• Journal of the Korean Chemical Society
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• v.32 no.3
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• pp.195-202
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• 1988

An electrochemical reduction on the 3-phenyl-4-nitrosydnone in acetonitrile solution has been studied by direct current, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. Before the cleavage of phenyl-N single bond a irreversible electron transfer-chemical reaction(EC) mechanism of nitro functional group proceeded to form amino (or-hydroxylamino) group by multielectron transfer which is followed to give phenyl hydrazine by single electron transfer-chemical reaction at the 2nd and 3rd irreversible reduction wave of high negative potential region. The cathodic half-wave potentials shown to be shift negative due to inhibitory effect of cetyl-trimethyl ammonium bromide micelle while reversible anodic peaks on the 2nd and 3rd reduction waves in the presence of NaLS at high negative potential region.

• Proceedings of the KIEE Conference
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• 2009.07a
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• pp.2119_2120
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• 2009

전압을 인가하였을 때 전계방향에 의해 가역적으로 색이 변화하는 현상을 전기변색(electrochromism)이라고 한다. 이러한 전기채색현상을 보이는 물질을 전기채색물질(electrochromism materials)이라고 하며, 전기채색 물질에 의한 소자를 전기채색소자(electrochromism device : ECD)라고 한다. 전기채색현상은 투과율(transmittance), 반사율(reflectance)의 가역적이며 가시적인 변화이고, 전기화학적인 산화환원 반응과 관련이 있다. 따라서 본 연구에서는 Titanate nanotube(TNT)를 제조하고 전기변색소자(ECD)에 응용하였다. SEM, XRD, UV-Vis등을 이용하여 재료학적 분석을 시행하였으며, 전기화학적 테스트로 cyclic voltammetry를 측정 하였다. 그 결과 TNT 분말은 직경 약 20~30 nm, 길이 약 500~600 nm 의 입자형상을 나타내었으며, X-선 회절시험결과 $H_2Ti_2O_5{\cdot}H_2O$의 층상구조를 나타내었다. 제조된 막은 FTO glass 위에 PEI/(TNT/TBAOH)$_{n-1}$/PDDA의 순으로 코팅되었다. 전기화학적 테스트를 위하여 2전극 시스템을 제작하였으며, 여러 종류의 액체 전해질을 제작하여 cycle voltammetry를 시행하였다. 그 결과, 각각의 전해질에서 "-"영역의 산화환원전위 피크가 뚜렷하게 나타났으며, 짙은 갈색으로의 채색현상을 나타냈다. 본 연구의 결과로서 TNT 박막을 이용한 ECD은 광조절 유리로서 뿐만 아니라, 여러 전기채색 디바이스에 응용될 것으로 사료된다.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2017.05a
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• pp.99.1-99.1
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• 2017

$TiO_2$는 기계적, 화학적 안정성이 높아 가혹한 화학적 환경 또는 고온 운전 조건에서 훌륭한 내구성을 보여주어 산업적으로 일찍이 널리 이용되어 왔다. 예를 들어, 염소발생 (chlorine evolution reaction) 또는 산소발생반응은 (oxygen evolution reaction) 염소 또는 산소 라디칼에 전극이 지속적으로 노출되기에 강한 내부식성을 지닌 전극재가 요구되었고, 그 결과 $TiO_2$를 골조로 한 불용성전극 (dimensionally stable anode)이 개발되어 이용되고 있다. 그러나, $TiO_2$는 절연성이 높은 금속 산화물 재료이기 때문에 넓은 표면적 획득 및 촉매제 사용을 통해 소재의 단점을 극복해야만 한다. 넓은 반응 표면적 획득의 한 방법으로써 전기화학적 양극산화 (electrochemical anodization)를 통한 $TiO_2$ 나노튜브 제조법은 경제적이면서도 구조 제어도 간편한 방법이다. $TiO_2$ 나노튜브는 100nm 전후의 기공 크기를 가짐과 동시에 매우 높은 종횡비를 지니고 있어 넓은 반응 표면적 획득에 특히 유리하다. 그러나, 이 높은 종횡비는 촉매 도입을 어렵게 하는 저해요소가 되기도 한다. 이러한 문제를 해결하기 위하여 다양한 방법들이 연구되었으나 대부분이 번거롭거나 비싼 후단공정을 필요로 한다. 본 연구에서는 $TiO_2$ 나노튜브에 촉매를 도핑하기 위한 간단한 전기화학적 방법으로, 단일공정 양극산화법 (single-step anodization)과 전압충격법 (potential shock), 그리고 저전압충격법 (under potential shock)을 연구하였으며 이에 적용 가능한 촉매제의 종류를 소개한다. 또한, 촉매의 성질에 따른 응용분야와 그 성능평가 결과를 제시한다.

• Journal of the Korean Chemical Society
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• v.35 no.1
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• pp.70-77
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• 1991

1-Benzyl-4-iodomethyl-2-azetidinone(BIMA) was synthesized and its electrochemical reduction was investigated by direct current, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. The irreversible two electron transfer on reductive dehalogenation of iodo group proceeded to form 1-benzyl-4-methyl-2-azetidinone by EEC electrode reaction mechanism at the first reduction step(-1.35 volts vs. Ag-AgCl). The polarographic reduction waves separated into two reduction steps due to anionic surfactant (sodium lauryl sulfate) effects, while the waves were shifted to the positive potential as the concentration of cationic surfactant (cetyltrimethylammonium bromide) increased. Upon the basis of results on the product analysis and interpretation of polarogram with pH variable, EEC electrochemical reaction mechanism was suggested.

