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Effect of the cathode gas diffusion layer on the water transport behavior and the performance of passive direct methanol fuel cells operating with neat methanol
Authors:QX Wu  TS Zhao  WW Yang
Affiliation:1. College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China;2. Center for Energy Storage and Conversion, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai 201210, PR China;1. Fuel Cell Research Center, Korea Institute of Energy Research (KIER), 152 Gajeong, Yuseong, 305-343 Daejeon, Republic of Korea;2. Department of Chemical and Biological Engineering, Korea University, 1 Anam 5, Seongbuk, 136-713 Seoul, Republic of Korea;3. Advanced Energy Technology, University of Science and Technology, 217 Gajeong, Yuseong, 305-350 Daejeon, Republic of Korea;1. Department of Mechanical Engineering, Islamic Azad University, Qaemshahr Branch, Qaemshahr, Iran;2. Fuel Cell Research Technology Group & Mechanical Engineering Department, Babol University of Technology, Babol, Iran;3. Department of Mechanical Engineering, Babol University of Technology, Babol, Iran
Abstract:The passive operation of a direct methanol fuel cell with neat methanol requires the water that is produced at the cathode to diffuse through the membrane to the anode to compensate the methanol oxidation reaction (MOR). Hence, the anode performance of this type of fuel cell can be limited by the water transport rate from the cathode to the anode. In this work we theoretically show that the water transport from the cathode to the anode depends primarily on the design of the cathode gas diffusion layer (GDL). We investigate experimentally the effects of the design parameters of the cathode GDL, including the PTFE (polytetrafluoroethylene) content in the backing layer (BL), and the carbon loading and the PTFE content in the microporous layer (MPL) on the water transport and the performance of the passive DMFC with the help of a reference electrode. The results indicate that on one hand, these parameters can be adjusted to decrease the water concentration loss of the anode performance, but on the other hand, they can also cause an increase in the oxygen concentration loss of the cathode performance. Hence, an optimal balance in minimizing the both concentration losses is the key to maximize the cell performance.
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