• 제목/요약/키워드: Pt anode

검색결과 141건 처리시간 0.027초

Anode processes on Pt and ceramic anodes in chloride and oxide-chloride melts

  • Mullabaev, A.R.;Kovrov, V.A.;Kholkina, A.S.;Zaikov, Yu.P.
    • Nuclear Engineering and Technology
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    • 제54권3호
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    • pp.965-974
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    • 2022
  • Platinum anodes are widely used for metal oxides reduction in LiCl-Li2O, however high-cost and low-corrosion resistance hinder their implementation. NiO-Li2O ceramics is an alternative corrosion resistant anode material. Anode processes on platinum and NiO-Li2O ceramics were studied in (80 mol.%) LiCl-(20mol.%)KCl and (80 mol.%)LiCl-(20 mol.%)KCl-Li2O melts by cyclic voltammetry, potentiostatic and galvanostatic electrolysis. Experiments performed in the LiCl-KCl melt without Li2O illustrate that a Pt anode dissolution causes the Pt2+ ions formation at 3.14 V and 550℃ and at 3.04 V and 650℃. A two-stage Pt oxidation was observed in the melts with the Li2O at 2.40 ÷ 2.43 V, which resulted in the Li2PtO3 formation. Oxygen current efficiency of the Pt anode at 2.8 V and 650℃ reached about 96%. The anode process on the NiO-Li2O electrode in the LiCl-KCl melt without Li2O proceeds at the potentials more positive than 3.1 V and results in the electrochemical decomposition of ceramic electrode to NiO and O2. Oxygen current efficiency on NiO-Li2O is close to 100%. The NiO-Li2O ceramic anode demonstrated good electrochemical characteristics during the galvanostatic electrolysis at 0.25 A/cm2 for 35 h and may be successfully used for pyrochemical treating of spent nuclear fuel.

Bismuth를 이용한 다층구조의 개미산 연료전지 연료전극 개발 (Development of a Formic Acid Fuel Cell Anode by Multi-layered Bismuth Modification)

  • 권영국;엄성현;이재영
    • Korean Chemical Engineering Research
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    • 제46권4호
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    • pp.697-700
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    • 2008
  • 본 연구에서는 개미산 연료전지의 연료극에서 Pt 촉매의 안정성과 활성을 높이기 위해 Bi를 UPD법을 이용하여 Pt 촉매 위에 증착시켰다. 증착된 Bi의 활용도를 높이기 위해 다층 전극구조를 적용하였으며, 전자탐침미세분석(EPMA) 결과에서 Bi가 장기성능 실험동안 촉매층에 안정적으로 존재하는 것을 확인할 수 있었다. 연료전지 성능실험에서는 Pt black 촉매 위에 Bi를 UPD한 다층 구조의 전극이 PtRu black 촉매보다 전류밀도 $150mA/cm^2$에서 약 200 mV정도 높은 성능을 나타냈다. Pt black을 40% Pt/C로 대체했을 경우 역시 높은 성능과 장기 안정성을 보였다.

Acid Treatments of Carbon Nanotubes and Their Application as Pt-Ru/CNT Anode Catalysts for Proton Exchange Membrane Fuel Cell

  • Kim, Min-Sik;Lim, Sin-Muk;Song, Min-Young;Cho, Hyun-Jin;Choi, Yun-Ho;Yu, Jong-Sung
    • Carbon letters
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    • 제11권4호
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    • pp.336-342
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    • 2010
  • Different oxidation treatments on CNTs using diluted 4.0 M $H_2SO_4$ solution at room temperature and or at $90^{\circ}C$ reflux conditions were investigated to elucidate the physical and chemical changes occurring on the treated CNTs, which might have significant effects on their performance as catalyst supports in PEM fuel cells. Raman spectroscopy, X-ray diffraction and transmission electron microscope analyses were made for the acid treated CNTs to determine the particle size and distribution of the CNT-supported Pt-Ru nanoparticles. These CNT-supported Pt-based nanoparticles were then employed as anode catalysts in PEMFC to investigate their catalytic activity and single-cell performance towards $H_2$ oxidation. Based on PEMFC performance results, refluxed Pt-Ru/CNT catalysts prepared using CNTs treated at $90^{\circ}C$ for 0.5 h as anode have shown better catalytic activity and PEMFC polarization performance than those of the commercially available Pt-Ru/C catalyst from ETEK and other Pt-Ru/CNT catalysts developed using raw CNT, thus demonstrating the importance of acid treatment in improving and optimizing the surface properties of catalyst support.

