阴极
氧化还原
水溶液
化学
吸附
乙腈
电解质
化学工程
硫黄
润湿
电流密度
无机化学
动力学
电池(电)
电极
图层(电子)
电化学
材料科学
分子
密度泛函理论
碘
作者
Shanshan Liu,Shouyue Wang,Guangwei He,Miao Qi,Yuheng Jin,Jingxia Qiu,Tao Zhang,Chunyang Miao,Sheng Li
标识
DOI:10.1002/batt.202500757
摘要
Aqueous Zn‐S batteries exhibit great potential owing to their intrinsic safety, cost‐effectiveness, and eco‐friendly nature. However, their advancement faces persistent challenges, including sluggish redox kinetics, parasitic side reactions, and poor cathode wettability. Herein, we propose a hybrid electrolyte composed of acetonitrile (ACN) ‐ H 2 O solvents, with an iodine (I 2 ) redox mediator, to address these issues. Compared to H 2 O, the ACN molecules exhibit a higher adsorption affinity toward sulfur, thereby facilitating the formation of an ACN‐enriched interfacial layer on the cathode. This layer mediates I 2 transport to the sulfur cathode, while I 2 ensures efficient sulfur redox conversion, synergistically promoting the reversible S/ZnS reactions. Notably, the I 2 concentration critically influences reaction kinetics and rate capability. Moreover, incorporating ACN enhances cathode wettability and mitigates side reactions, thereby improving cathode stability. Consequently, the Zn‐S battery delivers a high specific capacity of 1535 mAh g −1 at 0.1 C and a high energy density of 912 Wh kg −1 . Notably, it demonstrates exceptional rate capability, retaining a substantial capacity of 899 mAh g −1 at a high current density of 10 C (16.75 A g −1 ), while maintaining considerable cycling stability.
科研通智能强力驱动
Strongly Powered by AbleSci AI