An Electrochemical Impedance Spectroscopy Study on the Effects of the Surface- and Solution-Based Mechanisms in Li-O-2 Cells

作者：Knudsen Kristian B; Vegge Tejs; McCloskey Bryan D^*; Hjelm Johan^*

来源：Journal of the Electrochemical Society, 2016, 163(9): A2065-A2071.

DOI：10.1149/2.1111609jes

The maximum discharge capacity in non-aqueous Li-O-2 batteries has been limited to a fraction of its theoretical value, largely due to a conformal deposition of Li2O2 on the cathode surface. However, it has recently been established that additives that increase the shielding of either O-2(-) or Li+ will activate the formation of toroidal shaped Li2O2, thereby dramatically increasing cell capacity. Here we apply porous electrode theory to electrochemical impedance measured at the Li-O-2 cathode to investigate changes in the surface-and ionic resistance within the pores under conditions where either the surface-mechanism or the solution-mechanism is favored. Our experimental observations show that (i) an additional charge transfer process is observed in the impedance spectrum where the solution-based mechanism is favored; (ii) that the changes in the ionic resistance in the cathode during discharge (related to Li2O2 build up) is much greater in cells where the solution-based mechanism is activated and can qualitatively determine the extent of discharge product deposited within the pores of the cathode versus the deposition extent at the electrode/electrolyte interface; and (iii) that the observed "sudden-death" during discharge is a consequence of the increasing charge transfer resistance regardless of whether Li2O2 forms predominantly through either the surface-or solution-based mechanism.

• 出版日期2016