Influence of defective sites in Pt/C catalysts on the anode of direct methanol fuel cell and their role in CO poisoning: a first-principles study

  • Kwon, Soonchul;Lee, Seung Geol
    • Carbon letters
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    • 제16권3호
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    • pp.198-202
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    • 2015
  • Carbon-supported Pt catalyst systems containing defect adsorption sites on the anode of direct methanol fuel cells were investigated, to elucidate the mechanisms of H2 dissociation and carbon monoxide (CO) poisoning. Density functional theory calculations were carried out to determine the effect of defect sites located neighboring to or distant from the Pt catalyst on H2 and CO adsorption properties, based on electronic properties such as adsorption energy and electronic band gap. Interestingly, the presence of neighboring defect sites led to a reduction of H2 dissociation and CO poisoning due to atomic Pt filling the defect sites. At distant sites, H2 dissociation was active on Pt, but CO filled the defect sites to form carbon π-π bonds, thus enhancing the oxidation of the carbon surface. It should be noted that defect sites can cause CO poisoning, thereby deactivating the anode gradually.

Pt/C 및 Pt-Ru/C 촉매를 사용한 직접 메탄올 연료전지 연료극의 메탄올 산화 반응 특성 (Oxidation Characteristics of Methanol on Pt/C and Pt-Ru/C Catalyst for the Anode of Direct Methanol Fuel Cell)

  • 정두환;이창형;신동열
    • 에너지공학
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    • 제7권1호
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    • pp.35-43
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    • 1998
  • 본 연구에서는 Pt/C와 Pt-Ru/C 촉매를 이용하여 직접메탄올 연료전지용 연료극 전극을 제조하고 전극 및 메탄올 산화 특성에 대하여 고찰하였다. 전극은 SEM, TEM 및 열중량 분석을 통하여 특성을 조사하였다. 메탄올의 산화 특성은 1M CH3OH+1M H2SO4 용액에서 정전위/정전류계를 이용하여 반전지 시험 및 순환 전압-전류법으로 조사하였다. 연구결과를 통하여 메탄올 산화전극은 촉매층 내에 PTFE가 20w% 포함되었을 경우가 백금촉매의 이용률이 높고 우수한 성능을 보여 주었다. Pt-Ru/C 이원촉매는 Pt/C 촉매에 비하여 메탄올 산화특성이 우수하고 성능이 우수한 촉매임을 알 수 있었다. Pt/Ru/C와 Pt/C 촉매를 이용하여 제조한 전극의 메탄올 산화반응에 대한 활성화 에너지는 11.60 kJ/mol과 26.85 kJ/mol이었다.

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백금담지 촉매의 직접메탄올 연료전지 환원전극 적용 (Application of Pt/C (60 wt.%) on electrode catalyst layer of direct methanol fuel cell)

  • 조용훈;조윤환;박현서;정남기;성영은
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2007년도 춘계학술대회
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    • pp.188-190
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    • 2007
  • The MEA with the catalyst layer containing PtRu black and 60 wt. %Pt/C as their anode and cathode catalysts. For find to effect of carbon support, the MEA with platinum black for cathode catalyst was fabricated. The performance of the MEA with the catalyst layer containing (PtRu black:60 wt.% Pt/C) as their anode and cathode catalyst has shown competitively higher value than the performance of the MEA with the catalyst layer containing (PtRu black:Pt black) as their anode and cathode catalyst.

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Electrogeneration of Hypochlorite Ions using a Dimensionally Stable Anode-Type (Ti/PtPd(10%)Ox) Electrode

  • Teresa Zayas;Miriam Vega;Guillermo Soriano-Moro;Anabella Handal;Miguel Morales;Leonardo Salgado
    • Journal of Electrochemical Science and Technology
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    • 제15권2호
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    • pp.268-275
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    • 2024
  • The study examined the electrogeneration of hypochlorite ions (ClO-) via electrolysis of aqueous NaCl solutions using a dimensionally stable anode-type (DSA-type) electrode based on platinum and palladium oxides supported on titanium mesh (Ti/PtPd(10%)Ox). The electrogenerated ClO- was quantified on the basis of the absorption band at 292 nm (Aλ = 292) of the UV-Vis spectrum. The effect of initial pH, concentration of NaCl, cell potential difference and electrolysis time were investigated in this study. The results showed that the electrolysis of aqueous NaCl solutions increases the solution pH up to high values (≥ 8.0) that favor the formation of ClO- over chlorine or hypochlorous acid. The hypochlorite concentration increases significantly at pH values > 7.0 and shows a linear trend with increasing NaCl concentration and with increasing cell potential difference. When the cell potential and NaCl concentration are held constant, the maximum hypochlorite value during electrolysis depends on both the cell potential and NaCl concentration. The Ti/PtPd(10%)Ox anode favors the production of hypochlorite ions, making this anode a promising material for use in electrochemical oxidation of wastewater via an indirect mechanism.

