• Bulletin of the Korean Chemical Society
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• 제11권3호
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• pp.200-205
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• 1990

Chemically modified electrodes(CMEs), based on 2-imino-1-cyclopentane-dithiocarboxylic acid (icdc) containing carbon paste, have been characterized using cyclic voltammetric techniques. Ag(I) was chemically deposited on the CMEs, and voltammograms were obtained with the electrode in a separate buffer solution. The CME surface can be regenerated with exposure to acid and reused for deposition. In 10 deposition/measurement/regenerate cycles, the linear response have been reproduced up to $1{\times}10^{-6}$ M in linear sweep voltammetry and 1${\times}$10-8 M in differential pulse voltammetry with relative standard deviation of 5.2% and 12.4%, respectiveiy. The sensitivity increased with deposition time and scanning rate, and detection limit was $1{\times}10^{-7}M\;and\;1{\times}10^{-9}M$ at 20 minutes deposition in the linear sweep voltammetry and differential pulse voltammetry, respectively. The presence of some metal ions does not influence the silver ion response. Satisfactory results were obtained for the analysis of the silver ion for a variety of reference materials without interference of Hg ion at the condition of pH = 5-6.

• 분석과학
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• 제19권1호
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• pp.58-64
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• 2006

탄소반죽에 쑥조직을 혼입시켜 과산화수소 정량 바이오센서를 제작하고 그것의 전기화학적 성질을 조사하였다. 다른 생체조직을 이용하여 제작한 센서와 비교할 때, 생촉매 안정성이 뛰어났으며, 보다 큰 감응신호를 보여주었다. 조직의 함량 변화에 따른 신호의 변화는 넓은 범위에 걸쳐 직선성을 보여 주었고, Lineweaver-Burk 도시의 직선성은 전극 감응이 효소 촉매작용에 의하여 조절되고 있음을 보였다. 또 감응전류의 pH 의존성 변화는 센서가 두 종류의 동위효소를 포함하고 있음을 암시하였다.

• 마이크로전자및패키징학회지
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• 제29권4호
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• pp.35-40
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• 2022

본 연구에서는 실버 파우더의 입자 크기, 즉 평균입자 크기가 2㎛, 7㎛, 이들의 혼합(50:50wt%), 이렇게 3가지 실버 페이스트를 제조하여 점도 및 점탄성, 경화후에 잔류용제 유무 확인을 위한 TGA측정, Strain에 따른 저항변화 및 전극 표면구조 변화에 대해서 검토한 결과 다음과 같은 결론을 얻을 수 있었다. 이러한 결과를 정리하면 Strain에 따른 저항변화를 최소화하기 위해서는 실버 파우더의 입자를 2㎛정도인 것이 가장 바람직함을 알 수 있었다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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• pp.75.1-75.1
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• 2010

Dye sensitized solar cells(DSSCs) have been extensively studied due to their various advantages such as low production cost, colorful design, and eco-friendly process. Long optical path length is one of the most effective method to improve light harvest efficiency for DSSCs. Multi-layered $TiO_2$ nano-structured film with scattering layer has been studied to generate scattering effect by many researchers. It was expected that the difference of refractive index between $TiO_2$ particles and glass frit would generate the light scattering effect and provide the long optical path length. Therefore, to enhance the scattering effect, the frits of $Bi_2O_3-B_2O_3$-ZnO glass system that has the different refractive index were added to $TiO_2$ pastes in this study. First of all, the absorbance and haze factor of $TiO_2$ electrode with dyes and the refractive index of glass frit and $TiO_2$ were measured, respectively. To study the effect of frits, the efficiencies of DSSCs added glass frit and without glass frit were compared. Our results showed slightly higher efficiency with the different absorbance and haze factor of $TiO_2$ and glass frit. It was considered that the light scattering effect would be improved with adding frits to $TiO_2$ paste. Our preliminary studies will be useful for increasing efficiency of DSSCs.

• 전기화학회지
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• 제8권1호
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• pp.6-11
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• 2005

직접보로하이드라이드 연료전지는(direct borohydrides fuel cell. DBFC) 직접메탄을 연료전지가 갖는 메탄을 크로스오버(crossover)문제를 해결할 수 있어서, 휴대용 및 이동용 전원으로 활용하기 위하여 새롭게 대두되고있는 연료전지이다. 본 논문에서는 직접보로하이드라이드 연료전지의 전극제조 공정 확립을 위하여 여러 가지의 연료극 및 공기극 촉매를 선정하고 열가압법 (hot pressing)으로 전극을 제조하여 이에 대한 성능 특성을 고찰하였다. 공기극 촉매로는 Pt/C와 Pt black을 사용하였고, 연료극 촉매로는 Pt/C. Pt black, Au/C, $AB_5$ alloy를 사용하였다 제조된 전극 촉매는 XRD, SEM, EDS 등을 통한 특성 분석과 단위전지 운전을 통하여 I-V특성 분석이 이루어졌다. 다양한 촉매 조합을 통하여 촉매별 단전지 테스트를 한 결과 공기극 및 연료극 촉매를 Pt/C로 했을 때 가장 높은 성능인 366mW/mg을 얻을 수 있었다.

