• 한국신재생에너지학회:학술대회논문집
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• 2009.06a
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• pp.403-405
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• 2009

RF-스퍼터링법을 사용하여 메탄올 산화반응을 위해 박막형 전극을 제조하였다. 전극은 텅스텐 탄화물(WC)과 텅스텐 산화물($WO_3$), 그리고 백금(Pt) 타겟을 이용하였으며 그 구조적 특성과 전기화학적 특성을 TEM(Transmission electron microscopy와 CV(Cyclic Voltametry)를 통하여 촉매적 활성을 측정해 보았다. 같은 양의 백금과의 활성을 비교하고 활성을 확인하였다.

• Korean Chemical Engineering Research
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• v.46 no.4
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• pp.727-731
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• 2008

Mesoporous Pt-Au alloy films were successfully fabricated on ITO-coated glass by electrodeposition method using tri-blockcopolymer (P123) as a templating agent. The electrolyte consisted of 10 mM hydrogen hexachloroplatinate ($H_2PtCl_6$), 10 mM hydrogen tetrachloroaurate ($HAuCl_4$), and proper amount of P123. For comparison, control samples were electrodeposited without $HAuCl_4$ and P123. Film composition was determined by EDS(Energy Dispersive X-ray Spectroscopy), and the mesoporous structure was confirmed by TEM(Transmission Electron Microscopy). SEM(Scanning Electron Microscopy) was utilized to examine surface morphology, and it was observed that the addition of P123 affected the particle growth, resulting in the significant change of surface morphology. Methanol oxidation and CO oxidation were carried out to investigate electrocatalytic activities of synthesized samples. It was observed that the catalytic activity was strongly dependent on the film compositions. Compared with nonporous electrode prepared without P123 templating, mesoporous films prepared with P123 templating showed much higher catalytic activities and stability for both methanol oxidation and CO oxidation. These enhanced electrocatalytic activities were due to the high surface area and facilitated charge transfer of mesoporous films.

• Proceedings of the Korean Vacuum Society Conference
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• 2016.02a
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• pp.411.2-411.2
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• 2016

직접 메탄올 연료전지 (DMFCs)는 친환경적이고 낮은 작동 온도로 인한 빠른 구동, 높은 에너지 밀도 등 다양한 장점을 가지고 있어 차세대 에너지 변환소자로 많은 관심을 받고 있다. 직접 메탄올 연료전지는 메탄올을 연료로 사용하며, 메탄올이 보유하고 있는 화학적 에너지를 전기 에너지로 변환하는 장치로써 음극에서는 백금 촉매로 인한 메탄올 산화반응, 양극에서는 환원 반응이 일어나며 전기화학적 구동을 하게 된다. 하지만 일산화탄소 피독으로 인한 촉매 활성 저하, 메탄올의 cross over, 백금 촉매 사용으로 인한 고비용 등의 문제점을 가지고 있다. 따라서 많은 연구자들이 백금 사용량을 줄이고 백금 촉매를 고르게 분포하기 위해 값이 저렴하고 넓은 비표면적을 갖는 탄소계 (graphite, graphene, carbon nanotube, carbon nanofiber 등) 지지체 재료를 도입하고 있다. 이 중 탄소나노섬유 (carbon nanofibers, CNFs)는 우수한 전기전도도와 열적/화학적 안정성을 가지고 있으며, 특히 넓은 비표면적을 가지고 있어 백금 촉매의 지지체로서 많은 연구가 진행되고 있다[1]. 따라서 우리는 전기방사법을 활용하여 넓은 비표면적을 보유하는 다공성 탄소나노섬유를 성공적으로 합성하였다. 또한, 이를 백금 촉매의 지지체로 도입하여 직접 메탄올 연료전지를 위한 다공성 탄소나노섬유에 담지된 고분산성 백금 촉매를 제조하였다. 제조한 다공성 탄소나노섬유의 형상 및 구조 분석은 주사전자 현미경 (field-emission scanning electron microscopy)와 투과전자 현미경 (transmission electron microscopy)를 이용하여 분석하였고, 결정구조와 화학적 결합상태는 X-선 회절분석 (X-ray diffraction) 및 X-선 광전자 분광법 (X-ray photoelectron spectroscopy)를 이용하여 규명하였다. 전기화학적 특성은 순환 전압 전류법 (cyclic voltammetry)를 이용하였다. 이러한 실험 결과들을 바탕으로 다공성 탄소나노섬유에 담지된 고분산성 백금 촉매의 자세한 특성을 본 학회에서 다루도록 하겠다.

