Elucidating the Mechanism of Oxygen Reduction for Lithium-Air Battery Applications
Author(s) -
Cormac O. Laoire,
Sanjeev Mukerjee,
K. M. Abraham,
Edward J. Plichta,
Mary A. Hendrickson
Publication year - 2009
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/jp908090s
Subject(s) - electrolyte , chemistry , electrochemistry , lithium (medication) , inorganic chemistry , alkali metal , redox , cyclic voltammetry , battery (electricity) , electrode , glassy carbon , intercalation (chemistry) , oxygen , organic chemistry , thermodynamics , medicine , power (physics) , physics , endocrinology
Unlocking the true energy capabilities of the lithium metal negative electrode in a lithium battery has until now been limited by the low capacity intercalation and conversion reactions at the positive electrodes. Abraham et al. (Abraham, K. M.; Jiang, Z. J. Electrochem. Soc. 1996, 143, 1−5) overcame this limitation by removing these electrodes and allowing lithium to react directly with oxygen in the atmosphere, forming the Li-air battery. The Li/O2 battery redox couple has a theoretical specific energy of 5200 W h/kg and represents the ultimate, environmentally friendly electrochemical power source. In this work, we report for the first time the intimate role of electrolyte, in particular the role of ion conducting salts, in determining the reversibility and kinetics of oxygen reduction in nonaqueous electrolytes designed for such applications. Such fundamental understanding of this high energy density battery is crucial to harnessing its full energy potential. The kinetics and mechanisms of O2 reductio...
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