HRTEM and neutron diffraction study of LixMo5O17: From the ribbon (x=5) structure to the rock salt (x=12) structure
Creators
- 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.2011.02.001Additional 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
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 42086065
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ELECTROCHEMISTRY; LITHIUM COMPOUNDS; LITHIUM IONS; MOLYBDENUM OXIDES; NEUTRON DIFFRACTION; TRANSMISSION ELECTRON MICROSCOPY
- Descriptors DEC
- ALKALI METAL COMPOUNDS; CHALCOGENIDES; CHARGED PARTICLES; CHEMISTRY; COHERENT SCATTERING; DIFFRACTION; ELECTRON MICROSCOPY; IONS; MICROSCOPY; MOLYBDENUM COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; REFRACTORY METAL COMPOUNDS; SCATTERING; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.