• Applied Chemistry for Engineering
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• v.22 no.5
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• pp.545-550
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• 2011

We have synthesized a high electrically conductive 4-(2-(4-(acetylthio)phenyl)ethynyl)benzoic acid (APBA) with a conjugated aromatic structure as a bio fix linker, and then fabricated APBA self-assembled monolayer (SAM) with a self-assembly technique. The structure of the prepared APBA SAM was studied and electrochemical properties of APBA SAM immobilized with a ferrocene molecule were investigated. Also, we have examined the molecular orientation and oxidation-reduction redox characteristics of the mixed SAM consisting of APBA and butanethiol (BT) with a X-ray photo electron spectroscopy (XPS) and cyclicvoltammetry, respectively. Electrochemical activity of the mixed SAM was increased with increasing the mixed time. Especially, the maximum redox current was obtained at a mixed time of 36 hrs.

• Proceedings of the KAIS Fall Conference
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• 2002.05a
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• pp.166-169
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• 2002

본 연구는 콘크리트 배합시 염분의 함량이 구조물의 부식에 미치는 영향을 조사하기 위하여 수행되었다. 콘크리트는 물 : 포틀랜트 cemente : 자갈 : 모래의 비율을 1 : 1.78 : 5.35 : 4.73의 비율로 하여 배합하였으며 염분의 함량은 0-3.5wt%의 범위에서 철근의 부식을 연구하였다. 부식특성을 연구하기 위하여 부식전위를 2년간 측정하였으며 이를 콘크리트 파괴 후의 철근의 외관 부식도와 비교하였다. 옥내와 옥외에 두었을 때 부식속도의 차이는 없었으며 염분의 함량이 증가함에 따라 활성이 큰 전위값이 측정되었다. 전위값이 낮은 시편은 부동태 피막이 파괴되어 부식이 진행하고 있었으며, 전위값이 높은 시편에서는 부식생성물이 관찰되지 않았다. 본 실험의 결과로 보강용 강재의 부식손상 정도를 자연전위 측정방법을 통하여 콘크리트내 보강용 철근의 부식거동 및 부식속도에 대한 비괴적인 전기화학적 기술로서 구조물의 손상여부를 확인할 수 있었다.

• Journal of the Korean Electrochemical Society
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• v.18 no.3
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• pp.115-120
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• 2015

The mechanical and electrochemical properties of poly(ethylene oxide) (PEO)-coated Rayon separator were characterized using potassium polyacrylate (PAAK)-KOH electrolyte. The supercapacitive properties of activated carbon supercapacitor adopting the Rayon/PEO separator and PAAK-KOH electrolyte was also tested. As the PEO content increased, the mechanical strength increased. Room-temperature ionic conductivity of over $10^{-2}S\;cm^{-1}$ was obtained at the PEO content lower than 5 wt.%, applicable to a supercapacitor. As a result, the specific capacitance at $1000mV\;s^{-1}$ of the activated carbon supercapacitor adopting the Rayon/PEO separator and PAAK-KOH electrolyte was highly stable after 1000th cycle. This was due to high rate-capability provided by the fact that PEO coating could fix the entanglements among fiber filaments of Rayon.

