B.N.M. Dolah

Supercapacitor Electrodes from Activated Carbon Monoliths and Carbon Nanotubes

Binderless monoliths of supercapacitor electrodes were prepared by the carbonization (N2) and activation (CO2) of green monoliths (GMs). GMs were made from mixtures of self-adhesive carbon grains (SACG) of fibers from oil palm empty fruit bunches and a combination of 5 & 6% KOH and 0, 5 & 6% carbon nanotubes (CNTs) by weight. The electrodes from GMs containing CNTs were found to have lower specific BET surface area (SBET). The electrochemical behavior of the supercapacitor fabricated using the prepared electrodes were investigated by electrochemical impedance spectroscopy (EIS) and galvanostatic charge-discharge (GCD). In general an addition of CNTs into the GMs reduces the equivalent series resistance (ESR) value of the cells. A cell fabricated using electrodes from GM with 5% CNT and 5% KOH was found to have the largest reduction of ESR value than that from the others GMs containing CNT. The cell has steeper Warburgs slope than that from its respective non-CNT GM, which reflect the smaller resistance for electrolyte ions to move into pores of electrodes despite these electrodes having largest reduction in specific BET surface area. The cell also has the smallest reduction of specific capacitance (Csp) and maintains the specific power range despite a reduction in the specific energy range due to the CNT addition.

Effect of Compression Pressure on the Physical and Electrochemical Properties of Activated Carbon Monoliths Electrodes for Supercapacitor Application

Green Monoliths (GMs) of self-adhesive carbon grain from fibers of oil palm empty fruit bunches were prepared by compression pressure at 1.43 × 107, 1.91 × 107 and 2.39 × 107 kg/m2, respectively. Activated carbon monoliths ACM-A, ACM-B and ACM-C prepared by CO2 activation from these GMs, respectively, were used as electrodes in supercapacitor cells which employed stainless steel 316L current collector and H2SO4 electrolyte. Evaluation of the electrochemical properties showed that ACM-A, ACM-B and ACM-C cells had specific capacitance of 30, 9 and 5 F/g, total ESR of 3.21, 4.95 and 7.33 Ω, specific power (maximum) of 173.41, 107.58 and 33.82 W/kg, and specific energy (maximum) of 0.67, 0.15 and 0.09 Wh/kg. These properties are directly associated with the surface area of the ACMs, i.e. 419, 336 and 302 m2/g for the ACM-A, ACM-B and ACM-C, respectively, indicating a direct effect of compression pressure on the physical and electrochemical properties of ACMs electrodes.

Graphene/semicrystalline-carbon derived from amylose films for supercapacitor application

Graphene/semicrystalline-carbon in the form of carbon flakes is produced by carbonization up to 600, 700, 800, 900 and 1000°C, respectively, of the amylose films prepared by a casting method on copper foil substrate. The carbon flakes are characterized by X-ray diffraction (XRD) method to determine their microcrystallite interlayer spacing, width and stack-height; and Raman spectroscopy (RS) method to obtain structural information from the D-, D2- and G-bands peak-intensities. The XRD results show that increase in carbonization temperature lead to ~(1-3%), ~85% and ~30%increase in the microcrystallites interlayer spacing, width and stack-height, respectively, indicating that a larger growth of microcrytallite of carbon flakes occurs in the direction parallel to (001) plane or film planar surface. The specific surface area of carbon flakes estimated from the XRD results in decreases from ~4400 to ~3400 m2/g, corresponding to the specific capacitance between ~500 to ~400 F/g, which are well within the range of specific capacitance for typical electrodes carbon for supercapacitor application. The RS results show that the multilayer graphene co-exist with semicrystalline- carbon within the carbon flakes, with the multilayer graphene relative quantities increase with increasing carbonization temperature.

Electric double-layer capacitors with tea waste derived activated carbon electrodes and plastic crystal based flexible gel polymer electrolytes

We report a novel configuration of symmetrical electric double-layer capacitors (EDLCs) comprising a plastic crystalline succinonitrile (SN) based flexible polymer gel electrolyte, incorporated with sodium trifluoromethane sulfonate (NaTf) immobilised in a host polymer poly (vinylidine fluoride-co-hexafluoropropylene) (PVdF-HFP). The cost-effective activated carbon powder possessing a specific surface area (SSA) of ~ 1700 m2g-1 containing a large proportion of meso-porosity has been derived from tea waste to use as supercapacitor electrodes. The high ionic conductivity (~3.6×10-3 S cm-1 at room temperature) and good electrochemical stability render the gel polymer electrolyte film a suitable candidate for the fabrication of EDLCs. The performance of the EDLCs has been tested by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and galvanostatic charge-discharge studies. The performance of the EDLC cell is found to be promising in terms of high values of specific capacitance (~270 F g-1), specific energy (~ 36 Wh kg-1), and power density (~ 33 kW kg-1).

Effect of heat-treatment of manganese oxide deposited on stainless steel 316L current collector surface towards carbon based supercapacitor performance

Manganese oxide was deposited on the surface of stainless steel (SS) foil current collector (CC) using a simple immersion method followed by heat-treatment at three different temperatures (70, 200 and 400 °C) for 3 h. The CC deposited with manganese oxide without and with heat treatment were used in symmetrical supercapacitor cells using highly porous activated carbon electrodes and LiCl electrolyte. The heat-treatment changes the structure (from amorphous to crystalline phase) and surface morphology of manganese oxide deposited on the CC surface as evidenced by X-ray diffraction and field emission scanning electron microscopy studies. The electrochemical impedance spectroscopy, cyclic voltammetry and galvanic charge-discharge characterization results of the supercapacitor cells demonstrate that the heat-treatment temperature of 70 o C results in a maximum increase of ~70 % in specific capacitance, ~140 % in specific power and ~280 % in specific energy compared to the cell using CC deposited with manganese oxide at room temperature. Further, a 10-fold decrement in response time (from ~ 14 to ~ 1.4 s) is achieved for a heat-treatment at 70 o C which implies a ten times faster delivery of energy. These results show the superiority of CC deposited with manganese oxide heat-treated at 70 o C over the manganese oxide deposited at other temperatures.

Effect of carbonization temperature on the physical and electrochemical properties of supercapacitor electrode from fibers of oil palm empty fruit bunches

Self-adhesive carbon grains (SACG) was prepared from fibers of oil palm empty fruit bunches. The SACG green monoliths were carbonized in N2 environment at 400, 500, 600 and 700°C to produce carbon monoliths labeled as CM1, CM2, CM3 and CM4 respectively. The CMs were activated in CO2 surrounding at 800°C for 1 hour to produce activated carbon monolith electrodes (ACM1, ACM2, ACM3 and ACM4). The physical properties of the CMs and ACMs were investigated using X-ray diffraction, field emission scanning electron microscopy (FESEM) and N2 adsorption-desorption isotherm techniques. ACMs were used as electrode to fabricate symmetry supercapacitor cells and the cells’ performances were investigated using electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) standard techniques. In this paper we report the physical and electrochemical properties of the ACM electrodes by analyzing the influence of the carbonization temperature on these properties.