• Journal of the Korean Chemical Society
• /
• v.66 no.6
• /
• pp.436-441
• /
• 2022

Because the nanoporous electrodes has large electrochemical surface areas, extensive studies have been focused on their fabrication methods. In this paper, a method for introducing a nanoporous gold (NPG) structure on the surface of an ultramicroelectrode (UME) using potentiostatic anodization was investigated. A well-defined NPG structure was introduced on the surface of the UME when a potential of 1.3 V was applied in 0.1 M phosphate buffer solution (pH 8) containing 1 M KCl. The anodic oxidation efficiency was investigated by observing the effect of the applied potential, the reaction time, and the size of the electrode on the roughness factor (R_f) of the prepared NPG-UMEs. In a short time of about 10 minutes, NPG-UME with a large R_f value of about 2000 could be prepared, which could be effectively used for electrochemical glucose detection. The results shown in this work are expected to have great applicability when performing electrochemical analysis with a small sample volume.

• Journal of the Microelectronics and Packaging Society
• /
• v.25 no.4
• /
• pp.105-109
• /
• 2018

We studied graphene synthesis to porous Cu to improve the characteristics of carbon dioxide reduction of cu. Cu powders were formed through Thermal Chemical Vapor Deposition(TCVD) to Porous Cu/Graphene structures synthesized with graphene. As a result of electrochemical experiments using a 0.1 M $KHCO_3$ electrolyte at an applied potential of -1.0 V to -1.4 V, the current density of Porous Cu/Graphene was 1.8 times higher than that of Porous Cu. As a result of evaluating the product, CO and $H_2$ were generated to Porous Cu electrode. On the other hand, the product of porous Cu/Graphene produced CO, $CH_4$ and $C_2H_4$. It is considered that the graphene causes longer carbon dioxide adsorption time, which means that the intermediates formed during the reaction remain on the electrode surface for a longer time. As a result, it can be concluded that the production reaction of the C2 compound could be continuously performed.

• Journal of the Korean Electrochemical Society
• /
• v.7 no.2
• /
• pp.100-107
• /
• 2004

The nano or micro sized structures of conducting polymer had been prepared by synthesizing the desired polymer within the pores of template of nano or micro porous membrane filter. In this study, we had tried to fabricate conducting polymer microstructures on an electrode by using electrochemical deposition adopting template synthesis. Our attention was focused on two different things, attaching template on the electrode and fabricating microstructures only at limited areas of the electrode. A conducting polymer, PEDiTT (poly 3,4-ethylenedithi-athiophene) solution was blended with PVA(polyvinyl alcohol) solution and used as an conducting adhesive. After attaching template membrane, the electrode were immersed in 0.5M pyrrole in 0.1M KCI solution, and electrochemical polymerization was performed. The growth process of the microstructures studied by SEM. The electrochemical fabrication of conducting polymer was performed by using two-electrode system. A large working electrode and a micro scale disc electrode were used for the confined area synthesis. Polymerization potential was 4V in an electrolytic solution made of KCI in deionized water. The optimum polymerization conditions were, i.e. (4V/100sec) for $250{\mu}m$ electrode and (6V/30 sec) for $10{\mu}m$ electrode.

• Journal of Energy Engineering
• /
• v.2 no.2
• /
• pp.187-193
• /
• 1993

Porous matrices to contain and support phosphoric acid were prepared with PTFE as binder and SiC whisker or SiC powders of various particle size for phosphoric acid fuel cell(PAFC). Among the matrix characteristics the most important factors in stack performances were thought to be the bubble pressure and electrolyte wettability And then matrix was constructed to have pore size smaller than that of electrode. The bubble pressures and wettabilities of matrices manufactured with various size of SiC and different PTFE contents were investigated and related with the porosities measured by porosimeter, and then the optimum manufacturing condition of matrix for PAFC was determined.

