Carbon-based materials, particularly graphite, have been extensively studied for their potential in fabricating flexible conductive fabrics with high electrical conductivity, which are attractive for wearable electronics. In this study, we investigated the effects of polar solvents, graphite concentration, and temperature on the electrical properties of conductive cotton fabrics. Our results show that the type of polar solvent and graphite concentration strongly influence the electrical conductivity of the fabrics. By controlling the graphite concentration, a wide range of conductive cotton fabrics with different conductivity values can be produced. Additionally, temperature resistance studies revealed that the fabrics exhibit both semiconductor and metallic behavior in the temperature range from room temperature to 160 °C. These interesting properties make the conductive cotton fabrics suitable for use as electrical components in circuits with resistive and inductive loads. Furthermore, we fabricated a supercapacitor with electrodes based on dispersed graphite and an electrolyte of sodium chloride salt dissolved in deionized water. Our findings suggest that conductive cotton fabrics have great potential for use in high-performance wearable electronics and energy storage devices.

Energy storage for sustainable development and progress of power production industries is vitally important. The energy storage devices are under extensive research from last three decades to ensure the hand-on-hand coordination with power supply phenomenon and to reduce the energy loses in lines. The cost-effective materials are still highly demanding as an electrode material for energy storage devices. Biomass-derived carbon materials are best candidates due to their low cost, relatively high abundance, pollution-free nature. Here, we are reporting a facile two-step green approach to convert Himalayan horse chestnuts (HHCNs) into activated carbon materials. In first step, grinding and pyrolysis of the HHCNs were carried out, and then activation was performed using KOH to enhance the pore density and surface area. HHCNs-derived carbon was utilized as an electrode in electrical double-layer capacitors (EDLCs) with 1 M H2SO4 as an electrolyte. The macroporous structure along with hierarchical porous network acts as an efficient source of transportation of charges across the electrode and separator. Cyclic voltammetry test was taken from 10 to 100 mV/s current and within a range of 0–1 V applied potential; approximately rectangular CV shown mirror response towards current and shown typical EDLCs properties. The proximate analysis confirms the presence of heteroatoms like sulfur, oxygen, and nitrogen which act as carbon dopants. The wettability of HHCNs-derived carbon enhanced due to the various types of oxygen functionalities inherited from the lignin skeletal part. The nitrogen content is primarily responsible for the pseudo-capacitive behavior of HHCNs-codoped carbon. HHCNs-derived activated carbon materials has emerged as a promising electrode material for energy storage applications.

As the use of capacitors in electrical appliances and electrical control circuits increases, the related electrical fire is increasing. There are various parts such as resistors, coils, and capacitors that make up an electric circuit. Among them, the ignition of a capacitor with a temporary charging function is closely related to the structural characteristics of the capacitor. Capacitors can explode due to various reasons, and the high heat generated when they explode ignites the inflammable dielectric, which in turn burns the inflammable materials such as the surrounding electric wires and spreads into a fire. In this paper, the ignition mechanism is studied by conducting a reenactment experiment on the various probabilities that can be ignited in an electric capacitor, and the prevention measures to be applied to the fire prevention are presented.

본 연구에서는 싸이크론 헥산에서 PVC와 트리에틸디아민 (TEDA), 1,4-디메틸피페라진 (DMP) 및 1,4-비스(이미다졸-1-일메틸)벤젠을 각각 치환반응시켜서3가지 형태의 PVC 멤브레인, AEM-1, AEM-2, and AEM-3를 제조하였다. AEM-1, AEM-2, and AEM-3멤브레인의 성공적인 제조 여부를 이온전도도(S/cm), 물함수율 (%), 접촉각, 이온교환능력 (meq/g), 열분석, SEM 및 XPS 분석 통하여 확인하였다. 또한, 제조된 가교 음이온 PVC멤브레인을 사용하여 유기전해질에서 전기화학 캐퍼 시터 실험을 수행한 결과, 제조된 AEM-1, AEM-2 AEM-3 멤브레인의 경우 유기전해질에서 충/방전 실험결과 매우 안정적임을 확인 할 수 있었다. 이러한 결과로 치환반응 후에 용매 캐시팅법으로 제조 된 PVC기반 멤브레인 (AEM-1, AEM-2, 및 AEM-3)의 경우 유기전기화학캐퍼시터 (슈퍼캐퍼시터)용 분리막으로 사용될 수 있다.

