PURPOSES : This study is conducted to evaluate the development of materials for extinguishing ESS(Energy Storage System) fires in electric vehicles using industrial byproducts. METHODS : Grout containing an appropriate amount of fly ash, silica fume, blast furnace slag powder, and ferronikel slag, which are industrial byproducts, was prepared. The fluidity, stress, and mechanical properties were evaluated in accordance with standard test methods. RESULTS : The fluidity of the materials used for the evolution of ESS fires differed depending on the material of the industrial byproducts. In the case of blast furnace slag, its fluidity is low owing to viscosity even when it content is high, and the use of ferronikelsrag is shown to be suitable for the evolution of ESS fires in fluidity and curing tests. CONCLUSIONS : Fire-extinguishing materials using industrial byproducts require a long curing time but exhibit the fluidity required for ESS fire extinguishment. In particular, the curing and fluidity of Peronikel slag and fly ash are suitable for ESS fire extinguishing.

Lead-free perovskite ceramics, which have excellent energy storage capabilities, are attracting attention owing to their high power density and rapid charge-discharge speed. Given that the energy-storage properties of perovskite ceramic capacitors are significantly improved by doping with various elements, modifying their chemical compositions is a fundamental strategy. This study investigated the effect of Zn doping on the microstructure and energy storage performance of potassium sodium niobate (KNN)-based ceramics. Two types of powders and their corresponding ceramics with compositions of (1-x)(K,Na)NbO3-xBi(Ni2/3Ta1/3)O3 (KNN-BNT) and (1-x)(K,Na)NbO3-xBi(Ni1/3Zn1/3Ta1/3) O3 (KNN-BNZT) were prepared via solid-state reactions. The results indicate that Zn doping retards grain growth, resulting in smaller grain sizes in Zn-doped KNN-BNZT than in KNN-BNT ceramics. Moreover, the Zn-doped KNNBNZT ceramics exhibited superior energy storage density and efficiency across all x values. Notably, 0.9KNN-0.1BNZT ceramics demonstrate an energy storage density and efficiency of 0.24 J/cm3 and 96%, respectively. These ceramics also exhibited excellent temperature and frequency stability. This study provides valuable insights into the design of KNNbased ceramic capacitors with enhanced energy storage capabilities through doping strategies.

As the demand for flexible wearable electronic devices increases, the development of light, thin and flexible high-performance energy-storage devices to power them is a research priority. This review highlights the latest research advances in flexible wearable supercapacitors, covering functional classifications such as stretchability, permeability, self-healing and shapememory capabilities, as well as practical studies on energy harvesting capabilities.

In this study, we have fabricated the phenolic resin (PR)/polyacrylonitrile (PAN) blend-derived core-sheath nanostructured carbon nanofibers (CNFs) via one-pot solution electrospinning. The obtained core-sheath nanostructured carbon nanofibers were further treated by mixed salt activation process to develop the activated porous CNFs (CNF-A). Compared to pure PAN-based CNFs, the activated PR/PAN blend with PR 20% (CNF28-A)-derived core-sheath nanostructured CNFs showed enhanced specific capacitance of ~ 223 F g− 1 under a three-electrode configuration. Besides, the assembled symmetric CNF28-A//CNF28-A device possessed a specific capacitance of 76.7 F g− 1 at a current density of 1 A g− 1 and exhibited good stability of 111% after 5,000 galvanostatic charge/discharge (GCD) cycles, which verifies the outstanding long-term cycle stability of the device. Moreover, the fabricated supercapacitor device delivered an energy density of 8.63 Wh kg− 1 at a power density of 450 W kg− 1.

In today’s world, carbon-based materials research is much wider wherein, it requires a lot of processing techniques to manufacture or synthesize. Moreover, the processing methods through which the carbon-based materials are derived from synthetic sources are of high cost. Processing of such hierarchical porous carbon materials (PCMs) was slightly complex and only very few methods render carbon nano-materials (CNMs) with high specific surface area. Once it is processed, which paves a path to versatile applications. CNMs derived from biological sources are widespread and their application spectrum is also very wide. This review focuses on biomass-derived CNMs from various plant sources for its versatile applications. The major thrust areas of energy storage include batteries, super-capacitors, and fuel cells which are described in this article. Meanwhile, the challenges faced during the processing of biomass-derived CNMs and their future prospects are also discussed comprehensively.

