Negative electrode material for potassium-ion battery, preparation method thereof and negative electrode sheet
A technology of negative electrode material and negative electrode sheet, which is applied in the direction of battery electrodes, secondary batteries, circuits, etc., can solve the problems of short cycle life, low specific capacity, poor rate performance, etc., achieve long cycle life, increase specific capacity, improve Effect of Magnification Performance
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2018-10-16
- Estimated Expiration
- Not applicable · inactive patent
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Abstract
Description
technical field
[0001] The invention belongs to the field of electrochemistry and battery technology, and more specifically relates to a negative electrode material for a potassium ion battery, a preparation method thereof, and a negative electrode sheet. Background technique
[0002] Energy and environment are two eternal themes involved in the sustainable development of human society. In the face of energy and environmental issues, new clean energy technologies, especially energy storage technologies, are considered to be one of the effective ways. Compared with traditional Ni-MH batteries and lead-acid batteries, alkali metal ions (Li + / Na + / K + ) batteries have higher energy density and environmental friendliness, and have broad application prospects in the field of clean energy storage. Among them, lithium-ion batteries are widely used in communication equipment, electronic equipment, electric vehicles and other fields due to their environmental friendliness, safe...
Examples
preparation example Construction
[0040] According to a second aspect of the present invention, a kind of preparation method of negative electrode material for potassium ion battery is provided, comprising the following steps:
[0041] (1) Disperse chitin powder in a mixed solution of NaOH, urea and water, wherein NaOH accounts for 6wt%-14wt% of the mixed solution, urea accounts for 2wt%-6wt% of the mixed solution, and the freezing temperature is -20°C to - Keep at 45°C for 2 hours to 6 hours, and perform several freeze-thaw cycles until a transparent first solution is obtained;
[0042] (2) Add the first solution to the mixed solution of isooctane and Span 85, wherein the mass ratio of the first solution, isooctane and Span 85 is 16:40:1, stir at -10°C-0°C 0.5 hour-2 hours, obtain the second solution;
[0043] (3) Centrifuge the second solution to obtain the carbon microsphere precursor, wash the carbon microsphere precursor several times with ethanol and water to obtain the third solution, and freeze the th...
Embodiment 1
[0054] A preparation method for a negative electrode material for a potassium ion battery, comprising the following steps:
[0055] (1) Disperse the chitin powder in a mixed solution of NaOH, urea and water, wherein NaOH accounts for 10wt% of the mixed solution, urea accounts for 4wt% of the mixed solution, the freezing temperature is -30°C, keep for 4 hours, and freeze- Thaw several cycles until a clear first solution is obtained;
[0056] (2) Add the first solution to the mixed solution of excess isooctane and a small amount of Span 85 and mix well, wherein the mass ratio of the first solution, isooctane and Span 85 is 16:40:1. Stir for 0.5 hour to obtain the second solution;
[0057] (3) Centrifuge the second solution to obtain the carbon microsphere precursor, wash the carbon microsphere precursor several times with ethanol and water to obtain the third solution, freeze-dry the third solution at -30°C for 4 hours to obtain Nitrogen-doped porous carbon nanofibers;
[005...
Embodiment 2
[0079] A preparation method for a negative electrode material for a potassium ion battery, comprising the following steps:
[0080] (1) Disperse the chitin powder in the mixed solution of NaOH, urea and water, wherein NaOH accounts for 6wt% of the mixed solution, urea accounts for 6wt% of the mixed solution, the freezing temperature is -20°C, keep for 6 hours, and freeze- Thaw several cycles until a clear first solution is obtained;
[0081] (2) Add the first solution to the mixed solution of excess isooctane and a small amount of Span 85, mix well, and stir at -5°C for 1 hour to obtain the second solution;
[0082] (3) Centrifuge the second solution to obtain the carbon microsphere precursor, wash the carbon microsphere precursor several times with ethanol and water to obtain the third solution, freeze-dry the third solution at -20°C for 6 hours to obtain Nitrogen-doped porous carbon nanofibers;
[0083](4) The nitrogen-doped porous carbon nanofibers were heat-treated for 4...