4.8 Article

Membrane/Electrode Interface Design for Effective Water Management in Alkaline Membrane Fuel Cells

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 11, 期 38, 页码 34805-34811

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b08075

关键词

dual-side patterning; anion exchange membrane; alkaline membrane fuel cell; membrane-electrode assembly; water management

资金

  1. Institute for Basic Science of the Republic of Korea [IBS-R006-A2]
  2. Global Frontier R&D Program on Center for Multiscale Energy System - National Research Foundation of Korea [2016M3A6A7945505]
  3. Technology Development Program to Solve Climate Changes of the National Research Foundation (NRF) - Ministry of Science and ICT [2018M1A2A2061975]
  4. National Research Foundation of Korea [2019R1C1C1004462]
  5. National Research Foundation of Korea [2019R1C1C1004462] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The recent development of ultrathin anion exchange membranes and optimization of their operating conditions have significantly enhanced the performance of alkaline-membrane fuel cells (AMFCs); however, the effects of the membrane/electrode interface structure on the AMFC performance have not been seriously investigated thus far. Herein, we report on a high-performance AMFC system with a membrane/electrode interface of novel design. Commercially available membranes are modified in the form of well-aligned line arrays of both the anode and cathode sides by means of a solvent-assisted molding technique and sandwich-like assembly of the membrane and polydimethylsiloxane molds. Upon incorporating the patterned membranes into a single-cell system, we observe a significantly enhanced performance of up to similar to 35% compared with that of the reference membrane. The enlarged interface area and reduced membrane thickness from the line-patterned membrane/electrode interface result in improved water management, reduced ohmic resistance, and effective utilization of the catalyst. We believe that our findings can significantly contribute further advancements in AMFCs.

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