The Alkali-Metal Thermal to Electric Converter (AMTEC) can be used as a next-generation power generation technology related with a large thermal energy storage. In particular, this technology is expected for the higher efficiency by a cascade power generation with the thermoelectric generator(TEG), and the temperature distribution becomes a very important design parameter in this case. In this study, the temperature distribution of the AMTEC unit was analyzed through CFD analysis, and design points were discussed based on the results.

In preparation of porous carbon materials microwave oven brightening is one of the warming modes used ever. The various procedures that take place in microwave combustion process include carbonization, incitation, and recovery and thus carbon is defined. This paper compares ideal conditions of traditional warming methods, as well as their implementation potential, losses, and specifications. This porous carbon with heat treatment possesses various properties and they are well suited for energy applications which require constrained space such as hydrogen storage in solid-state and supercapacitors. The enhanced properties are chemical and thermal stability, ready availability, low framework density and ease of processability. The recent trend in class of porous carbons is Activated Carbons that are employed traditionally as adsorbents or catalyst supporters but currently, they found potent applications in fabricating for hydrogen storage materials and supercapacitors. These activated carbons are much enhanced form in class of porous carbon materials and they possess the capability to enable hydrogen economy, where the energy carrier is hydrogen. Therefore, the utility of activated carbons as a source for energy storage experiences a rapid growth at current trend and they possess significant advances. This investigation is based on detailed cost development data and electrical imperativeness applications.

Recently, due to high theoretical capacitance and excellent ion diffusion rate caused by the 2D layered crystal structure, transition metal hydroxides (TMHs) have generated considerable attention as active materials in supercapacitors (or electrochemical capacitors). However, TMHs should be designed using morphological or structural modification if they are to be used as active materials in supercapacitors, because they have insulation properties that induce low charge transfer rate. This study aims to modify the morphological structure for high cycling stability and fast charge storage kinetics of TMHs through the use of nickel cobalt hydroxide [NiCo(OH)2] decorated on nickel foam. Among the samples used, needle-like NiCo(OH)2 decorated on nickel foam offers a high specific capacitance (1110.9 F/g at current density of 0.5 A/g) with good rate capability (1110.9 - 746.7 F/g at current densities of 0.5 - 10.0 A/g). Moreover, at a high current density (10.0 A/g), a remarkable capacitance (713.8 F/g) and capacitance retention of 95.6% after 5000 cycles are noted. These results are attributed to high charge storage sites of needle-like NiCo(OH)2 and uniformly grown NiCo(OH)2 on nickel foam surface.

본 논문은 에너지를 실시간으로 저장할 수 있는 저장장치 중 열에너지 저장 콘크리트를 대상으로 재료의 미세구조와 물성(열전도 도)의 상관관계를 분석하는 연구를 수행하였다. 에너지 저장 콘크리트의 열전도 성능을 증가시키기 위해 혼화재인 그라파이트 (graphite)를 사용하였다. 그라파이트가 시멘트 질량의 10%와 15%를 치환한 시편과 일반 콘크리트(OPC) 시편을 제작하여 그라파이 트의 혼입에 따른 미세구조 변화 및 열전도도의 영향을 마이크로 스케일에서 분석하였다. 마이크로-CT를 활용하여 OPC와 그라파이 트를 사용한 콘크리트의 공극률을 비교하였으며, 확률함수를 사용하여 미세구조 특성을 정량화하였다. 미세구조 특성 차이가 열전도 도에 미치는 영향을 확인하기 위해 3차원 가상 시편을 제작하여 열해석을 수행하였으며, 이를 열평판법을 사용하여 측정한 열전도도 실험 결과와 비교하였다. 열해석 수행 시 그라파이트 재료가 지닌 열전도도 성능을 반영하기 위하여 해석 결과와 실험 결과를 기반으 로 고체상의 열전도도를 역해석을 통해 계산하였으며, 그라파이트가 시편의 열전도도에 미치는 영향에 대해 분석하였다.

