Multi-doped interconnected carbon nanospheres for high-performance supercapacitor

Author(s):  
Shiying Lin ◽  
Lanlan Mo ◽  
Tao Lyu ◽  
Feijun Wang

Abstract Heteroatom doping is an effective modification to improve electrochemical performance of carbon materials as electrodes in storage devices and multi-doping works better because of synergistic effect. In this report, a N/O/S multi-doped carbon nanospheres (SLS/PANI-700) are prepared from crosslinking hydrogel beads of polyaniline and sodium lignosulfonate. The addition of sodium lignosulfonate significantly improve the electrochemical performance of PANI-based carbon by changing micromorphology, building interconnected network and offering diverse doping. SLS/PANI-700 has ultrahigh specific surface area of 2861 m2 g−1, well-developed hierarchically porous structure, interconnected conducting carbon network and high N and O concentration. Take these advantages, it delivers very high capacitance of 487.7 F g−1 at 1 A g−1, a superior rate retention with capacitance of 373.6 F g−1 at a high current density of 20 A g−1 as electrode material. The assembled symmetric supercapacitor device exhibits a very high energy density of 43.68 Wh kg−1 at 488.98 W kg−1 and keeps 21.18 Wh kg−1 under a high power density of 8664.54 W kg−1. Based on these properties, SLS/PANI-700 possesses a great promising potential as electrode material for advanced supercapacitor.

Materials ◽  
2020 ◽  
Vol 13 (21) ◽  
pp. 4870
Author(s):  
Xiao Li ◽  
Jun Li ◽  
Ying Zhang ◽  
Peng Zhao ◽  
Ruyan Lei ◽  
...  

Ni(OH)2 derived from an MOF template was synthesized as an electrode material for supercapacitors. The electrochemical performance of the electrode was adjusted by effectively regulating the morphology of Ni(OH)2. The evolution of electrochemical performance of the electrode with morphology of Ni(OH)2 was highlighted in detail, based on which honeycomb-like Ni(OH)2 was successfully synthesized, and endowed the electrode with outstanding electrochemical performance. For the three-electrode testing system, honeycomb-like Ni(OH)2 exhibited a very high specific capacitance (1865 F·g−1 at 1 A·g−1, 1550 F·g−1 at 5 mV·s−1). Moreover, it also presented an excellent rate capability and cycling stability, due to 59.46 % of the initial value (1 A·g−1) being retained at 10 A·g−1, and 172% of initial value (first circle at 50 mV·s−1) being retained after 20,000 cycles. With respect to the assembled hybrid supercapacitor, honeycomb-like Ni(OH)2 also displayed superior electrochemical performance, with a high energy density (83.9 Wh·kg−1 at a power density of 374.8 W·kg−1). The outstanding electrochemical performance of Ni(OH)2 should be attributed to its unique honeycomb-like structure, with a very high specific surface area, which greatly accelerates the transformation and diffusion of active ions.


Energies ◽  
2019 ◽  
Vol 12 (6) ◽  
pp. 1143 ◽  
Author(s):  
Anil Yedluri ◽  
Tarugu Anitha ◽  
Hee-Je Kim

Hierarchical NiMoO4/NiMoO4 nanoflowers were fabricated on highly conductive flexible nickel foam (NF) substrates using a facile hydrothermal method to achieve rapid charge-discharge ability, high energy density, long cycling lifespan, and higher flexibility for high-performance supercapacitor electrode materials. The synthesized composite electrode material, NF/NiMoO4/NiMoO4 with a nanoball-like NF/NiMoO4 structure on a NiMoO4 surface over a NF substrate, formed a three-dimensional interconnected porous network for high-performance electrodes. The novel NF/NiMoO4/NiMoO4 nanoflowers not only enhanced the large surface area and increased the electrochemical activity, but also provided an enhanced rapid ion diffusion path and reduced the charge transfer resistance of the entire electrode effectively. The NF/NiMoO4/NiMoO4 composite exhibited significantly improved supercapacitor performance in terms of a sustained cycling life, high specific capacitance, rapid charge-discharge capability, high energy density, and good rate capability. Electrochemical analysis of the NF/NiMoO4/NiMoO4 nanoflowers fabricated on the NF substrate revealed ultra-high electrochemical performance with a high specific capacitance of 2121 F g−1 at 12 mA g−1 in a 3 M KOH electrolyte and 98.7% capacitance retention after 3000 cycles at 14 mA g−1. This performance was superior to the NF/NiMoO4 nanoball electrode (1672 F g−1 at 12 mA g−1 and capacitance retention 93.4% cycles). Most importantly, the SC (NF/NiMoO4/NiMoO4) device displayed a maximum energy density of 47.13 W h kg−1, which was significantly higher than that of NF/NiMoO4 (37.1 W h kg−1). Overall, the NF/NiMoO4/NiMoO4 composite is a suitable material for supercapacitor applications.