Owing to its low cost, easy fabrication process, and good ionic properties, aqueous supercapacitors are under strong consideration as next-generation energy storage devices. However, the limitation of the current collector is its poor electrochemical stability, leading to low energy storage performance. Therefore, a reasonable design of the current collector and the acidic electrolyte is a necessary, as well as interfacial engineering to enhance the electrochemical performance. In the present study, graphite foil, with excellent electrochemical stability and good electrical properties, is suggested as a current collector of aqueous supercapacitors. This strategy results in excellent electrochemical performance, including a high specific capacitance of 215 F g−1 at a current density of 0.1 A g−1, a superior high-rate performance (104 F g−1 at a current density of 20.0 A g−1), and a remarkable cycling stability of 98 % at a current density of 10.0 A g−1 after 9,000 cycles. The superior energy storage performance is mainly ascribed to the improved ionic diffusion ability during cycling.

Engineering the microstructure of the carbonaceous materials is a promising strategy to enhance the capacitive performance of supercapacitors. In this work, nanostructured Black Pearl (1500 BP) carbon which is a conductive carbon being commercially used in printing rolls, conductive packaging, conductive paints, etc. is analyzed for its feasibility as an electrode material for Electric Double-Layer Capacitors (EDLCs). To achieve that commercial Black Pearl (BP), carbon is treated with mild acid H3PO4 to remove the impurities and enhance the active sites by regulating the growth of agglomerates and creating micropores in the nano-pigments. Generally, the coalescence of nanoparticles owing to their intrinsic surface energy has tendency to create voids of different sizes that act like meso/micropores facilitating the diffusion of ions. The electrochemical performance of BP carbon before and after chemical activation is investigated in aqueous ( H2SO4, KOH and KCl) and a non-aqueous electrolyte (1 M TEMABF4 in acetonitrile) environment employing different electrochemical techniques such as Cyclic Voltammetry (CV), Galvanostatic charge/discharge (GCD) and Electrochemical Impendence Spectroscopy (EIS). The chemically activated BP carbon delivers the highest specific capacitance of ∼156 F g−1 in an aqueous electrolyte, 6 M KOH. The highest specific power, ~ 15.3 kW kg−1 and specific energy, 14.6 Wh kg−1 are obtained with a symmetric capacitor employing non-aqueous electrolyte because of its high working potential, 2.5 V.

Activated carbons (ACs) have been used as electrode materials of electric double-layer capacitors (EDLC) due to their high specific surface areas (SSA), stability, and ecological advantages. In order to make high-energy-density ACs for EDLC, petroleum pitch (PP) precarbonized at 500–1000°C in N2 gas for 1 h was used as the electrode material of the EDLC after KOH activation. As the pre-carbonization temperature increased, the SSA, pore volume and gravimetric capacitance tended to decrease, but the crystallinity and electrode density tended to increase, showing a maximum volumetric capacitance at a medium carbonization temperature. Therefore, it was possible to control the crystalline structure, SSA, and pore structure of AC by changing the pre-carbonization temperature. Because the electrode density increased with increasing of the pre-carbonization temperature, the highest volumetric capacitance of 28.4 F/cc was obtained from the PP pre-carbonized at 700°C, exhibiting a value over 150% of that of a commercial AC (MSP-20) for EDLC. Electrochemical activation was observed from the electrodes of PP as they were pre-carbonized at high temperatures above 700°C and then activated by KOH. This process was found to have a significant effect on the specific capacitance and it was demonstrated that the higher charging voltage of EDLC was, the greater the electrochemical activation effect was.

In this study, we used I-V spectroscopy, photoconductivity (PC) yield and internal photoemission (IPE) yield using IPE spectroscopy to characterize the Schottky barrier heights (SBH) at insulator-semiconductor interfaces of Pt/HfO2/p-type Si metal-insulator-semiconductor (MIS) capacitors. The leakage current characteristics of the MIS capacitor were analyzed according to the J-V and C-V curves. The leakage current behavior of the capacitors, which depends on the applied electric field, can be described using the Poole-Frenkel (P-F) emission, trap assisted tunneling (TAT), and direct tunneling (DT) models. The leakage current transport mechanism is controlled by the trap level energy depth of HfO2. In order to further study the SBH and the electronic tunneling mechanism, the internal photoemission (IPE) yield was measured and analyzed. We obtained the SBH values of the Pt/HfO2/p-type Si for use in Fowler plots in the square and cubic root IPE yield spectra curves. At the Pt/HfO2/p-type Si interface, the SBH difference, which depends on the electrical potential, is related to (1) the work function (WF) difference and between the Pt and p-type Si and (2) the sub-gap defect state features (density and energy) in the given dielectric.

