Published April 2011 | Version v1
Journal article

HRTEM and neutron diffraction study of LixMo5O17: From the ribbon (x=5) structure to the rock salt (x=12) structure

  • 1. Laboratoire CRISMAT, CNRS ENSICAEN, Universite Caen, 6 bd Marechal Juin, 14050 Caen (France)
  • 2. PSI Laboratoire, Swiss Light Source, CH-5232 Villigen (Switzerland)
  • 3. EMAT, University of Antwerpen, Groenenborgerlaan 171, B2020 Antwerpen (Belgium)

Description

Structure determination of the fully intercalated phase Li12Mo5O17 and of the deintercalated oxide Li5Mo5O17 has been carried out by electron microscopy and neutron powder diffraction. The reversible topotactic transformation between the ordered rock salt structure of the former and the ribbon structure of the latter (closely related to that of Li4Mo5O17) is explained on the following basis: both structures can be described as strips built up as an assembly of infinite ribbons of MoO6 octahedra that are five octahedra thick, and that differ by slight displacements of the octahedral ribbons. We show that the electrochemical behavior of the LixMo5O17 system is based on two sorts of Li+ sites; those that are located within the strips between the ribbons, and those that are located at the border of the strips. The high rate of Li intercalation in this oxide and its reversibility are discussed in terms of its peculiar structure. -- Graphical abstract: Structure determination of the fully intercalated phase Li12Mo5O17 and of the deintercalated oxide Li5Mo5O17 has been carried out by electron microscopy and neutron powder diffraction. The reversible topotactic transformation between the ordered rock salt structure of the former and the ribbon structure of the latter is explained on the following basis: both structures can be described as strips built up as an assembly of infinite ribbons of MoO6 octahedra that are five octahedra thick, and that differ by slight displacements of the octahedral ribbons. We show that the electrochemical behavior of the LixMo5O17 system is based on two sorts of Li+ sites; those that are located within the strips between the ribbons, and those that are located at the border of the strips. The high rate of Li intercalation in this oxide and its reversibility are discussed in terms of its peculiar structure. Research highlights: → Electron microscopy and neutron powder diffraction structure determination → We have explained the reversible topotactic transformation between an ordered rock salt structure and a ribbon structure → We show that the electrochemical behavior of the LixMo5O17 system is based on two sorts of Li+ sites → The high rate of Li intercalation in this oxide and its reversibility are discussed in terms of its peculiar structure.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jssc.2011.02.001

Additional details

Identifiers

DOI
10.1016/j.jssc.2011.02.001;
PII
S0022-4596(11)00055-7;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
184
Journal Issue
4
Journal Page Range
p. 790-796
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

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