Electrolyte Effect on the Electrochemical Performance of Mild Aqueous Zinc-Electrolytic Manganese Dioxide Batteries
Author(s) -
Huilin Pan,
Jacob F. Ellis,
Xiaolin Li,
Zimin Nie,
Hee Jung Chang,
David Reed
Publication year - 2019
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.9b09252
Subject(s) - electrolyte , cathode , pseudocapacitance , manganese , materials science , electrochemistry , aqueous solution , inorganic chemistry , zinc , energy storage , chemical engineering , diffusion , battery (electricity) , electrode , chemistry , supercapacitor , metallurgy , organic chemistry , power (physics) , physics , quantum mechanics , engineering , thermodynamics
Recently, mild aqueous rechargeable Zn-MnO 2 batteries have attracted increasing interest for energy storage due to the low cost of Zn and Mn resources, high safety, and environmental benignity. Extensive types of MnO 2 have been proposed as the cathodes in the literature, but the different reported performance and lack of a thorough understanding of reactions in MnO 2 cathodes greatly hinder the practical applications of mild aqueous Zn-MnO 2 batteries. Here, we revealed the correlation between the reaction mechanisms and the used electrolytes for the mild aqueous zinc-electrolytic manganese dioxide (EMD) batteries. In optimal Zn(TFSI) 2 -based electrolyte, the EMD cathode exhibits a mixed diffusion-controlled conversion reaction between EMD and H + and diffusion-free "pseudocapacitance"-like reactions. This mechanism enables excellent cycling stability of an EMD cathode over 5000 cycles with a capacity retention of 94.6%. This study provides a useful insight into developing reversible MnO 2 cathodes through rational control of reaction mechanisms for high performance mild aqueous Zn-MnO 2 batteries.
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