• 제목/요약/키워드: Catalytic electrode

검색결과 191건 처리시간 0.028초

Catalytic Effects of Heteroatom-doped Graphene Nanosheets on the Performance of Li-O2 Batteries

  • Bae, Youngjoon;Lim, Hee-Dae;Yun, Young Soo;Kang, Kisuk
    • Journal of Electrochemical Science and Technology
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    • 제5권2호
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    • pp.49-52
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    • 2014
  • Graphene nanosheets (GNS), nitrogen-doped graphene nanosheets (N-GNS), and sulfur-doped graphene nanosheets (S-GNS) were successfully synthesized, and their catalytic effects on the oxygen reduction reaction (ORR) in $Li-O_2$ batteries were compared. The S-GNS electrode exhibited the highest ORR catalytic activity, resulting in enhanced discharge capacity and power capability. We attributed the enhanced ORR catalytic activity to the increased defect sites on graphene.

고무 결합재를 이용한 식물조직 바이오센서의 간편한 제작과 응용성 (A rapid and easy fabrication of plant-tissue biosensor using rubber binder and its practicability test)

  • 이범규;류근배;윤길중
    • 분석과학
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    • 제22권5호
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    • pp.355-359
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    • 2009
  • An enzyme electrode bound by rubber solution was newly constructed and the test of its practicability were carried out. The binder of carbon powder was styrene-butadiene rubber dissolved in toluene and enzyme source was ground tissue of cabbage root. Volatilization of the solvent made the electrode material possess a mechanical robustness and a fast signal appearance. The electrode showed electrochemically irreversible characteristics and a powerful catalytic power (detection limit=$5.0{\times}10^{-5}M$, S/N=2). The double reciprocal plot of signal current and substrate concentration was ideally linear and the symmetry factor and exchange current density of the electrode used in this work were 0.35 and $4.93{\times}10^{-5}Acm^{-2}$ respectively.

염료 감응형 태양전지 효율에 미치는 백금 상대 전극 제조공정의 영향 (Effects of Deposition Method of Thermally Decomposed Platinum Counter Electrodes on the Performance of Dye-Sensitized Solar Cells)

  • 서현우;백현덕;김동민
    • 한국수소및신에너지학회논문집
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    • 제28권1호
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    • pp.63-69
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    • 2017
  • In this work, two different platinum (Pt) counter electrodes have been prepared by spin coating a Pt solution and screen printing a Pt paste on fluorine doped tin oxide (FTO) glass substrate followed by sintering at $380^{\circ}C$ for 30 min. Linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS) analyses of the Pt electrodes showed that the spin coated electrode was catalytically more active than the screen printed electrode. The above result agrees well with the surface morphology of the electrodes studied by atomic force microscopy (AFM) and the photovoltaic performance of the dye-sensitized solar cells (DSSCs) fabricated with the Pt electrodes. Moreover, calculation of current density-voltage (j-V) curves according to diode model with the parameters obtained from the experimental j-V curves and the EIS data of the DSSCs provided a quantitative insight about how the catalytic activity of the counter electrodes affected the photovoltaic performance of the cells. Even though the experimental situations involved in this work are trivial, the method of analyses outlined here gives a strong insight about how the catalytic activity of a counter electrode affects the photovoltaic performance of a DSSC. This work, also, demonstrates how the photovoltaic performance of DSSCs can be improved by tuning the performance of counter electrode materials.

CO 가스 산화를 위한 백금/다공성 골드 전극의 개발 (Preparation of Pt/porous Gold Electrode for CO Oxidation)

  • 신소향;김휘로;오천석;고재욱;김영훈
    • 한국가스학회지
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    • 제15권4호
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    • pp.27-32
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    • 2011
  • 가스 설비의 증가와 함께 가스 사용시 안전관리가 중요해 지고 있다. 그 일환으로 국가적인 차원에서 U-safety 시스템 도입이 추진되고 있으며, 이를 위해서는 실시간으로 현장에서 가스 누출에 대한 검지가 가능해야 한다. 탄화수소류로 주로 구성된 가스의 누출 감지는 열저항을 이용하는 방식이지만, 도관에 함께 매설될 시에는 폭발 가능성으로 인해 적용이 불가하다. 이에 상온에서 메탄이나 일산화탄소와 같은 탄화수소류를 전기화학적 촉매 반응으로 검지할 수 있는 방법이 필요하다. 본 연구에서는 다공성 골드 분말을 팰렛 형태로 제조하여 백금 나노입자를 전해 도금법으로 도핑하여, CO의 $CO_2$ 산화 반응을 유도할 수 있는 촉매 전극을 제조하였다. Pt/PAu 전극의 경우, 약 21%의 CO 전환률을 보여서 탄화수소류의 상온 촉매전환과 함께 전기화학적 센싱이 가능함을 보였다. 이는 추후 메탄 가스 검지에 적용할 수 있는 여지를 마련했다고 판단된다.

염료감응형 태양전지용 나노두께 Pt와 Ru 상대전극의 물성 (Property of Counter Electrode with Pt and Ru Catalyst Films for Dye-Sensitized Solar Cell)

  • 노윤영;유병관;유기천;고민재;송오성
    • 대한금속재료학회지
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    • 제50권3호
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    • pp.243-247
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    • 2012
  • A ruthenium (Ru) catalytic layer and a conventional Pt layer were assessed as counter electrodes (CE) for dye sensitized solar cells (DSSCs). Ru films with different thicknesses of 34, 46, and 90 nm were deposited by atomic layer deposition (ALD). Pt layers with the same thicknesses were prepared by sputtering. $0.45cm^2$ DSSCs were prepared and their properties were characterized by FE-SEM, cyclic voltammetry (CV), impedance spectroscopy (EIS), and current-voltage (I-V). FE-SEM revealed that the crystallized Ru films and Pt films had been deposited quite conformally. CV showed that the catalytic activity of Pt was much greater than that of Ru. In addition, although the catalytic activity of Pt did not depend on the thickness, that of Ru showed an increase with increasing thickness. Impedance analysis revealed high charge transfer resistance at the Ru interface and a decrease with increasing Ru thickness, whereas Pt showed low resistance with no thickness dependence. Despite the relatively small catalytic activity of Ru, the I-V result revealed the average energy conversion efficiency of Ru and Pt to be 2.98% and 6.57%, respectively. These results suggest that Ru can be used as counter electrodes in DSSCs due to its extremely low temperature process compatibility.

