Lithium carbon dioxide battery positive electrode catalyst and preparation method thereof
A carbon dioxide and battery positive electrode technology, which is applied to battery electrodes, fuel cell half-cells, secondary battery-type half-cells, circuits, etc., can solve the problems of large particle size, poor electrical conductivity, and weak electrocatalytic activity. Achieve the effect of increasing battery capacity, reducing cost, and increasing reactive area
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Embodiment 1
[0026] The preparation operation steps of the lithium carbon dioxide battery cathode catalyst with high electrochemical performance are as follows:
[0027] (1) Dissolve 105.1 mg (0.36 mmol) nickel nitrate hexahydrate and 11.65 mg (0.04 mmol) cobalt nitrate hexahydrate in 40 mL deionized water, stir for 5 minutes, add 150 mg carbon nanotubes, and ultrasonically disperse for 2 hours to obtain Suspension.
[0028] (2) Magnetically stir the suspension in a water bath at 50°C for 2 hours, slowly drop into 0.5 mol / L sodium hydroxide solution until the pH value reaches 10, transfer to room temperature and let it stand for 1 hour to obtain a black precipitated product .
[0029] (3) After the above-mentioned black precipitate was washed by centrifugation with deionized water and absolute ethanol for 5 times, it was dried at a temperature of 80 °C for 10 hours, and placed in a tube furnace for 5 o The heating rate of C / min was raised to 300 ° C, calcined in nitrogen for 2 hours, and...
Embodiment 2
[0036] The preparation operation steps of the lithium carbon dioxide battery cathode catalyst with high electrochemical performance are as follows:
[0037] (1) Dissolve 93.4 mg (0.32 mmol) nickel nitrate hexahydrate and 23.30 mg (0.08 mmol) cobalt nitrate hexahydrate in 40 mL deionized water, stir for 5 minutes, add 150 mg carbon nanotubes, and ultrasonically disperse for 2 hours to obtain Suspension.
[0038] (2) Magnetically stir the suspension in a water bath at 50°C for 2 hours, slowly drop into 0.5 mol / L sodium hydroxide solution until the pH value reaches 10, transfer to room temperature and let it stand for 1 hour to obtain a black precipitated product .
[0039] (3) After the above-mentioned black precipitate was washed by centrifugation with deionized water and absolute ethanol for 5 times, it was dried at a temperature of 80 °C for 10 hours, and placed in a tube furnace for 5 o The heating rate of C / min was raised to 300 ° C, calcined in nitrogen for 2 hours, and ...
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