Charge storage mechanism of MnO2 cathodes in Zn/MnO2 batteries using ionic liquid-based gel polymer electrolytes

Cathode reactions in Zn/MnO2 batteries using aqueous electrolytes have been usually interpreted by the reduction of Mn4+ to Mn3+ while protons and/or cations penetrate inside the cathode. However, until now, the MnO2 storage charge mechanism using a non-aqueous gel polymer electrolyte (GPE) has not...

Full description

Saved in:
Bibliographic Details
Published inElectrochemistry communications Vol. 60; pp. 190 - 194
Main Authors Tafur, Juan P., Abad, José, Román, Elisa, Fernández Romero, Antonio J.
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.11.2015
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Cathode reactions in Zn/MnO2 batteries using aqueous electrolytes have been usually interpreted by the reduction of Mn4+ to Mn3+ while protons and/or cations penetrate inside the cathode. However, until now, the MnO2 storage charge mechanism using a non-aqueous gel polymer electrolyte (GPE) has not been investigated. In this work, ionic liquid-based GPEs including BMIM Tf and ZnTf2 have been employed in Zn/MnO2 batteries. Different states of charge of MnO2 cathodes used in Zn/IL-GPE/MnO2 batteries have been analyzed by XPS and EDX techniques. XPS analysis showed that Mn4+ is reduced during the discharge process at the same time as Zn2+ cations are incorporated into the cathode. Besides, Zn2+ cations insertion is accompanied by triflate anions. [Display omitted] •MnO2 charge storage mechanism in a Zn/IL-GPE/MnO2 battery is analyzed.•XPS analysis demonstrated that Mn4+ is reduced to Mn2+ during discharging.•Zn2+ cations are incorporated into the cathode accompanied by triflate anions.•Mn2+ species are expulsed to the GPE during the discharge process.
ISSN:1388-2481
1873-1902
DOI:10.1016/j.elecom.2015.09.011