• 제목/요약/키워드: Fuel cell anode

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Advances in Materials for Proton Exchange Membrane based Fuel Cells

  • McGrath James E.
    • 한국고분자학회:학술대회논문집
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    • 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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    • pp.58-59
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    • 2006
  • Less than a decade ago, most alternate membrane materials for fuel cells relied upon a post-sulfonation process to generate ionic groups capable of transporting protons from the anode to the cathode. These random post sulfonations showed some promise, but in general they produced materials that were not sufficiently stable or protonically conductive at ion exchange capacities where aqueous swelling could be restricted. Our group began to synthesize disulfonated monomers that could be used to incorporate into random copolymer proton exchange membranes. The expected limitation was that the aromatic polymers might not be stable enough to withstand fuel cell conditions. However, this was mostly based upon an accelerated test known was the Fenton's Reagent Test, which did not seem to this author as being a reliable predictor of performance. A much better approach has been to evaluate the open circuit voltage (OCV) for alternate membranes, as well as the benchmark perfluorosulfonic acid systems. When this is done, the aromatic ionomers of this study, primarily based upon disulfonated polyarylene ether sulfones, show up quite well. Real time 3000 hours DMFC results have also been generated. Obtaining conductive materials at low humidities is another major issue where alternate membranes have not been particularly successful. In order to address this problem, multiblock copolymers with relatively high water diffusion coefficients have been designed, which show promise for conductivity at lowered humidity.

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복합 박막 증착 공정을 이용한 중저온 고체산화물 연료전지용 전해질 증착 (Deposition of Electrolyte for Intermediate Temperature Solid Oxide Fuel Cells by Combined Thin Film Deposition Techniques)

  • 하승범;지상훈;와카스 하산 탄비르;이윤호;차석원
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2011년도 추계학술대회 초록집
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    • pp.84.1-84.1
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    • 2011
  • Typical solid oxide fuel cells (SOFCs) have limited applications because they operate at high temperature due to low ionic conductivity of electrolyte. Thin film solid oxide fuel cell with yttria stabilized zirconia (YSZ) electrolyte is developed to decrease operating temperature. Pt/YSZ/Pt thin film SOFC was fabricated on anodic aluminum oxide (AAO). The crystalline structure of YSZ electrolyte by sputter is heavily depends on the roughness of porous Pt layer, which results in pinholes. To deposit YSZ electrolyte without pinholes and electrical shortage, it is necessary to deposit smoother and denser layer between Pt anode layer and YSZ layer by sputter. Atomic Layer Deposition (ALD) technique is used to deposit pre-YSZ layer, and it improved electrolyte quality. 300nm thick Bi-layered YSZ electrolyte was successfully deposited without electrical shortage.

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혼합 이온 및 전자 전도체-프로톤 전도성 전해질 복합 공기극을 적용한 프로토닉 세라믹 연료전지의 전기화학적 성능 평가 (Electrochemical Evaluation of Mixed Ionic and Electronic Conductor-Proton Conducting Oxide Composite Cathode for Protonic Ceramic Fuel Cells)

  • 신형식;이진우;최시혁
    • 한국수소및신에너지학회논문집
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    • 제35권1호
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    • pp.48-55
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    • 2024
  • The electrochemically active site of mixed ionic and electronic conductor (MIEC) as a cathode material is restricted to the triple phase boundary in protonic ceramic fuel cells (PCFCs) due to the insufficient of proton-conducting properties of MIEC. This study primarily focused on expanding the electrochemically active site by La0.6Sr0.4Co0.2Fe0.8O3-δ(LSCF6428)-BaZr0.4Ce0.4Y0.1Yb0.1O3-δ (BZCYYb4411) composite cathode. The electrochemical properties of the composite cathode were evaluated using anode-supported PCFC single cells. In comparison to the LSCF6428 cathode, the peak power density of the LSCF6428-BZCYYb4411 composite cathode is much enhanced by the reduction in both ohmic and non-ohmic resistance, possibly due to the increased electrochemically active site.

전자빔 물리증착을 이용한 고체 산화물 연료전지의 제조: II. 단전지 성능 (Fabrication of Solid Oxide Fuel Cells via Physical Vapor Deposition with Electron Beam: II. Unit Cell Performance)

  • 김형철;박종구;정화영;손지원;김주선;이해원;이종호
    • 한국세라믹학회지
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    • 제43권5호
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    • pp.299-303
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    • 2006
  • In this paper, anode supported SOFC with columnar structured YSZ electrolyte was fabricated via Electron Beam Physical Vapor Deposition (EBPVD) method. Liquid condensation process was employed for the preparation of NiO-YSZ substrate and the high power electron beam deposition method was used for the deposition of YSZ electrolyte film. Double layered cathode with LSM-YSZ and LSM was printed on electrolyte via screen-printing method and fired at $1150^{\circ}C$ in air atmosphere for 3 h. The electrochemical performance and the long-term stability of $5{\times}5cm^2$ single cell were investigated with DC current-voltage characteristics and AC-impedance spectroscopy. According to the investigation, $5{\times}5cm^2$ sized unit cell showed the maximum power density of around $0.76W/cm^2$ at $800^{\circ}C$ and maintained the stable performance over 400 h.

