Published October 30, 2011 | Version v1
Journal article

The cycle performance and capacity fading mechanism of a LiV3O8 thin-film electrode with a mixed amorphous-nanocrystalline microstructure

  • 1. Guangzhou Research Institute of Non-ferrous Metals, Guangzhou 510640 (China)
  • 2. School of Materials Science and Engineering, South China University of Technology, Guangzhou 510640 (China)

Description

Highlights: → The mixed amorphous-nanocrystalline microstructure LiV3O8 thin film underwent a slow degradation process during prolonged cycling. → This paper reveals the capacity fading mechanism for LiV3O8 film electrode. The composition of surface layer has been confirmed by XRD and TEM. → This research gives evaluable improvement proposal for further modifying LiV3O8 film electrode materials. - Abstract: The electrochemical behavior related to cycle performance and capacity fading for LiV3O8 thin-film positive electrodes has been investigated. These electrodes experience a slight capacity loss over an initial 200 cycles, and the capacity decreases rapidly upon further cycling. This two-stage capacity fading is related to the growth of a surface layer and exfoliation of active materials, which occurs at different stages of the cycling period. The growth of the surface layer is a major reason for the increased impedance. However, it can prevent the dissolution of active materials and retard further electrode degradation, which leads to the gentle decline in capacity over the initial 200 cycles. In the later cycling period, the exfoliation of active materials causes poor electronic contacts in the film and results in severe capacity fading.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2011.08.007

Additional details

Identifiers

DOI
10.1016/j.electacta.2011.08.007;
PII
S0013-4686(11)01204-7;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
56
Journal Issue
25
Journal Page Range
p. 9329-9336
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.