Visualizing and Understanding the Ionic Liquid-Mediated Polybromide Electrochemistry for Aqueous Zinc-Bromine Redox Batteries
Chao Wang, Qihong Xie, Guotao Wang, Yimeng Lyu, Qianhui Wang, Xinxi Ma, Haobo Wang, Taolian Guo, Yutong Wu, Jie Han
Abstract
Aqueous zinc–bromine redox systems possess multiple merits for scalable energy storage. Applying bromine complexing agents shows effectiveness in alleviating the key challenge of ubiquitous crossover of reactive liquid bromine species, while the underlying microscopic mechanism requires a deep understanding to engineer better complexing electrochemistry. Herein, taking a series of quaternary ammonium ionic liquids (methyl 4 NBr, ethyl 4 NBr, propyl 4 NBr, and butyl 4 NBr) as a redox mediator model, operando optical monitoring was used to visualize the dynamic electrochemical behaviors, unveiling the ionic liquid-mediated polybromide electrochemistry with a distinct chain length effect. A longer chain length possesses a stronger electrostatic interaction in the complexing product to effectively capture Br 2 . Operando results reveal the liquid nature of the reversibly electrogenerated polybromide microdroplets in the butyl 4 NBr-added redox system, which promoted the Br 3 – /Br – conversion kinetics and alleviated the self-discharge for improved battery performance. This work provides direct evidence and new insights into complexing electrochemistry for advancing Zn-Br 2 batteries.