Implications of CO2 Contamination in Rechargeable Nonaqueous Li-O2 Batteries
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作者:
Gowda, S. R.
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IBM Corp, Almaden Res Ctr, San Jose, CA 95120 USAIBM Corp, Almaden Res Ctr, San Jose, CA 95120 USA
Gowda, S. R.
[1
]
Brunet, A.
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IBM Corp, Almaden Res Ctr, San Jose, CA 95120 USA
Minatec, Grenoble INP, Phelma, F-38016 Grenoble 1, FranceIBM Corp, Almaden Res Ctr, San Jose, CA 95120 USA
Brunet, A.
[1
,2
]
Wallraff, G. M.
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IBM Corp, Almaden Res Ctr, San Jose, CA 95120 USAIBM Corp, Almaden Res Ctr, San Jose, CA 95120 USA
Wallraff, G. M.
[1
]
McCloskey, B. D.
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IBM Corp, Almaden Res Ctr, San Jose, CA 95120 USAIBM Corp, Almaden Res Ctr, San Jose, CA 95120 USA
McCloskey, B. D.
[1
]
机构:
[1] IBM Corp, Almaden Res Ctr, San Jose, CA 95120 USA
[2] Minatec, Grenoble INP, Phelma, F-38016 Grenoble 1, France
In this Letter, the effect of CO2 contamination on nonaqueous Li-O-2 battery rechargeability is explored. Although CO2 contamination was found to increase the cell's discharge capacity, it also spontaneously reacts with Li2O2 (the primary discharge product of a nonaqueous Li-O-2 battery) to form Li2CO3. CO2 evolution from Li2CO3 during battery charging was found to occur only at very high potentials (>4 V) compared to O-2 evolution from Li2O2 (similar to 3-3.5 V), and as a result, the presence of CO2 during discharge dramatically reduced the voltaic efficiency of the discharge-charge cycle. These results emphasize the importance of not only completely removing CO2 from air fed to a Li-air battery, but also developing stable cathodes and electrolytes that will not decompose during battery operation to form carbonate deposits.