability.

MnO2 Nanosheets Grown on Nitrogen-Doped Hollow Carbon Shells as a High-Performance Electrode for Asymmetric Supercapacitors.

A hierarchical hollow hybrid composite, namely, MnO2 nanosheets grown on nitrogen-doped hollow carbon shells (NHCSs@MnO2 ), was synthesized by a facile in situ growth process followed by calcination. The composite has a high surface area (251 m(2) g(-1) ) and mesopores (4.5 nm in diameter), which can efficiently facilitate transport during electrochemical cycling. Owing to the synergistic effect of NHCSs and MnO2 , the composite shows a high specific capacitance of 306 F g(-1) , good rate capability, and an excellent cycling stability of 95.2 % after 5000 cycles at a high current density of 8 A g(-1) . More importantly, an asymmetric supercapacitor (ASC) assembled by using NHCSs@MnO2 and activated carbon as the positive and negative electrodes exhibits high specific capacitance (105.5 F g(-1) at 0.5 A g(-1) and 78.5 F g(-1) at 10 A g(-1) ) with excellent rate capability, achieves a maximum energy density of 43.9 Wh kg(-1) at a power density of 408 W kg(-1) , and has high stability, whereby the ASC retains 81.4 % of its initial capacitance at a current density of 5 A g(-1) after 4000 cycles. Therefore, the NHCSs@MnO2 electrode material is a promising candidate for future energy-storage systems.

Designing 3D highly ordered nanoporous CuO electrodes for high-performance asymmetric supercapacitors.

The increasing demand for energy has triggered tremendous research efforts for the development of lightweight and durable energy storage devices. Herein, we report a simple, yet effective, strategy for high-performance supercapacitors by building three-dimensional pseudocapacitive CuO frameworks with highly ordered and interconnected bimodal nanopores, nanosized walls (∼4 nm) and large specific surface area of 149 m(2) g(-1). This interesting electrode structure plays a key role in providing facilitated ion transport, short ion and electron diffusion pathways and more active sites for electrochemical reactions. This electrode demonstrates excellent electrochemical performance with a specific capacitance of 431 F g(-1) (1.51 F cm(-2)) at 3.5 mA cm(-2) and retains over 70% of this capacitance when operated at an ultrafast rate of 70 mA cm(-2). When this highly ordered CuO electrode is assembled in an asymmetric cell with an activated carbon electrode, the as-fabricated device demonstrates remarkable performance with an energy density of 19.7 W h kg(-1), power density of 7 kW kg(-1), and excellent cycle life. This work presents a new platform for high-performance asymmetric supercapacitors for the next generation of portable electronics and electric vehicles.

Facile synthesis of ZnCo2O4nanowire cluster arrays on Ni foam for high-performance asymmetric supercapacitors

ZnCo2O4NWCAs on Ni foam as electrodes for high-performance asymmetric supercapacitors.

A NiAl layered double hydroxide@carbon nanoparticles hybrid electrode for high-performance asymmetric supercapacitors

A NiAl layered double hydroxide (LDH)@carbon nanoparticles (CNPs) hybrid electrode was fabricated via a facile and cost-effective approach and displays excellent pseudocapacitive behavior.

DNA-assisted assembly of carbon nanotubes and MnO2 nanospheres as electrodes for high-performance asymmetric supercapacitors

A DNA-assisted assembly approach is developed to fabricate a capacitor-type electrode material, DNA-functionalized carbon nanotubes (CNTs@DNA), and a battery-type electrode material, DNA@CNTs-bridged MnO2 spheres (CNTs@DNA-MnO2), for asymmetric supercapacitors. An energy density of 11.6 W h kg(-1) is achieved at a power density of 185.5 W kg(-1) with a high MnO2 mass loading of 4.2 mg cm(-2). It is found that DNA assembly plays a critical role in the enhanced supercapacitor performance. This is because while DNA molecules functionalize carbon nanotubes (CNTs) via π-π stacking, their hydrophilic sugar-phosphate backbones also promote the dispersion of CNTs. The resultant CNTs@DNA chains can link multiple MnO2 spheres to form a networked architecture that facilitates charge transfer and effective MnO2 utilization. The improved performance of the asymmetric supercapacitors indicates that DNA-assisted assembly offers a promising approach to the fabrication of high-performance energy storage devices.

Three-dimensional ordered macroporous MnO2/carbon nanocomposites as high-performance electrodes for asymmetric supercapacitors

MnO2/carbon composites with ultrathin MnO2 nanofibers (diameter of 5-10 nm) uniformly deposited on three dimensional ordered macroporous (3DOM) carbon frameworks were fabricated via a self-limiting redox process. The MnO2 nanofibers provide a large surface area for charge storage, whereas the 3DOM carbon serves as a desirable supporting material providing rapid ion and electron transport through the composite electrodes. Cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy (EIS) were used to characterize the capacitive performance of these composites. Optimization of the composition results in a composite with 57 wt% MnO2 content, which gives both a high specific capacitance (234 F g(-1) at a discharge current of 0.1 A g(-1)) and good rate capability (52% retention of the capacitance at 5 A g(-1)). An asymmetric supercapacitor was fabricated by assembling the optimized MnO2/carbon composite as the positive electrode and 3DOM carbon as the negative electrode. The asymmetric supercapacitor exhibits superior electrochemical performances, which can be reversibly charged and discharged at a maximum cell voltage of 2.0 V in 1.0 M Na2SO4 aqueous electrolyte, delivering both high energy density (30.2 W h kg(-1)) and power density (14.5 kW kg(-1)). Additionally, the asymmetric supercapacitor exhibits an excellent cycle life, with 95% capacitance retained after 1000 cycles.