Preparation method of high-capacity fluoride/porous carbon composite positive electrode material
A technology of porous carbon material and positive electrode material, which is applied in the field of preparation of high-capacity composite positive electrode material, can solve the problems of limited improvement of electrochemical performance, poor long-term cycle stability, easy particle agglomeration, etc. Excellent performance and high selectivity
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Embodiment 1
[0059] Include the following steps:
[0060] (1) 3g of anhydrous ferric fluoride (its particle size is 20 microns) and 1g of porous carbon fiber (the specific surface area of porous carbon fiber is 700m 2 / g, the average pore diameter is 5nm) placed in absolute ethanol, it was fully mixed through ultrasonic treatment for 8 hours, then filtered and dried to obtain the ferric fluoride / porous carbon composite precursor ( figure 1 , 2 );
[0061] (2) Disperse the precursor evenly and evenly at the bottom of the small beaker for one "spray-vacuum-dry" treatment, in which the amount of each spray is 2mL, and the volume ratio of water / ethanol in water is 1:1. Place in a sealed suction filter bottle with a vacuum of -0.1MPa for 5 minutes, the drying temperature during the treatment is 120°C, and the drying time is 2 hours;
[0062] (3) Place the product obtained after the "spray-vacuum-dry" treatment at 120°C for 60 hours for final dehydration treatment, and finally obtain nano-f...
Embodiment 2
[0065] The preparation method is the same as in Example 1, except that the quality of anhydrous ferric fluoride and porous carbon in the step (1) of Example 1 is changed to 2g and 2g respectively, and the phase characterization shows that the resulting product is a nano-ferric fluoride / porous carbon fiber composite material , the size of ferric fluoride is about 5nm, which is distributed on the surface and in the pores of the porous carbon fiber. .
[0066] The prepared materials were prepared according to the method in Example 1 to make a positive electrode sheet of a lithium-ion battery, and a simulated battery was assembled. Under the current density of 200mA / g, the prepared battery completed the charge and discharge test with a charge and discharge interval of 2-4.5V. The first reversible specific capacity of the battery is 210mAh / g, and the reversible specific capacity after 200 cycles is 143mAh / g.
Embodiment 3
[0068] The preparation method is the same as in Example 1, except that the quality of anhydrous ferric fluoride and porous carbon fiber in the step (1) of Example 1 is changed to 4g and 1g respectively, and the phase characterization shows that the resulting product is a nano-ferric fluoride / porous carbon fiber composite material , the size of ferric fluoride is about 5nm, which is distributed on the surface and in the pores of the porous carbon fiber.
[0069] The prepared materials were prepared according to the method in Example 1 to make a positive electrode sheet of a lithium-ion battery, and a simulated battery was assembled. Under the current density of 200mA / g, the prepared battery completes the charge and discharge test in the charge and discharge range of 2-4.5V (theoretical specific capacity at this voltage is 237mAh / g). The initial reversible specific capacity of the battery is 266mAh / g, and the reversible specific capacity after 200 cycles is 207mAh / g (relative to t...
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