Electrochemical properties of nano-sized Li4Ti5O12 powders synthesized by a sol-gel process and characterized by X-ray absorption spectroscopy

Nano-sized spinet Li4Ti5O12 powders were synthesized by a sol-gel process. The cubic spinel structure without impurity phase of the synthesized Li4Ti5O12 powders was confirmed by X-ray diffraction. The average grain size of the synthesized powders was found to be around 39 nm. In situ X-ray absorpti...

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Published inJournal of power sources Vol. 146; no. 1-2; pp. 204 - 208
Main Authors VENKATESWARLU, M, CHEN, C. H, DO, J. S, LIN, C. W, CHOU, T. C, HWANG, B. J
Format Conference Proceeding Journal Article
LanguageEnglish
Published Lausanne Elsevier Sequoia 26.08.2005
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Summary:Nano-sized spinet Li4Ti5O12 powders were synthesized by a sol-gel process. The cubic spinel structure without impurity phase of the synthesized Li4Ti5O12 powders was confirmed by X-ray diffraction. The average grain size of the synthesized powders was found to be around 39 nm. In situ X-ray absorption spectroscopy (XAS) has been performed on the Li4Ti5O12 electrode to investigate its change in the oxidation state and the local environment of the electrode during charging and discharging processes. The X-ray absorption near edge spectroscopy (XANES) analysis showed that the absorption edge energy shifts towards lower and higher energy, respectively, during discharge and charge ; processes, indicating the reversibility of the electrode is quite good. It was worthy to note that the discharging capacity and the charging capacity obtained for the nano-sized Li4Ti5O12 electrode in the potential range of 0.01-1.75 V are 255 and 242 mAh g, respectively. However, the specific charge capacity obtained in the potential range of 1.0-2.0 V is 126 mAh g-1. The spinel Li4Ti5012 electrode maintains the cubic spinet structure for repeated cycling resulting in good cyclability and the capacity retention.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0378-7753
1873-2755
DOI:10.1016/j.jpowsour.2005.03.016