Electrode material for lithium-air battery and preparation method of electrode material
An electrode material, air battery technology, applied in the direction of battery electrodes, circuits, electrical components, etc., can solve the problem of increasing battery cost, achieve the effect of reducing battery cost and improving utilization rate
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[0031] Example 1
[0032] Accurately weigh 200 mg of KB600 carbon powder, add 100 g of deionized water and stir until it is completely dispersed, and then adjust the pH of the suspension to 10 with a 0.1M aqueous sodium hydroxide solution. To the above reaction system, add 10ml KMnO with a concentration of 0.1M 4 And 1ml of 0.1M H 2 PtCl 6 The mixed solution, stir and mix well. Condensate and reflux in an oil bath at 60°C for 5 hours. After washing by suction, vacuum drying at 80°C for 24 hours, heat treatment at 350°C for 4 hours to obtain KB600-supported manganese platinum oxide compound.
[0033] Electrode material and PTFE (mass ratio 8:1), stir in ethanol, ultrasonically oscillate and mix uniformly to obtain a paste mixture. The electrode pancake is obtained by roller pressing and punched into 2cm 2 The wafer is cold pressed with the nickel mesh and dried to prepare the electrode.
[0034] Using the 2016 button battery case as the battery package, place the lithium sheet, the e...
Example Embodiment
[0037] Example 2
[0038] Accurately weigh 300 mg of XC-72 carbon powder, add 100 g of deionized water and stir until it is completely dispersed, and then adjust the pH of the suspension to 5 with a 0.1M aqueous hydrochloric acid solution. To the above reaction system, add 5ml KMnO with a concentration of 0.1M 4 And 2ml FeCl with a concentration of 0.1M 3 The mixed solution, stir and mix well. Condensate and reflux in an oil bath at 60°C for 5 hours. After washing by suction, vacuum dry at 80°C for 24 hours, and heat the sample at 300°C for 3 hours to obtain XC-72-supported manganese iron oxide compound.
[0039] The electrode was prepared by the method of Example 1, and the battery was assembled for performance evaluation.
Example Embodiment
[0040] Example 3
[0041] Accurately weigh 300 mg of carbon nanotubes, add 100 g of deionized water and stir until they are completely dispersed, and then adjust the pH of the suspension to 6 with a 0.1M aqueous hydrochloric acid solution. To the above reaction system, add 6ml KMnO with a concentration of 0.1M 4 And 2ml of 0.1M Co(NO 3 ) 2 The mixed solution, stir and mix well. The reaction was carried out for 5 hours in an ultrasonic environment, and the reaction temperature was constant at 30°C. After washing by suction, vacuum drying at 80°C for 24 hours, and heat treatment of the sample at 350°C for 3 hours to obtain manganese-cobalt-oxygen compounds supported by carbon nanotubes.
[0042] The electrode was prepared by the method of Example 1, and the battery was assembled for performance evaluation.
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