Journal
MATERIALS RESEARCH BULLETIN
Volume 47, Issue 1, Pages 79-84Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.materresbull.2011.09.024
Keywords
Layered coumpounds; Intercalation reactions; Electrochemical properties; Energy storage
Categories
Funding
- Japan Society for the Promotion of Science
- Grants-in-Aid for Scientific Research [23750237, 22245035] Funding Source: KAKEN
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Layered rocksalt-type LiFeO2 particles (O3-LiFeO2) with average particle sizes of ca. 40 and 400 nm were synthesized by an ion exchange reaction from alpha-NaFeO2 precursors. X-ray diffraction (XRD) patterns and scanning electron microscopy (SEM) images confirmed the formation of nanosized O3-LiFeO2. 40-nm LiFeO2 exhibited a higher discharge capacity (115 mAh g(-1)) than 400-nm LiFeO2 (80 mAh g(-1)), and also had better rate characteristics. The downsizing effect and cation disorder between the lithium and iron layers may have improved the electrochemical activity of the LiFeO2 particles. Transmission electron microscopy (TEM) observation indicated a phase transition from O3-LiFeO2 to a cubic lattice system during the electrochemical process. The cubic lithium iron oxide exhibited stable electrochemical reactions based on the Fe2+/Fe3+ and Fe2+/Fe-0 redox couples at voltages between 4.5 and 1.0 V. The discharge capacities of 40-nm LiFeO2 were ca. 115, 210, and 390 mAh g(-1) under cutoff voltages of 4.5-2.0 V, 4.5-1.5 V. and 4.5-1.0 V. respectively. (C) 2011 Elsevier Ltd. All rights reserved.
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