최근 대두된 난분해성 미량오염물질은 일반적인 수처리 공법으로는 제거가 잘 되지 않고 수 ng/L 단위로도 수중생태계와 인간에게 독성을 나타내므로 반드시 처리가 필요하다. 따라서 본 연구에서는 CNT (Carbon nanotube)를 이용하여 중공사막을 제조한 후, 그것을 전극으로 사용하여 미량오염물질을 전기화학적으로 산화 제거하였다. SEM, BET, flux, conductivity 결과를 통해 전극의 특성을 분석하였다. BPA(bisphenol A), Sulfamethoxazole(SMX), N,N-Diethyl-metatoluamide(DEET) 3가지 물질을 제거 대상 미량오염물질로 선정하였고 CHM 산화극 내부로 오염물질이 포함된 물을 흘려 보내주었을 때 5분 만에 100%의 제거효율을 보였다.

Silicon alloys are considered promising anode active materials to replace Li-ion batteries by graphite powder, because they have a relatively high capacity of up to 4200 mAh/g, and are environmentally friendly and inexpensive ECO-materials. However, its poor charge/discharge properties, induced by cracking during cycles, constitute their most serious problem as anode electrode. In order to solve these problems, Si-Ge-Al alloys with porous structure are designed as anode alloy powders, to improve cycling stability. The alloys are melt-spun to obtain the rapidly solidified ribbons, and then ball-milled to make fine powders. The powders are etched using 1 M HCl solution, which gives the powders a porous structure by removing the element Al. Subsequently, in this study, the microstructures and the characteristics of the etched powders are evaluated for application as anode materials. As a result, the etched porous powder shows better electrochemical properties than as-milled Si-Ge-Al powder.

In this study, we intensively investigated the effect of conductive additive amount on electrochemical performance of organic supercapacitors. For this purpose, we assembled coin-type organic supercapacitor cells with a variation of conductive additive(carbon black) amount; carbon aerogel and polyvinylidene fluoride were employed as active material and binder, respectively. Carbon aerogel, which is a highly mesoporous and ultralight material, was prepared via pyrolysis of resorcinolformaldehyde gels synthesized from polycondensation of two starting materials using sodium carbonate as the base catalyst. Successful formation of carbon aerogel was well confirmed by Fourier-transform infrared spectroscopy and N2 adsorptiondesorption analysis. Electrochemical performances of the assembled organic supercapacitor cells were evaluated by cyclic voltammetry, galvanostatic charge/discharge, and electrochemical impedance spectroscopy measurements. Amount of conductive additive was found to strongly affect the charge transfer resistance of the supercapacitor electrodes, leading to a different optimal amount of conductive additive in organic supercapacitor electrodes depending on the applied charge-discharge rate. A high-rate charge-discharge process required a relatively high amount of conductive additive. Through this work, we came to conclude that determining the optimal amount of conductive additive in developing an efficient organic supercapacitor should include a significant consideration of supercapacitor end use, especially the rate employed for the charge-discharge process.

Membrane based water and wastewater treatment becomes more and more popular; however, membrane fouling is still a critical obstacle for its extensive use. Most of the membranes being used are polymeric and have limitations in physical, chemical, and thermal stability, even though various novel materials were introduced. In this study, metal membranes were fabricated to solve those weak points of polymeric membranes. We evaluated the physical properties of a metal membrane, such as pore size distribution, surface morphology, and water flux, and finally used the membrane for electrochemical oxidation of municipal wastewater with simultaneous hydrogen fuel generation. The metal membrane removed 50-70% of the feed organic matter by electrochemical oxidation; 10-30 % removal by electrochemical oxidation plus 40% by membrane rejection.

The Chlor-alkali (CA) membrane cell is a major electrolysis system to produce valued chemicals such as chlorine gas and sodium hydroxide. The CA membrane process has been attracted in the industries, since it has relatively low energy consumption when compared with other CA processes. The key component in CA process is perfluorinated sulfonic acid ionomer membranes, which provide ion-selectivity and barrier properties to produced gases. Unfortunately, there is limited information to determine which factors should be satisfied for CA applications. In this study, the influences of PFSA membranes on CA performances are disclosed. They include ion transport behaviors, gas evolution capability, and chemical/electrochemical resistances under CA operation conditions.

In this work, we studied the effects of electrochemical oxidation treatments of carbon fibers (CFs) on interfacial adhesion between CF and epoxy resin with various current densities. The surface morphologies and properties of the CFs before and after electrochemical-oxidation-treatment were characterized using field emission scanning electron microscopy, atomic force microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and single-fiber contact angle. The mechanical interfacial shear strength of the CFs/epoxy matrix composites was investigated by using a micro-bond method. From the results, electrochemical oxidation treatment introduced oxygen functional groups and increased roughness on the fiber surface. The mechanical interfacial adhesion strength also showed higher values than that of an untreated CF-reinforced composite.

