Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6661854 | Journal of Electroanalytical Chemistry | 2018 | 11 Pages |
Abstract
Discharge by a surface route at the cathode of an aprotic metal-O2 battery typically results in surface passivation by the non-conducting oxide product. This leads to low capacity and early cell death. Here we investigate the cathode discharge reaction in the potassium-O2 battery and demonstrate that discharge by a surface route is not limited to growth of thin (<10â¯nm) metal oxide layers. Electrochemical analysis and in situ Raman spectroscopy confirmed that the product of the cathode reaction is a combination of KO2 and K2O2, depending on the applied potential. Use of the low donor number solvent, acetonitrile, allows us to directly probe the surface route. Rotating ring-disk electrode, electrochemical quartz crystal microbalance and scanning electron microscope characterisations clearly demonstrate the formation of a thick >1â¯Î¼m product layer, far in excess of that possible in the related lithium-O2 battery. These results demonstrate a high-capacity surface route in a metal-O2 battery for the first time and the insights revealed here have significant implications for the design of the K-O2 battery.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Yuhui Chen, Zarko P. Jovanov, Xiangwen Gao, Jingyuan Liu, Conrad Holc, Lee R. Johnson, Peter G. Bruce,