Published October 30, 2012 | Version v1
Journal article

Lithium storage in commercial MoS2 in different potential ranges

  • 1. Laboratory for Solid State Ionics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China)
  • 2. Institute of New Energy Material Chemistry, Nankai University, Tianjin 300371 (China)
  • 3. Beijing Key Laboratory of Environment Science and Engineering, School of Chemical Engineering and Environment, Beijing Institute of Technology, Beijing 100081 (China)
  • 4. Institute for Superconducting and Electronic Materials, University of Wollongong, Squires Way, Fairy Meadow, NSW 2519 (Australia)

Description

Transition metal sulfides are regarded as another type of high-performance anode materials following the transition metal oxides for lithium ion batteries. However, the lithium storage mechanisms of these sulfides are complicated. This work is intended to evaluate the electrochemical performances of molybdenum disulfide (MoS2) and find out its lithium storage mechanism at different lithium insertion stages. It is found that although the MoS2 shows excellent cycling stability in different voltage ranges, its structural transition is irreversible in the initial cycling. In contrast to the traditional beliefs, metallic Mo is found inert and Li2S/S is the redox couple in a deeply discharged MoS2/Li cell (0.01 V vs. Li/Li+). The metallic Mo nanoparticles are believed to be responsible for the enhanced cycling stability of the cell and act as the electronically conducting phase in the capacitive energy storage on the interfaces or grain boundaries of Mo/Li2Sx nanocomposite. In addition, the Mo/Li2S nanocomposite can be used as a cathode material for lithium–sulfur batteries.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2012.07.020

Additional details

Identifiers

DOI
10.1016/j.electacta.2012.07.020;
PII
S0013-4686(12)01136-X;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
81
Journal Page Range
p. 155-160
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.