Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/1874
Title: | HIGH-CAPACITY SOL−GEL SYNTHESIS OF LINIXCOYMN1−X−YO2 (0 ≤ X, Y ≤ 0.5) CATHODE MATERIAL FOR USE IN LITHIUM RECHARGEABLE BATTERIES |
Authors: | Nithya C Thirunakaran R Sivashanmugam A Kiruthika G V M Gopukumar S |
Keywords: | Lithium battery Sol–gel method Cathode material Galvanostatic cycling |
Issue Date: | 15-Oct-2009 |
Publisher: | American Chemical Society |
Abstract: | Succinic acid assisted sol−gel synthesized layered LiNixCoyMn1−x−yO2 (0 ≤ x, y ≤ 0.5) materials have been studied as cathode materials for lithium rechargeable batteries. TG/DTA studies were performed on the gel precursor and suggest the formation of a layered phase around 400 °C. The gel precursor was calcined at 850 °C and characterized by means of X-ray diffraction and FT-IR analyses and reveals that all of the synthesized materials are found to be well-crystallized with an α-NaFeO2 layered structure. The effect of Co content on the surface morphology has been examined by scanning electron microscopy, and X-ray photoelectron spectroscopy studies indicate that the oxidation states of nickel, cobalt, and manganese are +2, +3, and +4, respectively. The electrochemical galvanostatic charge/discharge cycling behavior of the synthesized layered materials has been evaluated in the voltage range of 2.7–4.8 V at C/10 and C/5 rates. LiCo0.1Ni0.4Mn0.5O2 cathode material delivered the highest average discharge capacity of ~175 mAh/g at C/10 rate over the investigated 50 cycles. |
URI: | https://pubs.acs.org/doi/abs/10.1021/jp907036a http://localhost:8080/xmlui/handle/123456789/1874 |
ISSN: | 1932-7447 |
Appears in Collections: | International Journals |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
HIGH-CAPACITY SOL−GEL SYNTHESIS OF LINIXCOYMN1−X−YO2 (0 ≤ X, Y ≤ 0.5) CATHODE MATERIAL FOR USE IN LITHIUM RECHARGEABLE BATTERIES.docx | 10.52 kB | Microsoft Word XML | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.