scholarly journals Fabrication of Eco-Friendly Solid-State Symmetric Ultracapacitor Device Based on Co-Doped PANI/GO Composite

Polymers ◽  
2019 ◽  
Vol 11 (8) ◽  
pp. 1315 ◽  
Author(s):  
Gul ◽  
Shah ◽  
Bilal

An eco-friendly solid-state symmetric ultracapacitor (Uc) device was fabricated using a polyaniline graphene oxide composite co-doped with sulfuric acid (H2SO4) and dodecyl benzene sulfonic acid (DBSA) or camphor sulfonic acid (CSA), as electrode material utilizing gold sheets as current collectors. The device showed specific capacitance value of 150 F/g at 1 A/g current density, with a capacitance retention value of 93.33% at higher current density (10 A/g), indicating a high rate capability. An energy density of 15.30 Whkg−1 with a power density of 1716 Wkg−1 was obtained at the current density of 1 A/g. The values of areal capacitance, power density, and energy density, achieved at the current density of 5 mAcm−2, were 97.38 mFcm−2, 9.93 mWhcm−2, and 1.1 Wcm−2, respectively. Additionally, the device showed very low solution and charge transfer resistance (0.885 Ω and 0.475 Ω, respectively). A device was also fabricated utilizing copper as current collector; however, a lower value of specific capacitance (82 F/g) was observed in this case.

Polymers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1678 ◽  
Author(s):  
Gul ◽  
Shah ◽  
Bilal

Conducting polymers and carbon-based materials such as graphene oxide (GO) and activated carbon (AC) are the most promising capacitive materials, though both offer charge storage through different mechanisms. However, their combination can lead to some unusual results, offering improvement in certain properties in comparison with the individual materials. Cycling stability of supercapacitors devices is often a matter of concern, and extensive research is underway to improve this phenomena of supercapacitive devices. Herein, a high-performance asymmetric supercapacitor device was fabricated using graphene oxide–polyaniline (GO@PANI) nanocomposite as positive electrode and activated carbon (AC) as negative electrode. The device showed 142 F g-1 specific capacitance at 1 A g-1 current density with capacitance retention of 73.94% at higher current density (10 A g-1). Most importantly, the device exhibited very high electrochemical cycling stability. It retained 118.6% specific capacitance of the starting value after 10,000 cycles at 3 Ag-1 and with coulombic efficiency of 98.06 %, indicating great potential for practical applications. Very small solution resistance (Rs, 0.640 Ω) and charge transfer resistance (Rct, 0.200 Ω) were observed hinting efficient charge transfer and fast ion diffusion. Due to asymmetric combination, potential window was extended to 1.2 V in aqueous electrolyte, as a result higher energy density (28.5 Wh kg-1) and power density of 2503 W kg-1 were achieved at the current density 1 Ag-1. It also showed an aerial capacitance of 57 mF cm-2 at current 3.2 mA cm-2. At this current density, its energy density was maximum (0.92 mWh cm-2) with power density (10.47 W cm-2).


Author(s):  
Tianrui Wang ◽  
Yupeng Su ◽  
Mi Xiao ◽  
Meilian Zhao ◽  
Tingwu Zhao ◽  
...  

AbstractCoTe@reduced graphene oxide (CoTe@rGO) electrode materials for supercapacitors were prepared by a one-step hydrothermal method in this paper. Compared with that of pure CoTe, the electrochemical performance of CoTe@rGO was significantly improved. The results showed that the optimal CoTe@rGO electrode material has a remarkably high specific capacitance of 810.6 F/g at a current density of 1 A/g. At 5 A/g, the synthesized material retained 77.2% of its initial capacitance even after 5000 charge/discharge cycles, thereby demonstrating good cycling stability. Moreover, even at a high current density of 20 A/g, the composite electrode retained 79.0% of its specific capacitance at 1 A/g, thus confirming its excellent rate performance. An asymmetric supercapacitor (ASC) with a wider potential window and higher energy density was assembled by using 3 M KOH as the electrolyte, the CoTe@rGO electrode as the positive electrode, and active carbon as the negative electrode. The operating voltage of the supercapacitor could be increased to 1.6 V, and its specific capacitance could reach 112.6 F/g at 1 A/g. The specific capacitance retention rate of the fabricated supercapacitor after 5000 charge/discharge cycles at 5 A/g was 87.1%, which confirms its excellent cycling stability. In addition, the ASC revealed a high energy density of 40.04 W·h/kg at a power density of 799.91 W/kg and a high power density of 4004.93 W/kg at an energy density of 33.43 W·h/kg. These results collectively show that CoTe@rGO materials have broad application prospects.


