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Cited 158 time in webofscience Cited 159 time in scopus
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Effect of Residual Lithium Compounds on Layer Ni-Rich Li[Ni0.7Mn0.3]O-2

Authors
Cho, Dae-HyunJo, Chang-HeumCho, WoosukKim, Young-JunYashiro, HitoshiSun, Yang KookMyung, Seung-Taek
Issue Date
Apr-2014
Publisher
ELECTROCHEMICAL SOC INC
Citation
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, v.161, no.6, pp.A920 - A926
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume
161
Number
6
Start Page
A920
End Page
A926
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/25904
DOI
10.1149/2.042406jes
ISSN
0013-4651
Abstract
In order to confirm reasons that deteriorate cathode performances, Ni-rich Li[Ni0.7Mn0.3]O-2 is modified by lithium isopropoxide to artificially provide lithium excess environment by forming Li2O on the surface of active materials. X-ray diffraction patterns indicate that the lithium oxide coating does not affect structural change comparing to the bare material. Scanning electron microscopy and transmission electron microscopy data show the presence of coating layers on the surface of Li[Ni0.7Mn0.3]O-2. Electrochemical tests demonstrate that the Li2O-coated Li[Ni0.7Mn0.3]O-2 exhibits a greater irreversible capacity with a small capacity because of the presence of insulating layers composed of lithium compounds on the active materials since these layers delay facile Li+ diffusion. Also, the Li2O layer forms byproducts such as Li2CO3, LiOH, and LiF, as are proved by X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry. The presence of residual lithium tends to bond with hydrocarbons induced from decomposition of electrolytic salt during electrochemical reactions. And the reaction, accelerated by the decomposition of electrolytic salt that produces the byproducts, causes the formation of passive layers on the surface of active material. As a result, the new layers consequently impede diffusion of lithium ions that deteriorate electrochemical properties.
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