锰
插层(化学)
水溶液
电化学
电解质
电池(电)
氧化还原
阴极
无机化学
化学
电极
材料科学
化学工程
有机化学
物理化学
冶金
功率(物理)
工程类
物理
量子力学
作者
Songshan Bi,Shuai Wang,Yue Fang,Zhiwei Tie,Zhiqiang Niu
标识
DOI:10.1038/s41467-021-27313-5
摘要
Abstract Aqueous rechargeable metal batteries are intrinsically safe due to the utilization of low-cost and non-flammable water-based electrolyte solutions. However, the discharge voltages of these electrochemical energy storage systems are often limited, thus, resulting in unsatisfactory energy density. Therefore, it is of paramount importance to investigate alternative aqueous metal battery systems to improve the discharge voltage. Herein, we report reversible manganese-ion intercalation chemistry in an aqueous electrolyte solution, where inorganic and organic compounds act as positive electrode active materials for Mn 2+ storage when coupled with a Mn/carbon composite negative electrode. In one case, the layered Mn 0.18 V 2 O 5 ·nH 2 O inorganic cathode demonstrates fast and reversible Mn 2+ insertion/extraction due to the large lattice spacing, thus, enabling adequate power performances and stable cycling behavior. In the other case, the tetrachloro-1,4-benzoquinone organic cathode molecules undergo enolization during charge/discharge processes, thus, contributing to achieving a stable cell discharge plateau at about 1.37 V. Interestingly, the low redox potential of the Mn/Mn 2+ redox couple vs. standard hydrogen electrode (i.e., −1.19 V) enables the production of aqueous manganese metal cells with operational voltages higher than their zinc metal counterparts.
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