钒
氧化还原
膜
化学
离子交换
流动电池
扩散
无机化学
离子
电极
分析化学(期刊)
色谱法
热力学
物理化学
有机化学
电解质
物理
生物化学
作者
Torben Lemmermann,Maik Becker,Maria Stehle,Marco Drache,Sabine Beuermann,Mohsen Sadeghi Bogar,Uwe Gohs,Ursula E. A. Fittschen,Thomas Turek,Ulrich Kunz
标识
DOI:10.1016/j.jpowsour.2022.231343
摘要
The vanadium crossover is the primary source of capacity fade in vanadium flow batteries (VFB). Available transport models for the vanadium crossover use significantly different diffusion coefficients for the vanadium species. Previously, we demonstrated that redox reactions between V3+ and VO2+ occur within cation exchange membranes. Therefore, it seems very likely that the neglect of redox reactions inside the membrane may lead to these inconsistencies. To investigate the reactions inside the membrane, a time-resolved in situ and in operando method based on potential probes, which have already been successfully used to measure potentials on and in electrodes, was developed. The probes were integrated into firmly pressed layers of several membranes. This work reports the new experimental design and presents the first results which give valuable insights into the transport processes and redox reactions inside the membrane.
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