2021 ◽  
Author(s):  
P.A. Le ◽  
Van Qui Le ◽  
Thi Viet Bac Phung ◽  
Nghia Trong Nguyen

Abstract Three-dimensional (3D) porous carbon material enhances the electrochemical performance of symmetrical solid-state supercapacitors which are prepared by using abundant biomass waste as electrodes and (PVA-Li2SO4) gel polymer electrolyte. A saving and simple carbonization method with KOH chemical activation is developed for synthesizing highly porous carbon from peanut shell with high specific surface area of 1348 m2 g–1, which can be reused the chemical activation solution. The electrodes making by such three-dimensional porous carbon in a 1 M Li2SO4 electrolyte demonstrates a maximum specific capacitance of 386 F g–1 at current density of 2 A g–1, energy density and power density of 53.61 Wh k g–1 and 1000 W kg–1, respectively. The symmetrical solid state supercapacitors with sandwich structure of (3D porous carbon P/PVA-Li2SO4/3D porous carbon P) exhibits a maximum specific capacitance of 116 F g-1 at current density of 0.5 A g–1. The energy density and power density are the value of 9 W h kg–1 and 380 W kg–1, respectively. Further, the supercapacitors also demonstrate good cycling stability 89 % retention after 7000 cycles.


Processes ◽  
2021 ◽  
Vol 9 (10) ◽  
pp. 1750
Author(s):  
Deepa Guragain ◽  
Romakanta Bhattarai ◽  
Jonghyun Choi ◽  
Wang Lin ◽  
Ram Krishna Gupta ◽  
...  

For electrochemical supercapacitors, nickel cobaltite (NiCo2O4) has emerged as a new energy storage material. The electrocapacitive performance of metal oxides is significantly influenced by their morphology and electrical characteristics. The synthesis route can modulate the morphological structure, while their energy band gaps and defects can vary the electrical properties. In addition to modifying the energy band gap, doping can improve crystal stability and refine grain size, providing much-needed surface area for high specific capacitance. This study evaluates the electrochemical performance of aluminum-doped Ni1−xAlxCo2O4 (0 ≤ x ≤ 0.8) compounds. The Ni1−xAlxCo2O4 samples were synthesized through a hydrothermal method by varying the Al to Ni molar ratio. The physical, morphological, and electrochemical properties of Ni1−xAlxCo2O4 are observed to vary with Al3+ content. A morphological change from urchin-like spheres to nanoplate-like structures with a concomitant increase in the surface area, reaching up to 189 m2/g for x = 0.8, was observed with increasing Al3+ content in Ni1−xAlxCo2O4. The electrochemical performance of Ni1−xAlxCo2O4 as an electrode was assessed in a 3M KOH solution. The high specific capacitance of 512 F/g at a 2 mV/s scan rate, 268 F/g at a current density of 0.5 A/g, and energy density of 12.4 Wh/kg was observed for the x = 0.0 sample, which was reduced upon further Al3+ substitution. The as-synthesized Ni1−xAlxCo2O4 electrode exhibited a maximum energy density of 12.4 W h kg−1 with an outstanding high-power density of approximately 6316.6 W h kg−1 for x = 0.0 and an energy density of 8.7 W h kg−1 with an outstanding high-power density of approximately 6670.9 W h kg−1 for x = 0.6. The capacitance retention of 97% and 108.52% and the Coulombic efficiency of 100% and 99.24% were observed for x = 0.0 and x = 0.8, respectively. First-principles density functional theory (DFT) calculations show that the band-gap energy of Ni1−xAlxCo2O4 remained largely invariant with the Al3+ substitution for low Al3+ content. Although the capacitance performance is reduced upon Al3+ doping, overall, the Al3+ doped Ni1−xAlxCo2O4 displayed good energy, powder density, and retention performance. Thus, Al3+ could be a cost-effective alternative in replacing Ni with the performance trade off.


