scholarly journals Design and synthesis of graphene/activated carbon/polypyrrole flexible supercapacitor electrodes

RSC Advances ◽  
2017 ◽  
Vol 7 (50) ◽  
pp. 31342-31351 ◽  
Author(s):  
Lanshu Xu ◽  
Mengying Jia ◽  
Yue Li ◽  
Shifeng Zhang ◽  
Xiaojuan Jin

A ternary composite of graphene/activated carbon/polypyrrole (GN/AC/PPy) used as an electrode active material for supercapacitors has been synthesized via vacuum filtration and anodic constant current deposition methods.

2018 ◽  
Author(s):  
Hakeem K. Henry ◽  
Sang Bok Lee

The PMo<sub>12</sub>-PPy heterogeneous cathode was synthesized electrochemically. In doing so, the PMo<sub>12</sub> redox-active material was impregnated throughout the conductive polymer matrix of the poly(pyrrole) nanowires. All chemicals and reagents used were purchased from Sigma-Aldrich. Anodized aluminum oxide (AAO) purchased from Whatman served as the porous hard template for nanowire deposition. A thin layer of gold of approximately 200nm was sputtered onto the disordered side of the AAO membrane to serve as the current collector. Copper tape was connected to the sputtered gold for contact and the device was sealed in parafilm with heat with an exposed area of 0.32 cm<sup>2</sup> to serve as the electroactive area for deposition. All electrochemical synthesis and experiments were conducted using a Bio-Logic MPG2 potentiostat. The deposition was carried out using a 3-electrode beaker cell setup with a solution of acetonitrile containing 5mM and 14mM of the phosphomolybdic acid and pyrrole monomer, respectively. The synthesis was achieved using chronoamperometry to apply a constant voltage of 0.8V vs. Ag/AgCl (BASi) to oxidatively polymerize the pyrrole monomer to poly(pyrrole). To prevent the POM from chemically polymerizing the pyrrole, an injection method was used in which the pyrrole monomer was added to the POM solution only after the deposition voltage had already been applied. The deposition was well controlled by limiting the amount of charge transferred to 300mC. Following deposition, the AAO template was removed by soaking in 3M sodium hydroxide (NaOH) for 20 minutes and rinsed several times with water. After synthesis, all cathodes underwent electrochemical testing to determine their performance using cyclic voltammetry and constant current charge-discharge cycling in 0.1 M Mg(ClO<sub>4</sub>)<sub>2</sub>/PC electrolyte. The cathodes were further characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), and x-ray photoelectron spectroscopy (XPS).


2021 ◽  
Vol 874 ◽  
pp. 159930
Author(s):  
Jiangfan Sun ◽  
Mingcai Yin ◽  
Yixian Li ◽  
Kaiyue Liang ◽  
Yaoting Fan ◽  
...  

2020 ◽  
Vol 1000 ◽  
pp. 50-57
Author(s):  
Jagad Paduraksa ◽  
Muhammad Luthfi ◽  
Ariono Verdianto ◽  
Achmad Subhan ◽  
Wahyu Bambang Widayatno ◽  
...  

Lithium-Ion Capacitor (LIC) has shown promising performance to meet the needs of high energy and power-density-energy storage system in the era of electric vehicles nowadays. The development of electrode materials and electrolytes in recent years has improvised LIC performance significantly. One of the active materials of LIC electrodes, activated carbon (AC), can be synthesized from various biomass, one of which is the water hyacinth. Its abundant availability and low utilization make the water hyacinth as a promising activated carbon source. To observe the most optimal physical properties of AC, this study also compares various activation temperatures. In this study, full cell LIC was fabricated using LTO based anode, and water hyacinth derived AC as the cathode. The LIC full cell was further characterized to see the material properties and electrochemical performance. Water hyacinth derived LIC can achieve a specific capacitance of 32.11 F/g, the specific energy of 17.83 Wh/kg, and a specific power of 160.53 W/kg.


2011 ◽  
Vol 347-353 ◽  
pp. 3456-3458
Author(s):  
Ren Qing Wang ◽  
Mei Gen Deng

Superscript text Commercial activated carbon was modified by surface treatment using nitric acid, The modified carbons were characterized by X-ray photoelectron spectroscopy (XPS).The resultant carbon electrode-based electric double-layer capacitors (EDLCs)were assembled with 1 mol/L (NH4)2SO4 as the electrolyte. The influence of introduced functional groups, such as hydroxyl and carbonyl, on the performance of EDLCs was studied by Constant current charge-discharge. These functional groups significantly improved the wettability of AC. As a result, the specific capacitance of the carbon modified with 40wt.%HNO3 achieved a specific capacitance of 223.45 F/g at a current density of 5mA/cm2, which is 100.9% higher than that of original AC.


Batteries ◽  
2019 ◽  
Vol 5 (1) ◽  
pp. 36 ◽  
Author(s):  
Tiphaine Plattard ◽  
Nathalie Barnel ◽  
Loïc Assaud ◽  
Sylvain Franger ◽  
Jean-Marc Duffault

Reliable development of LIBs requires that they be correlated with accurate aging studies. The present project focuses on the implementation of a weighted ampere-hour throughput model, taking into account the operating parameters, and modulating the impact of an exchanged ampere-hour by the well-established three major stress factors: temperature, current intensity (rated), and state of charge (SoC). This model can drift with time due to repeated solicitation, so its parameters need to be updated by on-field measurements, in order to remain accurate. These on-field measurements are submitted to the so-called Incremental Capacity Analysis method (ICA), consisting in the analysis of dQ/dV as a function of V. It is a direct indicator of the state of health of the cell, as the experimental peaks are related to the active material chemical/structural evolution, such as phase transitions and recorded potential plateaus during charging/discharging. It is here applied to NMC/graphite based commercial cells. These peaks’ evolution can be correlated with the here-defined Ah-kinetic and t-kinetic aging, which are chemistry-dependent, and therefore, has to be adjusted to the different types of cells.


1984 ◽  
Vol 62 (6) ◽  
pp. 527-531 ◽  
Author(s):  
P. J. Mulhern ◽  
R. R. Haering

Electrochemical cells based on the intercalation of lithium into Mo6S8 were examined by derivative constant current chronopotentiometry, in situ X-ray diffraction, and long-term cycling. About three-quarters of the capacity of such cells oeeurs between 2.0 and 2.1 V with most of the remainder near 2.45 V. Li/Mo6S8 cells have a long cycle life, good discharge rate capability, and an energy density of at least 260 W∙h/kg (1 W∙h = 3.6 kJ) of active material. Such cells can be made by starting with cathodes made from ternary Chevrel phase compounds. AyMo6S8 (A = Cu, Fe, Ni), and electrochemically converting these materials to form LixMo6S8.


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