• Proceedings of the Korean Institute of Surface Engineering Conference
• /
• 2018.06a
• /
• pp.28-28
• /
• 2018

수전해(electrochemical water splitting)는 연료전지의 가역적 역반응을 이용하여 물로부터 수소와 산소를 발생시키는 기술이다. 산소는 음극에서 발생하는데, 이 때 음극 표면은 고농도의 산소 음이온 및 라디칼에 장시간 노출된다. 때문에 기계적, 화학적 내구성이 우수한 전극재를 사용할 필요가 있다. 불용성 전극 (dimensionally stable anode, DSA)은 이러한 기술적 요구사항을 잘 만족하는 상용화 된 전극이다. 티타늄이나 티타늄 합금 표면에 촉매를 미량 반복 살포하여 산화물 형태의 매우 견고한 표면을 형성함으로서 내구성을 확보한다. 그러나, 보통 DSA 제조 기법의 특징에 따라 다공성 표면 구조를 사용하지는 않기 때문에 생산 과정이 복잡하고 비용이 많이 발생하는 문제를 여전히 나타내고 있다. 본 연구는 상기 문제를 개선하기 위한 수전해용 음극 제조 기술에 관한 연구이다. 티타늄과 티타늄 합금은 동일한 양극산화 기술 적용이 가능하다는 점을 이용하여 티타늄 기판으로부터 다공성 구조를 형성함으로써 바인더의 사용을 배제하였다. 단일공정양극산화기법 (single-step anodization)을 이용하여 $IrO_2$와 $RuO_2$를 도핑함으로써 TiO2에 촉매능을 부여하였다. 제조된 나노튜브들의 구조적 특징을 HR-TEM (High-resolution transmission electron microscope)과 FE-SEM (Field-emission scanning electron microscope)으로 분석하고 SAED (selective area electron diffraction) 패턴을 분석하여 전극재의 결정성을 확인하였다. 알칼라인 분위기에서 일으킨 산소발생반응 (oxygen evolution reaction, OER)의 LSV (linear sweep voltammetry) 결과를 XPS (X-ray photoelectron microscoscopy) 결과와 연관지어 촉매 표면 구조와 과전압의 관계를 해석하였다. LSV 결과로부터 Tafel 분석을 연달아 수행함으로써 전극의 속도결정단계를 정의하였다. 최종적으로 사이클 테스트 통하여 DSA로써의 성능을 평가하였다.

• 한국전기화학회:학술대회논문집
• /
• 2001.04a
• /
• pp.9-9
• /
• 2001

• 한국전기화학회:학술대회논문집
• /
• 2003.10a
• /
• pp.55-55
• /
• 2003

• Proceedings of the Korean Radioactive Waste Society Conference
• /
• 2004.06a
• /
• pp.352-352
• /
• 2004

산화물 형태의 사용후핵연료를 고온 용융염계에서 금속 형태로 전환하는 전기화학적 금속전환 공정 개발의 일환으로 $U_3O_8$ 분말로 충전된 다공성 마그네시아 용기 및 스테인레스강 고체전극으로 구성된 일체형 음극과 $SnO_2$ 재질의 양극을 사용하여 5kg $U_3O_8$/batch 규모의 mock-up 시험을 수행하였다. 백금 재질의 양극을 사용하였을 때 99% 이상의 금속전환율을 보인 동일한 전하량을 공급하고 실험을 중단한 결과 X-선 회절분석(XRD) 및 열중량 분석(TG)으로부터 스테인레스강 고체전극 부분에서는 거의 금속으로 전환되었으나 다공성 마그네시아 용기 부분에서는 비교적 금속전환율이 낮은 경향을 나타내었다.(중략)

• Applied Chemistry for Engineering
• /
• v.29 no.6
• /
• pp.759-764
• /
• 2018

3D porous carbon electrodes (cNPIM), prepared by solution casting of a polymer of intrinsic microporosity (PIM-1) followed by nonsolvent-induced phase separation (NIPS) and carbonization are presented. In order to effectively control the pore size of 3D porous carbon structures, cNPIM was prepared by varying the THF ratio of mixed solvents. The SEM analysis revealed that cNPIMs have a unique 3D macroporous structure having a gradient pore structure, which is expected to grant a smooth and easy ion transfer capability as an electrode material. In addition, the cNPIMs presented a very large specific surface area ($2,101.1m^2/g$) with a narrow micropore size distribution (0.75 nm). Consequently, the cNPIM exhibits a high specific capacitance (304.8 F/g) and superior rate capability of 77% in an aqueous electrolyte. We believe that our approach can provide a variety of new 3D porous carbon materials for the application to an electrochemical energy storage.

• 한국전기화학회:학술대회논문집
• /
• 2002.07a
• /
• pp.227-232
• /
• 2002