Tin is one of the most promising anode materials for next-generation lithium-ion batteries with a high energy density. However, the commercialization of tin-based anodes is still hindered due to the large volume change (over 260%) upon lithiation/delithiation cycling. To solve the problem, many efforts have been focused on enhancing structural stability of tin particles in electrodes. In this work, we synthesize tin nano-powders with an amorphous carbon layer on the surface and surroundings of the powder by electrical wire explosion in alcohol-based liquid media at room temperature. The morphology and microstructures of the powders are characterized by scanning electron microscopy, Xray diffraction, Raman spectroscopy, and transmission electron microscopy. The electrochemical properties of the powder for use as an anode material for lithium-ion battery are evaluated by cyclic voltammetry and a galvanometric dischargecharge method. It is shown that the carbon-coated tin nano-powders prepared in hexanol media exhibit a high initial charge specific capacity of 902 mAh/g and a high capacity retention of 89% after 50 cycles.

Sulphonated polysulphone (SPS) has been synthesized and subsequently applied as binder for graphene oxide (GO)-based electrodes for development of electrochemical supercapacitors. Electrochemical performance of the electrode was investigated using cyclic voltammetry in 1M Na2SO4 and 1M KOH solution. The fabricated supercapacitors gave a specific capacitance of 161.6 and 216.8 F/g with 215.4 W/kg and 450 W/kg of power density, in 1M Na2SO4 and 1M KOH solutions, respectively. This suggests that KOH is a better electrolyte than Na2SO4 for studying the electrochemical behavior of electroactive material, and also suggests SPS is a good binder for fabrication of a GO based electrode.

Fluorine-doped tin oxide (FTO) nanoparticles have been successfully synthesized using ultrasonic spray pyrolysis. The morphologies, crystal structures, chemical bonding states, and electrochemical properties of the nanoparticles are investigated. The FTO nanoparticles show uniform morphology and size distribution in the range of 6-10 nm. The FTO nanoparticles exhibit excellent electrochemical performance with high discharge specific capacity and good cycling stability (620mA h g−1 capacity retention up to 50 cycles), as well as excellent high-rate performance (250 mA h g−1 at 700mAg−1) compared to that of commercial SnO2. The improved electrochemical performance can be explained by two main effects. First, the excellent cycling stability with high discharge capacity is attributed to the nano-sized FTO particles, which are related to the increased electrochemical active area between the electrode and electrolyte. Second, the superb high-rate performance and the excellent cycling stability are ascribed to the increased electrical conductivity, which results from the introduction of fluorine doping in SnO2. This noble electrode structure can provide powerful potential anode materials for high-performance lithiumion batteries.

Electrochemical synthesis was employed to prepare a novel hydroxyapatite/graphene (HAP/ Gr) composite powder suitable for medical applications as a hard tissue implant (scaffold). The synthesis was performed in a homogeneous dispersion containing Na2H2EDTA·2H2O, NaH2PO4 and CaCl2 with a Ca/EDTA/PO4 3− concentration ratio of 0.25/0.25/0.15M, along with 0.01 wt% added graphene nanosheets, at a current density of 137 mA cm−2 and pH value of 9.0. The field emission scanning electron microscopy and transmission electron microscopy observations of the composite HAP/Gr powder indicated that nanosized hydroxyapatite particles were uniformly placed in the graphene overlay. Raman spectroscopy, Fourier transform infrared spectroscopy and X-ray diffraction confirmed graphene incorporation in the HAP/Gr powder. The electrochemically prepared HAP/Gr composite powder exhibited slight antibacterial effect against the growth of the bacterial strain Staphylococcus aureus.

The optical fibers tend to have poor machinability because of its hardness and brittleness. In the previous study, we applied the electrochemical discharge machining to fabricate the tip of the optical fiber. We could machine the optical fiber using the electrochemical discharge machining however the machined optical fiber tip had rough surface. In this study, we use electrochemical discharge machining with rotation tool which of the rough-grinding and finishing-grinding process to obtain a smooth surface of the side firing fiber. As a result, we are able to machine the optical fiber tip with smooth surface effectively from the proposed fiber machining process and the emission from the side-firing fiber clearly demonstrated the directional emission as the emission beam was reflected at 80 ° relative to the fiber axis.

상업적으로 이용되는 폴리스티렌계 이온교환막은 제조 공정이 쉽고 간단하지만 막이 가지는 취성 때문에 내구성이 약하다는 단점을 가지고 있다. 이를 보완하기 위하여 친수성 그룹인 poly(ethylene glycol)을 곁사슬로 가지고 있는 poly(ethylene glycol)methyl ether methacrylate를 공중합시켜 음이온 교환막을 합성하였다. 지지체로는 내화학성 및 기계적 강도가 우수한 다 공성 PE 지지체를 사용하였고, 여기에 다양한 조성의 vinylbenzyl chloride, styrene, poly(ethylene glycol)methyl ether methacrylate, divinylbenzene, benzoyl peroxide를 녹인 단량체 용액을 지지체 기공에 채운 뒤 열중합 가교시켜 trimethylamine을 이 용하여 음이온 교환기를 도입해 세공충전 음이온 교환막을 합성하였다. 또한 poly(ethylene glycol)methyl ether methacrylate의 곁사슬 길이와 각 단량체가 차지하는 비율의 변화가 음이온 교환막의 전기화학적 특성에 미치는 영향을 알아보았다.