Guojie Li, Yanwei Zhao, Bin Guo, Junlong Zhang, Jingmiao Jia, Aoxuan Wang, Chuntai Liu
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At the anode, in addition to boosting the wettability of the interface between the electrolyte and aluminum electrode, the altered surface of aluminum anode can also retard side reactions. At the same time, high concentration electrolyte (5 mol L<sup>−1</sup> Al(OTF)<sub>3</sub>) with a broad electrochemical window allows the battery system to attain a specific capacity of 452 mAh g<sup>−1</sup> at 50 mA g<sup>−1</sup> and an energy density of 542 Wh kg<sup>−1</sup>, with greatly increased cycle stability. At the cathode, the mechanism investigation reveals that δ-MnO<sub>2</sub> is reduced to soluble Mn<sup>2+</sup> during the first cycle discharge, whereas Al<sub><i>x</i></sub>Mn<sub>(1−<i>x</i>)</sub>O<sub>2</sub> generates during the charging process, acting as a highly reversible active material in the succeeding cycle. 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引用次数: 0
摘要
铝基水电池因其高质量和体积比容量、高稳定性和丰富的铝储量而被认为是下一代储能系统最有前途的候选材料之一,但自腐蚀和钝化膜的副反应严重阻碍了铝电池的发展。此外,理想的匹配电解质体系和阴极工作机理还有待探索。本文采用界面改性铝阳极、高浓度电解液和层状二氧化锰阴极构建了高比能铝锰水电池。在阳极处,铝阳极表面的改变除了可以提高电解液与铝电极界面的润湿性外,还可以延缓副反应。同时,具有宽电化学窗口的高浓度电解质(5 mol L−1 Al(OTF)3)使电池系统在50 mA g−1时获得452 mAh g−1的比容量和542 Wh kg−1的能量密度,大大提高了循环稳定性。在阴极,δ-MnO2在第一次循环放电过程中被还原为可溶的Mn2+,而AlxMn(1−x)O2在充电过程中生成,在随后的循环中作为高度可逆的活性物质。这项综合研究为铝基储能装置的发展铺平了道路。
Architecting a High Specific Energy Aqueous Aluminum–Manganese Battery
Aluminum-based aqueous batteries are considered one of the most promising candidates for the upcoming generation energy storage systems owing to their high mass and volume-specific capacity, high stability, and abundant reserves of Al. But the side reactions of self-corrosion and passive film severely impede the advancement of aluminum batteries. Besides, the ideal matched electrolyte system and cathode working mechanism still need to be explored. Herein, a high specific energy aqueous aluminum–manganese battery is constructed by interfacial modified aluminum anode, high concentration electrolyte and layered manganese dioxide cathode. At the anode, in addition to boosting the wettability of the interface between the electrolyte and aluminum electrode, the altered surface of aluminum anode can also retard side reactions. At the same time, high concentration electrolyte (5 mol L−1 Al(OTF)3) with a broad electrochemical window allows the battery system to attain a specific capacity of 452 mAh g−1 at 50 mA g−1 and an energy density of 542 Wh kg−1, with greatly increased cycle stability. At the cathode, the mechanism investigation reveals that δ-MnO2 is reduced to soluble Mn2+ during the first cycle discharge, whereas AlxMn(1−x)O2 generates during the charging process, acting as a highly reversible active material in the succeeding cycle. This comprehensive study paves the way for the development of aluminum-based energy storage devices.