Published August 25, 2003 | Version v1
Journal article

Synthesis of spinel LiMn2O4 powders for lithium ion battery by mechanical alloying of Li2O2 and Mn2O3

Description

Using the oxides of Li2O2 and Mn2O3 as starting materials, the spinel LiMn2O4 for lithium rechargeable batteries was directly synthesized by optimized mechanical alloying (MA). The prepared powders had low crystallinity, increased surface area and aggregates of particles smaller than 1 μm. To obtain well-crystallized pure spinel phase at lower temperature, the effects of subsequent firing temperature, times and the initial mixed molar ratio of Li/Mn on the synthesized phase were investigated and compared with the case of sample prepared by the conventional solid-state reaction. On firing at 700 deg. C for only 2 h of mechanically alloyed sample with a initial molar ratio of Li/Mn=0.55, a well-crystallized pure spinel phase was obtained, which exhibited the best electrochemical cycling performance. In contrast, the pure spinel without retained Mn2O3 could not be obtained by the solid-state reaction under the same firing conditions. The maximum discharge capacity of the sample by MA and firing at 700 deg. C was 125 mAh/g, and the capacity retention after 30 cycles was ∼95%

Additional details

Identifiers

DOI
10.1016/S0925-8388;
PII
S0925838803000665;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
358
Journal Issue
1-2
Journal Page Range
p. 294-301
ISSN
0925-8388
CODEN
JALCEU

INIS

Country of Publication
Netherlands
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
37045919
Subject category
S36: MATERIALS SCIENCE;
Descriptors DEI
ELECTROCHEMICAL CELLS; ELECTRODES; LITHIUM IONS; LITHIUM OXIDES; MANGANESE OXIDES; SPINELS; SYNTHESIS
Descriptors DEC
ALKALI METAL COMPOUNDS; CHALCOGENIDES; CHARGED PARTICLES; IONS; LITHIUM COMPOUNDS; MANGANESE COMPOUNDS; MINERALS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; TRANSITION ELEMENT COMPOUNDS

Optional Information

Copyright
Copyright (c) 2003 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.