Nanomaterials ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 1467
Author(s):  
Xuanni Lin ◽  
Zhuoyi Yang ◽  
Anru Guo ◽  
Dong Liu

High energy density batteries with high performance are significantly important for intelligent electrical vehicular systems. Iron sulfurs are recognized as one of the most promising anodes for high energy density lithium-ion batteries because of their high theoretical specific capacity and relatively stable electrochemical performance. However, their large-scale commercialized application for lithium-ion batteries are plagued by high-cost and complicated preparation methods. Here, we report a simple and cost-effective method for the scalable synthesis of nanoconfined FeS in porous carbon (defined as FeS@C) as anodes by direct pyrolysis of an iron(III) p-toluenesulfonate precursor. The carbon architecture embedded with FeS nanoparticles provides a rapid electron transport property, and its hierarchical porous structure effectively enhances the ion transport rate, thereby leading to a good electrochemical performance. The resultant FeS@C anodes exhibit high reversible capacity and long cycle life up to 500 cycles at high current density. This work provides a simple strategy for the mass production of FeS@C particles, which represents a critical step forward toward practical applications of iron sulfurs anodes.


2021 ◽  
Author(s):  
yajun JI ◽  
Fei Chen ◽  
Shufen Tan ◽  
Fuyong Ren

Abstract Transition metal oxides are generally designed as hybrid nanostructures with high performance for supercapacitors by enjoying the advantages of various electroactive materials. In this paper, a convenient and efficient route had been proposed to prepare hierarchical coral-like MnCo2O4.5@Co-Ni LDH composites on Ni foam, in which MnCo2O4.5 nanowires were enlaced with ultrathin Co-Ni layered double hydroxides nanosheets to achieve high capacity electrodes for supercapacitors. Due to the synergistic effect of shell Co-Ni LDH and core MnCo2O4.5, the outstanding electrochemical performance in three-electrode configuration was triggered (high area capacitance of 5.08 F/cm2 at 3 mA/cm2 and excellent rate capability of maintaining 61.69 % at 20 mA/cm2), which is superior to those of MnCo2O4.5, Co-Ni LDH and other metal oxides based composites reported. Meanwhile, the as-prepared hierarchical MnCo2O4.5@Co-Ni LDH electrode delivered improved electrical conductivity than that of pristine MnCo2O4.5. Furthermore, the as-constructed asymmetric supercapacitor using MnCo2O4.5@Co-Ni LDH as positive and activated carbon as negative electrode presented a rather high energy density of 220 μWh/cm2 at 2400 μW/cm2 and extraordinary cycling durability with the 100.0 % capacitance retention over 8000 cycles at 20 mA/cm2, demonstrating the best electrochemical performance compared to other asymmetric supercapacitors using metal oxides based composites as positive electrode material. It can be expected that the obtained MnCo2O4.5@Co-Ni LDH could be used as the high performance and cost-effective electrode in supercapacitors.


2019 ◽  
Vol 11 (1) ◽  
Author(s):  
Lu Wang ◽  
Junwei Han ◽  
Debin Kong ◽  
Ying Tao ◽  
Quan-Hong Yang

Abstract Lithium-ion batteries (LIBs), which are high-energy-density and low-safety-risk secondary batteries, are underpinned to the rise in electrochemical energy storage devices that satisfy the urgent demands of the global energy storage market. With the aim of achieving high energy density and fast-charging performance, the exploitation of simple and low-cost approaches for the production of high capacity, high density, high mass loading, and kinetically ion-accessible electrodes that maximize charge storage and transport in LIBs, is a critical need. Toward the construction of high-performance electrodes, carbons are promisingly used in the enhanced roles of active materials, electrochemical reaction frameworks for high-capacity noncarbons, and lightweight current collectors. Here, we review recent advances in the carbon engineering of electrodes for excellent electrochemical performance and structural stability, which is enabled by assembled carbon architectures that guarantee sufficient charge delivery and volume fluctuation buffering inside the electrode during cycling. Some specific feasible assembly methods, synergism between structural design components of carbon assemblies, and electrochemical performance enhancement are highlighted. The precise design of carbon cages by the assembly of graphene units is potentially useful for the controlled preparation of high-capacity carbon-caged noncarbon anodes with volumetric capacities over 2100 mAh cm−3. Finally, insights are given on the prospects and challenges for designing carbon architectures for practical LIBs that simultaneously provide high energy densities (both gravimetric and volumetric) and high rate performance.


