Lithium secondary battery using potassium-beta-ferrite as a new cathode active material

Citation
S. Ito et al., Lithium secondary battery using potassium-beta-ferrite as a new cathode active material, SOL ST ION, 115, 1998, pp. 17-21
Citations number
11
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
SOLID STATE IONICS
ISSN journal
01672738 → ACNP
Volume
115
Year of publication
1998
Pages
17 - 21
Database
ISI
SICI code
0167-2738(199812)115:<17:LSBUPA>2.0.ZU;2-R
Abstract
The possibility of K+-beta-ferrite as a cathode active material for lithium secondary battery was investigated. Discharge-charge characteristics based on the lithium insertion and extraction of K+-beta-ferrite have been studi ed by constructing an electrochemical cell Li/1 M LiClO4 PC/K1.33Fe11O17 (K +-beta-ferrite). The cyclic voltammograms for K+-beta-ferrite were unchange d after 10 cycles of operation. The OCV (open circuit voltage) before disch arge was 3.2 V vs. Li/Li+. The discharge potential maintained 2.3 V vs. Li/ Li+ up to ca. 200 mAh/g at 60 degrees C under a constant current density of 0.1 mA/cm(2). According to the chemical analysis, K+-beta-ferrite at each discharge step certainly contained lithium, in agreement with the lithium c ontent calculated by current integration. Lithium content y in K1+xLiyFe11O 17 was increased up to 11. After discharge, the spinel blocks were disorder ed, whereas the layer structure still remained in the XRD pattern. Lithium ions seem to mainly enter into gamma-Fe2O3 layers (spinel blocks) of K+-bet a-ferrite, because alkali layers could practically contain only 1.5 alkali ions for Fe11O17. The cell voltage in charge increased up to 4.5 V vs. Li/L i+ at 25 degrees C. The potential during charge was lowered to 3.7 V by rai sing the temperature to 60 degrees C. The XRD pattern of the cathode materi al at every step of charge was similar to that at 200 mAh/g of discharge. D egradation of discharge-charge characteristics was not observed after 10 cy cles of operation. (C) 1998 Elsevier Science B.V. All rights reserved.