Activated non-graphitizable hard carbon using orange peel with mesoporous structure has been prepared by pyrolyzation at 700, 800, 900 °C using chemical activation method. The activated orange peel-derived hard carbon has been characterized for its mesoporous and disordered structure. TG-DSC gives the information for the changes about sample composition and thermal stability of the materials. Increasing the carbonization temperature for orange peel precursor using NaOH as activating agent, elevates the pore diameter, which thereby facilitating the insertion of Na+. Raman and X-ray diffraction confirms the presence of disordered carbon. The surface morphology of the material was analyzed by scanning eletron microsope and nitrogen ( N2) adsorption and desorption analysis give the morphology, mesopore size (3.374, 3.39 and 4 nm) and surace area (60.164, 58.99 and 54.327 m2/g) of the orange peel-derived hard carbon. Hence, this work strongly evidences that the biomass-derived hard carbon with good porosity and paves way of superior electrochemical performance for emerging sodium ion batteries.

To improve ferroelectric properties of PZT, many studies have attempted to fabricate dense PZT films. The AD process has an advantage for forming dense ceramic films at room temperature without any additional heat treatment in low vacuum. Thick films coated by AD have a higher dielectric breakdown strength due to their higher density than those coated using conventional methods. To improve the breakdown strength, glass (SiO2-Al2O3-Y2O3, SAY) is mixed with PZT powder at various volume ratios (PZT-xSAY, x = 0, 5, 10 vol%) and coating films are produced on silicon wafers by AD method. Depending on the ratio of PZT to glass, dielectric breakdown strength and energy storage efficiency characteristics change. Mechanical impact in the AD process makes the SAY glass more viscous and fills the film densely. Compared to pure PZT film, PZT-SAY film shows an 87.5% increase in breakdown strength and a 35.3 % increase in energy storage efficiency.

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.

Zinc-ion Batteris (ZIBs) are recently being considered as energy storage devices due to their high specific capacity and high safety, and the abundance of zinc sources. Especially, ZIBs can overcome the drawbacks of conventional lithium ion batteris (LIBs), such as cost and safety issues. However, in spite of their advantages, the cathode materials under development are required to improve performance of ZIBs, because the capacity and cycling stability of ZIBs are mainly influenced by the cathode materials. To design optimized cathode materials for high performance ZIBs, a novel manganese oxide (MnO2) coated graphite sheet is suggested herein with improved zinc-ion diffusion capability thanks to the uniformly decorated MnO2 on the graphite sheet surface. Especially, to optimize MnO2 on the graphite sheet surface, amounts of percursors are regulated. The optimized MnO2 coated graphite sheet shows a superior zinc-ion diffusion ability and good electrochemical performance, including high specific capacity of 330.8 mAh g−1 at current density of 0.1 A g−1, high-rate performance with 109.4 mAh g−1 at a current density of 2.0 A g−1, and remarkable cycling stability (82.2 % after 200 cycles at a current density of 1.0 A g−1). The excellent electrochemical performance is due to the uniformly decorated MnO2 on the graphite sheet surface, which leads to excellent zinc-ion diffusion ability. Thus, our study can provide a promising strategy for high performance next-generation ZIBs in the near future.

Necessity of novel energy storage devices extensively increased due to consumption of high power in various devices. To address the issues, in this report, we are addressing with a composite Iron Sulfide/reduced Graphene Oxide ( Fe3S4/rGO) synthesized using the standard solvothermal method. X-ray diffraction and Field Emission Scanning Electron Microscope analysis results confirmed that Face-Centered cubic crystal structure of Fe3S4 and rGO’s surface is decorated with a mean diameter of < 50 nm Fe3S4 respectively. Transmission Electron Microscopy images show further evidence that dispersed Fe3S4 on the rGO surface. Fe3S4/ rGO exhibits specific capacitance of 560 F/g than its individual counterparts ( Fe3S4 = 200 F/g and rGO = 145 F/g) at 1 A/g of current density and maximum cyclic stability of 91% capacitance retention after 2000 cycles that may be the influence of synergy between the composite materials.

