Hierarchically porous carbon materials with high nitrogen functionalities are extensively studied as highperformance supercapacitor electrode materials. In this study, nitrogen-doped porous carbon textile (N-PCT) with hierarchical pore structures is prepared as an electrode material for supercapacitors from a waste cotton T-shirt (WCT). Porous carbon textile (PCT) is first prepared from WCT by two-step heat treatment of stabilization and carbonization. The PCT is then nitrogendoped with urea at various concentrations. The obtained N-PCT is found to have multi-modal pore structures with a high specific surface area of 1,299 m2 g−1 and large total pore volume of 1.01 cm3 g−1. The N-PCT-based electrode shows excellent electrochemical performance in a 3-electrode system, such as a specific capacitance of 235 F g−1 at 1 A g−1, excellent cycling stability of 100 % at 5 A g−1 after 1,000 cycles, and a power density of 2,500 W kg−1 at an energy density of 3.593 Wh kg−1. Thus, the prepared N-PCT can be used as an electrode material for supercapacitors.

The carbon spheres (CSs) synthesized by an ultrasonic-spray pyrolysis method were activated for supercapacitor electrode. There are plenty of cracks on the surface of the activated carbon spheres (ACSs), which expend with increasing the activation temperature and activator dosage. The specific capacitance of ACSs increases with the activation temperature and activator dosage and reach to maximal value at certain conditions. Importantly, the ACS sample activated at relatively low activation temperature (600 °C) and 7 of mass ratio of KOH to CSs has the highest specific capacitance (about 209 F g− 1 at 50 mA g− 1 of current density) and indicates the excellent cycling stability after 1000 consecutive charge–discharge cycles. Furthermore, the graphene sheets could be found in the samples that were activated at 1000 °C. And the electrode prepared by the sample has the very low series resistance because of the excellent conductivity of the formed graphene sheets.

Abstract In this study, we investigated that the activated carbon (AC)-based supercapacitor and introduced SIFSIX-3-Ni as a porous conducting additive to increase its electrochemical performances of AC/SIFSIX-3-Ni composite-based supercapacitor. The AC/SIFSIX-3-Ni composites are coated onto the aluminum substrate using the doctor blade method and conducted an ion-gel electrolyte to produce a symmetrical supercapacitor. The electrochemical properties of the AC/SIFSIX-3-Ni composite-based supercapacitor are evaluated through cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and galvanostatic charge/discharge tests (GCD). The AC/SIFSIX-3-Ni composite-based supercapacitor showed reasonable capacitive behavior in various electrochemical measurements, including CV, EIS, and GCD. The highest specific capacitance of the AC/SIFSIX-3-Ni composite-based supercapacitor was 129 F g−1 at 20 mV s−1.

Most recently, graphene-related composite-modified electrode surfaces are been widely employed to improve surface interactions and electron transfer kinetics. Hydrothermally prepared strontium pyro niobate (SPN) and reduced graphene oxide/ strontium pyro niobate (RGOSPN) nanostructures reveal excellent morphology. X-ray diffraction analysis of SPN and RGOSPN agree with standard data. Thermogravimetry–differential scanning calorimetry analyses show that RGOSPN has higher thermal stability than SPN. In addition, from the polarization–electric field (P–E) loop measurements, the estimated value of remnant polarization (Pr) and coercive electric field (Ec) of SPN are 0.039 μC cm−2 and − 2.90 kV cm−1 and that of RGOSPN nanocomposite are 0.0139 μC cm−2 and − 2.04 kV cm−1. Cyclic voltammetry measurements show that RGOSPN nanocomposite manifests the possibility of electrochemical reversibility beyond long cycles without change in performance. The redox cycle reveal that RGOSPN can be used as part of a composite electrode for hybrid capacitors dynamic conditions. Moreover, the specific capacitance of SPN and RGOSPN was calculated using galvanostatic charge–discharge (GCD) technique. The observed energy density of 9.1 W h kg−1 in RGOSPN is higher when compared with previous reported values.

The electrochemical reaction between lead borate glass frit doped with Sn metal filler and Ni-Cr wire of a J-type resistor during a term of Joule heating is investigated. The fusing behavior in which the Ni-Cr wire is melted is not observed for the control group but measured for the Sn-doped specimen under 30 V and 500 mA. The Sn-doped lead borate glass frit shows a fusing property compared with other metal-doped specimens. Meanwhile, the redox reaction significantly contributes to the fusing behavior due to the release of free electrons of the metal toward the glass. The electrons derived from the glass, which used Joule heat to reach the melting point of Ni-Cr wire, increase with increasing corrosion rate at interface of metal/ glass. Finally, the confidence interval is 95 ± 1.959 %, and the adjusted regression coefficient, R in the optimal linear graph, is 0.93, reflecting 93% of the data and providing great potential for fusible resistor applications.

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.

The synthesis of graphene and graphene quantum dots (GQDs) employing various approaches with a range of precursors, chemicals, and parameters has been reported. Most of the top-down and bottom-up techniques employ strong and hazardous chemical environments, complicated and tedious procedures, are time-consuming, and often require special equipment. Another drawback of the techniques reported is the production of agglomerated, inhomogeneous, and non-dispersible graphene in aqueous solvents or organic solvents, thus limiting its application. This work specifically and comprehensively describes the electrochemical exfoliation of graphene and GQDs, which is often considered as a simple one-step, facile, non-hazardous, and highly efficient technique yet favourable for mass production. A brief discussion on the advantageous and challenges of the electrochemical technique and applications of the electrochemically exfoliated graphene and GQDs is also presented.

