Ali Rinaldi, Olivia Wijaya, Denis Yu, Harry E Hoster (2013) How initial nucleation influences discharge capacities of Li-O2 cells 223rd ECS Meeting, Toronto, Ontario, Canada [Oral Contributions] Abstract: The Li-O2 system has been recognized as one of the candidates for next generation batteries. Several groups have reported Li-O2 cells with high capacity and good cycle stability [1-3]. However, there are also concerns about chemical and electrochemical reactions that occur during discharge and charge in different solvents and electrolytes [4-5]. In particular, the gradual formation of organic deposits as a result of the side reactions by the
reactive superoxide radical O2.- and Li2O2 with the solvents can impede the discharge and charge reactions.
The rates of both the main cathode reaction and the side reactions are influenced by composition and morphology of the cathode surface. The overall energy density of a Li-O2 cell is limited by the amount of solid Li2O2 formed at the cathode during discharge. Hence, it is important to
understand if that amount only depends on structure and composition of the permanent cathode backbone (here: carbon), or if also its own growth history is relevant. In this work, we will demonstrate that the morphology of Li2O2 layers formed on carbon cathodes at the beginning of discharge vary in roughness when grown at increasing kinetically relevant overpotentials.
Notes: [1] S. R. Younesi et al., J. Power Sources, 196, 9835 (2011).
[2] R. R. Mitchell et al., Energy Environ. Sci., 4, 2952, (2011).
[3] Z. Peng et al., Science, 337, 563, (2012).
[4] B. D. McCloskey et al., J. Phys. Chem. Lett., 2, 1161, (2011).
[5] B. D. McCloskey et al., J. Phys. Chem. Lett., 3, 3043, (2012).