溶解
双锰矿
水溶液
离子
氧化还原
材料科学
阴极
化学工程
反应机理
化学
无机化学
纳米技术
锰
氧化锰
物理化学
冶金
催化作用
有机化学
工程类
生物化学
作者
Sung Joo Kim,Daren Wu,Nahian Sadique,Calvin D. Quilty,Lijun Wu,Amy C. Marschilok,Kenneth J. Takeuchi,Esther S. Takeuchi,Yimei Zhu
出处
期刊:Small
[Wiley]
日期:2020-11-09
卷期号:16 (48)
被引量:79
标识
DOI:10.1002/smll.202005406
摘要
Abstract Aqueous Zn/α‐MnO 2 batteries have attracted immense interest owing to their high energy density, low cost, and safety, making them desirable for future large‐scale energy application. Despite these merits, the comprehensive understanding of their reaction mechanism has been elusive due to the limitations of standard bulk characterization. Here, via transmission electron microscopy, the dissolution‐mediated reaction mechanism of a Zn/α‐MnO 2 system is discovered and explored in full scope to involve reversible formation of Zn 4 SO 4 (OH) 6 · x H 2 O and “birnessite‐like” Zn‐MnO x phase upon cycling. Overall, α‐MnO 2 acts primarily as a source for cell activation through dissolution and thus is not directly involved in the Zn redox chemistry. This microscopic study offers a unique knowledge on the unconventional reaction chemistry of Zn/α‐MnO 2 batteries.
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