• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1996년도 춘계학술대회 논문집
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• pp.273-276
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• 1996

Polyphenylenediamine(PPD) film was prepared with dimethylsulfoxide after the synthesis of PPD by chemical polymerization. The molecular structure of conductive polymer synthesized were discussed by using SEM, FT-IR, NMR. The electrical conductivity measurements were carried out at room temperature. The electrical conductivity which was obtained from electrical instrument was 1.98${\times}$10$\^$-2/ S/cm at ambient temperature.

• Korean Chemical Engineering Research
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• 제57권3호
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• pp.425-431
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• 2019

As rechargeable metal-air batteries will be ideal energy storage devices in the future, an active cathode electrocatalyst is required with bi-functionality on both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) during discharge and charge, respectively. Here, a class of perovskite cathode catalyst with a micro-tubular structure has been developed by controlling bi-functionality from different Ru and Ni dopant ratios. A micro-tubular structure is achieved by the activated carbon fiber (ACF) templating method, which provides uniform size and shape. At the perovskite formula of $LaCrO_3$, the dual dopant system is successfully synthesized with a perfect incorporation into the single perovskite structure. The chemical oxidation states for each Ni and Ru also confirm the partial substitution to B-site of Cr without any changes in the major perovskite structure. From the electrochemical measurements, the micro-tubular feature reveals much more efficient catalytic activity on ORR and OER, comparing to the grain catalyst with same perovskite composition. By changing the Ru and Ni ratio, the $LaCr_{0.8}Ru_{0.1}Ni_{0.1}O_3$ micro-tubular catalyst exhibits great bi-functionality, especially on ORR, with low metal loading, which is comparable to the commercial catalyst of Pt and Ir. This advanced catalytic property on the micro-tubular structure and Ru/Ni synergy effect at the perovskite material may provide a new direction for the next-generation cathode catalyst in metal-air battery system.

• Journal of Electrochemical Science and Technology
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• 제2권2호
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• pp.85-90
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• 2011

Active oxygen species or free radicals are considered to cause extensive oxidative damage to biological macromolecules, which brings about a variety of diseases as well as aging. Electrolyzed reduced water(ERW) has been regarded as a ideal antioxidative agent in recent years. ERW is produced by passing a diluted salt solution through an electrolytic cell, within which the anode and cathode are separated by membrane. It can be produced reactive materials in ERW near the cathode during the electrolysis of water. ERW have the following advantages over other traditional cleaning agents: effective antioxidative agent, easy preparation, inexpensive, and environmentally friendly. The main advantage of ERW is its safety and antioxidative effect. ERW with strong reducing potential can be used to remove dirt and grease from items such as cutting boards and other kitchen utensils. The primary aim of this study is the activation mechanism of oxidation reduction potentials, ion conductivity, pH, and electrochemical properties with reactive materials in ERW.

• 한국분말재료학회지
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• 제25권4호
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• pp.296-301
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• 2018

In this study, an experiment is performed to recover the Li in $Li_2CO_3$ phase from the cathode active material NMC ($LiNiCoMnO_2$) in waste lithium ion batteries. Firstly, carbonation is performed to convert the LiNiO, LiCoO, and $Li_2MnO_3$ phases within the powder to $Li_2CO_3$ and NiO, CoO, and MnO. The carbonation for phase separation proceeds at a temperature range of $600^{\circ}C{\sim}800^{\circ}C$ in a $CO_2$ gas (300 cc/min) atmosphere. At $600{\sim}700^{\circ}C$, $Li_2CO_3$ and NiO, CoO, and MnO are not completely separated, while Li and other metallic compounds remain. At $800^{\circ}C$, we can confirm that LiNiO, LiCoO, and $Li_2MnO_3$ phases are separated into $Li_2CO_3$ and NiO, CoO, and MnO phases. After completing the phase separation, by using the solubility difference of $Li_2CO_3$ and NiO, CoO, and MnO, we set the ratio of solution (distilled water) to powder after carbonation as 30:1. Subsequently, water leaching is carried out. Then, the $Li_2CO_3$ within the solution melts and concentrates, while NiO, MnO, and CoO phases remain after filtering. Thus, $Li_2CO_3$ can be recovered.

