School of Science, Westlake University, 18 Shilongshan Road, Hangzhou, 310024, Zhejiang, China.
Institute of Natural Sciences, Westlake Institute for Advanced Study, Hangzhou, 310024, Zhejiang, China.
Angew Chem Int Ed Engl. 2021 Mar 1;60(10):5289-5298. doi: 10.1002/anie.202014610. Epub 2021 Jan 28.
Aqueous organic redox flow batteries (AORFBs) are a promising electrochemical technology for large-scale energy storage. We report a biomimetic, ultra-stable AORFB utilizing an amino acid functionalized phenazine (AFP). A series of AFPs with various commercial amino acids at different substituted positions were synthesized and studied. 1,6-AFPs display much higher stability during cycling when compared to 2,7- and 1,8-AFPs. Mechanism investigations reveal that the reduced 2,7- and 1,8-AFPs tend to tautomerize and lose their reversible redox activities, while 1,6-AFPs possess ultra-high stability both in their oxidized and reduced states. By pairing 3,3'-(phenazine-1,6-diylbis(azanediyl))dipropionic acid (1,6-DPAP) with ferrocyanide at pH 8 with 1.0 M electron concentration, this flow battery exhibits an OCV of 1.15 V and an extremely low capacity fade rate of 0.5 % per year. These results show the importance of molecular engineering of redox-active organics for robust redox-flow batteries.
水相有机氧化还原流电池(AORFBs)是一种很有前途的大规模储能电化学技术。我们报告了一种仿生的、超稳定的 AORFB,利用氨基酸功能化的吩嗪(AFP)。合成并研究了一系列具有不同取代位置的各种商业氨基酸的 AFP。与 2,7- 和 1,8-AFPs 相比,1,6-AFPs 在循环过程中表现出更高的稳定性。机理研究表明,还原的 2,7- 和 1,8-AFPs 倾向于互变异构并失去其可逆氧化还原活性,而 1,6-AFPs 在其氧化态和还原态均具有超高的稳定性。通过将 3,3'-(吩嗪-1,6-二基双(氮杂二基))二丙酸(1,6-DPAP)与 pH 8 下的亚铁氰化物以 1.0 M 电子浓度配对,该流电池表现出 1.15 V 的开路电压和极低的每年 0.5%的容量衰减率。这些结果表明,对氧化还原活性有机分子进行分子工程对于构建坚固的氧化还原流电池非常重要。