Activated carbons (ACs) were prepared by activation of coal tar pitch (CTP) in the range of 700°C-1000°C for 1-4 h using potassium hydroxide (KOH) powder as the activation agent. The optimal activation conditions were determined to be a CTP/KOH ratio of 1:4, activation temperature of 900°C, and activation time of 3 h. The obtained ACs showed increased pore size distribution in the range of 1 to 2 nm and the highest specific capacitance of 122 F/g in a two-electrode system with an organic electrolyte, as measured by a charge-discharge method in the voltage range of 0-2.7 V. In order to improve the performance of the electric double-layer capacitor electrode, various mixtures of CTP and petroleum pitch (PP) were activated at the optimal activation conditions previously determined for CTP. Although the specific capacitance of AC electrodes prepared from CTP only and the mixtures of CTP and PP was not significantly different at a current density of 1 A/g, the AC electrodes from CTP and PP mixtures showed outstanding specific capacitance at higher current rates. In particular, CTP-PP61 (6:1 mixture) had the highest specific capacitance of 132 F/g, and the specific capacitance remained above 90% at a high current density of 3 A/g. It was found that the high specific capacitance could be attributed to the increased micro-pore volume of ACs with pore sizes from 1 to 2 nm, and the high power density could be attributed to the increased meso-pore volume.

The effects of the mixing of an active material and a conductive additive on the electrochemical performance of an electric double layer capacitor (EDLC) electrode were investigated. Coin-type EDLC cells with an organic electrolyte were fabricated using the electrode samples with different ball-milling times for the mixing of an active material and a conductive additive. The ball-milling time had a strong influence on the electrochemical performance of the EDLC electrode. The homogeneous mixing of the active material and the conductive additive by ball-milling was very important to obtain an efficient EDLC electrode. However, an EDLC electrode with an excessive ball-milling time displayed low electrical conductivity due to the characteristic change of a conductive additive, leading to poor electrochemical performance. The mixing of an active material and a conductive additive played a crucial role in determining the electrochemical performance of EDLC electrode. The optimal ball-milling time contributed to a homogeneous mixing of an active material and a conductive additive, leading to good electrochemical performance of the EDLC electrode.

A hierarchical pore structured novolac-type phenol based-activated carbon with micropores and mesopores was fabricated. Physical activation using a sacrificialsilicon dioxide (SiO2) template and chemical activation using potassium hydroxide (KOH) were employed to pre-pare these materials. The morphology of the well-developed pore structure was character-ized using field-emissionscanning electron microscopy. The novolac-type phenol-based activated carbon retained hierarchical pores (micropores and mesopores); it exhibited high Brunauer-Emmett-Teller specificsurface areas and hierarchical pore size distributions. The hierarchical pore novolac-type phenol-based activated carbon was used as an electrode in electric double-layer capacitors, and the specificcapacitance and the retained capacitance ratio were measured. The specificcapacitances and the retained capacitance ratio were en-hanced, depending on the SiO2 concentration in the material. This result is attributed to the hierarchical pore structure of the novolac-type phenol-based activated carbon.

Well-distributed ruthenium (Ru) nanoparticles decorated on porous carbon nanofibers (CNFs) were synthesized using an electrospinning method and a reduction method for use in high-performance elctrochemical capacitors. The formation mechanisms including structural, morphological, and chemical bonding properties are demonstrated by means of field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). To investigate the optimum amount of the Ru nanoparticles decorated on the porous CNFs, we controlled three different weight ratios (0 wt%, 20 wt%, and 40 wt%) of the Ru nanoparticles on the porous CNFs. For the case of 20 wt% Ru nanoparticles decorated on the porous CNFs, TEM results indicate that the Ru nanoparticles with ~2-4 nm size are uniformly distributed on the porous CNFs. In addition, 40 wt% Ru nanoparticles decorated on the porous CNFs exhibit agglomerated Ru nanoparticles, which causes low performance of electrodes in electrochemical capacitors. Thus, proper distribution of 20 wt% Ru nanoparticles decorated on the porous CNFs presents superior specific capacitance (~280.5 F/g at 10 mV/s) as compared to the 40 wt% Ru nanoparticles decorated on the porous CNFs and the only porous CNFs. This enhancement can be attributed to the synergistic effects of well-distributed Ru nanoparticles and porous CNF supports having high surface area.

Activated carbon (AC) was synthesized from rice husks using the chemical activation method with KOH, NaOH, a combination of (NaOH + Na2CO3), and a combination of (KOH + K2CO3) as the chemical activating reagents. The activated carbon with the highest surface area (around 2000m2/g) and high porosity, which allows the absorption of a large number of ions, was applied as electrode material in electric double layer capacitors (EDLCs). The AC for EDLC electrodes is required to have a high surface area and an optimal pore size distribution; these are important to attain high specific capacitance of the EDLC electrodes. The electrodes were fabricated by compounding the rice husk activated carbons with super-P and mixed with polyvinylidene difluoride (PVDF) at a weight ratio of 83:10:7. AC electrodes and nickel foams were assembled with potassium hydroxide (KOH) solution as the electrolyte. Electrochemical measurements were carried out with a three electrode cell using 6 M KOH as electrolyte and Hg/HgO as the reference electrode. The specific capacitance strongly depends on the pore structure; the highest specific capacitance was 179 F/g, obtained for the AC with the highest specific surface area. Additionally, different activation times, levels of heating, and chemical reagents were used to compare and determine the optimal parameters for obtaining high surface area of the activated carbon.