• Corrosion Science and Technology
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• 제9권6호
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• pp.281-288
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• 2010

This study examined the carbon corrosion at Pt/C interface in proton exchange membrane fuel cell environment. The Pt nano particles were electrodeposited on carbon substrate, and then the corrosion behavior of the carbon electrode was examined. The carbon electrodes with Pt nano electrodeposits exhibited the higher oxidation rate and lower oxidation overpotential compared with that of the electrode without Pt. This phenomenon was more active at $75^{\circ}C$ than $25^{\circ}C$. In addition, the current transients and the corresponding power spectral density (PSD) of the carbon electrodes with Pt nano electrodeposits were much higher than those of the electrode without Pt. The carbon corrosion at Pt/C interface was highly accelerated by Pt nano electrodeposits. Furthermore, the polarization and power density curves of PEMFC showed degradation in the performance due to a deterioration of cathode catalyst material and Pt dissolution.

• Journal of Electrochemical Science and Technology
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• 제2권2호
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• pp.97-102
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• 2011

Different amounts of excess lithium in the range of x = 0~0.3 were added to $Li_{1+x}[Mn_{0.720}Ni_{0.175}Co_{0.105}]O_2$ cathode materials synthesized using the co-precipitation method to investigate its microstructure and electrochemical properties. Pure layered structure without impurities was confirmed in the XRD pattern analysis and increasing peak intensity of $Li_2MnO_3$ was observed along with the addition of over 0.2 mol Li. The initial discharge capacity of the stoichiometric composition was determined to be 246 mAh/g, while the discharge capacity of the addition of 0.1 mol Li was obtained to be 241 mAh/g, which was not significantly different from that of the stoichiometric composition. However, the discharge capacities decreased dramatically after the addition of 0.2 and 0.3 mol Li to 162 mAh/g and 146 mAh/g, respectively. In the rate capability test, the active $Li_{1+x}[Mn_{0.720}Ni_{0.175}Co_{0.105}]O_2$ cathode material of the stoichiometric composition showed a dramatic decrease in its discharge capacity with increasing C-rate, as evidenced by the result that the discharge capacity at 5C was 13% compared with 0.1C. On the other hand, the discharge capacity of compositions containing excess lithium was improved at higher current rates. The cycling test showed that the composition containing an excess of 0.1 mol Li had the most outstanding capacity retention.

• 자원리싸이클링
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• 제31권6호
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• pp.81-91
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• 2022

리튬이온 배터리의 사용은 전자기기 및 전기차 등의 생산량 증가로 인해 사용량이 크게 증가하고 있으며, 이와 맞물려 향후 폐배터리의 발생량 증가도 예상된다. 따라서 폐배터리를 구성하고 있는 여러 유가 자원 중 Ni, Co, Mn, Li 등이 함유되어 있는 양극 활물질이 매우 중요한 유가 자원으로, 이를 재활용하기 위한 많은 연구가 진행되고 있다. 양극 활물질 회수를 위해서 일반적으로 폐배터리로부터 블랙 매스(Black mass)를 회수하고, 이를 처리하여 주요 금속 자원을 회수한다. 블랙 매스를 회수하는 공정은 폐배터리를 수거-방전-해체-파쇄-분급의 순서로 이루어지며, 본 연구에서는 블랙 매스 회수를 위한 파쇄/분급 공정을 분석하였다. 파쇄/분급 공정을 통해 다양한 공정 산물의 입도 특성을 분석하고, 이 과정에서 생산된 산물의 입도별 형상을 현미경 및 SEM(Scanning Electron Microscopy)-EDS(Energy Dispersive Spectrometer)로 분석하였다. 분석 결과 블랙 매스로 회수되는 입자 중 74 ㎛의 미세한 입자들은 양극/음극 활물질이 전극으로부터 단체분리되어 존재하였지만, 100 ㎛ 이상의 입자들은 전극과 활물질이 붙어있는 상태에서 파쇄에 의해 입도가 감소되어 존재함을 확인하였다. 또한 배터리의 특징인 2종 혼합물(전극과 활물질)이 결합되어 있는 시료에 대해 파분쇄 특성을 모사할 수 있는 PBM(Population Balance Model) 을 개발하였으며, 2종 혼합물의 분쇄 상수를 도출하고 입도 분포 예측 성능을 검증하였다.

