• Bulletin of the Korean Chemical Society
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• 제31권8호
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• pp.2185-2189
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• 2010

Closely arranged CdSe and Zn doped CdSe vertical nanorod bundles were grown directly on FTO coated glass by using electrodeposition method. Structural analysis by XRD showed the hexagonal phase without any precipitates related to Zn. FE-SEM image showed end capped vertically aligned nanorods arranged closely. From the UV-vis transmittance spectra, band gap energy was found to vary between 1.94 and 1.98 eV due to the incorporation of Zn. Solar cell parameters were obtained by assembling photoelectrochemical cells using CdSe and CdSe:Zn photoanodes, Pt cathode and polysulfide (1M $Na_2S$ + 1M S + 1M NaOH) electrolyte. The efficiency was found to increase from 0.16 to 0.22 upon Zn doping. Electrochemical impedance spectra (EIS) indicate that the charge-transfer resistance on the FTO/CdSe/polysulfide interface was greater than on FTO/CdSe:Zn/polysulfide. Cyclic voltammetry results also indicate that the FTO/CdSe:Zn/polysulfide showed higher activity towards polysulfide redox reaction than that of FTO/CdSe/polysulfide.

• 한국환경과학회지
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• 제18권11호
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• pp.1235-1245
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• 2009

The purpose of this study is to investigate electro-generation of free Cl, $ClO_2$, $H_2O_2$ and $O_3$ and degradation of Rhodamine B in solution using Ru-Sn-Sb electrode. Electrolysis was performed in one-compartment reactor using a dimensionally stable anode(DSA) of Ru-Sn-Sb/Ti as the working electrode. The effect of applied current (0.5-3 A), electrolyte type (NaCl, KCl, HCl, $Na_2SO_4$ and $H_2SO_4$) and concentration (0.5-2.5 g/L), air flow rate (0-3 L/min) and solution pH (3-11) was evaluated. Experimental results showed that concentration of 4 oxidants was increased with increase of applied current, however optimum current for RhB degradation was 2 A. The generated oxidant concentration and RhB degradation of the of Cl type-electrolyte was higher than that of the sulfate type. The oxidant concentration was increased with increase of NaCl concentration and optimum NaCl dosage for RhB degradation was 1.75 g/L. Optimum air flow rate for the oxidants generation and RhB degradation was 2 L/min. $ClO_2$ and $H_2O_2$ generation was decreased with the increase of pH, whereas free Cl and $O_3$ was not affected by pH. RhB degradation was increase with the pH decrease.

• 대한화학회지
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• 제22권6호
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• pp.365-369
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• 1978

음극 환원상태에 있는 철과 양극산화로 부동상태에 있는 철의 표면에 대하여 반사율과 광학적(ellipsometry) 측정을 하였다. 환원상태와 부동상태에 있는 표면들 사이의 광학적 파라미터들 (${\Delta},\;{\psi}$ 및 반사율)의 차이를 측정하여 그로부터 부동상태에서 금속 표면을 덮고 있는 표면막의 두께와 광학적 상수들을 정할 수가 있었다. 포화 칼로멜전극에 대하여 -400mV에서 부동화된 표면의 산화막은 약 11${\AA}$의 두께와 ${\tilde{n}}$ = 2.8 - 0.8 i 의 광학상수를 갖고 있는 것으로 나타났다. 이로부터 부동상태의 표면막은 적지 않은 전자 전기전도성을 가지고 있음을 알 수 있다.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2008년도 제39회 하계학술대회
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• pp.1295-1296
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• 2008

