Improving the stability of the cathode interface is one of the critical issues for the development of high-performance Li/O2 batteries. The most critical feature to address is the development of electrolytes that mitigate side reactions that bring about cathode passivation. It is well known that superoxide anion (O2-) formed during O2 reduction plays a critical role. Here, we propose the scanning electrochemical microscopy (SECM) as analytical tool to screen the electrolyte of Li/O2 batteries. We demonstrate that by SECM it is possible to evaluate the stability of O2 - and of the cathode to the passivation process occurring during the oxygen redox reaction. Specifically, we report about a study carried out at glassy carbon electrode in 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (PYR14TFSI) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), and tetraethylene glycol dimethyl ether with LiTFSI, the latter ranging from salt insolvent to solvent-in-salt region.
Ruggeri, I., Arbizzani, C., Rapino, S., Soavi, F. (2019). Oxygen Redox Reaction in Ionic Liquid and Ionic Liquid-like Based Electrolytes: A Scanning Electrochemical Microscopy Study. THE JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 10, 3333-3338 [10.1021/acs.jpclett.9b00774].
Oxygen Redox Reaction in Ionic Liquid and Ionic Liquid-like Based Electrolytes: A Scanning Electrochemical Microscopy Study
Ruggeri, Irene;Arbizzani, Catia;Rapino, Stefania
;Soavi, Francesca
2019
Abstract
Improving the stability of the cathode interface is one of the critical issues for the development of high-performance Li/O2 batteries. The most critical feature to address is the development of electrolytes that mitigate side reactions that bring about cathode passivation. It is well known that superoxide anion (O2-) formed during O2 reduction plays a critical role. Here, we propose the scanning electrochemical microscopy (SECM) as analytical tool to screen the electrolyte of Li/O2 batteries. We demonstrate that by SECM it is possible to evaluate the stability of O2 - and of the cathode to the passivation process occurring during the oxygen redox reaction. Specifically, we report about a study carried out at glassy carbon electrode in 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (PYR14TFSI) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), and tetraethylene glycol dimethyl ether with LiTFSI, the latter ranging from salt insolvent to solvent-in-salt region.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.