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Highly Stable Carbon-Free Cathodes for Li-Air Batteries with Aqueous Alkaline Electrolyte: Electrochemical and Structural Investigations

Abstract

The operation of a secondary Li-air battery requires to run the battery in oxygen reduction reaction (ORR) as well as in oxygen evolution reaction (OER). OER represents the charge reaction and requires a sufficient catalyst for oxygen evolution. Currently carbon materials are widely used in cathodes of aqueous alkaline Li-air batteries due to their high electronic conductivity, stability, relatively low costs and catalytic activity towards oxygen reduction reaction (ORR). However, carbon-based cathode materials are non-stable in the potential range of OER as they start to corrode at potentials higher than open circuit voltage (OCV). Corrosion leads to high degradation corresponding to successive capacity loss and ultimately destruction of the cathode. To improve long-term stability and reduce side reactions such as H2 and CO2 evolution carbon-free bifunctional cathodes for aqueous alkaline Li-air batteries are of need. In this poster we present cathodes with a combination of Ag or Ni as conductive additive and Co3O4. Those were prepared with a dry-processed and solvent-free preparation method. Electrocatalytic activity regarding both ORR and OER was investigated by cyclic voltammetry (CV) for up to 300 cycles in half-cells. In addition structural and surface characteristics of the Ag/Co3O4 were investigated by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). These combined measurements give new insights in the materials oxidation states and the stability of Ag oxides in Ag/Co3O4 cathodes throughout a complete battery cycle. Cathodes with the combination of Ag and Co3O4 show high activity for both reactions ORR and OER and a significant improvement in performance compared to both pure Ag and pure Co3O4 cathodes. Long-term tests show superior stability of the bimetal cathodes

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