Modified carbon-free silver electrodes for the use as cathodes in lithium-air batteries with an aqueous alkaline electrolyte

被引:35
作者
Wittmaier, Dennis [1 ]
Wagner, Norbert [1 ]
Friedrich, K. Andreas [1 ]
Amin, Hatem M. A. [2 ]
Baltruschat, Helmut [2 ]
机构
[1] German Aerosp Ctr DLR, Inst Tech Thermodynam, D-70569 Stuttgart, Germany
[2] Univ Bonn, Inst Phys & Theoret Chem, D-53117 Bonn, Germany
关键词
Lithium-air battery; Oxygen reduction; Oxygen evolution; Silver electrode; Cobalt oxide electrode; Alkaline electrolyte; OXYGEN REDUCTION; POTENTIAL RANGE; BLACK ANODES; OXIDE; ELECTROCATALYST; CORROSION; HYBRID;
D O I
10.1016/j.jpowsour.2014.04.142
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Gas diffusion electrodes with silver catalysts show a high activity towards oxygen reduction reaction in alkaline media but a rather poor activity towards oxygen evolution reaction. For the use in future lithium air batteries with an aqueous alkaline electrolyte the activity of such electrodes must be improved significantly. As Co3O4 is a promising metal oxide catalyst for oxygen evolution in alkaline media, silver electrodes were modified with Co3O4. For comparison silver electrodes were also modified with IrO2. Due to the poor stability of carbon materials at high anodic potentials these gas diffusion electrodes were prepared without carbon support to improve especially the long-term stability. Gas diffusion electrodes were electrochemically investigated in an electrochemical half-cell arrangement. In addition to cyclic voltammograms electrochemical impedance spectroscopy (EIS) was carried out. SEM and XRD were used for the physical and morphological investigations. Investigations showed that silver electrodes containing 20 wt.% Co3O4 exhibited the highest performance and highest long-term stability. For comparison, rotating ring disc electrode experiments have been performed using model electrodes with thin catalyst layers, showing that the amount of hydrogen peroxide evolved is negligible. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:299 / 308
页数:10
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