4.7 Article

Pore-filled anion-exchange membranes for non-aqueous redox flow batteries with dual-metal-complex redox shuttles

期刊

JOURNAL OF MEMBRANE SCIENCE
卷 454, 期 -, 页码 44-50

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.memsci.2013.11.051

关键词

Pore-filled anion-exchange membranes; Redox flow battery; Non aqueous media; Dual-metal complex redox electrolyte; Crossover

资金

  1. Strategy Task of Energy Source Technology Development of the Korea Institute of Energy Technology Evaluation and Planning (KETEP)
  2. Korea government Ministry of Trade. Industry 8: Energy (MOITE) [2011201010007A]
  3. National Research Foundation of Korea (NRF)
  4. Korea government (MSIP) for the Center for Next Generation Dye-sensitized Solar Cells [2008-0061903]
  5. Korea Evaluation Institute of Industrial Technology (KEIT) [2011201010007A] 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

Pore-filled anion-exchange membranes (PFAEMs) were synthesized using thin porous polymer substrates for non-aqueous redox flow battery (RFB) applications. The PFAEMs which have a thickness of about 25 pm exhibited high ion conductivity and selectivity in both aqueous and non-aqueous media. In addition, they showed excellent mechanical properties as well as dimensional stability in a nonaqueous environment The non-aqueous RFB experiments utilizing novel Fe/Ni dual-metal complex redox electrolyte resulted in the respectable energy efficiencies (i.e. 87.3% and 772% in non-flowing and flowing cells, respectively) much higher than those of previous papers where other non-aqueous redox electrolytes were used. The PFAEMs showed much better ion selectivity in non-aqueous medium compared to that of the commercial membrane due to the relatively low swellability. The results demonstrated that the charge-discharge performances were largely enhanced by the mitigated crossover of metal complex as well as the low mass transport resistance through the membrane. (c) 2013 Elsevier B.V. All rights reserved,

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