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Effect of Vinylethylene Carbonate and Fluoroethylene Carbonate Electrolyte Additives on the Performance of Lithia-Based Cathodes
Author(s) -
Si Yeol Lee,
Yong Joon Park
Publication year - 2020
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b03932
Subject(s) - overpotential , electrolyte , cathode , electrochemistry , x ray photoelectron spectroscopy , carbon fibers , chemical engineering , carbonate , dimethyl carbonate , inorganic chemistry , materials science , chemistry , catalysis , electrode , composite material , organic chemistry , metallurgy , composite number , engineering
Nanolithia-based materials are promising lithium-ion battery cathodes owing to their high capacity, low overpotential, and stable cyclic performance. Their properties are highly dependent on the structure and composition of the catalysts, which play a role in activating the lithia to participate in the electrochemical redox reaction. However, the use of electrolyte additives can be an efficient approach to improve properties of the lithia-based cathodes. In this work, vinylethylene carbonate (VEC) and fluoroethylene carbonate (FEC) were introduced as electrolyte additives in cells containing lithia-based cathode (lithia/(Ir, Li 2 IrO 3 ) nanocomposite). The use of additives enhanced the electrochemical performance of the lithia-based cathodes, including the rate capability and cyclic performance. Especially, their available capacity increased without modifying the cathodes. Results of X-ray photoelectron spectroscopy (XPS) analysis confirmed that the additives form interface layers at the cathode surface, which contain Li 2 CO 3 , more carbon reactants, and more LiF than the interface layer formed with the pristine electrolyte. The Li 2 CO 3 and carbon reactants may improve rate capability by facilitating Li + transport, and LiF may stabilize the Li 2 O 2 (and/or LiO 2 ) produced by the oxygen redox reaction with lithia. Therefore, the additive-enhanced electrochemical performance of the cell is attributed to the effects of the interface layer derived from additive decomposition during cycling.

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