Characterization of Methanol Crossover through Nafion Membranes by Direct Cell Performance Measurement

  • Park, Kyung-Won;Kim, Young-Min;Kwon, Bu-kil;Choi, Jong-Ho;Park, In-Su;Sung, Yung-Eun
    • 전기화학회지
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    • 제5권4호
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    • pp.226-231
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    • 2002
  • Power densities produced by the permeation of methanol through membranes were directly measured by inserting the membrane in front of anode in a membrane-electrode-assembly of a direct methanol fuel cell (DMFC). The power density was closely related to the loss of power in the DMFC and was strongly affected by temperature. As the cell temperature was increased, the power density resulting from methanol crossover was increased. The increase in methanol crossover had be attributed to diffusion caused or affected by temperature. Methanol crossover a major effect on the performance of a DMFC at a relatively low temperature with $26\%\;loss\;at\;30^{\circ}C$. In order to reduce methanol crossover, a conventional Nafion membrane was modified by the incorporation of Pt or Pd. The reduction in methanol crossover was investigated in these modified membranes by our cell performance measurement. Pt and Pd particles incorporated in the Nafion membranes block methanol pathway and prevent methanol transport through the membranes, which was proved by combining with liquid chromatography.

고분자전해질 연료전지의 동작압력에 대한 가스 확산층의 위치 별 전류밀도 및 수분거동에 대한 수치해석 (Numerical Modeling of Current Density and Water Behavior at a Designated Cross Section of the Gas Diffusion Layer in a Proton Exchange Membrane Fuel Cell)

  • 강신조;김영배
    • 대한기계학회논문집B
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    • 제36권2호
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    • pp.161-170
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    • 2012
  • 고분자 전해질 연료전지에서 물 관리는 연료 전지성능에 영향을 미치는 중요한 요인이다. 공급되는 수분의 양이 적을 경우 수소이온의 이동을 담당하는 전해질의 건조현상으로, 수분의 양이 과다할 경우 반응이 일어나는 촉매층과 전해질 삼상 계면에서의 홍수현상으로 성능을 감소시키거나 동작을 멈추게 하므로 이 부분에 대한 많은 연구가 진행되고 있다. 본 논문에서는 연료전지 수분에 영향을 주는 요소 중, 연료극과 공기극에 공급되는 상대습도를 100%로, 동작온도를 $80^{\circ}C$로 설정한 후, 입구 측에 압력을 변화하면서, 다중물리응용 수치해석을 포함하고 유한요소를 통하여 비선형 편미분 방정식이 결부된 상용코드를 이용하여 전체적인 전기화학반응 및 성능에 대한 해석을 수행하고 공기극 측의 가스 확산층에 각 위치별 전류밀도 분포와 수분포화의 분포, 압력차에 의한 동작물질의 속도 등을 분석하여 보았다. 본 연구를 통하여 얻어진 결과는 연료전지의 성능은 압력의 세기에 따라 달라지며 압력이 높을수록 성능과 위치별 최대 전류밀도가 높게 나타났으며, 공기극의 가스 확산층에서의 수분함량은 높은 압력에서보다 낮은 압력에서 수분함량이 많은 것으로 나타났으며 특히 전극의 바로 아래 부분에서의 수분이 더 많이 응축되어 나타났으며 공기극 가스 확산층에서의 동작물질의 속도는 동작물질의 입구방향에서 출구측으로 진행할수록 그 변동 폭이 크게 나타났다.

전기화학반응을 수반한 유로채널 형상에 따른 마찰계수에 대한 연구 (Friction Factor in Micro Channel Flow with Electrochemical Reactions in Fuel Cell)

  • 조선아;이필형;한상석;최성훈;황상순
    • 전기화학회지
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    • 제10권4호
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    • pp.245-251
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    • 2007
  • 주어진 연료전지면적에서 반응면적이 넓을수록 성능이 향상되는 연료전지는 좁은 폭의 채널을 여러 개 존재하게 하는 구조를 선호하지만 채널 폭이 좁아질수록 압력이 커지는 문제가 고려되어져야 한다. 그러나 현재 채널 구조에 따른 압력에 대한 연구는 많이 진행되어져 왔지만 대부분 반응을 고려하지 않았으며, 반응을 고려한 경우에 어떤 경향을 나타내는지 알아보는 것이 연료전지 유로설계에 있어 매우 중요하다. 본 논문에서 화학반응을 고려한 평행류, 90도 밴드형, serpentine 세가지 종류의 유로채널를 가진 연료전지를 수치 해석하여 반응을 고려하지 않은 경우와 마찰계수(fRe), 속도, 압력강하를 비교하여 본 결과 parallel과 bend 형태의 채널은 반응을 고려한 경우 반응에 의한 밀도의 감소에 따라 근소하게 감소한 것을 알 수 있었다. 그러나 serpentine채널은 다공성매체인 확산층을 통해 인접한 채널로 가스가 이동하는 bypass flow 영향에 의하여 상대적으로 낮은 압력강하를 나타내는 것을 알 수 있었다.