In this study, the electrochemical behavior of Sm on the binary liquid Al-Ga cathode in the LiCl-KCl molten salt system is investigated. First, the co-reduction process of Sm(III)-Al(III), Sm(III)-Ga(III), and Sm(III)-Ga(III)-Al(III) on the W electrode (inert) were studied using cyclic voltammetry (CV), square-wave voltammetry (SWV) and open circuit potential (OCP) methods, respectively. It was identified that Sm(III) can be co-reduced with Al(III) or Ga(III) to form AlzSmy or GaxSmy intermetallic compounds. Subsequently, the under-potential deposition of Sm(III) at the Al, Ga, and Al-Ga active cathode was performed to confirm the formation of Sm-based intermetallic compounds. The X-ray diffraction (XRD) and scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS) analyses indicated that Ga3Sm and Ga6Sm intermetallic compounds were formed on the Mo grid electrode (inert) during the potentiostatic electrolysis in LiCl-KCl-SmCl3-AlCl3- GaCl3 melt, while only Ga6Sm intermetallic compound was generated on the Al-Ga alloy electrode during the galvanostatic electrolysis in LiCl-KCl-SmCl3 melt. The electrolysis results revealed that the interaction between Sm and Ga was predominant in the Al-Ga alloy electrode, with Al only acting as an additive to lower the melting point.

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.

Electronic textiles promise to provide an intelligent platform to enlarge the scope of wearable electronic applications. Therefore, the combination of flexible energy storage devies into wearable systems is a key for operating these electronic textiles during bending, knotting, and rolling. Nonetheless, the application of fibrous supercapacitors consisting of a gel-electrolyte and carbon fiber electrode is still obstructed by low capacitance, low rate-performance, and poor cycling stability owing to the inefficient interface between the gel-electrolyte and electrode. Here, a fibrous supercapacitor is obtained using an optimized gelelectrolyte that improves the ionic diffusion capability. The optimized fibrous supercapacitor shows a superior electrochemical performance, including high specific capacitance of 41 mF cm−2 at current density of 2.0 μA cm−2, high-rate performance with 17 mF cm−2 at a current density of 15.0 μA cm−2, and outstanding cycling stability (88% after 3,000 cycles at a current density of 200.0 μA cm−2). The excellent energy storage performance is mainly attributed to the optimzied interface between the gelelectrolyte and electrode material, leading to an improved ionic diffusion capability.

The porous carbons with high specific surface area and excellent electrochemical properties were prepared using three types of green needle coke as raw materials. Electrochemical performances of the porous carbons derived from different microstructure green needle coke were investigated. The XRD and Raman spectra demonstrated that the content of the ordered carbon microcrystals were decreased and the content of amorphous and cross-linked structure were increased in the porous carbons with comparison to the raw materials. The results of N2 adsorption–desorption analysis verified that the content of ordered microcrystalline structure in the raw materials evidently influence the specific surface area and pore size distribution of the porous carbons. The porous carbon with 1665 m2 g−1 specific surface area and 2.89 nm average pore size has shown that the specific capacitance was 288 F g−1 at the current density 1 A g−1. Furthermore, the capacity retention was 94.93% and the Coulombic efficiency was 92.87% after 5000 charge/discharge cycles.

본 연구는 절탄기 튜브의 저온부식 손상을 방지하기 위해 Inconel 625 용사재료를 활용하여 아크 열용사 코팅기술 적용 후 실링 처리를 실시하였다. 용사코팅(TSC) 층의 내식성 분석을 위해 0.5 wt% 황산 수용액에서 다양한 전기화학적 실험을 진행하였다. 양극분극 실험 후에는 주사전자현미경과 EDS 성분분석을 통해 부식 손상 정도를 파악하였다. 자연전위 계측 시 TSC+실링처리(TSC+Sealing)의 안정적인 전위 형성을 통해 실링처리 효과를 확인하였다. 양극분극 실험 결과 TSC와 TSC+Sealing에서 부동태 영역이 확인되었으며, 부식 손상 역시 관찰되지 않아 내식성이 개선되었다. 더불어 타펠분석에 의해 산출된 부식전위와 부식전류밀도 분석 결과 TSC+Sealing의 내식성이 가장 우수하게 나타났다.

In this study, soybean oil, which is used in a large variety of processed foods, is used as a carbon source. Soybean oil is successfully coated onto the surface of LiNi1/ 3Co1/3Mn1/3O2 (NCM) by a simple method. The physical and electrochemical properties of NCM/C hybrid materials are determined. As a result, a 5 nm thickness carbon coating layer is formed on the surface of the NCM, resulting in improved capability and cyclic performance in the battery. The NCM/C battery shows an initial discharge capacity of 159 mAh g−1 and 95% capacity retention after 100 cycles (a discharge capacity of 120 mAh g−1 and 94% retention are observed after 100 cycles for the NCM cathode).