전기차, 에너지저장시스템의 수요급증으로 에너지 저장장치에 대한 관심이 세계적으로 증가해왔다. 에너지 저장장치의 핵심원료인 리튬과 바나듐 등과 같은 에너지저장광물 자원을 안정적으로 공급하기 위하여 새로운 기술적 대안이 필요하다. 이미 리튬과 바나듐을 직접 확보할 수 있는 기술에 대한 여러 국가들의 연구개발 활동이 이루어지고 있다. 이에 따라 효과적인 연구개발 전략을 수립하기 위해서 특허 및 논문 분석을 통해 각국의 기술동향을 분석하고 향후 기술발전방향을 설정하는 것이 중요하다. 본 연구는 1970년부터 2019년 10월까지 출원 공개 또는 출원 등록된 한국, 미국, 유럽, 일본의 특허자료와 2000년 1월부터 2019년 10월까지의 논문을 대상 검색된 자료를 통해 신기술 개발 동향 및 국내외 연구개발 현황을 분석하였다. 분석결과, 현재 에너지저장광물과 관련된 기술의 성장단계는 태동기 단계에 있는 것으로 분석되었다. 따라서 기술시장 선도와 기술 경쟁력 강화를 위해 새로운 기술의 개발과 개발된 기술에 대한 실증을 병행하여 빠르게 기술을 고도화 하는 전략이 필요하다고 사료된다.

본 연구에서는 “이온젤” 이라고 불리는 고분자 기반의 PVA(polyvinyl alcohol) 기반의 고체 전 해질에 이온성 액체 BMIMBF4 (1-buthyl-3-methylimidazolium tetrafluoroborate)를 첨가하여 제조한 전 고체 전해질과 활성탄소와 금속유기골격체 복합재료 기반의 전극 재료를 이용하여 슈퍼커패시터를 제작 하였으며, 유기골격체의 유 무에 따른 전기화학적 특성을 분석하여 보았다. 슈퍼커패시터의 전기화학적 특 성은 순환전압전류법(CV), 전기화학적 임피던스 분광법(EIS) 및 전정류 충·방전법(GCD)을 통하여 비교 및 분석하여 보았다. 그 결과로, 금속유기골격체가 함유되지 않은 슈퍼커패시터의 전기용량값은 380 F/g 으로 확인 할 수 있었고, 이 값은 금속유기골격체를 첨가하였을 때 340 F/g로 감소하는 현상을 확인할 수 있었 다. 이러한 결과로 1 wt%의 금속유기골격체의 함유량은 전기화학적 특성 감소에 영향을 주는 것으로 사료 되며 이러한 결과를 바탕으로 금속유기골격체의 첨가량을 최적화 할 필요가 있다고 판단된다

고분자를 기반으로 하는 고체 전해질은 수퍼커패시터, 배터리, 센서, 액추에이터 등 다양한 전기화학 소자에 응용이 가능한 소재로써, 기존 고분자 전해질의 낮은 이온전도도를 향상시키기 위해서 다양한 이온성 액체 기반의 고체 전해질에 관한 연구가 활발히 진행 중에 있다. 이온성 액체의 높은 전기적 특성 및 전기화학적, 열적 안정성과 고분자의 우수한 기계적인 강도를 활용한 젤 상태의 고체 전해질인 이온젤은 차세대 웨어러블 및 플렉시블 전자소자에 응용되어 연구되고 있다. 따라서 본 연구에서는 이러한 이온성 액체와 고분자 기반의 고체 전해질을 제조하고 특성을 분석하여 탄소나노복합체 기반의 전극 에 적용하여 다양한 전자소자에 응용이 가능한 이온전도도 및 안정성이 향상된 이온성 액체 기반의 고체 전해질을 개발하고자 한다. 제조된 고체전해질은 전기화학적 임피던스법을 이용하여 이온 전도도를 측정 하여 보았으며 이온성 액체를 첨가하여 제조한 고체전해질의 이온 전도도가 1.26 x 10-1 S/cm 로 확인 되었다. 또한 제조된 고체 전해질을 이용하여 전고체형 수퍼커패시터를 제조하여 전기화학적 특성을 비교 하여 보았으며, 수퍼커패시터의 전기화학적 특성 역시 이온성 액체를 첨가하여 제조된 고체 전해질을 사 용하였을 때 향상된 전기화학적 특성을 나타내었다.