턴-오프 시 PT-IGBT의 애노드 전압 강하 모델링 (Modeling of Anode Voltage Drop for PT-IGBT at Turn-off)

  • 류세환;이호길;안형근;한득영
    • 한국전기전자재료학회논문지
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    • 제21권1호
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    • pp.23-28
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    • 2008
  • In this paper, transient characteristics of the Punch Through Insulated Gate Bipolar Transistor (PT-IGBT) have been studied. On the contrary to Non-Punch Through Insulated Gate Bipolar Transistor(NPT-IGBT), it has a buffer layer and reduces switching power loss. It has a simple drive circuit controlled by the gate voltage of the MOSFET and low on-state resistance of the bipolar junction transistor. The transient characteristics of the PT-IGBT have been analyzed analytically. Excess minority carrier and charge distribution in active base region, the rate of anode voltage with time are expressed analytically by adding the influence of buffer layer. The experimental data is obtained from manufacturer. The theoretical predictions of the analysis have been compared with the experimental data obtained from the measurement of a device(600 V, 15 A) and show good agreement.

Synthesis of Pd and Pt Based Low Cost Bimetallic Anode Electrocatalyst for Glycerol Electrooxidation in Membraneless Air Breathing Microfluidic Fuel Cell

  • Panjiara, Deoashish;Pramanik, Hiralal
    • Journal of Electrochemical Science and Technology
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    • 제12권1호
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    • pp.38-57
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    • 2021
  • The different weight ratios of Pd to Pt, i.e., 16:4, 10:10, 4:16 in Pd-Pt/C and Pd (20 wt. %) /C electrocatalysts with low metal loading were synthesized for glycerol electrooxidation in an air breathing microfluidic fuel cell (MFC). The cell performance on Pd-Pt (16:4)/C anode electrocatalyst was found best among all the electrocatalysts tested. The single cell when tested at a temperature of 35℃ using Pd-Pt (16:4)/C, showed maximum open circuit voltage (OCV) of 0.70 V and maximum power density of 2.77 mW/㎠ at a current density of 7.71 mA/㎠. The power density increased 1.45 times when cell temperature was raised from 35℃ to 75℃. The maximum OCV of 0.78 V and the maximum power density of 4.03 mW/㎠ at a current density of 10.47 mA/㎠ were observed at the temperature of 75℃. The results of CV substantiate the single cell performance for various operating parameters.

Electrochemical oxidation of sodium dodecylbenzenesulfonate in Pt anodes with Y2O3 particles

  • Jung-Hoon Choi;Byeonggwan Lee;Ki-Rak Lee;Hyun Woo Kang;Hyeon Jin Eom;Seong-Sik Shin;Ga-Yeong Kim;Geun-Il Park;Hwan-Seo Park
    • Nuclear Engineering and Technology
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    • 제54권12호
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    • pp.4441-4448
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    • 2022
  • The electrochemical oxidation process has been widely studied in the field of wastewater treatment for the decomposition of organic materials through oxidation using ·OH generated on the anode. Pt anode electrodes with high durability and long-term operability have a low oxygen evolution potential, making them unsuitable for electrochemical oxidation processes. Therefore, to apply Pt electrodes that are suitable for long-term operation and large-scale processes, it is necessary to develop a new method for improving the decomposition rate of organic materials. This study introduces a method to improve the decomposition rate of organic materials when using a Pt anode electrode in the electrochemical oxidation process for the treatment of organic decontamination liquid waste. Electrochemical decomposition tests were performed using sodium dodecylbenzenesulfonate (SDBS) as a representative organic material and a Pt mesh as the anode electrode. Y2O3 particles were introduced into the electrolytic cell to improve the decomposition rate. The decomposition rate significantly improved from 21% to 99%, and the current efficiency also improved. These results can be applied to the electrochemical oxidation process without additional system modification to enhance the decomposition rate and current efficiency.