电解质
材料科学
电池(电)
水溶液
溶解
流动电池
化学工程
电极
氧化还原
电化学窗口
电化学
容量损失
阴极
无机化学
阳极
法拉第效率
化学
离子电导率
冶金
有机化学
热力学
物理化学
功率(物理)
工程类
物理
作者
Chang Liu,Xiaowei Chi,Qi Han,Yu Liu
标识
DOI:10.1002/aenm.201903589
摘要
Abstract Aqueous batteries are facing big challenges in the context of low working voltages and energy density, which are dictated by the narrow electrochemical window of aqueous electrolytes and low specific capacities of traditional intercalation‐type electrodes, even though they usually represent high safety, low cost, and simple maintenance. For the first time, this work demonstrates a record high‐energy‐density (1503 Wh kg −1 calculated from the cathode active material) aqueous battery system that derives from a novel electrolyte design to expand the electrochemical window of electrolyte to 3 V and two high‐specific‐capacity electrode reactions. An acid‐alkaline dual electrolyte separated by an ion‐selective membrane enables two dissolution/deposition electrode redox reactions of MnO 2 /Mn 2+ and Zn/Zn(OH) 4 2− with theoretical specific capacities of 616 and 820 mAh g −1 , respectively. The newly proposed Zn–Mn 2+ aqueous battery shows a high Coulombic efficiency of 98.4% and cycling stability of 97.5% of discharge capacity retention for 1500 cycles. Furthermore, in the flow battery based on Zn–Mn 2+ pairs, more excellent stability of 99.5% of discharge capacity retention for 6000 cycles is achieved due to greatly improved reversibility of the Zn anode. This work provides a new path for the development of novel aqueous batteries with high voltage and energy density.
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