• Journal of the Korean Electrochemical Society
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• v.18 no.3
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• pp.107-114
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• 2015

Electrochemical fabrication of nanostructured Au surfaces has received increased attention. In the present work, electrochemical modification of Au surfaces for fabricating nanostructured Au surfaces in the absence of externally added precursors is presented, which is different to the previous methods utilizing electrochemical deposition of externally added precursors. Application of anodic potential at Au surfaces in phosphate buffers containing $Br^-$ resulted in the anodic dissolution of Au, which produced Au precursors at the electrode surfaces. The resulting Au precursors were further reduced at the surface to produce nanostructured Au structures. The effects of applied potential and time on the morphology of Au nanostructures were systematically examined, from which a unique backbone type Au nanostructures was produced. The backbone type Au nanostructures exhibited high surface-enhanced Raman activity. The present work would give insights into the formation of electrochemical fabrication of nanostructured Au surfaces.

• Korean Chemical Engineering Research
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• v.55 no.5
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• pp.593-599
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• 2017

In order to enhance ultra battery performances, the electrochemical characteristics of nano Pb/AC anode composite was investigated. Through nano Pb adsorption onto activated carbon, nano Pb/AC was synthesized and it was washed under vacuum process. The prepared anode materials was analysed by SEM, BET and EDS. The specific surface area and average pore size of nano Pb/AC composite were $1740m^2/g$ and 1.95 nm, respectively. The negative electrode of ultra battery was prepared by nano Pb/AC dip coating on lead plate. The electrochemical performances of ultra battery were studied using $PbO_2$ (the positive electrode) and prepared nano Pb/AC composite (the negative electrode) pair. Also the electrochemical behaviors of ultra battery were investigated by charge/discharge, cyclic voltammetry, impedance and rate capability tests in 5 M $H_2SO_4$ electrolyte. The initial capacity and cycling performance of the present nano Pb/AC ultra battery were improved with respect to the lead battery and the AC-coated lead battery. These experimental results indicate that the proper addition of nano Pb/AC into the negative electrode can improve the discharge capacity and the long term cycle stability and remarkably suppress the hydrogen evolution reaction on the negative electrode.

• Journal of the Korean Electrochemical Society
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• v.22 no.1
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• pp.13-21
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• 2019

Prussian blue analogues(PBAs) are comprised of cyano-bridged transition metal ions. The wide and unique open-framework structures of the PBAs enable reversible intercalation and deintercalation of various ions such as $Na^+$, $K^+$, $Mg^{2+}$, $Zn^{2+}$, etc. In addition, since PBAs are synthesized through coprecipitation reaction in aqueous solution at room temperature, they are produced economically and environmentally friendly. However, the formation of crystals proceeds rapidly, and defects such as vacancy and crystal water tend to be present in the crystals, thereby affecting key battery performance. Therefore, significant efforts to inhibit defects in PBAs have been made. In the case of vacancy, the reaction rate was controlled at the synthesis stage to reduce the formation of vacancy, and the crystal water was removed by heat treatment under vacuum. In addition, by adding transition metals that do not react within the structure of PBA, the structural instability during the electrochemical reaction was largely alleviated.

• Korean Chemical Engineering Research
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• v.43 no.6
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• pp.756-760
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• 2005

In this study, the effect of $N_2$-plasma treatment on carbon blacks (CBs) was investigated by analyzing acid-base surface values and surface functional groups of CBs. The surface characteristics of the CBs were determined by fourier transformed-infrared (FT-IR) spectrometer, X-ray photoelectron spectroscopy (XPS), and Boehm's titration method. Electrochemical properties of the plasma-treated CBs-supported Pt (Pt/CBs) catalysts were analyzed by cyclic voltammetry (CV) experiments. From the results of FT-IR and acid-base values, $N_2$-plasma treatment at 300 W intensity on the CBs led to the formation of the free radical. The peak intensity was increased with increasing the treatment time due to the formation of new basic functional groups(such as C-N, C=N, $-NH_3{^+}$, -NH, and =NH) by the free radical. Accordingly, the basic values were increased by the basic functional groups. However, after a specific reaction time, $N_2$-plasma treatment could hardly influence change of surface functional groups of CBs, due to the disappearance of free radical. Consequently, it was found that optimal treatment time was 30 second for electro activity of Pt/CBs catalysts.