Radical Charge Population and Energy: Critical Role in Redox Potential and Cycling Life of Piperidine Nitroxyl Radical Cathodes in Aqueous Zinc Hybrid Flow Batteries.
Hao FanJiahui ZhangMahalingam RavivarmaHongbin LiBo HuJiafeng LeiYangyang FengShizhao XiongCheng HeJianying GongTieyu GaoJiangxuan SongPublished in: ACS applied materials & interfaces (2020)
Redox-active 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) derivatives have recently been investigated to expand the choice of catholyte for aqueous flow batteries (AFBs). However, the effects of substituent R in 4-position on redox potential and corresponding capacity fading mechanism are still unclear. Here, we conduct comparative studies of four R-TEMPO with R = -OH, -NH2, -COOH, and -NHCOCH3 in zinc hybrid AFBs. Experimental and theoretical analyses reveal that low-radical head charge population sum and radical energy, depending on R in 4-position, play a critical role in enhancing redox potential and cycling life of R-TEMPO. The electronic effect brought along by N-acetyl could redistribute the charge and lower systematic energy, making the ring-opening joint sturdy and therefore suppress the side reactions. Accordingly, the 4-NHCOCH3-TEMPO/Zn battery achieves a high capacity retention of >99.65%/day and an open-circuit voltage of 1.71 V. Our findings on the effects of substituent are greatly anticipated to boost the high-energy density, long-life, and eco-friendly TEMPO-based AFBs.