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- (3cr) Scientific Challenges to Develop a Nonaqueous Secondary Li-Air Battery
To better understand electrolyte stability in the presence of the working electrochemical cathode reaction (i.e., Li+ + O2 + 2e- → Li2O2), quantitative Differential Electrochemical Mass Spectrometry (DEMS) was used to analyze Li-O2 cells employing various electrolytes and porous carbon paper as the cathode. In conjunction with the gas-phase DEMS analysis, electrodeposits formed during discharge were characterized using ex-situ analytical techniques. This poster will outline results which indicate that the reversibility of Li-O2 electrochemistry is strongly dependent on the choice of solvent employed in the cell.
In addition, lithium-oxygen discharge electrodeposits formed on smooth, glassy carbon electrodes were characterized by both electrochemical and surface analytical techniques. Ferrocene was used as an in-situ electrochemical redox probe to correlate cell performance with electrical passivation as a result of discharge product formation. These studies revealed that cell failure during discharge was coincident with exponentially decreasing charge transfer at the cathode surface. Ex-situ analysis of the electrodeposit using focused ion beam micromachining, combined with conductive atomic force microscopy, yielded results consistent with the in-situ findings.