• 대한화학회지
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• 제57권3호
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• pp.329-334
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• 2013

솔잎조직과 ferrocene을 각각 효소원 및 매개체로, CSM 고무를 흑연가루 결합재로 사용하여 전류법 과산화수소 정량 효소전극을 제작하고, 그것의 특성을 전기화학적인 방법으로 관찰하였다. 낮은 퍼텐샬 영역(-100 ~ -500 mV)에서 보여준 ln($i(1-e^{nf{\eta}})$) vs. ${\eta}$ 및 Lineweaver-Burk 도시의 좋은 직선성은 신호전류의 생성이 효소의 촉매작용에 의한 것임을 확인하여 주었다. 이 때 얻어진 대칭인자(${\alpha}$, 0.17), 한계전류($i_1$, 1.99 $A/cm^2$), 교환전류밀도($i_0$, $5.86{\times}10^{-5}\;A/cm^2$), 마이클 상수($K_M$, $1.68{\times}10^{-3}$ M) 및 기타 전극 파라메터들은 전극 표면에서 소나무 과산화효소가 정량적으로 성능을 발휘하고 있음을 보여 주었다. 이런 실험적 사실들은 솔잎조직이 상업용 과산화효소를 대치하여 실용 효소전극 제작에 사용될 수 있음을 보여 주었다.

• Journal of Electrochemical Science and Technology
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• 제12권2호
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• pp.173-187
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• 2021

In the present research, a simple electrochemical sensor based on a carbon paste electrode (CPE) modified with ZnO-Zn₂SnO₄-SnO₂ and graphene (ZnO-Zn₂SnO₄-SnO₂/Gr/CPE) was developed for the direct, simultaneous and individual electrochemical measurement of Acetaminophen (AC), Caffeine (Caf) and Ascorbic acid (AA). The synthesized nano-materials were investigated using scanning electron microscopy, X-ray Diffraction, Fourier-transform infrared spectroscopy, and electrochemical impedance spectroscopy techniques. Cyclic voltammetry and differential pulse voltammetry were applied for electrochemical investigation ZnO-Zn₂SnO₄-SnO₂/Gr/CPE, and the impact of scan rate and the concentration of H⁺ on the electrode's responses were investigated. The voltammograms showed a linear relationship between the response of the electrode for individual oxidation of AA, AC and, Caf in the range of 0.021-120, 0.018-85.3, and 0.02-97.51 μM with the detection limit of 8.94, 6.66 and 7.09 nM (S/N = 3), respectively. Also, the amperometric technique was applied for the measuring of the target molecules in the range of 0.013-16, 0.008-12 and, 0.01-14 μM for AA, AC and, Caf with the detection limit of 6.28, 3.64 and 3.85 nM, respectively. Besides, the ZnO-Zn₂SnO₄-SnO₂/Gr/CPE shows an excellent selectivity, stability, repeatability, and reproducibility for the determination of AA, AC and, Caf. Finally, the proposed sensor was successfully used to show the amount of AA, AC and, Caf in urine, blood serum samples with recoveries ranging between 95.8% and 104.06%.

• Bulletin of the Korean Chemical Society
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• 제33권8호
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• pp.2613-2618
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• 2012

Hydrothermal route have been used in different conditions for preparation of $Ni(OH)_2$ nanostructures. The NiO nanoparticles were obtained by calcining the $Ni(OH)_2$ precursor at $450^{\circ}C$ for 2 h. The effect of sodium dodecyl sulfonate (SDS) as surfactant on the morphology and size of $Ni(OH)_2$ nanoparticles were discussed in detail. X-ray diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM) and Fourier transform infrared (FT-IR) spectroscopy were used to characterize the products. The growth mechanism of the as-synthesized nanostructures was also discussed in detail based on the experimental results. Coming up, the NiO nanoparticle modified carbon paste electrode was applied to the determination of captopril in aqueous solution.

• Bulletin of the Korean Chemical Society
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• 제27권10호
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• pp.1613-1617
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• 2006

Optimum analytical conditions for cyclic voltammetry (CV) and square wave (SW) stripping voltammetry were determined using mercury-mixed carbon nanotube paste electrode (PE). The results approached the microgram working ranges of SW: 10.0-80.0 $ugL^{-1}$ and CV: 100-700 $ugL^{-1}$ Cd (II); working conditions of 300-Hz frequency, 100 mV amplitude, 1.6 V accumulation potential, 400 sec accumulation time, and 40 mV increment potential. First, analysis was performed through direct assay of cadmium ions deep into the fishs brain core and plant tissue in real time with a preconcentration time of 400 sec. The relative standard deviation of 10.0 $mgL^{-1}$ Cd (II) observed was 0.064 (n = 12) at optimum conditions. The low detection limit (S/N) was set at 0.6 $ugL^{-1}$ ($5.33{\times}10^{-9}$ M). The methods can be used in direct analysis in vivo or in real-time monitoring of plant tissue.

• 한국응용과학기술학회지
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• 제29권3호
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• pp.443-449
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• 2012

A investigation of electrochemical analysis of antibiotics Neomycin ($C_{23}H_{46}N_6O_{13}$) was searched using electrochemical square wave (SW) stripping and cyclic voltammetry (CV) using working sensor of the modified carbon nanotube combination electrodes, optimum diagnostic parameters were searched by anodic stripping, final conditions were attained to working range of 1.0-14.0 ng/L, detection limit (S/N) was found to be 0.6 ng/L. The developed method was discovered to be fitting in quality control in the food, pharmaceutical and other manufacturing sectors.