• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2002년도 하계학술대회 논문집 Vol.3 No.2
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• pp.1125-1128
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• 2002

Electrochemical capacitor made with metal oxide electrode uses rapid and reversible protonation/deprotonation of metal oxide material under the aqueous acidic solution, generally. Electrochemical stability window of aqueous electrolyte-type capacitor is narrow compared to that of organic electrolyte-type capacitor. Electrochemical characteristics of electrochemical capacitor made with metal oxide electrode and lithium cation based organic electrolyte were evaluated. Electrochemical capacitor based on $RuO_2$ electrode material and 1M $LiPF_6$ in mixed solvents of EC, DEC, and EMC has anodic and cathodic specific capacitance of 145 and 142 F/g-$RuO_2{\cdot}nH_2O$, respectively, by using cyclic voltammetry with scan rate of 2 mV/sec g-$RuO_2$ in potential range of 2.0~4.2V(Li|$Li^+$).

• 전기화학회지
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• 제9권1호
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• pp.6-9
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• 2006

The effect of $ZrO_2$-coating on the electrochemical properties of the cathode material $LiNi_{0.8}Co_{0.2}O_2$ was investigated using EPMA, TEM, and EIS. In particular, we facused on the distribution of the $ZrO_2$ on the particle surface to study the relation between electrochemical properties of the coated cathode and the distribution of the coating materials in the particle. Based on the results from the composition analysis and electrochemical tests, it was found that the coating layer consisted of nano-sized $ZrO_2$ particles attached non-uniformly on the particle surface and the $ZrO_2$ layer significantly improved the electrochemical properties of the cathode by suppressing the impedance growth at the interface between the electrodes and the electrolyte.

• Korean Chemical Engineering Research
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• 제55권3호
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• pp.379-384
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• 2017

LiCl 용융염에서 희토류 산화물의환원율을 높이기 위해 NiO와 혼합하여 전해환원을실시하였다. Cyclic voltammetry (CV) 실험을 통해 LiCl 용융염 내에서 혼합산화물의 전기화학적 환원거동을 조사하였다. 혼합산화물로 제작된 환원전극과 그라파이트 산화전극 사이에 일정한 작동전압을 인가하여 이론전하량 대비 다양한 전하량을 공급한 후 중간생성물의 결정구조를 XRD를 이용하여 분석하였다. NiO 산화물을 첨가함으로써 전기전도성이 좋은 Ni 금속 주위로 희토류 산화물이 환원되어 RE-Ni 합금형태의 금속으로 완전히 전환되었으며, 합금을 형성하는 반응 메커니즘을 제시하였다.

• Biotechnology and Bioprocess Engineering:BBE
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• 제10권6호
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• pp.505-509
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• 2005

For the purpose of developing a direct label-free electrochemical detection system, we have systematically investigated the electrochemical signatures of each step in the preparation procedure, from a bare gold electrode to the hybridization of label-free complementary DNA, for the streptavidin-modified electrode. For the purpose of this investigation, we obtained the following pertinent data; cyclic voltammogram measurements, electrochemical impedance spectra and square wave voltammogram measurements, in $Fe(CN)_6^{3-}/Fe(CN)_6^{4-}$ solution (which was utilized as the electron transfer redox mediator). The oligonucleotide molecules on the streptavidin-modified electrodes exhibited intrinsic redox activity in the ferrocyanide-mediated electrochemical measurements. Furthermore, the investigation of electrochemical electron transfer, according to the sequence of oligonucleotide molecules, was also undertaken. This work demonstrates that direct label-free oligonucleotide electrical recognition, based on biofunctional streptavidin-modified gold electrodes, could lead to the development of a new biosensor protocol for the expansion of rapid, cost-effective detection systems.

• 전기화학회지
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• 제5권3호
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• pp.164-167
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• 2002

본 연구에서는 ABS(Acrylonitrile-Butadiene-Styrene)을 주-고분자로 사용하여 산화안정성이 개선된 ABS/Polypyrrole 복합박막을 전기화학적 방법으로 합성하였다 우선 acetonitrile계의 용매로 주-고분자를 팽창시켰으며, pyrrole과 지지전해질이 백금전극에 미리 코팅된 ABS내부로 투과하여 백금 전극표면에 ABS/PPy복합체가 형성되도록 하였다. 결과적으로 전도성 ABS/PPy 복합박막은 polypyrrole과 비교하여 일정한 저항을 유지하였으며, 산화안정성도 향상되는 것으로 나타났다.

