While lithium-oxygen batteries have a high theoretical specific energy, the practical discharge capacity is much lower due to the passivation of the solid discharge product, LiO, on the electrode surface. Herein, we studied and quantified the deposition and dissolution kinetics of LiO using an electrochemical quartz crystal microbalance (EQCM). It is found that the orientation of the electrode greatly influences the formation path and deposition amount of LiO. We identified two distinct dissolution modes: surface dissolution and bulk fragmentation, with the latter 100 times faster than the former. By revealing the underlying factors affecting dissolution, 80% of LiO can dissolve within 3 minutes when a desorption potential of 2.9 V is applied. Consequently, we designed an intermittent-desorption discharge strategy, which increased the discharge capacity by an order of magnitude. This work shows that high practical specific energy of Li-O batteries can be achieved once problems of LiO dissolution are addressed.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11621826 | PMC |
http://dx.doi.org/10.1039/d4sc05911e | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!