C-coated Co-MOF hollow nanobelt for negative electrode material of potassium ion battery and preparation method and application
A battery negative electrode and potassium ion technology, applied in nanotechnology for materials and surface science, battery electrodes, secondary battery manufacturing, etc., can solve the problems of lithium scarcity and high cost hindering the development of LIBs, and achieve easy operation, The effect of reducing resistance and simple process
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[0035] As shown in the figure, a method for preparing a Co-MOF hollow nanobelt coated with a cathode material C for a potassium ion battery of the present invention includes the following steps:
[0036] S1. Under magnetic stirring, dissolve cobalt nitrate in methanol to obtain solution A, where the mass ratio of cobalt nitrate to methanol is (12.5-15):1;
[0037] S2. Under magnetic stirring, dissolve methylimidazole in solution A to obtain solution B, and the mass ratio of methylimidazole to cobalt nitrate is 1: (0.88-2);
[0038] S3. Stir solution B at room temperature for 24 hours to obtain product C;
[0039] S4. Centrifugal separation of product C at 10000-15000 rpm, repeated washing with deionized water and ethanol 3 times, and drying at 60-80°C for 12-24 hours to obtain precursor D;
[0040] S5. Anneal the precursor D in an argon atmosphere at a temperature of 400-600°C for 1 to 6 hours to obtain the precursor carbon-coated Co;
[0041] S6. Dissolve the precursor carbon-coated Co ...
Embodiment 1
[0052] (1) Under magnetic stirring, dissolve 291 mg of cobalt nitrate in 20 mL of methanol to obtain solution A;
[0053] (2) Under magnetic stirring, dissolve 582 mg of methyl imidazole in solution A to obtain solution B;
[0054] (3) Stir the B solution at room temperature for 24 hours to obtain product C;
[0055] (4) Centrifugal separation of C solution at 10000rpm, repeated washing with deionized water and ethanol 3 times, and drying at 60℃12 to obtain precursor D;
[0056] (5) Annealing the synthesized product D in an argon atmosphere at 400°C for 1 hour to obtain carbon-coated Co;
[0057] (6) Take the carbon-coated Co and dissolve it in 15 mL of ethanol and ultrasound for 30 minutes to obtain solution E;
[0058] (7) Weigh 0.8g PVP and fully dissolve it in 5mL DMF to obtain solution F;
[0059] (8) Under magnetic stirring, add solution E to solution F and stir for 24h at room temperature;
[0060] (9). Take 3 mL of mixed solution G with a syringe, spin it at a certain voltage and f...
Embodiment 2
[0063] ((1) Under magnetic stirring, dissolve 291 mg of cobalt nitrate in 20 mL of methanol to obtain solution A;
[0064] (2) Under magnetic stirring, dissolve 400 mg of methyl imidazole in solution A to obtain solution B;
[0065] (3) Stir the B solution at room temperature for 24 hours to obtain product C;
[0066] (4) Centrifugal separation of solution C at 10000 rpm, repeated washing with deionized water and ethanol for 3 times, and drying at 60°C for 12-24 hours to obtain precursor D;
[0067] (5) Annealing the synthesized product D in an argon atmosphere at 300°C for 3 hours to obtain carbon-coated Co;
[0068] (6) Take the carbon-coated Co and dissolve it in 15 mL of ethanol and ultrasound for 45 minutes to obtain solution E;
[0069] (7) Weigh 0.8g PVP and fully dissolve it in 5mL DMF to obtain solution F;
[0070] (8) Under magnetic stirring, add solution E to solution F and stir for 24h at room temperature;
[0071] (9). Take 3 mL of mixed solution G with a syringe, spin it at a...
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