• Applied Chemistry for Engineering
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• v.34 no.2
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• pp.180-185
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• 2023

To improve the efficiency of water electrolysis, it is essential to develop an oxygen evolution reaction (OER) electrocatalyst with high performance and long-term stability, accelerating the reaction rate of OER. In this study, a hollow metal-organic framework (MOF)-derived ruthenium-cobalt oxide catalyst was developed to synthesize an efficient OER electrocatalyst. As the synthesized catalyst increases the surface exposure of ruthenium, a low overpotential (386 mV) was observed at a current density of 10 mA/cm² with a low Tafel slope. It is expected to be able to replace noble metal catalysts by showing higher mass activity and stability than commercial RuO₂ catalysts.

• Applied Chemistry for Engineering
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• v.8 no.6
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• pp.1022-1028
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• 1997

This work was performed to study the characteristics of electrochemical intercalation reactions occurring at the interface between the organic electrolyte and tungsten trioxide thin film (thickness of $4000{\AA}$) prepared by e-beam evaporation method as cathodically coloring oxide with regard to the electrochromism by the intercalating reactions of the lithium cation in the 1M $LiClO_4/PC$ organic solution. The characteristics of electrochemical intercalation reactions were investigated by various DC electrochemical methods such as cathodic Tafel polarization test, multiple and the single sweep cyclic voltammetry and the coulomety titrations method. The surfaces of thin films were observed with the patterns of X ray diffraction after the coloring and bleaching reactions. In comparison with the previous results that $WO_3$ thin film intersely detached from the surface of electrode when the hydrogen cation was intercalated into $WO_3$ thin film in the o.1N $H_2SO_4$ aqueous solution, the intercalation reaction of lithium cation into $WO_3$ thin film in the 1M $LiClO_4/PC$ organic solution was shown that the stable bleaching and coloration was appeared within 1.0V of the applied overpotential. When the overpotential of electrochromic reaction for lithium cation in the 1M $LiClO_4/PC$ organic solution had been applied up to 1.5V, the accumulation phenomenon of lithium in amorphous $WO_3$ thin film layer occurred because the inserted lithium into amorphous $WO_3$ thin layer for coloring process was not fully removed from the thin layer to the electrolyte during bleaching process. It was found that there is a limitation of applied overpotential for coloring process by the reduction of the current densities of bleaching and coloration after few number of coloring and bleaching cycles.

• Corrosion Science and Technology
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• v.14 no.1
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• pp.19-24
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• 2015

Flow Accelerated Corrosion (FAC) causes unexpected accidents in a secondary side of a nuclear power plant. The secondary side pipes are mainly carbon steel tubes that have a protective magnetite ($Fe_3O_4$) layer on the inner surface. The stability of the protective magnetite layer depends on the parameters related to the FAC phenomena such as pH, temperature, flow rate, surface roughness etc. The dissolution of magnetite is basically the electrochemical reaction, but the most of the experiments of magnetite dissolution were carried out thermodynamically to determine the solubility of magnetite. The knowledge of the electrochemical properties of magnetite is required to understand the dissolution process of magnetite. This paper reviews the manufacture of the magnetite ($Fe_3O_4$) electrode, and summaries the electrochemical properties of the magnetite.

• Proceedings of the Korean Society of Precision Engineering Conference
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• 2003.06a
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• pp.1844-1847
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• 2003

Electrochemical micro-machining(EMM) is used to achieve a desired workpiece surface by dissolving the metal workpiece with an electrochemical reaction. This machining method can be applied to metal that is difficult to machining using other methods. The workpiece dissolves when it is positioned close to the tool electrode in electrolyte and current is applied. This aim of this work is to develop electrochemical micro-machining(EMM) technique for micro groove shape by establishing appropriate electrochemical parameters of machining

• 전기의세계
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• v.12
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• pp.12-23
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• 1963

전력연구소 전식연구실에서는 상기 지구의 전식작용이 예상되는 10여개점에서 예비조사를 한 결과 상수도관이 전식작용을 받고 있음을 확인하고, 순화동지구의 상수도관의 전식작용 실태조사에 착수하게 되었다. 지중 매설금속체의 부식에는 누설전류에 의한것 외에도 전기화학작용에 의한것 화학반응에 의한것, 물리적 작용에 상반되는것 등이 있다. 누설전류에 의한 것은, 실제의 경우, 전철이 궤조로 부터의 누설전류는 전해질로서 볼 수 있는 토야을 매체로 하여, 이것보다 저항이 적은 매설금속체에 유입하여, 변전소 근처에서 이것으로부터 유출 귀류한다.

• Journal of the Korean Chemical Society
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• v.22 no.6
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• pp.423-430
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• 1978

The initiation mechanism of trioxane polymerization catalyzed by Ti$Cl_4$ in nitrobenzene was investigated. The kinetic studies revealed that the rate of polymerization was drastically decreased by the addition of a minute amount of water or methanol. A third substance as cocatalyst was not required for the polymerization. Measurements of dielectric constants gave no evidence for the zwitterionic mechanism of the polymerization. The electric conductivity measurements of polymerization system and the initiator solution showed that the initiation was started by Ti$Cl_3^+$ cation, formed by a disproportionation of the initiator in nitrobenzene.