Issue 7, 2019

In Operando analysis of the charge storage mechanism in a conversion ZnCo2O4 anode and the application in flexible Li-ion batteries

Abstract

As a conversion-type electrode material, ZnCo2O4 (ZCO) is intensively researched due to its attractive high specific capacity. Much effort to study ZCO supported on a conductive matrix has been successful to overcome the inherent drawbacks of low conductivity and dramatic volume variation during the (de)lithiation process. Despite many reported studies, the lithiation storage mechanism in the ZCO electrode is not yet clearly elucidated. In this work, in operando synchrotron radiation diffraction and in operando X-ray absorption spectroscopy are used to study the lithium storage mechanism in the ZCO material. The initial conversion process of ZnCo2O4, involving multiple reactions based on intercalation, conversion and alloying is deeply elucidated. During the 1st lithiation intermediate phases such as LiCo2O3, CoO and ZnO are formed. On the other hand, upon delithiation, the conversion to ZnO and CoO (and not to the pristine ZnCo2O4) occurs. This is different from the previous conclusion, which claims that Co3O4 forms after the initial delithiation. Furthermore, a binder-free ZnCo2O4/carbon cloth composite electrode is also prepared, which exhibits higher rate performance and capacity retention, compared to the bare ZCO electrode.

Graphical abstract: In Operando analysis of the charge storage mechanism in a conversion ZnCo2O4 anode and the application in flexible Li-ion batteries

Supplementary files

Article information

Article type
Research Article
Submitted
29 Mar 2019
Accepted
27 May 2019
First published
28 May 2019
This article is Open Access
Creative Commons BY license

Inorg. Chem. Front., 2019,6, 1861-1872

In Operando analysis of the charge storage mechanism in a conversion ZnCo2O4 anode and the application in flexible Li-ion batteries

Z. Zhao, G. Tian, V. Trouillet, L. Zhu, J. Zhu, A. Missiul, E. Welter and S. Dsoke, Inorg. Chem. Front., 2019, 6, 1861 DOI: 10.1039/C9QI00356H

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