Comparison of Catalytic Activity for Methanol Electrooxidation Between Pt/PPy/CNT and Pt/C

  • Lee, C.G.;Baek, J.S.;Seo, D.J.;Park, J.H.;Chun, K.Y.
    • 전기화학회지
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    • 제13권4호
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    • pp.240-245
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    • 2010
  • This work explored the catalytic effect of Pt in multi-wall carbon nanotube and poly-pyrrole conductive polymer electrocatalysts (Pt/PPy/MWCNT). A home-made Pt/PPy/MWCNT catalyst was first evaluated by comparing its electrochemical active surface area (ESA) with E-Tek commercial catalysts by cyclic voltammetry in $H_2SO_4$ solution. Then, the methanol oxidation currents of Pt/PPy/MWCNT and the hydrogen peaks in $H_2SO_4$ solution were serially measured with microporous electrode. This provided the current density of methanol oxidation based on the ESA, allowing a quantitative comparison of catalytic activity. The current densities were also measured for Pt/C catalysts of E-Tek and Tanaka Precious Metal Co. The current densities for the different catalysts were similar, implying that catalytic activity depended directly on the ESA rather than charge transfer or electronic conductivity.

저온형 연료전지용 산소의 고활성 환원 촉매 제조 (Preperation of catalyst having high activity on oxygen reduction)

  • 김영우;김형진;이주성
    • 한국에너지공학회:학술대회논문집
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    • 한국에너지공학회 1992년도 학술발표회 초록집
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    • pp.39-40
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    • 1992
  • This paper dealt with the manufacturing of binary alloy catalyst and showed simple electrochemical method for determing catalytic activity of oxygen reduction in acid or alkaline electrolyte. The catalyst was prepared by impregnating transition metal salts on platinum or silver particles adsorbed before on carbon paper substrate. The electrochemical characteristics of the catalysts was investigated with carbon paper electrode or PTFE-boned porous electrode and then cathodic current densities and tafel slopes were compared. As a result, of all binary catalysts utilized in this work, Pt-Fe, Pt-Mo showed better oxygen reduction activity than pure platinum catalyst in acid electrolyte and Ag-Fe, Ag-Pt, and Ag-Ni-Bi-Ti catalyst did than pure silver catalyst in alkaline electrolyte. The current density of Pt-Fe electrode in acid electrolyte was one and half times higher than that of Pt electrode(~500mA/$\textrm{cm}^2$ at 0.7VvsNHE).

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$ZrO_2/Ti$ 막의 제조와 전기화학적 성질 (Preparation and electrochemical characterization of Ziconuim oxide)

  • 홍경미;손원근;김태일;박수길
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2005년도 추계학술대회 논문집 전기물성,응용부문
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    • pp.191-193
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    • 2005
  • This study has investigated the effects of the etching method of a Ti substrate for a metal oxide electrode on the electrochemical characteristics of the electrode. The HCl etching develops a fine and homogeneous roughness on the Ti substrate. Fabrication and material properties of the catalytic oxide electrode, which is known to be so effective to destruct refractory organics in aqueous waste, were studied. A method to enhance the fabrication reproducibility of the oxide electrode was tested for Ru, Zr, Sn oxide on the Ti substrate using SEM, XRD, Cyclic voltammetry.

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Physioelectrochemical Investigation of Electrocatalytic Activity of Modified Carbon Paste Electrode in Alcohol Oxidation as Anode in Fuel Cell

  • Shabani-Shayeh, Javad;Ehsani, Ali;Jafarian, Majid
    • 전기화학회지
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    • 제17권3호
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    • pp.179-186
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    • 2014
  • Methanol electro oxidation on the surface of carbon paste modified by $NiCl_2/6H_2O$ was studied in 1M NaOH by potentiostatic and potentiodynamic methods. Ni/C catalyst by the concentration of 5% Ni showed about twice higher electro catalytic activity than Ni metal. The amount of monolayer's on the surface of electrode is almost one order higher for Ni/C than Ni electrode. The kinetic parameters and the diffusion coefficient of methanol were derived from chronoamperometry (CA) and electrochemical impedance spectroscopy (EIS) measurements.

Preparation of Ru-C Nano-composite Film by MOCVD and Electrode Properties for Oxygen Gas Sensor

  • Kimura, Teiichi;Goto, Takashi
    • 한국분말야금학회:학술대회논문집
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    • 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part 1
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    • pp.358-359
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    • 2006
  • Ru-C nano-composite films were prepared by MOCVD, and their microstructures and their electrode properties for oxygen gas sensors were investigated. Deposited films contained Ru particles of 5-20 nm in diameter dispersed in amorphous C matrix. The AC conductivities associating to the interface charge transfer between Ru-C composite electrode and YSZ electrolyte were 100-1000 times higher than that of conventional paste-Pt electrodes. The emf values of the oxygen gas concentration cell constructed from the nano-composite electrodes and YSZ electrolyte showed the Nernstian theoretical values at low temperatures around 500 K. The response time of the concentration cell was 900 s at 500 K.

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