전사법으로 제조한 SOFC용 YSZ 전해질 전사지의 치밀화 및 전기화학적 특성 (Densification and Electrochemical Properties of YSZ Electrolyte Decalcomania Paper for SOFCs by Decalcomania)

  • 조해란;최병현;안용태;백성현;노광철;박선민
    • 대한금속재료학회지
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    • 제50권9호
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    • pp.685-690
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    • 2012
  • Decalcomania is a new method for SOFCs (solid oxide fuel cells) unit cell fabrication. A tight and dense $5{\mu}m$ Yttria-stabilized zirconia (8YSZ) electrolyte layer on anode substrate was fabricated by the decalcomania method. After 8YSZ as the electrolyte starting material was calcined at $1200^{\circ}C$, the particle size was controlled by the attrition mill. The median particle size (D50) of each 8YSZ was $39.6{\mu}m$, $9.30{\mu}m$, $6.35{\mu}m$, and $3.16{\mu}m$, respectively. The anode substrate was coated with decalcomania papers which were made by using 8YSZ with different median particle sizes. In order to investigate the effect of median particle sizes and sintering conditions on the electrolyte density, each sample was sintered for 2, 5 and 10 h, respectively. 8YSZ with a median particle size of $3.16{\mu}m$ which was sintered at $1400^{\circ}C$ for 10 had the highest density. With this 8YSZ, a SOFCs unit cell was manufactured with a $5{\mu}m$ layer by the decalcomania method. Then the unit cell was run at $800^{\circ}C$. The Open Circuit Voltage (OCV) and Maximum power density (MPD) was 1.12 V and $650mW/cm^2$, respectively.

저온형 SOFC용 GDC 전해질 두께에 따른 Open Circuit Voltage 향상 (Improvement of Open Circuit Voltage (OCV) depending on Thickness of GDC Electrolyte of LT-SOFCs)

  • 고현준;이종진;현상훈
    • 한국세라믹학회지
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    • 제47권2호
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    • pp.195-198
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    • 2010
  • It has been considered to apply GDC ($Gd_{0.1}Ce_{0.9}O_{1-X}$) for low-temperature SOFC electrolytes because it has higher ionic conductivity than YSZ at low temperature. However, open circuit voltage with using GDC ($Gd_{0.1}Ce_{0.9}O_{1-X}$) electrolyte in SOFCs, becomes lower than using YSZ (8 mol% Yttria stabilized Zirconia) electrolyte because GDC has electronic conductivity. In this work, the effect of changing GDC electrolyte thickness on the open circuit voltage has been investigated. Ni-GDC anode-supported unit cells were fabricated as follows. Mixed NiO-GDC powders were pressed and pre-sintered at $1200^{\circ}C$. And then, GDC electrolyte material was dip-coated on the anode and sintered at $1400^{\circ}C$. Finally the LSCF-GDC cathode material was screen-printed on the electrolyte and sintered at $1000^{\circ}C$. Electrolyte thickness was controlled by the number of dip-coating times. Open circuit voltage was measured depending on electrolyte thickness at $650^{\circ}C$ and found that the thicker GDC electrolyte was, the better OCV was.

기계적 합금화한 Ni-W(WC)의 미세구조 및 특성 (Microstructure and Characteristics of Mechanically Alloyed Ni-W(WC))

  • 신수철;장건익
    • 한국재료학회지
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    • 제8권12호
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    • pp.1133-1137
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    • 1998
  • MCFC(Molten Carbonate Fuel Cell) 작동온도인 $650^{\circ}C$에서 Ni 음극의 Creep 및 소결에 대한 저항성을 개선시키고자 Ni-W(WC) 복합재료를 기계적 합금법으로 제조하였다. 기계적 합금화한 분말의 XRD분석결과 밀링시간이 증가함에 따라 재료의 규칙적인 결정이 파괴되어 비정질화 되어가는 경향을 보였다. 소결은 $1280^{\circ}C$의 수소분위기에서 10시간 행하였다 소결된 시편의 dot-mapping 및 TEM 분석결과 Ni-W 계면에서의 2차상 관찰되지 않았으나 $0.1\mu\textrm{m}$ 이하의 W이 Ni 기지내에 미세하고 균일하게 분포되어 있는 것으로 나타났다. 이와같이 미세하고 균일하게 분포되어 있는 W은 고용강화 및 분산강화 효과를 통하여 Ni음극의 기계적 특성을 향상시킬 것으로 기대된다.

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