RSC Advances ◽  
2016 ◽  
Vol 6 (74) ◽  
pp. 70292-70302 ◽  
Author(s):  
Syed Khalid ◽  
Chuanbao Cao ◽  
Lin Wang ◽  
Youqi Zhu ◽  
Yu Wu

The volumetric energy density and power density of a novel solid state device (NiCo2O4//MnO2) are much higher than most reported devices.


2019 ◽  
Vol 12 (01) ◽  
pp. 1850104 ◽  
Author(s):  
Jinggao Wu ◽  
Qi Lai ◽  
Canyu Zhong

MoO3@CoMoO4 hybrid is fabricated by a facile one-step hydrothermal method and is used as anode for lithium-ion battery (LIB). Compared to pristine MoO3, galvanostatic charge–discharge tests show that the hybrid electrode delivered a remarkable rate capability of 586.69[Formula: see text]mAh[Formula: see text]g[Formula: see text] at the high current density of 1000[Formula: see text]mA[Formula: see text]g[Formula: see text] and a greatly enhanced cyclic capacity of 887.36[Formula: see text]mA[Formula: see text]h[Formula: see text]g[Formula: see text] after 140 cycles at the current density of 200[Formula: see text]mA[Formula: see text]g[Formula: see text] (with capacity retention, 85.3%). The superior electrochemical properties could be ascribed to the synergistic effect of MoO3 and CoO nanostructure that results in the lower charge transfer resistance and the higher Li[Formula: see text] diffusion coefficient, thus leading to high performance Li[Formula: see text] reversibility storage.


2019 ◽  
Vol 7 (10) ◽  
pp. 5333-5343 ◽  
Author(s):  
Wen Lu ◽  
Ze Yuan ◽  
Chunyang Xu ◽  
Jiqiang Ning ◽  
Yijun Zhong ◽  
...  

A self-templating strategy was used to prepare novel mesoporous Cu-doped Co9S8 rectangular nanotube arrays (Cu-Co9S8 NTAs) as an advanced electrode for all-solid-state asymmetric supercapacitors, which deliver a high energy density of 71.93 W h kg−1 at a power density of 750 W kg−1.


Polymers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1433 ◽  
Author(s):  
Ahmed S. F. M. Asnawi ◽  
Shujahadeen B. Aziz ◽  
Muaffaq M. Nofal ◽  
Muhamad H. Hamsan ◽  
Mohamad A. Brza ◽  
...  

In this study, the solution casting method was employed to prepare plasticized polymer electrolytes of chitosan (CS):LiCO2CH3:Glycerol with electrochemical stability (1.8 V). The electrolyte studied in this current work could be established as new materials in the fabrication of EDLC with high specific capacitance and energy density. The system with high dielectric constant was also associated with high DC conductivity (5.19 × 10−4 S/cm). The increase of the amorphous phase upon the addition of glycerol was observed from XRD results. The main charge carrier in the polymer electrolyte was ion as tel (0.044) < tion (0.956). Cyclic voltammetry presented an almost rectangular plot with the absence of a Faradaic peak. Specific capacitance was found to be dependent on the scan rate used. The efficiency of the EDLC was observed to remain constant at 98.8% to 99.5% up to 700 cycles, portraying an excellent cyclability. High values of specific capacitance, energy density, and power density were achieved, such as 132.8 F/g, 18.4 Wh/kg, and 2591 W/kg, respectively. The low equivalent series resistance (ESR) indicated that the EDLC possessed good electrolyte/electrode contact. It was discovered that the power density of the EDLC was affected by ESR.


Sign in / Sign up

Export Citation Format

Share Document