Constructing a high-performance cathode for aqueous zinc ion batteries via understanding the energy storage mechanism of MnO

被引:0
|
作者
Yan, Xue-Min [1 ]
Li, Hong [1 ]
Zhang, Bing-Ling [1 ]
Chen, Bo-Hong [2 ]
Xiao, Wei [1 ]
机构
[1] Yangtze Univ, Coll Chem & Environm Engn, Jingzhou 434023, Peoples R China
[2] Jiangxi Acad Sci, Inst Energy Res, Nanchang 330096, Peoples R China
基金
中国国家自然科学基金;
关键词
MnO-based cathode; Phase diagram; In-situ X-ray diffraction (XRD); Density functional theory (DFT); Energy storage behavior; OXIDATION;
D O I
10.1007/s12598-024-02938-9
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
MnO, a potential cathode for aqueous zinc ion batteries (AZIBs), has received extensive attention. Nevertheless, the hazy energy storage mechanism and sluggish Zn2+ kinetics pose a significant impediment to its future commercialization. In light of this, the electrochemical activation processes and reaction mechanism of pure MnO were investigated. Combining the Pourbaix diagram and phase diagram of Zn-Mn-O with experiment results, the essential energy storage behavior of MnO cathode can be explained as follows: (1) Zn2+ insertion/extraction into ZnMn2O4 derived from MnO-based active material, and (2) Zn2+ insertion/extraction into ZnMn2O4 (originated from the transition of Mn2+ -> Zn2Mn3O8 -> ZnMn2O4 in the electrolyte). To further ulteriorly enhance the electrochemistry performance of MnO, N-doped carbon fiber surrounding MnO nanoparticles was constructed, which can provide a conductive matrix with a high specific surface area preventing the undue stack of as-formed ZnMn2O4. Additionally, it creates a conductive highway for Zn2+ penetration through the electrode/electrolyte interphase, thanks to the electron-rich N that facilitate the reduction of the desolvation penalty. Thus, the results from this study provide a new angle for designing high-performance MnO-based cathodes for AZIBs.
引用
收藏
页码:218 / 229
页数:12
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