提龙
氧化还原
阴极
材料科学
电化学
水溶液
储能
化学工程
电子转移
锌
无机化学
锰
纳米技术
电极
作者
Sijia He,Yaozhi Liu,Hong Wu,Wenjun Zhao,Zhiqing Xue,Yue Zhang,Sibo Wang,Jing Wang,Xiaoxia Liu,Xiaoqi Sun
标识
DOI:10.1002/adfm.202519798
摘要
Abstract Rechargeable aqueous Zn‐MnO 2 batteries are promising for large‐scale energy storage. A two‐electron transfer reaction of MnO 2 /Mn 2+ is available for the cathode, delivering a high theoretical capacity of 616 mAh g −1 . However, this process requires protons, and its practical contribution in conventional mildly acidic zinc batteries is limited. Herein, an organic redox mediator of Tiron is demonstrated to realize dominant two‐electron transfer energy storage in MnO 2 cathode materials. The reversible hydroquinone/benzoquinone redox couple of Tiron allows facile spontaneous chemical reaction with MnO 2 to generate Mn 2+ as well as electrochemical redox in zinc cells according to combined in situ/ex situ analysis. Theoretical calculations further reveal that Tiron reduces the energy required for Mn release from the MnO 2 lattice. Therefore, Tiron not only boosts the two‐electron reaction of MnO 2 but also reactivates any dead materials. Thanks to these effects, the MnO 2 cathode achieves a high capacity of 525 mAh g −1 at 0.3 A g −1 , far exceeding 384 mAh g −1 in the baseline system. The lifespan also extends four times to 12 000 cycles at 5 A g −1 together with stable capacity retention. This work presents an effective strategy to encourage the high‐capacity reaction path of MnO 2 cathodes in aqueous zinc batteries.
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