• 한국응용과학기술학회지
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• 제33권1호
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• pp.83-91
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• 2016

ISG (Idle Stop & Go) 시스템이 적용되는 자동차에 적합한 납축전지를 개발하기 위해 전극재료인 3BS ($3PbO{\cdot}PbSO_4{\cdot}H_2O$)와 4BS ($4PbO{\cdot}PbSO_4$)의 생성조건과 활물질의 화성 방법에 따른 납축전지 초기 성능과 심방전에 미치는 영향에 대해 연구 하였다. 양극과 음극 활물질을 숙성반응 중 온도 제어로 최종 생성 활물질의 상이 변하며, 납축전지의 수명에 영향을 미친다는 것을 알 수 있었다. 초기 성능에는 3BS 활물질을 적용한 AGM 납축전지와 Flooded 납축전지가 우수한 성능을 나타내는 반면 4BS 활물질을 적용한 AGM 납축전지는 상대적으로 낮은 성능을 나타내었다. 또한, 활물질 화성 효율을 비교분석하기 위해 화성을 3 step과 9 step으로 구분하여 시험한 결과, 3BS로 제작된 AGM 납축전지에 비해 4BS 활물질을 적용한 AGM 납축전지의 초기 성능이 우수 하였다. DOD17.5% 수명시험으로 수명성능을 비교한 결과, 잦은 심방전이 요구되는 ISG 시스템에서 Flooded 납축전지는 적합하지 않았으나, AGM 납축전지는 적합한 결과를 나타내었다. 결론적으로 AGM 납축전지가 ISG 시스템 적용 자동차에 적합하였고, AGM 납축전지의 숙성, 화성 방법에 따라 수명 성능이 80% 차이를 나타내는 것으로 확인되었다.

• Journal of Information Display
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• 제7권1호
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• pp.1-6
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• 2006

A 10" carbon nanotube field emission display device was fabricated with a novel structure with a hopping electron spacer (HES) by screen printing technique. HES plays a role of preventing the broadening of electron beams emitted from carbon nanotubes without electrical discharge during operation. The structure of the novel tetrode is composed of carbon nanotube emitters on a cathode electrode, a gate electrode, an extracting electrode coated on the top side of a HES, and an anode. HES contains funnel-shaped holes of which the inner surfaces are coated with MgO. Electrons extracted through the gate are collected inside the funnel-shaped holes. They hop along the hole surface to the top extracting electrode. In this study the effects of the addition of HES on emission characteristics of field emission display were investigated. An active ozone treatment for the complete removal of residues of organic binders in the emitter devices was applied to the field emission display panel as a post-treatment.

• 한국분말재료학회지
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• 제26권4호
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• pp.340-344
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• 2019

Due to the rapid development of electricity, electronics, information communication, and biotechnology in recent years, studies are actively being conducted on nanopowders as it is required not only for high strengthening but also for high-function powder with electric, magnetic, and optical properties. Nonetheless, studies on nickel nanopowders are rare. In this study of the synthesis of nickel nanoparticles from $LiNiO_2$ (LNO), which is a cathode active material, we have synthesized the nanosized nickel powder by the liquid reduction process of $NiSO_4$ obtained through the leaching and purification of LNO. Moreover, we have studied the reduction reaction rate according to the temperature change of liquid phase reduction and the change of particle size as a function of NaOH addition amount using hydrazine monohydrate ($N_2H_4{\cdot}H_2O$) and NaOH.