TiO2 thin films for high energy density capacitors were prepared by r.f. magnetron sputtering at room temperature.Flexible PET (Polyethylene terephtalate) substrate was used to maintain the structure of the commercial film capacitors. Theeffects of deposition pressure on the crystallization and electrical properties of TiO2 films were investigated. The crystal structureof TiO2 films deposited on PET substrate at room temperature was unrelated to deposition pressure and showed an amorphousstructure unlike that of films on Si substrate. The grain size and surface roughness of films decreased with increasing depositionpressure due to the difference of mean free path. X-ray photoelectron spectroscopy (XPS) analysis revealed the formation ofchemically stable TiO2 films. The dielectric constant of TiO2 films was significantly changed with deposition pressure. TiO2films deposited at low pressure showed high dissipation factor due to the surface microstructure. The dielectric constant anddissipation factor of films deposited at 70mTorr were found to be 100~120 and 0.83 at 1kHz, respectively. The temperaturedependence of the capacitance of TiO2 films showed the properties of class I ceramic capacitors. TiO2 films deposited at10~30mTorr showed dielectric breakdown at applied voltage of 7V. However, the films of 500~300nm thickness depositedat 50 and 70mTorr showed a leakage current of ~10−8~10−9 A at 100 V.

The electrochemical performances of an asymmetric hybrid capacitor were investigated using LiFePO4 as the positive electrode and active carbon fibers(ACF) as the negative electrode. The electrochemical behaviors of a nonaqueous hybrid capacitor were characterized by constant current charge/discharge test. The specific capacitance using LiFePO4/ACF electrode turned out to be 0.87F/cm2 and the unit cell showed excellent cycling performance. This hybrid capacitor was able to deliver a specific energy as high as 178 Wh/kg at a specific power of 1,068 W/kg.

The power capacitors used as vehicle inverters must have a small size, high capacitance, high voltage, fast response and wide operating temperature. Our thin film capacitor was fabricated by alumina layers as a dielectric material and a metal electrode instead of a liquid electrolyte in an aluminum electrolytic capacitor. We analyzed the micro structures and the electrical properties of the thin film capacitors fabricated by nano-channel alumina and metal electrodes. The metal electrode was filled into the alumina nano-channel by electroless nickel plating with polyethylene glycol and a palladium catalyst. The spherical metals were formed inside the alumina nano pores. The breakdown voltage and leakage current increased by the chemical reaction of the alumina layer and PdCl2 solution. The thickness of the electroless plated nickel layer was 300 nm. We observed the nano pores in the interface between the alumina layer and the metal electrode. The alumina capacitors with nickel electrodes had a capacitance density of 100 nF/cm2, dielectric loss of 0.01, breakdown voltage of 0.7MV/cm and leakage current of 104μA.

In semiconductor memory, the kinds of voltage generator are high voltage generator, negative voltage generator, drain voltage generator and etc. The relevant circuits supported voltage generator, are clock generator, sense amplifier, voltage regulator and etc. The voltage generator consists of MOS diodes and MOS capacitors. To get the out voltage with sufficient charge, the MOS capacitors are big size. These MOS transistors can be adapted only on the EEPROM process. Thus, in this paper, we designed stacked metal capacitor. This capacitor is small size but can get much capacitance. This capacitor is designed to comb type using metal-line and poly-line. The size of designed capacitor is 208×52㎛2 and the capacitance is about 4㎊. The stacked metal capacitor can get much capacitance of 5～6 times than single plane capacitor. Also this capacitor will be easy adapted in sub-micro process technology of semiconductor memory. And this capacitor can be adapted on all memory process.

Mesoporous activated carbon (AC) was prepared from aged petroleum coke through chemical activation. The AC has a specific surface area of 1733 m2/g and a mean pore diameter of 2.37 nm. The volume fraction of 2 to 4nm pores is 56.74%. At a current density of 10 mA/cm2, a specific capacitance of 240 F/g is achieved representing the use factor of the surface area of 69.2%. And the electrical double layer capacitor (EDLC) based on the AC shows an excellent power performance. This result suggests that the presence of high fraction of mesopores can effectively increase the adsorption efficiency of the specific surface area of the AC and enhance the power performance of EDLC based on the efficient surface area of the AC.