Hydrogen peroxide ($H_2O_2$) biosensor is one of the most developing sensors because this kind of sensors is highly selective and responds quickly to the specific substrate. Hemoglobin (Hb) has been used as ideal biomolecules to construct hydrogen peroxide biosensors because of their high selectivity to $H_2O_2$. The direct electron transfer of Hb has widely investigated for application in the determination of $H_2O_2$ because of its simplicity, high selectivity and intrinsic sensitivity. An electrochemical detection for hydrogen peroxide was investigated based on immobilization of hemoglobin on DNA/Fe(pyterpy)$^{2+}$ modified gold electrode. The pyterpy monolayers were firstly an electron deposition onto the gold electrode surface of the quartz crystal microbalance (QCM). It is offered a template to attach negatively charged DNA. The fabrication process of the electrode was verified by quartz crystal analyzer (QCA). The experimental parameters such as pH, applied potential and amperometric response were evaluated and optimized. Under the optimized conditions, this sensor shows the linear response within the range between $3.0{\times}10^{-6}$ to $9.0{|times}10^{-4}$ M concentrations of $H_2O_2$. The detection limit was determined to be $9{\times}10^{-7}$ M (based on the S/N=3).

• Journal of Advanced Marine Engineering and Technology
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• 제24권5호
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• pp.58-68
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• 2000

When SS400 steel was welded with low hydrogen type and ilmennite type welding, the effect of post-weld heat treatment(PWHT) was investigated with parameters such as micro vickers hardness, corrosion potential, polarization behaviors, galvanic current, Al anode generating current and Al anode weight loss etc. Hardness of each parts(HAZ, BM, WM) by PWHT in case of low hydrogen type and ilmennite type welding was lower than that of each parts by As-welded However hardness of WM area in case of low hydrogen type and ilmennite type welding was the highest among those three parts regardless of PWHT, Whereas in case of ilmennite type welding, WM area was the highest potential among these three parts on galvanic potential series with As-welded while BM area was the highest potential among these three parts by PWHT on the contrary. And in case of low hydrogen type welding, galvanic corrosion and micro cell corrosion of welding parts was decreased with PWHT. However, It was increased with PWHT in case of ilmennite type welding. Moreover Al anode generating current and anode weight loss in case of low hydrogen type was decreased by PWHT compared to As-wedled but, which was increased than that of As-welded in case of ilmennite type welding. Therefore, it is suggested that Corrosion resistance property in case of low hydrogen type welding is increased by PWHT. However its property was devreased with PWHT in case of ilmennite type welding.

• 전기화학회지
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• 제6권1호
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• pp.23-27
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• 2003

본 연구는 휴대용 전원으로 사용 가능성이 높은 소형 직접메탄을 연료전지의 단위전지와 모노폴라 스택의 운전특성을 살펴본 것이다. 공기와 메탄올이 외부에서 강제로 공급되지 않는 수동형(passive)의 운전조건에서 최적 메탄을 농도는 4M이었으며, 촉매 담지량도 $8mg/cm^2$에서 가장 높은 성능을 나타내었다. 상온 상압 수동형 조건에서 얻은 최대 성능은 $55mW/cm^2$이었다. 6개의 단전지로 이루어진 모노폴라 스택에서는 셀간의 성능차이는 크게 나타나지 않았으며, 출력밀도는 $37mW/cm^2$이고, 1W의 출력을 보였다. 또한, 16셀로 구성된 2.4W급 모노폴라 스택을 제작하여 모형 자동차에 장착하고 시범 운전을 성공적으로 수행하였다.

• 전기화학회지
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• 제11권1호
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• pp.33-36
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• 2008

본 연구에서는 겔식 VRLA (valve regulated lead acid번지의 충전상태(SoC) 판단을 위해 임피던스 기법을 이용하여 조사하였다. 임피던스는 VRLA전지 (2V/1.2Ah)의 다양한 충전상태에서 진폭 10mV로 100kHz에서${\sim}$10mHz까지 측정하였다. 측정된 임피던스 데이터로부터 등가회로를 유도하고, CNLS (Complex Non-linear Least Squares) 법을 사용하여 분석하였다. 양극 쪽의 전하전이 저항과 전기이중층 커패시턴스가 음극보다 높았다. 겔 저항은 충전상태가 감소함에 따라 증가하며 이는 VRLA 전지의 충전상태를 판단하는데 중요한 파라미터임을 확인하였다.