2017 ◽  
Vol 41 (17) ◽  
pp. 9024-9032 ◽  
Author(s):  
Enke Feng ◽  
Hui Peng ◽  
Zhiguo Zhang ◽  
Jindan Li ◽  
Ziqiang Lei

As-fabricated foldable solid-state supercapacitors are suitable for highly fold-tolerant high-energy-density energy storage device applications.


2021 ◽  
Vol 236 ◽  
pp. 01016
Author(s):  
Congcong Huang ◽  
Yunhui Dong ◽  
Xingjun Dong

A facile route has been employed to synthesize a series of high performance activated carbons as the electrode material for supercapacitors. The structure of the carbons are characterized by N2 adsorption/desorption and FTIR spectroscopy. The electrochemical performances of the carbons as an electrode material were evaluated by cyclic voltammetry test and galvanostatic charge/discharge measurements. As a biomass derived carbon, KOH-1 exhibits high capacity, good rate capability and high energy density, indicating the promising application of hydrothermal combining with KOH activation method for biomass materials that used in supercapacitors


2020 ◽  
Vol 15 (1) ◽  
pp. 147-153
Author(s):  
Yucai Li ◽  
Yan Zhao ◽  
Dong Zhang ◽  
Shiwei Song ◽  
Jian Wang ◽  
...  

Electrochemical performance of the electrode materials is seriously dependent on the structure and morphology of the electrode material. In this work, the nanoflower-like Co3O4 samples are successfully prepared on Ni foam via a facile hydrothermal method. The as-fabricated Co3O4 samples exhibit superior electrochemical performance with a high specific capacitance of 382.6 C g-1 at 1 A g-1 and excellent capacitance retention. In addition, the as-fabricated device presents a high energy density of 23.6 Wh kg-1 at a power density of 508.6 W kg-1 and excellent cycle stability with a capacitance retention of 81.2% after 10000 cycles, indicating a promising application as electrodes for energy storage device.


Materials ◽  
2019 ◽  
Vol 12 (10) ◽  
pp. 1626 ◽  
Author(s):  
Muhammad Fahim ◽  
Anwar ul Haq Ali Shah ◽  
Salma Bilal

The use of electroactive polyaniline (PANI) as an electrode material for a symmetric supercapacitor has been reported. The material was synthesized via interfacial polymerization, using ammonium per sulfate, dodecylbenzene sulfonic acid (DBSA), and gasoline, respectively, in the oxidant, dopant, and novel organic phase, and was subsequently employed as an electrode material to design a binder-free symmetric capacitor. As properties of PANI rely on the method of synthesis as well as reaction parameters, the present combination of reactants, at pre-optimized conditions, in the interfacial polymerization, led to the formation of PANI exhibiting a high specific capacitance (712 Fg−1 at 0.5 Ag−1), a good rate capability (86% capacitance retention at 10 Ag−1), a very low solution resistance (Rs = 0.61 Ω), and a potential drop (IR = 0.01917 V). The device exhibited a high energy density of 28 Whkg−1, at a power density of 0.28 kWkg−1, and retained as high as 15.1 Whkg−1, at a high power density of 4.5 kWkg−1. Moreover, it showed an excellent cycling stability and retained 98.5% of coulombic efficiency after 5000 charge discharge cycles, without showing any signs of degradation of polymer.


Author(s):  
Karthikeyan Gunasekaran Govindarasu ◽  
Boopathi Ganesan ◽  
Ramani Venkatesan ◽  
Pandurangan Arumugam

AbstractDoping of heteroatom into well-structured mesoporous carbon architecture can significantly augment the capacitive performance. In this work, we report P-doped graphitic hollow carbon spheres (P-GHCS) grown over Fe-KIT-6 through the in situ approach using the catalytic CVD technique. The obtained P-GHCS possesses a relatively high surface area with uniform mesoporous structure, good graphitization with tunable P-doping contents. The highly favorable structure and desirable heteroatom doping were taken into account to evaluate the P-GHCS as a modified electrode material towards high-performance supercapacitor. The optimized P-GHCS-800 sample exhibits superior specific capacitance (Csp) 321 F g−1 at 0.2 A g−1 with outstanding cycling stability with 2.9% loss of its initial capacitance after 2000 cycles in 6 M KOH electrolyte background in the three-electrode computerized system. More importantly, the fabricated P-GHCS-800 symmetric supercapacitor device can withstand at a wide potential width of 2.0 V, together with remarkable cyclic stability (89.09%) after 2000 cycles at a current density of 1 A g−1 in aqueous 1 M Na2SO4 as electrolyte providing a relatively high energy density of 10.83 Wh kg−1 with a power density of 222.78 W kg−1. Additionally, we demonstrated the single symmetric supercapacitor cell which provided sufficient energy to turn on a red LED of 20 mW and emit light over a certain period of time opens up possible realistic applications.


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