• 전기화학회지
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• 제11권4호
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• pp.227-241
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• 2008

This article involves a unified treatment of equilibrium thermodynamics of the chemical reaction coupled with other interfacial (phase boundary) reactions. The modified (restrictive) chemical potential ${\mu}_k^+$, such as electrochemical potential, hydrostatic-chemical (mechanochemical) potential (exceptionally in the presence of the pressure difference) and surface-chemical potential, was first introduced under the isothermal and isobaric conditions. This article then enlightened the equilibrium conditions in case where the release of chemical energy is counterbalanced by the supply of electrical energy, by the supply of hydrostatic work (exceptionally in the presence of ${\Delta}p$), and finally by the release of surface energy, respectively, at constant temperature T and pressure p in terms of the modified chemical potential ${\mu}_k^+$. Finally, this paper focussed on the difference between chemical and electrochemical equilibria based upon the fundamentals of the isothermal and isobaric equilibrium conditions described above.

• 대한기계학회논문집A
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• 제26권7호
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• pp.1332-1339
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• 2002

This research was undertaken to clarify effects of thermal aging on electrochemical and mechanical properties of superaustenitic stainless steel and to detect the material degradation nondestructively. The steel was artificially aged at $300{\sim}650^{\circ}C$ for $240{\sim}10,000h$ and the mechanical properties were investigated at $-196{\sim}650^{\circ}C$ using small punch(SP) test. Also, the change in electrochemical properties caused by effects of thermal aging on superaustenitic stainless steel was investigated using electrochemical anodic polarization test in a KOH electrolyte. Carbides and ${\eta}-phase(Fe_2Mo)$ precipitated in the grain boundaries seem to deteriorate the mechanical properties by decreasing cohesive strength in the grain boundaries and to promote the current density observed in electrochemical polarization curves, The electrochemical and mechanical properties of superaustenitic stainless steel decreased significantly in the specimen aged at $650^{\circ}C$ corresponding to the sensitization temperature for conventional austenitic stainless steels.

• 공업화학
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• 제29권4호
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• pp.363-368
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• 2018

Polyoxometalates (POMs)는 뛰어난 특성과 전기 화학 응용 분야에 대한 많은 잠재력을 가지고 있다. POM은 매우 잘 녹는 성질 때문에 전기화학 소자에서 POM의 잠재력을 최대한 활용하기 위해서는 다양한 기능성 재료에 POM을 고정화하는 과정이 필수이다. 본 논문에서는 우리는 최근 개발된 고정화 방법인 나노 카본 및 전도성 고분자와 같은 전도성 나노 물질에 POM을 도입하는 기술들에 대해서 논하고자 한다. Langmuir-Blodgett 기술, 층별 자기 조립 및 전기화학 in-situ 중합을 사용하여 전도성 고분자 매트릭스 및 POM을 나노 카본으로 도입할 수 있는 다양한 고정화 전략을 소개한다. 또한 우리는 POM의 응용 분야인 물 산화용 전극 촉매, 리튬 이온 배터리, 슈퍼커패시터 및 전기화학적 바이오 센서 등의 다양한 전기 화학 응용 분야를 다룬다.

• Journal of Electrochemical Science and Technology
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• 제11권1호
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• pp.1-13
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• 2020

As research on secondary batteries becomes important, interest in analytical methods to examine the condition of secondary batteries is also increasing. Among these methods, the electrochemical impedance spectroscopy (EIS) method is one of the most attractive diagnostic techniques due to its convenience, quickness, accuracy, and low cost. However, since the obtained spectra are complicated signals representing several impedance elements, it is necessary to understand the whole electrochemical environment for a meaningful analysis. Based on the understanding of the whole system, the circuit elements constituting the cell can be obtained through construction of a physically sound circuit model. Therefore, this mini-review will explain how to construct a physically sound circuit model according to the characteristics of the battery cell system and then introduce the relationship between the obtained resistances of the bulk (R_b), charge transfer reaction (R_ct), interface layer (R_SEI), diffusion process (W) and battery characteristics, such as the state of charge (SOC), temperature, and state of health (SOH).

• 한국재료학회지
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• 제28권1호
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• pp.50-61
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• 2018

Various carbon aerogels (CAs) were prepared from polymerization of resorcinol and formaldehyde and applied as the electrode materials of an electric double layer capacitor (EDLC) with the aim of controlling the textural and electrochemical properties of CAs by the type of base catalyst and the ratio of resorcinol to catalyst (R/C). The CAs from $NaHCO_3$ and $KHCO_3$ with $H^+$ ions had higher specific surface areas but exhibited lower electrochemical properties than those from $K_2CO_3$ and $Na_2CO_3$, which had more uniform pore size distributions. The electrochemical properties of $Na_2CO_3$ were superior to those of $K_2CO_3$ probably because the polarizing power of $Na^+$ ions was higher than $K^+$ ions. With an increasing R/C ratio, the pore sizes of CA showed a tendency to increase but the uniformity of the pore size distribution got worse. For the four base catalysts, the highest electrochemical property was obtained at the R/C ratio of 500.