• Journal of Electrochemical Science and Technology
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• 제7권3호
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• pp.190-198
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• 2016

Application of fuel cell to produce renewable energy for commercial purpose is limited by the high cost of Pt based electrode materials. Development of inexpensive, high energetic electrode is the need of the hour to produce pollution free energy using bio-fuel through a fuel cell. Ni-Cu and Ni-CeO₂-Cu electrode materials, electro synthesized by pulse current have been developed. The surface morphology of the electrode materials is controlled by different deposition parameters in order to produce a high current from the electro-oxidation of the fuel, the ethanol. The developed materials are electrochemically characterized by Cyclic Voltammetry (CV), Chronoamperometry (CA) and Potentiodynamic polarization tests. The results confirm that the high current is due to their enhanced catalytic properties viz. high exchange current density (i₀), low polarization resistance (R_p) and low impedance. It is worthwhile to mention here that the addition of CeO₂ to Ni-Cu has outperformed Pt as far as the high electro catalytic properties are concerned; the exchange current density is about eight times higher than the same on Pt surface. The morphology of the electrode surface examined by SEM and FESEM exhibits that the grains are narrow and sub spherical with 3D surface, containing vacancies in between the elongated grains. The fact has enhanced more surface area for electro oxidation of the fuel, giving rise to an increase in current. Presence of Ni, CeO₂, and Cu is confirmed by the XRD and EDXS. Fuel cell fabricated with Ni-CeO₂-Cu material electrode is expected to produce clean electrical energy at cheaper rates than conventional one, using bio fuel the derived from biomass.

• Bulletin of the Korean Chemical Society
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• 제29권5호
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• pp.974-978
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• 2008

Removal of heavy metal ions ($Cd^{2+}$ and $Zn^{2+}$) by electrocoagulation (ECG) was investigated in an acidic condition, which is necessary for re-using or discharging the mediated electrochemical oxidation (MEO) media. Effects of various parameters such as electrolytes, current densities, and electrode materials were examined for a metal-contaminated MEO system using $Fe^{2+}/Fe^{3+}$ pairs as a mediator. It was found that ECG with Al electrodes is greatly affected by the presence of $Fe^{2+}$. [$Cd^{2+}$] and [$Zn^{2+}$] remain constant until [$Fe^{2+}$] reaches a certain concentration level (ca. 10 mM). This preferential removal of $Fe^{2+}$ during ECG with Al electrodes is not alleviated by controlling current densities, potential programs, and solution mixing. ECG with Fe electrodes, on the other hand, resulted in relatively fast removal of $Cd^{2+}$ and $Zn^{2+}$ under coexistence of $Fe^{2+}$, indicative of the different role between $Fe^{n+}$ generated from an electrode and $Fe^{2+}$ initially present in a solution. When ECG was performed with Fe electrodes until [$Fe^{n+}$] became the same as the concentration of initially present $Fe^{2+}$, [$Cd^{2+}$] and [$Zn^{2+}$] were reduced to one-tenth of the initial concentrations, suggesting the possibility of a continuous use of the medium for a subsequent MEO process.

• Bulletin of the Korean Chemical Society
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• 제32권1호
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• pp.49-52
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• 2011

A dinuclear copper(II) complex of [$Cu_2(aceace)_4$(dipyph)] [aceace = acetylacetone, dipyph = 1,4-di(4-pyridylethene-2-yl-)benzene] has been synthesized and characterized by elemental analysis, IR and X-ray single crystal diffraction. It crystallizes in the monoclinic system, space group P21/c, with lattice parameters a = 7.9584(16) $\AA$, b = 18.594(4) $\AA$, c = 15.063(4) $\AA$ $\beta=120.97(2)^o$ and $M_r$ = 807.85 ($C_{40}H_{44}Cu_2N_2O_8$), Z = 2. Each of the $Cu^{2+}$ ion adopts a square pyramid geometry and coordinates with four oxygen atoms from two aceace ligands and one nitrogen atom from dipyph bidentate ligand. Magnetic measurement shows that the Weiss constant and Curie constant for the title compound are -0.22 K and 0.1154 emu K/mol, respectively. Thermal stability data indicate that the title complex undergoes two steps decomposition and the residue is $Cu_2O_4$. In the potential range of -1.5 ~ 0.8 V, the title complex represents an irreversible electrochemical process.