Chai Jingchao, Lashgari Amir, Cao Zishu, Williams Caroline K, Wang Xiao, Dong Junhang, Jiang Jianbing Jimmy
Department of Chemistry, University of Cincinnati, P.O. Box 210172, Cincinnati, Ohio 45221-0172, United States.
Department of Chemical Engineering, University of Cincinnati, Cincinnati, Ohio 45221-0172, United States.
ACS Appl Mater Interfaces. 2020 Apr 1;12(13):15262-15270. doi: 10.1021/acsami.0c01045. Epub 2020 Mar 18.
Non-aqueous redox flow batteries (RFBs) are promising energy storage devices owing to the broad electrochemical window of organic solvents. Nonetheless, the wide application of these batteries has been limited by the low stability and limited solubility of organic materials, as well as the insufficient ion conductivity of the cell separators in non-aqueous electrolytes. In this study, two viologen analogues with poly(ethylene glycol) (PEG) tails are designed as anolytes for non-aqueous RFBs. The PEGylation of viologen not only enhances the solubility in acetonitrile but also increases the overall molecular size for alleviated crossover. In addition, a composite nanoporous aramid nanofiber separator, which allows the permeation of supporting ions while inhibiting the crossover of the designer viologens, is developed using a scalable doctor-blading method. Paired with ferrocene, the full organic material-based RFB presents excellent cyclability (500 cycles) with a retention capacity per cycle of 99.93% and an average Coulombic efficiency of 99.3% at a current density of 2.0 mA/cm. The high performance of the PEGylated viologen validates the potential of the PEGylation strategy for enhanced organic material-based non-aqueous RFBs.
非水系氧化还原液流电池(RFBs)由于有机溶剂具有较宽的电化学窗口,是很有前景的储能装置。尽管如此,这些电池的广泛应用受到有机材料稳定性低、溶解度有限以及非水电解质中电池隔膜离子传导率不足的限制。在本研究中,设计了两种带有聚乙二醇(PEG)尾链的紫精类似物作为非水系RFBs的阳极电解液。紫精的聚乙二醇化不仅提高了其在乙腈中的溶解度,还增大了整体分子尺寸以减轻交叉渗透。此外,采用可扩展的刮刀法制备了一种复合纳米多孔芳纶纳米纤维隔膜,该隔膜允许支持离子渗透,同时抑制设计的紫精的交叉渗透。与二茂铁配对,基于全有机材料的RFB在2.0 mA/cm的电流密度下表现出优异的循环性能(500次循环),每次循环的容量保持率为99.93%,平均库仑效率为99.3%。聚乙二醇化紫精的高性能验证了聚乙二醇化策略在增强基于有机材料的非水系RFBs方面的潜力。