JOURNAL ARTICLE

Implications of CO<sub>2</sub> Contamination in Rechargeable\nNonaqueous Li–O<sub>2</sub> Batteries

S. R. Gowda (1292022)A. Brunet (1292016)G. M. Wallraff (1292019)B. D. McCloskey (1277835)

Year: 2015 Journal:   OPAL (Open@LaTrobe) (La Trobe University)   Publisher: La Trobe University

Abstract

In this Letter, the effect of CO<sub>2</sub> contamination\non nonaqueous\nLi–O<sub>2</sub> battery rechargeability is explored. Although\nCO<sub>2</sub> contamination was found to increase the cell’s\ndischarge capacity, it also spontaneously reacts with Li<sub>2</sub>O<sub>2</sub> (the primary discharge product of a nonaqueous Li–O<sub>2</sub> battery) to form Li<sub>2</sub>CO<sub>3</sub>. CO<sub>2</sub> evolution from Li<sub>2</sub>CO<sub>3</sub> during battery charging\nwas found to occur only at very high potentials (>4 V) compared\nto\nO<sub>2</sub> evolution from Li<sub>2</sub>O<sub>2</sub> (∼3–3.5\nV), and as a result, the presence of CO<sub>2</sub> during discharge\ndramatically reduced the voltaic efficiency of the discharge–charge\ncycle. These results emphasize the importance of not only completely\nremoving CO<sub>2</sub> from air fed to a Li-air battery, but also\ndeveloping stable cathodes and electrolytes that will not decompose\nduring battery operation to form carbonate deposits.

Keywords:
Battery (electricity) Contamination Electrolyte Cathode Carbonate Alkaline battery Organic radical battery

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